Effect of N fertilisation rate, energy supplementation and supplementation strategy on efficiency of N utilisation in the sheep rumen.

The effect of nitrogen (N) fertilisation (200 vs. 400 kg N ha-1 year-1) of pasture cut in the beginning (end of May) and the end (end of August) of the grazing season and of simultaneous or separated feeding of maize and grass (400 kg N ha-1 year-1) on efficiency of N utilisation in the rumen has been studied using four rumen cannulated wethers. Doubling N fertiliser rate increased grass CP production by about 60%, but induced extensive excess of rumen degradable N, reflected in high urinary urea excretion (rpearson = 0.747). The latter was lower (74% at the maximum) when feeding less fertilised or older grass or when supplementing with maize silage. Although simultaneous feeding of maize silage with grass changed patterns of rumen ammonia concentrations, no change in urinary excretion of purine derivatives was observed. Hence, faecal or urinary N excretion was unaffected by the supplementation strategy. Microbial growth efficiency was estimated from urinary excretion of purine derivatives and fermented OM. The latter was calculated from total rumen CH4 production, based on rumen fermentation stoichiometry and taking into account proportional concentrations of individual volatile fatty acids. Higher levels of intake tended to improve rumen microbial growth efficiency slightly (rpearson = 0.406), which, however, could not compensate for the reduced effective rumen DM degradability (rpearson = -0.442). The latter was apparently associated with a partial shift of the fermentation from the rumen to the hindgut, as suggested from the negative correlation (rpearson = -0.745) between faecal RNA concentrations and rumen effective degradability.

Age and incubation time effects on in vitro caecal fermentation pattern in rabbits before and after weaning.

The caecal fermentation pattern was studied in four litters of rabbits. Rabbits were sequentially slaughtered at the age of 4 (before weaning), 6, 8 and 11 weeks. Their caecal contents were analyzed and incubated in vitro at 39 degrees C for 6 and 12 h. Net productions of short-chain fatty acids (SCFA), hydrogen and methane were determined. The average caecal weight increased three-times within two weeks after weaning, from 31.4 to 93.7 g. At the end of the experiment, the caecal weight was on average 134.4 g. A large variability of the SCFA concentration observed before weaning decreased after weaning. Measurements of caecal metabolite profiles and results of in vitro experiments indicated a certain decrease of propionate in favour of butyrate, associated with the weaning. The establishment of methanogens in rabbits was slow. Methanogenesis started in one out of four rabbits at the age of 6 weeks. Five weeks later, one of four rabbits still did not produce methane. The hydrogen recovery decreased between the 4th and the 6th week of age, due to the increase of the butyrate/propionate ratio. After the 6th week, the hydrogen recovery increased with age, apparently because of the increase in methane production. Hydrogen recovery tended to increase during incubation, suggesting a decrease of reductive acetogenesis. This increase was observed both in methanogenic and non-methanogenic rabbit caecal cultures. In former cultures, the ratio CH4/SCFA rose with time of incubation.

Attempts to induce reductive acetogenesis into a sheep rumen.

A rumen fistulated wether was used for continuous infusion of a 2-bromoethanesulfonic acid (BES) solution (2 g/d in 50 ml of water). The infusion was started after introduction of a pulse dose of BES (2 g) into the rumen. Immediately after introduction of the pulse dose, methane concentration in rumen gases was lowered from about 40 to less than 1%, with concomittant decreases and increases in the molar proportions of acetic and propionic acids respectively in the rumen volatile fatty acids. After 4 days of infusion however, and despite repeated pulse dosage of BES, methanogenesis adapted to BES and methane concentration in rumen gases reached 20%. Addition of BES to incubations of rumen contents with hay resulted in considerable inhibition of methanogenesis. Extra addition of methanol in such incubations increased both acetate and methane production, whereas addition of formate had no effect. In a second experiment using a second rumen fistulated whether, a 4 day control period was followed by 10 days of daily introduction of 11 of cattle cecal contents into the rumen. The cattle cecal contents were collected from slaughterhouse cattle, filtered and kept at -20 degrees C until use. Comparison of in vitro fermentation of thawed with fresh contents showed absence of methanogenesis but not of reductive acetogenesis after freezing and thawing. Evidence for the latter was sought by calculation of metabolic hydrogen recoveries from amounts of end products formed in incubations. In a similar way, evidence for induction of reductive acetogenesis was sought from incubations in vitro, carried out with rumen contents obtained before, during and after introduction of cecal contents into the rumen. No such evidence was obtained.

[Adaptation of rumen fermentation to monensin]. / Essai sur l'adaptation de la fermentation ruminale au monensin.

Adaptation of rumen fermentation to monensin feeding has been studied with rumen-fistulated sheep receiving a daily dose of 30 mg of monensin for a period of 21 d followed by a 28 d period during which 60 mg doses were administered. The ration consisted of 300 g of hay and 300 g of concentrates, fed at 9.00 h and 16.00 h. Monensin was placed in the rumen as an aqueous suspension, just prior to the morning feeding. Monensin infusion was preceded and followed by a period during which no monensin was infused. The following rumen fermentation parameters were determined: methane production, pH, volatile fatty acids (VFA) molar proportions, total volatile fatty acid concentration, lactate and ammonia concentrations and in sacco degradability of hay. Rumen gas expelled through the fistula was collected for 6 h per day and analysed. Total VFA concentration, molar proportions of individual VFA, pH, lactate and ammonia concentration were determined on rumen contents, sampled just prior the administration of monensin and 2 and 6 h later. In vitro incubations of 3 h were carried out with rumen fluid, sampled 1 h after feeding. In vivo and in vitro methane production was decreased by monensin feeding. The molar proportion of propionate in the rumen was increased, while acetate and butyrate percentages were lowered. The total VFA and ammonia concentrations were also decreased by monensin, but pH values were increased. In vitro production of propionate was stimulated by monensin administration and methanogenesis decreased. The organic matter in sacco degradability was not affected, probably because of the time difference between the introduction of bags and monensin in the rumen. These modifications of rumen fermentation persisted as long as monensin was given, indicating that in this experiment, there was no adaptation to the ionophore.