CONTENT - International Society of Zoological Sciences
CONTENT - International Society of Zoological Sciences
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.