Aural exostoses (surfer's ear) provide vital fossil evidence of an aquatic phase in Man's early evolution.

For over a century, otolaryngologists have recognised the condition of aural exostoses, but their significance and aetiology remains obscure, although they tend to be associated with frequent swimming and cold water immersion of the auditory canal. The fact that this condition is usually bilateral is predictable since both ears are immersed in water. However, why do exostoses only grow in swimmers and why do they grow in the deep bony meatus at two or three constant sites? Furthermore, from an evolutionary point of view, what is or was the purpose and function of these rather incongruous protrusions? In recent decades, paleoanthropological evidence has challenged ideas about early hominid evolution. In 1992 the senior author suggested that aural exostoses were evolved in early hominid Man for protection of the delicate tympanic membrane during swimming and diving by narrowing the ear canal in a similar fashion to other semiaquatic species. We now provide evidence for this theory and propose an aetiological explanation for the formation of exostoses.

Histological aspects of the mucosa of the spermaceti chamber of a dwarf sperm whale / Aspectos histológicos da mucosa da câmera do espermacete de cachalote-anão

The sound producing apparatus of the dwarf sperm whale (Kogia sima) presents a complex anatomic structure composed of melon, spermaceti, phonic lips, vocal cap, case, papillae, spermaceti chamber and other airspaces, as well as facial muscles involved in sound production. The spermaceti chamber rests on the caudal portion of the premaxilla, with part of its mucosa covered with spherical/oval-shaped structures (approximately 1 to 2 mm in diameter), compatible with vesicles (previously referred to as "papillae"). Macroscopical examination revealed whitish, firm, widely and irregularly distributed vesicular mucosa on the premaxillary portion of the spermaceti chamber of a K. sima specimen stranded on the coast of Santos (southeastern Brazilian coast). Upon microscopic examination, walls of connective tissue with abundant type I collagen forming vesicles with an internal space or cavity filled with a small amount of eosinophilic substance compatible with mucoproteic fluid were observed. The base of such vesicles presented glands within the connective tissue, probably responsible for fluid production. This study describes the histology of the mucosa of the spermaceti chamber of a K. sima specimen and characterizes the glands associated with fluid production.(AU)

O sistema de produção sonora do cachalote-anão (Kogia sima) apresenta uma complexa estrutura anatômica composta por melão, espermacete, lábios fônicos, "vocal cap", "case", papilas, câmara do espermacete e outros espaços aéreos, além de músculos faciais envolvidos na produção sonora. A câmara do espermacete localiza-se na porção caudal da pré-maxila, apresentando parte de sua mucosa recoberta por estruturas esférico-ovaladas de aproximadamente 1 a 2 mm de diâmetro, compatíveis com vesículas (previamente denominadas "papilas"). Ao exame macroscópico de um espécime de K. sima encalhado no litoral de Santos (sudeste da costa brasileira), foi identificada mucosa esbranquiçada e firme ao corte, ampla e irregularmente distribuída na porção pré-maxilar da câmara do espermacete. Ao exame microscópico foram observadas vesículas compostas por abundante tecido conectivo de colágeno tipo I, dando origem a um espaço interno ou cavidade, contendo pequena quantidade de substância eosinófila, compatível com fluido mucoprotêico. Estruturas glandulares foram observadas em tecido conjuntivo na base das vesículas, provavelmente responsáveis pela produção do fluido observado no interior das mesmas. Esse estudo caracteriza histologicamente a mucosa da câmara do espermacete de um espécime de K. sima e as glândulas relacionadas a sua produção secretória.(AU)

Sir John Struthers (1823-1899), Professor of Anatomy in the University of Aberdeen (1863-1889), President of the Royal College of Surgeons of Edinburgh (1895-1897).

Between 1841 and 1845 John Struthers attended both the University of Edinburgh and some of the various Extra-mural Schools of Medicine associated with Surgeons' Hall. While a medical student he became a Member of the Hunterian Medical Society of Edinburgh and later was elected one of their Annual Presidents. He graduated with the MD Edin and obtained both the LRCS Edin and the FRCS Edin diplomas in 1845. Shortly afterwards he was invited to teach Anatomy in Dr Handyside's Extra-mural School in Edinburgh. The College of Surgeons certified him to teach Anatomy in October 1847. He had two brothers, and all three read Medicine in Edinburgh. His younger brother, Alexander, died of cholera in the Crimea in 1855 while his older brother James, who had been a bachelor all his life, practised as a Consultant Physician in Leith Hospital, Edinburgh, until his death.When associated with Dr Handyside's Extra-mural School in Edinburgh, John taught Anatomy there until he was elected to the Chair of Anatomy in Aberdeen in 1863. Much of his time was spent in Aberdeen teaching Anatomy and in upgrading the administrative facilities there. He resigned from this Chair in 1889 and subsequently was elected President of Leith Hospital from 1891 to 1897. This was in succession to his older brother, James, who had died in 1891. Later, he was elected President of the Royal College of Surgeons of Edinburgh from 1895 to 1897 and acted as its Vice-President from 1897 until his death in 1899. In 1898, Queen Victoria knighted him. His youngest son, John William Struthers, was the only one of his clinically qualified sons to survive him and subsequently was elected President of the Edinburgh College of Surgeons from 1941 to 1943.

Neuroglobin of seals and whales: evidence for a divergent role in the diving brain.

Although many physiological adaptations of diving mammals have been reported, little is known about how their brains sustain the high demands for metabolic energy and thus O(2) when submerged. A recent study revealed in the deep-diving hooded seal (Cystophora cristata) a unique shift of the oxidative energy metabolism and neuroglobin, a respiratory protein that is involved in neuronal hypoxia tolerance, from neurons to astrocytes. Here we have investigated neuroglobin in another pinniped species, the harp seal (Pagophilus groenlandicus), and in two cetaceans, the harbor porpoise (Phocoena phocoena) and the minke whale (Balaenoptera acutorostrata). Neuroglobin sequences, expression levels and patterns were compared with those of terrestrial relatives, the ferret (Mustela putorius furo) and the cattle (Bos taurus), respectively. Neuroglobin sequences of whales and seals only differ in two or three amino acids from those of cattle and ferret, and are unlikely to confer functional differences, e.g. in O(2) affinity. Neuroglobin is expressed in the astrocytes also of P. groenlandicus, suggesting that the shift of neuroglobin and oxidative metabolism is a common adaptation in the brains of deep-diving phocid seals. In the cetacean brain neuroglobin resides in neurons, like in terrestrial mammals. However, neuroglobin mRNA expression levels were 4-15 times higher in the brains of harbor porpoises and minke whales than in terrestrial mammals or in seals. Thus neuroglobin appears to play a specific role in diving mammals, but seals and whales have evolved divergent strategies to cope with cerebral hypoxia. The specific function of neuroglobin that conveys hypoxia tolerance may either relate to oxygen supply or protection from reactive oxygen species. The different strategies in seals and whales resulted from a divergent evolution and an independent adaptation to diving.

Immunology of whales and dolphins.

The increasing disease susceptibility in different whale and dolphin populations has led to speculation about a possible negative influence of environmental contaminants on the immune system and therefore on the health status of marine mammals. Despite current efforts in the immunology of marine mammals several aspects of immune functions in aquatic mammals remain unknown. However, assays for evaluating cellular immune responses, such as lymphocyte proliferation, respiratory burst as well as phagocytic and cytotoxic activity of leukocytes and humoral immune responses have been established for different cetacean species. Additionally, immunological and molecular techniques enable the detection and quantification of pro- and anti-inflammatory cytokines in lymphoid cells during inflammation or immune responses, respectively. Different T and B cell subsets as well as antigen-presenting cells can be detected by flow cytometry and immunohistochemistry. Despite great homologies between marine and terrestrial mammal lymphoid organs, some unique anatomical structures, particularly the complex lymphoepithelial laryngeal glands in cetaceans represent an adaptation to the marine environment. Additionally, physiological changes, such as age-related thymic atrophy and cystic degeneration of the "anal tonsil" of whales have to be taken into account when investigating these lymphoid structures. Systemic morbillivirus infections lead to fatalities in cetaceans associated with generalized lymphoid depletion. Similarly, chronic diseases and starvation are associated with a loss of functional lymphoid cells and decreased resistance against opportunistic infections. There is growing evidence for an immunotoxic effect of different environmental contaminants in whales and dolphins, as demonstrated in field studies. Furthermore, immunomodulatory properties of different persistent xenobiotics have been confirmed in cetacean lymphoid cells in vitro as well as in animal models in vivo. However, species-specific differences of the immune system and detoxification of xenobiotics between cetaceans and laboratory rodents have to be considered when interpreting these toxicological data for risk assessment in whales and dolphins.

Histological, immunohistochemical and pathological features of the pituitary gland of odontocete cetaceans from the Western gulf of Mexico.

Pituitary glands were recovered from dolphins and small whales found stranded along the Texas coast of the Gulf of Mexico over a 15-year period (1991-2006). One hundred animals of 14 species were found to be suitable for inclusion in this study. Of these, 72 were Atlantic bottlenose dolphins (Tursiops truncatus). Other species included were the melon-headed whale (Peponocephala electra), spinner dolphin (Stenella longirostris), striped dolphin (Stenella coeruleoalba), pantropical spotted dolphin (Stenella attenuata), pygmy sperm whale (Kogia breviceps), dwarf sperm whale (Kogia sima), Risso's dolphin (Grampus griseus), the short finned pilot whale (Globicephala macrorhyncha), false killer whale (Pseudorca crassidens), Fraser's dolphin (Lagenorhynchus hosei), rough-tooth dolphin (Steno bredanensis), Gervais's beaked whale (Mesoplodon europaeus) and an infant sperm whale (Physeter catodon). The pituitary weights in T. truncatus ranged from 0.69 g in a 109-cm long neonate to 3.44 g in a large (277 cm) male. More typical weights were in the range of 0.95-2.35 g (mean=1.65+/-0.70 g) The cetacean pituitary consisted of two distinct parts, the adenohypophysis and the neurohypophysis, which were separated by a thin fibrous membrane in all species examined, in contrast to terrestrial mammals in which the parts are apposed and joined through a pars intermedia. Cell types were identified with conventional stains and immunohistochemistry. Cells positive for adrenocorticotropic hormone, follicle stimulating hormone, growth hormone, melanocyte stimulating hormone, luteinizing hormone and prolactin were identified with appropriate antibodies. Lesions, which were few, included one pituicytoma of the pars nervosa and a squamous cyst in T. truncatus, and colloid cysts in several species. Nodular aggregates of single cell types were common, probably representing a physiological variant.

Structure of the integument of southern right whales, Eubalaena australis.

Skin (integument) anatomy reflects adaptations to particular environments. It is hypothesized that cetacean (whale) integument will show unique anatomical adaptations to an aquatic environment, particularly regarding differences in temperature, density, and pressure. In this study, the gross and histological structure of the southern right whale integument is described and compared with terrestrial mammals and previous descriptions of mysticete (baleen whale) and odontocete (toothed whale) species. Samples were taken of the integument of 98 free-swimming southern right whales, Eubalaena australis, and examined by both light and electron microscopy. Results show that three epidermal layers are present, with the stratum corneum being parakeratotic in nature. As in bowhead whales, southern right whales possess an acanthotic epidermis and a notably thick hypodermis, with epidermal rods and extensive papillomatosis. However, unlike bowhead whales, southern right whales possess an uninterrupted hypodermal layer. Surprisingly, the integument of balaenids (right and bowhead mysticetes) in general is more like that of odontocetes than that of the more closely related balaenopterids (rorqual mysticetes). Similarities to odontocetes were found specifically in the collagen fibers in a fat-free zone of the reticular dermal layer and the elastic fibers in the dermal and hypodermal layers. Callosities, a distinctive feature of this genus, have a slightly thicker stratum corneum and are usually associated with hairs that have innervated and vascularized follicles. These hairs may function as vibrissae, thus aiding in aquatic foraging by allowing rapid detection of changes in prey density. Although the thick insulatory integument makes right whales bulky and slow-moving, it is an adaptation for living in cold water. Epidermal thickness, presence of epidermal rods, and callosities may act as barriers against mechanical injury from bodily contact with conspecifics or hard surfaces in the environment (e.g., rocks, ice).

Morphologic characteristics of pulmonary macrophages in cetaceans: particular reference to pulmonary intravascular macrophages as a newly identified type.

We examined the morphologic characteristics of pulmonary macrophages in 42 specimens of Odontoceti (Globicephala macrorhynchus, Grampus griseus, Tursiops truncatus, Stenella attenuata, Stenella coeruleoalba, Berardius bairdii), using light and electron microscopes as well as immunohistochemistry with SRA-E5. SRA-E5-positive alveolar macrophages and pulmonary interstitial macrophages contained graphitic soots, indicating the clearance of airborne, aspirated foreign bodies. Pulmonary intravascular macrophages (PIMs), positive with SRA-E5, were present within pulmonary capillaries, attaching to applied endothelial cells by cell junctions. They showed cytoplasmic tubular structures of micropinocytosis vermiformis and erythrophagocytosis, indicating their contributory role in the clearance of blood-borne particles. The uptake of pathogens by PIMs may be associated with the inducement of acute lung injury, especially bacterial infectious pneumonia. This study revealed for the first time the presence of PIMs in cetaceans.

Microanatomy of the lung of the bowhead whale Balaena mysticetus.

The lungs from six bowhead whales harvested by Alaskan Eskimos have been examined with light and electron microscopes. Airways ranging from 1 to 40 mm in luminal diameter are lined by a pseudostratified ciliated epithelium containing numerous mucus-secreting cells. The underlying lamina propria-tela submucosa of these airways contains tubuloalveolar glands, plasma cells, and lymphatic accumulations in addition to both elastic and collagenous fibrillar elements. Cartilage extends to the level of the respiratory airways, but smooth muscle is absent from airways larger than 3 mm, and tubuloalveolar glands are absent from airways smaller than 3 mm. Respiratory airways are lined by pseudostratified, simple cuboidal, and simple squamous epithelia. Alveolar ducts are lined by simple squamous epithelium exclusively. A connective tissue core composed mostly of elastic fibers supports the walls of the alveolar ducts. Neither smooth muscle nor cartilage has been observed in these structures. Alveoli contain the typeical cetacean double capillary bed separated by a thick septum composed mainly of collagenous connective tissue. Alveoli are lined by a simple squamous epithelium similar to that encountered in alveolar ducts and respiratory airways. This epithelium is composed of type I and II pneumocytes closely appressed to an underlying capillary network. The type II pneumocytes contain typical lamellar bodies and tubular myelin can be seen in the air spaces. The lung is surrounded by a thick (X = 2.5 mm) visceral pleura rich in blood vessels and elastic fibers.

Visión interna y directa del corazón de una ballena

Se presenta el estudio del corazón de la ballena picuda, varada en la Isla San Andrés, Colombia. Se realizó examen visual externo e interno del corazón de la ballena por visión directa y con fibroscopio. También se hizo endoscopia de las arterias coronarias. Se encontró gran similitud del corazón de la ballena picuda en relación con el del humano