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31 Relationship between nutritional status and prolactin levels in the
Common Eider, a capital incubator
FRANÇOIS CRISCUOLO
1
, OLIVIER CHASTEL², GEIR. WING GABRIELSEN
3
, ANDRÉ LACROIX
2
AND YVON LE MAHO
1
1
Centre d'Ecologie et Physiologie Energétiques, CNRS, 23 rue Becquerel, F-67087 Strasbourg Cedex 2, France;
2
Centre d'Etudes
Biologiques de Chizé, CNRS, F-79360 Villiers-En-Bois, France ;
3
Norwegian Polar Institute, The Polar Environmental Center, Hjalmar
Johansensgate l4, N-9296 Tromsø
Norway e-mail: f.criscuolo@c-strasbourg.fr
ABSTRACT
In Common Eider, only females incubate while fasting for 25 days. When their body condition is
deteriorated at hatching, females often abandon their ducklings. To therefore investigate how body
condition may mediate parental care in eiders, we studied the effect of a change in the duration of
incubation on their plasma prolactin, i.e. the main parental hormone in birds. Birds with shortened
incubation have higher body masses and showed higher levels of plasma prolactin levels at hatching
than the control group, suggesting that circulant prolactin at hatching is linked to body condition.
The females that underwent an extended incubation started to feed again and displayed a "normal"
body mass but unexpectedly a very high plasma prolactin concentration.
Key Words: Somateria mollissima, prolactin, Svalbard, incubation, feeding patterns
INTRODUCTION
Prolactin is involved in the initiation and maintenance of incubation
behaviour in birds (Hall 1991, Buntin 1996, Sharp et al. 1998), in
addition to its large variety of actions (i.e. in lipid metabolism, Hall et
al. 1986). Eggs act as tactile and visual stimuli in most birds, since
their removal results in a decrease in plasma prolactin and the
termination of parental behaviour (Buntin 1986, Hall & Goldsmith
1983, Ramsey et al. 1985). However, prolactin secretion can be
modulated by several factors such as food restriction (Hall et al. 1986)
or be endogenously timed as it has been showed in pelagic birds,
prolactin levels being maintained regardless of direct stimulations from
the nest or eggs (Hector & Goldsmith 1985, Lormée et al. 1999, Garcia et
al. 1996, Jouventin & Mauget 1996, Vleck et al. 2000). Incubation
behaviour competes with foraging, thus inducing restricted access to
food. Anorexia has evolved as a means to ensure greater nest attendance
(Mrosovsky & Sherry 1980), to enhance the chances of hatching
success. However, the amount of adult body reserves available to
incubate is a key factor in determining incubation constancy (Aldrich
& Raveling 1983, Chastel et al. 1995, Chaurand & Weimerskirch 1994,
Cherel et al. 1994). This suggests a potential control of prolactin
secretion (thus of parental behaviour) by adult body condition in capital
incubators, i.e. birds which does not feed during incubation.
The female Common Eider Somateria mollissima can indeed be
defined as a true capital incubator (Drent & Daan 1980) since it relies
entirely on its body nutrient reserves during 24-26 days of incubation
(Korschgen 1977). Moreover, the female behaves as a brood-tender
or not, depending on its remaining body reserves at hatching (Bustnes
& Erikstad 1991). Knowing that plasma prolactin concentration is
high in female eiders taking care of the brood (Criscuolo et al, in
press) as observed in other species (Ball 1991), we checked whether
prolactin is endogenously controlled (i.e. by adult body reserves). To
modify the female body condition at hatching, the incubation length
was experimentally shortened or prolonged by swapping eggs between
nest with different laying dates. Prolonged incubating females were
found to start feed again, since we observed successive dive cycles
during recesses at sea (Criscuolo et al. in press). Thus, for these females,
to test whether the nutritional status of the bird can influence its
prolactin concentration, we determined the plasma concentrations of
triacylglycerols as a sign of feeding and of β-hydroxybutyrate as a
sign of fasting (Le Maho et al. 1981).
METHODS
The study was conducted in Kongsfjorden, on the western coast of
the Svalbard Archipelago (78°55' N), on female eiders nesting on
Prins Heinrich Island (1998 and 2000) from early June to mid-July.
Antarctic Biology in a Global Context, pp 193-197.
Edited by A.H.L. Huiskes, W.W.C. Gieskes, J. Rozema, R.M.L. Schorno, S.M. van der Vies & W.J. Wolff.
©2003 Backhuys Publishers, Leiden, The Netherlands.