In Brazil, high-yield soybean [Glycine Max (L). Merrill] – corn (Zea mays L.) double cropping system might be nitrogen (N)-limited and additional N fertilization can be beneficial. Early application of N in soybean reduces the symbiotic N fixation (SNF) efficiency and/or establishment. One alternative to avoid SNF impairment is to apply N between the beginning pod (R3) and seed-fill (R5) stages through the use of controlled release fertilizers. In this study, N was applied at 50 kg ha−1 as common urea (CU) or controlled release urea (CRU) with different lag periods until N release starts (30 days, 60 days, or 1:1 mix of both lag times) in a randomized complete blocks design with six treatments and four replicates under tropical and subtropical conditions. CU was applied after soybean emergence (VE) or at the beginning pod (R3), and CRU only at VE. Using urea labeled with 15N isotope, we analyzed the N source used by soybean (fertilizer, soil, or SNF) and SNF parameters. On average, CRU – 30 days, CRU – 1:1 mix (30 + 60 days) and CU applied at the R3 stage increased grain yield by 9.2% (354 kg ha−1) compared to the control. N derived from all fertilizer treatment were almost 35 kg N ha−1, a high N recovery efficiency of 68%. The SNF was not impaired by CU and CRU and accounted for 71% (220 kg N ha−1) of total N uptake. In the conditions of the experiments, fertilization of 50 kg N ha−1 as CRU was shown to be effective to supply N in late soybean demand (R3 stage), increasing yield without damaging the SNF process in high-yield environments.

Durum wheat culture requires a high level of N fertilization to achieve ideal protein concentration for semolina and pasta quality, contributing to N losses. Optimizing plant N use efficiency could improve agro-environmental balance. In the current paper, we studied the impact of the marine (DPI4913) and fungal (AF086) extracts (biostimulants) applied on leaves on growth, N absorption and N fluxes in durum wheat in field and greenhouse experiments. In the field, 15NO3− and 15NH4+ were injected into the soil; in the greenhouse, N of the flag-leaf was labelled with 15NH4+. Flag-leaf senescence was studied by estimating leaf chlorophyll concentration. In greenhouse, biostimulants increased grain yield, total N in plant and the proportion of plant N in ears. When water was limited in greenhouse experiment, neither biostimulants had any effect. In the field, DPI4913 increased soil fertilizer-derived 15N accumulated in grains. In the greenhouse, biostimulants increased the proportion of 15N applied to the flag-leaf recovered in grains and accelerated leaf senescence. For plants treated with biostimulants, flag-leaf N resorption increased. Biostimulants had a larger positive impact on mineral N root uptake than on N remobilization. In conclusion, our study has shown that DPI4913 and AF086 can promote plant growth and grain yield, N uptake and remobilization. Thus, these biostimulants could be used to optimize durum wheat N fertilization and contribute to reduced N losses.

Protein turnover is an energy-consuming process that is essential for ensuring the maintenance of living organisms. Gold standard methods for whole-body protein turnover (WBPT) measurement have inherent drawbacks precluding their generalization for large farm animals and use during long periods. Here, we proposed a non-invasive proxy for the WBPT over a long period of time and in a large number of beef cattle. The proxy is based on the rate at which urine-N and plasma proteins are progressively depleted in terms of 15N after a slight decrease in the isotopic N composition of the diet (i.e. diet switch). We aimed to test the ability of this proxy to adequately discriminate the WBPT of 36 growing-fattening young bulls assigned to different dietary treatments known to impact the WBPT rate, with different protein contents (normal v. high) and amino acid profiles (balanced v. unbalanced in methionine). The 15N depletion rate found in plasma proteins represented their fractional synthesis rate, whereas the slow depletion rate found in urine was interpreted as a proxy of the WBPT. The proxy tested in urine suggested different WBPT values between the normal- and high-protein diets but not between the balanced and unbalanced methionine diets. In contrast, the proxy tested in plasma indicated that both dietary conditions affected the fractional synthesis rate of plasma proteins. We considered that the rate at which urine is progressively 15N-depleted following an isotopic diet switch could be proposed as a non-invasive proxy of the WBPT rate in large farm animals.

It is difficult to separate an age-dependent fall in nitrogen use efficiency (NUE; N balance/N intake) in growing ruminants from a progressively decrease in animal protein requirements over time. This study examined the effect of dietary protein content on N partitioning, digestibility and N isotopic discrimination between the animal and its diet (Δ15Nanimal-diet) evaluated at two different fattening periods (early v. late). Twenty-four male Romane lambs (age: 19 ± 4.0 days; BW: 8.3 ± 1.39 kg) were equally allocated to three dietary CP treatments (15%, 17% and 20% CP on a DM basis). Lambs were reared with their mothers until weaning, thereafter housed in individual pens until slaughter (45 kg BW). During the post-weaning period, lambs were allocated twice (early fattening (30 days post-weaning) and late fattening (60 days post-weaning)) to metabolic cages for digestibility and N balance study. When diet CP content increased, the average daily gain of lambs increased (P < 0.05) while the age at slaughter decreased (P = 0.01), but no effect was observed on feed efficiency (P > 0.10). Diet CP content had limited effect on lamb carcass traits. Higher fibre digestibility was observed at the early v. late fattening period (P < 0.001). The N intake and the urinary N excretion increased when diet CP content increased (P < 0.001) and when shifting from early to late fattening period (P < 0.001). Faecal N excretion (P = 0.14) and N balance (P > 0.10) were not affected by diet CP content. Nitrogen digestibility increased (P < 0.001) as the diet CP content increased and on average it was greater at late v. early fattening period (P = 0.02). The NUE decreased (P = 0.001) as the diet CP content increased and as the lamb became older (P < 0.001). However, the age-dependent fall in NUE observed was lower at high v. low dietary CP content (CP × age interaction; P = 0.04). The Δ15Nanimal-diet was positively correlated (P < 0.05) with N intake (r = 0.59), excretion of faecal N (r = 0.41), urinary N (r = 0.69) and total manure N (r = 0.64), while negatively correlated with NUE (r = −0.57). Overall, the experiment showed NUE was lower in older lambs and when lambs were fed high diet CP content, and that Δ15Nanimal-diet was a useful indicator not only for NUE but also for urinary N excretion, which is a major environmental pollution factor on farm.

The objective of this study was to evaluate the effects of oak tannin extract (OTE) added in forage before ensiling on dairy cows fed at 92% of their digestible protein requirements. Six multiparous lactating Holstein cows were used in a crossover design (two treatments × two periods). The control treatment (CON) was based on a diet including 50% of grass silage, whereas the experimental treatment (TAN) included grass silage sprayed with OTE (26 g/kg DM) just before baling. Milk yield (on average 24 kg fat protein corrected milk per day) was not affected, but both milk and rumen fatty acids profiles were impacted by OTE. Nitrogen intake (415 g N per cow per day) and nitrogen use efficiency (NUE; 0.25 on average) were not affected, but a shift from urine (−8% of N intake relatively to control, P = 0.06) to faecal N (+5%; P = 0.004) was observed with the TAN diet (P ≤ 0.05). Nitrogen apparent digestibility was thus reduced for TAN (−3%; P ≤ 0.05). The effect of OTE on ruminal and milk FA profiles suggests an impact on rumen microbiota. Nitrogen isotopic discrimination between animal proteins and diet (Δ15N) was evaluated as a proxy for NUE. While no differences in NUE were observed across diets, a lower Δ15N of plasma proteins was found when comparing TAN v. CON diets. This finding supports the concept that Δ15N would mainly sign the N partitioning at the metabolic level rather than the overall NUE, with the latter also being impacted by digestive processes. Our results agree with a N shift from urine to faeces, and this strategy can thus be adopted to decrease the environmental impact of ruminant protein feeding.

Animal proteins are naturally 15N enriched relative to the diet and the extent of this difference (Δ15Nanimal-diet or N isotopic fractionation) has been correlated to N use efficiency (NUE; N gain or milk N yield/N intake) in some recent ruminant studies. The present study used meta-analysis to investigate whether Δ15Nanimal-diet can be used as a predictor of NUE across a range of dietary conditions, particularly at the level of between-animal variation. An additional objective was to identify variables related to N partitioning explaining the link between NUE and Δ15Nanimal-diet. Individual values from eight publications reporting both NUE and Δ15Nanimal-diet for domestic ruminants were used to create a database comprising 11 experimental studies, 41 treatments and individual animal values for NUE (n=226) and Δ15Nanimal-diet (n=291). Data were analyzed by mixed-effect regression analysis taking into account experimental factors as random effects on both the intercept and slope of the model. Diets were characterized according to the INRA feeding system in terms of N utilization at the rumen, digestive and metabolic levels. These variables were used in a partial least squares regression analysis to predict separately NUE and Δ15Nanimal-diet variation, with the objective of identifying common variables linking NUE and Δ15Nanimal-diet. For individuals reared under similar conditions (within-study) and at the same time (within-period), the variance of NUE and Δ15Nanimal-diet not explained by dietary treatments (i.e. between-animal variation plus experimental error) was 35% and 55%, respectively. Mixed-effect regression analysis conducted with treatment means showed that Δ15Nanimal-diet was significantly and negatively correlated to NUE variation across diets (NUE=0.415 −0.055×Δ15Nanimal-diet). When using individual values and taking into account the random effects of study, period and diet, the relationship was also significant (NUE=0.358 −0.035×Δ15Nanimal-diet). However, there may be a biased prediction for animals close to zero, or in negative, N balance. When using a novel statistical approach, attempting to regress between-animal variation in NUE on between-animal variation in Δ15Nanimal-diet (without the influence of experimental factors), the negative relationship was still significant, highlighting the ability of Δ15Nanimal-diet to capture individual variability. Among the studied variables related to N utilization, those concerning N efficiency use at the metabolic level contributed most to predict both Δ15Nanimal-diet and NUE variation, with rumen fermentation and digestion contributing to a lesser extent. This study confirmed that on average Δ15Nanimal-diet can predict NUE variation across diets and across individuals reared under similar conditions.

Seed dispersal is a crucial process in most plant invasions, but is notoriously difficult to study. One technique to identify the maternal source of dispersed seeds and newly established seedlings is labeling with a stable isotope. We tested whether foliar application of 15N-labeled urea would result in sufficient 15N enrichment to discriminate among seeds and seedlings grown from those seeds of the invasive shrub Lonicera maackii (Amur honeysuckle). We subjected mature L. maackii to all combinations of three concentrations of 15N-labeled urea (0.025 g L−1 [0.003 oz gal−1], 0.20 g L−1, and a 0 g L−1 control) and three temporal treatments (one application in August, one application in September, and five applications spaced every three weeks from June through August). Seeds were collected September to November; some of these were analyzed for %15N and others allowed to germinate and grow into seedlings under two treatments (in potting mix in greenhouse and in woodlot soil outdoors). Seedlings were harvested midway through the next growing season. We found that seeds from plants subjected to the three different concentrations had significantly different %15N levels, and there was a significant interaction between concentration and temporal treatment: the highest seed %15N levels were from plants sprayed five times with 15N-labeled urea, and the second highest from plants sprayed once in September. Similar patterns in %15N levels were found in seedlings, except that those from the 0.025 g L−1 spray treatment were only distinguishable from controls for seedlings grown outdoors in woodlot soil. These findings demonstrate that a single foliar application of 15N in early September is sufficient to label both seeds and seedlings of this invasive shrub, enabling one to identify the source of field-collected seeds or seedlings. This provides a tool for studying patterns and processes in seed dispersal of Amur honeysuckle and potentially other invasive plants.

Animal tissues are naturally 15N enriched relative to their diet and the extent of this difference (Δ15Nanimal-diet) has been correlated to the efficiency of N assimilation in different species. The rationale is that transamination and deamination enzymes, involved in amino acid metabolism are likely to preferentially convert amino groups containing 14N over 15N. However, in ruminants the contribution of rumen bacterial metabolism relative to animal tissues metabolism to naturally enrich animal proteins in terms of 15N has been not assessed yet. The objective of this study was to assess the impact of rumen and digestion processes on the relationship between Δ15Nanimal-diet and efficiency of N utilization for milk protein yield (milk N efficiency (MNE); milk N yield/N intake) as well as the relationship between the 15N natural abundance of rumen bacteria and the efficiency of N use at the rumen level. Solid- and liquid-associated rumen bacteria, duodenal digesta, feces and plasma proteins were obtained (n=16) from four lactating Holstein cows fed four different diets formulated at two metabolizable protein supplies (80% v. 110% of protein requirements) crossed by two different dietary energy source (diets rich in starch v. fiber). We measured the isotopic N fractionation between animal and diet (Δ15Nanimal-diet) in these different body pools. The Δ15Nanimal-diet was negatively correlated with MNE when measured in solid-associated rumen bacteria, duodenal digesta, feces and plasma proteins, with the strongest correlation found for the latter. However, our results showed a very weak 15N enrichment of duodenal digesta (Δ15Nduodenal digesta-diet mean value=0.42) compared with that observed in plasma proteins (Δ15Nplasma protein-diet mean value=2.41). These data support the idea that most of the isotopic N fractionation observed in ruminant proteins (Δ15Nplasma protein-diet) has a metabolic origin with very little direct impact of the overall digestion process on the existing relationship between Δ15Nplasma protein-diet and MNE. The 15N natural abundance of rumen bacteria was not related to either rumen N efficiency (microbial N/available N) or digestive N efficiency (metabolizable protein supply/CP intake), but showing a modest positive correlation with rumen ammonia concentration. When using diets not exceeding recommended protein levels, the contribution of rumen bacteria and digestion to the isotopic N fractionation between animal proteins and diet is low. In our conditions, most of the isotopic N fractionation (Δ15Nplasma protein-diet) could have a metabolic origin, but more studies are warranted to confirm this point with different diets and approaches.

Nitrous oxide (N2O) is a potent greenhouse gas and the dominant anthropogenic stratospheric ozone-depleting emission. The tropospheric concentration of N2O continues to increase, with animal production systems constituting the largest anthropogenic source. Stable isotopes of nitrogen (N) provide tools for constraining emission sources and, following the temporal dynamics of N2O, providing additional insight and unequivocal proof of N2O source, production pathways and consumption. The potential for using stable isotopes of N is underutilised. The intent of this article is to provide an overview of what these tools are and demonstrate where and how these tools could be applied to advance the mitigation of N2O emissions from animal production systems. Nitrogen inputs and outputs are dominated by fertiliser and excreta, respectively, both of which are substrates for N2O production. These substrates can be labelled with 15N to enable the substrate-N to be traced and linked to N2O emissions. Thus, the effects of changes to animal production systems to reduce feed-N wastage by animals and fertiliser wastage, aimed at N2O mitigation and/or improved animal or economic performance, can be traced. Further 15N-tracer studies are required to fully understand the dynamics and N2O fluxes associated with excreta, and the biological contribution to these fluxes. These data are also essential for the new generation of 15N models. Recent technique developments in isotopomer science along with stable isotope probing using multiple isotopes also offer exciting capability for addressing the N2O mitigation quest.

We investigated if the commonly used aggregation of organisms into trophic guilds, such as detritivores and predators, in fact represent distinct trophic levels. Soil arthropods of a forest-meadow transect were ascribed a priori to trophic guilds (herbivores, detritivores, predators and necrovores), which are often used as an equivalent to trophic levels. We analysed natural variations in 15N/14N ratios of the animals in order to investigate the trophic similarity of organisms within (a priori defined) trophic guilds. Using trophic guilds as an equivalent to trophic level, the assumed stepwise enrichment of 15N by 3.4‰ per trophic level did not apply to detritivores; they were only enriched in 15N by on average 1.5‰ compared to litter materials. Predators on average were enriched in 15N by 3.5‰ compared to detritivores. Within detritvores and predators δ15N signatures varied markedly, indicating that these trophic guilds are dominated by generalist feeders which form a gradient of organisms feeding on different resources. The results indicate that commonly used trophic guilds, in particular detritivores and predators, do not represent trophic levels but consist of subguilds, i.e. subsets of organisms differing in resource utilization. In particular, in soil and litter food webs where trophic level omnivory is common, the use of distinct trophic levels may be inappropriate. Guilds of species delineated by natural variations of stable isotope ratios are assumed to more adequately represent the structure of litter and soil food webs allowing a more detailed understanding of their functioning.

We used stable isotope analysis (15N/14N) to characterize the trophic relationships of consumer communities of an aquatic food web (a permanent pond) and the adjacent terrestrial food web (secondary dry dipterocarp forest) from a seasonal tropical field site in north-eastern Thailand. In general, isotopic signatures of aquatic vertebrates were higher (δ15N range = 4.51–9.90‰) than those of invertebrates (δ15N range = 1.10–6.00‰). High 15N signatures identified water snakes and swamp eels as top predators in the pond food web. In the terrestrial food web 15N signatures of saprophagous litter invertebrates (diplopods, earthworms), termites, ants and beetle larvae were lower than in those of predatory invertebrates (scolopendrids, scorpions, whip spiders). Predatory terrestrial frogs and caecilians had lower 15N signatures than snakes, indicating that snakes are among the top predators in the terrestrial web. Based on the distribution of isotopic signatures, we estimated five trophic levels for both the aquatic and terrestrial food web. The food chains of a seasonal tropical site studied were rather short, which implies similarities to the structure of temperate food webs.

The origin of post-ruminal purine bases (PB) was studied in 24 growing lambs that were given a pelleted concentrate plus barley straw (C) or whole barley grain plus protein supplement (WB). Six lambs from each treatment were slaughtered at 10 and 30 days post weaning after 15N labelling of microbial nitrogen (N) and PB. Microbial contribution to digesta non-ammonia N (NAN) and PB was lower (P < 0·01) when estimated from duodenal rather than abomasal samples (0·36 v. 0·52 (s.e.d. 0·021) for NAN and 0·47 v. 0·77 (s.e.d. 0·029) for PB) as a result of endogenous contamination. In comparison with 15N, total PB/N led to higher estimates (P < 0·01) of microbial contribution to abomasal NAN in WB treatment (0·62 v. 0·46 s.e.d. 0·049). The difference was removed after correcting for microbial PB, while this effect was not observed with < the C diet, resulting in a marker by diet interaction (P < 0·05). Abomasal PB flow increased (P < 0·1) from 10 to 30 days after weaning mainly due to the higher proportion of microbial PB (0·70 v. 0·81 (s.e.d. 0·047)). Rumen apparent PB degradation did not differ between diets in older lambs, but it was proportionally 0·39 lower for WB treatment (P < 0·05) in younger lambs. When the microbial PB flow was estimated indirectly from labelled microbial N and the PB/N ratio of bacterial extracts the estimates were in agreement with those derived from PB-15N in the WB treatment but resulted in unrealistic values in lambs on diet C. Results suggest that significant proportions of dietary PB can escape rumen degradation which may lead to overestimation of microbial contribution to abomasal NAN when the PB/N ratio is used as marker. The extent of the overestimation is affected by the lamb age and grain processing.

Two-yr-old Scots pine (Pinus sylvestris) seedlings were grown in sand culture for 1 yr with a generous supply of a balanced nutrient solution. Trees were repotted into clean sand in February 1998 and given either a reduced or adequate nutrient supply containing enriched 15N, 41K and 26Mg to label nutrient uptake during spring 1998. Trees doubled their biomass during the experiment. Whole-tree net photosynthesis was reduced by 43% after 95 d in trees that received the lower nutrient supply (P < 0.001), although differences in biomass between the two treatments were less pronounced. Remobilization contributed 83, 82 and 52% of the N, K and Mg, respectively, used to support growth of new tissues in trees that received reduced nutrient supply. Those receiving the higher nutrient supply still obtained 44–59% of nutrients used for spring growth of new tissues from remobilization. Current nutrient supply had no significant effect on the amount of N or Mg remobilized to new tissues but K remobilization was less in trees that received the lower nutrient supply (P = 0.025). The importance of remobilization in young trees and problems associated with quantifying internal cycling of nutrients are discussed.

The natural abundance of 13C and 15N was measured in basidiocarps of at least 115 species in 88 genera of ectomycorrhizal, wood-decomposing and litter-decomposing fungi from Japan and Malaysia. The natural abundance of 13C and 15N was also measured in leaves, litter, soil and wood from three different sites. 15N and 13C were enriched in ectomycorrhizal and wood-decomposing fungi, respectively, relative to their substrates. Ectomycorrhizal and wood-decomposing fungi could be distinguished on the basis of their δ13C and δ15N signatures. Although there was high variability in the isotopic composition of fungi, the following isotope- enrichment factors (ε, mean±SD) of the fungi relative to substrates were observed:

εectomycorrhizal fungi/litter = 6.1±0.4‰ 15N

εectomycorrhizal fungi/wood = 1.4±0.8‰ 13C

εwood-decomposing fungi/wood = −0.6±0.7‰ 15N

εwood-decomposing fungi/wood = 3.5±0.9‰ 13C

The basis of isotope fractionation in C metabolism from wood to wood-decomposing fungus is discussed.

To investigate nitrogen assimilation in Lolium perenne L. colonized by the arbuscular mycorrhizal (AM) fungus Glomus fasciculatum (Thax. sensu Gerd.), nitrate uptake, key enzyme activities, and 15N incorporation into free amino acids were measured. After a 4-h labelling period with [15N]nitrate, 15N content was higher in roots and shoots of AM-plants than in those of control plants. Glutamine synthetase (GS) and nitrate reductase (NR) activities were increased in shoots of AM-plants, but not in roots. More label was incorporated into amino acids in shoots of AM plants. Glutamine, glutamate, alanine and γ-aminobutyric acid were the major sinks for 15N in roots and shoots of control and AM plants. Interactions between mycorrhizal colonization, phosphate and nitrate nutrition and NR activity were investigated in plants which received different amounts of phosphate or nitrate. In shoots of control plants, NR activity was not stimulated by high levels of phosphate nutrition but was stimulated by high levels of nitrate. At 4 mM nitrate in the nutrient solution, NR activity was similar in control and AM plants. We concluded that mycorrhizal effects on nitrate assimilation are not mediated via improved phosphate nutrition, but could be due to improved nitrogen uptake and translocation.

A pot experiment was designed to evaluate the interactive effects of multiple microbial inoculation treatments and rock phosphate (RP) application on N and P acquisition by alfalfa plants using 15N and 32P isotopes. The microbial inocula consisted of a wild type (WT) Rhizobium meliloti strain, its genetically modified (GM) derivative, which had an enhanced competitiveness, the arbuscular mycorrhizal (AM) fungus Glomus mosseae (Nicol. and Gerd.) Gerd. and Trappe, and a phosphate-solubilizing rhizobacterium (Enterobacter sp.). Inoculated micro-organisms became established in the root tissues and/or in the rhizosphere soil of alfalfa plants (Medicago sativa L.). The GM Rhizobium strain did not interfere with AM formation. Inoculated phosphate-solubilizing rhizobacteria established in the alfalfa rhizosphere, but the level of establishment was lower where the natural population of phosphate-solubilizing bacteria was stimulated by AM inoculation and RP application. The stimulation of these indigenous bacteria was also greater in the rhizosphere of alfalfa nodulated by the GM Rhizobium. Improvements in N and P accumulation in alfalfa corroborate beneficial effects of the improved GM Rhizobium on AM performance, in RP-amended plants. Inoculation with Enterobacter did not improve the AM effect on N or P accumulation in the RP-added soil, but it did in the non RP-amended controls. Measurements of the 15N[ratio ]14N ratio in plant shoots indicated enhanced N2 fixation rates in Rhizobium-inoculated AM-plants, over that achieved by the same Rhizobium strain in non-mycorrhizal plants. Regardless of the Rhizobium strain and of whether or not RP was added, AM-inoculated plants showed a lower specific activity (32P[ratio ]31P) than did their comparable non-mycorrhizal controls, suggesting that the plant was using otherwise unavailable P sources. The phosphate-solubilizing, AM-associated, microbiota could in fact release phosphate ions, either from the added RP or from the indigenous ‘less-available’ phosphate. Deficiency in Ca concentration in soil solution in the neutral test soil might benefit P solubilization. The proportion of plant P derived either from the labelled soil P (labile P pool) or from RP was similar for AM inoculated and non-mycorrhizal controls (without Enterobacter inoculation) for each Rhizobium strain, but the total P uptake, regardless of the P source, was far higher in AM-plants. Enterobacter inoculation seems to improve the use of RP in the rhizosphere of non-mycorrhizal plants inoculated with the WT Rhizobium.

The ability of ryegrass (Lolium perenne L.) to take up and utilize aspartic acid (Asp) and serine (Ser), and the effect of colonization of the roots by the arbuscular mycorrhizal (AM) fungus Glomus fasciculatum (Thax. sensu Gerd.) were studied. The seedlings were grown under controlled conditions in a series of micro-lysimeters. All plants were fed with a nutrient solution containing either nitrate, Asp or Ser as the sole N source. After 49 d, they were supplied with 15N labelled nitrate, Asp or Ser for 1 h and harvested.

AM colonization increased the growth and total N content of the plants in all cases. Similarly, the amount of Asp or Ser taken up was higher in AM than in control plants. There were no differences in biomass production between the nitrate and Ser-fed plants. However uptake rates were lower for Ser than for nitrate. Growth of the Asp-fed plants was significantly less than the other two treatments, and uptake of 15N-Asp was lower than uptake of 15N-Ser. Analysis of 15N incorporation into the amino acids extracted from the roots suggests the hydrolysis of Ser followed by re-assimilation of the resulting ammonia via the GS-GOGAT cycle. There were no differences in the patterns of accumulation of amino acids in the root-zone of control and AM-ryegrass. The implication of these results for the pathway of nitrogen transfer between plants is discussed.

Des sédiments d'un lac de gravière mésotrophe ont été mis à incuber au laboratoire pendant 15 jours en présence ou en l'absence de vers oligochètes. L'apport d'azote ammoniacal marqué par l'isotope lourd (15N) a permis de mesurer les flux entre les différents compartiments azotés (N organique, N-NH4 +, N-NO3 -). La nitrification apparaît négligeable alors que la dénitrification, un peu plus de 1 mg.m-2 h-1, est alimentée par les nitrates allochtones de la nappe. La perte d'azote ammoniacal par volatilisation est plus importante que la dénitrification mais elle est probablement influencée par le système d'aération. L'influence des oligochètes n'apparaît sensible qu'au niveau du couple minéralisation - réorganisation qu'elle active nettement.

Mycorrhizal mycelium was allowed to grow into a compartment from which roots were excluded. Ammonium or nitrate was supplied exclusively to the fungus and the respiration rate before and after nitrogen addition was measured. Mycelial respiration in the fungal compartment represented 11–29% of total fungal and root respiration. The mycelium in the fungal compartment received 20–29% of shoot net assimilation, and 43–64% of the carbon allocated to the mycelium was respired. The nitrogen-induced respiration increase ranged, in the fungal compartment, from 54 to 180%.

Milk and yoghurt proteins were 15N-labelled in order to measure the flow rate of exogenous N during digestion in the human intestine. After fasting overnight, sixteen healthy volunteers, each with a naso-jejunal tube, ingested either [15N]milk (n 7) or [15N]yoghurt (n 9). Jejunal samples were collected every 20 min for 4 h. A significant stimulation of endogenous N secretion was observed during the 20–60 min period after yoghurt ingestion and the 20–40 min period after milk ingestion. The endogenous N flows over a 4 h period did not differ between the groups (44·3 (SEM 6·5) mmol for milk and 63·5 (SEM 5·9) mmol for yoghurt). The flow rates of exogenous N indicated a delayed gastric emptying of the yoghurt N compared with N from milk. The jejunal non-protein N (NPN) flow rate increased significantly after milk and yoghurt ingestion due to an increase in the exogenous NPN flow rate. The NPN fraction of exogenous N ranged between 40 and 80%. The net gastro-jejunal absorption of exogenous N did not differ significantly between milk (56·7 (SEM 8·5)%) and yoghurt (50·9 (SEM 7)%). The high level of exogenous N hydrolysis is in accordance with the good digestibility of milk products. Fermentation modifies only the gastric emptying rate of N and does not affect the level of diet hydrolysis, the endogenous N stimulation or the digestibility rate.