Professional Documents
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Village Chicken Production Systems in Me
Village Chicken Production Systems in Me
Vol. 2(9), pp. 256 - 262, September 2013 2013 Wudpecker Journals
A cross-sectional survey was conducted in Metekel zone, Northwest of Ethiopia to assess village
chicken production systems, productive and reproductive performance of village chicken and
identifying constraints to village chicken production. Stratified random sampling technique was
used to select 160 farming households and administer a pre-tested and structured questionnaire.
The average flock size per household was 13.68±0.62. Only 48% of chicken owners prepared a
separate overnight houses/shelters for birds. The average age of indigenous pullets and cockerels
at first mating was 5.2±1.16 and 5.44±1.3 months, respectively. The total number of
clutches/hen/year was 4.29±0.17 with an average of 13.56±0.26 eggs/clutch. The average egg
hatchability was 84.74%. Seasonal disease outbreaks, mainly Newcastle disease, and predation
were the major causes of chicken loss in the districts. Household division of labor engages women
more on various chicken husbandry activities. Respondents prioritized lack of credit service, limited
skill of management practices and low productivity of the local chicken as major constraints to
chicken production. Thus, technical and institutional interventions are very crucial to alleviate the
prevailing constraints and transform the existing traditional/subsistence chicken production system
to semi-commercial production system in the study area.
INTRODUCTION
In most developing countries rural poultry play disease, thermo-tolerance, good egg and meat flavor,
significant roles of improving the nutritional status, hard eggshells, high fertility and hatchability (Aberra,
income, food security and livelihood of many 2000).
smallholders (Abubaker et al., 2007; Alders and Pym, According to Besbes (2009) and Hunduma et al.
2009). In Ethiopia, village chickens are an integral (2010), changing production systems and
component of the farming system of nearly all rural indiscriminate cross-breeding are the major treats to
families, and they account for about 99% of the poultry indigenous breeds. Recently, efforts are being made to
production system (Tadelle et al., 2003) and for more increase the productivity of indigenous chickens of
than 90% of the chicken and egg output of the country Ethiopia through selective breeding (Nigussie et al.,
(Nigussie et al., 2010). 2010). According to Solkner et al. (1998), success of
Village chicken production fits quite well with the such breeding programs on village chicken requires
conditions of rural households due small feed cost, defining the production environment and identifying
space requirement and low price of the animals breeding practices, production objectives and trait of
(Solomon, 2003). In addition, the local chicken sector choice of rural farmers. Moreover, to design appropriate
constitutes a significant contribution to human livelihood development intervention programs on village chicken
by being affordable sources of animal protein and production, characterization of the production system
contributes significantly to food security of poor and understanding the socio-economic implications are
households (Reta, 2009). crucial (Gueye, 1998; Pedersen, 2002).
Despite its importance, village chicken production Due to poor agricultural extension service, however,
system in Ethiopia is generally characterized by poor there is no documented information pertaining to the
performance of local chicken in terms of egg resource base, productivity and management of the
production, small egg size, slow growth rate, late chickens and the constraints in the study area. The
maturity, an instinctive inclination to broodiness and objective of the study was to assess production system,
high mortality of chicks (Teketel, 1986; Aberra, 2000; productive and reproductive performance of village
Nigussie et al., 2003; Solomon, 2003). On the other chickens and to identify production constraints in
hand, local chickens are known for their ability to resist Metekel zone.
257 Wudpecker J. Agric. Res.
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Zewdu et al. 258
Figure 1. Decision making, ownership and division of labor on village chicken husbandry in Metekel Zone, Ethiopia.
Table 1. Chicken flock structure by district and flock size (Mean±SE) per household in four districts of Metekel
zone, Ethiopia.
District
Chicken age group Grand mean
Pawe Dibate Wombera Guba
Chicks 0-8 weeks of age 6.68±0.94 6.17±0.58 3.6±0.65 4.05±0.77 5.12±0.38
Pullets 8-20 weeks of age 3.3±0.37 2.4±0.18 2.23±0.35 2.95±0.32 2.72±0.16
Cockerel 8-20 weeks of age 2.18±0.3 1.52±0.11 1.88±0.23 1±0.19 1.64±0.11
Layers > 20 weeks of age 3.28±0.44 2.12±0.19 1.92±0.18 2.85±0.31 2.54±0.15
Cocks >20 weeks of age 1.78±0.35 1.65±0.41 2.13±0.67 1.03±0.26 1.64±0.23
a ab b b
Total fock size 17.2±1.46 13.88±0.91 11.75±1.25 11.88±1.12 13.68±0.62
Means with different superscripts within a row are significantly different (P < 0.05).
Table 2. Feed resources and feeding practice of chickens in four districts of Metekel zone, Ethiopia.
District Total
Variables
Pawe Dibate Wombera Gublack Percent
Practice of supplementation (yes) 97.5 80 97.5 94.9 92.5
Feeds used for supplementation
Maize grain 77.5 55 77.5 47.5 64.4
Sorghum grain 72.5 42.5 62.5 95 68.1
Rice (paddy rice) 27.5 0 0 0 6.9
Broken maize, sorghum and rice grains 20 12.5 42.5 10 21.3
Spoiled grains 10 20 40 10 20
Food left over 57.5 52.5 50 35 48.8
Kitchen left over 7.5 0 57.5 10 18.8
Change due to supplementation (yes) 87.2 58.8 92.3 97.5 84.9
Season for shortage of grain supplements
Rainy season (May-October) 87.5 100 100 82.5 92.5
Dry season (November-May) 12.5 0 0 17.5 7.5
strategically administered supplements are likely to trying to improve the genetic potential of local chicken
increase production and minimize mortality once the through selection based on egg production history
other constraints have been tackled. (59.4%), body weight (44.3%) and feather colour
Results revealed that 92.5% of the households (25.5%). Selection were made on males (55.2%),
provide water for their chickens' regularly. Water females (20%) and both male and females (24.8%).
sources used by the households in the study area were Nigussie et al. (2010) reported that beside other
river (30.5%), spring (20.8%), tap water (19.5%), well quantitative traits, morphologic traits such as plumage
water (12.3%) and in different combinations of these color and comb type have significant economic values.
sources (16.9%). In addition to selection, 37.1% households were
upgrading the genetic potential of the local chicken
through crossbreeding with exotic breeds. Exotic
Housing breeds used for crossbreeding include Rhode Island
Red (RIR) (82.5%), White Leghorn (WL) (5.3%) and
Only 48% of the respondents constructed separate both RIR and WL (12.3%). The farmers had these
houses for their birds; the other 52% kept in various exotic birds mainly from Woreda agricultural office as
overnight sheltering places. Results also showed that poultry extension packages to improve the productivity
houses/night shelters were made using locally available of local chickens.
materials such as bamboo for making ceilings (86.7%),
mud blocks and hat (11.1%), a house made of iron
sheet roof (1.5%) and basket made of bamboo (0.7%). Performance of village chickens
The sites are secure overnight places to protect from
predators. According to Bell and Abdou (1995), large Production performance
proportion of village poultry in most African countries is
lost due to nocturnal predators. The average age of indigenous pullets and cockerels at
first mating was 5.2±1.16 and 5.44±1.3 months
respectively (Table 3). These findings are comparable
Breeding with the 5 and 7 months reported by Halima (2007) and
Moges et al. (2010) for indigenous birds in Northwest
Results revealed that 63.1% of the respondents were Ethiopia. The female chicken is generally reported to
Zewdu et al. 260
Table 3. Production performance of local chickens in four districts of Metekel zone, Ethiopia.
District Grand
Variables
Pawe Dibate Wombera Guba mean
st abc b abc c
Average age of cockerels at 1 mating (months) 5.41±1.53 5.83±1.37 5.51±1.14 4.92±0.90 5.44±1.30
st a a a a
Average age of local pullets at 1 mating (months) 5.22±1.18 5.26±1.10 5.42±1.26 4.9±1.09 5.2±1.16
a ab ab b
Average number of eggs/hen/ clutch 14.72±0.64 13.98±0.59 13.46±0.42 12.15±0.37 13.56±0.26
a b b b
Number of clutches/hen/ year 6.11±0.49 4.00±0.29 3.38±0.18 3.79±0.12 4.29±0.17
a b b b
Total egg production/hen/ year 93.19±6.79 56.03±4.74 45.38±2.79 46.10±2.03 59.51±2.66
a a a a
Weaning age (weeks) 7.49±0.56 9.55±0.77 9.00±1.26 8.03±0.48 8.51±0.40
a a a a
Reproductive life span of hens (year) 3.82±0.38 3.49±0.27 3.41±0.24 3.53±0.20 3.56±0.14
a a a a
Reproductive life span of male chicken (year) 4.53±0.43 3.92±0.26 3.18±0.15 3.51±0.22 3.79±0.15
a,b,c
Least square means with different superscripts within a raw are significantly different (P < 0.05)
Table 4. Hatchability and brooding performance of indigenous hens (using medium and large size broody hens), in four districts
of Metekel Zone, Ethiopia.
District
Variables Total
Pawe Dibate Wombera Guba
Choice of broody hen size
Large body size 84.8 90.5 87.5 85.7 87
Medium body size 15.2 9.5 12.5 14.3 13
Source of egg for brooding
Home laid 80 90 92.3 100 90.6
Hatchability by medium body size broody hen
Number of eggs set 12.73±0.36 11.65±0.39 12.86±0.45 10.30±0.34 11.8±3.21
Hatchability % 82.38 79.04 76.68 74.76 78.62
Hatchability by large body size broody hen
Number of eggs set 15.21±0.37 14.88±0.40 16.91±0.47 12.40±0.47 14.74±0.25
Hatchability % 89.1 82.81 80.91 84.41 84.74
mature late with values ranging from 6 months in Mali 22) with hatchability percentage of 82.6 and 89.1 at
and Nigeria (Sonaiya, 1989), 7 months in Tanzania Bure and Dale districts of Ethiopia, respectively.
(Katule, 1992), 8 months in Sudan (Wilson, 1979), and Results revealed that 82.5, 47.5, 38.5 and 12.5%
7 to 9 months in Benin (Assan, 1990). village chicken owners in Pawe, Dibate, Wombera and
The average egg production per hen per clutch of Guba, respectively, have a culture of selecting broody
local hens, under existing farmer management hens for egg incubation purposes. Overall, 87 and 13%
condition, was 13.56±0.26 (range 12.15-14.72). The of the respondents used large and medium body size
number of clutch periods recorded per year was as a selection criterion for broody hens. Similarly, a
4.29±0.17 (range 3.38-6.11) giving a total of 59.51±2.66 study by Moges et al. (2010) showed that 66.7% of the
(range 45.38-93.19) per hen per year (Table 3). The respondents use large body size as a selection criterion
number of eggs per clutch found in the current study for broody hens in Fogera district of Ethiopia.
falls within the range (9–19 eggs/clutch) reported by
Halima (2007) in Northwest Ethiopia. Moges et al.
(2010) also reported similar values, 15.7, 13.2 and Constraints on village chicken production
14.9eggs/hen/clutch and total egg production/hen/year
of 60, 53 and 55, in Bure, Fogera and Dale districts of Diseases, mainly Newcastle, and predation were the
Ethiopia, respectively. major constraints in all areas surveyed. Other
constraints included the lack of technical information,
capital and credit services to expand production
Reproductive performance through improved feeding, and housing. Both incidence
of chicken disease and predator attack were found to
Data on hatchability and brooding performance of be higher in the wet season (May to November) than in
indigenous hens are presented in Table 4. Over all, in the dry season (October to April). Newcastle disease
the four districts, the average number of eggs set per (Serkalem et al. 2005) and predator attack (Halima,
hen was 14.74±0.25 (range 12.40-16.91) with a 2007) have also been reported as a major constraints
hatchability of 84.7%. The average number of eggs set to chicken production in central and Northwest Ethiopia.
for natural incubation and hatchability percentage in Moreover, due to low productivity of village chickens,
this study are in agreement with the report of Moges et 98.1% of the farmers indicated their interest towards
al. (2010). These authors reported 13 eggs (ranged 7– having exotic breeds. Although 37.5 % households
261 Wudpecker J. Agric. Res.
crossbred the locals with exotic breeds, due to poor chicken production: Effects of gender on ownership,
management practices in terms of feeding, housing and and management responsibilities in some parts of
health provision, the farmers didn’t achieve sustainable Nigeria and Cameroon. Int. J. poultry Sci., 6(6):413-
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the cross-breeds. A study by Kitalyi (1998) also Alders RG, Pym RAE (2009). Village poultry: still
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Bell JG, Abdou I (1995). Dynamics of village poultry
The results of the present study show that village production in the Keita region of Niger. Nig. J. Anim.
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cultural or religious ceremonies. As in the other parts of EEA (Ethiopia Economic Association) (2002). Land
the country, the productivity of village chicken in the tenure and agricultural development in Ethiopia.
study area is generally low. Newcastle disease followed Ethiopia Economic Policy Research Institute, Addis
by predator attack was the major constraints to chicken Ababa.
production in the study area. Other constraints included Engda M (2000). Agro-climatic classification of
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Acknowledgments Gunaratne SP, Chandrasiri ADN, Mangalika Hemalatha
WAP, Roberts JA (1993). Feed resource base for
We thank district’s agriculture office experts and key scavenging village chickens in Sri Lanka. Trop. Anim.
informants of the community in the study area for Health and Prod., 25:249-257.
understanding and passing the purpose of the project Halima H (2007). Phenotypic and genetic
to the subordinates down to livestock farmers to the characterization of indigenous chicken populations in
Kebele level. We are also grateful to the interviewed North-West Ethiopia. PhD thesis. Faculty of natural
farmers for their active participation in sharing their and agricultural sciences, department of animal,
knowledge and time. wildlife and grassland Sciences. University of the
Free State, Bloemfontein, South Africa.
Hunduma D, Regassa C, Fufa D, Endalew B, Samson
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