Observations on the external morphology and vasculature of a fetal heart of the bowhead whale, Balaena mysticetus.

BACKGROUND: Specialized demands within the aquatic environment for over some 60 million years have shaped unique morphological expressions in the whales, dolphins, and porpoises (Cetacea). Detailed consideration of these features, particularly in the great whales, has often been constrained by difficulties in securing adequate specimens for study. We had the opportunity to examine external heart morphology in a rarely obtained and prepared specimen from the bowhead whale, Balaena mysticetus. METHODS: The external morphology and in situ relations of a formalin-perfused heart were examined grossly in a near-term bowhead fetus. Latex injections assisted visualization of coronary vasculature. Magnetic resonance imaging was used to clarify heart positioning within the thoracic cavity in two younger (early and mid-gestational) intact fetuses. RESULTS: The heart was globular in form, with a blunt apex and wide base; it was laterally broad relative to height yet considerably compressed between nearly planar atrial (diaphragmatic) and auricular (sternocostal) surfaces. The heart constituted 0.01 of body mass in the near-term fetus. Within the thoracic cavity, the heart tilted forward on its long axis, placing the great basal vessels in the region of the thoracic inlet. The aorta extended forward from mid-base in parallel with the pulmonary trunk, arched sharply to the left, producing in succession the brachiocephalic trunk, left common carotid artery, and the left subclavian artery. Bifurcation of the brachiocephalic trunk yielded the right common carotid and right subclavian arteries. The distal portion of the aortic arch was linked to the pulmonary trunk via the ductus arteriosus. The aorta then swung caudally over the heart base, descending beneath the bodies of the thoracic vertebrae. The ascending aorta featured three bulbous sinuses immediately distal to the three semilunar cusps of the aortic valve. Originating along the distal boundaries of the left and right sinuses were the left and right coronary arteries. The arteries were similar in size and, because each sent contributions along their respective coronary and interventricular grooves, the heart can be described as bilateral relative to arterial supply. Anastomoses were common within and between the two arteries. Venous return from the heart was comprised of the great, middle, and right cardiac veins, all three converging in the coronary sinus. The right cardiac vein also included tributaries that emptied directly into the right atrium. CONCLUSIONS: External heart morphology in the fetal bowhead whale examined was distinguished by a laterally broad conformation with significant compression between its cranial and caudal surfaces. Aortic bulb configuration in combination with an expandable aortic arch may support blood service to the heart during diastole. Vascular service to the heart featured a complex vessel network with extensive intraarterial and intravenous anastomoses that enable many alternate blood perfusion pathways and may be adaptive to water-column-pressure fluctuations experienced by a large diving mammal.

Toxaphene, PCB, DDT, and Chlordane Analyses of Beluga whale blubber.

Beluga whales bioaccumulate organochlorines from their environment. Blubber samples of Beluga Whales from Alaska's north coast contain organochlorines, including Toxaphene (polychlorinated camphenes) PCBs, DDTs and chlordane. Toxaphene was the organochlorine pesticide found in the highest concentration in all samples with the exception of the 6 year old male where PCBs were highest. The source of these organochlorines is likely global distillation from lower latitudes. Males had higher concentrations than females and the oldest male had higher concentration than the younger male. Females exhibit a decrease in concentrations with age. The fetus had about 10% higher concentrations for all organochlorines compared to the mother. Transplacental transfer of organochlorines and lactation lower the contaminant concentration in females. Older females have lower contaminate concentrations likely due to continual reproductive success. Consumption of older males will expose humans to higher levels of organochlorines.

Dolphin peripheral visual pathway in chronic unilateral ocular atrophy: complete decussation apparent.

Components of the peripheral visual pathway were examined in two bottlenose dolphins, Tursiops truncatus, each with unilateral ocular degeneration and scarring of 3 or more years' duration. In both animals, the optic nerve associated with the blind eye (right eye in Tg419 and left eye in Tt038) had a translucent, gel-like appearance upon gross examination. This translucency was also evident in the optic tract contralateral to the affected eye. In Tg419, myelinated axons of varying diameters were apparent in the left optic nerve, whereas the right optic nerve, serving the blind eye, appeared to be devoid of axons. In Tt038, myelinated axons were associated with the right optic nerve (serving the functional eye) and left optic tract but were essentially absent in the left optic nerve and right optic tract. Examined by light microscopy in serial horizontal sections, the optic chiasm of Tt038 was arranged along its central plane in segregated, alternating pathways for the decussation of right and left optic nerve fibers. Ventral to this plane, the chiasm was comprised of fibers from the left optic nerve, whereas dorsal to the central plane, fibers derived from the right optic nerve. Because of this architectural arrangement, the right and left optic nerves grossly appeared to overlap as they crossed the optic chiasm with the right optic nerve coursing dorsally to the left optic nerve. At the light and electron microscopic levels, the optic nerves and tracts lacking axons were well vascularized and dominated by glial cell bodies and glial processes, an expression of the marked glial scarring associated with postinjury axonal degeneration. The apparent absence of axons in one of the optic tract pairs (right in Tt038 and left in Tg419) supports the concept of complete decussation of right and left optic nerve fibers at the optic chiasm in the bottlenose dolphin.

Corpus callosum size in delphinid cetaceans.

The midsagittal surface area of the corpus callosum was determined by computer-assisted morphometry in juvenile and adult members of 13 species of the cetacean family Delphinidae. In 57 brains, absolute callosal areas ranged from 104 to 829 mm2. When compared to other mammal groups possessing a corpus callosum, callosal area in dolphins was smaller in relation to brain mass with a ratio range (mm2/g) of 0.08-0.31. The corpus callosum was decreased relative to brain mass in the larger-brained odontocetes, suggesting that increases in brain size were not necessarily allied with needs for equivalent increases in callosal linkage. One delphinid species, Tursiops truncatus, for which the largest single-species sample was available, was examined for sex differences in callosal size relative to brain mass. Among 10 males and 5 females the averaged ratio was not distinguishable between sexes.

Kinetics of healing of grafted and nongrafted wounds on the distal portion of the forelimbs of horses.

Full-thickness, circular, cutaneous wounds (5 cm in diameter) were created on the distal portion of the forelimbs of 6 horses. One wound on each horse was treated with 6 full-thickness punch grafts that were obtained from the horse's neck with a 6-mm skin biopsy punch and inserted in the graft sites on day 14 after wounding. The wound on the contralateral limb was not grafted. A combination of ticarcillin disodium and clavulanate potassium was applied to the wounds when bandages were changed to control bacterial infection. Areas of each wound were measured on days 1, 7, 9, 11, 13 through 15, 17 through 22, 24, 26, 29, and 32 after wounding. Three distinguishable phases of healing were observed (expansion, contraction, and epithelialization), and the time course of each phase was evaluated, using formulas of first-order processes. Rate constants of each phase were not significantly (P less than 0.05) affected by punch grafts.

Observations on the anatomy of the stomach and duodenum of the bowhead whale, Balaena mysticetus.

Gastric and cranial duodenal structure of the bowhead whale (Balaena mysticetus) was examined grossly and microscopically. The stomach was arranged in a series of four compartments. The first chamber, or forestomach, was a large nonglandular sac lined by a keratinized stratified squamous epithelium. It was followed by the fundic chamber, a large, somewhat globular and entirely glandular compartment. At the entrance of the fundic chamber, a narrow cardiac gland region could be defined. The remaining mucosa of the chamber contained the proper gastric glands. A narrow, tubular connecting channel, the third distinct gastric division, was lined by mucous glands and joined the fundic chamber with the final stomach compartment, or pyloric chamber. This fourth chamber was also tubular and lined by mucous glands but was of a diameter considerably larger than the connecting channel. The stomach terminated at the pyloric sphincter which consisted of a well-developed band of circular smooth-muscle bundles effecting a division between the pyloric chamber and small intestine. The small intestine began with the duodenal ampulla, a dilated sac considerably smaller than the fundic chamber of the stomach. The mucosa of this sac contained mucous glands throughout. The ampulla led without a separating sphincter into the duodenum proper which continued the intestine in a much more narrow tubular fashion. The mucosal lining of the duodenum was composed of villi and intestinal crypts. Although their occurrence varied among whales, enteroendocrine cells were identified within the mucous glands of the cardiac region, connecting channel, pyloric chamber, and cranial duodenum. The hepatopancreatic duct entered the wall of the duodenum shortly after the termination of the duodenal ampulla and continued intramurally along the intestine before finally joining the duodenal lumen.