A variety of skull shapes are frequently used for discrimination between animal species, breeds, and sexes. In this study, skulls of three different breeds of cats were examined by the geometric morphometric method, with the aim of revealing skull shape differences. For this purpose, 27 cats (6 British Shorthair, 7 Scottish Fold, and 14 Van cats) were used. The skulls of cats were modeled by computed tomography. Geometric morphometrics was applied using dorsal (8 landmarks, 63 semilandmarks) and lateral (8 landmarks, 63 semilandmarks) skull projections on these models. Centroid size differences between the breeds were statistically insignificant. However, the differences in shape were statistically significant for both the dorsal view and lateral view. Shape variation was less in the British Shorthair than in other breeds. Shape differences generally occurred around the orbit. In the skull of Scottish Folds, the orbit was situated more caudally than in other breeds. The British Shorthair had the largest orbital ring. In dorsal view, the Scottish Fold had the largest orbital diameter. The orbital ring of Van cats was smallest in both dorsal and lateral views. In the canonical variate analysis, it was seen that the breeds were separated from each other. The shape difference in the skull between different cat breeds could be revealed by geometric morphometrics. The results of this study provide useful information for taxonomy.

The aim of this work was to study the topography, morphology, vascularisation, histology and innervation of the lungs in the ground squirrel (Spermophilus citellus) and compare these data with those concerning the rat, mole rat, rabbit and mouse. The research was carried out on 15 animals. It was revealed that the right lung has four lobes (cranial, middle, caudal and accessory lobes), while the left lung is not divided into segments. The functional vessels are a. pulmonalis dextra et sinistra and vv. pulmonales (5–6), while the nutritive vessels of the lungs are a. bronchoesophagea dextra and v. bronchoesophagea dextra. Histological tissue sections of the lungs revealed that the wall of terminal bronchioles contains no cartilage and the mucosal epithelium is pseudostratified, cubic and ciliated. Clara cells (club cells, bronchiolar exocrine cells) are present but have no cilia. The lung alveolar diameter is 37 μm on average, and the thickness of the alveolar wall and the interalveolar septa is 1.38 μm. Destruction of the alveolar walls, accumulation of erythrocytes in the capillaries of alveolar septa and destruction of the cytolemma of the capillary endothelium were detected. In addition, connective tissue fibres and peripheral nerves were detected by silver impregnation.

The carapace morphology of tortoises is a crucial characteristic used for species identification, with features such as shell shape, roughness, and color patterns varying among species. Understanding this morphological diversity is valuable not only for taxonomic classification but also for more specialized clinical approaches. This study investigated the morphological differences in the shells of Leopard tortoises (Stigmochelys pardalis), African spurred tortoises (Centrochelys sulcata), and Greek tortoises (spur-thighed tortoises; Testudo graeca) raised in captivity. Using 3D scanners, the carapaces were modeled, and a 3D geometric morphometric method was employed to analyze shape variations and dimensional features, with landmarks applied automatically. Among the species studied, African spurred tortoises had the largest carapace size. Principal component analysis (PCA) identified PC1 and PC3 as critical factors in distinguishing between species based on morphological characteristics. Positive PC1 values, associated with a shorter carapace height, indicated a flatter or more compact shell shape. A higher PC3 value corresponded to a raised shape at the back of the shell, while a lower PC3 value indicated a raised shape at the front. Specifically, Leopard tortoises exhibited a higher carapace shape than the other species, while African spurred tortoises had shorter carapaces. An allometric effect was observed in the carapaces, where smaller specimens tended to be proportionately higher-domed, whereas larger shells displayed a lower height in shape. These findings highlight the significance of shape variations in tortoise shells, which emerge during adaptation and have important implications for taxonomy and clinical practice. Such differences should be carefully considered in veterinary care and species identification.

Poultry production is one of the most intensive sectors of animal production providing a significant source of animal protein through meat and eggs. However, increasing production intensity has brought challenges related to animal health, welfare, and product quality. In chickens (Gallus gallus domesticus), the sterno-pectoral region represents a key anatomical and functional unit that supports the birds’ body and is essential for locomotion and respiration. This region is particularly susceptible to the adverse effects of intensive selection and production in both broilers, i.e., meat production, and laying hens, i.e., egg production. Skeletal disorders of the sternum, predominantly observed in laying hens, and breast muscle myopathies, primarily affecting broilers, are typically investigated as separate conditions. However, their anatomical co-localization, shared developmental background, and common risk factors suggest they should be considered within a unified framework. The aim of this review is to integrate the current knowledge on skeletal and muscular disorders of the sterno-pectoral region, with emphasis on their interrelationships, underlying mechanisms, and implications for production efficiency and animal welfare. By identifying this region as a critical hotspot for production-related pathology, this review offers a more comprehensive perspective on the biological limits of intensive poultry production and highlights the importance of an integrated approach as the foundation for developing future breeding and production strategies.

Metatarsal bones and finger articles of roe deer and sheep are rarely used for animal identification. In practice there are frequent cases where on a corpse the head and distal parts of the limbs are missing. That is in order to prevent the identification of the bones, by which it is easiest to determine the animal species. For identification of metatarsal bones (Ossa metatarsi) as well as finger articles (Os?sa digitorum pedis seu phalanges digitorum) there were used distal parts of hindlimb bones, taken from 6 roe deers and 7 sheep. Afer the separation from the soft tissues, the bones were boiled in an autoclave, and for bleaching and degreasing they were kept in 3% solution of hydrogen peroxide (H2O2). The bones were air dried, and then photographed. In roe deer, four metatarsal bones are developed: the second (Os metatarsale secundum), the third (Os metatarsale tertium), the fourth (Os metatarsale quartum) and the fifth (Os metatarsale quintum). In sheep, the third (Os metatarsale tertium) and the fourth (Os metatarsale quartum) metatarsal bones are developed. Both in roe deer and sheep, the third and the fourth metatarsal bones are fused into one single bone - main metatarsal bone. In sheep, on dorsal and plantar side of these bones there are grooves which are more shallow and wider than in roe deer. In roe deer, hindlimbs have four fingers, and in sheep two. In roe deer there is also the difference in the number of articles on the second and fifth finger. In this animal the second and fifth finger have coalesced the first and second article (Ph1 + Ph2) and the third article(Ph3). Based on the third article of the third and fourth finger, it may be distinguished one animal from another. Margo solearis in roe deer is peaky and in sheep it is blunt. In roe deer Processus extensorius is peaky on Margo coronalis, while in shee it is blunt. In the cases when material (fresh meat, blood, hair) necessary for some laboratory methods is missing, there is used the method of animal species determination based on morphological differences between the bones of these two animals. By this method it can be with certainty determined which animal the bones belong to.