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International Journal of
eISSN: 2574-9862

Avian & Wildlife Biology

Research Article Volume 2 Issue 1

Comparison of nonlinear models describing growth curves of broiler chickens fed on different levels of corn bran

Abbas Masoudi, Arash Azarfar

Department of Animal Science, Lorestan University, Iran

Correspondence: Abbas Masoudi, Department of Animal Science, Lorestan University, Khoramabad, Lorestan, Iran

Received: May 13, 2017 | Published: June 13, 2017

Citation: Masoudi A, Azarfar A. Comparison of nonlinear models describing growth curves of broiler chickens fed on different levels of corn bran. Int J Avian & Wildlife Biol. 2017;2(1):334-39. DOI: 10.15406/ijawb.2017.02.00012

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Abstract

This study compared four nonlinear models to describe growth parameters of broiler chicken fed on different levels of corn bran. Two experiments were designed for this purpose. In the first experiment, 80 chickens (308 Ross strain) that had been fed on the same diet and weighed separately were used to determine the best model. Indicators of R2, ACI and the number of circulation of the model were used to confirm the best model. In the second experiment, 300 one-day-old Ross 308 broiler chickens were used in a completely randomized design with four treatments and five replicates. The treatments included control and diets contained 2.5, 5 and 7.5% corn bran. Results showed that the Gompertz function had the highest R2 and the lowest AIC and number of iterations. So, the Gompertz model best described the broiler growth curves. R2, AIC values and number of iterations of the Gompertz model were 0.9970, 648 and 5, respectively. Different levels of corn bran significantly affected mature body weight (Wf) and body weight at the inflection point (Wi) (P<0.05), but did not affect the initial body weight (W0), inflection point (Ti) and coefficient of relative growth (b) (P>0.05). Additionally, corn bran significantly decreased the growth rate on days 21, 28, 35 and 42 (P<0.05), but had no significant effect on the growth rate on days 7 and 14 (P>0.05). Overall, the results showed that the Gompertz model described the biological curves of broiler fed on corn bran better than other models. Also, growth parameters were affected by corn bran.

Keywords: corn bran, gompertz model, growth curve, nonlinear models

Introduction

The process of growth measured as body weight on a longitudinal time frame has often been summarized using mathematical models fitted to growth curves. One of the objectives of curve fitting is to describe the course of body weight increase over time with mathematical parameters that are biologically interpretable.1 In models of animal production systems, growth curves are used to provide estimates of daily feed requirements for growth. These estimates are used in providing total feed requirements, which sets an upper limit to feed intake when animals are given ad libitum access to feeds.2 The mathematical models for describing growth kinetics are important tools to examine biological parameters, such as body weight at specific time, maximum growth response, and body weight at maturity, growth rates, inflection point, and body weight at the inflection point. Numerous growth functions have been developed to describe and fit the nonlinear sigmoid relationship between growth and time or age. Growth characteristics of poultry have been described by some nonlinear mathematical models such as Gompertz, Brody, Bertalanffy, Weibull, negative exponential, Hyperbolastic Models and logistic growth functions in broiler chicken,3–5 ducks,6 pearl gray guinea fowl,7 turkey8 and Japanese quail.9

According to,10 fiber is a nutritionally, chemically and physically heterogeneous substance. It may be divided into insoluble fibers which are less viscous and fermentable and soluble fibers which are viscous and fermentable. Both insoluble and soluble fibers have different roles in the digestion and absorption processes in the gastrointestinal tract (GIT). Dietary fiber encompasses very various polymers with large differences in physicochemical properties that, when included in the diet, result in differences in ion exchange capacity, fermentation capability, digestive viscosity, and bulking effect in the GIT.11,12 The beneficial effects of fiber were also shown to be related to the decreased gizzard pH, which was accompanied by improved nutrient utilization to increase growth.13 In addition, fiber can provide a fermentative substrate for the large intestinal flora, and a healthy microflora could decline the incidence of intestinal problems such as necrotic enteritis.14 In terms of weight gain (WG),15 observed that the addition of 3% of either oat hull or sugar beet pulp improved weight gain from day 1 to day 21. Also,16 found that WG was increased by the inclusion of insoluble fiber in the broilers' diet. But,17 reported that an inclusion of 4% oat hull in the diet increased feed intake (FI) in broiler chickens without affecting18 reported that a high rate of fiber inclusion (up to 12-16%) could reduce the body weight due to depressed FI in chickens from day 14 to day 35. Also,19 observed that inclusions of 5 and 10% of insoluble fiber increased feed conversion ratio (FCR) and FI but reduced WG.

So, the objectives of this study was to compare five nonlinear models including logistic, Gompertz, Lopez, Richards and Von Bertalanfi for describing growth parameters of broiler chicken and to use the best model to describe growth parameters of broiler chicken fed on different levels of corn bran.

Materials and methods

Experiment 1

Chickens, diets and experimental design:Eighty male and female chicks (Ross 308) were

Raised in a deep litter system. Feed and water were provided ad libitum. The birds were fed on a starter diet (2,900 kcal of ME/kg and 21.5% CP) from day 1 through day 21, and a grower diet (3,050 kcal of ME/kg and 19.5% CP) from day 22 through day 42. Temperature started at 33°C and was reduced by 2.8 °C per week until 21 °C was attained. The birds were individually weighed at 0900 AM and body weights were recorded on every other day for 42 days. Six of the 80 birds died before the end of 42 d. The dead birds were not included in the study. The average body weights of the remaining 74 birds were used as the data for the growth curve to be modeled.

Nonlinear models: Four growth models including Logistic, Gompertz, Lopez and Richards were fitted to data using NLIN procedure of the SAS (SAS Institute Inc., 2001) for the evaluation of the growth parameters (Table 1). The models and equations are shown in. In all models,Wt refers to live body weight (g) at age t (day), W0 is the initial body weight (g), b is the coefficient of relative growth or maturing index (smaller b indicates later maturity, while larger b indicates earlier maturity); t is the age of bird (day) and Wf is the mature body weight (g). The derived parameters were, then, used to estimate the inflection point Ti (day); body weight at the inflection point (g; wi) and growth rate (GR; g/day).

 

Mathematical Expression

Weight at Inflection (W*)

Time to Inflection (t*)

Growth Rate (dw/dt)

Gompertz

w = w 0 * e x p ( ( 1 e x p ( b * t ) ) * ( l o g ( w f / w 0 ) ) ) MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qacaWG3bGaeyypa0Jaam4DaiaaicdacaGGQaGaamyzaiaadIha caWGWbWdamaabmaabaWaaeWaaeaapeGaaGymaiabgkHiTiaadwgaca WG4bGaamiCa8aadaqadaqaa8qacqGHsislcaWGIbGaaiOkaiaadsha a8aacaGLOaGaayzkaaaacaGLOaGaayzkaaWdbiaacQcapaWaaeWaae aapeGaamiBaiaad+gacaWGNbWdamaabmaabaWdbiaadEhacaWGMbGa ai4laiaadEhacaaIWaaapaGaayjkaiaawMcaaaGaayjkaiaawMcaaa GaayjkaiaawMcaaaaa@560B@

0.368 W f MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qacaaIWaGaaiOlaiaaiodacaaI2aGaaGioaiaadEfal8aadaWg aaqcfayaaKqzadWdbiaadAgaaKqba+aabeaaaaa@3EBB@

1 b [ ln ( l n ( W f W 0 ) ) ] MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qadaWcaaWdaeaapeGaaGymaaWdaeaapeGaamOyaaaadaWadaWd aeaapeGaaeiBaiaab6gadaqadaWdaeaapeGaamiBaiaad6gadaqada WdaeaapeWaaSaaa8aabaWdbiaadEfapaWaaSbaaKqbGeaapeGaamOz aaqcfa4daeqaaaqaa8qacaWGxbWdamaaBaaajuaibaWdbiaaicdaa8 aabeaaaaaajuaGpeGaayjkaiaawMcaaaGaayjkaiaawMcaaaGaay5w aiaaw2faaaaa@477C@

b W l n ( W f W ) MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qacaWGIbGaam4vaiaadYgacaWGUbWaaeWaa8aabaWdbmaalaaa paqaa8qacaWGxbWdamaaBaaabaqcLbmapeGaamOzaaqcfa4daeqaaa qaa8qacaWGxbaaaaGaayjkaiaawMcaaaaa@40E1@

Logistic

w = w 0 * W f / ( W 0 + ( W f W 0 ) * e x p ( b * t ) ) MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qacaWG3bGaeyypa0Jaam4DaiaaicdacaGGQaGaam4vaiaadAga caGGVaWdamaabmaabaWdbiaadEfacaaIWaGaey4kaSYdamaabmaaba WdbiaadEfacaWGMbGaeyOeI0Iaam4vaiaaicdaa8aacaGLOaGaayzk aaWdbiaacQcacaWGLbGaamiEaiaadchapaWaaeWaaeaapeGaeyOeI0 IaamOyaiaacQcacaWG0baapaGaayjkaiaawMcaaaGaayjkaiaawMca aaaa@5071@

0.5 W f MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qacaaIWaGaaiOlaiaaiwdacaWGxbWdamaaBaaajuaqbaWdbiaa dAgaa8aabeaaaaa@3B34@

1 b l n ( W f W 0 W 0 ) MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qadaWcaaWdaeaapeGaaGymaaWdaeaapeGaamOyaaaacaWGSbGa amOBamaabmaapaqaa8qadaWcaaWdaeaapeGaam4va8aadaWgaaqcfa saa8qacaWGMbaajuaGpaqabaWdbiabgkHiTiaadEfapaWaaSbaaKqb GeaapeGaaGimaaWdaeqaaaqcfayaa8qacaWGxbWdamaaBaaajuaiba Wdbiaaicdaa8aabeaaaaaajuaGpeGaayjkaiaawMcaaaaa@4581@

b W ( 1 W f W ) MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qacaWGIbGaam4vamaabmaapaqaa8qacaaIXaGaeyOeI0YaaSaa a8aabaWdbiaadEfapaWaaSbaaKqbGeaapeGaamOzaaqcfa4daeqaaa qaa8qacaWGxbaaaaGaayjkaiaawMcaaaaa@3FA5@

Lopez

w = ( w 0 * k * * b + w f * t * * b ) / ( k * * b + t * * b ) MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcLbsaqaaaaa aaaaWdbiaadEhacqGH9aqpjuaGpaWaaeWaaOqaaKqzGeWdbiaadEha caaIWaGaaiOkaiaadUgacaGGQaGaaiOkaiaadkgacqGHRaWkcaWG3b GaamOzaiaacQcacaWG0bGaaiOkaiaacQcacaWGIbaak8aacaGLOaGa ayzkaaqcLbsapeGaai4laKqba+aadaqadaGcbaqcLbsapeGaam4Aai aacQcacaGGQaGaamOyaiabgUcaRiaadshacaGGQaGaaiOkaiaadkga aOWdaiaawIcacaGLPaaaaaa@5364@

[ ( 1 + 1 b ) W 0 + ( 1 1 b ) W f ] 2 MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qadaWcaaWdaeaapeWaamWaa8aabaWdbmaabmaapaqaa8qacaaI XaGaey4kaSYaaSaaa8aabaWdbiaaigdaa8aabaWdbiaadkgaaaaaca GLOaGaayzkaaGaam4va8aadaWgaaqcfasaa8qacaaIWaaapaqabaqc fa4dbiabgUcaRmaabmaapaqaa8qacaaIXaGaeyOeI0YaaSaaa8aaba Wdbiaaigdaa8aabaWdbiaadkgaaaaacaGLOaGaayzkaaGaam4va8aa daWgaaqcfasaa8qacaWGMbaapaqabaaajuaGpeGaay5waiaaw2faaa WdaeaapeGaaGOmaaaaaaa@4AAA@

K [ b 1 b + 1 ] 1 b MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qacaWGlbWaamWaa8aabaWdbmaalaaapaqaa8qacaWGIbGaeyOe I0IaaGymaaWdaeaapeGaamOyaiabgUcaRiaaigdaaaaacaGLBbGaay zxaaWdamaaCaaajuaibeqaaKqba+qadaWccaqcfaYdaeaapeGaaGym aaWdaeaapeGaamOyaaaaaaaaaa@4204@

b ( t b 1 K b + t b ) ( W f W ) MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qacaWGIbWaaeWaa8aabaWdbmaalaaapaqaa8qacaWG0bWdamaa Caaajuaibeqaa8qacaWGIbGaeyOeI0IaaGymaaaaaKqba+aabaWdbi aadUeapaWaaWbaaeqajuaibaWdbiaadkgaaaqcfaOaey4kaSIaamiD a8aadaahaaqcfasabeaapeGaamOyaaaaaaaajuaGcaGLOaGaayzkaa WaaeWaa8aabaWdbiaadEfapaWaaSbaaKqbGeaapeGaamOzaaWdaeqa aKqba+qacqGHsislcaWGxbaacaGLOaGaayzkaaaaaa@4ACD@

Richards

w = ( w 0 * W f ) / ( W 0 * * n + ( W f * * n W 0 * * n ) * e x p ( b * t ) ) * * ( 1 / n ) MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qacaWG3bGaeyypa0ZdamaabmaabaWdbiaadEhacaaIWaGaaiOk aiaadEfacaWGMbaapaGaayjkaiaawMcaa8qacaGGVaWdamaabmaaba WdbiaadEfacaaIWaGaaiOkaiaacQcacaWGUbGaey4kaSYdamaabmaa baWdbiaadEfacaWGMbGaaiOkaiaacQcacaWGUbGaeyOeI0Iaam4vai aaicdacaGGQaGaaiOkaiaad6gaa8aacaGLOaGaayzkaaWdbiaacQca caWGLbGaamiEaiaadchapaWaaeWaaeaapeGaeyOeI0IaamOyaiaacQ cacaWG0baapaGaayjkaiaawMcaaaGaayjkaiaawMcaa8qacaGGQaGa aiOka8aadaqadaqaa8qacaaIXaGaai4laiaad6gaa8aacaGLOaGaay zkaaaaaa@5EA9@

Wf/(n+1)(1⁄n)

1 b l n ( W f n W 0 n n W 0 n ) MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qadaWcaaWdaeaapeGaaGymaaWdaeaapeGaamOyaaaacaWGSbGa amOBamaabmaapaqaa8qadaWcaaWdaeaapeGaam4va8aadaqhaaqcfa saa8qacaWGMbaapaqaa8qacaWGUbaaaKqbakabgkHiTiaadEfapaWa a0baaKqbGeaapeGaaGimaaWdaeaapeGaamOBaaaaaKqba+aabaWdbi aad6gacaWGxbWdamaaDaaajuaibaWdbiaaicdaa8aabaWdbiaad6ga aaaaaaqcfaOaayjkaiaawMcaaaaa@496E@

b W ( W f n W n n W f n ) MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq=Jc9 vqaqpepm0xbba9pwe9Q8fs0=yqaqpepae9pg0FirpepeKkFr0xfr=x fr=xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaqcfaieaaaaaa aaa8qacaWGIbGaam4vamaabmaapaqaa8qadaWcaaWdaeaapeGaam4v a8aadaqhaaqcfasaa8qacaWGMbaapaqaa8qacaWGUbaaaKqbakabgk HiTiaadEfapaWaaWbaaeqajuaibaWdbiaad6gaaaaajuaGpaqaa8qa caWGUbGaam4va8aadaqhaaqcfasaa8qacaWGMbaapaqaa8qacaWGUb aaaaaaaKqbakaawIcacaGLPaaaaaa@46B6@

Table 1 Mathematical description of growth models, biological parameters and growth evaluators.

The treatments included control and diets contained 2.5 (T1), 5 (T2) and 7.5 (T3) percentage of corn bran

Four models were fitted to the data by nonlinear regression using the NLIN procedure of SAS (2001). To select the best model, three principal criteria of adjustment, including  coefficient of determination (R2), number of iterations and Akaike information criterion (AIC) were used [20,21,22]. For each of these criteria, the optimum status was the highest level of the determinati on coefficient (pseudo R2), the smallest number of the iterations needed, and the lowest value of the Akaike information criterion [23]. The Akaike information criterion was calculated as;

AIC = n × ln ( SSE n ) + 2 P MathType@MTEF@5@5@+= feaagKart1ev2aqatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqiVu0Je9sqqrpepC0xMi=hEeeu0xXdbba9frFj0=OqFf ea0dXdd9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr 0=vqpWqaaeaabiGaciaacaqabeaadaqaaqaaaOqaaKqbacbaaaaaaa aapeGaaeyqaiaabMeacaqGdbGaeyypa0JaaeOBaiabgEna0kaabYga caqGUbWaaeWaa8aabaWdbmaalaaapaqaa8qacaqGtbGaae4uaiaabw eaa8aabaWdbiaab6gaaaaacaGLOaGaayzkaaGaey4kaSIaaGOmaiaa bcfaaaa@464A@

Where, p is the number of parameters +1, SSE is the residuals sum of squares and n is the number of observations.

Experiment 2

Chickens, diets and experimental design: Three hundred one-day-old Ross 308 male

Broiler chickens were used in a completely randomized design with four treatments and five replicates 15 chicks for each replicate), in days 1 to 42 of the growing phase.  The chickens received diets containing 0 (control), 2.5 (T1), 5 (T2) and 7.5% (T3) of corn bran. All chickens were fed on starter (1-21 days), and grower (22-42 days) diets according to Nutritional Requirements of Poultry.24 This diet was iso energitic and isonitogenic. The ingredients and nutrient contents of the diets are shown in (Table 2). Chickens in each pen were weighed together every three days. Prior to trial commencement, corn bran was purchased from a commercial supplier and was ground using hammer mill (2 mm screen) and analyzed for chemical composition (Table 3). Dry matter (DM), crude protein (CP) and Ether extract (EE) of fiber sources were determined as per the methods described by AOAC.25

 

Ingredient

Starter (1-21)

Grower (22-42)

Control

T1

T2

T3

Control

T1

T2

T3

Corn

54.86

50.70

46.54

42.39

59.32

55.98

52.66

49.32

Soybean Meal-44

38.64

39.29

39.96

40.60

33.75

33.86

33.96

34.07

Corn bran

0

2.5

5

7.5

0

2.5

5

7.5

Oil

1.70

2.76

3.84

4.89

3.12

3.91

4.71

5.50

Calcium carbonate

1.17

1.15

1.13

1.12

1.00

0.96

0.92

0.89

Dical. Phos.

1.90

1.9

1.88

1.87

1.47

1.46

1.45

1.43

Sodium bicarbonate

0.09

0.09

0.08

0.08

0.18

0.17

0.17

0.17

Vit & Min Premix

0.50

0.50

0.50

0.50

0.50

0.50

0.50

0.50

Common salt

0.32

0.32

0.32

0.31

0.27

0.27

0.26

0.26

DL-Methionine

0.33

0.33

0.33

0.33

0.21

0.22

0.22

0.22

L-Lysine

0.32

0.30

0.28

0.28

0.13

0.12

0.11

0.10

Theronin

0.17

0.16

0.14

0.13

0.05

0.05

0.04

0.04

Calculated composition

ME (Kcal/kg)

2900

2900

2900

2900

3050

3050

3050

3050

Protein (%)

21.50

21.50

21.50

21.50

19.50

19.50

19.50

19.50

Calcium (%)

0.96

0.96

0.96

0.96

0.79

0.79

0.79

0.79

Phos. (%)

0.48

0.48

0.48

0.48

0.63

0.64

0.64

0.65

Lysine (%)

1.28

1.28

1.28

1.28

1.03

1.00

1.03

1.03

Met+Cys(%)

0.95

0.95

0.95

0.95

0.80

0.80

0.80

0.80

Table 2 Chemical composition of corn bran (CB).

Chemical Composition of Corn Bran (CB)

Dry matter (%)

95.63

Organic mater

98.94

Ash (%)

1.06

Crude protein (%)

10.43

Ether extract (%)

1.02

Acid detergent fiber (%)

39.81

Neutral detergent fiber (%)

67.32

Calcium (%)

0.67

Table 3 N=57; Epidemiological distribution of the pathological fractures, traumatic fractures, and nonunion.

Statistical analyses: Data were analyzed using the general linear models (GLM) procedure of SAS (2001; SAS Inst. Inc., Cary, NC). Tukey-Kramer method was used to compare treatment means at P<0.05.

Results and discussion

Experiment 1

Growth models have been widely used to represent changes in size of body with age or time so that the genetic potential of animals for growth can be evaluated and nutrition can be matched to possible growth. Also, growth models are used to provide estimates of daily feed requirements for growth (Lopez et al., 2000). Comparisons of the models by R2, number of iterations and Akaike information criterion (AIC) are shown in Table 4. Regarding the goodness of fit criteria, all models were suitable for describing the growth of the broiler chicken. Among all nonlinear models used, the smallest AIC and the lowest number of iterations were calculated for the Gompertz function. The Gompertz model best described the growth curves for body weight of broiler chicken, with R2, AIC values and number of iterations being 0.9970, 648 and 5, respectively. The Gompertz model is one of the most common models to describe broiler growth curve. In this model, the growth curve is asymmetric around the point of maximum growth rate. However, the point of inflection in Gompertz model is fixed26,27 compared the  Logistic, Gompertz, Von Bertalanfi, Morgan-Mercer-Flodin (MMF)  and Weibull  growth models and suggested  that MMF, Weibull and Gompertz models can be useful for explaining  broiler chickens growth performance.  Compared the Richards, logistic, Gompertz and spline linear regression models for describing chicken growth curves. This researcher reported that the spline model had the poorest fit to the data as compared with the other three nonlinear models.

Models

W0

B

Wf

K\n

wi

Ti

Iterations

R2

AIC

Gompertz

31.73 (1.90)

0.053 (0.001)

3623 (68)

-

1334

29.28

5

0.9970

648

Logestic

77.68 (2.36)

0.122 (0.001)

2561 (25)

-

1281

28.36

9

0.9960

672

Lopez

47.49 (6.50)

2.119 (0.049)

5155 (291)

49.07 (2.34)

1396

30.25

13

0.9969

655

Richards

25.10 (4.53)

0.047 (0.005)

3956 (251)

-0.106 (0.064)

1374

14.90

10

0.9970

655

Table 4 N=57; Epidemiological distribution of the pathological fractures, traumatic fractures, and nonunion.

The parameters estimated by four models are presented in (Table 4). In this study, the Logestic model and Richards model exhibited the highest (77.68) and lowest (25.09) W0, respectively. Also, the Richards model had the lowest b parameter but the Lopez model had the highest one. The final weight (Wf) was estimated between 2561 g and 5155 g and the Lopez and Logestic model had the minimum and maximum Wf, respectively.28,29 found that Gompertz gave a higher estimate than the Logistic and Richards models for parameter A in male and female turkeys. Body weight at the inflection point (g; wi) was 1281 g for the Logestic model and 1396 g for the Lopez model, which were the lowest and highest wi, respectively. Time of inflection point was measured between 14.9 to 68.54 days. The Richard model had the lowest estimation and Von had the highest one. Approximate correlation matrix of Gompertz parameters is shown in (Table 5) Correlation between W0 and b parameters was high and negative (-0.9410502), but a high and positive correlation (0.8341997) was observed between W0 and Wf. However, b and Wf were correlated strongly and negatively (-0.9652989).

Parameter

W0

B

Wf

W0

1

-0.9410502

0.8341997

B

-0.9410502

1

-0.9652989

Wf

0.8341997

-0.9652989

1

Table 5 Approximate correlation matrix of the Gompertz parameters.

W0: the initial body weight (g); b: coefficient of relative growth; Wf: mature body weight (g)

Experiment 2

The effect of the different levels of corn bran on weekly body gain is presented in (Table 6) Results indicated the loss of body weight with the increase in corn bran from 0 to 7.5 percent in diet. In the end of period, i.e. day 42, the final body weight was lower when corn bran was included in the diet (P<0.05). Birds fed on control diet (0 % CB) had the highest final body weight (2324 g) while birds fed on diets containing 7.5% corn bran had the lowest final body weight at the end of the period (P<0.05).

Treatments

Day 7

Day 14

Day 21

Day 28

Day 35

Day 42

Control

138.9

353.7

777.0

1282.1a

1727.4a

2324.7a

T1

133.3

345.4

756.5

1179.4b

1615.0b

2151.6b

T2

132.2

335.4

741.7

1181.7b

1636.4b

2122.9b

T3

127.8

341.3

749.3

1202.7b

1622.8b

2111.7b

SEM

3.38

8.27

14.73

16.75

29.59

36.44

P-Value

0.201

0.448

0.433

0.002

0.037

0.002

Table 6 Effect of different levels of corn bran on weekly body weight (g).

The treatments included control (0%) and diets contained 2.5 (T1), 5 (T2) and 7.5 (T3) percentage of corn bran, SEM: standard error of treatment means.

The effect of different levels of corn bran on growth parameters including W0: the initial body weight (g), Wf: mature body weight (g), wi: body weight at the inflection point (g), b: coefficient of relative growth, and Ti: inflection point (day) is shown in (Table 7). Wf and wi of the treated chickens were significantly different (P<0.05). Birds fed on diet 1 (control) had the highest Wf and wi while birds fed on diet 4 had the lowest Wf and wi. However, there was no significant difference (P>0.05) between birds fed on diet 2 and control. Wf and wi decreased linearly with the increase in corn bran percent in diet (P<0.05). The different levels of corn bran did not affect W0, b and Ti (P>0.05). The estimated growth rates (GR) of the birds fed on different levels of fiber are shown in Table 8. Growth rate on days 21, 28, 35 and 42 was significantly affected by experimental treatments (P<0.05), but on days 7 and 14, it was not affected by treatments (P>0.05). The birds fed on diet containing 0 and 7.5 % corn bran displayed the highest and lowest GR, respectively. GR on days 21, 28, 35 and 42 decreased linearly with the increase in corn bran in diet (P<0.05).

Treatments

W0

B

Wf

wi

Ti

Control

38.97

0.0493

4195a

1543a

31.58

T1

41.09

0.0492

3810ab

1402ab

30.99

T2

32.63

0.0527

3524b

1296b

29.3

T3

31.89

0.0542

3426b

1260b

28.58

SEM

2.94

0.0016

172

62

0.952

P-Value

0.248

0.191

0.031

0.031

0.154

Linear

0.078

0.069

0.006

0.0061

0.078

Quadratic

0.699

0.678

0.454

0.4545

0.095

Table 7 The effect of different levels of fiber on growth parameters.

W0: the initial body weight (g); Wf: mature body weight (g); wi: body weight at the inflection point (g), b: coefficient of relative growth; Ti: inflection point (day); The treatments included control (0%) and diets containing 2.5 (T1); 5 (T2) and 7.5 (T3) percentage of corn bran; SEM: standard error of treatment means.

Treatments

GR7

GR14

GR21

GR28

GR35

GR42

Control

23.19

42.84

64.06

74.18a

74.59a

66.64a

T1

21.82

40.47

59.68

67.40b

67.44b

59.78ab

T2

22.85

41.5

60.67

67.82b

65.82b

56.35b

T3

22.71

42.38

60.97

67.24b

63.93b

53.93b

SEM

0.629

0.855

0.951

1.621

2.198

2.748

P-Value

0.512

0.272

0.012

0.012

0.016

0.033

Linear

0.880

0.930

0.051

0.010

0.004

0.007

Quadratic

0.372

0.089

0.021

0.075

0.272

0.477

Table 8 The effect of different levels of corn bran on growth rate (g/day).

Treatments included control (0%) and diets containing 2.5 (T1), 5 (T2) and 7.5 (T3) percentage of corn bran, GR: Growth Rate, SEM: Standard Error of Treatment Means.

Higher fiber concentrations in chick diets can have negative effects on nutrient digestion and absorption30 and may subsequently affect performance as seen in the ADG response of the broiler chicks in the current experiment. Insoluble fiber in monogastric diets has for long been considered as diluent of nutrients.31 The little or no degradation of insoluble fiber in chickens results in increased bulk of digest in the intestinal tract. This makes its effect on microbial population quite insignificant.32,33 Since diets high in insoluble fiber contain low energy, birds tend to increase feed consumption as a way to compensate for the reduced nutrient concentration in feed.34 There are suggestions that fiber decreases nutrient digestion because it encapsulates nutrients into the plant cell causing a reduction in the activity of digestive enzymes. In some cases, some fiber sources may cause pancreatic enlargement, leading to an increase in secretions.35 In a study on turkeys,36 indicated that an increase in the fiber content of the diet reduced performance so that an increase in the crude fiber content of the diet from 3 to 9% reduced body weight from 1 to 4 wk of age. Studied the effects of fiber sources by adding 3% oat husks and soybean hulls into a basal diet containing 2.5% crude fiber in comparison with the control diet containing 1.5% crude fiber.

They reported that adding raw fiber sources had no effect on average daily feed intake from day 1 to day 21 of the age, but it improved the average daily weight gain and feed conversion ratio (FCR). Adding fiber to the diet improves bowel function and development of the digestive system, increases the production of hydrochloric acid (HCl), bile acids and secretion of digestive juices,37 changes the composition and gastrointestinal tract micro flora population of poultry and pig laboratory conditions38 and breeding conditions.39-41 So, the positive effects of adding fiber on growth performance of broiler chickens is related to the improvement of the digestibility of nutrients and metabolic pathways changes.42 All this information is consistent with our hypothesis that the effects of dietary fiber on broiler performance depend on the source and level of fiber used.

Conclusion

In conclusion, different models were used to monitor the growth of birds in the poultry industry. This study used the logistic, Gompertz, Lopez and Richards models. The Gompertz growth model was the best describing the growth curves for body weight of broiler chickens. The estimated values of growth parameters in the experimental diets containing different levels of fiber were lower than the control group.

Acknowledgements

None.

Conflict of interest

The author declares no conflict of interest.

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