178 research outputs found

    Inferring muscle functional roles of the ostrich pelvic limb during walking and running using computer optimization

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    Owing to their cursorial background, ostriches (Struthio camelus) walk and run with high metabolic economy, can reach very fast running speeds and quickly execute cutting manoeuvres. These capabilities are believed to be a result of their ability to coordinate muscles to take advantage of specialized passive limb structures. This study aimed to infer the functional roles of ostrich pelvic limb muscles during gait. Existing gait data were combined with a newly developed musculoskeletal model to generate simulations of ostrich walking and running that predict muscle excitations, force and mechanical work. Consistent with previous avian electromyography studies, predicted excitation patterns showed that individual muscles tended to be excited primarily during only stance or swing. Work and force estimates show that ostrich gaits are partially hip-driven with the bi-articular hip–knee muscles driving stance mechanics. Conversely, the knee extensors acted as brakes, absorbing energy. The digital extensors generated large amounts of both negative and positive mechanical work, with increased magnitudes during running, providing further evidence that ostriches make extensive use of tendinous elastic energy storage to improve economy. The simulations also highlight the need to carefully consider non-muscular soft tissues that may play a role in ostrich gait

    The Microvasculature of the Guinea Pig Ureter. A Scanning Electron Microscopic Investigation

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    In 24 albinotic guinea pigs (Cavia porcellus) the gross vasculature and the microvascular architecture of the ureter were studied by light microscopy of tissue blocks and by scanning electron microscopy of vascular casts. The guinea pig ureter is supplied by the renal artery proximally, by the aorta and the internal iliac artery in its mid-segment, and by the uterine and prostatic as well as by the vesical arteries distally. The main arterial trunks run alongside the ureter before they branch to send perforating arterioles to the muscular coat and the mucosal lining. The draining venules are found on both sides of the ureter and form transverse anastomoses. Communications between the arterioles are also located on both sides, but longitudinally arranged. The capillary network of the mucosal lining shows an undulating pattern with tortuous vessels and lies just below the epithelium. The muscular coat and the adventitia have no prominent capillaries of their own. Large arteries are embedded in the adventitia, large veins in the lamina propria. In analogy to human anatomy the vascular arrangement found suggests that, if the ureters are excised in transplant surgery, a lateral incision should be used for the abdominal portion, while the pelvic portion is best approached by a medial incision

    The Vascularization of the Digestive Tract Studied by Scanning Electron Microscopy with Special Emphasis on the Teeth, Esophagus, Stomach, Small and Large Intestine, Pancreas, and Liver

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    The periodontal vessels in adult rats show a ladder-like pattern; in guinea pigs molars, by contrast, they present a honey-comb pattern. The vascular architecture in human teeth seems to be similar to that of rabbits. In guinea pigs, rats, rabbits and humans esophagus circumferential vessels give off perforating vessels. In human esophagus the number and diameter of the vessels in the submucous venous plexus decrease from proximal to distal. In the stomach the subepithelial capillary network shows a honey-comb pattern reflecting the arrangement of the gastric pits. A local portal system between the gastric glands and the surface mucosal cells for the transport of HCO3- ions has been suggested. In the small intestine of humans and rabbits the existence of a dual blood supply of the villus has meanwhile been established. It consists of pericryptal capillaries for the lower portion of the villus (tuft pattern) and a direct arterial supply up to the villus tip (fountain pattern). The colonic microvasculature closely resembles that of the stomach. In the pancreas the insulo-acinar portal system is physiologically significant in that it connects the venules draining the islets with the acini. Venous sphincters in the vascular system of the exocrine pancreas of the rat are of particular functional importance. The hepatic sinusoids are supplied both by the hepatic artery and the branches of the portal vein. The peribiliary plexus is supplied by the afferent vessels of the hepatic artery, the efferent vessels drain the plexus either into the sinusoids or into the lobular vein

    Esophageal Vasculature in the Guinea Pig: A Scanning Electron Microscope Study of Vascular Corrosion Casts

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    The esophageal vascularization of adult male and female albinotic Guinea pigs (Cavia porcellus) is studied by means of light microscopically evaluated serial sections and by scanning electron microscopy (SEM) of vascular corrosion casts. Bronchoesophageal artery (cervical portion), direct branches of tha aorta, recurrent branches of the intercostal arteries (thoracic portion) as well as of the left gastric artery (abdominal portion) supply the esophagus; internal jugular vein, inferior thyroid vein (cervical portion), azygos vein, intercostal veins (thoracic portion) and portal vein, gastroepiploic vein and cranial pancreatoduodenal vein (abdominal portion) drain it. Longitudinally arranged arterioles, venules and capillaries lying at the level of the lamina propria of the esophageal mucosa around the whole circumference of the organ are the most striking vascular features, whereby the venules are considered as those vessels from which esophageal varices arise under pathological conditions

    Sphincters in the Rat Pulmonary Veins. Comparison of Scanning Electron and Transmission Electron Microscopic Studies

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    The microvasculature of the rat lung was studied by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) of vascular corrosion casts and tissue sections. Particular emphasis was placed on postcapillary venules, pulmonary venules and small pulmonary veins (small interlobular veins). Casts of lung capillaries appeared inconspicuous with smooth surface. On the casts of pulmonary venules and small pulmonary veins, by contrast, series of narrow annular constrictions, present at regular distances of 20-25 ÎĽm, were seen. These constrictions may be drastic, narrowing down the caliber of the vessel up to 50%. In the constrictions the marks of circularly running tubular structures were seen and were interpreted as being caused by circular bands of smooth muscle cells. Tissue sections of the corresponding vascular wall showed the presence of single or grouped smooth muscle cells which regularly formed myoendothelial junctions. These smooth muscle cells are interpreted as sphincters, responsible for the constrictions seen on cast preparations. Axon terminals were not found in spatial relationship to these sphincters. It is suggested that the described venous sphincters are governed by blood-borne and/or endothelium-derived substances and may significantly influence the blood flow

    A high-quality annually laminated sequence from Lake Belau, Northern Germany: Revised chronology and its implications for palynological and tephrochronological studies

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    The annually laminated record of Lake Belau offers an exceptional opportunity to investigate with high temporal resolution Holocene environmental change, aspects of climate history and human impact on the landscape. A new chronology based on varve counts, 14C-datings and heavy metal history has been established, covering the last 9400 years. Based on multiple varve counting on two core sequences, the easily countable laminated section spans about 7850 varve years (modelled age range c. 9430 to 1630 cal. BP). Not all of the record is of the same quality but approximately 69% of the varves sequence is classified to be of high quality and only c. 5% of low quality. The new chronology suggests dates generally c. 260 years older than previously assumed for the laminated section of the record. The implications for the vegetation and land-use history of the region as well as revised datings for pollen stratigraphical events are discussed. Tephra analysis allowed the identification of several cryptotephra layers. New dates for volcanic eruptions are presented for the Lairg B event (c. 6848 cal. BP, 2s range 6930–6713 cal. BP), the Hekla 4 event (c. 4396 cal. BP, 2s range 4417–4266 cal. BP), and Hekla 3 eruption (c. 3095 cal. BP, 2s range 3120–3068 cal. BP)

    Hip joint articular soft tissues of non-dinosaurian Dinosauromorpha and early Dinosauria: evolutionary and biomechanical implications for Saurischia

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    Dinosauromorphs evolved a wide diversity of hind limb skeletal morphologies, suggesting highly divergent articular soft tissue anatomies. However, poor preservation of articular soft tissues in fossils has hampered any follow-on functional inferences. We reconstruct the hip joint soft tissue anatomy of non-dinosaurian dinosauromorphs and early dinosaurs using osteological correlates derived from extant sauropsids and infer trends in character transitions along the theropod and sauropodomorph lineagues. Femora and pelves of 107 dinosauromorphs and outgroup taxa were digitized using 3D imaging techniques. Key transitions were estimated using maximum likelihood ancestral state reconstruction. The hips of dinosauromorphs possessed wide a disparity of soft tissue morphologies beyond the types and combinations exhibited by extant archosaurs. Early evolution of the dinosauriform hip joint was characterized by the retention of a prominent femoral hyaline cartilage cone in post-neonatal individuals, with the cartilage cone independently reduced within theropods and sauropodomorphs. The femur of Dinosauriformes possessed a fibrocartilage sleeve on the metaphysis, which surrounded a hyaline core. The acetabulum of Dinosauriformes possessed distinct labrum and antitrochanter structures. In sauropodomorphs, hip congruence was maintained by thick hyaline cartilage on the femoral head, whereas theropods relied on acetabular tissues such as ligaments and articular pads. In particular, the craniolaterally ossified hip capsule of non- Avetheropoda neotheropods permitted mostly parasagittal femoral movements. These data indicate that the dinosauromorph hip underwent mosaic evolution within the saurischian lineage and that sauropodomorphs and theropods underwent both convergence and divergence in articular soft tissues, correlated with transitions in body size, locomotor posture, and joint loading

    More than one way to be a giant: Convergence and disparity in the hip joints of saurischian dinosaurs

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    ABSTRACT Saurischian dinosaurs evolved seven orders of magnitude in body mass, as well as a wide diversity of hip joint morphology and locomotor postures. The very largest saurischians possess incongruent bony hip joints, suggesting that large volumes of soft tissues mediated hip articulation. To understand the evolutionary trends and functional relationships between body size and hip anatomy of saurischians, we tested the relationships among discrete and continuous morphological characters using phylogenetically corrected regression. Giant theropods and sauropods convergently evolved highly cartilaginous hip joints by reducing supraacetabular ossifications, a condition unlike that in early dinosauromorphs. However, transitions in femoral and acetabular soft tissues indicate that large sauropods and theropods built their hip joints in fundamentally different ways. In sauropods, the femoral head possesses irregularly rugose subchondral surfaces for thick hyaline cartilage. Hip articulation was achieved primarily using the highly cartilaginous femoral head and the supraacetabular labrum on the acetabular ceiling. In contrast, theropods covered their femoral head and neck with thinner hyaline cartilage and maintained extensive articulation between the fibrocartilaginous femoral neck and the antitrochanter. These findings suggest that the hip joints of giant sauropods were built to sustain large compressive loads whereas those of giant theropods experienced compression and shear forces
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