The topography of the thoraco-abdominal viscera in the ostrich (Struthio camelus)

The topography of the thoraco-abdominal viscera in the ostrich was studied in 20 birds varying in age from 2 weeks to 12 months. The lungs occupied the dorsal third of the thorax, and the heart lay in the cranioventral thorax perpendicular to the long axis of the body. There was no pleural cavity. The liver was situated in the caudoventral part of the thorax, and the proventriculus occupied the left cranial part of the abdomen between the 7th vertebral rib and the acetabulum. The gizzard lay in the cranioventral part of the abdomen, resting on the sternum and abdominal floor. The duodenum formed a loop from right to left, with the pancreas lying between the 2 limbs of the loop. The coiled jejunum and ileum occupied the ventral part of the abdomen between the gizzard and pelvis. The two caeca lay on either side of the terminal ileum with their apices in the pelvis. The rectum was the longest part of the intestine and could be divided into a thick proximal segment situated in the right dorsal part of the abdomen, and a thin distal part that occupied the left caudodorsal part of the abdomen. The trilobed kidneys lay along the ventral surface of the synsacrum, with the adrenal glands at their cranioventral poles. The testes lay ventrally to the cranial divisions of the kidneys, whereas the left ovary was situated ventrally to the cranial division of the left kidney. The spleen lay wedged in between the right kidney, caudal vena cava and proventriculus. The thyroid glands were situated at the cranial borders of the subclavian arteries,and the thymus lay at the base of the neck.The articles have been scanned in colour with a HP Scanjet 5590; 600dpi. Adobe Acrobat XI Pro was used to OCR the text and also for the merging and conversion to the final presentation PDF-format

Ascites and the anatomy of the peritoneal sacs of broilers

Although the ascites syndrome of broilers is well documented, all the authors fail to describe exactly in which of the various coelomic cavities ascitic fluid is found. Determination of the precise location of this fluid is essential if the pathogenesis of the syndrome is to be understood and explained. Post-mortem examinations were done on 100 broilers that had ascites or had died of the ascites syndrome. In all of them large quantities of fluid were found in the ventral hepatic peritoneal cavities, moderate amounts in the right dorsal hepatic peritoneal cavities and small amounts in the intestinal peritoneal and pericardial cavities. No ascitic fluid was found in the left dorsal hepatic peritoneal cavity. The amount of ascitic fluid effusing from the liver was directly proportional to the surface area of the liver in a given peritoneal cavity.The articles have been scanned in colour with a HP Scanjet 5590; 600dpi. Adobe Acrobat XI Pro was used to OCR the text and also for the merging and conversion to the final presentation PDF-format.lmchunu2014mn201

A light microscopic and immunocytochemical study of the gastro-intestinal tract of the ostrich (Struthio camelus L.)

Although the histological features and endocrine cells of the gastro-intestinal tract of the chicken have been well studied, little is known about these features of the gut of the ostrich. The present study was undertaken to elucidate the histology and peptide-storing endocrine cells of the ostrich. As a rule the histological features of the gastro-intestinal tract of the ostrich corresponded to that of the fowl. However, certain differences were observed. The superficial proventricular glands were simple, branched tubular glands, while the deep proventricular glands were restricted to a slipper-shaped area and extended into the muscularis mucosae. The gizzard had a variably developed muscularis mucosae, a feature that seems to be unique to the ostrich. The villi of the small intestine were long and branched profusely, forming a labyrinthine surface. No Paneth cells were observed. The mucosa of the ceca and the first part of the rectum was thrown in large circular folds, forming a compressed spiral. Numerous melanocytes were seen in the submucosa and the connective tissue around the blood vessels of the muscle layers at the tips of the ceca. A well developed subserosa was present throughout the gastro-intestinal tract. Endocrine cells immunoreactive to somatostatin, glucagon, gastrin, bombesin, neurotensin, substance P and pancreatic polypeptide were detected in the gastro-intestinal tract of the ostrich. The topographical distribution of those endocrine cells immunoreactive to glucagon, bombesin, neurotensin and substance P differed from that of the chicken. The results of this investigation inferred that at least one of the gut peptides of the ostrich (secretin) to be structurally different from its counterparts in mammal and chicken. Molecular heterogeneity of somatostatin was observed in endocrine cells situated in the deep ventricular glands of the ostrich.The articles have been scanned in colour with a HP Scanjet 5590; 600dpi. Adobe Acrobat XI Pro was used to OCR the text and also for the merging and conversion to the final presentation PDF-format.mn201

The osteology of the African elephant (Loxodonta africana): vertebral column, ribs and sternum

The vertebral column, sternum and ribs of the African elephant were studied and illustrated. In the cervical series, the vertebrae are characterized by very short (compressed) vertebral bodies and short spinous processes. There are 20-21 thoracic vertebrae that carry ribs, and three lumbar vertebrae. The neural arches of the five sacral vertebrae fuse with each other as well as with the wings of the ilium, while the intervertebral discs do not ossify and the vertebral bodies remain separate. There are 19-21 caudal vertebrae. In the latter, the neural arches of only the first five to six vertebrae fuse dorsally, the vertebral foramens of the other vertebrae as well as the vertebral canal remain open dorsally. The body of the first rib is greatly expanded while that of the last three to four ribs are reduced. The cartilages of the first six ribs articulate with the sternum, the last five to six ribs do not bear costal cartilages and are not attached to the costal arch. The sternum consists of five sternabrae that form three approximately equal , but separate, segments. The first segment is formed by the first sternabra, the second segment is formed by the second to fourth sternabrae and the last segment is formed by the fifth sternabra. The first and second sternabrae articulate with each other by means of a synovial joint, the second to fourth sternabrae are fused to each other and the fourth and fifth sternabrae are loosely attached to each other by connective tissue.The articles have been scanned in colour with a HP Scanjet 5590; 600dpi. Adobe Acrobat X Pro was used to OCR the text and also for the merging and conversion to the final presentation PDF-format.mn201

Deep dissections of the veins of the bovine head : unpublished work by Prof. J.M.W. Le Roux (1926-1991)

The articles have been scanned in colour with a HP Scanjet 5590; 600dpi. Adobe Acrobat XI Pro was used to OCR the text and also for the merging and conversion to the final presentation PDF-format.mn201

Osteology of the pelvic limb of the African elephant (Loxodonta africana)

The pelvic girdle was characterized by large, transversely-placed ilial wings. The femur was the longest bone of the skeleton and its fovea capitis was situated caudomedially between the epiphyseal line and the articular surface of the femoral head. A wedge-shaped patella articulated with the femoral trochlea. The bones of the crus were approximately half as long as the femur and consisted of the sturdy tibia and slender fibula. The condyles of the tibia were concave and the femoro-tibial joint was congruent with rudimentary menisci. The tarsus consisted of seven bones which were arranged in three rows. There were five metatarsal bones. Only four digits were present, the third and fourth consisted of three phalanges each while the second and fourth digits were smaller and consisted of two phalanges each. The first digit was represented by one proximal sesamoid bone only. A large, cartilagenous rod or prehallux was attached to the first tarsal and metatarsal bones. Proximal sesamoid bones were present on the plantar aspect of the trochleae of metatarsal bones 1- V. The pes was found to be digitigrade and the digits rested on a thick pad of elastic connective tissue and fat.The articles have been scanned in colour with a HP Scanjet 5590; 600dpi. Adobe Acrobat XI Pro was used to OCR the text and also for the merging and conversion to the final presentation PDF-format.mn201

Osteology of the thoracic limb of the African elephant (Loxodonta africana)

The forelimb bones of 8 elephants (7 adults, 1 juvenile) were studied. In addition, the bones of the digits were dissected and studied in situ in a mature specimen. The scapula, humerus and bones of the antebrachium (particularly the ulna) are massive in comparison to the short, relatively small bones of the manus. There are 8 carpal bones, 5 metacarpal bones and 5 digits. Digits 2-4 consist of 3 phalanges each. The 5th digit consists of 2 phalanges, while the 1st is represented by a single phalanx which is tusk-like and pointed. The distal phalanges of digits 2-4 are very small and do not articulate with the middle phalanges. The proximal sesamoids are well developed and are present on the palmar aspect of all 5 metacarpophalangeal joints. All the bones are illustrated from at least 2 aspects.The articles have been scanned in colour with a HP Scanjet 5590; 600dpi. Adobe Acrobat XI Pro was used to OCR the text and also for the merging and conversion to the final presentation PDF-format.mn201

The skull and mandible of the African elephant (Loxodonta africana)

In the present study the bones of the skull, excluding the hyoid apparatus, are described. All the bones are aerated by sinuses. In the occipital bone the squamous part is aerated from the sinus of the parietal bone, the lateral part is aerated from the tympanic bulla and the basal part from the sinus of the basisphenoid bone. Condylar foramens and hypoglossal canals are absent. A small interparietal bone is present at birth. At an early age it fuses with the surrounding cranial bones. The squamous part of the temporal bone lies sagittally in young animals, but moves progressively to a transverse plane as the animals age. A foramen lacerum is represented by jugular and oval foramens and the carotid canal. The body of the basisphenoid bone is excavated by the massive maxillary tuberosity. The latter extends to the oval foramen and contains the developing molar teeth. The ethmoturbinate, nasal and lacrimal bones are exceptionally small. In old bulls the palatine processes of the incisive bones and their sinuses are gradually displaced by the palatine processes of the maxillae. The incisive part of the mandible does not carry any teeth and both lateral and medial mental foramina are present.The articles have been scanned in colour with a HP Scanjet 5590; 600dpi. Adobe Acrobat XI Pro was used to OCR the text and also for the merging and conversion to the final presentation PDF-format.mn201

Serum- and bone-mineral status of ostriches with tibiotarsal rotation

Tibiotarsal rotation in ostrich chicks is a serious problem that accounts for considerable financial loss to ostrich farmers. Serum- and bone-mineral analyses of 20 ostrich chicks with tibiotarsal rotation were compared with serum- and bone-mineral analyses of eight normal ostrich chicks of comparable age, sex and body mass, and raised under identical conditions. The serum-zinc values were significantly higher and the bone-calcium and phosphorus values significantly lower in the affected group than in the group of normal ostrich chicks. The results indicated poor mineralization of bone with subsequent reactive osteoid formation.The articles have been scanned in colour with a HP Scanjet 5590; 600dpi. Adobe Acrobat XI Pro was used to OCR the text and also for the merging and conversion to the final presentation PDF-format.mn201

Sperm-storage tubules in the vagina of the ostrich (Struthio camelus)

Sperm-storage tubules have been described in a number of species of birds. The presence of these tubules in the Rhea has been mentioned, but no description of these structures in ratites is available. The purpose of this study was to determine the presence and morphology of sperm-storage tubules in the vagina of the ostrich. The study was performed with the use of conventional light- and electron-microscopic techniques. Sperm-storage tubules were located in a 200-mm-wide band of the vagina adjacent to the utero-vaginal junction. The tubules were mostly branched and slightly coiled and lined by columnar epithelial cells. The cells contained a basal nucleus and displayed extensive apical junctional complexes. TEM revealed sperm in all the tubules examined.The articles have been scanned in colour with a HP Scanjet 5590; 600dpi. Adobe Acrobat XI Pro was used to OCR the text and also for the merging and conversion to the final presentation PDF-format.mn201