Abstract
The enteric methane conversion factor (Y m) is an important country‐specific value for the provision of precise enteric methane emissions inventory reports. The objectives of this meta‐analysis were to develop and evaluate the empirical Y m models for the national level and the farm level for tropical developing countries according to the IPCC's categorization. We used datasets derived from 18 in vivo feeding experiments from 1999 to 2015 of Zebu beef cattle breeds fed low‐quality crop residues and by‐products. We found that the observed Y m value was 8.2% gross energy (GE) intake (~120 g methane emission head−1 day−1) and ranged from 4.8% to 13.7% GE intake. The IPCC default model (tier 2, Y m = 6.5% ± 1.0% GE intake) underestimated the Y m values by up to 26.1% compared with its refinement of 8.4% ± 0.4% GE intake for the national‐level estimate. Both the IPCC default model and the refined model performed worse in predicting Y m trends at the farm level (root mean square prediction error [MSPE] = 15.1%–23.1%, concordance correlation coefficient [CCC] = 0.16–0.18, R 2 = .32). Seven of the extant Y m models based on a linear regression approach also showed inaccurately estimated Y m values (root MSPE = 16.2%–36.0%, CCC = 0.02–0.27, R 2 < .37). However, one of the developed models, which related to the complexity of the energy use efficiencies of the diet consumed to Y m, showed adequate accuracy at the farm level (root MSPE = 9.1%, CCC = 0.75, R 2 = .67). Our results thus suggest a new Y m model and future challenges for estimating Zebu beef cattle production in tropical developing countries.
Keywords: cattle, low‐quality feed, meta‐analysis, methane, tropical countries, Ym model
1. Introduction
With an estimated 999 million tons of carbon dioxide equivalent per annum, methane emissions from the enteric fermentation of beef cattle are a major human‐induced greenhouse gas emission (Opio et al., 2013). Enteric methane emissions represent a loss in the range of 2%–12% of the gross energy (GE) intake; that is, MJ methane energy loss per 100 MJ GE consumed by cattle, directly reducing the energy use efficiency of the diet consumed (Johnson & Johnson, 1995).
Currently, enteric methane emissions for cattle globally are estimated from energy requirements using the enteric methane conversion factor (Y m, % of GE intake), according to the IPCC (2006) standard. Practically, the Y m default model of “Y m = 6.5% ± 1.0% of GE intake” of IPCC (2006) (tier 2 level) is used worldwide to upscale national estimations and obtain accurate cattle population and related activity data. Average daily GE intake (MJ/day) and Y m are ordinarily used to estimate methane emission factors. For nonfeedlot cattle (fed concentrate diet <90% of total intake), the upper bounds of the default model are recommended for diets with poorer digestibility and energy values (IPCC, 2006). Because the Y m default model was developed from a dataset based on Bos taurus fed temperate feedstuffs, research that adopts country‐ or region‐specific Y m models is also significant for reducing possible errors in the estimates of Y m for different livestock and feed combinations (Lassey, 2007).
In addition to emissions at the national level, those at the farm level are also significant for applying methane mitigation strategies that may increase feed energy deposition in animals (Hristov et al., 2013). Y m values at the farm level show extremely high variability (Johnson & Johnson, 1995; Lassey, 2007). Indeed, models that describe this circumstance at the farm level are too complex to be used in national inventories at low tier levels. Overall, extant models for estimating enteric methane emissions can be classified into two principal groups: empirical (statistical) or dynamic mechanistic models (Kebreab, Johnson, Archibeque, Pape, & Wirth, 2008). In terms of the former, independent variables such as animal and diet as well as energy utilization efficiency have been selected to develop empirical Y m models (Blaxter & Clapperton, 1965; IPCC, 2006, Jaurena et al., 2015). Regarding the latter, a Danish‐specific Y m model has been developed using a mathematical description of ruminal fermentation biochemistry (Nielsen et al., 2011).
One challenge is the lack of data available to predict Y m for Zebu and Zebu crossbred beef cattle in tropical countries. This is a particular problem given that stocks of Zebu (Bos indicus) beef cattle in developing countries in tropical regions now account for more than half of the global beef cattle population (FAO, 2015). Both Kurihara, Magner, Hunter, and McCrabb (1999) and our previous studies (Chaokaur, Nishida, Phaowphaisal, & Sommart, 2015; Chuntrakort et al., 2014; Tangjitwattanachai, Phaowphaisal, Otsuka, & Sommart, 2015) have consistently found the Y m value of Zebu beef cattle production in tropical regions to be much higher than those estimated by IPCC (2006). As the diets fed to these Zebu beef cattle typically consist of poor‐quality crop residues and by‐products compared with those fed to B. taurus (Kearl, 1982; NRC, 2000, WTSR, 2010), extant Y m models may be inaccurate for the Zebu beef population.
Based on this gap in the body of knowledge on this topic, this meta‐analysis aimed to develop new and evaluate existing regional diet‐specific empirical Y m models for Zebu beef cattle production in tropical regions at the national level and the farm level from on‐farm accessible data.
2. Materials and Methods
2.1. Dataset construction
A dataset was constructed from 18 energy balance or feeding experiments conducted from 1999 to 2015 (total 53 observations (n) as the feeding treatment means; from peer‐reviewed papers, proceedings, theses, and unpublished results from our research station) of Zebu and Zebu crossbred beef cattle fed low‐quality crop residues and by‐products in tropical regions (Canesin et al., 2014; Chaokaur, Nishida, & Sommart, 2010; Chaokaur et al., 2015; Chuntrakort et al., 2014; Hayashi et al., 2010 [unpublished results]; Kaewpila, Suzuki, & Sommart, 2015; Kennedy & Charmley, 2012; Khuamankgorn, Namsele, Angthong, & Martosoth, 2009; Kongphitee, Udchachon, Otsuka, & Sommart, 2010; Kongphitee et al., 2015 [unpublished results]; Kurihara et al., 1999; Moonmat, Otsuka, Udchachon, & Sommart, 2009; Nitipot, Pattarajinda, & Sommart, 2010; Phromloungsri, Hayashi, Otsuka, Udchachon, & Sommart, 2012; Sitthiwong, 2010; Suzuki et al., 2008; Tangjitwattanachai et al., 2015; Tomkins, McGinn, Turner, & Charmley, 2011). Diets that contained feed additive reagents for mitigating Y m such as monensin were not included in the dataset, while starving animals and animals fed good‐quality forage and legumes or lipids supplements were also excluded. Enteric methane emissions were measured using an indirect respiration calorimeter (head hood) or a sulfur hexafluoride tracer technique. GE intake was measured by multiplying the GE content of the diet (determined using a bomb calorimeter) by dry matter intake (collected by total collection or a maker technique). Some previous studies have not reported nutritive values such as chemical composition, energy content, and feed digestibility, which are necessary as predictors for models in this meta‐analysis. Therefore, we investigated this missing information using animal feed information guidelines (Feedipedia, 2015, NRC, 2000, WTSR, 2010) including ether extract, neutral detergent fiber, and acid detergent fiber via the mean value of the feedstuffs. The procedures for determining the feed fractions are as follows (Mertens, 1997; Owens, Sapienza, & Hassen, 2010):
Further, the models for predicting feed fractions were as follows (Rittenhouse, Streeter, & Clanton, 1971):
where NFC, nonfiber carbohydrates (g/kg DM); Ash expressed as g/kg DM; CP, crude protein (g/kg DM); EE, ether extract (g/kg DM); NDF, neutral detergent fiber (g/kg DM); TDN, total digestible nutrients (g/kg); DMD, dry matter digestibility (g/kg); DE, digestible energy (MJ/kg DM); GE, gross energy (MJ g/kg DM); and OMD, organic matter digestibility (g/kg). Note that the model inputs from some of these predicted parameters can further create additional errors beyond the model formulation. The summary statistics of the dataset are shown in Table 1.
Table 1.
Summary statistics of the Zebu beef cattle dataset used to develop and evaluate the models (n = 53)
| Item | Mean | SD | Minimum | Maximum |
|---|---|---|---|---|
| Beef cattle | ||||
| Age (month) | 23 | 10 | 12 | 48 |
| Body weight (kg) | 277 | 80 | 113 | 432 |
| Diet composition (g/kg dry matter) | ||||
| Roughage proportion | 526 | 287 | 220 | 1,000 |
| Organic matter | 911 | 25 | 840 | 962 |
| Crude protein | 106 | 33 | 40 | 213 |
| Ether extract | 36 | 16 | 10 | 78 |
| Neutral detergent fiber | 507 | 142 | 293 | 756 |
| Acid detergent fiber | 296 | 93 | 162 | 472 |
| Nonfiber carbohydrates | 260 | 123 | 53 | 543 |
| Energy content (MJ/kg dry matter) | ||||
| Gross energy | 17.6 | 1.4 | 15.0 | 19.9 |
| Digestible energy | 11.9 | 1.7 | 8.3 | 14.8 |
| Metabolizable energy | 10.1 | 1.7 | 6.7 | 12.9 |
| Digestibility (g/kg) | ||||
| Dry matter digestibility | 643 | 70 | 464 | 746 |
| Organic matter digestibility | 677 | 72 | 508 | 790 |
| Total digestible nutrients | 604 | 86 | 454 | 737 |
| Feeding level | ||||
| Dry matter intake (kg/day) | 4.6 | 1.5 | 2.2 | 7.7 |
| Dry matter intake (% body weight) | 1.7 | 0.3 | 1.2 | 2.2 |
| Metabolizable energy intakea | 1.4 | 0.3 | 1.0 | 2.2 |
| Enteric methane emission | ||||
| Methane emission (g/day) | 123 | 53 | 38 | 311 |
| Y m (% gross energy intake) | 8.2 | 1.7 | 4.8 | 13.7 |
Expressed as multiple time of maintenance requirement (0.48 MJ ME/kg BW0.75, WTSR, 2010).
2.2. Extant Y m model selection
The extant Y m models from the published works (Blaxter & Clapperton, 1965; FAO, 2010; IPCC, 2006, Jaurena et al., 2015, Patra, 2013; Ramin & Huhtanen, 2013; Yan, Agnew, Gordon, & Porter, 2000) presented in Table 2 were selected to predict the Y m of the beef cattle dataset and to guide the model development. The model selection criteria were based on the model's possible use at the national or farm level as well as the existence of independent variables in the dataset. At the national level, the tier 2 Y m default models of the IPCC (2006) are used worldwide (Kebreab et al., 2008). These Y m estimates are a rough guide based on the beef farm practices in most developed and developing countries (IPCC, 2006). A default model (Y m = 6.5% ± 1.0% of GE intake, namely model A) was selected to emphasize the IPCC's recommendation for cattle fed low‐quality crop residues and by‐products in developing countries. At the farm level, regression models are typically used to estimate the Y m values related to the complex variable(s) of the animal and its diet. Seven regression models (namely model B, C, D, E, F, G, and H) were thus selected to increase the levels of the complexity variable(s).
Table 2.
Extant models selected to predict Y m values
| Model category | Model | Relationshipa | Description |
|---|---|---|---|
| National level | |||
| IPCC (2006) | Model A | Y m = 6.5 ± 1.0 | These IPCC guidelines for the tier 2 level are used to upscale the measurements of national and global inventories. The model is developed from a database including dairy cows in New Zealand, dairy heifers and steers in the United States, and beef cows in France (i.e., animals grazing in temperate pastures). It is the currently suggested emissions inventory method for the enteric fermentation of cattle population categories fed low‐quality crop residues and by‐products in developing countries |
| Farm level | |||
| Patra (2013) | Model B | Y m = 7.10 − 0.0192 × EE | This model is developed from a database including dairy and beef cattle fed a wide range of dietary composition in unspecified locations |
| Yan et al. (2000) | Model C | Y m = [0.0522 + 0.0694 × ADFI/DMI] × 100 | This model is developed from a database including dairy cows and steers offered grass silage‐based diets in Northern Ireland |
| FAO (2010) | Model D | Y m = 9.75 − 0.005 × DMD | This model has been previously used to predict methane emissions from dairy cattle production in Sweden and Nigeria. No information on the database is available |
| Jaurena et al. (2015) | Model E | Y m = Intercept alternativesb − 0.243 × DMI + 0.0059 × NDF + 0.0057 × DMD | This model is developed from a database including beef cattle fed a wide range of dietary composition in unspecified locations |
| Ramin and Huhtanen (2013) | Model F | Y m = [–0.60 − 0.70 × DMIbw + 0.076 × OMDm − 0.130 × EE + 0.046 × NDF + 0.044 × NFC]/10 | This model is developed from a database including dairy and beef cattle and sheep fed a wide range of dietary composition in unspecified locations |
| Yan et al. (2000) | Model G | Y m = [0.0877 − 0.0078 × (MEIm − 1.00)] × 100 | See description of model C |
| Blaxter and Clapperton (1965) | Model H | Y m = 1.30 + 11.2 × DE/GE − [2.37 − 5.00 × DE/GE] × MEIm | This model is developed from a database including cattle and sheep fed roughages or mixed diets in the United Kingdom |
Y m, methane conversion factor (% of GEI); DE, digestible energy (MJ/kg DM); GE, gross energy (MJ/kg DM); GEI, GE intake (MJ/day); MEIm, metabolizable energy intake as multiple time of maintenance requirement (0.48 MJ ME/kg BW0.75, WTSR, 2010); ADFI, acid detergent fiber intake (kg/day); DMI, dry matter intake (kg/day); DMD = dry matter digestibility(g/kg); DMIbw, dry matter intake (g/kg body weight); OMDm, organic matter digestibility (OMD) determined at a maintenance level of feeding (g/kg, OMDm = OMD (g/kg) + 1.83 × [DMIbw − 10]); NDF, neutral detergent fiber (g/kg DM); EE, ether extract (g/kg DM); NFC, nonfiber carbohydrates (g/kg DM).
All the intercept alternatives were used: fresh forage with level of concentrate less than 35% (of dry matter intake), and between 35% and 65% = 2.0, and 4.1 (respectively), conserved forages with level of concentrate less than 35%, between 35% and 65%, and more than 65% = 3.1, 2.3, and 1.5 (respectively), straw with level of concentrate less than 35%, between 35% and 65%, and more than 65% = 5.1, 4.4, and 1.0 (respectively).
2.2.1. Model development for the national level
This model (Table 3, namely model I) was simulated according to the tier 2 level of IPCC (2006), which developed a Y m model based on the quotient of mean methane energy emissions to mean GE intake across the measured herd, while the conversion from methane energy to flux in mass units was 55.56 MJ/kg (Lassey, 2007). Thus, the calculation was
| (1) |
where Y m, methane conversion factor (% of GE intake); CH4i, the ith observed methane energy emissions (MJ/day); GEIi, the ith observed GE intake (MJ/day); and n, number of observations. Based on the IPCC's recommendation, the Y m value for the national level can be estimated although the uncertainty in the mean (i.e., choices regarding what to include or exclude), which originally relate to the digestibility and energy values of the diet. The uncertainty in the mean was calculated as ±1.96 multiples of the standard error (IPCC, 2006).
Table 3.
List of models developed to predict the Y m values
| Model category | Modela | p‐Value | R 2 b | RMSPE %c | Largest VIFd |
|---|---|---|---|---|---|
| National level (n = 53) | |||||
| Model I | Y m = 8.4 ± 0.4 | – | – | – | – |
| Farm level (n = 36) | |||||
| Model J (dietary level) | Y m = 14.12(SE = 1.55, p < .01) − 0.073(SE = 0.018, p < .01) × EE − 0.006(SE = 0.002, p < .05) × NDF | <.01 | .34 | 17.4 | 1.29 |
| Model K (intake level) | Y m = 7.70(SE = 0.69, p < .01) − 8.33(SE = 3.40, p < .05) × EEI + 3.74(SE = 0.89, p < .01) × CPI | <.01 | .38 | 16.9 | 1.04 |
| Model L (digestibility level) | Y m = − 0.24 (SE = 2.53, p = .92) + 0.013(SE = 0.004, p < .01) × OMD | <.01 | .25 | 18.5 | – |
| Model M (integrated dietary, intake and digestibility level) | Y m = 8.65(SE = 1.05, p < .01) − 0.034(SE = 0.015, p < .05) × EE − 1.41(SE = 0.38, p < .01) × DMI + 2.57(SE = 0.54, p < .01) × DOMI | <.01 | .54 | 14.5 | 8.03 |
| Model N (energy level) | Y m = 37.70(SE = 5.00, p < .01) + 19.71(SE = 2.69, p < .01) × DE/GE − 50.70(SE = 6.55, p < .01) × ME/DE | <.01 | .71 | 12.0 | 1.24 |
Y m, methane (CH4) conversion factor (% of GE intake); EE, ether extract (g/kg DM); NDF, neutral detergent fiber (g/kg DM); EEI, ether extract intake (g/day); CPI, crude protein intake (g/day); OMD, organic matter digestibility (g/kg); DOMI, digestible organic matter intake (kg/day); GE, gross energy (MJ/kg DM); DE, digestible energy (MJ/kg DM); ME, metabolizable energy (MJ/kg DM).
R 2, coefficient of determination.
RMSPE, root‐mean‐square prediction error (% of the mean of observed Y m).
VIF, variance inflation factors (>10 indicates existing of collinearities among the independent variables).
2.2.2. Model development for the farm level
This investigation was carried out using a subsampling dataset (n = 36, termed the two‐thirds dataset) from the total dataset (n = 53). The models were developed using a multiple linear regression analysis, which relates the independent variable(s) to Y m. This investigation was conducted in a sequential manner to increase model complexity at each level and thus increase the model's predictive power, which is based on complex information (IPCC, 2006, Moraes, Strathe, Fadel, Casper, & Kebreab, 2014). According to the dataset availability and extent models (Table 2), five complexity levels were performed, namely dietary, intake, digestibility, integrated dietary, intake and digestibility, and energy levels (Table 3). All variables were computed under the selected most probable model at these levels of complexity. Specifically, the regression analysis for model complexity at each level was analyzed using the REG procedure (stepwise and collinearity diagnostics) of the SAS statistical software version 6.12 (SAS Institute Inc. Cary, NC, USA). The statistical model was
| (2) |
where Y m = methane conversion factor (% of GE intake); β0 = intercept, β1, β2, …, βn = slopes, X 1, X 2, …, X n = independent variables, and ɛ = error.
2.2.3. Cross‐evaluation
Three statistical parameters, namely the coefficient of determination (R 2), root‐mean‐square prediction error (RMSPE), and variance inflation factors (VIFs), were undertaken to evaluate the developed models against the observed Y m to assess model performance. The predicted Y m dataset for each model was developed using the model regressor. Model I, developed for the national level, was excluded as it did not exactly mimic the real regression system.
The R 2 (stepwise) and VIFs (collinearity diagnostics) were obtained during the model development process previously described via the REG procedure of the SAS. This R 2 was used as an index of the goodness of fit of the Y m models, determining the proportion of variance in the observed Y m explained by the model (Nakagawa & Schielzeth, 2013). Thus, R 2 of 1 indicates that the regression line perfectly fits the data, while an R 2 of 0 indicates that the line does not fit the data at all. The VIFs measure the inflation in the variances of the parameter estimates due to collinearities that exist among the independent variables (Belsley, Kuh, & Welsch, 1980). The largest VIF was used as the formal criterion for deciding if it is larger than 10 (i.e., sufficient to affect the predicted values; Moraes et al., 2014).
The RMSPE was calculated as
| (3) |
where O i = ith observed Y m value, P i = ith predicted Y m value, n = observation number, and = mean observed Y m value. The RMSPE was used as an index to describe the predictive accuracy of every developed model (Tedeschi, 2006). RMSPE values are expressed as a percentage of the observed Y m, and range from 0 to positive infinity. An RMSPE value equal to 0 indicates a perfect score in the predictive accuracy model.
2.3. Comparison of the extant and developed Y m models using on‐farm accessible data
This comparison aimed to evaluate the performance of the extant and developed models in predicting Y m using on‐farm accessible data (the one‐third dataset, n = 17). The predicted Y m values were constructed as a dataset by adding the independent variable(s) into the Y m models. Models A and I for the national level were again used. The predicted Y m values for models A and I were generated around their mean value using their specific uncertainty value, namely 6.5% ± 1.0% GE intake and 8.4% ± 0.4% GE intake, respectively. The mean was presumed to be the lower bounds if the diet had a greater DE/ME value (due to the negative relationship between the energy use efficiency and Y m values), and thus, the upper bounds were used on the opposite side.
Three parameters were used as model evaluation tools, namely the mean square prediction error (MSPE; Tedeschi, 2006), the concordance correlation coefficient (CCC; Lin,1989), and observed versus predicted values (Kebreab et al., 2008). These statistical analyses are widely used to assess biological models (Ellis, Bannink, France, Kebreab, & Dijkstra, 2010; Jaurena et al., 2015; Tedeschi, 2006).
The MSPE analysis was divided into RMSPE (3) and total MSPE. Total MSPE was decomposed to compile the sources of variation in the MSPE (Bibby & Toutenburg, 1977), consisting of errors in central tendency (ECT), errors due to regression (ER), and errors due to disturbances (ED). These four statistical parameters were calculated as
| (4) |
| (5) |
| (6) |
| (7) |
where = mean observed Y m value, = mean predicted Y m value, S P = standard deviation of the predicted Y m value, r = Pearson correlation coefficient, and S O = standard deviation of the observed Y m value. ECT, ER, and ED were expressed as a percentage of total MSPE.
The CCC and derivative statistics (Lin, 1989) consisting of r, bias correction factor (C b), and the location shift (μ) were calculated as
| (8) |
| (9) |
| (10) |
where the notations are as above. The CCC evaluates a model's predictive accuracy and precision at the same time (the degree to which the pairs of observed and predicted Y m values fall on the unity line). A CCC value equal to 1 indicates perfect agreement between the two variables (Tedeschi, 2006). This r measures precision (deviation of the observed from the predicted Y m values line) and C b (range = 0___1, perfect score = 1) measures accuracy (how far the predicted Y m values line deviates from the unity line) (Ellis et al., 2010). Moreover, μ (range = negative___positive infinities, perfect score = 0) is a measure of the location shift relative to the scale (the degree of the residual of means relative to the root of the product of two standard deviations). A positive μ value indicates underprediction, while a negative one indicates overprediction (Kebreab et al., 2008).
The observed versus predicted plots were analyzed using the method described by Ellis et al. (2010). Briefly, the slope was determined by regressing the observed Y m values (independent variable) against the predicted Y m values (dependent variable) using the REG procedure. This response aims to test the significance of the slope against 0, which assesses the existence of linear relationship between the observed and predicted values.
3. Results
3.1. Dataset description
The dataset for this meta‐analysis, including beef cattle characteristics (age and body weight), diet composition, digestibility, feeding level, and enteric methane emissions, is shown in Table 1. The GE content of diets ranged from 15.0 to 19.9 MJ/kg DM and averaged 17.6 MJ/kg DM. Enteric methane emissions were ~120 g head−1 day−1 (range 38–311 g head−1 day−1). The observed Y m value ranged from 4.8% to 13.7% of GE intake.
3.2. Development of the models
The Y m models developed and categorized using the levels of predictive possibility discussed herein are listed in Table 3. For the national level, the model simulated according to the IPCC yielded model I as the refinement (Y m = 8.4% ± 0.4% of GE intake) to the IPCC default model (Y m = 6.5% ± 1.0% GE intake). Based on a model comparison (Figure 1), the IPCC default model underestimated the Y m values of the Zebu beef cattle fed low‐quality crop residues and by‐products in tropical regions by up to 45.5%, 29.3%, and 17.3% at the lower, middle, and upper bounds, respectively.
Figure 1.

Methane conversion factor (Y m) of Zebu beef cattle fed low‐quality crop residues and by‐products in tropical regions as compared with the IPCC default values. The referent line (Y m = 7.5%) represented the limitation of the IPCC default model
For the farm level, the regression analysis yielded models J, K, L, M, and N (p < .01; Table 3) that represented the dietary (ether extract and neutral detergent fiber contents of the diet), intake (ether extract and crude protein intakes), digestibility (organic matter digestibility), integrated dietary, intake and digestibility (ether extract content, dry matter intake, and digestible organic matter intake), and energy (DE/GE and ME/DE) levels, respectively. The independent variable(s) in models J, K, L, and M did not fit well to predicted Y m values because they had too low R 2 (.25___.54), and relatively moderate RMSPE values (14.5%___18.5%). The multiple variables in model N had a moderate R 2 of .71 and a low RMSPE of 12.0%, and thus presumably had a moderate fit among all models. As it showed the largest VIF of 1.24, the clarity of the collinearity between the DE/GE and ME/DE variables was demonstrated.
3.3. Comparison of the extant and developed models using on‐farm accessible data
The MSPE analysis (Table 4) indicated that model N was the best performing model here (RMSPE = 9.1%, of which 99.7% of this error came from the disturbance). The CCC analysis also selected model N as that having the highest precision and accuracy (CCC = 0.75, r = .77, C b = 0.97) among the evaluated models. The positive and low μ value for model N (μ = 0.03) indicated a slightly underpredicted Y m value.
Table 4.
Mean predicted Y m values and analysis of the MSPE and CCC of the extant and developed Y m models (using the one‐third dataset, n = 17)
| Model category | Mean of predictedY m (±SE)a | MSPE analysisb | CCC analysisc | ||||||
|---|---|---|---|---|---|---|---|---|---|
| RMSPE% | ECT% | ER% | ED% | CCC | r | C b | μ | ||
| National level | |||||||||
| Model A | 6.56 (±0.135) | 23.1 | 64.6 | 0.6 | 34.8 | 0.18 | .52 | 0.33 | 1.78 |
| Model I | 8.42 (±0.054) | 15.1 | 7.0 | 14.2 | 78.8 | 0.16 | .53 | 0.31 | −0.62 |
| Farm level | |||||||||
| Model B | 6.42 (±0.086) | 24.8 | 67.0 | 3.2 | 29.8 | 0.11 | .54 | 0.20 | 2.43 |
| Model C | 7.34 (±0.185) | 20.1 | 20.4 | 16.7 | 62.9 | 0.04 | .06 | 0.70 | 0.75 |
| Model D | 6.58 (±0.088) | 25.1 | 53.9 | 4.8 | 41.3 | 0.02 | .07 | 0.23 | 2.18 |
| Model E | 7.80 (±0.414) | 22.2 | 2.5 | 51.3 | 46.2 | 0.27 | .28 | 0.95 | 0.20 |
| Model F | 7.01 (±0.130) | 18.6 | 48.6 | 2.0 | 49.4 | 0.23 | .57 | 0.45 | 1.28 |
| Model G | 8.48 (±0.053) | 16.2 | 8.4 | 0.2 | 91.4 | 0.06 | .21 | 0.30 | −0.73 |
| Model H | 10.14 (±0.422) | 36.0 | 47.9 | 32.2 | 19.9 | 0.02 | .05 | 0.51 | −0.14 |
| Model J | 8.32 (±0.289) | 14.1 | 3.6 | 14.4 | 82.0 | 0.54 | .55 | 0.98 | −0.19 |
| Model K | 8.08 (±0.148) | 12.2 | <0.1 | 4.6 | 95.4 | 0.48 | .63 | 0.76 | 0.01 |
| Model L | 8.08 (±0.221) | 18.6 | <0.1 | 28.1 | 71.9 | 0.06 | .06 | 0.93 | 0.01 |
| Model M | 8.08 (±0.230) | 11.3 | <0.1 | 0.6 | 99.4 | 0.62 | .66 | 0.95 | 0.01 |
| Model N | 8.06 (±0.254) | 9.1 | 0.2 | 0.1 | 99.7 | 0.75 | .77 | 0.97 | 0.03 |
Y m, methane conversion factor (% of GE intake); mean of the observed Y m is 8.09 (SE = ±0.321).
MSPE, mean square prediction error; RMSPE, root‐mean‐square prediction error (% of the observed mean); ECT, errors in central tendency (% of total MSPE); ER, errors due to regression (% of total MSPE); ED, errors due to disturbances (% of total MSPE).
CCC, concordance correlation coefficient; r, Pearson correlation coefficient; C b, bias correction factor; μ, location shift.
Once again, the analysis of the observed versus predicted values plots (Figure 2) indicated that only model N had moderate predictive power (R 2 = .67). For most of the models here, although the statistical significance of the slope was reached (p < .05 or <.01), predictive power was very low considering an R 2 less than .50.
Figure 2.

Predicted (y‐axis) versus observed (x‐axis) Y m values of the extant and developed models (using the one‐third dataset, n = 17)
4. Discussion
4.1. Perspectives of the dataset
Because of the importance of Y m in determining the accuracy of enteric methane emissions for national and global inventories (IPCC, 2006), we analyzed a range of Y m models of the associated beef cattle production system. The present dataset (Table 1) is different from that used to develop the IPCC (2006) Y m default model, by means of geographic areas of data, and especially the existence of cattle breeds and feed resources from tropical areas highlighted here. Our dataset covered a wide range beef cattle fed low‐quality crop residues and by‐products production systems in tropical regions (from growing to finishing). Zebu beef cattle in Thailand such as native Thai cattle have a low mature body weight of ~450 kg for females and ~550 kg for males, while Brahman cattle and Zebu beef cattle crossed with B. taurus can show a higher mature body weight (Marcondes, Tedeschi, Valadares Filho, & Gionbelli, 2013; Ogino et al., 2016). Nellore beef cattle, wide spread in Brazil and India, are also a small breed size, with a mature body weight of ~530 kg according to Marcondes et al. (2013). The diet compositions and nutritive values such as crude protein (40–213 g/kg DM), total digestible nutrients (454–737 g/kg), and ME content (6.7–12.9 MJ/kg DM) showed several available feeding systems for tropical developing countries. The mean enteric methane emission rate in our records (~120 g methane head−1 day−1) could result from frame size and voluntary feed intake of cattle (Smith, Lyons, Wagner, & Elliott, 2015).
The range of Y m values of 4.8%–13.7% of GE intake in this study agreed with that in Johnson and Johnson (1995). The many attempts to estimate Y m variability emphasize the difficulty because of the number of factors related to Y m (Blaxter & Clapperton, 1965; Hill, McSweeney, Wright, Bishop‐Hurley, & Kalantar‐Zadeh, 2016). What is certain is the positive relationship between plant fiber digestion and high acetic acid production sides as well as between plant fiber digestion and high methanogenesis yields in the rumen (IPCC, 2006, Jaurena et al., 2015). Roughage sources can change Y m because of the fiber compositions (Jaurena et al., 2015; Kennedy & Charmley, 2012). While dietary lipid is also undeniably a strong single indicator of Y m, the change is not constant (e.g., when sources of the lipid are different; Patra, 2013). Further, diets fed as single feed at varying levels of feeding also deduce Y m given the stimulated rates of passage or undigested feed in the rumen (Blaxter & Clapperton, 1965; Chaokaur et al., 2015). Using these factors as the single or multiple variables of a Y m model are typical, while rough estimates often fail to capture Y m for a variety of reasons including extrapolation (application of the model beyond the domain for which model predictions are known to be valid; IPCC, 2006, Bannink, van Schijndel, & Dijkstra, 2011). Studies have suggested that the application of models is positively associated with the degree of representativeness between a model's dataset and a real farm (Ellis et al., 2010, IPCC, 2006). Ideally, models which relate the diet particles and chemical component rates of passage and digestion in each enteric compartment at varying intake levels and the resulting hydrogen balance, volatile fatty acids, and microbial yields should generate Y m values that are reliable to direct measurements from cattle (IPCC, 2006). Thus, more representative and complex models can result in fairly different Y m accuracies (i.e., the degree of simulation of real systems).
Many attempts also promoted the methane mitigation through consideration of model's prediction characteristics. Recently, Jaurena et al. (2015) demonstrated that the categories of cattle (beef or dairy) and roughage (fresh forage, conserved forage, straw) are the primary factors affecting Y m values. Conventionally, it has been known that Y m values reduce as ME intake (Blaxter & Clapperton, 1965; Chaokaur et al., 2015), feed quality (starch content), energy content (IPCC, 2006; Johnson & Johnson, 1995; Kurihara et al., 1999), and fat content rise (Chuntrakort et al., 2014; Patra, 2013). Our previous studies showed that an increase in feeding level not only reduces Y m values, but also improves beef productivity; thus, reducing the intensity of enteric methane is a strategic feeding management approach (Chaokaur et al., 2015; Tangjitwattanachai et al., 2015).
4.2. Predicting Y m values at the national level for Zebu beef cattle in tropical regions
The predicted Y m values are used in a complex algorithm standardized by IPCC (2006). If inventory compliers are chosen at the tier 2 level, the aim is to control errors of less than 20% around the mean of the enteric methane emission inventory of a country. IPCC (2006) suggested that a 10% error in a variable will result in methane errors ranging up to 20% depending on the circumstances. Our result (Figure 1) showed room to improve Y m predictions for Zebu beef cattle fed low‐quality crop residues and by‐products in tropical regions. Compared with the refinement (model I), the default underestimated by up to 29.3% for the reference animal and diets (Y m = 6.5% vs. 8.4% GE intake). This finding confirmed the Y m degrees are different among different livestock and feed combinations (IPCC, 2006). However, the available data are sparse during the Y m default models. The 0.4% GE intake of uncertainty for predicted Y m was lower than the 1.0% reported under tier 2 because of the sample size effect (i.e., a larger sample size reduces its standard error). The sample size in the present dataset was larger than that of Lassey (2007) used to develop the IPCC's Y m default model, that is, n = 53 versus n = 14. Traditionally, the uncertainty of the refinement (model I) could also be replaced as 1.0% GE intake (IPCC, 2006). Beyond the scope of our study, as the available data are limited, such an improvement still needs cattle fed on tropical pastures as well a tier 3 model that includes a dynamic and mechanistic model of fermentation biochemistry in the enteric to calculate enteric methane emission inventories, instead of a tier 2 one (Bannink et al., 2011). The Y m tabulation for the cattle fed blooming grasses, legumes, and high‐quality crop residues should be related to the IPCC's data because there is evidence in Brazil and Australia that the Y m response to this diet is rather similar given the overall range of uncertainty (Kennedy & Charmley, 2012; Pedreira et al., 2013; Tomkins et al., 2015). Additionally, a main reason for this difference is the degree to which Y m depends on feed quality (Jaurena et al., 2015; Kurihara et al., 1999; Lassey, 2007).
4.3. Predicting the Y m values at the farm level for Zebu beef cattle in tropical regions
Predicting the Y m values at the farm level is a different task compared with tier 2. Indeed, describing the Y m trends from the direct measurements in cattle is challenging for a variety of reasons such as the importance of data on methane mitigation throughout the assessment of the carbon footprint values (Ogino et al., 2016). According to Kebreab et al. (2008), predicted values equal observed values in a perfect model. Thus, the best model should have a low RMSPE, high CCC, and high R 2 (observed vs. predicted). Some researchers have shown that regression models may also be capable of describing the changes in Y m values considering the effects of dietary changes (Blaxter & Clapperton, 1965; Jaurena et al., 2015; Patra, 2013; Ramin & Huhtanen, 2013; Yan et al., 2000). In particular, as the regression approach statistically relates the factors of animal and diet to Y m output, it was thus effective to refine to the IPCC (2006) default Y m model when predicting at the farm level because the latter is designed to enumerate national‐level emissions (Crosson et al., 2011). Our results (Table 4, Figure 2) showed that model N had adequate predictive performance among the examined models. The results recognized that a large scatter of Y m values that represent on‐farm data needs complexity for generating estimates, including DE/GE and ME/DE (energy use efficiencies of the diet consumed). The positive relationship between DE/GE and the Y m value agrees with the findings of Blaxter and Clapperton (1965). In the IPCC (2006) guidelines, DE/GE is recommended as an important factor for controlling variations in Y m, although it is excluded in the tier 2 model. For model N, the ME/DE appeared to be an additional implement beyond to other traditions. Indeed, the Y m value was sensitive to variation in ME/DE because methane is an energy loss that is represented in DE to ME content. Model N's assessment of an enteric methane inventory relies on the beef cattle herds and feedstock being well characterized. In tropical regions of developing countries, some farmers impose changes in beef herd composition and feeding regime to improve beef productivity. These considerations challenge the enteric methane inventory method (Lassey, 2007).
For the case of extent models, the lack of data representativeness of the cattle used in this analysis could be a major source of error. This kind of model error typically calls for extrapolation, which is associated with a lack of correspondence between the circumstances associated with the available data and those associated with the predictions (IPCC, 2006). In this case, the Y m data of the extent models may be available for situations in which high diet quality is stimulating at high voluntary intake load but not for situations involving the intake limited changes due to low diet quality (Table 1, dry matter intake varied from 1.2% to 2.2% body weight). Thus, the variables are only partly relevant to the desired Y m estimate. Another possible error is the measurement error, which may be random as a result of missing information (feed characteristics, includes ether extract, fibers, and digestibilities) from external sources. Overall, the results imply that the further prediction of Y m should focus on representing the effects of traditional variables such feed characteristics and intakes.
In conclusion, this meta‐analysis highlighted the advantages of some developed Y m models for Zebu beef cattle fed low‐quality crop residues and by‐products in tropical developing countries. The dataset reported the importance of Zebu beef cattle, diet composition, feeding level, enteric methane emission rate (~120 g head−1 day−1), and Y m model (8.4% ± 0.4% of GE intake) for the national level regarding the IPCC's tier 2 level application. We further showed that the IPCC default model (Y m = 6.5% ± 1% of GE intake) underestimates the Y m value by 1.9% of GE intake. At the farm level, seven of the extant models examined herein were inadequate for describing changes in the Y m value (RMSPE = 16.2%–36.0%, CCC = 0.02–0.27, R 2 = <.01–.37). Finally, although these findings contribute to our understanding of Zebu beef cattle populations in tropical regions and offer better model applications for estimating their presented Y m values, the lack of information obtained from feedlot and grazing herds is a limitation of this study. Thus, the scopes for further research should be to develop the Y m models using feedlot and grazing datasets to provide more implications in estimating enteric methane emissions of Zebu cattle.
Conflict of Interest
None declared.
Acknowledgments
We thank Khon Kaen University, the National Research Council of Thailand (NRCT2556___64), the Japan International Research Center for Agricultural Sciences, and the research article owners. We also thank the Food and Functional Food Research Cluster of Khon Kaen University (under the Higher Education Research Promotion and National Research University Project, Office of the Higher Education Commission) who supported Ph.D. student Mr. Chatchai Kaewpila with a scholarship fund (Ph.d.54126).
References
- Bannink, A. , van Schijndel, M. W. , & Dijkstra, J. (2011). A model of enteric fermentation in dairy cows to estimate methane emission for the Dutch National Inventory Report using the IPCC Tier 3 approach. Animal Feed Science and Technology, 166–167, 603–618. [Google Scholar]
- Belsley, D. A. , Kuh, E. , & Welsch, R. E. (1980). Regression diagnostics. Hoboken, NJ: John Wiley & Sons Inc. [Google Scholar]
- Bibby, J. , & Toutenburg, H. (1977). Prediction and improved estimation in linear models. Chichester, UK: John Wiley & Sons. [Google Scholar]
- Blaxter, K. L. , & Clapperton, J. L. (1965). Prediction of the amount of methane produced by ruminants. The British Journal of Nutrition, 19(4), 511–522. [DOI] [PubMed] [Google Scholar]
- Canesin, R. C. , Berchielli, T. T. , Messana, J. D. , Baldi, F. , Pires, A. V. , Frighetto, R. T. S. , … Reis, R. A. (2014). Effects of supplementation frequency on the ruminal fermentation and enteric methane production of beef cattle grazing in tropical pastures. Revista Brasileira de Zootecnia, 43(11), 590–600. [Google Scholar]
- Chaokaur, A. , Nishida, T. , Phaowphaisal, I. , & Sommart, K. (2015). Effects of feeding level on methane emissions and energy utilization of Brahman cattle in the tropics. Agriculture, Ecosystems & Environment, 199, 225–230. [Google Scholar]
- Chaokaur, A. , Nishida, T. , & Sommart, K. (2010). Effects of various levels of crude protein and metabolizable energy intake on heat production of Brahman cattle fed under humid tropical conditions In Crovetto G. M. (Ed.), Proceeding of the energy and protein metabolism and nutrition: 3rd EAAP International Symposium on Energy and Protein Metabolism and Nutrition, Parma, Italy (pp. 309–310). Wageningen, the Netherlands: Wageningen Academic Publishers. [Google Scholar]
- Chuntrakort, P. , Otsuka, M. , Hayashi, K. , Takenaka, A. , Udchachon, S. , & Sommart, K. (2014). The effect of dietary coconut kernels, whole cottonseeds and sunflower seeds on the intake, digestibility and enteric methane emissions of Zebu beef cattle fed rice straw based diets. Livestock Science, 161(1), 80–89. [Google Scholar]
- Crosson, P. , Shalloo, L. , O'Brien, D. , Lanigan, G. J. , Foley, P. A. , Boland, T. M. , & Kenny, D. A. (2011). A review of whole farm systems models of greenhouse gas emissions from beef and dairy cattle production systems. Animal Feed Science and Technology, 166–167, 29–45. [Google Scholar]
- Ellis, J. L. , Bannink, A. , France, J. , Kebreab, E. , & Dijkstra, J. (2010). Evaluation of enteric methane prediction equations for dairy cows used in whole farm models. Global Change Biology, 16(12), 3246–3256. [Google Scholar]
- FAO (2010). Greenhouse gas emissions from the dairy sector. Rome, Italy: Author. [Google Scholar]
- FAO (2015). The second report on the state of the world's animal genetic resources for food and agriculture. Rome, Italy: FAO Commission on Genetic Resources for Food and Agriculture Assessments. [Google Scholar]
- Feedipedia (2015). Animal feed resources information system, published on the website of INRA CIRAD AFZ and FAO. Retrieved from http://www.feedipedia.org/
- Hill, J. , McSweeney, C. , Wright, A.‐D. G. , Bishop‐Hurley, G. , & Kalantar‐Zadeh, K. (2016). Measuring methane production from ruminants. Trends in Biotechnology, 34(1), 26–35. [DOI] [PubMed] [Google Scholar]
- Hristov, A. N. , Oh, J. , Firkins, J. L. , Dijkstra, J. , Kebreab, E. , Waghorn, G. , … Tricarico, J. M. (2013). SPECIAL TOPICS‐Mitigation of methane and nitrous oxide emissions from animal operations: I. A review of enteric methane mitigation options. Journal of Animal Science, 91(11), 5045–5069. [DOI] [PubMed] [Google Scholar]
- IPCC (2006). 2006 IPCC guidelines for national greenhouse gas inventories. Hayama, Japan: Institute for Global Environmental Strategies (IGES). [Google Scholar]
- Jaurena, G. , Cantet, J. M. , Arroquy, J. I. , Palladino, R. A. , Wawrzkiewicz, M. , & Colombatto, D. (2015). Prediction of the Ym factor for livestock from on‐farm accessible data. Livestock Science, 177, 52–62. [Google Scholar]
- Johnson, K. A. , & Johnson, D. E. (1995). Methane emissions from cattle. Journal of Animal Science, 73(8), 2483–2492. [DOI] [PubMed] [Google Scholar]
- Kaewpila, C. , Suzuki, T. , & Sommart, K. (2015). Effect of whole kapok seed or chitosan supplementation on feed intake and methane emission of Thai native beef cattle fed rice straw In Lu Y., Takehara K., Beynen A. C., Yasuhiro K., & Haron W. (Eds.), Proceeding of the 5th International Conference on Sustainable Animal Agriculture for Developing Countries (SAADC2015) (p. 216). Nakorn Ratchasima, Thailand: Rajamangala University of Technology Isan. [Google Scholar]
- Kearl, L. C. (1982). Nutrient requirements of ruminants in developing countries. Logan, UT: International Feedstuffs Institute. [Google Scholar]
- Kebreab, E. , Johnson, K. A. , Archibeque, S. L. , Pape, D. , & Wirth, T. (2008). Model for estimating enteric methane emissions from United States dairy and feedlot cattle. Journal of Animal Science, 86(10), 2738–2748. [DOI] [PubMed] [Google Scholar]
- Kennedy, P. M. , & Charmley, E. (2012). Methane yields from Brahman cattle fed tropical grasses and legumes. Animal Production Science, 52(4), 225–239. [Google Scholar]
- Khuamankgorn, P. , Namsele, R. , Angthong, W. , & Martosoth, S. (2009). Determination of metabolizable energy of Rhodes grass (Chloris gayana) and Purple guinea grass (Panicum maximum TDn58) in beef cattle In Oshio S., Otsuka M. & Sommart K. (Eds.), Proceeding of the establishment of a feeding standard of beef cattle and a feed database for the Indochinese peninsula (pp. 30–32). Ibaraki, Japan: Japan International Research Center for Agricultural Sciences. [Google Scholar]
- Kongphitee, K. , Udchachon, S. , Otsuka, M. , & Sommart, K. (2010). Energetic efficiency of Thai native beef cattle fed rice straw or Ruzi straw base diet. Khon Kaen Agriculture Journal, 38(Suppl), 176–179. [Google Scholar]
- Kurihara, M. , Magner, T. , Hunter, R. A. , & McCrabb, G. J. (1999). Methane production and energy partition of cattle in the tropics. The British Journal of Nutrition, 81(3), 227–234. [PubMed] [Google Scholar]
- Lassey, K. R. (2007). Livestock methane emission: From the individual grazing animal through national inventories to the global methane cycle. Agricultural and Forest Meteorology, 142(2–4), 120–132. [Google Scholar]
- Lin, L. I. K. (1989). A concordance correlation coefficient to evaluate reproducibility. Biometrics, 45(1), 255–268. [PubMed] [Google Scholar]
- Marcondes, M. I. , Tedeschi, L. O. , Valadares Filho, S. C. , & Gionbelli, M. P. (2013). Predicting efficiency of use of metabolizable energy to net energy for gain and maintenance of Nellore cattle. Journal of Animal Science, 91(10), 4887–4898. [DOI] [PubMed] [Google Scholar]
- Mertens, D. R. (1997). Creating a system for meeting the fiber requirements of dairy cows. Journal of Dairy Science, 80, 1463–1481. [DOI] [PubMed] [Google Scholar]
- Moonmat, N. , Otsuka, M. , Udchachon, S. , & Sommart, K. (2009). Nutritive value and metabolizable energy evaluation of rice bran, kapok seed meal and coconut meal in Thai native beef cattle. Journal of Science and Technology Mahasarakham University, 29(4), 382–388. [Google Scholar]
- Moraes, L. E. , Strathe, A. B. , Fadel, J. G. , Casper, D. P. , & Kebreab, E. (2014). Prediction of enteric methane emissions from cattle. Global Change Biology, 20(7), 2140–2148. [DOI] [PubMed] [Google Scholar]
- Nakagawa, S. , & Schielzeth, H. (2013). A general and simple method for obtaining R2 from generalized linear mixed‐effects models. Methods in Ecology and Evolution, 4(2), 133–142. [Google Scholar]
- Nielsen, O.‐K. , Mikkelsen, M. H. , Hoffmann, L. , Gyldenkærne, S. , Winther, M. , Nielsen, M. , … Hansen, M. G. (2011). Denmark's National Inventory Report 2011—Emission climate, inventories 1990–2009—Submitted under the United Nations Framework Convention on Change and the Kyoto Protocol. Rønde, Denmark: National Environmental Research Institute, Aarhus University. [Google Scholar]
- Nitipot, P. , Pattarajinda, V. , & Sommart, K. (2010). Energy requirements of Zebu beef cattle: A meta‐analysis. Khon Kaen Agricuture Journal, 38(supplement), 184–188. [Google Scholar]
- NRC (2000). Nutrient requirements of beef cattle (7th ed.). Washington, DC: National Academy Press. [Google Scholar]
- Ogino, A. , Sommart, K. , Subepang, S. , Mitsumori, M. , Hayashi, K. , Yamashita, T. , & Tanaka, Y. (2016). Environmental impacts of extensive and intensive beef production systems in Thailand evaluated by life cycle assessment. Journal of Cleaner Production, 112, 22–31. [Google Scholar]
- Opio, C. , Gerber, P. , Mottet, A. , Falculli, A. , Tempio, G. , MacLeod, M. , … Steinfeld, H. (2013). Greenhouse gas emissions from ruminant supply chains—A global life cycle assessment. Rome, Italy: Food and Agriculture Organization of the United Nations. [Google Scholar]
- Owens, F. N. , Sapienza, D. A. , & Hassen, A. T. (2010). Effect of nutrient composition of feeds on digestibility of organic matter by cattle: A review. Journal of Animal Science, 88(Suppl 13), E151–E169. [DOI] [PubMed] [Google Scholar]
- Patra, A. K. (2013). The effect of dietary fats on methane emissions, and its other effects on digestibility, rumen fermentation and lactation performance in cattle: A meta‐analysis. Livestock Science, 155(2–3), 244–254. [Google Scholar]
- Pedreira, M. dos S. , de Oliveira, S. G. , Primavesi, O. , de Lima, M. A. , Frighetto, R. T. S. , & Berchielli, T. T. (2013). Methane emissions and estimates of ruminal fermentation parameters in beef cattle fed different dietary concentrate levels. Revista Brasileira de Zootecnia, 42(8), 592–598. [Google Scholar]
- Phromloungsri, A. , Hayashi, K. , Otsuka, M. , Udchachon, S. , & Sommart, K. (2012). Effects of energy intake level on methane production of Thai Native and Brahman crossbred cattle. Khon Kaen Agriculture Journal, 40(Suppl), S5–S11. [Google Scholar]
- Ramin, M. , & Huhtanen, P. (2013). Development of equations for predicting methane emissions from ruminants. Journal of Dairy Science, 96(4), 2476–2493. [DOI] [PubMed] [Google Scholar]
- Rittenhouse, L. R. , Streeter, C. L. , & Clanton, D. C. (1971). Estimating digestible energy from digestible dry and organic matter in diets of grazing cattle. Journal of Range Management, 24, 73–75. [Google Scholar]
- Sitthiwong, J. (2010). Evaluation of the nutritive values of Brachiaria hybrid grasses and a study on the energy requirements for Thai native cattle. PhD Thesis, Ubon Ratchathani University, Ubon Ratchathani, Thailand. [Google Scholar]
- Smith, F. A. , Lyons, S. K. , Wagner, P. J. , & Elliott, S. M. (2015). The importance of considering animal body mass in IPCC greenhouse inventories and the underappreciated role of wild herbivores. Global Change Biology, 21(10), 3880–3888. [DOI] [PubMed] [Google Scholar]
- Suzuki, T. , Phaowphaisal, I. , Pholsen, P. , Narmsilee, R. , Indramanee, S. , Nitipot, P. , … Nishida, T. (2008). In vivo nutritive value of Pangola grass (Digitaria eriantha) hay by a novel indirect calorimeter with a ventilated hood in Thailand. Japan Agricultural Research Quarterly, 42(2), 123–129. [Google Scholar]
- Tangjitwattanachai, N. , Phaowphaisal, I. , Otsuka, M. , & Sommart, K. (2015). Enteric methane emission, energetic efficiency and energy requirements for maintenance of beef cattle in the tropics. Japan Agricultural Research Quarterly, 49, 399–407. [Google Scholar]
- Tedeschi, L. O. (2006). Assessment of the adequacy of mathematical models. Agricultural Systems, 89(2–3), 225–247. [Google Scholar]
- Tomkins, N. W. , Denman, S. E. , Pilajun, R. , Wanapat, M. , McSweeney, C. S. , & Elliott, R. (2015). Manipulating rumen fermentation and methanogenesis using an essential oil and monensin in beef cattle fed a tropical grass hay. Animal Feed Science and Technology, 200, 25–34. [Google Scholar]
- Tomkins, N. W. , McGinn, S. M. , Turner, D. A. , & Charmley, E. (2011). Comparison of open‐circuit respiration chambers with a micrometeorological method for determining methane emissions from beef cattle grazing a tropical pasture. Animal Feed Science and Technology, 166–167, 240–247. [Google Scholar]
- WTSR (2010). Nutrient requirement of beef cattle in Indochinese Peninsula. Khon Kaen, Thailand: Klungnanavitthaya Press. [Google Scholar]
- Yan, T. , Agnew, R. E. , Gordon, F. J. , & Porter, M. G. (2000). Prediction of methane energy output in dairy and beef cattle offered grass silage‐based diets. Livestock Production Science, 64(2–3), 253–263. [Google Scholar]
