Literature DB >> 28311710

Adaptations of the reed frog Hyperolius viridiflavus (Amphibia, Anura, Hyperoliidae) to its arid environment : II. Some aspects of the water economy of Hyperolius viridiflavus nitidulus under wet and dry season conditions.

W Geise1, K E Linsenmair1.   

Abstract

Adaptations to aridity of the reedfrog Hyperolius viridiflavus nitidulus, living in different parts of the season-ally very dry and hot West African savanna, are investigated. 1. During the dry season mainly juveniles (weighing 200-600 mg) were found in the field. A very low rate of evaporative water loss (EWL; about 1.2% of the body weight/day under laboratory dry season conditions) enables the frogs to estivate unshaded on dry plants. There they are exposed to temperatures occasionally reaching 45° C and are to sustain high radiation loads. The EWL of wet season frogs (WSF) was on average 30 times higher. 2. In dry season frogs (DSF) a thin layer of desiccated mucus seals the body surface reducing water loss and securing tight attachment to the substrate. The DSF are not in a state of torpor but are able to become active at any moment. The highest tolerable water loss of DSF amounts to 50% of their initial body weight. Since uptake of water or food often is impossible for more than two months, the small DSF have to survive these harsh conditions with very limited reserves of energy and water. 3. The low EWL of DSF does not engender any cooling effects. Only above a certain high temperature limit, defined as the critical thermal maximum (CTM; 43-44°C) we found a steep increase of EWL-probably indicating evaporative cooling. The CTM is affected by the temperature during acclimatization. 4. In contrast to WSF cutaneous respiration is not found in DSF. All CO2 is delivered via the lungs by discontinuous ventilation. The simultaneous water loss via the respiratory tract makes up to 14.9+/-8.9% of the entire water loss. 5. A very fast water uptake (69.3+/-19.4%/h) via thin and vascular skin areas at the ventral flanks and the inner sides of the legs enables the frogs to use small quantities of water available for very short times only. This highly permeable skin is protected against desiccation by the typical squat resting position of the frogs. 6. DSF usually to neither urinate nor defecate; they are not proved to be uricotelic. Probably they store the nitrogenuous wastes as urea in the body fluids and as purines in the iridophores and connective tissues. It is suggested that there is no selective advantage for uricotelism in the small H. v. nitidulus.

Entities:  

Year:  1986        PMID: 28311710     DOI: 10.1007/BF00378769

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


  22 in total

1.  Determination of skin resistance and the role of the skin in controlling water loss in amphibians and reptiles.

Authors:  J R Spotila; E N Berman
Journal:  Comp Biochem Physiol A Comp Physiol       Date:  1976

2.  Metabolism of land snails (Otala lactea) during dormancy, arousal, and activity.

Authors:  C F Herreid
Journal:  Comp Biochem Physiol A Comp Physiol       Date:  1977

3.  Physiological correlates of basking in amphibians.

Authors:  H B Lillywhite
Journal:  Comp Biochem Physiol A Comp Physiol       Date:  1975-10-01

Review 4.  Osmoregulation in amphibians and reptiles.

Authors:  V H Shoemaker; K A Nagy
Journal:  Annu Rev Physiol       Date:  1977       Impact factor: 19.318

5.  Quantitative morphology of cold-blooded lungs: amphibia and reptilia.

Authors:  S M Tenney; J B Tenney
Journal:  Respir Physiol       Date:  1970-05

6.  Rate of water uptake through the integument of the desert toad, Bufo punctatus.

Authors:  L McClanahan; R Baldwin
Journal:  Comp Biochem Physiol       Date:  1969-01

Review 7.  Gas exchange and control of breathing in reptiles.

Authors:  M L Glass; S C Wood
Journal:  Physiol Rev       Date:  1983-01       Impact factor: 37.312

8.  Uricotelism and low evaporative water loss in a South American frog.

Authors:  V H Shoemaker; D Balding; R Ruibal; L L McClanahan
Journal:  Science       Date:  1972-03-03       Impact factor: 47.728

9.  Acid-base relationships in the blood of the toad, Bufo marinus. I. The effects of environmental CO2.

Authors:  R G Boutilier; D J Randall; G Shelton; D P Toews
Journal:  J Exp Biol       Date:  1979-10       Impact factor: 3.312

10.  THE EVAPORATION OF WATER FROM HELIX ASPERSA. I. THE NATURE OF THE EVAPORATING SURFACE.

Authors:  J MACHIN
Journal:  J Exp Biol       Date:  1964-12       Impact factor: 3.312

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  7 in total

1.  Adaptations of the reed frog Hyperolius viridiflavus (Amphibia, Anura, Hyperoliidae) to its arid environment : I. The skin of Hyperolius viridiflavus nitidulus in wet and dry season conditions.

Authors:  Frank Kobelt; K E Linsenmair
Journal:  Oecologia       Date:  1986-03       Impact factor: 3.225

2.  Adaptations of the reed frog Hyperolius viridiflavus (Amphibia, Anura, Hyperoliidae) to its arid environment : IV. Ecological significance of water economy with comments on thermoregulation and energy allocation.

Authors:  W Geise; K E Linsenmair
Journal:  Oecologia       Date:  1988-11       Impact factor: 3.225

3.  Adaptations of the reed frog Hyperolius viridiflavus (Amphibia, Anura, Hyperoliidae) to its arid environment : III. Aspects of nitrogen metabolism and osmoregulation in the reed frog, Hyperolius viridiflavus taeniatus, with special reference to the role of iridophores.

Authors:  R Schmuck; K E Linsenmair
Journal:  Oecologia       Date:  1988-04       Impact factor: 3.225

4.  Behavioural thermoregulation of the Andean toad (Bufo spinulosus) at high altitudes.

Authors:  U Sinsch
Journal:  Oecologia       Date:  2013-03-13       Impact factor: 3.225

5.  Adaptations of the reed frog Hyperolius viridiflavus (Amphibia: Anura: Hyperoliidae) to its arid environment. VI. The iridophores in the skin as radiation reflectors.

Authors:  F Kobelt; K E Linsenmair
Journal:  J Comp Physiol B       Date:  1992       Impact factor: 2.200

6.  Adaptations of the reed frog Hyperolius viridiflavus (Amphibia, Anura, Hyperoliidae) to its arid environment. VII. The heat budget of Hyperolius viridiflavus nitidulus and the evolution of an optimized body shape.

Authors:  F Kobelt; K E Linsenmair
Journal:  J Comp Physiol B       Date:  1995       Impact factor: 2.200

7.  Examining the relationship between sexual dimorphism in skin anatomy and body size in the white-lipped treefrog, Litoria infrafrenata (Anura: Hylidae).

Authors:  Collin S Vanburen; David B Norman; Nadia B Fröbisch
Journal:  Zool J Linn Soc       Date:  2019-11-06       Impact factor: 3.286

  7 in total

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