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Review

Mitigating Ammonia Deposition Derived from Open-Lot Livestock Facilities into Colorado’s Rocky Mountain National Park: State of the Science

1
Texas A&M AgriLife Research, Amarillo, TX 79106, USA
2
Department of Animal Science, Texas A&M University, College Station, TX 77843, USA
3
College of Engineering, West Texas A&M University, Canyon, TX 79016, USA
4
Department of Life, Earth and Environmental Sciences, West Texas A&M University, Canyon, TX 79016, USA
5
Livestock Nutrient Management Research Unit, Agricultural Research Service, The United States Department of Agriculture (USDA-ARS), Bushland, TX 79012, USA
6
Shaw Engineering, LLC, Lexington, TX 78947, USA
*
Author to whom correspondence should be addressed.
Retired.
Atmosphere 2023, 14(10), 1469; https://doi.org/10.3390/atmos14101469
Submission received: 14 August 2023 / Revised: 5 September 2023 / Accepted: 8 September 2023 / Published: 22 September 2023

Abstract

:
Northeast Colorado’s livestock operations have been identified as a major contributor to reactive nitrogen deposition in the Rocky Mountains National Park (RMNP). We present a review on the state of knowledge concerning the emission, transport, deposition, and mitigation of gaseous ammonia (NH3) from open-lot cattle feeding facilities located east of the Northern Front Range of the Rocky Mountains. Gaseous NH3 mitigation strategies discussed are related to diet manipulation and management practices. Crude protein content of 11% and condensed tannins of 8% reduced the NH3 emission by 43% and 57%, respectively. Ambiguous results for NH3 mitigation by using water sprinklers have been reported—an increase in NH3 emission by 27% and decrease of 27 to 56%. Manure harvesting should be evaluated in terms of maintaining proper moisture content, and not necessarily as a mitigation option. The use of chemical and physical manure amendments has shown a wide range in NH3 mitigation effectiveness, ranging from 19 to 98% for chemical and 0 to 43% for physical amendments, respectively. The review outlined the scientific basis, practicality, and expected efficacy of each management practice. The most plausible management practices to reduce NH3 emissions from corral surfaces in cattle feedyards are presented.

1. Introduction

Colorado’s Front Range of the Rocky Mountains lies along the Great Plains’ western edge, a classic rural–urban interface between the fast-growing cities of the Interstate 25 corridor and the agriculture-dominated land uses of eastern Colorado. That narrow interface is also an imaginary boundary between the sensitive, alpine ecosystems of the Front Range and the anthropogenically modified air masses along and east of the foothills. Among the many and varied land uses characteristic of the plains adjacent to and east of Interstate 25 are intensive animal agricultural production systems, prominently including concentrated animal feeding operations (CAFOs) such as open-lot cattle feedyards and dairies. Those livestock operations have been identified as a major contributor to reactive nitrogen deposition in Rocky Mountains National Park (RMNP).
The ruminant population of the Great Plains has not changed over the last 300–400 years although bison (Bison bison) have been replaced by beef and dairy cattle (Bos taurus and B. indicus). The primary differences between bison and cattle include characteristic adult liveweights (2600 vs. 1300 lbs per head for bison and cattle, respectively), characteristic diets (lower-protein, lower-energy grasses and forbs for bison vs. higher-energy, higher-protein diets for cattle), rumen adaptation to (and feed-to-gain conversion efficiency of) those diets, and characteristic management intensity (free-ranging and extensive vs. a combination of controlled-extensive and intensive production, respectively). We cannot yet document the extent to which any differences exist between the two genera in magnitude, location, and/or duration of ruminant-derived ammonia (NH3) emissions and their implications for NH3 deposition in RMNP, but it is reasonable to suppose that such differences exist and may be significant.
The meteorology of this region is complex due to the local topography (principally the South Platte River Valley and the high mountain ranges) and the consequent predominance of orographic influences, which include diurnal, thermally driven, and upslope/downslope conditions as well as less frequent, synoptic-scale, deeper, and upslope flows [1,2,3].
Superimposed on the regional meteorology are the fugitive, airborne emissions of NH3 from a wide variety of anthropogenic sources, in animal agriculture and beyond—and the subsequent transport and deposition of that NH3 into RMNP under ‘upslope’ conditions. The ecological significance of NH3 deposition in the RMNP is amplified, especially in the high elevations east of the Continental Divide, because the soils are thin and rocky; soluble nitrogen compounds accumulate and concentrate in snowpack and are released on short timescales during the spring melt; and the length of the growing season is greatly attenuated. Consequently, the RMNP ecosystem is quite sensitive to changes in macronutrient inputs from the atmosphere [4].
The increased wet and dry NH3 deposition and its effects on RMNP ecosystems have been studied for over three decades [5,6,7,8,9,10,11,12]. Wet deposition of reduced N comprises fine particulate ammonium (NH4+) salts or aerosols of acidic gases. These components have a relatively long atmospheric residence time, 4 to 15 days, and when removed by precipitation contribute to N deposition after long-range transport in remote ecosystems [13]. Dry deposition is the removal of N pollutants by sedimentation under gravity, diffusion processes, or turbulent transfer that results in interception [14]. Field measurement and modeling studies have shown that eastern Colorado annually has contributed more to the wet deposition of gaseous ammonia (NH30) and ammonium aqueous (NH4+) (61%) in RMNP than NH3 sources west of the Continental Divide (26–30%); sources within the park contributed to the remaining 9–13% [8,12]. According to modeling studies [9,12], sources west of the State of Colorado contribute about 30% of measured NH3, with California contributing approximately 13%, eastern Utah 10%, and the Snake River Valley of southern Idaho 7%. Regional contributions to dry N deposition into RMNP are still lacking. The larger, easterly contribution to N deposition in RMNP is apparently due to source proximity and relatively high aggregate emissions [12,15]; eastern Colorado hosts the fourth highest NH3 emission “hot spot” in the U.S. [16,17]. However, the larger eastern Colorado contributions are episodic, depending on meteorological conditions that lead air masses from this region into the RMNP. As a result, emissions transport from eastern Colorado into RMNP is correlated with the occurrence of upslope events (Figure 1) [12].
According to the Rocky Mountains Atmospheric Nitrogen and Sulfur Study (RoMANS) [18], wet N deposition is the major deposition process in RMNP during both spring and summer. The total dry deposition flux was significantly less than wet deposition flux for all species measured during spring and summer at the RoMANS’s core site. Wet deposition fluxes increased from spring to summer, specifically 135.6% for nitrate, 101.9% for NH4+, 48.9% for organic N, and 61.6% for sulfate. Dry deposition fluxes of nitric acid, ammonia, and sulfur dioxide also increased by 101.6%, 141.0%, and 16.5%, respectively, during the summer. Contrarily, dry deposition fluxes of particulate nitrate, NH4+, and sulfate decreased by 62.1%, 10.0%, and 16.1%, respectively [18].
There are roughly 2.6 million head of cattle in Colorado, including beef and dairy cattle (cows and calves) [19]. On average, the region of concern in this paper (northeast Colorado; specifically, Morgan, Logan, Larimer, and Weld Counties) has approximately 1,100,000 animals on feed in feedyards at any one time, and the majority of which are fed ~80 km east of RMNP in Weld County, the leading animal and agricultural producing county in Colorado [20].
The manure (feces plus urine) deposited continuously on a feedyard’s corral surface is a primary source of fugitive NH3 emissions, and the process of NH3 formation and volatilization begins immediately after urine and feces are excreted. Ammonia is produced by the urease-mediated (present in the feces) hydrolysis of nitrogenous compounds (urea and protein) in the urine. Urea in urine is the predominant, fast-hydrolyzing NH3 source in manure; more complex compounds, such as proteins and amino acids, are decomposed more slowly by microbes [21]. Once emitted into the atmosphere, in the presence of water and suitable anionic species (primarily oxides of S and N), NH3 enters rapidly into ionic reactions that form secondary aerosols as precipitates. The dynamics of those reactions, however, are complex and depend on environmental conditions and the relative concentrations of reactants, being extremely sensitive to temperature, moisture, pH [22,23], air pollutants (e.g., dust) [24], and wind as well as to the aerodynamic mechanisms that modulate NH3 emissions from different source classifications [12].
Some 70–90% of N fed to beef cattle is excreted in feces and urine [25]. Because protein sources are relatively expensive components of the mixed feed, the cattle-feeding industry has long sought research-based management practices to decrease NH3 emissions, first via dietary manipulations and growth-promoting technologies to increase nutrient- use efficiency by cattle (e.g., crude protein (CP), β-adrenergic agonists (β-AA), and condensed tannins (CT)), and from pen surfaces and the broader production system, such as amending pen-surface chemistry (alum or gypsum) and more frequent manure-harvesting operations. Only recently [26] has the use of sprinkler dust-control systems been proposed as a means of reducing NH3 emissions from the pen surface.
Few field-measured NH3 emissions studies have been conducted to date in Colorado’s cattle-feeding regions [26,27]. Most studies have been conducted in other cattle-feeding areas, such as Canada, United Kingdom, and especially the Texas Panhandle and the surrounding Southern High Plains in the United States (Figure 2). Because of regional differences (edaphic and climatic, animal density, dietary feedstocks, and proximity to RMNP) between Texas and Colorado’s Front Range, more research data from representative Colorado feedyards would enhance the regional understanding of NH3 dynamics in RMNP’s immediate source areas, thereby reducing the uncertainty associated with modeling results derived from assumptions imported from other cattle-feeding regions [28].
In 2007, the cattle-feeding industry committed (along with the broader agricultural and agribusiness sector in eastern Colorado) to support the RMNP Nitrogen Deposition Reduction Plan (NDRP), the goal of which is to reduce the 5-y average deposition flux of inorganic N into RMNP by 50% as compared to 2004 levels. The targeted wet-deposition flux into RMNP is 1.5 kg N ha−1 y−1 by 2032. This flux threshold, established through “hindcasting” by previous research, is the estimated critical load of wet-deposited N that can be assimilated by sensitive ecosystems within RMNP without irreversible changes to the Park’s flora and fauna [5]. The downward trajectory in deposition flux from 2004 to 2032 that is expected to result from the NDRP is known colloquially as the “glidepath” [11]. The Natural Resources Report (NDRP) [10,11] showed annual wet N deposition in 2018 and 2019 to be about 2.5 kg N ha−1 y −1, decreasing from 3.2 in 2017. However, the 5-y average (2.7 ± 0.22 kg N ha−1 y−1) remained 0.3 kg N ha−1 y−1 above the glidepath (2.4 kg N ha−1 y−1).
Gauging feedyards’ implementation of management practices to reduce NH3 emissions would be difficult. But the scientific community has identified important knowledge needs and gaps. Understanding the emission mechanisms and atmospheric-transport dynamics associated with NH3 deposition in RMNP will inform the selection and implementation of both tactics and strategies to reduce NH3 emissions from cattle feedyards in response to short- and long-range weather forecasts. Given the importance of ensuring that feedyard management recommendations are both affordable and demonstrably effective, with financial support from the USDA Natural Resources Conservation Service (NRCS) and the Colorado Livestock Association (CLA), we present herein the most recent state of the science on the dynamics of NH3 emissions in open-lot livestock facilities, the influence of diurnal and synoptic weather events on NH3 emission, transport, and deposition into RMNP, and the most plausible management practices to reduce fugitive NH3 emissions from corral surfaces in cattle feedyards. We outline the scientific basis, practicality, and expected efficacy of each candidate mitigation method.
Our literature review seeks to answer the overarching question “how might theoretically plausible methods to reduce NH3 emissions from open-lot cattle feedyards be practically applied in northeastern Colorado to reduce the delivery of atmospheric NH3 into RMNP during transient, upslope conditions?” That question presents four major objectives:
  • Understand the dynamics of NH3 emissions from pen surfaces in open-lot CAFOs characteristic of northeastern Colorado;
  • Describe the meteorological influences on NH3 emissions mechanisms from open-lot cattle feedyards, including both seasonal and daily components;
  • Describe the meteorological influences on the transport mechanisms from Colorado’s Front Range into RMNP, including both synoptic meteorological patterns and upslope conditions;
  • Evaluate recommended management practices to decrease NH3 emission in open-lot livestock facilities during upslope conditions, based on the USDA-NRCS list of best management practices, such as diet manipulation (CP, CT), growth-promoting technologies (β-AA, implants), feed additives (monensin), phase feeding, manure harvesting, water sprinkling, and pen surface amendments.

2. Materials and Methods

2.1. Literature Review Approach

We searched Google Scholar and Web of Science for the most relevant published literature on NH3 emission in feedyards. Initially, the topic “ammonia (emission)” yielded over 3,300,000 (1,600,000) documents. After adding the search terms “Cattle (beef)”, over 100,000 documents remained; adding the search terms “Feedlot (CAFO, AFO, feedyard)” and identifying papers pertaining to (a) feedlot NH3 emissions or (b) management practices to mitigate NH3, our search yielded ~150 papers that were clearly within the scope of this review topic. The data were summarized in tables according to the major management practices adopted by feedyards.

2.2. Relevance and Screening

We used data exclusively from primary research evaluating the following: (1) NH3 emissions from open-lot cattle feedyards, (2) the seasonality or temporality of those emissions, and (3) the effects of management practices to mitigate them. Data were considered eligible when published in refereed journal articles (132), dissertations and theses (1), and conference articles (6). Our primary focus was research conducted in the United States cattle-feeding sector.

3. Literature Review

3.1. NH3 Emission Dynamics in Open-Lot Surfaces

Ammonia is a colorless gas with a distinct pungent smell. It occurs naturally and is normally found in trace amounts in the atmosphere, where it is the dominant alkaline gas, combining readily with acidic compounds. It is produced by the decomposition or fermentation of animal and plant residues containing N, including livestock manure (urine and feces) [29]. The primary sources of livestock-derived NH3 emissions into the atmosphere are manure in CAFOs [30,31,32] and the associated waste management systems, including open manure storage and land application of manure products.
Bovines use dietary N less efficiently than most other species [33]. In open-lot cattle feedyards, between 70 and 90% of fed N is excreted in feces and urine [25]. Once excreted, urea is enzymatically hydrolyzed to CO2 and NH4+ and then volatilized to gaseous NH3 via well-documented reactions given below (Equations (1)–(3)):
C O ( N H 2 ) 2 + 2 H 2 O + U r e a s e ( N H 4 ) 2 C O 3
( N H 4 ) 2 C O 3 + 2 H + 2 N H 4 + + C O 2 + H 2 O
N H 4 + + O H N H 3 + H 2 O
A significant fraction of cattle manure N, primarily from urinary urea (CO(NH2)2), is converted to NH4+ and eventually lost to the atmosphere as NH3. Up to 90% of feedyard NH3 originates from urine deposited in animal pens [22,23], but the instantaneous magnitude of that loss depends strongly on weather conditions (temperature, precipitation, humidity, and wind), soil properties, pH, microbiological activities (e.g., urease activity), and management practices (Table 1 and Table 2). Ammonia volatilization increases linearly with total ammoniacal nitrogen concentration (TAN), and curvilinearly with temperature, wind speed, and slurry pH [24,34,35]. Temperature and pH have been reported to be the most important factors influencing NH3 volatilization [24], as the NH3/NH4+ ratio is equilibrium dependent (Figure 3, Figure 4 and Figure 5).
During winter, mineralization of organic N to NH3 is limited by low temperature, but as pen surfaces warm in spring and summer, the mineralization rate increases rapidly [57]. Increasing manure temperature (Equation (1)) accelerates microbial activity and favors the production of gaseous NH3 (Equation (2)) [12,58]. In summary, there are three major factors associated with an increase in NH3 volatilization as temperature increases: (1) a decrease in solubility of aqueous NH3, (2) an increase in ratio of aqueous NH3 to NH4+ in solution (NH4+/NH3 equilibrium), and (3) an increase mineralization rate of organic matter via biological activity [24].
The percentage of NH3-N loss from fed N during the summer was around 58%, and 39% in winter, which reflected an average annual loss of 52% (Table 1). On an annual basis, one beef cattle (animal unit) fed in confinement emits 104 g NH3-N per day (Table 2), which represents 52% higher NH3 emissions on average than what was previously reported for Colorado [27] in the early 1980s (50 g head−1 day−1). It is important to highlight the lack of current information related to NH3 emissions from Colorado’s feedyards, especially considering the evolution of the beef cattle industry.
In addition, at a constant temperature, higher pH favors the formation of NH3 over NH4+ and increases the potential for NH3 volatilization (Figure 3) [59,60]. The proportion of NH3 increases rapidly as pH exceeds 7, and at pH 10, virtually all of the total ammoniacal N exists as NH3 [23]. Manure’s buffering capacity is strong, especially due to the presence of bicarbonates and organic acids, which result in an increase in pH when in acidic systems (manure–soil–water; open-lot surface). Thus, maintaining manure with a low pH to mitigate NH3 emission is challenging. Increasing pH (Figure 3) and temperature (Figure 4) move the NH4+/NH3 equilibrium towards NH3 formation. Thus, the higher temperatures reached during summer enhance the NH3 volatilization in feedlots (Table 2). The drying process itself increases aqueous NH4+ concentrations, thereby enhancing NH3 volatilization; however, that may be temporarily reduced under optimum water content/corral surface moisture. The optimum water content for manure composting, for example, ranges between 50–70%, which allows maintenance of highly soluble NH3 in a dissolved state [61,62]. However, to reach an optimum moisture level in open-lot surface is challenge (if not impossible) as a dynamic environment is constantly receiving new fresh manure deposition and evaporating existing moisture.
Figure 3. NH4+, NH3, and TAN equilibrium as a function of pH, and the relationship between NH3 emission flux and pH for the simulated beef cattle feedyard data.
Figure 3. NH4+, NH3, and TAN equilibrium as a function of pH, and the relationship between NH3 emission flux and pH for the simulated beef cattle feedyard data.
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Figure 4. Ammonium and ammonia equilibrium as a function of temperature and pH (adapted from [61]).
Figure 4. Ammonium and ammonia equilibrium as a function of temperature and pH (adapted from [61]).
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Figure 5. NH3 emissions mechanisms and management levers available to alter those emissions. If a given arrow starts at variable A and points to variable B, then the sign (+ or −) on the tip of the arrow designates the direction that variable B moves if variable A increases.
Figure 5. NH3 emissions mechanisms and management levers available to alter those emissions. If a given arrow starts at variable A and points to variable B, then the sign (+ or −) on the tip of the arrow designates the direction that variable B moves if variable A increases.
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3.2. Meteorological Impacts on NH3 Emission and Transport Characteristics from Colorado’s Front Range into the Rocky Mountains

3.2.1. Synoptic Meteorological Pattern and Upslope Conditions

Colorado’s Front Range and the adjacent east slopes of the Rocky Mountains, including RMNP, are characterized by prevailing westerly (downslope) winds during much of the year. However, easterly upslope winds resulting from either synoptic-scale storm systems or diurnal, orogenic circulations are known to contribute to gas and particulate transport from eastern Colorado’s livestock facilities into the RMNP, where atmospheric deposition then enriches sensitive alpine ecosystems with reactive nitrogen [1,12,15].
The easterly transport mechanisms associated with various meteorological flow patterns are variable and complex due to many factors, such as the unique meteorological situation, mountain–valley circulation effects, high elevation, and varied terrain [63]. However, these meteorological effects vary seasonally and temporally and can be mostly predicted in advance by numerical weather prediction models. This has raised interest in combining short-term weather forecasts (e.g., Early Warning System; [1]) with the understanding of NH3 emission dynamics from open-lot corral surface [22,23] to improve management practices to reduce NH3 emission.
Two primary easterly transport processes are documented in the literature as mostly responsible for maintaining the N enrichment process of the RMNP. One of these process is the synoptic meteorological pattern that brings notable cool-season (particularly in the spring) rain and snowstorms to the Colorado Front Range, and the other process is the summertime mountain–plains circulation that occurs when the jet stream is too far north for its associated large-scale westerly winds to influence Colorado [1]. The most common period (40% of hours of the day) of upslope conditions in RMNP associated with synoptic-scale storm systems is in April, and least frequent in December (20% of hours of the day; [18]). Although easterly conditions are important, their association with precipitation events is fundamental for N deposition in RMNP. The coincidence of upslope conditions and precipitation events is most likely to occur in the winter and spring, whereas summer precipitation events are more prone to be associated with westerly winds [18]. However, unexpectedly high precipitable water values associated with cold fronts play also significant roles in the N deposition into the RMNP [1].
Boreal summers in Colorado promote fewer synoptic weather systems, which allows the diurnal cycle to exert a dominant control on meteorological flows along the mountain–plain interface. The weak synoptic conditions in the warm season have unique consequences for the transport, mixing (dilution), and photochemical processing of local emissions [3,64,65]. As the land surface cools during the evening, downslope drainage flows extend from the Continental Divide onto the eastern plains and are most pronounced in the canyons and river valleys [65]. As solar radiation heats the ground during the morning hours, upslope flows are formed, starting a few hours after sunrise in the foothills and slowly extending to the eastern plains about 3 h later. The upslope flows can reach the top of the Continental Divide by mid-afternoon on days with strong upslope. Flow reversal starts at the top of the Continental Divide in the late afternoon, which forms the convergence line that moves east in the evening hours. Downslope winds then dominate the entire region again around midnight [63,65]. Thus, vertical and horizontal dispersion associated with these cyclical mesoscale mountain circulations, driven by differential heating of mountains and plains, are considered a primary driver of the eastward convective transport towards mountains in the absence of large-scale synoptic weather systems [1].
There remains some uncertainty in the depth and relative magnitude of the easterly upslope transport associated with both synoptic storm systems and mountain–plains circulations into the RMNP, and the need to more accurately model the easterly flows in the complex terrain has been noted [15,66]. For example, Clow et al. (2015) [67] found higher summer dissolved inorganic nitrogen concentrations in the eastern portions of RMNP, presumably because local flow patterns result in greater easterly transport from the Front Range in these areas than in locales further to the west.

3.2.2. Major Meteorological Factors Influencing Local Surface NH3 Emission

To represent accurate weather processes and simulate potential scenarios of high NH3 deposition into the RMNP, it is also important to understand how variations in meteorological quantities associated with synoptic weather regimes, season, and time of day affect the local NH3 emissions and chemistry at ground level at the various emission sources in eastern Colorado. The soil and air temperatures, humidity/precipitation, and wind/atmosphere turbulence (Figure 1) strongly influence the emission and dispersion processes of NH3. Diurnal temperature change is considered one of the major weather factors influencing NH3 flux in Colorado because of the direct effect on the volatilization of TAN [18,28,63,68,69]. On an annual scale, NH3 mixing ratios in northeastern Colorado typically achieve a maximum in warmer summer months when the volatility of NH3 increases due to higher temperatures and to conditions that suppress partitioning to particle NH4+ [68,69,70]. Air temperature for this period ranges from 10.0 to 36.6 °C, with an overall mean of 24.9 °C [18,68]. Golston et al. [68] reported enhanced emissions from 0.08 to 0.55 mol NH3/mol−1 of air (106 ppm) in this region during summertime conditions, with the lowest and highest temperature reflecting the minimum NH3 emission from 12:00 a.m. to 6:00 a.m. and maximum around 12:00 p.m., respectively [18]. Evaluating NH3 mixing ratios at different heights during the summer, Tevlin et al. [2] observed at higher altitudes; specifically at 100 ± 5 approximately 8 to 22 ppb, and at 280 ± 5 m 6 to 11 ppb, which represented a gradual maximum between 9:00 a.m. and 4:00 p.m. local time, and at 10 ± 5 m (lower altitudes), the maximum was achieved earlier at 7:00 a.m., followed by a sharper increase at 9:00 a.m.; approximately ranging from 6 to 16 ppb.
Although summer is characterized by the highest NH3 emission fluxes, a slight increase in winter season NH3 concentrations at surface of observing sites (urban and rural area) in northeastern Colorado has been noticed as compared to fall and spring [69,70], which is attributed to the low-level temperature inversions that trap NH3 emissions closer to the surface within a shallower nocturnal and less well-ventilated winter boundary layer [2,69,70].
The difference in concentration between manure and atmosphere drives NH3 emission first through diffusive transfer from the ground surface, followed by convective mass transfer in the atmospheric boundary layer, where wind and atmospheric turbulence transport the NH3 according to the prevailing wind direction [71]. Overall, Colorado’s diurnal, orographically driven, evening winds are usually from the northwest (downslope), while during daytime (7:00 to 18:00) winds change to southeasterly (upslope), suggesting transport from the Front Range to the RMNP during the daytime [18]. The highest NH3 mixing ratios measured at multiple altitudes were observed when the wind arrives from the north and east, and the lowest ratios were observed when westerly and southwesterly winds were coming from the direction of the Rocky Mountains and cities along the foothills [2].
Li et al. [68] and Tevlin et al. [2,69] evaluated the vertical scale/profile (0–300 m) NH3 mixing ratios at the Boulder Atmospheric Observatory (BAO) Tower throughout the year of 2012 and during the summer of 2014, respectively. Overall, both studies observed comparable results with an increase in NH3 mixing ratios at the lower heights (4.69 µg m−3 (89%) during the day and 2.73 µg m−3 (141%) at night [2], and 4.63 µg m−3 at 10 m height through the year) [69]. However, the highest NH3 concentration at the vertical profile evaluated by Li et al. [69] was always observed at the 10 m height instead of closer to the surface, which decreased towards the surface (4.35 µg m−3) and towards higher altitudes (1.93 µg m−3), with the minimum concentration observed at the 300 m height.
Having measured those data year-round, Li et al. [69] could conclude that the highest concentrations across the profile were observed in summer, when the volatility of NH3 increases due to higher temperatures and vertical mixing is enhanced, which also may reflect a shift in the thermodynamic equilibrium of particulate-phase NH4NO3 toward its gas-phase precursors, NH3 and HNO3. Although higher NH3 ratios were observed during the summer, the greatest vertical concentration differences were observed in winter with a decrease of approximately 75%, with the average concentration near the surface higher than 4 µg m−3 and approximately 1 µg m−3 at 300 m, followed by autumn, with average of 1.9 µg m−3 near the surface and 4.5 µg m−3 at 300 m). Authors concluded that low-level temperature inversions which trap NH3 emissions closer to the surface (shallow winter boundary layer) are common in both seasons (autumn and winter) that can produce elevated surface concentrations. They also stated that is usual a gradient of decreasing concentration near the surface at this location, where local emissions are expected to be small, and the net local flux represents surface deposition.
To summarize, high values of wet N deposition in RMNP require elevated NH3 emissions, easterly winds transporting fugitive emissions toward RMNP, and conditions that favor precipitation followed by deposition, especially in the leeside of the park [1]. As easterly winds advect and lift pollutants up the east slope of the RMNP, the air cools and condenses to form clouds in the presence of moisture. Precipitation maxima in northern Colorado are associated with easterly winds and occur most frequently in spring and summer [6,7]. During precipitation events, clouds entrain Front Range pollution and deposit the pollutants over the mountains with precipitation [1].

3.3. Feeding and Management Practices to Mitigate NH3 Emissions from Open-Lot Livestock Facilities

The digestion of dietary proteins and other nitrogenous compounds is complex in ruminants because of ruminal fermentation [72]. The ruminal microorganisms can degrade some of the dietary nitrogen (also known as rumen-degradable protein, or RDP) and use the products for their own growth. According to Owens and Zinn [73], ruminal microbes themselves produce between 20 and 60% of their dry matter as CP. Accordingly, rumen microorganisms can use both dietary protein and non-protein nitrogen, as well as nitrogen recycled to the rumen. A portion of the NH3 produced in the rumen by the deamination of amino acids not used for microbial protein synthesis will be absorbed across the ruminal epithelium into the portal vein and converted mostly to urea by the liver [74]. Firkins and Reynolds (2005) [75] found that the net NH3 absorption was 42% of dietary nitrogen intake across 304 measurements in lactating dairy cows. The urea produced by the liver is partly excreted in the urine (20–60%), with the remainder recycled back to the gastrointestinal tract, and of this, 27–60% of the urea enters the rumen [76]. Feeding excess N results in increased NH3 absorption, increased urea production, and increased urea excretion in urine [74]. In fact, as N intake increases urine N excretion increases at a much greater rate than fecal N excretion [77]. The NH3 emissions from open-lot livestock facilities is primarily produced via the hydrolysis of urinary urea to NH4+ and CO2 that occurs on the feedlot pen surface [23,39].
Aiming to mitigate NH3-N deposition into RMNP, the USDA-NRCS has listed several recommended management practices for crops, dairy, and beef production. Because our primary objective is to evaluate recommended management practices to decrease NH3 emission in open-lot livestock facilities, we have used the USDA-NRCS’s list of best management practices (Table 3) to search the literature for scientific evidence of the most common/conventional management practices on NH3 abatement (Table 4, Table 5, Table 6, Table 7 and Table 8).
NH3 mitigation through feeding management ultimately aims to improve the efficiency of dietary N use by beef and dairy cattle, decreasing the amount of N compounds excreted, more specifically decreasing urinary excretion of urea-N. According to NASEM [72], in beef cattle, 40 to 80% of non-retained N is excreted in the urine, increasing as the dietary CP and/or RDP concentration increases in the diet. For that reason, NH3 emissions generally increase with increased N intake in protein-adequate diets. Decreasing CP concentration in the diet can potentially decrease NH3 emissions, but it also decreases average daily gain, which can increase days on feed, the amount of manure deposited in the pens, and consequent NH3 emissions.
Phase feeding is a nutritional management strategy in which the ingredients and chemical composition of the diet is modified over the growth stage of the animal so that the nutrient composition of the diet more closely meets the nutrient requirements of the animal [42]. The purpose of phase feeding is to supply a more accurate quantity of nutrients for each animal’s stage to decrease nutrient excretion and subsequent losses of these nutrients, especially N and P, to groundwater, surface, or to the atmosphere. As beef cattle grow and mature, many of their nutrient requirements as a percentage of the diet decrease, most notably protein [79]. However, according to NASEM [72], the practicality of phase feeding under the current feeding and management situations is equivocal because of potential logistic (additional supplements, diets, and feed truck scheduling), economic, and animal health obstacles. Clearly, more scientific discussions on the technoeconomic of phase feeding are still needed.
Including some feed additives (e.g., monensin and CT) and growth-promoting technologies, such as β-AA and implants, have shown benefits to the feedlot industry, including increased feed-to-gain performance and meat quality and reduced environmental impact through reduced NH3 and CH4 emissions. In addition, other management practices such as manure harvesting, dust control using water sprinklers or other irrigation systems, and surface manure amendments have also been evaluated, although results are still uncertain (Figure 5).

3.3.1. Feeding Management—Diet Manipulation: CP and CT

NH3 emissions from feedlot operations are sensitive to dietary CP concentrations [36,46,80]. When beef cattle are fed enough CP to meet their physiological and growth needs, about 25 to 50% of N intake is subsequently lost to the atmosphere as NH3 [22]. When CP exceeds cattle needs, the excess N is excreted, primarily as urea in the urine, thereby increasing NH3 emissions [81]. Kissinger et al. [82] found that 12% of the feed N is retained by cattle, and the remaining was assumed to be excreted to the pen surface, representing 67% of excreted N, which were lost as NH3 volatilized, as dissolved or suspended N in feedlot runoff, or retained in manure not removed from pens. One way to mitigate NH3 emissions from open-lot livestock facilities is by manipulating dietary CP. By reducing dietary CP content to match animal needs more closely, more urea recycling is stimulated, overall feed efficiency improves, and N losses are minimized [26]. According to previous studies, when CP in the feed was adjusted to around 11%, the NH3 emission due to the volatilization of the excreted N could be reduced by 42.8% (Table 4).
Table 4. NH3 mitigation by manipulating CP in feeding beef cattle in open-lot livestock facilities.
Table 4. NH3 mitigation by manipulating CP in feeding beef cattle in open-lot livestock facilities.
Study LocationCP
Range Value (%)
NH3 or N Excretion Mitigationp ValueReference
ResultRate (%)
Nebraska13.4 to phase-fed (10.5–12.0)N volatilization from N excretion: 158 to 108 g/head/d320.01Erickson et al. (2000) [44]
Texas13.0 to 10 Urine N excretion: 5.2 to 1.7 g/head/d67<0.01Cole et al. (2006) [42]
Texas16.3 to 12.2NH3 emission: 149 to 82 g/head/day45<0.05Todd et al. (2009) [83]
Texas13.0 to phase-fed (10.9–12.1%)N volatilization from N excretion: 101 to 86 g/head/day150.32Erickson and Klopfenstein (2010) [38]
Texas16.0, 13.5, and 11 Estimated NH3 emission: 169.9, 104.4 to 90.1 g/head/d47N/ATodd et al. (2013) [81]
Michigan13.0 to 10.0NH3 emission: 32.4 to 11.8 g/head/d64<0.01Chiavegato et al. (2015) [84]
Texas13.0 to 11.0NH3 flux:
1.69 to 0.79 g/m2/d
53<0.05Pandrangi et al. (2003) [85]
Texas13.0 to 11.5NH3-N flux from excretion:
1.95 to 1.24 g/m2/d
37<0.01Cole et al. (2005) [46]
Texas13.0 to 11.5NH3 flux (Lab):
0.18 to 0.10 g/m2/d
NH3 flux (Field):
0.49 to 0.33 g/m2/d
32–44<0.01 (Lab)
>0.05 (Field)
Todd et al. (2006) [80]
Colorado13.5 to 11.6NH3 flux:
7.2 to 6.3 g/m2/d
13<0.05Galles et al. (2011) [26]
Another way to mitigate NH3 emission is by including CT in the diets. CT are polyphenolic compounds synthesized by plants that bind and precipitate proteins [86]. Herbaceous plants such as alfalfa and cottonseed have CT present in their seed coats and hulls [87]. Phenolic hydroxyl groups of CT form complexes with macromolecules (primarily proteins), reducing degradation in the rumen [86]. CT are thought to increase the efficiency of urea recycled to the rumen, which lowers the ruminal production of NH3 [88]. It occurs because CT reduces N excretion in urine by shifting the excreted N from urine to feces [89]. For example, when a mixture of condensed and hydrolysable tannins was provided to dairy heifers at 0.15% of dry matter, urine N excretion was reduced by 12% [90]. Since volatilized NH3 is mainly from urine, significant mitigation of NH3 has been reported with CT feeding (0 to 57% NH3 mitigation rate; Table 5).
Table 5. NH3 mitigation from including CT in beef cattle feeding.
Table 5. NH3 mitigation from including CT in beef cattle feeding.
Study LocationCT SourceCT DoseNH3 or N Excretion MitigationRate (%)Feeding Descriptionp ValueReference
Result
ColombiaQuebracho, acacia, and chestnut0, 2, 4, and 8% dry weight.Quebracho (0 to 8%): 68 to 50 NH3 concentration mg/dL
Acacia (0 to 8%): 68 to 48 mg/dL
Chestnut (0 to 8%): 69 to 30 mg/dL
26–57CT (Quebracho, acacia, and chestnut) was added to soybean meal at levels of 0, 2, 4, and 8% of dry weight.<0.05Gonzalez et al. (2002) [91]
TexasNot identifiedCT rates of 0, 0.5 and 1.0% on a dry matter basis.0 to 0.5% CT: 64 to 33 ppm
0 to 1% CT: 64 to 37 ppm
42–47-<0.01Campbell et al. (2016) [92]
TexasNot identifiedCT extract at 0, 0.5, and 1.0% of diet, DM basisUrinary N excretion was not different among treatment.
0 to 1% CT: 82 (139) to 74 (136) g/d
Not significant Top-dressing a steam-flaked corn–based finishing diet (14.4% CP and NEg 1.47 Mcal/kg)≥0.39Ebert et al. (2017) [93]
CanadaAcacia mearnsiiFeeding 2.5% CT extract with high protein diets containing corn dried distillers’ grains and solubles (DG)Feeding 40% DG with CT decreased the excretion of total urinary N and urea N in urine by 17 and 21%, respectively.17–21-<0.01Koenig & Beauchemin (2018) [94]
ItalyMimosa and Gambier
Chestnut and Tara (hydrolysable CT)
Two CT (Mimosa and Gambier) and two hydrolysable CT (Chestnut and Tara) were added (4 g/100 g DM) to a basal feed.NH3 emission was mitigated with hydrolysable CT (control 249 to CT 179 mg/L rumen fluid) 28 -<0.01 Cappucci et al. (2020) [95]

3.3.2. Growth-Promoting Technologies: β-AA and Implants

β-AA, such as ractopamine and zilpaterol hydrochloride, are catabolic hormones that indirectly lead to decreased lipogenesis and increased lipolysis [96]. This feed additive is used by the feedlot industry to enhance the efficiency of gain and modify the carcass characteristics and meat quality [96]. Ractopamine also affects protein metabolism by increasing protein synthesis and decreasing protein degradation. β-AA activates adenylate cyclase, increases cyclic adenosine monophosphate (cAMP), and thereby activates protein kinase A (PKA) and other protein kinases. Thus, β-AA was thought to promote protein degradation and inhibit protein synthesis. However, previous studies have found that β-AA is attributed to elevated myofibrillar protein synthesis [97,98] and depressed myofibrillar protein degradation [99]. β-AA promotes protein synthesis in livestock, reducing N excretion. The reduced N excretion mitigated NH3 emission (11 to 17%) from β-AA feeding [100]. Ross [100] conducted an experiment to determine the efficacy of feeding ractopamine hydrochloride (RAC) for the last 42 days of the finishing period to reduce NH3 emissions and improve animal performance. Steers fed RAC vs. control rations showed lower NH3 emission by 17.21% from d 0 to 28 (p = 0.032) and a trend for lower emissions from d 0 to 42 by 11.07% (p = 0.070). Ractopamine simultaneously increased beef cattle performance reduced NH3 emissions [100].
A relatively new β-AA, called lubabegron (Experior; Elanco, Greenfield, IN, USA), was approved by the U.S. Food and Drug Administration in 2018 to be fed to finishing cattle during the last 14 to 91 days on feed, with the label to reduce NH3 emissions. To our knowledge, lubabegron is the first feed additive approved by the FDA with a label to reduce NH3 emissions. When fed at a dose of 1.5, 3.5, or 5.5 mg per kg DM, lubabegron increased average daily gain by 11.3%, 16.2%, and 14.2%; feed efficiency by 9%, 12%, and 11.4%; and hot carcass weight by 2.8%, 3.9%, and 4.2% during the last 56-d on feed compared with the control, respectively. Further, NH3 emissions were reduced by 1.3%, 6.0%, and 11.0% compared with the control when lubabegron was fed to cattle at 1.5, 3.5, or 5.5 mg per kg DM, respectively [101,102].
Previous studies demonstrated decreased NH3 and amino acid concentration when ractopamine was added to in vitro incubations of ruminal fluid, suggesting a decrease in proteolysis and deamination, and the potential need for greater ruminally degraded protein, although effects varied with protein source and method of grain processing [103].
Growth promoting implants are known as an anabolic hormone product. The active ingredients contained in implants belong to three major categories of endogenously produced hormones: androgens (male hormones), estrogens (female), progestins (pregnancy), progesterone (female), and estradiol (female). Implants increase the circulating levels of somatotropin (ST) and insulin-like growth factor-1 (IGF-1) [104,105], which in skeletal muscle are important for the proliferation and differentiation of bovine satellite cell needed to support the DNA to protein unit throughout growth [106]. Both of ST and IGF-1 are produced by the animal and have a marked effect on how nutrients are used by the animal to produce muscle, bone, and fat [105]. In addition, the mechanisms of the implant to increase growth performance of cattle include modification of priorities for nutrient use for protein vs. fat deposition, alteration of tissue turnover, modification of daily tissue deposition limits, and modification of nutrient supply [107,108].
It was reported that implants enhance both ADG and feed conversion; however, implanted cattle often have less marbling and lower quality grades [109,110,111]. An increase in protein synthesis with an implant would be expected to reduce N excretion, but no studies have been found to prove that hypothesis. The use of conventional productivity-enhancing technologies (monensin, tylosin, β-AA, and others) mitigate NH3 emissions by 11–13% [112,113], but the effect of implants alone has not been investigated.

3.3.3. Feed Additive: Monensin

Monensin is an ionophore that increases overall energy yield from feed, improves animal growth performance, and prevents Coccidiosis caused by ssp. in beef and dairy cattle. Monensin alters the volatile fatty-acid profile by changing the dominant bacterial species in the rumen from gram-positive bacteria, which favor acetate production, to gram-negative bacteria, which favor propionate production [114,115,116,117,118]. Monensin increases the ratio of propionate to acetate [117,119] and decreased the deamination of amino acids [117].
Monensin decreased NH3 concentration in ruminal fluid and increased bacterial protein [120]. By decreasing amino acid-fermenting bacteria, monensin has an amino acid-sparing effect, which results in decreased deamination of amino acids and NH3 concentration in the rumen, leading to increased flow of dietary amino acids to the abomasum [117,121,122].
Providing monensin in feedlot diets decreases DMI and improves feed efficiency of feedlot cattle [119,121,123,124]. In addition, monensin improves N metabolism of rumen bacteria andthe animal, and reduces ruminal degradation of peptides and amino acids, while increasing the flow of dietary protein origin to the small intestine [122,125,126]. Muntifering et al. [126] reported that the amount of N retained in beef steers fed a diet with monensin (33 mg kg−1) was increased from 19 to 24 g/d (+27%) as compared to a monensin-free control diet.
Although the reported effects of monesin seem to increase N availability and decrease N excretion, some studies did not determine a subsequent increase in animal performance [127] or a reduction in N excretion in manure [128]. In addition, the isolated effect of monensin on NH3 emission has not yet been reported, but, only, the mitigation of NH3 emissions through combination of monensin, tylosin, and β-AA.

3.3.4. Manure Harvesting

The purpose of manure harvesting is to prevent an increase in the production of odorous gases and dust control due to moisture saturation of the open corral surface, which receives constant manure excretion, and to avoid impairing the productivity and welfare of livestock from muddy conditions. If the moisture content of the pen surface is high due to the infrequency of manure harvesting, an environment is formed wherein the NH4+ in the manure (especially urine) is easily evaporated as NH3 into the atmosphere rather than absorbed into soil or bedding. It was reported that moisture content management through periodic manure harvesting reduced NH3 emissions by 14 to 44% [38,129] (Table 6). In addition, wet conditions foster negative health and well-being outcomes as the wet environment promotes microorganisms’ development and creates an uncomfortable environment for livestock to rest and move.
Table 6. Manure harvesting effectiveness in decreasing NH3 emissions in open-lot livestock facilities.
Table 6. Manure harvesting effectiveness in decreasing NH3 emissions in open-lot livestock facilities.
Study LocationStudy Scale Pen Cleaning FrequencyResultRatep ValueReference
NebraskaFieldMonthly cleaning (28 days) vs. cleaning after marketingN loss with monthly cleaning: 12–17 kg/head;
N loss with cleaning after marketing: 15–21 kg/head
Monthly cleaning reduced the total N loss by an average of 14%. <0.01Wilson et al. (2004) [129]
NebraskaFieldMonthly cleaning (28 days) vs. cleaning after marketing (135 days)Monthly cleaning N loss: 12–17 kg/head
N loss from cleaning end: 15–21 kg/head
19–44%<0.01Erickson and Klopfenstein (2010) [38] *
IowaFieldBeef bedded pack barn vs. cleaned and re-bedded one to two times per week (transition)Bedded pack: 68 mmol/L
Transition: 64 mmol/L
Not significant Not significantSpiehs et al. (2011) [130]
* Erickson et al. (2010) [38] used the measured data from Wilson et al. (2004) [129].

3.3.5. Manure Handling

Management of livestock manure has a direct impact on NH3 loss to air [131]. The management of livestock manure and the way it is stored affect manure decomposition, with a direct impact on NH3 [131] and greenhouse gas (GHG) emissions [132]. Manure is often stockpiled or composted prior to land application [21,22]. Stockpiles heap manure into stacks with no active management of the pile [23], while composted manure piles are turned periodically, entraining oxygen (O2) into the piles. Overall, it is expected that composted manure emits more aerobically produced gases, such as carbon dioxide (CO2) and NH3 [23,26], while stockpiled manure emits more anaerobically produced gases such as CH4 [25]. Manure composting reduces pathogenic microbes and weed seeds, reduces moisture content, reduces odor, stabilizes nutrients, and improves physical properties of manure that add value to manure as a soil amendment and organic fertilizer [133]. The impact of composting beef manure, although perhaps a means of reducing NH3 losses during land application, is associated with higher emission losses prior to the field application [131]. The end-product differs from raw manure due to the minimal N loss in storage or after land application [133]. It is estimated that more than 50% of the total N fed is lost as NH3 from the manure that accumulates within the feedlot [43,134]. Overall, 56 to 75% of the N content of beef cattle manure can be lost between the time it is excreted by the animal and when it is field applied [134]. Piled manure that was applied to the land lost 27% less NH3 than did manure taken directly from the pen. There was little NH3 lost from compost that was applied to land since the applied available-N was very low relative to the pen and piled manure [131]. Nitrogen loss during composting ranged from 19 to 42% related to the initial manure N content. Ammonia volatilization (calculated by difference) accounted for >92% of the N loss whereas combined runoff nitrate and ammonium loss was <0.5% [135].
The influence of handling treatment (fresh, stockpiled, or composted) on nutrient levels and mass balance estimates of feedlot manure was evaluated at Lethbridge, Alberta, and Brandon, Manitoba, in Canada, which showed that total nitrogen (TN) concentration was not affected by handling treatment but the percent of inorganic N was lower (p < 0.01) for compost (5.1%) than both fresh (24.7%) and stockpiled (28.9%) manure [136].
The N lost as NH3 and N2O emissions represented 26.4 and 3.8% of the initial N in windrow (turning), and 5.3 and 0.8% of that in the stockpile (non-turning), respectively, in a commercial feedyard in Australia [137].
Cumulative GHGs (except N2O) and NH3 emissions were higher from composted compared to stockpiled manure (all p  <  0.01) from cattle fed a typical finishing diet and 3-NOP (125–200 mg kg−1 dry matter (DM) feed), or both 3-NOP (125–200 mg kg−1 DM) and monensin (33 mg kg−1 DM) together, compared to a control (no supplements). NH3 fluxes averaged 2.9 g N m−2 d−1 and 2.2 g N m−2 d−1 from the composted and stockpiled manure for the first 104 days, respectively, which drastically decreased to 0.1 g N m−2 d−1 at 105 and 202 days for both practices evaluated. Within the respective handling methods, cumulative NH3 emissions extrapolated over the initial surface area of the piles (kg pile−1) averaged over all additives were 158% higher from the composted compared to the stockpiled manure (p < 0.001). Compared to the stockpiled manure, the NH3 kg N t−1 initial N was 142% higher (p < 0.001) from the composted manure [132].

3.3.6. Dust Control—Water Sprinklers/Irrigation System

Fugitive dust emissions are a high-profile environmental concern for open-lot cattle feedyards. Feedyard dust includes particles from manure, soil, hair, plant material, and insects [138]. It is composed of organic dust (proteins, complex carbohydrates), microorganisms (viruses, bacteria, and fungi), and cellular components like endotoxins [139,140]; it also carries odorous volatile organic compounds [141]. Dust from feedyard surfaces may create nuisance conditions, health hazards, and traffic hazards on adjacent highways [142,143]. Offensive odors are often associated with high dust concentrations [144] and can lead to an increase in neighbor complaints and a decrease in property values [145]. Therefore, NH3 emission in feedyards correlates with dust control, but the relationship between the two remains somewhat ambiguous.
Water sprinklers are recognized to decrease dust emissions and are thought to mitigate heat stress, but they have not been used in large scale with the aim to mitigate NH3 from open-lot corral surfaces. While the mechanism of NH3 volatilization suggests that adding water could increase the rate of N loss, other studies suggest that water has a depressive effect on volatilization rates [26]. The phenomenon of decreasing NH3 emission following a precipitation event could relate to simple leaching of aqueous NH4+ away from the surface layers where it is less susceptible to volatilization. Hutchinson et al. [27] suggested that precipitation events cause a dramatic increase in the size of the reservoir available for NH3 to exist in solution—diluting the NH4+ concentration and effectively decreasing the area of the air/water interface in the manure, the boundary at which volatilization occurs. A modeling exercise by Wu et al. [146] suggests that both mechanistic explanations are at work.
Contradictory results for NH3 mitigation by using water sprinklers have been reported (Table 7). Some studies evaluating water sprinklers in feedyards have reported an increase in NH3 generation by ~27% [85,147] after water application, but other studies have reported the mitigation of NH3 emissions ranging from 27 to 56% [26,148,149,150]. In view of the lack of consensus on the use of this management practice, there is a concern that the NH3 mitigation due to water sprinkler is temporary and causes more NH3 generation during the evaporation process, especially when a rapid evaporation of water due to the hot weather and windy climate in the feedyards is expected.
To fill this knowledge gap, we need:
  • More studies on the use of water sprinklers in open corral surface;
  • Elucidate short-term NH3 dynamics in open-lot feedyard;
  • Understand those dynamics in different soil and weather conditions;
  • Evaluate the major factors influencing short-term NH3 dynamics, such as sprinklers height, depth of water applied, and frequency of application, and
  • A deeper understanding of those dynamics will help livestock producers respond effectively to the Rocky Mountain National Park Early Warning System.
Table 7. Use of water sprinklers to decrease NH3 emissions in open-lot livestock facilities.
Table 7. Use of water sprinklers to decrease NH3 emissions in open-lot livestock facilities.
Study LocationStudy ScaleTreatmentNH3 Mitigationp ValueReference
Water Applied Rate (%)
UKIn vitro2 mm and 12 mm as layers of water applied after the urine application2 mm
12 mm (1)
+15
+81 (3)
N/AWhitehead et al. (1991) [150]
TexasIn vitroDay 7 (control)
Day 9 (270 mL water added)
270 mL (at 9 d) −1 to −27%N/APandrangi et al. (2003) [85]
Maaninka, FinlandIn vitro(1) no irrigation (control),
(2) 5 + 5 mm irrigation
(3) 20 mm irrigation
NH3 flux at control: 0.01~0.1 g/m2/h
NH3 flux with 20 mm irrigation: 0 to 0.04 NH3-N g/m2/h). (2)
~+56N/ASaarijärvi et al. (2006) [149]
ColoradoIn vitroWater layer application of 5 mm5 mm+27<0.01Galles (2011) [26]
(1) after urine application, (2) rainfall along with irrigation, (3) means more NH3 was emitted to the atmosphere, and + means NH3 was mitigated/less emission.

3.3.7. Manure Amendments

Manure amendments include both chemical and physical amendments. The mechanism for mitigating NH3 for each specific amendment is different in detail. Chemical amendments primarily suppress urea decomposition or the formation of aqueous NH30. Physical amendments act to block NH3 emission or absorb it prior to release from the pen surface.
Most of the proposed amendments for mitigating NH3 are chemicals applied to the pen surface. Much of the N excreted in the urine is in the form of urea, which is rapidly hydrolyzed to NH4+ and eventually NH3 gas by the urease enzyme produced by soil and fecal microbes [130]. Urease inhibitors can block the hydrolysis of urea to NH4+ [131,132] and thereby decrease NH3 production. Studies evaluating application of chemical amendment on open corral surfaces to mitigate NH3 emission have shown a wide range (19 to 98%) of effectiveness, which included urease inhibitors [130,132,133,134] and chemical compounds such as calcium chloride, humate, aluminum sulfate, and CT [135] (Table 8). The urease inhibitor reduced emissions between 26 and 66% in the laboratory and at the pilot scale but did not show significant mitigation in a farm-scale experiment. The manure amendments calcium chloride, humate, aluminum sulfate, and commercial NH3 inhibitors, lower the pH and thereby inhibit urease hydrolysis which reduce in vitro NH3 emission by 32 to 71% [135].
Widespread adoption of chemical amendments is low due to their high cost and the negligible financial benefit of NH3 suppression.
As physical amendments, biochar, bentonite, vermiculite, and zeolites have been used on pen surfaces to mitigate emissions by absorbing NH3 generated from beef, dairy, and swine manure.
Biochar is defined by Lehmann and Joseph [151] as a carbon-rich product derived from the pyrolysis of organic material at 300 to 800 °C. Biochar’s total surface charge and total concentration of functional groups act on the adsorption of NH3 or organic-N into biochar, cation or anion exchange reactions, and enhanced immobilization of N as a consequence of labile C addition in the biochar. The action of zeolite is based on its tetrahedral crystals containing silicon and aluminum in various proportions, forming a skeletal structure with unique ion-exchange properties enabling the removal of pollutants. The efficiency of this process depends mainly on the type of pollutant, the presence of oxygen, and the reaction temperature [152].
Several studies evaluating the effects of biochar and CT have shown significant results on mitigating NH3 emission from swine and dairy manure [137,138,139]. However, only Sepperer et al. [136] evaluated the effects on beef manure amended with CT, observing mitigation of NH3 emission from 75 to 95%. Szymula et al. [153] evaluated different sorbents to decrease NH3 emissions from fecal samples collected from dairy cows and found that the most effective reduction in NH3 was achieved using 3% biochar (42.56% of reduction), 3% bentonite, with zeolite in a 1:1 ratio (24.56% of reduction), and 3% addition of zeolite (10% of reduction) relative to the control.
Table 8. Effectiveness of manure amendments on decreasing NH3 emissions in feedyards.
Table 8. Effectiveness of manure amendments on decreasing NH3 emissions in feedyards.
Study LocationStudy ScaleType of AmendmentAmendment DoseNH3 Mitigation Rate (%)p ValueReference
NebraskaFieldUrease inhibitor: N-(n-butyl) thiophosphoric triamide (NBPT)22.8 kg/ha once per week for 42 d45N/AVarel et al. (1999) [154]
TexasIn vitroNBPT1 kg/ha for 21 d65<0.05Shi et al. (2001) [155]
NBPT2 kg/ha for 21 d66<0.05
Calcium chloride4500 kg/ha71<0.05
Humate9000 kg/ha68<0.05
Aluminum sulfate9000 kg/ha98<0.05
Commercial product (Ammonia Hold, Lonoke, AR)750 kg/ha32<0.05
TexasIn vitroNBPT1 kg/ha once per 8 d for 38 d 49<0.05Parker et al. (2004) [156]
NBPT2 kg/ha once per 8 days for 38 d66<0.05
TexasIn vitroNBPT5 kg/ha once per 4 d + 6 mm rainfall once per 4 d26<0.05Parker al. (2011) [157]
NBPT5 kg/ha once per 4 d33<0.05
TexasFieldNBPT1, 2, 4, 8, and 40 kg/ha for 42 dNot significant Parker al. (2016) [158]
AustriaIn vitroCT1 mL of manure was added with 1%, 5%, and 10% by weight of tannins adsorbent75–95Not significantSepperer et al. (2020) [159]

4. Conclusions

Our review combines the state of knowledge concerning the emission, transport, and deposition, and mitigation strategies of gaseous NH3 from open-lot cattle feeding facilities located east of the northern Front Range of the Rocky Mountains. Overall, up to 90% of feedyard NH3 originates from urine deposited in animal pens, but the instantaneous magnitude of that loss depends strongly on weather conditions (temperature, precipitation, humidity, and wind), soil properties, pH, microbiological activities (e.g., urease activity), and management practices. As easterly winds advect and lift pollutants up the eastern slope of RMNP, the air cools and condenses to form clouds. Precipitation maxima in northern Colorado are associated with easterly winds and occur most frequently in spring and summer. During precipitation events, clouds entrain Front Range pollution and deposit the pollutants over the mountains in the precipitation. Among dietary manipulation practices, CP and CT were the most effective in reducing NH3 emission (43 and 57%, respectively). However, more information is needed on the effectiveness of implants and monensin on NH3 mitigation. Manure moisture content management through periodic manure harvesting reduced NH3 emissions by 14 to 44%. The impact of water sprinklers has been ambiguous, showing both increases and decreases in NH3 emissions. Pen-surface amendments are promising but costly NH3 mitigators whose effectiveness at scale has not been conclusively demonstrated.

Author Contributions

Conceptualization, B.W.A. and C.B.B.; methodology, B.W.A., C.B.B. and M.L.; resources, B.W.A. and D.B.P.; writing—original draft preparation, C.B.B., M.L. and B.W.A.; writing—review and editing, B.W.A., J.A.K., D.B., D.B.P., E.T.C., K.D.C., C.B.B., M.L., V.N.G., M.R.B., K.J.B. and B.S.; visualization, C.B.B., B.W.A. and M.L.; writing, C.B.B., M.L., B.W.A., V.N.G. and J.A.K.; supervision, B.W.A. project administration, B.W.A. and D.B.P.; funding acquisition, B.W.A. and D.B.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the NRCS Conservation Innovation Grant (project number NR213A750013G037), and additional support was provided by Colorado Livestock Association.

Informed Consent Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest. The sponsors did not play any role in the study design, data collection, analysis, interpretation, and decision to write the manuscript or present the results.

Abbreviations

Definitions of key acronyms used in this paper.
ADG
average daily gain
AFO
animal feeding operations
BAO
Boulder Atmospheric Observatory Tower
BMP
best management practices
BSC
bovine satellite cell
CAFOs
concentrated animal feeding operations
CAMP
cyclic adenosine monophosphate
CLA
Colorado Livestock Association
CP
crude protein
CT
condensed tannins
DMI
dry matter intake
IGF-1
insulin-like growth factor-1
NASEM
National Academies of Sciences, Engineering, and Medicine
NBPT
urease
NDRP
Nitrogen Deposition Reduction Plan
NRCS
Natural Resources Conservation Service
PKA
protein kinase A
RAC
ractopamine hydrochloride
RDP
rumen degradable protein
RMNP
Rocky Mountains National Park
RoMANS
Rocky Mountains Atmospheric Nitrogen and Sulfur Study
RUP
rumen undegradable protein
ß-AA
ß-adrenergic agonists
ST
somatotropin
TAN
total ammoniacal nitrogen

References

  1. Piña, A.J.; Schumacher, R.S.; Denning, A.S.; Faulkner, W.B.; Baron, J.S.; Ham, J.; Ojima, D.S.; Collett, J.L. Reducing wet ammonium deposition in Rocky Mountain National Park: The development and evaluation of a pilot early warning system for agricultural operations in Eastern Colorado. Environ. Manag. 2019, 64, 626–639. [Google Scholar] [CrossRef] [PubMed]
  2. Tevlin, A.; Li, Y.; Collett, J.; McDuffie, E.; Fischer, E.; Murphy, J. Tall tower vertical profiles and diurnal trends of ammonia in the Colorado Front Range. J. Geophys. Res. Atmos. 2017, 122, 12468–412487. [Google Scholar] [CrossRef]
  3. Toth, J.J.; Johnson, R.H. Summer surface flow characteristics over northeast Colorado. Mon. Weather Rev. 1985, 113, 1458–1469. [Google Scholar] [CrossRef]
  4. Burns, D.A.; Fenn, M.E.; Baron, J.; Lynch, J.A.; Cosby, B.J. National Acid Precipitation Assessment Program Report to Congress: An Integrated Assessment; National Science Technology Council: Washington, DC, USA, 2011.
  5. Baron, J.S. Hindcasting nitrogen deposition to determine an ecological critical load. Ecol. Appl. 2006, 16, 433–439. [Google Scholar] [CrossRef]
  6. Baron, J.S.; Ojima, D.S.; Holland, E.A.; Parton, W.J. Analysis of nitrogen saturation potential in Rocky Mountain tundra and forest: Implications for aquatic systems. Biogeochemistry 1994, 27, 61–82. [Google Scholar] [CrossRef]
  7. Benedict, K.; Carrico, C.; Kreidenweis, S.; Schichtel, B.; Malm, W.; Collett, J., Jr. A seasonal nitrogen deposition budget for Rocky Mountain National Park. Ecol. Appl. 2013, 23, 1156–1169. [Google Scholar] [CrossRef]
  8. Benedict, K.B.; Day, D.; Schwandner, F.M.; Kreidenweis, S.M.; Schichtel, B.; Malm, W.C.; Collett, J.L., Jr. Observations of atmospheric reactive nitrogen species in Rocky Mountain National Park and across northern Colorado. Atmos. Environ. 2013, 64, 66–76. [Google Scholar] [CrossRef]
  9. Malm, W.C.; Schichtel, B.A.; Barna, M.G.; Gebhart, K.A.; Rodriguez, M.A.; Collett, J.L., Jr.; Carrico, C.M.; Benedict, K.B.; Prenni, A.J.; Kreidenweis, S.M. Aerosol species concentrations and source apportionment of ammonia at Rocky Mountain National Park. J. Air Waste Manag. Assoc. 2013, 63, 1245–1263. [Google Scholar] [CrossRef]
  10. Morris, K. Data Summary of Wet Nitrogen Deposition at Rocky Mountain National Park; Natural Resource Report NPS/NRSS/ARD/NRR—2018/1610; National Park Service: Fort Collins, CO, USA, 2018.
  11. Morris, K. 2018/2019 Data Summary of Wet Nitrogen Deposition at Rocky Mountain National Park; U.S. Department of the Interior, National Park Service: Washington, DC, USA, 2021.
  12. Thompson, T.M.; Rodriguez, M.A.; Barna, M.G.; Gebhart, K.A.; Hand, J.L.; Day, D.E.; Malm, W.C.; Benedict, K.B.; Collett, J.L., Jr.; Schichtel, B.A. Rocky Mountain National Park reduced nitrogen source apportionment. J. Geophys. Res. Atmos. 2015, 120, 4370–4384. [Google Scholar] [CrossRef]
  13. Asman, W.A.; Sutton, M.A.; Schjørring, J.K. Ammonia: Emission, atmospheric transport and deposition. New Phytol. 1998, 139, 27–48. [Google Scholar] [CrossRef]
  14. Beckett, K.P.; Freer-Smith, P.; Taylor, G. Urban woodlands: Their role in reducing the effects of particulate pollution. Environ. Pollut. 1998, 99, 347–360. [Google Scholar] [CrossRef]
  15. Gebhart, K.A.; Malm, W.C.; Rodriguez, M.A.; Barna, M.G.; Schichtel, B.A.; Benedict, K.B.; Collett, J.L.; Carrico, C.M. Meteorological and back trajectory modeling for the rocky mountain atmospheric nitrogen and sulfur study II. Adv. Meteorol. 2014, 2014, 414015. [Google Scholar] [CrossRef]
  16. Dammers, E.; McLinden, C.A.; Griffin, D.; Shephard, M.W.; Van Der Graaf, S.; Lutsch, E.; Schaap, M.; Gainairu-Matz, Y.; Fioletov, V.; Van Damme, M. NH3 emissions from large point sources derived from CrIS and IASI satellite observations. Atmos. Chem. Phys. 2019, 19, 12261–12293. [Google Scholar] [CrossRef]
  17. Van Damme, M.; Clarisse, L.; Whitburn, S.; Hadji-Lazaro, J.; Hurtmans, D.; Clerbaux, C.; Coheur, P.-F. Industrial and agricultural ammonia point sources exposed. Nature 2018, 564, 99–103. [Google Scholar] [CrossRef]
  18. Malm, W.; Collett, J., Jr.; Barna, M.; Gebhart, K.; Schichtel, B.; Beem, K.; Carrico, C.; Day, D.; Hand, J.; Kreidenweis, S. RoMANS: Rocky Mountain Atmospheric Nitrogen and Sulfur Study Report; U.S. Department of the Interior, National Park Service: Washington, DC, USA, 2009.
  19. USDA-NASS. Surveys-Cattle Inventory. Available online: https://www.nass.usda.gov/Surveys/Guide_to_NASS_Surveys/Cattle_Inventory/ (accessed on 26 July 2023).
  20. USDA/NASS. 2021 State Agriculture Overview for Colorado. Available online: https://www.nass.usda.gov/Quick_Stats/Ag_Overview/stateOverview.php?state=COLORADO (accessed on 26 July 2023).
  21. Sakirkin, S.; Cole, N.; Todd, R.; Auvermann, B. Ammonia Emissions from Cattle-Feeding Operations. Part 1 of 2: Issues and Emissions; Animal Agriculture and Air Quality Iowa State University: Ames, IA, USA, 2013. [Google Scholar]
  22. Hristov, A.N.; Hanigan, M.; Cole, A.; Todd, R.; McAllister, T.A.; Ndegwa, P.M.; Rotz, A. Ammonia emissions from dairy farms and beef feedlots. Can. J. Anim. Sci. 2011, 91, 1–35. [Google Scholar] [CrossRef]
  23. Waldrip, H.; Cole, N.; Todd, R. Nitrogen sustainability and beef cattle feedyards: II. Ammonia emissions. Prof. Anim. Sci. 2015, 31, 395–411. [Google Scholar] [CrossRef]
  24. Arogo, J.; Westerman, P.W.; Heber, A.J.; Robarge, W.P.; Classen, J.J. Ammonia Emissions from Animal Feeding Operations. In Animal Agriculture and the Environment: National Center for Manure and Animal Waste Management White Papers; ASABE: Berrien County, MI, USA, 2006. [Google Scholar]
  25. Cole, N.; Todd, R.; Auvermann, B.; Parker, D. Auditing and assessing air quality in concentrated feeding operations. Prof. Anim. Sci. 2008, 24, 1–22. [Google Scholar] [CrossRef]
  26. Galles, K.J. Practical Strategies for Reducing Ammonia Volatilization from Feedlots along Colorado’s Front Range; Colorado State University: Fort Collins, CO, USA, 2011. [Google Scholar]
  27. Hutchinson, G.; Mosier, A.; Andre, C. Ammonia and Amine Emissions from a Large Cattle Feedlot; 0047-2425; Wiley Online Library: Hoboken, NJ, USA, 1982. [Google Scholar]
  28. Shonkwiler, K.B. Micrometeorological Studies of a Beef Feedlot, Dairy, and Grassland: Measurements of Ammonia, Methane, and Energy Balance Closure; Colorado State University: Fort Collins, CO, USA, 2018. [Google Scholar]
  29. Preece, S.L.; Cole, N.A.; Todd, R.W.; Auvermann, B.W. Ammonia Emissions from Cattle Feeding Operations. In Texas A&M AgriLife Extension Service; E-632; Texas A&M University: Amarillo, TX, USA, 2011; pp. 1–15. [Google Scholar]
  30. Burchill, W.; Reville, F.; Misselbrook, T.H.; O’Connell, C.; Lanigan, G.J. Ammonia emissions and mitigation from a concrete yard used by cattle. Biosyst. Eng. 2019, 184, 181–189. [Google Scholar] [CrossRef]
  31. Nasiru, A.; Ibrahim, M.H.; Ismail, N. Nitrogen losses in ruminant manure management and use of cattle manure vermicast to improve forage quality. Int. J. Recycl. Org. Waste Agric. 2014, 3, 57. [Google Scholar] [CrossRef]
  32. Sommer, S.G.; Webb, J.; Hutchings, N.D. New emission factors for calculation of ammonia volatilization from European livestock manure management systems. Front. Sustain. Food Syst. 2019, 3, 101. [Google Scholar] [CrossRef]
  33. Oenema, O. Nitrogen budgets and losses in livestock systems. Int. Congr. Ser. 2006, 1293, 262–271. [Google Scholar] [CrossRef]
  34. Sommer, S.; Olesen, J. Effects of Dry Matter Content and Temperature on Ammonia Loss from Surface-Applied Cattle Slurry; 0047-2425; Wiley Online Library: Hoboken, NJ, USA, 1991. [Google Scholar]
  35. Olesen, J.; Sommer, S. Modelling effects of wind speed and surface cover on ammonia volatilization from stored pig slurry. Atmos. Environ. Part A. Gen. Top. 1993, 27, 2567–2574. [Google Scholar] [CrossRef]
  36. Todd, R.W.; Cole, N.A.; Rhoades, M.B.; Parker, D.B.; Casey, K.D. Daily, monthly, seasonal, and annual ammonia emissions from Southern High Plains cattle feedyards. J. Environ. Qual. 2011, 40, 1090–1095. [Google Scholar] [CrossRef]
  37. Rhoades, M.; Parker, D.; Cole, N.; Todd, R.; Caraway, E.; Auvermann, B.; Topliff, D.; Schuster, G. Continuous ammonia emission measurements from a commercial beef feedyard in Texas. Trans. ASABE 2010, 53, 1823–1831. [Google Scholar] [CrossRef]
  38. Erickson, G.; Klopfenstein, T. Nutritional and management methods to decrease nitrogen losses from beef feedlots. J. Anim. Sci. 2010, 88, E172–E180. [Google Scholar] [CrossRef]
  39. Cole, N.; Todd, R. Nitrogen and phosphorus balance of beef cattle feedyards. In Proceedings of the Texas Animal Manure Management Issues Conference, Round Rock, TX, USA, 29–30 September 2009; pp. 17–24. [Google Scholar]
  40. Todd, R.W.; Cole, N.A.; Clark, R.N.; Flesch, T.K.; Harper, L.A.; Baek, B.H. Ammonia emissions from a beef cattle feedyard on the southern High Plains. Atmos. Environ. 2008, 42, 6797–6805. [Google Scholar] [CrossRef]
  41. Flesch, T.; Wilson, J.; Harper, L.; Todd, R.; Cole, N. Determining ammonia emissions from a cattle feedlot with an inverse dispersion technique. Agric. For. Meteorol. 2007, 144, 139–155. [Google Scholar] [CrossRef]
  42. Cole, N.; Defoor, P.; Galyean, M.; Duff, G.; Gleghorn, J. Effects of phase-feeding of crude protein on performance, carcass characteristics, serum urea nitrogen concentrations, and manure nitrogen of finishing beef steers. J. Anim. Sci. 2006, 84, 3421–3432. [Google Scholar] [CrossRef]
  43. Todd, R.; Cole, N.; Harper, L.; Flesch, T.; Baek, B. Ammonia and gaseous nitrogen emissions from a commercial beef cattle feedyard estimated using the flux-gradient method and N: P ratio analysis. In Proceedings of the Symposium State of the Science: Animal Manure and Waste Management, San Antonio, TX, USA, 5–7 January 2005. [Google Scholar]
  44. Erickson, G.; Milton, C.; Klopfenstein, T. Dietary protein effects on nitrogen excretion and volatilization in open-dirt feedlots. In Animal, Agricultural and Food Processsing Wastes, Proceedings of the Eighth International Symposium, Des Moines, IA, USA, 9–11 October 2000; American Society of Agricultural Engineers: St. Joseph, MI, USA, 2000; pp. 297–304. [Google Scholar]
  45. Bierman, S.; Erickson, G.; Klopfenstein, T.; Stock, R.A.; Shain, D. Evaluation of nitrogen and organic matter balance in the feedlot as affected by level and source of dietary fiber. J. Anim. Sci. 1999, 77, 1645–1653. [Google Scholar] [CrossRef]
  46. Cole, N.; Clark, R.; Todd, R.; Richardson, C.; Gueye, A.; Greene, L.; Mcbride, K. Influence of dietary crude protein concentration and source on potential ammonia emissions from beef cattle manure. J. Anim. Sci. 2005, 83, 722–731. [Google Scholar] [CrossRef]
  47. Baek, B.-H.; Todd, R.; Cole, N.A.; Koziel, J.A. Ammonia and hydrogen sulphide flux and dry deposition velocity estimates using vertical gradient method at a commercial beef cattle feedlot. Int. J. Glob. Environ. Issues 2006, 6, 189–203. [Google Scholar] [CrossRef]
  48. McGinn, S.; Flesch, T.; Crenna, B.; Beauchemin, K.; Coates, T. Quantifying ammonia emissions from a cattle feedlot using a dispersion model. J. Environ. Qual. 2007, 36, 1585–1590. [Google Scholar] [CrossRef]
  49. Denmead, O.; Chen, D.; Griffith, D.; Loh, Z.; Bai, M.; Naylor, T. Emissions of the indirect greenhouse gases NH3 and NOx from Australian beef cattle feedlots. Aust. J. Exp. Agric. 2008, 48, 213–218. [Google Scholar] [CrossRef]
  50. Van Haarlem, R.; Desjardins, R.; Gao, Z.; Flesch, T.; Li, X. Methane and ammonia emissions from a beef feedlot in western Canada for a twelve-day period in the fall. Can. J. Anim. Sci. 2008, 88, 641–649. [Google Scholar] [CrossRef]
  51. Rhoades, M.B.; Auvermann, B.W.; Cole, N.A.; Todd, R.W.; Parker, D.B.; Caraway, E.A.; Schuster, G.; Spears, J. Ammonia concentration and modeled emission rates from a beef cattle feedyard. In Proceedings of the 2008 American Society of Agricultural and Biological Engineers, Providence, RI, USA, 29 June 29–2 July 2008; p. 1. [Google Scholar]
  52. Staebler, R.M.; McGinn, S.M.; Crenna, B.P.; Flesch, T.K.; Hayden, K.L.; Li, S.-M. Three-dimensional characterization of the ammonia plume from a beef cattle feedlot. Atmos. Environ. 2009, 43, 6091–6099. [Google Scholar] [CrossRef]
  53. Waldrip, H.M.; Todd, R.W.; Li, C.; Cole, N.A.; Salas, W.H. Estimation of ammonia emissions from beef cattle feedyards using the process-based model Manure-DNDC. Trans. ASABE 2013, 56, 1103–1114. [Google Scholar]
  54. McGinn, S.; Janzen, H.; Coates, T.; Beauchemin, K.; Flesch, T. Ammonia emission from a beef cattle feedlot and its local dry deposition and re-emission. J. Environ. Qual. 2016, 45, 1178–1185. [Google Scholar] [CrossRef]
  55. McGinn, S.; Flesch, T. Ammonia and greenhouse gas emissions at beef cattle feedlots in Alberta Canada. Agric. For. Meteorol. 2018, 258, 43–49. [Google Scholar] [CrossRef]
  56. Samuelson, K.; Hubbert, M.; Galyean, M.; Löest, C. Nutritional recommendations of feedlot consulting nutritionists: The 2015 New Mexico State and Texas Tech University survey. J. Anim. Sci. 2016, 94, 2648–2663. [Google Scholar] [CrossRef]
  57. Powlson, D. Understanding the soil nitrogen cycle. Soil Use Manag. 1993, 9, 86–93. [Google Scholar] [CrossRef]
  58. Nenes, A.; Pandis, S.N.; Pilinis, C. Continued development and testing of a new thermodynamic aerosol module for urban and regional air quality models. Atmos. Environ. 1999, 33, 1553–1560. [Google Scholar] [CrossRef]
  59. Montes, F.; Rotz, C.; Chaoui, H. Process modeling of ammonia volatilization from ammonium solution and manure surfaces: A review with recommended models. Trans. ASABE 2009, 52, 1707–1720. [Google Scholar] [CrossRef]
  60. Sawyer, C.N.; McCarty, P.L. Chemistry for Environmental Engineering; McGraw-Hill: New York, NY, USA, 1978. [Google Scholar]
  61. Cofie, O.; Nikiema, J.; Impraim, R.; Adamtey, N.; Paul, J.; Koné, D. Co-Composting of Solid Waste and Fecal Sludge for Nutrient and Organic Matter Recovery; IWMI: Colombo, Sri Lanka, 2016; Volume 3. [Google Scholar]
  62. Schreiner, A. Chemische Untersuchungen natürlicher Fliessgewässer. Quantitative Chemische Gewässeranalyse der Mosel, Gymnasium Konz: Konz, Germany 1997. Available online: http://www.ruschmidt.de/NAUCI2.htm (accessed on 26 July 2023).
  63. Flocke, F.; Pfister, G.; Crawford, J.H.; Pickering, K.E.; Pierce, G.; Bon, D.; Reddy, P. Air quality in the Northern Colorado front range metro area: The front range air pollution and photochemistry éxperiment (FRAPPÉ). J. Geophys. Res. Atmos. 2020, 125, e2019JD031197. [Google Scholar] [CrossRef]
  64. Church, D.C. The Ruminant Animal: Digestive Physiology and Nutrition; Waveland Press: Long Grove, IL, USA, 1993. [Google Scholar]
  65. Johnson, R.H.; Toth, J.J. A Climatology of the July 1981 Surface Flow over Northeast Colorado; Colorado State University Libraries: Fort Collins, CO, USA, 1982. [Google Scholar]
  66. Wetherbee, G.A.; Benedict, K.B.; Murphy, S.F.; Elliott, E.M. Inorganic nitrogen wet deposition gradients in the Denver-Boulder metropolitan area and Colorado Front Range–Preliminary implications for Rocky Mountain National Park and interpolated deposition maps. Sci. Total Environ. 2019, 691, 1027–1042. [Google Scholar] [CrossRef]
  67. Clow, D.W.; Roop, H.A.; Nanus, L.; Fenn, M.E.; Sexstone, G.A. Spatial patterns of atmospheric deposition of nitrogen and sulfur using ion-exchange resin collectors in Rocky Mountain National Park, USA. Atmos. Environ. 2015, 101, 149–157. [Google Scholar] [CrossRef]
  68. Golston, L.M.; Pan, D.; Sun, K.; Tao, L.; Zondlo, M.A.; Eilerman, S.J.; Peischl, J.; Neuman, J.A.; Floerchinger, C. Variability of ammonia and methane emissions from animal feeding operations in northeastern Colorado. Environ. Sci. Technol. 2020, 54, 11015–11024. [Google Scholar] [CrossRef] [PubMed]
  69. Li, Y.; Thompson, T.M.; Van Damme, M.; Chen, X.; Benedict, K.B.; Shao, Y.; Day, D.; Boris, A.; Sullivan, A.P.; Ham, J. Temporal and spatial variability of ammonia in urban and agricultural regions of northern Colorado, United States. Atmos. Chem. Phys. 2017, 17, 6197–6213. [Google Scholar] [CrossRef]
  70. Day, D.; Chen, X.; Gebhart, K.; Carrico, C.; Schwandner, F.; Benedict, K.; Schichtel, B.; Collett, J., Jr. Spatial and temporal variability of ammonia and other inorganic aerosol species. Atmos. Environ. 2012, 61, 490–498. [Google Scholar] [CrossRef]
  71. Ni, J. Mechanistic models of ammonia release from liquid manure: A review. J. Agric. Eng. Res. 1999, 72, 1–17. [Google Scholar] [CrossRef]
  72. National Academies of Sciences, Engineering, and Medicine. Nutrient Requirements of Beef Cattle; National Academies of Sciences, Engineering, and Medicine: Washington, DC, USA, 2016. [Google Scholar]
  73. Owens, F.; Zinn, R. Protein metabolism of ruminant animals. In The Ruminant Animal: Digestive Physiology and Nutrition; Simon & Schuster: Englewood Cliffs, NJ, USA, 1988; pp. 227–249. [Google Scholar]
  74. Reynolds, C.; Kristensen, N. Nitrogen recycling through the gut and the nitrogen economy of ruminants: An asynchronous symbiosis. J. Anim. Sci. 2008, 86, E293–E305. [Google Scholar] [CrossRef]
  75. Firkins, J.; Reynolds, C. Whole-animal nitrogen balance in cattle. In Nitrogen and Phosphorus Nutrition of Cattle: Reducing the Environmental Impact of Cattle Operations; CABI Publishing: Wallingford, UK, 2005; pp. 167–186. [Google Scholar]
  76. Lapierre, H.; Lobley, G. Nitrogen recycling in the ruminant: A review. J. Dairy Sci. 2001, 84, E223–E236. [Google Scholar] [CrossRef]
  77. Dijkstra, J.; Oenema, O.; Van Groenigen, J.; Spek, J.; Van Vuuren, A.; Bannink, A. Diet effects on urine composition of cattle and N2O emissions. Animal 2013, 7, 292–302. [Google Scholar] [CrossRef] [PubMed]
  78. USDA-NRCS. Conservation Management Practices. Available online: https://www.nrcs.usda.gov/resources/guides-and-instructions/conservation-practice-standards (accessed on 26 July 2023).
  79. National Research Council. Nutrient Requirements of Beef Cattle; Update; National Academies of Sciences, Engineering, and Medicine: Washington, DC, USA, 2000; p. 248.
  80. Todd, R.W.; Cole, N.A.; Clark, R.N. Reducing crude protein in beef cattle diet reduces ammonia emissions from artificial feedyard surfaces. J. Environ. Qual. 2006, 35, 404–411. [Google Scholar] [CrossRef]
  81. Todd, R.W.; Cole, N.A.; Waldrip, H.M.; Aiken, R.M. Arrhenius equation for modeling feedyard ammonia emissions using temperature and diet crude protein. J. Environ. Qual. 2013, 42, 666–671. [Google Scholar] [CrossRef]
  82. Kissinger, W.F.; Koelsch, R.K.; Erickson, G.E.; Klopfenstein, T.J. Characteristics of manure harvested from beef cattle feedlots. Appl. Eng. Agric. 2007, 23, 357–365. [Google Scholar] [CrossRef]
  83. Todd, R.; Cole, N.; Parker, D.; Rhoades, M.; Casey, K. Effect of feeding distiller’s grain on dietary crude protein and ammonia emissions from beef cattle feedyards. In Proceedings of the Texas Animal Manure Management Issues (TAMMI) Conference, Round Rock, TX, USA, 29 September 2009; pp. 37–44. [Google Scholar]
  84. Chiavegato, M.; Powers, W.; Palumbo, N. Ammonia and greenhouse gas emissions from housed Holstein steers fed different levels of diet crude protein. J. Anim. Sci. 2015, 93, 395–404. [Google Scholar] [CrossRef]
  85. Pandrangi, S.; Parker, D.B.; Greene, L.W.; Almas, L.K.; Rhoades, M.B.; Cole, N.A. Effect of dietary crude protein on ammonia emissions from open-lot beef cattle feedyards. In Proceedings of the 2003 ASAE Annual Meeting, Las Vegas, NV, USA, 27–30 July 2003; p. 1. [Google Scholar]
  86. Naumann, H.; Muir, J.; Lambert, B.; Tedeschi, L.; Kothmann, M. Condensed tannins in the ruminant environment: A perspective on biological activity. J. Agric. Sci. 2013, 1, 8–20. [Google Scholar]
  87. Waghorn, G.; Reed, J.; Ndlovu, L. Condensed tannins and herbivore nutrition. In Proceedings of the XVIII International Grassland Congress, Calgary, AB, Canada; 1999; p. 153. [Google Scholar]
  88. Reed, J.D. Nutritional toxicology of tannins and related polyphenols in forage legumes. J. Anim. Sci. 1995, 73, 1516–1528. [Google Scholar] [CrossRef]
  89. Kronberg, S.L.; Liebig, M.A. Condensed tannin in drinking water reduces greenhouse gas precursor urea in sheep and cattle urine. Rangel. Ecol. Manag. 2011, 64, 543–547. [Google Scholar] [CrossRef]
  90. Marshall, C.; Beck, M.; Garrett, K.; Castillo, A.; Barrell, G.; Al-Marashdeh, O.; Gregorini, P. The effect of feeding a mix of condensed and hydrolyzable tannins to heifers on rumen fermentation patterns, blood urea nitrogen, and amino acid profile. Livest. Sci. 2022, 263, 105034. [Google Scholar] [CrossRef]
  91. González, S.; Pabon, M.L.; Carulla, J. Effects of tannins on in vitro ammonia release and dry matter degradation of soybean meal. Lat. Am. Arch. Anim. Prod. 2002, 10, 97–101. [Google Scholar]
  92. Campbell, T.N.; Rhoades, M.B.; Bailey, E.A.; Parker, D.B.; Shreck, A.L. Manure ammonia and green house gas emissions from beef cattle fed condensed tannins. In Proceedings of the 2016 ASABE Annual International Meeting, Orlando, FL, USA, 17–20 July 2016; p. 1. [Google Scholar]
  93. Ebert, P.; Bailey, E.; Shreck, A.; Jennings, J.; Cole, N. Effect of condensed tannin extract supplementation on growth performance, nitrogen balance, gas emissions, and energetic losses of beef steers. J. Anim. Sci. 2017, 95, 1345–1355. [Google Scholar] [CrossRef] [PubMed]
  94. Koenig, K.M.; Beauchemin, K.A. Effect of feeding condensed tannins in high protein finishing diets containing corn distillers grains on ruminal fermentation, nutrient digestibility, and route of nitrogen excretion in beef cattle. J. Anim. Sci. 2018, 96, 4398–4413. [Google Scholar] [CrossRef] [PubMed]
  95. Cappucci, A.; Mantino, A.; Buccioni, A.; Casarosa, L.; Conte, G.; Serra, A.; Mannelli, F.; Luciano, G.; Foggi, G.; Mele, M. Diets supplemented with condensed and hydrolysable tannins affected rumen fatty acid profile and plasmalogen lipids, ammonia and methane production in an in vitro study. Ital. J. Anim. Sci. 2021, 20, 935–946. [Google Scholar] [CrossRef]
  96. Lean, I.J.; Thompson, J.M.; Dunshea, F.R. A meta-analysis of zilpaterol and ractopamine effects on feedlot performance, carcass traits and shear strength of meat in cattle. PLoS ONE 2014, 9, e115904. [Google Scholar] [CrossRef] [PubMed]
  97. Smith, S.; Garcia, D.; Anderson, D. Elevation of a specific mRNA in longissimus muscle of steers fed ractopamine. J. Anim. Sci. 1989, 67, 3495–3502. [Google Scholar] [CrossRef]
  98. Smith, S.B.; Davis, S.K.; Wilson, J.J.; Stone, R.T.; Wu, F.; Garcia, D.K.; Lunt, D.K.; Schiavetta, A.M. Bovine fast-twitch myosin light chain 1: Cloning and mRNA amount in muscle of cattle treated with clenbuterol. Am. J. Physiol.-Endocrinol. Metab. 1995, 268, E858–E865. [Google Scholar] [CrossRef]
  99. Wang, S.-Y.; Beermann, D. Reduced calcium-dependent proteinase activity in cimaterol-induced muscle hypertrophy in lambs. J. Anim. Sci. 1988, 66, 2545–2550. [Google Scholar] [CrossRef]
  100. Ross, E.G. Mitigation of Gaseous Emissions from Beef and Dairy Cattle Through Feed Additives and Manure Supplements. Ph.D. Thesis, UC Davis, Davis, CA, USA, 2021. [Google Scholar]
  101. Brown, M.S.; Cole, N.A.; Gruber, S.; Kube, J.; Teeter, J.S. Modeling and prediction accuracy of ammonia gas emissions from feedlot cattle. Appl. Anim. Sci. 2019, 35, 347–356. [Google Scholar] [CrossRef]
  102. Kube, J.C.; Holland, B.P.; Word, A.B.; Allen, J.B.; Calvo-Lorenzo, M.; McKenna, D.; Vogel, G. Effects of various doses of lubabegron on calculated ammonia gas emissions, growth performance, and carcass characteristics of beef cattle during the last 56 days of the feeding period. Transl. Anim. Sci. 2021, 5, txab137. [Google Scholar] [CrossRef]
  103. Walker, C.E.; Drouillard, J. Effects of ractopamine hydrochloride are not confined to mammalian tissue: Evidence for direct effects of ractopamine hydrochloride supplementation on fermentation by ruminal microorganisms. J. Anim. Sci. 2010, 88, 697–706. [Google Scholar] [CrossRef] [PubMed]
  104. Preston, R. Hormone containing growth promoting implants in farmed livestock. Adv. Drug Deliv. Rev. 1999, 38, 123–138. [Google Scholar] [CrossRef] [PubMed]
  105. Zobell, D.R.; Chapman, C.K.; Heaton, K.; Birkelo, C. Beef Cattle Implants; Utah State University Extension: Logan, UT, USA, 2000. [Google Scholar]
  106. Smith, Z.K.; Johnson, B.J. Mechanisms of steroidal implants to improve beef cattle growth: A review. J. Appl. Anim. Res. 2020, 48, 133–141. [Google Scholar] [CrossRef]
  107. Hutcheson, J.; Johnson, D.; Gerken, C.; Morgan, J.; Tatum, J. Anabolic implant effects on visceral organ mass, chemical body composition, and estimated energetic efficiency in cloned (genetically identical) beef steers. J. Anim. Sci. 1997, 75, 2620–2626. [Google Scholar] [CrossRef] [PubMed]
  108. Nichols, W.; Galyean, M.; Thomson, D.; Hutcheson, J. Effects of steroid implants on the tenderness of beef. Prof. Anim. Sci. 2002, 18, 202–210. [Google Scholar] [CrossRef]
  109. Ohnoutka, C.; Bondurant, R.; Boyd, B.; Hilscher, F.; Nuttelman, B.; Crawford, G.; Streeter, M.; Luebbe, M.; MacDonald, J.; Smith, Z. Evaluation of coated steroidal combination implants on feedlot performance and carcass characteristics of beef heifers fed for constant or varying days on feed. Appl. Anim. Sci. 2021, 37, 41–51. [Google Scholar] [CrossRef]
  110. Preston, R.; Herschler, R. Controlled release estradiol/progesterone anabolic implant in cattle. In Texas Tech University Agricultural Science & Technology Report No. T-5-317: 140; Texas Tech University: Lubbock, TX, USA, 1992. [Google Scholar]
  111. Selk, G. Implants For Suckling Steer And Heifer Calves And Potential Replacement Heifers; Research Report P; Oklahoma State University Extension: Stillwater, OK, USA, 1997. [Google Scholar]
  112. Aboagye, I.A.; Cordeiro, M.R.; McAllister, T.A.; May, M.L.; Hannon, S.J.; Booker, C.W.; Parr, S.L.; Schunicht, O.C.; Burciaga-Robles, L.O.; Grimson, T.M. Environmental performance of commercial beef production systems utilizing conventional productivity-enhancing technologies. Transl. Anim. Sci. 2022, 6, txac074. [Google Scholar] [CrossRef]
  113. Stackhouse, K.; Rotz, C.; Oltjen, J.; Mitloehner, F. Growth-promoting technologies decrease the carbon footprint, ammonia emissions, and costs of California beef production systems. J. Anim. Sci. 2012, 90, 4656–4665. [Google Scholar] [CrossRef]
  114. Chen, M.; Wolin, M. Effect of monensin and lasalocid-sodium on the growth of methanogenic and rumen saccharolytic bacteria. Appl. Environ. Microbiol. 1979, 38, 72–77. [Google Scholar] [CrossRef]
  115. Muir, L.A.; Barretto, A., Jr. Sensitivity of Streptococcus bovis to various antibiotics. J. Anim. Sci. 1979, 48, 468–473. [Google Scholar] [CrossRef]
  116. Russell, J. The importance of pH in the regulation of ruminal acetate to propionate ratio and methane production in vitro. J. Dairy Sci. 1998, 81, 3222–3230. [Google Scholar] [CrossRef] [PubMed]
  117. Russell, J.; Strobel, H. Effects of additives on in vitro ruminal fermentation: A comparison of monensin and bacitracin, another gram-positive antibiotic. J. Anim. Sci. 1988, 66, 552–558. [Google Scholar] [CrossRef] [PubMed]
  118. Russell, J.B.; Strobel, H. Effect of ionophores on ruminal fermentation. Appl. Environ. Microbiol. 1989, 55, 1–6. [Google Scholar] [CrossRef]
  119. Perry, T.; Beeson, W.; Mohler, M. Effect of monensin on beef cattle performance. J. Anim. Sci. 1976, 42, 761–765. [Google Scholar] [CrossRef]
  120. Yang, C.; Russell, J.B. The effect of monensin supplementation on ruminal ammonia accumulation in vivo and the numbers of amino acid-fermenting bacteria. J. Anim. Sci. 1993, 71, 3470–3476. [Google Scholar] [CrossRef] [PubMed]
  121. Bergen, W.G.; Bates, D.B. Ionophores: Their effect on production efficiency and mode of action. J. Anim. Sci. 1984, 58, 1465–1483. [Google Scholar] [CrossRef] [PubMed]
  122. McGuffey, R.; Richardson, L.; Wilkinson, J. Ionophores for dairy cattle: Current status and future outlook. J. Dairy Sci. 2001, 84, E194–E203. [Google Scholar] [CrossRef]
  123. Tedeschi, L.O.; Fox, D.G.; Tylutki, T.P. Potential environmental benefits of ionophores in ruminant diets. J. Environ. Qual. 2003, 32, 1591–1602. [Google Scholar] [CrossRef]
  124. Weiss, C.P.; Beck, P.A.; Richeson, J.T.; Tomczak, D.J.; Hess, T.; Hubbell, D.; Zhao, J. Effect of monensin intake during a stocker phase and subsequent finishing phase on rumen bacterial diversity of beef steers. J. Anim. Sci. 2019, 97, 163–164. [Google Scholar] [CrossRef]
  125. Castillo, C.; Benedito, J.; Méndez, J.; Pereira, V.; Lopez-Alonso, M.; Miranda, M.; Hernández, J. Organic acids as a substitute for monensin in diets for beef cattle. Anim. Feed. Sci. Technol. 2004, 115, 101–116. [Google Scholar] [CrossRef]
  126. Muntifering, R.B.; Theurer, B.; Swingle, R.; Hale, W. Effect of monensin on nitrogen utilization and digestibility of concentrate diet by steers. J. Anim. Sci. 1980, 50, 930–936. [Google Scholar] [CrossRef] [PubMed]
  127. Montgomery, S.; Drouillard, J.; Sindt, J.; Farran, T.; Labrune, H.; Hunter, R. Effects of monensin and tylosin concentrations in limit-fed, high-energy growing diets for beef cattle. Prof. Anim. Sci. 2003, 19, 244–250. [Google Scholar] [CrossRef]
  128. Benchaar, C.; Duynisveld, J.; Charmley, E. Effects of monensin and increasing dose levels of a mixture of essential oil compounds on intake, digestion and growth performance of beef cattle. Can. J. Anim. Sci. 2006, 86, 91–96. [Google Scholar]
  129. Wilson, C.B.; Erickson, G.E.; Macken, C.N.; Klopfenstein, T.J. Impact of Cleaning Frequency on Nitrogen Balance in Open Feedlot Pens; Nebraska Beef Cattle Report; University of Nebraska: Lincoln, NE, USA, 2004. [Google Scholar]
  130. Spiehs, M.; Woodbury, B.; Doran, B.; Eigenberg, R.; Kohl, K.; Varel, V.; Berry, E.; Wells, J. Environmental conditions in beef deep-bedded mono-slope facilities: A descriptive study. Trans. ASABE 2011, 54, 663–673. [Google Scholar] [CrossRef]
  131. McGinn, S.; Sommer, S.G. Ammonia emissions from land-applied beef cattle manure. Can. J. Soil Sci. 2007, 87, 345–352. [Google Scholar] [CrossRef]
  132. Owens, J.L.; Thomas, B.W.; Stoeckli, J.L.; Beauchemin, K.A.; McAllister, T.A.; Larney, F.J.; Hao, X. Greenhouse gas and ammonia emissions from stored manure from beef cattle supplemented 3-nitrooxypropanol and monensin to reduce enteric methane emissions. Sci. Rep. 2020, 10, 19310. [Google Scholar] [CrossRef]
  133. DeLuca, T.; DeLuca, D. Composting for feedlot manure management and soil quality. J. Prod. Agric. 1997, 10, 235–241. [Google Scholar] [CrossRef]
  134. Eghball, B.; Power, J. Beef cattle feedlot manure management. J. Soil Water Conserv. 1994, 49, 113–122. [Google Scholar]
  135. Eghball, B.; Power, J.F.; Gilley, J.E.; Doran, J.W. Nutrient, Carbon, and Mass Loss During Composting of Beef Cattle Feedlot Manure; 0047-2425; Wiley Online Library: Hoboken, NJ, USA, 1997. [Google Scholar]
  136. Larney, F.J.; Buckley, K.E.; Hao, X.; McCaughey, W.P. Fresh, stockpiled, and composted beef cattle feedlot manure: Nutrient levels and mass balance estimates in Alberta and Manitoba. J. Environ. Qual. 2006, 35, 1844–1854. [Google Scholar] [CrossRef]
  137. Bai, M.; Flesch, T.; Trouvé, R.; Coates, T.; Butterly, C.; Bhatta, B.; Hill, J.; Chen, D. Gas emissions during cattle manure composting and stockpiling. J. Environ. Qual. 2020, 49, 228–235. [Google Scholar] [CrossRef]
  138. Bush, K.J.; Heflin, K.R.; Marek, G.W.; Bryant, T.C.; Auvermann, B.W. Increasing stocking density reduces emissions of fugitive dust from cattle feedyards. Appl. Eng. Agric. 2014, 30, 815–824. [Google Scholar]
  139. Purdy, C.W.; Straus, D.C.; Parker, D.B.; Wilson, S.C.; Clark, R.N. Comparison of the type and number of microorganisms and concentration of endotoxin in the air of feedyards in the Southern High Plains. Am. J. Vet. Res. 2004, 65, 45–52. [Google Scholar] [CrossRef] [PubMed]
  140. Seedorf, J. An emission inventory of livestock-related bioaerosols for Lower Saxony, Germany. Atmos. Environ. 2004, 38, 6565–6581. [Google Scholar] [CrossRef]
  141. Wyatt, T.A.; Slager, R.E.; Devasure, J.; Auvermann, B.W.; Mulhern, M.L.; Von Essen, S.; Mathisen, T.; Floreani, A.A.; Romberger, D.J. Feedlot dust stimulation of interleukin-6 and-8 requires protein kinase Cε in human bronchial epithelial cells. Am. J. Physiol.-Lung Cell. Mol. Physiol. 2007, 293, L1163–L1170. [Google Scholar] [CrossRef] [PubMed]
  142. Sweeten, J.B. Feedlot Dust Control; Texas Agricultural Extension Service: College Station, TX, USA, 1982.
  143. Sweeten, J.B.; Parnell, C.B.; Etheredge, R.S.; Osborne, D. Dust emissions in cattle feedlots. Vet. Clin. N. Am. Food Anim. Pract. 1988, 4, 557–578. [Google Scholar] [CrossRef]
  144. Von Essen, S.G.; Auvermann, B.W. Health effects from breathing air near CAFOs for feeder cattle or hogs. J. Agromed. 2005, 10, 55–64. [Google Scholar] [CrossRef]
  145. Rahman, S.; Mukhtar, S.; Weiderholt, R. Managing Odor Nuisance and Dust From Cattle Feedlots; North Dakota State University: Fargo, ND, USA, 2008. [Google Scholar]
  146. Wu, J.; Nofziger, D.; Warren, J.; Hattey, J. Modeling ammonia volatilization from surface-applied swine effluent. Soil Sci. Soc. Am. J. 2003, 67, 1–11. [Google Scholar]
  147. Jackson, T.L.; Alban, L.A.; Wolfe, J.W. Ammonia Nitrogen Loss from Sprinkler Applications; Oregon State College: Corvallis, OR, USA, 1959. [Google Scholar]
  148. Chadwick, D. Emissions of ammonia, nitrous oxide and methane from cattle manure heaps: Effect of compaction and covering. Atmos. Environ. 2005, 39, 787–799. [Google Scholar] [CrossRef]
  149. Saarijärvi, K.; Mattila, P.; Virkajärvi, P. Ammonia volatilization from artificial dung and urine patches measured by the equilibrium concentration technique (JTI method). Atmos. Environ. 2006, 40, 5137–5145. [Google Scholar] [CrossRef]
  150. Whitehead, D.; Raistrick, N. Effects of some environmental factors on ammonia volatilization from simulated livestock urine applied to soil. Biol. Fertil. Soils 1991, 11, 279–284. [Google Scholar] [CrossRef]
  151. Lehmann, J.; Joseph, S. Biochar for environmental management: An introduction. In Biochar for Environmental Management; Routledge: Abingdon-on-Thames, UK, 2015; pp. 1–13. [Google Scholar]
  152. Mackiewicz, E.; Szynkowska, M.I.; Maniukiewicz, W.; Paryjczak, T. Removal of ammonia by the catalytic oxidation on MexOy/zeolite type catalysts. Przem. Chem. 2011, 90, 896–899. [Google Scholar]
  153. Szymula, A.; Wlazło, Ł.; Sasáková, N.; Wnuk, W.; Nowakowicz-Dębek, B. The use of natural sorbents to reduce ammonia emissions from cattle faeces. Agronomy 2021, 11, 2543. [Google Scholar] [CrossRef]
  154. Varel, V.H.; Nienaber, J.A.; Freetly, H.C. Conservation of nitrogen in cattle feedlot waste with urease inhibitors. J. Anim. Sci. 1999, 77, 1162–1168. [Google Scholar] [CrossRef] [PubMed]
  155. Shi, Y.; Parker, D.; Cole, N.; Auvermann, B.; Mehlhorn, J. Surface amendments to minimize ammonia emissions from beef cattle feedlots. Trans. ASAE 2001, 44, 677. [Google Scholar]
  156. Parker, D.B.; Pandrangi, S.; Greene, L.W.; Almas, L.K.; Cole, N.A.; Rhoades, M.B.; Koziel, J. Application rate and timing effects on urease inhibitor performance for minimizing ammonia emissions from beef cattle feedyards. In Proceedings of the 2004 ASAE Annual Meeting, Ottawa, ON, Canada, 1–4 August 2004; p. 1. [Google Scholar]
  157. Parker, D.; Rhoades, M.; Cole, N.; Sambana, V. Effect of urease inhibitor application rate and rainfall on ammonia emissions from beef manure. Trans. ASABE 2011, 55, 211–218. [Google Scholar] [CrossRef]
  158. Parker, D.B.; Rhoades, M.B.; Koziel, J.A.; Baek, B.-H.; Waldrip, H.M.; Todd, R.W. Urease inhibitor for reducing ammonia emissions from an open-lot beef cattle feedyard in the Texas High Plains. Appl. Eng. Agric. 2016, 32, 823–832. [Google Scholar]
  159. Sepperer, T.; Tondi, G.; Petutschnigg, A.; Young, T.M.; Steiner, K. Mitigation of ammonia emissions from cattle manure slurry by tannins and tannin-based polymers. Biomolecules 2020, 10, 581. [Google Scholar] [CrossRef]
Figure 1. Main drivers influencing NH3 transport from Colorado’s eastern plains into Rocky Mountain National Park (RMNP), followed by both wet and dry deposition. Increased air temperature and solar radiation heat the NH3-enriched manure on the corral surface, accelerating NH3 emissions at ground level; diffusion and convective mass transfer bring the NH3 into the atmospheric boundary layer; easterly (upslope) winds move NH3-laden air masses into RMNP. Colorado’s map shows the region of interest/concern highlighted in red.
Figure 1. Main drivers influencing NH3 transport from Colorado’s eastern plains into Rocky Mountain National Park (RMNP), followed by both wet and dry deposition. Increased air temperature and solar radiation heat the NH3-enriched manure on the corral surface, accelerating NH3 emissions at ground level; diffusion and convective mass transfer bring the NH3 into the atmospheric boundary layer; easterly (upslope) winds move NH3-laden air masses into RMNP. Colorado’s map shows the region of interest/concern highlighted in red.
Atmosphere 14 01469 g001
Figure 2. Number of journal articles on in situ NH3 emissions studies conducted in cattle-feeding regions in the U.S., Canada, and United Kingdom from 1982 to 2022.
Figure 2. Number of journal articles on in situ NH3 emissions studies conducted in cattle-feeding regions in the U.S., Canada, and United Kingdom from 1982 to 2022.
Atmosphere 14 01469 g002
Table 1. Percent NH3-N loss as a percentage of nitrogen fed to beef cattle confined in feedyards.
Table 1. Percent NH3-N loss as a percentage of nitrogen fed to beef cattle confined in feedyards.
Location of StudySummerWinterAnnualReference
% of N fed
Texas Panhandle68–7142–4452–59Todd et al. (2011) [36]
Texas Panhandle46–5531–5149Rhoades et al. (2010) [37]
Nebraska56–6436–64 Erickson and Klopfenstein (2010) [38]
Texas Panhandle5028 Cole and Todd (2009) [39]
Texas Panhandle683653Todd et al. (2008) [40]
Texas Panhandle63 Flesch et al. (2007) [41]
Texas Panhandle51–65 Cole et al. (2006) [42]
Texas Panhandle552741Todd et al. (2005) [43]
Nebraska5431 Erickson et al. (2000) [44]
Nebraska57–67 Bierman et al. (1999) [45]
Average583952
Range46–7127–5141–59
NH3-N refers to the percentage of N related to the entire ammonia molecule (NH3).
Table 2. Seasonal NH3-N emissions reported for cattle feedyards.
Table 2. Seasonal NH3-N emissions reported for cattle feedyards.
Location of StudyReference NH3-N Emission (g head−1day−1)
SpringSummerFallWinterAnnual
ColoradoHutchinson et al. (1982) [27] 50
Texas PanhandleTodd et al. (2005) [43] 74 * 44 *
Texas PanhandleCole et al. (2005) [46]108 66
Texas Panhandle Baek et al. (2006) [47] 167 * 13 *
Alberta, CanadaMcGinn et al. (2007) [48] 140
Texas PanhandleFlesch et al. (2007) [41]150
Narrabri, AustraliaDenmead et al. (2008) [49] 46
Alberta, Canadavan Haarlem et al. (2008) [50] 164–318
Texas PanhandleRhoades et al. (2008) [51]89
(58–123)
78
(72–86)
Texas PanhandleTodd et al. (2008) [40]118131 6897
Alberta, CanadaStaebler et al. (2009) [52] 245
Texas PanhandleRhoades et al. (2010) [37]97.5
(69–128) *
88
(82–96) *
70
(47–103) *
61
(47–76) *
79 *
Texas PanhandleTodd et al. (2011) [36] 135–207 78–93105–150
Texas PanhandleWaldrip et al. (2013) [53] 90–167
Alberta, CanadaMcGinn et al. (2016) [54] 85
Alberta, CanadaMcGinn et al. (2018) [55] 100–117
Average11313018759104
Range108–15074–207140–31813–9350–167
* Indicates the estimated NH3 emission using the given NH3 flux and stocking density. If stocking density was not given, an average value of 20.9 m2 head−1 [56] was used.
Table 3. Best management practices (BMP) for open-lot livestock facilities to decrease NH3 deposition into RMNP (USDA-NRCS; conservation management practices [78]) in Colorado.
Table 3. Best management practices (BMP) for open-lot livestock facilities to decrease NH3 deposition into RMNP (USDA-NRCS; conservation management practices [78]) in Colorado.
Category NRCS Code Management Practices
Feed management592Diet manipulation
CP
CT
Growth-promoting technologies
β-AA
Implants
Feed additives (monensin),
Phase feeding
Pen maintenanceN/AManure harvesting and pen drainage
Dust control375Water sprinkler
Manure amendment632Surface amendment and manure separation
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Brandani, C.B.; Lee, M.; Auvermann, B.W.; Parker, D.B.; Casey, K.D.; Crosman, E.T.; Gouvêa, V.N.; Beck, M.R.; Bush, K.J.; Koziel, J.A.; et al. Mitigating Ammonia Deposition Derived from Open-Lot Livestock Facilities into Colorado’s Rocky Mountain National Park: State of the Science. Atmosphere 2023, 14, 1469. https://doi.org/10.3390/atmos14101469

AMA Style

Brandani CB, Lee M, Auvermann BW, Parker DB, Casey KD, Crosman ET, Gouvêa VN, Beck MR, Bush KJ, Koziel JA, et al. Mitigating Ammonia Deposition Derived from Open-Lot Livestock Facilities into Colorado’s Rocky Mountain National Park: State of the Science. Atmosphere. 2023; 14(10):1469. https://doi.org/10.3390/atmos14101469

Chicago/Turabian Style

Brandani, Carolina B., Myeongseong Lee, Brent W. Auvermann, David B. Parker, Kenneth D. Casey, Erik T. Crosman, Vinícius N. Gouvêa, Matthew R. Beck, K. Jack Bush, Jacek A. Koziel, and et al. 2023. "Mitigating Ammonia Deposition Derived from Open-Lot Livestock Facilities into Colorado’s Rocky Mountain National Park: State of the Science" Atmosphere 14, no. 10: 1469. https://doi.org/10.3390/atmos14101469

APA Style

Brandani, C. B., Lee, M., Auvermann, B. W., Parker, D. B., Casey, K. D., Crosman, E. T., Gouvêa, V. N., Beck, M. R., Bush, K. J., Koziel, J. A., Shaw, B., & Brauer, D. (2023). Mitigating Ammonia Deposition Derived from Open-Lot Livestock Facilities into Colorado’s Rocky Mountain National Park: State of the Science. Atmosphere, 14(10), 1469. https://doi.org/10.3390/atmos14101469

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