S O Tamura

Abstract: 1. The routine oxygen consumption by Periophthalmus cantonensis and Boleophthalmus chinensis in water increased geometrically, whereas that in air increased logarithmically with temperature. At temperatures of more than 20 degrees C the oxygen uptake of both species was greater in water than in air. 2. When the fishes were able freely to select either an aquatic or terrestrial habitat, the total oxygen consumption of Periophthalmus and Boleophthalmus was 236 and 110 ml/kg, h at 20 degrees C respectively; 66% (Periophthalmus) and 70% (Boleophthalmus) of the total uptake was from water, and 34 and 30% of the total uptake was from air at 20 +/- 1 degrees C. 3. Oxygen uptake of fish limited to aquatic or terrestial life was less than when they could freely select their habitat; for Periophthalmus, uptake was reduced to 83% when confined in water and to 50% in air, and for Bolephthalmus, to 65% in water and to 43% in air. 4. The proportion of oxygen uptake by the gill in water was 52% for Periophthalmus and 59% for Boleophthalmus; in air the corresponding figures were 27 and 52%. 5. The proportions of oxygen uptake via the skin in water was 48% for Periophthalmus and 36% for Boleophthalmus; in air the corresponding figures were 76 and 43%. 6. It is concluded that, on land, Periophthalmus relies mainly on its skin and Boleophthalmus relies mainly on its gills.

Abstract: Summary 1. The exchange of oxygen and carbon dioxide between skin and environment is commonplace in the vertebrates. In many lower vertebrates, the skin is the major or even sole avenue for respiration. 2. As implied by the physical laws governing diffusion of gases, the skin diffusion coefficient, surface area, gas diffusion distance and transcutaneous gas partial pressures may independently or jointly affect cutaneous respiration. In vertebrates, each of these variables has undergone modification that may be related to dependence upon cutaneous gas exchange. 3. Both theoretical models and experimental data suggest that cutaneous gas exchange is limited by the rate of diffusion. However, changes in convection of the respiratory medium and of blood may partially compensate for diffusion limitation, and potentially function in the regulation of cutaneous gas exchange. 4. Typically, the skin is one of several gas exchangers, although many salamanders and some species in other vertebrate groups breathe solely through the skin. The cutaneous contribution to overall gas exchange is often most important in small animals, at cool temperatures, at low levels of activity and in normoxic and normocapnic conditions. Branchial and pulmonary respiration increasingly predominate in other circumstances. 5. Often, the skin figures more prominently in CO2, excretion than in O2, uptake. 6. Cutaneous gas exchange emerges in vertebrates as a process perhaps less effective and more constrained than branchial or pulmonary exchange but also less energetically costly. Its utility is indicated by its wide and successful exploitation in vertebrates occupying a diverse array of habitats.

Abstract: Amphibious mangrove killifish, Kryptolebias marmoratus (formerly Rivulus marmoratus), are frequently exposed to aerial conditions in their natural environment. We tested the hypothesis that gill structure is plastic and that metabolic rate is maintained in response to air exposure. During air exposure, when gills are no longer functional, we predicted that gill surface area would decrease. In the first experiment, K. marmoratus were exposed to either water (control) or air for 1 h, 1 day, 1 week, or 1 week followed by a return to water for 1 week (recovery). Scanning electron micrographs (SEM) and light micrographs of gill sections were taken, and morphometric analyses of lamellar width, lamellar length and interlamellar cell mass (ILCM) height were performed. Following 1 week of air exposure, SEM indicated that there was a decrease in lamellar surface area. Morphometric analysis of light micrographs revealed that there were significant changes in the height of the ILCM, but there were no significant differences in lamellae width and length between any of the treatments. Following 1 week of recovery in water, the ILCM regressed and gill lamellae were similar to control fish, indicating that the morphological changes were reversible. In the second experiment, V(CO(2)) was measured in fish continuously over a 5-day period in air and compared with previous measurements of oxygen uptake (V(O(2))) in water. V(CO(2)) varied between 6 and 10 micromol g(-1) h(-1) and was significantly higher on days 3, 4 and 5 relative to days 1 and 2. In contrast to V(O(2)) in water, V(CO(2)) in air showed no diurnal rhythm over a 24 h period. These findings indicate that K. marmoratus remodel their gill structures in response to air exposure and that these changes are completely reversible. Furthermore, over a similar time frame, changes in V(CO(2)) indicate that metabolic rate is maintained at a rate comparable to that of fish in water, underlying the remarkable ability of K. marmoratus to thrive in both aquatic and terrestrial habitats.

Abstract: There are a small number of fish species, both marine and freshwater, that exhibit a truly amphibious habit that includes periods of aerial exposure. The duration of emersion is reflected in the level of physical and physiological adaptation to an amphibious lifestyle. Fish that are only briefly out of water retain predominantly aquatic attributes whereas there are semi-terrestrial species that are highly adapted to prolonged periods in the aerial habitat. Desiccation is the main stressor for amphibious fish and it cannot be prevented by physiological means. Instead, amphibious fish resist excessive water loss by means of cutaneous modification and behavioural response. The more terrestrially adapted fish species can tolerate considerable water loss and may employ evaporation to aid thermoregulation. The amphibious habit is limited to fish species that can respire aerially. Aerial respiration is usually achieved through modification to existing aquatic pathways. Freshwater air-breathers may respire via the skin or gills but some also have specialized branchial diverticula. Marine species utilize a range of adaptations that may include modified gills, specialized buccopharyngeal epithelia, the intestine and the skin. Areas of enhanced respiratory activity are typified by increased vascularization that permits enhanced perfusion during aerial exposure. As with other adaptations the mode of nitrogenous elimination is related to the typical durations of emersion experienced by the fish. Intertidal species exposed on a regular cycle, and which may retain some contact with water, tend to remain ammoniotelic while reducing excretion rates in order to prevent excessive water loss. Amphibious fish that inhabit environments where emersion is less predictable than the intertidal, can store nitrogen during the state of emersion with some conversion to ureotelism or have been shown to tolerate high ammonia levels in the blood. Finally, the more amphibious fish are more adapted to moving on land and seeing in air. Structural modifications to the pectoral, pelvic, dorsal and anal fins, combined with a well-developed musculature permit effective support and movement on land. For vision in air, there is a general trend for fish to possess close-set, moveable, protruberant eyes set high on the head with various physical adaptations to the structure of the eye to allow for accurate vision in both air and water.

Abstract: Amphibious behaviour in fish has evolved separately many times since the first amphibious fishes, the rhipidistian crossopterygians, ventured onto land about 350 million years ago. This behaviour has resulted in the colonization and eventual domination by vertebrates of the terrestrial habitat. It is generally proposed that aquatic hypoxia, owing to metabolic oxygen consumption and organic decay, was the most important selective force in the evolution of air-breathing vertebrates (e.g. Randall et al., 1981). Modern amphibious fish species give an insight into the reasons for leaving and eventually abandoning the aquatic habitat. Amphibious fishes today leave the water for a variety of reasons associated with degradation of their aquatic habitat, or biotic factors within it. The possible causal factors which may elicit an emergence response are summarized in Fig. 1(a) and (b). Amphibious fish inhabiting closed systems, as typified by freshwater or intertidal pools, may leave water for any of the reasons detailed in Fig. 1(a). The relative importance of any one stimulus is likely to vary between different species. However, it is possible that in closed systems, adverse fluctuations in physico-chemical parameters will have a more important effect in eliciting amphibious behaviour than will biotic factors. In open systems, such as coastal waters or large freshwater bodies, effectively two routes of escape from adverse aquatic conditions are available to amphibious fish. They may move onto land, or alternatively they may move underwater to find better conditions. In such a system, where physico-chemical parameters remain relatively constant, abiotic factors are unlikely to have a significant influence on amphibious behaviour. The dominant stimulus in open systems is possibly the three-way interaction between predation, competition, and short-or long-term food availability (Fig. 1(b)). It is unlikely that any one of the factors discussed in this review will act alone in causing amphibious behaviour, and in this respect the available literature on fish leaving water is lacking. Much of it is fragmentary and partly anecdotal, and the limited amount of experimental work tends to concentrate on individual causal factors. There is evidently scope for detailed examination of emersion in a number of amphibious fishes, testing a matrix of environmental and biotic stimuli, in an attempt to determine in more detail the reasons for such behaviour.

Abstract: The oxygen consumption of excised skin (MO2 is.cut.) and the normal cutaneous oxygen uptake by the skin in situ from the external medium (MO2 ext.cut.) were investigated in seven species of teleosts in normoxic sea water: butterfish (Pholis gunnellus L.), cod (Gadus morhua L.), five-bearded rockling (Ciliata mustela L), shanny (Blennius pholis L.), flounder (Platichthys flesus L.), sole (Solea solea L.) and eel (Anguilla anguilla L.). In the butterfish, cod and rockling, all the oxygen absorbed by the skin is consumed by the skin tissue itself, whereas in the other species there is a net inward transcutaneous oxygen flux. The gain of oxygen through the skin is obtained either by a low MO2is.cut. (shanny, flounder) and/or by high MO2ext.cut. (sole and eel). The blind side of the sole is particularly efficient in oxygen uptake. The results are discussed in relation to the biota of the different species.