Song recognition in the grasshopper Chorthippus biguttulus is not impaired by shortening song signals: implications for neuronal encoding

1998 ◽  
Vol 183 (6) ◽  
pp. 729-735 ◽  
Author(s):  
B. Ronacher ◽  
R. Krahe
Zootaxa ◽  
2010 ◽  
Vol 2410 (1) ◽  
pp. 1 ◽  
Author(s):  
DENIZ SIRIN ◽  
OTTO VON HELVERSEN ◽  
BATTAL CIPLAK

The Chorthippus biguttulus group distributed in the west Palaearctic, while intensively examined in Europe, is poorly known in the glacial refugia such as Anatolia. This produces constraints in making accurate statements about evolution and the biogeography of the group. The C. brunneus subgroup of this lineage is examined using large amounts of morphological and song data from Anatolia (Asian Turkey) and representatives from Europe. Song and morphology in combination suggested three species to be found in Anatolia. The first is C. bornhalmi Harz which is also known from south-east Europe. The other two are new species: Chorthippus antecessor sp. n. and Chorthippus relicticus sp. n.. Morphologically, C. antecessor sp. n. is the most aberrant species of the C. brunneus subgroup, but is similar to C. bornhalmi in song. The specific song and morphology (the aberrant number of stridulatory pegs) define C. relicticus as a new species and both also indicate that it is closely related to C. brunneus and C. jacobsi. A song and morphology based phyloylogenetic assumption for C. brunneus subgroup suggests C. antecessor, C. bornhalmi and C. miramae to constitute one clade and C. brunneus, C. jacobsi and C. relicticus another. The scenario suggested for their evolution assume the following steps: (i) divergence of C. bornhalmi from a C. antecessor like ancestor, (ii) derivation of an ancestral population (which later give rise to C. brunneus + C. jacobsi + C. relicticus) from a C. bornhalmi like ancestor, and (iii) later fragmentation of this ancestral population to result in the present three species (C. brunneus + C. jacobsi + C. relicticus). All of these events seem to be correlated with the climatic cycles during Pleistocene. The conclusion is that the two new species are range-restricted, vulnerable species as is the case for many other taxa present in the Mediterranean Taurus biodiversity hotspot.


1996 ◽  
Vol 25 ◽  
pp. S203
Author(s):  
Nozomu Saito ◽  
Masao Maekawa
Keyword(s):  

2002 ◽  
Vol 64 (2) ◽  
pp. 245-250 ◽  
Author(s):  
Klaus Reinhold ◽  
Karin Reinhold ◽  
Kristina J. Jacoby

Behaviour ◽  
1994 ◽  
Vol 130 (1-2) ◽  
pp. 1-15 ◽  
Author(s):  
Bernard Lohr ◽  
Ronald Weisman ◽  
Stephen Nowicki

1995 ◽  
Vol 198 (9) ◽  
pp. 1817-1827 ◽  
Author(s):  
A Michelsen ◽  
K Rohrseitz

Physical mechanisms involved in directional hearing are investigated in two species of short-horned grasshoppers that differ in body length by a factor of 3­4. The directional cues (the effects of the direction of sound incidence on the amplitude and phase angle of the sounds at the ears) are more pronounced in the larger animal, but the scaling is not simple. At high frequencies (10­20 kHz), the sound pressures at the ears of the larger species (Schistocerca gregaria) differ sufficiently to provide a useful directionality. In contrast, at low frequencies (3­5 kHz), the ears must be acoustically coupled and work as pressure difference receivers. At 3­5 kHz, the interaural sound transmission is approximately 0.5 (that is, when a tympanum is driven by a sound pressure of unit amplitude at its outer surface, the tympanum of the opposite ear receives a sound pressure with an amplitude of 0.5 through the interaural pathway). The interaural transmission decreases with frequency, and above 10 kHz it is only 0.1­0.2. It still has a significant effect on the directionality, however, because the directional cues are large. In the smaller species (Chorthippus biguttulus), the interaural sound transmission is also around 0.5 at 5 kHz, but the directionality is poor. The reason for this is not the modest directional cues, but rather the fact that the transmitted sound is not sufficiently delayed for the ear to exploit the directional cues. Above 7 kHz, the transmission increases to approximately 0.8 and the transmission delay increases; this allows the ear to become more directional, despite the still modest directional cues.


1999 ◽  
Vol 202 (2) ◽  
pp. 121-133 ◽  
Author(s):  
J. Schul ◽  
M. Holderied ◽  
D.V. Helversen ◽  
O.V. Helversen

A recently proposed biophysical model for directional hearing in grasshoppers was tested using complex stimulus situations, with two loudspeakers, one on either side of the animal, synchronously emitting sinusoids with defined phase and amplitude relationships. Hearing responses were determined from whole nerve recordings and compared with the predictions of the model. In Schistocerca gregaria, there were only minor differences between the predictions of the model and measurements and, by reducing the value of the gain of the internal sound path measured previously, a close agreement was achieved between model and measured hearing responses. In Chorthippus biguttulus, larger discrepancies between model calculations using the values measured previously and neuronal response functions were found in both shape and amplitude. A better fit between measurements and model predictions was achieved by increasing the values of the internal delay over those measured previously. The measurements presented here indicate high inter-individual variability of the parameters of the internal pathway, with a range of 60 degrees for the internal phase delay. Calculating the directional characteristics using this range of values for the internal delay indicated that sufficient directional information was available down to 5 kHz. Increasing the value of the internal delay over that measured in an earlier study therefore provides an explanation for the discrepancy between the poor directional information attributed to C. biguttulus in that study and the excellent lateralization ability of males of this species at 5 kHz.


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