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ORIGINAL RESEARCH article

Front. Vet. Sci., 06 July 2023
Sec. Animal Nutrition and Metabolism
This article is part of the Research Topic Natural Phytochemicals To Enhance Animal Productivity And Health Status With Low Greenhouse Gas Emissions View all 6 articles

Maine organic dairy producers’ receptiveness to seaweed supplementation and effect of Chondrus crispus on enteric methane emissions in lactating cows

Diana C. ReyesDiana C. Reyes1Jennifer MeredithJennifer Meredith2Leah PuroLeah Puro3Katherine BerryKatherine Berry3Richard KersbergenRichard Kersbergen4Kathy J. SoderKathy J. Soder5Charlotte QuigleyCharlotte Quigley6Michael DonihueMichael Donihue2Dorn CoxDorn Cox3Nichole N. PriceNichole N. Price6Andre F. Brito
Andre F. Brito1*
  • 1Department of Agriculture, Nutrition, and Food Systems, University of New Hampshire, Durham, NH, United States
  • 2Department of Economics, Colby College, Waterville, ME, United States
  • 3Wolfe’s Neck Center for the Agriculture and the Environment, Freeport, ME, United States
  • 4Cooperative Extension, University of Maine, Orono, ME, United States
  • 5USDA-ARS, Pasture Systems and Watershed Management Research Unit, University Park, PA, United States
  • 6Bigelow Laboratory for Ocean Sciences, East Boothbay, ME, United States

Introduction: There is a growing interest in utilizing seaweed in ruminant diets for mitigating enteric methane (CH4) emissions while improving animal health. Chondrus crispus is a red seaweed that grows in the Gulf of Maine (United States) and has shown to suppress CH4 production in vitro. Organic dairy producers in Maine are currently feeding seaweed due to herd health promoting benefits. However, large-scale adoption depends on technical and financial factors, as well as validation from pilot studies.

Methods: A survey was developed to identify barriers and drivers towards the adoption of CH4-reducing algal-based feeds. Concurrently, a randomized complete block design study was conducted to investigate the effect of C. crispus on enteric CH4 emissions and milk production in a typical Maine organic dairy farm. Twenty-two organically certified Holstein and Jersey cows averaging 29 ± 6.8 kg of milk/d and 150 ± 69 days in milk, were blocked and randomly assigned to a control diet without C. crispus (0CC), or with 6% [dry matter (DM) basis] C. crispus (6CC). Samples were collected on the last week of the 2-wk covariate period, and wk 3, 5, 8, and 10 after initiation of treatments for a total of 12 weeks. Gaseous emissions were measured using a GreenFeed unit. Data were analyzed using the MIXED procedure of SAS with repeated measures over time.

Results: All survey respondents (n = 35; 54% response rate) were familiar with seaweeds as feed, and 34% were already users. Producers who were willing to pay 0.64 USD/cow/d on average for a CH4-reducing algal-based feed, also stated the need for co-benefits in terms of cattle health and performance as a requirement for adoption. Feeding 6CC decreased enteric CH4 production by 13.9% compared with 0CC (401 vs. 466 g/d). Further, milk yield (mean = 27.1 kg/d), CH4 intensity (mean = 15.2 g of CH4/kg of energy corrected milk), and concentrations and yields of milk fat and true protein were not affected by treatments.

Discussion: Producer receptiveness to CH4-reducing algal-based feeds will not only be dependent on purchase price, but also on co-benefits and simplicity of integration into existing feed practices. Feeding C. crispus at 6% of the diet DM decreased CH4 production in dairy cows by 13.9% without negative effects on milk yield and composition. Identifying the bioactive compounds in C. crispus is critical to understand the effect of this red seaweed on mitigating enteric CH4 emissions in dairy cows.

1. Introduction

The dairy industry is under increasing scrutiny regarding its role in global greenhouse gas emissions, mainly from enteric methane (CH4). There is a growing interest in incorporating algal-based feeds in ruminant diets motivated by their potential for reducing enteric CH4 emissions while improving animal health (13). Seaweed contains secondary compounds with broad bioactive properties, some well-known for their antimethanogenic activity [e.g., bromoform, phlorotannins (4)]. However, factors such as seaweed species, geographical location, processing, and dietary inclusion rates may affect the extent of CH4 suppression when feeding algae (5). The red seaweeds Asparagopsis taxiformis and Asparagopsis armata have been identified for their high antimethanogenic activity, decreasing CH4 production in sheep (6), dairy cows (2, 7), and beef cattle up to 80% (8). The mechanism of inhibition has been correlated to the accumulation of halogenated compounds such as bromoform (9). Nonetheless, these seaweeds do not grow in colder climates, are highly invasive, and yield low biomass (10). Therefore, scaling up production to be used in commercial dairy operations is challenging. Moreover, concerns have been raised related to high and variable iodine concentration in Asparagopsis species which may be transferred to milk and must be considered in future research (11). Currently, the brown seaweed Ascophyllum nodosum, commercialized as kelp meal, is the most popular algal-based feed used in organic dairy farms in the United States (1215). A recent survey revealed that 72.5% of the organic grass-fed dairy producers in the United States feed A. nodosum (15). Perceived benefits reported by producers in response to A. nodosum supplementation include improved body condition and overall animal appearance, as well as decreased reproductive problems, milk somatic cell count, and incidence of infectious bovine keratoconjunctivitis [i.e., pinkeye (12)]. However, feeding A. nodosum meal to organic dairy cows during the grazing season had minor effects on suppressing enteric CH4 emissions (16).

Supplementing an algal-based feed that would provide the benefit of reducing the impact of greenhouse gas emissions from farms may be appealing to organic dairy producers if animal production and health are not compromised. Chondrus crispus is a red seaweed that is wild harvested from the intertidal zone of the North Atlantic, including the Gulf of Maine (United States), that has exhibited potential to suppress CH4 production in vitro, and is available under organic certification. Results from a study conducted at the University of New Hampshire in which incremental amounts [0, 3, and 6%; diet dry matter (DM) basis] of C. crispus were fed to organic dairy cows given a baleage-based diet, showed a linear decrease in enteric CH4 production, with the greatest dietary level resulting in an 8.4% reduction in CH4 compared with the control diet (17). However, further research is needed to validate the effect of C. crispus on enteric CH4 emissions and production performance under different production systems. Moreover, beyond scientific validation, diverse technical, financial, and social factors may dictate the receptiveness of dairy producers towards algal-based feeds. Therefore, research that incorporates the concerns of stakeholders and the marketability of seaweed products are increasingly necessary (18, 19). Our first objective was to quantitatively survey the willingness of organic dairy producers in Maine (United States) to adopt an algal-based feed that decreases enteric CH4 emissions. Our second objective was to conduct an animal case study feeding trial to investigate the effect of C. crispus on enteric CH4 emissions and production performance in lactating dairy cows from a herd representative of a typical organic dairy farm of the state of Maine.

2. Materials and methods

2.1. Survey development and administration

The survey was developed with the aim of determining Maine organic dairy producers’ perception and willingness for adoption of an algal-based feed that would decrease enteric CH4 emissions. The survey was approved by the Colby College Institutional Review Board (Approval Number 2021-099). The survey was first announced to 65 organic dairy producers through a flyer (Appendix A), followed by the survey instrument, which was conducted telephonically by interviewers from Colby College (Waterville, Maine) between March and June 2021. The questionnaire (Appendix B) included the following sections: (1) general farm and herd production descriptors, (2) feeding and management practices that could potentially contribute to the design of an effective algal-based feed, and (3) current seaweed supplementation practices and their willingness to adopt and pay for a hypothetical supplement that had been proven to reduce enteric CH4 emissions. Survey data were described with summary statistics including means and standard deviations (Appendix C). Data were analyzed using Stata (version 17, StataCorp LLC).

2.2. Animal case study feeding trial

An animal case study feeding trial examining the effect of the red seaweed C. crispus on enteric CH4 emissions and milk production and composition in dairy cows was conducted at Wolfe’s Neck Center for Agriculture and the Environment. This is a 243-hectare certified organic and preserved coastal farm located in Freeport, Maine (43°49′50.7′N, 70°04′17′W), with an educational and regenerative farming mission. At the time of the study, the organic dairy herd consisted of 32 lactating dairy cows (Holstein, Jersey, and crossbred) producing an average of 27.4 kg milk/d, with 22 animals selected to participate in the study. All experimental procedures were reviewed and approved by the University of New Hampshire Institutional Animal Care and Use Committee (IACUC protocol # 200502).

2.2.1. Cows, experimental design, and treatments

Eighteen Holstein and 4 Jersey cows (averaging 144 ± 72 and 175 ± 53 days in milk in the beginning of the study, respectively), were used in a 12-wk randomized complete block design study conducted from February to May 2021. Cows were blocked (n = 4 blocks) according to breed and days in milk, and within block, randomly assigned to a control diet without C. crispus supplementation (0CC) or a diet containing (DM) basis 6% C. crispus (6CC). The seaweed (Wild North Atlantic Irish Moss; Vitamin Sea, Scarborough, Maine) was harvested in the summer of 2020, air-dried indoors for 24 to 72 h, by spreading it over a plastic film, frequently turning it to remove moisture, and finally milled to pass through a 3-mm screen (small flake size). Cows were housed in a compost-bedded pack barn with dried pine shavings as bedding, and milked twice daily at 0530 and 1630 h, with milk yield recorded throughout the experiment using electronic milkmeters (SCR, Madison, WI). Diets were formulated with a forage to concentrate ratio (% of diet DM) of 67:33 with each component of the ration fed separately. The forage component of the diet was a mixture of chopped, first and second cut grass-legume baleage mix (mostly grass) and alfalfa baleages. A ground corn-based concentrate pellet made up the remainder of the diet. The seaweed was mixed by hand with the concentrate and fed 4 times/d (before and after the morning and afternoon milkings) individually when cows were restrained in headlocks for approximately 20 min to ensure complete seaweed consumption.

2.2.2. Sampling and analyses

Milk and gaseous samples were taken on the last week of the 2-week covariate period, and week 3, 5, 8, and 10 after treatments began. Body weight (BW) was measured for 3 consecutive days before the beginning of the experiment and at the end of each sampling week with a SmartScale (C-Lock Inc., Rapid City, SD). Estimated DM intake (DMI) was determined using the Nutrient Requirements of Dairy Cattle (2001) equation:

D M I k g / d = 0.372 × F C M + 0.0968 × B W 0.75 × 1 e 0.192 × W O L + 3.67

where FCM = 4% fat corrected milk (kg/d), BW0.75 is metabolic BW in kg, and WOL = week of lactation (20). Feed samples (forage, concentrate, and seaweed) were collected weekly, composited by month, and analyzed for DM, crude protein (CP), neutral detergent fiber, acid detergent fiber, acid detergent lignin, ether extract, ash, and minerals, following wet chemistry procedures used by Dairy One Forage Laboratory [Ithaca, NY; (21)]. The iodine concentration of C. crispus was analyzed via quadrupole inductively coupled plasma mass spectrometry at the Bigelow Laboratory for Ocean Sciences, Trace Metal Biogeochemistry Laboratory (East Boothbay, ME). The presence of bromoform and other brominated compounds (including dibromomethane) in C. crispus was analyzed by Bigelow Analytical Services (East Boothbay, ME). Samples of C. crispus were extracted in methanol using a bead-beating protocol. Fifty to 200 mg of sample was weighed out into 1.5-mL microcentrifuge tubes containing ~0.8 g of 2.0 mm Zirconia Oxide beads. One mL of methanol extractant containing the internal standard (naphthalene) was added and the samples were bead-beat for 15 min at 30 Hz. The tubes were then centrifuged at ~21,000 g for 5 min and the supernatant transferred to autosampler vials and analyzed on a Shimadzu GCMS-QP2010 (Shimadzu Scientific Instruments Inc., Columbia, MD). The column used was a 30 m × 0.25 mm × 1.4 μm film thickness Restek Rtx 502.2 (Restek Corporation U.S., Bellefonte PA). The injection temperature was 200°C, and the ion source and interface temperatures were both 220°C. The GC–MS column oven temperature was programmed to start at 40°C for 4 min, increase at a rate of 15°C to 80°C, increase at 30°C to a final temperature of 200°C, and hold for 5 min. The injection volume was 5 μL. Helium was used as carrier gas at a constant pressure of 10.5 psi, giving a column flow rate of 1.13 mL/min. For quantification, the major fragment ions were mass/charge ratio (m/z) 173 and 128 for bromoform and naphthalene, respectively. The limit of detection was 0.012 μg bromoform/g of seaweed (dry weight).

Milk samples were collected during 4 consecutive milkings starting on Monday afternoon of each sampling week, composited based on individual milk yield, preserved with a 2-bromo-2-nitropropane-1,3 diol tablet, and refrigerated at 4°C until analyses. Composited milk samples were shipped to Dairy One Laboratory (Ithaca, NY) and analyzed for concentrations of fat, true protein, and milk urea N (MUN) by Fourier transform infrared spectroscopy using a MilkoScan model 6,000 (Foss Inc., Hillerød, Denmark). Production of 4% FCM and energy corrected milk (ECM) were calculated using the equations reported by Gaines and Davidson (22) and Tyrrell and Reid (23), respectively. Cows had access to a portable automated open-circuit gas quantification unit (i.e., GreenFeed system, C-Lock Inc., Rapid City, SD) for gaseous measurements [CH4 and carbon dioxide (CO2)] throughout the experiment. GreenFeed calibrations were performed weekly using a zero [nitrogen (N2); baseline gas] and a span gas mixture (CO2 and CH4) as outlined by Hristov et al. (24), and a CO2 recovery test was conducted once a month, with a mean (±SD) recovery of 103 ± 3.9%. The same ground corn-based concentrate pellet from the diet (4.4 mm diameter) was used as a bait to attract cows to the unit. In 24 h, cows were allowed a maximum of 6 visits of up to 6 min each (average visit time = 05:24 min), with 4 h intervals between visits, and no more than 12 pellet drops of 33 ± 1.05 g (as fed) per visit.

2.2.3. Statistical analysis

Data (excluding estimated DMI) were analyzed for a randomized complete block design with repeated measures over time using the MIXED procedure of SAS (version 9.4, SAS Institute Inc., Carey, NC). Yields of milk and concentrations and yields of milk components, and gaseous measurements were used as covariate variables in the statistical model reported below:

Y i j k l = μ + B i + T j + W k + β C i j k l + T × W j k + ε i j k l

where Yijkl = dependent variable, μ = overall mean, Bi = random effect of the ith block, Tj = fixed effect of the jth treatment, Wk = fixed effect of the kth sampling week, β = the regression coefficient of the covariate C, Cijkl = the covariate variable for the lth cow within the ith block of the jth treatment of in the kth week, T × Wjk = interaction between the jth treatment and the kth week, and εijkl = residual error. The SAS command REPEATED was used for modeling distinct residual variances, and the covariance structure with the lowest Bayesian information criterion value was retained in the final model. The following covariance matrices were tested: variance components, spatial power, compound symmetry, autoregressive (1), and heterogeneous autoregressive (1). Cow nested within treatment was defined as the subject of the repeated measures and treated as a random effect in the model. Least square means were separated by pairwise t-test using the PDIFF option of the MIXED procedure of SAS if p ≤ 0.05. Furthermore, least square means within sampling week were partitioned with the SLICE command of SAS and separated by pairwise t-test when diet × week interactions were p ≤ 0.05. Significance was declared at p ≤ 0.05 and tendencies at 0.05 < p ≤ 0.10.

3. Results and discussion

3.1. Survey

In total, 35 organic dairy producers participated in the survey (including the Wolfe’s Neck Center for Agriculture and the Environment dairy farm), yielding a response rate of 54%. The organic dairy sector in Maine is diverse (mean ± standard deviation; Appendix C, Supplementary Table C1) in terms of herd size (53 ± 47 lactating cows), productivity (21.1 ± 6.98 kg milk/cow/d), and milk contract price (0.68 ± 0.15 USD/kg of milk). Similarly, dietary inclusion of pasture is highly variable (65.3 ± 21.7%) and it was a key determinant of producer receptiveness to the algal-based feed as discussed below. Nearly half of the respondents (48.6%) reported willingness to pay on average 0.64 USD (± 1.33) per cow daily for an algal-based feed that had been proven to reduce enteric CH4 emissions (Appendix C, Supplementary Table C1). This would represent an additional feed cost of 4,523.38 USD per year to the average farm (53 lactating cows). It is noteworthy to mention that the self-reported price producers were willing to pay (0.64 USD/cow/d) may have been inflated by hypothetical survey bias and further research investigating consumer and producer preference is needed before the marketability of a supplement can be determined. The producers that were willing to pay for an algal-based feed were characterized by having 16% less dietary inclusion of pasture and 10% greater milk contract price (p < 0.05; Table 1). These differences indicate that the best predictors of voluntary supplement demand within the market are farm revenue and convenience of delivery. On the other hand, farm size was not significantly correlated with willingness to pay or with an increased value for the hypothetical supplement (p = 0.34).

TABLE 1
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Table 1. Maine organic dairy producer differences in willingness to pay for an enteric methane-reducing seaweed supplement1,2.

All respondents were familiar with algal-based feeds, and 34% were already feeding them (i.e., A. nodosum meal) to their herds, and were paying an average of 0.45 USD/cow/d. They reported diverse perceived benefits such as improved reproductive health, provision of micronutrients, and decreased incidence of pink eye and ringworm, thus in line with Antaya et al. (12), who reported that 58% of US northeastern organic dairy producers feed A. nodosum meal due to decreased reproductive problems, milk somatic cells count, and pink eye incidence. Of the 23 producers who were no longer feeding seaweed, 7 had discontinued use due to price increase, 2 because of complications obtaining and storing these feeds, and 4 due to a lack of perceived benefits.

Barriers for implementing the hypothetical CH4-reducing algal based feed are presented in Table 2. Beyond the price of the supplement, organic dairy producers who reported qualifications for their willingness to adopt were most likely to cite the existence of co-benefits such as improved milk production as a precondition for their adoption. One respondent expressed “Just using for CH4 production is a strong maybe, but if it helped with milk production and other factors, we would make sure to at least consider it.” Lastly, of the 6 who were unambiguously unwilling to adopt the hypothetical supplement, 5 expressed skepticisms about the link between dairy CH4 emissions and climate change and 1 was concerned that the scale of their farm was too small to make a difference.

TABLE 2
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Table 2. Qualifications to Maine organic dairy producers’ willingness to adopt1 a methane-reducing seaweed supplement.

Producers were also asked about the top 3 challenges they face as organic dairy producers in Maine. More than 54% listed rising input costs as a primary concern, with labor shortages, failing infrastructure, and supply chain issues also being listed by more than a third of the sample. Conversely, only 4 producers cited a changing climate or climate regulations in their list. Companies within the dairy processing sector anticipate stricter climate regulations and are voluntarily making corporate social responsibility commitments to proactively lower their climate footprint (25). However, organic dairy producers are already operating at low profit margins and seem willing to prioritize CH4-reducing innovations only when mandated by their contracted milk buyers, when the animal health co-benefits compensate them for the additional expense, or when climate-conscious consumers are willing to pay a premium for their product.

3.2. Animal case study feeding trial

The ingredient and nutritional composition of the experimental diets are presented in Table 3. The ingredient composition of the concentrate pellet is shown in Table 4, and the nutritional composition of C. crispus and other dietary ingredients is presented in Table 5. Iodine concentration is typically greater in brown versus red seaweeds (26). However, lower iodine values were reported for A. nodosum [mean = 654 ± 212 mg/kg of DM (12, 16, 27)] relative to A. taxiformis [2,270 mg/kg of DM (8)]. This discrepancy may be attributed to intrinsic species differences, effects of seasonality, geographical location, and harvesting and processing methods (28). Considering that iodine can be transferred from feed into milk, the high concentration of iodine in seaweeds in studies conducted with lactating dairy cows, have raised animal and human-health concerns (29). Although high iodine intake is well tolerated by most healthy individuals, people with underlying thyroid conditions or susceptible groups (e.g., elderly and neonates), may develop goiter (thyroid enlargement), hyperthyroidism, or hypothyroidism (30, 31). In the United States, the recommended dietary allowance for adults is 150 μg/d, and the tolerable upper intake level is 1,100 μg/d (32). According to the European Food Safety Authority (33), milk iodine concentrations should remain below 500 μg/L to minimize toxicity risks. However, as recently summarized by Brito (34), milk iodine concentrations above the 500-μg/L threshold have been reported in response to dietary supplementation of A. nodosum (12, 27), A. taxiformis (2), and C. crispus (35) to dairy cows. Consequently, it is imperative to develop technologies that enable dairy producers to feed safe and predictable algal-based feeds to decrease the risk of excess iodine intake by cows and humans.

TABLE 3
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Table 3. Ingredient and nutritional composition [% of diet dry matter (DM)] of diets with Chondrus crispus at 6% DM (6CC) or without (0CC).

TABLE 4
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Table 4. Ingredient composition of the concentrate pellet fed during the animal case study feeding trial.

TABLE 5
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Table 5. Nutrient profile of dietary ingredients [% of dry matter (DM) unless otherwise noted].

In the present animal case study feeding trial, individual DMI was not measured due to constraints in farm facilities. Alternatively, we estimated an average DMI of 20.6 and 19.6 kg/d for 0CC and 6CC, respectively, using an empiric model (Table 6). The decline in estimated DMI resulting from feeding 6CC is challenging to interpret due to the limitations of the model. However, a study conducted at the University of New Hampshire in which organic certified Jersey cows were fed incremental amounts of C. crispus (0, 3, and 6% diet DM basis) showed a linear decrease in DMI (20.7, 19.3, and 18.9 kg/d for 0, 3, and 6%, respectively), potentially associated with palatability issues (17). A similar response was observed when the red seaweed A. taxiformis was fed to lactating dairy cows (2).

TABLE 6
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Table 6. Emissions of carbon dioxide (CO2) and enteric methane (CH4)1, estimated dry matter intake (DMI), milk yield and composition, and body weight (BW) in lactating dairy cows supplemented with Chondrus crispus at 6% diet dry matter (6CC) or without (0CC).

A treatment by week interaction (p = 0.04) was observed for milk production (Table 6), but treatments did not differ from each other during weeks 3, 5, 8, and 10 (Figure 1), suggesting that the effect of lactation progression was different for the 2 treatments. Likewise, a treatment by week interaction was detected for MUN concentration (p = 0.05; Figure 2). Cows in 6CC treatment had lower (p = 0.04) MUN concentration than those in the 0CC treatment during wk. 8 (11.6 vs. 10.5 mg/dL), and a tendency (p = 0.10) for reduced MUN concentration during wk. 5 (11.2 vs. 10.4 mg/dL). It is well known that dietary CP concentration is the main driver of MUN (36). However, dietary CP concentration was similar between treatments (Table 4) and likely did not account for the observed decrease in MUN with feeding 6CC on weeks 5 and 8. Concentrations and yields of milk fat and milk true protein, as well as 4% FCM and ECM yields were not affected (p > 0.05) by treatments possibly because the difference in estimated DMI was small when comparing 0CC versus 6CC diets (Table 6). The observed lack of effect of C. crispus on lactational performance in the current study is consistent with our recent work (17).

FIGURE 1
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Figure 1. Weekly milk yield in cows supplemented either 0 or 6% dry matter of the red seaweed Chondrus crispus. Treatment effect, p = 0.55; week effect, p < 0.001; interaction of treatment by week, p = 0.04.

FIGURE 2
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Figure 2. Weekly milk urea N concentration in cows supplemented either 0 or 6% dry matter of the red seaweed Chondrus crispus. Treatment effect, p = 0.35; week effect, p < 0.001; interaction of treatment by week, p = 0.05. *Indicates statistical tendency (p = 0.1) and **difference between treatments (p = 0.04).

Enteric CH4 production decreased by 13.9% in dairy cows fed the 6CC (401 g/d) versus the 0CC (466 g CH4/d) as shown in Table 6. This response surpassed the 8.4% reduction in enteric CH4 production (from 383 to 351 g CH4/d) observed in our previous research in which Jersey cows were fed incremental amounts (0, 3, and 6% of the diet DM) of C. crispus (17). Such discrepancy in response magnitude between our 2 studies may be explained by using different batches of C. crispus, as well as differences in the basal diets, dairy breed, management practices, and concentration of antimethanogenic compounds present in C. crispus tissues. In our recent study (17), the linear decline in enteric CH4 production was accompanied by a linear reduction in DMI as C. crispus inclusion increased in the diet DM. The positive correlation between DMI and enteric CH4 production is well established in the literature (19). Estimated DMI was 4.9% lower with feeding 6CC versus 0CC in the current experiment, which may have contributed to the observed drop in CH4 production. However, DMI was not individually measured herein and estimated DMI data should be interpreted cautiously, particularly because the equation (20) used to calculate DMI does not account for specific diet nutrient characteristics. Both CO2 production (mean = 11.8 kg/d), and CH4 intensity (mean = 15.2 g of CH4/kg of ECM) did not differ between treatments, thus in line with our recent research (17).

Certain red seaweeds have been reported for having high antimethanogenic activity in vitro (37, 38) and in vivo (2, 7). For instance, dietary supplementation with A. armata and A. taxiformis at 1 and 0.5% (organic matter basis, respectively) effectively suppressed enteric CH4 production in dairy cows by 67.2 and 34.4%, respectively, relative to a control diet (0% seaweed inclusion) (2, 7). These responses were attributed to the presence of halogenated or brominated compounds (e.g., bromoform) that bioaccumulate in the tissues of some red seaweeds (4). A recent genomic sequencing reported that C. crispus possesses the enzymes required to synthesize halogenated compounds (39). However, in the present study, none of the C. crispus samples tested had detectable levels of bromoform, nor any other brominated metabolites. Thus, it is possible that unknown bioactive compounds may be involved and should be identified to better understand the potential of C. crispus to decrease enteric CH4 emissions in dairy cows. By extrapolating the 13.9% reduction in CH4 production from this feeding trial to the current size of Maine’s organic dairy sector and average estimates of annual CH4 emitted per cow [100 kg/cow (40)], we estimate that nearly 50,000 kg of CH4 originating from 3,600 cows would be suppressed each year. At current estimates of the social cost of CH4 [i.e., 1,756 USD/ton of CH4 emitted (41)], this is an annual external benefit of over 87,000 USD from Maine organic dairies alone. Nonetheless, to effectively engage and maximize widespread adoption of algal-based feeds by producers, it may be necessary to implement subsidies or participation in carbon offset markets when available.

4. Conclusion

There has been much discussion regarding the utilization of seaweeds in dairy cattle diets. This study surveyed Maine’s organic dairy producers for their willingness to adopt an antimethanogenic algal-based feed. About 93% of organic dairy producers in our survey cited deteriorating infrastructure, rising costs, and instability in the supply chain as pressing concerns before they mentioned climate change and climate regulation. Therefore, producer’s receptiveness to implement seaweeds in dairy diets will hinge not only on costs but also on the documentation of co-benefits, government policies and subsidies, and the ease of integration into existing feeding management practices. Concurrently, we conducted an animal case study feeding trial to evaluate the antimethanogenic potential of the red seaweed C. crispus in a typical Maine organic dairy farm. Feeding C. crispus at 6% of the diet DM decreased enteric CH4 production in dairy cows by 13.9% with no adverse effect on milk production and composition. Further research exploring C. crispus bioactive compounds will help to better understand the effect of this red seaweed on mitigating enteric CH4 emissions in ruminants.

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving human participants were reviewed and approved by Colby College Institutional Review Board. The patients/participants provided their written informed consent to participate in this study. The animal study was reviewed and approved by University of New Hampshire Institutional Animal Care and Use Committee.

Author contributions

AB, CQ, and NP contributed to conception and design of study. JM and MD designed and implemented the producer survey. DR, LP, KB, RK, and CQ carried out the animal feed trial, taking samples, feeding animals, etc. DR and AB performed the statistical analysis of the animal feed trial data and JM and MD of the survey. KS and DC contributed with facilities/equipment. DR and JM wrote the first draft of the manuscript. All authors contributed to the article and approved the submitted version.

Funding

This work was supported by the Shelby Cullom Davis Charitable Fund and the Sustainable Agriculture Systems grant no. 2021-69012-35919 from the USDA National Institute of Food and Agriculture. Partial funding was provided by the New Hampshire Agricultural Experiment Station (Durham, NH; Scientific Contribution Number 2985). This work was further supported by the USDA-National Institute of Food and Agriculture Hatch Multistate NC-2042 (Project Number NH00670-R; Kansas City, MO).

Acknowledgments

The authors acknowledge the Colby College students who conducted phone interviews Georgia Dettmann, Sophya Guwn, Natalie Simonton, and Jack Tomlin, and Wolfe’s Neck Center for Agriculture and the Environment farm crew for animal care and research support.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fvets.2023.1153097/full#supplementary-material

References

1. Allen, VG, Pond, KR, Saker, KE, Fontenot, JP, Bagley, CP, Ivy, RL, et al. Tasco: influence of a brown seaweed on antioxidants in forages and livestock – a review. J Anim Sci. (2001) 79:E21–31. doi: 10.2527/jas2001.79E-SupplE21x

CrossRef Full Text | Google Scholar

2. Stefenoni, HA, Räisänen, SE, Cueva, SF, Wasson, DE, Lage, CFA, 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) 104:4157–73. doi: 10.3168/jds.2020-19686

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Makkar, HPS, Tran, G, Heuzé, V, Giger-Reverdin, S, Lessire, M, Lebas, F, et al. Seaweeds for livestock diets: a review. Anim Feed Sci Technol. (2016) 212:1–17. doi: 10.1016/j.anifeedsci.2015.09.018

CrossRef Full Text | Google Scholar

4. Paul, NA, Nys, R, and Steinberg, PD. Chemical defence against bacteria in the red alga Asparagopsis armata: linking structure with function. Mar Ecol Prog Ser. (2006) 306:87–101. doi: 10.3354/meps306087

CrossRef Full Text | Google Scholar

5. Beauchemin, KA, Ungerfeld, EM, Abdalla, AL, Alvarez, C, Arndt, C, Becquet, P, et al. Invited review: current enteric methane mitigation options. J Dairy Sci. (2022) 105:9297–326. doi: 10.3168/jds.2022-22091

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Li, X, Norman, HC, Kinley, RD, Laurence, M, Wilmot, M, Bender, H, et al. Asparagopsis taxiformis decreases enteric methane production from sheep. Anim Prod Sci. (2018) 58:681–8. doi: 10.1071/AN15883

CrossRef Full Text | Google Scholar

7. Roque, BM, Salwen, JK, Kinley, R, and Kebreab, E. Inclusion of Asparagopsis armata in lactating dairy cows’ diet reduces enteric methane emission by over 50 percent. J Clean Prod. (2019) 234:132–8. doi: 10.1016/j.jclepro.2019.06.193

CrossRef Full Text | Google Scholar

8. Roque, BM, Venegas, M, Kinley, RD, de Nys, R, Duarte, TL, Yang, X, et al. Red seaweed (Asparagopsis taxiformis) supplementation reduces enteric methane by over 80 percent in beef steers. PLoS One. (2021) 16:e0247820. doi: 10.1371/journal.pone.0247820

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Machado, L, Magnusson, M, Paul, NA, Kinley, R, de Nys, R, and Tomkins, N. Identification of bioactives from the red seaweed Asparagopsis taxiformis that promote antimethanogenic activity in vitro. J Appl Phycol. (2016) 28:3117–26. doi: 10.1007/s10811-016-0830-7

CrossRef Full Text | Google Scholar

10. Silva, CO, Lemos, MFL, Gaspar, R, Gonçalves, C, and Neto, JM. The effects of the invasive seaweed Asparagopsis armata on native rock pool communities: evidences from experimental exclusion. Ecol Indic. (2021) 125:107463. doi: 10.1016/j.ecolind.2021.107463

CrossRef Full Text | Google Scholar

11. Muizelaar, W, Groot, M, van Duinkerken, G, Peters, R, and Dijkstra, J. Safety and transfer study: transfer of Bromoform present in Asparagopsis taxiformis to Milk and urine of lactating dairy cows. Foods. (2021) 10:584. doi: 10.3390/foods10030584

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Antaya, NT, Soder, KJ, Kraft, J, Whitehouse, NL, Guindon, NE, Erickson, PS, et al. Incremental amounts of Ascophyllum nodosum meal do not improve animal performance but do increase milk iodine output in early lactation dairy cows fed high-forage diets. J Dairy Sci. (2015) 98:1991–2004. doi: 10.3168/jds.2014-8851

CrossRef Full Text | Google Scholar

13. Hardie, CA, Wattiaux, M, Dutreuil, M, Gildersleeve, R, Keuler, NS, and Cabrera, VE. Feeding strategies on certified organic dairy farms in Wisconsin and their effect on milk production and income over feed costs. J Dairy Sci. (2014) 97:4612–23. doi: 10.3168/jds.2013-7763

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Sorge, US, Moon, R, Wolff, LJ, Michels, L, Schroth, S, Kelton, DF, et al. Management practices on organic and conventional dairy herds in Minnesota. J Dairy Sci. (2016) 99:3183–92. doi: 10.3168/jds.2015-10193

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Snider, MA, Ziegler, SE, Darby, HM, Soder, KJ, Brito, AF, Beidler, B, et al. An overview of organic, grassfed dairy farm management and factors related to higher milk production. Renew Agric Food Syst. (2021) 37:624–32. doi: 10.1017/S1742170521000284

CrossRef Full Text | Google Scholar

16. Antaya, NT, Ghelichkhan, M, Pereira, ABD, Soder, KJ, and 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. doi: 10.3168/jds.2019-16478

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Reyes, DC, Sacramento, JP, Geng, Y, Silva, LH, Price, N, Quigley, C, et al. Effect of the brown seaweed Chondrus crispus on milk yield and enteric methane emissions in dairy cows. J Dairy Sci. (2021) 104:100.

Google Scholar

18. 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. Front Vet Sci. (2020) 7:597430. doi: 10.3389/fvets.2020.597430

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Min, BR, Lee, S, Jung, H, Miller, DN, and Chen, R. Enteric methane emissions and animal performance in dairy and beef cattle production: strategies, opportunities, and impact of reducing emissions. Animals (Basel). (2022) 12:948. doi: 10.3390/ani12080948

CrossRef Full Text | Google Scholar

20. NRC. Nutrient Requirements of Dairy Cattle. Washington, D.C.: National Research Council (2001). 519 p.

Google Scholar

21. Dairy One Inc. Analytical Procedures; (2022), [1–12 pp]. Available at: https://dairyone.com/download/forage-forage-lab-analytical-procedures/?wpdmdl=13889&refresh=639de5ff36fe61671292415 (Accessed October 17, 2022).

Google Scholar

22. Gaines, WL, and Davidson, FA. Relation between Percentage of Fat Content and Yield of Milk. Urbana-Champaign, Illinois: University of Illinois Agricultural Experiment Station (1923).

Google Scholar

23. Tyrrell, HF, and Reid, JT. Prediction of the energy value of Cow's Milk1, 2. J Dairy Sci. (1965) 48:1215–23. doi: 10.3168/jds.S0022-0302(65)88430-2

CrossRef Full Text | Google Scholar

24. Hristov, AN, Oh, J, Giallongo, F, Frederick, T, Weeks, H, Zimmerman, PR, et al. The use of an automated system (GreenFeed) to monitor enteric methane and carbon dioxide emissions from ruminant animals. JoVE. (2015) 103:e52904. doi: 10.3791/52904

CrossRef Full Text | Google Scholar

25. Lazarus, O, McDermid, S, and Jacquet, J. The climate responsibilities of industrial meat and dairy producers. Clim Chang. (2021) 165:30. doi: 10.1007/s10584-021-03047-7

CrossRef Full Text | Google Scholar

26. Teas, J, Pino, S, Critchley, A, and Braverman, LE. Variability of iodine content in common commercially available edible seaweeds. Thyroid. (2004) 14:836–41. doi: 10.1089/thy.2004.14.836

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Silva, LHP, Reis, SF, Melo, ATO, Jackson, BP, and Brito, AF. Supplementation of Ascophyllum nodosum meal and monensin: effects on diversity and relative abundance of ruminal bacterial taxa and the metabolism of iodine and arsenic in lactating dairy cows. J Dairy Sci. (2022) 105:4083–98. doi: 10.3168/jds.2021-21107

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Evans, FD, and Critchley, AT. Seaweeds for animal production use. J Appl Phycol. (2014) 26:891–9. doi: 10.1007/s10811-013-0162-9

CrossRef Full Text | Google Scholar

29. Brito, AF. Assessing the potential of milk iodine intake to mitigate iodine deficiency in pregnant women of the United States via supplementation of Ascophyllum nodosum meal to dairy cows: a sensitivity analysis. J Dairy Sci. (2020) 103:6798–809. doi: 10.3168/jds.2019-17429

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Zimmermann, MB, Jooste, PL, and Pandav, CS. Iodine-deficiency disorders. Lancet. (2008) 372:1251–62. doi: 10.1016/S0140-6736(08)61005-3

CrossRef Full Text | Google Scholar

31. Katagiri, R, Yuan, X, Kobayashi, S, and Sasaki, S. Effect of excess iodine intake on thyroid diseases in different populations: a systematic review and meta-analyses including observational studies. PLoS One. (2017) 12:e0173722. doi: 10.1371/journal.pone.0173722

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Institute of Medicine (US) Panel on Micronutrients. Dietary Reference Intakes for Vitamin A, Vitamin K, Arsenic, Boron, Chromium, Copper, Iodine, Iron, Manganese, Molybdenum, Nickel, Silicon, Vanadium, and Zinc: Dietary Reference Intakes. Washington (DC): National Academies Press (US) (2001).

Google Scholar

33. EFSA. Scientific opinion on the safety and efficacy of iodine compounds (E2) as feed additives for all animal species: calcium iodate anhydrous and potassium iodide, based on a dossier submitted by Ajay Europe SARL. EFSA J. (2013) 11:3099. doi: 10.2903/j.efsa.2013.3099

CrossRef Full Text | Google Scholar

34. Brito, AF. Effects of Seaweeds on Dairy Production. 2022 Cornell Nutrition Conference, 2022-10-18; (2022).

Google Scholar

35. Reyes, DC, Sacramento, JP, Geng, YC, Silva, LHP, Twining, B, Honisch, B, et al. Effect of the red seaweed Chondrus crispus on nutrient digestibility and iodine metabolism in lactating dairy cows. J Dairy Sci. (2022) 105:70.

Google Scholar

36. Nousiainen, J, Shingfield, KJ, and Huhtanen, P. Evaluation of Milk urea nitrogen as a diagnostic of protein feeding. J Dairy Sci. (2004) 87:386–98. doi: 10.3168/jds.S0022-0302(04)73178-1

CrossRef Full Text | Google Scholar

37. Machado, L, Magnusson, M, Paul, NA, de Nys, R, and Tomkins, N. Effects of marine and freshwater macroalgae on in vitro Total gas and methane production. PLoS One. (2014) 9:e85289. doi: 10.1371/journal.pone.0085289

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Kinley, RD, de Nys, R, Vucko, MJ, Machado, L, and Tomkins, NW. The red macroalgae Asparagopsis taxiformis is a potent natural antimethanogenic that reduces methane production during in vitro fermentation with rumen fluid. Anim Prod Sci. (2016) 56:282–9. doi: 10.1071/AN15576

CrossRef Full Text | Google Scholar

39. Collén, J, Porcel, B, Carré, W, Ball, SG, Chaparro, C, Tonon, T, et al. Genome structure and metabolic features in the red seaweed Chondrus crispus shed light on evolution of the Archaeplastida. Proc Natl Acad Sci U S A. (2013) 110:5247–52. doi: 10.1073/pnas.1221259110

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Mitloehner, F. Making Cattle More Sustainable, Cows and Climate Change. Washington, D.C.: UC Davis News and Media Relations (2019).

Google Scholar

41. Interagency Working Group. Technical Support Document: Social Cost of Carbon, Methane, and Nitrous Oxide Interim Estimates Under Executive Order 13990. United States: Interagency Working Group on Social Cost of Greenhouse Gases (2021).

Google Scholar

Keywords: alternative feed, greenhouse gases, milk quality, mitigation, survey

Citation: Reyes DC, Meredith J, Puro L, Berry K, Kersbergen R, Soder KJ, Quigley C, Donihue M, Cox D, Price NN and Brito AF (2023) Maine organic dairy producers’ receptiveness to seaweed supplementation and effect of Chondrus crispus on enteric methane emissions in lactating cows. Front. Vet. Sci. 10:1153097. doi: 10.3389/fvets.2023.1153097

Received: 28 January 2023; Accepted: 15 June 2023;
Published: 06 July 2023.

Edited by:

Yosra Ahmed Soltan, Alexandria University, Egypt

Reviewed by:

Matthew R. Beck, United States Department of Agriculture (USDA), United States
Mohammad Ramin, Swedish University of Agricultural Sciences, Sweden

Copyright © 2023 Reyes, Meredith, Puro, Berry, Kersbergen, Soder, Quigley, Donihue, Cox, Price and Brito. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Andre F. Brito, andre.brito@unh.edu

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.