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Members of this species are made conspicuous by their colouration, remarkable defensive body thorns and the loud mating calls of the males. Through capture, marking, and recapture, we determined singing\u2010site characteristics in two different natural habitats: an RF and a DF. Using nearest neighbour analysis, we found male distribution tends to uniformity in forest habitats, but in the RF, male distribution is more random. Males also showed preference for high singing sites and these were correlated with host plant height. Although host plants in DF were taller than those in the RF, male\u2019s perch preference was independent from the habitat; and in RF, males select lower perches. To investigate if male spacing was a function of the calling song, we manipulated two groups of males from a different population, one group deafened (tympanic membranes torn), and another control group with tympanic membranes intact. Insects were released from a single location in the two different zones of similar area. After a number of days we measured male displacement, and found that the deafened group distribution tended to aggregation, while the control group spread throughout the experimental zone with a random distribution. These results suggest that male spacing behaviour is one of the functions of the calling song. Based on a pre\u2010established phylogenetic framework of the genus <jats:italic>Panacanthus<\/jats:italic>, we discuss some implications for the evolution of the calling song of <jats:italic>P. pallicornis<\/jats:italic> in both RF and DF.<\/jats:p>","DOI":"10.1111\/j.1439-0310.2007.01428.x","type":"journal-article","created":{"date-parts":[[2007,11,20]],"date-time":"2007-11-20T17:37:09Z","timestamp":1195580229000},"page":"1158-1172","source":"Crossref","is-referenced-by-count":6,"title":["Determinants of Male Spacing Behaviour in <i>Panacanthus pallicornis<\/i> (Orthoptera: Tettigoniidae)"],"prefix":"10.1111","volume":"113","author":[{"given":"Juliana","family":"Chamorro\u2010R","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fernando","family":"Montealegre\u2010Z","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ranulfo","family":"Gonz\u00e1lez\u2010O","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2007,11,20]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.1093\/aesa\/57.6.736"},{"key":"e_1_2_6_3_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00176170"},{"key":"e_1_2_6_4_1","first-page":"227","volume-title":"Cricket Behavior and Neurobiology","author":"Bennet\u2010Clark H. 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Males of this species produce sustained pulses with a sharp low frequency peak of \u223c5 kHz and a broad band spectrum between 15 and 25 kHz. Simultaneous recordings of movement and sound indicate that the entire stridulatory file is used for sound production and there is nearly a 1:1 correspondence between the number of cycles in a song and the number of teeth on the file. There is an overall tendency for both the spacing of teeth to increase along the file and the velocity of wing closure to increase as the scraper traverses the file. There is considerable variation,however, in the evenness of tooth spacing and in the instantaneous velocity of wing closure during sound production. The production of sustained pulses appears to depend on resonance in the right tegmen, with the left tegmen acting primarily as a damping element. This resonance is not strongly coupled to the scraper and, unlike crickets, the timing of file-scraper interactions,and therefore the phasing of energy input to wing oscillations, is variable. Similarly, the quality of the sound spectrum varies over the course of a single stridulatory wing-stroke. Based on measurements of tooth spacing on the stridulatory file and cycle-by-cycle frequency of sound output, we predicted the velocity of wing movement that would provide consistent phasing of file-scraper interactions with respect to sound-radiating wing oscillations and compared this with measurements of wing velocity. Acceleration of wing velocity during stridulation results in a closer match to the velocity required for optimal phasing during a portion of the call, and this corresponds with higher amplitudes of radiated sound and the excitation of higher order modes of vibration (evident as distinct harmonic peaks in spectrograms). Our results suggest that in katydid stridulation, the movement of the scraper along the file is not regulated by an escapement mechanism as it is in crickets. Instead, katydids that produce pure-tone songs sweep their wings over a range of velocities, within which some portion matches file tooth spacing to give optimal phasing of energy input to excite a resonance in the right tegmen.<\/jats:p>","DOI":"10.1242\/jeb.01526","type":"journal-article","created":{"date-parts":[[2005,3,21]],"date-time":"2005-03-21T23:13:21Z","timestamp":1111446801000},"page":"1219-1237","source":"Crossref","is-referenced-by-count":66,"title":["The mechanics of sound production in<i>Panacanthus pallicornis<\/i>(Orthoptera: Tettigoniidae: Conocephalinae): the stridulatory motor patterns"],"prefix":"10.1242","volume":"208","author":[{"given":"Fernando","family":"Montealegre-Z","sequence":"first","affiliation":[{"name":"Department of Zoology, University of Toronto at Mississauga, 3359 Mississauga Road, Mississauga, Ontario, Canada, L5L 1C6"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andrew C.","family":"Mason","sequence":"additional","affiliation":[{"name":"Integrative Behaviour and Neuroscience Group, Department of Life Sciences,University of Toronto at Scarborough, 1265 Military Trail, Scarborough,Ontario, Canada, M1C 1A4"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"237","reference":[{"key":"2021042510465853000_REF1","doi-asserted-by":"crossref","unstructured":"Anstee, J. 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Stridulatory file teeth in crickets: taxonomic and acoustic implications(Orthoptera: Gryllidae). J. Insect Morph. 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The evolutionary origin of spines is considered as a defensive mechanism in\n                    <jats:italic>Panacanthus<\/jats:italic>\n                    ; both morphological and behavioural (i.e. acoustic) traits allow inferences about relationships. Phylogenetic analysis produced one most parsimonious cladogram eighty\u2010two steps long, with the ensemble consistency index\u2003=\u20030.84.\n                    <jats:italic>Panacanthus cuspidatus<\/jats:italic>\n                    and\n                    <jats:italic>P. pallicornis<\/jats:italic>\n                    (formerly\n                    <jats:italic>Storniza<\/jats:italic>\n                    Walker 1869,\n                    <jats:italic>Martinezia<\/jats:italic>\n                    Bolivar 1881) are properly incorporated in\n                    <jats:italic>Panacanthus<\/jats:italic>\n                    . On morphology,\n                    <jats:italic>Panacanthus<\/jats:italic>\n                    is more related to the Neotropical\n                    <jats:italic>Copiphora<\/jats:italic>\n                    and\n                    <jats:italic>Lirometopum<\/jats:italic>\n                    than to the Old World\n                    <jats:italic>Lesina<\/jats:italic>\n                    . Character analysis reveals that in\n                    <jats:italic>Panacanthus<\/jats:italic>\n                    the ancestral condition of calling song resonance (the production of musical sounds) has given rise to a more nonresonant (transient) stridulation. A correlation between the production of more complex sound waves and spinous protection of the body (especially the pronotum) is noted. Because early workers grouped\n                    <jats:italic>Panacanthus<\/jats:italic>\n                    with other spiny genera, based on pronotal morphology, we present a critique of the evolutionary and ecological implications of the development of defensive spines in this genus. This approach may be applied to other taxa using a similar protective mechanism. We advise against arrangement of the pronotal, cephalic and femoral armature as a homologous characteristic across subfamilies. Several pronotal processes and modifications evolved independently in other genera of Conocephalinae, Hetrodinae, Pseudophyllinae and Phaneropterinae. The pronotal structure of\n                    <jats:italic>Panacanthus<\/jats:italic>\n                    is unique and may be taken as a synapomorphic characteristic of all its species and as an autapomorphic feature of the genus.\n                  <\/jats:p>","DOI":"10.1111\/j.1365-3113.2004.00223.x","type":"journal-article","created":{"date-parts":[[2003,12,24]],"date-time":"2003-12-24T05:26:13Z","timestamp":1072243573000},"page":"21-57","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":41,"title":["The spiny devil katydids,\n                    <i>Panacanthus<\/i>\n                    Walker (Orthoptera: Tettigoniidae): an evolutionary study of acoustic behaviour and morphological traits"],"prefix":"10.1111","volume":"29","author":[{"given":"Fernando","family":"Montealegre\u2010Z.","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Glenn K.","family":"Morris","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2003,12,24]]},"reference":[{"key":"e_1_2_15_2_1","volume-title":"Animal Behaviour: an Evolutionary Approach","author":"Alcock J.","year":"1989"},{"key":"e_1_2_15_3_1","unstructured":"Alexander R.D.(1956)A comparative study of sound production in insects with special reference to the singing Orthoptera and Cicadidae of the Eastern United States.PhD Dissertation Ohio State University."},{"key":"e_1_2_15_4_1","doi-asserted-by":"publisher","DOI":"10.1163\/156853961X00042"},{"key":"e_1_2_15_5_1","doi-asserted-by":"crossref","first-page":"495","DOI":"10.1242\/jeb.52.3.495","article-title":"The mechanics of stridulation in bush crickets (Tettigonoidea, Orthoptera) I. 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