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CONTENT - International Society of Zoological Sciences

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S17 ICZ2008 - Abstracts<br />

Nest biology <strong>of</strong> Monoeca haemorrhoidalis (Smith, 1854)<br />

(Apidae) at the Atlantic Rainforest <strong>of</strong> Southern Brazil<br />

Léo Correia da Rocha-Filho 1 and Gabriel A. R. Melo 2<br />

1 Departamento de Biologia, Universidade de São Paulo, Av.<br />

Bandeirantes 3900, Monte Alegre, 14040-901, Ribeirão Preto, SP,<br />

Brazil ; 2 Departamento de Zoologia, Setor de Ciências Biológicas,<br />

Centro Politécnico, Universidade Federal do Paraná, 81531-990,<br />

Curitiba, PR, Brazil<br />

The genus Monoeca is distributed over almost the entire<br />

Neotropical region, with ten described species. The nesting biology<br />

<strong>of</strong> a few species, Monoeca sp., M. schrottkyi, M. lanei and M.<br />

xanthopyga, has been studied by previous authors. The aim <strong>of</strong> this<br />

study was to investigate the nesting ecology <strong>of</strong> M. haemorrhoidalis.<br />

This study was conducted between Setember/2005 and<br />

January/2007, in an area <strong>of</strong> Atlantic Rainforest. Four nest<br />

aggregations were studied, as well as other smaller aggregations<br />

<strong>of</strong> M. haemorrhoidalis also found along the reserve trail. M.<br />

haemorrhoidalis females construct their nests in clay soil, in dense<br />

aggregations, with density values varying from 4 to 27 nests/m 2 .<br />

The period <strong>of</strong> nest construction and cell provisioning started at the<br />

end <strong>of</strong> October/2005 and stopped by the end <strong>of</strong> February/2006.<br />

During this period, plant species <strong>of</strong> the families Orchidaceae,<br />

Styracaceae and, mainly, Malpighiaceae, were the most important<br />

pollen and floral oils resources that were utilized in brood cell<br />

provisioning. Males and females gathered nectar in a great variety<br />

<strong>of</strong> plant species. M. haemorrhoidalis is a univoltine and seasonal<br />

species and its nest habits are similar to those already observed<br />

for other Monoeca species.<br />

Natural enemies and other species associated with Monoeca<br />

haemorrhoidalis (Smith, 1854) (Apidae)<br />

Léo Correia da Rocha-Filho 1 and Gabriel A. R. Melo 2<br />

1 Departamento de Biologia, Universidade de São Paulo, Av.<br />

Bandeirantes 3900, Monte Alegre, 14040-901, Ribeirão Preto, SP,<br />

Brazil<br />

2 Departamento de Zoologia, Setor de Ciências Biológicas, Centro<br />

Politécnico, Universidade Federal do Paraná, 81531-990, Curitiba,<br />

PR, Brazil<br />

The bee species Monoeca haemorrhoidalis, the largest one in the<br />

genus, occurs in the Atlantic rainforest <strong>of</strong> southeastern and<br />

southern Brazil. This study focused in the interactions between M.<br />

haemorrhoidalis and its natural enemies and associates. Nest<br />

aggregations were studied in an area at the transition between<br />

Dense and Mixed subtropical Rainforest, in southern Brazil. During<br />

the nest activities, between October/2005 and February/2006,<br />

thirty-two animal species were observed at the nesting sites.<br />

Nonetheless, association with M. haemorrhoidalis was confirmed<br />

only for the cleptoparasitic species Protosiris gigas (Apidae),<br />

Heterostylum maculipennis (Bombyliidae) and Megaselia sp.<br />

(Phoridae), Tetraolytta gerardi and Tetraonyx distincticollis<br />

(Meloidae), the predators Pyrogaster moestus (Lampyridae) and<br />

Pachycondyla harpax (Formicidae), the cleptobiont species<br />

Acromyrmex niger (Formicidae) and the parasitoids Physocephala<br />

bipunctata (Conopidae), Pseudomethoca melanocephala e<br />

Hoplocrates specularis (Mutillidae). Moreover, pathogenic fungi<br />

developed in stored food <strong>of</strong> brood cells and in M. haemorrhoidalis<br />

cocoons and Meloidae larvae, causing the death <strong>of</strong> these species.<br />

The cleptoparasitic bee P. gigas was one <strong>of</strong> the main causes <strong>of</strong> M.<br />

haemorrhoidalis mortality. During the peak <strong>of</strong> activity <strong>of</strong> P. gigas, M.<br />

haemorrhoidalis had a substantial decrease in its nest construction.<br />

This can be an important adaptation <strong>of</strong> the host species against its<br />

cleptoparasite.<br />

- 58 -<br />

Phenotypic plasticity, genotype x environment interaction,<br />

and the (un)reliability <strong>of</strong> animal mating signals<br />

Michael D. Greenfield<br />

IRBI (Institut de Recherche sur la Biologie de l’Insecte), CNRS<br />

UMR 6035, Université François Rabelais, Parc de Grandmont,<br />

Tours 37200, France<br />

The potential for animals to ‘deceive’ one another via ‘dishonest’<br />

signals remains a major question in behavioral ecology. The<br />

current view, that on average an individual’s signals are reliable<br />

indications <strong>of</strong> potential ability, is based on the argument that<br />

receivers would be selected to ignore signals that are habitually<br />

unreliable, which, in turn, would select against the production <strong>of</strong><br />

such signals. Formal analyses as well as observations and<br />

experimental findings are largely consistent with this generalization.<br />

A very different, and more insidious, problem for reliable<br />

communication, particularly in mating, is posed by the plasticity <strong>of</strong><br />

signal traits across environments: Because genotypes may<br />

respond in different ways to environmental changes across space<br />

or time, a given genotype may exhibit the ‘superior’ (mating) signal<br />

in one environment but the ‘inferior’ one in another. Thus, (mating)<br />

signals may not be reliable indications if the environment changes<br />

across generations or <strong>of</strong>fspring disperse to different environments.<br />

This conundrum does not necessarily challenge the primacy <strong>of</strong><br />

signal reliability, but it points out fundamental weaknesses in our<br />

understanding <strong>of</strong> signal evolution that result from ignoring<br />

unpredictable environmental variation. Here, I present findings on<br />

genotype x environment interaction (gei) in the male courtship<br />

song <strong>of</strong> the ultrasonic pyralid moth Achroia grisella. I show how<br />

signal unreliability can arise and discuss the restricted<br />

circumstances under which reliability might yet persist. I then<br />

present recent findings on genetic variance, phenotypic plasticity,<br />

and gei in female response and preference in A. grisella, and I<br />

show how reliability in animal communication can increase or<br />

decrease when both male signal and female response traits are<br />

subject to gei.<br />

Prenatal stress influences behavioural features in young birds<br />

Floriane Guibert 1 , Cécilia Houdelier 1 , Sophie Lumineau 1 , Kurt<br />

Kotrschal 2 , Erich Möstl 3 and Marie-Annick Richard-Yris 1<br />

1<br />

UMR CNRS 6552 Ethologie animale et humaine, Université de<br />

Rennes 1, 35042 Rennes, France<br />

2 Konrad-Lorenz-Forschungsstelle, University <strong>of</strong> Vienna, A-4645<br />

Grünau, Austria<br />

3<br />

University <strong>of</strong> Veterinary Medicine, Department <strong>of</strong> Natural<br />

<strong>Sciences</strong>, Biochemistry, Veterinärplatz 1, A-1210 Vienna, Austria<br />

The individual’s behavioural development is notably influenced by<br />

his social environment and particularly by his mother. This<br />

maternal effect occurs after youngster’s birth but also before. In<br />

mammals, prenatal maternal stress influences the setting up <strong>of</strong><br />

youngster’s behaviour; this influence results from the modulation <strong>of</strong><br />

the mother’s plasmatic levels <strong>of</strong> steroid hormones. In birds, a<br />

similar maternal influence also exists, implicating a modulation <strong>of</strong><br />

steroids levels in the egg. Indeed, egg’s hormonal levels are<br />

influenced by laying females’ environment and an artificial steroids’<br />

enrichment <strong>of</strong> eggs modulates the behavioural phenotype <strong>of</strong><br />

resulting chicks. However, no study has investigated yet the whole<br />

mechanism <strong>of</strong> maternal prenatal influence in birds (i.e. from the<br />

mother to the <strong>of</strong>fspring). Thus, our aim was to analyse the impact<br />

<strong>of</strong> stress on the laying female on her eggs’ hormonal composition<br />

and on the behavioural features <strong>of</strong> her <strong>of</strong>fspring. Therefore, we<br />

applied stressors on laying females in a precocious bird, the<br />

Japanese quail. Our results showed that the prenatally stressed<br />

chicks appeared to be more emotive with a higher social<br />

motivation and also a slight increase <strong>of</strong> steroids in the eggs <strong>of</strong><br />

stressed females. Thus, in this study, we show for the first time<br />

that, in birds, stress on the laying female has a significant impact<br />

on the behaviour <strong>of</strong> her <strong>of</strong>fspring via a hormonal change in her<br />

eggs.

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