Literature DB >> 20143234

Freshwater elasmobranchs: a review of their physiology and biochemistry.

James S Ballantyne1, J W Robinson.   

Abstract

Only 5% of elasmobranch species live in freshwater (FW) compared to more than 40% of known teleost species. The factors affecting the poor penetration of elasmobranchs into FW environments are currently unknown, however, an important consideration may be the high urea requirement of many proteins in marine elasmobranchs. Urea is an important osmolyte in marine elasmobranchs and must be reduced in dilute environments. There are three identifiable stages in the successful colonization of FW. The euryhaline marine species freely entering and leaving FW represent the initial stage of FW colonization. In this group, there is an apparent inability to eliminate all urea due to protein integrity issues and this results in energy and nitrogen losses that may constrain growth and reproduction. The second stage is represented by those species that live entirely in FW but must also retain some urea. This group also suffers from the same constraints as the first group. These two groups have kidneys and sensory organs that more closely resemble strictly marine forms. The third and final stage is represented by the Potamotrygonid stingrays where the need for urea in FW has been eliminated. Consequently nitrogen and energy losses are reduced and those sections of the kidney needed for urea conservation have been eliminated. The driving force for such modifications is a reduction in urea levels and the concomitant saving of energy needed for urea synthesis. Other physiological adaptations associated with survival in FW include giving birth to live young, the capacity of sperm to be activated in freshwater and modifications of the electrosensory system to function in a low conductivity environment. The need for many anatomical, metabolic and physiological modifications for FW existence may constrain the rapidity and hence the frequency of FW colonization, compared to the situation in the more advanced osmoregulating teleosts. Once optimally adapted to FW, recolonization of sea water by elasmobranchs is problematic due to the loss of urea synthetic capacity and renal structures for urea retention.

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Year:  2010        PMID: 20143234     DOI: 10.1007/s00360-010-0447-0

Source DB:  PubMed          Journal:  J Comp Physiol B        ISSN: 0174-1578            Impact factor:   2.200


  105 in total

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Authors:  T B THORSON
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4.  Renal ammoniagenesis and acid excretion in the dogfish, Squalus acanthias.

Authors:  P A King; L Goldstein
Journal:  Am J Physiol       Date:  1983-10

5.  Marine (Taeniura lymma) and freshwater (Himantura signifer) elasmobranchs synthesize urea for osmotic water retention.

Authors:  Yuen K Ip; Wai L Tam; Wai P Wong; Shit F Chew
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Authors:  J G Richards; G J F Heigenhauser; C M Wood
Journal:  J Comp Physiol B       Date:  2003-07-08       Impact factor: 2.200

8.  Urea transport in kidney brush-border membrane vesicles from an elasmobranch, Raja erinacea.

Authors:  Robyn L Morgan; Patricia A Wright; James S Ballantyne
Journal:  J Exp Biol       Date:  2003-09       Impact factor: 3.312

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Authors: 
Journal:  J Exp Biol       Date:  1995       Impact factor: 3.312

10.  Oxygenational properties and phosphorylated metabolic intermediates in blood and erythrocytes of the dogfish, Squalus acanthias.

Authors:  R M Wells; R E Weber
Journal:  J Exp Biol       Date:  1983-03       Impact factor: 3.312

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