The study was approved by the Animal Care and Use Committee of Rajamangala University of Technology Isan, Thailand (approval no. 01-67-002). According to the National Research Council of Thailand Guidelines for Ethics of Animal Experimentation, approval was required for rumen fluid collection because the primary objective of this study involved the laboratory evaluation of ruminant feeds. All procedures were conducted in accordance with the applicable regulations and guidelines. The study adhered to the Animal Research: Reporting of in vivo Experiments 2.0 guidelines. Throughout the experimental period, all animals were monitored daily for clinical signs of mimosine toxicity and adverse health effects, including alopecia, excessive salivation, lethargy, and abnormal weight loss. No adverse clinical signs were observed during the study.

The experiment was conducted during the rainy season in August 2024 in Roi Et Province, Thailand. Fresh young leaves of L. leucocephala and rhizomes of Z. officinale were harvested locally at approximately 45 days of age. The feeding trial and laboratory analyses were performed under tropical conditions in Thailand.

Four female Thai native beef cattle with an initial body weight (BW) of 230 ± 10 kg and approximately 2 years of age were randomly assigned to four dietary treatments according to a 4 × 4 Latin square design. The treatments consisted of a control group without LGP supplementation and groups receiving LGP at 50, 100, and 150 g/head/day.

The concentrate allowance was provided at 1.0% of BW on a DM basis. To ensure accurate feeding rates throughout the study, the daily concentrate allocation for each animal was recalculated according to individual BW measured at the beginning and end of each experimental period. Because of the short 21-day duration of each period, average daily gain was not evaluated as a primary parameter; however, no significant BW loss was observed.

Animals received LGP according to their assigned treatments and were fed two equal portions of locally sourced rice straw (Oryza sativa L.) at 07:00 and 16:00 h daily. The basal diet was formulated to meet the maintenance and growth requirements of Thai native beef cattle. The chemical compositions of the concentrate mixture, rice straw, and LGP are presented in Table 1. Based on the daily intake proportions, the nutrient composition of the total diet provided sufficient energy and protein to meet the maintenance requirements of the experimental animals.

Each experimental period lasted 21 days, comprising 14 days for dietary adaptation and 7 days for sample collection and nutrient digestibility measurements. During the experiment, the cattle were housed individually in well-ventilated stalls measuring approximately 2 × 3 m, with concrete floors covered with rubber mats, under natural daylight and ventilation. Clean drinking water was available ad libitum throughout the experiment.

Before the start of the trial, all animals underwent a comprehensive health examination, including routine vaccination against Foot and Mouth Disease and treatment for internal and external parasites with ivermectin to ensure optimal health.

The chemical compositions and nutrient contents of the experimental diets and LGP are listed in Table 1.

Fresh young leaves of L. leucocephala and rhizomes of Z. officinale were harvested locally in Roi Et Province, Thailand. Following collection, the leaves and chopped ginger rhizomes were dried in a hot-air oven at 60°C for 48 h until a constant weight was achieved. The dried materials were then ground using a Cyclotec Mill (Tecator, Hoganas, Sweden) and passed through a 1-mm screen.

Pellets were prepared by combining 75% L. leucocephala leaves, 15% ginger powder, 9% cassava chips, and 1% molasses using a pellet machine. This ratio of active phytogenic ingredients was selected to provide an optimal supply of CT and essential oils to effectively modulate rumen fermentation without impairing microbial nutrient degradability. Following pellet formation, pellets measuring approximately 6-8 mm in diameter were sun-dried for 2-3 days to reduce moisture content and ensure stability during storage and feeding.

Although mimosine and SP concentrations were not quantified because of laboratory limitations, previous studies have demonstrated that the combination of sun drying, oven drying at 60°C, and heat generated during pellet production substantially reduces mimosine concentrations to safe levels. Cassava chips and molasses were incorporated primarily as pellet binders and highly fermentable energy sources, and their nutrient contributions were inherently included in the proximate composition of the final pellets (Table 1). To maintain stability and prolong shelf life, the pellets were stored in sealed moisture-proof containers at room temperature throughout the feeding trial.

Feeds were weighed daily to determine the intake of concentrate, rice straw, and LGP for each dietary treatment. Feed, fecal, and urine samples were collected during the last 7 days of each experimental period. Following oven drying, samples were ground to pass through a 1-mm screen and analyzed for DM, ash, and CP according to Association of Official Analytical Chemists procedures [14]. Acid-insoluble ash was determined according to Van Keulen and Young [15]. Acid detergent fiber (ADF) and neutral detergent fiber contents were analyzed according to the method of Van Soest et al. [16].

The concentrations of CT and flavonoids in LGP were determined using the Folin-Ciocalteu reagent by measuring absorbance at 765 nm [17].

Spot urine samples were obtained by manual stimulation of the vulva to induce urination, whereas fecal samples were collected directly from the rectum. Samples were collected at 0 and 4 h after the morning feeding. Total daily urine output was estimated from creatinine concentration, assuming a constant creatinine excretion rate of 0.88 mmol/kg BW^0.75. Microbial purine absorption was estimated from the excretion of purine derivatives. Allantoin and creatinine concentrations were measured by high-performance liquid chromatography, and microbial nitrogen supply was calculated using the equations, assumptions, and recovery factors described by Chen and Gomes [18].

Rumen fluid and jugular blood samples were collected at 0 and 4 h after feeding. To minimize stress and discomfort, rumen fluid was collected using a soft flexible stomach tube connected to a vacuum pump, with the sample volume limited to 200 mL. Immediately after collection, ruminal temperature and pH were measured using a handheld pH meter (HI8424 Microcomputer; Hanna Instruments, Woonsocket, RI, USA).

Rumen fluid was filtered through four layers of cheesecloth and divided into two portions. In the first portion, NH₃-N and VFA concentrations were determined by mixing 45 mL of rumen fluid with 5 mL of 1 M H₂SO₄ followed by centrifugation at 1,600 × g for 15 min. The NH₃-N concentration was determined by the micro-Kjeldahl method [14], whereas VFA concentrations were analyzed using high-performance liquid chromatography [19].

CH₄ production was estimated from VFA concentrations according to Moss et al. [20] using the following equation:

CH₄ production (mol/100 mol total VFA) = 0.45 (acetate) − 0.275 (propionate) + 0.40 (butyrate).

For microbial enumeration, 1 mL of filtered rumen fluid was immediately transferred into 9 mL of 10% formalin solution to preserve microbial cells. Bacterial and protozoal populations were counted directly using a hemocytometer under a phase-contrast microscope, as described by Galyean [21]. To ensure accuracy and reliability, microscopic counts were performed in duplicate, and at least 10 microscopic fields were examined for each sample. To ensure precision and reproducibility, all chemical and microbial analyses were conducted in triplicate.

Blood samples (5 mL) were collected from the jugular vein at 0 and 4 h after feeding, placed in tubes containing ethylenediaminetetraacetic acid, and analyzed for blood urea nitrogen (BUN) according to Crocker [22].

Before statistical analysis, the assumptions of analysis of variance were evaluated. Residual normality was assessed using the Shapiro-Wilk test, and homogeneity of variances was examined to verify the suitability of the statistical model. The use of four animals in a 4 × 4 Latin square design represents standard practice for in vivo rumen metabolism studies and balances statistical power with the ethical principle of minimizing animal use.

Potential outliers were evaluated using studentized residuals, and no observations exceeded the ±3 standard deviation threshold. Therefore, all observations were retained for the final analysis.

Data were analyzed using the MIXED procedure in SAS version 9.4 (SAS Institute Inc., Cary, NC, USA) with a variance-covariance structure based on a 4 × 4 Latin square design. The statistical model was:

where Yijk represents the observation, μ is the overall mean, Ai is the random effect of animal (i = 1, 2, 3, and 4), Pj is the random effect of experimental period (j = 1, 2, 3, and 4), Tk is the fixed effect of treatment (k = 1, 2, 3, and 4), and eijk is the residual error.

Differences among treatment means were determined using Tukey's multiple comparison procedure [23], and significance was declared at p < 0.05. Orthogonal polynomial contrasts were used to evaluate linear and quadratic treatment responses.

The feed ingredients and chemical compositions of the concentrate mixture, rice straw, and LGP used in the experiment are presented in Table 1. As expected for standard basal diets, the concentrate and rice straw contained 14.7% and 2.2% CP, respectively. Notably, the formulated LGP exhibited a favorable nutritional profile, containing 24.6% CP, 32.5% neutral detergent fiber, and 25.2% ADF. In addition, LGP served as a substantial source of bioactive compounds, providing 6.8% CT and 2.4% flavonoids. L. leucocephala is a widely distributed leguminous species in tropical regions with a high protein content and is commonly used as a feed resource for ruminants.

The effects of dietary treatments on feed intake and nutrient digestibility are presented in Table 2. Supplementation with LGP had no effect on rice straw intake, concentrate intake, or total feed intake among treatment groups (p > 0.05). However, increasing LGP levels (p < 0.05) increased the digestibility of DM and neutral detergent fiber. In contrast, the digestibility of OM, CP, and ADF was not affected by LGP supplementation (p > 0.05).

When expressed as a percentage of BW, total daily DM intake ranged from approximately 2.5% to 2.7% across treatments, which is within the normal range for beef cattle. Feed intake is influenced by the chemical composition and physical characteristics of the diet, which in turn affect animal productivity. The absence of significant differences in feed intake among treatments indicates that LGP supplementation did not adversely affect feed consumption.

The effects of dietary treatments on rumen fermentation characteristics, blood metabolites, and microbial populations are presented in Table 3. Supplementation with LGP had no effect on ruminal temperature, pH, or blood urea nitrogen (BUN) concentration (p > 0.05). Rumen fermentation, microbial growth, and microbial activity were maintained within the optimal pH range of 6.7-6.8. Increasing the level of LGP supplementation did not significantly affect NH₃-N concentrations, which remained within the normal range of 13.7-18.5 mg/dL. BUN concentrations were closely associated with ruminal NH₃-N concentrations, although no significant differences in BUN concentrations were observed among treatments.

Increasing LGP supplementation levels resulted in higher propionic acid concentrations and lower estimated CH₄ production (p < 0.05), particularly at 150 g/head/day. However, total VFA concentration, acetic acid concentration, butyric acid concentration, and the acetic acid-to-propionic acid ratio did not differ significantly among treatment groups (p > 0.05).

Furthermore, increasing levels of LGP supplementation increased bacterial populations (p < 0.05) and decreased protozoal populations (p < 0.05), as shown in Table 3.

The effects of dietary treatments on microbial protein synthesis are presented in Table 4. Supplementation with LGP had no significant effect on absorbed or excreted urinary purine derivatives (p > 0.05). However, microbial protein synthesis and efficiency of microbial nitrogen synthesis increased significantly (p < 0.05) when cattle received 150 g/head/day of LGP.

The high CP content observed in LGP was primarily attributed to the inclusion of L. leucocephala, a widely available leguminous species in tropical regions that is commonly used as a high-quality protein feed for ruminants. This finding is consistent with Melesse et al. [7], who reported that L. leucocephala leaves contain high levels of CP (24.5%), total phenols (6.5%), and CT (2.3%), and provide an excellent supply of essential amino acids compared with other multipurpose tree foliage. Beyond its protein content, LGP was a rich source of phytonutrients, containing 6.8% CT and 2.4% flavonoids. These polyphenolic compounds, particularly tannins, play an important role in ruminal protein utilization. Zhang et al. [24] demonstrated that, under normal ruminal pH conditions, these active components bind with dietary proteins to form stable complexes, thereby reducing excessive microbial protein degradation in the rumen.

Dietary chemical composition, physical characteristics, and other related factors typically influence DM intake, which subsequently affects livestock productivity. In this study, no significant differences in feed intake were observed among treatment groups, indicating that LGP supplementation maintained normal feed consumption. This sustained intake may be attributed to the synergistic formulation of LGP, which likely counteracted the potential negative effects commonly associated with high-tannin diets. While CT from L. leucocephala contributes to dietary protein protection, ginger provides bioactive compounds, including gingerols and shogaols, that stimulate digestive enzyme activity. This combination may enhance diet palatability and reduce the intake-depressing effects commonly associated with single-source high-tannin supplementation.

Throughout the in vivo trial, no clinical signs of mimosine toxicity, such as alopecia, excessive salivation, depressed appetite, or visible goiter, were observed in any experimental animal. This absence of clinical toxicity supports the safety of the formulated pellet and the thermo-mechanical processing approach used in the study. Furthermore, the significant improvements in DM and neutral detergent fiber digestibility may be mechanistically attributed to the combined effects of CT and ginger bioactives. The targeted suppression of rumen protozoa by CT and flavonoids in LGP likely reduced bacterial predation, allowing greater proliferation of cellulolytic and fibrolytic bacteria. Consequently, enhanced bacterial activity, together with stimulation of salivary secretion and microbial enzymatic activity by ginger bioactives, may have improved structural carbohydrate degradation and overall nutrient digestibility.

These results are consistent with those of Phesatcha et al. [25], who reported an increase in total DM intake after supplementation with Flemingia macrophylla pellets. Similarly, Totakul et al. [26] showed that crossbred bulls did not alter feed consumption when supplemented with Cnidoscolusa conitifolius leaf pellets. Increasing LGP supplementation levels improved palatability and influenced rumen fermentation. Improvements in feed conversion ratio, growth rate, nutrient digestibility, and palatability have also been reported when plants, particularly ginger, were used to stimulate feed intake [27]. In the present study, LGP enhanced DM and neutral detergent fiber digestibility, likely because reduced protozoal populations decreased predation on fibrolytic bacteria. The bioactive compounds naturally present in ginger may also enhance animal health and growth by stimulating gastric secretions and digestive enzyme activity, thereby supporting feed utilization and production.

The addition of CT and SP may negatively affect nutrient digestibility, particularly protein digestion, when included at excessive levels. However, a moderate reduction in ruminal protein degradation can be beneficial if tannin-CP complexes dissociate in the lower digestive tract, thereby allowing subsequent protein digestion. Matra et al. [28] reported improved CP digestibility in dairy cows fed dragon fruit peel pellets. Although significant increases in DM and neutral detergent fiber digestibility were observed in this study (p < 0.05), the relatively high standard error, particularly for DM digestibility, should be noted. Such variability is common in in vivo studies using low-quality basal roughages, such as rice straw, and reflects inherent individual variation among animals within a small Latin square design. Nevertheless, the significant treatment effect indicates that the synergistic action of phytogenic compounds in LGP was sufficient to improve rumen microbial activity and feed degradation.

Rumen fermentation, microbial growth, and microbial activity were maintained within a pH range of 6.7-6.8. Improved rumen fermentation may be supported by maintaining ruminal pH through the strategic inclusion of feedstuffs containing phenolic acids [29]. Increasing LGP supplementation did not significantly alter NH₃-N concentrations, which remained within the normal range of 13.7-18.5 mg/dL. BUN concentrations were closely associated with ruminal NH₃-N concentrations, although no significant differences in BUN were observed among treatments. Phesatcha et al. [30] reported that CT improved nutrient utilization by forming protein-tannin complexes, decreasing ruminal feed protein degradation, and reducing ammonia production. In contrast, Matra et al. [28] found that ruminal NH₃-N increased when Holstein crossbred bulls received dragon fruit peel pellets at 400 g/animal/day. In the present study, BUN concentrations ranged from 10.3 to 12.0 mg/dL and did not differ significantly among treatments, suggesting efficient use and absorption of available ruminal NH₃-N for microbial synthesis. Similarly, Phesatcha et al. [25] reported normal BUN concentrations when tree leaf pellets were added to the diet as a CT source.

Patra and Saxena [31] reported that bioactive compounds can alter propionate formation when hydrogen is available in excess. Hydrogen is a major substrate for methanogenesis, whereas its use in propionate formation provides an alternative hydrogen sink. Therefore, inhibition of acetogenic bacteria and redirection of hydrogen toward propionate synthesis represent potential biological roles of tannins. A lower acetate-to-propionate ratio is generally associated with increased propionate concentration. Several studies have demonstrated that leguminous fodder shrubs can alter VFA profiles. Totakul et al. [26] reported that supplementation with Cnidoscolus leaf pellets increased propionate concentration and decreased the acetate-to-propionate ratio. Similar findings were reported by Phesatcha et al. [30], who observed increased propionate and reduced acetate proportions after leaf pellet supplementation.

Diets supplemented with CT and SP enhanced rumen fermentation, reduced CH₄ production, decreased protozoal populations, and increased propionate production. Propionate concentration often increases when rumen methanogenesis is suppressed, as observed in this study. The shift in the VFA profile from acetate-to-propionate, along with reduced CH4 formation and redirected hydrogen utilization, may improve the energy availability to the host animal. These results are consistent with recent in vitro studies showing that Z. officinale mitigates CH₄ emissions by altering rumen microbial activity [10]. Moreover, the synergistic use of phytogenic compounds has been shown to modify in vitro fermentation parameters and translate into reduced in vivo CH₄ emissions while maintaining performance in dairy and beef cattle [32]. Similarly, phytogenic-based additives can suppress methanogenesis by shifting fermentation pathways toward propionate production [2].

The observed shift in rumen fermentation, particularly increased propionate and decreased CH₄ production, is closely associated with the chemical properties of the phytogenic compounds. Rumen protozoa have a symbiotic relationship with methanogenic archaea, providing them with a habitat and hydrogen. The antiprotozoal actions of CT and flavonoids may disrupt this symbiosis and impair methanogenesis. Concurrently, to maintain thermodynamic balance in the rumen ecosystem, metabolic hydrogen may be redirected toward propionate synthesis. This competitive hydrogen sink can reduce CH₄ emissions while providing more glucogenic energy to the host animal. Montoya-Flores et al. [8] reported a 14% reduction in CH₄ production when Leucaena was included at a comparable level, which was attributed to the bioactive compounds present in Leucaena. Although formal correlation analysis between protozoal populations and CH₄ production was not performed because CH₄ was estimated indirectly using stoichiometric equations, the concurrent reduction in both parameters is consistent with established biological mechanisms. This parallel decline supports disruption of the symbiotic relationship between rumen ciliate protozoa and methanogenic archaea and further demonstrates the efficacy of LGP in favorably modifying the rumen microbiome.

Although LGP contained a relatively high CT concentration of 6.8%, the low daily supplementation rate, with a maximum of 150 g/head/day, ensured that total dietary CT remained below the threshold generally associated with impaired protein digestibility and well below commonly recommended safe inclusion limits. In addition, cattle in tropical regions, including Thai native beef cattle, may possess natural rumen adaptation. Their rumen microbiome often harbors mimosine-degrading bacteria, such as Synergistes jonesii, which can detoxify mimosine and its goitrogenic metabolites, including 3,4-dihydroxypyridine and 2,3-dihydroxypyridine. Thus, the formulation likely leveraged the beneficial effects of phytogenic compounds without approaching the threshold for mimosine-induced toxicity.

Essential oils in ginger may influence feed digestion and rumen fermentation. Saponins, which are among the bioactive constituents of ginger, may increase beneficial bacteria while decreasing protozoal populations. Higher LGP supplementation increased bacterial populations and reduced protozoal populations. Phesatcha et al. [30] similarly reported decreased protozoal and ruminal methanogen populations when beef cattle were supplemented with Mitragyna leaf pellets. The reduction of protozoa is a recognized mechanism by which bioactive compounds in both Leucaena and ginger suppress methanogenic archaea associated with protozoa, thereby improving nitrogen utilization and post-ruminal protein flow [5].

The reduction in protozoal populations, suppression of methanogenesis, and concurrent enhancement of microbial protein synthesis observed with LGP supplementation suggest a biological synergy among its constituent bioactive compounds. Leucaena is rich in CT, which can bind to the cell coat of ciliate protozoa and dietary proteins, impair cell membrane permeability, and inhibit enzyme activity. In parallel, the phytochemical profile of ginger, including flavonoids, gingerols, shogaols, and saponins, may complement this effect by disrupting lipid bilayers of methanogenic and protozoal cell membranes. This combination may create a dual-action inhibitory effect on cellular integrity, resulting in a more pronounced defaunation effect and greater bacterial proliferation and microbial protein synthesis than either ingredient alone. The rich phytochemical profile of these combined feedstuffs may therefore optimize fermentation kinetics and support higher microbial protein synthesis [4].

Ebeid et al. [33] reported that ginger supplementation improved digestion by increasing cellulolytic bacterial populations and enhancing salivary secretion, thereby increasing the secretion and activity of digestive enzymes. Ginger may benefit gastrointestinal ecology, improve feed stability, and limit the growth of pathogenic microorganisms, although excessive antimicrobial activity can reduce diet fermentability. Plant secondary metabolites and antiprotozoal actions of ginger components may therefore contribute to reduced total protozoal populations. Norrapoke and Pongjongmit [34] also reported that Mahad leaf pellet supplementation containing 15.6% CT significantly decreased protozoal populations in beef cattle.

The overall efficacy of LGP appears to be closely linked to dose-dependent synergy. At the optimal supplementation level of 150 g/head/day, which provided approximately 112.5 g of Leucaena leaves and 22.5 g of ginger powder, this study observed favorable ruminal outcomes. This dose increased propionate concentration and microbial protein synthesis while reducing protozoal populations and enteric CH₄ emissions. Importantly, these effects occurred without adverse outcomes commonly associated with high-tannin interventions, such as reduced feed intake or compromised ruminal pH. Therefore, 150 g/head/day may represent a practical biological threshold at which complementary bioactives maximize fermentation efficiency while maintaining ruminal homeostasis.

Nitrogen intake increased with higher LGP supplementation, likely due to protein complex formation. Hung et al. [35] demonstrated that microbial nitrogen synthesis efficiency was enhanced by supplementation with Leucaena leaf pellets containing 24% CP. Rumen bypass protein also improved when dietary protein and CT levels increased with LGP supplementation. Rumen microorganisms play a central role in protein production, and changes in microbial growth directly influence amino acid availability. In the present study, LGP significantly increased microbial protein synthesis and the efficiency of microbial nitrogen synthesis.

The enhancement of microbial protein synthesis and microbial nitrogen synthesis efficiency can be explained by two major mechanisms. First, reversible binding of CT to dietary proteins at normal ruminal pH forms stable CT-protein complexes. This process protects protein from rapid ruminal degradation and synchronizes nitrogen release with carbohydrate fermentation for optimal microbial growth. Second, reduced protozoal predation on bacteria increases the net flow of intact microbial cells from the rumen to the lower gut. Together, these mechanisms improve the overall efficiency of microbial nitrogen synthesis. Viennasay and Wanapat [36] reported that Flemingia supplementation enhanced microbial nitrogen synthesis and its efficiency in lactating dairy cows, whereas Phesatcha et al. [37] found that supplementing beef cattle with pellets containing insect protein and phytonutrient plants improved microbial nitrogen synthesis efficiency.

Beyond the direct suppression of methanogenesis, the synergy between ginger bioactives and Leucaena CT may involve specific physical and enzymatic interactions related to CT-protein complex formation. While appropriate CT levels protect dietary protein from ruminal degradation, excessive CT can irreversibly bind proteins, reducing lower-gut digestibility. Ginger bioactives may counteract this risk through two mechanisms. First, gingerols can stimulate salivary secretion, and saliva contains proline-rich proteins that have a high affinity for tannins. Increased salivary flow may therefore buffer excess CT and prevent excessive inhibition of dietary protein digestion in the rumen. Second, after reversible CT-protein complexes dissociate in the acidic environment of the abomasum, gingerols may stimulate lower-gut protease secretion, improving breakdown and absorption of liberated amino acids. This dual-action mechanism may explain the increased microbial nitrogen flow and sustained nutrient digestibility observed in LGP-supplemented cattle.

The synergistic efficacy of LGP should be interpreted in relation to previous studies that evaluated these phytogenic sources independently. Several previous in vivo studies using Leucaena alone reported a risk of reduced DM and structural carbohydrate digestibility at high inclusion levels due to excessive CT-protein binding [8]. In contrast, the present study demonstrated significantly improved digestibility of DM and neutral detergent fiber, suggesting that ginger bioactives in LGP may have counteracted potential CT-induced microbial inhibition. Similarly, although in vitro studies have documented the antimethanogenic and antimicrobial effects of ginger extracts, their practical in vivo application may be limited by the rapid ruminal degradation of volatile compounds. In contrast, the pelleted LGP matrix may help stabilize these bioactives and achieve a marked reduction in protozoal populations, along with increased microbial protein synthesis, at a conservative supplementation level of 150 g/head/day. Therefore, the combined formulation appears to provide greater rumen-modulatory benefits than either Leucaena or ginger alone.

From a practical perspective, LGP functions as a ready-to-use technology for resource-limited tropical farmers. Its reliance on standard pelleting equipment and locally available ingredients suggests strong potential for cooperative-level scale-up and broader commercialization. By using locally abundant materials from Roi Et Province and evaluating their efficacy in Thai native beef cattle fed a low-quality rice straw-based diet, this formulation directly addresses practical nutritional constraints in tropical smallholder systems. The innovation of this study extends beyond combining ingredients; it includes the development of a specific pelleted matrix. Unlike most previous studies that evaluated Leucaena as loose leaves or unprocessed meal, this study used cassava chips and molasses as binders, together with mechanical processing and sun drying. This thermo-mechanical approach may improve pellet integrity, storage stability, and ease of feeding, while potentially enhancing the bioavailability of volatile gingerols and further reducing residual mimosine within the pellet matrix.

Mimosine toxicity remains a recognized limitation in Leucaena utilization, but LGP may provide a dual mitigation strategy. In addition to physical mimosine reduction through drying and pelleting, enhanced fermentation and bacterial proliferation stimulated by ginger bioactives may further support ruminal detoxification of residual mimosine and its secondary metabolites. Consequently, this phytogenic formulation may promote sustainable and adoptable feeding practices in tropical regions.

The CT concentration must also be interpreted in relation to total dietary intake. Although LGP contained 6.8% CT, the maximum supplementation rate of 150 g/head/day diluted the net CT contribution to only a small fraction of total dietary DM. This level is likely within a beneficial range, allowing CT to act as a phytogenic rumen modifier without reaching concentrations that negatively affect feed intake or nutrient digestibility.

Despite these promising findings, several limitations should be acknowledged. First, the 4 × 4 Latin square design, although appropriate for evaluating ruminal fermentation, included only four animals, short experimental periods of 21 days, and exclusively female cattle. These factors limit direct extrapolation to long-term production outcomes, including average daily gain, final BW, carcass traits, and responses in male cattle. Second, although the physical integrity of LGP was adequate for handling and daily feeding, formal evaluation of pellet characteristics, including hardness, durability, and water stability, was not performed. Third, residual mimosine and specific ginger bioactives in the final pellet were not quantified because of analytical constraints. Finally, classical methods such as hemocytometer counting and VFA-based stoichiometric estimation do not identify specific microbial taxa or measure absolute CH₄ emissions.

Future studies should therefore include long-term growth trials to validate practical application and economic benefits. Direct quantification of CH₄ using respiration chambers or related technologies, comprehensive mimosine adaptation studies, quantification of residual mimosine and ginger bioactives, and advanced molecular microbiome analysis are also recommended to clarify the long-term physiological, microbial, environmental, and economic impacts of this synergistic pellet.