Reducing methane emissions from cattle in Australia will be dependent upon finding a strategy that can be readily adopted by its northern beef industry. The majority of the herd are located in this region and they graze low-quality tropical (C4) pastures, resulting in high methane output. There are few mitigation options that can be readily applied to extensively grazed cattle. The addition of nitrate to the diet of cattle has been shown to reduce methane production and may be an applicable strategy in northern Australia. Nitrogen is often the primary limiting nutrient in low-quality tropical pastures and it is common practice by industry to supplement with urea. Supplying an equivalent dose of nitrogen using nitrate as an alternative to urea has been demonstrated in cattle without adverse impacts upon animal productivity or health. These findings may not be directly applicable to grazing cattle in northern Australian because the diets and feeding management are not representative of the region. Nitrite toxicity can result from feeding nitrates to livestock and there is evidence that the composition of the total diet and feeding pattern influences the risk of toxicity. If nitrate supplementation in grazing beef cattle in northern Australia can be demonstrated to reduce methane and be applied safely, adoption rates will still depend on carbon market pricing. Current modelling suggests that the cost of supplementing beef cows with nitrate in northern Australia would be at least double the cost of urea supplementation.
1 November 2021 in Food and Bioproducts Processing
This experiment has quantified the methane abatement potential of nitrate in the context of extensively managed cattle. The experimental protocol consisted of two, 4 × 4 Latin square design using eight rumen fistulated Bos indicus steers fed Flinders grass (Iseilema spp.) hay ad libitum. The treatments were Control (nil nitrogen supplement), urea (32.5 g/day urea) and two levels of calcium nitrate: CaN1 and CaN2 (to provide 4.6 g and 7.9 g NO3/kg DM equivalent to ~0.46% and 0.80% of DM, respectively). Complete supplement intake was ensured by dosing any supplement that had not been voluntarily consumed, through the rumen fistula, 1 h after feeding. Enteric methane production was measured using open circuit respiration chambers. Methane yield (g/kg DM intake) from the CaN2 treatment tended to be lower (P < 0.07) than either the Control or urea treatments. There were no significant differences in methane yield between Control, urea or CaN1 treatments. Mean blood methaemoglobin concentrations were significantly (P < 0.001) higher for CaN2 animals compared with the Control, urea or CaN1 treatments. In addition, a significant time effect after dosing (P < 0.001) and a significant interaction between treatment and time after dosing (P < 0.001) was apparent. Overall mean total volatile fatty acid concentration was 74.0 ± 1.53 mM with no significant treatment effect, but a significant effect for both time of sampling (3 h vs 6 h) within days and among 7 sampling days. The inclusion of calcium nitrate as a non-protein-N source significantly reduced the molar proportions of butyrate (P < 0.001), iso-butyrate (P < 0.05) and iso-valerate (P < 0.001) compared with the Control. The provision of nitrate supplements, providing both a NPN and an alternative sink for H that would otherwise support enteric methanogenesis, has some potential. In extensive grazing systems effective methane abatement strategies are required. The elevated concentration of MetHb using CaN2 suggests that the strategy of replacing urea with nitrate in supplements fed to extensively managed cattle in the northern rangelands may be inappropriate where supplement intake cannot be controlled on an individual animal basis and forage quality is seasonally variable.
This study tested the hypothesis that Bacillus amyloliquefaciens strain H57 (H57) improves preference by reducing the development of microbial volatile organic compounds (mVOCs) in feed pellets. Sixteen bull calves were, for 4 weeks, provided equal access to a panel of 8 automated feed bunks in a single paddock with some hay. Each bunk contained pellets with (H57) or without (Control) the H57, each aged for 4 months at either ambient or chiller temperature. Each treatment was changed to a new bunk pair position weekly. Relative preference was determined according to weight of pellets remaining per hour per treatment bunk pair per 24 h. Pellets were analysed for volatile organic compounds (VOCs) and the concentrations tested for correlation with relative preference. Calves showed the lowest preference (p < 0.0001) for the Control/Ambient treatment whereas preference for all other treatments (H57/Ambient; H57/Chiller; Control/Chiller) was similar. The Control/Ambient treatment odour profile grouped differently to the other 3 treatments which grouped similarly to each other. Up to 16 mVOCs were determined to have potential as pre-ingestive signals for the extent of microbial spoilage. Further studies are required to find which combination of these mVOCs, when added to pellets, results in feed aversion.
Mould and bacterial contamination releases microbial volatile organic compounds (mVOCs), causing changes in the odour profile of a feed. Bacillus amyloliquefaciens strain H57 (H57) has the potential ability to inhibit microbial growth in animal feeds. This study tested the hypothesis that H57 influences the odour profile of stored feedlot pellets by impeding the production of mVOCs. The emission of volatile organic compounds (VOCs) of un-inoculated pellets and those inoculated with H57, stored either at ambient temperature (mean 22 °C) or at 5 °C, was monitored at 0, 1, 2, and 3 months by gas chromatography–mass spectrometry. Forty VOCs were identified in all the pellet samples analysed, 24 of which were potentially of microbial and 16 of non-microbial origin. A score plot of the principal component analysis (PCA) showed that the VOC profiles of the pellets stored at ambient temperature changed more rapidly over the 3 months than those stored at 5 °C, and that change was greater in the un-inoculated pellets when compared to the inoculated ones. The bi-plot and correlation loading plots of the PCA indicated that the separation of the un-inoculated pellets from the other treatments over the 3 months was primarily due to nine mVOCs. These mVOCs have been previously identified in grains spoiled by fungi, and could be considered potential markers of the types of fungi that H57 can protect pellets against. These data indicate the ability of H57 to maintain the odour profile and freshness of concentrated feed pellets. This protective influence can be detected as early as 3 months into ambient temperature storage.
Context: The Australian government has approved a greenhouse gas (GHG) offset method that requires cattle to consume nitrate in the form of a lick block. Field studies demonstrating the effectiveness of this methodology have not been previously reported. Aims: This experiment was conducted to determine the effects on productivity and health when nitrate lick blocks were provided as a supplement to grazing beef cattle. We hypothesised that beef cattle given access to nitrate lick blocks would have similar productivity compared with cattle offered urea lick blocks. Methods: Bos indicus breeding cows (n = 76) grazed a 467-ha paddock near Charters Towers, Queensland, between May and November 2014. A two-way remote automatic drafting system enabled allocation of cattle to different treatments while grazing in a common paddock. Treatments were 30% urea lick blocks (30U), or molasses nitrate lick blocks (MNB). At monthly intervals liveweight (LW), body condition score (BCS), and blood methaemoglobin concentration were recorded. Estimates of individual supplement intake were made on three separate occasions using a lithium marker technique. Results: Mean daily supplement intake (±s.e.m.) of 30U (122 ± 13 g) was greater (P < 0.001) than MNB (67 ± 8 g). Lesser MNB intake was associated with greater variability for individual supplement intake, a greater proportion of non-consumers of supplement during July (P < 0.05) and reduced voluntary supplement intake until October (P < 0.001). Increasing MNB consumption during October and November was accompanied by elevated blood methaemoglobin concentration (P < 0.001). It was estimated that cattle offered MNB had insufficient supplementary nitrogen intake throughout the study to resolve rumen degradable nitrogen deficiency from grazed forage. Consequently, cattle provided access to MNB demonstrated conceptus free liveweight loss and lesser BCS compared with cattle treated with 30U (P < 0.001). Conclusion: Nitrate lick blocks were ineffective as a dual-purpose non-protein nitrogen supplement and methane mitigant for beef cattle grazing poor quality forage. Further field experiments are required to determine if there may be situations where this GHG offset methodology is efficacious. Implications: Caution is advised in implementing GHG mitigation methods that involve the use of nitrate lick blocks.