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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.

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