Effect of uniconazole and limited water on growth,water relations,and mineral nutrition of “Lalandei” Pyracantha

Pyracantha (Pyracantha coccinea M. J. Roem. Lalandei) plants were treated with uniconazole at 0.5 mg ai container^–1 as a medium drench, 150 mg ai L^–1 as a foliar spray, or left untreated. Plants from all treatments were placed under three water regimes: drought acclimated, nonacclimated and later exposed to drought, or nonstressed. Acclimated plants were conditioned by seven 4-day stress cycles (water withheld), while nonacclimated were well watered prior to a single 4-day stress cycle at the same time as the seventh drought cycle of acclimated plants. Nonstressed plants were well watered throughout the study. Nonstressed plants had higher leaf water potentials and leaf conductances than acclimated and nonacclimated plants, and transpiration rates were higher in nonacclimated than acclimated plants. Uniconazole did not affect leaf water potential, leaf conductance, or transpiration rate. Acclimated plants had smaller leaf areas and leaf, stem, and root dry weights than nonacclimated or nonstressed plants. Plants drenched with uniconazole had the lowest stem and root dry weights. Acclimated plants also contained higher N concentrations than nonacclimated or nonstressed plants, and higher P concentrations than nonacclimated plants. Uniconazole medium drench treatments increased levels of Mn and P. Calcium concentration was increased in plants receiving either medium drench or foliar applications.     

Effect of GA4+7 on growth and cellular change in uniconazole-treated hibiscus

Hibiscus rosa-sinensis Jane Cowl in 1.5–1 pots were given a soil drench of 0.2 mg uniconazole, pruned 2 weeks later, and treated with a foliar application of GA₄₊₇ at 0, 25 (once or four times every 2 weeks), 50 (once or twice every 4 weeks), or 100 mg L^-1. One application of GA₄₊₇ at 100 mg L^-1, two applications at 50 mg L^-1, and four applications at 25 mg L^-1 were more active in partially restoring stem elongation and caused nearly normal leaf production than other GA treatments, but promoted the abscission of the lower leaves. The size of the individual leaves, but not stem diameter, increased following GA₄₊₇ application. Multiple applications of GA₄₊₇ stimulated flowering of the retarded plants. Uniconazole resulted in short pedicels bearing short cells with increased diameter, as well as larger pith, vascular, and cortical tissues than the untreated control. Four applications of 25 mg L^-1 GA₄₊₇ to uniconazole-treated plants resulted in long pedicels, having long cells similar to the control. Results of the histological study suggest that uniconazole either slowed cell division or caused cell division to cease early.     

The effects of ancymidol,abscisic acid,uniconazole and paclobutrazol on somatic embryogenesis of asparagus

Summary The effects of ancymidol, abscisic acid (ABA), uniconazole, and paclobutrazol on asparagus somatic embryogenesis were evaluated. Calli induced from seedlings of genotype G447 were transferred to embryo induction medium (MS plus 3% sucrose, 0.1 mg L^–1 NAA, 0.5 mg L^–1 kinetin and 3% gelrite), with different concentrations of these compounds. After 8 weeks, the recovered bipolar or globular embryos were placed on germination medium (MS plus 6% sucrose, 0.1 mg L^–1 NAA, 0.1 mg L^–1 kinetin, 0.75 mg L^–1 ancymidol, 40 mg L^–1 adenine sulphate dihydrate, 0.17 mg L^–1 sodium phosphate monobasic and 3% gelrite) for conversion to plantlets. Inclusion of ancymidol, ABA, uniconazole and paclobutrazol in the embryo induction medium did not affect the total number of somatic embryos produced relative to the control without these compounds. However, ancymidol, ABA and uniconazole significantly improved embryo development by increasing the production of bipolar embryos 250–750% and decreasing that of globular embryos 8–35% relative to the control. The bipolar embryos produced with any of the four compounds in the embryo induction medium converted to plantlets at rates 700–1100% greater than the control. None of the globular embryos converted to plantlets. Ancymidol (0.75 mg L^–1) and ABA (0.05 mg L^–1) were the most effective treatments; 61 and 46 bipolar embryos g^–1 callus were produced, and 38% and 37% of the bipolar embryos converted to plantlets, respectively. These results indicated that ancymidol, ABA, uniconazole and paclobutrazol significantly enhanced the production of asparagus somatic embryos and their conversion to plantlets, and ancymidol and ABA were more effective than uniconazole and paclobutrazol.Abbreviations Ancymidol a-cyclopropyl-a(4-methoxyphenyi)-5-pyrimidine methanol - NAA 1-naphthaleneacetic acid - Paclobutrazol I-(4-chlorophenyl)-4,4-dimethyl-2(1H-1,2,4-triazol-1-yl)-pentan-3-ol - Uniconazole (E)-(p-chlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-1-pentan-3-ol - ABA abscisic acid - GA gibberellic acid     

Modification of hibiscus growth by treating unrooted cuttings and potted plants with uniconazole or paclobutrazol

Unrooted cuttings ofHibiscus rosasinensis L. Seminole Pink were soaked for 5 s in a solution containing 25, 50, 75, or 100 mg L^–1 uniconazole or paclobutrazol, rooted, and then potted and allowed to grow without pinching. Uniconazole was more effective than paclobutrazol in suppressing stem growth and number and length of lateral shoots. Uniconazole and paclobutrazol, at the 25 mg L^–1 concentration, resulted in stem growth 75 and 25%, respectively, of the control, with further reduction at higher rates. Flowering was delayed by the highest rate of uniconazole but not paclobutrazol. Flower number was reduced by both retardants, without any effect on flower size. Plants treated with uniconazole had short pedicels regardless of the rates, whereas paclobutrazol did not affect pedicel length. A second experiment used unrooted cuttings being soaked in a solution containing 0, 12.5, 25, or 50 mg L^–1 uniconazole or having the lower 2.5 cm of the stem dipped in a solution containing 0, 50, 100, or 200 mg L^–1 uniconazole. Plants were pinched after potting. Soaking resulted in more efficient height control than dipping. Lateral shoot number was reduced by soaking but not dipping. All treated plants had smaller stem diameters. Flower size was unaffected regardless of method of treatment and the type of retardant applied. In a third experiment, soil drenches with uniconazole at a rate as low as 0.05 mg/pot resulted in excessive growth retardation. Soil drenches with paclobutrazol at 0.05–0.20 mg/pot reduced shoot growth, flower number, and pedicel length, but did not affect days to bloom.     

Effects of Plant Growth Regulators on Seed Filling,Endogenous Hormone Contents and Maize Production in Semiarid Regions

In this study, we determined whether the application of uniconazole alone or combined with ethephon could enhance the seed-filling rates in maize by regulating the endogenous hormone contents. Uniconazole was applied to the foliage at concentrations of 0 (CK), 25 (U₂₅), 50 (U₅₀) and 75 (U₇₅) mg L⁻¹ at the 12-leaf stage. In addition, uniconazole was applied to the foliage at the 12-leaf stage and ethephon at 10 days after silking stage at concentrations of 0 (CK), 25 mg L⁻¹ uniconazole + 100 mg L⁻¹ ethephon (U₂₅ + E₁₀₀), 50 mg L⁻¹ uniconazole + 200 mg L⁻¹ ethephon (U₅₀ + E₂₀₀) and 75 mg L⁻¹ uniconazole + 300 mg L⁻¹ ethephon (U₇₅ + E₃₀₀). Uniconazole applied alone or in combination with ethephon significantly improved ear characters and grain yield. Uniconazole applied alone or combination with ethephon significantly improved the dry matter accumulation in seeds and seed-filling rates. Uniconazole significantly increased the abscisic acid (ABA) and zeatin (Z) + zeatin riboside (ZR) contents of seeds, but reduced the gibberellic acid (GA) contents. The application of uniconazole combined with ethephon decreased the ABA, Z + ZR and GA contents in seeds. The ABA and Z + ZR contents were significantly positively correlated, whereas the GA content was negatively correlated with the maximum seed weight, maximum seed-filling rate and mean seed-filling rate. The application of uniconazole alone significantly improved the seed-filling rates in maize by regulating the endogenous hormone contents. Thus, we conclude that uniconazole application at 50 mg L⁻¹ in the 12-leaf stage can enhance the maize production.

     

Seed potato (Solanum tuberosum L.) yield and tuber number increase after foliar applications of cytokinins and gibberellic acid under field and glasshouse conditions

The purpose of these experiments is to determine the effects of foliar applications of benzylaminopurine (BAP) and gibberellic acid (GA) on tuber number production of seed potatoes. In field experiments conducted during 1989/90 cv. Mailén was used and BAP, 50 mg·l^–1 was foliarly applied at (1) tuber initiation, 36 days after emergence (DAE); (2) 54 DAE; and, (3) 64 DAE. Under glasshouse conditions, in 1991/92 cv. Spunta was used and BAP 50 mg·l^–1+GA 50 mg·l^–1 were applied 30 and 37 days after planting/transplanting. In 1992 cv. Huinkul, Kennebec and Spunta were used and BAP 50 mg·l^–1+GA 50 mg·l^–1 and Biozyme (Techic SA), a commercial product with auxin (IAA, 32.2 mg·l^–1), gibberellic acid (GA₃, 32.2 mg·l^–1) and cytokinins (zeatin, 83.2 mg·l^–1) at 5 ml·l^–1 were applied. In cv. Mailén, a higher tuber number in the seed fraction (<80 g) was found when BAP was applied at each of the three crop stages, while applications 54 and 62 DAE also increased tuber number in the 80–400 g fraction. As a result of BAP applications, tuber yield was also significantly increased. In the glasshouse experiments, cv. Spunta showed a significant increase in minituber production in 3 out of 4 cases, either if the mother plant came from in vitro generated plantlets or minitubers, or if GA + BAP or Biozyme was applied. It can be concluded that the use of these PGRs under both field and glasshouse conditions in cvs. Mailén and Spunta can result in increased tuber number in the seed fraction.     

Uniconazole-induced alleviation of freezing injury in relation to changes in hormonal balance, enzyme activities and lipid peroxidation in winter rape

Winter rape (Brassica napus L. cv. 601) seedlings were treated with 50 mg.l-1 of foliar-applied uniconazole and then exposed to freezing stress with a light/dark temperature regime of 2 °C/–3 °C for 5 days at the seedling stage. Stressed plants contained lower endogenous GA3 and IAA contents than the controls, while zeatin and ABA contents and ethylene levels were significantly increased. Uniconazole-treated plants had lower endogenous GA3 and IAA contents, and higher zeatin and ABA contents and ethylene levels. Leaf chlorophyll content and respiratory capacity of roots were reduced significantly after plants were subjected to freezing stress, and foliar sprays of uniconazole retarded the degradation of chlorophyll and increased respiratory capacity of roots. Uniconazole-induced freezing tolerance was accompanied by increased activities of various antioxidant enzymes, including superoxide dismutase, catalase and peroxidase. Foliar applications of uniconazole reduced electrolyte leakage and malondialdehyde accumulation caused by freezing stress, suggesting that uniconazole may have decreased freezing-induced lipid peroxidation and membrane damage.     

Excretion of photosynthetically fixed organic carbon by metalimnetic phytoplankton

The effects of light intensity, oxygen concentration, and pH on the rates of photosynthesis and net excretion by metalimnetic phytoplankton populations of Little Crooked Lake, Indiana, were studied. Photosynthetic rates increased from 1.42 to 3.14 mg C·mg^–1 chlorophylla·hour^–1 within a range of light intensities from 65 to 150E·m^–2·sec^–1, whereas net excretion remained constant at 0.05 mg C·mg^–1 chlorophylla·hour^–1. Bacteria assimilated approximately 50% of the carbon released by the phytoplankton under these conditions. Excreted carbon (organic compounds either assimilated by bacteria or dissolved in the lake water) was produced by phytoplankton at rates of 0.02–0.15 mg C·mg^–1 chlorophylla·hour^–1. These rates were 6%–13% of the photosynthetic rates of the phytoplankton. Both total excretion of carbon and bacterial assimilation of excreted carbon increased at high light intensities whereas net excretion remained fairly constant. Elevated oxygen concentrations in samples incubated at 150E· m^–2·sec^–1 decreased rates of both photosynthesis and net excretion. The photosynthetic rate increased from 3.0 to 5.0 mg C·mg^–1 chlorophylla· hour^–1 as the pH was raised from 7.5 to 8.8. Net excretion within this range decreased slightly. Calculation of total primary production using a numerical model showed that whereas 225.8 g C·m^–2 was photosynthetically fixed between 12 May and 24 August 1982, a maximum of about 9.3 g C·m^–2 was released extracellularly.     

Simultaneous biodegradation ofp-cresol and phenol by the basidiomycetePhanerochaete chrysosporium

Summary The fungusPhanerochaete chrysoporium BKM-F-1767 was able to degrade high concentrations ofp-cresol (up to 150 mg L^–1) provided that glucose was added as a carbon and energy source and conditions favourable to ligninolytic enzyme activities were used, i.e. a nitrogen-limited medium. The fungus also simultaneously degradedp-cresol (50 mg L^–1) and phenol (50 mg L^–1) in a mixture at similar rates. Kinetics ofp-cresol biodegradation were almost identical whether the compound was tested individually or in a mixture with phenol.     

Nutritional and hormonal requirements of Ginkgo biloba embryo-derived callus and suspension cell culture

Calli were obtained from Ginkgo biloba embryos grown on Murashige and Skoog (MS) medium. The G. biloba cells could grow on either MS or Gamborg B5 mineral salt medium supplemented with sucrose (3% and 2%, respectively) and naphthaleneacetic acid (NAA) and kinetin (K) in concentrations ranging from 0.1 to 2.0 mg·L^–1. Best growth and maintenance of callus cultures were achieved using MS medium supplemented with 2 mg·L^–1 NAA and 1 mg·L^–1 K (N₂K₁MS). Light was required to maintain healthy growth of the callus tissue.In both MS and B5 based media, sucrose was hydrolyzed extracellularly before being taken up by Ginkgo cell suspension cultures. Specific growth rates of 0.13 d^–1 and 0.08 d^–1 were obtained in MS medium supplemented with 1 mg·L^–1 NAA, 0.1 mg·L^–1 K and 30 g·L^–1 sucrose (N₁K_0.1MS) and B5 medium supplemented with the same growth regulator regime and 20 g·L^–1 sucrose (N₁K_0.1B5) respectively. Complete phosphate and ammonium uptake was observed in 11 days when cultured in MS medium and 10 days and 4 days respectively when cultured in B5 medium. During the culture, G. biloba cells consumed only 64% and 29% of the nitrate content of N₁K_0.1MS and N₁K_0.1B5 media respectively. Maximum dry biomass concentrations were 13.4 g·L^–1 and 7.9 g·L^–1, and yields on carbohydrate were 0.39 and 0.45 in N₁K_0.1MS and N₁K_0.1B5 media respectively. The better performance of MS cultures came from the higher sucrose and nitrogen salts concentrations of this medium.Abbreviations B5 Gamborg mineral salt medium - d.w. Dry weight - K Kinetin - MS Murashige and Skoog mineral salt medium - N or NAA Naphthaleneacetic acid - N_iK_jMS i and j are the respective concentrations (mg·L^–1) of NAA and K - n Number of experimental points - r Linear regression correlation coefficient     

Growth and Flowering Responses of Sea Marigold to Daminozide,Paclobutrazol, or Uniconazole Applied as Drenches or Sprays

Borrichia frutescens (L.) DC., sea marigold, is a woody perennial shrub native to the Gulf and Atlantic coasts of North America and has potential as a landscape shrub or groundcover. This study assesses application rates of three commercially available plant growth regulators (PGRs) on B. frutescens during container production. In one experiment, plants were drenched with 0, 0.5, 1, 2, or 4 mg active ingredient (a.i.) pot^?1 of uniconazole or 0, 5, 10, 20, or 40 mg a.i. pot^?1 of paclobutrazol, and in a second experiment, plants were sprayed with solutions of either 0, 25, 50, 100, or 200 mg a.i. L^?1 of uniconazole, 0, 50, 100, 200, or 400 mg a.i. L^?1 of paclobutrazol, or 0, 2500, 5000, 10000, or 20000 mg a.i. L^?1 of daminozide. Drench-applied paclobutrazol (40 mg a.i. pot^?1) reduced shoot mass and root mass (52.9 and 48.5 %, respectively). Both paclobutrazol (40 mg a.i. pot^?1) and uniconazole (2 mg a.i. pot^?1) reduced leaf number by as much as 56.7 and 23.8 %, respectively. Height was reduced 54.9 % by paclobutrazol at 40 mg a.i. pot^?1 and 34.9 % by uniconazole at 2 mg a.i. pot^?1. Drench application of paclobutrazol and uniconazole reduced internode extension by 50.1 and 41.4 %, respectively. At the levels tested, daminozide, paclobutrazol, and uniconazole were generally ineffective at controlling growth when applied as a spray. Drench application of paclobutrazol or uniconazole can be used to control height during container production of B. frutescens, whereas spray application rates need to be tested at higher concentrations or multiple applications to achieve desired control.     

Paclobutrazol or uniconazol applied early in the previous season promotes flowering of field-grown Rhododendron and Kalmia

Field-grown large leaf Rhododendron and Kalmia latifolia were treated with one of three concentrations of paclobutrazol or uniconazol in April, June, or August in the second year from propagation. The elongation of stems was measured as was the number of flower buds initiated. Spray applications in April or June increased flowering at the lowest concentrations tested; 4 mg · L^–1 paclobutrazol and 1.5 mg · L^–1 uniconazol. Flowering was induced in cultivars that normally did not flower, and the number of flower buds per plant was increased in cultivars that normally flowered. All treatments that induced flowering also reduced stem elongation. Spray application in August failed to enhance flowering. At the concentrations tested, uniconazol was more effective than paclobutrazol in increasing the number of flower buds and reducing stem elongation of Rhododendron. For Kalmia, there was less response to the concentration of growth retardant, and the two chemicals enhanced flowering equally.     

Degradation of carbondisulphide by a Thiobacillus isolate

During experiments investigating the purification of waste gas a bacterium capable of using carbon disulphide (CS₂) als sole energy source was isolated. It could be identified as a Thiobacillus sp.; however, the species remains unclear. Both the properties of T. thioparus and T. thiooxidans have been observed. Since the organism could be used for removing CS₂ in the environment, the degradation kinetics have been investigated by different methods. Substrate concentrations of up to 100 mg CS₂·l^–1 were oxidized at maximum rates of 2.5 mg CS₂·g^–1 protein·min^–1 at pH 7.0 and at 30°C. CS₂ levels above 150 mg CS₂·l^–1 caused termination of degradative activity. Correspondence to: Ch. Plas     

Turbidity enhances feeding abilities of larval Pacific herring,Clupea harengus pallasi

Fishes inhabiting estuaries, rivers, and embayments are subject to turbid conditions. Larvae of many fishes utilize estuaries as nursery areas. For visual plankton feeders such as larval fishes, turbidity may reduce search and reaction distances, resulting in lowered feeding abilities. In this study feeding Pacific herring larvae, Clupea harengus pallasi, were exposed to suspensions of estuarine sediment and Mount Saint Helens volcanic ash at concentrations ranging from 0 mg · l^–1 to 8 000 mg · l^–1. In all experiments, maximum feeding incidence and intensity occurred at levels of suspension of either 500 mg · l^–1 or 1000 mg · l^–1 with values significantly greater than controls (0 mg · l^–1). Feeding decreased at greater concentrations. The suspensions may enhance feeding by providing visual contrast of prey items on the small perceptive scale used by the larvae. Larval residence in turbid environments such as estuaries may serve to reduce predation from larger, visual planktivores, while searching ability in the small larval perceptive field is not decreased.     

Uniconazole inhibits stress-induced ethylene in wheat and soybean seedlings

Previous studies have shown that uniconazole inhibits ethylene synthesis and protects plants from various stresses. The present research was conducted to delineate the mechanism of ethylene inhibition by uniconazole [(E)-(p-chlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-1-penten-3-ol]. Following heat stress of 48°C for 3 h, the shoots of the control wheat seedlings became desiccated, and the seedlings lost 23% of their fresh mass 8 h after stress. The control soybean seedlings had epinastic unifoliate leaves 5 h after foliar application (4.4 g.a.i./ha) of the herbicide triclopyr [(3,5,6-trichloro-2-pyridinyl)oxyacetic acid]. Soil drench applications of uniconazole, a potent member of the triazole family, reduced these symptoms associated with heat and herbicide stress in wheat (5.0 mg/L) and soybean (0.4 mg/L) seedlings, respectively.Basal ethylene production was inhibited 32 and 48% by uniconazole in the wheat and acotyledonous soybean seedlings, respectively. Following a 48°C heat stress, 1-aminocyclopropane-1-carboxylic acid (ACC) levels increased 40% in both the control and uniconazole-treated wheat seedlings. After triclopyr application, ACC levels increased 400% in both the control and uniconazoletreated soybean seedlings. The increased ACC levels, following stress, were accompanied by increased ethylene production from the control, but not from the uniconazole-treated wheat and acotyledonous soybean seedlings. Uniconazole treatment did not significantly change the basal or stress-induced N-malonyl-1-aminocyclopropane-1-carboxylic acid (MACC) levels compared to controls. These results suggest that uniconazole inhibits ethylene synthesis by interfering with the conversion of ACC to ethylene in wheat and acotyledonous soybean seedlings. Ethylene production and ACC conversion were not inhibited by uniconazole in excised soybean cotyledons. These results indicate that different ethylene-forming enzyme (EFE) systems operate in the soybean acotyledonous seedling and cotyledon, and the system in the former is inhibited by uniconazole.     

Sources and sinks of dissolved organic carbon in a forested swamp catchment

Concentrations of dissolved organic carbon (DOC) were measured in precipitation, throughfall, stemflow, and soil, peat and stream water in a 50 ha catchment with a central 5 ha swamp at Mont St. Hilaire, Quebec. DOC concentrations in precipitation were low (2.0 mg L^–1), but increased in passage through the tree canopies as throughfall (9.1–14.6 mg L^–1) and stemflow (23.1–30.1 mg L^–1). For the period July 1–November 15, 1987, 0.5 g DOC m^–2 was imported as precipitation, and forest canopies contributed a further 1.4–1.7 g m^–2 2 to the soil surface. DOC concentrations were higher (46.0 and 67.6 mg L^–1) in upland soil organic horizons, but decreased with depth because subsoil mineral horizons acted as a major sink of DOC. A laboratory experiment using leaf leachate revealed that subsoil horizons were able to adsorb DOC, with equilibrium DOC concentrations ranging from 3 to 19 mg L^–1. Soil organic carbon appeared to be an important determinant of equilibrium DOC concentrations. The swamp was a major source of DOC, with an overall average DOC concentration of 58.6 mg L^–1 and showed strong spatial and temporal variations related to hydrologic and thermal regimes. During base flow periods, stream DOC concentrations were small (< 3 mg L^–1), dominated by water fed from springs draining upland soils. During high flows, stream DOC concentrations increased through the contribution of DOC-rich water originating in the swamp. Sources, sinks and transport of DOC are thus a function of a complex set of inter-related biotic and abiotic process.     

Effects of constitutive expression of nitrate reductase in transgenic Nicotiana plumbaginifolia L. in response to varying nitrogen supply

Transformed Nicotiana plumbaginifolia plants with constitutive expression of nitrate reductase (NR) activity were grown at different levels of nitrogen nutrition. The gradients in foliar NO ₃ ^– content and maximum extractable NR activity observed with leaf order on the shoot, from base to apex, were much decreased as a result of N-deficiency in both the transformed plants and wild type controls grown under identical conditions. Constitutive expression of NR did not influence the foliar protein and chlorophyll contents under any circumstances. A reciprocal relationship between the observed maximal extractable NR activity of the leaves and their NO ₃ ^– content was observed in plants grown in nitrogen replete conditions at low irradiance (170 mol photons·m^–2 ·s^–1). This relationship disappeared at higher irradiance (450 mol photons·m^–2·S^–1) because the maximal extractable NR activity in the leaves of the wild type plants in these conditions increased to a level that was similar to, or greater than that found in constitutive NR-expressors. Much more NO ₃ ^– accumulated in the leaves of plants grown at 450 mol photons·m^–2·s^–1 than in those grown at 170 mol photons·m^–2·s^–1 in N-replete conditions. The foliar NO ₃ ^– level and maximal NR activity decreased with the imposition of N-deficiency in all plant types such that after prolonged exposure to nitrogen depletion very little NO ₃ ^– was found in the leaves and NR activity had decreased to almost zero. The activity of NR decreased under conditions of nitrogen deficiency. This regulation is multifactoral since there is no regulation of NR gene expression by NO ₃ ^– in the constitutive NR-expressors. We conclude that the NR protein is specifically targetted for destruction under nitrogen deficiency. Consequently, constitutive expression of NR activity does not benefit the plant in terms of increased biomass production in conditions of limiting nitrogen.Abbreviations Chl chlorophyll - N nitrogen - NR NADH-nitrate reductase - WT wild type     

Effect of Putrescine and Paclobutrazol on Growth, Physiochemical Parameters, and Nutrient Acquisition of Salt-sensitive Citrus Rootstock Karna khatta (Citrus karna Raf.) under NaCl Stress

Salinity is a serious problem in arid and semiarid areas and citrus trees are classified as salt-sensitive. Because putrescine (Put) and paclobutrazol (PBZ) are known to act as plant protectants under environmental stresses, we examined the effect of Put and PBZ on the physiochemical parameters of the salt-susceptible citrus rootstock Karna khatta under NaCl stress. PBZ was applied at 0, 250, and 500 mg L⁻¹ as a soil drench 1 week prior to salinization. A computed amount of NaCl salt to develop soil salinity of 3 dS m⁻¹ (3 g NaCl kg⁻¹ soil) and foliar spray of Put at 0 or 50 mg L⁻¹ were applied. The electrical conductivity (EC) of the garden soil (0.35 dS m⁻¹) was used as control. Application of PBZ and/or Put reduced the membrane injury index and increased relative water content, photosynthetic rate, and pigments content under saline conditions compared to what occurred in plants exposed to NaCl in the absence of PBZ or Put. Application of PBZ or Put alone or in combination also improved the activities of SOD and peroxidase and proline content under saline conditions. Application of PBZ and/or Put also increased K⁺ and reduced Na⁺ and Cl⁻ concentrations in leaf tissues. It is proposed that PBZ and/or Put could improve the tolerance of salt-susceptible Karna khatta by regulating absorption and accumulation of ions and improving antioxidant enzyme activities.     

Modification of hibiscus growth by treating unrooted cuttings and potted plants with uniconazole or paclobutrazol

Unrooted cuttings ofHibiscus rosasinensis L. “Seminole Pink” were soaked for 5 s in a solution containing 25, 50, 75, or 100 mg L^?1 uniconazole or paclobutrazol, rooted, and then potted and allowed to grow without pinching. Uniconazole was more effective than paclobutrazol in suppressing stem growth and number and length of lateral shoots. Uniconazole and paclobutrazol, at the 25 mg L^?1 concentration, resulted in stem growth 75 and 25%, respectively, of the control, with further reduction at higher rates. Flowering was delayed by the highest rate of uniconazole but not paclobutrazol. Flower number was reduced by both retardants, without any effect on flower size. Plants treated with uniconazole had short pedicels regardless of the rates, whereas paclobutrazol did not affect pedicel length. A second experiment used unrooted cuttings being soaked in a solution containing 0, 12.5, 25, or 50 mg L^?1 uniconazole or having the lower 2.5 cm of the stem dipped in a solution containing 0, 50, 100, or 200 mg L^?1 uniconazole. Plants were pinched after potting. Soaking resulted in more efficient height control than dipping. Lateral shoot number was reduced by soaking but not dipping. All treated plants had smaller stem diameters. Flower size was unaffected regardless of method of treatment and the type of retardant applied. In a third experiment, soil drenches with uniconazole at a rate as low as 0.05 mg/pot resulted in excessive growth retardation. Soil drenches with paclobutrazol at 0.05–0.20 mg/pot reduced shoot growth, flower number, and pedicel length, but did not affect days to bloom.     

The nitrogen cycle in lodgepole pine forests,southeastern Wyoming

Storage and flux of nitrogen were studied in several contrasting lodgepole pine (Pinus contorta spp.latifolia) forests in southeastern Wyoming. The mineral soil contained most of the N in these ecosystems (range of 315–860 g · m^–2), with aboveground detritus (37.5–48.8g · m^–2) and living biomass (19.5–24.0 g · m^–2) storing much smaller amounts. About 60–70% of the total N in vegetation was aboveground, and N concentrations in plant tissues were unusually low (foliage = 0.7% N), as were N input via wet precipitation (0.25 g · m^–2 · yr^–1), and biological fixation of atmospheric N (<0.03 g · m^–2 · yr^–1, except locally in some stands at low elevations where symbiotic fixation by the leguminous herbLupinus argenteus probably exceeded 0.1 g · m^–2 · yr^–1).Because of low concentrations in litterfall and limited opportunity for leaching, N accumulated in decaying leaves for 6–7 yr following leaf fall. This process represented an annual flux of about 0.5g · m^–2 to the 01 horizon. Only 20% of this flux was provided by throughfall, with the remaining 0.4g · m^–2 · yr^–1 apparently added from layers below. Low mineralization and small amounts of N uptake from the 02 are likely because of minimal rooting in the forest floor (as defined herein) and negligible mineral N (< 0.05 mg · L^–1) in 02 leachate. A critical transport process was solubilization of organic N, mostly fulvic acids. Most of the organic N from the forest floor was retained within the major tree rooting zone (0–40 cm), and mineralization of soil organic N provided NH₄ for tree uptake. Nitrate was at trace levels in soil solutions, and a long lag in nitrification was always observed under disturbed conditions. Total root nitrogen uptake was calculated to be 1.25 gN · m^–2 · yr^–1 with estimated root turnover of 0.37-gN · m^–2 · yr^–1, and the soil horizons appeared to be nearly in balance with respect to N. The high demand for mineralized N and the precipitation of fulvic acid in the mineral soil resulted in minimal deep leaching in most stands (< 0.02 g · m^–2 · yr^–1). These forests provide an extreme example of nitrogen behavior in dry, infertile forests.