Livestock Research for Rural Development 29 (5) 2017 Guide for preparation of papers LRRD Newsletter

Citation of this paper

Phenotypic analysis of underutilized poultry species in Kenya

J W Macharia, M N Mberu, L Wamuyu, T Imboma1, J K Lichoti2, K J Ngeiywa2 and S C Ommeh

Institute for Biotechnology Research (IBR), Jomo Kenyatta University of Agriculture and Technology (JKUAT). P.O. Box 62000, City Square 00200, Nairobi-Kenya.
sommeh@jkuat.ac.ke
1 Department of Zoology, National Museums of Kenya. P.O. Box 40658, GPO 00100, Nairobi-Kenya.
2 State Department of Livestock; Directorate of Veterinary Services, Ministry of Agriculture, Livestock and Fisheries. P.O. Box Private Bag, Kangemi, Nairobi-Kenya.

Abstract

Poultry are playing an increasingly important role in ensuring food security especially in developing countries. They are a source of dietary protein as well as a source of income. In Kenya, there is an overreliance on chicken to provide poultry products like meat and eggs. Other poultry species such as domestic ducks (Carina moschata and Anas plathyrynchos), geese (Anser anser and Anser cygnoides), pigeons ( Columba livia) and turkey (Meleagris gallopavo), in this paper referred to as minor poultry, have not been adequately exploited. This study aimed to characterize the phenotypic traits of these minor poultry species. Quantitative parameters measured were live body weight and shank length, while the qualitative traits of shank colour and skin colour were observed and recorded. Data analysis was done using Excel spread sheets and R Core Version 3.1.2.

Geese showed no variation in the qualitative traits scored as all birds sampled had white skin and yellow shanks. Ducks on the other hand exhibited the largest variations in shank colour with six different colours being identified. Ninety-eight percent of the ducks sampled had pink skin colour whereas the remaining two percent were white. More than half of the number of turkeys (fifty-six percent) had white skin colour and almost three quarters (seventy-two percent) had pink shanks. The dominant phenotypes identified in the pigeons sampled were eighty-seven percent with pink skin colour and ninety-four percent with pink shank colour. Males exhibited higher body weights as compared to the females (p≥0.05) in these four species. Shank lengths were significantly longer in males than females (p≥0.05) in all the species except in geese. Results from this study could be used by the National Poultry Improvement Program to establish breeding and improvement programs for minor poultry species. These underutilized poultry species could play a greater role in improving nutrition and alleviating poverty in Kenya, particularly in the rural areas.

Key words: diversity, ecotypes, emerging livestock, family poultry, indigenous poultry


Introduction

Indigenous poultry populations reared using backyard production systems account for more than 80% of poultry in some developing countries (Conan et al 2012; Pym et al 2006). Women tend to be the main participants in poultry keeping with most rural families rearing one or more species (Guèye 2005). To rural populations, poultry are often the only source of animal protein and an invaluable source of income. In Kenya, poultry are reared mainly for egg and meat production. Of the 32 million birds estimated to be reared in the country, 98% are chicken (76% consisting of free range indigenous chicken while 22% are commercial layers and broilers). The remaining 2% comprises other poultry species such as duck, geese, turkey, pigeon, guinea fowl, quail and farmed ostrich, which are becoming increasingly important (Government of Kenya 2010). The indigenous chicken and local ecotypes of ducks, geese, turkey, pigeons and guinea fowl are mostly reared in mixed flocks by small scale farmers who use village production systems (Guèye 2000; FAO 2008). The poultry roam freely and scavenge for their food with no feed supplementation and farmers provide housing only during the night to protect them from predators. Village poultry are highly adapted to the local conditions where they live, which is essential to achieving a sustainable, low-input production system.

 Phenotypic traits are sometimes linked to specific adaptations (FAO 2012). Morphological characterization of local ecotypes of minor poultry species is therefore important if we are to exploit them fully. Income from the sale of meat and the eggs from the minor poultry species could play a vital role in poverty alleviation for rural communities especially for women, the youth and under privileged groups (Adzitey and Adzitey 2011). Ecotypes possessing unique traits need to be conserved as a reservoir for genetic materials for future breed improvements (FAO 2012). Rural poultry reared in backyard systems are rarely vaccinated (Spradbrow 2005) and may possess innate immunity to poultry diseases. Ommeh et al (2010) identified a SNP in the Mx gene of indigenous chicken that confers resistance to avian viral infections in vitro. It will be significant if any of the minor poultry reared under village production systems are found to have resistance to common chicken diseases.

As the Kenya poultry population estimates (GoK 2010) above indicate, there is a vast overreliance on chicken with the other poultry species being largely underutilized. Ducks (mainly Muscovy ducks), geese, pigeons and turkey are found in various parts of the country in small numbers for local meat consumption and also for ornamental purposes (FAO 2008). Most farmers keep these poultry as ornaments and their productivity is generally low due to poor husbandry (Ogada et al 2016). A study on the phenotypic traits of minor poultry could be the initial step toward reaping benefits from ducks, geese, pigeons and turkeys in this country.

Previous similar studies include that conducted by Panyako et al (2016) on the phenotypic traits of domestic and wild guinea fowls in Kenya. Djebbi et al (2014) studied the phenotypic traits of turkey in Tunisia. In India, Banerjee et al (2013) studied the morphological traits of ducks and geese. Bhowmik et al (2014) studied the morphometric measurements, productive and reproductive performance of Jalali Pigeons in Bangladesh. Moraa et al (2015) carried out a similar study on the phenotypic traits relevant to adaptation to hot environments in indigenous chicken while Aswani et al (2017) also characterized phenotypes associated with body growth and egg production in local chickens from three agro-climatic zones of Kenya. This is the first study in Kenya to look into characterizing the phenotypic traits of ducks, geese, pigeons and turkey. An initial countrywide survey was conducted amongst farmers and middlemen in over 20 counties including Nairobi, Uasin Gishu, Kiambu, Makueni and Kwale. Farmers visited were found to keep ducks, geese, pigeons and turkey in mixed flocks with chicken. Middlemen interviewed confirmed that interest in these minor poultry which fetch premium prices was growing rapidly. Poultry sampled for this study were from Western Kenya where more households were found to keep ducks, geese, pigeons, and turkey in addition to chicken. The findings on the phenotypic traits of Kenyan local ecotypes of ducks, geese, pigeons and turkey could facilitate the establishment breeding and improvement programs for these poultry. This would impact the livelihoods of rural families by improving nutrition and alleviating poverty.


Materials and methods

Study sites

This study was conducted between 2014-2016 in Siaya, Busia and Bungoma counties of Western Kenya. Siaya county lies between latitude 0° 26’ to 0° 18’ north and longitude 33° 58’ east and 34° 33’ west. Busia County lies between latitude 0º and 0º 45 north and longitude 34º 25 east. Bungoma County lies between latitude 0° 25’ and 0° 53’ north and longitude34° 21’ and 35° 04’ east. Western Kenya has two rainy seasons with average rainfall from 750mm-1800mm per annum. Average temperature ranges between 15-30°C. Total sampling of poultry owned by households was done rather than random sampling from their flock.

Figure 1. Map of study area (Source: http://d-maps.com/carte.php)
Study clearance

Permit of “No objection” number RES/POL/VOL.XXVII/162 was obtained from the Directorate of Veterinary Services, Ministry of Agriculture, Livestock and Fisheries in Kenya in order to conduct the study.

Data collection

A cross-sectional survey was conducted in villages within Siaya, Busia and Bungoma counties. Homesteads in the area were visited at random and only homesteads where domesticated ducks, geese, turkey and pigeons were found were considered for the study. From the chosen households, only farmers willing to participate were included in the survey. Interviews were conducted in collaboration with local agricultural extension officers to gain knowledge from the farmers on their experiences with rearing the minor poultry species. Sample numbers were chosen as per Hale et al (2012) because the same samples were part of a larger molecular study on minor poultry. A total of 136 poultry were sampled from the chosen homesteads based on the availability of the target species. The qualitative traits of skin colour and shank colour were identified through visual observation. The quantitative traits (body morphometric measurements) were taken once. Individual poultry were weighed using a scale and the body live weight recorded. Shank length, which is the distance from the upper most shank joint to the toe, was measured using a flexible measuring tape graduated in centimeters and a venier caliper graduated in millimeters. The Open Data Kit (ODK) application accessible on android mobile phones was used to record and store the data collected.

The sample numbers for the minor poultry species are shown in Table 1.

Table 1. Sample numbers for minor poultry

Species

Sample Number

Ducks

45

Geese

24

Pigeons

46

Turkey

21

Total

136

NB: Sample numbers were chosen as per Hale et al (2012) because the same samples were part of a larger molecular study on minor poultry

Data analysis

Data was analyzed using Microsoft Excel and ANOVA tests in R Core statistical software (R commander) version 3.1.2 to determine mean measurements of various quantitative traits in each population. Results are presented in the form of bar graphs, tables and percentages.


Results and discussion

Observed phenotypes

The four minor poultry species had diverse phenotypes that were noted during the survey as shown in Figure 2 below.

Figure 2. Observed phenotypes of turkey, pigeon, geese and duck.

Meleagris gallopavo (Turkey): A-White Holland, B-Royal Palm, C-Black
Columba livia
(Pigeon): D-Rock Pigeon, E-Black/Grey, F-White
Anser anser
(Geese): G-white feathered, H-Brown/Grey and White feathered, I-Brown feathered
Carina moschata
(Muscovy duck): J-Black feathered, K-White feathered, L-Black and White feathered
NB: Feather colours of the ducks, geese and turkey indicated cross breeding.
The pigeons encountered were feral and thus could not be assigned to a specific breed.

Skin and shank colour

Figure 3. Skin colour distribution amongst the minor poultry species from Kenya


Figure 4. Shank colour distribution amongst minor poultry species in Kenya

We noted that sampled geese showed no variation in skin and shank colour. They all had white skin colour and yellow shank colour. This is in partial agreement with Banerjee et al (2013) who reported white skin colour but both yellow and orange shanks in the geese sampled. The most common phenotypes were white, white with brown feathers and grey with some white feathers. All the geese were of the Anser anser species which are descendants of the graylag goose (FAO 2002; Albarella 2005). The white feathered geese are kept as ornamental birds and guardians in the homestead because they make noise when they spot strangers. Those with grey and brown feathers are kept for their meat.

We observed that the over half (56%) of the turkeys in the three counties had white skin colour with the red skin colour at 11%. The feather colours observed were white and black mixed with white as also reported of Mexican backyard turkey by Camacho-Escobar et al (2008).

The most prominent shank colour was pink (72%) and the least common was red (11%). The variations noted were fewer than those identified by Camacho-Escobar (2008) in Mexican turkey.

All the domestic ducks encountered in the study area were found to be Muscovy ducks (Carina moschata), which are known by their fleshy red outgrowths found around the eyes and beaks as described by Yakubu (2013). Muscovy ducks are characterized by black and white or Sepia coloured feathers. We noted all the ducks had white skin colour with one exception having pink skin colour. The shank colour in ducks showed the most variation with six different colours. Some of these variations in shank colour that have previously been reported are grey with yellow markings, plain grey and yellow as described by Banerjee et al (2013).

Pink was the predominant colour noted for the shank and skin colour of pigeons.87% had pink skin colour and 94% pink shank colour. The pigeons were feral and had a wide range of feather colours including white, grey, brown and black. Other than one Rock Pigeon, the pigeons could not be classified into exact breeds as the exhibited a mixture of characteristics due to cross breeding. This phenotypic diversity could also indicate genetic diversity which can be attributed to mating between the different breeds. A number of pigeon and dove species are found in Kenya including the Rock Pigeon (Columba livia),the Speckled Pigeon (Columba guinea), the Lemon dove (Columba larvata) , the Rameron/Olive Pigeon (Columba arquatrix) , the Delegorgues Pigeon (Columba delegorguei)) among others (Zimmerman et al 1999).

Shank length and body weight

Table 2 represents the measurements of body traits taken in Siaya, Bungoma and Busia counties.

Table 2. Interaction between body weight and shank length of the four poultry groups.

Trait

Sex

Mean (Std. dev.)

P

Duck

Body weight (kg)

Female N=23

1.97 (0.40)

1.27e-11 ***

Male N=22

3.38 (0.61)

Shank length (cm)

Female N=23

7.02 (0.46)

9.89e-10 ***

Male N=22

8.42 (0.72)

 

Geese

Body weight (kg)

Female N=12

3.27 (0.46)

0.0293 *

Male N=12

3.73 (0.49)

Shank length (cm)

Female N=12

10.16 (0.61)

0.0517

Male N=12

10.78 (0.83)

 

Turkey

Body weight (kg)

Female N=9

3.39 (0.89)

4.55e-05 ***

Male N=9

7.20 (1.86)

Shank length (cm)

Female N=9

13.5 (0.72)

3.18e-08 ***

Male N=9

16.94 (0.72)

 

Pigeons

Body weight (kg)

Female N=23

0.26 (0.04)

0.0391 *

Male N=23

0.85 (0.03)

Shank length (cm)

Female N=23

3.51 (0.29)

0.0337 *

Male N=23

3.70 (0.29)

* Significant at 0.05,   **Significant at 0.01 and   *** Significant at 0.001.
All the surveyed birds were adults over 12 months old.

We observed that mean body weight measurements (kg) were significantly higher in males than in females (p≥0.05) for all groups of poultry studied, with the largest difference between male and female body weight recorded in turkey. This provides evidence of sexual dimorphism, observations that are in agreement with Olver (1977). The average body weight of Muscovy ducks observed was higher compared to that observed by Banerjee et al (2013)and Omojola (2007), but lower than those reported by Yakubu( 2013).The average body weight of the geese as assessed in the study is within the range reported by Sahin and Yardimci (2009).We also noted that males had longer mean shank lengths in all the four poultry species as compared to female shank length. Sex and body weight had significant interaction as shown in p values in the four types of poultry sampled with the highest interaction seen in turkeys.


Conclusion

Challenges
Recommendations
Opportunities available


Acknowledgements

We would like to thank the Directorate of Veterinary Services under the Ministry of Agriculture, Livestock and Fisheries for supporting this research. We also appreciate the co-operation extended to us by the local extension officers and the farmers that facilitated data collection. This research was funded through a research grant JKU/2/4/RP/181 awarded to Dr. Sheila Ommeh by Jomo Kenyatta University of Agriculture and Technology.


References

Adeola A C, Ommeh S C, Murphy R W, Wu S H, Peng M S and Zhang Y P 2015 Mitochondrial DNA variation of Nigerian domestic helmeted guinea fowl. Animal Genetics 46(5):576–579.

Adzitey F and Adzitey S 2011 Duck production: Has a potential to reduce poverty among rural households in Asian communities-a review. Journal of World’s Poultry Research, 1(1), 7–10.

Albarella Umberto 2005 Alternate fortunes? The role of domestic ducks and geese from from Roman to Medieval times in Britain. Documenta Archaeobiologiae III. Feathers, Grit and Symbolism (ed. by G.Grupe & J.Peters), Pgs 249-58

Aswani P B, Lichoti J K, Masanga J, Oyier P A, Maina S G, Makanda M, Moraa G K, Alakonya A E, Ngeiywa K J and Ommeh S C 2017 Characterisation of the phenotypes associated with body growth and egg production in local chickens from three agro-climatic zones of Kenya. Livestock Research for Rural Development. Volume 29, Article #032. Retrieved on 1st February, 2017 from http://www.lrrd.org/lrrd29/2/aswa29032.html

Banerjee S 2013 Morphological traits of duck and geese breeds of West Bengal, India. Animal Genetic Resources/Ressources Génétiques animales/Recursos Genéticos Animales, 52(2), 1–16.

Bennun L, Dranzoa C and Pomeroy D 1996 The Forest Birds of Kenya and Uganda, 85(1), 23–48.

Bhowmik N, Mia M M and Rahman M A 2014 Morphometric Measurements, Productive And Reproductive Performance Of Jalali Pigeon. International Journal of Development Research Vol 4, Issue 4, 908-911.

Buckland R and Guy G 2002 Goose Production FAO Animal Production and Health Paper 154. Retrieved on 9 th February 2017, from ftp://ftp.fao.org/docrep/fao /005/y4359e/Y4359e01.pdf

Camacho-Escobar M A, Hernandez-Sanchez V, Ramirez-Cancino L, Sánchez-Bernal E I and Arroyo-Ledezma J 2008 Characterization of backyard guajolotes ( Meleagris gallopavo gallopavo ) in tropical zones of Mexico. Livestock Research for Rural Development. Volume 20, Article #50. Retrieved November 19, 2008, from http://www.cipav.org.co/lrrd/lrrd20/4/cama20050.htm

Conan A, Goutard F L, Sorn S and Vong S 2012 Biosecurity measures for backyard poultry in developing countries: a systematic review. BMC Veterinary Research Volume 8, Issue1, Pg 240.

Djebbi A, M’hamdi N and Chriki A 2014 Phenotypic Characterization Of The Indigenous Turkey ( Meleagris Gallopavo ) In The North West Regions of Tunisia. ScientiaAgriculturae, (April 2014). Retrieved on 9th January 2017 from http://doi.org/10.15192/PSCP.SA.2014

FAO 2008 Poultry Sector Country Review Kenya. FAO Animal Production and Health Livestock Country Reviews. Retrieved 11th March, 2016 from ftp://ftp.fao.org/docrep/fao/011/ai319e/ai319e00.pdf

FAO 2012 Phenotypic characterization of animal genetic resources. http://www.fao.org/docrep/015/i2686e/i2686e00.htm

Government of Kenya 2010 Agricultural Sector Development Strategy 2010-2020.

Guèye E F 2000 Women and family poultry production in rural Africa. Development in Practice Volume 10, 2000 - Issue 1

Guèye E F 2005 Gender aspects in family poultry management systems in developing countries. World’s Poultry Science Journal, 61(1), 39–46.

Hale M L, Burg T M and Steeves T E 2012 Sampling for Microsatellite-Based Population Genetic Studies: 25 to 30 Individuals per Population Is Enough to Accurately Estimate Allele Frequencies. PLoS ONE Volume 7, Issue 9.

Moraa G K, Oyier P A, Maina S G, Makanda M, Ndiema E K, Alakonya A E, Lichoti J and Ommeh S C 2015 Assessment of phenotypic traits relevant for adaptation to hot environments in indigenous chickens from four agro-climatic zones of Kenya. Livestock Research for Rural Development. Volume 27, Article #200. http://www.lrrd.org/lrrd27/10/omme27200.html

Ogada S, Lichoti J, Oyier P A, Imboma T, Peng M S, Ngeiywa K J and Ommeh S C 2016 A survey on disease prevalence, ectoparasite infestation and chick mortality in poultry populations of Kenya.Livestock Research for Rural Development. Volume 28, Article #230. Retrieved January 19, 2017, from http://www.lrrd.org/lrrd28/12/omme28230.html

Olver P J 1977 Evolution equations possessing infinitely many symmetries. Journal of Mathematical Physics, 18(6), 1212.

Ommeh S, Jin L N, Eding H, Muchadeyi F C, Sulandari S, Zein M S A, Danbaro G, Wani C E, Zhao S G, Nie Q H, Zhang X Q, Ndila M, Preisinger R, Chen G H, Yousif I A, Heo K N, Oh S J, Tapio M, Masiga D, Hanotte O, Jianlin H and Weigend S 2010 Geographic and Breed Distribution Patterns of an A/G Polymorphism Present in the Mx Gene Suggests Balanced Selection in Village Chickens. International Journal of Poultry Science 9 (1)

Omojola A 2007 Carcass and Organoleptic Characteristics of Duck Meat as Influenced by Breed and Sex. Journal, International Science, Poultry, (November). Retrieved on 10th November 2016, from http://doi.org/10.3923/ijps.2007.329.334

Panyako P M, Imboma T, Kariuki D W, Makanda M, Oyier P A, Malaki P, Ndiema E K, Obanda V, Agwanda B, Ngeiywa K J, Lichoti J and Ommeh S C 2016 Phenotypic characterization of domesticated and wild helmeted Guinea fowl of Kenya. Livestock Research for Rural Development Volume 28, Issue 9. Retrieved on 1st November 2016 http://lrrd.cipav.org.co/lrrd28/9/omme28158.html

Pym R, Bleich E G and Hoffmann I 2006 The relative contribution of indigenous chicken breeds to poultry meat and egg production and consumption in the developing countries of Africa and Asia. … of the XII European Poultry …. Retrieved on 12th November 2016 http://www.cabi.org/animalscience/uploads/file/animalscience/additionalfiles/wpsaverona/10222.pdf

Sahin E H and Yardimci M 2009 Effects of Kefir as a Probiotic on Growth Performance and Carcass Characteristics in Geese (Anser anser). Journal of Animal and Veterinary Advances. Volume 5 No.2, Pages 207-212.

Spradbrow P 2005 Appropriate vaccination and therapies for rural poultry flocks in developing countries and their relevance to developed countries. World’s Poultry Science Journal, 61(1), 47–54.

Yakubu A 2013 Characterisation of the local Muscovy duck in Nigeria and its potential for egg and meat production. World’s Poultry Science Journal, 69(4), 931–938.

Zimmerman D, Turner D and Pearson D 1999 Birds of Kenya & Northern Tanzania. Christopher Helm, London Pgs 286-362


Received 26 January 2017; Accepted 20 March 2017; Published 1 May 2017

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