Abstract. Physiological aspects like heat balance, gas exchange, osmoregulation, and digestion of the early Permian aquatic temnospondyl Archegosaurus decheni, which lived in a tropical freshwater lake, are assessed based on osteological correlates of physiologically relevant soft-tissue organs and by physiological estimations analogous to air-breathing fishes. Body mass (M) of an adult Archegosaurus with an overall body length of more than 1m is estimated as 7kg using graphic double integration. Standard metabolic rate (SMR) at 20°C (12kJh−1) and active metabolic rate (AMR) at 25°C (47kJh−1) were estimated according to the interspecific allometry of metabolic rate (measured as oxygen consumption) of all fish (VO2 = 4. 8M0. 88) and form the basis for most of the subsequent estimations. Archegosaurus is interpreted as a facultative air breather that got O2 from the internal gills at rest in well-aerated water but relied on its lungs for O2 uptake in times of activity and hypoxia. The bulk of CO2 was always eliminated via the gills. Our estimations suggest that if Archegosaurus did not have gills and released 100% CO2 from its lungs, it would have to breathe much more frequently to release enough CO2 relative to the lung ventilation required for just O2 uptake. Estimations of absorption and assimilation in the digestive tract of Archegosaurus suggest that an adult had to eat about six middle-sized specimens of the acanthodian fish Acanthodes (ca. 8cm body length) per day to meet its energy demands. Archegosaurus is regarded as an ammonotelic animal that excreted ammonia (NH3) directly to the water through the gills and the skin, and these diffusional routes dominated nitrogen excretion by the kidneys as urine. Osmotic influx of water through the gills had to be compensated for by production of dilute, hypoosmotic urine by the kidneys. Whereas Archegosaurus has long been regarded as a salamander-like animal, there is evidence that its physiology was more fish- than tetrapod-like in many respects.
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Do air-breathing fish suffer branchial oxygen loss in hypoxic water?
In hypoxia, air-breathing fish obtain O2from the air but continue to excrete CO2into the water. Consequently, it is believed that some O2obtained by air-breathing is lost at the gills in hypoxic water.Pangasionodon hypophthalmusis an air-breathing catfish with very large gills from the Mekong River basin where it is cultured in hypoxic ponds. To understand howP. hypophthalmuscan maintain high growth in hypoxia with the presumed O2loss, we quantified respiratory gas exchange in air and water. In severe hypoxia (PO2: ≈ 1.5 mmHg), it lost a mere 4.9% of its aerial O2uptake, while maintaining aquatic CO2excretion at 91% of the total. Further, even small elevations in water PO2rapidly reduced this minor loss. Charting the cardiovascular bauplan across the branchial basket showed four ventral aortas leaving the bulbus arteriosus, with the first and second gill arches draining into the dorsal aorta while the third and fourth gill arches drain into the coeliacomesenteric artery supplying the gut and the highly trabeculated respiratory swim-bladder. Substantial flow changes across these two arterial systems from normoxic to hypoxic water were not found. We conclude that the proposed branchial oxygen loss in air-breathing fish is likely only a minor inefficiency.
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- Award ID(s):
- 1755187
- PAR ID:
- 10502234
- Publisher / Repository:
- The Royal Society
- Date Published:
- Journal Name:
- Proceedings of the Royal Society B: Biological Sciences
- Volume:
- 290
- Issue:
- 2006
- ISSN:
- 0962-8452
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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