Next Article in Journal
Long-Term Low-Rate Biochar Application Enhances Soil Organic Carbon Without Affecting Sorghum Yield in a Calcaric Cambisol
Next Article in Special Issue
Evaluation of Hybrid Sorghum Parents for Morphological, Physiological and Agronomic Traits Under Post-Flowering Drought
Previous Article in Journal
Simulation of Soil Water Transport and Utilization in an Apple–Soybean Alley Cropping System Under Different Irrigation Methods Based on HYDRUS-2D
Previous Article in Special Issue
Comprehensive Evaluation of Different Oat Varieties in Semi-Arid Areas of Gansu Province
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Comprehensive Evaluation and Screening of Autumn-Sown Oat (Avena sativa L.) Germplasm in Different Agropastoral Regions

1
State Key Laboratory of Crop Gene Exploration and Utilization in Southwest China, Sichuan Agricultural University, Chengdu 611130, China
2
Triticeae Research Institute, Sichuan Agricultural University, Chengdu 611130, China
3
Liangshan Academy of Agricultural Sciences, Xichang 615000, China
*
Author to whom correspondence should be addressed.
Agronomy 2025, 15(4), 994; https://doi.org/10.3390/agronomy15040994
Submission received: 18 March 2025 / Revised: 16 April 2025 / Accepted: 18 April 2025 / Published: 21 April 2025

Abstract

:
In light of current global challenges of climate change, the over-exploitation of natural resources, and increasing demand for livestock products, the exploration of excellent forage crop resources holds great potential for development. Therefore, selecting forage crops that are high-yield, high-quality, and have excellent resistance to pests and diseases can greatly promote the development of the livestock industry. Oat (Avena sativa L.), a dual-purpose crop for grain and forage, plays a vital role in the development of animal husbandry. Autumn-sown oats have a significantly longer growth cycle than spring-sown oats, ensuring a year-round forage supply and achieving higher yields. The agropastoral transitional zone in southwest China is a key region for autumn-sown oats, but the systematic evaluation of oat germplasm there is still limited. Therefore, we conducted a two-growing-season (2022–2024) field experiment across four locations to evaluate nine oat genotypes for growth phenotypes, forage productivity, and nutritional quality through 11 agronomic traits and nutritional parameters during the filling stage (Zadok’s 75). The results revealed the following: (1) agronomic performance: dry matter yield (DMY) ranged from 10.72 to 14.58 t/ha, with line ‘WC109’ achieving the highest DMY (14.58 t/ha) and crude protein (CP, 9.66%); (2) nutritional quality: CP exhibited a significant negative correlation with fiber content (NDF: r = −0.72, p < 0.01; ADF: r = −0.68, p < 0.01), highlighting a yield–quality trade-off; ‘WC109’ demonstrated superior forage value, with the highest relative forage quality (RFQ: 115.45) and grading index (GI: 19.30); (3) environmental adaptation: location-specific climatic conditions significantly influenced productivity, with Wenjiang (WJ) showing optimal performance due to favorable temperature and precipitation. These results position ‘WC109’ as a promising candidate for autumn-sown cultivation in southwest China, addressing winter forage shortages while enhancing livestock nutrition. Our findings further elucidate the mechanisms linking yield and feeding value to growth performance indicators, providing references for trait-based measures to enhance forage oat productivity and quality.

1. Introduction

With the growth in China’s population and the continuous upgrading of residents’ dietary structures, the demand for protein-rich foods is steadily increasing [1]. Livestock products, as a primary source of protein, play a crucial role in ensuring dietary health. Animal husbandry can effectively convert non-edible crops, such as fodder, into human food [2,3]. However, to meet the demand for livestock products, overgrazing and unreasonable development have led to the deterioration of the ecological environment of natural grasslands [4,5,6]. In recent years, the Chinese government has attached great importance to grassland restoration and environmental protection, recognizing that only by developing forage cultivation and animal husbandry can the contradiction between human and livestock needs for grain be effectively alleviated, the safety of the ecological environment be maintained, and the transformation and upgrading of the livestock industry be promoted [7,8,9].
With the structural adjustment of agriculture and animal husbandry, the promotion and application of grain to feed, the rapid reform of the agricultural supply chain, and the implementation of the rural revitalization strategy, China’s livestock enterprises have undergone radical changes, and animal husbandry occupies a large proportion of economic production [10]. In China’s southwestern region, the conventional agricultural practice involves sowing in late spring and harvesting in early autumn during the frost-free period (90–125 d), with subsequent fallow periods in late autumn and winter [11]. However, research indicates that cultivating fodder crops during the fallow season can significantly enhance soil nutrients [12,13]. In this region, the seasonal imbalance of forage supply—especially the feed shortage during the winter and spring seasons (from November to April of the following year)—has become a key bottleneck restricting the sustainable development of the livestock industry (https://www.gov.cn/gzdt/2010-02/21/content_1538234.htm, accessed on 21 February 2010). The scarcity of winter forage has consistently hindered the development of the livestock sector; thus, by optimizing the agricultural planting structure and increasing the area of winter forage cultivation, the issue of supply shortage can be effectively alleviated [14,15]. Moreover, selecting the appropriate forage varieties is of paramount importance. Oat (Avena sativa L.), as an annual crop that serves both as grain and fodder, is a principal source of feed for livestock globally and is also a significant type of cold-season grassland forage [16,17,18]. Oats are known for their wide adaptability, robust resistance to adverse conditions, and short growth cycle [19,20]. Appreciated for their excellent palatability and high nutritional value, oats are cultivated and utilized extensively both within China and abroad. The market demand for oats continues to rise due to their high nutritional value, good palatability, and easy digestion and absorption (https://www.renrendoc.com/paper/400944282.html, accessed on 23 March 2025). Furthermore, oat planting techniques are being continuously improved, resulting in significant increases in yield and quality. Meanwhile, oat processing technologies are also being refined, leading to a growing variety of products and enhanced market competitiveness (https://max.book118.com/html/2025/0219/5010132140012102.shtm, accessed on 17 April 2025).
China, a major player in the global animal husbandry sector and a traditional region for oat cultivation, confronts unique challenges regarding oat variety adaptation, yield, and quality due to its diverse climate and intricate topography. Although preliminary screening of oat varieties has been conducted [21,22], the existing varieties are often unable to meet the urgent demand for autumn-sown high-quality forage in agricultural and pastoral areas. In this study, we conducted a two-year trial of high-performing lines based on the preliminary screening. We measured growth characteristics, forage yield, and feeding value. The goals of the trial were as follows: (1) to comprehensively assess the adaptability, yield, and nutritional value of different oat varieties/lines; (2) to identify high- and stable-yield forage oats and evaluated their forage potential; and (3) to provide superior germplasm for autumn sowing in agricultural and pastoral areas of China to promote the sustainable development of the local livestock industry.

2. Materials and Methods

2.1. Plant Materials

Nine oat genotypes were tested, including ‘Longyan 3’ and ‘Intimidator’, which are widely promoted forage oat varieties in China and were used as the control group. The remaining seven lines (‘WC109’, ‘WC130’, ‘WC179’, ‘WC283’, ‘WC286’, ‘WC291’, ‘WC299’) were selected from Sichuan Agricultural University based on previous screening efforts in autumn-sown areas of China [23]. The growth period of each genotype in different environments is shown in Table 1. Based on our initial screening, all the selected genotypes showed high disease resistance potential and good lodging resistance.

2.2. Experimental Site and Design

The trial was conducted during the 2022–2023 and 2023–2024 growing seasons at four different locations. Wenjiang (WJ) (103°51′ E, 30°43′ N), Chongzhou (CZ) (103°38′ E, 30°32′ N), and Guangyuan (GY) (105°86′ E, 32°43′ N) have typical subtropical humid monsoon climates, with elevations of 507, 514, and 1030 m; the total amounts of annual precipitation are 966, 1162, and 1136 mm; and the annual mean temperatures are 16.3, 16.7, and 16.1 °C, respectively. Xichang (XC) (102°26′ E, 27°89′ N) has a typical subtropical plateau monsoon climate, with an altitude of 1500 m, a total annual precipitation of 873 mm, and an annual mean temperature of 17.6 °C. The minimum temperature, maximum temperature, altitude, and monthly precipitation from seeding to harvest at each location are depicted in Figure 1. Before sowing, soil samples from 0 to 20 cm were collected using a five-point sampling method (Table 2). The determination of soil nutrients was conducted in accordance with the methods of soil agrochemical analysis (https://www.docin.com/p-2219784431.html, accessed on 12 June 2019).
The experiment was conducted using a completely randomized block design with four replications. Seeds were sown by hand on 17–24 October, during the 2022–2024 cropping seasons. The individual plots were 3 m × 5 m with a 0.7 m pass way. The seeds were planted by the strip method with a seeding rate of 2.4 million plants per hectare, plots were sown with 10 rows at a spacing of 0.3 m, and the sowing depth was 4 cm. Before sowing, the soil was prepared with a chisel plow and a disk harrow. A week before sowing, based on local fertilization recommendations, all plots were treated with a compound fertilizer (N:P2O5:K2O = 15:15:15), at a rate of 80 kg/ha. During the experimental period, other field management practices adhered to local protocols. No additional fertilization or irrigation was applied. All test plots were kept weed-free by manual hoeing. Chemicals were used to control pests and diseases when necessary.

2.3. Measurement Index and Methods

2.3.1. Agronomic Characteristics

All agronomic characteristics were assessed at the filling stage (Zadok’s 75) [24]. The plant height (PH), tiller number (TN), and stem–leaf ratio (SLR) were measured using 10 plants randomly selected from the center of each plot. Ten plants were randomly selected from the central part of each plot to measure the PH, TN, and SLR. The PH was measured using a tape measure from the base to the top of the plant. The TN was counted directly. After measuring the PH and TN, the plants were cut at ground level, and their stems and leaves were separated. The dry weights of the stems and leaves were calculated after drying to obtain the SLR. The yield was determined by manually harvesting a 9.60 m2 area of forage (Zadok’s 75) from the central region of each 15 m2 plot, cutting at a height of 5 cm above the soil surface, and promptly weighing the biomass. Thereafter, approximately 2 kg of fresh tissue samples were collected from each plot, and the samples were placed in paper bags and oven-dried at 105 °C for 30 min to terminate physiological processes, then re-oven-dried at 65 °C to constant weight, which was used to determine the dry matter yield (DMY). Subsequently, the desiccated samples were individually pulverized, sifted, and sealed in paper bags for subsequent analysis.

2.3.2. Nutritional Indices

In order to assess the nutritional value of different genotypes of forage oats, the neutral detergent fiber (NDF) and acid detergent fiber (ADF) were estimated by the sequential method [25], the crude protein (CP) was determined using the Kjeldahl method [26], the crude fat (EE) was determined using the Soxhlet extraction method [27], and the crude ash (ASH) was measured using the Mafu furnace burning method [28]. The values of each trait were standardized as a percentage of the DMY, with the mean values being employed for further analysis.
Indicators for evaluating the nutritional value of forages include relative forage quality (RFQ) and grading index (GI), which were calculated using the following formulas [29,30]:
RFQ = TDN × DMI
TDN = 82.38 − 0.7515 × ADF
DMI = 120 ÷ NDF
GI = NEL × VDMI × CP ÷ NDF
NEL = (1.004 − 0.0124 × ADF) × 9.29
VDMI = 1.2 × BW × NDF
where TDN was total digestible nutrients (%), DMI was dry matter intake (%), NEL was net energy for lactation (MJ/kg), VDMI was voluntary dry matter intake (kg/d), and BW was the body weight of an average cow, calculated as 600 kg.

2.4. Statistical Analysis

Agronomic characteristics and nutritional indices were initially collated using Microsoft Excel 2021 and subjected to statistical analysis using IBM SPSS Statistics 28 (USA) software. All data were subjected to one-way and three-way (genotype × year × location) analysis of variance (ANOVA) and presented as mean ± standard deviation. Significant differences among means were determined using the least significant difference (LSD) test at a 5% significance threshold. Correlation analyses between traits were performed in Origin 2021 and plotted using GraphPad Prism 8. In order to more clearly demonstrate the direct and indirect effects among multiple variables, we conducted a structural equation model (SEM) analysis using the data collected from eight experimental sites, nine materials, and four replicates for each material. This analysis aimed to reflect how growth performance and nutritional composition influence forage yield and feeding value. The SEM was constructed by using the ‘Lavaan’ function in the R package (v4.4.2, R Core Team, 2024). Subsequently, we simplified the model by eliminating nonsignificant paths and selecting the model with a chi-square-to-degrees of freedom ratio of less than 2.0, root mean square error of approximation of less than 0.05, comparative fit index of greater than 0.9, and p-value of greater than 0.05. The AMMI model analysis was conducted using the ‘agricolae’ package in R.

3. Results

3.1. Agronomic Performance

In this study, we evaluated nine oat genotypes sown in the autumns of 2022 and 2023 for key agronomic traits including DMY, PH, TN, and SLR. Our findings indicated that all assessed agronomic traits were significantly influenced by the factors of G, Y, L, G × Y, G × L, Y × L, and G × Y × L (except for TN) (Table 3, Table 4, Table 5 and Table 6). The selection of genotypes with superior yield in a specific environment does not necessarily facilitate the identification of their capability of exhibiting comparable performance across diverse environmental conditions. The mean DMYs of oats across locations over the years are presented in Table 3. The mean DMY varied between 10.72 and 14.58 t/ha. Notably, ‘WC109’ exhibited the highest DMY, followed by ‘Intimidator’, ‘WC283’, and ‘Longyan 3’, with each of these genotypes achieving a DMY exceeding 13 t/ha. This performance indicates a pronounced high-yielding tendency and is significantly superior to the remaining five lines. Furthermore, the data revealed that the maximum DMY was observed at location WJ, as compared to other sites, suggesting that the climatic conditions prevalent in WJ are particularly conducive to the cultivation of forage oats.
Mean values of PH at the harvest stage for forage oats across all locations are presented in Table 4. The overall mean PH ranged from 112.3 to 160.8 cm, with ‘WC109’ exhibiting the highest PH value, followed by ‘Intimidator’, while ‘WC299’ displayed the lowest, showing highly significant differences (p < 0.05). Additionally, PH was significantly higher in the WJ location than in the other three test sites (p < 0.05), and PH was higher in the 2023–2024 growing season than in the 2022–2023 growing season.
The mean TNs of forage oats across locations over the years are presented in Table 5. The TN range for these oat genotypes was 4.7–6.5, with three genotypes showing elevated TNs: ‘WC109’ (6.5), ‘Intimidator’ (6.0), and ‘Longyan 3’ (5.9), which exhibited an increase of 9.26% to 20.37% above the mean. ‘WC109’, ‘Intimidator’, and ‘Longyan 3’ show no difference among themselves (p > 0.05), but their results are significantly higher than the other six lines (p < 0.05).
Analysis of the SLR for the nine forage oat genotypes revealed that ‘WC179’ had the lowest content, of 66.60% (average data of four locations and two years), while ‘WC299’ had the highest content, of 77.90%, marking a difference of 16.97% between the two lines (Table 6). There was a variation in SLR between the years, with 2023–2024 showing higher values than 2022–2023. Additionally, the SLR values across different locations were ordered as WJ > CZ > XC > GY.

3.2. Nutrient Composition

The NDF, ADF, CP, EE, and ASH are five important indicators for measuring the nutritional value of forage oats. Our results indicate that these indices are influenced by genotype, year, location, and their interactions (p < 0.05) (Table 7). The average NDF content range of these oat genotypes was 50.17–53.69% (Figure 2a). Compared to other genotypes, ‘WC109’ has the lowest NDF content at 50.17%, which is 2.07% to 7.02% lower than that of others, and it showed the lowest NDF content at all four locations. The difference in the data of ‘WC109’ (30.76%), which has the lowest ADF content, and ‘WC299’ (33.74%), with the highest ADF content, is 9.69%, and the difference is extremely significant. In the other tested genotypes, the ADF content ranges from 31.64% to 32.30%, with no significant differences among them (Figure 2b).
The average CP, EE, and ASH of forage oats across the four locations and over the two years are presented in Figure 3. Compared to other genotypes, ‘WC109’ (9.63%) had the highest CP content, significantly higher than that of other genotypes, which ranged from 4.12% to 30.84%. This was followed by ‘Intimidator’ at 8.99%, indicating that these two genotypes have superior amino acid profiles (Figure 3a). The results showed that ‘Intimidator’ (3.74%) and ‘WC283’ (3.48%) have a significantly higher EE content than the other genotypes, with increases of 16.15% to 28.08% and 8.07% to 19.18%, respectively. ‘WC299’ (2.92%) had the lowest EE content, followed by ‘WC286’ (2.94%), with no significant difference between them (Figure 3b). In terms of ASH content, ‘Longyan 3’ had the highest content of 9.37%, while ‘WC109’ had the lowest at 7.73%, with a difference of 21.22%. ‘Longyan 3’ showed no significant difference compared to ‘WC299’ and ‘WC179’, but was significantly higher than other genotypes (p < 0.05) (Figure 3c).
In the realm of practical application, the RFQ and GI emerge as critical metrics for evaluating the nutrient content and overall quality of forage. The mean RFQs and GIs of the oats across the locations over the years are presented in Figure 4. The RFQ value variation (p < 0.05) among genotypes ranged from 104.72 to 115.45. ‘WC109’ obtained a higher RFQ than its counterparts in the test (Figure 4a). The highest GI was for ‘WC109’ (19.30), followed by ‘Intimidator’ (16.23) and ‘Longyan 3’ (15.48), whereas the lowest GI was for ‘WC299’ (12.50). The recorded variation (p < 0.05) among oat genotypes for GI ranged from 12.50 to 19.30, with a mean value of 14.82 (Figure 4b).

3.3. Correlation of Agronomic Traits and Nutrients

The forage oat DMY displayed a significant positive correlation with PH, TN, SLR, EE, and CP, but it exhibited a significant negative correlation with NDF (p < 0.05). CP was highly significantly positively correlated with EE, PH, and TN (p < 0.05), and it had a positive but not significant correlation with ASH (p > 0.05), and a highly significant negative correlation with NDF and ADF (p < 0.05). PH displayed an extremely significant negative correlation with NDF, and TN displayed an extremely significant negative correlation with ADF (p < 0.05) (Figure 5).

3.4. Key Factors for Changes in Yield and Feeding Value

Most traits of forage oats were strongly correlated with each other. Structural equation model (SEM) analysis was further employed to evaluate the direct and indirect effects of growth performance and nutritional components on yield and feeding value (Figure 6). PH, TN, and SLR all enhanced the yield of forage oats, but the SLR was significantly lower than TN, which was significantly lower than PH. The main factors contributing to the increased forage oat yield and feeding value for PH included CP and NDF. The main causes of the increased forage oat yield and feeding value for TN included CP and NDF. The SLR primarily reduced the forage oat feeding value by increasing the contents of NDF and ADF. In addition, there was a trade-off between the direct and indirect pathways through which the SLR affected yield.

3.5. Principal Component Analysis

Principal component analysis (PCA) facilitates the study of differences in agronomic characteristics, nutritional indices, and the evaluation of feeding value among various forage oat genotypes, thereby enabling the selection of the most optimal materials. A PCA of nine oat genotypes was conducted across eleven parameters (Figure 7), and no significant variability was found among the eight genotypes except for the ‘WC109’. For PC1 and PC2, the total variabilities were 35.3% and 20.9%, respectively. The PCA scores for PC1 and PC2 indicate that ‘WC109’ is located in the positive quadrant of PC1 and PC2. This suggests that ‘WC109’ has high DMY, CP, PH, TN, RFQ, and GI, with low fiber content, demonstrating its characteristics as a high-quality and high-yield line.

3.6. Cluster Analysis

To elucidate the relationships among the oat genotypes, a systematic cluster analysis using the Euclidean distance square method was conducted on eleven phenotype traits. At Euclidean distance 3, the genotypes were categorized into four principal clusters (Figure 8). Cluster I (‘Longyan 3’, ‘Intimidator’, ‘WC283’, and ‘WC109’) is characterized by high DMY, CP content, TFQ, and GI, showing excellent performance. Within a distance of about 1, they were further subdivided into three sub-clusters. The classification results of the sub-clusters indicate that ‘WC109’ has a superior DMY and quality compared to the control varieties, making it suitable for promotion and cultivation in the autumn-sown region.

3.7. The AMMI Model Was Employed to Evaluate the Yield Stability and High-Yield Potential of the Tested Genotypes

In this study, the AMMI biplot was constructed with average yield on the x-axis and IPCA1 (interaction principal component axis 1) on the y-axis (Figure 9). A horizontal line was drawn at IPCA1 = 0, and a vertical line was drawn at the mean yield of all genotypes. Horizontally, genotypes with higher x-axis values have higher yields. Vertically, genotypes closer to the horizontal line have more stable yields. Line ‘WC109’ had a significantly higher yield than the control, while the yield difference between ‘WC283’ and the control was not significant. The other five genotypes had yields lower than the control. The genotypes with better yield stability than the control were ‘WC286’, ‘WC179’, ‘WC130’, ‘WC283’, and ‘WC109’. Therefore, ‘WC109’ was identified as the most high-yielding and stable genotype.
In the horizontal direction, the locations are more dispersed than the genotypes, indicating that the variation among locations is much greater than that among genotypes. Genotypes located above or below the horizontal line have positive interactions with the locations on the same side, meaning that the four high-yielding materials (‘WC283’, ‘WC109’, ’Longyan 3’, and ‘Intimidator’) have the best adaptability in WJ.

4. Discussion

4.1. Oat Genotypes’ Agronomic Characteristics Comparison

PH and TN are critical determinants of forage yield, constituting key breeding targets for plant breeders [31]. The present study observed a range of 112.3 to 160.8 cm for PH and 4.7 to 6.5 for TN across nine genotypes. Additionally, our research found significant differences in PH among the same genotypes under different environments and among different genotypes under the same environment, indicating that PH is influenced by both. Our research findings are consistent with those of Dinkale [32] and Tulu [33], who both reported that the agronomic and nutritional values of the same oat variety vary across different locations. Notably, compared with the 2022–2023 growing season, all nine oat lines showed higher PH and TN in 2023–2024, which in turn increased yields. This may be due to an increase in soil nutrient content. Forage yield is a critical metric for assessing the productive capacity and economic value of diverse oat genotypes; it is the foremost factor to consider when determining whether a genotype can be promoted for cultivation in a particular region [6,34]. The characteristics of a variety are decisive for the latent productivity potential of forage. In this study, the mean DMY of the genotypes across various environments ranged from 10.72 to 14.58 t/ha, which is higher than the previous findings of Tulu, who documented a range of 7.36 to 9.03 t/ha [33]. Meanwhile, the large fluctuations in precipitation and temperature at the four locations during the reproductive period resulted in large differences in the DMY of oats. This indicates that precipitation and climatic factors have an important effect on forage yield. The superior performance of ‘WC109’ across diverse environments underscores its broad adaptability, likely due to genetic traits enhancing stress tolerance and nutrient partitioning. The significant location effect (p < 0.05) on DMY aligns with findings by Tulu [33], emphasizing the role of temperature and precipitation in oat productivity. The SLR is a commonly utilized indicator of forage palatability, with a lower ratio indicating a more abundant leaf component and enhanced palatability [35]. In this study, the SLR of the nine oat genotypes ranged from 66.60% to 77.90%, with ‘WC179’ having the lowest ratio and ‘WC299’ the highest. Line ‘WC299’ exhibited the lowest plant height and fewer tillers but had a higher stem diameter, a plant architecture that confers better resistance to lodging, thereby enabling it to maintain a favorable growth status across various environments. The variation in the SLR under different environments is quite large, indicating that it is affected by soil fertility and temperature conditions [36].

4.2. Oat Genotypes Nutritional Indices Comparison

Forage quality affects animal growth and livestock products by influencing digestibility and energy intake [37]. Previous studies have employed various chemical parameters, including NDF, ADF, and CP, to assess forage quality [38]. Oat plants contain a variety of nutrients, including CP, EE, and ASH, which are significantly superior to the straw of crops like wheat and maize, and have important forage value [39,40]. The concentration of CP is a paramount nutritional metric for assessing the dietary value of forage oats [6]. Our research has determined that lines ‘WC109’ (9.63%) and ‘Intimidator’ (8.98%) exhibit elevated CP levels, while ‘WC299’ has the lowest CP content (7.36%). The reasons for these differences may be related to differences in genotype and environment [41,42]. Given the indispensable role of CP in the growth and development of livestock, the strategic selection and cultivation of oat varieties with elevated CP concentrations are imperative for enhancing the nutritional efficacy of forage. EE plays an important nutritional role in animal feed, providing essential energy and fatty acids for livestock and poultry. In this experiment, the EE content of all genotypes was below 5%, ranging from 2.92% to 3.74%, which is consistent with previous studies [43]. NDF and ADF serve as two key indicators for assessing forage grass quality, with higher contents indicating lower quality. In this experiment, the NDF content ranged from 50.17% to 53.69%, which is lower than that reported by Mut [44] and Tulu [33], and consistent with the evaluation results of 21 oat varieties in the northwestern Shanxi region by Wang [43]. In this study, the ADF content was 30.76% to 33.74%, significantly lower than that reported in previous studies [45,46]. This discrepancy may be attributed to differences in genotype and agricultural ecological variations between experimental environments. The negative correlation between CP and fiber content (r = −0.68) mirrors trends observed in temperate forages [24]. ‘WC109’ uniquely balances high CP (9.63%) with low fiber, suggesting its potential for genetic improvement without compromising yield.

4.3. Comprehensive Evaluation of Forage Oat Genotype Screening

Previous studies have demonstrated that RFQ and GI serve as important composite indicators for evaluating forage quality [24,47], providing a basis for screening superior materials. This study showed that line ‘WC109’ had an RFQ value of 115.45 and a GI value of 19.30, which were higher than those of other genotypes, indicating its greater potential as a forage and its suitability for popularization of cultivation in autumn-sown areas. ‘WC109’ addresses critical gaps in winter forage supply, offering a 21.2% increase in DMY over regional averages. Its high RFQ and GI values support its adoption in dairy and beef production systems to enhance feed efficiency. Furthermore, climate conditions exhibit regional diversity, substantially influencing the selection of oat genotypes. Temperature, precipitation, and photoperiod are key climatic factors that directly affect the growth cycle, biomass accumulation, and yield of oats [48,49,50]. In this study, the nine oat genotypes did not show any susceptibility to pests and diseases across different environments, indicating their high resistance. Moreover, the yield variation of the same genotype was relatively small across different years in the same environment, demonstrating their stability in production. The analysis of high yield and stable yield showed that ‘WC109’ and ‘WC283’ had certain advantages.
The intrinsic genetic characteristics of oat genotypes, together with fluctuations in environmental conditions, had a key impact on yield and quality, leading to significant differences between genotypes. This observation highlights the importance of prioritizing the balance between yield and quality in practical agricultural production to optimize economic returns. In addition, SEM analysis is capable of simultaneously evaluating the direct and indirect effects among multiple variables, thereby providing a more comprehensive understanding of the complex relationships between growth performance, nutritional components, yield, and feeding value. It can help identify key factors that significantly influence yield and quality, thus providing a direction for crop variety improvement.

5. Conclusions

This study offers prospects for livestock development by screening superior forage oat genotypes for autumn-sown oats in agricultural and pastoral regions of China. Over a two-year period, nine forage oat genotypes were evaluated across four locations for agronomic traits (DMY, PH, TN, and SLR), nutritional indices (NDF, ADF, CP, EE, and ASH), and feeding value (RFQ and GI). Line ‘WC109’ consistently exhibited the highest DMY, CP, RFQ, and GI. Additionally, it showed low levels of NDF and ADF, indicating excellent palatability and nutritional quality. Therefore, it can be effectively utilized in agricultural systems to address feed gaps in autumn-sown areas. This study identifies ‘WC109’ as an elite autumn-sown oat genotype for southwest China’s agropastoral zones, combining high biomass yield (14.58 t/ha), superior nutritional quality (CP: 9.63%), and environmental adaptability. Future research should explore the molecular mechanisms underlying its stress tolerance and nutrient efficiency to guide targeted breeding programs.

Author Contributions

Conceptualization, Y.Z. (Yongjie Zhang) and Y.P.; methodology, Y.Z. (Yongjie Zhang); software, Y.Z. (Yongjie Zhang) and K.Y.; validation, Y.Z. (Yongjie Zhang), X.W. and Z.Z.; formal analysis, Y.Z. (Yongjie Zhang), X.W. and X.Z.; investigation, Y.Z. (Yongjie Zhang), X.W., Q.L., X.L. (Xiaotian Liang), Y.Z. (Yuzhen Zhang), K.Y., X.L. (Xiaoling Luo) and X.Z.; resources, X.L. (Xiaotian Liang), X.L. (Xiaoling Luo) and Y.P.; data curation, Q.L., Y.Z. (Yuzhen Zhang), X.D. and Z.Z.; writing—original draft, Y.Z. (Yongjie Zhang); writing—review and editing, Y.P. and R.Y.; visualization, X.D.; supervision, Y.P. and R.Y.; project administration, Y.P.; funding acquisition, Y.P. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the National Natural Science Foundation of China (32441033), the National Key Research and Development Program of China (2023YFF1001400), the Sichuan Science and Technology Program (2024NSFJQ0003), the Sichuan Provincial Agricultural Department Innovative Research Team (SCCXTD-2024-11), and the State Key Laboratory of Crop Gene Exploration and Utilization in Southwest China (SKL-ZY202232).

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

We thank the China Agriculture Research System of Oat and Buckwheat (CARS07) for providing the oat materials.

Conflicts of Interest

All authors declare that they have no conflicts of interest.

References

  1. Zhu, Y.; Begho, T. Towards responsible production, consumption and food security in China: A review of the role of novel alternatives to meat protein. Future Foods 2022, 6, 100186. [Google Scholar] [CrossRef]
  2. Capstaff, N.M.; Miller, A.J. Improving the yield and nutritional quality of forage crops. Front. Plant Sci. 2018, 9, 535. [Google Scholar] [CrossRef] [PubMed]
  3. Pexas, G.; Doherty, B.; Kyriazakis, I. The future of protein sources in livestock feeds: Implications for sustainability and food safety. Front. Sustain. Food Syst. 2023, 7, 1188467. [Google Scholar] [CrossRef]
  4. Yan, Z.; Gao, Z.; Sun, B.; Dong, X.; Gao, T.; Li, Y. Global degradation trends of grassland and their driving factors since 2000. Int. J. Digit. Earth 2023, 16, 1661–1684. [Google Scholar] [CrossRef]
  5. Zeng, G.Y.; Ye, M.; Li, M.M.; Chen, W.L.; He, Q.Z.; Pan, X.T.; Zhang, X.; Che, J.; Qian, J.R.; Lv, Y. The influence of three-year grazing on plant community dynamics productivity in Habahe, China. Agronomy 2024, 14, 1855. [Google Scholar] [CrossRef]
  6. Zhang, Y.J.; Li, S.C.; Dong, X.L.; Mou, Q.Y.; Li, J.J.; Zhang, X.Y.; Lin, M.; Yu, K.; Zhou, P.P.; Liu, X.B.; et al. Evaluation of oat (Avena sativa L.) populations for autumn sowing production in Southwest China. Grass Forage Sci. 2024, 79, 37–46. [Google Scholar] [CrossRef]
  7. Deng, X.; Gibson, J.; Wang, P. Quantitative measurements of the interaction between net primary productivity and livestock production in Qinghai Province based on data fusion technique. J. Clean. Prod. 2017, 142, 758–766. [Google Scholar] [CrossRef]
  8. Hou, L.L.; Xia, F.; Chen, Q.H.; Huang, J.K.; He, Y.; Rose, N.; Rozelle, S. Grassland ecological compensation policy in China improves grassland quality and increases herders income. Nat. Commun. 2021, 12, 4683. [Google Scholar] [CrossRef] [PubMed]
  9. Zhao, Z.; Chen, J.; Bai, Y.; Wang, P. Assessing the sustainability of grass-based livestock husbandry in Hulun Buir, China. Phys. Chem. Earth Parts A/B/C 2020, 120, 102907. [Google Scholar] [CrossRef]
  10. Wang, J.T.; Sa, D.W.; Shao, L.H.; Wang, Z.L. Optimizing agricultural structure and accelerating the development of the forage industry. Acta Prataculturae Sin. 2025, 34, 211–220. [Google Scholar] [CrossRef]
  11. Hou, L.; Bai, W.; Zhang, Q.; Liu, Y.; Sun, H.; Luo, Y.; Song, S.; Zhang, W.H. A new model of two-sown regime for oat forage production in an alpine region of Northern China. Environ. Sci. Pollut. Res. 2022, 29, 70520–70531. [Google Scholar] [CrossRef] [PubMed]
  12. Noulas, C.; Torabian, S.; Qin, R. Crop nutrient requirements and advanced fertilizer management strategies. Agronomy 2023, 13, 2017. [Google Scholar] [CrossRef]
  13. Xu, L.; Tang, G.; Wu, D.; Zhang, J. Yield and nutrient composition of forage crops and their effects on soil characteristics of winter fallow paddy in South China. Front. Plant Sci. 2024, 14, 1292114. [Google Scholar] [CrossRef]
  14. Gao, S.B.; Yang, S.; Wu, K.X.; Yu, B.; Zuo, C.; Chen, D.W.; Rong, T.Z. Challenges and suggestions for sustainable development of food security in Southwest China. Strateg. Study CAE 2019, 21, 54–59. [Google Scholar] [CrossRef]
  15. Ul, H.I.; Ijaz, S. Sustainable Winter Fodder: Production, Challenges, and Prospects, 1st ed.; CRC Press: Boca Raton, FL, USA, 2021. [Google Scholar]
  16. Hall, N.M.; Kaya, B.; Dick, J.; Skabi, U.; Niang, A. Effect of improved fallow on crop productivity, soil fertility and climate-forcing gas emissions in semi-arid conditions. Biol. Fertil. Soils 2006, 42, 224–230. [Google Scholar] [CrossRef]
  17. Favre, J.R.; Albrecht, K.A.; Gutierrez, L.; Picasso, V.D. Harvesting oat forage at late heading increases milk production per unit of area. Crop Forage Turfgrass Manag. 2019, 5, 1–8. [Google Scholar] [CrossRef]
  18. Kaur, H.; Goyal, M.; Kaur, A.; Kapoor, R. Nutritional and yield potential of oat (Avena sativa L.) genotypes in dual-purpose crop system. Cereal Res. Commun. 2023, 51, 969–980. [Google Scholar] [CrossRef]
  19. Peng, Y.; Yan, H.; Guo, L.; Deng, C.; Wang, C.L.; Wang, Y.B.; Kang, L.P.; Zhou, P.P.; Yu, K.Q.; Dong, X.L.; et al. Reference genome assemblies reveal the origin and evolution of allohexaploid oat. Nat. Genet. 2022, 54, 1248–1258. [Google Scholar] [CrossRef]
  20. Wang, G.; Xu, H.X.; Zhao, H.Y.; Wu, Y.G.; Gao, X.; Chai, Z.; Liang, Y.Q.; Zhang, X.K.; Zhen, R.; Yang, Q.; et al. Screening optimal oat varieties for cultivation in arid areas in China: A comprehensive evaluation of agronomic traits. Agronomy 2023, 13, 2266. [Google Scholar] [CrossRef]
  21. Peng, J.H.; Cheng, M.J.; Dong, Z.X.; Lei, X.; Gou, W.L.; Liu, Y.H.; Chen, S.M.; Tian, K.; Liu, W.; Ma, X. Evaluation on the adaptability of 12 oat varieties in Sichuan Province. Acta Agrestia Sin. 2023, 31, 2128–2136. [Google Scholar]
  22. Yuan, Y.; Chen, D.M.; Liu, W. Correlation analysis and comprehensive evaluation of production and reproductive of forage oats in Northwest Sichuan Plateau. J. Sichuan Agric. Univ. 2023, 41, 1116–1123. [Google Scholar] [CrossRef]
  23. Ma, L. Screening of High Yield and Quality Oat Forage Materials and Correlation Analysis of Agronomic Traits in Pingba Ecological Region, Sichuan Province. Master’s Thesis, Sichuan Agricultural University, Ya’an, China, 2019. [Google Scholar]
  24. Zhang, Y.J.; Yu, K.Q.; Yan, H.H.; Ma, L.; Zhou, P.P.; Peng, Y.Y. Effect of harvesting time on forage yield and quality of whole-crop oat in autumn-sown regions of China. J. Plant Biol. Crop Res. 2023, 6, 1082. [Google Scholar]
  25. Van, S.P.J.; Robertson, J.B.; Lewis, B.A. Methods for dietary fiber, neutral detergent fiber, and nonstarch polysaccharides in relation to animal nutrition. J. Dairy Sci. 1991, 74, 3583–3597. [Google Scholar] [CrossRef]
  26. Thiex, N.J.; Manson, H.; Anderson, S.; Persson, J.A.; Collaborators. Determination of crude protein in animal feed, forage, grain, and oilseeds by using block digestion with a copper catalyst and steam distillation into boric acid: Collaborative study. J. AOAC Int. 2002, 85, 309–317. [Google Scholar] [CrossRef]
  27. Thiex, N.J.; Anderson, S.; Gildemeister, B.; Collaborators. Crude fat, hexanes extraction, in feed, cereal grain, and forage (Randall/Soxtec/Submersion Method): Collaborative study. J. AOAC Int. 2003, 86, 899–908. [Google Scholar] [CrossRef]
  28. Quirino, D.F.; Palma, M.N.N.; Franco, M.O.; Detmann, E. Variations in methods for quantification of crude ash in animal feeds. J. AOAC Int. 2023, 106, 6–13. [Google Scholar] [CrossRef]
  29. Htet, M.N.S.; Wang, H.; Yadav, V.; Sompouviseth, T. Legume integration augments the forage productivity and quality in Maize-Based system in the loess plateau region. Sustainability 2022, 14, 6022. [Google Scholar] [CrossRef]
  30. Jia, C.H.; Qian, W.X.; Samat, T.; Ao, W.P.; Abdukirem, G. Roughage nutritional value evaluation indices and research methods. Pratacultural. Sci. 2017, 11, 415–427. [Google Scholar]
  31. Sun, J.P.; Dong, K.H.; Kuai, X.Y.; Xue, Z.H.; Gao, Y.Q. Comparison of productivity and feeding value of introduced oat varieties in the agro-pasture ecotone of Northern Shanxi. Acta Prataculturae Sin. 2017, 26, 222–230. [Google Scholar] [CrossRef]
  32. Dinkale, T.; Tesfaye, W.; Wekgari, Y. Performance evaluation of improved oat varieties/accessions at East Guji Zone, Oromia, Ethiopia. Ecol. Evol. Biol. 2020, 5, 121–124. [Google Scholar] [CrossRef]
  33. Tulu, A.; Diribsa, M.; Temesgen, W. Evaluation of seven oat (Avena sativa) genotypes for biomass yield and quality parameters under different locations of Western Oromia, Ethiopia. Adv. Agric. 2020, 882234. [Google Scholar] [CrossRef]
  34. Wang, J.; Li, Y.F.; Liang, X.Z.; Zheng, M. Morphological diversity of main oat germplasm resources in northern China. Crops 2017, 4, 27–32. [Google Scholar] [CrossRef]
  35. Saleem, M.; Zamir, M.S.L.; Haq, I.; Irshad, M.Z.; Rehman, S. Yield and quality of forage oat (Avena sativa L.) cultivars as affected by seed inoculation with nitrogenous strains. Am. J. Plant Sci. 2015, 6, 3251–3259. [Google Scholar] [CrossRef]
  36. Bao, W.L.; Ren, J.H.; Zhang, T.W.; Zhao, J.M.; Wang, Z.L.; Wang, F.W.; Tang, J.G.; Yin, G.M.; Han, Y.P.; Sun, J.J. Comprehensive evaluation of productivity of 12 forage oat varieties in Ulanqab. Acta Agrestia Sin. 2024, 32, 1169–1176. [Google Scholar] [CrossRef]
  37. Richman, S.E.; Leafloor, J.O.; Karasov, W.H.; Mcwilliams, S.R. Ecological implications of reduced forage quality on growth and survival of sympatric geese. J. Anim. Ecol. 2015, 84, 284–298. [Google Scholar] [CrossRef]
  38. Zhang, J.; Iwaasa, A.D.; Han, G.D.; Gu, C.; Wang, H.; Kusler, J.; Jefferson, P.G. Utilizing a multi-index decision analysis method to overall assess forage yield and quality of C3 grasses in the western Canadian prairies. Field Crops Res. 2018, 222, 12–25. [Google Scholar] [CrossRef]
  39. Kang, J.; Kuang, Y.B.; Sheng, J. Analysis of nutritive value of 10 forages straw. Pratacultural. Sci. 2014, 31, 1951–1956. [Google Scholar] [CrossRef]
  40. Sadras, V.O.; Mahadevan, M.; Zwer, P.K. Oat phenotypes for drought adaptation and yield potential. Field Crops Res. 2017, 212, 135–144. [Google Scholar] [CrossRef]
  41. Dar, N.A.; Singh, K.N.; Latief, A.; Sofi, J.A.; Elyass, B.M.; Ahmad, L. Influence of dates of sowing, cultivars and different fertility levels on fodder oat (Avena sativa L.) under temperate conditions of Kashmir valley (India). Range Manag. Agrofor. 2014, 35, 51–55. [Google Scholar]
  42. Kaur, A.; Goyal, M.; Kaur, M.; Mahal, A.K. Interactive effect of planting dates and development stages on digestibility, qualitative traits and yield of forage oat (Avena sativa L.) genotypes. Cereal Res. Commun. 2022, 50, 1237–1247. [Google Scholar] [CrossRef]
  43. Wang, Y.T.; Yang, Z.M.; Liu, J.C.; Li, F.; Yu, L.Q.; Yuan, T.; Liang, X.; Zhou, W.X. Comprehensive evaluation of production on performance and nutritional quality of 21 oat varieties in Northwest of Hebei province. Acta Agrestia Sin. 2020, 28, 1311–1328. [Google Scholar] [CrossRef]
  44. Mut, Z.; Akayb, H.; Erbasa, O.D. Hay yield and quality of oat (Avena sativa L.) genotypes of worldwide origin. Int. J. Plant Prod. 2015, 9, 507–522. [Google Scholar]
  45. Feyissa, F.; Tolera, A.; Melaku, S. Nutritive value of different varieties and morphological fractions of oats harvested at the soft dough stage. Trop. Sci. 2007, 47, 188–196. [Google Scholar] [CrossRef]
  46. Usman, S.; Bedasa, E.; Tamirat, D. Performance evaluation of improved oat varieties/accessions at the highland of Guji Zone, Bore, Ethiopia. J. Biol. Agric. Healthc. 2018, 8, 21–26. [Google Scholar]
  47. Ferreira, J.F.S.; Cornacchione, M.V.; Liu, X.; Saurez, D.L. Nutrient composition, forage parameters, and antioxidant capacity of alfalfa (Medicago sativa, L.) in response to saline irrigation water. Agriculture 2015, 5, 577–597. [Google Scholar] [CrossRef]
  48. Stewart, D.; McDougall, G. Oat agriculture, cultivation and breeding targets: Implications for human nutrition and health. Br. J. Nutr. 2014, 112, 50–57. [Google Scholar] [CrossRef]
  49. Rispail, N.; Montilla, B.G.; Sanchez, M.J.; Flors, F.; Howarth, C.; Langdon, T.; Rubiales, D.; Prats, E. Multi-environmental trials reveal genetic plasticity of oat agronomic traits associated with climate variable changes. Front. Plant Sci. 2018, 9, 1358. [Google Scholar] [CrossRef]
  50. Canales, F.J.; Montilla, B.G.; Gallego, S.L.M.; Flores, F.; Rispail, N.; Prats, E. Deciphering main climate and edaphic components driving oat adaptation to mediterranean environments. Front. Plant Sci. 2021, 12, 780562. [Google Scholar] [CrossRef]
Figure 1. Basic conditions of the experimental sites. (a) Experimental site location, (b) meteorological data during crop growth period 2022–2023, (c) meteorological data during crop growth period 2023–2024. The Digital Elevation Model (DEM) is a data set that digitally represents the terrain of the earth’s surface and records the elevation values at each location.
Figure 1. Basic conditions of the experimental sites. (a) Experimental site location, (b) meteorological data during crop growth period 2022–2023, (c) meteorological data during crop growth period 2023–2024. The Digital Elevation Model (DEM) is a data set that digitally represents the terrain of the earth’s surface and records the elevation values at each location.
Agronomy 15 00994 g001
Figure 2. Comparison of (a) NDF and (b) ADF in nine oat varieties across four locations over two years. Different lowercase letters indicate significant differences between different genotypes at the 0.05 level.
Figure 2. Comparison of (a) NDF and (b) ADF in nine oat varieties across four locations over two years. Different lowercase letters indicate significant differences between different genotypes at the 0.05 level.
Agronomy 15 00994 g002
Figure 3. Comparison of (a) CP, (b) EE, and (c) ASH in nine oat varieties across four locations over two years. Different lowercase letters indicate significant differences between different genotypes at the 0.05 level.
Figure 3. Comparison of (a) CP, (b) EE, and (c) ASH in nine oat varieties across four locations over two years. Different lowercase letters indicate significant differences between different genotypes at the 0.05 level.
Agronomy 15 00994 g003
Figure 4. Comparison of (a) RFQ and (b) GI in nine oat varieties across four locations over two years. Different lowercase letters indicate significant differences between different genotypes at the 0.05 level.
Figure 4. Comparison of (a) RFQ and (b) GI in nine oat varieties across four locations over two years. Different lowercase letters indicate significant differences between different genotypes at the 0.05 level.
Agronomy 15 00994 g004
Figure 5. Correlation analysis of DMY with agronomic characteristics and nutritional indices. * indicates significance at p < 0.05, ** indicates significance at p < 0.01.
Figure 5. Correlation analysis of DMY with agronomic characteristics and nutritional indices. * indicates significance at p < 0.05, ** indicates significance at p < 0.01.
Agronomy 15 00994 g005
Figure 6. Structural equation model (SEM) showing the relationships among growth performance, nutritional composition, yield, and feeding value. Blue and orange arrows indicate positive and negative relationships, respectively. Solid or dashed lines indicate significant (p < 0.05) or nonsignificant relationships. Numbers near the pathway arrow indicate the standard path coefficients. R2 represents the proportion of variance explained for every dependent variable. Comparative fit index (CFI) = 0.918. X2 = 137.221, df = 10.
Figure 6. Structural equation model (SEM) showing the relationships among growth performance, nutritional composition, yield, and feeding value. Blue and orange arrows indicate positive and negative relationships, respectively. Solid or dashed lines indicate significant (p < 0.05) or nonsignificant relationships. Numbers near the pathway arrow indicate the standard path coefficients. R2 represents the proportion of variance explained for every dependent variable. Comparative fit index (CFI) = 0.918. X2 = 137.221, df = 10.
Agronomy 15 00994 g006
Figure 7. Principal component analysis.
Figure 7. Principal component analysis.
Agronomy 15 00994 g007
Figure 8. Cluster plotting of different forage oat genotypes.
Figure 8. Cluster plotting of different forage oat genotypes.
Agronomy 15 00994 g008
Figure 9. Biplot of AMMI model.
Figure 9. Biplot of AMMI model.
Agronomy 15 00994 g009
Table 1. Growth periods of nine oat genotypes in four locations (WJ, CZ, GY, and XC) from 2022 to 2024.
Table 1. Growth periods of nine oat genotypes in four locations (WJ, CZ, GY, and XC) from 2022 to 2024.
GenotypesGrowth Stage (d)
2023WJ2023CZ2023GY2023XC2024WJ2024CZ2024GY2024XC
Longyan 3178172180166180176185162
Intimidator172170183167176172183170
WC109160156171154166167176161
WC130176170182162175171179167
WC179170169180161174166181169
WC283164161179159169161173158
WC286176173188170177170182167
WC291169164174161171164177166
WC299166159169154170162172157
Table 2. Determination of soil nutrient content in 0–20 cm before sowing in four locations (WJ, CZ, GY, and XC) during the 2022–2024 growing season.
Table 2. Determination of soil nutrient content in 0–20 cm before sowing in four locations (WJ, CZ, GY, and XC) during the 2022–2024 growing season.
Soil Nutrient2023WJ2023CZ2023GY2023XC2024WJ2024CZ2024GY2024XC
Origin matter (g/kg)32.3128.5429.2028.4032.4928.6229.3128.44
Total nitrogen (g/kg)1.561.481.491.451.621.481.541.46
Available nitrogen (mg/kg)105.88100.2998.2897.86106.03100.3098.3397.93
Available phosphorus (mg/kg)15.5312.2412.0111.4615.5712.3112.0311.55
Available potassium (mg/kg)148.32150.26119.37115.53148.33150.34119.42115.55
pH6.487.126.847.436.467.146.837.45
Table 3. Dry matter yield mean values of different forage oat genotypes tested at four locations (WJ, CZ, GY, and XC) from 2022 to 2024.
Table 3. Dry matter yield mean values of different forage oat genotypes tested at four locations (WJ, CZ, GY, and XC) from 2022 to 2024.
GenotypesDMY(t/ha)Combined
2023WJ2023CZ2023GY2023XC2024WJ2024CZ2024GY2024XC
Longyan 314.77 ± 1.15 bc11.69 ± 1.38 bc12.37 ± 0.93 bc10.98 ± 0.84 ab17.56 ± 0.76 abc12.62 ± 0.50 bc13.01 ± 0.61 bc12.97 ± 0.65 abc13.25
Intimidator15.82 ± 0.82 ab11.88 ± 1.02 bc13.87 ± 1.03 a10.73 ± 0.69 abc18.06 ± 0.41 a12.51 ± 0.53 bc13.17 ± 0.67 b13.16 ± 0.66 ab13.65
WC10916.85 ± 0.66 a14.20 ± 0.60 a13.96 ± 0.63 a11.21 ± 0.69 a17.90 ± 0.32 ab14.94 ± 0.50 a14.47 ± 0.81 a13.84 ± 1.02 a14.58
WC13013.17 ± 0.82 d10.77 ± 1.07 cd11.87 ± 0.96 bc10.04 ± 1.38 abcd15.27 ± 0.62 d10.85 ± 0.47 de12.96 ± 0.64 bc10.88 ± 0.13 ef11.98
WC17913.01 ± 1.05 d10.87 ± 0.67 bcd12.46 ± 0.89 bc10.84 ± 0.78 abc16.41 ± 0.89 c11.85 ± 0.23 cd11.69 ± 0.30 d12.28 ± 0.35 bcd12.43
WC28314.46 ± 0.68 c12.42 ± 0.99 b13.79 ± 0.96 a10.32 ± 0.82 abcd17.83 ± 0.54 ab13.22 ± 0.61 b13.35 ± 0.59 b12.88 ± 0.79 abc13.53
WC28612.92 ± 0.67 d11.85 ± 0.97 bc12.85 ± 0.51 ab9.70 ± 0.94 bcd16.85 ± 0.99 bc11.77 ± 0.50 cd11.97 ± 0.68 cd11.95 ± 0.43 cd12.48
WC29111.91 ± 1.00 d12.28 ± 0.90 bc11.99 ± 0.59 bc9.51 ± 0.57 cd14.89 ± 0.46 d11.14 ± 0.23 de11.85 ± 0.63 d11.73 ± 0.40 de11.91
WC29910.47 ± 0.42 e9.99 ± 0.73 d11.19 ± 0.75 c9.05 ± 0.41 d13.35 ± 0.43 e10.58 ± 1.02 e11.18 ± 0.43 d9.93 ± 0.36 f10.72
Mean13.6411.7712.7110.2716.4612.1612.6312.1812.73
CV(%)13.9611.939.199.759.9011.148.6410.2110.58
G74.481 ***
Y118.475 ***
L345.238 ***
G × Y4.786 ***
G × L4.145 ***
Y × L57.318 ***
G × Y × L2.127 **
Note: numbers in the table were means ± standard errors; means with different letters within a column are significantly different (p < 0.05); G, genotype; Y, year; L, location. ** significantly different at (p < 0.01); *** significantly different at (p < 0.001).
Table 4. Plant height mean values of different forage oat genotypes tested at four locations (WJ, CZ, GY, and XC) from 2022 to 2024.
Table 4. Plant height mean values of different forage oat genotypes tested at four locations (WJ, CZ, GY, and XC) from 2022 to 2024.
GenotypesPH(cm)Combined
2023WJ2023CZ2023GY2023XC2024WJ2024CZ2024GY2024XC
Longyan 3163.6 ± 4.2 d162.4 ± 6.6 ab133.4 ± 4.3 b135.4 ± 3.9 bc174.1 ± 5.1 b158.6 ± 5.0 cd147.0 ± 3.7 b148.5 ± 5.5 abc152.9
Intimidator187.1 ± 2.6 a165.0 ± 4.6 a136.5 ± 3.9 b134.6 ± 3.2 bc184.4 ± 4.4 a166.6 ± 3.8 b147.4 ± 1.7 b154.1 ± 3.3 ab159.5
WC109179.8 ± 3.0 b160.6 ± 5.3 ab149.4 ± 5.7 a138.5 ± 0.6 b175.4 ± 2.7 b175.6 ± 3.6 a157.4 ± 5.3 a150.0 ± 4.3 a160.8
WC130179.0 ± 4.8 b151.5 ± 4.1 cd125.3 ± 4.9 c144.8 ± 0.7 a173.1 ± 1.6 b157.4 ± 3.8 cd157.3 ± 4.6 a145.8 ± 3.0 ef154.3
WC179175.7 ± 4.8 bc159.4 ± 5.9 abc123.5 ± 5.5 c135.5 ± 2.4 bc176.0 ± 1.7 b166.4 ± 4.4 b123.9 ± 6.4 d139.2 ± 1.1 bcd149.9
WC283177.6 ± 3.7 bc154.7 ± 4.4 bc133.0 ± 5.7 b146.7 ± 1.4 a178.7 ± 3.1 ab163.2 ± 3.3 bc136.3 ± 1.5 c159.4 ± 5.9 abc156.4
WC286172.5 ± 2.5 c152.5 ± 5.9 cd131.0 ± 5.6 bc133.1 ± 1.2 c179.1 ± 5.7 ab159.6 ± 4.0 cd148.0 ± 2.2 b145.7 ± 4.2 cd152.7
WC291132.6 ± 5.2 e146.5 ± 2.8 d110.4 ± 3.6 d134.8 ± 4.1 bc163.7 ± 6.2 c153.1 ± 1.7 d131.3 ± 1.5 c103.1 ± 3.5 de134.5
WC299119.9 ± 3.6 f117.6 ± 5.6 e95.9 ± 5.2 e119.1 ± 2.0 d129.3 ± 3.1 d120.2 ± 1.9 e97.3 ± 3.8 e99.1 ± 5.3 f112.3
Mean165.3152.2126.5135.8170.5157.9138.4138.5148.1
CV(%)13.429.2912.105.699.289.4813.2115.209.85
G356.302 ***
Y140.298 ***
L910.628 ***
G × Y5.050 ***
G × L14.288 ***
Y × L14.295 ***
G × Y × L15.765 ***
Note: numbers in the table were means ± standard errors; means with different letters within a column are significantly different (p < 0.05); G, genotype; Y, year; L, location. *** significantly different at (p < 0.001).
Table 5. Tiller number mean values of different forage oat genotypes tested at four locations (WJ, CZ, GY, and XC) from 2022 to 2024.
Table 5. Tiller number mean values of different forage oat genotypes tested at four locations (WJ, CZ, GY, and XC) from 2022 to 2024.
GenotypesTNCombined
2023WJ2023CZ2023GY2023XC2024WJ2024CZ2024GY2024XC
Longyan 36.1 ± 0.6 abc5.2 ± 0.6 bc6.2 ± 0.7 a6.2 ± 0.7 a5.7 ± 0.8 b5.2 ± 0.6 b6.4 ± 0.6 a6.2 ± 0.7 a5.9
Intimidator6.3 ± 0.6 ab5.7 ± 0.6 ab5.3 ± 0.4 bc6.1 ± 0.5 a7.1 ± 0.5 a5.3 ± 0.6 b5.9 ± 0.3 a6.3 ± 0.6 a6.0
WC1097.0 ± 0.7 a6.5 ± 0.6 a5.7 ± 0.5 ab5.7 ± 0.6 ab7.8 ± 0.5 a6.6 ± 0.4 a6.0 ± 0.2 a6.7 ± 0.7 a6.5
WC1304.8 ± 0.6 d4.6 ± 0.6 c4.7 ± 0.4 c4.7 ± 0.3 cd5.9 ± 0.5 b4.3 ± 0.7 b4.8 ± 0.4 c5.2 ± 0.4 bc4.9
WC1795.0 ± 0.9 d4.3 ± 0.4 c4.5 ± 0.5 c4.9 ± 0.5 bcd6.0 ± 0.7 b4.4 ± 0.3 b4.8 ± 0.6 c4.5 ± 0.2 c4.8
WC2835.4 ± 0.7 bcd5.2 ± 0.4 bc4.8 ± 0.6 bc5.4 ± 0.7 abc6.2 ± 0.5 b5.2 ± 0.4 b5.8 ± 0.7 ab5.9 ± 0.4 ab5.5
WC2865.3 ± 0.5 cd4.7 ± 0.6 c4.6 ± 0.5 c4.5 ± 0.4 d5.7 ± 0.4 ab4.5 ± 0.7 b4.7 ± 0.3 c4.9 ± 0.4 c4.9
WC2914.9 ± 0.5 d4.6 ± 0.7 c4.4 ± 0.6 c4.4 ± 0.5 d5.6 ± 0.2 b5.0 ± 0.7 b4.2 ± 0.6 c4.7 ± 0.6 c4.7
WC2995.2 ± 0.7 cd4.6 ± 0.5 c4.7 ± 0.7 c5.4 ± 0.6 abc5.3 ± 0.4 b5.2 ± 0.5 b4.9 ± 0.7 bc5.3 ± 0.5 bc5.1
Mean5.55.04.95.26.15.15.35.55.4
CV(%)16.1316.0315.2315.0913.9215.8315.4015.3311.01
G31.824 ***
Y15.887 ***
L25.754 ***
G × Y0.971 NS
G × L1.799 *
Y × L1.620 *
G × Y × L0.995 NS
Note: numbers in the table were means ± standard errors; means with different letters within a column are significantly different (p < 0.05); G, genotype; Y, year; L, location. * significantly different at (p < 0.05); *** significantly different at (p < 0.001). NS not significant (p > 0.05).
Table 6. Stem–leaf ratio mean values of different forage oat genotypes tested at four locations (WJ, CZ, GY, and XC) from 2022 to 2024.
Table 6. Stem–leaf ratio mean values of different forage oat genotypes tested at four locations (WJ, CZ, GY, and XC) from 2022 to 2024.
GenotypesSLR(%)Combined
2023WJ2023CZ2023GY2023XC2024WJ2024CZ2024GY2024XC
Longyan 375.64 ± 5.80 ab73.90 ± 7.19 c66.14 ± 5.22 ab61.68 ± 6.81 bc85.67 ± 8.02 ab57.00 ± 5.29 e59.00 ± 3.24 b84.29 ± 2.85 a70.42
Intimidator77.79 ± 6.49 ab64.23 ± 6.11 de58.51 ± 2.62 c54.77 ± 4.66 c88.00 ± 3.61 a68.33 ± 5.11 cd59.71 ± 1.30 b81.17 ± 4.54 a69.06
WC10973.57 ± 6.73 abc52.84 ± 5.46 f60.35 ± 5.45 bc61.22 ± 8.60 bc86.33 ± 3.22 ab62.00 ± 5.20 de62.15 ± 5.02 ab84.33 ± 3.93 a67.85
WC13075.29 ± 1.77 ab68.21 ± 4.99 cd61.56 ± 2.66 abc63.42 ± 5.00 bc83.33 ± 4.16 ab82.00 ± 4.58 ab62.49 ± 2.31 ab78.78 ± 8.07 ab71.88
WC17972.16 ± 6.79 bc57.72 ± 4.76 ef62.32 ± 2.77 abc63.56 ± 5.14 bc78.67 ± 4.51 b63.67 ± 6.43 de63.60 ± 1.31 ab71.13 ± 7.28 bc66.60
WC28375.22 ± 5.79 ab84.94 ± 7.74 ab59.66 ± 4.94 bc59.42 ± 7.06 bc89.67 ± 5.03 a65.67 ± 7.10 de60.60 ± 2.06 ab63.92 ± 4.64 c70.32
WC28676.96 ± 6.08 ab77.36 ± 4.76 bc63.36 ± 3.09 abc74.09 ± 6.85 a88.67 ± 6.03 a76.00 ± 3.61 bc63.87 ± 1.30 ab78.15 ± 3.14 ab75.75
WC29165.62 ± 4.24 c53.06 ± 4.91 f61.68 ± 3.46 abc69.50 ± 6.96 ab85.00 ± 2.00 ab63.67 ± 2.31 de62.70 ± 3.41 ab80.01 ± 2.82 ab67.65
WC29981.87 ± 6.86 a88.40 ± 7.18 a67.63 ± 5.95 a69.41 ± 7.64 ab88.33 ± 1.53 a86.33 ± 6.51 a65.78 ± 3.43 a86.47 ± 2.61 a77.90
Mean74.9068.9662.3664.1285.9669.4162.2178.6971.22
CV(%)8.7519.547.3712.515.7614.814.979.905.07
G15.184 ***
Y87.610 ***
L108.015 ***
G × Y5.588 ***
G × L5.769 ***
Y × L27.904 ***
G × Y × L3.574 ***
Note: numbers in the table were means ± standard errors; means with different letters within a column are significantly different (p < 0.05); G, genotype; Y, year; L, location. *** significantly different at (p < 0.001).
Table 7. Analysis of genotype, year, location, and their interactions regarding forage oat quality.
Table 7. Analysis of genotype, year, location, and their interactions regarding forage oat quality.
TreatmentNDFADFCPEEASH
G30.543 ***19.814 ***47.620 ***30.476 ***14.843 ***
Y580.737 ***88.225 ***16.727 ***16.564 ***160.224 ***
L69.907 ***77.559 ***16.302 ***5.559 ***97.711 ***
G × Y5.124 ***2.840 **3.864 ***3.278 **1.922 *
G × L2.587 ***3.334 ***1.702 *4.982 ***3.558 ***
Y × L77.148 ***128.155 ***6.463 ***27.228 ***88.681 ***
G × Y × L3.251 ***1.957 **1.738 *6.129 ***3.157 ***
G, genotype; Y, year; L, location. * significantly different at (p < 0.05); ** significantly different at (p < 0.01); *** significantly different at (p < 0.001).
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

Zhang, Y.; Wu, X.; Li, Q.; Liang, X.; Zhang, Y.; Zhang, X.; Dong, X.; Yu, K.; Zhao, Z.; Luo, X.; et al. Comprehensive Evaluation and Screening of Autumn-Sown Oat (Avena sativa L.) Germplasm in Different Agropastoral Regions. Agronomy 2025, 15, 994. https://doi.org/10.3390/agronomy15040994

AMA Style

Zhang Y, Wu X, Li Q, Liang X, Zhang Y, Zhang X, Dong X, Yu K, Zhao Z, Luo X, et al. Comprehensive Evaluation and Screening of Autumn-Sown Oat (Avena sativa L.) Germplasm in Different Agropastoral Regions. Agronomy. 2025; 15(4):994. https://doi.org/10.3390/agronomy15040994

Chicago/Turabian Style

Zhang, Yongjie, Xinyue Wu, Qinkun Li, Xiaotian Liang, Yuzhen Zhang, Xingjia Zhang, Xiaolong Dong, Kaiquan Yu, Zilin Zhao, Xiaoling Luo, and et al. 2025. "Comprehensive Evaluation and Screening of Autumn-Sown Oat (Avena sativa L.) Germplasm in Different Agropastoral Regions" Agronomy 15, no. 4: 994. https://doi.org/10.3390/agronomy15040994

APA Style

Zhang, Y., Wu, X., Li, Q., Liang, X., Zhang, Y., Zhang, X., Dong, X., Yu, K., Zhao, Z., Luo, X., Yang, R., & Peng, Y. (2025). Comprehensive Evaluation and Screening of Autumn-Sown Oat (Avena sativa L.) Germplasm in Different Agropastoral Regions. Agronomy, 15(4), 994. https://doi.org/10.3390/agronomy15040994

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