Submit or Track your Manuscript LOG-IN

Evaluation of Production and Reproductive Traits of Mamourah Egyptian Local Chicken and Crossbreed Tanta G-1

AAVS_10_12_2571-2577

Research Article

Evaluation of Production and Reproductive Traits of Mamourah Egyptian Local Chicken and Crossbreed Tanta G-1

Ahmed Rizk1, Gomaa Said Ramadan2*, Alaa Eldin Abdou3, Ossama Ahmed El-Weshahy1, Omer sayed Rashed1

1Animal Production Research Institute, Agriculture Research Center., Ministry of Agriculture, Egypt; 2Animal Production Department, Agriculture and Biology Research Institute, National Research Centre, El Buhouth St., 1231 Dokki, Cairo, Egypt; 3Department of Animal Production Faculty of Agriculture, Cairo University, Giza, Egypt.

Abstract | This experiment was conducted to study the progress in productive performance of Tanta G-1 selected for high body weight at 8 weeks of age compared with the Mamourah local strain. The selection was applied for three generations. Body weight at sexual maturity (BWSM), age at sexual maturity (ASM), and egg production traits (EP) from 36 - 42 weeks of age were also applied. Our results showed that the average body weight for Tanta G-1 and Mamourah chicken strains was 866.45 grams and 558.75 grams in the first generation. In the second generation, the Tanta G-1 line’s body weight was 1006.50 grams against 555.10 grams for the Mamourah strain, while in the third generation the average body weight in the Tanta G-1 line was 1068.93 grams versus 551.25 grams in the Mamourah strain at the age of 8 weeks. This difference between the two lines was significant (P≤0.05). Body weight at sexual maturity was 3155.16 g,1525.00g for males and females in generation one, 3137.35g,1526.24g in generation two, and 3119.91g,1526.83g in generation 3 respectively for Tanta G- 1 and Mamourah chickens strain respectively. In the first generation age at sexual maturity for Tanta G- 1 was 172 days, while it was 157 days for the Mamourah strain. The weight of the first egg weight was (45.46g) for Tanta G- 1, while it was 34.84g for the Mamourah strain (34.84g). The overall mean fertility percentage for Tanta G-1 female egg was 87.92 %, while it was 88.94 % for the Mamourah strain and the difference was significantly different (P≤0.05). The overall mean hatchability percentage was 76.15% and 75.03%, for Mamourah and Tanta G- 1 line respectively.

 

Keywords | Local strain, Selection, body weight, Correlated response, productive performance, Reproductive performance.


Received | October 15, 2022; Accepted | November 01, 2022; Published | November 20, 2022

*Correspondence | Gomaa Said Ramadan, Animal Production Department, Agriculture and Biology Research Institute, National Research Centre, El Buhouth St., 12311 Dokki, Cairo, Egypt; Email: [email protected]

Citation | Rizk A, Ramadan GS, Abdou AE, El-Weshahy OA, Rashed OS (2022). Evaluation of production and reproductive traits of mamourah egyptian local chicken and crossbreed tanta g-1. Adv. Anim. Vet. Sci. 10(12): 2571-2577.

DOI | http://dx.doi.org/10.17582/journal.aavs/2022/10.12.2571.2577

ISSN (Online) | 2307-8316

 

BY%20CC.png 

Copyright: 2022 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

Native strains of chickens play an important role to produce meat and eggs. Native strains of chickens have low body weight and slow growth rate and need more time to reach marketing weight. (Sopannarath and Bunchasak, 2015; Jaturasitha et al., 2016). The future success of the broiler industry depends on the bird being able to continue to perform at present levels but with minimized negative effects on fitness traits, which reduces the management resources required (Pollock, 1999). Information on phenotypic and genetic parameters for production traits and traits related to health is needed for the design of breeding programs aimed at improving the balance between production and health traits (Zerehdaran, 2005). Live Body weight (LBW) and carcass traits were under intensive selection for more than half a century, and are considered the most important economic traits in broiler breeding programs. Progress in rapid growth has been accompanied by an increase in abdominal fat deposition in broilers (Baéza et al., 2012; Crossley and Altimiras, 2012).

The genetic control of growth, in chickens, will provide an opportunity for genetic enhancement of production performance and physiology (Li et al., 2005). However, improving the body weight of native chickens by genetic selection is a slow and time-consuming practice. Therefore, crossbreeding is a better option to obtain birds with a faster growth rate that are adapted to local environmental conditions (Segura-Correa et al., 2004).

Crossbreeding in chickens is a technique for producing superior hybrid to improve body weight, egg production traits, and reproductive performance through independent culling level (Nassar, 2017), and fitness. To take advantage of hybrid vigor, crossbreeding is regarded as an effective strategy for the generation of commercial stocks in the chicken business. A two-way hybrid between a commercial breed and an enhanced local breed is usually used in cross-breeding, to combine greater production features with hardiness. (Debes, 2017; El-Tahawy, 2020). The current study aimed to improve the productivity of the local strains by improving body weight and egg production traits.

MATERIALS AND METHODS

Ethical approval

The present study has been conducted in accordance with the guidelines of the Ethics Committee of the Faculty of Agriculture of Cairo University.

This experiment was conducted at Animal Production Research Institute, Agriculture Research Center to develop a new synthetic local broiler breeder male line. Local Egyptian strain Mamourah females (Abd_ElGawad et.al., 1979) were housed individually and artificially inseminated with grandparent male line male Indian River strain (Aviagen, 2018). Pedigreed eggs for each sire and dam were collected to obtain the base generation named the Tanta line. Hatched chicks were wing banded, pedigreed for sir and dam, sexed, and weighed individually.

An inter-C-mating system with no full or half-sibs mating was applied. Two hatched chicks were taken. The first hatch considered the selected line named Tanta G-1 line while the second hatch served as a random-bred control line (Mamourah strain). Feed and water are provided ad libitum from hatch until 8 weeks of age. The light was provided 24 hours per day. The selection procedure for high body weight at 8 weeks was applied for the next generation in the Tanta G-1 line.

Experimental measurements

In each generation, chicks were weighed individually biweekly. Also, body weight at sexual maturity (BWSM), age at sexual maturity (ASM), egg production numbers (EN), and egg weight (EW) were recorded for (Tanta G-1) line and Mamourah strain. Fertility and Hatchability percentage was also recorded.

Statistical analysis

Analysis of variance was carried out using, the General Linear Model procedure of the (X L stat, 2014). Significant differences were separated by Duncan’s multiple range test (Duncan, 1955). The significance level was set at 5%. The following model was used in each generation:

Yijk = μ + Li + Sj + LSij + eijk Where:

Yijk = the Kth observation of the jth sex within the ith line.

μ = the overall mean.

Li = the effect of the ith line.

Sj = the effect of the jth sex

LSij = the interaction between the ith

e = the random error.

RESULTS AND DISCUSSION

Body weight and growth performance

After three generations of selection for high live body weight, the Tanta G-1 line increased significantly (P < 0.05) in body weight at 8 weeks of age compared with the Mamourah strain. The average body weight of Tanta G-1 and Mamourah strain at 8 weeks of age were 1172.25g and 618.50g respectively (Table 1). These results agreed with Rashid et al. (2012) reported that body weight at 6 weeks of age was 485 g and 396 g for males and females of the Cairo B2 line selected for high live body weight respectively. Also, Nassar (2013) reported that body weight at 6 weeks of age for Cairo B-2 and the random-bred control lines were 1085 and 700g respectively, in the seventh generation of selection for high live body weight.

Also, our results indicate that the body weight of the Tanta G-1 line increased significantly (p<0.05) at different ages after three generations of selection compared with the control line Mamourah strain. These results agreed with Joseph et al. (2005), Schmidt et al. (2006), Nassar (2017), Ramadan et al. (2014), and Ramadan (2019). Joseph et al., (2005), Schmidt et al. (2006), and Nassar, (2013) reported that selection for high body weight in broiler breeders includes maternal effects which have a positive association with the live body weight of its progenies after hatch. Also, Nassar (2017) reported that body weight for the Giza M-2 line increased significantly (p < 0.05) at different ages compared with the control line.

Also, our results agreed with many authors whose recorded breed and strain differences in body weight (Taha et al., 2012), Omer (2012), Ajayi and Ejiofor, (2009), and Ramadan (2019). The typical LBW via the creation of Giza M-2 and RBC (Random bred control) LINE lines 862 g compared 550 g at 6 weeks of age (983 g vs. 625 g), and 983 g vs. 625 g (G5), with substantial differences, respectively for the two lines (Nassar, 2017). In the same direction, El-Tahawy (2020) reported that at 0, 4, 8, and 12 weeks of age, the bird’s body weight was 35.3 g, 226.1 g, 560.2 g, and 924.6 g, respectively.

Soliman et al. (2020) reported that for all variables tested, genotype comparisons revealed statistically significant differences. When compared to the commercial Lohmann strain (LL) and other crossbreds, the Alexandria (AA) strain produced significantly higher body weight at 8 weeks of age (AL and LA). In body weight at sexual maturity, however, the commercial strain (LL) greatly outperformed the local strain (AA) and both crossbreds (AL and LA) (1829.25 vs. 1669.16, 1649.72, and 1563.74 g, respectively).

Tanta G-1 males exhibited considerably higher LBW than Mamourah males over all generations and at all ages, according to the findings. Furthermore, at hatch, 14 days, 28 days, 42 days, and 56 days of age, Tanta G-1 males had significantly (P≤0.05) larger LBW than Mamourah males (Figure 1). At 8 weeks of age, the average LBW of Tanta G-1 males and Mamourah males’ lines were 921.50 g vs. 612.16 g (G1), 1074.24 g vs. 619.83 (G2), and 1172.25 g vs. 618.50 g (G3), respectively.

 

Tanta G-1 females exhibited considerably higher LBW than Mamourah females over all generations and at all ages, according to the findings). Tanta G-1 females had considerably (P≤0.05) higher LBW at hatch, 14 days, 28 days, 42 days, and 56 days of age compared with the Mamourah female line (Figure 1). The average LBW of Tanta G-1 females and Mamourah females’ lines by generation at 8 weeks of age were 811.37 g vs. 464.33 g (G1), 938.73 g vs 490.16 (G2) and 965.62 g vs. 484.00 g (G3), respectively.

Faruque et al. (2017) discovered that intensive management system selection improved the BW of indigenous chickens in the second generation, with weight gains of 107.34, 175.95, and 150.70g for ND, HI, and NN genotypes at 8 weeks of age, and BW increases of 202.91, 337.36, and 72.82 g for ND, HI, and NN genotypes at 40 weeks of age. Nassar (2017) also indicated a positive reaction in LBW and egg productivity in the Giza M-2 line as a result of the breeding effort.

Significant sexual dimorphism, in body weight, was apparent at all ages studied except at hatch. From the second week of age until the 6 weeks of age, males had significantly (P≤0.05) higher body weight than females Table (2). At 4 and 8 weeks of age, sex had a significant impact on body weight. At all ages, males were substantially heavier than females (Soliman et al., 2020).

Sultana et al. (2021) found that the mean BW of Non-descript deshi (ND), Hilly (HI), and Naked Neck (NN) hens grew from 349.99, 380.07, 340.43 g in G0 to 609.09, 704.15, and 591.39g in G7 at 8 weeks of age, and from 1240.71, 1448.30, 1218.34g in G0 to 1530.82, 1901.43, and 1511.66 g in G6 at 40 weeks of age. Over the seven generations of selection, ND, HI, and NN gained 259.10, 324.08, and 250.96 g at 8 weeks of age, and 290.11, 453.13, and 293.32 g at 40 weeks of age, respectively. As a result, the effect of generations of selection on body weight (p≤0.001) was highly significant. Sultana (2019) discovered that at both 8 and 4 weeks of age, generation of selection increased the body weight. Intensive management system selection enhanced the BW of indigenous chickens in the second generation, according to Faruque et al. (2017).

Age and body weight at sexual maturity

Body composition plays a crucial role in sexual development, and the connection between LBW and reproduction in restricted-fed broiler breeder females is not straightforward (Bornstein et al., 1984). However, because LBW is a primary predictor of both of those factors, it is commonly assumed that high uniformity reduces variability in ASM and EW (Wilson, 1991; Hocking, 2004). To achieve optimal reproductive performance in broiler breeder pullets, maintaining a high level of LBW homogeneity is a primary goal during the raising stage (Hocking, 2004).

Results indicated that the Tanta G-1 line had significantly higher body weight at sexual maturity (BWSM) for the first three generations in comparison to those of the Mamourah line (Table 3). This may be due to the selection

 

Table 1: Live body weight (g) LSM and SE at different ages of the 3rd generation of both the Tanta G-1 line and the Mamourah strains.

Trait Age(day)
S.O.V Hatch (gm) 14dys (gm) 28 days (g) 42 days (g) 56 days(g)
Strain          
Tanta G-1

41.13a

189.00a

331.06a

644.60a

1068.93a

Mamouraha

31.47b

115.50b

188.00b

366.75b

551.25b

SE 0.07 1.37 1.98 2.95 3.49
Sex          
Male

36.39a

157.37a

281.93a

568.37a

895.37a

Female

36.21a

147.12b

237.12b

442.37b

724.81b

SE 0.072 1.372 1.988 2.955 3.942
Strain*Sex          

Tanta G-1

41.16a

194.25a

352.87a

724.75a

1172.25a

Tanta G-1

40.08a

183.75b

309.25b

563.25b

965.62b

Mamourah

31.60b

120.50c

211.00c

412.00c

618.50c

Mamourah

31.35b

110.50d

165.00d

321.50d

484.00d

SE 0.11 1.94 2.814.17 4.17 5.24
Probabilities          
Strain 0.00001 0.00001 0.00001 0.00001 0.00001
Sex 0.0878 0.00001 0.00001 0.00001 0.00001
Strain*Sex 0.00001 0.00001 0.00001 0.00001

0.00001

a…d. Means, within age and source of variation (S.O.V), with different superscripts, are significantly different (Duncan, 1955).

 

Table 2: Sexual dimorphism of the Tanta G-1 line and Mamourah strain from generation 1(G1) to generation 3 (G3).

  Sex Generation
G1 G2 G3
Mamouraha        
8 week LBW (g) Female 496.33 490.16 484
Male 621.16 619.83 618.5
Sex differences   110.13 135.5 206.63
TantaG-1        
8 week LBW (g) Female 811.37 938.75 965.62
Male 921.5 1074.25 1172.25
Sex differences   124.83 129.67 134.5
Lines different   307.7 451.4 517.68
Lines different (%)   35.51 44.85

48.43

 

for high LBW at 8 weeks of age in the Tanta G-1 line. A major objective of the genetic selection in the Tanta G-1 line has been to increase LBW at earlier ages and this strategy has changed LBW at different points along the growth curve including BWSM. On the other hand, there were significant differences between the Tanta G-1 and the (MAMOURAH) strain in ASM in the first three generations compared to the Mamourah strain Soliman et al. (2020) When compared to the commercial strain (LL), the local strain (AA) laid the first egg significantly later (182.78 vs. 151.40 d). However, when compared to the native strain (AA), the crossbred (LA) lay much earlier (172.83 vs. 182.78 d) The results of Soliman et al. (2020) agreed with the results found in our study. Debes (2017) found that the Silver Montazah (SM) strain was the heaviest (P≤0.05) at sexual maturity (1550.76g) when compared to the other pure strains, but the two-way hybrid (SM X LSL) had a higher BWSM (1553.22 g) than (MT XLS) (1479.91g). This could be owing to the genetic differences between these breeds. According to Iraqi et al. (2016), the body weight at sexual maturity in the line Benha chickens (Line B) was 1742 g.

 

Table 3: Weight at sexual maturity, age at sexual maturity, egg number during first 36-week of age, average egg weight for the eggs produced during the first 36 weeks of age, the weight of the first egg (LSM ± SE) of the Tanta G-1 line and Mamourah strain in the generation’s studies.

Generation Traits BWSM (g) ASM (days) EN90 EW (g) FEW (g)
G1 Mamouraha

1525.66b±37.16

154.1b±0.54

58a±0.35

51.36b±0.21

35.03b±0.25

Tanta G-1

3155.16a±18.58

172.72a±0.1

58a±0.17

60.41a±0.10

45.61a±0.11

G2 Mamouraha

1526.24b±20.44

156.6b±0.23

58a±0.25

51.58b±0.19

34.84b±0.16

Tanta G-1

3137.35a±12.43

172.0a±0.20

58a±0.16

60.21a±0.12

45.42a±0.13

G3 Mamouraha

1526.83b±8.80

159.26b±0.19

58a±0.15

51.80b±0.13

34.65b±0.10

Tanta G-1

3119.91a±6.28

171.79a±0.14

58a±0.15

60.08a±0.09

45.37a±0.07

BWSM= body weight at sexual maturity, ASM= age at sexual maturity, EN= egg number, EW= egg weight, FEW= weight of first egg.,

* Means within traits, with different superscripts are significantly different (P≤0.05).

 

Table 4: Fertility and hatchability percentage of Tanta G-1 line and Mamourah strain for the first three generations combined data.

Lines Fertility (%) Hatchability (%)
Mamourah

88.94a

76.1500a

Tanta G-1

87.92b

75.0375b

SE 0.158 0.1456
Probability <0.0001 <0.0001

a..b, means within traits, with different superscripts are significantly different (P≤0.05).

Egg number and Egg weights

In comparison to the Mamourah strain, the Tanta G-1 line had considerably greater FEW, and EW than the Mamourah strains (P≤0.05) (Table 3). Table 3 shows the EN of the Tanta G-1 and Mamourah strains for the first 36 weeks of age. The number of eggs produced, by the first three-generation, during the first 90 days of production, is presented in Table 3. The egg production means for the first three-generation female was 58 eggs for both lines. This number was found to be within the range of 27 to 69 eggs reported for the local Egyptian.

The increase in EN in the Mamourah strains until 42 weeks is due to the high age of sexual maturity of the Tanta G1 strain compared to the Mamourah strain. Therefore, we must focus on future generations on through independent culling levels to improve egg production for the selected line compared to the control line. And also, may be due to the negative correlation between high body weight and reproductive performance (Luo et al., 2007) Nassar (2017) reported that in comparison to the RBC line, the EN, FEW, and EW of the Giza M-2 line were significantly greater (P0.05). The EN of Giza M-2 and RBC lines are shown for the first 36 weeks of age. The increase in EN in the Giza M-2 line is attributable to our decision to raise EN (via independent culling levels) in all generations of the Giza M-2 line. Furthermore, when compared to the RBC line, Giza M-2 had a much greater FEW. In addition, the Giza M-2 line showed a greater EW throughout the first 36 weeks of age than the RBC line. Soliman et al. (2020) although both crossbreds (AL and LA) lay significantly more eggs than the local strain (AA) (53.14 and 52.29 g vs. 47.47 g), they consistently weighed less than the commercial strain (LL) (57.55 g). The egg mass followed the same pattern. The crossbreds (AL and LA) deposited significantly more eggs (2452.69 and 2231.51 g) than the local strain (1630.67 g), while the local strain (1630.67 g) laid significantly more eggs. They were not as numerous as the commercial strain (3394.82 g). Also, Nassar (2017) also found that the Giza M-2 line had considerably greater EN and FEW than the RBC line (P0.05). According to Younis et al. (2014), the average egg number for the base, first, and second generation over the first 90 days of laying was 43.9, 52.7, and 61.9 eggs for the selected line, and 43.6, 44.8, and 46.1 eggs for the control line, respectively.

Fertility and hatchability percentage

The overall mean fertility of Tanta G-1 chicken eggs was 87.92 percent (Table 4), whereas the fertility of Mamourah chicken eggs was 88.94 percent. This difference was significantly statistical. Overall mean hatchability across total incubated and viable eggs were determined to be 76.15 and 75.03 percent, for Mamourah and Tanta G-1 respectively, as shown in Table 4. Also, this difference was significantly statistical this difference between the two lines due to the negatively correlated between high body weight and reproductive performance (Nassar 2017, Luo et al., 2007) Sapkota et al. (2020) Fertility and hatchability traits play an important role in overall profitability. Fertility of Sakini chickens Fertility, hatchability, and survivorship all improved significantly (p0.05) in chosen generations when compared to the base population, but no significant differences were found within the different populations. Thus, indigenous Sakini chicken in this experiment fared better in terms of survivorship, fertility, and hatchability in subsequent generations, indicating that there is plenty of room for selective breeding within the indigenous population to boost Sakini chicken productivity in Nepal. Sapkota et al. (2020).

CONCLUSION

This study’s findings the production performance (live weight at various weeks) and reproductive traits such as age at first laying, weight at first laying, egg number, egg weight, and egg production. The results clearly showed that the Tanta G-1 chickens outperformed Mamourah chickens in terms of growth, but that Mamourah chickens outperformed Tanta G-1 in terms of fertility and hatchability in subsequent generations, indicating that there is a lot of variation for selective breeding within the indigenous population to improve these economically important traits. Finally, to produce commercially hybrid lines, better adapted to the volatile climate changes in Egypt’s environmental conditions and more resistant to endemic poultry diseases we suggested used Tanta G-1 males in crossing with other female lines.

conflict of interest

The authors have declared no conflict of interest.

authors contribution

Conceptualization: Gomaa Said Ramadan, Omer Sayed Rashed; investigation: Gomaa Said Ramadan, Ossama el-WeshAhy; resources: Ahmed Rezk, Alaa Abdo, Omer Sayed Rashed, Osamaa El -Weshahy; analysis: Gomaa Said Ramadan; writing—original draft preparation: Gomaa Said Ramadan; writing-review, and editing: Gomaa, Said Ramadan, Omer Sayed Rashed. All authors have read and agreed to the published version of the manuscript.

REFERENCES

Abd El-Gawad Elham, A. Z. Khalil, Magda M. Balat (1979). Genetic analysis of new breed of chickens “Mamourah”. Egypt. J. Genet. Cytol. 8: 303 – 314.

Addinsoft, XLSTAT (2014). Data analysis and statistics with Microsoft Excel, Paris, France, 2014.

Ajayi FO, Ejiofor O (2009). Effects of Genotype X Sex Interaction on Growth and Some Development Characteristics of Ross and Anak Broiler Strains in. Asian Journal of Poult. Sci., 3(2): 51-56. https://doi.org/10.3923/ajpsaj.2009.51.56

Aviagen (2018). Indian River Guide. Accessed Sept. 2020. http://ap.aviagen.com/brands/indian-river/products/indian-river-meat.

Baéza E., Arnould C., Jlali M., Chartrin P., Gigaud V., Mercerand F., Berri C. (2012). Influence of increasing slaughter age of chickens on meat quality, welfare, and technical and economic results. J. Anim. Sci., 90(6): 2003-2013. https://doi.org/10.2527/jas.2011-4192

Bornstein S, Plavnik I., Lev Y (1984). Body weight and/or fatness as potential determinants of the onset of egg production in broiler breeder hens. British Poult. Sci., 25(3): 323-341. https://doi.org/10.1080/00071668408454873

Crossley II, D. A., Altimiras J. (2012). Effect of selection for commercially productive traits on the plasticity of cardiovascular regulation in chicken breeds during embryonic development. Poult. Sci., 91(10): 2628-2636. https://doi.org/10.3382/ps.2012-02344

Debes AAEM (2017). Effect of Crossing Between Lohman Selected Leghorn with Two Developed Strains of Chickens for Improving Some Egg Production Traits. Egyptian Poult. Sci. J. 37(4). https://doi.org/10.21608/epsj.2017.5652

Duncan DB (1955). Multiple ranges and multiple F tests. Biometrics., 11: 1-42. https://doi.org/10.2307/3001478

El-Tahawy WS (2020). Analysis of heterotic components in a cross-bred between two Egyptian local chicken strains. Egyptian Poult. Sci. J., 40(2): 525-535.

Faruque S, Bhuiyan AKFH, Ali M, Joy ZF (2017). Breeding for the improvement of indigenous chickens of Bangladesh: evaluation of performance of first generation of indigenous chicken. Asian J. Med. Biolog. Res., 3(1): 72-79. https://doi.org/10.3329/ajmbr.v3i1.32039

Hocking P. M. (2004). Roles of body weight and feed intake in ovarian follicular dynamics in broiler breeders at the onset of lay and after a forced molt. Poult. Sci., 83(12): 2044-2050. https://doi.org/10.1093/ps/83.12.2044

Iraqi MM, Khalil MH, El_Attrouny MM (2016). The Phenotypic and Productive Characterization of Benha-Line Chicken Under Egyptian Conditions. Egyptian Poult. Sci. J., 36(2). https://doi.org/10.21608/epsj.2016.5423

Jaturasitha S, Chaiwang N, Kreuzer M (2016). Thai native chicken meat: an option to meet the demands for specific meat quality by certain groups of consumers; a review. Anim. Prod. Sci., 57(8): 1582-1587. https://doi.org/10.1071/AN15646

Joseph NS, Moran ETJ (2005). Characteristics of eggs, embryos, and chicks from broiler breeder hens selected for growth or meat yield. J. Appl. Poult. Res., 14:275–280. https://doi.org/10.1093/japr/14.2.275

Li H., Deeb N., Zhou H., Ashwell C. M., Lamont S. J. (2005). Chicken quantitative trait loci for growth and body composition associated with the very low-density apolipoprotein-II gene. Poult. Sci., 84(5): 697-703. https://doi.org/10.1093/ps/84.5.697

Luo PT, Yang RQ, Yang N (2007). Estimation of genetic parameters for cumulative egg numbers in a broiler dam line by using a random regression model. Poult. Sci., 86(1): 30-36. https://doi.org/10.1093/ps/86.1.30

Naser FS (2017). Productive Performance in Local Chicken After Five Generations of Crossing and Selection for High Live Body Weight. Egyptian Poult. Sci. J., 37(3): 779-813. https://doi.org/10.21608/epsj.2017.7733

Nassar FS (2013). Improving Broiler Performance Through Modern Biotechnological Methods. Ph.D. THESIS, Fac. Agric., Cairo Univ., Egypt, 137 P.

Pollock D. L. (1999). A geneticist’s perspective from within a broiler primary breeder company. Poult. Sci., 78(3): 414-418 https://doi.org/10.1093/ps/78.3.414.

Ramadan GS, Moghaieb RE, EL-Ghamry AA, EL-Komy EM, Nassar FS, Abdou AM, Mona M, Stino FKR (2014). Effect of Selection for High Live Body Weight on Slaughter Performance of Broiler Breeders Egy. Poult. Sci., 34(1) :289-304. https://doi.org/10.21608/epsj.2014.5317

Ramadan GS (2019). Molecular Markers as a tool for selection in local Egyptian chickens. Ph.D. THESIS, Fac. Agric., Cairo Univ., Egypt, 146 P.

Rashed OS (2012). Improving meat production in native Chickens Ph.D. THESIS, Fac. Agric., Cairo Univ., Egypt, 99 P.

Sapkota S, Kolakshyapati MR, Devkota NR, Bhattarai N, Gorkhali NA (2020). Selective Breeding to Improve Productive and Reproductive Performances and Survivability of Indigenous Sakini Chicken. J. Nepal Agric. Res. Council, 6: 62-69. https://doi.org/10.3126/jnarc.v6i0.28116

Schmidt GS, Figueiredo EA, Ledur MC (2006). Genetic gain for body weight, feed conversion, and carcass traits in selected broiler strains. Bra. J. Poult. Sci., 8:29-32. https://doi.org/10.1590/S1516-635X2006000100004

Segura-Correa J. C., Sarmiento-Franco L., Magaña-Monforte J. G., Santos-Ricalde R. (2004). Productive performance of Creole chickens and their crosses raised under semi-intensive management conditions in Yucatan, Mexico. Brit. Poult. Sci., 45(3): 342-345. https://doi.org/10.1080/00071660410001730833

Soliman MA, Khalil MH, El-Sabrout K, Shebl MK (2020). Crossing effect for improving egg production traits in chickens involving local and commercial strains, Vet. World., 13 (3): 407-412. https://doi.org/10.14202/vetworld.2020.407-412

Sopannarath P, Bunches C (2015). Betong chicken (KU line) or KU Betongchicken. Kasetsart Ext. J. 61: 13-21.

Sultana S, Faruque S, Bhuiyan MSA, Bhuiyan AKFH (2021). Progress in the performance of indigenous chickens selected for economic traits in Bangladesh. J. Agric., Food Environ. (JAFE)| ISSN (Online Version): 2708-5694 2.1: 50-54. https://doi.org/10.47440/JAFE.2021.2109

Sultana S (2019). Selection for Improvement of Indigenous Chicken of Bangladesh. M.Sc. Thesis, Department of Animal Breeding and Genetics, Bangladesh Agricultural University, Bangladesh.

Taha AE, El-Edel MA, El-Lakany HF, Shewita RS (2012). Growth performance and immune response against Newcastle and avian influenza vaccines in Egyptian chicken strains. Glob. Vet., 9: 434-440.

Wilson HR (1991). Interrelationships of egg size, chick size, post-hatching growth, and hatchability. World’s Poult. Sci. J., 47: 5 – 20. https://doi.org/10.1079/WPS19910002

Younis HH, Abd El-Ghany FA, Awadein NB (2014). Genetic improvement of egg production traits in Dokki-4 strain. 1-Correlated response, heritability, genetic and phenotypic correlations for egg production and egg quality traits. Egyptian Poult. Sci., 34: 345-362. https://doi.org/10.21608/epsj.2014.5320

Zerehdaran S. (2005). Genetic improvement for production and health in broilers. Ph.D. Thesis, Animal Breeding and Genetics Group, Department of Animal Science, Wageningen University, Netherlands, 132P.

Advances in Animal and Veterinary Sciences

December

Vol. 12, Iss. 12, pp. 2301-2563

Featuring

Click here for more

Subscribe Today

Receive free updates on new articles, opportunities and benefits


Subscribe Unsubscribe