Northern Leopard Frog

Northern Leopard Frog
Conservation status
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Class: Amphibia
Order: Anura
Family: Ranidae
Genus: Rana
Species: R. pipiens
Binomial name
Rana pipiens
Schreber, 1782
Synonyms

Lithobates pipiens
Dubois, 2006

The Northern Leopard Frog (Rana pipiens)[1][2][3] is a species of leopard frog from the true frog family, native to parts of Canada and United States. It is the state amphibian of Minnesota and Vermont.

Contents

Physical description

The Northern Leopard Frog is a fairly large species of frog reaching about 11 cm (4.3 in) in length. It varies from green to brown in dorsal colour with large dark circular spots on its back, sides and legs. Each spot is normally bordered by a lighter ring. A pair of dorsolateral folds starting from the back of the eye run parallel to each other down the back. These dorsolateral folds are often lighter or occasionally pinkish in colour. There is also a pale stripe running from the nostril, under the eye and tympanum, terminating at the shoulder. The ventral surface is white or pale green. The iris is golden and toes are webbed. Tadpoles are dark brown or grey, with light blotches on the underside. The tail is pale tan.

Color Variations

The Northern Leopard frog has several different color variations. The most common being the green morph and the brown morph. There is another morph know as the burnsi morph. Individuals with the burnsi morph coloration lack spots on their back, but retain them on their legs. They are bright green and have yellow dorsal folds.

Ecology and behavior

Northern Leopard Frogs have a wide range of habitats. They are found in permanent ponds, swamps, marshes and slow moving streams throughout forest, open and urban areas. They normally inhabit water bodies with abundant aquatic vegetation. They are well adapted to cold and can be found above 3,000 m (9,800 ft) asl. Males make a short snore-like call from water during spring and summer. The northern leopard frog breeds in the spring (March–June). Up to 6500 eggs are laid in water, and tadpoles complete development within the breeding pond. Tadpoles are light brown with black spots, and development takes 70–110 days, depending on conditions. Metamorph frogs are 2–3 cm (0.79–1.2 in) and resemble the adult.

This species was once quite common through parts of western Canada until declines started occurring during the 1970s. The population decline is thought to have been caused by pollution drift from the United States falling in the form of acid rain. Many populations of Northern Leopard Frogs have not yet recovered from these declines.

Northern Leopard Frogs are preyed upon by many different animals such as snakes, raccoons, other frogs and even humans. They do not produce distasteful skin secretions and rely on speed to evade predation.

They eat a wide variety of animals including crickets, flies, worms, and smaller frogs. Using their large mouths, they can even swallow birds and garter snakes. This species is similar to the Pickerel frog (Rana palustris) and the Southern Leopard Frog (Rana sphenocephala).

Research

Medical

The Northern Leopard Frog produces specific ribonucleases in its oocytes. Those enzymes are potential drugs for cancer. One such molecule called ranpirnase (onconase) is in clinical trials as a treatment for pleural mesothelioma and lung tumours. Another called amphinase was recently described as a potential treatment for brain tumors.[4]

Neuroscience

The Northern Leopard Frog has been a preferred species for making discoveries about basic properties of neurons since before the 1950s. The neuromuscular junction of the sciatic nerve fibers of the sartorius muscle of this frog has been the source of a lot of initial data about the nervous system.[5][6][7][8][9][10]

Muscle physiology and biomechanics

The Northern Leopard Frog is a popular species for in vitro experiments in muscle physiology and biomechanics due to the ease of accessibility for investigators in its native range and the ability of the sartorius muscle to stay alive in vitro for several hours. Furthermore, the reliance of the frog on two major modes of locomotion (jumping and swimming) allows for understanding how muscle properties contribute to organismal performance in each of these modes.

See also

References

  1. ^ Hillis, David M. (2007). "Constraints in naming parts of the Tree of Life". Molecular Phylogenetics and Evolution 42 (2): 331–8. doi:10.1016/j.ympev.2006.08.001. PMID 16997582. 
  2. ^ Hillis, David M.; Wilcox, Thomas P. (2005). "Phylogeny of the New World true frogs (Rana)". Molecular Phylogenetics and Evolution 34 (2): 299–314. doi:10.1016/j.ympev.2004.10.007. PMID 15619443. http://www.cnah.org/pdf_files/215.pdf. 
  3. ^ Pauly, Gregory B.; Hillis, David M.; Cannatella, David C. (2009). "Taxonomic Freedom and the Role of Official Lists of Species Names". Herpetologica 65 (2): 115–28. doi:10.1655/08-031R1.1. http://www.cnah.org/pdf_files/1225.pdf. 
  4. ^ Frog molecule could provide drug treatment for brain tumors
  5. ^ Fatt, P; Katz, B (1952). "Spontaneous subthreshold activity at motor nerve endings". The Journal of physiology 117 (1): 109–28. PMC 1392564. PMID 14946732. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1392564. 
  6. ^ Del Castillo, J; Katz, B (1954). "Quantal components of the end-plate potential". The Journal of physiology 124 (3): 560–73. PMC 1366292. PMID 13175199. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1366292. 
  7. ^ Katz, B; Miledi, R (1965). "The Measurement of Synaptic Delay, and the Time Course of Acetylcholine Release at the Neuromuscular Junction". Proceedings of the Royal Society of London. Series B 161 (985): 483–95. doi:10.1098/rspb.1965.0016. PMID 14278409. 
  8. ^ Kuffler, SW; Yoshikami, D (1975). "The number of transmitter molecules in a quantum: An estimate from iontophoretic application of acetylcholine at the neuromuscular synapse". The Journal of physiology 251 (2): 465–82. PMC 1348438. PMID 171380. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1348438. 
  9. ^ Hille, B (1967). "The selective inhibition of delayed potassium currents in nerve by tetraethylammonium ion". The Journal of general physiology 50 (5): 1287–302. doi:10.1085/jgp.50.5.1287. PMC 2225709. PMID 6033586. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2225709. 
  10. ^ Anderson, CR; Stevens, CF (1973). "Voltage clamp analysis of acetylcholine produced end-plate current fluctuations at frog neuromuscular junction". The Journal of physiology 235 (3): 655–91. PMC 1350786. PMID 4543940. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1350786. 

Further reading

External links