Relationship Between Body Weight and Linear Body Measurements at Various Stages of Permanent Tooth Eruption in Indigenous Matebele Female Goats of Zimbabwe
Research Article
Relationship Between Body Weight and Linear Body Measurements at Various Stages of Permanent Tooth Eruption in Indigenous Matebele Female Goats of Zimbabwe
Never Assan1,2, Michael Musasira3, Maphios Mpofu3, Nicholas Mwayera4, Kwena Mokoena5, Thobela Louis Tyasi5*
1Zimbabwe Open University, Faculty of Agriculture, Department of Agriculture Management, Bulawayo Regional Campus, Bulawayo, Zimbabwe; 2Professor Extraordinaire, University of South Africa, College of Agriculture and Environmental Sciences, Department of Agriculture and Animal Health, South Africa; 3Matopos Research Station, Ministry of Lands and Agriculture, Department of Research and Extension, Private Bag 5137, Bulawayo, Zimbabwe; 4Zimbabwe Open University, Faculty of Agriculture, Department of Mathematics, Mutare Regional Campus, Bulawayo, Zimbabwe; 5School of Agricultural and Environmental Sciences, Department of Agricultural Economics and Animal Production, University of Limpopo, Private Bag X1106, Sovenga 0727, Limpopo, South Africa.
Abstract | This study aimed to evaluate the influence of dental age on predicting body weight (BWT) using Linear body measurements (LBM) in 168 indigenous Matebele goat females of Zimbabwe. LBM and BWT were recorded at various stages of permanent incisor eruption (PE): second pair (I2), third pair (I3), fourth pair (I4), full mouth (FM), and broken mouth (BM). The LBMs were measured using a ruler and centimeter-calibrated tailor’s tape, while BWT was measured using an electronic weighing scale in kilograms. The correlation between BWT and LMBs was assessed using Pearson’s correlation and regression were used for data analysis. The highest correlation was observed between body length (BL) and rump height (RH) (r = 0.70), while BWT and heart girth (HG) showed a significant correlation (r = 0.68) (p<0.05) at I2 stage. Simple regression models demonstrated good predictive power on BWT at the FM stage for HG (R2 = 74%), BL (R2 = 65%), and WT (R2 = 53%) (p<0.05). The predictive power of multiple regression models for I3 was slightly reduced when non-significant components were removed. The findings suggest that HG is the best predictor of BWT during the I3 to FM tooth eruption phases, supporting genetic improvement and selection of replacement females based on LBM. The study concludes that dentition-based age determination influences the correlation between BWT and LBMs in female indigenous goats, with the strongest correlation observed between I2 and I4 eruption periods. Combining HG and RH can optimize body weight prediction for I3 females by reducing variables in the model. The results highlight the importance of dentition-based age estimation and morphometric feature-based body weight prediction in small ruminants, particularly in small-scale animal agriculture where scales and record-keeping are often lacking.
Keywords | Body weight, Dentition, Linear body measurements, Indigenous matebele goat, Zimbabwe
Received | May 10, 2024; Accepted | June 19, 2024; Published | August 15, 2024
*Correspondence | Thobela Louis Tyasi; 5School of Agricultural and Environmental Sciences, Department of Agricultural Economics and Animal Production, University of Limpopo, Private Bag X1106, Sovenga 0727, Limpopo, South Africa; Email: [email protected]
Citation |Assan N, Musasira M, Mpofu M, Mwayera N, Mokoena K, Tyasi TL. 2024. Relationship between body weight and linear body measurements at various stages of permanent tooth eruption in indigenous matebele female goats of Zimbabwe. Adv. Anim. Vet. Sci. 12(9): 1818-1828.
DOI | https://dx.doi.org/10.17582/journal.aavs/2024/12.9.1818.1828
ISSN (Online) | 2307-8316; ISSN (Print) | 2309-3331
Copyright: 2024 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
The Matebele goat, a medium to large breed, is primarily found in Matabeleland North, Matabeleland South, and some parts of Midlands province (Devendra and Burns, 1983). It is a medium to large breed with a height of around 65cm at withers and mature weights ranging from 35kg to 55kg (Matopos Research Station, 2003). The typical birth weight for kids is 2.5kg, with weaning weights ranging from 12kg to 16kg. Both male and female Matebele goats have powerful legs for bi-pedal browsing and a short and moderate neck proportional to body length (Sikosana and Senda, 2007). The indigenous Matabele goat is often crossbred with other breeds, like the Kalahari buck, to produce desirable offspring (Assan and Makuza, 2005). Efforts are being made to conserve and promote the use of indigenous goat breeds in Zimbabwe, with breed standards established to guide farmers and promote conservation (Assan, 2007). The indigenous Matabele goat is a crucial component of Zimbabwe’s smallholder farming sector, with a significant population presence in this area.
Body weight is another critical factor in animal husbandry, as it serves as a reference point for carrying out a range of procedures, including breeding and selection, marketing, and managing the animal’s health, including supplementation and medicine dosage, particularly during dry spells. An accurate estimation of body weight is crucial to maximize profitability (Skapetas et al., 2006). Linear body measurements can be used to estimate live weight easily and inexpensively (Aduku et al., 1991). Evaluating the live weight of goats can be accomplished easily and affordably by using linear body measurements, as demonstrated by research conducted by Tadesse et al. (2012) and Chitra et al. (2012). Establishing a reliable live weight method for field application is essential, as emphasized by Muhammad et al. (2021). The lack of weighing scales has made it difficult for farmers to manage dosage regimens, choose suitable breeding animals, and determine acceptable supplementing proportions (Ravimurugan, et al., 2013).
Age estimation and body weight prediction are essential practices in small-scale animal agriculture, particularly in goats (McGregor, 2011). Dentition is used for goats, but teeth eruption can be the most accurate method in resource-limited areas (Wilson and Durkin, 1984). Age affects edible body parts, meat offal, and carcass yield, making it crucial to know an animal’s age before processing it (Mahilet, 2012). However, small-scale animal agriculture faces problems such as a shortage of scales for weighing animals and poor record keeping for determining animal age (Yakubu et al., 2011). These factors make it difficult for farmers to manage dosage regimens, choose suitable breeding animals, and determine acceptable supplementing proportions (Ravimurugan et al., 2013). In the informal market, farmers who rely on the informal market have lost revenue from the sale of their animals due to the lack of records that could be used to determine the age of the animals. The pricing of goats of unknown age is particularly challenging in the informal market (Van Rooyen et al., 2007).
The study highlights the importance of the relationship between body weight and linear body at different stages of permanent tooth eruption as part of characterization of indigenous Matabele goat females, aiding conservation efforts and preserving genetic diversity in this breed. Linear body measurements such as body length, height-at-withers, and heart girth can be used to accurately predict body weight in goats, which is essential for management decisions (Mokoena et al., 2022). Selection for breeding due to the strong correlation between body weight and linear measurements suggests that selection for breeding can be based on these easily measurable traits (Dige et al., 2022). The relationship can be used for monitoring growth and development in goats, enabling farmers to identify any growth-related issues (Yakubu et al., 2011). Understanding the relationship between body weight and linear measurements can inform nutrition and feeding strategies to optimize growth and productivity. The relationship between body weight and linear measurements can be used to estimate the age of goats, particularly in the absence of birth records (Idamokoro et al., 2018). The study’s findings can be used in genetic improvement programs to develop breeds with desirable body weight and linear measurement traits.
Tsegaye et al. (2013) suggest that predicting live weight from body measurements is efficient, quicker, and less costly in rural areas lacking the necessary facilities for breeders. Linear body measurements were used to calculate and predict goats’ weight without weighing, using a stepwise multiple balance and a prediction equation (Atta and El Khidir, 2004; Adeyinka and Mohammed, 2006a; Fajemilehin and Salako, 2008; Olatunji-akioye and Adeyemo, 2009; Agamy et al., 2015; Sam et al., 2016; Yakubu et al., 2015). This method can explain live body weight for males and females at maximum variation in the dependent variable (Lawrence and Fowler, 1997). The relationship between live weight and heart girth in animals growing over a wide weight range is curvilinear, and morpho-biometrical traits with high correlations with body weight can be used for selection purposes in meat production and to predict live weight in the field when scales are unavailable, especially in villages or smallholder farms (Thiruvenkadan, 2005; Ojedapo et al., 2007). A linear regression model with a 0.934 coefficient of determination can predict the body weight of Red Sokoto goats in the field and for selection purposes, considering indices like body length, chest girth, shoulder width, cannon circumference, and neck circumference (de Villiers et al., 2009). The study found a strong correlation between body weight and linear body measurements, with heart girth being the most suitable linear measurement for predicting body weight (Sam et al., 2016).
A few studies have explored the relationship between body weight, linear body measurements, and tooth eruption in female goats, with most being cross-sectional (Bello and Adam, 2012). Tooth eruption stages are not well-defined, making it difficult to standardize the relationship (Matika et al., 1992). The relationship may vary across breeds, but breed-specific studies are scarce (Tsegaye et al., 2013). Nutrition’s impact on this relationship is poorly understood, and environmental factors like climate, management practices, and health status may influence it (Tsegaye et al., 2013). Standardized measurement protocols make comparisons challenging (Abd-Allah et al., 2019). Most studies focus on kids and yearlings, with limited information on adult females (Idamokoro et al., 2018). Some studies may not use appropriate statistical models to account for the complex relationships between these variables (Yakubu et al., 2011; Eyduran et al., 2017). Addressing these knowledge gaps through well-designed studies can provide valuable insights.
The potential research questions to investigate the relationship between body weight and linear body measurements at different tooth eruption stages in female goats: Is there a significant correlation between body weight and linear body measurements (height, length, chest circumference) at different tooth eruption stages in female goats? It is hypothesized that body weight increases linearly with each stage of tooth eruption, with specific dentition stages having a greater impact on one sex. Body weight is positively correlated with the number of permanent teeth erupted and significantly increases once a certain stage is reached. The study aims to develop models that predict body weight and age in female indigenous Matebele goats based on linear body measurements at different stages of tooth eruption, and to determine if there are sex-specific differences in this relationship.
Materials and Methods
Ethical approval
The study was approved by the Zimbabwe Open University Animal Research Ethics Committee (Projects 2023).
Study period and area
The study was conducted in April 2023. The research was undertaken 30km Southwest of Bulawayo, at Matopos Research Station (20 0 23’ S, 310 30’ E), Zimbabwe. The area experiences high temperatures ranging in the hottest months to 21.6 0C and 11.4 0C and low rainfall (<450mm) (Hagreveas et al., 2004; Homann et al., 2007). The research area is a rangeland with sweet veld vegetation with good nutritional value to sustain ruminants (Ward et al., 1979; Ncube, 2005; Van Rooyen et al., 2007).
Study design and measurements
The study used a cross-sectional design were the animals were observed once per animal. The BW and linear body measurement (LBMs) properties of 168 indigenous Matebele females at different stages of permanent tooth eruption were obtained from a randomly selected experimental flock kept at Matopos Research Station. The ages of the study’s indigenous Matebele females were approximated using dentition. The study analyzed indigenous Matebele females aged 2-5 years based on their dentition, using categories I2 (second pair permanent incisors emerged), I3 (third pair permanent incisors emerged), and I4 (fourth pair of permanent incisors emerged full mouth) and BM (broken mouth lost or broken).
The study examined Linear body measurements (LBMs), namely heart girth (HG), body length (BL), wither height (WTH) and rump height (RH) following FAO (2011) recommendations. Measurements were recorded in centimeters and evaluated using a flexible tape and wood ruler, while BW was described in kilograms using a weighing scale that does not cause pain to animals. Data were extracted following Animal Ethics Committee protocols. The study measured animals in the morning before grazing on pastures. All animals experienced a fast period before weighing, with minimal variation due to gut-fill. To maintain consistency, measurements were taken by the same person and performed early in the morning before the flock left for grazing.
Figure 1, Below shows the LBMs in indigenous matabele female goats.
The four linear body measurements were taken into consideration in this study.
Heart Girth (HG): Chest circumference, behind the posterior edge of the shoulders at the point of least perimeter.
Withers height (WTH): Distance from the top of the withers to the ground.
Body Length (BL): Body length from the anterior edge of the shoulder to the posterior edge of the ischium.
Table 1: Descriptive statistics for body weight (kg) and linear body measurements (cm) at different permanent tooth eruption stages.
PTE |
Trait |
Mean |
SE |
SD |
CV (%) |
Incisor (I2) (N=28) |
BWT (Kg) |
23.30 |
0.52 |
2.34 |
22.22 |
HG |
69.30 |
1.20 |
5.38 |
22.30 |
|
WH |
48.30 |
0.42 |
1.86 |
22.58 |
|
BL |
46.40 |
0.77 |
3.42 |
22.51 |
|
RH |
58.70 |
0.58 |
2.57 |
22.56 |
|
BWT (Kg) |
31.28 |
0.71 |
3.86 |
18.39 |
|
HG |
77.55 |
0.72 |
3.88 |
18.56 |
|
WH |
51.08 |
0.68 |
3.70 |
18.37 |
|
BL |
52.07 |
0.69 |
3.69 |
18.69 |
|
RH |
60.86 |
0.86 |
4.62 |
18.61 |
|
BWT (Kg) |
27.90 |
0.66 |
4.19 |
15.75 |
|
HG |
74.20 |
0.53 |
3.33 |
15.91 |
|
WH |
48.55 |
0.53 |
3.33 |
15.91 |
|
BL |
47.53 |
0.61 |
3.84 |
15.88 |
|
RH |
57.50 |
0.88 |
5.58 |
15.77 |
|
FM(N=33) |
BWT (Kg) |
31.13 |
1.60 |
4.51 |
35.47 |
HG |
77.75 |
1.33 |
3.77 |
35.27 |
|
WH |
50.75 |
0.94 |
2.66 |
35.33 |
|
BL |
53.38 |
1.52 |
4.31 |
35.27 |
|
RH |
60.38 |
1.59 |
4.50 |
35.33 |
|
BM (N=25) |
BWT (Kg) |
33.86 |
0.65 |
3.87 |
16.79 |
HG |
77.91 |
0.68 |
4.04 |
16.83 |
|
WH |
50.69 |
0.47 |
2.75 |
17.09 |
|
BL |
52.14 |
1.13 |
6.70 |
16.86 |
|
RH |
62.69 |
0.56 |
3.32 |
16.86 |
Permanent tooth eruption stages (PTE): (I2) = 2nd pair permanent incisors emerged; Incisor (I3) =3rd pair permanent incisors emerged; SD= Standard deviation; Incisor (I4) =4th pair permanent incisors emerged; FM= Full mouth; BM= Broken mouth (Lost or broken); HG= heart girth; BWT = body weight; WH = withers height; BL = body length; RH= rump height; N =number per each category; SE = standard error, CV=coefficient of variation.
Rump height (RH): The distance from the surface of a platform to the rump using a measuring stick as described for height at withers.
Statistical analysis
The study analyzed data from indigenous Matabele female goats of Zimbabwe, focusing on body weight, heart girth, wither height, body length, and rump height. Means, standard deviations, and coefficients of variation were obtained, and bivariate correlations were found. Descriptive statistics were used to present phenotypic measurements at
different stages of permanent tooth eruption, and Pearson’s correlation coefficient was used to estimate associations. Simple and multiple regression was used to establish a formula to predict the BWT using linear body measurements (SPSS 2010). All the findings were tested at 0.05 significant value. The simple linear regression of body weight on linear body parameters below was performed:
Model: Y = α + βX
Where;
Y = dependent variable (BWT), X = independent variable (HG, WTH, BL, RH), α = the intercept, β = regression coefficient.
The below multiple linear regression was adopted:
Model: Y = a + b1X1 + b2X2 + b3X3 + b4X4
Where;
Y = dependent variable (BWT), a = intercept, b1 − b4 = coefficient of regression, and X1 − X4 = independent variables (HG, WTH, BL, RH).
Results and Discussion
Descriptive statistics for linear body measurements and body weight at different permanent tooth eruption stages
The evaluation of live weight in goats can be carried out easily and affordably by linear body measurements, as demonstrated by Tadesse et al. (2012) and Chitra et al. (2012). It is essential, therefore, to establish a live weight determination procedure that can be employed in the field (Muhammad et al., 2021). Many studies across various animal species have investigated the relationship between live weight and biometric measurements. These studies include Abdelhadi and Babiker (2009); Gunawan and Ja (2011); Agung et al. (2018) (on cattle); Cam et al. (2010a); Musa et al. (2012) (on sheep); Machebe and Ezekwe (2010); Sungirai et al. (2014); Birteeb et al. (2015) (on pigs); Mendes et al. (2005) (on poultry); Variedades (2010) (on turkey); Ojo et al. (2013) (on Guinea fowl); Yakubu et al. (2015) (on ducks); Sadick et al. (2020) (on broiler chicken); Tyasi et al. (2020) (on layers chicken); and Vilakazi et al. (2020) (on indigenous chicken). However, the calculations that result from this research can be intricate or complex to interpret, as the coefficients for each body measurement gathered comprise unique decimal numbers. The study’s objective is to assess the age of animals using the rate of permanent incisor eruption and to relate this to assessing BWT using LBM in Matebele goat females. Age estimation based on dentition and body weight prediction based on morphometric features are essential practices in small ruminant management. These practices can help address the primary challenges facing small-scale animal agriculture, such as the scarcity of scales for weighing animals and poor record-keeping for determining the age of animals. Accurate estimation of age and body weight is crucial for maximizing profitability and ensuring the health and well-being of the animals. The study’s findings may be influenced by factors such as goat breed, season, age, sex, and management approach, as well as the specific season and data collected.
Phenotypic correlation of linear body measurements and body weight
Table 2. displays the correlation coefficients between BWT and LBMs in indigenous Matebele goat does in Zimbabwe. PE phases influence the phenotypic correlation of biometric body measurements with BWT. When a female goat reaches the mature stage, her phenotypic connection with BWT is highest at incisor (I4) = 4th pair permanent incisors emergencies. At this time, the phenotypic correlation of LBM characteristics with BWT was in a downward sequence: HG (r = 0.80), BL (r = 0.70), WH (r = 0.69), and RH (r = 0.57). The stronger correlation between BWT and HG in this dental group was likely because HG contributed more to body weight due to its morphology, which includes muscles, viscera, and bones (Thiruvenkadan, 2005). The present study’s findings contradict those of Hassan and Ciroma (1990), who found a connection between heart girth and body weight.
The lowest phenotypic correlation of LBM characteristics with BWT emerged at the PE second set of permanent incisors (I2), with the following values: BL (r = 0.45), HG (r = 0.37), WH (r = 0.23), and RH (r = 0.21). A weak and negative correlation was observed between HG and WH, BL and RH at this stage of tooth eruption. This suggests that while HG grows, WH, BL, and RH may decrease, albeit at a moderate rate, or may grow slowly. Indigenous Matebele goat female HG exhibited a high positive correlation with BW in most tooth eruption classes, except for I2, with the following values: (I3) (r = 0.68), (I4) (r = 0.80), FM (r = 0.72), and BM (r = 0.71). The findings correspond with Atta and El Khidir, 2004; Thiruvenkadan, 2005; Afolayan et al., 2006; Alade et al., 2008; and Cam et al., 2010b, who revealed a strong phenotypic relationship between HG and BWT.
Table 2: Bivariate Pearson correlation coefficients between linear body measurements and body weight.
PTE |
TRAIT |
BWT |
HG |
WH |
BL |
RH |
(I2) |
||||||
BWT |
1 |
|||||
HG |
0.37 |
1 |
||||
WH |
0.23 |
-043 |
1 |
|||
BL |
0.45 |
-0.40 |
0.85 |
1 |
||
RH |
0.21 |
-0.45 |
0.87 |
0.81 |
||
(I3) |
||||||
BWT |
1 |
|||||
HG |
0.68 |
1 |
||||
WH |
0.12 |
0.47 |
1 |
|||
BL |
0.36 |
0.38 |
0.20 |
1 |
||
RH |
0.61 |
0.51 |
0.37 |
0.70 |
1 |
|
(I4) |
||||||
BWT |
1 |
|||||
HG |
0.80 |
1 |
||||
WH |
0.69 |
0.66 |
1 |
|||
BL |
0.70 |
0.74 |
0.84 |
1 |
||
RH |
0.57 |
0.46 |
0.76 |
0.65 |
||
FM |
||||||
BWT |
1 |
|||||
HG |
0.72 |
1 |
||||
WH |
0.64 |
0.54 |
1 |
|||
BL |
0.45 |
0.51 |
0.68 |
1 |
||
RH |
0.44 |
0.58 |
0.74 |
0.37 |
1 |
|
BM |
||||||
BWT |
1 |
|||||
HG |
0.71 |
1 |
||||
WH |
0.09 |
0.15 |
1 |
|||
BL |
0.18 |
0.16 |
-0.03 |
1 |
||
RH |
0.36 |
0.25 |
0.23 |
0.01 |
1 |
Permanent tooth eruption stages (PTE): (I2) = 2nd pair permanent incisors emerged; Incisor (I3) =3rd pair permanent incisors emerged; Incisor (I4) = 4th pair permanent incisors emerged; RH = rump height; FM= Full mouth; r = non-significant at (r > 0.50); BM = Broken mouth (Lost or broken); BWT = body weight; HG = heart girth; BL = body length; Phenotypic correlation (r): r = significant at (r < 0.50); WH = withers height.
This implies a substantial relationship between HG and BWT as a potential predictor of body weight. The favourable relationship that exists between BWT and HG at this stage of tooth eruption showed that this biometric feature may be utilized to assess the BWT of indigenous Matebele goat females accurately.
According to a study by Khargharia et al. (2015), there is a positive statistical correlation between body weight (BWT) and body length (BL) (r = 0.86) and heart girth (HG) (r = 0.79) in Indian Assam Hill goats. These findings are consistent with those obtained from the eruption of the 4th pair of permanent incisors (I4). The high correlation between BWT and HG, BL, and wither height (WH) suggests that these linear body measurement traits could be used to estimate BWT without a weighing scale in the fields.
Okpeku et al. (2011) reported a positive relationship between BWT and wither height (r = 0.66) and heart girth (r = 0.54) in Nigerian WAD goats. These findings agree with the current study’s findings for the 4th pair of permanent incisors (I4). The association between BWT and linear body measurements (LBMs) was found to be positive, ranging from r = 0.09 to r = 0.80, indicating that there was no multicollinearity because they were all under 0.90 (Dakhlan, 2019).
Simple and multiple regression equations for predicting body weight
Simple regression equations with their coefficients of determination (R2) obtained from body weight and linear body measurements of indigenous Matebele goat ewes at different permanent tooth eruption stages are presented in Table 3. In I2, the single contribution to the variation in BWT was low and not significant, ranging from R2 (0.03 to 0.15). In I3, the contribution to the variation in BWT was less than 50%, and in descending order, HG (47%), RH (38%), WH (24%), and BL (13%). In I4, however, HG was the highest contributor to BWT, followed by BL, WH, and RH (64, 50, 47, and 32%, respectively).
For HG (74%), BL (65%), and WH (53%), simple regression models exhibited strong predictive power with respect to BWT at the FM stage. Conversely, RH exhibited a poor coefficient of determination (6%), even at the same stage of PEs. For the BM stage, only HG had an R2 greater than 50% (R2 = 53%), whereas the others had low R2 (RH = 16%, BL = 5%, and WH = 3%). Except for RH in FM and BM and BL in the BM tooth eruption group, simple regression models for LBM on BWT in (I2) were statistically non-significant at first but turned statistically significant as PE progressed. Sam et al. (2016) discovered that heart girth may be utilized to predict body weight at different ages based on permanent incisor eruption using simple linear regression analysis.
Multiple regression, on the other hand, demonstrated great accuracy when additional factors were included in the female goat estimation model (R2 = 0.694). The present research also confirmed this, as shown by our findings in Tables 3 and 4. Their predictive value of R2 = 0.694 is close to the R2 = 0.697 obtained in the current investigation for the fourth pair of permanent incisors in the female group.
Table 3: Simple regression between body weight and body measurements of indigenous Matebele goat ewes at different permanent teeth eruption stage.
PTE |
Regression Equation |
R2 (%) |
SE |
P-Value |
(I2) |
BWT= 13.954 + 0.135 HG |
0.09 |
2.28 |
0.1840NS |
BWT= 11.06+0.251WH |
0.04 |
2.35 |
0.3995NS |
|
BWT= 10.888 +0.268BL |
0.15 |
2.21 |
0.00881NS |
|
BWT= 13.625+0.165RH |
0.03 |
1.89 |
0.4445NS |
|
(I3) |
BWT= -21.494 +0.680HG |
0.47 |
2.87 |
0.0000** |
BWT= 14.725+0.468WH |
0.24 |
3.29 |
0.0070** |
|
BWT= 11.307+ 0.384 BL |
0.13 |
3.66 |
0.0500* |
|
BWT= -0.009 + 0.514RH |
0.38 |
3.10 |
0.0000** |
|
(I4) |
BWT= -46.712+ 1.005HG |
0.64 |
2.56 |
0.0000** |
BWT= -14.082 + 0.865WH |
0.47 |
3.08 |
0.0000** |
|
BWT= -8.871 + 0.774BL |
0.50 |
2.99 |
0.0000** |
|
BWT= 3.358 + 0.427RH |
0.32 |
3.49 |
0.0000** |
|
FM |
BWT= -48.773 +1.028HG |
0.74 |
2.51 |
0.0064** |
BWT= -31.671 + 1.237WH |
0.53 |
3.34 |
0.0400* |
|
BWT= -13.928 + 0.844BL |
0.65 |
2.90 |
0.0160** |
|
BWT= 16.390 + 0.244RH |
0.06 |
4.73 |
0.5620ns |
|
BM |
BWT= -20.859 +0.702HG |
0.53 |
2.67 |
0.0000** |
BWT= 22.554+0.222WH |
0.03 |
3.87 |
0.3624NS |
|
BWT= 27.410+0.124BL |
0.05 |
3.83 |
0.2164NS |
|
BWT= 4.408+0.469RH |
0.16 |
3.59 |
0.0929NS |
Permanent tooth eruption stages (PTE): (I2) = 2nd pair permanent incisors emerged; Incisor (I3) = 3rd pair permanent incisors emerged; WH = withers height; BL = body length; Incisor (I4) = 4th pair permanent incisors emerged; FM = Full mouth; RH = rump height; BM = Broken mouth (Lost or broken); BWT = body weight; **significant at (p<0.01); R2 = coefficient of determination; SE = standard error, *significant at (p<0.05); HG = heart girth; NS = non-significant.
The contribution of RH was not significant in I2, while HG and BL were significant in the current study (BWT = -10.126+0.316HG**-0.434WH+0.801BL**-0.076RH). HG and BL were highlighted as the best predictors of live weight in Nigerian Red Sokoto goats (Adeyinka and Mohammed, 2006b). This finding is partly consistent with the current results. Dakhlan et al. (2020), studying female Ettawa Grade goats, found that the combination of HG and BL in the body weight estimate regression model is consistent with the current research.
Table 4, displays a range of multiple regression equations and their corresponding R2 values, which were derived from the BWT and other variables. The best fit was found in FM, although individual variables were not statistically
Table 4: Preliminary multiple regression equation for predicting body weight of indigenous Matebele goat ewes at different permanent teeth eruption stage.
PTE |
Regression Equation |
R2 (%) |
R2(adj) |
SE |
(I2) |
BWT= -10.126+0.316HG*-0.434WH+0.801BL*-0.076RH |
0.599 |
0.492 |
1.669 |
(I3) |
BWT= -20.286+0.607HG*-0.307WH-0.054BL+0.377RH* |
0.624 |
0.561 |
2.558 |
(I4) |
BWT= -45.917+0.765HG**+0.149WH+0.054BL+0.126RH |
0.697 |
0.663 |
2.435 |
FM |
BWT= -53.043+0.886HG+0.862WH-0.021BL+-0.340RH |
0.845 |
0.689 |
2.714 |
BM |
BWT= -28.931+0.640HG**-0.087WH+0.038BL+0.245RH |
0.580 |
0.524 |
2.668 |
Permanent tooth eruption stages (PTE): (I2) = 2nd pair permanent incisors emerged; Incisor (I3) =3rd pair permanent incisors emerged; HG = heart girth; Incisor (I4) = 4th pair permanent incisors emerged; R2 = coefficient of determination; FM = Full mouth; BM = Broken mouth (Lost or broken); BWT = body weight; WH = withers height; RH = rump height; **significant at (p<0.01); BL = body length; SE = standard error; *significant at (p<0.05); all LBMs in a model without a superscript are non-significant.
Table 5: Optimal regression equation for predicting body weight of indigenous Matebele goat ewes at different permanent teeth eruption stage.
PTE |
Regression Equation |
R2 (%) |
R2(adj) |
SE |
(I2) |
BWT= -10.126+0.316HG**-0.434WH+0.801BL**-0.076RH |
0.599 |
0.482 |
1.669 |
BWT=-23.45+0.266HG+0.486RH |
0.286 |
0.202 |
2.092 |
|
(I3) |
BWT= -20.286+0.607HG**-0.307WH-0.054BL+0.377RH* |
0.624 |
0.561 |
2.558 |
BWT=-25.033+0.495HG+0.294RH |
0.556 |
0.522 |
2.671 |
|
(I4) |
BWT= -45.917+0.765HG**+0.149WH+0.054BL+0.126RH |
0.697 |
0.663 |
2.435 |
BWT= -46.712+ 1.005HG |
0.638 |
0.628 |
2.557 |
|
FM |
BWT= -53.043+0.886HG+0.862WH-0.021BL+-0.340RH |
0.845 |
0.689 |
2.714 |
BWT= -48.773 +1.028HG |
0.735 |
0.691 |
2.900 |
|
BM |
BWT= -28.931+0.640HG**-0.087WH+0.038BL+0.245RH |
0.580 |
0.524 |
2.668 |
BWT= -20.859 +0.702HG |
0.538 |
0.524 |
2.667 |
Permanent tooth eruption stages (PTE): (I2) = 2nd pair permanent incisors emerged; Incisor (I3) =3rd pair permanent incisors emerged; **significant at (p<0.01); RH= rump height; Incisor (I4) =4th pair permanent incisors emerged; HG= heart girth; FM= Full mouth; BM= Broken mouth (Lost or broken); R2= coefficient of determination; BWT = body weight; WH = withers height; BL = body length; *significant at (p<0.05); SE= standard error; all LBMs in a model without a superscript are non-significant.
significant. The next best fit was found in I4, followed by I3 and I2, with BM having the lowest R2 value. The simple regression of heart girth on BWT was consistent with previous studies, and the R2 for basic modeling of HG and other LBM was relatively high. However, the study found that estimating live weight using two or more body measures did not yield higher accuracy than using heart circumference alone. The findings of Iqbal et al. (2013) were similar, where multiple regression provided the greatest predictors for BW in female Beetal goats with an R2 of 0.69.
Table 5. provides an optimal regression model for estimating the body weight of native Matebele goat ewes at different permanent tooth eruption stages. The multiple regression model in I2 lost 31% of its R2 value when non-significant components (WH and RH) were removed, falling from 60% to 29%. Similarly, removing non-significant components from I3 reduced the predictive power by 6%, and removing them from I4 had a negligible effect. The variables removed were WH, BL, and RH. Although none of the factors used in the multiple regression equation were significant for FM, this model provided the best fit (R2 = 0.845). It was noted that the full model with all LBMs included gave the best result for (I2) (R2 = 0.599); however, under field conditions, using all LBMs is impossible since the main aim of predicting BW from LBMs is to easily predict BW from LBMs.
In this case, farmers might opt for a simple model, such as BWT = -23.45 + 0.266 HG + 0.486 RH, with a compromised low predictive power (R2 = 0.286). Fitting HG alone produced an identical best coefficient of determination of R2 = 0.735 with a loss of value of 11% in the optimal model. The removal of non-significant variables from the BM multiple regression model had no effect on the coefficient of determination. Yakubu and Salako (2009) proposed a method of eliminating non-significant variables to generate optimal equations. The following optimal regression models for predicting the body weight of indigenous Matebele goat ewes at different stages of permanent tooth eruption were established for the current study: In Model (I2): BWT = -23.45+ 0.266 HG + 0.486 RH (R2 = 0.286). NB: This model indicates that at an early stage of tooth eruption, most morphological traits will not be well developed to warrant any measurement for use in predicting body weight. For (I3): Optimal Model: BWT =-25.033+0.495HG+0.294RH (R2 = 0.556), Model (I4): BWT = -46.712+1.005HG (R2 = 0.638), Model FM: BWT = -48.773 +1.028HG (R2 = 0.735), and Model BM: BWT = -20.859 +0.702HG (R2 = 0.538). This study’s findings are consistent with those published by Dea et al. (2019), Seid et al. (2016), Selolo et al. (2015), and Khargharia et al. (2015). Based on dentition-based age determination, HG is the most reliable indicator of body weight in female goats. The precision of determination improves when comparing I3 with FM. This stage corresponds to adulthood, at which point all body measurements are fully taken. The low prediction value in BM (broken mouth) can be attributed to muscle loss induced by animals in this group who fail to use feed adequately owing to tooth loss. BM animals cannot always eat enough to keep their bodies in excellent shape.
Conclusion
The study investigates the correlation between body weight and linear body measurements in indigenous Matebele female goats during permanent tooth eruption, concluding that dentition-based age determination influences this correlation. Dentition and LBMs can be combined to determine BWT accurately. The indigenous Matebele female goats showed a strong correlation between LBM and BWT during permanent tooth eruptions, while HG was found to be the most accurate predictor of BWT between I3 and FM teeth eruption phases. Combining HG and RH can optimize BWT prediction for I3 females. The study provides new insights into the relationship between these measurements’ protocols and their morphological development, which could benefit female goat replacement management and future breeding programs.
Implications
However, the study’s findings should be interpreted with caution due to potential limitations in sample size and other methodological factors. The study’s limitations may limit its generalizability. Despite its limitations, the study offers important insights into the link between body weight and linear body measures during permanent tooth eruption in female goats that are scarce in the literature. Future research on teeth eruption should use larger sample sizes and longitudinal designs to improve accuracy and consider individual variability. It should evaluate multiple phases, manage dietary aspects, and use machine learning algorithms for data analysis. Collaborating with other researchers is crucial for merging data and knowledge, as regional and environmental factors may be considered in data collection from multiple locations.
Acknowledgments
The authors express their sincere gratitude to the Matopos Research Station for allowing them to utilize their goats for data collection.
novelty statement
The estimation of body weight at different ages of indigenous goats is limited. This study identified linear body measurements that might be used by goat farmers at different ages of goats.
Author’s contributions
Never Assan designed and drafted the manuscript. Nicholas Mwayera, Micheal Musasera and Maphios Mpofu collected and analysed the data. Louis Tyasi and Kwena Mokoena revised the manuscript. All authors read and approved the final manuscript.
Conflict of interest
The authors have stated that they have no competing interests.
References
Abd-Allah S, Abd-El Rahman HH, Shoukry MM, Mohamed MI, Salman FM, Abedo AA (2019). Some body measurements as a management tool for Shami goats raised in subtropical areas in Egypt. Bull Natl. Res. Cent., 43(1): 0-5. https://doi.org/10.1186/s42269-019-0153-3
Abdelhadi OMA, Babiker SA (2009). Prediction of zebu cattle live weight using live animal measurements. Livest. Res. Rural Dev., 21(8): 1-7.
Adeyinka IA, Mohammed ID (2006b). Accuracy of body weight prediction in nigerian red sokoto goats raised in North Eastern Nigeria using linear body measurement. Pak. J. Biol. Sci., 9(15): 2828-2830. https://doi.org/10.3923/ pjbs.2006.2828.2830.
Adeyinka LA, Mohammed ID (2006a). Relationship of live weight and linear body measurement in two breeds of goats of Northern Nigeria. J. Anim. Vet. Adv., 5:891-893.
Aduku AO, Aganga AA, Okoh AN, Ingawa SA, Phillip DOA (1991). Contribution of offals to the gross value of goat carcasses in Nigeria. Small Rumin. Res., 6(1-2):179-184. https://doi.org/10.1016/0921-4488(91)90022-I
Afolayan RA, Adeyinka IA, Lakpini CAM (2006). The estimation of live weight from body measurements in Yankasa sheep. Czech J. Anim. Sci., 51(8):343-348. https://doi.org/10.17221/3948-CJAS
Agamy R, Abdel-Moneim AY, Abd-Alla MS, Abdel-Mageed II, Ashmawi GM (2015). Using linear body measurements to predict body weight and carcass characteristics of three Egyptian fat-tailed sheep breeds. Asian J. Anim. Veterinary Adv., 10:335-344. https://doi.org/10.3923/ajava.2015.335.344
Agung PP, Putra WPB, Anwar S, Wulandari AS (2018). Body weight estimation of Bali cattle in Banyumulek Techno Park West Nusa Tenggara using several morphometric parameters. Bull. Anim. Sci., 42:20-25. DOI:10.21059/buletinpeternak. v42i1.29840. https://doi.org/10.21059/buletinpeternak.v42i1.29840
Alade NK, Raji AO, Atiku MA (2008). Determination of appropriate model for the estimation of body weight in goats. JABS. 3(4):52-57.
Assan N (2007). The effect of non-genetic factors on slaughter weight and carcass traits in indigenous Matebele goats in Zimbabwe. Afr. J. Agric. Res. Vol., 2(1): 12-15.
Assan N, Makuza SM (2005). The effect of non-genetic factors on birth weight and weaning weight in three sheep breeds of Zimbabwe. Asian-Aust. J. Anim. Sci., 18 (2): 151-157. https://doi.org/10.5713/ajas.2005.151
Atta M, El Khidir OA (2004). Use of heart girth, wither height and scapuloischial length for prediction of live weight of Nilotic sheep. Small Rum. Res., 55:233–237. https://doi.org/10.1016/j.smallrumres.2004.01.005
Bello AA, Adama TZ (2012) Studies on body weight and linear body measurements of castrates and non-castrate Savan-nah Brown goats. Asian J. Anim. Sci., 6:140-146. https://doi.org/10.3923/ajas.2012.140.146
Birteeb PT, Tetteh IO, Salifu AS (2015). Growth performance and weight estimation of large white piglets weaned at different ages. Research & Reviews. RRJoVST. 4(3): 15-23.
Cam MA, Olfaz M, Soydan E (2010a). Body measurements reflect body weights and carcass yields in Karayaka sheep. Asian J. Anim. Vet. Adv., 5: 120-127. https://doi.org/10.3923/ajava.2010.120.127
Cam MA, Olfaz M, Soydan E (2010b). Possibilities of using morphometrics characteristics as a tool for body weight prediction in Turkish hair goats (Kilkeci). Asian J. Anim. Vet. Adv., 5(1): 52-59. https://doi.org/10.3923/ajava.2010.52.59
Chitra R, Rajendran S, Prasanna D, Kirubakaran A (2012). Prediction of body weight using appropriate regression model in adult female Malabari goat. Vet. World. 5:409-411. https://doi.org/10.5455/vetworld.2012.409-411
Dakhlan A (2019). Experimental design and data analysis using R. Graha Ilmu. Yogyakarta.
Dakhlan A, Saputra A, Hamdani MDI, Sulastri A (2020). Regression models and correlation analysis for predicting body weight of female Ettawa grade goat using its body measurements. Adv. Anim. Vet. Sci., 8(11): 1142-1146. https://doi.org/10.17582/journal.aavs/2020/8.11.1142.1146
de Villiers J F, Gcumisa S T, Gumede S A (2009). Estimation of live body weight from the heart girth measurement in KwaZulu-Natal goats. Applied Animal Husbandry & Rural Development 2009, Volume 2. Retrieved June 5, 2013, from http://www.mdukatshani.com/resources/Weight%20band%20English.pdf.
Dea D, Melesse A, Mekasha Y (2019). Application of morphometric traits and body indices in assessing the type and function of local goats reared in two districts of Gamo-Gofa Zone, South. Ethiopian J. Anim. Prod., 19(1): 73-90.
Devendra C, Burns M (1983). Comparative slaughter performance and meat quality of Rutana, Gumuz and Washera sheep of Ethiopia supplemented with different levels of concentrate. Open J. Anim. Sci., 10(1):12-19.
Dige MS, Rout PK, Singh MK, Bhusan S, Kaushik R, Gowane GR (2022). Estimates of genetic parameters for linear body measurements and prediction of body weight in goat. J. Anim. Breed Genet., 139(4):423-433. https://doi.org/10.1111/jbg.12677
Eyduran E, Zaborski D, Waheed A, Celik S, Karadas K, Grzesiak W. (2017). Comparison of the predictive capabilities of several data mining algorithms and multiple linear regression in the prediction of body weight by means of body measurements in the indigenous Beetal goat of Pakistan. Pak. J. Zool., 49(1): 257-265. https://doi.org/10.17582/journal.pjz/2017.49.1.257.265
Fajemilehin OKS, Salako AE (2008). Body measurement characteristics of the west African dwarf (WAD) goat in deciduous forest zone of Southwestern Nigeria. Afr. J. Biotechnol., 7(14): 2521-2526.
FAO (2011). Draft guidelines on phenotypic characterization of animal genetic resources. In: Commission on genetic resources for food and Agriculture, 31th regular session, 18-22 July 2011, Rome.
Gunawan A, Jakaria R (2011). Application of linear body measurements for predicting weaning and yearling weight in Bali cattle. J. Anim. Prod., 12:163-168.
Hagreveas SK, Bruce D, Beffa LM (2004). Disaster mitigation options for livestock production in communal farming systems in Zimbabwe. In: Background information and literature review. Bulawayo, Zimbabwe: ICRISAT and FAO Rome, Italy, 56.
Hassan A, Ciroma A (1990). Bodyweight measurements relationship in Nigerian Red Sokoto goats. Available online: https://cgspace.cgiar.org/items/1158c646-32ca-43a9-b339-b89fc4cb2e8b (accessed on 08 February, 2024).
Homann S, Van Rooyen AF, Moyo T, Nengomahsa Z (2007). Goat production and marketing: Baseline information for semi-arid Zimbabwe. P.O. Box 776. Bulawayo,
Idamokoro EM, Muchenje V, Masika PJ. (2018). Influence of genotype, sex and age on selected body measurements of Nguni, Boer and Non-descript goat kids reared under an extensive system of farming in South Africa Trop. Agric., 95(3): 284-294.
Iqbal M, Javed K, Ahmad N (2013). Prediction of body weight through body measurements in Beetal goats. Pak. J. Sci., 65(4): 458-461.
IBM SPSS (2010): Statistical packages for social sciences for windows: base system user’s guide. – IBM statistics, 19. Chicago: SPSS Inc. doi:10.2527/jas.2013-6967
Khan H, Muhammad F, Ahmad R, Nawaz G, Rahimullah A, Zubair M (2006). Relationship of body weight with linear body measurements in goats. J. Agric. Biol. Sci., 1:51-54.
Khargharia G, Kadirvel G, Kumar S, Doley S, Bharti PK, Mukut D (2015). Principal component analysis of morphological traits of Assam Hill goat in eastern Himalayan India. J. Anim. Plant Sci., 25(5): 1251-1258.
Lawrence TL, Fowler VR. (1997). Growth of farm animals. Wallingford, Oxon, UK: CAB International; pp. 330.
Machebe NS, Ezekwe AG (2010). Predicting body weight of growing-finishing gilts raised in the tropics using linear body measurements. Asian J. Exp. Biol. Sci., 1:162-165.
Mahilet D (2012). Characterization of Hararghe Highland goat and their production system in Eastern Hararghe. MSc thesis, submitted to the school of graduate studies of Haramaya University, Ethiopia.
Matika O, Sibanda R, Beffa, ML (1992). Eruption of permanent incisors in indigenous goats and sheep. In: Rey, B., S.H.B. Lebbie, and L. Reynolds (eds). Small Ruminant Research and Development in Africa proceedings of the first biennial conference of the African small ruminant research network, ILRAD, Nairobi, Kenya, 10-14 December, 1990.pp. 499-504.
Matopos Research Station (2003). Fact Sheet: Animal Genetic Resources (AnGR) Survey.
McGregor BA (2011). Incisor development, wear and loss in sheep and their impact on ewe production, longevity and economics: A review. Small Rumin. Res., 95(2-3): 79-87. https://doi.org/10.1016/j.smallrumres.2010.11.012. https://doi.org/10.1016/j.smallrumres.2010.11.012
Mendes M, Karabayir A, Pala A (2005). Path analysis of the relationship between various body measures and live weight of American Bronze turkeys under three different lighting programs. Tarim Bilim Derg. 11: 184-188. https://doi.org/10.1501/Tarimbil_0000000408
Mokoena K, Molabe KM, Sekgota MC, Tyasi TL (2022). Predicting body weight of Kalahari Red goats from linear body measurements using data mining algorithms. Vet World. 15(7):1719-1726. https://doi.org/10.14202/vetworld.2022.1719-1726
Muhammad HA, Garba Y, Ogah DM (2021). Multivariate analysis of morphometric differentiation in the red Sokoto and Boer goats. Adv. Anim. Vet., 9(4): 595-603. https://doi.org/10.17582/journal.aavs/2021/9.4.595.603
Musa AM, Idam NZ, Elamin KM (2012). Regression analysis of linear body measurements on live weight in Sudanese Shugor Sheep. Online J. Anim. Feed Res., 2(1): 27-29.
Ncube S (2005). The role of proanthocyanidins and related flavonoids in the utilization of sorghum grain varieties as feed for ruminant in the semi-arid areas of Zimbabwe. PhD. Thesis, University of Zimbabwe, Mt Pleasant, Harare, Zimabwe.
Ojedapo LO, Adedeji TA, Olayeni TB, Adedeji OS, Abdullah AR, Ojebiyi OO (2007): Influence of age and sex on body weight and some body linear measurements of extensively reared WAD goats in derived savannah zone of Nigeria. J. Anim. Vet. Adv., 6: 114-117.
Ojo V, Fayeye TR, Ayorinde KL, Olojede H (2013). Relationship between body weight and linear body measurement in Japanese qual (Cortunix cortunix japonica). J. Sci. Res., 6:175-181. https://doi.org/10.3329/jsr.v6i1.16368
Okpeku M, Yakubu A, Peters S, Ozoje M, Ikeobi C, Adebambo O, Imumorin I (2011). Application of multivariate principal component analysis to morphological characterization of indigenous goats in southern Nigeria. Acta Agric. Slov., 98 (2): 101-109. https://doi.org/10.2478/v10014-011-0026-4
Olatunji-akioye A, Adeyemo OK (2009). Liveweight and chest girth correlation in commercial sheep and goat herds in Southwestern Nigeria. Int. J. Morphol., 27:49-52. https://doi.org/10.4067/S0717-95022009000100009
Rashijane LT, Mbazima VG, Tyasi TL (2012). Prediction of Body Weight from Linear Body Measurement Traits of Boer Goats Raised at Farm Tivolie, Limpopo Province, South Africa. Am. J. Anim. Vet. Sci., 16 (4): 278-288. https://doi.org/10.3844/ajavsp.2021.278.288
Ravimurugan T, Thiruvenkadan AK, Sudhakar K, Panneerselvam S, Elango A (2013). The estimation of body weight from body measurements in Kilakarsal Sheep of Tamil Nadu India. Iran. J. Appl. Anim. Sci., 3(2): 357-360.
Sadick AM, Aryee G, Poku PA, Kyere CG (2020). Relationship between body weight and linear body measurements in the Cobb broiler chicken. WJBPHS. 4(2): 1-6. https://doi.org/10.30574/wjbphs.2020.4.2.0087
Sam I, Ekpo J, Ukpanah U, Eyoh G, Warrie M (2016). Relationship between linear body measurement and live body weight in West African Dwarf goats in Obio Akpa. J. Biol. Agric. Healthcare, 6(16): 118-124.
Seid A, Kebede K, Effa K (2016). Morphological characterization of indigenous goats in Western Ethiopia: implication for community-based breeding programs. Anim. Genet. Resour., 58: 53-62. https://doi.org/10.1017/S2078633616000047
Selolo TC, Mashiloane ML, Norris D, Ng’ambi JW, Brown D (2015). Morphological differentiation of indigenous goats in different agro-ecological zones of Vhembe district, Limpopo province, South Africa. Indian J. Anim. Res., 49 (I4): 527-531. https://doi.org/10.5958/0976-0555.2015.00052.7
Sikosana JLN, Senda TS (2007). Goat farming as a business: A farmer’s manual to successful goat production and marketing. Supported by SNV, Netherlands Development Organization.49pp.
Singh SG, Kaur A, Kumar B (2020). Predicting the body weight using appropriate regression model in beetal goat kids. Theriog. Insig., 10(1): 01-06. https://doi.org/10.30954/2277-3371.01.2020.1
Skapetas B, Sinapis E, Hatziminaouglou J, Karalazos A, Katanos J (2006). Effect of age at slaughter on carcass characteristics and carcass composition in lambs of mountain Greek breeds. Czech J. Anim. Sci., 51(7):311-317. https://doi.org/10.17221/3944-CJAS
Sungirai M, Masaka L, Benhura TM (2014). Validity of Weight Estimation Models in Pigs Reared under Different Management Conditions. Vet. Med. Int., 1-5. http://dx.doi.org/10.1155/2014/530469. https://doi.org/10.1155/2014/530469
Tadesse A, Gebremariam T, Gangwar SK (2012). Application of linear body measurements for predicting body weight of Abergelle goat breed in Tigray region, Northern-Ethiopia. J. BioSci. Biotechnol., 1:314-319.
Thiruvenkadan AK (2005). Determination of best-fitted regression model for estimation of body weight in Kanni Adu Kids under farmer’s management system. Livest. Res. Rural Dev., 17: 1-11.
Tsegaye D, Belay B, Haile A (2013). Linear body measurements as predictor of body weight in Hararghe Highland goats under farmers’ environment: Ethiopia. Global Veterinaria, 11(5): 649-656.
Tyasi TL, Makgowo KM, Mokoena K, Rashijane LT, Mathapo MC, Danguru LW, Molabe KM, Bopape PM, Mathye ND, Maluleke D (2020). Multivariate adaptive regression splines data mining algorithm for prediction of body weight of Hy-line silver brown commercial layer chicken breed. Adv. Anim. Vet. Sci., 8(8): 794-799. https://doi.org/10.17582/journal.aavs/2020/8.8.794.799
Van Rooyen AF, Freeman A, Moyo S, Rohrback D (2007). Livestock development in southern Africa. Future Research and Investment Priorities. ICRISAT Bulawayo, Zimbabwe.
Variedades DT (2010). Morphostructural characteristics of three varieties of greybreasted helmeted guinea fowl in Nigeria. Int. J. Morphol., 28(2): 557-562 https://doi.org/10.4067/S0717-95022010000200036
Vilakazi NB, Ncobela CN, Kunene NW, Panella F (2020). Determining the morphological structure of indigenous chickens using multivariate principal component analysis of body measurements. Appl. Anim. Husb. Rural Dev. 13: 69-75. https://www.sasas.co.za/wp-content/ uploads/2020/09/Vilakazi-BN_2020-Vol-13-1.pdf
Ward HK, Richardson FD, Denny RP, Dye PJ (1979). Matopos Research Station: A perspective: Rhod. agric. J., 76(1): 5-18.
Wilson RT, Durkin JW (1984). Age at permanent incisors eruption in indigenous goats and sheep in semi-arid Africa. Livest. Prod. Sci., 11(I4): 451-455. https://doi.org/10.1016/0301-6226(84)90056-3
Yakubu A, Ladokun AO, Adua, MM (2011). Bioprediction of body weight from zoometrical traits of non-descript goats using linear and non-linear models in North Central Nigeria. Livest. Res. Rural Dev. 23:130.
Yakubu A, Muhammed MM, Ari MM, Musa-Azara IS, Omeje JN (2015). Correlation and path coefficient analysis of body weight and morphometric traits of two exotic genetic groups of ducks in Nigeria. Bangladesh J. Vet. Anim. Sci., 44: 1-9. https://doi.org/10.3329/bjas.v44i1.23112
Yakubu A, Salako AE (2009). Path coefficient analysis of body weight and morphological traits of Nigerian indigenous chickens. Egypt. Poult. Sci., 29: 837-850.
To share on other social networks, click on any share button. What are these?