Givaudan-Roure Lecture - Association for Chemoreception Sciences
Givaudan-Roure Lecture - Association for Chemoreception Sciences
Givaudan-Roure Lecture - Association for Chemoreception Sciences
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53 Poster [ ] Olfaction: Animal Behavior<br />
AESTHETASCS, THE OLFACTORY SENSILLA, ARE<br />
MEDIATORS OF CHEMOSENSORY ACTIVATION OF<br />
ANTENNULAR FLICKING IN THE SPINY LOBSTER,<br />
PANULIRUS ARGUS<br />
Daniel P.C. 1 1Biology, Hofstra University, Hempstead, NY<br />
Lobster antennules bear a number of different sensilla sensitive to<br />
odorants. We have found that two antennular behaviors, grooming<br />
(Wroblewska et al., Chem. Senses 27:769-778, 2002) and flicking (Fox<br />
et al. Chem. Senses 28:555, 2003), are mediated by aesthetascs and/or<br />
asymmetric setae located in the “tuft” region of the lateral flagellum.<br />
Flicking also requires “non-tuft” setae scattered across the lateral and<br />
medial flagella. Schmidt et al. (this meeting) have found through<br />
ablation experiments that grooming is solely activated by asymmetric<br />
setae. The present study used similar techniques to determine the<br />
relative importance of aesthetascs and asymmetric setae to activation of<br />
flicking behavior. Two groups of lobsters were sham-ablated by<br />
removing a row of guard setae and then tested <strong>for</strong> antennular responses<br />
to L-glutamate (the major chemical stimulus eliciting grooming), and<br />
squid extract (concentration). This was followed by either ablation of<br />
asymmetric setae (N=8) or ablation of aesthetascs (N=6) after which the<br />
behavioral assay was repeated. Lobsters with asymmetric setae<br />
removed no longer groomed in response to glutamate but showed no<br />
reduction in flick rate to squid extract compared to their responses to<br />
the same odorants following sham ablation. In contrast, lobsters with<br />
aesthetascs removed showed no reduction in grooming to glutamate but<br />
no longer increased flick rates to squid extract. These results, along<br />
with those from the earlier study, suggest that olfactory and<br />
nonolfactory pathways are utilized in eliciting flicking behavior in<br />
which processing occurs via the olfactory lobes and the lateral<br />
antennular neuropils.<br />
54 Poster [ ] Olfaction: Animal Behavior<br />
BEHAVIORAL DISCRIMINATION OF AMINO ACIDS IN<br />
ZEBRAFISH (DANIO RERIO)<br />
Valentincic T. 1, Miklavc P. 1 1Department of Biology, University of<br />
Ljubljana, Ljubljana, Slovenia<br />
Based on the dissimilar patterns of glomerular activation during<br />
amino acid stimulation in recent calcium-imaging studies in zebrafish<br />
(Friedrich and Korsching, 1997), it is possible, but previously untested,<br />
that this species is capable of discriminating behaviorally different<br />
amino acids. As per<strong>for</strong>med in catfish, olfactory discrimination was<br />
studied by conditioning zebrafish with a food reward that was presented<br />
90 seconds after the conditioning amino acid solution was injected into<br />
the aquarium. Tests <strong>for</strong> discrimination began after ~50 conditioning<br />
sessions. Conditioned zebrafish, which associated a specific amino acid<br />
odor with a food reward, searched <strong>for</strong> food longer and more intensely<br />
(measurements of the swimming path by video-tracking or counting the<br />
turns >90 degrees during 90 seconds) than after stimulation with a nonconditioned<br />
amino acid. We used 3x10-5M L-Ala, L-Val and L-Arg,<br />
respectively, as conditioning stimuli and the following as test stimuli:<br />
Gly, L-Ala, L-Ser, L-Phe, L-Tyr, L-Trp, L-His, L-Asn, L-Val, L-Ile, L-<br />
Leu, L-Met, L-Arg, L-Lys, L-Glu, L-Asp, L-Pro and D-Ala . With the<br />
exception of the L-Val conditioning stimulus and the L-Ile test<br />
stimulus, zebrafish discriminated all the conditioning stimuli from the<br />
test stimuli. Our results clearly indicated that the amino acids that<br />
previously showed similar glomerular activity patterns (e.g. L-Val and<br />
L-Ile), were not discriminated behaviorally by zebrafish, but those in<br />
which the glomerular activation patterns were distinct were readily<br />
discriminated.<br />
Friedrich, R.W. and Korsching, S., 1997. Combinatorial and<br />
chemotopic odorant coding in the zebrafish olfactory bulb visualised by<br />
optical imaging. Neuron 18:737-752.<br />
14<br />
55 Poster [ ] Olfaction: Animal Behavior<br />
OLFACTORY COMMUNICATION: EVOLVING NEW BLENDS<br />
AND NOVEL PREFERENCES<br />
Vickers N.J. 1, Hillier K. 1, Groot A. 2, Gould F.L. 2 1Biology, University<br />
of Utah, Salt Lake City, UT; 2Entomology, North Carolina State<br />
University, Raleigh, NC<br />
Male moths are often extremely sensitive and narrowly tuned to the<br />
blend of components emitted by conspecific females. The sexual<br />
communication channel is there<strong>for</strong>e under strong stabilizing selective<br />
pressure. How then do new female blends and male preferences evolve?<br />
Two closely related moth species, Heliothis virescens and Heliothis<br />
subflexa, can be hybridized under laboratory conditions in order to<br />
study the genetic basis of behavior and olfactory characteristics that<br />
accompany species divergence. Males of these two species prefer<br />
qualitatively distinct blends that include either Z9-14:Ald (H. virescens)<br />
or Z9-16:Ald (H. subflexa). In addition, H. subflexa males require Z11-<br />
16:OH. These behavioral preferences are correlated with the specificity<br />
of olfactory receptor neurons and central interneurons arborizing within<br />
the glomeruli of the male-specific macroglomerular complex. Wind<br />
tunnel studies have shown that Z9-14:Ald/Z9-16:Ald preference<br />
segregates in a 1:1 ratio in backcross males. Preliminary genetic (QTL)<br />
analyses have revealed that this trait is associated with a single<br />
autosomal chromosome suggesting that a major gene may control this<br />
phenotype, perhaps coupled to the expression of odorant receptors.<br />
Other divergent characters in this system, such as Z11-16:OH-agonism<br />
and Z11-16:OAc-antagonism, may involve odorant receptors but also<br />
likely involve shifts in the glomerular targets of receptor axons and<br />
interpretation of olfactory in<strong>for</strong>mation by higher brain centers.<br />
Supported by NSF IBN-9905683 to NJV.<br />
56 Poster [ ] Olfaction: Animal Behavior<br />
OLFACTORY RECOGNITION IN CANINES<br />
Puchalski D. 1, Leitch A. 1, Hornung D. 1 1Biology Department, St.<br />
Lawrence University, Canton, NY<br />
The overall objective of this work was to assess the specificity of the<br />
olfactory cues that canines use when identifying humans. That is, once<br />
a dog is trained to identify the smell of a human (the target), will the<br />
dog be confused by the smell of the target´s siblings or by the smell of<br />
other people who use the target´s soap or deodorant? A 1-year-old<br />
golden retriever was trained to pick her owner´s scent out of three<br />
possible choices. After a trial had been initiated by “go” the dog would<br />
smell each of three boxes containing T-shirts impregnated with human<br />
scent. The target was randomly assigned to one of the boxes. The boxes<br />
were constructed such that the dog could not use visual cues. The dog<br />
signaled recognition of the target´s smell by a sit/stay response. The<br />
dog was trained to correctly identify the target over 90% of the time.<br />
When there was no target present the dog would repeatedly sample the<br />
three boxes and 80% of the time give no recognition signal. The dog<br />
was rewarded only <strong>for</strong> correct target responses. Probe trials consisting<br />
of the scent of the target´s siblings or of the scent of other humans who<br />
had used the soap and/or deodorant of the target were inserted into the<br />
testing sessions. There was no reward given during a probe trial. The<br />
dog gave the recognition response more often to the smell of the<br />
target´s siblings as compared to the smell of non-related humans.<br />
Likewise the dog gave the recognition response more often when nonrelated<br />
humans used either the soap or deodorant of the target. These<br />
results suggest that both genetic factors (such as HLA typing) and<br />
added smells (such as soap) may have some bearing on canine olfactory<br />
recognition of humans.