|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Energy and Communication in Three Species of Hylid Frogs: Power Input, Power Output and Efficiency
1 Department of Biology, College of the Holy Cross Worcester, MA 01610, USA; Department of Zoology, University of Florida, Gainesville, FL 32611, USA
2 Department of Zoology, University of Florida Gainesville, FL 32611, USA; Department of Wildlife and Range Sciences, and US Fish and Wildlife Service, University of Florida, Gainesville, FL 32611, USA
3 Department of Biology, College of the Holy Cross Worcester, MA 01610, USA
1. Rates of oxygen consumption for calling, rest and locomotion were measured for three species of treefrogs from the south-east United States: Hyla cinerea (Schneider), H. gratiosa LeConte and H. squirella Bosc.
2. Anaerobic metabolism was slight during calling but large during forced hopping in H. squirella. It is assumed that calling in all three species is primarily aerobic.
3. For all species, oxygen consumption during calling rivalled or exceeded that for locomotion in a closed chamber. Calling apparently is at least as costly as closed-chamber locomotion, if anaerobic contributions to hopping are ignored.
4. The mass-specific costs of producing calls are similar in most species of hylids whose calling energetics have been studied.
5. As in other species of hylids, abdominal trunk muscle masses in male H. squirella and H. gratiosa were large - approximately 10% of the total body mass.
6. Complete sound fields (with measures of variation) were mapped for each species. Each species is an essentially omnidirectional radiator with only a slight flattening of the field behind the head.
7. Efficiencies of sound production (acoustic power/metabolic power) were calculated for each species and compared with values from other frogs, insects and loudspeakers. Efficiencies in hylids vary between 0.8 and 4.9%.
8. Factors that contribute to determining the efficiency of sound production are reviewed. Small animals such as frogs and insects must either use low-efficiency radiators or use high-frequency sounds that do not propagate over great distances. It is possible that low-efficiency transducers maximize the area over which an animal is heard per unit of energy expended.
Key words: energetics, acoustics, treefrogs, efficiency, metabolism, oxygen consumption, coustic power output, advertisement calls
Accepted on March 31, 1989
This article has been cited by other articles:
![]() |
V. L. Salazar and P. K. Stoddard Sex differences in energetic costs explain sexual dimorphism in the circadian rhythm modulation of the electrocommunication signal of the gymnotiform fish Brachyhypopomus pinnicaudatus J. Exp. Biol., March 15, 2008; 211(6): 1012 - 1020. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. N. Prestwich and K. O'Sullivan Simultaneous measurement of metabolic and acoustic power and the efficiency of sound production in two mole cricket species (Orthoptera: Gryllotalpidae) J. Exp. Biol., April 15, 2005; 208(8): 1495 - 1512. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Girgenrath and R. L. Marsh Season and testosterone affect contractile properties of fast calling muscles in the gray tree frog Hyla chrysoscelis Am J Physiol Regulatory Integrative Comp Physiol, June 1, 2003; 284(6): R1513 - R1520. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. J. Bailey and S. Yang Hearing asymmetry and auditory acuity in the Australian bushcricket Requena verticalis (Listroscelidinae; Tettigoniidae; Orthoptera) J. Exp. Biol., September 15, 2002; 205(18): 2935 - 2942. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. R. Moon, J. J. Hopp, and K. E. Conley Mechanical trade-offs explain how performance increases without increasing cost in rattlesnake tailshaker muscle J. Exp. Biol., March 1, 2002; 205(5): 667 - 675. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Oberweger and F. Goller The metabolic cost of birdsong production J. Exp. Biol., January 10, 2001; 204(19): 3379 - 3388. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Ressel Ultrastructural design of anuran muscles used for call production in relation to the thermal environment of a species J. Exp. Biol., January 4, 2001; 204(8): 1445 - 1457. [Abstract] [PDF] |
||||
![]() |
J. McLister Physical factors affecting the cost and efficiency of sound production in the treefrog Hyla versicolor J. Exp. Biol., January 1, 2001; 204(1): 69 - 80. [Abstract] [PDF] |
||||
![]() |
K. S. Pfennig Female spadefoot toads compromise on mate quality to ensure conspecific matings Behav. Ecol., March 1, 2000; 11(2): 220 - 227. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Dantzker, G. Deane, and J. Bradbury Directional acoustic radiation in the strut display of male sage grouse Centrocercus urophasianus J. Exp. Biol., January 11, 1999; 202(21): 2893 - 2909. [Abstract] [PDF] |
||||
![]() |
M Girgenrath and R. Marsh Power output of sound-producing muscles in the tree frogs Hyla versicolor and Hyla chrysoscelis J. Exp. Biol., January 11, 1999; 202(22): 3225 - 3237. [Abstract] [PDF] |
||||