Gross Anatomical Studies of the Oropharyngeal Cavity in Eurasian Hobby (Falconinae: Falco Subbuteo, Linnaeus 1758)

There is no descriptive information about morphology of the oropharyngeal cavity of Eurasian Hobby. There is a common oropharyngeal cavity of Eurasian Hobby as reported in all avian species. The oral cavity of the Eurasian Hobby takes the triangular cone shape, while the roof of the oral cavity was formed by an incomplete hard palate, which presents by a long median choanal cleft, which connects the oropharynx to the nasal cavity. The choanal cleft divided into two parts; the rostral long narrow part and the caudal wide part. The infundibular cleft is very narrow, small, shorter, and more caudal midline slit-like opening. There were numerous conical backward papillae were scattered singly or arranged in five rows on the roof of the oral cavity. The arranged five rows of conical papillae; first row was the transverse huge caudomedially directed conical palatine papillae, encircled the choanal cleft. The second and third rows are longitudinal rows of the caudomedially directed papillae, were located parallel to the rostral narrow part of choana on each side. The fourth row is semicircular row of caudomedially directed conical palatine papillae, while the fifth row is oblique line of palatine papillae. The roof of pharynx has two semicircular papillary rows on the caudal border of the pharyngeal folds. The elongated tongue is non-protrusible and not extended to fill the limit of the lower beak. The laryngeal mound contains middle, elongated opening (glottis) which connected to the trachea and not guarded by the epiglottis

Histological characterisation of the skin of the Paraechinus hypomelas, Brandt, 1836 (Erinaceidae: Eulipotyphla)

Background: The current study represents the first description of the histological characterisations of the normal skin of Brandt’s hedgehog (paraechinus hypomelas). Materials and methods: Skin samples were collected from abdomen, back, nostril and cloacal regions. Results: The skin consisted of 3 layers including epidermis, dermis and hypodermis. The epidermis was covered by a layer of keratinised squamous epithelium mainly in the back region, but the skin keratinisation was present with a little amount or may was absent in other regions. Histologically, the total thickness of skin was maximum on the back and minimum on the cloacal regions. The epidermis consisted of 4 layers and stratum lucidum was absent in all regions. Beneath the epidermis, the dermis layer was constituted of dense connective tissue in which the hair follicles, sweat glands, sebaceous glands, arrector pilli muscles and blood vessels were present. The sweat and sebaceous glands were more populated in the nostril region. The hair follicles were located in the epidermal and dermal regions. Vibrissae were only in the nostrils region and characterised from other hairs by their large and well innervated hair follicle which was surrounded by the blood sinus. Conclusions: The present findings show that in Brandt’s hedgehog (paraechinus hypomelas) the back and cloacal regions have thickest and thinnest skin respectively as compared to the nostril and abdominal regions. In addition, sebaceous and sweat glands were mainly populated in the nostril regio

Morphological examination of the accessory sex glands of the Barki bucks (Capra hircus)

The present investigation was prepared to describe the accessory sex glands of the Barki bucks grossly and by light microscopy. There are four sex glands: ampullary, vesicular, prostate, and bulbourethral. The ampullary gland is an enlargement of the terminal part of the ductus deferens, its glandular part has branched tubuloalveolar glands, and its secretory alveoli lined with a pseudo-stratified epithelium composed of cuboidal to columnar cells. The vesicular gland takes the appearance of a cluster of grapes and the left vesicular gland is enlarged and higher than the right one. The vesicular gland is a lobulated tubuloalveolar gland with wide intralobular space and the gland contain a secretory unit which lined by pseudo-stratified columnar epithelium, and the interlobular ductules lined by the stratified epithelium, while the interlobular duct lined by simple cuboidal epithelium moreover, the lining epithelium of secretory part consists of tall columnar cells. The prostate gland consists only of the disseminated part and is enclosed by a connective tissue capsule that was thin dorsally, thick laterally, and reduced in thickness ventrally. The prostatic acini are lined by simple cuboidal epithelium. The bulbourethral gland was similar in size to the walnut and surrounded by a capsule and there are interlobular connective tissue septa that divided the gland into lobes and lobules of different sizes. The bulbourethral gland contains secretory units lined by the tall simple columnar epithelium of mucous type with basely located nuclei and eosinophilic cytoplasm contain granular secretion. The gross and microscopic examination of the four accessory sex glands gave valuable information in the future pathology diagnosis of the accessory sex glands of the Barki bucks

Structural and Functional adaptation of the lingual papillae of the Egyptian fruit bat (Rousettus aegyptiacus): Specific Adaptive feeding Strategies

The current investigation was directed to clarify the correlations between the feeding strategy and lingual structure of the Egyptian fruit bat captured from the Egyptian east desert. The current work depends on twelve adult Egyptian fruit bats that observed grossly and with the help of the stereo, light, and scanning electron microscope. There were three types of the lingual papillae; one mechanical filiform and two gustatory (fungiform and circumvallate). There were seven subtypes of filiform papillae were recognized on the seven lingual regions. There were scanty numbers of fungiform papillae distributed among the filiform papillae on the lingual tip and two lateral parts of apex and body while fungiform papillae completely absent in the median part. There were three circumvallate papillae. The central bulb of circumvallate papillae surrounded by one layer of two segmented circular annular bad. The lingual tip had cornflower-like and diamond-shaped filiform papillae. Histochemical results revealed that the lingual glands were a stronger AB-positive reaction and gave dark blue color, while the reaction for the PAS-stain was negative. Also, the glands exhibited a blue color as an indication of positive AB reactivity with combined AB-PAS staining

Gross Anatomical Studies of the Oropharyngeal Cavity in Eurasian Hobby (Falconinae: Falco Subbuteo, Linnaeus 1758)

There is no descriptive information about morphology of the oropharyngeal cavity of Eurasian Hobby. There is a common oropharyngeal cavity of Eurasian Hobby as reported in all avian species. The oral cavity of the Eurasian Hobby takes the triangular cone shape, while the roof of the oral cavity was formed by an incomplete hard palate, which presents by a long median choanal cleft, which connects the oropharynx to the nasal cavity. The choanal cleft divided into two parts; the rostral long narrow part and the caudal wide part. The infundibular cleft is very narrow, small, shorter, and more caudal midline slit-like opening. There were numerous conical backward papillae were scattered singly or arranged in five rows on the roof of the oral cavity. The arranged five rows of conical papillae; first row was the transverse huge caudomedially directed conical palatine papillae, encircled the choanal cleft. The second and third rows are longitudinal rows of the caudomedially directed papillae, were located parallel to the rostral narrow part of choana on each side. The fourth row is semicircular row of caudomedially directed conical palatine papillae, while the fifth row is oblique line of palatine papillae. The roof of pharynx has two semicircular papillary rows on the caudal border of the pharyngeal folds. The elongated tongue is non-protrusible and not extended to fill the limit of the lower beak. The laryngeal mound contains middle, elongated opening (glottis) which connected to the trachea and not guarded by the epiglottis

Ultrastructural features on the oral cavity floor (tongue, sublingual caruncle) of the Egyptian water buffalo (Bubalus bubalis): gross, histology and scanning electron microscope

The present work was focused on the morphological characters of the lingual caruncles, and tongue with its papillae of Egyptian water buffalo (Bubalus bubalis) using the gross, light, and scanning electron microscope. The ventral surface of the sublingual caruncle carried a small opening of the duct of both monostoamtic and mandibular salivary gland. The lingual mucosa of dorsal, lateral border, some extent to ventral surface of apex had lingual papillae (filiform, fungiform), while the lingual mucosa of body especially at torus linguae had conical papillae, but circumvallate papillae observed at the caudal part of body and root. The dorsal surface of apex and body carried numerous long thread-like with blunt apex caudally directed filiform papillae that covered with keratinized scales without secondary papillae. The degree of keratinization classified filiform papillae into rostral part of high keratinization and caudal less keratinization. Conical papillary surface carried exfoliated epithelium with longitudinal groove on its rostral surface and had CT core does not reach the level surface of epithelium and carried secondary papillae. Fungiform papillae scattered among filiform papillae on the dorsal and ventral surface of apex and its convex surface had exfoliated keratinized epithelium. Circumvallate papillae surrounded by circular deep groove that bordered by vallum that carried small secondary papillae that ended into the primary groove. Taste buds of circumvallate papillae opened in the lateral lining epithelium facing the groove. Von Ebner's glands were observed in CT under papillae especially toward the groove and their ducts open into the base of the groove

Deflection Analysis of a Nonlocal Euler–Bernoulli Nanobeam Model Resting on Two Elastic Foundations: A Generalized Differential Quadrature Approach

This paper provides a general formularization of the nonlocal Euler–Bernoulli nanobeam model for a bending examination of the symmetric and asymmetric cross-sectional area of a nanobeam resting over two linear elastic foundations under the effects of different forces, such as axial and shear forces, by considering various boundary conditions’ effects. The governing formulations are determined numerically by the Generalized Differential Quadrature Method (GDQM). A deep search is used to analyze parameters—such as the nonlocal (scaling effect) parameter, nonuniformity of area, the presence of two linear elastic foundations (Winkler–Pasternak elastic foundations), axial force, and the distributed load on the nanobeam’s deflection—with three different types of supports. The significant deductions can be abbreviated as follows: It was found that the nondimensional deflection of the nanobeam was fine while decreasing the scaling effect parameter of the nanobeams. Moreover, when the nanobeam is not resting on any elastic foundations, the nondimensional deflection increases when increasing the scaling effect parameter. Conversely, when the nanobeam is resting on an elastic foundation, the nondimensional deflection of the nanobeam decreases as the scaling effect parameter is increased. In addition, when the cross-sectional area of the nanobeam varies parabolically, the nondimensional deflection of the nonuniform nanobeam decreases in comparison to when the cross-sectional area varies linearly

The tongue of the red-eared slider (Trachemys scripta elegans): morphological characterization through gross, light, scanning electron, and immunofluorescence microscopic examination

Abstract The red-eared slider (Trachemys scripta elegans) is renowned for its remarkable adaptations, yet much of its complex biology remains unknown. In this pioneering study, we utilized a combination of gross anatomy, scanning electron microscopy (SEM), light microscopy, and immunofluorescence techniques to examine the tongue’s omnivorous adaptation in this species. This research bridges a critical knowledge gap, enhancing our understanding of this intriguing reptile. Gross examination revealed a unique arrowhead-shaped tongue with a median lingual fissure and puzzle-piece-shaped tongue papillae. SEM unveiled rectangular filiform, conical, and fungiform papillae, with taste pores predominantly on the dorsal surface and mucous cells on the lateral surface of the papillae. Histologically, the tongue’s apex featured short rectangular filiform and fungiform papillae, while the body exhibited varying filiform shapes and multiple taste buds on fungiform papillae. The tongue’s root contained lymphatic tissue with numerous lymphocytes surrounding the central crypt, alongside lingual skeletal musculature, blood and lymph vessels, and Raffin corpuscles in the submucosa. The lingual striated muscle bundles had different orientations, and the lingual hyaline cartilage displayed a bluish coloration of the ground substance, along with a characteristic isogenous group of chondrocytes. Our research represents the first comprehensive application of immunofluorescence techniques to investigate the cellular intricacies of the red-eared slider’s tongue by employing seven distinct antibodies, revealing a wide array of compelling and significant findings. Vimentin revealed the presence of taste bud cells, while synaptophysin provided insights into taste bud and nerve bundle characteristics. CD34 and PDGFRα illuminated lingual stromal cells, and SOX9 and PDGFRα shed light on chondrocytes within the tongue’s cartilage. CD20 mapped B-cell lymphocyte distribution in the lingual tonsil, while alpha smooth actin (α-SMA) exposed the intricate myofibroblast and smooth muscle network surrounding the lingual blood vessels and salivary glands. In conclusion, our comprehensive study advances our knowledge of the red-eared slider’s tongue anatomy and physiology, addressing a significant research gap. These findings not only contribute to the field of turtle biology but also deepen our appreciation for the species’ remarkable adaptations in their specific ecological niches