The development of photopic and scotopic vision in the frog (Rana temporaria)

1964 ◽  
Vol 4 (3-4) ◽  
pp. 241-IN4 ◽  
Author(s):  
W.R.A. Muntz
2011 ◽  
Vol 4 (2) ◽  
pp. 192-194
Author(s):  
Georgy A. Lada ◽  
V. Y. Nedosekin

A small isolated population of tesselated snake, Natrix tesselata was found in the Upper Don (Lipetsk Region, Russia). It is the first record of this species in the Central Chernozem Territory of Russia, which is separated from the northern border of the main range by the distance of about 200 km. An isolated population of common frog, Rana temporaria and phenetically peculiar population of fire-bellied toad, Bombina bombina are found here too. Faunistic aspect of new herpetological records is discussed.


2015 ◽  
Vol 36 (4) ◽  
pp. 417-424 ◽  
Author(s):  
Alexandre Boissinot ◽  
Pierre Grillet ◽  
Aurélien Besnard ◽  
Olivier Lourdais

Traditional farming landscape in western Europe is made of a complex mosaic of pastures, cultures, ponds and hedgerows connected with woods. Previous observations in the common frog species suggest that lowland populations are closely associated to wood cover and our aim was to test the validity of this assumption. We studied common frog occurrence and abundance in western central France (Deux-Sèvres department) close to the southern margin of lowland distribution. Our results pointed out that the proportion of woods surface around sampled areas (1 ha) was a critical determinant of common frog presence and abundance. Extensive farming, which maintains a mosaic of small woods, may provide a robust conservation tool for this species.


Author(s):  
Svetlana A. Kaurova ◽  
Victor K. Uteshev ◽  
Andrew B. Gapeyev ◽  
Natalia V. Shishova ◽  
Edith N. Gakhova ◽  
...  

1996 ◽  
Vol 270 (4) ◽  
pp. R821-R829 ◽  
Author(s):  
U. Krause ◽  
G. Wegener

The gastrocnemius muscle of the frog (Rana temporaria) has a high capacity for anaerobic glycolysis from glycogen. Glycolytic metabolites and effectors of phosphofructokinase, particularly the hexose bisphosphates, were followed in muscle during exercise (swimming between 5 s and 5 min), recovery (rest for up to 2 h after 5 min of swimming), and repeated exercise (swimming for up to 60 s after 2 h of recovery). Glycogen phosphorylase and phosphofructokinase were swiftly activated with exercise. The hexose bisphosphates followed markedly different time courses. Fructose 1,6-bisphosphate was transiently increased in both exercise and repeated exercise. This appears to be an effect rather than a cause of phosphofructokinase activation. Glucose 1,6-biphosphate was accumulated only while phosphofructokinase was active and was unchanged at other times. Fructose 2,6-biphosphate showed a 10-fold transient increase on exercise in rested frogs, almost disappeared from the muscle during recovery, and did not change during repeated exercise. Fructose 2,6-biphosphate is a potent activator of phosphofructokinase in vitro under near physiological assay conditions, and it may serve this function also in vivo during exercise. Glucose 1,6-biphosphate could be an activator of phosphofructokinase in repeated exercise when fructose 2,6-biphosphate is not available.


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