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Sustainability of the Dairy Industry: Emissions and Mitigation Opportunities

Authors:

Abstract

Dairy cattle provide a major benefit to the world through upcycling human inedible feedstuffs into milk and associated dairy products. However, as beneficial as this process has become, it is not without potential negatives. Dairy cattle are a source of greenhouse gases through enteric and waste fermentation as well as excreting nitrogen emissions through their feces and urine. However, these negative impacts vary widely due to how and what these animals are fed. In addition, there are many promising opportunities for further reducing emissions through feed and waste additives. The present review aims to further expand on where the industry is today and the potential avenues for improvement. This area of research is still not complete and additional information is required to further improve our dairy systems impact on sustainable animal products.
SYSTEMATIC REVIEW
published: 18 October 2021
doi: 10.3389/fanim.2021.760310
Frontiers in Animal Science | www.frontiersin.org 1October 2021 | Volume 2 | Article 760310
Edited by:
Pasquale De Palo,
University of Bari Aldo Moro, Italy
Reviewed by:
Andrea Bragaglio,
University of Bari Aldo Moro, Italy
Andrea Vitali,
University of Tuscia, Italy
*Correspondence:
Frank M. Mitloehner
fmmitloehner@ucdavis.edu
Specialty section:
This article was submitted to
Animal Physiology and Management,
a section of the journal
Frontiers in Animal Science
Received: 18 August 2021
Accepted: 17 September 2021
Published: 18 October 2021
Citation:
Peterson CB and Mitloehner FM
(2021) Sustainability of the Dairy
Industry: Emissions and Mitigation
Opportunities.
Front. Anim. Sci. 2:760310.
doi: 10.3389/fanim.2021.760310
Sustainability of the Dairy Industry:
Emissions and Mitigation
Opportunities
Carlyn B. Peterson and Frank M. Mitloehner*
Department of Animal Science, University of California, Davis, Davis, CA, United States
Dairy cattle provide a major benefit to the world through upcycling human inedible
feedstuffs into milk and associated dairy products. However, as beneficial as this process
has become, it is not without potential negatives. Dairy cattle are a source of greenhouse
gases through enteric and waste fermentation as well as excreting nitrogen emissions
through their feces and urine. However, these negative impacts vary widely due to how
and what these animals are fed. In addition, there are many promising opportunities for
further reducing emissions through feed and waste additives. The present review aims to
further expand on where the industry is today and the potential avenues for improvement.
This area of research is still not complete and additional information is required to further
improve our dairy systems impact on sustainable animal products.
Keywords: cows, sustainability, greenhouse gases, methane, ammonia, enteric emissions, waste emissions
INTRODUCTION
Dairy production is considered a major societal asset globally due to its economic and nutritional
benefits. In 2019 alone global milk production totaled 851.8 million tons in milk equivalents
(Outlook, 2020). This contributes to substantial trade impacts, totaling about 76.7 million tons
in 2019, as well as major per capita consumption at about 111.4 kg/year globally (Outlook,
2020). There are over 245 million dairy cows worldwide that on average produce 2,300 kg
per year; although average production is less informative as there is such a major disparity
between production in different countries (FAO, 2009). This vast amount of milk production
has a major global benefit—for human health, society, and the economy. In countries with
developing economies livestock serve many purposes including: a source of household income,
a financial asset for women, a source of food security, risk management, and a direct link to
human health (Herrero et al., 2013). These benefits increase substantially when viewed from a
macro lens. Global dairy imports totaled over $42.2 billion in 2014 and global dairy exports
expanded 175% from 2005 to 2014 (Davis and Hahn, 2016). There are many dairy commodities
being produced and traded as part of these exports with whole milk powder being the highest,
followed by skim milk powder, butter, and cheese (Outlook, 2020). India is the largest dairy
producer globally, with 22% of global production and 52,841,810 total dairy cattle, the US
is second in production, followed by China, Pakistan, and Brazil (FAO, 1997; Knips, 2005).
While the US may not be the largest global milk producer, the total economic benefit of the
dairy industry is substantial, totaling $628.27 billion dollars in 2018 (O’Keefe, 2018). There are
currently 9,336,000 dairy cows in the U.S. that on average produce 10,610 kg of milk each year,
which amassed to over 99,056,409 kg of milk in 2019 (USDA, 2020). The US dairy sector also
generates over 2.9 million jobs either through direct or indirect support (O’Keefe, 2018). The
Peterson and Mitloehner Sustainability of the Dairy Industry
top five milk producing states in the US are California,
Wisconsin, Idaho, New York, and Texas, with California
accounting for nearly 20% of national production (Sumner and
Matthews, 2019; USDA, 2020). The dairy industry is such a major
part of California’s economy that in 2019 the associated impact
from milk production and processing was about $57.7 billion
dollars, providing over 179,900 jobs (Sumner and Matthews,
2019). Dairy is the leading agricultural commodity produced
in California, accounting for nearly 13% of the $49.9 billion
dollars in cash receipts generated for the top ranked agriculture
producing state (CDFA, 2019). Not only is the dairy industry a
major driver of the economy but its products serve a substantial
nutritional benefit to the growing human population.
Milk and dairy products are a well-known source of calcium,
vitamins, and other selected minerals as well as being a
complete high-quality protein. One of the most well-documented
nutritional benefits of dairy products is for bone health—
particularly for its ability to prevent osteoporosis and other
bone diseases. In particular the calcium in milk positively affects
bone mass in children and when coupled with vitamin D, as
seen in fortified milk products, will prevent bone loss and
osteoporotic fractures in aging populations (Caroli et al., 2011).
For low-income countries struggling with nutritional deficiencies
in children, studies have shown that supplementation with
dairy products causes a significant increase in vitamin B-12
plasma concentrations, improves cognition, growth and activity
(Allen, 2003; Siekmann et al., 2003). In addition, maternal milk
intake during pregnancy is positively associated with infant
birth weight, and subsequent bone mineral content during
childhood (Gil and Ortega, 2019). Other milk components,
including bioactive peptides present in the whey components
of milk were shown to benefit the immune system due to their
antimicrobial and immunomodulatory properties (Madureira
et al., 2010). Consumption of dairy products has shown
an inverse relationship with cardiovascular disease in that
consumption of milk and dairy is associated with a lower
incidence of type-2 diabetes and improvements in glucose
homeostasis (Hirahatake et al., 2014). While milk is relatively
high in saturated fat it has been shown that milk intake
did not increase cardiovascular risk (Visioli and Strata, 2014).
Furthermore, milk intake was associated with reduced risk of
childhood obesity as well as improved body composition and
weight loss in adults (Thorning et al., 2016). Dairy intake was
also shown to be inversely associated with incidence of cancer
including colorectal, bladder, gastric, and breast cancer and was
not shown to be associated with any other additional forms
of cancer (Thorning et al., 2016). Although dairy production
serves many benefits to overall nutrition, human health, and the
economy, there has been increasing concern about the impact of
dairy on the environment.
Impact of Dairies on Climate Change and
Air Quality
The earth’s surface has undergone massive increases in
temperature, primarily in the last three decades, and the last 30
years we have seen the warmest period ever recorded (IPCC,
2014). In addition to this temperature increase, there have been
other major changes to the climate including trends of increasing
ocean temperature, rising sea level, as well as a major increase in
greenhouse gas emissions (IPCC, 2014). Another phenomenon
that has occurred over the last few centuries is an increase in
ocean uptake of CO2, causing ocean acidification and a decrease
in surface water pH, as well as a rapid decrease in glaciers and
ice sheets around the globe. These major changes in the climate
are primarily due to anthropogenic (human caused) emissions
of GHGs that have steadily increased since the beginning of the
industrial revolution in the 1750s (Place and Mitloehner, 2010).
Atmospheric concentrations of CO2, CH4, and N2O are also
the highest they have been in at least the last 800,000 years,
with about 78% of these CO2emissions resulting from industrial
processes and the combustion of fossil fuels (IPCC, 2014). Several
studies have indicated that the production of livestock, including
the stages of growing, transport, processing, and consumption
have a relatively large impact on climate change (de Vries and
de Boer, 2010; Milani et al., 2011). Dairy cattle in particular
were shown to impact the environment through their potential
negative contributions to air, water, and land (Naranjo et al.,
2020).
In regards to the environment, the US Dairy industry has
seen substantial improvements over the years. In particular it
has seen a great increase in milk production primarily due
to dramatic increases in milk production per cow, increase in
average cow numbers per farm, as well as an overall decrease
in total animal numbers (Wolf, 2003; Barkema et al., 2015).
Some other major changes over the last 50 years include a shift
to a primarily Holstein dairy herd (90%), an increased heifer
growth rate, decreased age at first calving, and an increase in the
use of artificial insemination (Capper et al., 2009). Nutrition of
dairy animals has also allowed for a substantial improvement in
production via use of total mixed-rations balanced for nutrient
and energy requirements accounting for each animals age and
stage of lactation (National Research Council, 2001). Genetic
selection has also been a major driver in increased productivity,
longevity, and efficiency of dairy cows, further reducing the
environmental impact per unit of milk production (Pryce
and Haile-Mariam, 2020). These improvements in nutrition
and genetics, in conjunction with improvements to herd
management, accomplished primarily through increasing density
on dairy farms, have resulted in a fourfold increase in milk yield
from the mid-1940s until 2007 (Von Keyserlingk et al., 2013).
This efficiency of milk production has continued to improve to
2014 where 1 kg of energy and protein corrected milk (ECM) for
California emitted between 1.12 and 1.16 kg of CO2equivalents
(CO2e) in 2014 compared with 2.11 kg of CO2e in 1964, resulting
in a 45% reduction in CO2e (Naranjo et al., 2020). The dairy
industry has continued to still further these improvements. Dairy
production systems in 2017 compared with 2007 have reduced
their inputs by 25.2% for animal numbers, 17.3% for total feed,
20.8% for land, and 30.5% for water of one million metric ton
of energy-corrected milk, furthering the exceptional productivity
gains and environmental progress of the industry (Capper and
Cady, 2020). Even with these major advancements made over
the last century, dairy systems still impact the environment
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Peterson and Mitloehner Sustainability of the Dairy Industry
through: GHG emissions from enteric fermentation, manure
management, and feed production, water use for feed production
and milk processing, water quality with contaminants including
nitrogen (N) and phosphorous (P) from manure, as well as the
requirement for land used in feed production (Naranjo et al.,
2020). In addition to the direct impacts of cattle, such as N
and P as a result of dairy production systems, there are also
environmental impacts associated with dairy processing and
subsequent production (Milani et al., 2011).
Manure Emissions From Dairy Cattle
Dairy manure has the potential to negatively impact the
environment. Nitrogen not retained by the animal or secreted
in milk will be excreted in the urine and feces of the animal
(Hristov et al., 2019). Urine is more susceptible to losses of N to
the environment from the animal waste as compared with fecal
N (Dijkstra et al., 2013, 2018a). Dairy waste is a significant source
of N and P that when land applied in excess of crop requirements
can cause contamination of surface water (Knowlton and Cobb,
2006). This excess N and P in water causes a rapid bloom in
the growth of algal populations that consume dissolved oxygen
in water, termed eutrophication, which reduces the available
dissolved oxygen required for growth of aquatic animal life
(Knowlton and Cobb, 2006). Excess N can also contaminate
ground water through leaching. This poses a problem for human
and animal health as consumed nitrate from drinking water
is converted to nitrite in the digestive tract, which replaces
oxygen in hemoglobin and leads to cyanosis (oxygen starvation)
(Knowlton and Cobb, 2006).
Air quality also affects human and animal health as well as
the environment, and dairy cattle have been known to contribute
to poor air quality. One such compound that affects air quality
produced by dairy cattle is NH3. Ammonia is produced when
N in urea from the animal’s urine reacts with urease present in
feces (Place and Mitloehner, 2010). Ammonia production from
dairy waste is dependent on a variety of factors including: urea
content in urine, pH, and temperature, as well as the enzymatic
activity of urease (Muck, 1982; Sun et al., 2008). In addition
to NH3losses from fresh waste, volatilization can occur during
waste application to soil as a fertilizer, as well as during the
long term housing and storage of manure (Bussink and Oenema,
1998). Total losses of NH3can be between 0.82 and 250 g
NH3/cow/day, with the total loss dependent on the amount and
composition of animal waste as well as the environment and
management conditions of the manure storage (Bussink and
Oenema, 1998; Hristov et al., 2011). Dairy waste management
strategies greatly influence air emissions of NH3. The greatest
NH3emissions occur after field application, followed by the
manure management strategies, for example, separated liquid
and solids, aerated, straw covered, untreated, then anaerobic
digested (Amon et al., 2006).
Nitrogen in waste can also contribute to GHG production
through the formation and volatilization of nitrous oxide
(N2O). Nitrous oxide is created during incomplete microbial
denitrification process where nitrate is converted to N gas with
the potential to create N2O, an extremely volatile byproduct
(Place and Mitloehner, 2010). Land applied dairy manure on
cropland as well as the long term storage of manure in lagoons
can contribute to emissions of N2O (Velthof et al., 1998; Place
and Mitloehner, 2010). The N2O emissions during storage
depend on the N and carbon content of the manure (Amon et al.,
2006). Nitrous oxide production and subsequent volatilization
is also dependent on environment and management. Higher
temperatures as well as surface coverings contribute to increasing
emissions, whereas anaerobic conditions, such as those found
in lagoon systems, have lower N2O emissions (Dustan, 2002).
The process of long term storage of manure seems to also
contribute a larger proportion of N2O emissions compared with
land application with aerated, straw covered, digested, separated,
and untreated manure contributing decreasing amounts of N2O
emissions (Amon et al., 2006).
Another substantial GHG produced by dairy cattle waste
is methane (CH4). The amount of CH4emitted by dairy
waste is dependent on the amount of carbon, hydrogen, and
oxygen present in the waste, making manure storage, diet, and
bedding major contributors to total CH4production (Place and
Mitloehner, 2010). A smaller proportion of CH4is also produced
in the hindgut of the animal via post ruminal digestion and
fermentation (Ellis et al., 2008). This CH4is mostly absorbed
from the hindgut (89%) and eventually eructated by the animal
or excreted with the manure (11%) (Murray et al., 1976; Immig,
1996; de la Fuente et al., 2019). Manure CH4emissions are
substantially higher from long term storage compared with field
application (Amon et al., 2006). These emissions are highest from
straw covered manure and emissions decrease with untreated
manure, followed by separation, aeration, and digested manure
management methods (Amon et al., 2006).
Dairy waste can also produce volatile organic compounds
(VOC). Volatile organic compounds are a class of chemicals
that when reacted with oxides of N and sunlight contribute
to ozone formation (Place and Mitloehner, 2010). There were
73 detectable VOCs from slurry wastewater lagoons with the
most common VOCs being methanol, acetone, propanal, and
dimethylsulfide (Filipy et al., 2006; Shaw et al., 2007). As
with other waste emissions, VOCs from dairy waste increase
with ambient air temperature with summer months having the
highest rates of VOC emissions (Filipy et al., 2006). The largest
contribution of VOCs on dairy systems come from fermented
feedstuffs (i.e., silage) (Place and Mitloehner, 2010).
Effect of Nutrition on Emissions From Dairy
Cattle
Dairy cattle enteric emissions have been shown to contain a
variety of gases. For example dairy cattle emit CO2as a byproduct
of aerobic cellular respiration, which is the GHG with the greatest
contribution to climate change (Place and Mitloehner, 2010).
However, this gas is not considered a net contributor to the rise in
GHGs due to the CO2having been previously recycled from the
atmosphere by fixation during photosynthesis in plants, which
are then consumed by the cattle (Steinfeld et al., 2006). Dairy
cattle can also produce N2O from enteric emissions as a result of
the NO3reduction process that takes place by the microbes in the
rumen (Kaspar and Tiedje, 1981). Due to the small production of
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Peterson and Mitloehner Sustainability of the Dairy Industry
enteric N2O, these emissions are not always considered in dairy
emission analyses (Casey and Holden, 2005).
The most significant enteric emission compound from dairy
cattle is CH4. Methane acts as a hydrogen sink in the rumen and
is an end product of CO2reduction by methanogenic archaea
(Janssen and Kirs, 2008). Methanogens serve an important role
in rumen health by removing this hydrogen that can be toxic
to some bacterial communities and also causes the disease state
rumen acidosis (Beauchemin et al., 2009). In addition to being
a potent GHG, CH4also accounts for a 2–12% loss of potential
energy available to the animal that could otherwise be used for
maintenance and productive purposes as growth gestation, or
lactation (Moe and Tyrrell, 1979).
Dairy cattle diets have a significant impact on enteric
emissions, mostly CH4. As there is large variability in the
ingredient and chemical composition of diets fed to dairy cattle,
nutrition and feeding strategies have the greatest potential for
reducing CH4emissions, with potential reported reductions
between 2.5 and 15% (Knapp et al., 2014). The amount of CH4
produced is dependent on many factors including intake and
chemical composition of the carbohydrate, retention time of feed
in the rumen, rate of fermentation of different feedstuffs, as well
as the rate of methanogenesis (Beauchemin et al., 2009). Altering
feed digestibility and chemical composition cause a shift in the
proportions of volatile fatty acids (VFA) with the predominant
VFAs being propionate, butyrate, and acetate (Knapp et al., 2014).
This shift in VFA proportion is important because propionate
also acts as a hydrogen sink so shifting from acetate and butyrate
formation to propionate will consume reducing equivalents
and help preserve the pH balance in the rumen (Hungate,
2013). An overall reduction in CH4emissions or a shift in
VFAs can be accomplished through a variety of altered feeding
strategies. More energy dense or more digestible feedstuffs result
in additional energy available to the animal and generate less
CH4from fermentation (Knapp et al., 2014). An increase in
starch proportion of the diet, such as through an increase in
concentrate levels, also results in a more rapid fermentation
of these feedstuffs and therefore decreased CH4production
(Moe and Tyrrell, 1979; Johnson and Johnson, 1995). Feeding
higher starch diets requires increased grain production, which
can cause additional consumption of fossil fuel and fertilizers
that results in an increase in N2O and CO2; however, this
system is usually offset by the substantial decrease in overall
in CH4emissions (Johnson et al., 2002; Lovett et al., 2006).
Feeding of cereal forages can also favor propionate production
and reduce CH4emissions due to the higher starch concentration
(Beauchemin et al., 2009). Higher concentrations of legumes,
such as alfalfa, when compared with grass forage based diets can
also lead to an overall decrease in CH4emissions (McCaughey
et al., 1999). Age of harvest of forage also has a significant
impact on emissions, with advancing maturity resulting in more
lignified and less fermentable substrate contributing to increasing
emissions associated with higher ruminal acetate (Pinares-Patiño
et al., 2003). In addition to alterations in forage or concentrate
composition and ratio, supplementation of lipids to dairy cattle
diets can also mitigate enteric emissions (Hristov et al., 2013b).
Replacing concentrates with lipids results in a decrease in
fermentable substrate by the microbes in the rumen and can
also decrease total protozoa and methanogen populations (Ivan
et al., 2004). An inclusion of high-oil by-products, such as
distillers grains or oilseed meals, can result in decreased CH4
emissions (Hristov et al., 2013b). Research on ensiled feeds in
relation to enteric emissions is generally lacking, although it is
anticipated that corn silage will mitigate emissions due to its
higher starch content (Gerber et al., 2013). Furthermore, when
directly comparing grass-versus corn silage, a higher inclusion of
corn silage seems to mitigate enteric CH4emissions (Mills et al.,
2008; Doreau et al., 2012). There are many potential methods
to mitigate enteric emissions through alterations to nutrition
strategy and composition.
Manure emissions are also significantly impacted by various
dairy cattle feeding strategies. One of the main issues with
altering feeding strategies to reduce enteric emissions is that
fermentable substrate in the manure can increase, as has been
seen with increasing the concentrate to forage ratio in the diet
(Hindrichsen et al., 2006; Beauchemin et al., 2009). This response
has also been seen with the supplementation of certain fatty
acids (Kreuzer and Hindrichsen, 2006). To alleviate this issue,
feeding concentrate with higher lignified fiber has been shown
to mitigate both enteric and manure-derived emissions (Kreuzer
and Hindrichsen, 2006; Aguerre et al., 2012). These changes
to concentrate ratio do not have an impact on N containing
manure emissions, as would be expected (Hindrichsen et al.,
2006; Aguerre et al., 2012). The greatest impact of diet on waste
emissions can be seen when feeding low crude protein (CP)
diets to dairy animals, which results in decreased excreted N and
subsequent NH3volatilization (Cardenas et al., 2007; Lee et al.,
2012; Edouard et al., 2019). Comparing fresh grass with prepared
hay at the same CP content, feeding hay causes a higher overall N
and C/N ratio excreted but waste from grass fed animals tends to
volatilize more NH3emissions (Külling et al., 2003). Corn silage
inclusion in diets has also caused changes to manure emission
profiles. For example when comparing corn silage versus grass
silage, corn silage tended to reduce urinary N excretion (Mills
et al., 2008). When adding corn silage to alfalfa silage based diets
there is also an improvement in N efficiency leading to a decrease
in N losses in urine and subsequent decreases in available NH3
and N2O volatilization (Gerber et al., 2013). Higher sugar forages
also reduce N excretions, which also have the potential to limit
the N available to be volatilized as gaseous emissions (Miller et al.,
2001; Parsons et al., 2012; Gerber et al., 2013). Overall a variety
of feeding strategies can be employed to help mitigate emissions
from enteric and waste sources of dairy animals.
Mitigation Strategies for Dairy Cow Enteric
Gas Emissions
In addition to changes to the diet ingredient composition, there
are also additives to diets that may mitigate enteric emissions.
While there are various types of strategies to alter enteric
sourced emissions this section will focus primarily on methods
to alter CH4. One promising strategies for CH4reduction is
via feed supplementation of the methanogenic inhibitor, 3-
Nitrooxypropanol (3-NOP). 3-Nitrooxypropanol is a structural
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Peterson and Mitloehner Sustainability of the Dairy Industry
analog to methyl-coenzyme M, which acts on methyl-coenzyme
M reductase (MCR), a nickel enzyme involved in the final
reduction stages of methanogenesis (Duin et al., 2016). In the
rumen system 3-NOP was shown to mimic methyl-coenzyme M
and target the active site of MCR, thus inhibiting the enzymes
activity and subsequently causing a decrease in CH4production
(Duin et al., 2016). Research demonstrated that feeding 3-NOP
to cattle decreased enteric CH4emissions up to 95% in vitro
(Martínez-Fernández et al., 2014) and 84% in vivo (Vyas et al.,
2016). 3-NOP was tested in vivo in multiple ruminant models
including sheep (Martínez-Fernández et al., 2014), beef cattle
(Romero-Perez et al., 2015; Vyas et al., 2016), as well as Holstein
dairy cattle (Reynolds et al., 2014; Hristov et al., 2015; Lopes
et al., 2016; Haisan et al., 2017). Reynolds et al. (2014) fed 3-
NOP at a rate of either 500 or 2,500 mg/d via rumen fistula
before each feeding and using respiration calorimetry found a
reduction of 6.6 and 9.8% in CH4emissions, respectively. They
also found a decrease in dry matter intake (DMI) and an increase
in milk protein at the higher dose, without other changes in
production parameters. Haisan et al. (2017) also fed 2,500 mg/d
and using the SF6 systems measured a reduction in emissions
from 17.8 to 7.18 g/kg of DMI without adverse effects to milk
or DMI. Hristov et al., 2015 fed 3-NOP at a rate of 40, 60, or 80
mg/kg of DMI and measured reductions via a GreenFeed system
of 25, 31, and 32%, respectively. They also found no changes
to DMI or milk production with an increase in protein yield
following supplementation. Similarly, Lopes et al. (2016) also
fed 60 mg/kg of DMI and found a 31% decrease in emissions
with an increase in milk fat concentration. Dijkstra et al. (2018b)
evaluated the overall efficacy of 3-NOP in research trials and
determined that greater 3-NOP dose results in a greater reduction
of CH4emissions. These trials also used different diets, which did
not seem to effect the impact of 3-NOP on emissions. However,
this molecule has yet to be evaluated for its efficacy among
different dairy breeds and the potential side effects of its use have
not fully elucidated. Additionally, it has yet to be determined
whether 3-NOP has any unintended consequences of carryover
to the excreta of supplemented animals.
Nitrates offer great promise for their potential to mitigate
CH4and have been well studied for their use in beef cattle
diets with more recent literature focusing on the potential for
use in dairy cattle. Nitrate in the diet serves as a non-protein
N source that acts as an electron receptor resulting in effective
and consistent reduction of enteric emissions. However, nitrate
has the potential to induce methemoglobinaemia and is a known
carcinogen (Lee and Beauchemin, 2014). Nitrate toxicity can
generally be avoided when the rumen ecosystem is allowed time
to adapt (Hristov et al., 2013b). Even with the potential for
toxicity, the benefits of 16–50% reduction in CH4emissions
continue to drive research feeding nitrates (Leng and Preston,
2010). Van Zijderveld et al. fed nitrate at a rate of 21 g/kg DMI
and measured a persistent reduction in CH4of 16% via use of
open-circuit indirect calorimetry chambers (Van Zijderveld et al.,
2011). They did not measure changes in milk yield or DMI for
the supplemented animals. Similar research conducted by other
authors found a reduction in emissions of CH4/d from 363 g
for control animals to 263 g for nitrate supplemented animals
also at 21 g/kg DMI (Klop et al., 2016). They also measured
a reduction in milk protein concentration as well as DMI for
nitrate-supplemented cows. When high levels of nitrate (20 g/
kg DMI) were supplemented in a similar study design they
found a 31% reduction in CH4along with a decrease in DMI
during nitrate feeding (Lund et al., 2014). Another study found
a 28% decrease in methanogenesis after feeding nitrate at 2.3% of
DM to nonlactating cows, however they also found a significant
decrease in feed intake from the supplemented animals (Guyader
et al., 2015). Another trial reported a 10% decrease in DMI,
coupled with a 17% decrease in CH4where dairy cattle diets were
supplemented with nitrate at 1.5% of DMI (Meller et al., 2019).
A meta-analysis found a persistent reduction in CH4emissions
in both in vitro and in vivo studies (Lee and Beauchemin, 2014).
Similar to 3-NOP, TMR composition did not seem to have a
major effect on nitrate supplementation as these studies all saw
a significant decrease in emissions with vastly different diets.
Plant biological compounds have also been explored for their
potential to reduce emissions. Condensed tannins are secondary
phenolic compounds that generally discourage consumption by
herbivories and also concentrate N in the plant (Waghorn, 2008).
When consumed by dairy cattle these tannins bind protein
in the rumen, which reduces the degradation of protein and
enhances protein flow to the intestines (Beauchemin et al.,
2009). Tannin source appeared to make a major difference in
subsequent mitigation of CH4emissions from dairy cattle. For
example, the Hedysarum coronarium species supplemented at
27 g /kg DMI resulted in lower CH4emissions by dairy cattle
(Woodward et al., 2002). Whereas, Schinopsis quebracho-colorado
supplemented at 0, 1, or 2% of dietary DM did not have any
effect on enteric emissions or dry matter intake of beef cattle
(Beauchemin et al., 2007). Additional studies looking at Lotus
pedunculatus (fed at 10% of dry matter) and Medicago sativa (fed
at 0.1% of dry matter) tannin supplementation found decreased
CH4emissions from both strains of condensed tannins, although
DMI was not measured, which were attributed to reducing
hydrogen production and direct inhibition on methanogenic
archaea (Tavendale et al., 2005). A meta-analysis identified a
general anti-methanogenic effect of tannins across different
sources and that the variation in methane reduction seen in
previous studies may have been due to the low tannin levels
used in those trials (Jayanegara et al., 2012). They also found that
dietary tannins tended to increase DMI but decrease total tract
digestibility, apparent CP digestibility, and neutral detergent fiber
digestibility. As with previous feed supplementation, these trials
did not quantify emission changes to waste sources. Additional
research into tannins in various diets as well as its effect on milk
production and manure CH4emissions needs to be explored.
In addition to tannins, secondary plant compounds called
essential oils have been explored for their antimicrobial
properties. Essential oils are naturally occurring volatile
components in plants that provide the plant specific color
and flavor characteristics (Benchaar et al., 2008). Essential
oils reduced CH4production through inhibiting growth and
energy metabolism of selected bacteria and archaea including
methanogens (Benchaar et al., 2008). Over 250 essential oils have
been identified and contain mixtures of terpenoids, a variety of
Frontiers in Animal Science | www.frontiersin.org 5October 2021 | Volume 2 | Article 760310
Peterson and Mitloehner Sustainability of the Dairy Industry
low molecular weight aliphatic hydrocarbons, alcohols, acids,
aldehydes, acrylic esters, N, sulfur, coumarins, and homologs
of phenylpropanoids (Beauchemin et al., 2009). These essential
oils underwent in vitro screening for their potential to reduce
rumen CH4emissions and while 35 were found to be effective
only six were found to have significant decreases in emissions
without disrupting digestibility (Bodas et al., 2008). It is difficult
to directly compare essential oils because of the number of
different compounds as well as the difference in study design
and species studied. In addition, few essential oils have been
thoroughly evaluated in vivo.Benchaar and Greathead (2011)
performed additional in vitro testing and found decreased CH4
production following supplementation with oregano, rhubarb,
thyme, cinnamon, horse radish, frangula, and garlic. Tekippe
et al. (2011) fed oregano leaf at a rate of 500 g/d to lactating dairy
cattle and measured rumen CH4production 8 h after feeding.
They found a decrease in total CH4yield but did not see adverse
effects on DMI or milk yield with the added benefit of increased
milk fat content. In a follow up study by Hristov et al. (2013a)
they fed lactating dairy cows 250, 500, and 750 g of oregano leaf
per day and found a linear reduction in methane per unit of DMI
coupled with a linear decrease in DMI but no differences in any
milk production parameters. In addition to particular isolates
of essential oils, there are also commercial essential oil blends
being marketed for their potential to reduce enteric CH4. One
essential oil blend is Agolin SA created in Bière, Switzerland
that is comprised of coriander oil, geranyl acetate, and eugenol.
Agolin was tested in vitro and found a significant initial decrease
in rumen CH4, but the effect did not persist over time (Klop et al.,
2017b). Another Agolin in vitro trial found similar results where
there was an initial reduction in methane, but the effect was not
constant over the total 72 h incubation period (Castro-Montoya
et al., 2015). These authors also conducted feeding trials with
the Agolin essential oil product. Castro-Montoya et al. (2015)
found a trend in reduction of daily emissions relative to intake
and (Klop et al., 2017a) found initial decrease in CH4/DMI
only for the first 2 weeks of feeding Agolin, after which Agolin
did not impact CH4. In addition, Klop et al. (2017a) reported
a decrease in DMI over the second half of the supplementation
period. Hart et al. (2019) also supplemented lactating dairy cattle
with Agolin essential oils and measured a reduction in CH4
emissions per pen. Changes to DMI, milk production, or fat
composition after feeding of essential oils have also been reported
following Agolin supplementation. For example, Santos et al.,
2010 reported numerically lower DMI with an increase in milk
fat production, a 0.03 kg/day increase in fat production, from
Agolin supplemented cows, whereas Elcoso et al. (2019) saw an
increase in ECM supplemented animals without differences in
DMI. However, for Santos et al. (2010) the Agolin treatment was
applied to the pen and not the individual animal. Elcoso et al.
(2019) also estimated rumen CH4production from fermented
rumen fluid and found supplemented animals to be lower,
but there was an interaction between the time and treatment.
Hart et al. (2019) also found a greater milk yield and ECM for
Agolin supplemented animals. Clearly the large discrepancy
in responses across research studies for Agolin emphasizes
the need for additional research to determine if the essential
oil product has application at the farm level to reduce enteric
CH4emissions.
Mitigation Strategies for Dairy Cow
Manure Gas Emissions
While there are many ways in which to alter manure emissions
depending on the desired outcome this literature search will focus
on methods to alter CH4emissions specifically, of which there
are quite a few promising strategies. One manure amendment
strategy includes the use of biochar. Biochar is a general term
applied to products produced by thermal decomposition from
a variety of biomass substrates for agricultural applications
including the added benefit of optimizing the process of
composting (Godlewska et al., 2017). Biochar was shown to have
a multitude of benefits including improving the overall process
of composting, improving N conservation, facilitating nutrient
transformation, and favoring oxygen supply (Vandecasteele et al.,
2016; Chen et al., 2018; Mao et al., 2018). Other studies
demonstrated that biochar improved soil physicochemical
properties, benefited nutrient conservation as well as boosted
crop production (Li et al., 2015; Mao et al., 2017; Wu et al.,
2017). While the benefits of biochar as amendments to poultry
and pig manure have been well-documented (Agyarko-Mintah
et al., 2017; Chen et al., 2017; He et al., 2019), its use in dairy
cattle manure management has been less thoroughly studied.
Jindo et al. (2012) added biochar to cattle manure to measure
microbial communities, causing a significant increase in the C/N
ratio from the additional of high carbon biochar materials, but
they did not measure emissions from these systems. Duan et al.
(2019) applied wood or wheat straw biochar with and without
bacterial supplementation to cattle manure compost. While this
study did not measure CH4emissions specifically, they found
that biochar in addition to bacterial amendments enhanced the
compost overall and that Bacteroidales,Flavobacteriales, and
Bacilli were the communities with the highest abundance in
the samples. Awasthi et al. (2020) also tested biochar with and
without a bacterial inoculum applied to fresh cattle manure in
a reactor and found treatments with the inclusion of biochar
produced substantially less CH4as compared with the control.
Overall, the impact and mechanism of action of biochar on CH4
emissions from dairy waste specifically deserves further study.
Bacterial inoculums, as well as the supplementation of
bacterial produced enzymes, have been well-researched in the
literature for their potential to alter CH4emissions. Bacteria
are involved in many of the breakdown processes that occur in
manure management systems including reactions of hydrolysis,
acidogenesis, acetogenesis, and methanogenesis, the latter
of which has the potential to increase methane production
(Juodeikiene et al., 2017). While increased CH4may seem
in conflict with the present literature review, this manure
management strategy can be applied to systems where CH4can
be captured and transformed into biofuel or other renewable
resources. One such example is through anaerobic digestion in
which organic material is degraded by microbes in the absence
of oxygen (Rodriguez Chiang, 2011). A variety of bacterial
communities have been researched for their potential to change
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Peterson and Mitloehner Sustainability of the Dairy Industry
CH4emissions from various substrates. Juodeikiene et al. studied
Lactobacillus delbrüeckii, and found an increase in methane of
76% from dairy wastewater from milk processing, as compared
with 38% without the addition of bacteria (Juodeikiene et al.,
2017). Xu et al. pretreated corn straw with Bacillus subtilis, and
increased CH4production 17.35% above the untreated control
(Xu et al., 2018). He et al. also supplemented microalgal biomass
with Bacillus licheniformis, and bacterial supplementation
increased CH4production from 9.2 to 22.7% (He et al.,
2016). Commercial products have also been marketed for
their application in manure management systems, including
BiOWiSH products. BiOWiSH products contain a proprietary
mixture of Bacillus and Lactobacillus, including Bacillus subtilis,
Bacillus amyloliquefaciens, Bacillus licheniformis, Bacillus
pumilus, Pediococcus acidilactici, Pediococcus pentosaceus,
Lactobacillus plantarum, Bacillus meagerium, Bacillus coagulans,
and Paenibacillus polymyxia, a product covered by a patent
outlined by Carpenter et al. (2014). The process to create
BiOWiSH involves individually fermenting each organism,
followed by harvesting and then drying of each organism.
Finally, the dried organism ground to produce a powder with a
final moisture content <5% and a final bacterial concentration
between 105and 1011 colony forming units (CFU) per gram of
dried product. While these products have not been evaluated for
their effect on CH4specifically, these products claim to digest
sludge, and reduce biological oxygen demand, total suspended
solids, total Kjeldahl N, and odor from manure lagoons. The
BiOWiSH product has been applied to dairy waste systems and
showed promise for manure mitigation including: a reduction in
total suspended solids and a degradation and removal of N(Lee,
2012; Pal, 2012; Holland, 2017). However, BiOWiSH has not
been studied with respect to its effects on CH4emissions from
dairy wastewater systems.
Gypsum based products have been applied to dairy waste
systems for manure amendments. One of the more common
forms of gypsum used for manure amendment is flue gas
desulphurization gypsum that is a by-product of wet gas
desulphurization from coal-fired power stations (Febrisiantosa
et al., 2018). This gypsum has a low heavy metal content and
contains high concentrations of S, Si, and Ca that are essential
minerals nutrients required by plants (Guo et al., 2016). Gypsum
has been fairly well-characterized for its effects on N containing
compounds. Tubail et al. found gypsum supplemented dairy
manure lost significantly less N as compared with the control
dairy manure without supplementation (Tubail et al., 2008).
Li et al. applied gypsum to pig manure compost and found
significant reductions in NH3and enhanced mineral and total
N contents (Li et al., 2018). Hao et al. applied gypsum to
beef cattle manure and found a significant reduction in CH4
emissions from the medium and high doses of gypsum as
compared with the control (Hao et al., 2005). Yang et al. studied
kitchen waste compost and found the addition of gypsum to
dramatically reduce CH4emissions by 85.8% (Yang et al., 2015).
While these study designs don’t quite have the same application
as is intended in this literature review, the potential for use
of gypsum as a manure amendment is promising. There are
also commercial additives being marketed for their potential
to mitigate CH4emissions, including SOP Srl, a company that
makes the SOP Lagoon products. SOP Lagoon consists of calcium
sulfate dihydrate (agricultural gypsum) that is processed with
the company’s proprietary technology. The product’s claim is
to improve liquid manure management through inhibiting the
production and release of GHGs (e.g., CH4and N2O) and
criteria pollutants (e.g., NH3) while also reducing the odor
intensity from liquid manure. Borgonovo et al. first tested
the gypsum-based commercial additive, “SOP LAGOON,” on
fresh dairy manure and found the additive to be effective in
reducing direct NH3and GHG emissions, including a significant
mitigation of CH4emissions (Borgonovo et al., 2019). Recent
literature by Peterson et al. applied SOP Lagoon to liquid
stored dairy cattle manure over a 2 week period and found
similar results including significant reductions in NH3emissions
(22.7% for the supplemented systems as compared with an
unsupplemented control) (Peterson et al., 2020). With the strong
literature documenting the potential for gypsum to decrease CH4
emissions, this seems like a viable manure amendment strategy.
In addition to the previously described additives, a variety of
additional organic substrates have been applied as amendments
in diverse applications. These additional amendments include
lime and coal fly ash (Fang et al., 1999; Wong et al., 2009),
zeolite (Awasthi et al., 2016; Chan et al., 2016), bentonite (Wang
et al., 2016), clay (Chen et al., 2018), and medical stone (Awasthi
et al., 2017; Wang et al., 2017), among others. These amendments
require further research to evaluate their potential use in dairy
manure specifically as well as the resulting CH4emissions after
their application.
CONCLUSIONS
There is an increasing amount of literature and research data
concerning strategies to further reduce livestock’s impact on the
environment. However, there is no one method of environmental
sustainability in these systems and even still there are many
unanswered questions. Future research needs to better quantify
full reduction potential and elucidate the mechanism of actions
of these compounds including 3-NOP, tannins, essential oils,
bacterial inoculums, and biochar, among others. Furthermore,
slight alterations to dairy cattle diets can cause major changes
in both enteric and waste emissions. Research on mitigating the
environmental impact of dairy cattle will allow dairy producers
to contribute to a more sustainable dairy production system.
DATA AVAILABILITY STATEMENT
The original contributions presented in the study are included
in the article/Supplementary Material, further inquiries can be
directed to the corresponding authors.
AUTHOR CONTRIBUTIONS
CP wrote the manuscript draft. All authors contributed to the
article and approved the submitted version.
Frontiers in Animal Science | www.frontiersin.org 7October 2021 | Volume 2 | Article 760310
Peterson and Mitloehner Sustainability of the Dairy Industry
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... There is a mutual consistency that climate change is a phenomenon due to concentration of CO 2 and GHGs emissions in the environment (Malhi et al., 2021;Jeon et al., 2023;Fan & Ma, 2024). Over population, urbanization, and industrialization increased the quantity of CO 2 and GHGs emissions in the environment worldwide after the 1970s (Malhi et al., 2021;Peterson & Mitloehner, 2021). Fluctuation in natural disasters i.e., floods, drought, fog, earthquakes, hailstorm, landslide, land sinking etc. also increased due to abovementioned reasons across countries (Malhi et al., 2021;Negi et al., 2025). ...
... Milk production is positive to maintain the sustainability of nutritional and diet security of people in India. India has greater share of dairy producers in the world (Peterson & Mitloehner, 2021;Gaillard & Dervillé, 2022). It has the largest livestock resources in the world (Ranuzzi & Srivastava, 2012;. ...
... Milk and dairy farming are critical components of India's rural agricultural development and ensure food security of people (Jatav, 2024b;FAO, 2025). It ensures nutritional security as providing calcium, vitamins and minerals to humanity (Peterson & Mitloehner, 2021;Ravindran et al., 2024). Thus, livestock rearing business and harvesting livestock are helpful to sustain food security (Bashir et al., 2013;Mittal et al., 2019;Gaillard & Dervillé, 2022;Jatav, 2024b). ...
Chapter
This study measures the sensitivity in total milk production (TMP) due to frequency of climate change in India. TMP of a respective state is considered as an output, while monthly average maximum and minimum temperature, precipitation, and annual actual rainfall are used as climatic factors in empirical investigation. Thereupon, specific agricultural inputs like fertilizer and credit facilities from the banking sector are employed as control variables in the empirical model. The coefficients of independent variables with TMP are observed using a log-linear regression equation. Thereupon, it estimates the predicted milk production of India in different climate change perceptions. Projected results indicate a declining trend in TMP in different climate change perspectives. Irrigated area, credit facilities, gross cropped area and fertilizer application showed a positive impact on TMP. Dairy farmers should adopt appropriate mitigation practices to abate negative impact of climate change on milk production.
... Specific measures include reducing water consumption, improving water quality, and reducing greenhouse gas emissions. The industry is also exploring regenerative agriculture practices to protect soil health, enhance carbon sequestration, and enhance the nutrient density of dairy products (Peterson & Mitloehner, 2021). ...
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Unbalanced relations between all participants of the food chain in the dairy business hinder the development of the livestock sector. Implementation of cluster policy in dairy cattle breeding enables the development of a competitive reference standard using benchmarking analysis. For the full and comprehensive development of the dairy cluster, it is necessary to observe organisational independence to meet the economic interests of all participants. The developed mechanism acts as the basis of a new area of economic analysis that measures synergetic results possible only within the framework of cluster system economic interaction in dairy cattle breeding.
... International process standards, defined by the International Organization for Standardization (ISO) in collaboration with national standard bodies and government agriculture departments, are essential for optimizing techniques and strategies to mitigate GHG emissions, ensuring safety and regulatory compliance [73]. Biochar is one manure amendment strategy that can reduce GHG emissions by transforming waste biomass from dairy farms to a carbon-rich product [94,95]. The International Biochar Initiative biochar standard in the US and the European Biochar Certificate are widely acknowledged as the most prevalent standards globally, all operating as voluntary industry standards [96]. ...
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... Calculation of emissions in conventional and organic dairy farming was conducted using the 2023 data of the Central Statistical Office on the number of cows in small and mediumsized dairy farms [37]. The number of cows is divided into categories (1-9), (10)(11)(12)(13)(14)(15)(16)(17)(18)(19)(20)(21)(22)(23)(24)(25)(26)(27)(28)(29), (30)(31)(32)(33)(34)(35)(36)(37)(38)(39)(40)(41)(42)(43)(44)(45)(46)(47)(48)(49), and ...
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Methane is the main greenhouse-gas contributor to global warming in the livestock sector; it is generated by anaerobic fermentation in the different sections of the gut, and the methane concentration differs significantly among species. Methane is produced only by certain types of microorganisms called methanogens. The species composition of methanogenic archaea population is largely affected by the diet, geographical location, host and the section of the gut. Consequently, methane production, either measured as total grams emitted per day or per bodyweight mass, differs greatly among animal species. The main difference in methanogenic activity among different gut sections and animal species is the substrate fermented and the metabolic pathway to complete anaerobic fermentation of plant material. The three main substrates used by methanogens are CO2, acetate and compounds containing methyl groups. The three dominant orders of methanogens in gut environments are Methanomicrobiales, Methanobacteriales and Methanosarcinales. They normally are present in low numbers (below 3% of total microbiome). The present review will describe the main metabolic pathways and methanogens involved in CH4 production in the gut of different host-animal species, as well as discuss general trends that influence such emissions, such as geographical distribution, feed composition, section of the gut, host age and diurnal and season variation. Finally, the review will describe animal species (large and small domestic ruminants, wild ruminants, camelids, pigs, rabbits, horses, macropods, termites and humans) specificities in the methanogen diversity and their effects on methane emission.
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Ammonia (NH3), methane (CH4), nitrous oxide (N2O), and carbon dioxide (CO2) emissions from livestock farms contribute to negative environmental impacts such as acidification and climate change. A significant part of these emissions is produced from the decomposition of slurry in livestock facilities, during storage and treatment phases. This research aimed at evaluating the effectiveness of the additive “SOP LAGOON” (made of agricultural gypsum processed with proprietary technology) on (i) NH3 and Greenhouse Gas (GHG) emissions, (ii) slurry properties and N loss. Moreover, the Life Cycle Assessment (LCA) method was applied to assess the potential environmental impact associated with stored slurry treated with the additive. Six barrels were filled with 65 L of cattle slurry, of which three were used as a control while the additive was used in the other three. The results indicated that the use of the additive led to a reduction of total nitrogen, nitrates, and GHG emissions. LCA confirmed the higher environmental sustainability of the scenario with the additive for some environmental impact categories among which climate change. In conclusion, the additive has beneficial effects on both emissions and the environment, and the nitrogen present in the treated slurry could partially displace a mineral fertilizer, which can be considered an environmental credit.
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Dairy systems are a source of pollutant emissions, such as greenhouse gases ( GHG ) and NH 3 that are associated with impacts on the environment. Gas emissions in barns are related mainly to diet intake and chemical composition, N excretion and manure management. A reduction in dietary N is known to be an effective way to reduce N excretion and the resulting NH 3 emissions. However, most studies consider manure in liquid form with frequent removal from the barn. In deep litter systems, several processes can occur during the accumulation of solid manure that result in variable gas emissions. The objective of this experiment was to investigate the influence of the interaction between dietary CP (low or high) and manure management (liquid or solid) on gas emissions (NH 3 , N 2 O, CH 4 ) at the barn level. Dietary treatments provided either low ( LowN ; 12% CP) or high ( HighN ; 18% CP) degradable protein to modify the amount of total ammonia nitrogen ( TAN ) excreted. The cows were housed for two 8-week periods in two mechanically ventilated rooms equipped to manage manure either in liquid ( LM ; slurry) or solid form ( SM ; deep litter). In the LM treatment, N balance was measured for 4 days. As expected, animals fed the LowN diet ingested 35% less N and excreted 65% less N in their urine, with no reduction in faecal N excretion and N secretion in milk. On the LowN diet, excretion of urea-N and NH 3 -N emissions were reduced regardless of the manure management. On the HighN diet, urinary urea-N excretion was three times as high, while NH 3 -N emissions were 3.0 and 4.5 times as high in LM and SM, respectively. Manure management strongly influenced CH 4 -C emissions, which were 30% higher in SM than in LM, due to the accumulation of litter. Moreover, gas emissions from solid manure increased over the accumulation period, except for NH 3 on the LowN diet. Finally, our results suggest that methods used for national inventories would become more accurate by considering the variability in TAN excretion, which is the primary factor that influences NH 3 emissions.
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Objective Our objective was to assess the effect on milk yield and feed efficiency of a combination of essential oils (eugenol, geranyl acetate, and coriander). Materials and Methods Forty-eight Holstein cows (621 ± 61.3 kg of BW and 167 ± 83.8 DIM, 15 primiparous and 33 multiparous) were allocated to 2 treatments for 8 consecutive weeks in a completely randomized design. Treatments consisted of no supplementation (CTRL) or supplementation (AGL) of 1 g/d of Agolin Ruminant (Agolin, Bière, Switzerland) in the TMR. All cows were fed a common TMR (just differing in the presence or absence of Agolin Ruminant) twice daily. Milk production, milk composition, and feed intake of individual cows were recorded daily, and feed efficiency was calculated. Rumen fluid samples were collected from all cows throughout the study to determine pH and VFA profile and estimate methane concentrations. Results and Discussion Compared with CTRL, cows fed AGL produced more ECM after 4 wk of exposure to treatments, and because DMI did not differ between treatments, feed efficiency increased over time. Estimated rumen methane concentrations of cows fed AGL were lower compared with those fed CTRL during wk 4 to 8. Implications and Applications It is concluded that Agolin Ruminant increased milk production and feed efficiency after 4 wk of feeding the additive. This improvement could be attributed to a marginal improvement of rumen fermentation as indicated by decreases in in vitro estimates in rumen methane production.
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Milk and dairy products contain multiple nutrients and contribute significantly to meet the nutritional requirements for protein, calcium, magnesium, phosphorus, potassium, zinc, selenium, vitamin A, riboflavin, vitamin B-12, and pantothenic acid. However, consumption of dairy is decreasing and moving away from the advised level in many countries and the potential benefits of milk and dairy products for health have come under question. This, in spite that numerous studies report health benefits associated with dairy consumption. The present supplement aims to assess and summarize scientific evidence regarding the impact of dairy intake on health and all-cause mortality, and on the prevention of diverse chronic diseases, mainly from meta-analyses of observational studies and randomized controlled trials (RCTs). There seem to positive associations between moderate maternal milk intake during pregnancy and infant birth weight, length and bone mineral content during childhood. Moreover, consumption of dairy products in older subjects may reduce the risk of frailty and decrease the risk for sarcopenia. The highest consumption of dairy products did not show a clear association with total osteoporotic fracture and hip fracture risk; however, a diminished risk of vertebral fracture was found. Analysis of the differences between high and low dairy consumption and for dose-response found no association between dairy product consumption and risk of all-cause mortality. Total and low-fat dairy consumption is associated with a reduced risk of developing metabolic syndrome and current evidence supports that consumption of dairy does not adversely affect the risk of cardiovascular outcomes and may even have a subtle protective effect. Moreover, evidence has been provided of an inverse association between the consumption of dairy products and ischemic heart disease and myocardial infarction. Also, the evidence suggests that dairy consumption, particularly low-fat dairy and yogurt is associated with a lower risk of type 2 diabetes. Likewise, moderate compared with medium consumption of dairy is associated lower risk for colorectal and bladder cancer and has no association with prostate cancer. Finally, consumption of milk or dairy products did not show a proinflammatory effect on healthy subjects, overweight/obese individuals, or individuals with other metabolic abnormalities, and fortification of dairy products with phytosterols and ω-3 fatty acids seems to be a good approach to improve cardiometabolic risk biomarkers. In conclusion, the systematic reviews and meta-analyses of the present supplement support adequate milk consumption at various stages of life and in the prevention/control of various noncommunicable chronic diseases.
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The present study evaluates the effectiveness of different types of biochar additives and bacterial inoculation on gaseous emission, nutrient preservation, and relevant functional bacterial community during cow manure composting. The result revealed that biochar and bacterial consortium inoculation effectively inhibited gaseous emission and improved carbon and nitrogen sequestration, remarkably enriching the abundance of the functional bacteria community. Notably, superior efficacy was found in 12% wheat straw biochar and bacterial consortium amendment composting of T6 with the lowest cumulative CO2-C and NH3-N (308.02 g and 12.71 g, respectively), minimal total C and N losses, and the highest bacterial population. Additionally, gaseous emission exhibited a strong correlation between physicochemical properties with intersection of 66.78% and a unique substrate utilizing bacterial communities. Consequently, the integrated application of biochar and bacterial consortium inoculation was suggested as an efficient method to adjust microbial activity and facilitate cellulose-rich waste degradation, enabling efficient management of organic waste from cow manure and wheat straw by composting.