Seed dormancy and germination of Ficus lundellii and tropical forest restoration

We investigated seed dormancy and germination in Ficus lundellii Standl. (Moraceae), a native species of Mexico's Los Tuxtlas tropical rain forest. In an 8-h photoperiod at an alternating diurnal (16/8 h) temperature of 20/30 degrees C, germination was essentially complete (96%) within 28 days, whereas in darkness, all seeds remained dormant. Neither potassium nitrate (0.05-0.2%) applied continuously nor gibberellic acid applied either continuously (10-200 ppm) or as a 24 hour pretreatment (2000 ppm) induced germination in the dark. Germination in the light was not reduced by a 24-h hydrochloric acid (0.1-1%) pretreatment, but it was reduced both by a 24-h pretreatment with either H(2)O(2) (0.1-5 M) or 5% HCl, or by more than 5 days of storage at 40 degrees C (4.5% seed water content). In a study with a 2-dimensional temperature gradient plate, seeds germinated fully and rapidly in the light at a constant temperature of 30 degrees C, and fully but less rapidly in the light at alternating temperatures with low amplitudes (< 12 degrees C) about the optimal constant temperature. The base, optimal and ceiling temperatures for rate of germination were estimated as 13.8, 30.1 and 41.1 degrees C, respectively. In all temperature regimes, light was essential for the germination of F. lundellii seeds.     

Acquired thermotolerance of jack pine, white spruce and black spruce seedlings

The acquired thermotolerance of first-year seedlings of jack pine (Pinus banksiana Lamb.) hardened at 36, 38, 40 or 42 degrees C for 90, 180 or 360 minutes and of black spruce (Picea mariana (Mill.) B.S.P.) hardened at 34, 36, 38 or 40 degrees C for 30, 90, 180 or 360 minutes was determined by comparison of needle damage to that of non-hardened seedlings (25 degrees C) following exposure to temperatures of 49 and 47.5 degrees C, respectively. Compared to seedlings kept at 25 degrees C, heat injury sustained from exposure to high temperatures was markedly reduced following hardening for 180 minutes at 36 and 38 degrees C in jack pine and black spruce, respectively. Increasing the exposure time at 36 degrees C in jack pine, and at 36 to 40 degrees C in black spruce, also reduced needle damage. The duration of increased thermotolerance was investigated in jack pine, black spruce and white spruce (Picea glauca (Moench) Voss) by comparing heat injury from high temperatures in non-hardened seedlings and in seedlings hardened at 38 degrees C for 180 minutes a day for either 1, 3 or 6 days. In all three species, the duration of acquired thermotolerance increased with the number of days of heat hardening. For jack pine and white spruce seedlings hardened at 38 degrees C for 6 days, increased thermotolerance persisted for at least 14 and 10 days, respectively, after the end of the hardening treatment. In contrast, the thermotolerance of black spruce seedlings hardened at 38 degrees C for 6 days remained elevated for only 4 days.     

Acclimation of loblolly pine (Pinus taeda) seedlings to high temperatures

To determine the extent to which loblolly pine seedlings (Pinus taeda L.) acclimate to high temperatures, seedlings from three provenances-southeastern Texas (mean annual temperature 20.3 degrees C), southwestern Arkansas (mean annual temperature 16.2 degrees C) and Chesapeake, Maryland (mean annual temperature 12.8 degrees C)-were grown at constant temperatures of 25, 30, 35 or 40 degrees C in growth chambers. After two months, only 14% of the seedlings in the 40 degrees C treatment survived, so the treatment was dropped from the experiment. Provenance and family differences were not significant for most measured variables. Total biomass was similar in the 25 and 30 degrees C treatments, and less in the 35 degrees C treatment. Foliage biomass was higher, and root biomass lower, in the 30 degrees C treatment compared with the 25 degrees C treatment. Net photosynthesis and dark respiration of all seedlings were measured at 25, 30 and 35 degrees C. Both net photosynthesis and dark respiration exhibited acclimation to the temperature at which the seedlings were grown. For each temperature treatment, the highest rate of net photosynthesis was measured at the growth temperature. Dark respiration rates increased with increasing measurement temperature, but the basal rate of respiration, measured at 25 degrees C, decreased from 0.617 &mgr;mol m(-2) s(-1) in the 25 degrees C treatment to 0.348 &mgr;mol m(-2) s(-1) in the 35 degrees C treatment, resulting in less carbon loss in the higher temperature treatments than if the seedlings had not acclimated to the growth conditions. Temperature acclimation, particularly of dark respiration, may explain why total biomass of seedlings grown at 30 degrees C was similar to that of seedlings grown at 25 degrees C.     

Ecophysiological characteristics of the seed of the tropical forest pioneer Urera caracasana (Urticaceae)

Urera caracasana (Jacq.) Griseb is a small, fast-growing evergreen pioneer tree which colonizes openings in the tropical rain forest of 'Los Tuxtlas', Veracruz, Mèxico. Annual seed production by 10 trees was estimated to range from 0.4 x 10(5) to 1.6 x 10(6) seeds per tree. Fifteen species of resident and migratory birds were observed to visit the plants and disperse the seeds. Most seeds imbibed in petri dishes placed on the forest floor beneath a small opening in the canopy, where the red/far-red ratio of the light was around 1.0, germinated within 2 weeks. Germination beneath the forest canopy, where the red/far-red ratio of the light was approximately 0.2, was much slower and did not exceed 40%. A minimum of 4 h daily exposure to unfiltered natural light was required for rapid germination in the forest. In the laboratory rapid germination at 25 degrees C required a minimum of 4 h white light. However, if temperature during the light period was 35 degrees C, 30 min exposure to white light daily was sufficient to induce germination. Seeds that failed to germinate when imbibed for 60-360 days in petri dishes placed on the forest floor beneath the forest canopy, germinated rapidly in the laboratory when held at 25 degrees C and exposed daily to 12 h white or red light. Seeds imbibed for 120 days or more beneath the forest canopy were also induced to germinate by 12 h daily exposure to far-red light when this was combined with a 35/25 degrees C day/night temperature regime. Seeds buried in vermiculite-filled nylon mesh bags disappeared rapidly with few remaining after 2 months. Seeds that survived remained viable and germinated when incubated in petri dishes at 25 degrees C. Initially, buried seeds required light for germination. However, after 17 months' burial, seeds germinated in darkness when transferred to the laboratory and incubated on agar at 25 degrees C.     

Temperature Relations of Germination in Acer platanoides L. Seeds

The aim of this study was to describe the effect of temperature on the germination response of Acer platanoides L. seeds and the possible influence of dormancy. Moist chilled seeds (fruits) from eight trees were germinated at eight constant temperatures from 3 to 32C for 30 days. The highest germination was obtained at temperatures below 10C and the highest rate of germination was between 22 and 28C. The critical lower temperature for germination was estimated to be -2.6C, and the critical upper temperature between 30 and 35C. Temperatures above 10-15C increasingly inhibited the germination of seeds. Some of the non-germinated seeds were able to germinate after a second chilling period, possibly as a consequence of further release of primary dormancy and an indicated secondary dormancy. Seed survival decreased with increasing temperatures above 15C. The rate of germination was correlated with the accumulated thermal time at suboptimal temperatures. In conclusion, a constant temperature of 10C is recommended for testing the germination of seeds of A . platanoides.     

Effect of seed treatment for laboratory germination of Albizia chinensis

Seeds of Albizia chinensis(Osb.) Merr. in addition to water were also treated with different treatments by incubating in ethyl alcohol, acetone, and petroleum ether at room temperature for different du...     

Target seed moisture content,chilling and priming pretreatments influence germination temperature response in Alnus glutinosa and Betula pubescens

Abstract

The response of common alder [Alnus glutinosa (L.) Gaertn.] and downy birch (Betula pubescens Ehrh.) seeds to germination temperature was examined following chilling and priming. Seeds of two seed lots of each species were subjected to combinations of chilling (4±1°C) and priming (20°C) treatments in fully imbibed (FI) state or a lower target seed moisture content (TMC) level (30% and 35% in alder and birch, respectively). After treatment, the seeds were allowed to germinate for 56 days at constant temperatures of 7.5, 10, 15, 20, 25 or 30°C. The response to temperature and pretreatment differed between species, but the effect was consistent in each seed lot within each species. In alder, the TMC seeds germinated well across the full range of temperatures, whereas there was an optimum temperature (22–23°C) for seeds given the FI pretreatment. Priming had no significant effect on the germination response of the TMC seeds in alder, but priming greatly improved germination in the FI seeds, especially at the lower germination temperatures (optimum 18–19°C). In contrast, in birch, the TMC seeds germinated better across the full temperature range, but the optimal germination temperature (15°C) was the same for all seed pretreatments. Priming improved germination in both the FI and TMC seeds in birch.     

Seed Development, Maturation and Storage Behaviour of Mimusops elengi L.

Mass maturity (end of the seed-filling phase) occurred at about 72 days after flowering (DAF) in developing seeds of Mimusops elengi, at which time seed moisture content had declined to about 55%. The onset of ability to germinate was detected at 56 DAF and seeds showed 98% germination by 84 DAF. Tolerance of desiccation to 10% moisture content was first detected at 70 DAF and was maximal by 84 DAF. Delaying collection by a further 14 days to 98 DAF, when fruits began to be shed, reduced seed viability, particularly for seeds first dried to 10% moisture content. Hence the best time for seed collection appears to be about 14 days before fruits shed. In a separate investigation with six different seed lots, desiccation below about 8–12% moisture content reduced viability (considerably in some lots). The viability of dry seeds (below about 10% moisture content) stored hermetically was reduced at cool temperatures (5 °C and below), and none survived storage at sub-zero temperatures. The results suggest that Mimusops elengi shows intermediate seed storage behaviour and that the optimal hermetic seed storage environment is about 10% moisture content at 10 °C, while short-term, moist, aerated storage at high (40%) moisture content is also feasible.     

Effects of near-lethal heat stress on bud break, heat-shock proteins and ubiquitin in dormant poplar (Populus nigra Charkowiensis x P. nigra incrassata)

We assessed the effects of near-lethal heat stress on bud break, heat-shock proteins (HSPs) and ubiquitin in hybrid poplar (Populus nigra (L.) Charkowiensis x P. nigra (L.) incrassata). Shoots, with 10-15 buds each, were collected from September to March and exposed to temperatures between 20 and 60 degrees C for 2 h. Shoots were then placed in a greenhouse at 18-22 degrees C with supplemental light and cumulative bud break was recorded over a 4-week period. Samples of bud tissues were collected during and up to 96 h after heat treatment for protein analysis. De novo synthesis of proteins was monitored by exposing excised buds to [(35)S]-methionine for 3 h before, during, or after heat treatment. Heat treatments of 40-45 degrees C resulted in both a release from endodormancy and a decrease in thermal units needed for bud break during ecodormancy. The response to near-lethal heat stress was complex and was affected by intrinsic thermal sensitivity. Heat treatments were least effective during August and became progressively more effective as endodormancy progressed. In the later stages of ecodormancy, a heat treatment of 45 degrees C either inhibited bud break or killed the buds. Although temperatures of 42.5 to 45 degrees C inhibited incorporation of [(35)S]-methionine into proteins for at least 48 h, several HSPs were synthesized in response to temperatures of 40-45 degrees C. Immunoblots indicated that one of the heat-induced proteins was immunologically related to HSP70. Increases in free and conjugated forms of ubiquitin were also observed in response to heat treatment. Production of HSPs and ubiquitin, however, was not consistently associated with the heat treatments that induced the highest percentage of bud break. The roles of heat-induced protein degradation, HSPs, and ubiquitin in overcoming dormancy by near-lethal heat stress are discussed.     

Effect of elevated temperatures on carbon dioxide exchange in Picea rubens

We examined some of the physiological reasons that may underlie past and expected future migrations of red spruce (Picea rubens Sarg.) by evaluating the effects of high temperatures on photosynthesis and respiration of trees growing on Whiteface Mountain, NY. At temperatures of 35-40 degrees C, the trees exhibited a zero or negative carbon balance. Higher temperatures resulted in cellular disorganization and death. Temperatures around 30 degrees C resulted in reduced CO(2) uptake, a condition that could decrease future reproductive output and competitive stature. We conclude that thermal intolerance explains, at least in part, the absence of red spruce at low elevations and latitudes where temperatures of >/= 30 degrees C occur. We suggest that the thermosensitivity of this species is important with respect to global climate trends and migration patterns.     

Abscisic acid and the regulation of embryo dormancy in the genus Acer

Germination of Acer pseudoplatanus L. and Acer platanoides L. seeds was increased by moist storage of the intact fruits (seed + pericarp) at 5 degrees C, but not at 17 degrees C. In both species, germinative capacity of isolated embryos (seeds with testa removed) was increased by moist storage of fruits at either 5 or 17 degrees C. Thus dormancy loss by intact seeds and excised embryos was not necessarily correlated. Loss of dormancy in isolated embryos was associated with a reduction in free abscisic acid (ABA) content. Embryos from freshly harvested fruits of A. pseudoplatanus had a higher germinative capacity and a lower free ABA content than embryos from freshly harvested fruits of A. platanoides. Morever, germinative capacity increased, and free ABA content decreased, more rapidly with length of fruit storage in A. platanoides embryos than in A. pseudoplatanus embryos.     

Rapid temperature acclimation of leaf respiration rates in Quercus alba and Quercus rubra

We conducted controlled (chamber) and natural (field) environment experiments on the acclimation of respiration in Quercus alba L. and Quercus rubra L. Three-year-old Louisiana, Indiana and Wisconsin populations of Q. alba were placed in growth chambers and exposed to alternating 5-week periods of cool (20 degrees C mean) and warm (26 degrees C mean) temperatures. We measured respiration rates on fully expanded leaves immediately before and approximately every 2 days after a switch in mean temperature. In a second chamber experiment, 3-year-old potted Q. alba seedlings were exposed to alternating warm (26 degrees C mean) and cool (16 degrees C mean) temperatures at 4-day intervals. Leaf dark respiration rates were measured on days 2, 3 and 4 after each change in temperature. In a third, field-based study, we measured leaf respiration rates in the same three sources of Q. alba and in Arkansas, Indiana and Minnesota sources of Q. rubra before and after a natural 16 degrees C change in mean daily ambient temperature. We observed rapid, significant and similar acclimation of leaf respiration rates in all populations of Q. alba and Q. rubra. Cold-origin populations were no more plastic in their acclimation responses than populations from warmer sites. All geographic sources showed lower respiration rates when measured at 24 degrees C after exposure to higher mean temperatures. Respiration rates decreased 13% with a 6 degrees C increase in mean temperature in the first chamber study, and almost 40% with a 10 degrees C increase in temperature in the second chamber study. Acclimation was rapid in all three studies, occurring after 2 days of exposure to changed temperature regimes. Acclimation was reversible when changes in ambient temperature occurred at 4-day intervals. Respiration response functions, ln(R) = ln(beta0) + beta1T, were statistically different among treatments (cool versus warm, first chamber study) and among sources in a pooled comparison. Pair-wise comparisons indicated statistically significant (P<0.05) differences in cool- versus warm-measured temperature/respiration response functions for Indiana and Wisconsin sources of Q. alba. Log-transformed base respiration rates were significantly lower during periods of higher mean temperatures. Indiana Q. alba showed a significantly higher beta1 when plants were grown at 16 degrees C than when grown at 26 degrees C. Acclimation in Q. alba was unaccompanied by changes in leaf nitrogen concentration, but was associated with a change in leaf total nonstructural carbohydrate concentration. Total nonstructural carbohydrate concentration was slightly, but statistically, lower (13.6 versus 12%, P<0.05) after a 10 degrees C increase in temperature.     

Frost hardiness of Picea rubens growing in spruce decline regions of the Appalachians

It has been proposed that pollutants predispose Picea rubens Sarg. growing in the high Appalachians to frost damage. The pattern of autumn hardening of P. rubens growing at Whiteface Mountain, NY, and Newfound Gap, NC, was monitored by detaching shoots at 1-3 weekly intervals, air freighting them to Scotland, and freeze-testing them. The temperatures that produced freezing injury from August 1986 to January 1987 were compared with minimum air temperatures recorded in those months at nearby meteorological stations over 22 previous years. There was only weak evidence that the onset or degree of frost hardening was inadequate to protect the trees from direct freezing injury (as opposed to winter desiccation). Historically, minimum air temperatures occasionally fell below the lethal temperature for a 10% kill (LT(10)), but they rarely fell below the LT(50). The trees hardened rapidly in the autumn (max. 2.2 degrees C day(-1)) to between -30 degrees C and -40 degrees C by January (LT(50)), including trees showing visible decline on Clingman's Dome, TN. Individual trees differed in hardiness by up to 10 degrees C. It is concluded that any pollutant-induced susceptibility to freezing injury is insufficient, on its own, to account for forest decline in the Appalachians.     

Germination of stratified and non-stratified seeds of red alder at two germination temperatures

Two- to four-week stratification of red alder seeds slightly increased the speed of germination but did not improve total germination under alternating warm temperatures (30°C/20°C), yet significantly improved speed and total germination under cool temperatures (15°C/5°C) that simulated early spring outdoor nursery bed conditions. Only seeds that received four-week stratification achieved complete germination at the cooler temperatures. Strong seed source variation in response to seed treatments was observed at the cool regime. The Yacolt source germinated well regardless of seed treatments, even without stratification, while five other sources needed two to four weeks of stratification to achieve above 50% germination. Possible reasons for this variation are discussed.     

Limits of tolerance to high temperatures causing direct and indirect damage to black spruce

The heat tolerance of actively growing 13-15-week-old black spruce (Picea mariana (Mill.) B.S.P.) was determined by exposing seedlings to temperatures of 40 to 60 degrees C for durations of 5 seconds to 3 hours by direct immersion in a hot water bath. Direct and indirect heat damage to needles were differentiated by assessing damage 5 minutes (direct) and 3 weeks (indirect) after exposure to high temperature. Both direct and indirect damage increased exponentially with the duration of exposure to high temperatures. However, indirect damage occurred at lower temperatures and with shorter periods of exposure than direct damage. Arrhenius plots of length of exposure versus exposure temperature revealed that the energy of activation for indirect damage was 384 kJ mol(-1), 36% higher than for direct damage. Both direct and indirect damage were less in seedlings preconditioned by a heat shock treatment (3 hours of exposure to an air temperature of 38 degrees C on each of 6 days prior to immersion in the water bath). Preconditioned seedlings withstood higher temperatures and longer durations of high temperature exposure than seedlings not preconditioned by heat shock.     

Temperature response of leaf photosynthetic capacity in seedlings from seven temperate tree species

Seedlings of seven temperate tree species (Acer pseudoplatanus L., Betula pendula Roth, Fagus sylvatica L., Fraxinus excelsior L., Juglans regia L., Quercus petraea Matt. Liebl. and Quercus robur L.) were grown in a nursery under neutral filters transmitting 45% of incident global irradiance. During the second or third year of growth, leaf photosynthetic capacity (i.e., maximal carboxylation rate, Vcmax, maximal photosynthetic electron transport rate, Jmax, and dark respiration, Rd) was estimated for five leaves from each species at five or six leaf temperatures (10, 18, 25, 32, 36 and 40 degrees C). Values of Vcmax and Jmax were obtained by fitting the equations of the Farquhar model on response curves of net CO2 assimilation (A) to sub-stomatal CO2 mole fraction (ci), at high irradiance. Primary parameters describing the kinetic properties of Rubisco (specificity factor, affinity for CO2 and for O2, and their temperature responses) were taken from published data obtained with spinach and tobacco, and were used for all species. The temperature responses of Vcmax and Jmax, which were fitted to a thermodynamic model, differed. Mean values of Vcmax and Jmax at a reference temperature of 25 degrees C were 77.3 and 139 micromol m(-2) s(-1), respectively. The activation energy was higher for Vcmax than for Jmax (mean values of 73.1 versus 57.9 kJ mol(-1)) resulting in a decrease in Jmax/Vcmax ratio with increasing temperature. The mean optimal temperature was higher for Vcmax than for Jmax (38.9 versus 35.9 degrees C). In addition, differences in these temperature responses were observed among species. Temperature optima ranged between 35.9 and above 45 degrees C for Vcmax and between 31.7 and 43.3 degrees C for Jmax, but because of data scatter and the limited range of temperatures tested (10 to 40 degrees C), there were few statistically significant differences among species. The optimal temperature for Jmax was highest in Q. robur, Q. petraea and J. regia, and lowest in A. pseudoplatanus and F. excelsior. Measurements of chlorophyll a fluorescence revealed that the critical temperature at which basal fluorescence begins to increase was close to 47 degrees C, with no difference among species. These results should improve the parameterization of photosynthesis models, and be of particular interest when adapted to heterogeneous forests comprising mixtures of species with diverse ecological requirements.     

The effect of seed pretreatment and sowing date on the nursery emergence of Sitka spruce (Picea sitchensis [Bong.] Carr.) seedlings

Sitka spruce seeds which had been: (1) untreated (U), (2) prechilled(P), or (3) prechilled and then redried and stored for 16 months(R), were sown into progressively warmer seed beds on four datesat monthly intervals from March to June. At each sowing date,samples of seed were germinated in the laboratory at optimum(20°C) and sub-optimum (10°C) temperatures. Prechillingand prechilling + redrying both increased the rate and totalamount of germination compared with untreated seed at each testtemperature. However in the nursery, the beneficial effectsof pretreating Sitka spruce seed were restricted to sowing inMarch and April when soil temperatures were sub-optimal forthe germination of untreated seeds. Pretreatment resulted inrapid seedling emergence at soil temperatures between 10°Cand 15°C, whereas untreated seed germinated slowly and seedlingemergence continued until high soil temperatures in June killedungerminated seeds. The pattern of seedling emergence from theredried seed was similar to that from the prechilled seed, exceptfor a lag in the start of seedling emergence probably due tothe extra time needed for redried seed to imbibe water in theseed beds. Thus redrying caused insignificant loss of seed performanceon the nursery. Seed sown in May and June experienced average temperatures closeto the optimum for germination of 20°C, however daily maximaregularly exceeded 35°C resulting in the cessation of seedlingemergence in all three seed treatments, and the loss of newlyemerged seedlings. Periods of warm weather from June onwardswere the main factors limiting the final number and size ofseedlings.     

Pigment composition and location in honey locust (Gleditsia triacanthos) seeds before and after desiccation

Gleditsia triacanthos L. pods were harvested at San Lorenzo del Escorial, Madrid, Spain, before and after seed desiccation. Maturing green pods, harvested from trees, contained soft light-green seeds, whereas fully mature brown pods, collected on the ground, contained hard dark-green seeds. Based on visual inspection of seeds, it was determined that the green color is located in the cotyledons and embryo of soft seeds but mainly in the seed coat of hard seeds. High performance liquid chromatographic analysis indicated that both hard and soft seeds contained the same set of photosynthetic pigments as fully developed leaves, but in different proportions. The hard and soft seeds mainly differed in their chlorophyll a to chlorophyll b ratio and in the composition of the xanthophyll cycle pool of pigments. Fluorescence at -196 degrees C revealed that the molecular organization of the pigment molecules in the seed coat of hard seeds differed from that in intact cotyledons of soft seeds and intact green leaves. The -196 degrees C fluorescence spectra also revealed the presence of a small heterogenous pool of non-photoactive protochlorophyll(ide)s, similar to those found in dark-grown tissues of gymnosperms and angiosperms.     

Chlorophyll fluorescence and CO(2) assimilation of black spruce seedlings following frost in different temperature and light conditions

Effects of artificial frosts on light-saturated photosynthesis (A(max)) and ground, maximal and variable fluorescence variables (F(o), F(m), and F(v) and F(v)/F(m)) were monitored on 1-year-old foliage of black spruce seedlings (Picea mariana (Mill.) BSP) grown at high (25 degrees C), moderate (15 degrees C) and low (5 degrees C) temperatures and moderate (240 &mgr;mol m(-2) s(-1)) and low (80 &mgr;mol m(-2) s(-1)) irradiances. Photoinhibition of 1-year-old foliage was greater in seedlings grown in moderate light than in seedlings grown in low light. Photoinhibition increased with decreasing growth chamber temperature at both irradiances. Most changes in F(v)/F(m) were caused by changes in F(v). Exposure to -4 degrees C decreased both F(v)/F(m) and A(max) compared with control values. The effect of the -4 degrees C frost treatment was greater in seedlings grown in low light than in seedlings grown in moderate light, probably because seedlings grown in moderate light were already partially photoinhibited before the frost treatment. Following -4 degrees C treatment, neither F(v)/F(m) nor A(max) recovered in seedlings grown in low light. Light-saturated photosynthesis decreased with decreasing growth chamber temperature. Light-saturated photosynthesis was more sensitive to the -3 and -4 degrees C frost treatments in seedlings grown at 25 degrees C than in seedlings grown at 15 and 5 degrees C. The A(max) of seedlings grown at 15 degrees C was sensitive only to the -4 degrees C frost treatment, whereas A(max) of seedlings grown at 5 degrees C was not sensitive to any of the frost treatments. Recovery of A(max) following frost took longer in seedlings grown at high temperatures than in seedlings grown at low temperatures. For seedlings grown at the same temperature but under different irradiances, both A(max) and F(v)/F(m) reflected damage to the photosynthetic system following a moderate frost. However, for seedlings grown at the same irradiance but different temperatures, A(max) provided a more sensitive indicator of frost damage to the photosynthetic system than F(v)/F(m) ratio.     

濒危树种极东锦鸡儿(Caragana fruticosa)种子的萌发特性

以濒危树种极东锦鸡儿成熟种子为材料,研究极东锦鸡儿种子物理性状和温度对其种子萌发及幼苗生长的影响。结果表明:极东锦鸡儿种荚结实率较低,且约有1/4种子受虫害;成熟种子含水量为6.6%,千粒重18.6 g。种子长、宽和厚存在一定变异。种子长度平均为0.42 cm,宽度平均为0.27 cm,厚度平均为0.24 cm,长宽比为0.64。种皮透水性良好。不同温度条件对种子发芽率具有极显著影响。25℃条件下种子发芽率最高,为38.33%。随着温度的升高或降低,种子发芽率降低。发芽试验的第八天是计算种子发芽势的适宜时期。不同温度条件对极东锦鸡儿幼苗高度的影响极显著,对胚根长度影响显著。25℃有利于幼苗高度和胚根长度的增加,较高温度(30℃)有利于幼苗生物量增加。