Leaching of nitrogen forms from controlled‐release nitrogen fertilizers

Abstract

Application of soluble forms of nitrogen (N) fertilizers to sandy soils may cause leaching of nitrate N (NO₃‐N) resulting in contamination of groundwater. The leaching loss of N may be reduced to a certain extent by the use of controlled‐release N formulations. A leaching column study was conducted to evaluate the leaching of urea, ammonium N (NH₄‐N), and NO₃‐N forms from selected urea‐based controlled‐release formulations (Meister, Osmocote, and Poly‐S) and uncoated urea under eight cycles of intermittent leaching and dry conditions. Following leaching of 1,760 mL of water (equivalent to 40 cm rainfall) through the soil columns, the recovery of total N (sum of all forms) in the leachate accounted for 28, 12, 6, or 5% of the total N applied as urea, Poly‐S, Meister, and Osmocote, respectively. Loss of urea‐N from all fertilizer sources was pronounced during the initial leaching events (with the exception of Meister). Cumulative leaching of urea‐N was 10% for uncoated urea while <1.7% for the controlled‐release formulations. Cumulative leaching of NH₄‐N was 6.2% for uncoated urea while <0.5% for the controlled‐release formulations. Cumulative leaching loss of NO₃‐N was 3.78% for Osmocote, 4.6% for Meister, 10.4% for urea, and 10.5% for Poly‐S. This study demonstrates a significant reduction in leaching of N forms from controlled‐release formulations as compared to that from the soluble form.     

Uptake of ammonium‐nitrogen by blueberry plants

Blueberry plants (Vaccinium ashei Reade cv. Tifblue) and Citrus natsudaidai Hayata were compared in terms of their ability to regulate the uptake of ammonium‐nitrogen (NH₄‐N). Plants of both species were grown in N‐free nutrient solutions for three days and then transferred to nutrient solutions that contained various concentrations of NH4‐N. Blueberry plants showed increases in rates of uptake of NH₄‐N 8 to 24 h after application of NH₄‐N. At concentrations of NH₄‐N above 200 (μM, uptake rates decreased to the initial value 24 h after application of NH₄‐N and then increased. By contrast, seedlings of Citrus natsudaidai showed constant rates of uptake of NH₄‐N during the experiment. These results indicate that blueberry plants are able to repress the uptake of NH₄‐N periodically when they are exposed to high concentrations of external NH₄‐N, but not seedlings of Citrus natsudaidai.     

Determination of dissolved organic nitrogen using persulfate oxidation and conductimetric quantification of nitrate‐nitrogen

Abstract

Nitrogen (N) in forest soil extracts and surface waters may be dominantly in organic compounds as dissolved organic nitrogen (DON). Due to various difficulties associated with measuring total N (as TKN) by the Rjeldahl digest, this important vehicle for nutrient movement is rarely monitored. By coupling two relatively new methods and optimizing them for use in soil studies, we developed an alternative method for measuring DON. Analysis of pure compounds and field samples shows that persulfate oxidation combined with conductimetric quantification of nitrate (NO₃) provides a highly accurate measure of dissolved N content. With relatively inexpensive equipment and reagents, a single technician can digest and assay over a hundred samples a day. This rapid, simple, and accurate assay may make it possible to routinely monitor DON where it had previously been impractical. This in turn could substantially enhance understanding about the form and quantity of N involved in nutrient fluxes.     

Influence of organic compounds on nitrogen‐fertilizer solubilization

Abstract

In the attempt to find new products which release nutrients in gradual forms, the behavior of two commercial fertilizers was studied, Nitrophoska® (N) and urea (U), covered with two organic materials, humic acid (HA) and alginic acid (AA). The release of nitrogen from the fertilizers was determined by electroultrafiltration (EUF). These applied materials on the fertilizer surface resulted in a slowing of the release of nitrogen, although strictly speaking, these compounds do not function as coated fertilizers. Their effectiveness depends on the fertilizer, for with Nitrophoska®, the addition of alginic acid was more effective, while for urea, the addition of humic acid slowed the release of nitrogen.     

Effects of supplemental‐nitrogen on the quality of rice proteins

A study was conducted on the effect of supplemental nitrogen (N) (20 hg/ha) applied as a foliar spray or to the soil on seed production, protein percentage, and protein fractions of rice. Plants were grown in a greenhouse over two different periods of time, i.e., August 1988 to January 1989 (Period I), and December 1988 to April 1989 (Period II). Nitrogen was applied to the leaves 10 and 20 days after anthesis (DAA), and to the soil at anthesis and at 15 DAA. Average temperature was 28.7°C during Period I and 32°C during Period II, corresponding to 18.7 and 22.0 growing degree‐day/day (GDD/day), respectively. The difference in GDD/day reduced the plant cycle from 130 days during Period I to 109 days during Period II. Plants grown during Period II had larger numbers of spikelets, a higher percentage of “full grown grains”;, and higher grain weight. Although percentage crude protein was about the same for the two periods, prolamin content was increased and the albumin+globulin fraction was decreased during Period II, but with no difference in glutelin content. The increase in number of spikelets, percent full grains, and grain weight appeared to result in a greater energy demand for plants grown during Period II. This may explain the increase in prolamins, since prolamin synthesis requires less energy than globulin or albumin synthesis. There was a simultaneous decrease in albumin and globulin synthesis during Period II. The content of glutelins, which represent the major reserve proteins in rice grains, was constant during both periods.     

Effect of different nitrogen‐forms and iron‐chelates on the development of stinging nettle

The development of stinging nettle (Urtica dioica L.) grown on culture solution containing with either ammonium or nitrate ions, or urea, was investigated under iron deficiency conditions, and with added FeEDTA or FeCto. Both seed‐cultured and vegetatively‐cultured stinging nettle plants produced normally developed green shoots when nitrate and 4 μM FeEDTA or FeCto were supplied. Stinging nettle plants were able to utilize Fe‐citrate, Fe‐ascorbate, and Fe‐malate effectively at the same concentration as well. When K3Fe(CN)6 was supplied, which is impermeable to the plasmalemma, and therefore is used to measure the reductive capacity of the roots, stinging nettle plants became chlorotic because the complex was stable at the pH of the culture solution. Urea did not induce chlorosis but inhibited growth. The plants died when ammonium was supplied as a sole N source. Applying bicarbonate and ammonium together prevented the plants from dying, but the plants became chlorotic. Total exclusion of iron from the culture solution resulted in iron‐deficiency stress reactions as has been described for other dicotyledonous plants (Strategy II).     

Effect of nitrogen on the growth and photo‐synthetic activity of salt‐stressed barley

Pot experiments were conducted in the greenhouse to study the effect of nitrogen (N) nutrition on photosynthesis and water relations of barley plants under salinity conditions. Nitrogen decreased the sodium (Na) content and increased the potassium (K) content in shoots. The net photosynthetic rate of leaves increased significantly with added N increasing from 0 to 100 mg N/kg soil. The activity of ribulose 1,5 bisphosphate carboxylase (RuBPC_ase) in leaves of high‐salt plants was lower, and in leaves of the low‐salt plants higher than that in control plants. The photosynthetic rate was reduced by sodium chloride (NaCl) and was significantly correlated with total soluble protein per unit leaf area. At each N level, stomatal conductance in leaves was reduced considerably by salt. Proline content of leaves increased with increasing N level. It was higher in leaves of salt‐treated plants than in those of control plants. The osmotic potential of leaves decreased with increasing N applied, and the turgor pressure of high N plants remained higher under salt treatment condition.     

Use of reflectometry for determination of nitrate‐nitrogen in well water

Recurrent monitoring of water wells is necessary to ensure that nitrate‐nitrogen (NO3‐N) concentrations in groundwater do not exceed 10 mg/L, the maximum contaminant level set by the U.S. Environmental Protection Agency. Continuous chemical analysis is often a time consuming and expensive process. A recently developed ‘Reflectoquant Analysis System’, which employs reflectometry techniques, may offer a simple and accurate method for NO3‐N analysis. The objective of this study was to evaluate the ‘Reflectoquant Analysis System’ as an alternative method for determination of NO3‐N in well water. Water samples were collected from 42 wells in Oklahoma. The samples were analyzed using the ‘Reflectoquant Analysis System’, automated cadmium reduction (Griess‐Ilosvay), ion chromatography, and phenoldisulfonic acid procedures. The linear range of the ‘Reflectoquant Analysis System’ is 1.1 to 50.6 mg/L NO3‐N. Samples exceeding this range must be diluted before analysis is performed. Excluding two wells where NO3‐N was >50.6 mg/L, simple correlation was high (r > 0.91) among the four procedures evaluated. In addition, slopes and intercepts from linear regression of NO3‐N among procedures were not significantly different. Population means obtained using the four methods were very similar. For this sample of wells, the ‘Reflectoquant Analysis System’ was precise and provided NO3‐N analysis of water samples equivalent to standard methods. Other advantages of the ‘Reflectoquant Analysis System’ are short analytical times, reduced operator training period, and competitive costs compared to standard methods.     

Effects of supplemental nitrogen on nitrogen‐assimilation enzymes,free amino nitrogen,soluble sugars,and crude protein of rice

Abstract

An upland rice variety IAC‐47 was grown in a greenhouse to determine the effect of foliar nitrogen (N) supplementation during grain development on the activity of the N assimilation enzymes, nitrate reductase (NR) and glutamine synthetase (GS), on free amino‐N content and leaf soluble sugars, and on grain crude protein content. At 10 and 20 days after anthesis (DAA), the leaves were fertilized with a liquid fertilizer containing 32% N as 12.8% urea, 9.6% ammonium (NH₄), and 9.6% nitrate (NO₃) in increasing rates corresponding to 0,20+20, 40+40, and 60+60 kg N ha^‐1. Leaves were collected twice (at 12 DAA and 14 DAA for GS activity, sugar and amino‐N content, and at 11 and 13 DAA for NRA) after each application of leaf N. The late foliar application of N increased significantly grain crude protein without a corresponding decrease in grain weight. The NR activity (NRA) increased after the foliar application of N. In the flag leaf, 60+60 kg N ha^‐1 (21 DAA) resulted in higher NRA (20x over the control), while GS activity was smaller than the control. At 22 DAA there was an increase in GS activity in the flag leaf at 20+20 N level. However, the GS activity decreased as applied N levels increased. Also at the 20+20 level, there were increases in free amino‐N in the flag leaf and second leaf at the final harvest. Throughout the experiment, plants at the 60+60 N level had the lowest levels of soluble sugars. Increases in crude protein were highest at 40+40 N level (27.9%), followed by 60+60 (18.7%).     

Time of availability influences mixed‐nitrogen‐induced increases in growth and yield of wheat 1

Previous studies have indicated that under hydroponic conditions, spring wheat (Triticum aestivum) plants produce higher grain yields, more tillers, and increased dry matter when continuously supplied with mixtures of NO₃ and NH₄ than when supplied with only NO₃. The objective of this study was to determine if mixed N needs to be available before or after flowering, or continuously, in order to elicit increases in growth and yield of wheat. During vegetative development, plants of the cultivar ‘Marshal’ were grown in one of two nutrient solutions containing either a 100/0 or 50/50 mixture of NO₃ to NH₄ and, after flowering, half the plants were switched to the other solution. At physiological maturity, plants were harvested, separated into leaves, stems, roots, and grain and the dry matter and N concentration of each part determined. Yield components and the number of productive tillers were also determined. Availability of mixed N at either growth stage increased grain yield over plants receiving continuous NO₃, but the increase was twice as large when the mixture was present during vegetative growth. When the N mixture was available only during vegetative growth the yield increase was similar to that obtained with continuous mixed N. The yield increases obtained with mixed N were the result of enhanced tillering and the production of more total biomass. Although plants receiving a mixed N treatment accumulated more total N than those grown solely with NO₃, the greatest increase occurred when mixed N was available during vegetative growth. Because availability of mixed N after flowering increased the N concentration over all NO₃ and pre‐flowering mixed N plants, it appears that the additional N accumulation from mixed N needs to be coupled with tiller development in order to enhance grain yields. These results confirm that mixed N nutrition increases yield of wheat and indicate that the most critical growth stage to supply the N mixture to the plant is during vegetative growth.     

Influence of nitrate‐nitrogen and ammonium‐nitrogen on calcium (45Ca2+) absorption in sorghum root tips

Abstract

Root‐tip, 1‐cm of Sorghum bicolor (L.) Moench cv SC283, SC574, GP‐10, and Funk G522DR were exposed to calcium (⁴⁵Ca²⁺) at pH 5.5 for 2‐hr in the presence of nitrate‐nitrogen (NO3^?‐N) or ammonium‐nitrogen (NH4+‐N). Nitrate (0.1 mM) induced significantly increased ⁴⁵Ca uptake in Funk G522DR, SC283, and GP‐10 while 0.01 mM NO₃ ^?‐N induced significantly increased ⁴⁵Ca'uptake in SC574, but ⁴⁵Ca absorption was significantly decreased at 1 mM NO₃—N. In the presence of the NH4⁺ ion, ⁴⁵Ca uptake was increased up to 8X that of the NH₄ ⁺‐N untreated roots. When ammonium chloride (NH₄CI) was used, the Cl^? tended to induce an increased ⁴⁵Ca uptake. Cultivar variation was present.     

Lichen mycobionts of mycorrihizal symbiosis with nitrogen‐fixation of showy partridge pea

Effective mycorrhizal colonization is characteristic for nodulated Cassia genera that are adaptive to subhumid areas throughout the world. Growth, regeneration, and nitrogen (N) fixation occurs within regions of extreme soil and climatic environments that preclude persistent survival of other Leguminosae. Objectives of this study were to determine effective mycobiont components and adjunctive soil fertility factors governing growth, nodulation, and symbiotic N fixation of the important forage species, Showy Partridge Pea [Cassia Chamaecrista fasciculate (L.) Michx.] The perennial foliose lichen, Parmelia incurva, ubiquitous within extreme harsh drought and temperature regions, was utilized for mycorrizal mycobionts. Largest above ground plant growth, nodulation, and nitrogen fixation resulted with mycorrhizal colonization within lichen amended soil that received no other soil fertility treatments. Responses attained with phosphorus (P) and calcium (Ca) plant nutrient soil additions, without mycorrhizal mycobiont additions, were approximately half or less of effective mycorrhizal colonized plants. In general, yield response of mycorrhizal plants was reduced with plant nutrient additions throughout this study. Nitrate reductase (NR) and nitrate‐nitrogen (NO₃‐N) levels were significantly higher within nodule cytosol of nonmycorrhizal plants. Ureidoglycolate enzyme transformers and nodule cytosol ureide components were significantly greater for mycorrhizal colonized plants. These included urease (URC), allantoinase (ALTH), allantoicase (ALTC), and total ureides. However, differences were not significant for cytosol contents of pyruvate, amine‐amide N, aspartate transaminase (AST), glutamate dehydrogenase (GDH), glutamine synthetase (GS), and glutamate oxoglutarate trasaminase (GOGAT). Representative histological microscopy of mycorrhizal colonized Showy Partridge Pea are presented. Effective mycobiont propagules associative with lichen associations are apparently opportune commensal species and only functional as site specific sycophants governed by variable environmental conditions with lichen dissipation.     

On‐farm monitoring of soil and crop nitrogen status by nitrate‐selective electrode

Abstract

Nitrate‐nitrogen concentration in fresh petiole sap, as measured by a portable, battery‐operated, nitrate‐selective electrode, was highly correlated with NO₃‐N concentration in dry petiole tissue of broccoli [Brassica oleracea L. (Italica group), r² = 0.84], celery [Apium graveolens L. var. dulce (Mill.) Pers., r² = 0.88], lettuce (Lacluca saliva L., r² = 0.77), pepper (Capsicum annuum var. annuum L., r² = 0.89), tomato (Lycopersicon esculentum Mill., r² = 0.83), and watermelon [Citrulius lanatus (Thunb.) Matsum. & Nakai, r² = 0.88]. This relationship was linear over a wide range of NO₃‐N values and was generally unaffected by site, crop, cultivar, or growth stage, provided that petiole tissue analyzed was from recently matured leaves. Sap was analyzed directly without dilution or filtration. The slope of the regression equation differed widely among crops. Selective electrode analysis of NO₃‐N concentration of soil solution samples obtained by suction lysimetry was also highly correlated with conventional laboratory technique (r² = 0.87). The nitrate‐selective electrode appeared to be a useful tool for on‐farm monitoring of soil and crop N status.     

Response of summer‐planted potatoes to level of applied nitrogen and water

The irrigation and nitrogen (N) requirements of potatoes (cv. Delaware) were determined using sprinklers in a line‐source design on a Spearwood sand. Irrigation water was applied at 73 to 244% of the daily pan evaporation (Epan) and N at 0 to 800 kg N ha^‐1 (total applied) as NH₄NO₃ in 10 applications post‐planting. There was a significant yield (total and marketable) response to irrigation, at all levels of applied N, and N at all levels of applied water (P<0.001). The interaction between irrigation and N was also significant (P<0.001). There was no significant yield response to irrigation from 149% Epan (i.e., W3 treatment) to 244% Epan (i.e., W6 treatment). Irrigation at 125 and 150% of Epan was required for 95 and 99% of maximum yield, respectively, as determined from fitted Mitscherlich relationships. Critical levels of N required for 95 (417 kg ha^‐1) and 99% (703 kg ha^‐1) of maximum yield were also determined from a Mitschlerlich relationship fitted to the average of the W3 to W6 treatments. The percent total N and nitrate‐N in petioles of youngest fully expanded leaves required for 95 and 99% of maximum yield was 1.78 and 2.11, respectively, at the 10 mm tuber stage, and 0.25 and 0.80% at the 10mm plus 14 day stage (from quadratic regressions). There was a significant (P≤0.001) increase in N uptake by tubers with level of applied N from 57 kg ha^‐1 at 0 kg applied N ha^‐1 to 190 kg ha^‐1 at 800 kg applied N ha^‐1 (from a Mitscherlich relationship fitted to the average of W3 to W6 treatments). After accounting for N uptake from soil reserves (57 kg N ha^‐1), apparent recovery efficiency (RE) of fertilizer N by tubers [RE=(Up‐Uo/Np) where Up=uptake of N by the crop, Uo=uptake in absence of applied N and Np is the level of applied N, expressed as a fraction] declined from 0.28 at 100 kg applied N ha^‐1 to 0.17 at 800 kg applied N ha^‐1. There was a linear increase in ‘after cooking darkening’ (i.e., greying) of tubers with increasing level of applied N. Conversely, ‘sloughing’ (i.e., disintegration) of tubers decreased (inverse polynomial) with increasing level of applied N. Rate of irrigation had no effect on these cooking qualities. Reducing applied irrigation and N from levels required for 99% of maximum yield to levels required for 95% of maximum yield would not lead to a significant reduction in profit. This would increase apparent recovery efficiency of applied N by plants, maintain tuber quality, and reduce the impact of potato production on the water systems of the Swan coastal plain.     

Influence of sulphur and nitrogen fertilizer applications and within‐season sampling time on measurement of total sulphur in orchardgrass by six different methods

Abstract

Six different methods for measuring total sulphur concentrations in plant material were applied to orchardgrass samples derived from three cuts of a field trial with combinations of sulphur and nitrogen fertilizer applications. The results from the methods were grouped into three pairs of high, intermediate and low measured total sulphur concentrations. Highest concentrations were obtained using an oxygen flask and the LECO CNS‐2000 automated dry combustion methods, intermediate concentrations with an alkaline digestion and the Fisher automated dry combustion instrument, and lowest with two perchloric acid digestion methods. The low results with the two perchloric acid methods likely occurred from sulphur volatilization and incomplete organic sulphur compound destruction. The results from the pairs of methods with similar total concentrations did not yield the same significant cut, sulphur and nitrogen main and interaction effects when analysis of variance was applied to the treatment results. The two dry combustion methods agreed reasonably closely regarding the main and interaction effects, but calculated recovery of applied sulphur varied. It is apparent that current methods do not agree precisely in their ability to measure total sulphur in plant material types, and for the same type of plant grown under different climate conditions and fertilizer treatments. It was concluded that values by LECO CNS‐2000 instrument provided the best measurement of total sulphur for fertilizer response trials.     

Nutrient charge,composition of media and nitrogen‐form affect growth of vinca

Growth of vinca [Catharanthus roseus (L.) G. Don ‘Grape Cooler'] was compared under several cultural conditions. Conditions investigated included two types of media (a peat‐lite mix and a mix containing 25% pine bark) and five types of nutrient charges in the peat‐lite media (sulfated micros, chelated micros, sulfated or chelated micros with pH adjustment to 5.5, and no charge). Nitrogen (N) source effect on growth was also investigated. Plants were grown at five different ratios of nitrate‐N to ammonium‐N. Greatest growth as measured by shoot length and shoot dry weight occurred in the peat‐lite media at either the sulfated micro or chelated micros adjusted to pH 5.5 and at the highest ratios of nitrate‐N to ammonium‐N. Root dry weight and growth were negatively affected by high levels of ammonium‐N in the fertilizer solution.     

Reducing nitrogen leaching‐losses from containerized plants: The effectiveness of controlled‐release fertilizers

Abstract

To evaluate the effectiveness of controlled‐release fertilizer (CRF) for reducing nitrogen (N) leaching‐losses from containerized greenhouse crops, three experiments were conducted where CRFs were applied in different ways and compared to water‐soluble fertilizer (WSF). In each experiment, ‘First Lady’ marigold (Tagetes erecta L.) plants in 0.5‐liter pots of a soilless growth medium were fertilized with the same amount of ? from 20N‐4.3P‐16.6K WSF, Osmocote 14N‐6.2P‐11.6K CRF, or Nutricote 14N‐6.2P‐11.6K CRF fertilizers. The volume of irrigation water applied to all treatments was the same in each experiment. Nitrogen content, as NH₄‐N and NO₃‐N in container leachates, and plant growth were measured and used to compare WSF with CRFs incorporated in the growth medium, or as applied to the surface, in either one large application or two small doses. A single large application of CRF at planting resulted in as much or more ? leaching than the regular application of WSF. Effectiveness of CRFs in limiting ? leaching was greatly increased by making two smaller applications, the first at planting and the second 15 to 35 days later. More ? was recovered in the leachate when CRFs were incorporated in the growth medium compared to surface application. Regardless of fertilizer type, application method, timing of application, or for each individual experiment, NO₃‐N was the predominant ? form found in the leachate and more than one‐half of the total amount of ? leached during each experiment was recovered within 30 days of planting.     

Partitioning of biomass in water‐ and nitrogen‐stressed cotton during pre‐bloom stage

The partitioning of biomass between aboveground parts and roots, and between vegetative and reproductive plant parts plays a major role in determining the ability of cotton (Gossypium hirsutum L.) to produce a crop in a given environment. We evaluated the single and combined effects of water and N supply on the partitioning of biomass in cotton plants exposed to two N supply levels, 0 and 12 mM of N, and two water regimes, well irrigated and water‐stressed at an early reproductive stage. The N treatments began when the third true leaf was visible, while water deficit treatments were imposed over the N treatments when the plants were transferred into controlled‐environment chambers at a leaf area near 0.05 m². Both water deficits and N deficits inhibited total biomass accumulation and its partitioning in cotton. Water deficit alone and N deficit alone inhibited the growth of leaves, petioles, and branches, but did not inhibit growth of the stem and enhanced the accumulation of biomass in squares. When water deficit was superimposed on N deficit, leaf growth was inhibited, although to a lesser extent than when it was the sole stress factor, and the accumulation of biomass in squares was also inhibited. Yet, the dry weight of squares in plants exposed to water and N deficits was greater than that of non‐stressed plants. Water and N deficits, either alone or in combination, did not inhibit the growth of the tap root. Growth of lateral roots was not inhibited either by water deficit alone or in combination with N deficit, but was enhanced when plants were exposed to N deficit alone. Exposure to water deficit alone or in combination with N deficit decreased the shoot:root ratio through the inhibition of shoot growth. Exposure to N deficit alone decreased the shoot:root ratio through the combination of shoot growth inhibition and root growth enhancement.     

Deep‐freezing pretreatment and time of extraction of soil samples for inorganic nitrogen determination

Abstract

Soil samples for inorganic nitrogen (N) determination are usually deep‐frozen to prevent microbial transformations of N between sampling and analysis. For analysis, frozen soils are thawed, which may also lead to transformations of N. A specially manufactured mill for grinding frozen soil was tested to minimize these transformations. Whether the time of extraction of the samples could be extended to 20 hr to better accomondate routine work and to make the clay aggregates to disperse better during extraction was also investigated. Freezing of the samples did not produce different results to fresh soils from ammonium nitrogen (NH₄ ⁺‐N) or nitrate nitrogen (NO₃ ^‐‐N) determination. Thawing of the samples increased the concentration of NO₃ ^‐‐N in the extracts and grinding increased that of NH₄ ⁺‐N. When either thawing or grinding was applied, the total inorganic nitrogen concentration was about the same. Thawing of the ground samples increased concentrations of NO₃’‐N and NH₄ ⁺‐N in the extracts. Extending the time of extraction from 0.5 or 1 hr to 20 hr increased the concentration of NH₄ ⁺‐N in the extracts, while NO₃ ^‐‐N content was also increased slightly. It was concluded that sample pretreatment may cause serious errors in the determination of inorganic N even by methods which have proven most successful to prevent microbial transformations of nitrogen, unless the soils are extracted immediately after sampling. The period of extraction should not exceed two hours.     

Effects of N‐source,light intensity and temperature on nitrogen metabolism of bahiagrass

Under greenhouse conditions, a study was made on the effects of nitrogen (N) source (N)O₃ or NH₄), mode of application (single vs. split) and nitrification inhibition on the N‐uptake and metabolism, of bahiagrass.

Variations in light and temperature in the greenhouse affected the N‐metabolism of bahiagrass plants. Nitrate fed plants had nitrate reductase activity (NRA) pattern different from that of NH₄‐fed plants. Amino‐N accumulation patterns were similar for plants under both N‐sources, although amino‐N levels in leaves of NH₄‐fed plants were much smaller than that of NO₃ plants. Nitrate accumulation in leaves showed inverse trend to that of roots in plants fed both NO₃ or NH₄. To the sharp peaks in NO₃ levels in roots due to increases in light and temperature corresponds a sharp decrease of its levels in leaves.

For both both NO₃ or NH₄ treatments, soluble‐N accumulated most in the rhizomes of bahiagrass plants, whereas protein N accumulated most in leaves, suggesting that rhizomes had a buffering effect on the NO₃ fluxes to leaves. This presumably resulted in a lag in the NRA response of the NO₃‐fed plants to increases in light and temperature.