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PubMedDate not supplied

Determining of nitrogen absorption and nitrogen secretion in different sections of the pig's intestine by digesta exchange between 15N labelled and unlabelled animals.

In an experiment with 3 pigs (initial live weight 30 kg, each fitted with 2 re-entrant fistulas in duodenum and ileum, one labelled with 15N), the duodenal and ileum digesta was exchanged. The N and 15N contents were estimated in faeces, urine, duodenal and ileum digesta of all experimental animals as well as in special organs and in the contents of different tract sections. The 15N excess (15N') of N compounds secreted into the gut lumen was determined using the 15N' in pancreas, gut mucosa and TCA-soluble blood serum. From measuring the digesta passage through the 3 sections of the digestive tract: 1. mouth ... duodenum, 2. duodenum ... ileum, 3. ileum ... after (Krawielitzki et al., 1989) the absorption and secretion rates of nitrogen were calculated. Secretion into the 1st section amounted to 5.3 g N/d (= 15% of intake) and the absorption to approximately 1% of intake. In the 2nd section the corresponding dates were 8.9 resp. 38.6 g N/d (= 25 resp. 110% of N intake), and in the 3rd one 1.9 resp. 8.4 g N/d (= 5.6 resp. 24% of N intake). Total absorption amounted to 134% of N intake and the over all re-absorption of endogenous N compounds secreted into the gut lumen to about 90%. During the passage the amount of endogenous N (g/d) decreased from 5.3 at the duodenum to 3.8 at the ileum to 1.6 in the faeces, but the relative portion increased (13 resp. 35 resp. 39%). An incorporation into body proteins occurred only from N compounds absorbed in the 1st and in the 2nd section. N (or 15N) absorbed in the large intestine was almost quantitatively excreted by urine. The method of digesta exchange between cannulated labelled and unlabelled pigs seems to be a suitable method to estimate absorption and secretion of exogenous and endogenous N portions in various sections of the digestive tract.

Animals↗
PubMed1995

[Energy and nitrogen metabolism of pregnant and lactating sows and suckling piglets. 7. Energy and nitrogen metabolism in suckling piglets].

In 23 litters, each with 10 or 11 piglets, the energy and nitrogen metabolism was measured on base of 218 body analyses in suckling piglets and on base of 96 total metabolism experiments in early weaned piglets, combined with 134 body analyses. The studies were carried out as part of a complex experimental program for the factorial derivation of energy and protein requirement of piglets and for measuring the milk production of lactating sows. The energy maintenance requirement of suckling piglets (sow's milk nutrition, I) and of early weaned piglets (sow's milk replacement on the basis of cow's milk, II) amounted to 468 (I) and 451 kJ (II) metabolizable energy per kg LW0.75 . d, the utilization of of metabolizable energy for energy deposition to 70(I) and 72% (II). With mean live weight gains (LWG) of 161 and 162 g per animal and day the cost per kg LWG amounted to 19.9 and 20.4 MJ gross energy, 19.3 and 19.4 MJ metabolizable energy as well as 14.4 and 14.2 MJ net energy-fat in suckling and early weaned piglets resp. The mean energy content of the LWG amounted to 8.9 (I) and to 7.9 MJ/kg (II).

Animals↗
PubMed1975

Protein requirements of men in a hot climate: decreased urinary nitrogen losses concomitant with increased sweat nitrogen losses during exposure to high environmental temperature.

In two separate experiments 8 healthy young men were given an egg-milk formula at a level of 0.7 g protein/kg per day, and were exposed to high environmental temperature (34--37 C, 7 hours daily) or cool temperature (21--26 C, all day), alternately. In the first experiment a 16-day hot period was followed by a 20-day cool period and finally by a 20-day hot period. Daily urinary nitrogen (N) loss of the last 8 days of cool period, 82.2 mg/kg, was significantly higher than that of the last 8 days of the 20-day hot period 69.7 mg/kg. Daily skin N loss was significantly lower during the last 8 days of the cool period (3.5 mg/kg) than during the last 8 days of the 20-day hot period (11.9 mg/kg). Urinary N and skin N lossess were negatively correlated (r equal to -0.905) in these periods. In the second experiment a 28 day hot period was followed by a 20-day cool period. Skin N loss diminished from 12.3 mg/kg daily during the last 12 days of the 28-day hot period to 4.1 mg/kg during the last 12-days of the cool period. At the same time, urinary N loss increased significantly from 81.4 mg/kg during the 28-day hot period to 95.2 mg/kg during a cool period. Urinary N and skin N losses were again negatively correlated (r equal to -0.620) during these periods. Results of these studies indicate that when skin N loss increases during high temperature, urinary N loss decreases gradually, but total N loss does not increase.

Adult↗
PubMed1978

Effect of fiber from fruits and vegetables on metabolic responses of human subjects I. Bowel transit time, number of defecations, fecal weight, urinary excretions of energy and nitrogen and apparent digestibilities of energy, nitrogen, and fat.

Twelve men 37 to 58 years of age consumed two diets for a period of 26 days each in a cross-over design. The high fiber diet contained fruits and vegetables and the lower fiber diet contained fruit and vegetable juices. Neither diet contained whole grain cereals or nuts. Some nutrients were added to the low fiber diet in order to make the diets equivalent insofar as possible in all respects except fiber. The inclusion of fruits and vegetables in the diet decreased bowel transit time, increased fecal weight, increased number of defecations, increased fecal excretions and decreased apparent digestibilities of energy, nitrogen, and fat. Six of the 12 subjects had diastolic blood pressure of 80 or more when consuming the low fiber diet. The diastolic blood pressures of these six men were significantly lower when the high fiber diet was consumed.

Adult↗
PubMed1985

Urine nitrogen as an independent validatory measure of dietary intake: a study of nitrogen balance in individuals consuming their normal diet.

In order to determine the value of 24 h urine nitrogen (N) excretion as a way of validating dietary methods of measuring protein intake in individuals, daily N intake and excretion has been measured in eight healthy subjects while consuming their usual, varying, diets for 28 days. Daily duplicates of all food eaten were obtained and consecutive 24 h collections of urine and feces were made throughout and analyzed for N by the Kjeldahl method. The completeness of the 24 h urine collections was verified by the use of PABA and of feces by radiopaque pellets. N losses in blood and from the skin were measured. The within person variation in dietary intake ranged from 14 to 26% (coefficient of variation, CV) while urine N was more constant, varying from 11 to 18% (CV) within individuals. In these subjects eight 24 h urine collections, verified for their completeness, were sufficient to estimate dietary N intake to within 81 +/- 5% (SD) as assessed by 18 day dietary records.

Adult↗
PubMed2003

Vertical leaf nitrogen distribution in relation to nitrogen status in grassland plants.

Vertical gradients of leaf nitrogen (N) per unit leaf area (NLA) are viewed as plastic responses that optimize N utilization with respect to carbon assimilation. However, it has been shown that plant species, sowing density and N availability affect the steepness of the NLA gradient relative to the photon flux density (PFD) gradient. This paper tests the hypothesis that such variation is related to the N status of the plant. The N status was analysed using the concept of the critical N concentration (Ncrit) in which shoot N per unit dry mass (NSM) decreases with shoot mass, and a negative deviation of actual NSM from Ncrit indicates N shortage in the plant. The hypothesis was tested with contrasting grassland species Medicago sativa, Dactylis glomerata and Taraxacum officinale by varying PFD and N availability, plant density and hierarchical positions of individuals within stands. Combinations of all treatments showed a general negative correlation between the N allocation coefficient (i.e. the slope of the NLA-PFD relationship) and NSM for all three species. Thus, NLA, relative to PFD, gradients became steeper with increasing shoot mass and increasing N shortage in the plant. These data are consistent with the view that internal N availability is an important factor in modifying the NLA gradient.

Biomass↗
PubMed1975

Labile nitrogen reserves in the ruminant. Metabolic changes in growing cattle employing a nitrogen depletion-repletion treatment.

A metabolism study was conducted in which eight growing steers were subjected to a nitrogen (N) depletion-repletion regime. Three consecutive time periods were used to standardize, to deplete, and to replete body N. Diets fed in the respective periods provided by analysis 6 and 16% protein equivalent, respectively, from corn gluten or urea. Metabolic parameters were monitored during weeks 3 and 5 of standardization, weeks 1, 3, and 5 of depletion, and weeks 1 through 7 of repletion. Growth-rate trends started to deviate downward from linearity during the last 2 weeks of depletion; a trend that was not reversed until week 3 of repletion. Apparently digested N was defined by regression equations in which truly digested N was 94 and 83% of ingested N and metabolic fecal N totaled 0.64 and 0.48 g N/100 g ingested dry matter for corn gluten and urea N, respectively. The relationship between total urinary N losses and truly digested N was determined in which biological value equaled 60 and endogenous urinary N losses totaled 0.34 g N/kg0.60/day (equivalent to 0.040 g N/kg/day). Retained N decreased from 1.09 g during standardization to 0.16 g/kg0.60/day after 1 week of depletion. A subsequent improvement in retained N to 0.36 g in week 3 was followed by a decrease to 0.19 g/kg0.60/day after week 5 of depletion. In repletion, lowest and highest retained N occurred during weeks 1 and 4. Changes in retained N were produced by changes in urinary urea N excretion. Ammonia N accounted for 20, 21, and 24% of the total urinary N voided during standardization, depletion, and repletion. Except for urinary urea N losses that were greater and inversely related to fecal losses in urea-fed steers, dietary N source did not influence the excretion of ammonia, creatinine, or residual N.

Ammonia↗
PubMed1975

Labile nitrogen reserves and plasma nitrogen fractions in growing cattle.

The existence and magnitude of labile nitrogen (N) reserves were studied in growing cattle using a dietary N depletion-repletion technique. Blood parameters and urinary N excretion patterns were monitored. Blood hematocrit (Ht) did not respond to reduced ingested N until after week 3 of depletion at which time it began to fall. About 3 weeks of repletion regime was required before Ht values increased again. Plasma protein and albumin decreased from 6.05 and 2.70 g during standardization to 5.44 and 2.44 g/100 ml after 5 weeks of depletion and did not approach predepletion levels until week 6 of repletion. Plasma urea N decreased from 16 mg in standardization to 0.08 mg/100 ml in depletion and required 3 weeks of repletion treatment to attain a peak of 18 mg/100 ml. Labile N reserves were determined by integrating the areas from total urinary N excretion curves obtained during depletion and repletion periods. On a live body weight basis labile N represented 5.6% of total body N. When computed on an empty body weight basis (does not include weight of gastrointestinal tract), labile N totalled 6.0%. The magnitude of labile N stroes as a percentage of total body N was 44% greater in steers with a mean body weight of 280 kg compared with animals weighing 144 kg.

Animals↗
PubMed1980

Protein requirements of normal infants at the age of about 1 year: maintenance nitrogen requirements and obligatory nitrogen losses.

With 34 normal, healthy male infants aged 9-17 months, a total of 61 nitrogen (N) balance studies was conducted with N intake between 12 and 180 mg/kg/day. By regression analysis, the crude N maintenance requirements, either with whole egg or cow's milk protein, were estimated to be about the same, 106 and 103 mg/kg/day, respectively. The 97.5% confidence limits for the requirements were 128 (egg) and 142 (milk) mg/kg, respectively. Sums of the obligatory urinary and fecal N for the egg and milk protein series were 75 and 71 mg/kg as compared with 76 mg/kg of actually measured figure. Ratio of the maintenance N requirement to the obligatory N loss was 1.4. In another 15 N balance study, for which N intake from milk formulae ranged between 220 and 320 mg/kg/day, the mean apparent N retention was 25% of the intake. Total integumental N losses (skin + hair + nail) of infants fed 217-522 mg N/kg/day amounted to 7.8 +/- 2.9 mg/kg daily. Egg protein had somewhat higher digestibility than cow's milk protein, 92 versus 87%, but has lower biological value, 76 versus 82. Net protein utilization (NPU) estimated from the regression line was about the same for both proteins, 71 and 69, respectively.

Dietary Proteins↗
PubMed2004

Differential responses of growth and nitrogen uptake to organic nitrogen in four gramineous crops.

The capability to utilize different forms of nitrogen (N) by sorghum (Sorghum bicolor), rice (Oryza sativa), maize (Zea mays), and pearl millet (Pennisetum glaucum) was determined in pot experiments. Seedlings were grown for 21 d without N, or with 500 mg N kg(-1) soil applied as ammonium nitrate, rice bran or a mixture of rice bran and straw. No treatment-dependent changes of root length, surface area, and fractal dimension were observed. Shoot growth and N uptake in maize and pearl millet correlated with the inorganic N (ammonium and nitrate) concentration in the soil, suggesting that these species depend upon inorganic N uptake. On the other hand, shoot growth and N uptake patterns in sorghum and rice indicated that these two species could compensate low inorganic N levels in the organic material treatments by taking up organic N (proteins). Analysis of N uptake rates in solution culture experiments confirmed that sorghum and rice roots have higher capabilities to absorb protein N than maize and pearl millet.

Kinetics↗
PubMed2001

Nitrogen forms in bark, wood and foliage of nitrogen-fertilized Pinus sylvestris.

Cycling of soluble non-protein N compounds is thought to be indicative of the N-nutritional status of trees. We determined the major N forms in bark, wood and foliage and estimated the dependence of prevalent N forms on N availability in Pinus sylvestris L. trees from northern Sweden. Trees subjected to severe N limitation and trees that had been fertilized with an average 64 kg N ha(-1) year(-1) for 25 years were analyzed. Bark and wood samples were collected by tangentially cryo-sectioning the trunk into 30-microm thick sections, from the bark to the functional xylem. Soluble amino compounds were extracted from the sections for analysis. Sap samples from twigs were obtained by centrifugation, and bark samples from twigs were obtained by tissue extraction. In both needles and bark, arginine dominated the amino-N pool. Because arginine concentrations in needles increased with N fertilization, arginine dominance of the amino-N pool in needles was higher in N-fertilized trees than in control trees. In bark, N fertilization resulted in a large increase in glutamine concentration, so that glutamine accounted for a larger proportion of the amino-N pool in bark in N-fertilized trees than in control trees. Glutamine dominated the amino-N pool in wood of control trees. Nitrogen fertilization resulted in an increased proportion of arginine in the wood amino-N pool. We conclude that the composition of the amino-N pools in bark, wood and foliage is highly sensitive to N supply. The composition of the amino-N pools can contribute to the regulation of tree N-nutritional status, which is mediated by shoot to root signalling by long-distance transport of amino compounds.

Cycadopsida↗
PubMed2004

Nitrogen storage and its interaction with carbohydrates of young apple trees in response to nitrogen supply.

Bench-grafted 'Fuji/M.26' apple (Malus domestica Borkh.) trees received a constant nitrogen (N) supply (10.7 mM) from bud break to the end of June, and were then fertigated with 0, 5, 10, 15 or 20 mM N in a modified Hoagland's solution for 2 months during the summer. In mid-October, half of the trees fertigated at each N concentration were sprayed twice with 3% urea, whereas the remaining trees served as controls. All trees were harvested after natural leaf fall and were stored at 2 degrees C. Five trees from each of the N treatment combinations were destructively sampled during dormancy to determine the composition of N and total nonstructural carbohydrates (TNC). As the N supply from fertigation increased, amounts of N in both free amino acids and proteins increased, whereas C/N ratios decreased. Foliar urea applications in the fall significantly increased amounts of N in both free amino acids and proteins, but decreased their C/N ratios. Arginine, the most abundant amino acid in both free amino acids and in proteins, accounted for an increasing proportion of N in free amino acids and proteins with increasing N supply from fertigation or foliar urea application. The ratio of protein N to free amino acid N decreased from about 27.1 to 3.2 as N supply from fertigation increased from 0 to 20 mM, and decreased further to 3.0 in response to foliar urea applications in the fall. Concentrations of glucose, fructose, sucrose and TNC decreased as the N supply from fertigation increased, whereas concentrations of sorbitol and starch remained relatively unchanged. Foliar urea applications decreased the concentration of each TNC component and the TNC concentration in each N fertigation treatment. A negative linear relationship was found between carbon in TNC and N in proteins and free amino acids. The sum of carbon in TNC, proteins and free amino acids remained constant in response to N supply from fertigation. However, foliar urea applications decreased the sum of carbon in proteins, free amino acids and TNC because about 21% of the decrease in TNC carbon was not recovered in free amino acids or proteins. Young apple trees store N and carbon dynamically in response to N supply. As N supply increases, an increasing proportion of N is found in the form of free amino acids, which have a low carbon cost, although proteins remain the main form of N storage. Furthermore, part of the carbon from TNC is incorporated into amino acids and proteins, decreasing the carbon stored as TNC and increasing the carbon stored as amino acids and proteins.

Carbohydrate Metabolism↗
PubMed2004

Relationships between light, leaf nitrogen and nitrogen remobilization in the crowns of mature evergreen Quercus glauca trees.

We estimated the amount of nitrogen (N) remobilized from 1-year-old leaves at various positions in the crowns of mature Quercus glauca Thunb. ex Murray trees and related this to the production of new shoots. Leaf N concentration on an area basis (Na) and total N (Nt= Na x lamina area of all leaves on a shoot) were related to photosynthetic photon flux (PPF) on the leaves of current-year and 1-year-old shoots. When new shoots (S02 shoots; flushed in 2002) flushed, only a portion of the leaves on the previous year's shoots (S01 shoots; flushed in 2001) were shed. After the S02 shoots flushed, S01 shoots were defined as 1-year-old shoots (S01* shoots). Both Na and Nt were positively correlated with PPF for S01 shoots, but not for S01* shoots. The fraction of remobilized N (% of the maximum Na in S01 leaves) from remaining leaves was 5-35%, with the fraction size being positively correlated with the number of S02 shoots on an S01* shoot (new shoot number). However, the mean fraction of remobilized N from fallen leaves was 45% and was unrelated to new shoot number. The total amount of N remobilized from both fallen and remaining leaves was 1-20 mg per S01* shoot. Total remobilized N was positively correlated with new shoot number. There was a statistically significant positive relationship between the light-saturated net photosynthetic rate on a leaf area basis (Amax) and Na for both S01* and S02 leaves. However, when we compared leaves with similar Na, Amax of S01* leaves was only half that of S02 leaves, indicating that 1-year-old leaves had lower instantaneous N-use efficiency (Amax per unit Na) than current-year leaves. Ratios of chlorophyll a:b and Rubisco:chlorophyll were lower in S01* leaves than in S02 leaves, indicating that 1-year-old leaves were acclimatized to lower light environments. Thus, in Q. glauca, the N allocation theory (i.e., that N is distributed according to local PPF) applied only to the current-year shoots. Although the amount of foliar N in 1-year-old shoots was not strongly affected by the PPF on 1-year-old leaves, it was affected by interactions with current-year shoots.

Light↗
PubMed2006

Seasonal changes in photosynthesis, nitrogen content and nitrogen partitioning in Lindera umbellata leaves grown in high or low irradiance.

Seasonal changes in photosynthetic capacity, leaf nitrogen (N) content and N partitioning were studied from before leaf maturation (spring) until death (autumn) in high- and low-light-exposed leaves of a deciduous shrub, Lindera umbellata var. membranacea (Maxim.) Momiyama growing in a natural forest in northeast Japan. In spring, light-saturated photosynthetic rate (Pmax) was low despite high leaf N and Rubisco contents, indicating that the photosynthetic apparatus was not yet functionally developed. Rubisco seemed to be only partially active. In summer and autumn, Pmax per unit leaf N increased and changes in Pmax were correlated with changes in leaf N and two photosynthetic components, Rubisco and chlorophyll. Changes in these components paralleled the changes in leaf N. During leaf senescence, about 70% of leaf N was resorbed. Metabolic proteins that accounted for the majority of leaf N in summer were highly degradable and more than sufficient to explain the high N-resorption efficiency. Structural proteins represented only a small part of leaf N and were relatively resistant to degradation and thus contributed little to N resorption. Leaf N partitioning between metabolic and structural proteins determined the amount of retranslocatable N, but did not strictly determine the N content of a dead leaf or N-resorption efficiency.

Carbon Dioxide↗
PubMed1999

Organization and expression of nitrogen-fixation genes in the aerobic nitrogen-fixing unicellular cyanobacterium Synechococcus sp. strain RF-1.

Sixteen nif and 'nif-associated' genes (expressed only under conditions of nitrogen fixation) in Synechococcus sp. strain RF-1 have been cloned and sequenced. All of the nif and nif-associated genes identified in Synechococcus RF-1 were arranged in a continuous cluster spanning approximately 18 kb and containing seven operons. The nifH operon (nifH-nifD-nifK) has been reported previously. nifB, fdxN, nifS, nifU and nifP were found to be located upstream of the nifH operon. nifB-fdxN-nifS-nifU were expressed as an operon. A nifP-like gene was found to be located just upstream of nifB. nifE, nifN, nifX, nifW and the nif-associated hesA, hesB and 'fdx' were found to be located downstream from nifK. The genes located downstream from nifK are arranged nifE-nifN-nifX-orf-nifW-hesA-hesB-'+ ++fdx' and span approximately 7 kb. The function of the ORF situated between nifX and nifW is not known. However, it was identified as a counterpart of ORF-2 in Anabaena sp. strain PCC 7120 based on the deduced amino acid sequence. Northern hybridization and primer extension analysis indicated that the nif and nif-associated genes are organized in nifE-nifN, nifX-orf, nifW-hesA-hesB and 'fdx'-containing operons, respectively. According to the results of this study and previous reports, the genes are expressed in a rhythmic pattern with peaks during the dark phase when the culture is grown in a 12 h light/12 h dark regimen. The rhythm persisted after the culture was transferred to continuous illumination.

Aerobiosis↗
PubMed2001

Economic analysis as a basis for large-scale nitrogen control decisions: reducing nitrogen loads to the Gulf of Mexico.

Economic analysis can be a guide to determining the level of actions taken to reduce nitrogen (N) losses and reduce environmental risk in a cost-effective manner while also allowing consideration of relative costs of controls to various groups. The biophysical science of N control, especially from nonpoint sources such as agriculture, is not certain. Widespread precise data do not exist for a river basin (or often even for a watershed) that couples management practices and other actions to reduce nonpoint N losses with specific delivery from the basin. The causal relationships are clouded by other factors influencing N flows, such as weather, temperature, and soil characteristics. Even when the science is certain, economic analysis has its own sets of uncertainties and simplifying economic assumptions. The economic analysis of the National Hypoxia Assessment provides an example of economic analysis based on less than complete scientific information that can still provide guidance to policy makers about the economic consequences of alternative approaches. One critical value to policy makers comes from bounding the economic magnitude of the consequences of alternative actions. Another value is the identification of impacts outside the sphere of initial concerns. Such analysis can successfully assess relative impacts of different degrees of control of N losses within the basin as well as outside the basin. It can demonstrate the extent to which costs of control of any one action increase with the intensity of application of control.

Agriculture↗
PubMed2001

Prediction of nitrogen responses of corn by soil nitrogen mineralization indicators.

Soil nitrogen mineralization potential (N min) has to be spatially quantified to enable farmers to vary N fertilizer rates, optimize crop yields, and minimize N transfer from soils to the environment. The study objectives were to assess the spatial variability in soil N min potential based on clay and organic matter (OM) contents and the impact of grouping soils using these criteria on corn grain (Zea mays L.) yield, N uptake response curves to N fertilizer, and soil residual N. Four indicators were used: OM content and three equations involving OM and clay content. The study was conducted on a 15-ha field near Montreal, Quebec, Canada. In the spring 2000, soil samples (n = 150) were collected on a 30- x 30-m grid and six rates of N fertilizer (0 to 250 kg N ha(-1)) were applied. Kriged maps of particle size showed areas of clay, clay loam, and fine sandy loam soils. The N min indicators were spatially structured but soil nitrate (NO3-) was not. The N fertilizer rate to reach maximum grain yield (N max), as estimated by a quadratic model, varied among textural classes and Nmin indicators, and ranged from 159 to 250 kg N ha(-1). The proportion of variability (R2) and the standard error of the estimate (SE) varied among textural groups and N min indicators. The R2 ranged from 0.53 to 0.91 and the SE from 0.13 to 1.62. Corn grain N uptake was significantly affected by N fertilizer and the pattern of response differed with soil texture. For the 50 kg N ha(-1) rate, the apparent N min potential (ANM) was significantly larger in the clay loam (122 kg ha(-1)) than in the fine sandy loam (80 kg ha(-1)) or clay (64 kg ha(-1)) soils. The fall soil residual N was not affected by N fertlizer inputs. Textural classes can be used to predict N max. The N min indicators may also assist the variable rate N fertilizer inputs for corn production.

Agriculture↗
PubMed2003

Modeling grain nitrogen accumulation and protein composition to understand the sink/source regulations of nitrogen remobilization for wheat.

A functional explanation for the regulation of grain nitrogen (N) accumulation in cereal by environmental and genetic factors remains elusive. Here, new mechanistic hypotheses of grain N accumulation are proposed and tested for wheat (Triticum aestivum). First, we tested experimentally the hypothesis that grain N accumulation is mostly source regulated. Four contrasting cultivars, in terms of their grain N concentrations and yield potentials, were grown with non-limiting N supply. Grain number per ear was reduced by removing the top part of the ear at anthesis. Reduction in grain number gave a significant increase in N content per grain for all cultivars, showing that grain N accumulation was source regulated. However, on a per ear basis, cultivars with a high grain number fully compensated their N accumulation for reduced grain number at anthesis. Cultivars with a lower grain number did not compensate completely, and grain N per ear was decreased by 16%. Second, new mechanistic hypotheses of the origins of grain N source regulation and its response to environment were tested by simulation. The hypotheses were: (a). The regulation by N sources of grain N accumulation applies only for the storage proteins (i.e. gliadin and glutenin fractions); (b). accumulation of structural and metabolic proteins (i.e. albumin-globulin and amphiphilic fractions) is sink-regulated; and (c). N partitioning between gliadins and glutenins is constant during grain development and unmodified by growing conditions. Comparison of experimental and simulation results of the accumulation of grain protein fractions under wide ranges of N fertilization, temperatures, and irrigation supported these hypotheses.

Acclimatization↗