Nitrite and Ammonium Toxicity on Lettuce Grown under Hydroponics

Abstract

Nitrite (NO₂ ^?‐N) toxicity symptoms have been observed on lettuce (Lactuca sativa) at various locations in California. The objective was to evaluate the symptoms of ammonium (NH₄ ⁺‐N) and nitrite (NO₂ ^?‐N) toxicity on Sundevil iceberg lettuce and Paragon romaine lettuce and to determine lettuce growth and biomass production under different levels of NO₂ ^?‐N. Hydroponic studies under greenhouse conditions were conducted using nutrient solutions containing nitrate (NO₃ ^?‐N) and two other forms of nitrogen (NO₂ ^?‐N and NH₄ ⁺‐N) applied at a constant concentration (50 mg NL^?1) or using different NO₂ ^?‐N levels (0, 5, 10, 20, 30, and 40 mg N L^?1) and a constant NO₃ ^?‐N level (30 mg N L^?1). Crown discoloration (brownish color) was observed for lettuce grown in both NO₂ ^?‐N and NH₄ ⁺‐N solutions approximately 3 weeks after transplanting into the hydroponic systems. Lettuce grown in NO₃ ^?‐N solution produced larger biomass and greater number of leaves per plant than lettuce grown in NO₂ ^?‐N or NH₄ ⁺‐N solutions. Increasing the concentration of NO₂ ^?‐N suppressed plant height, fresh and dry biomass yield, and number of leaves and increased the root vascular discoloration. Lettuce growth was reduced more than 50% at NO₂ ^?‐N concentrations greater than 30 mg N L^?1. Even at 5 mg NO₂ ^?‐N L^?1, growth was reduced 14 and 24% for romaine and iceberg lettuce, respectively, relative to that obtained in nitrate solution. Although concentrations between 5 and 40 mg NO₂ ^?‐N L ^?1 reduced dry biomass similarly for both lettuce types, toxicity symptoms were more severe in iceberg lettuce than in romaine.     

Nitrate and ammonium nutrition in chicory and rocket salad plants

To evaluate chicory (Cichorium intybus L.) and rocket salad [Eruca vesicaria (L.) Cav.subsp. sativa (Mill.)] capability to use ammonium‐nitrogen (NH₄‐N) even in the absence of nitrate‐nitrogen (NO₃‐N) in the nutrient solution, and the chances they offer to reduce leaf NO₃ content, cultivated rocket and two cultivars of chicory ('Frastagliata’, whose edible parts are leaves and stems, and ‘Clio’, a leaf hybrid) were hydroponically grown in a growth chamber. Three nutrient solutions with the same nitrogen (N) level (4 mM) but a different NH₄‐N:NO₃‐N (NH₄:NO₃) ratio (100:0, 50:50, and 0:100) were used. Rocket growth was inhibited by NH₄ nutrition, while it reached the highest values with the NH₄:NO₃ ratio 50:50. Water and N‐use efficiencies increased in rocket with the increase of NO₃‐N percentage in the nutrient solution. In the best conditions of N nutrition, however, rocket accumulated NO₃ in leaves in a very high concentration (about 6,300 mg kg^‐1 fresh mass). For all the morphological and yield features analyzed, chicory resulted to be quite unresponsive to N chemical forms, despite it took more NO₃‐N than NH₄‐N when N was administered in mixed form. By increasing NO₃‐N percentage in the nutrient solution, NO₃ leaf content increased (5,466 mg kg^‐1 fresh mass with the ratio NH₄:NO₃ 0:100). On average, both chicory cultivars accumulated 213 mg NO₃ kg^‐1 fresh mass with the ratio NH₄:NO₃ 100:0 and, differently from rocket, they showed that by using NH₄ produce can be obtained very low in NO₃ content.     

Evaluating Bearberry Nitrogen Nutrition Using Hydroponic Cultures: Establishing Preliminary DRIS Norms

Abstract

This study was designed to explore nitrogen (N) nutrition in bearberry plants (Arctostaphylos uva‐ursi L.) using a hydroponic culture system. Two experiments were performed in which the total N concentration (34, 52, and 73 mg L^?1) and N‐NO₃ ^?:N‐NH₄ ⁺ ratio (50/50, 60/40, and 70/30 in %) in the nutrient solution were varied and effects on nutrient uptake [N, phosphorus (P), potassium (K), calcium (Ca), and magnesium (Mg)] and foliar composition determined. Highest‐quality plants were yielded using a N level of 73 mg L^?1 and a N‐NO₃ ^?:N‐NH₄ ⁺ ratio of 50/50. Standard nutrient values for foliar tissue were obtained for bearberry plants growing in these hydroponic cultures for their use as preliminary norms in the diagnosis and recommendation integrated system (DRIS). In a subsequent complementary experiment, these norms were used in the DRIS procedure and applied to plants growing in solutions of varying K concentrations. It was found that the DRIS norms established in the hydroponic experiments were able to account for changes in nutrient limiting factors produced in response to the varying K concentrations in the nutrient solution. The results obtained will be useful for the nutritional diagnosis of bearberry plants.     

DOUGLAS-FIR SEEDLING RESPONSE TO A RANGE OF AMMONIUM: NITRATE RATIOS IN AEROPONIC CULTURE

The objective of the experiment was to identify the most favorable nitrogen (N) source ratio of ammonium (NH₄ ⁺) and nitrate (NO₃ ^?) for aeroponically-grown Douglas-fir when pH was maintained at pH 4.0. Seedlings were grown in controlled environments with solutions containing 0:100, 20:80, 40:60, 60:40, 80:20 or 100:0 NH₄ ⁺:NO₃ ^? ratios. Nutrient additions in the aeroponic culture units were controlled by solution conductivity set points. Seedling growth and nutrient allocation was observed for 45 days. Different NH₄ ⁺:NO₃ ^? ratios resulted in significant differences in the rate of N addition, growth, morphology, and nutrient allocation. Seedlings grown in solutions containing 60 or 80% NO₃ ^? were characterized by a combination of high growth and photosynthetic rates, high and stable internal plant N concentrations, and sufficient levels of other essential nutrients. High proportions of NH₄ ⁺ in solution resulted in low rates of N addition, stunted lateral root growth, and may have been toxic.     

Effect of biochar on nutrient retention and nectarine tree performance: A three‐year field trial

We performed a series of experiments in controlled conditions to assess the potential of hardwood‐derived biochar either as a source or as a removing additive of macronutrients [nitrate‐nitrogen (NO₃‐N), ammonium‐N (NH₄‐N), potassium (K), phosphorus (P), and magnesium (Mg)] in solution. In addition, a 3‐year field trial was carried out in a commercial nectarine orchard to evaluate the effect of increasing soil‐applied biochar rates on tree nutritional status, yield, fruit quality, soil pH, soil NO₃‐N, and NH₄‐N concentration and soil water content. In controlled conditions, the concentrations of K, P, Mg, and NH₄‐N in solution were significantly increased and positively correlated with biochar rates. Biochar was ineffective in removing NO₃‐N, K, P, and Mg from enriched solutions, while at the rate of 40 g L^?1 biochar removed almost 52% of the initial NH₄‐N concentration. In a mature, irrigated, fertilized, commercial nectarine orchard (Big Top/GF677) on a sandy‐loam soil in the Italian Po Valley, soil‐applied biochar at the rates of 5, 15, and 30 t ha^?1 were effective in reducing the leached amount of NH₄‐N in the top 0.25 m soil layer over 13 months, as estimated by ion exchange resin lysimeters. Nevertheless, independent of the rate, biochar did not affect soil pH, soil N mineral availability, soil moisture, tree nutritional status, yield, and fruit quality. We conclude that, unless an evident constraint is identified, in non‐limiting conditions (e.g., water availability and soil fertility), potential benefits from biochar application in commercial orchards are hidden or negligible.     

Effects of ammonium and inorganic carbon enrichment on growth and yield of a hydroponic tomato crop

Effects of varying the proportions of NO₃^— and NH₄⁺ in the growth medium on seedling growth and tomato fruit yield (Lycopersicon esculentum L. cv. Trust F1) were investigated in greenhouse hydroponic experiments. The presence of NH₄⁺ as the sole N source (11 mM) was toxic: it curtailed growth and decreased chlorophyll content of the leaves. However, at low concentration (10 % of total N), the presence of NH₄⁺, with or without added dissolved inorganic carbon (DIC), increased vegetative growth and fruit yield by ˜ 15 %, and enhanced taste/flavor of the fruits. In DIC‐enriched treatment, pH was maintained at 5.8 by addition of KHCO₃ or as CaCO₃. The presence of NH₄⁺, at 10 % of total N, inhibited NO₃^— uptake rates by ˜ 27 %. The rates of uptake of NO₃^— and NH₄⁺ were comparable (13.3 and 14.2 mmol plant^—1 d^—1, respectively, in the presence of DIC, and 14.7 and 14.0 mmol plant^—1 d^—1, respectively, in the absence of DIC), despite such a large difference in their concentrations in the nutrient feed solution. A higher proportion of NH₄⁺ (up to 50 % of total N) had no further significant effect upon early vegetative growth, but in a long‐term experiment resulted in a high incidence of blossom end‐rot (BER) disease, thereby severely curtailing fruit yield. The presence of even 1.1 mM NH₄⁺ reduced Ca²⁺ and Mg²⁺ accumulation in the leaves as well as in fruits.     

Comparison of hydroponic solutions for poinsettia nutritional studies 1

Poinsettia cultivars Supjibi and Freedom were grown in eight hydroponic solutions to develop a baseline solution for further nutritional studies. Four solutions contained nitrogen (N) from Ca(NO₃)₂‐4H₂O and KNO₃ (denoted as ‐NH₄) and four contained Ca(NO₃)₂‐4H₂O, KNO₃, nitric acid, and NH₄NO₃ as the N sources (denoted as +NH₄). The four ‐NH₄ and +NH₄ solutions were further divided by an IX or 2X rate of micronutrients [boron (B), copper (Cu), iron (Fe), manganese (Mn), molybdenum (Mo), and zinc (Zn)] (denoted as IX or 2X). A factorial of these four solutions at 2 concentrations (100 mg L¹ of N and potassium (K) and 15 mg L¹ phosphorus (P), or 300 mg L¹ of N and K and 46 mg L^‐1 P) was studied. Greater leaf and stem dry weight for both ‘Supjibi’ and ‘Freedom’ was observed in plants grown with the +NH₄ solutions, with a larger increase occurring with’ Supjibi’. Leaf NH₄‐N content for both cultivars was higher for both the 100 and 300 mg L^‐1 N and K fertilization rates when NH₄‐N was included. The leaf K content was highest for the plants grown with the +NH/2X solution for ‘Supjibi’, for both fertilization rates, and leaf K content increased as the K application rate increased. Results indicate that for nutritional studies with poinsettias, hydroponic solutions should include between 12.5% to 33% of the N in the NH₄ form, a calcium magnesium (Ca:Mg) ratio of 2:1, and a micronutrient concentration of (mg I/¹) 0.5, 0.02, 6.6, 0.5, 0.1, and 0.05, respectively, for B, Cu, Fe, Mn, Mo, and Zn, for adequate plant growth.     

Comparison between nitrate and ammonium nutrition in fennel,celery, and Swiss chard

Abstract

To evaluate the chance to reduce leaf NO₃ content and to increase capability to use NH₄‐N even in the absence of NO₃‐N in the nutrient solution, plants of two Apiaceae species, fennel (Foeniculum vulgare Miller var. azoricum Mill. Thell.) and celery (Apium graveolens L. var. dulce Mill. Pers.), and of one species of Chenopodiaceae, Swiss chard (Beta vulgaris L. var. vulgaris), were hydroponically grown in a growth chamber with three different NH₄‐N: NO₃‐N (NH₄: NO₃) ratios (100: 0,50: 50, and 0: 100), but with the same total N level (4 mM) for 14 days. Swiss chard growth was inhibited by NH₄ nutrition and reached the highest values with the NH₄: NO₃ ratio 0: 100. For all the morphological and yield features analyzed, fennel and celery resulted to be quite unresponsive to nitrogen (N) chemical form. Water use efficiency increased in Swiss chard and decreased in fennel and celery with the increase of NO₃‐N percentage in the nutrient solution. The dependency of N uptake rate on shoot increment per unit root was more conspicuous for Swiss chard than fennel and celery. All species took more NO₃‐N than NH₄‐N when N was administered in mixed form. In the best conditions of N nutrition, Swiss chard accumulated NO₃ in leaves in high concentration (3,809 mg kg"¹ fresh mass). On average, fennel and celery accumulated 564 mg NO₃ kg^?1 fresh mass with the ratio NH₄: NO₃100: 0 and showed that by using NH₄ produce having very low NO₃ content can be obtained. By increasing NO₃‐N percentage in the nutrient solution; NO₃ leaf content of fennel and celery increased remarkably (7,802 mg kg^?1 fresh mass with the ratio N H₄: NO₃ 0: 100).     

Chloride interference in total nitrogen analysis by the Kjeldahl method

Abstract

Very low recovery of NH₄+‐N was observed in total N determination of (NH₄)₂SO₄ in KC1 solutions by a semimicro Kjeldahl method using permanganate and reduced iron to recover NO₃‐ and NO₂‐, whereas complete recovery was obtained in analysis of NH₄+‐N in water, and of NO₃ ^?‐N or NO₂ ^?‐N in either water or KC1 solutions. The loss of NH₄ ⁺‐N observed with KC1 was attributed to the formation of NCl₃ upon reaction of NH₄ ⁺ with Cl₂ generated during oxidation of Cl^? by MnO₄ ^?. This difficulty is avoided by using K₂SO₄ instead of KC1 for extraction of inorganic N from soil. Complete recovery was obtained by adding ¹⁵N‐labeled NH₄+, NO₃‐, or NO₂‐ to 0.5 M K₂SO₄ soil extracts, and total ¹⁵N analyses of the labeled extracts were in good agreement with values calculated from the additions of ¹⁵N and the total N contents of the soil extracts.     

N form and concentration: Effects on reproductive development,growth and N content of southern peas 1

Southern peas [Vigna unguiculata, (L.) Walp.] cultured with 100% NH⁺ ₄ produced no viable flowers, while treatments in which NO^‐ ₃ composed 50% or more of the N form were not significantly different in the number of flowers formed. Flower abortion was least with 100% NO^‐ ₃ at the lower N concentration and with 75% and 100% NO^‐ ₃ at the higher N concentration. Further increments of NH⁺ ₄ resulted in greater flower abortion. The trends in flower survival were reflected in the number of pods and number of seed/plant. At the lower N concentration, the addition of NH⁺ ₄ slowed pod maturity, while at the higher N concentration pod maturity was hastened with the addition of up to 50% NH⁺ ₄. The dry weight and N content of tissues were generally greater with the higher N concentration and with N combinations containing predominantly NO^‐ ₃, but trends varied with the plant part being analyzed. Ammonium appears to adversely influence reproductive development and/or NO^‐ ₃ is essential to complete the reproductive development of southern peas. The observed differences in the response of southern peas to N form may account for previously reported discrepancies concerning the effectiveness of N fertilization on growth and yield parameters. Also, vegetative growth and vegetative N content appear to be poor indicators of final seed yields of southern peas if NH⁺ ₄ supplies a significant portion of the N form utilized by the plant.     

Evaluation of methods for nitrogen‐15 analysis of inorganic nitrogen in soil extracts: I. Steam‐distillation methods

Abstract

A study was conducted to evaluate conventional steam‐distillation techniques for N‐isotope analysis of inorganic forms of N in soil extracts. Extracts obtained with 2 M KCl from 10 diverse soils were treated with: (i) (¹⁵NH₄)₂SO₄ and KNO₃, (ii) (NH₄)₂SO₄ and K¹⁵NO₃, or (iii) KNO₃and Na¹⁵NO₂. Steam distillations were performed sequentially to determine NH₄ ⁺‐N and NO₃ ^‐‐N, and were also carried out to determine (NO₃ ^‐ + NO₂ ^‐)‐N or (NH₄ ⁺ + NO₃ ^‐ + NO₂ ^‐)‐N; a pretreatment with sulfamic acid was used to determine NO₃ ^‐‐N in the presence of NO₂ ^‐‐N. Recovery of added N ranged from 95 to 102%. Significant isotopic contamination was observed in sequential distillation of unlabeled NO₃ ^‐‐N following labeled NH₄ ⁺‐N; otherwise, analyses for ¹⁵N were usually within 1% of the values calculated by isotope‐dilution equations.     

Growth and nutrition of pansy as influenced by N‐form ratio and temperature

Abstract

Pansy (Viola xwittrockiana Gams.) producers often observe nutrient disorders among plants grown during warm periods (>18°C) of the growing season. These disorders typically are not seen when production temperatures are optimal (≥18°C) even though fertility regimes may remain the same. Our objectives were to assess the effects of temperature and nitrogen (N) fertility on growth and nutrition of pansy. Pansies cultivar ‘Crown White’ were grown until lateral branches had open flowers. Treatments consisted of two temperatures (12 and 22°C) and three NO₃ ^?:NH₄ ⁺ molar % ratios (100:0, 62:38, and 25:75) with a total concentration of 100 mg N L^?1. A modified Hoagland's solution was used with NO₃ ^?‐N supplied as Ca(NO₃)₂ and KNO₃ and with NH₄ ⁺‐N as (NH₄)₂SO₄. Cumulative nutrient absorption and foliar nutrient content were determined when plant lateral branches flowered. Root and shoot growth were limited when NH₄ ⁺ was present in solutions at high ambient air temperature (22°C), but not at low temperature (12°C). Individual absorption and accumulation of plant nutrients varied with N regimes and temperatures. Overall, pansies absorbed more total N, NH₄ ⁺, NO₃ ^?, calcium (Ca), potassium (K), magnesium (Mg), phosphorus (P), zinc (Zn), and less iron (Fe) and manganese (Mn) at 12°C than at 22°C. In addition, absorption of NO₃ ^? by pansy was negligible if any NH₄ ⁺ was present in solutions at 22°C. Results suggest that pansy growers should adjust fertility programs according to production temperatures to avoid possible nutritional disorders and maximize plant growth. If maximum growth is to be obtained in warm temperatures, the use of NH₄ ⁺‐containing fertilizers should be reduced or eliminated. However, the choice of NO₃ ^?:NH₄ ⁺ ratio for nutrition may be less important under cool growing conditions.     

Effect of nitrate addition on efficient use of ammonium sulfate fertilizer on corn under saline conditions. I. Pot experiment

Abstract

Plant growth in saline soils is regulated by the availability of nitrogen (N). High soil nitrate (NO₃)‐N can lead to poor water quality. Many workers think that NO₃‐N as a source for N can contribute to better plant growth in saline soils. The purpose of this work was to determine the necessity of NO₃‐N and the ratio of NO₃/ammonium (NH₄) in the N fertilizer which gives higher productivity of the biomass yield of corn. Corn (Zea mays L.) plants (Var. LG11) were grown under saline soil conditions (8.5 dS m^‐1), soils taken from the Euphrates valley (ACSAO Research Station) at Deir‐Ez‐Zor, east of Syria, from the surface layer of soil (0–25 cm). Five levels of N were applied in two forms, ammonium sulfate [¹⁵(NH₄)₂SO₄] with enrichment (1.5% a) as the NH₄‐N form and calcium nitrate [Ca(NO₃)₂] as the NO₃‐N form, besides fixed amounts of phosphorus (P) and potassium (K) for all N treatments. The corn plants were harvested at the flowering stage (56 days old), oven dried, weighed, and analyzed for total N and ¹⁵N recovery. The results indicated that the dry matter weight for treatments which received a combination of NH₄‐N and NO₃‐N gave higher dry matter yield than a single treatment of one source of N. But, NO₃‐N was more effective in improving yield than NH₄‐N. Nitrogen recoveries on the basis of added and absorbed N derived from fertilizer were significantly more affected by NO₃‐N than NH₄‐N.     

Rapid assessment of the rate of nitrogen immobilisation in organic components of potting media: II. Nitrogen drawdown index and plant growth

Abstract

In several experiments, cabbage seedlings were grown in soilless potting media produced using a range of aged and composted pinebarks, peat and sawdusts. Their growth was compared with the Nitrogen Drawdown Indexes (NDI) of the media, measured by a standard method previously reported. Growth was highly correlated with NDI when N was applied via pre‐plant additions and/or liquid drenches.

Aged pinebarks and composted hardwood sawdusts, with high N immobilisation potential, have NDI values near zero and consume N at about 300 mg/L each week. Adequate plant growth is difficult to obtain in these media. Media with NDI values of around 0.5 consume about 40 mg/L N each week. Pre‐plant amendment with N equivalent to that in 0.5–1.0 g/L NH₄NO₃ is desirable and weekly feeding with a solution containing 200–400 mg/L N will give maximum growth rate. Weekly feeding with solutions containing 100–150 mg/L N provides sufficient N for excellent plant growth in peat‐based media, whose NDI values are 0.95–1.0.     

Growth and chloroplast ultrastructure of two citrus rootstock seedlings in response to ammonium and nitrate nutrition 1

Abstract

It is important to understand the differential response of citrus rootstock to various rates of nitrogen (N) forms in order to evaluate the tree response to N availability under different production conditions. In this study, the effects of N sources (NH₄‐N or NO₃‐N), and rates (5, 15, 45, and 135 mg N L^?1) on two citrus rootstock seedlings (Swingle citrumelo, SC; Cleopatra mandarin, CM) growth (110 d) and N concentrations in various parts of seedling were investigated in a nutrient solution experiment. The effects of N nutrition on the chloroplast ultrastructure of leaves were examined at the end of the experiment. Rootstock and N sources significantly influenced the growth of leaves, stems, and roots. The growth of all seedling parts of both rootstocks decreased with an increase in concentration of NH₄‐N in the solution. In contrast, there was a positive relationship between the seedling growth and the concentration of NO₃‐N in the nutrient solution with marked response observed as the NO₃‐N concentration increased from 5 to 15 mg L^?1 The experiment demonstrated a distinct growth suppression effect with an increase in concentration of NH₄‐N in the nutrient solution, particularly SC rootstock. Chloroplast ultra‐structure of the leaves showed evidence of injury of the seedlings which received N entirely as NH₄ ⁺ form, but the injury was not seen when the seedlings received N as the NO₃‐N form. The disruption of chloroplast ultrastructure increased with increased rate of NH₄‐N. The most conspicuous characteristic of ammonium toxicity was the massive accumulation of strands granules and phytoferritin which is clearly an evidence of NH₃ toxicity. The results are important for understanding the implications of N source on seedling growth and chloroplast structure of citrus leaves.     

Influence of ammonium: Nitrate ratios on the growth and nitrogen uptake of pearl millet

Pearl millet [Pennisetum glaucum (L.) R. Br.] is a potentially high‐yielding grain crop for the Southern Coastal Plain region of the USA. Information on the growth and N nutrition of pearl millet is limited; therefore, this study was initiated with the objective of studying pearl millet growth, N content, N uptake patterns and N‐form preference. Plants were grown in solution culture using a modified Hoagland's solution. Solutions were changed weekly and transpirational losses replaced daily. The N‐form ratios were 1:0, 3:1, 1:1, 1:3 and 0:1 NH₄ ⁺ to NO₃ ^‐ Uptake was determined by difference between the initial and final solutions. Nitrate and NH₄ ⁺ uptake patterns were different from each other and were influenced by the ratio of NH₄ ⁺ to NO₃ ^‐. After the plants had been transferred to the solutions, ammonium was preferred for the first two weeks, with NO₃ ^‐ preferred thereafter. Nitrate uptake was highest during the grain filling period. Plant growth as measured by leaf, stem, root, and seed weight, plant height, average seed weight, and head length was generally reduced as NH₄ ⁺ increased. The largest reduction was observed between the 3:1 and 1:0 ratios. Ammonium nutrition had an overall negative effect on pearl millet growth. Ammonium fertilization of pearl millet under conditions that increase absorption of NH₄ ⁺ over NO₃ ^‐ may have a negative effect on pearl millet growth and development.     

Effects of plant age on nitrogen uptake and distribution by greenhouse plants

Water‐soluble nitrogen (N) fertilizer is intensively used in greenhouse crop production. Any N not used by a crop is subject to leaching as nitrate (NO₃‐N), which may pollute groundwater. A close correlation between N supply and N uptake by plants would increase the efficiency of N fertilization and minimize the possibility of NO₃‐N pollution. The objectives of this study were to measure N uptake by American marigold (Tagetes erecta L. ‘First Lady') and New Guinea Impatiens (NGI) (Impatiens hawkeri Bull. ‘Selenia') during growth, to determine the effect of plant age on N uptake, to determine if the two species have a preference for NO₃‐N or ammonium (NH₄‐N), and to determine the total N required for 70 days of growth.The plants were grown in solution culture using solutions supplying 120 mg each of NO₃‐N and NH₄‐N. At ten day intervals, six cultures were chosen at random for nutrient solution analysis and plant sampling for dry weight and tissue analysis. Nitrate‐N uptake was greater than NH₄‐N uptake throughout the experiment for both marigold and NGI. Total N uptake by marigold was greater during the first 50 days after transplanting with maximum N uptake during the period 30 to 50 days. In contrast, N uptake by NGI was greater during the period 40 to 70 days after transplanting. Maximum N uptake for NGI occurred during the period 60 to 70 days. Results of this study suggest that early N fertilization of marigold could be more important for their growth and quality than N applied later. For NGI, N fertilization later in the crop's development appears to be more important than early on. The total N absorbed by marigold during the experiment was 1.1 gm N plant^‐1; for NGI the quantity was 0.5 gm N plant‐¹.     

Effect of nitrate/ammonium ratio on biomass production,nitrogen accumulation,and use efficiency in sorghums of different origin

Plant nitrogen (N) uptake, growth, and N use efficiency may be affected by N form (NO₃ ^‐or NH₄ ⁺) available to the root. The objectives of this study were to determine the effect of mixed N form on dry matter production and partitioning, N uptake, and biomass N use efficiency defined as total dry matter produced per unit plant N (NUE₁) in U.S. and tropical grain sorghums [Sorghum bicolor (L.) Moench]. The U.S. derived genotype CK 60 and three tropical genotypes, Malisor‐7, M 35–1, and S 34, were evaluated in a greenhouse trial using three nutrient solutions differing in their NO₃ ^‐/NH₄ ⁺ ratio (100/0, 75/25, 50/50). Shoot and root biomass, N accumulation, and NUE, were determined at 10‐leaf and boot stages. Averaged over all genotypes, shoot and root biomass decreased when NH₄ ⁺ concentration was increased in the solution. Shoot biomass was reduced by 11% for 75/25 and 26% for 50/50 ratios, as compared to 100/0 NO₃ ^‐/NH₄ ⁺. Similarly, root biomass reduction was about 34% and 45% for the same ratios, respectively. Increasing NH₄ ⁺ concentration also altered biomass partitioning between shoot and root as indicated by decreasing root/shoot ratio. Total plant N content and NUE₁ were also reduced by mixed N source. Marked genotypic variability was found for tolerance to higher rates of NH₄ ⁺. The tropical line M 35–1 was well adapted to either NO₃ ^‐ as a sole source, or to an N source containing high amounts of NH₄ ⁺. Such a characteristic may exist in some exotic lines and may be used to improve genotypes which do not do well in excessively wet soil conditions where N uptake can be reduced.     

Effect of nitrogen nutrition on salt tolerance of Pisum sativum during vegetative growth

The influence of different nitrogen (N) forms on salt tolerance of Pisum sativum L. was investigated. Plants of the pea cultivar “Resal” were subjected to 0 (control) or 90 mM NaCl and one of the following nitrogen forms: 5 mM mineral N supplied as either NO , NH , or NH₄NO₃ or N supplied by biological N₂ fixation (inoculated with Rhizobium leguminosarum bv. viciae). Root and shoot biomass were determined 15, 30, 45, and 60 d after emergence, and Na⁺, K⁺, and Cl^– concentrations were determined by capillary electrophoresis. Nitrogen sources induced significant differences in plant growth and in ion accumulation and distribution and in differentially affected salt tolerance. In the absence of salt, the largest biomass accumulation was obtained with NH₄NO₃. In the presence of NaCl, NO ‐fed plants experienced less salt toxicity than plants supplied with other N sources, as indicated by lower Na⁺ and Cl^– and higher K⁺ concentrations in the shoot. The results also suggest that it is possible to establish an effective symbiosis under saline conditions, provided that a salt‐tolerant Rhizobium isolate with good N₂‐fixing ability is used. The use of the appropriate N‐fertilizer source can enhance the growth of Pisum sativum. Hence, NH₄NO₃ may be preferably used under non‐saline and NO under moderately saline conditions.     

Influence of the Modification of Nutritional Parameters in Aglaonema commutatum: K+, Ca2+, Mg2+ and Na+

Abstract

This trial was carried out to establish an appropriate nutrient solution for Aglaonema commutatum and to investigate the nutritional effects generated by modifications in the solution. Six treatments were tested: control (T₀; pH 6.5, E.C. 1.5 dS m^?1, 6 mmol L^?1 NO₃ ^?‐N, and 6 mmol L^?1 K⁺); high nitrogen (N) level (T₁; 9 mmol L^?1 6:3 NO₃ ^?–NH₄ ⁺); N form (T₂; 6 mmol L^?1 N‐NH₄ ⁺); high K⁺ level (T₃; 12 mmol L^?1 K⁺); high electrical conductivity (T₄; E.C. 4 dS m^?1, 25 mmol L^?1 NaCl), and basic pH (T₅; pH 8). At the end of the cultivation, leaf, shoot, and root dry weights and elemental concentrations were determined. Nutrient contents and total plant uptake were calculated from the dry weights and nutrient concentrations. Plant K⁺ uptake increased with application of K⁺ or basic nutrient solution. The uptake and transport of calcium (Ca) were enhanced by the use of NO₃ ^?‐N and inhibited by the presence of other cations in the medium (NH₄ ⁺, K⁺, Na⁺) and by basic pH. Magnesium (Mg) uptake increased with NO₃ ^?‐N application and with pH. Sodium (Na) uptake was the highest in the saline treatment (T₄), followed by the basic pH treatment. Sodium accumulation was detected in the roots (natrophobic plant), where the plant generated a physiological barrier to avoid damage. Dry weight did not differ significantly (p<0.05) among treatments except in the NaCl treatment. These results may help in the formulation of nutrient solutions that take into account the ionic composition of irrigation water and the physiological requirements of plants.