Geotria australis: Bice, C., Górski, K., Closs, G., Franklin, P., David, B., West, D, Crow, S., Allibone, R, Ling, N. & Hitchmough, R.

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1982 ◽  
Vol 97 (1) ◽  
pp. 253-261
Author(s):  
D. J. Macey ◽  
I. C. Potter

1. Oxygen dissociation curves of the whole blood of larvae and adults of the Southern Hemisphere lamprey Geotria australis have been determined between pH 6.8 and 8.2 at 5, 15 and 25 degrees C. 2. The P50's at temperatures of 5, 15 and 25 degrees C and a pH of 7.75 were respectively 0.57, 0.92 and 1.19 mmHg in larvae and 6.9, 10.3 and 19.0 mmHg in adults. 3. The relatively very high affinity of larval blood for oxygen may reflect an adaptation to low environmental oxygen tensions. 4. The Bohr shift was not significantly affected by either temperature or life-cycle stage. 5. The slope (n) in Hill plots increased with temperature and oxygen saturation, and was greater in adults than in larvae.


1987 ◽  
Vol 247 (2) ◽  
Author(s):  
Sara Rodr�guez ◽  
PabloA. Rodr�guez ◽  
Carlos Banse ◽  
Est�banM. Rodr�guez ◽  
Andreas Oksche

1995 ◽  
Vol 100 (3) ◽  
pp. 413-422 ◽  
Author(s):  
J.Michael Conlon ◽  
Per F. Nielsen ◽  
John H. Youson ◽  
Ian C. Potter

1990 ◽  
Vol 14 (1) ◽  
pp. 39-48
Author(s):  
Anna C. Feldwick ◽  
W.John Penhale ◽  
David J. Macey

2020 ◽  
Vol 26 (3) ◽  
pp. 301 ◽  
Author(s):  
K. R. Paton ◽  
M. H. Cake ◽  
D. J. Bird ◽  
I. C. Potter

The anadromous Geotria australis, one of only three lamprey species representing the early agnathan (jawless) stage of vertebrate evolution in Australia and New Zealand, is declining in abundance. Its adults were caught soon after they had entered rivers on their non-trophic upstream migration and maintained in laboratory tanks for 13–15 months through to spawning. As adult G. australis are susceptible to haemorrhagic septicaemia, they were treated prophylactically and maintained in 3-m3 aquaria supplied with a flow-through charcoal filtration system and UV steriliser. Air temperature and the light:dark regime were constantly adjusted to parallel those in the environment. Males developed the very large suctorial disc and gular pouch characteristic of maturity and both sexes matured at the same time as in the wild. While males frequently showed aggressive behaviour towards each other, the same male and female mated on several occasions. The male coiled around the female and, with his urogenital papilla close to the female’s cloaca, twisted and vibrated, leading to egg release. These eggs formed coagulated clusters as in the wild, with many progressing through to the eight-cell stage. Remarkably, numerous G. australis were still alive 95–392 days after the end of the short spawning period, and one male after a further 119 days. Postspawning survival would be facilitated inter alia by extensive proteolysis, reflected in a shortening of the body. The data in this paper emphasise that G. australis is a highly atypical lamprey and provides invaluable information for conserving this declining species.


1988 ◽  
Vol 252 (1) ◽  
pp. 167-172 ◽  
Author(s):  
D J Macey ◽  
M H Cake ◽  
I C Potter

This study aimed to elucidate the way in which larvae of the lamprey Geotria australis counteract the potential problems of the very high concentrations of non-haem iron they contain and thereby avoid the deleterious effects associated with iron overload in other vertebrates. Particular attention has been paid to ascertaining whether increasing concentrations of iron are accompanied by (i) change to a less readily available form of iron and (ii) an increase in the activity of those detoxifying enzymes responsible for minimizing the production of harmful hydroxyl radicals via the Haber-Weiss reaction. The mean concentrations of haemosiderin and ferritin in larval G. australis were each far higher in the nephric fold than in either the liver or intestine, but all these concentrations were much greater than those in rat liver. Since haemosiderin releases iron far more slowly than ferritin, the iron it contains is much less readily available to catalyse the Haber-Weiss reaction. It is thus relevant that (i) non-haem iron in the nephric fold occurred to a greater extent as large dense haemosiderin granules than as ferritin molecules and (ii) the proportion of iron in the form of haemosiderin rose with increasing concentration of total non-haem iron. A strong correlation was also recorded between the activity of superoxide dismutase in the nephric fold and the concentrations of total non-haem iron and its haemosiderin and ferritin components. This demonstrates that enzyme detoxification of O2.- rises with increasing amounts of iron. The exceptional iron concentrations in the nephric fold were not reflected by a greater measured activity of superoxide dismutase than that found in other tissues. However, the nephric fold was shown to contain an augmentation factor which is presumed to enhance the activity of this enzyme in vivo. The activity of catalase and glutathione peroxidase, which catalyse the breakdown of H2O2 to O2 and water, were each significantly correlated with the concentration of ferritin.


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