CONTENT - International Society of Zoological Sciences
CONTENT - International Society of Zoological Sciences
CONTENT - International Society of Zoological Sciences
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S17 ICZ2008 - Abstracts<br />
Reproductive behavioral plasticity in Père David’s deer<br />
Zhigang Jiang 1,2 , Yan Zeng 1,2 , Zhenyu Zhong 3 , Chunwang Li 1 and<br />
Linyuan Zhang 3<br />
1<br />
Key Laboratory <strong>of</strong> Animal Ecology and Conservation Biology,<br />
Institute <strong>of</strong> Zoology, Chinese Academy <strong>of</strong> <strong>Sciences</strong>, Beijing,<br />
100101, China.<br />
2<br />
Graduated School <strong>of</strong> Chinese Academy <strong>of</strong> <strong>Sciences</strong>, Beijing,<br />
China 100049, China.<br />
3<br />
Beijing Père David’s Deer Park<br />
Père David’s deer is a polygamous species; one to several stags<br />
rut at the same time, a “Harem master” defends the receptive<br />
female herd and tries to monopolize the opportunity <strong>of</strong> mating.<br />
However, reproductive behavior in Père David’s deer is highly<br />
plastic. First, the males have different rut tactics: “Harem master<br />
tactic”, “Challenger tactic” and “Bachelor tactic”, rut season is<br />
extended for a long period, e.g. rut lasts as long as two months in<br />
the Beijing Père David deer population. Thus, the time to<br />
commence rut is plastic in stags. Female “estrus window”, which is<br />
composed <strong>of</strong> the individual females in estrus, drifts among years.<br />
That means unknown factor controls the estrus in the females, or<br />
females are able to adjust their estrus. We conducted a study on<br />
the reproductive behavior <strong>of</strong> Père David’s deer from 1994 to 2005.<br />
We observed the behaviors <strong>of</strong> males and females and used five<br />
polymorphic microstatellite loci which were screened out from 84<br />
pairs <strong>of</strong> species-transferred primers to study the mating system in<br />
the reintroduced Père David’s deer populations in China. The<br />
study identified multi stags sired <strong>of</strong>fspring in the population.<br />
“Harem masters” could not monopolize breeding opportunities,<br />
Challengers also had chance to breed. While the plasticity in<br />
female estrus window presumably is related to female cryptic sex<br />
choice, on the other hand, to be a “Harem master” is not the “The<br />
winner takes all” tactics. The multi-paternity in Père David’s deer<br />
indicates the rut tactics like “Challenger tactic” has its evolutionary<br />
fitness as well.<br />
Relationships between morphological traits, behavioural<br />
characteristics, and habitat selection in Iranian Wheatears<br />
using Fourth-Corner Problem analysis<br />
Mohammad Kaboli 1 , Mansour Aliabadian 2 , Saina Habibi 1 , Parisa<br />
Mehrandish 1 and Roger Prodon 3<br />
1<br />
Department <strong>of</strong> Fishery and Environment, Faculty <strong>of</strong> Natural<br />
Resources, University <strong>of</strong> Tehran, Tehran, Iran<br />
2<br />
Department <strong>of</strong> Biology, Faculty <strong>of</strong> Science, Ferdowsi University <strong>of</strong><br />
Mashhad, Mashhad, Iran<br />
3<br />
Laboratoire Ecologie et Biogéographie des Vertébrés (EPHE),<br />
Centre d’Ecologie Fonctionnelle et Evolutive, UMR 5175, 1919<br />
route de Mende, 34293 Montpellier cedex 5, France<br />
Ecological segregation in the Wheatear genus Oenanthe is a<br />
complex and intriguing question. Here we studied habitat variables,<br />
behavioural characteristics and morphological traits <strong>of</strong> 11<br />
Wheatear species that are distributed sympartrically in Iran. We<br />
recorded 19 behavioural characteristics and measured 36 habitat<br />
variables within a 100-m radius around observed birds. We also<br />
measured 21 biometrical variables in each species. We compared<br />
variable-to-variable correlation between these three data matrices<br />
using Legendre et al.’s Fourth-Corner Problem method. We first<br />
related, through the matrix A1 (presence/absence <strong>of</strong> species in<br />
sampling sites), the morphological traits <strong>of</strong> the species (mean<br />
values <strong>of</strong> the variables for each species; matrix Cmorphology) to the<br />
habitat features measured on each sampling site (matrix Bhabitat).<br />
We then related, through A1, the behavioural traits <strong>of</strong> the species<br />
(mean values <strong>of</strong> the variables for each species; matrix Cbehaviour) to<br />
the habitat features measured on each sampling site (matrix<br />
Bhabitat). We lastly related, through A2, the morphological traits <strong>of</strong><br />
the species (matrix Cmorphology) to the behavioural variables<br />
measured, on each sampling site, on the "principal" species <strong>of</strong><br />
Wheatears <strong>of</strong> the site (matrix Bbehaviour). Our results showed that<br />
morphological traits, particularly flight and foot-leg apparatuses,<br />
represent a good synthesis <strong>of</strong> overall behaviour traits. Since<br />
Morphological traits result from compromise between different<br />
selection pressures like foraging mode and migration pattern,<br />
seems plays an important role in determining the ecological range<br />
<strong>of</strong> a species. Likewise, habitat features are also correlated with<br />
behavioural traits, but less tightly.<br />
- 60 -<br />
This correlation between behaviour and habitat could be explained<br />
by this fact that many behavioural variables are defined on the<br />
habitat-basis (e.g. types <strong>of</strong> perch used). But the proportion <strong>of</strong><br />
significant relationships between habitat and behaviour remains<br />
the same when we consider only the "purely" behavioural variables<br />
(type, speed, and frequency <strong>of</strong> movements). Finally, The match<br />
between morphology and habitat is relatively loose that may partly<br />
be due to the fact that habitat variables are more likely depend on<br />
proximal factors, especially the sampling conditions (e.g., unequal<br />
frequency <strong>of</strong> different landscape features in different sampling<br />
areas, random component <strong>of</strong> the detection <strong>of</strong> the species).<br />
Control <strong>of</strong> copula duration: how males and females control<br />
sperm transfer<br />
Joshka Kaufmann, Jean-François Le Galliard and David Laloi<br />
Laboratoire Ecologie & Evolution - UMR 7625, Université Pierre et<br />
Marie Curie / ENS / AgroParisTech / CNRS, Paris, France<br />
In polygynandrous mating systems, sexual conflict can arise on the<br />
number <strong>of</strong> partners and on the reproductive investment <strong>of</strong> each<br />
sex. Particularly, traits that control sperm transfer can have quite<br />
different optima with regard to female and male fitness. Indeed,<br />
female behaviour may have evolved to ensure fertilization, favour<br />
preferred male through longer copulation or promote postcopulatory<br />
mate choice. Males may strategically allocate their<br />
sperm according to female reproductive quality, level <strong>of</strong> sperm<br />
competition and further mating opportunities. Behavioural<br />
mechanisms have been poorly studied in taxa, such as reptiles,<br />
where sperm transfer is driven by copula duration rather than by<br />
the number <strong>of</strong> copulations. In the present study, we investigate in<br />
the common lizard whether males and females control copula<br />
duration. In a sequential mating context, we study how mate<br />
choice and copulatory behaviours vary with individual quality (e.g.<br />
coloration, social dominance, fitness-related physical<br />
performances) and mating history. We principally disentangle the<br />
respective role <strong>of</strong> both sexes in this conflict for sperm transfer.<br />
Both sexes become more choosy in second mating opportunities,<br />
female preference being based on male ventral coloration while<br />
males prefer virgin females. Our results show that females control<br />
copula duration and hence sperm transfer and may therefore bias<br />
paternity. Nevertheless, no evidence was found that females<br />
favour high-quality males through longer copulation. Here, we<br />
suggest that female lizards may use both pre-copulatory mate<br />
choice and control <strong>of</strong> copula duration to maximize the genetic<br />
benefits <strong>of</strong> multiple mating.<br />
Is discrimination <strong>of</strong> song quality by shortened-wings female<br />
Canaries (Serinus canaria) reduced ?<br />
Alexandre Lerch and Laurent Nagle<br />
Laboratory <strong>of</strong> Ethology and Comparative Cognition, Université de<br />
Paris X-Nanterre ; Bat BSL, 1er étage; 200, avenue de la<br />
République, 92 000, Nanterre cedex 01, France<br />
Because <strong>of</strong> their greater investment in reproduction, females are<br />
supposed to be choosier than males when mating (Trivers, 1972).<br />
While numerous studies investigated this aspect <strong>of</strong> mate choice,<br />
most <strong>of</strong> them have focused on male traits that maintain female<br />
preferences (Jennion & Petrie, 1997).<br />
Nevertheless, consensus between females in the selection <strong>of</strong> male<br />
phenotypic features is not the rule, and more subtle mechanisms<br />
take place. Indeed, variations in female preferences do exist,<br />
especially in some contexts <strong>of</strong> predation (Simcox et al., 2005) or<br />
costly competition (Fawcett and Johnstone, 2003). In birds, a case<br />
<strong>of</strong> reduced discrimination for male coloration has been reported in<br />
female zebra Finches with shortened wings (Burley & Foster,<br />
2006).<br />
In canaries (Serinus canaria), song is known to be the main<br />
secondary sexual feature, and a special phrase (« A » phrase) is<br />
reported to elicit a high level <strong>of</strong> sexual responses by females<br />
(Vallet et al., 1998). In our study, we investigate the power <strong>of</strong><br />
discrimination toward songs <strong>of</strong> different quality, in a group <strong>of</strong><br />
female canaries tested in two conditions: 1) with intact wings<br />
(control group) and 2) with cut wings. Our preliminary results<br />
suggest that birds with shortened wings show a weaker preference<br />
toward high quality songs.