Figures
Abstract
There has been considerable interest in the use of red seaweed, and in particular Asparagopsis taxiformis, to increase production of cattle and to reduce greenhouse gas emissions. We hypothesized that feeding seaweed or seaweed derived products would increase beef or dairy cattle performance as indicated by average daily gain (ADG), feed efficiency measures, milk production, and milk constituents, and reduce methane emissions. We used meta-analytical methods to evaluate these hypotheses. A comprehensive search of Google Scholar, Pubmed and ISI Web of Science produced 14 experiments from which 23 comparisons of treatment effects could be evaluated. Red seaweed (Asparagopsis taxiformis) and brown seaweed (Ascophyllum nodosum) were the dominant seaweeds used. There were no effects of treatment on ADG or dry matter intake (DMI). While there was an increase in efficiency for feed to gain by 0.38 kg per kg [standardized mean difference (SMD) = 0.56; P = 0.001] on DerSimonian and Laird (D&L) evaluation, neither outcome was significant using the more rigorous robust regression analysis (P >0.06). The type of seaweed used was not a significant covariable for ADG and DMI, but A. nodosum fed cattle had lesser feed to gains efficiency compared to those fed A. taxiformis. Milk production was increased with treatment on weighted mean difference (WMD; 1.35 ± 0.44 kg/d; P <0.001); however, the SMD of 0.45 was not significant (P = 0.111). Extremely limited data suggest the possibility of increased percentages of milk fat (P = 0.040) and milk protein (P = 0.001) on (D&L) WMD evaluation. The limited data available indicate dietary supplementation with seaweed produced a significant and substantial reduction in methane yield by 5.28 ± 3.5 g/kg DMI (P = 0.003) on D&L WMD evaluation and a D&L SMD of −1.70 (P = 0.001); however, there was marked heterogeneity in the results (I2 > 80%). In one comparison, methane yield was reduced by 97%. We conclude that while there was evidence of potential for benefit from seaweed use to improve production and reduce methane yield more in vivo experiments are required to strengthen the evidence of effect and identify sources of heterogeneity in methane response, while practical applications and potential risks are evaluated for seaweed use.
Citation: Lean IJ, Golder HM, Grant TMD, Moate PJ (2021) A meta-analysis of effects of dietary seaweed on beef and dairy cattle performance and methane yield. PLoS ONE 16(7): e0249053. https://doi.org/10.1371/journal.pone.0249053
Editor: Juan J. Loor, University of Illinois, UNITED STATES
Received: March 11, 2021; Accepted: June 29, 2021; Published: July 12, 2021
Copyright: © 2021 Lean et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting information files.
Funding: The authors received no funding for this work.
Competing interests: The authors have declared that no competing interests exist.
Introduction
There has been considerable interest in the use of red seaweed, and in particular Asparagopsis taxiformis to increase production of cattle and to reduce greenhouse gas emissions [1, 2]. However, several different seaweeds have been fed to cattle and include brown seaweeds (Ascophyllum nodosum), and Saragssum wightii. A commercial product ‘Tasco’ has been developed based on A. nodosum [3].
To date, there have been several reviews that have provided qualitative overviews of the production responses and the extent of inhibition of methane emissions when seaweed was included in the diets of beef and dairy cattle [4, 5]. However, there has been no comprehensive quantitative review of this subject. Given that studies have evaluated the effects of seaweeds on beef cattle production, on dairy cattle production, and on methane emissions, there is potential to evaluate the use of seaweeds in cattle production and methane emissions using meta-analytical methods. We hypothesized that feeding seaweed or seaweed derived products would increase beef or dairy cattle performance as indicated by average daily gain (ADG), feed efficiency measures, milk production, and milk constituents, and reduce methane emissions.
Materials and methods
Literature search
A comprehensive search of the English language literature used the US National Library of Medicine National Institutes of Health through PubMed (http://www.ncbi.nlm.nih.gov/pubmed), Google Scholar (http://scholar.google.com/), and the ISI Web of Science (http://apps.webofknowledge.com). The search was conducted on 21 January 2021 and searches were based on the following key words with no limits included: seaweed and cattle. We searched the reference lists of papers obtained to identify other studies. One additional paper was identified from a personal communication.
For Google Scholar, 28,400 citation results occurred, and the screening of papers stopped when 50 sequential citations were not relevant, whereas only 58 and 55 results occurred from Pubmed and ISI Web of Science, respectively. In one case, the authors of an article were contacted to clarify results and to provide additional information.
Inclusion criteria
Papers were primarily screened on their citation title by 2 reviewers and secondarily screened based on the full text. Experiments were included in the analysis if they met the following inclusion criteria developed by Scibus (Camden, NSW, Australia): were full manuscripts from peer-reviewed journals; experiments were in vivo and the animals studied were cattle; the experiments evaluated use of seaweed or seaweed derived products for dietary supplementation of cattle; they were randomized; they had a description of the randomization processes employed; they had appropriate analysis of data; they contained sufficient data to determine the effect size for production outcomes (e.g., the number of cattle or pens in each treatment and control group); they had a measure of effect so that the data were amenable to effect size (ES) analysis for continuous data (e.g., standardized mean difference, SMD); and they had a measure of variance (SE or SD) for each effect estimate or treatment and control comparisons. Studies that could not be adequately interpreted, used purposive and non-representative sampling methods or where authors did not respond to clarify their approach, were excluded. Note, one article was included from the pre-print server for Biology, bioRxiv (https://www.biorxiv.org/).
Fig 1 depicts a PRISMA diagram [6] of the flow of data collection for the meta-analysis. The PRISMA checklist is provided in S1 File. After the initial search and screening 62 different papers (experiments) were identified and papers without a full text (5) were excluded providing 57 papers that were assessed for eligibility. A total of 43 were excluded for the following reasons: the abstract was in English but the full article was in another language (3 experiments), the experiment was in vitro (8 experiments), the article was a review or book chapter (7 articles), the experiment had group feeding resulting in pseudo-replication (2 experiments), the experiment was off topic or had irrelevant outcomes (20 experiments), the experiment lacked measures of variance (2 experiments), or had an inadequate Latin Square wash-out period (1 experiment). A list of articles excluded with the reason is provided in S1 Table. A total of 14 experiments with 23 treatment comparisons were included in the meta-analysis. That is, papers were considered as ‘experiments’ and there were multiple comparisons within some experiments. A list of the experiments and comparisons included in the meta-analysis is provided in Table 1.
The n refers to the number of records for identification and screening that includes experimental articles, abstracts, books, review papers, theses, patents and other records, whereas for the eligibility and included stages n refers to the number of experimental articles, that is experiments.
Data extraction
All data extracted from each of the experiments that met the inclusion criteria were audited by up to three reviewers. The descriptive data extracted included experiment design, and details about the experiment and the animals used. Design details included the number of: animals or pens, animals/group, and pens/group; experimental and analytical unit (animal or pen). Experimental details included: the number of days on feed, the number of days treatment products were fed, the dose of treatment administered, and diet and delivery methods of product. Animal details included: class of cattle (steers or heifers, or dairy cows), production system (dairy or beef), initial body weight of control and treatment groups, and type of housing and feeding systems. Key descriptive data are provided in Table 1. All but three experiments were conducted using total mixed rations, 2 were pasture, and one partial mixed ration. Three of the methane experiments used Greenfeed devices (GreenFeed; C-Lock Inc., Rapid City, SD), and one a respiratory chamber.
Output variables extracted for meta-analysis included: final body weight (FBW, kg), ADG (kg/head/d), dry matter intake (DMI; kg/head/d), gross feed efficiency [ratio of feed to gain (F:G)], milk yield (kg/d), milk fat percentage, milk protein percentage, and methane yield (g/kg DMI) (Tables 2 and 3).
Statistical analysis
Data were structured to allow a classical meta-analytical evaluation of differences in responses of the experimental groups. Many of the experiments in this analysis used multiple treatment comparisons (nesting), and therefore the data had a hierarchical structure. For this reason, meta-regression using multi-level models was used to evaluate the effects of experiment and treatment by taking into account this hierarchical structure [18–20].
Initial data exploration included production of basic statistics using Stata (Version 16, StataCorp. LP, College Station, TX) to examine the data for errors and to estimate the means and measures of dispersion. Normality of the data was examined for continuous variables, by visual and statistical appraisal.
Stata was also used to analyze differences in responses by SMD analysis which is also called ES analysis. These methods have been published in detail in [21] and [22]. The difference between treatment and reference groups means, which is termed ‘treatment’ in the following description, was standardized using the SD of reference and treatment groups. The SMD estimates were pooled using the DerSimonian and Laird random effects models (D&L) [23] and, in the case of methane yield, with the more conservative Knapp-Hartung method (K-H) [24]. Only random effects models were used, as previous work concluded that when there was uncertainty in the evaluative units caused by clustering of observations, the random effects model was appropriate [25].
Robust regressions models (RR) were produced that account for the nested effect of comparisons within experiment [18] and analysed using “robumeta” (Stata) as applied by [26]. The RR were developed to account for the two-stage cluster sampling inherent when the ES estimates are derived from a total of n = k1 + k2 + ··· + km estimates from comparisons that were collected by sampling m clusters of experiments, that is several comparison estimates are derived from the same experiment [18]. Hence, sampling kj ≥ 1 estimates within the jth cluster for j = 1,…, m. Briefly, in this test the mean ES from a series of experiments is described as follows: In this case, the regression model has only an intercept b1 and the weighted mean has the form:
where m is the total number of experiments, k the total number of comparisons in the extracted database and wij is the weighting for comparisons within experiments and Tij is the vector of the ES estimates of comparisons within experiments. If all the estimates in the same experiment are given identical weights, the robust variance estimate (vR) reduces to:
where Ťj is the unweighted mean of the estimates in the jth cluster, b1 is the estimate of the weighted mean, and wj is the total weight given to estimates in the jth cluster. This is a kind of weighted variance which reduces to (m-1)/m2 times the variance, when the weights within experiment are identical, and (since the correlation coefficient = 1 in this case) the robust regression standard error equals 1/ m times the variance of Ťj estimated when the weights are equal. Several important aspects of the robust model are highlighted by [18] and the underlying assumptions that; the correlation structure of the Tj does not need be known to compute the pooled ES or VR, only that the vectors of estimates from different experiments are independent and that regularity conditions are satisfied; the experiment or comparison level regressors do not need to be fixed; the theorem is asymptotic based on the number of experiments, rather than the number of comparisons; and the theorem is relatively robust to regularity assumptions.
A random-effects weighted mean difference (WMD) between treatment and reference was estimated, with the weighting reflecting the inverse of the variance of the treatments included according to the nostandard method in the metan model of Stata to allow an interpretation of treatment effects in familiar units (e.g. kg of FBW), rather than ES.
Forest plots were produced for both WMD and SMD results for each outcome variable that incorporated the D&L and RR estimates. The forest plots provided further allow a comparison of A. taxiformis, A. nodosum, and ‘other’ sources of seaweed evaluated with the D&L and RR methods. Additionally, plots were produced for initial body weight.
Variations among the comparison level SMD were assessed using a chi-squared (Q) test of heterogeneity. Heterogeneity in comparisons reflects underlying differences in clinical diversity of the research site and interventions, differences in experimental design and analytical methods, and statistical variation around responses. The clinical diversity of the site includes all the non-study design aspects of variation, such as facility design, environment, and cattle management that may be measured and controlled for in meta-analysis but are often not reported or measured. Identifying the presence and sources of the heterogeneity improves understanding of the responses to the interventions used. An α level of 0.10 was used because of the relatively poor power of the χ2 test to detect heterogeneity among small numbers of trials [27]. Heterogeneity of results among the comparisons was quantified using the I2 statistic [28]. The I2 provides an estimate of the proportion of the true variance of effects of the treatment, that is the true variance, tau2 (τ2) divided by the total variance observed in the comparison [29] that reflect measurement error. Negative values of I2 are assigned a value of 0, consequently the value I2 lies between 0 and 100%. An I2 value between 0 and 40% might not be important, 30 to 60% may represent moderate heterogeneity, 50 to 90% might represent substantial heterogeneity, and 75 to 100% might represent considerable heterogeneity [30]. Both I2 and τ2 are provided to allow readers the opportunity to evaluate both metrics.
A key focus of meta-analysis is to identify and understand the sources of heterogeneity or variation of response among comparisons. However, given the limited number of experiments available the only meta-regression analyses suitable were for category of seaweed intervention for ADG and DMI and production system for DMI.
Presence of publication bias was investigated using funnel plots which are a simple scatter plot of the intervention effect estimates from individual comparisons plotted against comparison precision. The name ‘funnel plot’ arises because precision of the intervention effect increases as the size and precision of a comparison increases. Effect estimates from comparisons with a small number of animal units will scatter more widely at the bottom of the graph and the spread narrows for those with higher numbers of units. In the absence of bias, the plot should approximately resemble a symmetrical (inverted) funnel.
Results and discussion
The literature that was amenable to quantitative review on seaweed use in cattle was reasonably limited with only 14 full texts suitable (Fig 1; Table 1). The experiments used were all published after the year 2000, indicating that they are relatively current. Although these were current some production data indicated only modest production performance (Tables 2 and 3). Funnel plots produced indicated that publication bias was not likely (S1 Fig). The limited number of comparisons and even fewer experiments limited the type of meta-regressions that could be performed and the use of RR. Only 2 experiments, one on a dairy and one on a beef production system, used Latin Square designs and this precluded evaluation of the effect of study design. As the SD of these were similar to the randomized controlled designs adjustments to the error terms for these were not made.
Differences in FBW were significant for treatment for both RR SMD and RR WMD suggesting that the FBW was lower for treated cattle and was not influenced by production system (Table 4). These findings were not supported by differences in ADG with all models showing little difference in ADG (Table 4; Fig 2). The numerically lower initial body weight for treated cattle supports the contention that FBW differences were substantially influenced by initial BW differences (WMD D&L = −3.08 kg; 95% CI = −7.62 to 1.46; P = 0.183; SMD D&L = −0.28; 95% CI = −0.57 to 0.02; P = −0.57 to 0.02). The comparisons contributing to the observations on FBW and ADG differ but had considerable overlap as 9 comparisons were shared. There was no evidence of difference between A. taxiformis and A. nodosum interventions on FBW or ADG (Table 4).
The solid vertical line represents a mean difference of zero or no effect. Points to the left of the line represent a reduction in ADG, while points to the right of the line indicate an increase. Each square around the point effect represents the mean effect size for that comparison and reflects the relative weighting of the comparison to the overall effect size estimate. The larger the box, the greater the comparison contribution to the overall WMD estimate. The weights that each comparison contributed are in the right-hand column. The upper and lower limit of the line connected to the square represents the upper and lower 95% CI for the WMD. The overall pooled WMD and 95% CI pooled using the DerSimonian and Laird (D+L) [23] and robust meta-analytical random effects models [18, 26] are indicated by the respective diamonds at the bottom. The heterogeneity measure, I2 is a measure of residual variation among comparisons included in the meta-analysis. The ADG was not heterogeneous as indicated by the overall I2 of 0%.
There was no effect of treatment on DMI (Table 4; Fig 3) and neither the effects of dairy or beef production system nor type of seaweed significantly influenced results (Table 4). Interestingly, these results were heterogenous among comparisons indicting substantial variations in experimental measurement (I2 > 60%; Table 4). The F:G was evaluated in 10 comparisons. The F:G was reduced by a significant 0.38 kg per kg with an SMD of 0.60 (Table 4); however, these are the less conservative D&L measures; the RR estimates were not significant with WMD -0.41 kg and SMD -0.56. The A. nodosum fed cattle had lesser gains in efficiency compared to the A. taxiformis fed cattle (Table 4). Differences in the significance of the WMD and SMD reflect differences in the algorithms used to calculate these. While the SMD provides a better estimate of significance the WMD, when it can be calculated, provides more familiar units.
Effects for Ascophyllum nodosum and Asparagopsis taxiformis and ‘Other’ seaweed interventions are provided as well as an overall effect. The solid vertical line represents a mean difference of zero or no effect. Points to the left of the line represent a reduction in DMI, while points to the right of the line indicate an increase. Each square around the point effect represents the mean effect size for that comparison and reflects the relative weighting of the comparison to the overall WMD estimate. The larger the box, the greater the comparison contribution to the overall estimate. The weights that each comparison contributed are in the right-hand column. The upper and lower limit of the line connected to the square represents the upper and lower 95% CI for the WMD. The overall pooled WMD and 95% CI pooled using the DerSimonian and Laird (D+L) [23] and robust meta-analytical random effects models [18, 26] are indicated by the respective diamonds at the bottom. The heterogeneity measure, I2 is a measure of residual variation among comparisons included in the meta-analysis. The DMI was substantially heterogeneous as indicated by the overall I2 of 60.9%.
Milk production was evaluated in only 6 experiments; however, the results were a significant D&L WMD of 1.35 kg/d increase with treatment. However, the D&L SMD of 0.45 was not significant and was heterogenous (I2 = 65.1%; Table 4). There were no significant effects on percentages of milk fat or milk protein on SMD, which were both heterogenous (I2 = 66.2% and 73.8%, respectively). However, the WMD for both milk fat and protein percentages were significantly increased by 0.06% (Table 4). The milk production results contrast with the lack of effect on ADG of treatment, but may be consistent with the efficiency improvement in F:G. The differences in SMD and WMD results reflect sparse data and differences in the weighting between these measures.
There is considerable interest in the potential for Asparagopsis to reduce methane emissions and methane yield [1, 2, 14, 31]. The very limited data available for the meta-analysis provide support for the effect to reduce methane yields in vivo with a D&L WMD of −5.28 ± 3.5 g/kg of DMI, D&L SMD of −1.70 or K-H SMD of −1.94 indicating a substantial reduction in methane yields. There was marked heterogeneity in the results (I2 > 80%; Table 4; Fig 4). In one comparison the reduction in methane yield with treatment was 97% [2]. These results are consistent with the observations made in in vitro studies on the effects of A. taxiformis on methane emissions [4] providing further evidence methane emissions is markedly reduced. The mechanism for the reduction in methane emissions and methane yields has been attributed to the bromoform and di-bromochloromethane content of the seaweeds [32, 33] that inhibit methane emissions. However, there are concerns that halogenated gases associated with the bromoforms could cause damage to the ozone layer [4, 34]. At the higher dose of 0.5% inclusion of A. taxiformis, [14] found that DMI and milk production and energy corrected milk production were significantly lower than controls and that the milk contained markedly increased concentrations of iodine (> 5 times the control) and bromide (approximately 8 times the control). In the experiment of [14], the concentration of iodine in milk of cows given 0.5% A. taxiformis was approximately 3 mg/L, and assuming that a child <3 yr old can drink milk at 1 L/d this is approximately 15 times the upper tolerable intake level [35].
The solid vertical line represents a mean difference of zero or no effect. Points to the left of the line represent a reduction in methane yield, while points to the right of the line indicate an increase. Each square around the point effect represents the mean effect size for that comparison and reflects the relative weighting of the comparison to the overall effect size estimate. The larger the box, the greater the comparison contribution to the overall estimate. The weights that each comparison contributed are in the right-hand column. The upper and lower limit of the line connected to the square represents the upper and lower 95% CI for the effect size. The overall pooled effects size or SMD and 95% CI pooled using the DerSimonian and Laird (D+L) [23] and robust meta-analytical random effects models [18, 26] are indicated by the respective diamonds at the bottom. The heterogeneity measure, I2 is a measure of residual variation among comparisons included in the meta-analysis. Methane yield was considerably heterogeneous as indicated by the overall I2 of 84.0%.
Although the present analysis indicates that the supplementary feeding of A. taxiformis to beef and dairy cattle has some positive effects on animal production and desirable inhibitory effects on methane yields, questions are raised, albeit in a single study, that relate to iodine concentration in A. taxiformis and the potential challenges this may bring regarding resultant iodine concentration in milk when feeding A. taxiformis to lactating dairy cows.
More in vivo experiments are required to strengthen the evidence of production and methane effects in both beef and dairy cows fed under partial mixed ration and pasture-based systems. These studies should use a range of Asparagopsis preparations/sources, examine effects on feed intake, and identify sources of heterogeneity in methane response, while practical applications and potential risks are evaluated for seaweed use.
Supporting information
S1 Fig.
Contour-enhanced funnel plot for effects of seaweed intervention in cattle on (A) final body weight, (B) average daily gain, (C) dry matter intake, (D) feed to gain, (E) gain to feed, (F) milk volume, (G) milk fat percent, (H) milk protein percent, and (I) methane yield. The grey broken lines represent the 90, 95, and 99% CI for treatment comparisons. Effect estimates from small comparisons will scatter more widely at the bottom of the graph and the spread narrows for larger comparisons. In the absence of heterogeneity or bias the plot should approximately resemble a symmetrical (inverted) funnel with comparisons lying within these lines. If there is bias, for example because smaller comparisons without statistically significant effects remain unpublished, this will lead to an asymmetrical appearance of the funnel plot and a gap will be evident in the bottom left-hand corner of the graph.
https://doi.org/10.1371/journal.pone.0249053.s001
(PDF)
S1 Table. List of references that were rejected at secondary screening and the reasons.
https://doi.org/10.1371/journal.pone.0249053.s002
(XLSX)
Acknowledgments
The authors acknowledge Erica Mo for her assistance in data extraction. We thank the authors of [2] for provision of data.
References
- 1. Roque BM, Venegas ME, Kinley R, deNys R, Neoh TL, Duarte TL, et al. Red seaweed (Asparagopsis taxiformis) supplementation reduces enteric methane by over 80 percent in beef steers. bioRxiv. 2020.
- 2. Kinley RD, Martinez-Fernandez G, Matthews MK, de Nys R, Magnusson M, Tomkins NW. Mitigating the carbon footprint and improving productivity of ruminant livestock agriculture using a red seaweed. Journal of Cleaner Production. 2020:120836.
- 3. Williams J, Spiers D, Thompson-Golden L, Hackman T, Ellersieck M, Wax L, et al. Effects of Tasco in alleviation of heat stress in beef cattle. Prof Ani Sci. 2009;25:109–17.
- 4. Abbott DW, Aasen IM, Beauchemin KA, Grondahl F, Gruninger R, Hayes M, et al. Seaweed and seaweed bioactives for mitigation of enteric methane: Challenges and opportunities. Animals. 2020;10:2432. pmid:33353097
- 5. Vijn S, Compart DP, Dutta N, Foukis A, Hess M, Hristov AN, et al. Key considerations for the use of seaweed to reduce enteric methane emissions from cattle. Frontiers in Veterinary Science. 2020;7:1135. pmid:33426018.
- 6. Moher D, Liberati A, Tetzlaff J, Altman DG, The PG. Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement. PLOS Medicine. 2009;6:e1000097. pmid:19621072.
- 7. Allen VG, Pond KR, Saker KE, Fontenot JP, Bagley CP, Ivy RL, et al. Tasco-forage: III. Influence of a seaweed extract on performance, monocyte immune cell response, and carcass characteristics in feedlot-finished steers. J Anim Sci. 2001;79:1032–40. pmid:11325177.
- 8. Anderson M, Blanton J Jr, Gleghorn J, Kim S, Johnson J. Ascophyllum nodosum supplementation strategies that improve overall carcass merit of implanted English crossbred cattle. Asian Austral J Anim. 2006;19:1514–8.
- 9. Antaya NT, Ghelichkhan M, Pereira ABD, Soder KJ, Brito AF. Production, milk iodine, and nutrient utilization in Jersey cows supplemented with the brown seaweed Ascophyllum nodosum (kelp meal) during the grazing season. J Dairy Sci. 2019;102:8040–58. pmid:31279546.
- 10. Carter J, Stovall T, Gill D, Confer A, Smith R, Ball R. Nutritional benefits of feeding a pelleted supplement manufactured from north atlantic seaweed to transit-stressed feedlot cattle: Animal performance and medical costs. Anim Sci Res Report P-980. 2000:65–9.
- 11. Cvetkovic B, Shirley JE, Brouk MJ. Impact of dried seaweed meal on heat-stressed lactating dairy cattle. Dairy Day. 2004:59–61.
- 12.
Gravett RB. The effects of Ascophyllum nodosom on immune function, performance, and carcass characteristics of sheep and cattle: Masters Thesis Texas Tech University; 2000.
- 13. Kidane A, Nesheim IL, Larsen HJ, Thuen E, Jensen SK, Steinshamn H. Effects of supplementing mid-lactation dairy cows with seaweed and vitamin E on plasma and milk α-tocopherol and antibody response to immunization. J Agric Sci. 2015;153:929–42.
- 14. Stefenoni H, Räisänen S, Cueva S, Wasson D, Lage C, Melgar A, et al. Effects of the macroalga Asparagopsis taxiformis and oregano leaves on methane emission, rumen fermentation, and lactational performance of dairy cows. J Dairy Sci. 2021;104:Article in Press. pmid:33516546.
- 15. Bendary M, Bassiouni M, Ali M, Gaafar H, Shamas AS. Effect of premix and seaweed additives on productive performance of lactating friesian cows. Int Res J Agric Sci Soil Sci. 2013;3:174–81.
- 16. Sharma A, Datt C. Supplementation effect of red seaweed powder on dry matter intake, body weight and feed conversion efficiency in crossbred cows. Journal of Entomology and Zoology Studies. 2020;8:1056–9.
- 17. Singh BK, Chopra RC, Rai SN, Verma MP, Mohanta RK. Nutritional evaluation of seaweed on nutrient digestibility, nitrogen balance, milk production and composition in sahiwal cows. Proc Natl Acad Sci, India, Sect B Biol Sci. 2015;87:437–43.
- 18. Hedges LV, Tipton E, Johnson MC. Robust variance estimation in meta-regression with dependent effect size estimates. Res Synth Methods. 2010;1:39–65. pmid:26056092.
- 19. Van den Noortgate W, López-López JA, Marín-Martínez F, Sánchez-Meca J. Three-level meta-analysis of dependent effect sizes. Behav Res Methods. 2013;45:576–94. pmid:23055166.
- 20. St-Pierre N. Invited review: Integrating quantitative findings from multiple studies using mixed model methodology. J Dairy Sci. 2001;84:741–55. pmid:11352149.
- 21. Lean IJ, Rabiee AR, Duffield TF, Dohoo IR. Invited review: Use of meta-analysis in animal health and reproduction: Methods and applications. J Dairy Sci. 2009;92:3545–65. pmid:19620636.
- 22. Golder HM, Lean IJ. A meta-analysis of lasalocid effects on rumen measures, beef and dairy performance, and carcass traits in cattle. J Anim Sci. 2016;94:306–26. pmid:26812337.
- 23. DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986;7:177–88. pmid:3802833.
- 24. Knapp G, Hartung J. Improved tests for a random effects meta-regression with a single covariate. Stat Med. 2003;22:2693–710. pmid:12939780.
- 25. White IR, Thomas J. Standardized mean differences in individually-randomized and cluster-randomized trials, with applications to meta-analysis. Clinical Trials. 2005;2:141–51. pmid:16279136.
- 26. Tanner-Smith EE, Tipton E. Robust variance estimation with dependent effect sizes: Practical considerations including a software tutorial in Stata and SPSS. Res Synth Methods. 2014;5:13–30. pmid:26054023.
- 27.
Egger M, Smith GD. Principles of and procedures for systematic reviews. In: Egger M, Smith GD, A GD, editors. Systematic reviews in health care meta-analysis in context. 23–42. London: British medical journal books; 2001.
- 28. Higgins JPT, Thompson SG. Quantifying heterogeneity in a meta-analysis. Stat Med. 2002;21:1539–58. pmid:12111919.
- 29. Borenstein M, Higgins JPT, Hedges LV, Rothstein HR. Basics of meta-analysis: I2 is not an absolute measure of heterogeneity. Res Synth Methods. 2017;8:5–18. pmid:28058794
- 30.
Higgins JPT, Green S. Cochrane handbook for systematic reviews of interventions version 5.1.0 [updated march 2011]. 2011 [cited 11/30/16]. The Cochrane Collaboration, [cited 11/30/16]. www.cochrane-handbook.org.
- 31. Chagas JC, Ramin M, Krizsan SJ. In vitro evaluation of different dietary methane mitigation strategies. Animals. 2019;9:1120. pmid:31835803.
- 32. Machado L, Magnusson M, Paul NA, Kinley R, de Nys R, Tomkins N. Identification of bioactives from the red seaweed Asparagopsis taxiformis that promote antimethanogenic activity in vitro. J Appl Phycol. 2016;28:3117–26.
- 33. Van Nevel C, Demeyer D. Control of rumen methanogenesis. Environ Monit Assess. 1996;42:73–97. pmid:24193494.
- 34. Eckard R, Clark H. Potential solutions to the major greenhouse-gas issues facing Australasian dairy farming. Anim Prod Sci. 2020;60:10–6.
- 35.
National Institutes of Health: Office of Dietary Supplements (NIH). Iodine: Fact sheet for health professionals 2020 https://ods.od.nih.gov/factsheets/Iodine-HealthProfessional/.