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First published online December 14, 2007
Journal of Experimental Biology 211, 49-57 (2008)
Published by The Company of Biologists 2008
doi: 10.1242/jeb.012229
Heat increment of feeding in double-crested cormorants (Phalacrocorax auritus) and its potential for thermal substitution
1 Institut Pluridisciplinaire Hubert Curien (IPHC), Département Ecologie,
Physiologie et Ethologie (DEPE), UMR 7178 CNRS-ULP, 23 Rue Becquerel, F-67087
Strasbourg Cedex 2, France
2 NRF Centre of Excellence at the Percy FitzPatrick Institute, University of
Cape Town, Rondebosch 7701, South Africa
3 Department of Zoology, University of British Columbia, 6270 University
Boulevard, Vancouver, British Columbia, V6T 1Z4, Canada
* Author for correspondence (e-mail: manfred.enstipp{at}c-strasbourg.fr)
Accepted 27 October 2007
Diving endotherms inhabiting polar regions face potentially high
thermoregulatory costs. Unless properly insulated, these animals will lose
vast amounts of heat when diving in cold water, which has to be balanced by
heat production. Heat generated as a by-product of digestion (heat increment
of feeding, HIF) or from exercising muscles might be important in maintaining
thermal balance under such conditions, as it would reduce the need for
shivering thermogenesis. Recording the rate of oxygen consumption
(
O2),
respiratory exchange ratio (RER), and stomach temperature, we studied the
magnitude and duration of HIF in seven double-crested cormorants
(Phalacrocorax auritus) following the voluntary ingestion of a single
herring (Clupea pallasi) while birds rested in air. Conducting trials
at thermoneutral (21.1±0.2°C) and sub-thermoneutral temperatures
(5.5±0.7°C), we investigated the potential of HIF for thermal
substitution. After the ingestion of a 100 g herring at thermoneutral
conditions,
O2was elevated
for an average of 328±28 min, during which time birds consumed
2697±294 ml O2 in excess of the resting rate. At
sub-thermoneutral conditions, duration (228±6 min) and magnitude
(1391±271 ml O2) of
O2elevation were
significantly reduced. This indicates that cormorants are able to use the heat
generated as by-product of digestion to substitute for regulatory
thermogenesis, if heat loss is sufficiently high. Altering meal size during
sub-thermoneutral trials, we also found that HIF in cormorants was
significantly greater after larger food intake. Based on these experimental
results, a simple calculation suggests that substitution from HIF might reduce
the daily thermoregulatory costs of double-crested cormorants wintering in
coastal British Columbia by
38%. Magnitude of HIF and its potential for
thermal substitution should be integrated into bioenergetic models to avoid
overestimating energy expenditure in these top predators.
Key words: heat increment of feeding, thermal substitution, cormorant, thermoregulation, ecological energetics, respirometry, time–energy budget
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