S. Muetzel

Effect of forage conservation method on ruminal lipid metabolism and microbial ecology in lactating cows fed diets containing a 60:40 forage-to-concentrate ratio

The effect of forage conservation method on ruminal lipid metabolism and microbial ecology was examined in 2 complementary experiments in cows. Treatments comprised fresh chopped grass, barn-dried hay, or untreated (UTS) or formic acid-treated silage (FAS) prepared from the same grass sward. Preparation of conserved forages coincided with the collection of samples from cows offered fresh grass. In the first experiment, 5 multiparous Finnish Ayrshire cows (229 d in milk) were used to compare the effects of feeding diets based on grass followed by hay during 2 consecutive 14-d periods separated by a 5-d transition during which extensively wilted grass was fed. In the second experiment, 5 multiparous Finnish Ayrshire cows (53 d in milk) were assigned to 1 of 2 blocks and allocated treatments according to a replicated 3×3 Latin square design with 14-d periods to compare the effects of hay, UTS, and FAS. Cows received 7 or 9 kg/d of the same concentrate in experiments 1 and 2, respectively. Conservation of grass by drying, but not ensiling, decreased forage fatty acid content primarily due to losses of 18:2n-6 and 18:3n-3. Compared with grass, feeding hay had no effect on dry matter intake (DMI), rumen pH, or fermentation characteristics, other than increasing ammonia content, but lowered whole-tract organic matter and fiber digestibility (experiment 1). Relative to hay, silage increased DMI, rumen volatile fatty acid (VFA) concentrations, and molar proportions of butyrate, and decreased molar acetate proportions (experiment 2). Compared with UTS, FAS increased DMI, had no effect on rumen ammonia or VFA concentrations, but tended to lower rumen pH and the molar ratio of lipogenic to glucogenic VFA. Conservation method had no substantial effect on ruminal or whole-tract digestibility coefficients. Compared with fresh grass and silages, hay decreased lipolysis and biohydrogenation (BH) of dietary unsaturates in the rumen, resulting in similar flows of 18:2n-6 and 18:3n-3, but lower amounts of trans-11 18:1 and Δ11,13 18:2 at the omasum. The extent of silage fermentation had minimal influence on ruminal lipid metabolism. Treatments were not associated with changes in the relative abundance of specific bacteria known to be capable of BH or rumen protozoal numbers. In conclusion, conservation method altered forage lipids, the extent of lipolysis and BH in the rumen, and the flow of fatty acids at the omasum, in the absence of substantial changes in ruminal Butyrivibrio populations.

Methane emissions from young and mature dairy cattle

Daily methane (CH4) emissions (g) and CH4 yield (g/kg dry matter intake) were measured from 10 dairy heifers ( 6 years old) fed ryegrass (Lolium perenne) chaffage indoors. The CH4 emissions were estimated using the sulfur hexafluoride tracer technique in four ~5-day periods beginning in June 2008 and repeated 4, 6 and 7 months later. Respiratory chambers were used in four ~13-day periods beginning in November 2008 and repeated 2, 5 and 6 months later. Third and fourth sulfur hexafluoride tracer periods overlapped with the first and second chamber measurement periods, respectively. Averaged over the four measurement periods the CH4 yields determined using both techniques were similar for heifers and cows. The mean CH4 yield estimated by the sulfur hexafluoride tracer technique was 25.3 ± 0.52 for heifers and 24.1 ± 0.55 for mature cows, whereas the mean CH4 yield measured in respiratory chambers was 23.7 ± 0.66 for heifers and 23.6 ± 0.66 for mature cows. Averaged over the eight measurements irrespective of technique, CH4 yields for heifers (24.5 ± 0.42) and cows (23.8 ± 0.43) were similar. There was also no difference between CH4 methods for assessing CH4 yield during the overlapping measurement periods. It was concluded that no consistent differences in CH4 yield existed between heifers and mature cows. Therefore, we do not recommend adoption of an age-related emission factor for cattle in the national inventory calculations for New Zealand.

Methane emissions from sheep fed fresh pasture

Methane emissions from ruminants are the major single source of greenhouse gases in New Zealand and considerable effort has gone into the measurement and prediction of these emissions. This paper analyses methane emissions measured in respiration chambers from adult sheep and lambs fed fresh-cut pasture of different quality. Results show that the major driver of methane production (pCH4, g/d) is dry matter intake (DMI, kg/d). Pasture quality affected methane emissions only in animals less than 1 year of age. A single equation to be used for all sheep based on DMI alone (ln(pCH4) = 0.792(0.0275) ln(DMI) + 3.1(0.03)) or a two-equation approach with an equation for sheep >1 year based on DMI (ln(pCH4) = 0.826(0.0438) ln(DMI) + 3.15(0.017)) and one for sheep <1 year based on DMI and the metabolisable energy content (ME, MJ/kg) of the diet (ln(pCH4) = 0.749(0.0190)ln(DMI) + 0.051(0.0064)ME + 2.45(0.069)) is proposed.

Effects of endophytic and saprophytic fungi on in vitro methanogenesis

Abstract The predominance of pasture in the diet of ruminants in New Zealand presents specific challenges for mitigation of enteric methane emissions. However, there is preliminary evidence from both laboratory and animal-based studies that some fungi may suppress enteric methanogenesis. This study determined the antimethanogenic potential of a range of endophytic (Neotyphodium species) and saprophytic (Geotrichum, Monascus, Mortierella and Penicillium species) fungi. Candidate fungi were selected on the basis of their production of various classes of secondary compounds and screened in an in vitro batch-culture fermentation assay. No strains of endophyte in ryegrass or tall fescue suppressed methanogenesis compared with their endophyte-free controls. The supernatant fractions from three strains of Mortierella wolfii were the most promising fungi identified. They suppressed methanogenesis as effectively as an inhibitor of methanogenesis (bromoethane sulphonate at 30 µmoles/L), without also reducing overall fermentation. These strains should be investigated further by screening fresh cultures grown under contrasting conditions to establish some variation in putative bioactive compounds.

Effect of dietary fish oil supplements alone or in combination with sunflower and linseed oil on ruminal lipid metabolism and bacterial populations in lactating cows

Fish oil (FO) alters ruminal biohydrogenation causing trans fatty acid (FA) intermediates to accumulate, but the effects of 18-carbon polyunsaturated FA supply on ruminal long-chain FA metabolism and microbial communities in cattle fed FO are not well established. Four cows fitted with rumen cannula were used in a 4 × 4 Latin square with 21-d experimental periods to evaluate the effects of FO alone or in combination with plant oils high in 18:2n-6 or 18:3n-3 on rumen microbial ecology and flow of FA at the omasum. Treatments comprised a basal grass silage-based diet containing no additional oil (control) or supplements of FO (200 g/d) or FO (200 g/d) plus 500 g/d of sunflower oil (SFO) or linseed oil (LFO). Flow of FA was determined using the omasal sampling technique. The relative abundance of key biohydrogenating bacteria was assessed by quantitative PCR on 16S rRNA genes in omasal digesta. Fish oil-supplemented treatments increased the amounts of trans-18:1, trans-18:2, and 20- to 22-carbon polyunsaturated FA escaping the rumen. Relative to the control, oil supplements had no effect on the amount of 18:0 leaving the rumen, but LFO decreased the flow of 18:0 at the omasum compared with SFO. Both SFO and LFO increased trans-18:1 relative to FO, whereas LFO resulted in the highest trans-18:2 and 20- to 22-carbon FA flow. Supplements of FO plus plant oils shifted biohydrogenation toward trans-10 18:1 formation. Compared with FO alone, the ruminal metabolism of 22:6n-3 in the rumen of lactating cows is more extensive on diets containing higher amounts of 18-carbon polyunsaturated FA. However, the biohydrogenation of 22:5n-3 was less extensive in LFO than SFO, but showed no difference between FO and diets containing plant oils. Ruminal outflow of 20:5n-3 was not altered when plant oils were added to FO. Alterations in the amount of intermediates at the omasum or ruminal biohydrogenation pathways were not accompanied by major changes in analyzed bacterial populations. In conclusion, dietary supplements of FO alone or in combination with plant oils increase the amount of biohydrogenation intermediates containing 1 or more trans double bonds escaping the rumen, which may have implications for host metabolism and the nutritional quality of ruminant foods.

Symposium review: Uncertainties in enteric methane inventories,measurement techniques, and prediction models

Ruminant production systems are important contributors to anthropogenic methane (CH4) emissions, but there are large uncertainties in national and global livestock CH4 inventories. Sources of uncertainty in enteric CH4 emissions include animal inventories, feed dry matter intake (DMI), ingredient and chemical composition of the diets, and CH4 emission factors. There is also significant uncertainty associated with enteric CH4 measurements. The most widely used techniques are respiration chambers, the sulfur hexafluoride (SF6) tracer technique, and the automated head-chamber system (GreenFeed; C-Lock Inc., Rapid City, SD). All 3 methods have been successfully used in a large number of experiments with dairy or beef cattle in various environmental conditions, although studies that compare techniques have reported inconsistent results. Although different types of models have been developed to predict enteric CH4 emissions, relatively simple empirical (statistical) models have been commonly used for inventory purposes because of their broad applicability and ease of use compared with more detailed empirical and process-based mechanistic models. However, extant empirical models used to predict enteric CH4 emissions suffer from narrow spatial focus, limited observations, and limitations of the statistical technique used. Therefore, prediction models must be developed from robust data sets that can only be generated through collaboration of scientists across the world. To achieve high prediction accuracy, these data sets should encompass a wide range of diets and production systems within regions and globally. Overall, enteric CH4 prediction models are based on various animal or feed characteristic inputs but are dominated by DMI in one form or another. As a result, accurate prediction of DMI is essential for accurate prediction of livestock CH4 emissions. Analysis of a large data set of individual dairy cattle data showed that simplified enteric CH4 prediction models based on DMI alone or DMI and limited feed- or animal-related inputs can predict average CH4 emission with a similar accuracy to more complex empirical models. These simplified models can be reliably used for emission inventory purposes.