Research Article

Evaluation of Growth Performance, Morphometric, Histomorphological Characteristics, and Meat Texture of IPB-D3 Chickens Reared Under Intensive Systems

Rizki Fitrawan Yuneldi1, Andhika Yudha Prawira1*, Isyana Khaerunnisa1, Ahmad Furqon1, Dwi Lestari2, Ni Luh Putu Rischa Phadmacanty1, Wawan Kuswandi3, Rizka Primasari Rambe3, Putri Vianisa3, Harits Shafwan Rafa3, Muzaki Alfa Rizqi3, Rojib Rojib3, Tiurma Pasaribu2, Anneke Anggraeni2, Cece Sumantri3

1Research Center for Applied Zoology, Research Organization for Life Sciences and Environment, National Research and Innovation Agency (BRIN), Bogor, Indonesia; 2Research Center for Animal Husbandry, Research Organization for Agriculture and Food, National Research and Innovation Agency (BRIN), Bogor, Indonesia; 3Department of Animal Production and Technology, Faculty of Animal Science, IPB University, Bogor, Indonesia.

Abstract | IPB-D3 chicken is a locally developed fast-growing composite line derived from Pelung, Sentul, Kampung, and Broiler strains. However, the integrated characterization of growth, muscle structure, and meat quality remains limited. This study aimed to evaluate the growth performance, morphometric, histomorphological characteristics, and meat texture of IPB-D3 chickens reared under intensive systems. Chicken body weight was measured once a week, and morphometry was performed every two weeks. Sampling was conducted at 1–3 months of age (n = 5–6 per age group). Chickens were slaughtered using the halal method for carcass analysis, muscle histomorphology, and breast meat texture. The results showed rapid growth performance in IPB-D3 chickens, with higher body weight in males than females and clear sexual dimorphism emerging after 6 weeks of age. The carcass ratio increased significantly, and the breast dominated meat deposition. Fasciculus area and myofiber cross-sectional area increased significantly without changes in the number of myofibers per fasciculus, indicating that muscle growth was dominated by hypertrophy, with a strong correlation between body weight and pectoralis, femoralis, and tibialis muscle parameters. Meat texture showed an increase in firmness, cohesion, gumminess, and chewiness, and a decrease in springiness with increasing age. In conclusion, IPB-D3 chickens exhibit rapid growth with clear sexual dimorphism from 6 to 12 weeks of age, accompanied by progressive carcass improvement and a predominance of breast meat deposition. Muscle growth occurs through hypertrophy that correlates with an increase in meat texture density, indicating efficient growth performance and stable meat texture.

Keywords | Growth performance, Histomorphology, IPB-D3 chicken, Meat texture, Morphometric, Muscle


Received | February 28, 2026; Accepted | March 31, 2026; Published | May 11, 2026

*Correspondence | Andhika Yudha Prawira, Research Center for Applied Zoology, Research Organization for Life Sciences and Environment, National Research and Innovation Agency (BRIN), Bogor, Indonesia; Email: [email protected]

Citation | Yuneldi RF, Prawira AY, Khaerunnisa I, Furqon A, Lestari D, Phadmacanty NLPR, Kuswandi W, Rambe RP, Vianisa P, Rafa HS, Rizqi MA, Rojib R, Pasaribu T, Anggraeni A, Sumantri C (2026). Evaluation of growth performance, morphometric, histomorphological characteristics, and meat texture of IPB-D3 chickens reared under intensive systems. Adv. Anim. Vet. Sci., 14(4):977-987.

DOI | https://dx.doi.org/10.17582/journal.aavs/2026/14.5.977.987

ISSN (Online) | 2307-8316

Copyright: 2026 by the authors. Licensee ResearchersLinks Ltd, England, UK.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).



INTRODUCTION

The increasing market demand for chicken meat has driven innovations in developing new local chicken breeds and strains that grow to high productivity in a relatively short time (Adelta et al., 2023). Local chickens play a vital role in the rural economy in most developing countries (Padhi, 2016). The superior traits of local Indonesian chickens form the basis for the creation of new crossbred chickens to meet community needs (Padhi et al., 2016). Composite chickens are developed through crossbreeding multiple breeds to combine desirable parental traits (Prawira et al., 2026). One of the results of this crossbreeding of local Indonesian chickens was the development of the IPB-D3 chicken, originating from a cross between male Pelung-Sentul and female Kampung-Broiler (Cobb parent stock) chickens, in an effort to obtain superior characteristics of local Indonesian chickens through a rigorous selection process (Sumantri et al., 2020). Furthermore, through several generations and selection processes, a fast-growing Indonesian composite chicken strain suitable as parent stock was established, namely the IPB-D3 chicken.

The IPB-D3 chicken has been extensively studied, with research focusing on growth performance, egg production, morphometrics, nutritional supplementation, genetics, immune response, and general histomorphological characteristics (Rahman et al., 2024; Hawari et al., 2024; Galib et al., 2024; Ratnawati et al., 2025; Romantis and Sumantri, 2024; Rizqi et al., 2024, 2025; Vianisa et al., 2025; Kuswandi et al., 2025; Prawira et al., 2026). However, comprehensive histomorphological characterization of skeletal muscle tissue in relation to growth performance, morphometric, and meat texture remains limited. Histomorphological characterization of muscle tissue in IPB-D3 chickens is crucial to understanding the genetic contributions inherited from their parents (Pelung, Sentul, Kampung, and Broiler), as each parental line exhibits distinct muscle fiber composition and growth patterns. Although the muscle structure of each has been reported separately, integrated histomorphological evaluation in IPB-D3 chickens has not been widely investigated.

According to Prawira et al. (2026), the first histological characterization of IPB-D3 chickens showed that both free-range and intensive rearing systems yielded similar growth performance. Free-range rearing enhanced muscle hypertrophy and type IIX fiber development, while intensive rearing increases collagen deposition. This indicates that IPB-D3 chickens can adapt to various production environments. However, this study had several limitations, including an unequal sex ratio and a limited sample size. Further studies are needed to comprehensively evaluate growth performance from day-old chicks (DOC) to 3 months of age, morphometrics, detailed muscle histomorphology (pectoralis, femoralis, and tibialis muscles), and meat texture characteristics. Therefore, this study aimed to evaluate the growth performance, morphometric, histomorphological characteristics, and meat texture of IPB-D3 chickens reared under intensive systems.

MATERIALS AND METHODS

Study period and location

The research was conducted from April 2025 to January 2026. The IPB-D3 chickens were housed at the Field Laboratory of Animal Breeding and Genetics, Faculty of Animal Science, IPB University, Dramaga, Bogor, located at approximately 250 m above sea level. Histomorphology analysis was conducted at the Veterinary and Zoology Laboratory, Anatomy and Histology Section, KST Soekarno, National Research and Innovation Agency (BRIN), Cibinong, Indonesia. Breast meat texture analysis was conducted at the Food Laboratory at KST Gunung Kidul (Umar Anggara Jenie), Research Center for Food Technology and Processing, BRIN, Indonesia.

Animal, housing, diet, and experimental design

The study used a total of 65 fifth-generation IPB-D3 chickens, consisting of 5 replications (38 males and 27 females). The chickens were reared intensively under a flock system from day-old chicks (DOC) until 13 weeks of age in indoor cages. The starter house measured 10 × 7 × 3 m, while the grower house measured 32 × 5.14 × 3 m, with each flock maintained in separate enclosures measuring 7 × 2.32 m (starter phase) and 6.5 × 1.85 m (grower phase), containing approximately 30 chickens per flock. The temperature of the cage was set at approximately 28°C. Temperature and humidity were monitored and controlled using a thermometer and an environmental control system. Ventilation was supported by side curtains, which were opened during high temperatures, and exhaust fans operated at 15-minute intervals to improve airflow. Additionally, the litter (husks) was replaced weekly to maintain hygiene. Feeding was conducted in two phases. The starter phase chickens (0–14 days) were fed a commercial diet (Hi-Pro-Vite 511, Phokpand, Indonesia) containing 20% crude protein, 5% crude fat, 5% crude fiber, 0.5% phosphorus, and 0.8–1.1% calcium. The grower phase (15 days to 13 weeks of age) was fed a commercial diet (Hi-Pro-Vite 512, Phokpand, Indonesia), which provided a diet containing 19% crude protein, 5% crude fat, 6% crude fiber, 0.45% phosphorus, and 0.8–1.1% calcium. Feed was offered twice daily (morning and evening), and water was provided ad libitum.

During the rearing process, data were collected on the body weight and morphometric characteristics of each chicken. Body weight was recorded weekly, whereas morphometric measurements were obtained every two weeks. Morphometric measurements included chest circumference, chest width, chest depth, body length, body height, wing length, neck length, thigh length, drumstick length, shank length, tibia circumference, and shank circumference.

Slaughtering and sample collection

Sampling was conducted in the first, second, and third months, with six male chickens initially included at each time point. During the first month, one individual was identified as female and was therefore excluded from the analysis. Consequently, the final number of samples was five, six, and six male chickens for the first, second, and third months, respectively. Sample selection was based on the average weekly body weight of male chickens at the time point closest to the scheduled sampling. The selected chickens were weighed to determine their body weight before slaughter. Subsequently, muscle samples (3 × 3 cm) were excised from the pectoralis (Pec), femoralis (Fem), and tibialis (Tib) before carcass processing. All muscle samples were fixed in 10% neutral buffered formalin (NBF) for 48 h.

Subsequently, carcasses were scalded by immersion in water at 70°C for 10-20 s to remove feathers (Mrajji et al., 2021). Defeathering was performed manually at 1-2 months of age, whereas birds at 3 months of age were processed using an automatic defeathering machine. Carcass and visceral weights were recorded, after which carcasses were partitioned into individual parts, including wings, breast, thigh, drumstick, and back, and each part was weighed separately. Deboning was performed on the breast, thigh, drumstick, and the meat and bone fractions were weighed separately. All samples were stored at –20°C until analyzed.

Histomorphology analysis

Muscle samples from the Pec, Fem, and Tib were processed into tissue blocks using the standard paraffin (Merck, Darmstadt, Germany)-embedding method. The paraffin blocks were sectioned at a thickness of 5 µm using a microtome. The sections were subsequently stained with hematoxylin and eosin (H&E, Merck, Darmstadt, Germany). Slides were observed using an Olympus CX43 microscope at 10× and 20× magnification, and images were captured under standardized brightness and white balance settings. The measured parameters included fasciculus area (FA), myofiber cross-sectional area (MCSA), and the number of myofibers per fasciculus (NMOF) (Yuneldi et al., 2023, 2024; Prawira et al., 2026). The measurements were obtained using ImageJ software (Version 1.53k, National Institutes of Health, USA). Calibration was performed using a micrometer to ensure measurement accuracy. The parameters measured in HE staining included the fasciculus area (average of 10 fasciculus), myofiber cross-sectional area (average of 60 myofibers), and the number of myofibers per mm² (5 fields per sample) (Prawira et al., 2026).

Breast meat texture analysis

Meat texture analysis was performed on left breast samples stored at –20°C for 10 days, before analysis, the samples were thawed at room temperature and subjected to texture profile analysis (TPA) using a TA.XT plus C (Godalming, Surrey, UK) equipped with a P/6 probe under the following conditions: double compression to 50% of the sample height, test speed 0.5 mm/s, pre-test speed 300 mm/min, preload force 1.0 N, and a 0.5 s interval between compressions; firmness, adhesiveness, resilience, cohesion, springiness, gumminess, and chewiness were recorded as textural parameters (Hariyadi et al., 2025; Yuneldi et al., 2024).

Statistical analysis

Data were tested for normality (Shapiro-Wilk) and homogeneity of variances (Levene’s test) before analysis. Variables that satisfied parametric assumptions were compared using one-way ANOVA. The analysis was confirmed using Duncan’s test. When the assumption of homogeneity of variance was violated, Welch’s ANOVA followed by the Games–Howell post hoc test was applied. For non-normally distributed data, the Kruskal–Wallis test followed by Bonferroni-adjusted pairwise comparisons. All statistical analyses were performed using Statisty (online platform) and JASP software (Version 0.95.4). Multivariate analysis, including principal component analysis (PCA) and heatmap visualization, was performed using the online ClustVis software (Version 2.0) (Metsalu and Vilo, 2015).

RESULTS AND DISCUSSION

Growth performance and morphometrics of IPB-D3 chickens

Over the 13 weeks, IPB-D3 chickens exhibited progressive growth, with the highest weekly body weight gain occurring at week 2. Final body weight at week 13 was greater in males (1242.87 g) than in females (1020.35 g) (Figure 1). The growth profile of IPB-D3 chickens is relatively rapid. These results are consistent with research by Sumantri and Darwati (2017), who found that IPB-D3 chickens at 10 weeks of age weighed 1256 g for males and 1042 g for females (Salsabila et al., 2022). In fourth-generation IPB-D3 chickens, the average body weight of males at 12 weeks of age was 1021.44 g, and that of females was 684.33 g (Galib et al., 2024). According to Prayogi (2011), this pattern aligns with reports on local Indonesian chickens, such as Pelung chickens, where Pelung chickens weigh 1162 g at 12 weeks of age. The interaction between age and sex indicates that morphology develops progressively with physiological maturation. However, compared with commercial broilers, IPB-D3 chickens exhibit a more moderate yet sustainable growth curve. Modern broilers reach maximum growth rates more quickly, but are often associated with metabolic disorders and myopathy due to extreme hypertrophy (Zuidhof et al., 2014; Petracci et al., 2015).

 

Table 1: Morphometric comparison between males and females at different ages in IPB-D3 chickens reared under intensive systems.

Variables (cm)

Average SD, Weeks

2

4

6

8

10

12

Male

Female

Male

Female

Male

Female

Male

Female

Male

Female

Male

Female

Chest circumference

9.65 ± 1.27

9.57 ± 1.38

13.09 ± 1.19

12.82 ± 0.69

16.49 ± 1.76*

15.50 ± 1.32

19.48 ± 2.69

18.45 ± 2.25

24.13 ± 2.14**

21.81 ± 1.51

26.39 ± 1.72**

23.98 ± 1.35

Chest width

2.28 ± 0.41

2.27 ± 0.33

3.23 ± 0.32

3.18 ± 0.34

4.18 ± 0.55

4.12 ± 0.45

4.58 ± 0.64

4.69 ± 0.73

5.19 ± 0.54**

4.65 ± 0.58

5.79 ± 0.46*

5.45 ± 0.41

Chest depth

3.27 ± 0.53

3.24 ± 0.57

4.60 ± 0.51

4.57 ± 0.44

6.23 ± 0.60

5.92 ± 0.43

7.45 ± 0.98**

6.62 ± 0.74

8.84 ± 0.60**

7.89 ± 0.67

9.92 ± 0.80**

9.03 ± 0.71

Body length

14.19 ± 1.64

13.87 ± 2.02

19.77 ± 2.22

19.25 ± 1.54

25.17 ± 2.54

25.07 ± 1.33

28.53 ± 2.02

27.95 ± 1.56

34.55 ± 1.85**

32.05 ± 1.24

35.67 ± 1.79**

33.65 ± 1.27

Body hight

18.25 ± 2.21

17.83 ± 2.28

26.88 ± 2.92

25.78 ± 3.02

33.52 ± 2.88

32.95 ± 2.92

38.69 ± 3.14*

37.00 ± 2.72

47.78 ± 3.70**

44.69 ± 2.43

51.73 ± 4.34**

47.25 ± 3.26

Wing length

7.45 ± 0.97

7.53 ± 0.98

10.79 ± 0.85

10.41 ± 0.90

12.41 ± 1.14

12.82 ± 5.07

15.50 ± 1.00

15.10 ± 1.14

18.07 ± 1.26**

16.52 ± 1.08

19.40 ± 2.27**

17.35 ± 1.39

Neck length

3.60 ± 0.61

3.27 ± 0.83

5.23 ± 0.57

5.21 ± 0.49

7.09 ± 0.57

7.11 ± 0.27

8.50 ± 0.93*

7.91 ± 0.96

10.32 ± 1.04**

9.42 ± 0.85

11.80 ± 0.67*

11.34 ± 0.79

Thigh length

3.02 ± 0.52

2.92 ± 0.50

4.30 ± 0.37

4.24 ± 0.31

5.70 ± 0.48*

5.46 ± 0.32

6.69 ± 1.12

6.42 ± 0.59

7.84 ± 0.55**

7.14 ± 0.69

9.23 ± 0.62**

8.56 ± 0.44

Drumstick length

3.78 ± 0.62

3.64 ± 0.62

5.12 ± 0.48

5.09 ± 0.53

6.96 ± 0.69*

6.52 ± 0.89

7.99 ± 0.86*

7.43 ± 0.59

9.58 ± 1.10**

8.61 ± 0.94

11.18 ± 0.73**

10.44 ± 0.64

Shank length

2.51 ± 0.45

2.42 ± 0.45

3.46 ± 0.41

3.42 ± 0.40

4.81 ± 0.47*

4.51 ± 0.42

5.86 ± 0.80

5.60 ± 0.40

7.23 ± 0.81**

6.28 ± 0.52

8.56 ± 0.58**

7.63 ± 0.39

Tibia circumference

2.38 ± 0.52

2.29 ± 0.51

3.40 ± 0.70

3.32 ± 0.77

4.31 ± 0.70

4.33 ± 1.00

5.44 ± 0.76**

4.50 ± 0.77

7.00 ± 1.24**

6.07 ± 0.95

6.83 ± 0.93*

6.15 ± 1.00

Shank circumference

1.75 ± 0.28

1.69 ± 0.41

2.22 ± 0.36

2.23 ± 0.31

2.89 ± 0.46

2.86 ± 0.32

3.33 ± 0.42*

3.08 ± 0.31

3.87 ± 0.48**

3.45 ± 0.36

3.93 ± 0.27**

3.51 ± 0.32

 

Note: A single asterisk (*) indicates a significant difference at 0.01 ≤ P < 0.05, whereas a double asterisk (**) indicates a significant difference at P < 0.01.

 

Sex-related differences in the morphometric profile became significant at week 6 and increased further at weeks 8 and 12. At 8 weeks of age, chest depth and tibia circumference showed highly significant differences between sexes. By weeks 10 and 12, all measured morphometric parameters differed significantly (Table 1). The increasing morphometric differences between the sexes after week 6 suggest that body-size-based selection may be an effective strategy to improve production performance. The results of this study indicate that the morphometric measurements of IPB-D3 chickens at 12 weeks of age are generally higher than those reported by Rizqi et al. (2024), although the observed growth pattern remains consistent. Across all variables, males are larger than females, indicating clear sexual dimorphism in skeletal and muscle development. This difference may be associated with hormonal and genetic regulation of skeletal muscle growth. Androgens, such as testosterone, promote muscle hypertrophy through increased protein synthesis, while growth factors such as IGF-1 support muscle cell proliferation and differentiation. Additionally, differential expression of genes involved in myogenesis may contribute to variations in muscle mass and fiber characteristics between sexes (Emmert et al., 2024; Murach et al., 2023). The chest circumference variable, as an indicator of pectoral muscle development, is directly correlated with meat production potential, so higher values reflect good growth performance.

Principal component analysis (PCA) revealed positive associations among body weight, morphometric, and meat weights of the breast, thigh, and drumstick at 1–3 months of age. The PCA pattern indicated relatively homogeneous clustering at 1 and 2 months, whereas greater variation was observed at 3 months. Heatmap visualization demonstrated that growth performance and meat yield traits at 1–3 months were not directly correlated with testis size (Figure 2). These results are similar to the pattern of more pronounced body weight in 2nd to 3rd months of age in fourth-generation IPB-D3 chickens, indicating accelerated growth after the initial adaptation phase (Galib et al., 2024). Increasing heterogeneity in growth with age has been reported in poultry, with individual growth patterns becoming more diverse after the starter phase (Buzala and Janicki, 2016; Darmani Kuhi et al., 2003), and variation in response to age is influenced by genetic factors between strains (Whittle et al., 2025).

 

The carcass ratio increased significantly from 1 to 3 months of age. In addition, carcass ratio to the body part showed a uniform value at 1–3 months of age, but there were significant differences between the three body parts, namely, the breast was generally more than the thigh and drumstick. Thus, the ratio of the amount of meat attached to the bone in these parts showed the thigh part having the most compared to the chest and drumstick (Figure 3). The increase in carcass ratio from 1 to 3 months of age indicates an acceleration in muscle tissue deposition relative to body weight, reflecting a shift in growth priority from organ development to skeletal muscle hypertrophy as the rapid growth phase is reached. During this period, there is an intensive increase in muscle protein synthesis, resulting in a significant increase in the proportion of tissue to carcass weight. These results are consistent with reports by Park et al. (2021) and Deng et al. (2022), which state that increasing slaughter age is directly correlated with increases in carcass weight and meat yield due to muscular system maturation and increased efficiency of nutrient conversion into muscle tissue. This is supported by other studies that increasing chicken age contributes to increased weight of major commercial cuts, particularly the breast and thigh, which are important determinants of carcass value (Bongiorno et al., 2022; Zuidhof et al., 2014). The dominant contribution of breast meat to the carcass reflects the high hypertrophic capacity of the pectoralis muscle as a major component of the commercial carcass, while the higher meat-to-bone ratio in the upper thigh indicates efficient muscle deposition relative to skeletal growth, which increases slaughter value. These results are consistent with the principle of allometric growth in broiler chickens, where the main muscle groups experience a higher rate of protein deposition compared to supporting tissues, resulting in carcass distribution becoming increasingly concentrated in areas with high economic value with increasing age

 

 

(Park et al., 2021; Deng et al., 2022). The combination of increased carcass ratio, breast muscle dominance, and thigh yield efficiency indicates that IPB-D3 chickens exhibit an efficient, coordinated muscle growth pattern under intensive rearing systems, thereby supporting their potential as a composite chicken breed with competitive carcass performance.

Histomorphology characteristics and meat texture

Fasciculus area (FA) in the pectoralis (Pec) muscle differed significantly among ages, with a greater increase from 1 to 2 months (2.40 × 10⁴) than from 2 to 3 months (1.64 × 10⁴). In the femoralis (Fem) and tibialis (Tib) muscles, FA at 1 month differed significantly from that at 2 and 3 months. Myofiber cross-sectional area (MCSA) in the Tib muscle differed significantly across all ages. In the Pec muscle, MCSA at 3 months differed significantly from that at 1 and 2 months, whereas in the Fem muscle, a significant difference was observed between 1 and 3 months. For the number of myofibers per fasciculus (NMOF), the Pec muscle differed significantly from the Fem muscle at 1 month. At 2 and 3 months, the Pec muscle differed significantly from both the Fem and Tib muscles (Table 2 and Figure 4). Correlation analysis showed that FA and MCSA were positively and significantly correlated with growth and carcass traits across all muscle parts. In the breast muscle (Table 3), FA and MCSA were significantly correlated with body weight, chest measurements, carcass weight, and breast meat weight (r = 0.60–0.90), whereas NMOF showed no significant correlations. In the thigh muscle (Table 4), FA (r = 0.83–0.89) and MCSA (r = 0.67–0.72) were positively correlated with body weight, thigh length, carcass weight, thigh weight, and thigh meat weight, while NMOF was not significantly associated with these traits. In the drumstick muscle (Table 5), FA (r = 0.75–0.88) and MCSA (r = 0.73–0.88) remained positively correlated with drumstick length, drumstick circumference, carcass weight , and drumstick weight. In contrast, NMOF showed significant negative correlations (r = −0.55 to −0.58).

 

Table 2: Histomorphology of pectoralis, femoralis, and tibialis muscles at 1, 2, and 3 months of age in IPB-D3 chickens reared under intensive systems.

Variables

Average ± SD, Month

1

2

3

FA (x 104 µm2)

Pec

4.74 ± 0.56a

7.14 ± 0.83b

8.78 ± 2.44c,α

Fem

2.89 ± 1.19a

5.62 ± 0.35b

6.11 ± 0.61b,β

Tib

2.65 ± 0.18a

5.82 ± 0.61b

5.85 ± 0.29b,β

MCSA (x 102 µm2)

Pec

3.74 ± 1.08a

4.55 ± 0.59a

5.82 ± 0.13b

Fem

3.22 ± 0.58a

6.20 ± 1.94ab

7.09 ± 2.96b

Tib

3.29 ± 1.29a

6.76 ± 2.20b

7.82 ± 2.04c

NMOF

Pec

132.72 ± 19.49α

143.93 ± 13.41α

150.97 ± 12.52α

Fem

91.92 ± 28.60β

100.17 ± 12.36β

94.50 ± 10.16β

Tib

99.40 ± 12.70αβ

85.40 ± 27.68β

88.10 ± 5.57β

 

Different superscripts (a,b,c) within the same row for each variable indicate significant differences (P < 0.05). Different superscripts (α, β) within the same column at the same month and within the same variable (different muscles) indicate significant differences (P < 0.05). FA= Fasciculus area; MCSA= Myofiber cross-sectional area; NMOF= Number of myofibers per fasciculus; Pec= Pectoralis; Fem= Femoralis; Tib= Tibialis.

 

Table 3: Correlation index of chest traits.

Variables

Body weight

Chest circumference

Chest width

Chest depth

Carcass weight

Breast weight

Breast meat weight

FA

0.87*

0.90*

0.81*

0.48

0.87*

0.88*

0.88*

MCSA

0.87*

0.86*

0.74*

0.60*

0.87*

0.88*

0.89*

NMOF

0.31

0.38

0.42

0.06

0.28

0.24

0.23

 

Note: An asterisk (*) indicates a statistically significant Pearson correlation (P < 0.05). FA = Fasciculus area; MCSA = Myofiber cross-sectional area; NMOF = Number of myofibers per fasciculus.

 

Table 4: Correlation index of thigh traits.

Variables

Body weight

Thigh length

Carcass weight

Thigh weight

Thigh meat weight

FA

0.86*

0.89*

0.84*

0.84*

0.83*

MCSA

0.71*

0.72*

0.68*

0.69*

0.67*

NMOF

-0.07

-0.02

-0.07

-0.08

-0.11

 

Note: An asterisk (*) indicates a statistically significant Pearson correlation (P < 0.05). FA = Fasciculus area; MCSA= Myofiber cross-sectional area; NMOF= Number of myofibers per fasciculus.

 

The increase in FA and MCSA without changes in NMOF indicates that muscle growth in IPB-D3 chickens is predominantly driven by post-hatch hypertrophy. This mechanism is widely recognized in poultry, where postnatal muscle growth primarily occurs through fiber hypertrophy and is closely associated with subsequent meat quality traits

 

Table 5: Correlation index of drumstick traits.

Variables

Body weight

Drumstick length

Drumstick circumference

Carcass weight

Drumstick weight

FA

0.83*

0.88*

0.80*

0.81*

0.75*

MCSA

0.87*

0.83*

0.73*

0.88*

0.83*

NMOF

-0.55*

-0.58*

-0.57*

-0.57*

-0.55*

 

Note: An asterisk (*) indicates a statistically significant Pearson correlation (P<0.05). FA= Fasciculus area; MCSA= Myofiber cross-sectional area; NMOF= Number of myofibers per fasciculus.

 

(Petracci and Cavani, 2011). This pattern is consistent with the fundamental concept of avian muscle biology, which holds that myofiber number is largely established during the embryonic phase, whereas postnatal growth primarily occurs through the enlargement of existing fibers (Velleman, 2015). The strong correlations between histomorphology parameters and carcass weight further support a direct structural association between muscle microstructure and production performance. Zhang et al. (2024) reported that muscle fiber characteristics are key determinants of carcass yield and quality, with hypertrophy representing the dominant growth mechanism under intensive rearing systems. Such progressive hypertrophic growth appears to maintain tissue architectural integrity, in contrast to the extreme growth patterns often observed in commercial broilers (Baldi et al., 2020). Comparative analyses of FA, MCSA, and NMOF in the Pec and Fem muscles of 24-week-old IPB-D3 chickens reared under intensive and free-range systems, as well as comparisons with broiler, Pelung, Sentul, and Kampung chickens at various ages, have been reported by Prawira et al. (2026). This result in FA, MCSA, and NMOF in the Tib muscle of 12-week-old IPB-D3 chickens (MCSA = 7.82 × 10² µm²; NMOF = 88.01) was lower than that reported for the gastrocnemius muscle of 49-day-old broilers, which exhibited a MCSA of approximately 1,400 µm² (≈ 14 × 10² µm²) and 106.1 myofibers per bundle. However, the MCSA of the Tib muscle in IPB-D3 chickens was higher than that reported in 12-week-old Sentul chickens, in which the drumstick muscle showed an MCSA of approximately 28.99 µm ≈ 6.6 × 102 µm² . These comparisons highlight the variability in muscle fiber dimensions among chicken genotypes, which are influenced by genetic background, age, nutrition, and muscle type (Honda et al., 2019). Gu et al. (2024), emphasized that accurate measurement of the total number of myofibers (TNM) is essential for developing effective genetic selection strategies aimed at improving meat quality. Meat quality is closely associated with histomorphological and biochemical muscle characteristics (Rehfeldt et al., 2000; Wegner et al., 2000). Understanding fiber size variation is therefore critical, as larger muscle fibers are generally associated with reduced tenderness due to increased muscle density (Joo et al., 2017).

 

Table 6: Breast meat texture of IPB-D3 chickens reared under an intensive system.

Variables

Average ± SD, Month

1

2

3

Firmness (N)

1.86 ± 0.13a

3.52 ± 1.91ab

4.65 ± 1.61b

Adhesiveness (g.sec)

-0.12 ± 0.03

-0.10 ± 0.04

-0.17 ± 0.07

Resilience (%)

15.68 ± 0.82

17.07 ± 2.00

17.66 ± 1.13

Cohesion

0.47 ± 0.05a

0.53 ± 0.03b

0.53 ± 0.02b

Springiness (%)

84.76±8.02b

77.93 ± 4.96b

67.66 ± 4.83a

Gumminess

86.13±8.43a

192.54±106.87ab

249.47±88.15b

Chewiness

72.07±9.86a

141.89 ± 73.25ab

169.84±65.56b

 

Different superscripts (a,b) within the same row indicate significant differences at P < 0.05.

 

Table 7: Correlation between breast meat texture and pectoralis muscle microstructure.

Variables

Firmness

Adhesiveness

Resilience

Cohesion

Springiness

Gumminess

Chewiness

FA

0.69*

-0.53*

0.48

0.37

-0.73*

0.67*

0.60*

MCSA

0.54*

-0.53*

0.33

0.31

-0.68*

0.52*

0.45

NMOF

0.45

-0.06

0.54*

0.70*

0.00

0.49*

0.54*

 

Note: An asterisk (*) indicates a statistically significant Pearson correlation (P < 0.05). FA= Fasciculus area; MCSA= Myofiber cross-sectional area; NMOF= Number of myofibers per fasciculus.

 

Texture analysis of the breast meat showed an increasing trend from 1 to 3 months of age. Significant differences (P < 0.05) were observed between 1 and 3 months, where firmness, cohesion, gumminess, and chewiness increased, whereas springiness decreased at 1 and 2 months compared with 3 months (Table 6). Correlation analysis revealed moderate associations between microstructure muscle characteristics and meat texture variables (Table 7). The texture of IPB-D3 chicken breast meat showed a progressive increase in firmness (1.86 to 4.65 N), gumminess (86.13 to 249.47), and chewiness (72.07 to 169.84), accompanied by a decrease in springiness (84.76 to 67.66%) from 1 to 3 months of age. This profile reflects an increase in tissue deformation resistance in line with muscle structural maturation. Myofiber hypertrophy likely enhances the contribution of myofibrillar components to load-bearing capacity; however, mechanical properties are not determined solely by fiber diameter. Intramuscular collagen within the perimysial–endomysial compartments plays a central role in determining hardness and chewiness during maturation (Wattanachant et al., 2004; Krzywdzińska-Bartkowiak et al., 2016). Structural and physicochemical modifications in muscle fibers and connective tissue are associated with variations in meat texture (Krzywdzińska-Bartkowiak et al., 2016). Progressive collagen cross-link stabilization increases tissue stiffness and reduces elasticity (Nishimura, 2010; 2015; Purslow, 2018; Zhu et al., 2023). Although collagen was not directly quantified, previous findings in intensively reared IPB-D3 chickens reported increased intramuscular collagen deposition (Prawira et al., 2026), which may explain the greater mechanical resistance observed in this study. Compared with other chicken types, IPB-D3 exhibited texture values that were higher than those typically reported for commercial broilers but lower than those observed in older or slow-growing local breeds. In Pelung chickens aged 40–56 weeks, reported values were hardness 134.43 N, springiness index 0.667, and chewiness 29.08 N (Yuneldi et al., 2024). Similarly, Bangkok chickens at 3 months showed hardness 177.44 N and a springiness index of 0.52 (Sidiqi et al., 2023). In contrast, male commercial broilers at 42 days showed substantially lower values. Ross 308 exhibited hardness 22.6 N, cohesiveness 0.4, springiness 1.6 cm, chewiness 13.8 N×cm, and gumminess 8.5 N, whereas Cobb 500 showed hardness 15.8 N, cohesiveness 0.4, springiness 1.8 cm, chewiness 9.5 N×cm, and gumminess 5.4 N (Kokoszyński et al., 2022). These differences reflect the combined effects of growth rate and connective tissue maturation on the mechanical properties of meat. Overall, advancing age and connective tissue maturation are positively associated with increased meat stiffness in IPB-D3 chickens.

Another factor influencing the texture of IPB-D3 chickens is the scalding procedure (70°C). According to Wattanachant et al. (2005), this heating process has the potential to increase absolute firmness values through protein denaturation and collagen shrinkage. However, because all groups underwent the same procedure, this effect did not influence the pattern of relative differences between ages. The texture profile of IPB-D3 chickens indicates that the increase in firmness and chewiness, and the decrease in springiness during the 1–3 months of growth, primarily reflect the interaction between myofiber hypertrophy and the gradual, steady maturation of intramuscular collagen.

Certain limitations should be acknowledged. Scalding (70°C) was performed prior to plucking, which may have influenced the breast meat texture profile. Future studies should avoid scalding or apply standardized processing conditions to enable more accurate comparisons of texture parameters. Additional analyses, including mineral composition of meat and bone, collagen evaluation using picrosirius red or Masson’s trichrome staining, immunohistochemical detection of myostatin and MYH1, and molecular assessment of related gene expression, are recommended to provide a more comprehensive understanding of muscle development and meat quality.

CONCLUSION

It can be concluded that IPB-D3 chickens exhibit a relatively rapid growth pattern, with clear sexual dimorphism: males consistently attain higher body weight and superior morphometric development than females from 6 weeks of age onward. Carcass yield increased progressively with age, primarily driven by enhanced breast muscle deposition, while the thigh maintained the highest meat-to-bone ratio. Muscle development was predominantly characterized by hypertrophy, as evidenced by enlargement of the fasciculus area (FA) and myofiber cross-sectional area (MCSA) without changes in the number of myofibers per fasciculus (NMOF). These microstructural adaptations were associated with progressive modifications in breast meat texture, including increased firmness, cohesion, gumminess, and chewiness, along with reduced springiness. The findings demonstrate consistent growth performance and progressive structural development of meat properties up to 12 weeks of age under Replaced with intensive rearing systems.

ACKNOWLEDGEMENT

This research was funded by the National Research and Innovation Agency (BRIN) in collaboration with the Indonesia Endowment Fund for Education Agency (LPDP) through the Riset dan Inovasi untuk Indonesia Maju – Kompetisi (RIIM Kompetisi) Batch 7 funding scheme in 2024, under the Decree of the Deputy for Research and Innovation Facilitation of BRIN No. 61/II.7/HK/2024 and Contract No. B-3864/II.7.5/KS.00/4/2025. The authors also acknowledge the scientific facilities and technical support provided by the Advanced Characterization Laboratories, Yogyakarta, National Research and Innovation Agency (BRIN), through E-Layanan Sains BRIN.

NOVELTY STATEMENT

Previous studies on IPB-D3 chickens have reported growth performance, body morphometrics, carcass traits, and muscle characterization of the breast, thigh, and drumstick. However, the texture properties of breast meat have not been previously investigated. In addition, earlier muscle characterization studies used unequal sex ratios and small sample sizes, and no comprehensive data are available on the characteristics of breast, thigh, and drumstick muscles at 1, 2, and 3 months of age. Therefore, the present study provides the first integrated evaluation of growth performance, morphometric traits, carcass characteristics, detailed histomorphological muscle features, and breast meat texture of IPB-D3 chickens at 1, 2, and 3 months of age reared under intensive systems.

AUTHOR’S CONTRIBUTION

AYP, RFY, IK, AF, DL, NLPRP, WK, RPR, PV, HSR, MAR, RR, TP, AA, and CS contributed to the conceptualization of the study, experimental design, data collection, sample collection, and manuscript revision. AYP conducted data processing and statistical analysis. AYP and RFY performed the histomorphology sample analysis and drafted the manuscript. All authors read and approved the final version of the manuscript.

Ethical approval

All research procedures were approved by the ethical clearance of the National Research and Innovation Agency (BRIN), Indonesia (Approval No. 191/KE.02/SK/09/2025).

Generative AI and AI assisted technology statement

The authors declare that no generative AI and AI assisted technology was used in the creation of this manuscript.

Conflict of interest

The authors have declared no conflict of interest.

REFERENCES

Adelta KB, Arief II, Sumantri C, Wulandari Z (2023). Meat quality characteristics of IPB-D1 chicken and the final stock from different locations. J. Ilmu Ternak Vet., 28(3): 197–207. https://doi.org/10.14334/jitv.v28i3.3121.

Baldi G, Soglia F, Petracci M (2020). Current status of poultry meat abnormalities. Meat Muscle Biol., 4(2): 1–7. https://doi.org/10.22175/mmb.9503

Bongiorno V, Schiavone A, Renna M, Sartore S, Soglia D, Sacchi P, Gariglio M, Castillo A, Mugnai C, Forte C, Bianchi C, Mioletti S, Gasco L, Biasato I, Brugiapaglia A, Sirri F, Zampiga M, Gai F, Marzoni M, Cerolini S, Dabbou S (2022). Carcass yields and meat composition of male and female Italian slow-growing chicken breeds: Bianca di saluzzo and Bionda piemontese. Animal, 12 (3): 1–20. https://doi.org/10.3390/ani12030406

Buzala M, Janicki B (2016). Review: Effects of different growth rates in broiler breeder and layer hens on some productive traits. Poult. Sci., 95(9): 2151–2159. https://doi.org/10.3382/ps/pew173

Darmani Kuhi H, Kebreab E, Lopez S, France J (2003). An evaluation of different growth functions for describing the profile of live weight with time (age) in meat and egg strains of chicken. Poult. Sci., 82(10): 1536–1543. https://doi.org/10.1093/ps/82.10.1536

Deng S, Xing T, Li C, Xu X, Zhou G (2022). The effect of breed and age on the growth performance, carcass traits and metabolic profile in breast muscle of Chinese indigenous chickens. Foods, 11(3): 1–18. https://doi.org/10.3390/foods11030483

Emmert ME, Emmert AS, Goh Q, Cornwall R (2024). Sexual dimorphisms in skeletal muscle: Current concepts and research horizons. J. Appl. Physiol., 137(2): 274–299. https://doi.org/10.1152/japplphysiol.00529.2023

Galib I, Sumantri C, Darwati S, Murtini S (2024). Weight performance of 4th generation IPB-D3 local chickens aged 1–3 months and its heritability value. J. Ilmu Prod. Teknol. Has. Peternak., 12(1): 14–20. https://doi.org/10.29244/jipthp.12.1.14-20

Gu S, Gao J, Li Z, Zhang S, Wen C, Sun C, Yan W, Hou Z, Yang N, Li J (2024). Comparative analysis of myofiber characteristics, shear force, and amino acid contents in slow- and fast-growing broilers. Foods, 13(24): 1–14. https://doi.org/10.3390/foods13243997

Hariyadi S, Rusman TE, Asmarani RR., Badrun RM, Firmansyah AM, Wahyono T (2025). Textural and chemical changes in chicken meat treated with irradiation and coriander powder. J. Anim. Health Prod., 13(3): 508–520. https://doi.org/10.17582/journal.jahp/2025/13.3.508.520

Hawari MF, Sumantri C, Darwati S (2024). Egg production and quality of IPB-D3 chicken and its repeatability estimation. J. Ilmu Prod. Teknol. Has. Peternak., 12(1): 8–13. https://doi.org/10.29244/jipthp.12.1.8-13

Honda M, Tsuchimochi H, Hitachi K, Ohno S (2019). Transcriptional cofactor Vgll2 is required for functional adaptations of skeletal muscle induced by chronic overload. J. Cell. Physiol., 234(9): 15809–15824. https://doi.org/10.1002/jcp.28239

Joo SH, Lee KW, Hwang YH, Joo ST (2017). Histochemical characteristics in relation to meat quality traits of eight major muscles from hanwoo steers. Korean J. Food Sci. Anim. Resour., 37(5): 716–725. https://doi.org/10.5851/kosfa.2017.37.5.716

Kokoszyński D, Żochowska-Kujawska J, Kotowicz M, Sobczak M, Piwczyński D, Stęczny K, Majrowska M, Saleh M (2022). Carcass characteristics and selected meat quality traits from commercial broiler chickens of different origin. Anim. Sci. J., 93(1): 1–10. https://doi.org/10.1111/asj.13709

Krzywdzińska-Bartkowiak M, Rezler R, Gajewska-Szczerbal H (2016). The influence of meat muscle structural properties on mechanical and texture parameters of canned ham. J. Food Eng., 181: 1–9. https://doi.org/10.1016/j.jfoodeng.2016.02.015

Kuswandi W, Budiman C, Khaerunnisa I, Sumantri C (2025). Rearing system and immune status influence the small intestinal microbiota of IPB-D3 chickens: A full-length 16S rRNA metagenomic approach. Vet. World, 18(8): 2206–2221. https://doi.org/10.14202/vetworld.2025.2206-2221

Metsalu T, Vilo J (2015). ClustVis: A web tool for visualizing clustering of multivariate data using Principal Component Analysis and heatmap. Nucl. Acids Res., 43(1): 566–570. https://doi.org/10.1093/nar/gkv468

Mrajji O, Wazna ME., Boussoualem Y, Bouari AE, Cherkaoui O (2021). Feather waste as a thermal insulation solution: Treatment, elaboration and characterization. J. Ind. Text., 50(10): 1674-1697. https://doi.org/10.1177/1528083719869393

Murach KA, Bagley JR, Phillips SM (2023). Skeletal muscle hypertrophy and regulatory mechanisms. Nat. Rev. Mol. Cell Biol., 24: 607–624. https://doi.org/10.1038/s41580-023-00606-x

Nishimura T (2010). The role of intramuscular connective tissue in meat texture. Anim. Sci. J., 81(1): 21–27. https://doi.org/10.1111/j.1740-0929.2009.00696.x

Nishimura T (2015). Role of extracellular matrix in development of skeletal muscle and postmortem aging of meat. Anim. Sci. J., 86(2): 1–8. https://doi.org/10.1016/j.meatsci.2015.05.015

Padhi MK, Chatterjee RN, Rajkumar U, Niranjan M, Haunshi S (2016). Evaluation of a three-way cross chicken developed for backyard poultry in respect to growth, production and carcass quality traits under intensive system of rearing. J. Appl. Anim. Res., 44(1): 390–394. https://doi.org/10.1080/09712119.2015.1091336

Padhi MK (2016). Importance of indigenous breeds of chicken for rural economy and their improvements for higher production performance. Scientifica, 2016(1): 2604685. https://doi.org/10.1155/2016/2604685

Park SY, Byeon DS, Kim GW, Kim HY (2021). Carcass and retail meat cuts quality properties of broiler chicken meat based on the slaughter age. J. Anim. Sci. Technol., 63(1): 180–190. https://doi.org/10.5187/jast.2021.e2

Petracci M, Cavani C (2011). Muscle growth and poultry meat quality issues. Nutrients, 4(1): 1–12. https://doi.org/10.3390/nu4010001

Petracci M, Mudalal S, Soglia F, Cavani C (2015). Meat quality in fast-growing broiler chickens. World’s Poult. Sci. J., 71(2): 363–374. https://doi.org/10.1017/S0043933915000367

Prawira AY, Yuneldi RF, Khaerunnisa I, Furqon A, Lestari D, Phadmacanty NLPR, Budiman C, Sumantri C (2026). Growth performance and muscle histological characteristics of IPB-D3 chickens reared under intensive and free-range systems. Vet. World, 19(1): 282–294. https://doi.org/10.14202/vetworld.2026.282-294

Prayogi HS (2011). The improvement of Indonesian native chicken; estimation of genetic parameters, response to selection, and disease resistance ability. J. Ilmu-Ilmu Peternak., 21(1): 1–5.

Purslow PP (2018). Contribution of collagen and connective tissue to cooked meat toughness: Some paradigms reviewed. Meat Sci., 144: 127–134. https://doi.org/10.1016/j.meatsci.2018.03.026

Rahman WN, Darwati S, Sumantri C (2024). Comparison of carcass and non-carcass weight percentage between IPB-D2 chickens and IPB-D3 chickens at different slaughter age. IOP Conf. Ser. Earth Environ. Sci., pp. 1–8. https://doi.org/10.1088/1755-1315/1364/1/012087

Ratnawati D, Darwati S, Murtini S, Sumantri C (2025). Productivity of IPB-D2 and IPB-D3 chickens with repeatability of Newcastle disease antibody titer. J. Ilmu Pertan. Indones., 30(1): 140–146. https://doi.org/10.18343/jipi.30.1.140

Rehfeldt C, Fiedler I, Dietl G, Ender K (2000). Myogenesis and postnatal skeletal muscle cell growth as influenced by selection. Livest. Prod. Sci., 66(2): 177–188. https://doi.org/10.1016/S0301-6226(00)00225-6

Rizqi MA, Sumantri C, Darwati S (2024). Morphometrics of IPB D1, IPB D2 and IPB D3 chickens aged 4 to 12 weeks. J. Ilmu Prod. Teknol. Has. Peternak., 12(3): 158–166. https://doi.org/10.29244/jipthp.12.3.158-166

Rizqi MA, Sumantri C, Darwati S (2025). Growth performance of IPB D2 with IPB D3 chicken line crossing and its reciprocal. IOP Conf. Ser. Earth Environ. Sci., pp. 1–8. https://doi.org/10.1088/1755-1315/1484/1/012025

Romantis S, Sumantri C (2024). Effects of supplementation with different nutrient contents of vitamin e diets on the performance and health status of IPB-D3 candidate chicken strains. J. Ilmu-Ilmu Peternak., 34(1): 118–125. https://doi.org/10.21776/ub.jiip.2024.034.01.13

Salsabila N, Sumiati S, Suryati T (2022). Suplementasi vitamin E pada level nutrien ransum berbeda untuk meningkatkan pertumbuhan dan mengatasi cekaman panas pada ayam lokal IPB-D3. J. Ilmu Nutr. Teknol. Pakan., 20(2): 58–65. https://doi.org/10.29244/jintp.20.2.58-65

Sidiqi AAA, Airin CM, Sarmin S, Astuti P (2023). A combination of Anadara nodifera shell and milkfish thorns powder effectively promote springiness index, serum testosterone, and breast muscle testosterone in Bangkok rooster. HAYATI J. Biosci., 30(4): 701–710. https://doi.org/10.4308/hjb.30.4.701-710

Sumantri C, Darwati S (2017). Pekembangan terkini riset ayam unggul IPB-D1. Pros. Semin. Nas. Ind. Peternak., pp. 1–6.

Sumantri C, Khaerunnisa I, Gunawan A (2020). The genetic quality improvement of native and local chickens to increase production and meat quality in order to build the Indonesian chicken industry. IOP Conf. Ser. Earth Environ. Sci., pp. 1–13. https://doi.org/10.1088/1755-1315/492/1/012099

Velleman SG (2015). Relationship of skeletal muscle development and growth to breast muscle myopathies: A review. Avian Dis., 59(4): 525-531. https://doi.org/10.1637/11223-063015-Review.1

Vianisa P, Murtini S, Furqon A, Sumantri C (2025). Immunocompetence index performance of the IPB-D3 candidate line under different rearing systems. J. Ilmu-Ilmu Peternak., 35(2): 281–290. https://doi.org/10.21776/ub.jiip.2025.035.02.11

Wattanachant S, Benjakul S, Ledward DA (2004). Composition, color, and texture of Thai indigenous and broiler chicken muscles. Poult. Sci., 83(1): 123–128. https://doi.org/10.1093/ps/83.1.123

Wattanachant S, Benjakul S, Ledward, DA (2005). Effect of heat treatment on changes in texture, structure and properties of Thai indigenous chicken muscle. Food Chem., 93(2): 337–348. https://doi.org/10.1016/j.foodchem.2004.09.032

Wegner J, Albrecht E, Fiedler I, Teuscher F, Papstein HJ, Ender K (2000). Growth- and breed-related changes of muscle fiber characteristics in cattle. J. Anim. Sci., 78(6): 1485–1496. https://doi.org/10.2527/2000.7861485x

Whittle RH, Karcher DM, Erasmus MA, Weimer SL (2025). Effects of genetic strain, stocking density, and age on broiler behavior. Poult. Sci., 104(2): 104723. https://doi.org/10.1016/j.psj.2024.104723

Yuneldi RF, Airin CM, Saragih HTS, Prawira AY, Astuti P (2024). Testosterone hormone levels and breast muscle performance of Pelung chickens after zinc sulfate and synthetic testosterone supplementation. Vet. World, 17(10): 2365–2369. https://doi.org/10.14202/vetworld.2024.2365-2369

Yuneldi RF, Airin CM, Saragih HTS, Sarmin S, Astuti P, Alimon AR (2023). Growth, pectoralis muscle performance, and testis of pelung cockerels (Gallus gallus gallus [Linnaeus, 1758]) supplemented with blood clam shell powder (Anadara granosa [Linnaeus, 1758]). Vet. World, 16(3): 474–482. https://doi.org/10.14202/vetworld.2023.474-482

Zhang D, Xu F, Liu Y (2024). Research progress on regulating factors of muscle fiber heterogeneity in poultry: A review. Poult. Sci., 103(9): 104031. https://doi.org/10.1016/j.psj.2024.104031

Zhu X, Puolanne E, Ertbjerg P (2023). Changes of raw texture, intramuscular connective tissue properties and collagen profiles in broiler wooden breast during early storage. Foods, 12(7): 1530. https://doi.org/10.3390/foods12071530

Zuidhof MJ, Schneider BL, Carney VL, Korver DR, Robinson FE (2014). Growth, efficiency, and yield of commercial broilers from 1957, 1978, and 2005. Poult. Sci., 93(2): 2970–2982. https://doi.org/10.3382/ps.2014-04291