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CONTENT - International Society of Zoological Sciences

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S15 ICZ2008 - Abstracts<br />

Temporal and amplitude parameters affecting mate choice<br />

selectivity in Nezara viridula (L.) (Heteroptera: Pentatomidae).<br />

Maarten de Groot, Andrej Čokl and Meta Virant-Doberlet<br />

Department <strong>of</strong> Entomology, National Institute <strong>of</strong> Biology, Večna pot<br />

111, Ljubljana, Slovenia<br />

While on the same plant, males and females <strong>of</strong> the southern green<br />

stink bug Nezara viridula use species and sex specific vibrational<br />

signals transmitted through the substrate for recognition and<br />

localization <strong>of</strong> conspecifics. We investigated the selectivity <strong>of</strong> the<br />

behavioural responses <strong>of</strong> males to natural and altered female<br />

calling song (FCS) in one- and two-side play-back experiments on<br />

bean plants. We tested the influence <strong>of</strong> two temporal parameters<br />

(signal and interval duration) and signal amplitude on triggering <strong>of</strong><br />

recognition (male calling) and searching. For all altered FCSs,<br />

significantly more males were calling than searching. The results<br />

show that the signal and interval duration were positively<br />

correlated with the male calling and searching. In general, in twoside<br />

playback experiments with natural and altered FCSs <strong>of</strong> equal<br />

amplitude, more males responded with calling and searching<br />

behaviour than in one-side stimulation experiments. In this<br />

situation only signals with shorter than normal interval induced less<br />

response, while duration <strong>of</strong> the signal had no effect on male<br />

responsiveness. In two-side playback experiments with signals <strong>of</strong><br />

different amplitudes, more males were searching when stimulated<br />

bilaterally by natural FCS. Fewer males were calling and searching<br />

when altered FCSs were played back simultaneously. Results<br />

indicate that males’ behavioural responses decreased in line with<br />

the decrease <strong>of</strong> natural FCS amplitude. In conclusion, males are<br />

able to discriminate between natural and altered FCS when played<br />

simultaneously. Furthermore, the structural and intensity<br />

differences <strong>of</strong> the FCS are important factors which underlie the<br />

complex mate searching behaviour <strong>of</strong> N. viridula males.<br />

Phenotypic plasticity and flexibility in the crowing behaviour<br />

<strong>of</strong> a vocal non-learner species: the domestic Japanese quail<br />

(Coturnix c. japonica)<br />

Sébastien Derégnaucourt and Manfred Gahr<br />

Max Planck Institute for Ornithology, Postfach 1564, D82305<br />

Starnberg (Seewiesen), Germany<br />

Previous studies have shown that species-specific behaviours<br />

gradually emerge, via incomplete patterns, to the final complete<br />

adult form. A classical example in the acoustic domain is birdsong,<br />

a learned behaviour. In contrast to birdsong development, little is<br />

known about ontogenetic changes <strong>of</strong> the vocalizations <strong>of</strong> vocal<br />

non-learners species. This was the purpose <strong>of</strong> our study, using the<br />

crowing behaviour <strong>of</strong> the domestic Japanese quail (Coturnix c.<br />

japonica) as an example. Young males were maintained in social<br />

isolation from the age <strong>of</strong> 3 weeks to 4 months, and their complete<br />

crowing activity was continuously recorded. We observed<br />

developmental changes in crow structure, both at the temporal and<br />

at the spectral levels. Speed and trajectories <strong>of</strong> these<br />

developmental changes did exhibit an unexpected high interindividual<br />

variability. These ontogenetic changes present some<br />

similarity to that <strong>of</strong> song in songbirds, both in general<br />

developmental changes in vocalization structure and in plasticity <strong>of</strong><br />

form development. We also observed some daily changes in the<br />

temporal pattern <strong>of</strong> the crow: crows emitted at night were longer<br />

than crows emitted during the day. Such vocal changes were also<br />

observed when quails were transferred from a regular light-dark<br />

cycle to constant light: crows emitted in constant light were shorter<br />

than crows emitted in a normal light-dark cycle. These results<br />

suggest that, like in songbirds, melatonin, which is produced in<br />

darkness, might affect the temporal pattern <strong>of</strong> birds’ vocalizations.<br />

Studies on vocal non-learners could shed light on the specificity<br />

and evolution <strong>of</strong> vocal learning.<br />

- 50 -<br />

Mechanisms <strong>of</strong> avian songs and calls<br />

Ole Næsbye Larsen<br />

Institute <strong>of</strong> Biology, University <strong>of</strong> Southern Denmark, DK-5230<br />

Odense M, Denmark<br />

The avian vocal organ, the syrinx, is a specialized structure<br />

located rather inaccessibly in an air sac close to the heart where<br />

the trachea bifurcates into the two primary bronchi. The syrinx <strong>of</strong><br />

different avian taxa varies so much in position and morphology that<br />

it has been used for taxonomy. It consists <strong>of</strong> a skeletal framework,<br />

flexible membranes or s<strong>of</strong>t tissue masses, labia, stretched<br />

between elements <strong>of</strong> this framework, and the syringeal muscles.<br />

Until a decade ago most <strong>of</strong> our knowledge about syringeal<br />

mechanics was based on such indirect evidence as<br />

electromyography, emitted sound, and anatomy. The use <strong>of</strong> thin,<br />

flexible endoscopes has made direct observation <strong>of</strong> the syrinx<br />

possible in situ. The effects <strong>of</strong> direct muscle stimulation on the<br />

syringeal aperture have identified adductor and abductor muscles,<br />

confirming results from electromyographic studies. Endoscopic<br />

observations have revealed the dynamics <strong>of</strong> syringeal<br />

reconfiguration during phonation, which in most bird species<br />

investigated results in simultaneous movement <strong>of</strong> s<strong>of</strong>t tissue<br />

masses (the medial and lateral labia in songbirds and lateral<br />

tympaniform membranes in non-songbirds) into the bronchial<br />

lumen where they collide. High-speed video-filming during sound<br />

production has revealed that sound pulses coincide with short<br />

duration formation <strong>of</strong> slots between the s<strong>of</strong>t tissue masses forming<br />

a pneumatic valve, which suggests that the avian sound<br />

generating mechanism is a similar to that in the human larynx.<br />

Lately studies have revealed surprising properties <strong>of</strong> the syringeal<br />

muscles and physical models <strong>of</strong> the syrinx have given us new<br />

insight into the workings <strong>of</strong> this fascinating organ.<br />

Testosterone early treatment affects production <strong>of</strong> song<br />

learning in male zebra finches<br />

Albertine Leitão and Manfred Gahr<br />

Max Planck Institute for Ornithology, Eberhard-Gwinner-Str. 82319<br />

Seewiesen, Germany<br />

Songbirds as well as humans exhibit vocal learning. In male zebra<br />

finches the sensory and motor phases overlap. Juveniles start to<br />

sing and memorize the father’s song from 25 post-hatching days<br />

(PHD) and they have to be exposed at least ten days with the<br />

tutor’s song to be able to produce an accurate copy <strong>of</strong> the tutor,<br />

when adult ca. 90PHD. Song learning and production are<br />

controlled by a discrete neural circuit, which undergoes pr<strong>of</strong>ound<br />

developmental changes during the time when song is learned.<br />

First singing starts when synaptic connections between two song<br />

control areas, HVC and RA, are established, sometime after<br />

PHD25. To understand how testosterone influences different<br />

stages <strong>of</strong> behavioural and neural development, we implanted<br />

juvenile males at PHD16 with testosterone (T) or placebo (P)<br />

pellets. We removed the tutor at PHD25 and monitored<br />

continuously their vocalizations until adulthood. We compared<br />

song development in T and P groups with birds implanted with<br />

placebo but that were kept exposed to the tutor’s song until PHD35<br />

(C, control) and with juveniles implanted with testosterone that<br />

were raised in acoustic isolation (no tutor). We found that<br />

administration <strong>of</strong> T induces a shift in the onset <strong>of</strong> song production:<br />

birds implanted with T started to sing at 19PHD, instead <strong>of</strong> 25 for C<br />

and P groups. Moreover, while not exposed to the tutor’s song at<br />

the ‘critical’ period T birds were nonetheless able to learn the<br />

tutor’s song as C birds did. P birds produced a song similar to<br />

isolate birds. We discuss these behavioural changes with our<br />

findings in the organisation <strong>of</strong> the neural vocal system.

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