This study was carried out on the tongues of 12 adult normal healthy Egyptian fruit bats of both sexes. The tongue is protrusible, elongated flat with a rounded apex and its wide and thickness increase gradually toward the lingual root. There are four types of lingual papillae; two mechanical and two gustatory. The tongue divided into three parts (anterior, middle and posterior), each part subdivides into three regions; two lateral regions and median region, in addition to the lingual apex to the anterior region. The lingual papillae close to the median region of the tongue were posteriorly directed toward the pharynx, while theses present on the lateral regions of the tongue are directed medioposteriorly. There are sex subtypes of the filiform papillae; three on the anterior part (small, conical and giant), two on the middle part (cornflower and leaf-like papillae) while the posterior part contain rosette shape filiform papillae, in addition to transitional papillae and conical papillae. Two gustatory papillae represented by; small number of fungiform papillae which scattered among the filiform papillae on lingual apex and two lateral regions of the anterior and middle part of tongue, while the three circumvallate papillae on the posterior part were arranged in a triangle form.
This study represents the first attempt to describe ultrastructural features of teeth in different three ages of white grouper (Epinephelus aeneus) grossly and by the aid of the electron microscope. The current study depends on 18 oropharyngeal cavity of E. aeneus from each age-stages. There are common and special characterization between each age. Five teeth bands in the roof (incisive, canine, upper molar, palatine, and vomer), while two bands in the floor (incisive, molar). The apical teeth part resembles the arrowhead that bordered by groove distally. In 5 cm age, small upper incisive teeth had two appearance (straight and curved), and vomer teeth arranged in triangular in only one row (while, in 12 cm fish arranged in two rows and in 15 cm fish arranged in more than two rows), the palatine teeth began rostrally as one row then two rows and terminated by one row, while in other two ages began by two, then three and ended by two rows. There is no canine teeth in lower jaw in all age. In 12 cm fish, the rostral row of lower incisive teeth usually contain small straight teeth,
The current work is designed to give the first trial to characterize the ultrastructural lineaments of the oral cavity floor in juvenile and adult white grouper. The present work depends on 10 oral cavities floor from each age. The common features joined the oral cavities floor of the juvenile and adult fish summarized in; oral cavity floor had two teeth bands (lower incisive and lower molar), tongue with its two lateral spinated lines, lower velum, ridges, the lower lip divided into a single anterior part and two lateral part, and the absence of lower canine teeth. The oral surface of semilunar lower velum had round fungiform papillae that carried taste buds type I. The non-protrusible elongated tongue had a clear apex, body, and root with the absence of any taste buds. The dorsal lingual surface of the body had two lateral spinated lines, a single ridge and microtubercles. The smooth dorsal lingual surface of the root did not carry any ridges. The notched lower velum at the middle of the free border was observed in juveniles and adults. Meanwhile, there are some variations between juvenile and adult as; absence of lower incisive ridge only in juvenile, pointed tongue with sublingual ridge observed in juvenile while round without sublingual ridge in adult fish, moreover the presence of velvar ridges observed only in adult fish. The obtained findings provided essential data to aquaculture of this fish species in Egypt by determining the food particle types that are favorite to this fish. HighlightsThe common features joined the oral cavities floor of the juvenile and adult fish summarized in; oral cavity floor had two teeth bands (lower incisive and lower molar), tongue with its two lateral spinated lines, lower velum, ridges, the lower lip divided into a single anterior part and two lateral part, and the absence of lower canine teeth. The oral surface of semilunar lower velum had round fungiform papillae that carried taste buds type I. The dorsal lingual surface of the body had two lateral spinated lines, a single ridge and microtubercles. The smooth dorsal lingual surface of the root did not carry any ridges. Meanwhile, there are some variations between juvenile and adult as; absence of lower incisive ridge only in juvenile, pointed tongue with sublingual ridge observed in juvenile while round without sublingual ridge in adult fish, moreover the presence of velvar ridges observed only in adult fish.
The present investigation was conducted to provide a full anatomical description of the stifle joint of donkeys using 3D computed tomography imaging technique, in addition to the classic anatomical methods, such as radiography and cross‐anatomical sectioning. The radiography and CT imaging of stifle joint were interpreted in comparison with cross‐sectional anatomical sections. Volume‐rendering reconstruction techniques (3D‐CT) were used to describe the anatomical structure of stifle joint. The used twelve adult healthy donkeys were free from any musculoskeletal disorders. Four donkeys were used for the gross anatomical observations, four for CT and radiography and two live animals for determination the site of injections. The results of this study revealed that the complex stifle joint was formed from three joints: femorotibial, femoropatellar and proximal tibiofibular. The articular surfaces were described for each joint, and the synovial layer of the articular capsule formed three main joint sacs: femoropatellar, medial femorotibial and lateral femorotibial sacs. The ligaments of stifle joint were recorded, and meniscal ligaments included cranial and caudal ligaments of medial and lateral menisci and meniscofemoral ligament of lateral meniscus. The cruciate ligaments were also described and they included the cranial and caudal cruciate ligaments, while the patellar ligament included the medial, middle and lateral patellar ligaments. The arterial supply and the site of injection of the stifle joint were described. In conclusion, the 3D reconstruction CT provided well‐defined baseline reference image for the stifle joint of donkeys for anatomist, radiologist, surgeons and researchers.
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 2 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.
The digit of the donkey as a draught animal is commonly susceptible to much affection. The purpose of the present study was to provide a detailed anatomic reference of radiographic and computed tomographic images in conjunction with cross and sagittal sections of the normal fetlock, pastern and coffin joints of the donkey for anatomists, surgeons and veterinary students. Eight adult donkeys of both sexes free from any joints affection were used in our study. The digit of two donkeys had undergone radiographic and computed tomographic scanning; the other donkey's specimens were used to anatomical dissection and sectional anatomy. In the computed tomography (CT) of the fetlock joint all bone structures of the joint appeared also the soft tissue structures that could be identified and evaluated on the different soft tissue window planes included the common digital extensor tendon, lateral digital extensor tendon, superficial digital flexor tendon (SDFT), deep digital flexor tendon (DDFT), straight, oblique, and cruciate distal sesamoidean and intersesamoidean ligaments. For the pastern joint the structures that can be identified including the proximal phalanx, DDFT and digital cushion. In the coffin joint the collateral sesamoidean ligament (CSL) is difficult to identify on CT images.
The present work aims to provide more anatomical information on the stifle joint of the investigated species using computed tomography with gross anatomical cross-sections. The current work analyzed the stifle joint of the pelvic limbs of 12 adult donkeys, goats and dogs of both genders. The medial condyle of the femur was larger than the lateral one in the donkey, while it was smaller and lower than the lateral one in the goat and in the dog. The unsuitable femoral and tibial condyles were adapted by the presence of menisci. In the donkey, the medial meniscus was crescentic in shape, but it was semicircular in the goat, while in the dog, the medial and lateral menisci were C-shaped. In the donkey, the medial meniscus was larger than the lateral one, but in the goat and in the dog, the lateral meniscus was the largest, and more concave and thicker. The lateral meniscus was semicircular in the donkey, but it was shaped like an elongated kidney in the goat. In the goat and in the dog, the central border of two menisci was thin, concave and notched centrally. The meniscal ligaments included cranial and caudal ligaments of the medial and lateral menisci, and meniscofemoral ligament of the lateral meniscus. In the dog, the cranial ligament of the medial meniscus was absent, and the medial meniscus had no bony attachment to the tibia but it attached to the transverse intermeniscal ligament, which connected the cranial horn of the medial meniscus with the cranial ligament of the lateral meniscus. The meniscofemoral ligament connected the caudal pole of the lateral meniscus with the intercondyloid fossa of the femur.
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