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Nitrogen in global animal production and management options for improving nitrogen use efficiency.

Animal production systems convert plant protein into animal protein. Depending on animal species, ration and management, between 5% and 45 % of the nitrogen (N) in plant protein is converted to and deposited in animal protein. The other 55%-95% is excreted via urine and feces, and can be used as nutrient source for plant (= often animal feed) production. The estimated global amount of N voided by animals ranges between 80 and 130 Tg N per year, and is as large as or larger than the global annual N fertilizer consumption. Cattle (60%), sheep (12%) and pigs (6%) have the largest share in animal manure N production. The conversion of plant N into animal N is on average more efficient in poultry and pork production than in dairy production, which is higher than in beef and sheep production. However, differences within a type of animal production system can be as large as differences between types of animal production systems, due to large effects of the genetic potential of animals, animal feed and management. The management of animals and animal feed, together with the genetic potential of the animals, are key factors to a high efficiency of conversion of plant protein into animal protein. The efficiency of the conversion of N from animal manure, following application to land, into plant protein ranges between 0 and 60%, while the estimated global mean is about 15%. The other 40%-100% is lost to the wider environment via NH3 volatilization, denitrification, leaching and run-off in pastures or during storage and/or following application of the animal manure to land. On a global scale, only 40%-50% of the amount of N voided is collected in barns, stables and paddocks, and only half of this amount is recycled to crop land. The N losses from animal manure collected in barns, stables and paddocks depend on the animal manure management system. Relative large losses occur in confined animal feeding operations, as these often lack the land base to utilize the N from animal manure effectively. Losses will be relatively low when all manure are collected rapidly in water-tight and covered basins, and when they are subsequently applied to the land in proper amounts and at the proper time, and using the proper method (low-emission techniques). There is opportunity for improving the N conversion in animal production systems by improving the genetic production potential of the herd, the composition of the animal feed, and the management of the animal manure. Coupling of crop and animal production systems, at least at a regional scale, is one way to high N use efficiency in the whole system. Clustering of confined animal production systems with other intensive agricultural production systems on the basis of concepts from industrial ecology with manure processing is another possible way to improve N use efficiency.

Animal Feed↗

Assessment of the efficiency of nitrogen utilization in the infant cebus monkey (Cebus albifrons) by nitrogen balance.

Nitrogen (N) balance and growth were utilized to assess the efficiency of N utilization in the infant cebus monkey (Cebus albifrons). The efficiency of N utilization as calculated from N balance data was 35%. The efficiency of N utilization for growth was 37% as determined by weight change over a 28-day trial and by body composition data from the literature. These results indicate, therefore, that growth and N balance are comparable indicators of N utilization in these primates.

Animals↗

Nitrogen dioxide and respiratory illness in children. Part IV: Effects of housing and meteorologic factors on indoor nitrogen dioxide concentrations.

In a prospective study of infants' exposure to nitrogen dioxide (NO2)* and respiratory illness, NO2 concentrations were measured in more than 1,400 homes in Albequerque, NM, From January 1988 through June 1991 (Health Effects Institute Research Report Number 58, Parts I, II and III). This report characterizes the variability in indoor NO2 concentrations across seasons and years, and identifies factors associated with variation in concentrations between homes and across seasons. In regression analyses of winter data, NO2 levels in the infants' bedrooms were predominately determined by the presence of gas cooking ranges with continuously burning pilot lights, the presence of wall or floor furnaces, the use of the stove for space heating, and the square footage of the living space. These findings are consistent with previously published analysis of data from homes in other U.S. cities. Relatively small differences in seasonal NO2 levels were observed across years. The correlation coefficient (r) of bedroom NO2 levels obtained in the same homes was 0.66 over two winters and 0.48 over two summers. For homes that had gas cooking ranges with continuously burning pilot lights, the NO2 bedroom concentrations differed, on average, less than 5 parts per billion (ppb) across winters. These differences were hypothesized to be caused by differences in the use of indoor NO2 sources, ventilation, and ambient (outdoor) NO2 levels. We were, however, unable to demonstrate an association between year-to-year differences in seasonal indoor NO2 concentrations and reported use of cooking range, furnace, or heater, or ambient NO2 levels, or temperature.

Air Pollution, Indoor↗

Nucleophile assistance of electron-transfer reactions between nitrogen dioxide and chlorine dioxide concurrent with the nitrogen dioxide disproportionation.

The reaction of chlorine dioxide with excess NO(2)(-) to form ClO(2)(-) and NO(3)(-) in the presence of a large concentration of ClO(2)(-) is followed via stopped-flow spectroscopy. Concentrations are set to establish a preequilibrium among ClO(2), NO(2)(-), ClO(2)(-), and an intermediate, NO(2). Studies are conducted at pH 12.0 to avoid complications due to the ClO(2)(-)/NO(2)(-) reaction. These conditions enable the kinetic study of the ClO(2) reaction with nitrogen dioxide as well as the NO(2) disproportionation reaction. The rate of the NO(2)/ClO(2) electron-transfer reaction is accelerated by different nucleophiles (NO(2)(-) > Br(-) > OH(-) > CO(3)(2-) > PO(4)(3-) > ClO(2)(-) > H(2)O). The third-order rate constants for the nucleophile-assisted reactions between NO(2) and ClO(2) (k(Nu), M(-2) s(-1)) at 25.0 degrees C vary from 4.4 x 10(6) for NO(2-) to 2.0 x 10(3) when H(2)O is the nucleophile. The nucleophile is found to associate with NO(2) and not with ClO(2) in the rate-determining step to give NuNO(2)(+) + ClO(2)(-). The concurrent NO(2) disproportionation reaction exhibits no nucleophilic effect and has a rate constant of 4.8 x 10(7) M(-1) s(-1). The ClO(2)/NO(2)/nucleophile reaction is another example of a system that exhibits general nucleophilic acceleration of electron transfer. This system also represents an alternative way to study the rate of NO(2) disproportionation.

Journal Article↗

Activity of nitrogen-containing and non-nitrogen-containing bisphosphonates on tumor cell lines.

We synthesized and tested three series of bisphosphonates for their activity in inhibiting the growth of three human tumor cell lines: MCF-7 (breast), NCI-H460 (lung), and SF-268 (CNS). The first series of compounds consisted of 49 nitrogen-containing bisphosphonates, the most active species being a tetrakispivaloyloxymethyl (POM) ester, having an (average) IC(50) of 6.8 microM. The second series of compounds consisted of nine terphenylbisphosphonates, the most active species also being a POM ester, having an IC(50) of 2.2 microM. The third series of compounds consisted of seven halogen or cyanophenylbisphosphonates, the most active species again being a POM ester, having an IC(50) of 500 nM. Taken together, these results are of interest because they show that bisphosphonate esters can have potent activity against a variety of tumor cell lines, with the most active terphenyl- and halophenyl-containing species having IC(50) values approximately 10-40x lower than the most potent commercially available bisphosphonates.

Antineoplastic Agents↗

Preparation of nitrogen-containing pi-deficient heteroaromatic Grignard reagents: oxidative magnesiation of nitrogen-containing pi-deficient halogenoheteroaromatics using active magnesium.

The oxidative magnesiation of nitrogen-containing pi-deficient halogenoheteroaromatics using active magnesium was accomplished. Both magnesiation followed by addition of a carbonyl compound (Grignard reaction) and magnesiation in the presence of a carbonyl compound (Barbier reaction) were carried out to afford the corresponding product. Especially, the latter method enabled fused halogenodiazines such as 4-chloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine or 2-chloroquinoxaline to magnesiate at a mild temperature (-20 to 30 degrees C).

Journal Article↗

Impacts of water and nitrogen supplies on the physiology, leaf demography and nitrogen dynamics of Betula pendula.

We determined the response of Betula pendula Roth. trees to a restricted water supply, and quantified the interactions between tree N and water status on leaf demography and internal N cycling. In April 1993, 3-year-old trees were planted in sand culture and four treatments applied: high-N supply (56 mg tree(-1) week(-1)) with either 2 dm(3) water week(-1) (HN+) or 0.9 dm(3) water week(-1) (HN-), or low-N supply (14 mg tree(-1) week(-1)) with 2 dm(3) (LN+) or 0.9 dm(3) (LN-) water week(-1). Until 1994, the N supplied to trees was enriched with (15)N to 5.4 atom %. During 1993, there were few differences in the growth or leaf demography of trees in the LN+ and LN- treatments, but the high-N treatment increased tree growth. Leaf mass and area were initially similar in trees in the HN+ and HN- treatments, but the trees in the HN- treatment had a smaller root system. Net assimilation rate under saturating light was higher in trees in the HN+ treatment than in trees in the LN+ treatment. There was an N x water supply interaction as a result of trees in the HN- treatment closing their stomata by the beginning of August. However, there was no difference in gas exchange characteristics of leaves in the LN+ and LN- treatments. Although leaf senescence and abscission started in the HN- treatment by mid-August and continued for about 90 days, whereas leaf abscission in the other treatments did not start until the beginning of October and only lasted 25-30 days, the trees in the HN+ and HN- treatments remobilized similar amounts of (15)N for leaf growth in the spring of 1994. There were no differences in predawn water potential among treatments and no evidence of osmotic adjustment. We conclude that B. pendula trees avoid rather than tolerate drought. The interaction between the effects of nitrogen and water supplies on leaf demography and internal cycling of N are discussed.

Journal Article↗

Kinetics of nitrogen uptake by Populus tremuloides in relation to atmospheric CO(2) and soil nitrogen availability.

Sustained increases in plant production in response to elevated atmospheric carbon dioxide (CO(2)) concentration may be constrained by the availability of soil nitrogen (N). However, it is possible that plants will respond to N limitation at elevated CO(2) concentration by increasing the specific N uptake capacity of their roots. To explore this possibility, we examined the kinetics of (15)NH(4) (+) and (15)NO(3) (-) uptake by excised roots of Populus tremuloides Michx. grown in ambient and twice-ambient CO(2) concentrations, and in soils of low- and high-N availability. Elevated CO(2) concentration had no effect on either NH(4) (+) or NO(3) (-) uptake, whereas high-N availability decreased the capacity of roots to take up both NH(4) (+) and NO(3) (-). The maximal rate of NH(4) (+) uptake decreased from 12 to 8 &mgr;mol g(-1) h(-1), and K(m) increased from 49 to 162 &mgr;mol l(-1), from low to high soil N availability.Because NO(3) (-) uptake exhibited mixedkinetics over the concentration range we used (10-500 &mgr;mol l( -1)), it was not possible to calculate V(max) and K(m). Instead, we used an uptake rate of 100 &mgr;mol g(-1) h(-1) as our metric of NO(3) (-) uptake capacity, which averaged 0.45 and 0.23 &mgr;mol g(-1) h(-1) at low- and high-N availability, respectively. The proximal mechanisms for decreased N uptake capacity at high-N availability appeared to be an increase in fine-root carbohydrate status and a decrease in fine-root N concentration. Both NH(4) (+) and NO(3) (-) uptake were inversely related to fine-root N concentration, and positively related to fine-root total nonstructural carbohydrate concentration. We conclude that soil N availability, through its effects on fine-root N and carbohydrate status, has a much greater influence on the specific uptake capacity of P. tremuloides fine roots than elevated atmospheric CO(2). In elevated atmospheric CO(2), changes in N acquisition by P. tremuloides appeared to be driven by changes in root architecture and biomass, rather than by changes in the amount or activity of N-uptake enzymes.

Journal Article↗

Utilization of Previously Accumulated and Concurrently Absorbed Nitrogen during Reproductive Growth in Maize : Influence of Prolificacy and Nitrogen Source.

A prolific maize (Zea mays L.) genotype was grown to physiological maturity under greenhouse conditions to examine the effects of reproductive sink demand on (a) the remobilization of N accumulated during vegetative growth, and (b) the partitioning of N accumulated concurrent with ear development. One- and two-eared plants were treated with either a NO(3) (-) or NH(4) (+) source of (15)N-labeled N during reproductive growth. Plants with two ears enhanced grain production, N remobilization from the stalk and roots, and N translocation to the grain from concurrently assimilated N. But, remobilization of leaf-N was unaffected by ear number. In addition, N uptake and total dry matter accumulation during the reproductive period were also unaffected, although P uptake was greater in the two-eared plants. Less than 15% of the total K(+) uptake was accumulated after silking while during this time more than 40% of the total N and more than 50% of the total P were absorbed. The data also indicate that with NO(3) (-) nutrition, internal recirculation of K(+) between shoots and roots may play a prominent role in the transport of nitrogenous solutes during grain development. N source had no effect on dry matter production and N uptake of both one- and two-eared plants. However, slightly greater partitioning of labeled-N from the NH(4) (+) source to the grain was observed in the two-eared plants.

Journal Article↗

The Nitrogen Use Efficiency of C(3) and C(4) Plants: II. Leaf Nitrogen Effects on the Gas Exchange Characteristics of Chenopodium album (L.) and Amaranthus retroflexus (L.).

The effect of leaf nitrogen (N) on the photosynthetic capacity and the light and temperature response of photosynthesis was studied in the ecologically similar annuals Chenopodium album (C(3)) and Amaranthus retroflexus (C(4)). Photosynthesis was linearly dependent on leaf N per unit area (N(a)) in both species. A. retroflexus exhibited a greater dependence of photosynthesis on N(a) than C. album and at any given N(a), it had a greater light saturated photosynthesis rate than C. album. The difference between the species became larger as N(a) increased. These results demonstrate a greater photosynthetic N use efficiency in A. retroflexus than C. album. However, at a given applied N level, C. album allocated more N to a unit of leaf area so that photosynthetic rates were similar in the two species. Leaf conductance to water vapor increased linearly with N(a) in both species, but at a given photosynthetic rate, leaf conductance was higher in C. album. Thus, A. retroflexus had a greater water use efficiency than C. album. Water use efficiency was independent of leaf N in C. album, but declined with decreasing N in A. retroflexus.

Journal Article↗

The Nitrogen Use Efficiency of C(3) and C(4) Plants : III. Leaf Nitrogen Effects on the Activity of Carboxylating Enzymes in Chenopodium album (L.) and Amaranthus retroflexus (L.).

The relationships between leaf nitrogen content per unit area (N(a)) and (a) the initial slope of the photosynthetic CO(2) response curve, (b) activity and amount of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) and phosphoenolpyruvate carboxylase (PEPC), and (c) chlorophyll content were studied in the ecologically similar weeds Chenopodium album (C(3)) and Amaranthus retroflexus (C(4)). In both species, all parameters were linearly dependent upon leaf N(a). The dependence of the initial slope of the CO(2) response of photosynthesis on N(a) was four times greater in A. retroflexus than in C. album. At equivalent leaf N(a) contents, C. album had 1.5 to 2.6 times more CO(2) saturated Rubisco activity than A. retroflexus. At equal assimilation capacities, C. album had four times the Rubisco activity as A. retroflexus. In A. retroflexus, a one to one ratio between Rubisco activity and photosynthesis was observed, whereas in C. album, the CO(2) saturated Rubisco activity was three to four times the corresponding photosynthetic rate. The ratio of PEPC to Rubisco activity in A. retroflexus ranged from four at low N(a) to seven at high N(a). The fraction of organic N invested in carboxylation enzymes increased with increased N(a) in both species. The fraction of N invested in Rubisco ranged from 10 to 27% in C. album. In A. retroflexus, the fraction of N(a) invested in Rubisco ranged from 5 to 9% and the fraction invested in PEPC ranged from 2 to 5%.

Journal Article↗