spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

First published online October 18, 2006
Journal of Experimental Biology 209, 4363-4370 (2006)
Published by The Company of Biologists 2006
doi: 10.1242/jeb.02485
This Article
Right arrow Summary Freely available
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Dangles, O.
Right arrow Articles by Casas, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Dangles, O.
Right arrow Articles by Casas, J.

Ontogeny of air-motion sensing in cricket

O. Dangles1,2, D. Pierre1, C. Magal1, F. Vannier1 and J. Casas1,*

1 Université de Tours, IRBI UMR CNRS 6035, Parc Grandmont, 37200 Tours, France
2 IRD (R072), c/o CNRS LEGS, BP1, 91198 Gif-sur-Yvette cedex, France


Figure 1
View larger version (48K):

[in a new window]
 
Fig. 1. (A) Photographs of the wood cricket (Nemobius sylvestris) showing the location of the cercal sensory system at the end of the abdomen (black arrows); Scale bar, 2 mm. (B,C) Scanning electron microscopy images illustrating the change in cercal receptors size and number throughout development in N. sylvestris: (B) first instar; Scale bar, 20 µm; (C) adult; Scale bar, 100 µm. Images are of the basal region of the left cercus. Cl, clavate hairs; Tr, trichoid hairs; Fi, filiform hairs.

 

Figure 2
View larger version (4K):

[in a new window]
 
Fig. 2. Relationship between the density of filiform hair receptors and the instar of N. sylvestris. Linear regression: y=-43.0x+469.3; r2=0.91, Spearman's P<0.001.

 

Figure 3
View larger version (30K):

[in a new window]
 
Fig. 3. Length-frequency distribution of all cercal filiform hairs inserted on the cercus throughout development in N. sylvestris (from instar I to adult; Ad). Adjustment curves represent the decomposition of the mixture distribution into Gaussian distributions. Parameter estimations and goodness-of-fit for each distribution are given in Table 1.

 

Figure 4
View larger version (17K):

[in a new window]
 
Fig. 4. Pair correlation function G(r) of the cercal filiform hair point pattern throughout development (instar I to adult; Ad) in N. sylvestris. The broken line gives the function for the null model of complete spatial randomness.

 

Figure 5
View larger version (12K):

[in a new window]
 
Fig. 5. Cercal hair canopy response to increasing air velocity as a function of signal frequency throughout development (instar I to adult; Ad) in N. sylvestris. (A) Peak air velocity 0.05 cm s-1, (B) peak air velocity 5 cm s-1.

 

Figure 6
View larger version (7K):

[in a new window]
 
Fig. 6. Characteristics of optimal performances of the cercal sensory system throughout development (instars I to adults; Ad) in N. sylvestris. (A) Canopy response at best-tuned frequency; (B) value of the best tuned frequency at v=5 cm s-1.

 





© The Company of Biologists Ltd 2006