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 />
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.