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Research article · 2026 · Full text

International Journal of Horticulture and Food Science

Effect of growth stage on chemical composition and nutritional quality of different oat (Avena sativa) cultivars

VD PimparkarSP PoulA.A. Bhagat

Volume 8(3) · Pages 82–85 · DOI: 10.33545/26631067.2026.v8.i3a.499 ↗

Research areasCrop Yield and Soil FertilityRuminant Nutrition and Digestive PhysiologyFood composition and properties

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Abstract

Author-written

The present study was undertaken to evaluate the effect of growth stage on the chemical composition and nutritional quality of different oat (Avena sativa L.) cultivars under rabi conditions. Eight oat cultivars were assessed at two growth stages, viz., 60 and 90 Days After Sowing (DAS), using a factorial randomized block design. The results revealed that growth stage exerted a significant influence on all major nutritional parameters. Advancement in maturity resulted in a significant (p<0.01) increase in dry matter, crude fibre, Neutral Detergent Fibre (NDF), Acid Detergent Fibre (ADF), cellulose, lignin, and silica, whereas crude protein, ether extract, total ash, calcium, and phosphorus contents declined significantly. Nitrogen free extract showed non-significant variation across growth stages. Significant genotypic differences were observed among cultivars for most of the parameters studied. Among the cultivars, RO-2000-19 exhibited superior nutritional quality, characterized by higher crude protein and lower fibre and silica content, while RO-2000-16 recorded higher dry matter and fibre fractions, indicating greater biomass accumulation but comparatively lower nutritive value. The study highlights a clear inverse relationship between forage maturity and nutritional quality, emphasizing the importance of optimal harvest timing. Harvesting at 60 DAS was found to be more suitable for obtaining nutritionally superior forage. The findings underscore the combined importance of growth stage and cultivar selection in optimizing forage quality and improving livestock productivity.

Summary

Source-checked

Plain-language reading of the full paper, prepared with AI and checked against the text. Each point links to the authors' own words.

  1. Why it matters

    • Oat is a critical winter forage crop for livestock because it provides high biomass, is palatable, and has high nutritional value. View evidence ↗

      Why it matters

      Oat is a critical winter forage crop for livestock because it provides high biomass, is palatable, and has high nutritional value.

      In the paper's own words

      “Oat (Avena sativa L.) is one of the most important winter forage crops widely cultivated for livestock feeding due to its high biomass yield, palatability, and superior nutritive value.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • The nutritional quality of oat forage depends on its chemical makeup, specifically its protein, fiber fractions, ash, and carbohydrates. View evidence ↗

      Why it matters

      The nutritional quality of oat forage depends on its chemical makeup, specifically its protein, fiber fractions, ash, and carbohydrates.

      In the paper's own words

      “The nutritive value of oat forage is determined by its chemical composition, including Crude Protein (CP), fiber fractions such as Neutral Detergent Fiber (NDF) and Acid Detergent Fiber (ADF), ether extract, ash, and soluble carbohydrates.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
    • The timing of the harvest (growth stage) is one of the most important factors influencing the nutritional quality of the forage. View evidence ↗

      Why it matters

      The timing of the harvest (growth stage) is one of the most important factors influencing the nutritional quality of the forage.

      In the paper's own words

      “One of the most critical factors affecting the nutritional quality of oat forage is the stage of growth at harvest.”

      Page 1

      Found in: Introduction

      Read it in the full textOpen PDF at page 1 ↗
  2. The question

    • The study aimed to evaluate how growth stage affects the chemical composition and nutritional quality of various oat cultivars to identify the best cultivars and the ideal harvest time. View evidence ↗

      The question

      The study aimed to evaluate how growth stage affects the chemical composition and nutritional quality of various oat cultivars to identify the best cultivars and the ideal harvest time.

      In the paper's own words

      “Therefore, the present study was undertaken to evaluate the effect of growth stage on chemical composition and nutritional quality of different oat (Avena sativa) cultivars, with the objective of identifying suitable cultivars and optimum harvesting stage for maximizing forage quality.”

      Page 2

      Found in: Introduction

      Read it in the full textOpen PDF at page 2 ↗
  3. What they did

    • The research was carried out at the Forage Crop Research Project in Rahuri, Maharashtra, India. View evidence ↗

      What they did

      The research was carried out at the Forage Crop Research Project in Rahuri, Maharashtra, India.

      In the paper's own words

      “The experiment was conducted at the Forage Crop Research Project, Mahatma Phule Krishi Vidyapeeth (MPKV), Rahuri, Maharashtra, India.”

      Page 2

      Found in: Experimental site

      Read it in the full textOpen PDF at page 2 ↗
    • The study evaluated eight different oat cultivars, including seven RO-series cultivars and Kent as a check. View evidence ↗

      What they did

      The study evaluated eight different oat cultivars, including seven RO-series cultivars and Kent as a check.

      In the paper's own words

      “Eight oat (Avena sativa) cultivars were evaluated: RO-2000-2, RO-2000-7, RO-2000-19, RO-2000-1, RO-2000-11, RO-2000-16, RO-2000-12, and Kent (check).”

      Page 2

      Found in: Introduction

      Read it in the full textOpen PDF at page 2 ↗
    • Samples were collected at two distinct growth stages: 60 days after sowing (Stage I) and 90 days after sowing (Stage II). View evidence ↗

      What they did

      Samples were collected at two distinct growth stages: 60 days after sowing (Stage I) and 90 days after sowing (Stage II).

      In the paper's own words

      “Samples were collected at: • 60 days after sowing (Stage I) • 90 days after sowing (Stage II)”

      Page 2

      Found in: Conclusion

      Read it in the full textOpen PDF at page 2 ↗
    • The researchers used a Factorial Randomized Block Design with eight cultivars, two growth stages, and three replications. View evidence ↗

      What they did

      The researchers used a Factorial Randomized Block Design with eight cultivars, two growth stages, and three replications.

      In the paper's own words

      “The experiment was laid out in a Factorial Randomized Block Design (FRBD) with: • 8 cultivars (Factor A) • 2 growth stages (Factor B) • 3 replications”

      Page 2

      Found in: Experimental design and layout

      Read it in the full textOpen PDF at page 2 ↗
  4. What they found

    • Dry matter (DM) content increased significantly as the plants matured, rising from 86.55% at 60 days to 89.90% at 90 days. View evidence ↗

      What they found

      Dry matter (DM) content increased significantly as the plants matured, rising from 86.55% at 60 days to 89.90% at 90 days.

      In the paper's own words

      “The mean DM content increased from 86.55% at Stage I (60 DAS) to 89.90% at Stage II (90 DAS).”

      Page 2

      Found in: Results and Discussion Dry Matter (DM)

      Read it in the full textOpen PDF at page 2 ↗
    • Crude fiber (CF) content increased significantly from 23.73% at Stage I to 27.60% at Stage II. View evidence ↗

      What they found

      Crude fiber (CF) content increased significantly from 23.73% at Stage I to 27.60% at Stage II.

      In the paper's own words

      “Crude fibre content increased significantly with growth stage (p < 0.01) (Table 1), rising from 23.73% at Stage I to 27.60% at Stage II.”

      Page 3

      Found in: Crude Fibre (CF)

      Read it in the full textOpen PDF at page 3 ↗
    • Total ash content declined significantly from 11.71% at Stage I to 9.71% at Stage II. View evidence ↗

      What they found

      Total ash content declined significantly from 11.71% at Stage I to 9.71% at Stage II.

      In the paper's own words

      “Total ash content decreased significantly with maturity (p < 0.01) (Table 1), declining from 11.71% at Stage I to 9.71% at Stage II.”

      Page 3

      Found in: Ether Extract (EE)

      Read it in the full textOpen PDF at page 3 ↗
    • Neutral Detergent Fiber (NDF) increased significantly from 52.38% at Stage I to 59.36% at Stage II. View evidence ↗

      What they found

      Neutral Detergent Fiber (NDF) increased significantly from 52.38% at Stage I to 59.36% at Stage II.

      In the paper's own words

      “NDF content increased significantly with growth stage (p < 0.01) (Table 2), from 52.38% at Stage I to 59.36% at Stage II.”

      Page 3

      Found in: Results and Discussion Dry Matter (DM)

      Read it in the full textOpen PDF at page 3 ↗
    • Lignin content increased significantly from 2.31% at Stage I to 3.00% at Stage II. View evidence ↗

      What they found

      Lignin content increased significantly from 2.31% at Stage I to 3.00% at Stage II.

      In the paper's own words

      “Lignin content increased significantly with growth stage (p < 0.01) (Table 2), from 2.31% at Stage I to 3.00% at Stage II.”

      Page 3

      Found in: Lignin

      Read it in the full textOpen PDF at page 3 ↗
    • Calcium (Ca) content decreased from 0.09% at Stage I to 0.08% at Stage II. View evidence ↗

      What they found

      Calcium (Ca) content decreased from 0.09% at Stage I to 0.08% at Stage II.

      In the paper's own words

      “The mean Ca content was 0.085%, decreasing from 0.09% (Stage I) to 0.08% (Stage II).”

      Page 3

      Found in: Mineral composition 7.1 Calcium (Ca)

      Read it in the full textOpen PDF at page 3 ↗
    • Phosphorus (P) content decreased from 0.14% at Stage I to 0.11% at Stage II. View evidence ↗

      What they found

      Phosphorus (P) content decreased from 0.14% at Stage I to 0.11% at Stage II.

      In the paper's own words

      “Phosphorus content also showed significant variation (p < 0.01) (Table 3), with mean value of 0.13%. Stage-wise values were 0.14% (Stage I) and 0.11% (Stage II).”

      Page 3

      Found in: Phosphorus (P)

      Read it in the full textOpen PDF at page 3 ↗
    • Among the cultivars, RO-2000-19 was identified as the superior genotype due to its highest crude protein and lowest silica content. View evidence ↗

      What they found

      Among the cultivars, RO-2000-19 was identified as the superior genotype due to its highest crude protein and lowest silica content.

      In the paper's own words

      “Table 4 delineates cultivar-wise nutritional stratification, clearly indicating RO-2000-19 as the superior genotype, characterized by highest crude protein and lowest silica content”

      Page 4

      Found in: Conclusion

      Read it in the full textOpen PDF at page 4 ↗
    • RO-2000-16 had the highest dry matter, crude fiber, and silica, indicating high biomass but lower nutritional quality. View evidence ↗

      What they found

      RO-2000-16 had the highest dry matter, crude fiber, and silica, indicating high biomass but lower nutritional quality.

      In the paper's own words

      “In contrast, RO-2000-16 exhibited maximum dry matter, crude fibre, and silica, signifying greater structural biomass but inferior feeding quality.”

      Page 4

      Found in: Conclusion

      Read it in the full textOpen PDF at page 4 ↗
  5. What it means

    • The authors conclude there is a trade-off between yield and quality, recommending harvesting at 60 days after sowing to maximize nutritional value. View evidence ↗

      What it means

      The authors conclude there is a trade-off between yield and quality, recommending harvesting at 60 days after sowing to maximize nutritional value.

      In the paper's own words

      “Overall, the findings establish a clear trade-off between forage yield and nutritional quality, emphasizing that early harvesting (around 60 DAS) is optimal for maximizing nutritive value, while later stages favor biomass accumulation.”

      Page 4

      Found in: Conclusion

      Read it in the full textOpen PDF at page 4 ↗
    • The authors recommend combining strategic cultivar selection with optimal harvest timing to improve livestock productivity. View evidence ↗

      What it means

      The authors recommend combining strategic cultivar selection with optimal harvest timing to improve livestock productivity.

      In the paper's own words

      “Therefore, strategic selection of cultivar in conjunction with appropriate harvest timing is critical for optimizing forage utilization and enhancing livestock productivity.”

      Page 4

      Found in: Conclusion

      Read it in the full textOpen PDF at page 4 ↗

Visual summary

3 visuals

Illustrations explain the paper; charts are replotted from the paper's own table values.

AI-generated illustration
AI-generated conceptual illustration (oat plants (Avena sativa)). It explains the idea and does not show study data.↗ Enlarge
Trade-off between Yield and Quality
AI-generated conceptual illustration (oat plants (Avena sativa)). It explains the idea and does not show study data.

AI-generated conceptual illustration (oat plants (Avena sativa)). It explains the idea and does not show study data.

Open full-size image ↗

Trade-off between Yield and Quality

AI-generated conceptual illustration (oat plants (Avena sativa)). It explains the idea and does not show study data.

View source evidence ↗
Replotted from source data
Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.↗ Enlarge
Stage I (60 DAS) and Stage II (90 DAS): DM vs CF vs Ash
Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

Open full-size image ↗

Stage I (60 DAS) and Stage II (90 DAS): DM vs CF vs Ash

Replotted from Table 1 (page 2) of the original paper. Every bar is the paper's own table value.

View source evidence ↗
Replotted from source data
Replotted from Table 3 (page 3) of the original paper. Every bar is the paper's own table value.↗ Enlarge
Stage I and Stage II: Calcium vs Phosphorus
Replotted from Table 3 (page 3) of the original paper. Every bar is the paper's own table value.

Replotted from Table 3 (page 3) of the original paper. Every bar is the paper's own table value.

Open full-size image ↗

Stage I and Stage II: Calcium vs Phosphorus

Replotted from Table 3 (page 3) of the original paper. Every bar is the paper's own table value.

View source evidence ↗

Figures & tables

From the original paper
Effect of growth stage on proximate composition (%)Table 1Page 2Fiber fractions (%) of oat cultivarsTable 2Page 3Mineral composition (%) of oat cultivarsTable 3Page 3Best and poorest cultivars (nutritional ranking)Table 4Page 4
FULL TEXT Original article · reflowed for reading

Introduction

Oat (Avena sativa L.) is one of the most important winter forage crops widely cultivated for livestock feeding due to its high biomass yield, palatability, and superior nutritive value. It plays a crucial role in bridging the gap between demand and availability of green fodder, particularly in mixed farming systems where dairy and draught animals require balanced nutrition. Oat forage is characterized by a favorable combination of crude protein, digestible carbohydrates, and mineral content, making it an essential component of ruminant feeding systems (Hanoğlu, 2024) [1] . In recent years, increasing emphasis has been placed on improving forage quality alongside yield, as the nutritional composition of fodder directly influences animal productivity, health, and overall farm profitability. The nutritive value of oat forage is determined by its chemical composition, including Crude Protein (CP), fiber fractions such as Neutral Detergent Fiber (NDF) and Acid Detergent Fiber (ADF), ether extract, ash, and soluble carbohydrates. These components collectively influence digestibility, intake, and energy availability in ruminants (Gaytán-Aleman, 2025) [2] . One of the most critical factors affecting the nutritional quality of oat forage is the stage of growth at harvest. As the plant matures, significant biochemical and structural changes occur. Early growth stages are characterized by higher concentrations of crude protein, minerals, and soluble carbohydrates, whereas later stages show increased accumulation of structural carbohydrates such as cellulose, hemicellulose, and lignin. This shift results in reduced digestibility and feeding value. Several studies have demonstrated that crude protein and ash content decline with maturity, while fiber fractions increase, thereby negatively affecting forage quality (Liu, 2015 & Coblentz, 2010) [3,5] .

Moreover, the increase in cell wall constituents with advancing maturity is associated with decreased digestibility and metabolizable energy. The rise in NDF and ADF concentrations reduces the availability of nutrients to rumen microbes, ultimately lowering feed efficiency (Coblentz, 2010) [5] . Concurrently, lignification and silica deposition further restrict microbial degradation of plant tissues, making mature forage less digestible. Therefore, determining the optimal harvest stage is essential to balance forage yield and nutritional quality. Apart from growth stage, genotypic variation among oat cultivars also plays a significant role in determining forage quality. Different cultivars exhibit variability in chemical composition, fiber content, and digestibility characteristics. Recent studies have highlighted substantial genetic variability in oat with respect to nutritional traits, suggesting the potential for selecting superior cultivars for improved forage quality and animal performance (Singh, 2024) [4] . In addition, agronomic and environmental factors such as fertilization, climate, and management practices further influence forage quality. Optimizing these factors, along with selecting appropriate cultivars and harvest stages, is essential for enhancing the efficiency of forage-based livestock systems (Duan, 2024) [6] . Despite extensive research on oat forage, there is still a need for systematic evaluation of different oat cultivars across distinct growth stages under specific agro-climatic conditions, particularly in regions where fodder scarcity is a major constraint. Understanding the interaction between genotype and growth stage is crucial for identifying cultivars that can maintain better nutritional quality over time. Therefore, the present study was undertaken to evaluate the effect of growth stage on chemical composition and nutritional quality of different oat (Avena sativa) cultivars, with the objective of identifying suitable cultivars and optimum harvesting stage for maximizing forage quality.

Materials and Methods

Materials and Methods

Experimental site

The experiment was conducted at the Forage Crop Research Project, Mahatma Phule Krishi Vidyapeeth (MPKV), Rahuri, Maharashtra, India.

Experimental material

Experimental material

Experimental design and layout

The experiment was laid out in a Factorial Randomized Block Design (FRBD) with: Whole plants were harvested, chopped (2-3 cm), sun-dried, and ground to pass through a 2 mm sieve.

Chemical analysis a) Proximate analysis (AOAC, 2012)

b) Fiber fractions (Van Soest and Moore, 1968) [8] • Neutral Detergent Fiber (NDF)

Statistical analysis

Data were analyzed using Factorial Randomized Block Design (FRBD)

Results and Discussion Dry Matter (DM)

Dry matter content increased significantly with advancement of growth stage (p < 0.01) (Table 1). The mean DM content increased from 86.55% at Stage I (60 DAS) to 89.90% at Stage II (90 DAS). Among cultivars (Table 1), DM ranged from 87.23% (RO-2000-1) to 89.05% (RO-2000-16). The non-significant interaction effect indicates that all cultivars followed a similar trend of increasing DM with maturity. This increase reflects progressive accumulation of structural biomass and reduction in moisture content, consistent with findings of Coblentz et al. (2010) [5] . [11,5] .

Table 1. Effect of growth stage on proximate composition (%)
ParameterStage I (60 DAS)Stage II (90 DAS)Significance
DM86.5589.90**
CP11.529.22**
EE2.962.50**
CF23.7327.60**
NFE50.7051.00NS
Ash11.719.71**

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Table 1
Effect of growth stage on proximate composition (%)

Effect of growth stage on proximate composition (%)

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Ether Extract (EE)

Ether extract content was significantly affected by cultivar and growth stage (p < 0.01) (Table 1). The mean EE content decreased from 2.96% at Stage I to 2.50% at Stage II. Among cultivars (Table 1), EE varied from 2.39% (RO-2000-16) to 3.01% (RO-2000-7). The decline in EE with maturity may be attributed to reduced lipid concentration as structural biomass increases (Cherney & Marten, 1982) [9] .

Crude Fibre (CF)

• Crude fibre content increased significantly with growth stage (p < 0.01) (Table 1), rising from 23.73% at Stage I to 27.60% at Stage II. • Among cultivars (Table 1), CF ranged from 23.72% (Kent) to 26.90% (RO-2000-16). The significant interaction effect indicates that cultivars differed in their rate of fiber accumulation. • The increase in CF is associated with increased lignification and deposition of structural carbohydrates, as reported by Van Soest (1994) [12] .

Nitrogen Free Extract (NFE)

• Nitrogen free extract content showed significant variation among cultivars (p < 0.05) but stage effect was non-significant (Table 1). [11] .

Fiber fractions 5.1 Neutral Detergent Fibre (NDF)

• NDF content increased significantly with growth stage (p < 0.01) ( 2). The increase reflects higher cell wall content and reduced digestibility (Van Soest, 1994) [12] .

Acid Detergent Fibre (ADF)

• ADF increased significantly with maturity (p < 0.01) (Table 2), from 28.85% (Stage I) to 32.43% (Stage II). • Among cultivars, ADF ranged from 29.48% (RO-2000-19) to 31.72% (RO-2000-1) (Table 2). The significan interaction effect indicates genotype-specific variation.

Table 2. Fiber fractions (%) of oat cultivars
ParameterMean rangeSignificance (Strain)Significance (Stage)
NDF55.12 - 57.05NS**
ADF29.48 - 31.72****
Hemicellulose23.98 - 26.23NS**
Cellulose24.85 - 28.58****
Lignin2.55 - 2.83***
Silica2.32 - 2.70****

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Fiber fractions (%) of oat cultivars↗ Enlarge
Table 2
Fiber fractions (%) of oat cultivars

Fiber fractions (%) of oat cultivars

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Hemicellulose

Hemicellulose content increased significantly (p < 0.01) from 23.53% (Stage I) to 26.93% (Stage II) (Table 2). Differences among cultivars were non-significant.

Cellulose

Cellulose content increased significantly with maturity (p < 0.01) (Table 2), from 24.41% to 29.35%. Among cultivars, cellulose ranged from 24.85% (RO-2000-19) to 28.58% (RO-2000-16).

Lignin

Lignin content increased significantly with growth stage (p < 0.01) (Table 2), from 2.31% at Stage I to 3.00% at Stage II. Among cultivars, lignin ranged from 2.55% (RO-2000-1) to 2.83% (RO-2000-7 and RO-2000-16). Increased lignin reduces digestibility due to restricted microbial access (Jung & Allen, 1995) [10] .

Silica

Silica content increased significantly (p < 0.01) (Table 2), from 2.32% (Stage I) to 2.77% (Stage II). Among cultivars, silica ranged from 2.32% (RO-2000-19) to 2.70% (RO-2000-16).

Mineral composition 7.1 Calcium (Ca)

Calcium content differed significantly among cultivars and growth stages (p < 0.01) (Table 3). The mean Ca content was 0.085%, decreasing from 0.09% (Stage I) to 0.08% (Stage II). Highest Ca content was observed in Kent, while lowest in RO-2000-1, RO-2000-7 and RO-2000-12.

Table 3. Mineral composition (%) of oat cultivars
ParameterStage IStage IIMeanSignificance
Calcium0.090.080.085**
Phosphorus0.140.110.13**

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Table 3
Mineral composition (%) of oat cultivars

Mineral composition (%) of oat cultivars

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Phosphorus (P)

Phosphorus content also showed significant variation (p < 0.01) (Table 3), with mean value of 0.13%.

Stage-wise values were 0.14% (Stage I) and 0.11% (Stage II). Among cultivars, highest P was recorded in Kent (0.17%), while lowest (~0.10%) in some cultivars.

Conclusion

The present investigation clearly demonstrated that growth stage exerts a predominant influence on the chemical composition and nutritive value of oat (Avena sativa) cultivars, with maturity-associated changes significantly altering forage quality. Advancement from 60 to 90 days after sowing resulted in a marked increase in structural carbohydrates (crude fibre, NDF, ADF, cellulose, lignin, and silica) accompanied by a concomitant decline in crude protein, ether extract, ash, and mineral content (Ca and P). These compositional shifts reflect progressive lignification and cell wall development, ultimately reducing the nutritive value of the forage. Significant genotypic variation was also observed, indicating the potential for selection of superior cultivars. Among the tested entries, RO-2000-19 consistently exhibited superior nutritional attributes, characterized by higher crude protein and lower fibre and silica content, whereas RO-2000-16 showed greater dry matter accumulation but inferior quality due to elevated structural constituents. Overall, the findings establish a clear trade-off between forage yield and nutritional quality, emphasizing that early harvesting (around 60 DAS) is optimal for maximizing nutritive value, while later stages favor biomass accumulation. Therefore, strategic selection of cultivar in conjunction with appropriate harvest timing is critical for optimizing forage utilization and enhancing livestock productivity.

Figures and tables from the paper

Table 4. Best and poorest cultivars (nutritional ranking)
TraitBest cultivarValuePoor cultivarValue
CPRO-2000-19HighestRO-2000-2Lowest
DMRO-2000-16HighestRO-2000-1Lowest
CFKentLowestRO-2000-16Highest
LigninRO-2000-1LowestRO-2000-7/16Highest
SilicaRO-2000-19LowestRO-2000-16Highest

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Table 4
Best and poorest cultivars (nutritional ranking)

Best and poorest cultivars (nutritional ranking)

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References

11 in the original paper
  1. Hanoğlu Oral H. Forage yields and nutritive values of oat and triticale pastures for grazing sheep in early spring. PeerJ. 2024;12:e17840. DOI:10.7717/peerj.17840.
  2. Gaytán-Aleman L, Mendoza-Carreola J, CalderónLeyva G, Arellano-Rodriguez F, Angel-García O, Contreras-Villarreal V, et al. Nutrient composition, digestibility, and intake of diets chosen by goats that grazed alfalfa and oat field residues. J Appl Anim Res. 2025;53(1):2486265.
  3. Liu K, Mahmood K. Nutrient composition and protein extractability of oat forage harvested at different maturity stages as compared to grain. J Agric Sci. 2015;7(12):50.
  4. Singh S, Koli P, Ahmed S, Kumar N, Rana M, Singhal R, et al. Exploring the genetic variability in yield, nutritional and digestibility traits in oat grains through ruminant nutrition. Heliyon. 2024;10(10).
  5. Coblentz WK, Walgenbach RP. Fall growth, nutritive value, and estimation of total digestible nutrients for cereal-grain forages in the north-central United States. J Anim Sci. 2010;88(1):383-399.
  6. Duan L, Ju Z, Ma X, Pan J, Mustafa AEZM, Jia Z. Research on enhancing the yield and quality of oat forage: Optimization of nitrogen and organic fertilizer management strategies. Agronomy. 2024;14(7):1406.
  7. Van Soest PJ, Jones LHP. Effect of silica in forages upon digestibility. J Dairy Sci. 1968;51(10):1644-1648.
  8. Cherney JH, Marten GC. Small grain crop forage potential: II. Interrelationships among biological, chemical, morphological, and anatomical determinants of quality. Crop Sci. 1982;22(2):240-245.
  9. Jung HG, Allen MS. Characteristics of plant cell walls affecting intake and digestibility of forages by ruminants. J Anim Sci. 1995;73(9):2774-2790.
  10. Khorasani GR, Jedel PE, Helm JH, Kennelly JJ. Influence of stage of maturity on yield components and chemical composition of cereal grain silages. Can J Anim Sci. 1997;77(2):259-267.
  11. Van Soest PJ. Nutritional ecology of the ruminant. Ithaca (NY): Cornell University Press; 1994.