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Predictive Equations of Carcass Characteristics and Primal Cut Weights of Native Mexican Guajolotes Using Body Measurements

ABSTRACT

This study was conducted to develop predictive equations for carcass characteristics and primal cut weights of native Mexican guajolotes using body measurements (BM). For this study, a total of 36 male guajolotes (Meleagris gallopavogallopavo), aged 6 to 10 months, and mean slaughter body weight (SBW) of 4543.14 ± 656.60 g, were used. The birds were kept under traditional extensive conditions. ThefollowingBMswererecorded24 h before slaughter: thoracicperimeter (TP), body circumference (BC), body length (BL), wing length (WL), keel length (KL), shank length (SL) and shank diameter (SD). After slaughter, hot carcass weight (HCW), cold carcass weight (CCW), hot dressing percentage (HDP), cold dressing percentage (CDP), organs and viscera weight (VIS) and abdominal fat weight (AFW) were recorded. The carcasses were dissected in to five primal cut (breast, thigh, drumstick, back and wing). The SBW and BMs showed moderate to high positive correlations (p<0.01; 0.34≤r<0.97) with carcass characteristics and primal cut weights. In the equations generated to predict HCW, CCW, HDP, CDP, VIS and AFW, the R2 ranged from 0.40 to 0.96, and the predictor variables were SBW, KL, BC, WL and SL. Regarding the equations developed to predict the primal cut weights, R2 ranged from 0.58 to 0.91. In these models, SBW, BC, SD, WL and KL explained most of the observed variation. The prediction equations obtained in the study had moderate to high accuracy; therefore, they can be used by researchers, technicians and poultry producers to obtain information on the carcass composition of native Mexican guajolotes.

Keywords:
Body measurements; carcass characteristics; mathematical equations; native guajolotes; primal cut weights

INTRODUCTION

In today’s poultry production, carcass tissue composition is an economically important factor to the increasing demand for specific cuts of meat (Faridi et al., 2012Faridi A, Sakomura NK, Golian A, Marcato SM. Predictingbody and carcasscharacteristicsof 2 broilerchickenstrainsusingsupport vector regression and neural networkmodels. PoultryScience 2012;91:3286-3294.). The weights and proportions of meat in the carcass, which are quantified by traits such as the retail product, are indicators of the quality of the carcasses based on the quantity of product to be marketed (Silva et al., 2012Silva SJ, Urdapilleta TJ, Sterman FJB, Gomes RC, Leme PR, Navajas EA. Prediction of retail beef yield, trimf at and proportion of high-valued cuts in Nellore cattle using ultrasound live measurements. Revista Brasileira de Zootecnia 2012;41:2025-31.). Therefore, the emphasis in meat poultry production is on the quality and yield of the main parts of the carcass (Faridi et al., 2012).

The most accurate standard method for determining carcass tissue composition in meat species is physical separation of the tissues or by dissection (Lorenzo et al., 2018Lorenzo JM, Guedes CM, Zdolec N, Sarriés MV, Franco D, De Palo P, et al. Prediction of foal individual primal cuts yield using video image analysis. South African Journal of Animal Science 2018;48:6.). However, it is an expensive, laborious procedure, and requires a lot of time and specialized labor (Faridi et al., 2012Faridi A, Sakomura NK, Golian A, Marcato SM. Predictingbody and carcasscharacteristicsof 2 broilerchickenstrainsusingsupport vector regression and neural networkmodels. PoultryScience 2012;91:3286-3294.). In addition, it promotes a significant waste of meat (Lin et al., 2018Lin FB, Zhu F, Hao JP, Yang FX, Hou ZC. In vivo prediction of the carcass fatness using live body measurements in Pekinducks. Poultry Science 2018;97:2365-2371.; Batista et al., 2021Batista AC, Santos V, Afonso J, Guedes C, Azevedo J, Teixeira A, et al. Evaluation of an image analysis approach to predicting primal cuts and lean in light lamb carcasses. Animals 2021;11:1368.). Therefore, some indirect methods have been proposed to estimate the yield and tissue composition of the carcass of farm animals, such as digital image analysis (Bozkurt et al., 2008Bozkurt Y, Aktan S, Ozkaya S. Digital image analysis to predict carcass weight and some carcass characteristics of beef cattle. Asian Journal of Animal and Veterinary Advances 2008;3:129-37.; Lorenzo et al., 2018; Batista et al., 2021), X-ray computed tomography (Navajas et al., 2010Navajas EA, Richarson RI, Fisher AV, Hyslop JJ, Ross DW, Prieto N, et al. Predicting beef carcass composition usingt issue weights of a primal cut assessed by computed tomography. Animal 2010;4:1810-17.), and real-time ultrasonography (Melo et al., 2003Melo JE, Motter MM, Morao LR, Huguet MJ, Canet Z, Miquel MC. Use of in-vivo measurements to estimate breast and abdominal fat content of a free-range broiler strain. Animal Science 2003;77:23-31.; Teixeira et al., 2008Teixeira A, Joy M, Delfa R. In vivo estimation of goat carcass composition and body fat partition by real-time ultrasonography. Journal of AnimalScience 2008;86:2369-76.). Although these techniques are promising for the subjective evaluation of carcass composition, their use is limited to laboratory conditions and the required equipment is expensive, which represents a challenge for developing countries. On the other hand, several authors (Bochno et al., 2000Bochno R, Rymkiewicz J, Szeremeta J. Regression equations for in vivo estimation of the meat content of Pekin duck carcases. British Poultry Science 2000;41:313-7.; Kleczek et al., 2006Kleczek K, Wawro K, Wilkiewicz-Wawro E, Makowski W. Multiple regression equations to estimate the content o fbreast muscles, meat, and fat in Muscovyducks. Poultry Science 2006;85:1318-26.; Yakubu et al., 2009Yakubu A, Idahor KO, Agade YI. Using factor scores in multiple linear regression model for predicting the carcass weight of broiler chickens using body measurements. Revista UDO Agrícola 2009;9:963-7.; Tyasi et al., 2018Tyasi TL, Qin N, Niu X, Sun X, Chen X, Zhu H, et al. Prediction of carcass weight from body measurement traits of Chinese indigenous Dagu male chickens using path coefficient analysis. Indian Journalof Animal Sciences 2018;88:744-8.; Costa et al., 2020Costa RG, Lima AGVO, Ribeiro NL, Medeiros AN, Medeiros GR, Gonzaga Neto S, et al. Predicting the carcass characteristics of Morada Nova lambs using biometric measurements. Revista Brasileira de Zootecnia 2020;49:e20190179.; Gomes et al., 2021Gomes MB, Neves MLMW, Barreto LMG, Ferreira MA, Monnerat JPIdS, Carone GM, et al. Prediction of carcass composition through measurements in vivo and measurements of the carcass of growing Santa Inês sheep. PLoS ONE 2021;16:e0247950.) showed that the development of regression equations using somebody measurements represents an indirect, accurate and non-invasive method to predict carcass components. Additionally, this technique allows information to be collected from animals in vivo, without the need for sacrifice, so it can be useful for selective breeding and genetic improvement (Banerjee, 2011Banerjee S. Prediction of carcass cuts using some non-invasive predictors on broiler ducks reared in hot and humid climate of Eastern India. World Applied Sciences Journal 2011;12:642-51.; Erensoy et al., 2020Erensoy K, Noubandiguim M, Cilavdaroglu E, Sarica M, Yamak US. Correlations between breast yield and morphometric traits in broiler pure lines. Brazilian Journal of Poultry Science 2020;22:1-8.).

The Guajolote (Meleagris gallopavogallopavo) is a poultry native to Mexico that has an acceptable productive yield, high rusticity and resistance to diseases, as well as a good capacity for adaptation that allows it to thrive in various adverse climatic conditions (Portillo-Salgado et al., 2022Portillo-Salgado R, Herrera-Haro JG, Bautista-Ortega J, Chay-Canul AJ, Cigarroa-Vázquez FA. Guajolote - a poultry genetic resource native to Mexico. World's Poultry Science Journal 2022;78.). Male guajolotes are characterized by their ability to produce meat as they have good muscle development and produce little fat in the carcass (Juárez-Caratachea, 2004Juárez-Caratachea A. Efecto del peso corporal en el rendimiento de la masa muscular en el pavo nativo mexicano. Revista Cubana de Ciencia Agrícola 2004;38:405-9.). Instead, female guajolotes are used only for the incubation of eggs, their own or those of Creole hens, due to their excellent maternal ability in protecting their chicks in outdoor conditions (Portillo-Salgado et al., 2020). The Guajolote production is an important poultry activity in suburban and rural communities because it contributes to the nutritional and economic sustenance of families. The birds are raised in semi-technified, extensive or backyard conditions (Portillo-Salgado et al., 2022). The consumption of Guajolote meat has a long tradition in Mexico and in other Central American countries. Although this meat is mostly consumed during in december, through out the year it is used in the preparation of typical regional dishes that are offered in social and family festivities because it has a desirable flavor and aroma (Ramírez-Rivera et al., 2012Ramírez-Rivera E, Camacho-Escobar M, García-López J, Reyes-Borques V, Rodríguez-Dela Torre M. Sensory analysis of Creole turkey meat with flash profile method. Open Journal of Animal Sciences 2012;2:1-10.). In native guajolotes, the most important primal carcass cuts are the breast, drumsticks and thighs, and represent approximately 30% of the total muscle mass of the bird (Juárez-Caratachea, 2004). However, other components of the carcass are also used, such as the back and wings.

Therefore, the hypothesis of this study was that body measurements taken in vivo could be used to predict carcass characteristics and primal cut weights in native Mexican guajolotes. Since there is littles cientific literature on the use of body measurements to estimate carcass composition of native Mexican guajolotes, the objective of this study was to develop predictive equations for carcass characteristics and primal cut weights using body measurements of native Mexican guajolotes.

MATERIAL AND METHODS

Experimental site and animals

The animals included in this study were handled in accordance with the guidelines and ethical standards for the use and care of animals intended for research established by the Animal Welfare Committee (Comité de Bienestar Animal (COBIAN)) of the Colegio de Postgraduados (Approvalnumber: 002/21). The experiment was carried out in an experimental poultry unit (19° 29’ N, 90° 32’ W; 24 masl), located in the locality of Sihochac, Campeche, Mexico.

In the experiment, a total of 36 male guajolotes, aged 6 to 10 months, and mean slaughter body weight (SBW) of 4543.14 ± 656.60 g, were used. The birds were randomly collected in different poultry production units from rural communities in the municipality of Champotón, Campeche, where they were traditionally raised in extensive conditions (Portillo-Salgado et al., 2018Portillo-Salgado R, Herrera-Haro JG, Bautista-Ortega J, Ortega-Cerrilla ME, Sánchez-Villarreal A, Bárcena-Gama JR. Análisis descriptivo de las prácticas locales de cría y manejo del guajolote nativo (Meleagrisgallopavo L.) en Campeche, México. Agroproductividad 2018;11:88-94.). They had access to the outside during the day (7:00 to 18:00 h), while at night they were confined in a roofed pen, with concrete walls and floor, the latter was covered with 10 cm thickwood chip bed. Feeders and drinkers were provided in the pen. The feed, provided in mashform, consisted of a mixed diet that included: 60% corn, 20% wheat bran, and 20% soybean meal, and had 17% crude protein (CP) and 11.90 MJ metabolizable energy (ME/kg) (NRC,1994). The grazing areas were covered with the grasses Cynodondactylon, Urochloabrizanthacv. Marandu, and Pennisetumpurpureum. Feed and water were available ad libitum.

Body measurements

Body measurements (BM) were taken in vivo on each guajolote 24 h before slaughter using a plastic measuring tape graduated in cm and a millimeter digital vernier (TRUPER®). Birds were placed upright on a flat surface. BMs were taken as previously described by Cigarroa-Vázquez et al. (2013Cigarroa-Vázquez F, Herrera-Haro JG, Ruíz-Sesma B, Cuca-García JM, Rojas-Martínez RI, Lemus-Flores C. Phenotypic characterization of the indigenous turkey (Meleagrisgallo pavo) and production system in the north-central region of Chiapas, México. Agrociencia 2013;47:579-91.), these were: thoracic perimeter (TP), body circumference (BC), body length (BL), wing length (WL), keel length (KL), shank length (SL) and shank diameter (SD). All measurements were made by the same person for consistency purposes and to avoid undesirable measurement errors.

Slaughter of animals

All birds were sacrificed on the same day after a 12 h fasting period, during which they received only cleanwater. The slaughter was carried out in accordance with the Official Mexican Standards (NOM-008-ZOO-1994, NOM-009-ZOO-1994 and NOM-033-ZOO-1995) established for the humane slaughter of animals intended for meat production. Before slaughter, the body weight (SBW) of the birds was recorded using a precision digital scale(±1 g). The birds were humanely killed by exsanguination, and the carcasses were then scalded in hot water (60-65 °C) for 2 min to facilitate manual plucking. The head and legs were cut off, and the viscera and internal organs (VIS), comprising blood, liver, empty gizzard, heart, kidneys, lungs, intestines, gall bladder, and spleen, were collected and weighed. Likewise, the weight of abdominal fat (AFW) attached to the carcass was recorded. Subsequently, the carcasses were weighed to obtain the hot carcass weight (HCW), and they were stored at +4 °C for 24 h to obtain the cold carcass weight (CCW). The percentages (%) of hot (HDP) and cold (CDP) dressing were determined in relation to the SBW. Carcass dissection was performed as described by Hahn & Spindler (2002Hahn G, Spindler M. Method of dissection of turkey carcases.World's Poultry Science Journal 2002;58:179-97.). The primal cuts selected were the breast, thigh, drumstick, back and wing.

Statistical analysis

Initially, the descriptive statistics of the variables were obtained using the MEANS procedure of the SAS statistical program, ver. 9.4 (SAS Inst. Inc., Cary, NC). For exploratory analysis of relationships between dependent (carcass characteristics and primal cut weights) independent variables (body measurements), Pearson correlation coefficients (r) were obtained using the CORR procedure of SAS. Simple and multiple linear regressions were developed to estimate functional relationships between variables using the REG procedure of SAS. The STEPWISE and Mallow’s Cp options were used in the REG procedure to determine the significant variables (p<0.05) that were included in the statistical models. The STEPWISE process added and removed explanatory variables in the models to strike a balance between model simplicity (parsimony) and predictive performance. The goodness of fit of the models was determined using the determination coefficient (R2), root mean square error (RMSE), Akaikés Information Criterion (AIC) and Bayesian Information Criterion (BIC). Models with the lowest RMSE, AIC and BIC, and highest R2 were defined as the best models (Rivera-Alegríaet al., 2022).

RESULTS AND DISCUSSION

To date, this is the first study conducted to evaluate the use of body measurements as an indirect, practical, and non-invasive method to predict carcass characteristics and primal cut weights of native Mexican guajolotes. The mathematical models developed in this type of study, in addition to estimating the tissue composition of the carcass in poultry of different breeds and sexes, also contribute to establishing the optimal marketage (Faridi et al., 2012Faridi A, Sakomura NK, Golian A, Marcato SM. Predictingbody and carcasscharacteristicsof 2 broilerchickenstrainsusingsupport vector regression and neural networkmodels. PoultryScience 2012;91:3286-3294.).

The results of the descriptive analysis of the variables are shown in Table 1. The mean SBW was 4543.14 ± 656.60 g, with a CV of 14.45% among birds. The observed variability is related to the susceptibility of this variable to external influences such as climatic conditions (Silva et al., 2019Silva SJ da, Santos DG do, Neto JVE, Lana ÂMQ, Silva Roberto FF da, Ribeiro PHC. Biometric measurements of Santa Inês meat sheep reared on Brachiaria brizantha pastures in Northeast Brazil. PLoS ONE 2019;14(7):e0219343.); however, a diversified database is desirable for better accuracy (Gomes et al.,2021Gomes MB, Neves MLMW, Barreto LMG, Ferreira MA, Monnerat JPIdS, Carone GM, et al. Prediction of carcass composition through measurements in vivo and measurements of the carcass of growing Santa Inês sheep. PLoS ONE 2021;16:e0247950.). Regarding HCW and CCW, they showed mean values of 2781.43 ± 496.91 g and 2747.57 ± 487.51 g, respectively, both with a CV > 17%. The high variation observed in HCW and CCW may be due to the values of SBW of the birds. Based on these results, the HDP and CDP were estimated, which in turn had values of around 60%, with a CV of 4.70% for both parameters. Previously, Juárez-Caratachea (2004Juárez-Caratachea A. Efecto del peso corporal en el rendimiento de la masa muscular en el pavo nativo mexicano. Revista Cubana de Ciencia Agrícola 2004;38:405-9.) reported higher percentages of hot and cold dressing (78.94 and 75.91%, respectively), which were related to the higher slaughter body weigh to the native guajolotes used in that study (7.93 ± 0.69 kg). In poultry production, the dressing percentage is an important criterion for the evaluation of slaughter value of the carcass (Mueller et al., 2018Mueller S, Kreuzer M, Siegrist M, Mannale K, Messikommer RE, Gangnat IDM. Carcass and meat quality of dual-purpose chickens (Lohmann Dual, Belgian Malines, Schweizerhuhn) in comparison to broiler and laye chicken types. Poultry Science 2018;97:3325-36.; Nematbakhsh et al., 2021Nematbakhsh S, Selamat J, Idris LH, Razis AFA. Chicken authentication and discrimination via live weight, body size, carcass traits, and breast muscle fat content clustering as affected by breed and sex varieties in Malaysia. Foods 2021;10:1575.). Overall, carcass characteristics showed moderate variability (<25%), except AFW which had a CV of 92.11% among birds. In this regard, Nematbakhsh et al. (2021) found that the variation in body fat content in broilers can be explained by breed, slaughter age and maturity stage of the birds. Internal fat is considered to be the most variable body component in farm animals (Bautista-Díaz et al., 2020Bautista-Díaz E, Mezo-Solis JA, Herrera-Camacho J, Cruz-Hernández A, Gomez-Vazquez A, Tedeschi LO, et al. Prediction of carcass traits of Hair sheep lambs using body measurements. Animals 2020;10:1276.). On the other hand, the primal cut weights extracted from the carcass showed moderate variability (10.59-33.39%). The greatest variation was observed in back and breast weights, which showed a CV of 33.39% and 28.30%, respectively. This variability may be associated with the lack of genetic improvement practices due to the fact that these native poultry have remained unselected over the years since they are raised in extensive or backyard conditions (Juárez-Caratachea et al., 2019). However, Juárez-Caratachea (2004) suggests that variability among native guajolotes with respectto a particular trait represents an advantage in the systematic selection of the best individuals for the purpose of improving this characteristic. Finally, the BMs showed low variability (4.20-10.15%), which is consistent with the results in other studies (Ríos et al., 2016Ríos UA, Román PSI, Vélez IA, Cabrera TE, Cantú CA, De la Cruz CL, et al. Analysis of morphological variables in Mexican backyard turkeys (Meleagris gallopavo gallopavo). Revista Mexicana de Ciencias Pecuarias 2016;7:377-89.; Portillo-Salgado et al., 2020Portillo-Salgado R, Cigarroa-Vázquez FA, Herrera-Haro JG, Vázquez-Martínez I. Prediction of body weight of native Mexican guajo lotes trough morphometric measurements. ITEA-Información Técnica Económica Agraria 2020;116:150-60.), which reported moderate or low morphological variability in the populations of native guajolotes reared in rural regions of Mexico.

Table 1
Descriptive analysis of the body measurements, carcass characteristics and primal cut weights in native Mexican guajolotes (n = 36).

The results of the Pearson correlation coefficients (r) are shown in Table 2. The SBW and BMs showed moderate to high positive correlations (p<0.01; 0.34≤r<0.97) with carcass characteristics and primal cut weights, except for WL, which had a positive correlation (p<0.01) onlywith BRW (r = 0.35). These high correlations indicate elevated meat production capacity, and these measurements can thus be used as selection tools (Silva et al., 2019Silva SJ da, Santos DG do, Neto JVE, Lana ÂMQ, Silva Roberto FF da, Ribeiro PHC. Biometric measurements of Santa Inês meat sheep reared on Brachiaria brizantha pastures in Northeast Brazil. PLoS ONE 2019;14(7):e0219343.). However, SL presented a negative correlation (p<0.01) with AFW (r = -0.56) and BAW (r = -0.33). This means that birds with shorter shanks have a greater weight of abdominal fat and back, and vice versa. Juárez-Caratachea (2004Juárez-Caratachea A. Efecto del peso corporal en el rendimiento de la masa muscular en el pavo nativo mexicano. Revista Cubana de Ciencia Agrícola 2004;38:405-9.) reported, in native male guajolotes, that SBW presented moderate to high positive correlations (0.38≤r<0.90) with carcass characteristics and breast, leg and thigh weights. The strong relationship between bodyweight and the breast and thigh weights is due to the fact that in these parts of the carcass there is greater deposition of muscle tissue (Ogah, 2011Ogah DM. In vivo prediction of live weight and carcass traits using body measurements in indigenous guinea fowl. Biotechnology in Animal Husbandry 2011;27:1827-36.). Other studies in chickens (Melo et al., 2003Melo JE, Motter MM, Morao LR, Huguet MJ, Canet Z, Miquel MC. Use of in-vivo measurements to estimate breast and abdominal fat content of a free-range broiler strain. Animal Science 2003;77:23-31.; Yang et al., 2006Yang Y, Mekki DM, Lv SJ, Yu JH, Wang LY, Wang JY, et al. Canonical correlation analysis of body weight, body measurement and carcass characteristics of JinghaiYellow chicken. Journal of Animal and VeterinaryAdvances 2006;5: 980-4.; Mendeş & Akkartal, 2009; Yakubu et al., 2009Yakubu A, Idahor KO, Agade YI. Using factor scores in multiple linear regression model for predicting the carcass weight of broiler chickens using body measurements. Revista UDO Agrícola 2009;9:963-7.; Erensoy et al., 2020Erensoy K, Noubandiguim M, Cilavdaroglu E, Sarica M, Yamak US. Correlations between breast yield and morphometric traits in broiler pure lines. Brazilian Journal of Poultry Science 2020;22:1-8.), ducks (Bochno et al., 2000Bochno R, Rymkiewicz J, Szeremeta J. Regression equations for in vivo estimation of the meat content of Pekin duck carcases. British Poultry Science 2000;41:313-7.; Kleczek et al., 2006Kleczek K, Wawro K, Wilkiewicz-Wawro E, Makowski W. Multiple regression equations to estimate the content o fbreast muscles, meat, and fat in Muscovyducks. Poultry Science 2006;85:1318-26.; Kokoszyňski et al., 2019Kokoszyňski D, Wasilewski R, Saleh M, Piwczyňski D, Arpášova H, Hrnčar C, et al. Growth performance, body measurements, carcass and some internal organs characteristics of pekin ducks. Animals 2019;9:963.), and guinea fowl (Ogah, 2011) also reported high and significant correlations between bodyweight and body measurements with carcass characteristics and primal cut weights. This suggests that bodyweight and body measurements could be used as reliable predictors of carcass composition.

Table 2
Pearson correlationcoefficients(r) amongthe variables used in thedevelopmentoftheequations.

The regression equations developed to predict carcass characteristics and primal cut weights are presented in Tables 3 and 4. For HCW, two equations explained (p<0.001) between 95 [Eq.1] and 96% [Eq. 2] of the observed variation. Of these, Equation [2], which included SBW and KL as predictors, was the best model to predict HCW because it had lower values of RMSE (98.84), AIC (324.41), and BIC (326.95). Instead, for CCW, the SBW explained (p<0.001) by itself a 95% of the variation observed in the model [Eq. 3], with RMSE, AIC and BIC values of 104.40, 327.32 and 329.55, respectively. It was observed that the SBW contributed a high percentage of the variation for HCW and CCW. These findings are consistent with previous studies in poultry (Bochno et al.,2000Bochno R, Rymkiewicz J, Szeremeta J. Regression equations for in vivo estimation of the meat content of Pekin duck carcases. British Poultry Science 2000;41:313-7.; Raji et al., 2010Raji AO, Igwebuike JU, Kwari ID. Regression models for estimating breast, thigh and fat weight and yield of broilers from non invasive body measurements. Agriculture and Biology Journal of North America 2010;1:469-75.; Banerjee, 2011Banerjee S. Prediction of carcass cuts using some non-invasive predictors on broiler ducks reared in hot and humid climate of Eastern India. World Applied Sciences Journal 2011;12:642-51.), which reported that body weight accounted for a high proportion of the variation in carcass weight. However, the inclusion of body measurements in the models, such as chest circumference, breast width, body length, wing length and keel length, improves their accuracy (Yakubu et al., 2009Yakubu A, Idahor KO, Agade YI. Using factor scores in multiple linear regression model for predicting the carcass weight of broiler chickens using body measurements. Revista UDO Agrícola 2009;9:963-7.; Ogah, 2011Ogah DM. In vivo prediction of live weight and carcass traits using body measurements in indigenous guinea fowl. Biotechnology in Animal Husbandry 2011;27:1827-36.; Behiry et al., 2019Behiry FM, Hassanin MNF, Ali AEA, El-Kamash EM, Bahnas MM. Using some body measurements as predictors of live body weight and carcass traits in four broilers straits. Egyptian Poultry Science Journal 2019;39:835-49.). In the same way, the models to predict HDP [Eqs. 4 and 5] were fitted using the SBW and KL as predictor variables. However, Equation [5], compared toEquation [4], had the best goodness of fit due to its lower values of RMSE (2.09 vs 2.14), AIC (54.75 vs 55.28) and BIC (57.39 vs 57.32), as well as the highest prediction capacity (R2 = 0.49). For the prediction of CDP, a single Equation [6] was fitted, with R2 = 0.40; in this case, only SBW was included as a predictor. The equations developed to predict VIS [7-10] showed an R2 that ranged between 0.62 and 0.79. In these models, SBW, BC, WL and KL were included as predictor variables, with Equation [10] having the best goodness of fit (RMSE = 60.96, AIC = 292.33 and BIC = 295.94), and explained 79% of the variation observed in the model. Regarding the prediction of AFW, the variables that were included in the models [Eqs. 11 and 12] were SBW and SL, providing an increase in R2 from 0.44 to 0.61. However, Equation [12] which included both variables presented lower RMSE (7.50), AIC (143.98) and BIC (146.52) values. In broilers, Melo et al. (2003Melo JE, Motter MM, Morao LR, Huguet MJ, Canet Z, Miquel MC. Use of in-vivo measurements to estimate breast and abdominal fat content of a free-range broiler strain. Animal Science 2003;77:23-31.) reported that abdominal fat weight can be predicted with good accuracy (R2 = 0.74) using a regression equation that included live weight and abdominal fat surface. In another study (Raji et al., 2010), using the same type of poultry, a prediction model was developed for fat weight that presented an R2 of 0.86, using the chest girth, chest depth, chest width, live weight and wing length, as predictor variables. Similarly, Kleczek et al. (2006Kleczek K, Wawro K, Wilkiewicz-Wawro E, Makowski W. Multiple regression equations to estimate the content o fbreast muscles, meat, and fat in Muscovyducks. Poultry Science 2006;85:1318-26.) reported that carcass fat weight of male Muscovy ducks can be estimated from a regression model that included bodyweight, humerus length and chest depth. The high precision of the model developed in the study was confirmed with the coefficients of multiple correlation (r = 0.87) and determination (R2 = 0.75). Recently, Lin et al. (2018Lin FB, Zhu F, Hao JP, Yang FX, Hou ZC. In vivo prediction of the carcass fatness using live body measurements in Pekinducks. Poultry Science 2018;97:2365-2371.) fitted an equation to predict abdominal fat weight in Pekinducks using live weight, skin fat thickness, chest width and neck length, showing a r = 0.58 and R2 = 34.65%.

Table 3
Regressions equations to predict the carcass characteristics using body measurements in native Mexican guajolotes (n = 36).
Table 4
Regressions equations to predict the primal cuts weights using body measurements in native Mexican guajolotes (n = 36).

In the prediction of BRW, in addition to the SBW, two body measurements (BC and SD) were added to the models [Eqs. 13-15] (Table 4). Equation [13], using SBW as the only predictor, explained 87% of the variation observed in the model. However, the inclusion of body measurements provided a light increase in R2 of 4%, reaching a precision of 91% and lower values of RMSE (77.51), AIC (308.28) and BIC (311.28). Previously, Rymkiewicz & Bochno (1998Rymkiewicz J, Bochno R. Estimation of breast muscle weight in chickens on the basis of live measurements. Archives Geflügelk 1998;63:229-233.) suggested the use of live weight and thickness of breast muscles, in a practical and accurate model (R2 = 0.972) for the prediction of breast meat weight in broilers. Similarly, Melo et al. (2003Melo JE, Motter MM, Morao LR, Huguet MJ, Canet Z, Miquel MC. Use of in-vivo measurements to estimate breast and abdominal fat content of a free-range broiler strain. Animal Science 2003;77:23-31.) reported that the best model for the prediction of breast weight in broilers was the simple regression of live weight because it had an R2 of 0.85, with a residual standard error of 32.34 g. In male Muscovyducks, Kleczek et al. (2006Kleczek K, Wawro K, Wilkiewicz-Wawro E, Makowski W. Multiple regression equations to estimate the content o fbreast muscles, meat, and fat in Muscovyducks. Poultry Science 2006;85:1318-26.) proposed a regression equation that included bodyweight, breast-bone crest length and chest girth to estimate breast muscle weight. The model showed a multiple correlation coefficient between the dependent variable and the set of independent variables of 0.77, while the R2 was 59.29%. For female ducks, the cited authors suggested an equation that included bodyweight, breast-bonecrest length, and breast muscle thickness. The developed model presented higher values of the multiple correlation coefficient (0.80) and of R2 (64.16%), than the equation based on data for males. For the estimation of THW, SBW was the only independent variable that was included in the prediction model [Eq. 16], which had an R2 of 0.58. Raji et al. (2010Raji AO, Igwebuike JU, Kwari ID. Regression models for estimating breast, thigh and fat weight and yield of broilers from non invasive body measurements. Agriculture and Biology Journal of North America 2010;1:469-75.) found that thigh weight of male broilers was predicted with high accuracy (r = 0.91; R2 = 0.83) based on live weight, chest width and chest girth, while for females the independent variables were chest girth, chest width, live weight and chest depth (r = 0.94; R2 = 0.88). Regarding the DRW prediction, the variables that were included in the models were SBW and SD [Eqs. 17 and 18]. It was observed that the SBW alone can explain 78% of the variation of the dependent variable, but with the inclusion of SD in Equation [18], the precision had a light increase (R2 = 0.81) and the model showed a best fit (RMSE = 27.41, AIC = 234.64, BIC = 237.18). Three equations were generated to predict BAW [Eqs. 19-21], which showed an R2 ranging between 0.79 and 0.83. In this case, SBW associated with WL and SD were selected as predictor variables. Finally, the models developed to predict WIW [Eqs. 22-25] explained from 64 to 80% of its variation, being the model of Equation [25] the one that had a slightly better goodness of fit (RMSE = 20.16, AIC = 214.88 and BIC = 218.49). Although both back and wings are considered low-value carcasscuts, it is known that in poultry up to 32% of total lean meat is found in these body parts, as well as in the neck (Bochno et al., 2003; 2005).

CONCLUSION

In conclusion, our results suggest that slaughter body weight can be used together with the body measurements as predictive variables of carcass characteristics and primal cut weight of native Mexican guajolotes. The prediction equations obtained in the study had moderate to high accuracy (R2> 0.40 ≤ and ≤ 0.96); therefore, they can be used by researchers, technicians and poultry producers to obtain information on the carcass composition of native guajolotes. Further studies should evaluate the use of these equations under different production conditions.

ACKNOWLEDGEMENTS

The authors thank the Consejo Nacional de Ciencia y Tecnología (CONACYT) of Mexico for the scholarship to the first author, as well as the support through MAP Champotón project for the partial funding provided to buy feed. Also, the authors appreciate the support received from Colegio de Postgraduados, Campus Campeche.

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Publication Dates

  • Publication in this collection
    08 Aug 2022
  • Date of issue
    2022

History

  • Received
    12 Apr 2022
  • Accepted
    02 May 2022
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