Journals / Türk Tarım - Gıda Bilim ve Teknoloji dergisi / 2020 / Cilt: 8 - Sayı: 1

Effect of In Ovo Injection of Organic Zinc, Manganese and Copper on Hatchability Parameters and Some Tissues’ Properties in Quail Breeder

Pages
95–98
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

These results demonstrated that in ovo injection with MinMix2 increased heart and liver weights and chick and wing lengths while in ovo mineral injection decreased yolk sac.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:This study has been carried out to investigate that the effect of different levels of in ovo zinc, manganese and copper mineral mix injection on the hatchability and some tissue characteristics in the Japanese quail breeder eggs.
📊
Key Findings & Data:In the study a total 400 Japanese quail breeder eggs which have similar weight have been randomly distributed to four different experimental groups: C as control non-injected (C), MinMix1 has been injected with 15+15+3 μg Zn-Mn-Cu mineral mix + 0.2 ml physiological serum per egg, MinMix2 has been injected with 30+30+6 μg Zn-Mn-Cu mineral mix + 0.2 ml physiological serum per egg and MinMix3 has been injected with 45+45+9 μg Zn-Mn-Cu mineral mix + 0.2 ml physiological serum per egg.
💡
Conclusion & Impact:These results demonstrated that in ovo injection with MinMix2 increased heart and liver weights and chick and wing lengths while in ovo mineral injection decreased yolk sac.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

This study has been carried out to investigate that the effect of different levels of in ovo zinc, manganese and copper mineral mix injection on the hatchability and some tissue characteristics in the Japanese quail breeder eggs. In the study a total 400 Japanese quail breeder eggs which have similar weight have been randomly distributed to four different experimental groups: C as control non-injected (C), MinMix1 has been injected with 15+15+3 μg Zn-Mn-Cu mineral mix + 0.2 ml physiological serum per egg, MinMix2 has been injected with 30+30+6 μg Zn-Mn-Cu mineral mix + 0.2 ml physiological serum per egg and MinMix3 has been injected with 45+45+9 μg Zn-Mn-Cu mineral mix + 0.2 ml physiological serum per egg. The effect of treatment on hatchability, hatching weight and tibia weight, leg, beak and tibia lengths has been found to be unimportant. The yolk sac weight was lower in the injected groups compared to the control group, whereas the heart and liver weights, chick and wing lengths have significantly increased with the in ovo mineral mix injection. The hatching of chicks in the injected groups has started earlier than the control group and the hatchings of these groups were completed earlier, except for the MinMix3 group. These results demonstrated that in ovo injection with MinMix2 increased heart and liver weights and chick and wing lengths while in ovo mineral injection decreased yolk sac.

🔖

Cite This Article

ŞENTÜRK, E. T., YILDIZ, A. Ö. (2020). Effect of In Ovo Injection of Organic Zinc, Manganese and Copper on Hatchability Parameters and Some Tissues’ Properties in Quail Breeder. Türk Tarım - Gıda Bilim ve Teknoloji dergisi, Cilt: 8 - Sayı: 1, 95–98. https://ajindex.com/articles/331032

References (12)

  1. Abdulqader AFA, Olgun O, Yıldız AÖ. 2017. In Ovo Besleme. Hayv. Üret. 58, 58-65.
  2. Beattie JH, Avenell A. 1992. Trace element nutrition and bone metabolism. Nutr. Res. Rev. 5, 167-88.
  3. Bhanja S, Goel A, Pandey N, Mehra M, Majumdar S, Mandal A. 2015 In ovo carbohydrate supplementation modulates growth and immunity‐related genes in broiler chickens. J Anim Phys. Anim. Nutr. 99, 163-73.
  4. Bhanja S, Mandal A, Agarwal S, Majumdhar S, Bhattacharyya A, Kadam MM. 2008. In ovo glucose injection for higher chick weight and gastrointestinal tract development. Ind. Vet. J.l 85, 289-92.
  5. Bhanja S, Sudhagar M, Goel A, Pandey N, Mehra M, Agarwal S, Mandal A. 2014. Differential expression of growth and immunity related genes influenced by in ovo supplementation of amino acids in broiler chickens. Czech J. Anim. Sci. 59, 399-408.
  6. Chen W, Wang R, Wan H, Xiong X, Peng P, Peng J. 2009. Influence of in ovo injection of glutamine and carbohydrates on digestive organs and pectoralis muscle mass in the duck. Brit. Poult. Sci. 50, 436-42.
  7. Dollwet H, Sorenson J. 1988. Roles of copper in bone maintenance and healing. Biol. Trace Elem. Res. 18, 39-48.
  8. Favero A, Vieira S, Angel C, Bos-Mikich A, Lothhammer N, Taschetto D, Cruz R, Ward T. 2013. Development of bone in chick embryos from Cobb 500 breeder hens fed diets supplemented with zinc, manganese, and copper from inorganic and amino acid-complexed sources. Poult. Sci. 92, 402-11. Ferket P. 2011. In ovo feeding and the promise of perinatal nutrition. In: Proceedings of Alltech International Nutrition Symposium, Lexington, Kentucky, United States of America. Festa RA, Thiele DJ. 2011. Copper: an essential metal in biology. Current Biology 21, R877-R83. Goel A, Bhanja SK, Mehra M, Mandal A, Pande V. 2016. In ovo trace element supplementation enhances expression of growth genes in embryo and immune genes in post‐hatch broiler chickens. J. Sci. Food Agri. 96, 2737-45.
  9. Goel A, Bhanja SK, Pande V, Mehra M, Mandal A. 2013. Effects of in ovo administration of vitamins on post hatch-growth, immunocompetence and blood biochemical profiles of broiler chickens. Ind. J. Anim. Sci. 83, 916-21.
  10. Gupta A, Lutsenko S. 2009. Human copper transporters: mechanism, role in human diseases and therapeutic potential. Fut. Med. Chem. 1, 1125-42.
  11. Johnston P, Liu H, O'Connell T, Phelps P, Bland M, Tyczkowski J, Kemper A, Harding T, Avakian A, Haddad E. 1997. Applications in in ovo technology. Poult. Sci. 76, 165-78.
  12. Jose N, Elangovan A, Awachat V, Shet D, Ghosh J, Da