Response of Mutant Sunflower Lines to Heat Shock

The effects of heat shock (HS) (40°C for 1 h) on the level of malondialdehyde (MDA), the terminal product of lipid peroxidation, superoxide dismutase (SOD) activity, catalase activity, and total peroxidase activity (TPA) were studied in root meristems and chloroplasts of several sunflower (Helianthus annuusL.) lines that carried nuclear or plastome chlorophyll mutations. HS either lowered or did not affect the MDA level in the root meristem and in the chloroplasts from the first true leaf, as compared to the untreated plants. In both treatments, the root and leaf enzyme activities varied in the sunflower lines. In the root meristem, catalase was the most sensitive to HS, whereas, in the chloroplasts from HS-treated sunflower lines, HS activated either TPA or SOD.     

Defoliation and Regrowth in the Graminaceous Plant: The Role of Current Assimilate

Infra-red gas analysis and a quantitative radiocarbon tracertechnique were used to measure photosynthesis, and the export,distribution and utilization of current assimilate in the regrowthof leaf tissue and the growth of stem and root of partially-defoliateduniculm barley plants. After defoliation, which removed allleaf tissue above the ligule of leaf 3, the rate of photosynthesisof the remaining two older leaves fell to 90–95 per centof that of control leaves, but they exported more of their assimilatedcarbon to meristems elsewhere in the plant during the first48 h after the defoliation. The level of export from the twoolder leaves began to decline when new leaf tissue regrew fromthe shoot apex, and fell below that of the control leaves 4days after defoliation. The two older leaves supplied the assimilateused in the regrowth of new leaf tissue immediately after defoliation:previously they had exported most of their assimilate to root.There was no evidence that ‘reserves’ were mobilizedto meet the needs of regrowth at leaf meristems or, indeed,of the growth in stem and root; current photosynthesis suppliedsufficient assimilate to account for all observed growth. Ingeneral, the plants responded to defoliation with a rapid andmarked re-allocation of assimilate from root to leaf meristems,with the result that root growth was severely retarded but newleaf tissue grew at 70–100 per cent of the rate observedin control plants.     

Net CO2 output by CAM plants in the light: the role of leaf conductance

Triadimefon [1-(4-chlorophenoxy)-3,3-dimethyl-l-(l,2,4-triazol-l-yl)-2-butanone] is a triazoie fungicide which protects bean ( Phaseolus vulgaris L. cv. Spring Green) plants from heat and chilling injury. When the plants were exposed to heat shock by dipping the shoots in hot (50°C) distilled water for 2 min or exposing the plants to cold (1°C) for 8 h the primary leaves showed visual symptoms of injury 2 days after treatment and thereafter there was a progressive decline in chlorophyll and an increase in electrolyte leakage indicative of a loss of membrane integrity. There was a loss of metabolic (respiratory) activity in the root meristems when the roots were dipped in hot (48°C) water. All these symptoms of heat and chilling injury in the controls were either delayed or prevented by root application of triadimefon.     

Production and nitrogen responses of the African dwarf shrub Indigofera spinosa to defoliation and water limitation

Summary The dwarf shrub Indigofera spinosa Forsk. (Papilionacea), a native forage species of arid Northwest Kenya, was propogated from seed, grown in a controlled environment, and subjected to three treatments of defoliation and watering frequencies in a factorial experimental design. Biomass production and nitrogen accumulation in tissue components were measured to determine defoliation responses in a water-limited environment. We hypothesized that plants would maintain biomass and nitrogen flows despite removal of aboveground meristems and tissues by defoliation. Principal experimental results included a slight reduction (11%; P=0.08) of total biomass production by clipping ca. 1/3 or 2/3 of new leaves and stems and all apical meristems every month. Total aboveground production was not affected by clipping, while final root biomass was reduced 17% by the 2/3 clipping. The least water stressed plants were affected most negatively by defoliation, and the unclipped plants responded more negatively to greater water limitation. Plants achieved partial biomass compensation through alterations in shoot activity and continued allocation of photosynthate to roots. A smaller fraction of leaf production was directed to litter in clipped plants although clipping only removed the youngest tissues, suggesting that clipping increased leaf longevity. In turn, each leaf probably contributed a greater total quantity of photosynthate. Photosynthetic rates were also likely to have been increased by clipping water-stressed plants. In contrast to biomass, plants overcompensated for nitrogen lost to defoliation. Total nitrogen uptake by individual plants was stimulated by defoliation, as there was more total nitrogen in leaves and stems. Increased nitrogen uptake was achieved by clipping stimulation of total uptake per unit of root rather than of total root mass.     

PRIMORDIAL LEAF AND PHYTOHORMONE EFFECTS ON EXCISED SHOOT APICAL MERISTEMS OF COLEUS BLUMEI BENTH.

Coleus blumei Benth. apical meristems and apical meristems +1, +2, +3 primordial leaf pairs were cultured to examine phytohormone influences on development and correlative effects of developing primordial leaves on in vitro responses. The meristem with no phytohormones or low levels of IAA could not develop in vitro. At least 0.1 mg/l IAA and optimumly 1-2 mg/l IAA were required for development into complete plants. IAA from 0.1 to 3 mg/l also resulted in root development with no apparent leaf or shoot formation. Levels of IAA higher than 3 mg/l were inhibitory to development. Kinetin, as a substitute for naturally occurring cytokinins, alone (0.0003 to 3 mg/l) resulted in development of rosettes of leaves. In the presence of IAA (***1 mg/l) and kinetin (0.003 mg/l) plants, rosettes, individual leaves with roots, and roots developed from isolated meristems. Glutamine and adenine sulfate both appeared inhibitory to meristem development. With +1, +2, +3 developing primordial leaf pairs left attached to the apical dome, three pairs were required for plant formation in the absence of phytohormones. In the presence of IAA, two pairs of primordial leaves resulted in plant formation; whereas, with IAA and low levels of kinetin one pair of primordial leaves was enough. Higher levels of kinetin were inhibitory to plant development with primordial leaves present. ABA appeared to be inhibitory to development of meristems and meristems +1, +3 primordial leaves at low concentrations and resulted in death at ***1 mg/l. Developing primordial leaves appear to supply the apical meristem with a balance of phytohormones during growth. Meristem development into a plant first involved formation of leaf primordia. Establishment of a bipolar axis with root formation followed.     

Leaf Diffusive Conductance and Tap Root Cell Turgor Pressure of Sugarbeet

Abstract. The interrelationships of leaf diffusive conductance, tap root cell turgor pressure and the diameter of the tap root of sugarbeet were studied. The study was conducted on well-watered plants growing in pots under artificial light in the glasshouse. In a typical experiment, on illumination (400 μmol m⁻² s⁻¹) leaf conductance increased from 0.6 to 7.4 mm s⁻¹. Cell turgor pressure in the tap root decreased from 0.8 MPa to 0.45 MPa and the root diameter (9.0 cm) contracted by 145μm. Removal of light resulted in the reversal of each of the above parameters to their previous values. Quantitively similar results were obtained when sugar beet plants were uprooted and the response of each of the parameters was measured. The sequence of events however was different. On stimulation by light, changes in leaf diffusive conductance preceded the turgor and root diameter changes (which were simultaneous) by some 15–20min. In contrast, on uprooting the simultaneous changes in root turgor pressure and diameter preceded the changes in leaf conductance. The lag times between changes in diffusive conductance and turgor pressure in the root were between 20 and 30 min.
Tap root turgor pressure and diameter correlated strongly and permitted the calculation of an apparent whole root volumetric elastic modules (55–63 MPa). The small changes in tissue volume relative to the transpiration rate suggest that the tap root is not a significant source of transpirational water during the day.     

Carbohydrate Metabolism in Leaf Meristems of Tall Fescue : II. Relationship to Leaf Elongation Rates Modified by Nitrogen Fertilization

Our objective was to examine alterations in carbohydrate status of leaf meristems that are associated with nitrogen-induced changes in leaf elongation rates of tall fescue (Festuca arundinacea Schreb.). Dark respiration rates, concentrations of nonstructural carbohydrates, and soluble proteins were measured in leaf intercalary meristems and adjacent segments of elongating leaves. The two genotypes used differed by 43% in leaf elongation rate. Application of high nitrogen (336 kilograms per hectare) resulted in 140% higher leaf elongation rate when compared to plants receiving low nitrogen (22 kilograms per hectare). Leaf meristems of plants receiving high and low nitrogen had dark respiration rates of 5.4 and 2.9 microliters O₂ consumed per milligram structural dry weight per hour, respectively. Concentrations of soluble proteins were lower while concentrations of fructan tended to be slightly higher in leaf meristems of low-nitrogen plants when compared to high-nitrogen plants. Concentrations of reducing sugars, nonreducing sugars, and takadiastase-soluble carbohydrate of leaf meristems were not affected by nitrogen treatment. Total nonstructural carbohydrates of leaf meristems averaged 44 and 39% of dry weight for low- and high-nitrogen plants, respectively. Within the leaf meristem, approximately 74 and 34% of the pool of total nonstructural carbohydrate could be consumed per day in high- and low-nitrogen plants, respectively, assuming no carbohydrate import to the meristem occurred. Plants were able to maintain high concentrations of nonstructural carbohydrates in leaf meristems despite a 3-fold range in leaf elongation rates, suggesting that carbohydrate synthesis and transport to leaf intercalary meristems may not limit leaf growth of these genotypes.     

Phosphorus supply and the growth of frequently defoliated white clover (Trifolium repens L.) in dry soil

A previous study found that increased phosphorus (P) supply to frequently defoliated white clover plants, growing in a low-P, dry soil, alleviated water stress symptoms and increased plant recovery on rewatering. In this study we determined how these stresses influence white clover growth. Measurements were made of the leaf canopy, stolon infrastructure and root system of the white clover plants growing in a low-P soil. Treatments included the factorial combination of four levels of P supply, two defoliation frequencies and two soil water treatments. White clover growth declined markedly when P-deficient plants were exposed to frequent defoliation and dry soil conditions. Leaf area was more affected than other parameters, in that the combination of stresses reduced leaf area to 2% of maximum observed for infrequently defoliated plants growing in high-P soil, with adequate water. Increased P supply generally increased the growth of all plant parts. Frequently defoliated plants growing in dry soil produced similar or greater leaf mass and leaf area as plants from similar treatments growing in wet soil, when the P supply increased to 50 mg P kg-1 soil. Higher P rates were able to negate the effect of dry soil on these frequently defoliated plants, as a result of larger water and P uptake. Also, the frequently defoliated plants with restricted root growth did not respond to a small increase in P supply (17 mg P kg-1 soil) for the leaf growth, irrespective of whether they were growing in wet or dry soil. Infrequently defoliated plants with greater root growth, compared to frequently defoliated plants, more than doubled their leaf mass with this P treatment.     

Regeneration of whole plants from apical meristems of Pinus radiata

A methodology to regenerate whole plants of Pinus radiata from apical meristems of 3- and 7-year-old trees was developed. Meristematic domes with two or three leaf primordia were excised from surface-sterilized branch tips of field-grown plants and cultured in LP medium with half strength macronutrients (1/2 LP) and full strength micronutrients. The early growth of meristems required approximately 12 weeks, including a recovery stage during the first 2 weeks. After 8 weeks, some meristems developed abnormal phenotypes and died during the subsequent stages of development. However, healthy meristems elongated and formed shoots when they were transferred to LP medium supplemented with MS vitamins, 30 mg l^–1 casein hydrolysate, and 0.4 g l^–1 agar plus 2.85 g l^–1 Gelrite. Meristems that developed vigorous shoots were used for rooting experiments when they were 2 cm in length. Whole plants were obtained after 5 days of root induction in water-agar medium containing 8.2 M IBA and 5.4 M NAA and 1 month culture in LP medium with 10 g l^–1 sucrose. Plants regenerated from meristems were further propagated by rooting of cuttings. Of the rooted cuttings, 10% were morphologically juvenile.     

The use of anther-derived haploids in Nicotiana

Immature anthers from monosomic Nicotiana tabacum L. (“Purpurea”) plants were cultured on a chemically defined agar medium. Plantlets obtained from these anthers were transferred first to a rooting media and subsequently to soil in greenhouse pots. Six nullihaploid plant types have been isolated, two of which have been positively identified as nullihaploids C and E. Chromosome numbers (n?1=23) were verified somatically from root tip and corolla tissues and meiotically by observing PMC's at metaphase I. The chromosome number was doubled in one of the lines by culturing leaf midvein tissue on a modified anther culture media. The nullisomic chromosome number (2n?2=46) was determined in root tips, and the nullisomic condition of 23 bivalents was observed in metaphase I PMC's.     

东北山地灌木沼泽植物铜、锌分布特征及季节动态

研究了东北山地灌木沼泽主要植物--细叶沼柳、五蕊柳、丛苔草和修氏苔草中Cu、Zn分布、积累及其季节动态.结果表明:Cu含量变动范围为6～12 mg·kg-1,细叶沼柳和五蕊柳各器官Cu含量为根》枝》叶;丛苔草和修氏苔草为茎》叶》根,Cu主要积累在灌木的根系和苔草的茎叶中,灌木和苔草中Cu含量相差较小.Zn含量变动在30～250 mg·kg-1之间,细叶沼柳和五蕊柳各器官Zn含量为叶》枝》根,尤其是叶和枝中都在150 mg·kg-1以上;丛苔草和修氏苔草各器官Zn含量为根》茎》叶.Zn多积累在灌木的叶和苔草的根中,且灌木各器官Zn含量明显高于苔草.细叶沼柳和五蕊柳各器官对Zn的富集系数均大于1.45,显示出较强的Zn富集能力.4种供试植物在生长初期地上部分Cu、Zn含量较高,且随着季节变化呈波动式降低趋势,而根中则表现出生长初期和末期Cu、Zn含量较高的特点.     

Transient gene expression in vegetative shoot apical meristems of wheat after ballistic microtargeting

A method has been established that allows the targeted delivery of DNA-carrying gold particles to vegetative shoot apical meristems of cereal species. Meristems of 8- to 10-day-old seedlings of wheat ( Triticum aestivum ), rice ( Oryza sativa ) and sorghum ( Sorghum bicolor ) were manually exposed by removal of the coleoptile and the first three to four leaves. Using ballistic microtargeting, equal-sized gold particles of different diameters ranging from 1.0 to 2.0 µm were propelled to meristems by pulses of compressed nitrogen ranging from 9 to 13 MPa. When accelerated by 13 MPa, particles of 1.4 µm or larger penetrated to cells of L2 in 80% of the bombarded wheat meristems. Expression vectors containing either the gene for β-glucuronidase ( gusA ) or genes regulating the anthocyanin biosynthesis ( Bperu and C1 from maize) were delivered to wheat meristems. The level of transient gene expression was dependent on the osmotic pressure of the MS-based medium that was used to mount the explants for shooting: an increase of the sucrose concentration from 2 to 10% in the medium resulted in an increase of transient gene expression from 5 to 25% of the bombarded meristems. Although particles of 1.4 µm were efficiently delivered to L1 and L2, transient gene expression occurred predominantly in the L1 layer. In contrast, up to 10% of the bombarded meristems had expressing cells in L2 when particles of 2.0 µm were used. Ten days after bombardment, GUS-positive sectors in meristems and in leaf primordia were observed. When destructive GUS detection was omitted, between 80 and 90% of the bombarded ex-plants recovered in vitro on basal MS medium and then regenerated to fertile plants in the greenhouse.     

Effects of Kinetin on Growth of the Apical Meristem and Floral Differentiation in Chenopodium rubrum L.

Kinetin (1•10^–4 M and 1•10^–3 M) was appliedto the plumules of 6-day-old Chenopodium rubrum plants. Effectson growth, anatomical structure and organogenesis in the apicalmeristem were followed. Floral differentiation as affected bykinetin was also investigated in plants induced to flower byshort-day treatment. Kinetin increased mitotic activity in the apical meristems inboth induced and non-induced plants. The effect was most pronouncedin the peripheral and subcentral zone. An increase in nucleolussize and a higher degree of pyroninophilia in the peripheralzone was also observed, indicating a localized promotion ofRNA synthesis. A higher rate of leaf initiation and a stimulationof leaf and stem growth was subse quentiy recorded. The growthof axillary meristems and of bud primordia was promoted onlyat the lower concentration of kinetin (1•^10–4 M),in both photoperiodically-induced and non-induced plants. However,the pattern of lateral bud growth differed from that found innormal floral differentiation. In kinetintreated plants, thebud primordia are isolated from the summit of the shoot apexby a succession of rapidly growing leaves. The enhancement ofleaf growth leads to correlative inhibition of axillary budpriniordia and results, finally, in a suppression of floraldifferentiation. The inhibitory effect of kinetin on floweringwas compared with that of auxin. Inhibition of flowering occurredin both cases but is achieved in two different ways.     

The Strategy of Carbon Utilization in Uniculm Barley I. THE CHEMICAL FATE OF PHOTOSYNTHETICALLY ASSIMILATED 14C

Following exposure of the youngest mature leaf of uniculm barleyto ¹⁴CO₂, groups of plants were harvested over a 72 h periodto determine the fate of 14C in the photosynthesizing leaf andin growing leaves and roots. Initially, ¹⁴C was mainly presentin sucrose with a little in starch and charged compounds; transportout of the fed leaf was rapid and, by 7 and 24 h, 56 and 93%respectively of the ¹⁴C had been translocated about equallyto growing leaves and roots. Sucrose entering meristems wasquickly metabolized to protein and structural carbohydrate (40and 60% of the ¹⁴C in these organs at 7 and 24 h respectively),while the remainder was converted to short-term storage productsor intermediary metabolites. By the end of the first day c.35% of the 14C originally assimilated had been lost in respiration. The metabolism of the leaf appeared to be organized on a diurnalbasis, for it exported nearly all its carbon within 24 h ofassimilation. In contrast, some of the assimilate imported intogrowing leaves and, to a lesser extent, roots was not immediatelyused for growth but persisted as temporary metabolites and wassubsequently used for growth in the following days.     

Effects of temperature on oxidative stress defense systems, lipid peroxidation and lipoxygenase activity in Phalaenopsis.

Higher plants growing in natural environments experience various abiotic stresses. The aim of this study was to determine whether exposure to temperature-stress would lead to oxidative stress and whether this effect varied with different exposure periods. The thermal dependencies of the activities of protective enzymes, photosynthetic efficiency (Fv/Fm), protein, non-protein thiol (NP-SH), cysteine content, lipoxygenase (LOX) activity (EC 1.13.11.12) and malondialdehyde (MDA) content at 25-40 degrees C were determined for 4, 24 and 48 h in leaf and root segments of Phalaenopsis. The increase in MDA level and LOX activity may be due to temperature-associated oxidative damage to leaf and root segments. Temperature-stress induced not only activities of active oxygen species (AOS) scavenging enzymes but also protein, NP-SH and cysteine content in both leaf and root segments at 30 degrees C for 4 and 24 h (except for 48 h in some cases) compared to 25 degrees C-and greenhouse-grown leaf and root segments indicating that antioxidants enzymes played an important role in protecting plant from temperature-stress. However, activities of dehydroascorbate reductase (DHAR, EC 1.8.5.1), glutathione peroxidase (GPX, EC 1.11.1.9) and glutathione-S-transferase (GST, EC 2.5.1.18) in leaf and root, glutathione reductase (GR, EC 1.6.4.2) in leaf and guaiacol peroxidase (G-POD, 1.11.1.7) in root segments were induced significantly at 40 degrees C compared to 25 degrees C and greenhouse-grown plants suggesting that these enzymes play protective roles at high temperature. In contrast, activities of superoxide dismutase (SOD, EC 1.15.1.1) and monodehydroascorbate reductase (MDHAR, EC 1.6.5.4) in leaf and root, catalase (CAT, EC 1.11.1.6) in root, GR in root, and protein, cysteine, NP-SH content in both root and leaf and Fv/Fm ratio were diminished significantly at 40 degrees C compared to 25 degrees C-and greenhouse-grown plants. These indicate that these enzymes were apparently not involved in detoxification process and sensitive at higher temperature. Also, the close relation between activities of enzymes with their metabolites at 30 degrees C than 40 degrees C indicated that the antioxidants enzymes and metabolites both may play an important role in protecting cells against the temperature-stress.     

The Arabidopsis OBERON1 and OBERON2 genes encode plant homeodomain finger proteins and are required for apical meristem maintenance

Maintenance of the stem cell population located at the apical meristems is essential for repetitive organ initiation during the development of higher plants. Here, we have characterized the roles of OBERON1 (OBE1) and its paralog OBERON2 (OBE2), which encode plant homeodomain finger proteins, in the maintenance and/or establishment of the meristems in Arabidopsis. Although the obe1 and obe2 single mutants were indistinguishable from wild-type plants, the obe1 obe2 double mutant displayed premature termination of the shoot meristem, suggesting that OBE1 and OBE2 function redundantly. Further analyses revealed that OBE1 and OBE2 allow the plant cells to acquire meristematic activity via the WUSCHEL-CLAVATA pathway, which is required for the maintenance of the stem cell population, and they function parallel to the SHOOT MERISTEMLESS gene, which is required for preventing cell differentiation in the shoot meristem. In addition, obe1 obe2 mutants failed to establish the root apical meristem, lacking both the initial cells and the quiescent center. In situ hybridization revealed that expression of PLETHORA and SCARECROW, which are required for stem cell specification and maintenance in the root meristem, was lost from obe1 obe2 mutant embryos. Taken together, these data suggest that the OBE1 and OBE2 genes are functionally redundant and crucial for the maintenance and/or establishment of both the shoot and root meristems.     

Diurnal oscillatory movements of growing leaves of tobacco

The analysis of diurnal oscillatory movements of tobacco leaves was used in the diagnosis of viral infection of plants. The oscillatory helices circumscribed by a growing leaf of a healthy plant were regular, but some deviations, particularly in the transition points, were recorded. In order to make clear the cause of these irregularities of trajectory, the course of elongation of leaf petiole and blade in relation to localization and shift of zones of elongation during ontogenesis was analysed. The present analysis is similar to that described by the author's earlier experiments with pea roots. Oscillatory curves circumscribed by petiole, projected on a horizontal plane, were compared with curves circumscribed by the blade tip. The analysis of the leaves of different ages enabled us to study this process in dependence on growth rate. It was confirmed that oscillations are a result of elongation; the extent of oscillations is quantitatively dependent on the growth rate. An analysis of the zones of growth showed that in petiole the active meristems are localized near to its base while in the leaf lamina they move gradually during the ontogenesis from the apical to the basal part of the leaf blade. Active meristems of young rapidly growing leaves are localized approximately in the middle of the blade while those of old leaves were found in close proximity to the base of the lamina. The growth rate of petiole can be expressed in hundreds of mm per hour (4.8×10^?2 mm h^?1); half of this value was recorded for its apical part. The growth rate of leaf blade was found approximately ten times higher (3.2×10^?1 mm h^?1). The oscillatory movements of growing leaf consists of two integrate components: of oscillations originating in the base of the petiole and of oscillations of leaf blade the centrum of which is localized in the basal third of the blade. The arrangement of the experiments did not enable us to determine to what extent the phototropic response of leaf blade participates in leaf movements. The movements of leaves of an intact plant are evidently affected by rhythmic stem oscillations. Stem is an integral part of a system which participates in the transfer of information in plants.     

Ectopic expression of the Arabidopsis MINI ZINC FINGER1 and MIF3 genes induces shoot meristems on leaf margins

A leaf undergoes determinate growth from a primordium on flank of the shoot apical meristem. Several intrinsic pathways restrict meristematic activity in the leaf of Arabidopsis; however, other factors remain to be defined. We report here that the overexpression of MINI ZINC FINGER1 (MIF1) or MIF3 disrupted the leaf determinate growth by inducing ectopic shoot meristems on leaf margins. These ectopic meristems occurred along margins of late rosette leaves at serration sinuses in an ERECTA-dependent manner. Expression of STM was activated in these ectopic meristems but not other leaf regions. The formation of ectopic meristems was independent of the BP gene but suppressed by exogenous gibberellic acid. In addition, reduced auxin response along leaf margins and subsequent response peak in the sinus were correlated with the occurrence of ectopic meristems. Our results suggest that the sinus of leaf serration is a quiescent domain possessing the potential for meristem formation. MIF1- or MIF3-overexpressing transgenic plants may provide a new genetic system for dissecting the molecular mechanism that maintains leaf determinate growth, and for understanding the interactions between hormone actions and meristematic activity.