Next Article in Journal
Screening of Varieties Resistant to Late-Spring Coldness in Wheat and Effects of Late-Spring Coldness on the Ultrastructure of Wheat Cells
Next Article in Special Issue
Silicon Fertilizer Addition Can Improve Rice Yield and Lodging Traits under Reduced Nitrogen and Increased Density Conditions
Previous Article in Journal
Soybean-Oil-Modified Petrochemical-Source Polyester Polyurethane Improves the Nutrient Release Performance of Coated Urea
Previous Article in Special Issue
Linkages of Enzymatic Activity and Stoichiometry with Soil Physical-Chemical Properties under Long-Term Manure Application to Saline-Sodic Soil on the Songnen Plain
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

The Effects of Manure Application and Herbivore Excreta on Plant and Soil Properties of Temperate Grasslands—A Review

1
Landesamt für Bergbau, Energie und Geologie (LBEG), Referat L3.2, Stilleweg 2, 30655 Hannover, Germany
2
Julius Kühn Institute (JKI)—Federal Research Centre for Cultivated Plants, Institute for Crop and Soil Science, Bundesallee 58, 38116 Braunschweig, Germany
*
Author to whom correspondence should be addressed.
Agronomy 2023, 13(12), 3010; https://doi.org/10.3390/agronomy13123010
Submission received: 27 September 2023 / Revised: 26 October 2023 / Accepted: 2 December 2023 / Published: 7 December 2023

Abstract

:
This review provides an overview of grassland studies on the effects of manure application and herbivore excreta on plant and soil properties in temperate grasslands. Grass biomass from grazing or mowing is mainly used for animal products such as milk or meat, as well as for energy or raw materials for biorefineries. Manure application or grazing has a significant impact on several plant and soil properties. There are effects on soil chemical properties, such as increased carbon sequestration, improved nutrient availability, and increased pH. Additionally, several physical soil properties are improved by manure application or grazing. For example, bulk density is reduced, and porosity and hydraulic conductivity are greatly improved. Some biological parameters, particularly microbial biomass and microbial and enzyme activity, also increase. The use of manure and grazing can, therefore, contribute to improving soil fertility, replacing mineral fertilizers, and closing nutrient cycles. On the other hand, over-application of manure and overgrazing can result in a surplus of nutrients over plant needs and increase losses through emission or leaching. The lost nutrients are not only economically lost from the nutrient cycle of the farm but can also cause environmental damage.

1. Introduction

Currently, 31.7% of the European Union’s utilized agricultural area is used as grassland [1], which is mainly of anthropogenic origin [2]. Grassland use has developed primarily where site conditions are unfavorable for crop production. For example, sites may be too wet, too dry, too steep, or too stony [3,4]. Grasslands provide several ecosystem services to human society, such as primary production, carbon sequestration, biodiversity conservation, flood control, water filtration and purification, and recreation and tourism [5]. Managed grasslands play an essential role in securing food supplies [6]. In addition to food production, grass biomass can be used as a feedstock for biogas production and as a solid biofuel, as well as a raw material for several other bioproducts [7,8].
Since the last century, and especially since 1970, the human population has grown rapidly [9], which has led to a growing demand for animal products, such as increased meat and milk consumption [10,11]. Therefore, in order to produce more livestock products, the productivity of grassland has often been increased [12]. Livestock production—especially dairy production—is extraordinarily important for human food production [13] and will continue to intensify to meet growing demand [10]. In addition to milk and meat, livestock production also produces manure [14].
The increasing amount of manure makes it necessary to reconsider manure as a valuable nutrient source rather than a waste compared to mineral fertilizers [15]. Nutrients removed as forage or feed and not replaced by crop residues, atmospheric deposition, or N fixation must be returned through fertilizer inputs; otherwise, soil fertility and productivity will decline [16]. When manure is applied to the soil, it provides a slow-release source of several nutrients that improve soil fertility and support plant growth [17,18]. Organic fertilizers contain the same basic nutrients, such as N, P, and K, as mineral fertilizers [19]. The use of organic manure can reduce the need for synthetic chemical fertilizers, which can be expensive and have environmental drawbacks [15]. In addition, mineral P fertilizers derived from rocks are a finite resource [20]. Therefore, the use of nutrient-rich manure is a sustainable alternative that reduces chemical dependency [15,21]. Consequently, organic manure can reduce input costs for farmers [22]. It is in line with the principles of agroecology and promotes environmentally friendly, resource-efficient, and long-term sustainable agriculture [15]. As an additional result, it can open up markets for organic and sustainably grown products, which often command higher prices.
Organic matter in manure is also rich in carbon [23]. When incorporated into the soil, it can contribute to carbon sequestration, helping to mitigate climate change [23]. Organic manure helps improve soil structure and water-holding capacity [24]. Therefore, it increases the soil’s ability to retain moisture and nutrients, reducing the risk of soil erosion and increasing drought resistance.
In addition to the many positive effects of manure application, there are also negative aspects to consider. Manure spreading can produce strong odors that can be unpleasant for people living near agricultural land [25]. Spreading manure evenly over grassland can be technically challenging, especially on uneven terrain. Uneven application can result in patchy plant growth [26]. Proper timing of application is also very important so that (1) plants are in the growing season and able to take up the nutrients being released, and (2) weather and soil conditions are appropriate so that the amount of manure applied remains in the soil and does not wash out [27]. Improper manure application and overgrazing can lead to overfertilization and soil compaction, both of which can severely degrade soil and water quality [28,29]. It can also result in feed contamination, which degrades feed quality and can lead to reduced feed intake and poor animal performance [30].
Fertilization with organic fertilizers applied directly during grazing as animal excreta or in the form of manure is a common practice in grassland management [31]. The nutrient content of manure needs to be measured or determined prior to application, whereas nutrient and organic matter inputs during grazing are more or less unknown and very heterogeneously distributed [32]. The interactions between applied nutrients and organic matter of organic fertilizers, soil fertility, plant growth, and herbage nutrient content are complex due to many biological, biochemical, and physical processes [33].
The objective of this review is to provide an overview of the effects of organic fertilization on the properties of temperate grasslands. In addition to changes in properties, topics covered in this paper include the basics of grasslands and their use and factors for optimizing the effects of fertilization by adjusting management practices.

2. Grassland Management

2.1. Grassland Use

Typical uses of grassland include mowed meadows, grazed pastures, and mown pastures as a combination of both [3,34,35]. Mown pastures are grasslands that are harvested by mowing several times per year [36] to produce hay or silage [35,37]. Pastures are grasslands that are grazed year-round or for a limited period, usually spring and summer. Typical grazing animals are cattle, sheep, horses, and goats [3]. During grazing, up to 90% of the nutrients consumed by ruminants are returned to the soil in the form of excreta [38]. Mown pastures are usually both grazed and mowed in the same year [39], but sometimes they are mowed or grazed only once a year [2] and typically mowed once at the end of the season [34].

2.2. Intensity of Grassland Management

Currently, there is a wide variation in the management intensity of grasslands. It ranges from extensive to intensively managed grasslands [2,40]. This depends on the amount of fertilizer, mowing frequency and/or grazing duration, and livestock density [34]. Table 1 shows typical levels of land use intensity in terms of fertilization, harvest, and livestock density. Extensive grasslands provide more regulating ecosystem services than intensive grasslands and are, therefore, often part of agri-environmental or compensation programs that prohibit or limit fertilization rates and require a late harvest date [6]. In contrast, very high forage quality is achieved on intensively managed grasslands [41].
As the number of cuts increases, the intensity of grassland management increases. The variation ranges from extensive grassland with one cut per year to four cuts and more for intensively managed grassland. Two to three cuts are considered as medium-intensive management [36].
Another characterization of management intensity is based on the number and amount of fertilizer applications. While pastures are mainly fertilized with livestock excreta [49,50,51], meadows and mown pastures are typically fertilized with both organic and mineral fertilizers [52]. In extensive systems, zero to two fertilizer applications are typical [42], and up to five applications per year in intensively managed grasslands [43]. A typical application rate in intensive farming systems in studies ranged from 181 kg N ha−1 [46] to 640 kg N ha−1 [45]. For extensive management, it has been reported that there is no fertilization [44] to 97 kg N ha−1 [42].
The grazing intensity of pastures ranges from 500 kg live weight or two heifers per ha as extensive management to 1000 kg live weight or four heifers per ha as intensive management [53]. Another classification of grazing management intensity is based on livestock density, referred to as livestock units (LU). According to Wang et al. [47], 0.8 LU is considered low intensity, 1.8 LU as medium intensity, and 3.4 LU as high intensity. Typical husbandry systems for extensive grazing in Europe are suckler cows [42] and sheep [54,55]. Diary husbandry is the most common form of intensive grazing system [42,54,56]. A typical average N input from herbivores under intensive grazing is 144 kg N ha−1, and under extensive grazing, it is 128 kg N ha−1 and 117 kg N ha−1, respectively, for organic farming [48].
While intensive management systems result in higher yields [57], energy consumption, e.g., for grass drying and the use of mineral and organic fertilizers, are much higher compared to extensive management systems [48].

2.3. Conventional versus Organic Farming

Grassland farming systems are managed in both conventional and organic manner. Conventional farming systems use multiple fertilizers, herbicides, and pesticides. This results in higher yields. On the other hand, the costs are higher compared to organic farming, and the impact on the environment can be negative. Organic farming aims to reduce external inputs, using organic sources as nutrient inputs and promoting sustainable soil management. However, the yield of organic farming systems is often lower, resulting in higher product prices [58]. Compared to intensive conventional farming, organic farming requires about half the product-related energy inputs; e.g., organic farms in Germany use 65% less energy than conventional farms [48]. In particular, fertilizer use is reduced to about two-thirds compared to conventional farming [59].

3. Application of Organic Fertilizers

3.1. Organic Fertilizer Properties

The nutrient content of organic fertilizers varies depending on the type of organic fertilizer [60], livestock species [61,62], husbandry system [63,64,65], and feed composition [65,66,67].
The types of organic fertilizers most often used in agriculture are as follows:
  • Slurry—a combination of the liquid and solid fractions of excreta;
  • Semi-solid manure—mainly the feces separated into liquid and solid fractions;
  • Solid manure, also called farmyard manure—feces combined with litter or straw [68].
According to Gisiger [60], solid organic fertilizer has the highest C and P content, while the amount of N and K in urine is higher. An increase in the solid fraction of the organic fertilizer leads to a higher P content and a simultaneous decrease in K and N [60,64]. Therefore, N (45–80%) and K (70–90%) are mainly excreted in urine, and between 20% and 55% of N, together with more than 95% of P and Ca are excreted in solid manure [62]. Composted manure has a lower C content but contains more N than non-composted manure [24]. The feed composition—especially protein and cellulose contents—affected not only the amount of nutrients but also the microbiological composition in organic fertilizers [66]. Higher protein content leads to increased N and P content [65] and has a positive effect on microbial communities [66]. However, ammonia (NH3) volatilization increases [65,67]. The higher energy content of feed with more protein reduces the dry matter (DM) content of manure due to higher digestibility [65]. A lower protein content leads to a decrease in N [65,66] and S and a lower amount of NH3 [66]. Other components such as Ca, Mg and Na are correlated with the amount of total N. van der Stelt et al. [65] found that the higher the N content, the lower the amount of free Ca and Mg due to exchange processes with ammonium (NH4). Mg content increases with increasing K due to a negative effect on the digestibility of Mg [65].
Table 2 summarizes the results of the nutrient content of different types of manure from the Manure Standards Project (https://msdb.netlify.app/ accessed on 5 December 2023).

3.2. Application Techniques and Their Effects

Several techniques are available for organic fertilizer application that have different emission losses of nutrients, especially N [69]. Typical techniques are broadcast applications on the soil surface, such as splash plate or band spreading techniques, low trajectory slurry applications, such as trailing shoe or shallow injection methods [70,71], and narrow band applications [72]. Huijsmans et al. [72] found that NH3 losses during slurry application were reduced by up to 74% using shallow injection compared to broadcast application. Groot et al. [73] confirmed that shallow injection was always the most efficient application method in terms of N losses. Overall, NH3 volatilization of total N varied from 27% to 98% with broad band application, 8% to 50% with narrow band application, and 1% to 25% with shallow injection. Precision application techniques such as shallow injection can be used to reduce NH3 losses not only for manure and slurry [74] but also for other organic fertilizers such as digestate [75]. Due to reduced N losses, more N was available for plants when slit and injection techniques were used [32].
It should be noted that in some European countries, such as Germany [76] and the Netherlands, the use of some application techniques is restricted [32]. High-emission techniques such as broad band application are prohibited in these countries, and therefore the use of low-emission techniques is mandatory [32,76].
Table 3 provides an overview of N losses, N recovery, and N loss reduction with different application techniques in temperate grasslands.

3.3. Timing of Application

The timing of fertilization is important to avoid nutrient losses. Mineral fertilizer is usually applied at the beginning of the growing season in spring and manure after the first cut [81]. Compared to spring fertilization at the beginning of the growing season, autumn fertilization resulted in higher losses by volatilization, leaching, and denitrification due to more frequent precipitation events and lower N uptake by plants. On the other hand, spring application prolongs the storage time of manure, which can also lead to higher nutrient losses [82]. Based on a study by Smith et al. [83], N losses are up to 43% in September and up to 53% in October. Sørensen and Rubæk [82] found that N is slowly mineralized and nitrified in the period after organic fertilizer application. Therefore, N losses may occur in the period after application. According to He et al. [84], to avoid nutrient losses, organic fertilizer amounts should be divided into smaller amounts, resulting in less nutrient leaching and less N2O emission.

4. Plant Properties

4.1. Yield

Nutrient availability, especially N, is a limiting factor for plant growth. The DM yield of grass is correlated with the N yield (DM yield = N yield 59.872 − (N yield)2 × 0.076) and is, therefore, most affected by N application in the form of mineral and organic fertilizers [85].
With the application of cattle manure, the grass yield was between 20% [86] and 56% [87] higher than without fertilization. DM yield was highest in the second year of fertilization [86]. The higher DM yield depends on the availability of nutrients for plant growth, which is provided over time by the mineralization of organic fertilizers [87]. Both aboveground and belowground biomass increased with organic manure application, with aboveground biomass increasing disproportionately with increasing N [88].
In a study by Kacorzyk and Głąb [89], the effect of N application from sheep manure on DM yield was significant, but P and K applications showed only moderate effects. Not only is the total or plant-available content of nutrients important, but the proportions of nutrients, especially an inappropriate N:P ratio in plants, can also limit plant growth. The higher the N:P ratio, the more P was the limiting nutrient, and the lower the N:P ratio, the more N was the limiting nutrient.
The DM yield of grass was also affected by the application technique used to apply manure to the fields. The use of injection techniques significantly increased DM yield as a function of N content in the manure due to a higher efficiency of N conversion to DM [32]. However, the higher the N level, the lower the positive effect of injection application [85].
According to Augustenborg et al. [90], dung excretion during grazing has a positive effect on DM yield, similar to mineral fertilization. The effect of grazing on DM yield depends on the grazing system and intensity. In particular, moderate grazing and rotational systems have a positive effect on biomass build-up, and the yield can be higher, both quantitatively and economically, than when hay or silage is harvested. Important advantages of pasture are the reduced need for additional fertilization, no losses during harvest, storage and transport, and lower costs for machinery [56]. Patches, mainly caused by urine deposition, show increasing concentrations of various nutrients such as N, S, and K in herbage and soil, thus increasing DM yield [91]. Typical nutrient hotspots where patches can develop are in shaded areas and around mineral and water sources [38]. Deposition of excreta led to both increased plant growth and avoidance of grazing [92].

4.2. Quality

As mentioned above, the use of manure as fertilizer has a positive effect on DM yield, although the effect on forage quality is uncertain. While Simić et al. [93] found no significant effect on quality aspects such as better digestibility, Štýbnarová et al. [87] observed a significant increase in crude protein by 9% to 29% depending on the grass species. Crude concentration protein increased with manure fertilization compared to unfertilized grassland. Higher N content improved forage quality by reducing the C:N ratio, resulting in higher availability for digestion and, thus, higher digestibility [38].
According to Rammer and Lingvall [68], manure application affects not only the quality of grass and forbs in terms of nutrient content and digestibility but also the quality of silage. Silage can be contaminated with manure during harvesting after application, especially when surface technology is used. This affects the microbial communities, leading to an increase in bacteria and bacterial activity and favoring the growth of undesirable microorganisms during ensiling.
Grass from pastures tended to be of higher quality than grass silage [56]. Grazing intensity had no significant effect on grass quality, such as lignin, N percentage, or C:N ratio [94]. In a study by Schellberg et al. [50], N uptake from excreta during grazing increased digestibility between 70% and 79% and crude protein content in plants between 10% and 25%. In a rotational grazing system, the nutritional value of plants may decrease due to maturation processes [38].

4.3. Plant Composition and Diversity

Organic fertilization causes changes in plant composition [86]. This increased nutrient availability may favor certain plant species that are more responsive to these nutrients, leading to changes in plant composition and a decrease in plant species diversity [39]. Nitrogen-rich species respond better to organic fertilizers, suppressing and eliminating less competitive nitrogen-poor species, and few of these nitrogen-deficient adapted species can survive. The opposite is true for very nutrient-poor soils. Here, gaps in the vegetative cover can allow undesirable species to spread, especially noncompetitive invasive species. In these areas, intermediate levels of fertilization can contribute to higher plant species diversity [95]. Organic soils also showed lower species richness and a slight positive effect on species richness with increasing fertilization [95].
According to a study by Kacorzyk and Głąb [89], both investigated doses of sheep manure (69 kg N ha−1, 103 kg N ha−1) resulted in a higher proportion of grasses than other plant species such as herbs and legumes. Similar results were found by Knežević et al. [96] that some species, especially grasses, tended to grow faster than other species, such as broadleaf weed species or herbs and legumes such as white clover after fertilization. As a result, grasses became the dominant species while the others declined. The proportion of herbs can be reduced by more than a third within two years. While P and K mainly influence the proportion of herbs, legumes are more affected by applied N. Tampere et al. [97] found that high application rates above 120 kg N ha−1 led to the disappearance of white clover. These high N application rates compensated for this loss through higher grass yield but had no significant effect on total yield. According to Kacorzyk and Głąb [89], organic fertilization can lead to an increase in legume percentage as long as the N application rate is lower than 69 kg ha−1. However, the type of application technique had no effect on plant composition [32].
In a study by Socher et al. [39], grazing had a very negative effect on biodiversity in organic soils and a slightly positive effect on less organic soils. It affects plant composition through the release of nutrients through urine or feces [53]. According to Kayser and Isselstein [91], the uneven distribution of nutrients and less grazed areas have created patches where special species can be established. Often, taller plant species can grow here and complement smaller ones [53]. Different patch types under different grazing intensities led to increased biodiversity but with a higher impact under extensive grazing than under intensive grazing [53]. This was due to the preference of cattle for smaller patches, which decreases with increasing LU [53,92].
Table 4 provides an overview of the yield, quality, and plant composition of temperate grasslands depending on manure application.

5. Soil Chemical Properties

5.1. Soil Carbon (C)

The terrestrial carbon (C) pool, particularly in grassland soils, is one of the most important C sinks on earth [102]. There are several different factors that affect C sequestration in grassland soils, including management practices, the amount of N and other nutrients [103,104,105], soil physical properties [102], soil organisms [106,107], and environmental factors such as air temperature and water availability. According to Jones et al. [103], manure is an important source of C, although its application can increase dissolved organic carbon (DOC) levels and thus C decomposition rates through the priming effect related to increased respiration. Overall, manure application leads to increased C sequestration despite increased soil respiration due to a positive C balance [29]. C accumulation in the soil results directly from the applied manure and secondarily from increased microbial biomass and higher amounts of plant residues such as litter and roots [108].
Depending on management, grassland can have high CO2 uptake during the growing season and thus act as a sink for C. The rate of CO2 uptake can vary from year to year [109]. The type of fertilizer affects soil respiration and, thus, CO2 emissions. According to a study by Jones et al. [103], the respiration rate is increased by 27% for cattle manure and 41% for poultry manure compared to the control without manure application.
Organic C can be converted to CH4 by anaerobic digestion [16,110] or emitted directly by livestock [108]. Anaerobic digestion primarily occurs when manure is applied in liquid form, especially on flooded soils or after runoff into surface waters [111]. However, Jones et al. [103] found no direct effect of manure application on CH4 emissions, except for temporary peaks immediately after cattle manure application. This CH4 flux originates directly from the manure and is, therefore, largely independent of soil respiration. Only between 0.1% and 0.4% of the total CH4 emissions originated from soil respiration.
Leaching of DOC is a relatively small but continuous loss and is of great importance for C and GHG balances [112]. Jones et al. [103] found that DOC is continuously increased by manure application. When comparing agricultural manures, DOC increased more after poultry manure application than after cattle manure application. In addition to the type and amount of manure applied, the amount of DOC leached depends on various conditions such as climate and edaphic conditions, e.g., soil structure and texture, pH, and vegetation, especially root distribution and litter quality [113].
Grazing tends to have a positive effect on soil organic carbon (SOC) content due to organic C input via excreta, depending, for example, on landscape position, soil properties, grazing management [114], and climatic factors [115]. Approximately 25% to 40% of C uptake is returned to the soil as excreta [108]. Moderate grazing intensity has the most positive effect on C accumulation, followed by rotational grazing and, finally, high grazing intensity [94]. Depending on management intensity, mowing may result in higher C export compared to grazing, leading to lower C sequestration rates on pastures if C export is not offset by organic fertilizers or other C inputs [116]. However, even under very extensive grazing, C content decreased due to higher rates of SOC decomposition. This was due to low C supply and, thus, depletion of the soil C pool [44]. Paz-Ferreiro et al. [117] suggest that increased nutrient availability, especially N, stimulated soil respiration. Excreta increased CH4 emissions through deposition effects [116], while emissions decreased over time with aging. According to a study by Voglmeier et al. [118], emissions occurred up to 20 days after deposition. Leaching losses of C as DOC were small compared to emission losses of CO2 [119]. Jones et al. [116] found in their study that only 2.1% of total C was lost through leaching under grazing management, as grazing primarily increases CO2 emissions.
Table 5 shows the changes in C storage and C losses as a function of organic fertilizer application on temperate grasslands.

5.2. Soil Nitrogen (N)

N is a very important nutrient in the global biogeochemical cycle and is crucial for plant growth and living organisms [38,124,125].
Bittman et al. [126] found that a high proportion of sequestered N comes from microbial N, which can be further increased by manure application. Microbial N is 1.5 to 1.6 times higher at an organic manure application rate of 100 kg N ha−1 a−1 than at a rate of 50 kg N ha−1 a−1.
NH3 volatilization depends on several factors, such as DM and NH4+-N content, manure and soil pH, soil moisture, and available soil C [127]. However, experiments with different DM contents in solid manure and slurry have shown that the DM content of manure has no significant effect on NH3 emissions [128], while a study by Misselbrook et al. [74] found increasing NH3 emissions with increasing DM. According to Sun et al. [110], coarse-grained solids slow the penetration of manure into the soil, resulting in increased NH3 emissions. In addition, higher temperatures and solar radiation led to an increase, while rain and snow events reduced it. However, application to water-filled soils increased NH3 emissions due to low infiltration rates. Twigg et al. [128] found that about 70% of NH3 losses occurred in the first eight days after manure application to grassland, while about 90% occurred between the first 32 h and 48 h after application. Overall, about one-third of the total NH3 is emitted in the first five days.
Manure application increases N2O fluxes, which are considered to be the main pathway for N losses from grassland soils [129]. The type of manure affects N2O emissions, e.g., through readily available C and N that stimulate microbial activity. In general, manure application causes the highest N2O emissions compared to other N2O sources on grassland [118]. After manure application, NH4+ and NO3 concentrations increased rapidly due to increased enzyme activity, resulting in increased N2O emissions [129]. Jahangir et al. [130] found a significant increase in N2O emissions due to higher denitrification rates after manure application. In their study, the denitrification rate in the A horizon increased from 25% to up to 61%.
N leaching usually occurs in the form of NO3 [131], which can be lost as leachate and surface runoff or converted to gaseous form and emitted as THG [130]. The risk of leaching depends on the type of fertilizer, with slurry N being more susceptible to leaching but also more rapidly available for plant uptake compared to solid manure N. This can lead to higher leaching losses, especially outside the main grassland growing season in fall and winter [83].
Pastures tend to have high levels of NO3 in the soil. N comes mainly from animal excreta and supplemental manure but also from mineral fertilizers and SOC [130]. During grazing, more than 70% of N uptake is returned to the soil as excreta. Excretion is unevenly distributed. There is usually a high surplus of N at excretion sites. According to a study by Anger et al. [132], between 350 and 1300 kg N ha−1 a−1 can be excreted on a patch. Plants are not able to take up this amount of N.
Depending on the LU, grazing has a strong effect on N sequestration and mineralization. The higher the LU, the higher the mineralization, and thus, N sequestration also decreases when N input is less than N output [94]. The proportion of NH3 emissions from grazing was very high, with values between 17% and 37% of the total NH3 emission losses from livestock [133]. In contrast, Misselbrook et al. [134] estimated that only about 8% of total NH3 emissions came from cattle grazing. Grazing increased NH3 emissions, especially on urine patches, due to favorable mineralization conditions such as higher soil moisture and pH on these patches [38]. NH3 losses can be highly variable. Petersen et al. [135] found a range of 3% to 52% N losses from urine. Higher grazing intensity led to higher NH3 emissions due to more excretion on the pasture [136]. The same is true for N2O emissions, as the N content in urine is higher than in feces [118,137].
Table 6 shows changes in N storage and N losses in temperate grasslands as a function of organic fertilizer type, and Table 7 shows these changes as a function of the timing of organic fertilizer application.

5.3. Other Soil Nutrients

5.3.1. Phosphorus (P)

Phosphorus (P) is an important element in plant nutrition, as increased P availability leads to better plant growth due to higher N mineralization rates [140]. On grassland farms, P is typically applied as manure, solid manure, or compost [141], increasing the soil P pool.
P can be leached in both dissolved and particulate organic or inorganic form [82]. P losses can especially occur when manure is applied near the surface [142]. However, an unfavorable timing of fertilization—especially before rainfall—or P surplus in the soil can lead to eutrophication of surface waters [131]. At high application rates, especially in coarse-textured soils with many macropores, leaching can be high because P sorption to free sites in the soil matrix is low. In contrast, in fine-textured soils with less macropore flow, the risk of P leaching is lower as long as there is sufficient P sorption capacity [82]. Hahn et al. [142] found in their study that under dry conditions, hydrophobic components in manure reduce the infiltration rate and, therefore, increase the risk of surface runoff when rain starts. On the other hand, as soil saturation increases, the infiltration rate decreases, and more runoff and P losses occur. With increased rainfall or irrigation, there is more colloidal dispersion, which mobilizes a greater amount of particulate-bound P. Over time, the amount of dissolved active P decreases due to increased sorption of P in the soil, manure decomposition, and bioturbation. According to Laurenson and Houlbrooke [143], approximately 6% of applied P is lost to surface runoff in the first seven days after manure application. Over the next two months, runoff losses decreased by 76% due to a reduction in surface dissolved P. Therefore, manure application and other management practices on grasslands need to be optimized to reduce P leaching losses [142]. For example, manure injection and banding, as well as proper timing of application, can reduce soil sealing and thus P loss.
According to several studies, grazing does not seem to have a major effect on P leaching [100,144,145]. In the study by Härdtle et al. [145], P leaching only differed between 0.2 kg P ha−1 a−1 and 0.4 kg P ha−1 a−1 without grazing and up to 0.5 kg P ha−1 a−1 with grazing. Chardon et al. [144] found that 76% of the P was still present in the plots at the end of their study. The low P leaching rate under grazing can be explained by the high sorption capacity of the soil and the low P deposition rates [145].

5.3.2. Potassium (K)

K is an important nutrient for several physiological interactions, such as stomatal regulation [91], and is the second most important nutrient for plants after N. K is of agronomic interest but not of serious environmental concern. In contrast to N and P, it has little effect on groundwater quality, and the EU limit of 12 mg l−1 is not yet toxicologically approved [146]. Depending on the management system, surpluses can occur, especially in intensive grassland systems, or deficiencies, mainly in organic and extensive grassland systems [91].
Plant uptake is the main form of K output from the soil system. Due to the high removal of plant biomass and thus high K removal rates, K losses by leaching are low on mowed grassland [91]. Alfaro et al. [147] found that K leaching losses averaged only 6% of total output compared to 88% to 98% by plant uptake. However, according to Kayser and Isselstein [91], due to the high amount of concentrated feed used in intensive dairy farming, there is a high probability of a K surplus when applying the resulting farm manure that cannot be taken up by plants—and therefore a high level of available K leading to increasing losses. The amount of applied K varied between 100 and 130 kg K ha−1 a−1 on extensively managed and 175 and 250 kg K ha−1 a−1 on intensively managed (up to four cuts) meadows.
The different types of organic fertilizers had only a small effect on K leaching. According to studies by Kayser and Isselstein [91] and Tampere et al. [97], the application of cattle slurry alone increased K leaching losses from grassland over the years. The type of application and application during or after the growing season had no effect on K leaching.
The most important factor influencing K leaching is the balance between K and N. N fixation influences K uptake by plants and, therefore, K leaching. N application rates had little effect on total K leaching, with a tendency to increase or decrease leaching over the years. The highest leaching losses occurred without N fertilization, depending on the plant composition. An imbalance between N and K can have a negative effect on the ensiling quality of grass [97,146].
On pastures, the amount of K in the soil due to excretion by herbivores can range from 180 kg K ha−1 a−1 to 500 kg K ha−1 a−1, which exceeds plant requirements [91]. According to a study by Kayser et al. [146], about 90% of the total K uptake during grazing was immediately returned to the soil through urine. This resulted in inefficient K recycling and leaching losses. Leaching from urine patches was mainly due to macropore flow and depended mainly on soil surface properties. K leaching from urine patches was highest in summer but only for a few days after application. Kayser et al. [146] suggested that high K leaching in summer is induced by heavy rainfall events.

5.3.3. Calcium (Ca) and Magnesium (Mg)

Ca is an important element for the stability of soil aggregates, particularly by binding clay particles together [148]. Mg is the central element of green plant pigment and helps to regulate water balance [149].
According to a study by Whalen and Chang [150], the amount of Ca and Mg is increased by manure application. However, because anions and acidic compounds bound most of the ions, only a small amount was available for plant uptake, depending on the rate of manure application. Leaching was the main pathway for Ca and Mg losses [91]. The leaching of Ca2+ and Mg2+ ions is not seen as an environmental problem but as a loss of valuable nutrients [151]. Whenever anions such as nitrates are leached, there are an equal number of cations that act as counterions. In particular, Ca and Mg are counterions of nitrate. Therefore, Ca and Mg are leached in addition to nitrate and other anions [91].
Di and Cameron [151] estimated that 60% to 99% of Ca2+ and Mg2+ ions ingested during grazing are returned by excretion. In their study, leaching losses of Ca2+ were determined to be 213 kg Ca ha−1 a−1 and 17 kg Mg ha−1 a−1 of Mg2+. Most of these leaching losses occurred on urine patches.
Table 8 shows the losses of P, K, Ca, and Mg from different manure applications in temperate grassland.

5.4. Soil pH Value

Soil pH is a major driver of several transformations in soils. Changing pH can affect the chemical form of nutrients [38]. Manure contains a certain amount of 0.3 to 110.7 g/kg Ca2+ and 0.1 to 11.5 g/kg Mg2+, depending on the origin of the manure [153]. According to the study by Naramabuye and Haynes [153], poultry manure contained the highest amount of Ca2+ and Mg2+ ions, followed by pig and cattle manure. Therefore, manure application has a long-term effect on increasing the pH of grassland soils due to the presence of Ca2+ and Mg2+ [12,153] and the oxidation of organic anions during manure decomposition, resulting in a higher buffering capacity [12]. In addition to Ca2+ and Mg2+ ions, other carbonates, bicarbonates, and organic acids with carboxyl and hydroxyl groups present in manure also affect buffering capacity [154]. Decomposition processes produce organic anions in the form of phenolic material that can bind protons from the soil and thus increase the soil pH of grassland soils [153].
Acidification of manure, where the addition of acid lowers the pH of the manure, is increasingly being used to reduce GHG and NH3 emissions from manure. The typical pH was below six when H2SO4 was used and below five when lactic or hydrochloric acid was used. The altered conditions and effects of reduced pH should be considered in the subsequent availability of nutrients [155].

5.5. Soil Bulk Density

Bulk density affects several soil parameters important for crop production, including hydraulic conductivity, gas diffusion, nutrient uptake, and root growth [156,157]. According to a study by Miller et al. [156], bulk density is positively affected by manure application due to increasing SOC content, which is associated with decreasing bulk density.
According to Mestdagh et al. [158], grazed soils tended to have lower bulk densities than mowed grassland soils. In their study, SOC content was 6% to 7% higher under grazing than under mowing. However, a change in soil bulk density can be explained not only by a change in SOC but also by mechanization or trampling [158,159]. According to Pietola et al. [159], trampling can increase soil bulk density. This can alter the positive effect of higher SOC content [158].

5.6. Soil Porosity

Soil porosity is mostly based on the soil type, organic matter, decomposition, mineralization processes [160], and tillage [161].
Manure application and, thus, increasing SOC content also changes the pore size distribution [161,162]. Kirchmann and Gerzabek [162] found a general increase with manure application. In particular, the proportion of fine macropores between 60 and 600 µm increased rapidly.
Although grazing increases SOC content [158], it can lead to a decrease in porosity due to clogging of surface pores and increased compaction [159,163]. The authors found a decrease in pores >30 µm from 11.2% to 9.5% by trampling. Since Greenwood et al. [164] found an increase in soil porosity years after cessation of grazing, the negative effect of trampling and the positive effect of wetting and drying cycles were much greater than the effect of animal excreta during grazing.

5.7. Soil Hydraulic Properties

According to Dlapa et al. [161], manure application to grassland soils increased water retention due to increasing SOC content. The authors found in their study that SOC content had an even stronger effect on water retention than texture and clay content, as coarse soil with high SOC content had higher water retention than fine-textured soil with low SOC content.
Near-saturated soil hydraulic conductivity is also increased in grassland soils after manure application due to increased biological activity [163]. The increased biological activity, e.g., by earthworms [165], resulted in more continuous and less tortuous pores, which allowed better water flow [163].
Grazing can reduce soil water conductivity—especially near saturation conductivity—due to partial compaction and clogged surface pores [163]. This resulted in an 85% to 90% reduction in water infiltration on clay soils [159]. Greenwood et al. [164] found a significant improvement in soil physical properties after excluding grazing due to the elimination of soil compaction by animals. For example, pasture soils without grazing had higher unsaturated hydraulic conductivity than pasture soils with grazing. When grazing was stopped, they could not find significant differences between the pasture that had not been grazed for 2.5 years and the pasture that had not been grazed for 27 years. Thus, the improvement processes seemed to occur very quickly after the cessation of grazing.

5.8. Size of Soil Aggregates

Organic manure application increases the proportion of aggregates in grassland soils. Linsler et al. [166] found a higher proportion of aggregates in soils with manure application compared to plots without manure application. The concentration of smaller aggregates tended to decrease after manure application. This was due to the formation of larger aggregates from smaller aggregates with the binding or cementing agents from the organic fertilizer [167]. The amino sugars of soil microbial communities, especially bacteria, serve as binding agents. They bind soil primary particles to form microaggregates, which are then bound together to form macroaggregates. These aggregates serve as niches for the microbial communities, providing them with better growth conditions. This was a positive feedback loop [168]. According to Wortmann and Shapiro [169], the formation of macroaggregates depends on the organic fertilizer applied. Feedlot solid manure and compost stimulated the formation of large macroaggregates >2 mm by 200% and more compared to control plots with no application. The effect of compost was about 240% greater than that of manure.
Manure application also leads to higher water stability of aggregates. The hydrophobic organic compounds are thought to be the cause of the improvement in water stability. Aggregate stability is higher in irrigated soils than in dryland plots due to higher soil moisture content [150].
Soil aggregation due to manure application also results in less runoff and, therefore, less P loss, which was observed two weeks after application. This effect persisted for more than one year [169].
During grazing, SOC content increased, resulting in increased formation and stability of large aggregates >2 mm and small aggregates <0.5 mm [170]. The author found that these effects occurred only at grazing intensities of 0.8 LU ha−1. Higher intensities of 1.8 LU ha−1 and 3.4 LU ha−1, respectively, resulted in higher rates of organic C decomposition and, thus, larger aggregates.

6. Soil Biological Properties

6.1. Soil Organisms

In grassland soils, microbial biomass accounts for about 45% of the humic fraction and is mainly favored by the high C content of grassland soils [106]. Due to the high content of labile forms of C, manure application has a positive effect on microbes [126], depending on the type of manure [61]. While SOC changes slowly, soil microbial biomass often develops rapidly after the application of organic amendments [171]. In particular, the application of manure together with straw stimulates fungal activity [31].
The C content of manure [171], with SOC content [172], is the most important factor for the growth of microbial populations, turnover rates, and microbial mortality rates, in addition to climatic conditions. However, Neufeld et al. [173] did not find significant differences in soil microbial growth between different forms of manure application—liquid or solid—despite different SOC content. However, in a study by Bittman et al. [174], manure application over several years, especially dairy manure, increased overall microbial biomass, especially fungal biomass. Bacterial biomass decreased over the years because common soil bacteria such as Pseudomonas spp. had better growth conditions on the labile organic substrates in the manure, while fungi grew faster on recalcitrant substrates such as lignin. Zhelezova et al. [175] showed the effects of manure application depending on the applied manure and soil type. Here, the number of fungi in poultry and pig manure was twice as high as in cattle manure. In addition, microbial populations changed over time depending on soil type. Because the microbial communities were rapidly activated in Chernozem, there was little change in taxonomy. In contrast, in Retisol, the microorganisms were only slightly activated in the first few months, but taxonomy changed significantly over time. Overall, a large number of manure-derived microorganisms survived in the soil. A similar result was found by Sayre et al. [176]. While the population of manure-derived microorganisms in the soil increased, the population of other microorganisms decreased. On some plots, there was a complete change after two years. In contrast, in the study by Semenov et al. [177], most of the manure-derived bacteria in the soil died within nine weeks. At the same time, the soil microbiota was mainly activated by manure application.
According to Conant et al. [178], mechanisms such as microbial immobilization, formation of recalcitrant litter, and small or inactive microbial populations can limit N mineralization. As N levels increase, these mechanisms are prevented, and N mineralization is accelerated. Soil N is directly related to soil C. Therefore, changes in C result in changes in N. A study by Laughlin et al. [179] showed that at high C levels induced by manure application, fungi tended to become dominant. They were the most important actor for N transformation, especially under permanent grassland, and therefore the dominant species for N2O emissions. According to a study by Vries et al. [180], high fungal biomass reduced N losses due to higher N uptake by plants and N immobilization. Simpson et al. [106] found that more than 80% of organic N comes from microbial sources. While microbes require N to grow, they immobilized soil N when there was insufficient soluble N available. This occurred in cycles as microbes died and decayed over time, while N was released and returned to the soil [38]. Therefore, microbes were considered a labile pool of plant nutrients with a turnover time of one to three years [171]. Due to high C:N ratios in decomposing organic matter, N immobilization outweighs N mobilization in grassland soils [52]. Microbial growth was more influenced by nutrient availability, especially N, than by energy substrates [181].
Hu et al. [182] found that 60% of the total microorganisms under pastures were bacteria. The number of Gram-negative bacteria was twice that of Gram-positive bacteria. On the other hand, according to a study by Semenov et al. [177], fog Gram-negative bacteria died in the soil. The majority of surviving bacteria were Gram-positive. According to Mencel et al. [183], the mass of bacteria in pastures decreased with soil depth. Due to decreasing organic matter and nitrogen, the number of Gram-positive bacteria decreased in particular. While the number of bacteria decreased with depth, actinobacteria are stable up to 30 cm depth. Soils from extensive or lightly grazed pastures had higher bacterial content than intensively grazed systems. Since grazing intensity changes the plant species composition, the bacterial population and diversity also change. Hu et al. [182] found that fungal populations, like bacteria, decreased under high grazing intensity and with soil depth. In addition, fungi were higher in total number and relative to bacteria under light grazing. However, according to Musiał, Kryszak, Grzebisz, Wolna-Maruwka, and Łukowiak [184], the increase in fungal population was five times higher after mowing than after grazing.

6.2. Changes in Microbial and Enzyme Activity after Manure Application

Enzymatic activities depend on various factors such as soil texture and moisture, substrate, temperature, and humic substances [185]. Nevertheless, manure application had a direct effect on microbial and enzyme activity in grassland soils [173], independent of other factors such as climatic conditions or soil properties [24]. Enzyme activity is essential for nutrient recycling in grassland soils, especially for N and P [186]. Dong et al. [187] showed the importance of the form of added N for enzyme activities. In organic treatments, the phenol oxidase and peroxidase had 19% and 43%, respectively, the highest increase of all treatments. N-acquiring enzymes were stimulated regardless of the form of fertilization. Based on a study by Neufeld et al. [173], the type of manure had no significant effect on microbial and enzyme activity. However, each type of manure application had a positive effect on microbial activity, although the liquid and solid manures had different levels of C and N. Enzymes were not directly bound to living microbes, as they could bind to organic and clay particles and remain active [173].
According to Mencel et al. [183], enzyme activities are higher under pastures. Due to animal excretion, the SOM and different macro- and microelements increased. This increased the number and activity of different microorganisms. A higher botanical composition in pastures led to a higher composition of bacteria species, inhibiting the roots from specific enzymatic reactions, which accumulated in the soil.
Table 9 provides an overview of the effects of different manure applications on microbial activity and growth in temperate grassland soils.

7. Summary and Conclusions

Temperate grasslands—mostly of anthropogenic origin—are used for meadows, pastures, or mown pastures. Different management practices (intensity, organic versus conventional farming, fertilization techniques, and timing) and the application of organic fertilizers—especially manure—have a strong influence on several grassland characteristics (e.g., forage yield and quality) and on several soil properties, including chemical, physical and biological properties. Fertilization with organic fertilizers is a common practice in grassland management to increase nutrients for optimal plant growth and to increase SOC content to improve soil properties. Fertilization is essential to maintain grassland fertility. Only with high fertility, achieved through fertilization, is it possible to produce high yields of good forage quality from grassland. Manure replenishes nutrient content and improves soil fertility by increasing nutrient storage, pH, physical conditions for water infiltration and root growth, and microbial activity. There is an effect on soil chemical properties such as C and N storage and the content of other nutrients, in this case, P, K, Ca, and Mg. Soil physical properties are improved by manure application. Bulk density is reduced, and porosity and hydraulic conductivity are improved. In addition, larger soil aggregates are formed, and aggregate stability is increased. Biological properties also increase, especially microbial biomass and microbial and enzyme activity.
However, additional factors must be considered when evaluating the impact of organic fertilizers on forage yield and quality. In particular, light and water have a major impact on nutrient yield and value. When water is limited, aboveground biomass does not respond to nutrient application, while when light is limited, belowground biomass response to N is limited.
On the other hand, manure can create a nutrient surplus beyond plant needs and increase losses through greenhouse gas emissions or leaching. The lost nutrients are not only economically lost from the nutrient cycle of the farm, but they can also cause environmental damage. Nutrient losses can be prevented or minimized by using advanced application techniques, such as injection technology, and by applying at times when crops have high nutrient needs and not exceeding nutrient requirements.
Optimizing the use of organic fertilizers by applying the 4R principles of ‘right source’, ‘right rate’, ‘right time’, and ‘right place’ is the best way to improve economic conditions and reduce GHG emissions and leaching [191].
The effects of organic fertilization on temperate grasslands and the advantages over mineral fertilization are more or less well understood, but there is still a lack of widespread implementation in common agricultural practice and acceptance by farmers and society.

8. Recommendation

For sustainable agriculture, it is important to close nutrient cycles and use resources efficiently. Organic manures and animal excreta are valuable nutrient resources and can replace mineral fertilizers. This review provides an overview of their effects on grassland properties and some ideas for their sustainable use:
  • The use of organic fertilizers should be given priority over the use of mineral fertilizers, in accordance with legal requirements, so as not to double the burden on the environment.
  • Mineral fertilizers should be used only when necessary and as an additional source of nutrients.
  • Manure should be used in a way that maximizes its usefulness as a valuable fertilizer and minimizes its negative impact on the environment.
  • Manure fertilization should be based on up-to-date data on the amount and composition of all relevant nutrients, especially nitrogen and phosphorus.
  • To avoid over-fertilization and the loss of valuable nutrients through leaching or greenhouse gas emissions, soil status should be known, at least for nitrogen and phosphorus.
  • Fertilization planning should be based on soil data and long-term yield data, which determine the actual nutrient demand of plants.
  • Organic fertilizers should be applied only during the growing season when plants have high nutrient requirements.
  • Nutrient losses due to leaching and greenhouse gas emissions must be avoided by using appropriate application techniques, such as broad band spreaders or injection techniques.
  • Organic fertilizers should be used instead of mineral fertilizers to increase carbon inputs and thus improve many soil parameters, which at the same time increases soil fertility and resilience to climate change impacts such as droughts or heavy rainfall.
  • Organic fertilizers should be applied in a manner and at a rate that promotes active soil life.
  • Livestock densities should be adapted so that the positive effects of excreta on soil and plant parameters and their diversity are not negated by trampling and increased biomass decomposition.
  • Knowledge transfer between scientists, policy makers, and farmers should be intensified at local, national, and global levels.

Author Contributions

A.B.: Conceptualization (equal); Investigation (lead); Writing—original draft (lead); Writing—review and editing (supporting). K.K.: Conceptualization (equal); Investigation (supporting); Supervision (lead); Writing—original draft (supporting); Writing—review and editing (lead). All authors have read and agreed to the published version of the manuscript.

Funding

This overview study was conducted during the period of the SuMaNu- Sustainable Manure and Nutrient Management for reduction of nutrient loss in the Baltic Sea Region-project platform, which was co-financed by Interreg Baltic Sea Region Programme and European Regional Development Fund of EU.

Data Availability Statement

For this study, we used only publicly available data from the listed references and from the Manure Standards project (see https://msdb.netlify.app/ accessed on 5 December 2023). No new data was created for this study.

Acknowledgments

We thank all project colleagues of SuMaNu project platform for fruitful discussions and suggestions on the content of the paper. The authors would also like to thank Leonie Kuka for editing the manuscript.

Conflicts of Interest

All authors declare that they have no competing interests related to any of the topics or materials discussed in this manuscript.

References

  1. Eurostat. Crop Production in EU Standard Humidity (from 2000 onwards): Utilised Agricultural Area by Categories; Online Data Code: TAG00025, 2021. Available online: https://ec.europa.eu (accessed on 23 October 2023).
  2. Gilhaus, K.; Boch, S.; Fischer, M.; Hölzel, N.; Kleinebecker, T.; Prati, D.; Rupprecht, D.; Schmitt, B.; Klaus, V.H. Grassland management in Germany: Effects on plant diversity and vegetation composition. Tuexenia 2017, 37, 379–397. [Google Scholar] [CrossRef]
  3. Dengler, J.; Birge, T.; Bruun, H.H.; Rašomavičius, V.; Rūsiņa, S.; Sickel, H. Grasslands of Northern Europe and the Baltic States. In Encyclopedia of the World’s Biomes; Elsevier: Amsterdam, The Netherlands, 2020; pp. 689–702. ISBN 9780128160978. [Google Scholar]
  4. DiPaolo, D.A. Grassland and Shrublands—An Overview. In Encyclopedia of the World’s Biomes; Elsevier: Amsterdam, The Netherlands, 2020; pp. 414–423. ISBN 9780128160978. [Google Scholar]
  5. Zhao, Y.; Liu, Z.; Wu, J. Grassland ecosystem services: A systematic review of research advances and future directions. Landsc. Ecol. 2020, 35, 793–814. [Google Scholar] [CrossRef]
  6. Schaub, S.; Finger, R.; Leiber, F.; Probst, S.; Kreuzer, M.; Weigelt, A.; Buchmann, N.; Scherer-Lorenzen, M. Plant diversity effects on forage quality, yield and revenues of semi-natural grasslands. Nat. Commun. 2020, 11, 768. [Google Scholar] [CrossRef] [PubMed]
  7. Ceotto, E. Grasslands for bioenergy production. A review. Agron. Sustain. Dev. 2008, 28, 47–55. [Google Scholar] [CrossRef]
  8. Kizeková, M.; Hopkins, A.; Kanianska, R.; Makovníková, J.; Pollák, Š.; Pálka, B. Changes in the area of permanent grassland and its implications for the provision of bioenergy: Slovakia as a case study. Grass Forage Sci. 2018, 73, 218–232. [Google Scholar] [CrossRef]
  9. Galloway, J.N.; Townsend, A.R.; Erisman, J.W.; Bekunda, M.; Cai, Z.; Freney, J.R.; Martinelli, L.A.; Seitzinger, S.P.; Sutton, M.A. Transformation of the nitrogen cycle: Recent trends, questions, and potential solutions. Science 2008, 320, 889–892. [Google Scholar] [CrossRef] [PubMed]
  10. Hill, D.N.; Popova, I.E.; Hammel, J.E.; Morra, M.J. Transport of Potential Manure Hormone and Pharmaceutical Contaminants through Intact Soil Columns. J. Environ. Qual. 2019, 48, 47–56. [Google Scholar] [CrossRef] [PubMed]
  11. Xu, R.; Tian, H.; Pan, S.; Dangal, S.R.S.; Chen, J.; Chang, J.; Lu, Y.; Skiba, U.M.; Tubiello, F.N.; Zhang, B. Increased nitrogen enrichment and shifted patterns in the world’s grassland: 1860–2016. Earth Syst. Sci. Data 2019, 11, 175–187. [Google Scholar] [CrossRef]
  12. Kidd, J.; Manning, P.; Simkin, J.; Peacock, S.; Stockdale, E. Impacts of 120 years of fertilizer addition on a temperate grassland ecosystem. PLoS ONE 2017, 12, e0174632. [Google Scholar] [CrossRef]
  13. Heyburn, J.; McKenzie, P.; Crawley, M.J.; Fornara, D.A. Effects of grassland management on plant C:N:P stoichiometry: Implications for soil element cycling and storage. Ecosphere 2017, 8, e01963. [Google Scholar] [CrossRef]
  14. Petersen, S.O.; Sommer, S.G.; Béline, F.; Burton, C.; Dach, J.; Dourmad, J.Y.; Leip, A.; Misselbrook, T.; Nicholson, F.; Poulsen, H.D.; et al. Recycling of livestock manure in a whole-farm perspective. Livest. Sci. 2007, 112, 180–191. [Google Scholar] [CrossRef]
  15. Janzen, R.A.; McGill, W.B.; Leonard, J.J.; Jeffrey, S.R. Manure as a resource—Ecological and economic considerations in balance. Trans. ASAE 1999, 42, 1261–1274. [Google Scholar] [CrossRef]
  16. van der Meer, H.G. Optimising manure management for GHG outcomes. Aust. J. Exp. Agric. 2008, 48, 38. [Google Scholar] [CrossRef]
  17. Lewu, F.B.; Volova, T.; Thomas, S.; Rakhimol, K.R. (Eds.) Controlled Release Fertilizers for Sustainable Agriculture; Academic Press: Cambridge, MA, USA, 2021; ISBN 978-0-12-819555-0. [Google Scholar]
  18. Shaji, H.; Chandran, V.; Mathew, L. Chapter 13—Organic Fertilizers as a Route to Controlled Release of Nutrients. In Controlled Release Fertilizers for Sustainable Agriculture; Lewu, F.B., Volova, T., Thomas, S., Rakhimol, K.R., Eds.; Academic Press: Cambridge, MA, USA, 2021; pp. 231–245. ISBN 978-0-12-819555-0. [Google Scholar]
  19. Henuk, Y.; Dingle, J. Poultry manure: Source of fertilizer, fuel and feed. World’s Poult. Sci. J. 2003, 59, 350–360. [Google Scholar] [CrossRef]
  20. van Middelkoop, J.C.; van der Salm, C.; Ehlert, P.A.I.; de Boer, I.J.M.; Oenema, O. Does balanced phosphorus fertilisation sustain high herbage yields and phosphorus contents in alternately grazed and mown pastures? Nutr. Cycl. Agroecosystems 2016, 106, 93–111. [Google Scholar] [CrossRef]
  21. Pecio, A.; Jarosz, Z. Long-term effects of soil management practices on selected indicators of chemical soil quality. Acta Agrobot. 2016, 69, 1–21. [Google Scholar] [CrossRef]
  22. Dong, S.; Sui, B.; Shen, Y.; Meng, H.; Zhao, L.; Ding, J.; Zhou, H.; Zhang, X.; Cheng, H.; Wang, J. Investigation and analysis of the linkage mechanism and whole process cost of livestock manure organic fertilizer. Int. J. Agric. Biol. Eng. 2020, 13, 223–227. [Google Scholar] [CrossRef]
  23. Gross, A.; Glaser, B. Meta-analysis on how manure application changes soil organic carbon storage. Sci. Rep. 2021, 11, 5516. [Google Scholar] [CrossRef]
  24. Liu, S.; Wang, J.; Pu, S.; Blagodatskaya, E.; Kuzyakov, Y.; Razavi, B.S. Impact of manure on soil biochemical properties: A global synthesis. Sci. Total Environ. 2020, 745, 141003. [Google Scholar] [CrossRef]
  25. Pain, B.F.; Misselbrook, T.H.; Clarkson, C.R.; Rees, Y.J. Odour and ammonia emissions following the spreading of anaerobically-digested pig slurry on grassland. Biol. Wastes 1990, 34, 259–267. [Google Scholar] [CrossRef]
  26. Prins, W.H.; Snijders, P.J.M. Negative Effects of Animal Manure on Grassland Due to Surface Spreading and Injection. In Animal Manure on Grassland and Fodder Crops. Fertilizer or Waste? Proceedings of an International Symposium of the European Grassland Federation, Wageningen, The Netherlands, 31 August–3 September 1987; van der Meer, H.G., Unwin, R.J., van Dijk, T.A., Ennik, G.C., Eds.; Springer: Dordrecht, The Netherlands, 1987; pp. 119–135. ISBN 978-94-009-3659-1. [Google Scholar]
  27. Sindhöj, E.; Krysztoforski, M.; Kuka, K.; Luostarinen, S.; Melnalksne, Z.; Mjöfors, K.; Riiko, K.; Tamm, K.; Ylivainio, K.; Sarvi, M. Technologies and Management Practices for Sustainable Manure Use in the Baltic Sea Region; RISE Research Institutes of Sweden: Upsala, Sweden, 2020. [Google Scholar]
  28. Soussana, J.-F.; Lemaire, G. Coupling carbon and nitrogen cycles for environmentally sustainable intensification of grasslands and crop-livestock systems. Agric. Ecosyst. Environ. 2014, 190, 9–17. [Google Scholar] [CrossRef]
  29. Jones, S.K.; Rees, R.M.; Skiba, U.M.; Ball, B.C. Greenhouse gas emissions from a managed grassland. Glob. Planet. Chang. 2005, 47, 201–211. [Google Scholar] [CrossRef]
  30. Bicudo, J.R.; Goyal, S.M. Pathogens and manure management systems: A review. Environ. Technol. 2003, 24, 115–130. [Google Scholar] [CrossRef] [PubMed]
  31. van Eekeren, N.; de Boer, H.; Bloem, J.; Schouten, T.; Rutgers, M.; de Goede, R.; Brussaard, L. Soil biological quality of grassland fertilized with adjusted cattle manure slurries in comparison with organic and inorganic fertilizers. Biol. Fertil. Soils 2009, 45, 595–608. [Google Scholar] [CrossRef]
  32. Schils, R.; Kok, I. Effects of cattle slurry manure management on grass yield. NJAS-Wagening. J. Life Sci. 2003, 51, 41–65. [Google Scholar] [CrossRef]
  33. Reijneveld, J.A.; Abbink, G.W.; Termorshuizen, A.J.; Oenema, O. Relationships between soil fertility, herbage quality and manure composition on grassland-based dairy farms. Eur. J. Agron. 2014, 56, 9–18. [Google Scholar] [CrossRef]
  34. Blüthgen, N.; Dormann, C.F.; Prati, D.; Klaus, V.H.; Kleinebecker, T.; Hölzel, N.; Alt, F.; Boch, S.; Gockel, S.; Hemp, A.; et al. A quantitative index of land-use intensity in grasslands: Integrating mowing, grazing and fertilization. Basic Appl. Ecol. 2012, 13, 207–220. [Google Scholar] [CrossRef]
  35. Vogt, J.; Klaus, V.H.; Both, S.; Fürstenau, C.; Gockel, S.; Gossner, M.M.; Heinze, J.; Hemp, A.; Hölzel, N.; Jung, K.; et al. Eleven years’ data of grassland management in Germany. Biodivers. Data J. 2019, 7, e36387. [Google Scholar] [CrossRef]
  36. Stybnarova, M.; Hakl, J.; Bilosova, H.; Micova, P.; Latal, O.; Pozdisek, J. Effect of cutting frequency on species richness and dry matter yield of permanent grassland after grazing cessation. Arch. Agron. Soil Sci. 2016, 7, 1–12. [Google Scholar] [CrossRef]
  37. Schrama, M.J.J.; Cordlandwehr, V.; Visser, E.J.W.; Elzenga, T.M.; de Vries, Y.; Bakker, J.P. Grassland cutting regimes affect soil properties, and consequently vegetation composition and belowground plant traits. Plant Soil 2013, 366, 401–413. [Google Scholar] [CrossRef]
  38. Dubeux, J.C.; Sollenberger, L.E. Nutrient Cycling in Grazed Pastures. In Management Strategies for Sustainable Cattle Production in Southern Pastures; Elsevier: Amsterdam, The Netherlands, 2020; pp. 59–75. ISBN 9780128144749. [Google Scholar]
  39. Socher, S.A.; Prati, D.; Boch, S.; Müller, J.; Klaus, V.H.; Hölzel, N.; Fischer, M. Direct and productivity-mediated indirect effects of fertilization, mowing and grazing on grassland species richness. J. Ecol. 2012, 100, 1391–1399. [Google Scholar] [CrossRef]
  40. Mayel, S.; Jarrah, M.; Kuka, K. How does grassland management affect physical and biochemical properties of temperate grassland soils? A review study. Grass Forage Sci. 2021, 76, 215–244. [Google Scholar] [CrossRef]
  41. Binnie, R.C.; Chestnutt, D.M.B. Effect of regrowth interval on the productivity of swards defoliated by cutting and grazing. Grass Forage Sci. 1991, 46, 343–350. [Google Scholar] [CrossRef]
  42. Drennan, M.J.; McGee, M. Performance of spring-calving beef suckler cows and their progeny to slaughter on intensive and extensive grassland management systems. Livest. Sci. 2009, 120, 1–12. [Google Scholar] [CrossRef] [PubMed]
  43. Fu, J.; Gasche, R.; Wang, N.; Lu, H.; Butterbach-Bahl, K.; Kiese, R. Dissolved organic carbon leaching from montane grasslands under contrasting climate, soil and management conditions. Biogeochemistry 2019, 145, 47–61. [Google Scholar] [CrossRef]
  44. Ammann, C.; Flechard, C.R.; Leifeld, J.; Neftel, A.; Fuhrer, J. The carbon budget of newly established temperate grassland depends on management intensity. Agric. Ecosyst. Environ. 2007, 121, 5–20. [Google Scholar] [CrossRef]
  45. Fornara, D.A.; Wasson, E.-A.; Christie, P.; Watson, C.J. Long-term nutrient fertilization and the carbon balance of permanent grassland: Any evidence for sustainable intensification? Biogeosciences 2016, 13, 4975–4984. [Google Scholar] [CrossRef]
  46. Metzger, C.M.H.; Heinichen, J.; Eickenscheidt, T.; Drösler, M. Impact of land-use intensity on the relationships between vegetation indices, photosynthesis and biomass of intensively and extensively managed grassland fens. Grass Forage Sci. 2017, 72, 50–63. [Google Scholar] [CrossRef]
  47. Wang, J.; Zhao, C.; Zhao, L.; Wen, J.; Li, Q. Effects of grazing on the allocation of mass of soil aggregates and aggregate-associated organic carbon in an alpine meadow. PLoS ONE 2020, 15, e0234477. [Google Scholar] [CrossRef]
  48. Haas, G.; Wetterich, F.; Köpke, U. Comparing intensive, extensified and organic grassland farming in southern Germany by process life cycle assessment. Agric. Ecosyst. Environ. 2001, 83, 43–53. [Google Scholar] [CrossRef]
  49. Allard, V.; Newton, P.C.D.; Lieffering, M.; Clark, H.; Matthew, C.; Soussana, J.-F.; Gray, Y.S. Nitrogen cycling in grazed pastures at elevated CO2: N returns by ruminants. Glob. Chang. Biol. 2003, 9, 1731–1742. [Google Scholar] [CrossRef]
  50. Orr, R.J.; Griffith, B.A.; Champion, R.A.; Cook, J.E. Defaecation and urination behaviour in beef cattle grazing semi-natural grassland. Appl. Anim. Behav. Sci. 2012, 139, 18–25. [Google Scholar] [CrossRef]
  51. Schellberg, J.; Südekum, K.-H.; Gebbing, T. Effect of herbage on N intake and N excretion of suckler cows. Agron. Sustain. Dev. 2007, 27, 303–311. [Google Scholar] [CrossRef]
  52. Ondrášek, Ľ.; Čunderlík, J. Effects of organic and mineral fertilisers on biological properties of soil under seminatural grassland. Plant Soil Environ. 2008, 54, 329–335. [Google Scholar] [CrossRef]
  53. Ludvíková, V.; Pavlů, V.; Pavlů, L.; Gaisler, J.; Hejcman, M. Sward-height patches under intensive and extensive grazing density in an Agrostis capillaris grassland. Folia Geobot. 2015, 50, 219–228. [Google Scholar] [CrossRef]
  54. Haygarth, P.M.; Chapman, P.J.; Jarvis, S.C.; Smith, R.V. Phosphorus budgets for two contrasting grassland farming systems in the UK. Soil Use Manag. 1998, 14, 160–167. [Google Scholar] [CrossRef]
  55. Marsden, K.A.; Holmberg, J.A.; Jones, D.L.; Chadwick, D.R. Sheep urine patch N2O emissions are lower from extensively-managed than intensively-managed grasslands. Agric. Ecosyst. Environ. 2018, 265, 264–274. [Google Scholar] [CrossRef]
  56. Hanson, G.D.; Ford, S.A.; Parsons, R.L.; Cunningham, L.C.; Muller, L.D. Increasing Intensity of Pasture Use with Dairy Cattle: An Economic Analysis. J. Prod. Agric. 1998, 11, 175–179. [Google Scholar] [CrossRef]
  57. Conant, R.T.; Six, J.; Paustian, K. Land use effects on soil carbon fractions in the southeastern United States. I. Management-intensive versus extensive grazing. Biol. Fertil. Soils 2003, 38, 386–392. [Google Scholar] [CrossRef]
  58. Hathaway-Jenkins, L.J.; Sakrabani, R.; Pearce, B.; Whitmore, A.P.; Godwin, R.J. A comparison of soil and water properties in organic and conventional farming systems in England. Soil Use Manag. 2011, 27, 133–142. [Google Scholar] [CrossRef]
  59. Klaus, V.H.; Hölzel, N.; Prati, D.; Schmitt, B.; Schöning, I.; Schrumpf, M.; Fischer, M.; Kleinebecker, T. Organic vs. conventional grassland management: Do 15N and 13C isotopic signatures of hay and soil samples differ? PLoS ONE 2013, 8, e78134. [Google Scholar] [CrossRef] [PubMed]
  60. Gisiger, L. Organic manuring of grassland*. Grass Forage Sci. 1950, 5, 63–79. [Google Scholar] [CrossRef]
  61. Larkin, R.P.; Honeycutt, C.W.; Griffin, T.S. Effect of swine and dairy manure amendments on microbial communities in three soils as influenced by environmental conditions. Biol. Fertil. Soils 2006, 43, 51–61. [Google Scholar] [CrossRef]
  62. Shand, C.A.; Coutts, G. The effects of sheep faeces on soil solution composition. Plant Soil 2006, 285, 135–148. [Google Scholar] [CrossRef]
  63. Nicholson, F.A.; Chambers, B.J.; Smith, K.A. Nutrient composition of poultry manures in England and Wales. Bioresour. Technol. 1996, 58, 279–284. [Google Scholar] [CrossRef]
  64. Rieck-Hinz, A.M.; Miller, G.A.; Schafer, J.W. Nutrient Content of Dairy Manure from Three Handling Systems. J. Prod. Agric. 1996, 9, 82–86. [Google Scholar] [CrossRef]
  65. van der Stelt, B.; van Vliet, P.C.J.; Reijs, J.W.; Temminghoff, E.J.M.; van Riemsdijk, W.H. Effects of dietary protein and energy levels on cow manure excretion and ammonia volatilization. J. Dairy Sci. 2008, 91, 4811–4821. [Google Scholar] [CrossRef]
  66. Ziemer, C.J.; Kerr, B.J.; Trabue, S.L.; Stein, H.; Stahl, D.A.; Davidson, S.K. Dietary protein and cellulose effects on chemical and microbial characteristics of Swine feces and stored manure. J. Environ. Qual. 2009, 38, 2138–2146. [Google Scholar] [CrossRef]
  67. Latshaw, J.D.; Zhao, L. Dietary protein effects on hen performance and nitrogen excretion. Poult. Sci. 2011, 90, 99–106. [Google Scholar] [CrossRef]
  68. Rammer, C.; Lingvall, P. Influence of farmyard manure on the quality of grass silage. J. Sci. Food Agric. 1997, 75, 133–140. [Google Scholar] [CrossRef]
  69. Nicholson, F.A.; Groves, S.J.; Chambers, B.J. Pathogen survival during livestock manure storage and following land application. Bioresour. Technol. 2005, 96, 135–143. [Google Scholar] [CrossRef]
  70. van der Ploeg, J.D.; Groot, J.; Verhoeven, F.; Lantinga, E.A. Interpretation of results from on-farm experiments: Manure-nitrogen recovery on grassland as affected by manure quality and application technique. 2. A sociological analysis. NJAS-Wagening. J. Life Sci. 2007, 54, 255–268. [Google Scholar] [CrossRef]
  71. Bourdin, F.; Sakrabani, R.; Kibblewhite, M.G.; Lanigan, G.J. Effect of slurry dry matter content, application technique and timing on emissions of ammonia and greenhouse gas from cattle slurry applied to grassland soils in Ireland. Agric. Ecosyst. Environ. 2014, 188, 122–133. [Google Scholar] [CrossRef]
  72. Huijsmans, J.; Hol, J.; Hendriks, M. Effect of application technique, manure characteristics, weather and field conditions on ammonia volatilization from manure applied to grassland. NJAS-Wagening. J. Life Sci. 2001, 49, 323–342. [Google Scholar] [CrossRef]
  73. Groot, J.; van der Ploeg, J.D.; Verhoeven, F.; Lantinga, E.A. Interpretation of results from on-farm experiments: Manure-nitrogen recovery on grassland as affected by manure quality and application technique. 1. An agronomic analysis. NJAS-Wagening. J. Life Sci. 2007, 54, 235–254. [Google Scholar] [CrossRef]
  74. Misselbrook, T.H.; Nicholson, F.A.; Chambers, B.J. Predicting ammonia losses following the application of livestock manure to land. Bioresour. Technol. 2005, 96, 159–168. [Google Scholar] [CrossRef]
  75. Nicholson, F.A.; Bhogal, A.; Rollett, A.; Taylor, M.; Williams, J.R. Precision application techniques reduce ammonia emissions following food-based digestate applications to grassland. Nutr. Cycl. Agroecosystems 2018, 110, 151–159. [Google Scholar] [CrossRef]
  76. Keidel, L.; Lenhart, K.; Moser, G.; Müller, C. Depth-dependent response of soil aggregates and soil organic carbon content to long-term elevated CO2 in a temperate grassland soil. Soil Biol. Biochem. 2018, 123, 145–154. [Google Scholar] [CrossRef]
  77. Häni, C.; Sintermann, J.; Kupper, T.; Jocher, M.; Neftel, A. Ammonia emission after slurry application to grassland in Switzerland. Atmos. Environ. 2016, 125, 92–99. [Google Scholar] [CrossRef]
  78. Rodhe, L.; Pell, M.; Yamulki, S. Nitrous oxide, methane and ammonia emissions following slurry spreading on grassland. Soil Use Manag. 2006, 22, 229–237. [Google Scholar] [CrossRef]
  79. Thorman, R.E.; Nicholson, F.A.; Topp, C.F.E.; Bell, M.J.; Cardenas, L.M.; Chadwick, D.R.; Cloy, J.M.; Misselbrook, T.H.; Rees, R.M.; Watson, C.J.; et al. Towards Country-Specific Nitrous Oxide Emission Factors for Manures Applied to Arable and Grassland Soils in the UK. Front. Sustain. Food Syst. 2020, 4, 359. [Google Scholar] [CrossRef]
  80. Misselbrook, T.H.; Smith, K.A.; Johnson, R.A.; Pain, B.F. SE—Structures and Environment. Biosyst. Eng. 2002, 81, 313–321. [Google Scholar] [CrossRef]
  81. Uusi-Kämppä, J.; Mattila, P.K. Nitrogen losses from grass ley after slurry application surface broadcasting vs. injection. Agric. Food Sci. 2010, 19, 327. [Google Scholar] [CrossRef]
  82. Sørensen, P.; Rubæk, G.H. Leaching of nitrate and phosphorus after autumn and spring application of separated solid animal manures to winter wheat. Soil Use Manag. 2012, 28, 1–11. [Google Scholar] [CrossRef]
  83. Smith, K.A.; Beckwith, C.P.; Chalmers, A.G.; Jackson, D.R. Nitrate leaching following autumn and winter application of animal manures to grassland. Soil Use Manag. 2002, 18, 428–434. [Google Scholar] [CrossRef]
  84. He, W.; Dutta, B.; Grant, B.B.; Chantigny, M.H.; Hunt, D.; Bittman, S.; Tenuta, M.; Worth, D.; VanderZaag, A.; Desjardins, R.L.; et al. Assessing the effects of manure application rate and timing on nitrous oxide emissions from managed grasslands under contrasting climate in Canada. Sci. Total Environ. 2020, 716, 135374. [Google Scholar] [CrossRef] [PubMed]
  85. Schröder, J.J.; Uenk, D.; Hilhorst, G.J. Long-term nitrogen fertilizer replacement value of cattle manures applied to cut grassland. Plant Soil 2007, 299, 83–99. [Google Scholar] [CrossRef]
  86. Simić, A.; Marković, J.; Bojan Stojanović, S.V.; Violeta Mandić, Z.B.; Dželetović, Ž. The use of different N sources for the treatment of permanent grassland and effect on forage quality. Emir. J. Food Agric. 2019, 31, 180–187. [Google Scholar] [CrossRef]
  87. Štýbnarová, M.; Mičová, P.; Fiala, K.; Karabcová, H.; Látal, O.; Pozdíšek, J. Effect of Organic Fertilizers on Botanical Composition of Grassland, Herbage Yield and Quality. Agriculture (Pol’nohospodárstvo) 2014, 60, 87–97. [Google Scholar] [CrossRef]
  88. Cleland, E.E.; Lind, E.M.; DeCrappeo, N.M.; DeLorenze, E.; Wilkins, R.A.; Adler, P.B.; Bakker, J.D.; Brown, C.S.; Davies, K.F.; Esch, E.; et al. Belowground Biomass Response to Nutrient Enrichment Depends on Light Limitation Across Globally Distributed Grasslands. Ecosystems 2019, 22, 1466–1477. [Google Scholar] [CrossRef]
  89. Kacorzyk, P.; Głąb, T. Effect of ten years of mineral and organic fertilization on the herbage production of a mountain meadow. J. Elem. 2012, 22, 219–233. [Google Scholar] [CrossRef]
  90. Augustenborg, C.A.; Carton, O.T.; Schulte, R.; Suffet, I.H. Response of silage yield to land application of out-wintering pad effluent in Ireland. Agric. Water Manag. 2008, 95, 367–374. [Google Scholar] [CrossRef]
  91. Kayser, M.; Isselstein, J. Potassium cycling and losses in grassland systems: A review. Grass Forage Sci. 2005, 60, 213–224. [Google Scholar] [CrossRef]
  92. Pavlů, K.; Kassahun, T.; Nwaogu, C.; Pavlů, L.; Gaisler, J.; Homolka, P.; Pavlů, V. Effect of grazing intensity and dung on herbage and soil nutrients. Plant Soil Environ. 2019, 65, 343–348. [Google Scholar] [CrossRef]
  93. Simić, A.; Stojanović, B.; Vučković, S.; Marković, J.; Božičković, A.; Bijelić, Z.; Mandić, V. Application of farmyard manure in grassland production. AGR 2016, 1, 20–27. [Google Scholar] [CrossRef]
  94. Chen, W.; Huang, D.; Liu, N.; Zhang, Y.; Badgery, W.B.; Wang, X.; Shen, Y. Improved grazing management may increase soil carbon sequestration in temperate steppe. Sci. Rep. 2015, 5, 10892. [Google Scholar] [CrossRef]
  95. Yoshihara, Y.; Furusawa, S.; Sato, S. Recent pasture management determines biodiversity and productivity, and past management determines forage quality. Écoscience 2016, 23, 89–96. [Google Scholar] [CrossRef]
  96. Knežević, M.; Leto, J.; Perčulija, G.; Bošnjak, K.; Vranić, M. Effects of liquid manure application on yield, quality and botanical composition of grassland. Cereal Res. Commun. 2007, 35, 637–640. [Google Scholar] [CrossRef]
  97. Tampere, M.; Kauer, K.; Keres, I.; Loit, E.; Selge, A.; Viiralt, R.; Raave, H. The effect of fertilizer and N application rate on nitrogen and potassium leaching in cut grassland. Zemdirb. Agric. 2015, 102, 381–388. [Google Scholar] [CrossRef]
  98. Głąb, T.; Kacorzyk, P. Root distribution and herbage production under different management regimes of mountain grassland. Soil Tillage Res. 2011, 113, 99–104. [Google Scholar] [CrossRef]
  99. Jones, S.K.; Rees, R.M.; Skiba, U.M.; Ball, B.C. Influence of organic and mineral N fertiliser on N2O fluxes from a temperate grassland. Agric. Ecosyst. Environ. 2007, 121, 74–83. [Google Scholar] [CrossRef]
  100. Saarijärvi, K.; Virkajärvi, P.; Heinonen-Tanski, H.; Taipalinen, I. N and P leaching and microbial contamination from intensively managed pasture and cut sward on sandy soil in Finland. Agric. Ecosyst. Environ. 2004, 104, 621–630. [Google Scholar] [CrossRef]
  101. van Dobben, H.F.; Quik, C.; Wamelink, G.W.; Lantinga, E.A. Vegetation composition of Lolium perenne-dominated grasslands under organic and conventional farming. Basic Appl. Ecol. 2019, 36, 45–53. [Google Scholar] [CrossRef]
  102. Jones, M.B.; Donnelly, A. Carbon sequestration in temperate grassland ecosystems and the influence of management, climate and elevated CO2. New Phytol. 2004, 164, 423–439. [Google Scholar] [CrossRef]
  103. Jones, S.K.; Rees, R.M.; Kosmas, D.; Ball, B.C.; Skiba, U.M. Carbon sequestration in a temperate grassland; management and climatic controls. Soil Use Manag. 2006, 22, 132–142. [Google Scholar] [CrossRef]
  104. Fornara, D.A.; Banin, L.; Crawley, M.J. Multi-nutrient vs. nitrogen-only effects on carbon sequestration in grassland soils. Glob. Chang. Biol. 2013, 19, 3848–3857. [Google Scholar] [CrossRef]
  105. Cenini, V.L.; Fornara, D.A.; McMullan, G.; Ternan, N.; Lajtha, K.; Crawley, M.J. Chronic nitrogen fertilization and carbon sequestration in grassland soils: Evidence of a microbial enzyme link. Biogeochemistry 2015, 126, 301–313. [Google Scholar] [CrossRef]
  106. Simpson, A.J.; Simpson, M.J.; Smith, E.; Kelleher, B.P. Microbially derived inputs to soil organic matter: Are current estimates too low? Environ. Sci. Technol. 2007, 41, 8070–8076. [Google Scholar] [CrossRef]
  107. Liang, C.; Cheng, G.; Wixon, D.L.; Balser, T.C. An Absorbing Markov Chain approach to understanding the microbial role in soil carbon stabilization. Biogeochemistry 2011, 106, 303–309. [Google Scholar] [CrossRef]
  108. Soussana, J.-F.; Loiseau, P.; Vuichard, N.; Ceschia, E.; Balesdent, J.; Chevallier, T.; Arrouays, D. Carbon cycling and sequestration opportunities in temperate grasslands. Soil Use Manag. 2004, 20, 219–230. [Google Scholar] [CrossRef]
  109. Soussana, J.F.; Allard, V.; Pilegaard, K.; Ambus, P.; Amman, C.; Campbell, C.; Ceschia, E.; Clifton-Brown, J.; Czobel, S.; Domingues, R.; et al. Full accounting of the greenhouse gas (CO2, N2O, CH4) budget of nine European grassland sites. Agric. Ecosyst. Environ. 2007, 121, 121–134. [Google Scholar] [CrossRef]
  110. Sun, F.; Harrison, J.H.; Ndegwa, P.M.; Johnson, K. Effect of Manure Treatment on Ammonia and Greenhouse Gases Emissions Following Surface Application. Water Air Soil Pollut. 2014, 225, 310. [Google Scholar] [CrossRef]
  111. Soussana, J.F.; Tallec, T.; Blanfort, V. Mitigating the greenhouse gas balance of ruminant production systems through carbon sequestration in grasslands. Animal 2010, 4, 334–350. [Google Scholar] [CrossRef] [PubMed]
  112. Kindler, R.; Siemens, J.A.; Kaiser, K.; Walmsley, D.C.; Bernhofer, C.; Buchmann, N.; Cellier, P.; Eugster, W.; Gleixner, G.; Grũnwald, T.; et al. Dissolved carbon leaching from soil is a crucial component of the net ecosystem carbon balance. Glob. Chang. Biol. 2011, 17, 1167–1185. [Google Scholar] [CrossRef]
  113. Sanderman, J.; Amundson, R. A comparative study of dissolved organic carbon transport and stabilization in California forest and grassland soils. Biogeochemistry 2009, 92, 41–59. [Google Scholar] [CrossRef]
  114. Xu, S.; Jagadamma, S.; Ashworth, A.J.; Singh, S.; Owens, P.R.; Moore, P.A. Long-term effects of pasture management and fenced riparian buffers on soil organic carbon content and aggregation. Geoderma 2021, 382, 114666. [Google Scholar] [CrossRef]
  115. Eze, S.; Palmer, S.M.; Chapman, P.J. Soil organic carbon stock in grasslands: Effects of inorganic fertilizers, liming and grazing in different climate settings. J. Environ. Manag. 2018, 223, 74–84. [Google Scholar] [CrossRef]
  116. Jones, S.K.; Helfter, C.; Anderson, M.; Coyle, M.; Campbell, C.; Famulari, D.; Di Marco, C.; van Dijk, N.; Tang, Y.S.; Topp, C.F.E.; et al. The nitrogen, carbon and greenhouse gas budget of a grazed, cut and fertilised temperate grassland. Biogeosciences 2017, 14, 2069–2088. [Google Scholar] [CrossRef]
  117. Paz-Ferreiro, J.; Medina-Roldán, E.; Ostle, N.J.; McNamara, N.P.; Bardgett, R.D. Grazing increases the temperature sensitivity of soil organic matter decomposition in a temperate grassland. Environ. Res. Lett. 2012, 7, 14027. [Google Scholar] [CrossRef]
  118. Voglmeier, K.; Six, J.; Jocher, M.; Ammann, C. Soil greenhouse gas budget of two intensively managed grazing systems. Agric. For. Meteorol. 2020, 287, 107960. [Google Scholar] [CrossRef]
  119. Ghani, A.; Sarathchandra, U.; Ledgard, S.; Dexter, M.; Lindsey, S. Microbial decomposition of leached or extracted dissolved organic carbon and nitrogen from pasture soils. Biol. Fertil. Soils 2013, 49, 747–755. [Google Scholar] [CrossRef]
  120. Ammann, C.; Spirig, C.; Leifeld, J.; Neftel, A. Assessment of the nitrogen and carbon budget of two managed temperate grassland fields. Agric. Ecosyst. Environ. 2009, 133, 150–162. [Google Scholar] [CrossRef]
  121. Chadwick, D.R.; Pain, B.F.; Brookman, S.K.E. Nitrous Oxide and Methane Emissions following Application of Animal Manures to Grassland. J. Environ. Qual. 2000, 29, 277–287. [Google Scholar] [CrossRef]
  122. Köster, J.R.; Cárdenas, L.M.; Bol, R.; Lewicka-Szczebak, D.; Senbayram, M.; Well, R.; Giesemann, A.; Dittert, K. Anaerobic digestates lower N2O emissions compared to cattle slurry by affecting rate and product stoichiometry of denitrification—An N2O isotopomer case study. Soil Biol. Biochem. 2015, 84, 65–74. [Google Scholar] [CrossRef]
  123. Rochette, P.; Gregorich, E.G. Dynamics of soil microbial biomass C, soluble organic C and CO2 evolution after three years of manure application. Can. J. Soil. Sci. 1998, 78, 283–290. [Google Scholar] [CrossRef]
  124. Galloway, J.N.; Dentener, F.J.; Capone, D.G.; Boyer, E.W.; Howarth, R.W.; Seitzinger, S.P.; Asner, G.P.; Cleveland, C.C.; Green, P.A.; Holland, E.A.; et al. Nitrogen Cycles: Past, Present, and Future. Biogeochemistry 2004, 70, 153–226. [Google Scholar] [CrossRef]
  125. Wheeler, M.M.; Dipman, M.M.; Adams, T.A.; Ruina, A.V.; Robins, C.R.; Meyer, W.M. Carbon and nitrogen storage in California sage scrub and non-native grassland habitats. J. Arid. Environ. 2016, 129, 119–125. [Google Scholar] [CrossRef]
  126. Bittman, S.; Forge, T.; Kowalenko, C. Responses of the bacterial and fungal biomass in a grassland soil to multi-year applications of dairy manure slurry and fertilizer. Soil Biol. Biochem. 2005, 37, 613–623. [Google Scholar] [CrossRef]
  127. Li, J.; Shi, Y.; Luo, J.; Houlbrooke, D.; Ledgard, S.; Ghani, A.; Lindsey, S. Effects of form of effluent, season and urease inhibitor on ammonia volatilization from dairy farm effluent applied to pasture. J. Soils Sediments 2014, 14, 1341–1349. [Google Scholar] [CrossRef]
  128. Twigg, M.M.; House, E.; Thomas, R.; Whitehead, J.; Phillips, G.J.; Famulari, D.; Fowler, D.; Gallagher, M.W.; Cape, J.N.; Sutton, M.A.; et al. Surface/atmosphere exchange and chemical interactions of reactive nitrogen compounds above a manured grassland. Agric. For. Meteorol. 2011, 151, 1488–1503. [Google Scholar] [CrossRef]
  129. Jin, T.; Shimizu, M.; Marutani, S.; Desyatkin, A.R.; Iizuka, N.; Hata, H.; Hatano, R. Effect of chemical fertilizer and manure application on N2O emission from reed canary grassland in Hokkaido, Japan. Soil Sci. Plant Nutr. 2010, 56, 53–65. [Google Scholar] [CrossRef]
  130. Jahangir, M.; Khalil, M.I.; Johnston, P.; Cardenas, L.M.; Hatch, D.J.; Butler, M.; Barrett, M.; O’flaherty, V.; Richards, K.G. Denitrification potential in subsoils: A mechanism to reduce nitrate leaching to groundwater. Agric. Ecosyst. Environ. 2012, 147, 13–23. [Google Scholar] [CrossRef]
  131. Watson, C.J.; Foy, R.H. Environmental Impacts of Nitrogen and Phosphorus Cycling in Grassland Systems. Outlook Agric. 2001, 30, 117–127. [Google Scholar] [CrossRef]
  132. Anger, M.; Hüging, H.; Huth, C.; Kühbauch, W. Nitrat-Austräge auf intensiv und extensiv beweidetem Grünland, erfasst mittels Saugkerzen- und Nmin-Beprobung I Einfluss der Beweidungsintensität. Z. Pflanzenernaehr. Bodenk. 2002, 165, 640–647. [Google Scholar] [CrossRef]
  133. Fischer, K.; Burchill, W.; Lanigan, G.J.; Kaupenjohann, M.; Chambers, B.J.; Richards, K.G.; Forrestal, P.J. Ammonia emissions from cattle dung, urine and urine with dicyandiamide in a temperate grassland. Soil Use Manag. 2016, 32, 83–91. [Google Scholar] [CrossRef]
  134. Misselbrook, T.H.; van der Weerden, T.J.; Pain, B.F.; Jarvis, S.C.; Chambers, B.J.; Smith, K.A.; Phillips, V.R.; Demmers, T. Ammonia emission factors for UK agriculture. Atmos. Environ. 2000, 34, 871–880. [Google Scholar] [CrossRef]
  135. Petersen, S.O.; Sommer, S.G.; Aaes, O.; Søegaard, K. Ammonia losses from urine and dung of grazing cattle. Atmos. Environ. 1998, 32, 295–300. [Google Scholar] [CrossRef]
  136. Voglmeier, K.; Jocher, M.; Häni, C.; Ammann, C. Ammonia emission measurements of an intensively grazed pasture. Biogeosciences 2018, 15, 4593–4608. [Google Scholar] [CrossRef]
  137. Bell, M.J.; Rees, R.M.; Cloy, J.M.; Topp, C.F.E.; Bagnall, A.; Chadwick, D.R. Nitrous oxide emissions from cattle excreta applied to a Scottish grassland: Effects of soil and climatic conditions and a nitrification inhibitor. Sci. Total Environ. 2015, 508, 343–353. [Google Scholar] [CrossRef]
  138. Webb, J.; Anthony, S.G.; Brown, L.; Lyons-Visser, H.; Ross, C.; Cottrill, B.; Johnson, P.; Scholefield, D. The impact of increasing the length of the cattle grazing season on emissions of ammonia and nitrous oxide and on nitrate leaching in England and Wales. Agric. Ecosyst. Environ. 2005, 105, 307–321. [Google Scholar] [CrossRef]
  139. van Vliet, L.J.P.; Bittman, S.; Derksen, G.; Kowalenko, C.G. Aerating grassland before manure application reduces runoff nutrient loads in a high rainfall environment. J. Environ. Qual. 2006, 35, 903–911. [Google Scholar] [CrossRef] [PubMed]
  140. Reed, S.C.; Seastedt, T.R.; Mann, C.M.; Suding, K.N.; Townsend, A.R.; Cherwin, K.L. Phosphorus fertilization stimulates nitrogen fixation and increases inorganic nitrogen concentrations in a restored prairie. Appl. Soil Ecol. 2007, 36, 238–242. [Google Scholar] [CrossRef]
  141. McDowell, R.W.; Gray, C.W.; Cameron, K.C.; Di, H.J.; Pellow, R. The efficacy of good practice to prevent long-term leaching losses of phosphorus from an irrigated dairy farm. Agric. Ecosyst. Environ. 2019, 273, 86–94. [Google Scholar] [CrossRef]
  142. Hahn, C.; Prasuhn, V.; Stamm, C.; Schulin, R. Phosphorus losses in runoff from manured grassland of different soil P status at two rainfall intensities. Agric. Ecosyst. Environ. 2012, 153, 65–74. [Google Scholar] [CrossRef]
  143. Laurenson, S.; Houlbrooke, D.J. Nutrient and microbial loss in relation to timing of rainfall following surface application of dairy farm manure slurries to pasture. Soil Res. 2014, 52, 513. [Google Scholar] [CrossRef]
  144. Chardon, W.J.; Aalderink, G.H.; van der Salm, C. Phosphorus leaching from cow manure patches on soil columns. J. Environ. Qual. 2007, 36, 17–22. [Google Scholar] [CrossRef]
  145. Härdtle, W.; von Oheimb, G.; Gerke, A.-K.; Niemeyer, M.; Niemeyer, T.; Assmann, T.; Drees, C.; Matern, A.; Meyer, H. Shifts in N and P Budgets of Heathland Ecosystems: Effects of Management and Atmospheric Inputs. Ecosystems 2009, 12, 298–310. [Google Scholar] [CrossRef]
  146. Kayser, M.; Müller, J.; Isselstein, J. Potassium leaching from cut grassland and from urine patches. Soil Use Manag. 2007, 23, 384–392. [Google Scholar] [CrossRef]
  147. Alfaro, M.A.; Jarvis, S.C.; Gregory, P.J. Potassium budgets in grassland systems as affected by nitrogen and drainage. Soil Use Manag. 2003, 19, 89–95. [Google Scholar] [CrossRef]
  148. Vargas, G.; Verdejo, J.; Rivera, A.; Suárez, D.; Youlton, C.; Celis-Diez, J.L.; Le Bissonnais, Y.; Dovletyarova, E.A.; Neaman, A. The effect of four calcium-based amendments on soil aggregate stability of two sandy topsoils. J. Plant Nutr. Soil Sci. 2019, 182, 159–166. [Google Scholar] [CrossRef]
  149. Kleiber, T.; Golcz, A.; Krzesiński, W. Effect of Magnesium Nutrition of Onion (Allium cepa L.). Part I. Yielding and Nutrient Status. Ecol. Chem. Eng. S 2012, 19, 97–105. [Google Scholar] [CrossRef]
  150. Whalen, J.K.; Chang, C. Macroaggregate Characteristics in Cultivated Soils after 25 Annual Manure Applications. Soil Sci. Soc. Am. J. 2002, 66, 1637–1647. [Google Scholar] [CrossRef]
  151. Di, H.J.; Cameron, K.C. Effects of the nitrification inhibitor dicyandiamide on potassium, magnesium and calcium leaching in grazed grassland. Soil Use Manag. 2004, 20, 2–7. [Google Scholar] [CrossRef]
  152. Alfaro, M.A.; Gregory, P.J.; Jarvis, S.C. Dynamics of Potassium Leaching on a Hillslope Grassland Soil. J. Environ. Qual. 2004, 33, 192. [Google Scholar] [CrossRef] [PubMed]
  153. Naramabuye, F.X.; Haynes, R.J. Short-term effects of three animal manures on soil pH and Al solubility. Soil Res. 2006, 44, 515. [Google Scholar] [CrossRef]
  154. Whalen, J.K.; Chang, C.; Clayton, G.W.; Carefoot, J.P. Cattle Manure Amendments Can Increase the pH of Acid Soils. Soil Sci. Soc. Am. J. 2000, 64, 962–966. [Google Scholar] [CrossRef]
  155. Sokolov, V.K.; VanderZaag, A.; Habtewold, J.; Dunfield, K.; Wagner-Riddle, C.; Venkiteswaran, J.J.; Crolla, A.; Gordon, R. Dairy manure acidification reduces CH4 emissions over short and long-term. Environ. Technol. 2021, 42, 2797–2804. [Google Scholar] [CrossRef]
  156. Miller, J.J.; Sweetland, N.J.; Chang, C. Soil physical properties of a Chernozemic clay loam after 24 years of beef cattle manure application. Can. J. Soil. Sci. 2002, 82, 287–296. [Google Scholar] [CrossRef]
  157. Hargreaves, P.R.; Baker, K.L.; Graceson, A.; Bonnett, S.; Ball, B.C.; Cloy, J.M. Soil compaction effects on grassland silage yields and soil structure under different levels of compaction over three years. Eur. J. Agron. 2019, 109, 125916. [Google Scholar] [CrossRef]
  158. Mestdagh, I.; Lootens, P.; van Cleemput, O.; Carlier, L. Variation in organic-carbon concentration and bulk density in Flemish grassland soils. Z. Pflanzenernaehr. Bodenk. 2006, 169, 616–622. [Google Scholar] [CrossRef]
  159. Pietola, L.; Horn, R.; Yli-Halla, M. Effects of trampling by cattle on the hydraulic and mechanical properties of soil. Soil Tillage Res. 2005, 82, 99–108. [Google Scholar] [CrossRef]
  160. Hassink, J.; Whitmore, A.P.; Kubát, J. Size and density fractionation of soil organic matter and the physical capacity of soils to protect organic matter. Eur. J. Agron. 1997, 7, 189–199. [Google Scholar] [CrossRef]
  161. Dlapa, P.; Hriník, D.; Hrabovský, A.; Šimkovic, I.; Žarnovičan, H.; Sekucia, F.; Kollár, J. The Impact of Land-Use on the Hierarchical Pore Size Distribution and Water Retention Properties in Loamy Soils. Water 2020, 12, 339. [Google Scholar] [CrossRef]
  162. Kirchmann, H.; Gerzabek, M.H. Relationship between soil organic matter and micropores in a long-term experiment at Ultuna, Sweden. Z. Pflanzenernaehr. Bodenk. 1999, 162, 493–498. [Google Scholar] [CrossRef]
  163. Schwartz, R.C.; Evett, S.R.; Unger, P.W. Soil hydraulic properties of cropland compared with reestablished and native grassland. Geoderma 2003, 116, 47–60. [Google Scholar] [CrossRef]
  164. Greenwood, K.L.; MacLeod, D.A.; Scott, J.M.; Hutchinson, K.J. Changes to soil physical properties after grazing exclusion. Soil Use Manag. 1998, 14, 19–24. [Google Scholar] [CrossRef]
  165. Schjønning, P.; Iversen, B.V.; Munkholm, L.J.; Labouriau, R.; Jacobsen, O.H. Pore characteristics and hydraulic properties of a sandy loam supplied for a century with either animal manure or mineral fertilizers. Soil Use Manag. 2005, 21, 265–275. [Google Scholar] [CrossRef]
  166. Linsler, D.; Geisseler, D.; Loges, R.; Taube, F.; Ludwig, B. Effects of tillage and application of cattle slurry on carbon pools and aggregate distribution in temperate grassland soils. J. Plant Nutr. Soil Sci. 2014, 177, 388–394. [Google Scholar] [CrossRef]
  167. Zhanhui, Z.; Congzhi, Z.; Jiabao, Z.; Changhua, L.; Qicong, W. Fertilizer impacts on soil aggregation and aggregate-associated organic components. Plant Soil Environ. 2018, 64, 338–343. [Google Scholar] [CrossRef]
  168. Ding, X.; Liang, C.; Zhang, B.; Yuan, Y.; Han, X. Higher rates of manure application lead to greater accumulation of both fungal and bacterial residues in macroaggregates of a clay soil. Soil Biol. Biochem. 2015, 84, 137–146. [Google Scholar] [CrossRef]
  169. Wortmann, C.S.; Shapiro, C.A. The effects of manure application on soil aggregation. Nutr. Cycl. Agroecosyst. 2008, 80, 173–180. [Google Scholar] [CrossRef]
  170. Wang, H.; Wu, J.; Li, G.; Yan, L. Changes in soil carbon fractions and enzyme activities under different vegetation types of the northern Loess Plateau. Ecol. Evol. 2020, 68, 140. [Google Scholar] [CrossRef] [PubMed]
  171. Goyal, S.; Mishra, M.M.; Dhankar, S.S.; Kapoor, K.K.; Batra, R. Microbial biomass turnover and enzyme activities following the application of farmyard manure to field soils with and without previous long-term applications. Biol. Fertil. Soils 1993, 15, 60–64. [Google Scholar] [CrossRef]
  172. Hopkins, D.W.; Waite, I.S.; O’Donnell, A.G. Microbial biomass, organic matter mineralization and nitrogen in soils from long-term experimental grassland plots (Palace Leas meadow hay plots, UK). Eur. J. Soil Sci. 2011, 62, 95–104. [Google Scholar] [CrossRef]
  173. Neufeld, K.R.; Grayston, S.J.; Bittman, S.; Krzic, M.; Hunt, D.E.; Smukler, S.M. Long-term alternative dairy manure management approaches enhance microbial biomass and activity in perennial forage grass. Biol. Fertil. Soils 2017, 53, 613–626. [Google Scholar] [CrossRef]
  174. Bittman, S.; Kowalenko, C.G.; Hunt, D.E.; Schmidt, O. Surface-Banded and Broadcast Dairy Manure Effects on Tall Fescue Yield and Nitrogen Uptake. Agron. J. 1999, 91, 826–833. [Google Scholar] [CrossRef]
  175. Zhelezova, A.D.; Semenov, V.M.; Ksenofontova, N.A.; Krasnov, G.S.; Tkhakakhova, A.K.; Nikitin, D.A.; Semenov, M.V. Effects of distinct manure amendments on microbial diversity and activity in Chernozem and Retisol. Appl. Soil Ecol. 2024, 193, 105152. [Google Scholar] [CrossRef]
  176. Sayre, J.M.; Wang, D.; Lin, J.Y.; Danielson, R.E.; Scow, K.M.; Mazza Rodrigues, J.L. Repeated manure inputs to a forage production soil increase microbial biomass and diversity and select for lower abundance genera. Agric. Ecosyst. Environ. 2023, 354, 108567. [Google Scholar] [CrossRef]
  177. Semenov, M.V.; Krasnov, G.S.; Semenov, V.M.; Ksenofontova, N.; Zinyakova, N.B.; van Bruggen, A.H. Does fresh farmyard manure introduce surviving microbes into soil or activate soil-borne microbiota? J. Environ. Manag. 2021, 294, 113018. [Google Scholar] [CrossRef]
  178. Conant, R.T.; Paustian, K.; Del Grosso, S.J.; Parton, W.J. Nitrogen pools and fluxes in grassland soils sequestering carbon. Nutr. Cycl. Agroecosystems 2005, 71, 239–248. [Google Scholar] [CrossRef]
  179. Laughlin, R.J.; Rütting, T.; Müller, C.; Watson, C.J.; Stevens, R.J. Effect of acetate on soil respiration, N2O emissions and gross N transformations related to fungi and bacteria in a grassland soil. Appl. Soil Ecol. 2009, 42, 25–30. [Google Scholar] [CrossRef]
  180. de Vries, F.T.; van Groenigen, J.W.; Hoffland, E.; Bloem, J. Nitrogen losses from two grassland soils with different fungal biomass. Soil Biol. Biochem. 2011, 43, 997–1005. [Google Scholar] [CrossRef]
  181. Jingguo, W.; Bakken, L.R. Competition for nitrogen during mineralization of plant residues in soil: Microbial response to C and N availability. Soil Biol. Biochem. 1997, 29, 163–170. [Google Scholar] [CrossRef]
  182. Hu, X.; Li, X.-Y.; Zhao, Y.; Gao, Z.; Zhao, S.-J. Changes in soil microbial community during shrub encroachment process in the Inner Mongolia grassland of northern China. CATENA 2021, 202, 105230. [Google Scholar] [CrossRef]
  183. Mencel, J.; Mocek-Płóciniak, A.; Kryszak, A. Soil Microbial Community and Enzymatic Activity of Grasslands under Different Use Practices: A Review. Agronomy 2022, 12, 1136. [Google Scholar] [CrossRef]
  184. Musiał, M.; Kryszak, J.; Grzebisz, W.; Wolna-Maruwka, A.; Łukowiak, R. Effect of Pasture Management System Change on In-Season Inorganic Nitrogen Pools and Heterotrophic Microbial Communities. Agronomy 2020, 10, 724. [Google Scholar] [CrossRef]
  185. Boeddinghaus, R.S.; Nunan, N.; Berner, D.; Marhan, S.; Kandeler, E. Do general spatial relationships for microbial biomass and soil enzyme activities exist in temperate grassland soils? Soil Biol. Biochem. 2015, 88, 430–440. [Google Scholar] [CrossRef]
  186. Shi, Y.; Ziadi, N.; Hamel, C.; Bittman, S.; Hunt, D.; Lalande, R.; Shang, J. Soil microbial bio-mass, activity, and community composition as affected by dairy manure slurry applications in grassland production. Appl. Soil Ecol. 2018, 125, 97–107. [Google Scholar] [CrossRef]
  187. Dong, L.; Berg, B.; Gu, W.; Wang, Z.; Sun, T. Effects of different forms of nitrogen addition on microbial extracellular enzyme activity in temperate grassland soil. Ecol. Process. 2022, 11, 36. [Google Scholar] [CrossRef]
  188. Egan, G.; Crawley, M.J.; Fornara, D.A. Effects of long-term grassland management on the carbon and nitrogen pools of different soil aggregate fractions. Sci. Total Environ. 2018, 613–614, 810–819. [Google Scholar] [CrossRef]
  189. Elfstrand, S.; Hedlund, K.; Mårtensson, A. Soil enzyme activities, microbial community composition and function after 47 years of continuous green manuring. Appl. Soil Ecol. 2007, 35, 610–621. [Google Scholar] [CrossRef]
  190. Hopkins, D.W.; Shiel, R.S. Size and activity of soil microbial communities in long-term experimental grassland plots treated with manure and inorganic fertilizers. Biol. Fertil. Soils 1996, 22, 66–70. [Google Scholar] [CrossRef]
  191. Shah, S.H.H.; Li, Y.; Wang, J.; Collins, A.L. Optimizing farmyard manure and cattle slurry applications for intensively managed grasslands based on UK-DNDC model simulations. Sci. Total Environ. 2020, 714, 136672. [Google Scholar] [CrossRef] [PubMed]
Table 1. Land use intensity of grassland.
Table 1. Land use intensity of grassland.
ManagementIntensive
Grassland
Medium Intensive GrasslandExtensive GrasslandReference
Cutting frequency per year4 and more2–31[36]
Quantity of fertilizer applications per yearUp to 53–40–2[42,43]
Amount of fertilizer applications per yearUp to 640 kg N ha−1n.s.0–181 kg N ha−1[42,44,45,46]
Grazing intensity3.4 LU1.8 LU0.8 LU[47]
Input of herbivores144 kg N ha−1n.s.128 kg N ha−1[48]
n.s.: not specified.
Table 2. Nutrient contents in different types of manure (laboratory analysis results of Manure Standards Project: https://msdb.netlify.app/ accessed on 23 October 2023).
Table 2. Nutrient contents in different types of manure (laboratory analysis results of Manure Standards Project: https://msdb.netlify.app/ accessed on 23 October 2023).
Animal GroupManure TypeDMSDnTot-NSDnTot-PSDnKSDnpHSDn
(%)(%) (% FM)(% FM) (% FM)(% FM) (% FM)(% FM)
Beef cattledeep litter26.993.78110.550.21110.080.04110.670.28118.680.404
Beef cattlesemi-solid manure15.741.4770.300.0670.130.0470.000.0008.240.407
Beef cattleslurry8.781.72130.340.09130.080.02130.410.08137.780.4012
Beef cattlesolid manure26.8612.3870.570.1570.110.0170.620.2778.470.387
Dairy cowssemi-solid manure15.623.24460.320.07460.120.05460.060.0017.780.6545
Dairy cowsslurry8.362.99790.280.11790.060.02790.280.10787.630.3874
Dairy cowssolid manure21.577.19560.500.18560.130.06560.580.23408.380.4953
Suckler cowsdeep litter23.224.64140.570.17140.100.04140.820.37148.390.5610
Heifers/calvessemi-solid manure15.781.99180.310.07180.130.04180.000.0008.010.5618
Heifers/calvessolid manure21.447.07270.410.08270.130.05270.510.16128.060.5427
Pigs integrateddeep litter27.494.1450.700.1450.220.0851.170.6658.400.405
Pigs integratedliquid fraction2.690.8250.090.0950.040.0550.000.0007.810.265
Pigs integratedslurry3.291.5470.290.1570.080.0470.150.0367.320.447
Pigs integratedsolid manure25.725.7270.470.2870.250.1670.330.0838.170.717
Fattening pigsslurry5.493.06340.440.21340.080.04300.210.07287.610.5031
Broilersdeep litter54.7716.94142.650.78140.580.13131.390.44136.401.218
Laying henssolid manure43.2522.98111.460.53110.470.35110.710.1837.810.919
Sheepdeep litter33.2816.93110.680.27110.170.07110.990.40118.860.3410
% FM percent fresh matter, SD: Standard deviation.
Table 3. Overview N losses in percent (%) with different application techniques of manure on temperate grassland.
Table 3. Overview N losses in percent (%) with different application techniques of manure on temperate grassland.
Application TechniqueTotal N Losses by NH3 Volatilisation (%)Reduction in N Losses (%)Reference
Broadcast application27–98-[73]
27.3–84.5-[77]
21-[72]
19.1-[75]
40-[78]
Cattle slurry (Spring)17.7–24.8-[79]
Cattle slurry (Autumn)5.9–23.9-
Farmyard manure (Spring)0.4–2.6-
Farmyard manure (Autumn)1.3–1.7-
Narrow-band application8.9–32.0-[72]
-26[80]
Cattle slurry (Spring)7.7–18.9-[79]
Cattle slurry (Autumn)6.4–22.1-
Trailing hose4–2851[77]
Railing shoe4–1253[77]
-57[80]
-40–50[75]
Shallow injection776[77]
1.5–15.7-[72]
-73[80]
-40–50[75]
Table 4. Changes in yield, quality, and plant composition on temperate grassland under different manure applications.
Table 4. Changes in yield, quality, and plant composition on temperate grassland under different manure applications.
TreatmentApplication
(kg N ha−1 a−1)
Yield
(t DM ha−1)
Quality
(g N kg−1 DM)
Diversity
(Species m−2)
Reference
Grazing3367.50–8.6326.1–31.3-[41]
Manure application3368.17–8.6622.7–27.2-
Sheep manure 1035.92--[98]
Sheep grazing 1845.42 --
Pig slurry 160±8--[45]
Pig slurry 320±14--
Pig slurry64020--
Cattle slurry130±9--
Cattle slurry 270±15--
Cattle slurry54019--
Cattle slurry3007.5--[99]
Poultry manure30010.1--
Cattle slurry conv.14411.8-22[48]
Cattle slurry ext.12810.5-26–28
Cattle slurry org.11710.7->32
sheep manure 693.55/2.15 *19.78/23.95 *-[89]
Sheep manure 1034.07/2.52 *19.20/23.32 *-
Liquid manure 76–1128.68- [96]
Grazing 19982206.0236.7-[100]
Grazing 19992207.9434.9-
Cut 19982208.8124.4-
Cut 19982208.9827.8-
Untreated cattle slurry3030.262 t N ha−1--[85]
Digested cattle slurry3060.270 t N ha−1--
Cattle slurry, injected3110.247 t N ha−1--
Cattle slurry, surface3030.206 t N ha−1--
Farmyard manure (FYM)3070.234 t N ha−1--
Farmyard manure n.a.2.95/1.38 **--[93]
FYM conventional280--12[101]
FYM organic140--16
Cattle slurry (CS)20211.11--[31]
CS low protein2068.78--
CS composted with hay1838.13--
Cattle FYM2179.56--
* First/second cut. ** First year/second year. n.a.: not available.
Table 5. Changes in C storages and C losses on temperate grassland with different treatments of fertilization with organic fertilizer.
Table 5. Changes in C storages and C losses on temperate grassland with different treatments of fertilization with organic fertilizer.
TreatmentApplication
(kg N ha−1 a−1)
C StorageCO2 EmissionsCH4 EmissionsReference
LCM *, 4 cuts110147 g C m−2 a−11.8 µmol m−2 s−1-[44]
No fert., 3 cuts0−57 g C m−2 a−13.1 µmol m−2 s−1-
LCM, 4 cuts11064.7–183 t C ha−1--[120]
No fert., 3 cuts061.0–173 t C ha−1--
Dairy cow slurry50--0.58 kg ha−1[121]
Pig slurry50--0.13 kg ha−1
Pig slurry 1600.39 t C ha−1 a−1--[45]
Pig slurry 3200.28 t C ha−1 a−1--
Pig slurry6400.31 t C ha−1 a−1--
Cattle slurry1300.43 t C ha−1 a−1--
Cattle slurry 2700.65 t C ha−1 a−1--
Cattle slurry 5400.86 t C ha−1 a−1--
Dairy cattle slurry130–540-11. 6–12 t CO2 eq-
Beef cattle slurry130–540-9.1–9.5 t CO2 eq-
Cattle slurry150/150 **-14.03/15.9 t CO2 C ha−11.0/6.4 kg ha−1[29]
Poultry manure150/150 **-17.22/17.22 t CO2 C ha−10.3/0.7 kg ha−1
Cattle slurry1508.4 t C ha−17.49–12.71 t CO2 C ha−10–6.4 kg ha−1[103]
Poultry manure15031.3 t C ha−17.0–13.77 t CO2 C ha−1−0.1–0.7 kg ha−1
Cattle slurry conv.144-1.280 t CO2 eq5.102 t CO2 eq[48]
Cattle slurry ext.128-0.666 t CO2 eq4.535 t CO2 eq
Cattle slurry org.117-0.428 t CO2 eq4.114 t CO2 eq
Anaerobic digestate80.12-669.5 mg (kg soil DM)−1-[122]
Cattle slurry246.3-2030.5 mg (kg soil DM)−1-
Stockpiled dairy manure190154.1 mg C kg−1733.1 mg C kg−1-[123]
Rotted dairy manure187186.9 mg C kg−1796.9 mg C kg−1-
* Liquid cattle manure. ** 2002/2003.
Table 6. Changes in N storages and N losses on temperate grassland with different treatments of fertilization with organic fertilizer.
Table 6. Changes in N storages and N losses on temperate grassland with different treatments of fertilization with organic fertilizer.
TreatmentApplication
(kg N ha−1 a−1)
N Storage(t N ha−1)NH3 EmissionsN2O EmissionsN LeachingReference
LCM *, 4 cuts1106.9–19.4 40–70 kg N ha−11.4–1.9 kg N ha−10–3.5 kg N ha−1[120]
No fert., 3 cuts06.6–18.6-0.4–0.6 kg N ha−10–3.5 kg N ha−1
Dairy cow slurry50--0.34 kg N ha−1-[121]
Pig slurry50--0.57 kg N ha−1-
Pig slurry6400.03---[45]
Cattle slurry1300.03---
Cattle slurry2700.05---
Cattle slurry5400.08---
Cattle slurry conv.144-129 kg N ha−13.017 t CO2 eq-[48]
Cattle slurry ext.128-113 kg N ha−11.808 t CO2 eq-
Cattle slurry org.117-104 kg N ha−11.776 t CO2 eq-
Cattle slurry150--0.147–0.319 t CO2 eq -[103]
Poultry manure150--1.179–6.612 t CO2 eq -
Cattle slurry1502.85–2.98-10.1–16.2%[99]
Poultry manure1502.81–5.2-2200 g N ha−1 d−11.9–7.0%
Anaerobic digestate---5.77% of total N0–4.9%[122]
Cattle slurry--8.87% of total N0.3–17.5%
Pig FYM--1.1–2.8%0.15–0.3%-[79]
Poultry manure-5.7–10.4%0.58–2.37%-
Pig slurry-20.7–24.9%0.32–1.79%-
Grazing dairy cows120--1.05–1.07 kg ha−1 a−1-[118]
Dairy cow slurry120--0.47–0.57 kg ha−1 a−1-
Slurry spreading250-1041/1258 ** kg N farm−1--[138]
Slurry + grazing250-485/410 ** kg N farm−1--
FYM 250-774/945 ** kg N farm−1--
FYM + grazing250-485/410 ** kg N farm−1--
* Liquid cattle manure. ** 150/180 days housed. ↑ Increase of the emissions.
Table 7. Changes in N storages and N losses on temperate grassland at different times of fertilization with organic fertilizer.
Table 7. Changes in N storages and N losses on temperate grassland at different times of fertilization with organic fertilizer.
Treatment
Type of Manure
Treatment
Time
Application
(kg N ha−1 a−1)
NH3 EmissionsN2O Emissions
(kg ha−1)
N LeachingReference
UrineIn spring480-1.903-[137]
In summer420-5.034-
In autumn435-2.014-
DungIn spring1020-2.035-
In summer680-1.996-
In autumn720-1.538-
DungIn spring-5.3%--[133]
In summer-2.8%--
In autumn-3.5%--
UrineIn spring69514.9%--
In summer-9.8%--
In autumn-8.7%--
Cattle slurryApril/June 2002300/170-2.5-[29]
April/June 2002380/150-1.2-
Poultry manure2002150-52.1-
2003150-9.3-
Slurry August–April [134]
<4% DM-15%--
4–8% DM-37%--
>8% DM-59%--
Slurry May–July-60%--
Solid manure-76%--
Dirty water-15%--
Poultry manure-45%--
Cut1998220--1.7 kg ha−1[100]
1999220--0.7 kg ha−1
2000----12 kg ha−1
Grazing1998220--1.4 kg ha−1
1999220--1.1 kg ha−1
2000-- 46.3 kg ha−1
Cattle slurrySeptemberØ 200--6.3–26.3%[83]
OctoberØ 200--15.5–29.4%
NovemberØ 200--10.1–16.2%
DecemberØ 200--1.9–7.0%
JanuaryØ 200--0–4.9%
Farmyard manureJuneØ 200--0.3–17.5%
OctoberØ 200--2.9–17.5%
Cattle slurryAutumn 2011245.6–14.8%0.99–1.03-[79]
Spring 201267–777.7–24.8%0.72–1.20-
Autumn 20127122.1–23.9%0.77–1.1817.0 kg ha−1
Spring 20137715.6–18.9%0.44–0.61-
Farmyard manureAutumn 20111311.3–1.7%1.283.4 kg ha−1
Spring 20121220.4–2.6%0.72–1.28-
Dairy slurry control199888.60.48 kg ha−1-0.19 kg ha−1[139]
199995.90.08 kg ha−1-0.016 kg ha−1
Pig slurry
control
200059.60.05 kg ha−1-0.01 kg ha−1
20011132.22 kg ha−1-0.012 kg ha−1
Dairy slurry aerated199888.60.05 kg ha−1-0.02 kg ha−1
199995.90.03 kg ha−1-0.018 kg ha−1
Pig slurry aerated200059.60.02 kg ha−1-0.009 kg ha−1
20011130.05 kg ha−1-0.048 kg ha−1
Table 8. Losses of P and K from temperate grassland under different manure applications.
Table 8. Losses of P and K from temperate grassland under different manure applications.
TreatmentManure TypeApplication
Amount
Special
Technique
PKReference
Grazing 1999--No drainage-5 kg ha−1 a−1[152]
Grazing 2000--No drainage-13 kg ha−1 a−1
Grazing 1999--Drainage-5 kg ha−1 a−1
Grazing 2000--Drainage-9 kg ha−1 a−1
Fertilization 1999Cattle FYM122 kg K ha−1No drainage-19 kg ha−1 a−1
Fertilization 2000Cattle FYM304 kg K ha−1 No drainage-31 kg ha−1 a−1
Fertilization 1999Cattle FYM122 kg K ha−1Drainage-7 kg ha−1 a−1
Fertilization 2000Cattle FYM304 kg K ha−1 Drainage-23 kg ha−1 a−1
IntensiveCattle slurry34.6 kg P ha−1-5.3 kg ha−1-[48]
ExtensiveCattle slurry30.9 kg P ha−1-4.5 kg ha−1-
OrganicCattle slurry23.2 kg P ha−1-−2.3 kg ha−1-
Fertilization on medium-P siteDairy manure-1 d sprinkler3.72 mg L−1-[142]
-1 d watering can1.17 mg L−1-
-8 d sprinkler0.95–2.09 mg L−1-
-8 d watering can0.84–0.90 mg L−1-
Fertilization on high-P siteDairy manure-1 d sprinkler0.75–1.93 mg L−1-
-1 d watering can2.17–2.31 mg L−1-
-8 d sprinkler2.04–5.25 mg L−1-
-8 d watering can1.20–1.40 mg L−1-
FertilizationCattle slurry425 kg K ha−1 a−1--149 kg ha−1[146]
Grass-clover sward.166 kg K ha−1 a−1--89 kg ha−1
Application in summerCattle urine60 g K m−2--2.4–4.2 g m−2
Application in AutumnCattle urine74 g K m−2--4.7–7.1 g m−2
Cut 3 timesDairy manure14.5 kg PGrass cover14 g ha−1-[100]
GrazingDairy manure14.5 kg PGrass cover11 g ha−1-
1998Dairy manure6.4 g P, 21.4 g K DM−1Fertilization without aeration1.50 kg ha−15.96 kg ha−1[139]
1999Dairy manure11.2 g P, 53.6 g K DM−10.06 kg ha−10.62 kg ha−1
2000Dairy manure12.5 g P, 16.5 g K DM−10.06 kg ha−10.22 kg ha−1
2001Swine manure-0.89 kg ha−15.32 kg ha−1
1998Dairy manure6.4 g P, 21.4 g K DM−1Fertilization with aeration1.13 kg ha−10.72 kg ha−1
1999Dairy manure11.2 g P, 53.6 g K DM−10.06 kg ha−10.27 kg ha−1
2000Dairy manure12.5 g P, 16.5 g K DM−10.02 kg ha−10.13 kg ha−1
2001Swine manure-n.a.1.17 kg ha−1
n.a.: not available.
Table 9. Impact of different manure applications on microbial activity and growth in temperate grassland soils.
Table 9. Impact of different manure applications on microbial activity and growth in temperate grassland soils.
TreatmentNutrientsImpact on MicrobesImpact on BacteriaImpact on FungiReference
Addition of organic nutrients by rabbit grazing-↑ not significant[188]
Green manure application2052 C/65 N (kg ha−1)34.3 nmol g soil−11.8 nmol g soil−1[189]
Manure application2212 C/104 N (kg ha−1)36.8 nmol g soil−11.3 nmol g soil−1
Sawdust application + Ca(NO3)22054 C/81 N (kg ha−1)37.4 nmol g soil−11.7 nmol g soil−1
Manure application20 t ha−1
54.4 C/4.49 N (mg g soil−1)
--[190]
Manure application400 C/59 N (kg ha−1)--[172]
Acetate as C source (replacement for manure)2.5 mL as solution[179]
Stockpiled dairy manure100 t ha−1--[123]
Rotted dairy manure100 t ha−1Slightly higher ↑--
Cattle slurry3361 OM/98 N (kg ha−1) 56 μg C g dry soil−115 μg C g dry soil−1[31]
Cattle slurry low protein3718 OM/104 N (kg ha−1) 57 μg C g dry soil−114 μg C g dry soil−1
Cattle slurry composted with hay4161 OM/170 N (kg ha−1)53 μg C g dry soil−116 μg C g dry soil−1
Cattle FYM6347 OM/171 N (kg ha−1)52 μg C g dry soil−117 μg C g dry soil−1
↑ Increase, ↓ Decrease, ↕ Increase and decrease.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Brummerloh, A.; Kuka, K. The Effects of Manure Application and Herbivore Excreta on Plant and Soil Properties of Temperate Grasslands—A Review. Agronomy 2023, 13, 3010. https://doi.org/10.3390/agronomy13123010

AMA Style

Brummerloh A, Kuka K. The Effects of Manure Application and Herbivore Excreta on Plant and Soil Properties of Temperate Grasslands—A Review. Agronomy. 2023; 13(12):3010. https://doi.org/10.3390/agronomy13123010

Chicago/Turabian Style

Brummerloh, Arne, and Katrin Kuka. 2023. "The Effects of Manure Application and Herbivore Excreta on Plant and Soil Properties of Temperate Grasslands—A Review" Agronomy 13, no. 12: 3010. https://doi.org/10.3390/agronomy13123010

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop