Literature DB >> 28312769

Metabolic oxygen regulation and conformity during submergence in the salamandersSiren lacertina, Amphiuma means, andAmphiuma tridactylum, and a comparison with other giant salamanders.

Jeffrey T Duke1, Gordon R Ultsch1.   

Abstract

The giant salamanders of North America include 4 genera, all of which are aquatic. We have compared the efficacy of aquatic O2 uptake among them by measuring theVO2 while submerged and determining the responses to progressive hypoxia at 10-240 mmHg at 20° C. Both species ofAmphiuma were metabolic O2 conformers over the entire range ofPO2. About half ofSiren lacertina were conformers over this range, and half were regulators with an average critical O2 tension of 92 mmHg. There were no short-term changes (days) in the response ofSiren to progressive hypoxia, but one animal switched from conformation to regulation after 4-5 months. Neither genus is considered to have an exceptionally low metabolic rate. The "whole-body O2 conductance", defined asΔVO2/ΔPO2(µl O2 · g-1 · h-1 · mmHg-1) in the range of metabolic O2 conformity, was least in the species most dependent upon air-breathing and most likely to be found in hypoxic waters (e.g., 0.076 forAmphiuma), and greatest in those that airbreathe less frequently and/or are found in relatively normoxic waters (e.g., 0.429 forNecturus). These conductances are considered to be adaptive in terms of preventing O2 loss through the skin, or in facilitating its uptake, as correlated with the O2 tensions normally prevailing in the environment of each species.

Entities:  

Year:  1990        PMID: 28312769     DOI: 10.1007/BF00665589

Source DB:  PubMed          Journal:  Oecologia        ISSN: 0029-8549            Impact factor:   3.225


  14 in total

1.  Gas exchange and habitat selection in the aquatic salamanders Necturus maculosus and Cryptobranchus alleganiensis.

Authors:  G R Ultsch; J T Duke
Journal:  Oecologia       Date:  1990-06       Impact factor: 3.225

2.  Effects of environmental O2 on blood flow and diffusing capacity in amphibian skin.

Authors:  G M Malvin; M P Hlastala
Journal:  Respir Physiol       Date:  1989-05

3.  Pulmonary, branchial and cutaneous gas exchange in the mud puppy, Necturus maculosus maculosus (Rfinesque).

Authors:  R W Guimond; V H Hutchison
Journal:  Comp Biochem Physiol A Comp Physiol       Date:  1972-06-01

4.  Trimodal gas exchange in the large aquatic salamander, Siren lacertina (Linnaeus).

Authors:  R W Guimond; V H Hutchison
Journal:  Comp Biochem Physiol A Comp Physiol       Date:  1973-10-01

5.  Respiration of some urodele and anuran amphibia. I. In water, role of the skin and gills.

Authors:  J W Shield; P J Bentley
Journal:  Comp Biochem Physiol A Comp Physiol       Date:  1973-09-01

6.  Gas exchange and metabolism in the Sirenidae (Amphibia: Caudata)--I. Oxygen consumption of submerged sirenids as a function of body size and respiratory surface area.

Authors:  G R Ultsch
Journal:  Comp Biochem Physiol A Comp Physiol       Date:  1974-02-01

7.  Cutaneous respiration in the Congo eel Amphiuma means (Amphibia: Urodela).

Authors:  P J Bentley
Journal:  Comp Biochem Physiol A Comp Physiol       Date:  1975-01-01

8.  Quantitative studies on the morphology of respiratory surfaces in amphibians.

Authors:  J Czopek
Journal:  Acta Anat (Basel)       Date:  1965

9.  Respiratory surface area as a factor controlling the standard rate of O2 consumption of aquatic salamanders.

Authors:  G R Ultsch
Journal:  Respir Physiol       Date:  1976-05

10.  Respiratory properties of blood in a strictly aquatic and predominantly skin-breathing urodele, Cryptobranchus alleganiensis.

Authors:  R G Boutilier; D P Toews
Journal:  Respir Physiol       Date:  1981-11
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