The effect of swimming depth on respiratory behavior of the honey gourami, Colisa chuna (Pisces, Belontiidae)

1986 ◽  
Vol 64 (9) ◽  
pp. 1893-1896 ◽  
Author(s):  
David J. Bevan ◽  
Donald L. Kramer

We tested the hypothesis that fish capable of bimodal respiration would respond to the increased travel costs of surfacing by decreasing their frequency of air breathing. Honey gouramis were permitted to move freely in a 220 cm deep aquarium, but their preferred depths were manipulated by changing the location of shelter and feeding sites. With increased depth the interval between air breaths increased. This supports the argument that travel to and from the surface is a significant cost for air-breathing fish. It provides evidence that respiratory behavior can be affected by factors not directly involved in the physiology of gas exchange. Furthermore, it suggests that retention of water-breathing capacity in air-breathing species may reduce the costs of breathing through adaptive changes in partitioning.

1987 ◽  
Vol 65 (2) ◽  
pp. 348-353 ◽  
Author(s):  
David J. Bevan ◽  
Donald L. Kramer

Clarias macrocephalus are continuous, facultative air breathers. Individuals (7.6–20.9 g) survived more than 25 days in normoxic water without surface access. Buoyancy decreased and water-breathing frequency increased when surface access was denied, but growth rate and the frequency of air-breathing attempts did not change. We examined air-breathing and water-breathing frequency in shallow (60 cm) and deep (235 cm) water under normoxic (8.0 mg O2∙L−1) and hypoxic (0.3, 0.7, 1.2, and 2.0 mg O2∙L−1) conditions to examine how changes in the travel costs of breathing affected the use of each respiratory mode. Air-breathing and water-breathing frequency increased as dissolved oxygen decreased from 8.0 to 2.0 mg O2∙L−1. Below this level air breathing continued to increase, but water breathing dropped sharply. At higher levels of dissolved oxygen (8.0 and 2.0 mg O2∙L−1), fish in deep water had lower air-breathing and higher water-breathing frequencies than fish in shallow water. Vertical distance travelled and time spent in air breathing increased with increasing depth and with decreasing level of dissolved oxygen. These results support the hypotheses that travel is a significant cost of aerial respiration and that fish respond to increases in this cost by decreasing their use of atmospheric oxygen when dissolved oxygen concentration permits them to do so.


1986 ◽  
Vol 64 (10) ◽  
pp. 2133-2136 ◽  
Author(s):  
Roger S. Smith ◽  
Donald L. Kramer

The interbreath interval for aerial and aquatic ventilation was determined for seven Florida gars (Lepisosteus platyrhincus, Pisces, Lepisosteidae) before, during, and after exposure to the simulated threat of predation by a mounted great blue heron (Ardea herodius, Aves, Ardeidae). During exposure to the heron, air-breath interval increased by 118% while water-breath interval decreased by 13% as compared with the pre-heron period. This provides evidence that ecological factors not directly involved in the physiology of gas exchange can influence respiratory partitioning in fishes. It also supports the hypothesis that retention of water-breathing capacity in air-breathing fish can reduce the risk of aerial predation in these species.


1990 ◽  
Vol 63 (1) ◽  
pp. 117-139 ◽  
Author(s):  
Peter Greenaway ◽  
Caroline Farrelly
Keyword(s):  

1968 ◽  
Vol 49 (2) ◽  
pp. 437-452 ◽  
Author(s):  
CLAUDE LENFANT ◽  
KJELL JOHANSEN

1. Respiratory properties of blood and pattern of aerial and aquatic breathing and gas exchange have been studied in the African lungfish, Protopterus aethiopicus. 2. The mean value for haematocrit was 25%. Haemoglobin concentration was 6.2 g% and O2 capacity 6.8 vol. %. 3. The affinity of haemoglobin for O2 was high. P50 was 10 mm. Hg at PCOCO2, 6 mm. Hg and 25 °C. The Bohr effect was smaller than for the Australian lungfish, Neoceratodus, but exceeded that for the South American lungfish, Lepidosiren. The O2 affinity showed a larger temperature shift in Protopterus than Neoceratodus. 4. The CO2 combining power and the over-all buffering capacity of the blood exceeded values for the other lungfishes. 5. Both aerial and aquatic breathing showed a labile frequency. Air exposure elicited a marked increase in the rate of air breathing. 6. When resting in aerated water, air breathing accounted for about 90% of the O2 absorption. Aquatic gas exchange with gills and skin was 2.5 times more effective than pulmonary gas exchange in removing CO2. The low gas-exchange ratio for the lung diminished further in the interval between breaths. 7. Protopterus showed respiratory independence and a maintained O2 uptake until the ambient O2 and CO2 tensions were 85 and 35 mm. Hg respectively. A further reduction in O2 tension caused an abrupt fall in the oxygen uptake. 8. Gas analysis of blood samples drawn from unanaesthetized, free-swimming fishes attested to the important role of the lung in gas exchange and the high degree of functional separation in the circulation of oxygenated and deoxygenated blood.


1988 ◽  
Vol 66 (1) ◽  
pp. 109-123 ◽  
Author(s):  
G. Shelton ◽  
P. C. Croghan

Control of breathing and gas exchange has been extensively investigated in unimodal animals, particularly mammals, in which ventilation is characteristically a regular and continuous process and gas exchange approximates to a steady-state system. Both static and dynamic models have been developed in control-theory analyses. Similar analyses are possible in unimodal fish, though few have been carried out. Control in bimodal animals, such as air-breathing fish and amphibians, is more difficult to understand and model. The evolutionary change from water to air breathing in vertebrates involves not only the adjustment of many control processes but also the development, in the early stages, of non steady states in gas exchangers, blood, and tissues. A simple control-system model, differing from mammalian counterparts in its greater emphasis on storage functions and its intermittently activated controller, is described for two suggested stages in the evolution of air breathing. The first of these stages is air gulping, in which a fixed and rather brief pattern of air breathing is activated by internal signals generated as a result of the inadequacy of the gills to provide sufficient oxygen for tissue metabolism. The second stage is that of burst breathing, in which lung ventilation is both begun and ended by internal signals so that burst duration is variable. The effects of adjusting parameters on variables of evolutionary importance, such as dive duration, burst duration, store renewal, and metabolic rate, can be examined in these two versions of the model. Refinements to incorporate arterial and venous compartments in the circulatory system, the shunting of venous and arterial blood streams in the heart, realistic oxygen dissociation curves, controller inputs from a wider range of sources, and the capacity to respond to some conditions with changes in ventilation rate as well as in burst and dive durations, are being developed. They should make the complex, non-steady-state interactions between gas exchangers, circulating blood, and tissues easier to understand and indicate the likely steps toward the evolution of steady-state systems seen in birds and mammals.


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