Morphological, densitometric and mechanical properties of mandible in 5-month-old Polish Merino sheep
BMC Veterinary Research volume 13, Article number: 12 (2016)
Among bones building the axial and appendicular skeleton, the mandible is characterized by unique morphological and functional traits. The aim of the study was to evaluate morphological, densitometric and mechanical properties of mandible in 5-month-old Polish Merino sheep. Using quantitative computed tomography, volumetric bone mineral density (vBMD) and calcium hydroxyapatite density of the cortical bone (CbCa-HA), mean vBMD (MvBMD) and total bone volume were determined. Using computed tomography cross-sectional scans of the mandible, cross-sectional area, second moment of inertia, mean relative wall thickness and cortical index were determined. Three-point bending test was applied to determine mechanical properties. Serum concentration of insulin-like growth factor I (IGF-I) and bone-specific alkaline phosphatase (BAP) was also measured.
All the investigated morphometric, densitometric and mechanical parameters of the right and left mandibular halves were not significantly different (P > 0.05). There was no correlation of final body weight, MvBMD, CbCa-HA, BAP and IGF-I with all the analyzed parameters of mandible (P > 0.05). However, positive correlations between the other investigated morphometric, densitometric and mechanical parameter of mandible were found (P < 0.05).
Relationships between morphological, densitometric and mechanical parameters of the mandible indicate that the elaborated experimental model may serve for further studies on metabolic responses of skeletal system to physiological, nutritional, pharmacological, toxicological and environmental factors.
Osteoporosis in animals and humans is a metabolic disorder of skeletal system characterized by low bone mass and microarchitectural deterioration of bony tissue with consequent increased risk of bone fracture [1–3]. Considering that peak bone mass (PBM) in mature mammals is genetically determined in 70–80%, approximately 20–30% of the variation in PBM is determined by environmental factors such as nutrition, physical activity, exposure to sunlight, external temperature and other . Thus, manipulations of the environmental factors during growth and development period in vertebrates may result in the attainment of higher bone mass of skeletal system expressed by superior bone mineral density, morphological and the mechanical properties of bones . Among bones building the axial and appendicular skeleton, mandible is characterized by unique morphological and functional traits. Whereas vertebral bodies consist mainly trabecular bone, long bones are composed of trabecular and cortical bone types . Mandible in mammals is built of cortical bone mainly and it is equipped with teeth physiologically . It is susceptible to bone loss occurring with age and in response to endocrine and metabolic impairments, medications or locally acting factors [8–11]. In humans, after 50 years of age, there is an observed bone loss of the cortical bone compartment with subsequent thinning of the lower jaw and an increase in its porosity. The rate of mandibular bone loss is sex-dependent, with females having a lower mandibular size, volume and bone mass compared to males [12, 13]. Considering the importance of mandibular functions in animals and humans, the aim of the study was to elaborate original experimental model for experimental studies focused on bone metabolism regulation. There is a dearth of information on the basic anatomical and physiological characteristics of the mandible of lambs. Thus, in this study, morphological, densitometric, and mechanical properties of mandible in 5-month-old Polish Merino male sheep was investigated.
Experimental design and sampling procedure
The study was carried out on growing Polish Merino male lambs (N = 7) which were reared intensively from birth to 5 months of age under standard rearing conditions. Lambs and ewes were provided with drinking water ad libitum and fed a standard diet. During neonatal and postnatal period (up to 10 weeks of life) ram lambs were fed maternal milk. Between the fourth week and the fifth month of life, lambs were fed commercial concentrate and hay ad libitum. At the age of 5 months of life, the animals were euthanized to obtain whole mandible for morphometric, densitometric and mechanical analyses. Bone samples were isolated postmortally and cleaned of remaining soft tissues, including periosteum. Morphological properties of the whole mandible (including teeth) such as bone weight and bone length were measured. To avoid sample dehydration, mandibles were wrapped in plastic bags and stored frozen at –25 °C until further analyses. Bone samples were thawed at room temperature for 2 h before further morphometric, densitometric and mechanical analyses.
Densitometric evaluation of mandible
Quantitative computed tomography (QCT) technique and Somatom Emotion Siemens apparatus (Siemens, Erlangen, Germany), equipped with Somaris/5 VB10B software (version B10/2004A) were used to determine volumetric bone mineral density (vBMD) of the cortical bone (Cd), mean volumetric bone mineral density (MvBMD) and total bone volume (Bvol) of the whole mandible with teeth (Volume Evaluation application package, Siemens, Erlangen, Germany). The measurement of Cd was performed on cross-sectional scan of mandibular body positioned in the half distance of the diastema (half distance between canine (the fourth incisor) and premolar, approximately 50 mm measuring from the extremity of the mandible determined by the external alveolar margin of the first lower incisor) (Fig. 1a and b). Using the same measuring scan and Osteo CT application package (Software Version B10/2004A), calcium hydroxyapatite (Ca-HA) density of the cortical bone (CbCa-HA) compartment was determined (Fig. 1c). Volumetric bone mineral density of the cortical bone of mandible and CbCa-HA were measured on the same cross-sectional scans for both the right and left mandibular halves. Mean volumetric bone mineral density of mandible and Bvol were determined using volume-of-interest (VOI) limited by minimum and maximum density of the investigated samples at 0 and 3071 Hounsfield units, respectively. The measurements of MvBMD and Bvol were performed for the whole mandible (combined right and left halves) and the results obtained reflect MvBMD measured for all the anatomical structures including teeth.
Determination of geometrical properties of mandible
Geometrical properties of the right and left mandibular body were determined on the basis of measurements of horizontal and vertical diameters (both external and internal) of the mid-diastemal cross-sections of the bone (the same measuring scans which were used for densitometric evaluation) obtained from computed tomography multiplanar reconstructions (Fig. 1d). The values of cross-sectional area (A), second moment of inertia (Ix), mean relative wall thickness (MRWT) and cortical index (CI) were determined in accordance to the following mathematical formulas:
Mechanical analysis of mandible
Using an INSTRON 3367 apparatus and Bluehill 2 software (Instron Corp., Canton, USA) the relationship between the loading force and bone displacement in the three-point bending test was recorded. Right and left halves of mandible (separated at the mandibular symphysis) were placed separately on flat bone supports on the lateral mandibular surface and the measuring head loaded bone samples on the medial surface at 50% of its length with the constant speed of 50 mm/min. Mechanical parameters such as maximum elastic strength (Wy) and ultimate strength (Wf) of both mandibular halves were determined. The distance between bone supports was set at 40% of mandible length.
Biochemical analysis of serum
Blood samples were collected from the lambs at 5 months of age for serum analysis. Insulin-like growth factor I (IGF-I) was determined in serum using IGF-I ELISA kit and two-site IEMA (Immunodiagnostic Systems Ltd., Boldon, Tyne & Wear, UK). Serum concentration of bone-specific alkaline phosphatase (BAP) was measured using Ostase® BAP immunoenzymometric assay (IEMA; Immunodiagnostic Systems Ltd., Boldon, Tyne & Wear, UK). Results of biochemical evaluation of serum were obtained with the use of Benchmark Plus microplate spectrophotometer supplied with Microplate Manager Software Version 5.2.1 (Bio-Rad Laboratories, Inc., Hercules, CA, USA).
Statistical analysis of data collected was performed using Statistica software (version 6.0). Data are presented as means ± SEM. The comparison of mean values of the investigated variables between right and left halves of the mandible was performed using paired Student’s t-test for dependent variables. P-value < 0.05 was considered as statistically significant for all comparisons. Pearson's correlation coefficient (r) was determined between all the investigated mandibular variables, final body weight, IGF-1 and BAP serum concentrations and P < 0.05 was considered as statistically significant.
Results of morphological, densitometric and mechanical properties of the mandible in 5-month-old ram lambs are presented in Table 1. All the investigated morphometric, densitometric and mechanical parameters of right and left mandibular halves were not significantly different (P > 0.05). The values of Pearson’s correlation coefficient between all the investigated parameters of mandible, final body weight, and serum concentration of BAP and IGF-1 in 5-month old sheep are shown in Table 2. Mandibular weight was observed to be positively correlated with mandibular length, Bvol, Cd, A, Ix and Wy (P < 0.05). Mandibular length was positively correlated with Bvol and Cd (P < 0.05). Total bone volume was positively correlated with Cd, A, Ix, and Wf (P < 0.05). Cross-sectional area and Ix were found to be positively correlated (r = 0.97; P < 0.001) and both parameters were positively correlated with Cd (P < 0.05). Volumetric bone mineral density of the cortical bone was found to be also positively correlated with Wy and Wf (P < 0.05). Positive correlations between MRWT and CI as well as between Wy and Wf were found (all P < 0.05).
In this study, a new experimental model to investigate bone metabolism regulation and skeletal system properties in mammals was introduced. Using quantitative computed tomography technique, for the first time Bvol and MvBMD of mandible in sheep was determined. While Bvol represents morphometric parameter, MvBMD is a densitometric parameter characterizing all anatomical structures of the mandible, including the teeth. Similarly to bone weight determination, both Bvol and MvBMD measurements were performed for whole mandible without its separation into two halves. The methodological advantage resulting from the determination of Bvol and MvBMD for whole mandible is that both these parameters may be evaluated both ex vivo and in vivo, while mandibular weight may be determined precisely on ex vivo isolated samples only. As opposed to the parameters characterizing whole mandible, densitometric, geometric and mechanical properties in this bone were determined for the right and left halves separately. As the results of densitometric evaluation of the right and left mandibular body, it was shown that Cd and Ca-HA values were not significantly different in both these halves of the bone. Noteworthy is the fact that anatomical shape and structure of mandible in sheep and physiological occurrence of the diastema enable volumetric bone mineral density determination (in terms of Cd and Ca-HA) exclusively for cortical bone compartment. The reference measuring point of the densitometric parameters in mandible is recommended at the half length of the diastema, since at this point also geometrical parameters for the right and left halves may be evaluated . In this study, computed tomography evaluations of serial cross-sections of the whole mandible along its longitudinal axis have not provided the reference point for the separate determination of vBMD of the trabecular bone compartment. Moreover, it was not possible to exclude non-invasively teeth from bone tissue of the mandible for measurements of bone weight, Bvol and MvBMD. As opposed to sheep model, studies in pigs have revealed that vBMD of the cortical bone in mandible may be measured on cross-sectional scan of the mandibular body positioned just after the 4th premolar tooth . It is interesting that at this reference point in mandible of pigs, cortical bone area and mechanical properties may be also evaluated. The loading head acts on the mandible in pigs exactly at this reference point in three-point bending test . Mechanical testing of mandible in sheep using three-point bending test can not be performed in the reference point used for Cd and Ca-HA determinations, which makes this model different from the mandibular models in pigs. Both densitometric parameters are measured approximately 5 cm from proximal extremity of mandible in sheep (determined by the external alveolar margin of the first lower incisor), while the loading head should act on bone sample at 50% of its length [14, 16]. In this study, the length of mandible varied between 205 and 228 mm. The separation of the right and left halves of the mandible enabled their separate evaluation. Bone length measured for the right and left halve of mandible did not revealed significant differences. Analogical results were obtained evaluating geometrical parameters of mandible. Cross sectional area, Ix, MRWT and CI had no significant differences in the values obtained in both mandibular halves. As opposed to anatomical traits of mandible in other animal species like pig, dog, fox and rodents, oval shape of the cross section of the middle part of the diastema in sheep enables determination of geometrical parameters in accordance to the principles applied in case of long bones such as tibia, femur, humerus and ribs [16, 19–23]. While A and Ix are considered as geometrical indices of mechanical endurance of bone shaft to acting forces, MRWT and CI reflect the amount of bone tissue accumulated in the midshaft ring in relation to the medullary cavity size [14–16]. Besides morphological, densitometric and geometrical parameters, mechanical testing of both halves of mandible was performed in this study. Based on three-point bending test, neither Wy nor Wf were found to be differentiated between the right and left halves of mandible. Considering the observed lack of the differences of mechanical endurance of the right and left halves of mandible and the fact that mandible in sheep may be classified as flat bone, precise mechanical testing of the bone may include the three-point and four-point bending tests; however, in such case both halves undergo structural disintegration . Separate evaluation of the right and left halves of mandible gives possibility to take average from both measurements, improving methodological precision. Moreover, separate evaluation of bone weight, Bvol and MvBMD for the right and left halves of mandible is possible; however, all these measurements must be repeated after the separation of bone halves at the symphysis.
In this study, the correlations between all the investigated parameters of mandible, final body weight and serum BAP and IGF-1 concentration were evaluated. Final body weight and serum indices of bone metabolism were not significantly correlated with the other investigated parameters of mandible in lambs and these observations are similar to the results obtained in pigs were such correlations also were not found. However, in the previous study on pigs, serum IGF-1 concentration was associated with the final body weight . Lack of correlations of MvBMD and Ca-HA with all the other investigated parameters were stated in this study that is partially in agreement with studies on pigs, where MvBMD of mandible were not correlated with final body weight, bone weight, bone length and Bvol. However, except for the insignificant correlation between Bvol and Cd in pigs, all the other evaluated parameters of mandible were significantly positively correlated . The current study revealed also that mandibular weight and volume are positively correlated with morphometric, densitometric and mechanical properties of mandible, while mandibular length, A and Ix were correlated only with morphometric (bone weight and volume) and densitometric (Cd) indices. Volumetric bone mineral density of the cortical bone was positively correlated with morphometric parameters (bone weight, length, Bvol, A and Ix) and has shown the most prognostic value for bone mechanical strength prediction, since its value was positively correlated with both Wy and Wf. Besides listed above relationships, significant positive correlations between geometrical (A and Ix as well as MRWT and CI) and mechanical (Wy and Wf) parameters of mandible were stated.
The results obtained in this study indicate that mandible in sheep provide possibility to investigate effects of experimental manipulations on bone tissue metabolism and skeletal system properties with a use of physiological, nutritional, pharmacological, toxicological and environmental factors. Even though mandibular samples were harvested from ram lambs in this study, the same analytical procedures may be applied for mandible from ewes. Except for ovariectomy-induced osteopenia and osteoporosis, experimental evaluation of mandible from ram lambs may provide valuable data on prevention and treatment of metabolic bone disorders resulting from malnutrition, glucocorticoid treatment, androgen deficiency, mineral and vitamin deficiency and impaired environmental conditions. Metabolic effects of positive or negative factors influencing bone tissue properties in mammals may be more apparent when acting during systemic growth and development period than later in skeletally matured or older animals . The elaborated experimental model in this study is characterized by numerous advantages in comparison to other animal models. In rodents, serial blood collection, small size of mandible and existing differences in bone growth and mineralization pattern in comparison to humans make these experimental models and data interpretation less attractive than in case of sheep or other small ruminants [26–29]. Bone size, histological characteristic and bone remodeling activity, as well as bone metabolism responses to hormonal manipulations in sheep skeleton is similar to humans [30, 31]. Moreover, in sheep serial blood sampling, housing, handling and experimental procedures are relatively easy to perform and similarity of the hormonal profile with humans favors sheep model for studies on bone metabolism [32, 33]. The other rationale for the use of mandible in experimental studies on bone metabolism regulation results from impact of bone loss in maxillofacial bones on health and quality of the stomatognathic system and whole body both in animals and humans. Maxillar and mandibular bone loss most commonly results from periodontal disease, resorption of alveolar ridges following tooth extraction, or a combination of both . Apart from these similarities, the differences such as gastrointestinal structure and digestion process in ruminants and quadruped posture must be also considered as potential limitations in some experimental approaches using the sheep model. However, during the neonatal and postnatal period of systemic growth and development, gastrointestinal tract anatomy and digestion and absorption processes in sheep are similar to monogastric mammals like pigs, dogs and humans. The quadruped posture in sheep appears not to be a limitation in studies on bone metabolism regulation and bone quality with the use of mandibular model, since the body posture has no impact on craniofacial bones characteristics [13, 23, 33].
In conclusion, this study presents basic morphological, densitometric and mechanical characteristics of mandible in 5-month-old Polish Merino sheep. Significant differences of the evaluated parameters between the right and left halves of the mandible were not shown. Common relationships between morphological, densitometric and mechanical parameters of the mandible indicate that the originally elaborated experimental model may serve for further studies on metabolic responses of bone tissue and skeletal system to physiological, nutritional, pharmacological, toxicological and environmental factors influencing bone tissue metabolism. Moreover, quantitative computed tomography may be also used for in vivo and ex vivo evaluation of morphometric and densitometric properties of bones of the stomatognathic system in sheep.
Bone-specific alkaline phosphatase
Total bone volume
- CbCa-HA :
Calcium hydroxyapatite density of the cortical bone
Volumetric bone mineral density of the cortical bone
Insulin-like growth factor I
Second moment of inertia
Mean relative wall thickness
Mean volumetric bone mineral density
Peak bone mass
Quantitative computed tomography
Volumetric bone mineral density
Maximum elastic strength
Anonymous. Prevention and management of osteoporosis. World Health Organ Tech Rep Ser. 2003;921:1–164.
Webster AB. Welfare implications of avian osteoporosis. Poult Sci. 2004;83:184–92.
Thompson KG. Skeletal diseases of sheep. Small Rumin Res. 2008;76:112–9.
Eastell R, Lambert H. Diet and healthy bones. Calcif Tissue Int. 2002;70:400–4.
Tatara MR. Neonatal programming of skeletal development in sheep is mediated by somatotrophic axis function. Exp Physiol. 2008;93:763–72.
Seeman E, Wahner HW, Offord KP, Kumar R, Johnson WJ, Riggs BL. Differential effects of endocrine dysfunction on the axial and the appendicular skeleton. J Clin Invest. 1982;69:1302–9.
Tatara MR, Szabelska A, Krupski W, Tymczyna B, Luszczewska-Sierakowska I, Bieniaś J, Ostapiuk M. Morphometric, densitometric and mechanical properties of mandibular deciduous teeth in 5-month-old Polish Merino sheep. BMC Vet Res. 2014;10:45.
Groen JJ, Duyvensz F, Halsted JA. Diffuse alveolar atrophy of the jaw (non-inflammatory form of paradental disease) and pre-senile osteoporosis. Gerontol Clin. 1960;2:68–86.
Bellido M, Lugo L, Castañeda S, Roman-Blas JA, Rufián-Henares JA, Navarro-Alarcón M, Largo R, Herrero-Beaumont G. PTH increases jaw mineral density in a rabbit model of osteoporosis. J Dent Res. 2010;89:360–5.
Tymczyna B, Bachanek T, Tatara MR, Krupski W, Tyczyna-Sobotka M, Łuszczewska-Sierakowska I. Interrelationships between morphometric, densitometric, and mechanical properties of mandible in 6-month-old male pigs. Bull Vet Inst Pulawy. 2012;56:177–81.
Raubenheimer EJ, Noffke CE, Hendrik HD. Recent developments in metabolic bone diseases: a gnathic perspective. Head Neck Pathol. 2014;8:475–81.
Ulm CW, Solar P, Ulm MR, Matejka M. Sex-related changes in the bone mineral content of atrophic mandibles. Calcif Tissue Int. 1994;54:203–7.
Drozdowska B, Michno M, Michno A. The relationships between mandibular bone mass and skeletal osteopenia/osteoporosis – a review. Nowa Stomatol. 2002;3:127–30.
Ferretti JL, Capozza RF, Mondelo N, Zanchetta JR. Interrelationships between densitometric, geometric and mechanical properties of rat femora: inferences concerning mechanical regulation of bone modelling. J Bone Miner Res. 1993;8:1389–96.
Brodzki A, Silmanowicz P, Tatara MR, Brodzki P, Orzelski M. Cortical index (CI) of dogs’ femur assessment in determining mechanical and geometrical properties of the skeletal system. Med Weter. 2004;60:1056–60.
Tatara MR, Sierant-Rożmiej N, Krupski W, Majcher P, Śliwa E, Kowalik S, Studziński T. Quantitative computed tomography for the assessment of mineralization of the femur and tibia in turkeys. Med Weter. 2005;61:225–8.
Krupski W, Tatara MR, Szabelska A, Łuszczewska-Sierakowska I, Tymczyna B. Interrelationships between morphometric, densitometric and mechanical properties of mandible in 5-month old Polish Merino sheep. Bone Abstracts. 2013;1:PP79.
Tymczyna B, Tatara MR, Krupski W, Tymczyna-Sobotka M, Łuszczewska-Sierakowska I, Bachanek T. Relationships between biochemical bone metabolism indices and morphometric, densitometric and mechanical properties of mandible in 6-month-old pigs. Ann Agric Environ Med. 2012;19:535–9.
Tatara MR, Krupski W, Majcher P, Studziński T. Long-term denervation of the humerus in turkeys as an experimental model for osteopenia. Poult Sci. 2005;84:718–22.
Krupski W, Tatara MR. Interrelationships between densitometric, morphometric, and mechanical properties of the tibia in turkeys. Bull Vet Inst Pulawy. 2007;51:621–6.
Tatara MR, Krupski W, Śliwa E, Maciejewski R, Dąbrowski A. Fundectomy-evoked osteopenia in pigs is mediated by the gastric-hypothalamic-pituitary axis. Exp Biol Med. 2007;232:1449–57.
Tatara MR, Tygesen MP, Sawa-Wojtanowicz B, Krupski W, Majcher P, Harrison AP. Bone development: the effect of short term alpha-ketoglutarate administration on long term mechanical properties of ribs in ram lambs. Small Rumin Res. 2007;67:179–83.
Tatara MR, Krupski W, Tymczyna B, Majcher P, Rosenbeiger P, Niedziela D. Interrelationships between densitometric, morphometric, and mechanical properties of the femur in male Polish Merino sheep. Bull Vet Inst Pulawy. 2011;55:795–9.
Abu-Serriah M, Kontaxis A, Ayoub A, Harrison J, Odell E, Barbenel J. Mechanical evaluation of mandibular defects reconstructed using osteogenic protein-1 (rhOP-1) in a sheep model: a critical analysis. Int J Oral Maxillofac Surg. 2005;34:287–93.
Tatara MR, Krupski W, Majer-Dziedzic B, Szabelska A. Novel and current approaches to dietary and non-dietary bone metabolism regulation. In: Watson RR, Mahadevan D, editors. Handbook of nutrition and diet in therapy of bone diseases. Wageningen: Wageningen Academic Publishers; 2016. p. 129–90.
Long J, Tang W, Fan YB, Tian WD, Feng F, Liu L, Zheng XH, Jing W, Wu L. Effects of rapid distraction rate on new bone formation during mandibular distraction osteogenesis in goats. Injury. 2009;40:831–4.
Jing XL, Farberg AS, Monson LA, Donneys A, Tchanque-Fossuo CN, Buchman SR. Radiomorphometric quantitative analysis of vasculature utilizing micro-computed tomography and vessel perfusion in the murine mandible. Craniomaxillofac Trauma Reconstr. 2012;5:223–30.
Bozzini CE, Champin GM, Alippi RM, Bozzini C. Biomechanical properties of the mandible, as assessed by bending test, in rats fed a low-quality protein. Arch Oral Biol. 2013;58:427–34.
Shimizu Y, Ishida T, Hosomichi J, Kaneko S, Hatano K, Ono T. Soft diet causes greater alveolar osteopenia in the mandible than in the maxilla. Arch Oral Biol. 2013;58:907–11.
Fortune CL, Farrugia W, Tresham J, Scoggins BA, Wark JD. Hormonal regulation of osteocalcin plasma production and clearance in sheep. Endocrinology. 1989;124:2785–90.
Pastoureau P, Arlot ME, Caulin F, Barier JP, Meunier PJ, Delmas PD. Effects of oophorectomy on biochemical and histological indices of bone turnover in ewes. J Bone Miner Res. 1989;4 Suppl 1:477.
Lill CA, Fluegel AK, Schneider E. Effect of ovariectomy, malnutrition and glucocorticoid application on bone properties in sheep: a pilot study. Osteoporos Int. 2002;13:480–6.
Turner AS. The sheep as a model for osteoporosis in humans. Vet J. 2002;163:232–9.
Turner AS. Animal models of osteoporosis - necessity and limitations. eCM. 2001;1:66–81.
Study financed by Medical University of Lublin.
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All data generated or analyzed during this study are included in this published article.
AS was responsible for the concept of the study, collection and interpretation of data, statistical analysis, references collection, and writing the manuscript. MT was responsible for the concept of the study, supervised all stages of the study, participated in animal management, collection and interpretation of data, as well as writing the manuscript. WK performed QCT analysis of bones and was responsible for interpretation of data and supervised all stages of the study. All authors participated in the preparation of, and have approved the final version of the manuscript.
The authors declare that they have no competing interests.
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The experimental procedures used in this study were approved by The Local Ethics Committee on Animal Experimentation of Medical University in Lublin, Poland (Permission number 6/2008).
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Szabelska, A., Tatara, M.R. & Krupski, W. Morphological, densitometric and mechanical properties of mandible in 5-month-old Polish Merino sheep. BMC Vet Res 13, 12 (2016). https://doi.org/10.1186/s12917-016-0921-3