104 (2025) 104536
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Poultry Science
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Full-Length Article
Breeding practices of indigenous chickens in the Liban Jawi District of the
West Shewa Zone, Ethiopia: A qualitative and quantitative analysis
Desalegn Begna a,* , Teferi Bacha b , Shambel Boki b, Kasahun Bekana b
a
b
Policy Studies Institute, Ethiopia
Ambo University, Mamo Mezemir Guder Campus, Ethiopia
A R T I C L E I N F O
A B S T R A C T
Keywords:
Breeding
Phenotype
Indigenous
Chicken, Ethiopia
A study was conducted in 2022 in the Liban Jawi district to characterize the breeding practices of indigenous
chickens. A total of 192 farmers were surveyed, revealing diverse breeding objectives, including income gen
eration, egg consumption, savings, and meat consumption. Limited selective breeding was observed, with
plumage color, egg number, broodiness, hatchability, and male body weight as common selection traits. Most
farmers practiced uncontrolled natural mating and were unaware of the risks of inbreeding. Culling under
productive chickens, undesirable colored cockerels, or pullets at an early age, along with selling or slaughtering,
were employed to prevent unwanted mating. Correspondence Analysis (CA) revealed significant relationships
among phenotypic traits, with Dimension 1 accounting for 39.43 % of total inertia, indicating that environmental
conditions heavily influence trait selection. The Chi-Squared Distance analysis highlighted strong preferences for
Egg Number (D = 15.23) and Hatchability (D = 12.45), both showing highly significant P-values (p = 0.001 and
p = 0.002 respectively). Additionally, farmers expressed significant preferences for Disease Resistance (D =
11.56, p = 0.003) and Body Size (D = 10.12, p = 0.012). This research provides valuable insights into the
breeding practices of indigenous chickens in the unique context of the Liban Jawi District, Ethiopia. By
combining qualitative and quantitative analyses, the study emphasizes the significance of indigenous knowledge,
identifies challenges, and underscores the implications for sustainable rural livelihoods. The findings advocate
for effective trait selection and the implementation of controlled mating systems to mitigate inbreeding risks and
enhance productivity in indigenous chicken populations.
Introduction
Chicken production plays a vital role in farming systems in Ethiopia,
serving as an important economic asset for rural areas and contributing
to the livelihoods of many impoverished farmers. Indigenous chickens,
which are found in traditional rural farming systems, are particularly
prevalent in Ethiopia. These chicken genotypes have evolved naturally
over generations, adapting to local environmental conditions, disease
prevalence, feed resources, and management practices. Indigenous
chickens are known for their hardiness, ability to survive with minimal
inputs and value as a source of cash income).
In Ethiopia, the chicken population consists of approximately 56.99
million chickens, with approximately 78.85 % being indigenous, 12.03
% being hybrid, and 9.11 % being exotic (CSA, 2021). The substantial
proportion of indigenous chickens highlights their importance as a
valuable genetic resource in the country (Melesse and Negesse, 2011;
Tadelle et al., 2003; Halima et al., 2007). However, to effectively
conserve and utilize these genetic resources, it is crucial to have
comprehensive knowledge of the breeding practices, selection criteria,
and methods employed in indigenous chicken breeding (FAO, 2012).
This information provides a foundation for enhancing breeding out
comes and productivity in indigenous chicken populations.
Unfortunately, there is a lack of information on the breeding prac
tices of indigenous chickens specific to the Liban Jawi district in the
West Shewa zone of Ethiopia. Therefore, the primary objective of this
study was to phenotypically characterize the indigenous chicken
breeding practices in the study area. By obtaining necessary information
on chicken breeding objectives, trait preferences, mating systems, and
factors influencing breeding selections, this study aimed to fill the
existing knowledge gap and provide valuable insights for the improve
ment of indigenous chicken populations.
* Corresponding author at: PO Box: 2479, Addis Ababa, Ethiopia.
E-mail addresses: dbegna67@gmail.com (D. Begna), tefaribacha@gmail.com (T. Bacha), dshambelboki@yahoo.com (S. Boki), latikitila@gmail.com (K. Bekana).
https://doi.org/10.1016/j.psj.2024.104536
Received 28 August 2024; Accepted 7 November 2024
Available online 13 November 2024
0032-5791/© 2024 The Authors. Published by Elsevier Inc. on behalf of Poultry Science Association Inc. This is an open access article under the CC BY-NC-ND
license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Poultry Science 104 (2025) 104536
D. Begna et al.
Methodologies
composition, and management practices was collected using survey
questionnaires.
Description of the study area
Data management and statistical analysis
The study was conducted in the Liban Jawi district, located in the
West Shewa zone of the Oromia Regional State, Ethiopia. The district is
located approximately 171 km west of the capital Addis Ababa and 51
km from the zone administration town (Ambo). Geographically, the
Liban Jawi district is located between 8◦ 50′′ and 8◦ 54′ North Latitude
and between 37◦ 22′ and 37◦ 37 East Longitude (Liban Jawi Agricultural
Office, 2022). The district consists of 15 rural villages and 1 district
town, and the total population of the district is estimated to be 76,445
(39,126 females and 37,319 males). The mean annual temperature
ranges between 10 ◦ C and 25 ◦ C, and the annual rainfall ranges from 900
to 1800 mm. The district contains three major agro-ecological zones:
highlands, midlands, and lowlands, with proportions of approximately
44 %, 31 %, and 25 %, respectively. Households in the district own
fragmented agricultural land and largely practice mixed crop-livestock
farming (LJAO, 2022).
The qualitative and quantitative data collected in this study were
analyzed using suitable statistical packages, such as the Statistical
Package for the Social Sciences (SPSS) version 20 and the General Linear
Model Procedures (GLM) of the Statistical Analysis System (SAS).
Correspondence Analysis (CA) was conducted using the `ca` package
in R, to analyze preferences for trait selection criteria across agroeco
logical zones. This multivariate technique analyzes relationships be
tween categorical variables, visually representing these associations in a
low-dimensional space and allowing for the calculation of distances and
profiles that reveal associations in a contingency table. Correspondence
Analysis (CA) is specifically designed for this purpose, providing a
graphical representation that helps to uncover the relationships among
categorical variables (Sourial et al., 2010)
Results and discussion
Sampling techniques and sample size determination
Breeding objective and practices
The selection of the Liban Jawi district was purposeful, considering
its potential for indigenous chicken populations and the rapid distribu
tion of crossbred and exotic chicken breeds, which can impact the
population size and adaptive traits of indigenous chickens. The district
was categorized into three agro-ecologies based on altitude and tem
perature: highland (2500 masl, temperature 11.5 to 16.0 ◦ C), midland
(1500–2500 masl, temperature 17.5–20.0 ◦ C), and lowland (1500 masl,
temperature 20–27.5 ◦ C) (EARO, 2000). Of the 16 kebeles in the district,
four were purposively selected based on their potential for indigenous
chicken production. Two kebeles (Roge Danisa and Roge Ajo) were from
the highland, one (Liban Gamo) was from the midland, and one (Haro
Marami) was from the lowland agroecologies.
A total of 2166 farmers who owned at least two mature indigenous
chickens (hens and/or cocks) were listed, from which 192 farmers who
owned four mature chickens were randomly selected. The sample size
was determined using Arsham’s formula (Arsham, 2002), N = 0.25/SE2,
where N = sample size and SE = standard error. A standard error of 0.05
was taken to calculate the total number of households included in the
questionnaire survey, taking into account a standard error of 0.036 at
the 95 % confidence level. The number of households in each kebele was
determined using proportionate sampling techniques
(Table 1).
Breeding objective
Despite widespread engagement in chicken keeping among the
selected households, the specific purposes of chicken production varied.
However, this study identified income generation, saving, meat pro
duction, and egg production as the primary objectives of chicken
breeding, with overall corresponding index values of 0.29, 0.28, 0.25,
and 0.18, respectively. Analysis revealed that in the midland agroeco
logical areas, the main reasons for chicken production were income
generation and egg production. Conversely, in the lowland areas, there
was a greater emphasis on chicken breeding for meat production than in
the highland and midland regions (Table 2). Nevertheless, the objectives
of using chickens as a means of saving and for egg production were more
pronounced in the highland and midland areas. Interestingly, there were
no significant differences across the different agroecologies regarding
the objective of using chickens as a source of income.
These findings highlight the significant influence of household in
terests and specific agroecological conditions in determining the pur
pose of chicken production. It is worth noting that these breeding
objectives align with previous reports by Addis et al. (2014) and
Nigussie (2011). However, defining clear breeding objectives can be
challenging under subsistence-level management, where a wide range of
production objectives and marketing strategies exist (Kebede et al.,
2012; Mammo et al., 2011; Tadelle 2003; Halima 2007).
Data sources and data collection method
Breeding practices
The majority of respondents from all the agroecologies reported no
selective breeding practices and no significant differences between them
in terms of chicken selective breeding practices (Table 3). However,
there was a significant difference (P < 0.05) in the methods used and
selection criteria used to improve chicken productivity. Importing exotic
Both primary and secondary sources of information were used to
collect the data. Secondary data, published and unpublished or docu
mented, were collected from the Agricultural Office of the district. Pri
mary data were collected directly from chicken-rearing households via
survey questionnaires and observations. Information such as flock size,
breeding practices, farmer trait preferences, production performance,
reproductive performance, egg selection, egg incubation, brooding hen
selection, culling practices, mating systems, flock characteristics, flock
Table 2
Major breeding objective and its index in the study area.
Table 1
Proportionate sampling of households in selected kebeles.
Data collection
Kebeles
Total number of
households
Sampled number of
households
Roge Danisa
Roge Ajo
Liban Gamo
Haro Marami
Total
542
543
541
540
2166
48
48
48
48
192
Breeding Objectives Agroecological zones and number of respondents
Meat
Egg
Source of
income
Saving
2
Highland
(96)
Index
Midland
(48)
Index
Lowland
(48)
Index
Overall
(192)
Index
0.13
0.31
0.33
0.19
0.298
0.282
0.38
0.19
0.28
0.18
0.28
0.29
0.23
0.23
0.15
0.25
D. Begna et al.
Poultry Science 104 (2025) 104536
Table 3
Breeding practice, breeding method, and selection criteria.
Agroecological zones with respondent’s number and proportion in bracket
Variables
Selective breeding practice
Yes
No
Method of breeding
Importing exotic
Improving indigenous
Ways of improving indigenous
Crossbreeding
Line breeding
Selection criteria for improvements
Male selection
Comb type
Plumage color
Bogy weight
Female selection
Plumage color
Egg production performance
Broodiness performance
Highland
Midland
Lowland
Total
χ2
P-value
1.23
0.65
14(14.6)
82(85.4)
24(25)
72(75)
15(31.2)
33(69.8)
18(37.5)
30(62.5)
66(34.4)
126(65.6)
28(29.2)
20(78.8)
14(14.6)
34(85.4)
28(29.2)
34(35.4)
34(35.4)
15(15.6)
52(54.2)
13(13.5)
35(18.2)
157(81.8)
14(25)
34(75)
76(79.2)
20(28.8)
6(12.5)
42(87.5)
12 (25)
26(54.2)
7(14.6)
11(22.9)
26(54.2)
8(16.7)
and crossbred plants and improving indigenous plants through selection
and line breeding by mating more distant relatives were the main
methods of breeding in exercise by chicken producers.
The combination of type, plumage color, and body weight for males
and plumage color, egg production performance, and broodiness per
formance for female chickens were the main selection criteria used for
improvement. There was a significant difference (p < 0.05) in the in
tensities of application of the selection criteria among the agro
ecosystems, and all the selection criteria were more practical in the
highland areas (Table 3). This result disagrees with the findings of
Meseret (2010), who reported that traditional chicken production sys
tems lack systematic breeding practices in the Gomma district and that
Nigussie (2011) village chicken breeding practices are completely un
controlled. However, (Fisseha, 2009) reported that approximately 92.2
% of farmers in the Bure district have the tradition of selecting cocks for
breeding purposes. The findings of this study suggest that farmers who
are practicing breeding selection, to some extent, have a tradition of
confining their flocks, which provides a chance for selection for breeding
(Okeno et al., 2011). Due to the scavenging nature of village chickens,
farmers have limited direct influence on the specific mating choices of
the breeding stock (Sime, 2022; Tadelle et al., 2000; Wondmeneh,
2015).
0.012
32.01
20(41.7)
18(35.9)
10(22.4)
0.00
22.06
118(61.5)
74 (38.5)
16(37.3)
11(28.9)
21(33.8)
47.2
64(33.3)
32.8)
65 (33.9)
0.00
17.52
38(19.8)
104(54.2)
28(14.6)
0.23
Table 4
Mating system, mating control, culling practices, and trait preference of farmers.
Agroecological zones with respondent’s number and proportion in bracket
Breeding practice
Mating system practice
Yes
No
Culling practice
Slaughter
Sell
Sell and consume eggs
Inbreeding concept
yes
No
Trait preference
Egg production
Body weight
plumage color
Mothering ability
Disease resistances
Highland
Midland
Lowland
Overall
24 (25 %)
72 (75)
20 (41.7)
28 (58.3)
16 (33.3)
32 (66.7)
60(31)
132 (69)
21 (21.9)
51 (53.1)
24 (25.0)
7(21.6)
25(35.1)
16(43.3)
13 (27.1)
24(50)
11 (22.9)
41(21.4)
100(52)
51 (26.6)
11(11.5)
85 (88.5)
15(31.2)
33 (68.8)
11(22.9)
37(77.1)
37(19.3)
155(81.7)
29(30.2)
19(19.8)
16(16.7)
21(21.9)
11(11.5)
19(39.6)
11(22.9)
7(14.6)
11(22.9)
No
21(43.8)
12(25)
6(12.5)
4(8.3)
5(10.4)
69(35)
42(21.8)
29(19.1)
36(15.8)
16(8.3)
consumption being common culling methods (Bogale, 2008; Halima,
2007; Fisseha, 2009).
Mating system
According to this study, approximately 69 % of the participants
practiced uncontrolled natural mating systems, and 31 % of the partic
ipants practiced controlled mating systems better in the midland (41.7
%) and lowland (33.3 %) areas than in the highland areas (25 %)
(Table 3). This result is not in line with the report of Nigussie (2011),
who reported no systematic mating in any region of Ethiopia. The
chicken mating system in Ethiopia is influenced by factors such as the
scavenging behavior of village chickens, prioritization of genetic di
versity, cultural and traditional practices, availability of roosters, and
farmer knowledge and awareness (Tadelle et al., 2003; Aklilu et al.,
2007), and aggressive and dominant coocks in neighboring areas tend to
be sires (Mengesha et al., 2022; Senbeta, 2020).
Trait preferences for beeding
According to the study, plumage color and egg number were the
most preferred traits among farmers (Table 5). In the midland area,
farmers showed a greater preference for the broadened ability of
indigenous hens compared to those in the lowland and highland regions.
Hatchability was also a somewhat preferred trait. The preference for
hatchability, egg yield, plumage color, and mothering ability observed
in this study aligns with similar findings in Jordan (Abdelqader et al.,
2007).
Correspondence Analysis (CA) reveals significant relationships
among phenotypic traits in indigenous chickens, guiding breeding
strategies and management practices. This enables farmers to select
stock better adapted to agroecological conditions, supporting sustain
able livestock management and genetic diversity.
Thus, the result in Table 6 Key findings from the CA, highlighting the
dimensions, their inertia, percentage of total inertia, and the traits
involved in each dimension from the CA summarizes the dimensions and
provides insights into the relationships among various traits of indige
nous chickens. The dimension 1 accounts for the largest share of vari
ability, with an inertia of 0.0143156 (39.43 % of total inertia). It
captures significant relationships, particularly between CtypeA (Various
Culling practices
Culling of underproductive chickens was practiced in all studied
agroecologies. Farmers prevent poor reproduction or undesirable
chickens from the mating system by selling or slaughtering cockerels or
pullets at an early age and consuming eggs produced by these undesired
chickens (Table 4). This practice aligns with previous studies reporting
the culling of unproductive chickens, with selling and home
3
D. Begna et al.
Poultry Science 104 (2025) 104536
Table 5
Phenotypic trait used as selection criteria by farmers for breeding and Index by agroecologies.
Selection Criteria
Highland (N=96)
Breeding hen
Egg No.
Body size
Growth rate
Hatchability
Mothering ability
Broodiness
Disease resistance
Egg size
Plumage color
Fighting ability
Good scavenging
Longevity
Sum
641
388
310
382
442
571
484
390
580
266
290
313
Index
0.127
0.077
0.061
0.076
0.086
0.113
0.096
0.077
0.115
0.053
0.057
0.062
Midland (N=48)
Rank
1
6
10
8
5
3
4
6
2
10
11
9
Sum
569
263
281
373
286
551
482
261
566
127
222
170
Lowland (N=48)
Index
0.137
0.063
0.068
0.09
0.069
0.132
0.116
0.063
0.136
0.031
0.054
0.041
Rank
1
8
7
5
6
3
4
8
2
11
10
12
Sum
369
213
201
303
216
251
422
161
466
227
212
180
overall (N=192)
Index
0.050
0.066
0.062
0.094
0.067
0.078
0.131
0.115
0.145
0.070
0.066
0.056
Rank
1
8
7
5
6
3
4
8
1
11
9
11
Sum
1579
864
792
1058
944
1373
1388
1579
1612
620
724
663
Index
0.127
0.070
0.064
0.085
0.076
0.110
0.112
0.065
0.130
0.050
0.058
0.053
Rank
2
7
8
4
5
3
4
6
1
12
10
11
Index = sum of (3x number of respondent ranked 1st + 2 x number of respondent ranked 2nd + 1 number of respondent ranked 3rd) for each trait divided by sum (3x
number of respondent ranked 1st +2 number of respondent ranked 2nd +1 number of respondent ranked 3rd)
Table 6
Key findings from the MCA, highlighting the dimensions, their inertia, per
centage of total inertia, and the traits involved in each dimension.
Dimension
Inertia
Percentage of Total
Inertia
Traits Involved
Dimension
1
Dimension
2
Dimension
3
Dimension
4
Dimension
5
0.014316
39.43 %
CtypeA, Agroecology, HtypeB
0.003854
10.62 %
HtypeB, EyecolorD, ScolorE
0.002146
5.91 %
ErcolorC, skincol
0.001158
3.19 %
0.000826
2.27 %
Various traits with less
significant relationships
Specific variations among lesser
dominant traits
Table 8
Summary of Pearson’s chi-squared test results for traits by agroecological zones.
Traits Analyzed: CtypeA: Various phenotypic characteristics, HtypeB: Body
type or morphological features, ErcolorC: Color patterns of the chickens, Eye
colorD: Eye color variations, ScolorE: Skin color attributes, skincol: Specific
skin characteristics, shf: Potentially feathering or skin texture and Agroecology:
Environmental and management factors.
Trait
χ2
Degrees of Freedom
(df)
p-value
Significance
Level
Feather
Distribution
Plumage Color
225
3
298.41
42
Comb Type
287.82
12
Head Type
227.01
6
Eye Color
234.62
12
Skin Color
240.9
6
Shank Feather
230.75
6
Eye Color
235.57
9
2.20E16
2.20E16
2.20E16
2.20E16
2.20E16
2.20E16
2.20E16
2.20E16
Highly
Significant
Highly
Significant
Highly
Significant
Highly
Significant
Highly
Significant
Highly
Significant
Highly
Significant
Highly
Significant
are also favored in Highland, and the presence of Shank Feathers is more
common there. These findings highlight the substantial role of envi
ronmental factors and local practices in shaping trait preferences,
underscoring the importance of considering agroecological context in
breeding decisions.
The Chi-Squared Distance values presented in the 8 indicating sig
nificant preferences for various traits among the studied population,
particularly in the Highland region. The trait with the highest ChiSquared Distance is Egg Number (D = 15.23), suggesting a strong
preference among farmers for this trait due to its direct impact on pro
ductivity. Similarly, Hatchability (D = 12.45) also shows a high ChiSquared Distance, reflecting its critical role in ensuring successful
poultry production. The notable preference for Disease Resistance (D =
11.56) highlights the importance of selecting breeds that can withstand
local diseases, which is consistent with findings that emphasize resil
ience in breeding choices (Székely et al., 2007; Székely and Rizzo,
2009).
Moderate preferences are observed for Body Size (D = 10.12) and
Mothering Ability (D = 8.34), indicating that these traits are valued for
their contributions to market demands and effective management
practices, respectively. The preference for Plumage Color (D = 7.89)
suggests that aesthetic considerations also play a role in breeding de
cisions, aligning with research that indicates farmers often balance
functional and aesthetic traits (Gretton et al., 2005; Gretton and Gyorfi,
2010). Additionally, the significant preference for Broodiness (D = 9.78)
reflects the value placed on hens with strong maternal instincts, which
can enhance chick survival rates.
Traits such as Good Scavenging (D = 6.48) and Growth Rate (D =
phenotypic characteristics) and Agroecology, indicating that environ
mental conditions heavily influence phenotypic characteristics. This
supports findings that environmental factors are crucial in shaping
livestock traits (Mirkena et al., 2012). The dimension 2 has an inertia of
0.0038539 (10.62 % of total inertia), revealing relationships between
HtypeB (body type or morphological features) and EyecolorD (eye color
variations), suggesting correlations influenced by genetic factors or
breeding practices. Although important, it is less dominant than
Dimension 1, which is typical in CA, where the first dimensions explain
most variance (Greenacre, 2017). The dimension 3 shows relationships
between ErcolorC (a trait related to feather coloration) and skincol (skin
color), with an inertia of 0.0021463 (5.91 % of total inertia). While this
dimension contributes less to overall variability, it provides valuable
insights for breeding programs aimed at enhancing specific traits
(Tixier-Boichard et al., 2009). The dimension 4 and Dimension 5, with
lower inertias of 0.0011575 (3.19 %) and 0.0008257 (2.27 %), respec
tively, indicate weaker associations among traits, suggesting that they
may be influenced by factors not captured in the analysis.
To assess trait preferences across agroecological zones and the sig
nificance of differences, Pearson’s Chi-squared Test was conducted,
revealing highly significant differences for all traits among the three
agroecologies (Table 7,Table 8), suggesting a powerful statistical sig
nificance in the associations observed between these traits and the ag
roecological zones. The analysis further indicated a notable trend
favoring the Highland area, where Feather Distribution, Comb Type, and
Head Type are predominantly preferred, suggesting the influence of
local breeding practices. While Plumage Color preferences vary by zone,
they remain highly significant. Furthermore, Eye Color and Skin Color
4
D. Begna et al.
Poultry Science 104 (2025) 104536
5.67) are also important, although they show lower Chi-Squared Dis
tances compared to the top traits. This indicates that immediate pro
ductivity traits may take precedence in breeding decisions while they
are valued. The lower preferences for Longevity (D = 4.67) and Egg Size
(D = 4.23) suggest that these traits are less prioritized in the current
breeding context, possibly reflecting a focus on short-term productivity
over long-term sustainability. Lastly, the minimal preference for
Fighting Ability (D = 3.11) indicates a shift towards selecting for more
productive and less aggressive breeds. Overall, these findings under
score the influence of local practices and environmental factors on trait
selection in agricultural contexts, highlighting the need for breeding
strategies that align with farmers’ priorities and the specific challenges
they face (Heller et al., 2013, 2016).
Table 10
Chi-squared distance values for trait preferences among agroecological zones.
Incubation practice
The study revealed that 76.6 % of respondents practiced incubation
without specific egg selection, while 23.4 % engaged in egg selection
based on size. Regarding broody hens, 31.8 % of respondents selected
them for incubation, considering factors such as body size and broodi
ness ability history. This finding aligns with previous studies conducted
by Meseret (2010) in the Gomma district and Fisseha (2009).
Furthermore, the farmers demonstrated knowledge of impending
broodiness behavior, employing methods such as hanging down and
disturbing the hen. Additional strategies included sending the hen to a
neighbor, removing the brooding nest, and immersing the hen in cold
water as common approaches to discourage broodiness (preference for
brooding hens based on body size and broodiness history, and the
presence of traditional knowledge and methods for identifying
impending broodiness (Table 9,10 and 11)
The findings align with Nigussie’s (2011) research, indicating
limited egg selection practices for breeding, a preference for brooding
hens based on body size and broodiness history, and the presence of
traditional knowledge and methods for identifying impending
broodiness.
Lowland
Total
39
(81.2)
147
(76.6)
Egg selection
Yes
Midland
No
25(25.2)
Broody hen selection
Yes
71(74.8)
22
(43.8)
27
(56.2)
73(76)
Bases of broody hen selection
Body size
Impending broodiness
Yes
62(64.6)
No
43(44.8)
53(55.2)
43(44.8)
Sending to neighbors
16(16.7)
Taking away brooding nest
Immersing in cold water
Disturbing the hen
15(15.1)
2(4.6)
22(18.8)
15
(31.8)
11
(22.9)
6(12.5)
5(10.4)
11
(22.4)
78(40.6)
114
(59.4)
22
(45.8)
26
(54.2)
11
(22.9)
37
(77.1)
10
(20.8)
15
(31.3)
5(10.4)
6(12.5)
12(25)
0.45
0.25
0.1
0.35
0.4
0.3
0.28
0.15
0.2
0.05
0.12
0.18
0.3
0.2
0.15
0.25
0.18
0.22
0.27
0.1
0.35
0.02
0.08
0.12
15.23
10.12
5.67
12.45
8.34
9.78
11.56
4.23
7.89
3.11
6.48
4.67
- The purposes of chicken production vary among households, with a
greater emphasis on meat production observed in lowland areas.
- Selective breeding practices are limited, indicating a lack of active
engagement in improving specific traits.
- Uncontrolled natural mating is the dominant mating system in the
district.
- Farmers practice culling underproductive chickens to maintain
desired productivity and quality standards.
- There are specific preferences for traits such as plumage color and
egg number within chicken populations.
- The main breeding constraints include chicken diseases, predators,
feed shortages, and the uncontrolled dissemination of exotic breeds.
- Correspondence Analysis reveals significant relationships among
phenotypic traits, emphasizing the influence of environmental con
ditions on livestock characteristics and supporting sustainable
management practices.
- Pearson’s Chi-squared Test shows highly significant differences in
trait preferences across agroecological zones, notably favoring traits
in the Highland area.
- Strong preferences for traits like Egg Number and Hatchability
highlight their critical roles in productivity and the importance of
selecting breeds that can withstand local diseases.
130
(67.7)
18
(37.5)
30
(62.5)
Egg Number
Body Size
Growth Rate
Hatchability
Mothering Ability
Broodiness
Disease Resistance
Egg Size
Plumage Color
Fighting Ability
Good Scavenging
Longevity
Based on this study, the following conclusions can be drawn
regarding chicken breeding practices in the Liben Jawi district:
62(31.8)
26
(54.2)
22
(45.8)
Chi-Squared Distance
Conclusions
45(23.4)
18
(37.5)
30
(62.5)
34(35.4)
Broodiness ability history
9(18.8)
22(22.9)
No
Ways of Impending
Hanging down the hen
11
(22.9)
37
(77.1)
Column Profile
Conclusions and recommendations
Agroecological zones with respondent’s number
and proportion in bracket
High lanD
Row Profile
Major chicken breeding constraints
Table 7 presents the main constraints on chicken breeding. The most
common breeding constraints identified were chicken diseases, uncon
trolled dissemination of exotic breeds, predators, and feed shortages.
The study also revealed differences in the prevalence of chicken diseases
across different agroecologies. It has been reported that chicken disease
incidence varies across different regions and farming systems (Zewdu
et al., 2013; Tesfaye, D. 2014). Predation by domestic and wild cats, as
well as wild birds, was reported as a major issue in the study districts.
These findings are consistent with previous studies conducted in
different parts of the country, highlighting wild birds, cats, diseases,
predators, and feed shortages as significant constraints on chicken
production across various regions (Hunduma et al., 2010; Wondu et al.,
2013).
Table 9
The incubation practice by the agroecological zones.
Incubation practices
Trait
76(39.6)
116
(60.4)
68(35.4)
Recommendations
42(21.9)
To improve chicken breeding practices in the Liben Jawi district,
promote sustainable livelihoods, encourage selective breeding, enhance
disease management, implement predator control measures, improve
access to quality feed, raise awareness about breeding best practices,
26(13.6)
11(5.7)
45(23.4)
5
D. Begna et al.
Poultry Science 104 (2025) 104536
Table 11
Major indigenous chicken production constraints in the study area.
Agroecological zones with respondent’s number and proportion in bracket
Major constraints
Highland (96)
Midland (48)
Lowland (48)
Overall (192)
χ2
P-v
Disease
Uncontrolled dissemination of exotic breed
Predators
Lack of feed resource
Lack of marketing access
Major predators attacking chicken
Domestic cat
Wild cat
Wild birds (eagle)
Dog
34.80 %
25.20 %
17.70 %
14.20 %
8.10 %
33.30 %
28.80 %
21.30 %
8.80 %
7.80 %
35.00 %
26.90 %
13.80 %
16.10 %
8.20 %
37.00 %
30.80 %
17.80 %
10.60 %
3.80 %
21.3
9.78
14.6
11.1
7.2
12.2
0.04
0.23
0.021
0.04
0.01
0.001
68.80 %
11.50 %
14.60 %
5.10 %
70.80 %
14.60 %
10.40 %
4.20 %
72.90 %
6.20 %
12.50 %
8.40 %
70.30 %
10.90 %
13.00 %
5.80 %
N = no of respondent, HL = Highland, MLS = midland, LL = lowland, P-V = P value
Table 7
Chi-squared distance values for traits by agroecological zones.
Trait
Highland
Chi-Squared Distance (D)
P-value
Midland
Chi-Squared Distance (D)
P-value
Lowland
Chi-Squared Distance (D)
P-value
Egg Number
Hatchability
Disease Resistance
Body Size
Mothering Ability
Broodiness
Plumage Color
Good Scavenging
Growth Rate
Longevity
Egg Size
Fighting Ability
15.23
12.45
11.56
10.12
8.34
9.78
7.89
6.48
5.67
4.67
4.23
3.11
0.001
0.002
0.003
0.012
0.020
0.005
0.030
0.045
0.060
0.080
0.090
0.150
10.15
9.30
7.50
8.20
6.80
5.90
6.00
5.20
4.50
3.80
4.00
2.50
0.005
0.010
0.025
0.015
0.040
0.055
0.050
0.065
0.075
0.120
0.100
0.200
8.75
7.20
6.50
5.90
5.25
4.80
4.20
5.10
3.80
3.00
3.50
2.00
0.007
0.015
0.030
0.050
0.060
0.070
0.090
0.065
0.110
0.150
0.130
0.220
conserve local chicken breeds, and support farmer cooperatives.
This study provides insights into the current state of chicken
breeding practices in the Liben Jawi district and highlights areas where
interventions and improvements can be made to enhance productivity,
disease management, and sustainable livelihoods for farmers.
Availability of data and material
Funding
Authors’ contributions
The research did not receive specific funding but was self-sponsored
and performed as part of the MSc thesis of the authors.
Desalegn: conducted the critical review, and wrote the whole
manuscript, Teferi conceptualized the ideas; conducted a research and
investigation process, Shambel: oversight and leadership responsibility
for the research activities
The data supporting the findings of this study are primarily included
in the article. Additional data that may not be included can be made
available by contacting the corresponding author upon request.
Disclosures
The authors declare that they have no conflicts of interest. This
research was conducted with the sole purpose of advancing scientific
knowledge and understanding in the field of indigenous chicken
breeding practices.
Preprints
Authors confirm no preprint previously
Acknowledgments
Ethics approval
The authors would like to extend their appreciation to Mamo
Mezemir Campus of Ambo University, Ethiopia for granting permission
to conduct the MSc study.
N/A
Consent to participate
References
The participants involved in this study have provided their informed
consent to voluntarily take part in the research.
Abdelqader, A.., Wollny, C.B.A., Gauly, M., 2007. Characterization of local chicken
production systems and their potential under different levels of management
practice in Jordan. Trop. Anim. Health Prod. 39, 155–164, 2007.
Addis, M., Tadelle, D., Gizaw, S., Dessie, T., 2014. Village chicken production system in
Ethiopia: use patterns and performance evaluation and chicken products and
socioeconomic functions. Livestock Res. Rural Dev. 26 (6). https://www.lrrd.or
g/lrrd26/6/addis26093.htm.
Aklilu, H.A., 2007. Village Poultry in Ethiopia: Sociotechnical Analysis and Learning
with Farmers. Wageningen University, Wageningen, the Netherlands, p. 178 (Ph.D.
thesis).
Consent for publication
The authors of this manuscript provide their consent for its publi
cation in the designated journal
6
D. Begna et al.
Poultry Science 104 (2025) 104536
Arsham H. (2002). Questionnaire Design and Surveys Sampling, SySurvey: the Online
Survey Tool. SySurvey, Baltimore, MD.
Bogale, K., 2008. In Situ Characterization of Local Chicken Eco-Type for Functional
Traits and Production System in Fogera Woreda, Amhara Regional State. Msc.Thesis
Submitted to. Haramaya University, Haramaya, Ethiopia.
CSA, 2021. Agricultural sample survey. Report on Livestock and Livestock
Characteristics Addis Ababa. Ethiopian Statistical Agency (CSA, Ethiopia.
EARO, 2000. Ethiopian Agricultural Research Organization (EARO). National Poultry
Research Strategy.
FAO, 2012. Draft guidelines on phenotypic characterization of animal genetic resources
Commission on Genetic Resources for Food and Agriculture. 13th Regular Session,
1822, July 2011. Rome (available at http://www.fao.org/docrep/meetin, 651e.pdf).
Fisseha, M., 2009. Marketing System of Local Chicken Ecotypes in Bure Wereda, North
west AmhaStudies on Production Andra. M.Sc. Thesis. Hawassa University, Hawassa,
Ethiopia.
Fisseha, M., 2009. Studies on Production and Marketing Systems of Local Chicken
Ecotypes in Bure District, North‒West Amhara. M.Sc.Thesis. Hawassa University,
Ethiopia, pp. 533–557.
Greenacre, M., 2017. Correspondence analysis in practice. CRC Press.
Gretton, A., Gyorfi, L., 2010. Consistent estimation of the Hilbert-Schmidt norm of the
cross-covariance operator. The Annals of Statistics 38 (4), 1930–1953. https://doi.or
g/10.1214/09-AOS754.
Gretton, A., Fukumizu, K., Herbrich, R., Schölkopf, B., 2005. A kernel statistical test of
independence. Adv Neural Inf Process Syst 18, 585–592.
Halima, H.assen., 2007. Phenotypic and Genetic Characterization of Indigenous Chicken
Populations in North‒West Ethiopia. Ph.D. Thesis, Submitted to the. Faculty of
Natural and Agricultural Sciences Department of Animal Wildlife and Grassland
Sciences University of the Free State, Bloemfontein, South Africa, p. 186.
Heller, R., Gyorfi, L., Karg, M., 2016. Testing independence in high dimensions with a
kernel-based approach. Statistics in Medicine 35 (11), 1870–1887. https://doi.
org/10.1002/sim.6812.
Heller, R., Heller, R., Karg, M., 2013. A new method for testing the independence of two
random variables. Journal of Multivariate Analysis 116, 125–140. https://doi.
org/10.1016/j.jmva.2013.02.002.
Hunduma, D., Chala, R., Dawo, F., Bekana, E., Leta, S., 2010. Major constraints and
health management of village poultry production in Rift Valley of Oromia, Ethiopia.
Am.Euras. J. Agric. Envir on, Sci. 9 (5), 529–533.
Kebede, K., Gebre-Michael, D., Tadelle, D., 2012. Village chicken production systems in
Ethiopia: 1. Flock characteristics and performance. Ethiopian J. Anim. Prod. 12 (1),
47–61.
LJAO, 2022. Liben Jawi Agricultural office (LJAO) Annual Report (unpublished).
Mammo, M.engesha., Berhan, T., Tadelle, D.essie., 2011. village Chicken Constraints and
Traditional Management Practices in Jamma District south wollo, Ethiopia.
Melesse, A., Negesse, T., 2011. Phenotypic and morphological characterization of
indigenous chicken population in southern region of Ethiopia Anim. Genet. Resour.
Inf. 49, 19–31.
Mengesha, Y., Kebede, E., Getachew, A., 2022. Review of Chicken Productive and
Reproductive Performance and Its Challenges in Ethiopia. Journal of Animal Science
and Technology, 64. Published by Taylor & Francis, Abingdon, UK, pp. 1–12.
Meseret M.olla. (2010). Characterization of village chicken production and marketing
system in Gomma wereda, jimma zone, Ethiopia, M.sc. thesis Meseret Molla Bogale
jimma university, Ethiopia.
Mirkena, T, Duguma, G, Willam, A, Wurzinger, M, Haile, A, Rischkowsky, B, Okeyo, AM,
Tibbo, M, Solkner, J, 2012 Jun. Community-based alternative breeding plans for
indigenous sheep breeds in four agro-ecological zones of Ethiopia. J Anim Breed
Genet 129 (3), 244–53. 10.1111/j.1439-0388.2011.00970.x. Epub 2011 Oct 15.
PMID: 22583329.
Nigussie, D., 2011. Breeding programs for indigenous production and Health, technical
livestock sector chicken in Ethiopia, Analysis of diversity in brief: Ethiopia. No. 1.
Okeno, T., Kahi, A., Peters, K., 2011. Characterization of indigenous chicken production
systems in Kenya. Trop. Anim. Health Prod. 44, 601–608. https://doi.org/10.1007/
s11250-011-9942-x.
Senbeta, E.K., 2020. Chicken reproductive performances in Ethiopia. Turkish J. Agric. Food Sci. Technol. 8, 755–1762. https://doi.org/10.24925/turjaf.v8i8.17551762.3501.
Sime, A. G. (2022). Review on poultry production, processing, and utilization in
Ethiopia. 10.17352/2455-815X.000156).
Sourial, G.F., Galal, S., Nizar, M.A., Osman, M.A., Shalaby, M.H., Aboul-Ela, M.B., 2010.
Correspondence analysis of factors affecting the diversity of local animal genetic
resources in Egypt. Animal Genetic Resources 46, 17–24.
Székely, G.J., Rizzo, M.L., 2009. Distance correlation: A new concept in statistical
dependence. The Annals of Applied Statistics 3 (2), 1236–1265. https://doi.org/
10.1214/09-AOAS285.
Székely, G.J., Rizzo, M.L., Bakirov, N.K., 2007. Measuring and testing dependence by
correlation of distances. The Annals of Statistics 35 (3), 2769–2794. https://doi.org/
10.1214/009053607000000505.
Tadelle, D., Million, T., Alemu, Y., Peters, K.J., 2003. Village chicken production systems
in Ethiopia: flock characteristics and performance. Livestock Res. Rural Dev. 15, 9.
http://www.lrrd.org/lrrd15/1/tadea151.htm.
Tadelle, D., Alemu, Y., Peters, K.J., 2000. Indigenous chickens in Ethiopia: genetic
potential and attempts at improvement. World’s Poult. Sci. J. 56 (1), 52–54. https://
doi.org/10.1079/wps20000005.
Tesfaye, D., 2014. Challenges and opportunities of village chicken production in
Ethiopia. World’s Poult. Sci. J. 70 (3), 581–590. https://doi.org/10.1017/
S0043933914000340.
Tixier-Boichard, M., Besse, P., Rognon, X., 2009. Genetic diversity in poultry species: A
review. World’s Poultry Science Journal 65 (3), 1–12.
Wondmeneh, E.W., 2015. Genetic Improvement in Indigenous Chicken of Ethiopia. Ph.D.
Thesis. Wageningen Institute of Animal Sciences, Animal Nutrition Group,
Wageningen University, Wageningen.
Wondu, M., Mehiret, M., Berhan, T., 2013. Characterization of Urban poultry production
system in Northern Gondar, Amhara Regional State, Ethiopia. Agric. Biol. J. North
Am. 4, 192–198. https://doi.org/10.5251/abjna.2013.4.3.192.198.
Zewdu, Solomon A.ltaye., Kassa, B.inyam., Agza, B.ilatu., Alemu, F.erede., 2013. Village
chicken production systems in Metekel zone, Northwest Ethiopia. Wudpecker J.
Agric. Res., 2, 2315–7259.
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