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. 2025 Dec 28;105(3):106356. doi: 10.1016/j.psj.2025.106356

Comparative analysis of classical growth models and artificial neural networks in predicting egg production parameters in three commercial broiler parent stocks

Zahra Moradi Gharajeh 1, Hassan Darmani Kuhi 1,, Navid Ghavi Hossein-Zadeh 1
PMCID: PMC12828518  PMID: 41529496

Abstract

In the rapidly evolving poultry industry, effective management is dependent on precise forecasting of production metrics. As producers seek to maximize yield while minimizing costs, the ability to accurately predict egg production parameters becomes essential. Traditional growth models have long been employed for this purpose, but with advancements in computational techniques, artificial neural networks (ANNs) present a promising alternative. This paper examines the efficacy of various classical growth models, Gamma, compartmental, logistic, curvilinear Gompertz, Richards, and Morgan models, alongside a multi-layer feed-forward ANN model in predicting weekly and cumulative production metrics of three distinct commercial broiler parent stock (Ross, Arbor Acres, and Cobb). The analysis revealed that the Morgan model performed as the most accurate for modeling cumulative data, showcasing a superior fit characterized by high adjusted R² values and low RMSE, AIC, and BIC. In contrast, the Logistic - curvilinear model demonstrated high precision for weekly data. The ANN significantly surpassed the best traditional Logistic curvilinear and Morgan models in predicting weekly and cumulative production metrics based on RMSE, AIC, and BIC criteria (RMSE = 100% both for weekly and cumulative productive metrics, AIC = 91.6% for weekly and 58.3% cumulative productive metrics, and BIC = 66.6% both for weekly and cumulative productive metrics). Although the findings underscore the strength of the classical growth model for cumulative data forecasts in poultry production systems, the advantages of ANNs in the prediction of egg production metrics represent a vital advancement toward more responsive flock management strategies. By integrating classical growth models with ANN approaches, poultry producers can enhance decision-making processes, leading to improved productivity and sustainability. The integration of these methodologies provides a powerful framework for accurate forecasting, ultimately advancing the poultry industry's capacity for efficient production management.

Keywords: Egg production, Artificial neural network (ANN), Growth model, Broiler parent stock, Prediction accuracy

Introduction

Effective management of egg production in layer breeder strains is crucial for optimizing production and ensuring sustainable productivity in the poultry industry (Ghazanfari et al., 2011). Accurate predictions of egg mass, hatching egg production, and overall egg production over time can assist in improving resource allocation, flock management, and profitability by increasing revenue, decreasing costs, or a combination of both. Understanding the egg production curve in broiler breeder hens is key to developing effective nutritional strategies and enhancing management practices. Growth models and artificial intelligence-based approaches, such as artificial neural networks (ANN), provide powerful tools for accurately predicting these properties, contributing to better decision-making and overall performance improvement in poultry operations (Faraji-Arough et al., 2023).

Hatchability is one of the key indicators in poultry production and is highly influenced by egg quality and weight. Various studies have shown that larger eggs generally have higher hatchability rates, and the chicks hatched from them tend to have greater body weights (Alabi et al., 2012a, 2012b). Since egg size is directly related to embryonic growth, residual yolk content, and chick quality, paying attention to this factor can significantly improve the economic efficiency of poultry farms. An increase in egg weight not only enhances hatchability rates but also leads to the production of stronger and healthier chicks, thereby reducing post-hatch mortality (Farooq et al., 2003). Egg weight is a critical trait for assessing both the quality and grading of eggs and is measurable without breaking the shell (Wilson and Suarez, 1993; Farooq et al., 2001). The proportions of internal components (albumen, yolk, and shell) are directly related to the egg's weight, and these proportions can vary significantly depending on the hen’s strain (Pandey et al., 1986). Additionally, the age of the hen plays a vital role in determining egg weight, with a general trend of increasing egg weight as the hen matures, eventually stabilizing toward the end of the laying cycle (Moreno et al., 2024). This indicates that egg weight should be considered not only as a quality indicator but also as a biologically relevant factor in the productive performance of laying hens.

Egg mass is a key factor in reproductive success in poultry, directly influencing hatchability, chick weight, and early growth. Larger eggs are generally associated with higher hatchability rates and heavier, stronger chicks (Krist, 2011; Kumar et al., 2024). This characteristic is also linked to incubation duration, embryonic metabolism, and hatchling size at the time of hatching (Rahn and Ar, 1974; Deeming and Birchard, 2007). From an evolutionary perspective, egg mass represents a trade-off between offspring quality and quantity, and its relationship with body size varies depending on the physiological and ecological traits of the species (Deeming, 2007).

Egg production is defined as the number of eggs laid within a specific period or cumulatively, and mathematical models are essential for describing the laying curve and assessing egg production across different periods (Narinc et al., 2013). There is limited research focusing on modeling egg production in breeder hens due to the longer duration required to track egg production (Narinc et al., 2014).

The egg production curve in hens is similar to the lactation curve in cows (Wood, 1967), and the functions used to describe the lactation curve have also been adapted for modeling egg production (Wolc et al., 2015). These models typically include biologically significant parameters that help in understanding the egg production process (Savegnago et al., 2011).

The Gamma model is the most widely used due to its simplicity and good fit with the data, though compartmental and Logistic-curvilinear models are also employed (Wood, 1967; Gavora et al., 1982; Narinc et al., 2013). The application of appropriate mathematical models is crucial for predicting egg production and making economic decisions in the poultry industry (Aggrey, 2002; Savegnago et al., 2011).

Productive performance in broiler breeder hens is influenced by a complex interaction of genetic, physiological, nutritional, and environmental factors. Understanding and predicting these biological responses are essential for improving management strategies and maximizing production efficiency. While traditional growth models effectively describe the overall production trend, they are limited in capturing the nonlinear and dynamic interactions inherent in biological systems (van der Klein et al., 2020). The inherent variability and interdependence among productive traits highlight the need for advanced modeling approaches capable of capturing and learning complex relationships within biological data. In this context, ANN offer a flexible and powerful alternative, as they can model nonlinear patterns, adapt to complex biological behaviors, and provide more accurate predictions without requiring predefined mathematical assumptions (Ghazanfari et al., 2011). Therefore, integrating ANN with traditional growth models can enhance our understanding of production dynamics and support more precise decision-making in broiler breeder breeding and management programs. Establishing this link between biological principles and model-based prediction is crucial for developing strategies to optimize nutrient use, improve growth performance, and support genetic improvement programs.

Despite many advantages, traditional models have limitations in capturing complex relationships in the data, whereas ANN have demonstrated the ability to model nonlinear relationships and complex patterns in agricultural settings, improving prediction accuracy without explicit assumptions (Zhang et al., 2002). The ANN is an advanced method capable of simulating complex nonlinear relationships between inputs and outputs. Key advantages of ANN include their adaptability to changing inputs and outputs, fault tolerance, and interpolation capabilities (Zhang et al., 2007). Recently, Oliveira et al. (2022) successfully applied ANN models to predict egg-production traits in commercial laying breeder hens, demonstrating their high accuracy and effectiveness in modeling complex biological processes. Bishop (2006) emphasized that the inherent parallel and simultaneous processing capabilities of neural networks significantly improve computational efficiency, leading to their widespread use in solving complex problems across various fields. Multi-layer neural networks, as advanced nonlinear models, can simulate intricate relationships between inputs and outputs by utilizing nonlinear activation functions and adjusting weights across different layers. These networks are highly effective in identifying complex patterns, improving predictions, and supporting decision-making processes. The flexibility and adaptability of these networks make them highly suitable for addressing complex nonlinear challenges, control issues, and predicting critical economic factors such as egg production (Oliveira et al., 2022), growth and reproductive performance (Mehri, 2013), and nutritional requirements (Kaewtapee et al., 2021; Mehri, 2014).

This study provides a novel contribution by simultaneously evaluating the predictive performance of both classical nonlinear models and an ANN across multiple traits and commercial egg-type strains. Unlike previous studies that typically focus on a single trait or genetic line, our comparative approach integrates information across diverse breeder strains and production-related traits, offering a more comprehensive assessment of model efficiency and biological interpretation. This integrated framework enhances our understanding of model performance across genetically diverse populations and supports more precise decision-making in both nutrition and breeding programs.

Materials and methods

Data source

The dataset used in this study was compiled from published information on the objective performance of three widely used commercial broiler parent stocks (Ross 308, Cobb, and Arbor Acres) (Aviagen.com, 2021a, Aviagen.com, 2021b; Cobb-Vantress.com, 2025). For each strain, performance records were obtained from breeder management databases covering the hens' production phase for 40 consecutive weeks, beginning at 23 weeks for Ross 308, 24 weeks for Cobb, and 25 weeks for Arbor Acres, and ending at 62, 63, and 64 weeks of age for each strain, respectively. All data were manually entered into Excel spreadsheets and verified for accuracy and consistency before analysis. The traditional models and ANN were fitted to the data using the nonlinear regression procedure of SigmaPlot (SPSS, 1998) and the ANN option of GMPpro software. This study used only previously published datasets and commercial management records with no new animal experimentation. All original data were collected under ethical standards established in the respective primary sources; therefore, additional institutional animal care or ethics approval was not required for the present secondary analysis.

Modelling weekly egg production metrics

This analysis undertakes a comparative evaluation of three traditional egg production models, Gamma, Compartmental, and the Logistic-curvilinear models, in predicting weekly egg production metrics. Each model presents unique methodologies and assumptions regarding the dynamics of egg production, making it essential to assess their effectiveness in representing key production metrics. The metrics included in this study were: weekly egg production (%), reflecting the percentage of hens laying eggs within a given week; weekly egg mass (g), quantifying the total weight of eggs laid per hen over a week; weekly hatching egg (%), indicating the proportion of eggs suitable for incubation; and weekly egg weight (g), representing the average weight of individual eggs. The structure and properties of the models are as follows:

Gammay=axbecx

In the gamma model, y is the interested egg production metric, a is the initial production, b is the rate of increase to the peak, c is the rate of decrease after the peak, and x is the number of weeks of egg production. Additionally, the week of peak production (b/c) and persistency of peak production (–(b 1)×lnc) can be derived from the model parameters.

Compartmentaly=a(ebxecx)

In the case of the compartmental model, y is the interested egg production metrics, a is the asymptotic value of egg production at the peak of egg-laying, b is the rate of production decrease after the peak (eggs/hen day decrease per week), c is the intermediate rate of weekly increase in egg-laying, and x is the number of weeks of egg production.

Logisticcurvilineary=a(ebx1+ec(xd))

In which, the biological interpretations of the relevant parameters for Logistic-curvilinear are: y = the interested egg production metrics, a = a scale parameter, b = the rate of decrease in laying ability, c = the reciprocal indicator of the variation in sexual maturity, d = the mean age of sexual maturity of the hens, and x is weeks of egg production.

Modelling cumulative egg production

In the study of avian reproductive performance, cumulative egg production traits are pivotal metrics. These traits include: cumulative egg production (%), cumulative egg mass (kg), cumulative hatching egg (%), and cumulative egg weight (kg). Understanding these parameters is crucial for optimizing breeding strategies and improving overall productivity in poultry farming. To analyze the relationships between the aforementioned cumulative egg production metrics and week of egg production, five nonlinear models were employed. Below are the models used in this analysis:

Gammay=axbecx
Logisticcurvilineary=a(ebx1+ec(xd))
Gompertzy=bexp[(lnab)(1ecx)]
Richardsy=ab[an+(anbn)ecx]1/n
Morganw=(bkc+axc)/(kc+xc)

In which the biological interpretations of the relevant parameters for Gamma, Compartmental, and the Logistic-curvilinear models are as noted earlier. For Gompertz, Richards, and Morgan: y = the interested egg production metric, b = initial value of cumulative egg production metrics, a = asymptotic value of cumulative egg production metric; x = weeks of egg production, c, k, and n are parameters that define the shape of the egg production curve.

Artificial neural networks (ANN)

In addition to the traditional models, a multilayer perceptron (MLP) feed-forward ANN was developed to predict egg production performance. The ANN was used both for weekly and cumulative production data. Its architecture consisted of four layers: one input layer, two hidden layers, and one output layer. The ANN structure was configured with one input neuron, three neurons in the first hidden layer, two in the second hidden layer, and one output neuron (1-3-2-1). A hyperbolic tangent activation function was employed in both the hidden and output layers. Additionally, 33% of the dataset was allocated for validation to enhance the model's reliability. The ANN was trained to predict the egg production traits. After ANN training and the selection of the most adjusted network model for each trait of interest, the ANN models’ efficacy was tested. The predicted values for training and validation data sets were compared with the actual observed data to assess the ANN performance. The ANN was trained using JMP Pro software, which automatically allocated 33% of the dataset for validation to prevent overfitting. Because the model used a single biological input variable and a low-complexity architecture (1–3–2–1), no additional cross-validation cycles or regularization techniques were required.

Statistical criteria

Various statistical criteria were used to assess the accuracy and reliability of both the traditional growth models and the ANN models. These criteria included the adjusted coefficient of determination (R2 adj), root mean square error (RMSE), as well as model selection criteria such as Akaike’s information criterion (AIC) and Bayesian information criterion (BIC). The calculations for these statistical measures were performed as follows:

  • 1) R2 adj=1-[(n-1/n-p) (1-R2)]

where: R2 adj represents the adjusted coefficient of determination, n is the total number of observations, p denotes the number of parameters in the model, and R2 is the standard coefficient of determination. The R2 value itself is derived from the ratio of the residual sum of squares (RSS) to the total sum of squares (TSS), providing a measure of how well the model explains the variability in the observed data.

  • 1) RMSE=√(RSS/(n-p-1))

Where RSS is the residual sum of squares, n is the number of observations, and p is the number of parameters in the model.

  • 2) MAD = ∑ (Ai-Fi)/n

  • 3) MAPE =1/n ∑ | (Ai-Fi)/Ai | ×100

  • 4) AIC = n × ln (RSS) + 2P

  • 5) BIC = n ln (RSS/n) + p ln(n)

Where Ai is the actual value, Fi is the forecasted value, RSS is the residual sum of squares, n is the number of observations, and p is the number of parameters in the models. Except for R2 adj, where higher values indicate a better fit of the model to the data, for the remaining studied criteria, the best model is the one with the lowest values.

Results

A summary of the performance of the models based on statistically significant parameters (P < 0.05) estimated by each model in terms of percentage of the total fits is demonstrated in Table 1.

Table 1.

A summary of the performance of the models based on statistically significant parameters (P < 0.05) estimated by each model in terms of the percentage of the total fits.

Parameter
Weekly egg production Model a b c d k n
Gamma 100 100 100 - - -
Compartmental 100 100 100 - - -
Logistic-curvilinear 100 100 100 100 - -
Cumulative egg production Gamma 100 100 100 - - -
Compartmental 0 0 0 - - -
Logistic-curvilinear 100 100 100 100 - -
Gompertz 100 100 100 - - -
Richards 33.3 83.3 83.3 - - 100
Morgan 83.3 100 83.3 - 100 -

The results for the percentage of models' superiority based on AIC and BIC (Table 2, Table 3) demonstrated that the ANN provided the highest accuracy for weekly data across all strains and traits, which indicates the ANN's capacity to capture complex patterns within the data enables it to outperform the other models according to the goodness of fit criteria. When examining cumulative data, the Morgan model is shown as the most effective among classical growth models. This suggests a potential ability of the classical model, especially Morgan, in scenarios where accumulated effects over time are more relevant than immediate fluctuations. Although other classical models’ efficacy, such as Gamma, Logistic-curvilinear, and Richards, were acceptable in most cases, they were less consistent than the ANN and Morgan.

Table 2.

Comparison of goodness of fit showing the efficacy of egg production curves and ANN to predict egg production traits in Ross 308, Cobb, and Arbor Acres parent stocks.

Ross 308
Cobb
Arbor Acres
Traits Model Parameter R2 adj RMSE 1 AIC 2 BIC 3 R2 adj RMSE 1 AIC 2 BIC 3 R2 adj RMSE 1 AIC 2 BIC 3
Egg Mass (kg) Gamma Weekly 0.8393 0.0049 −134.39 −276.88 0.8679 0.0044 −145.23 −297.00 0.8286 0.0052 −132.56 −275.05
Cumulative 0.9996 0.2013 −58.118 −200.60 0.9997 0.0250 −72.41 −224.17 0.9997 0.0291 −63.81 −206.29
Compartmental Weekly 0.9169 0.0025 −160.93 −303.42 0.9165 0.0028 −164.39 −316.16 0.9060 0.0028 −154.51 −299.00
Cumulative 0.9942 3.2558 −53.217 −89.271 0.9933 0.5568 57.79 −93.97 0.9948 0.4493 45.67 −96.81
Logistic Curvilinear Weekly 0.9809 0.0005 −218.19 −358.99 0.9576 0.0013 −192.24 −342.27 0.9665 0.0010 −196.64 −337.43
Cumulative 0.9981 1.0462 9.806 −130.99 0.9979 0.1718 9.86 −138.11 0.9980 0.1734 9.03 −131.76
Gompertz Cumulative 0.9966 1.9130 −31.94 −110.54 0.9969 0.2575 25.41 −126.35 0.9965 0.3066 30.39 −112.09
Richard Cumulative 0.9996 0.2046 −55.46 −196.26 0.9997 0.0237 −73.33 −223.36 0.9996 0.0303 −60.74 −201.54
Morgan Cumulative 0.9999 0.0444 −116.58 −257.38 0.9999 0.0056 −133.28 −281.26 0.9999 0.0065 −121.97 −262.77
ANN (training) Weekly 0.9998 0.0010 −252.68 −324.81 0.9999 0.0003 −338.32 −418.30 0.9912 0.0004 −292.45 −364.58
Cumulative 0.9999 0.0009 −180.44 −265.15 0.9999 0.0288 −90.86 −174.75 0.9999 0.0002 −212.12 −296.83
ANN (Validation) Weekly 0.9990 0.0008 −140.66 −171.22 0.9996 0.0012 −129.43 −159.98 0.9915 0.0013 −128.70 −159.26
Cumulative 0.9999 0.0004 −108.18 −145.13 0.9998 0.0436 −43.10 −79.81 0.9999 0.0003 −109.75 −146.69
Egg production
(Eggs/birdk)
Gamma Weekly 0.8022 1.7226 99.42 −43.06 0.8270 1.6606 103.69 −48.07 0.7892 1.8457 102.18 −40.30
Cumulative 0.9995 10.1685 170.44 27.95 0.9995 10.1310 179.64 27.87 0.9995 10.9746 173.49 31.00
Compartmental Weekly 0.8972 0.8953 73.24 −69.24 0.8985 0.9737 81.27 −70.49 0.8958 0.9123 73.99 −68.48
Cumulative 0.9943 120.0242 267.17 126.68 0.9938 125.8439 285.46 133.69 0.9949 11.5799 266.61 124.12
Logistic Curvilinear Weekly 0.9927 0.0631 −31.39 −172.19 0.9841 0.1507 4.36 −145.66 0.9944 0.0483 −42.08 −182.88
Cumulative 0.9970 48.8881 234.68 93.88 0.9974 46.4799 245.06 95.03 0.9977 51.3181 236.62 95.82
Gompertz Cumulative 0.9960 85.5029 255.61 113.12 0.9960 82.3034 267.62 115.85 0.9958 93.4855 259.18 116.69
Richard Cumulative 0.9995 9.7671 170.27 29.47 0.9995 9.1009 176.58 26.54 0.9995 10.9421 174.81 34.01
Morgan Cumulative 0.9999 2.1360 109.46 −31.33 0.9999 1.8803 110.35 −39.68 0.9999 2.2442 111.44 −29.35
ANN (training) Weekly 0.9999 0.0571 −82.49 −155.28 0.9992 0.0382 −71.78 −153.29 0.9996 0.0243 −89.20 −161.84
Cumulative 0.9999 0.0533 −39.03 −69.72 0.9999 0.0356 −14.27 −45.78 0.9999 0.0533 −62.58 −136.20
ANN (Validation) Weekly 0.9997 0.1479 −88.10 −160.76 0.9965 0.0458 −30.17 −60.99 0.9983 0.0368 −35.97 −66.70
Cumulative 0.9999 0.1015 −43.63 −74.29 0.9999 0.0874 −75.45 −156.76 0.9999 0.1015 −48.66 −79.28
Hatching egg (%) Gamma Weekly 0.9919 2.3470 111.68 −30.80 0.9850 1.6210 102.67 −49.09 0.9975 0.4015 41.17 −101.31
Cumulative 0.9994 11.7403 176.19 33.70 0.9994 10.8915 182.68 30.91 0.9994 11.7214 176.12 33.63
Compartmental Weekly 0.8158 53.0031 236.48 93.99 0.4912 55.0108 250.70 98.93 0.7854 34.4327 219.23 −76.74
Cumulative 0.9921 144.31 276.55 134.06 0.9926 127.2044 285.91 134.14 0.9934 120.0300 269.18 126.69
Logistic Curvilinear Weekly 0.9809 5.4259 146.75 5.95 0.9948 0.5522 58.89 −91.13 0.9963 0.5911 58.07 82.72
Cumulative 0.9978 39.6647 226.32 85.52 0.9974 43.5697 242.35 92.32 0.9978 39.8097 226.47 85.67
Gompertz Cumulative 09962 69.44 247.29 104.80 0.9959 430.8478 260.76 108.99 0.9960 73.5391 249.58 107.09
Richard Cumulative 0.9994 10.5974 173.53 32.73 0.9994 9.6940 179.23 29.20 0.9994 11.0310 175.13 34.33
Morgan Cumulative 0.9999 0.8546 72.82 −67.97 0.9999 2.4061 120.70 −29.32 0.9999 0.6992 64.79 −76.00
ANN (training) Weekly 0.9998 0.0907 −31.21 −110.34 0.9996 0.0727 −42.71 −115.37 0.9998 0.0721 −39.05 −115.61
Cumulative 0.9999 0.0347 −71.66 −144.82 0.9999 0.0247 −97.34 −177.86 0.9999 0.0814 −34.64 −112.42
ANN(Validation) Weekly 0.9999 0.0999 −24.99 −52.93 0.9995 0.0987 −11.70 −43.48 0.9999 0.0262 −41.53 −69.29
Cumulative 0.9999 0.0456 −27.63 −55.52 0.9999 0.0848 −14.95 −46.41 0.9999 0.0658 −18.86 −46.97
Egg weight Gamma Weekly 0.9970 0.6342 59.45 −83.03 0.9936 1.5503 100.80 −50.96 0.9970 0.5447 53.37 −89.11
Cumulative 0.9999 0.000004 −411.61 −554.10 0.9999 0.00001 −380.83 −532.60 0.9999 0.00001 −381.17 −523.66
Compartmental Weekly 0.9293 14.8293 185.53 43.04 0.9012 23.8893 215.67 63.90 0.9459 9.7517 168.76 26.27
Cumulative 0.9999 0.0005 −225.05 −367.54 0.9999 0.0003 −257.168 −408.936 0.9999 0.0003 −244.63 −387.12
Logistic Curvilinear Weekly 0.9995 0.0942 −15.38 −156.18 0.9994 0.1467 3.218 −146.81 0.9977 0.4006 42.52 −98.27
Cumulative 0.9991 0.0030 −152.47 −293.27 0.9991 0.0036 −152.30 −300.28 0.9991 0.0030 −152.47 −293.27
Gompertz Cumulative 0.9975 0.0086 −112.41 −254.90 0.9977 0.0094 −113.51 −265.28 0.9976 0.0082 −114.23 −256.72
Richard Cumulative 0.9999 0.00005 −316.46 −457.26 0.9999 0.00003 −349.72 −499.75 0.9999 0.00005 −316.46 −457.26
Morgan Cumulative 0.9999 0.000008 −387.11 −527.91 0.9999 0.000001 −493.78 −641.76 0.9999 0.00001 −360.41 −501.21
ANN (training) Weekly 0.9999 0.0465 −57.75 −131.72 0.9999 0.0275 −89.11 −169.88 0.9999 0.0293 −80.01 −152.87
Cumulative 0.9999 0.00003 −267.82 −352.53 0.9999 0.00004 −262.26 −346.97 0.9999 0.00004 −263.27 −347.98
ANN (Validation) Weekly 0.9999 0.0383 −47.33 −77.96 0.9999 0.0252 −46.31 −76.95 0.9999 0.0317 −40.00 −70.68
Cumulative 0.9999 0.00003 −144.58 −181.53 0.9999 0.00007 −133.37 −170.32 0.9999 0.00000004 −237.45 −274.25
1

Root Mean squared error.

2

Akaike’s information criterion.

3

Bayesian information criterion.

Table 3.

Percentage of cases in which the model specified in the row was superior to the model specified in the column based on Akaike’s information criterion (AIC) and Bayesian information criterion (BIC).

Parameter
Model Gama Compartmental Logistic-curvilinear
Weekly egg metrics Gama AIC - 50 16.7
BIC - 50 16.7
Compartmental AIC 50 - 0
BIC 50 - 0
Logistic-curvilinear AIC 83.3 100 -
BIC 83.3 100 -
ANN(training) AIC 100 100 91.6
BIC 100 100 58.3
ANN(validation) AIC 83.3 75 66.6
BIC 33.3 50 16.6
Cumulative egg metrics Gama Compartmental Logistic-curvilinear Gompertz Richards Morgan
Gama AIC - 100 100 100 50 16.6
BIC - 100 100 100 75 16.6
Compartmental AIC 0 - 33.3 33.3 0 0
BIC 0 - 25 25 0 0
Logistic-curvilinear AIC 0 64.7 - 91.6 0 0
BIC 0 75 - 100 0 0
Gompertz AIC 50 36.7 9.4 - 0 0
BIC 25 75 0 - 0 0
Richards AIC 50 100 100 100 - 0
BIC 25 100 100 100 - 0
Morgan AIC 83.4 100 100 100 100 -
BIC 83.4 100 100 100 100 -
ANN(training) AIC 75 100 100 100 75 66.6
BIC 66.6 75 100 100 66.6 66.6
ANN(validation) AIC 66.6 75 83.3 100 66.6 50
BIC 50 66.6 75 75 50 33.3

Percentage of cases in which the model specified in the row was statistically superior to the model specified in the column.

Limitations on space prevent the presentation of the results for all data sets. Therefore, as an example, model behavior for Ross 308 parent stock data set is illustrated in Figs. 1 and 7. The results indicate that the growth functions and ANN could be fitted to the data without difficulty by nonlinear regression. Although in some cases, the compartmental model was not able to show a suitable fit to the data, the other models provided an excellent fit. Poorer fits of the Gamma and Logistic-curvilinear occurred less with the cumulative data than the weekly data, which is in line with the results obtained for the ANN (Table 1, Table 2, Table 3, Fig. 2, Fig. 3).

Fig. 1.

Fig 1

Weekly egg mass (g), egg production (eggs/ bird /week), hatching egg (%), and egg weight (g) curves of Ross 308 parent stock.

Fig. 7.

Fig 7

Residual vs. predicted plot by artificial neural network for cumulative training and validating data sets of Ross 308 parent stocks.

Fig. 2.

Fig 2

Cumulative egg mass (kg), egg production (eggs/bird), hatching egg (ess/bird), and egg weight curves (kg) of Ross 308 parent stock.

Fig. 3.

Fig 3

Cumulative egg mass (kg), egg production (eggs/bird), hatching egg (eggs/bird), and egg weight (kg) curves of Ross 308 parent stocks.

The ANN accurately captured the actual variations in both weekly and cumulative data (Fig. 4, Fig. 5, Fig. 6, Fig. 7), with predictions closely matching the observed values.

Fig. 4.

Fig 4

Actual vs. predicted plot by artificial neural network for weekly training (a) and validating (b) data sets of Ross 308 parent stocks.

Fig. 5.

Fig 5

Actual vs. predicted plot by artificial neural network for cumulative training (a) and validating (b) data sets of Ross 308 parent stocks.

Fig. 6.

Fig 6

Residual vs. predicted plot by artificial neural network for weekly training and validating data sets of Ross 308 parent stocks.

The higher percentages of fitted cases (Table 2, Table 3) in which the ANN was superior to the best traditional Logistic-curvilinear and Morgan models according to the RMSE, AIC and BIC criteria (RMSE = 100% both for weekly and cumulative productive metrics, AIC = 91.6% for weekly and 58.3% for cumulative datasets, and BIC = 66.6% both for weekly and cumulative datasets), represent the capacity of the ANN to outperform the conventional models. The AIC and BIC are crucial statistical measures used to evaluate the quality of different models while penalizing for complexity. A lower AIC or BIC value indicates a better-fitting model. Thus, the higher percentages observed for the ANN suggest a robust explanatory capability that surpasses its traditional counterparts due to its better ability to represent the real physiological and reproductive responses of breeder hens to feeding level, age, and strain differences. From a management perspective, the improved accuracy means that flock reproductive performance can be predicted more precisely, allowing earlier detection of production drops or efficiency losses. Such predictive ability enables producers to adjust feeding programs, lighting schedules, or strain selection in time, leading to better resource use and improved overall reproductive productivity in broiler parent stocks.

Discussion

The poultry industry faces continuous pressure to improve production efficiency through advanced management techniques. Accurate prediction of egg production parameters plays a pivotal role in sustainable flock management. Classical growth models have long been employed to forecast production trends; however, recent advancements in machine learning, particularly ANN, offer promising alternatives that may enhance predictive capabilities (Roush et al., 2006; Khojastehkey et al., 2021). Accurate prediction of key production parameters, such as egg mass, hatching egg production, egg weight, and overall egg production throughout the production cycle, plays a crucial role in optimizing flock management and enhancing productivity in the poultry industry.

This study explores the performance of classical growth models and ANNs in predicting weekly and cumulative production patterns across three commercial parent stocks of broiler chicks. Gamma, Compartmental, and Logistic curvilinear models were applied to analyze the weekly data, while Gamma, Compartmental, Logistic curvilinear, Gompertz, Richards, and Morgan models were used for the cumulative data. A multi-layer feed-forward perceptron neural network structure was also employed for the ANN model. Model performance was assessed using adj, RMSE, AIC, and BIC criteria.

The outcomes of the current study align with those reported by Darmani Kuhi and France (2019), who successfully applied classical growth functions to model cumulative egg production in laying and breeder hens. Traditional analysis methods often exhibit sensitivity to missing records, which can lead to skewed results and misinterpretations in production trends. In this regard, the application of non-linear growth functions presents a compelling alternative for analyzing cumulative egg yield records. Unlike conventional models, these non-linear approaches demonstrate an inherent resilience to missing data points. This characteristic is particularly advantageous in agricultural settings where data collection may be sporadic or incomplete due to various factors such as environmental changes or operational challenges. The smoother trend depicted by cumulative production curves fitted with non-linear functions offers a more robust representation of egg yield over time and is less influenced by outliers or abnormal records. Abnormal records can be a result of several problems, such as measurement faults and biological disruptions in animal performance occurring when birds are threatened by some severe condition that limits expression of their genetic potential, e.g., nutritional deficit, metabolic or infectious disorders (Jefferson, 2005).

Despite the fact that flexible growth functions do not always produce statistically significant parameter estimates (Table 3), it is crucial to recognize that this aspect should not be the only determining factor in the selection process for a model (Darmani Kuhi and France, 2019). Considering the Compartmental model, for example, even when the statistical criteria did not indicate a suitable fit across the different data sets, fitting the Compartmental model consistently resulted in statistically significant parameter estimates.

The superior performance of the ANN model is likely due to its ability to capture complex and nonlinear interactions among nutrition, genetic potential, and reproductive physiology in broiler breeder hens. These relationships often involve multifactorial effects between nutritional and physiological factors; for example, the combination of feed level, body weight, and age can nonlinearly influence egg production and fertility, as also reported by Van Emous et al. (2021). From a management perspective, the outputs of the ANN can serve as an effective decision-support tool for flock management. Accurate prediction of weekly and cumulative egg production trends allows early detection of performance declines, enabling timely adjustments to feeding programs, lighting schedules, or breeder management strategies. Moreover, these predictions can assist in optimizing resource utilization, improving feed efficiency, and reducing production costs under different nutritional or environmental conditions.

Although the ANN model demonstrated high predictive accuracy in predicting production traits of broiler parent stocks, certain limitations should be acknowledged. The model was developed using data from a specific set of breeder strains and management conditions, which may limit its generalizability to other genetic lines or production systems. Furthermore, it relied primarily on historical production and physiological data without incorporating real-time environmental or behavioral inputs. Future research should focus on integrating ANN models with emerging technologies such as the Internet of Things (IoT) and real-time monitoring systems to collect continuous data on environmental parameters, bird behavior, and feeding activity. Such integration could enhance predictive precision and support more dynamic and intelligent management decisions for broiler parent flocks (Cruz et al., 2024).

Overall, the findings of this study confirm the high potential of ANNs as powerful tools for modeling and predicting egg production parameters in laying hens, while also acknowledging the applicability of classical models in predicting the egg production metrics.

Conclusion

Based on the comparative analysis of various growth models and ANNs for predicting productive parameters across three commercial broiler breeder strains, ANNs consistently demonstrated the highest accuracy and the lowest prediction error, especially in weekly data modeling. In the analysis of production metrics, the ANN demonstrated a significant advantage over the best traditional Logistic curvilinear and Morgan models based on RMSE, AIC, and BIC criteria (RMSE = 100% both for weekly and cumulative productive metrics, AIC = 91.6% for weekly and 58.3% for cumulative datasets, and BIC = 66.6% both for weekly and cumulative datasets. Classical models such as Morgan and Richard performed well in modeling cumulative data, sometimes approaching the predictive accuracy of ANN. Overall, it can be concluded that both approaches, classical growth functions and neural networks, can serve as complementary and effective tools in modeling egg production, depending on the type of data and analytical objectives. While classical models, due to their simplicity and interpretability, are more suitable for quick and transparent analyses, neural networks offer superior predictive accuracy and the capability to model complex, nonlinear relationships. Integrating both methods could provide a powerful strategy for optimizing flock performance and enhancing productivity in poultry production systems by implementing them in breeding programs or management software.

Ethics approval statement

This study did not involve direct experimentation on animals, and therefore, ethics approval was not required.

CRediT authorship contribution statement

Zahra Moradi Gharajeh: Methodology, Formal analysis, Data curation. Hassan Darmani Kuhi: Writing – original draft, Methodology, Formal analysis, Conceptualization. Navid Ghavi Hossein-Zadeh: Writing – review & editing, Formal analysis.

Disclosures

There is no Conflict of Interest

Footnotes

Supplementary material associated with this article can be found, in the online version, at doi:10.1016/j.psj.2025.106356.

Appendix. Supplementary materials

mmc1.docx (26.2KB, docx)

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