CONTENT - International Society of Zoological Sciences
CONTENT - International Society of Zoological Sciences
CONTENT - International Society of Zoological Sciences
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S16 ICZ2008 - Abstracts<br />
What makes a termite queen – from ecology to genes<br />
Judith Korb<br />
Behavioral Biology, University <strong>of</strong> Osnabrück, D-49069 Osnabrück,<br />
Germany<br />
Termites are the oldest social insects. Despite their apparent<br />
similarity to ants, they evolved social life independently, probably<br />
from a wood-nesting cockroach ancestor. We studied the ultimate<br />
and proximate factors influencing cooperation in a drywood termite,<br />
Cryptotermes secundus, with an ancestral life type <strong>of</strong> dwelling in<br />
dead wood. Associated with this life type is a flexible development<br />
in which workers can become sterile soldiers, winged sexuals that<br />
disperse and found a new colony, or replacement reproductives<br />
that inherit the natal breeding position when the same sex<br />
individual <strong>of</strong> the colony dies. We showed that the ‘decision’ <strong>of</strong><br />
individuals to stay in the colony or leave it as winged sexual is<br />
influenced by ecological factors, such as food availability or<br />
parasite pressure, and social factors such as colony size. However,<br />
it is not affected by the number <strong>of</strong> young present in the nest. These<br />
results together with the finding that the workers do not care for<br />
young, suggest that the workers do not stay to raise siblings.<br />
Rather they seem to stay because they can inherit the colony as<br />
replacement reproductive. Proposing that the opportunity to<br />
become a replacement reproductive builds a major backbone for<br />
the evolution <strong>of</strong> termite sociality, we investigated genes involved in<br />
reproductive development. In a cross-species comparison we<br />
isolated three genes which were generally highly overexpressed in<br />
female replacement reproductives. These genes are good<br />
candidates to play a crucial role in caste determination and<br />
reproductive division <strong>of</strong> labor.<br />
Molecular basis <strong>of</strong> foraging and defense behaviors in the ant<br />
Pheidole pallidula<br />
Christophe Lucas 1,2 and Maria B. Sokolowski 1<br />
1 Department <strong>of</strong> Biology, University <strong>of</strong> Toronto, 3359 Mississauga<br />
Rd. Mississauga, Ont. L5L 1C6, Canada<br />
2 present address: Department <strong>of</strong> Ecology and Evolution,<br />
University <strong>of</strong> Lausanne, Biophore, CH-1015 Lausanne,<br />
Switzerland<br />
Social insects are spectacular examples <strong>of</strong> behavioral adaptations<br />
with sterile sisters performing specialized work in the colony.<br />
However, little is known about the molecular basis <strong>of</strong> their<br />
behavioral specialization and flexibility.<br />
The ant Pheidole pallidula has two sub-castes <strong>of</strong> workers, majors<br />
and minors, which are specialized in defense and foraging<br />
respectively. However, majors are able to help minors in foraging<br />
activities depending on the needs <strong>of</strong> the colony. Thus, there is<br />
plasticity in the subcaste behavioral repertoires.<br />
Here we investigate the molecular underpinnings <strong>of</strong> subcaste<br />
specialization and plasticity in foraging and defense by studying<br />
the foraging (for) gene. The behavioral effects <strong>of</strong> for which<br />
encodes a cGMP dependent protein kinase (PKG) were first<br />
described in Drosophila melanogaster, where for allelic variation<br />
affects foraging behaviors (Osborne et al. 1997). In Apis melifera,<br />
for expression is different between foragers and nurses (Ben-<br />
Shahar et al. 2002). Here we show that for is involved in<br />
behavioral flexibility and specialization <strong>of</strong> P. pallidula's sub-caste.<br />
Specifically, majors have higher PKG enzyme activities than<br />
minors, their PKG activities are lower in the presence <strong>of</strong> a foraging<br />
stimulus and higher in the presence <strong>of</strong> an alien intruder.<br />
Furthermore, pharmacological activation <strong>of</strong> PKG decreases<br />
foraging and increases defense behaviors. Finally, both the<br />
number and localization <strong>of</strong> neuron clusters in which FOR-PKG is<br />
expressed differ between the brains <strong>of</strong> majors and minors.<br />
Together these results suggest that the foraging gene modulates<br />
responses to task-related stimuli in the ant colony.<br />
Ben-Shahar Y, Robichon A, Sokolowski MB, Robinson GE (2002)<br />
Influence <strong>of</strong> gene action across different time scales on behavior.<br />
Science 296:741-744.<br />
Osborne K, Robichon A, Burgess E, Butland S, Shaw RA,<br />
Coulthard A, Pereira HS, Greenspan RJ, Sokolowski MB (1997)<br />
Natural behavior polymorphism due to a cGMP-dependant protein<br />
kinase <strong>of</strong> Drosophila. Science 277:834-836.<br />
- 54 -<br />
Evolution <strong>of</strong> queen size polymorphism in the neotropical ants<br />
Ectatomma Smith 1958<br />
Alejandro Nettel 1 , Chantal Poteaux-Leonard 1 , Dominique<br />
Fresneau 1 and Jean-Paul Lachaud 2<br />
1 Laboratoire d‘Ethologie Expérimentale et Comparée (LEEC)<br />
CNRS UMR 7153 - Université Paris 13. 99, avenue J-B. Clément,<br />
93430, Villetaneuse, France<br />
2 Centre de Recherches sur la Cognition Animale (CRCA) UMR<br />
5169 - Université Paul-Sabatier, 118 route de Narbonne, Bât. IVR3,<br />
31062 Toulouse, France<br />
The evolutionary implications <strong>of</strong> ant queen-size polymorphism, a<br />
phenomenon sparsely present throughout the Formicidae, is a<br />
central question in the study <strong>of</strong> the reproductive strategies <strong>of</strong> social<br />
insects. This polymorphism entails the presence <strong>of</strong> normal sized<br />
queens, macrogynes, and size-reduced queens, microgynes.<br />
Microgynes have been related to different evolutionary trajectories<br />
including parasite queens (inquilinism), alternative dispersal<br />
agents at a lower energetic cost, and dependent colony-founding<br />
specialists. Parasitic forms are thought to originate from queenpolymorphic<br />
populations that undergo sympatric speciation. Two<br />
different instances <strong>of</strong> microgyny have been described within two<br />
widely distributed species <strong>of</strong> the neotropical genus Ectatomma.<br />
Microgynes in E. tuberculatum are parasites and have recently<br />
been described as a new species, E. parasiticum. On the other<br />
hand, evidence suggests that E. ruidum microgynes are a<br />
dispersal-related morph. These two cases <strong>of</strong> queen-size<br />
dimorphism have been described only for colonies from southern<br />
Mexico. The aim <strong>of</strong> our study is to understand the evolution <strong>of</strong><br />
microgyny in Ectatomma by answering the questions: Is there<br />
evidence <strong>of</strong> a common origin <strong>of</strong> microgyny in E. ruidum and E.<br />
tuberculatum? If not, is microgyny a recent, derived characteristic<br />
within each species? Our results based on the molecular<br />
phylogeny <strong>of</strong> the whole Ectatomma genus using mitochondrial and<br />
nuclear sequences show that microgyny has evolved twice<br />
independently and that dissimilar processes were involved in the<br />
origin <strong>of</strong> mycrogyne-bearing populations in E. ruidum and E.<br />
tuberculatum. We present our results and their implications to our<br />
understanding <strong>of</strong> the evolution <strong>of</strong> alternative reproductive<br />
strategies in ants.<br />
Genomic response to sex: A microarray-based study <strong>of</strong><br />
queens in the ant Cardiocondyla obscurior<br />
Jan Oettler 1 and John Wang 2<br />
1<br />
Universität Regensburg, Biologie I, Germany<br />
2<br />
University <strong>of</strong> Lausanne, Department <strong>of</strong> Ecology and Evolution,<br />
Suisse<br />
Previous research documented a dramatic effect <strong>of</strong> mating on<br />
aging in the ant C. obscurior: Queens that have been mated with<br />
sterilized males show a similar lifespan compared to queens<br />
mated with fertile males. By contrast, virgin queens have a much<br />
lower life expectancy (50% lower). We were interested in why<br />
those queens that were mated with sterilized males still show<br />
physiological traits <strong>of</strong> fully functional queens although fecundity is<br />
as low as in virgin queens, i.e. why does aging appear to be<br />
uncoupled from fecundity. To begin investigating the molecular<br />
basis for this uncoupling, we used a cDNA microarray developed<br />
for the closely related Solenopsis invicta to pr<strong>of</strong>iled gene<br />
expression differences between virgin queens, queens mated to<br />
normal males and queens mated to sterilized males. We found<br />
many differentially regulated genes among the three different<br />
queen classes, and <strong>of</strong> particular interest in our preliminary analysis,<br />
some <strong>of</strong> these genes are involved in metabolism and juvenile<br />
hormone production.