Substrate vibrations mediate behavioral responses via femoral chordotonal organs in a cerambycid beetle
© The Author(s). 2016
Received: 31 May 2016
Accepted: 10 August 2016
Published: 26 August 2016
Vibrational senses are vital for plant-dwelling animals because vibrations transmitted through plants allow them to detect approaching predators or conspecifics. Little is known, however, about how coleopteran insects detect vibrations.
We investigated vibrational responses of the Japanese pine sawyer beetle, Monochamus alternatus, and its putative sense organs. This beetle showed startle responses, stridulation, freezing, and walking in response to vibrations below 1 kHz, indicating that they are able to detect low-frequency vibrations. For the first time in a coleopteran species, we have identified the sense organ involved in the freezing behavior. The femoral chordotonal organ (FCO), located in the mid-femur, contained 60–70 sensory neurons and was distally attached to the proximal tibia via a cuticular apodeme. Beetles with operated FCOs did not freeze in response to low-frequency vibrations during walking, whereas intact beetles did. These results indicate that the FCO is responsible for detecting low-frequency vibrations and mediating the behavioral responses. We discuss the behavioral significance of vibrational responses and physiological functions of FCOs in M. alternatus.
Our findings revealed that substrate vibrations mediate behavioral responses via femoral chordotonal organs in M. alternatus.
KeywordsBehavior Vibration Sense organ Coleoptera
Many animals are sensitive to substrate-borne vibrations. Vibration detection is an important sense that is used for intra- and interspecific interactions in diverse animal taxa [1, 2]. Specifically, vibrations transmitted through plants propagate well, allowing plant-dwelling animals to detect approaching conspecifics or predators without relying on other signals [3, 4]. Insects exhibit a range of behaviors in response to vibrations [1, 2]. A ‘startle response’ is a fast jerky movement with short latency elicited by vibrations; it is considered to be a preparatory behavior that enables locomotion to follow in a smooth behavioral sequence [5–7]. Vibrations may also elicit abrupt cessation of ongoing movements, such as freezing behavior or thanatosis (long-lasting freezing) [6–12]. The functional significance of vibration detection can be classified into: i) predator–prey interactions, including prey localization and antipredatory behavior, and ii) social interactions, including sexual signals, aggressive signals, and heterospecific signals [1, 2, 4, 13–17].
Although a number of studies have shown that coleopteran insects detect vibrations, and that they exhibit behavioral responses [11–16], the sense organs mediating such responses are largely unknown. An electrophysiological study showed that unidentified sensory neurons originating from the tibia and tarsus responded to low-frequency vibrations in Scarabaeidae, Carabidae, and Silphidae . Studies of orthopteran insects showed that the primary organs sensitive to vibrations are internal mechanoreceptors, called ‘chordotonal organs’, located in the legs and other body appendages; these organs are also known to participate in the motor control of joints [8, 19–23].
The Japanese pine sawyer beetle, Monochamus alternatus (Coleoptera: Cerambycidae), is the vector of the pine wood nematode, which kills pine trees . In this study, we investigated the behavioral responses of M. alternatus to vibrations and identified a chordotonal organ in the leg that detects vibrations transmitted through the tree.
Dead pine trees, Pinus thunbergii and Pinus densiflora, infested with larvae of Monochamus alternatus were collected at the Forestry and Forest Products Research Institute and its Chiyoda Experimental Station in Ibaraki Prefecture, Japan in February to March during the 2006–2013 period, and were kept within a screen-caged house in natural conditions. In June through July, adults emerging from the dead pine logs were collected and kept separately in plastic cups (ca. 10 cm diam., 6 cm high) at 25 °C and 50–60 % relative humidity with a 16:8-h L:D cycle. A few twigs (ca. 10 cm long) of P. thunbergii and P. densiflora were provided as diet and replaced every 3–7 days. Male and female mature adults (>2 weeks old) were used. All behavioral experiments were performed at room temperature (23–26 °C) during the light-on period.
Vibration stimuli and behavioral responses
Pulsed sine waves of 100 ms duration ranging from 25 Hz to 10 kHz were shaped by commercial software (0105; NF Corp., Yokohama, Japan). The duration included 5 ms rise and 5 ms fall times, irrespective of frequency. The vibration stimuli, continuously looped back by a function generator (WF1945; NF Corp.) at intervals of 900 ms, were applied to a beetle via a vibration exciter (type 4809; Brüel & Kjær, Nærum, Denmark) connected to a type 2718 power amplifier. Frequencies (Hz) and amplitudes (zero-to-peak accelerations, m/s2) of vibrations were measured by attaching a piezoelectric charge accelerometer (type 4371 or 4393; Brüel & Kjær) to the center of the steel plate on which the beetle was placed. The signals were amplified by a type 2692 conditioning amplifier and displayed on an oscilloscope (DS-8822P; Iwatsu Test Instruments Corp., Tokyo, Japan).
Behavioral responses of M. alternatus to vibration stimuli were observed under various conditions (Experiments 1–3), as follows.
Instead of the steel plate of Experiment 1, a rod of naturally dried pine trunk (3 cm diam., 30 cm long) attached to the vibration exciter with a screw (5 mm diam., 13 mm long) was hung from the ceiling of a soundproof box (90 × 90 × 70 cm) with a thick rope (Fig. 1b). The pine rod was tilted at ca. 70 ° from the horizontal. A beetle was gently transferred to the edge of the rod. Continuous waves of 100 Hz were applied to the beetle via the rod after it was allowed to rest or walk. Freezing responses during walking (i.e., cessation of walking), or initiation of walking from a stationary position were observed in intact beetles. Prior to the behavioral tests, vibration amplitudes as accelerations on the surface of the rod at 15 cm from the exciter were determined to be 0.03 m/s2. The numbers of freezing or walking behaviors in the presence of vibrations were compared with those in the absence of vibrations (control) using Fisher’s exact probability test.
A naturally dried pine rod was attached vertically to the vibration exciter, which was placed on the desktop vibration isolator (Fig. 1c). Freezing responses during walking were observed in beetles with operated femoral chordotonal organs (FCOs), in sham-operated beetles (with femoral integument damaged with microscissors), and in intact beetles. The conditions used in this experiment were more suitable for observing the response than those in Experiment 2, because it allowed the beetles to walk up and down the rod. The FCO- and sham-operated beetles were allowed to recover for at least 1 day. As described in Experiment 1, the amplitude of stimuli at a set frequency was gradually raised from 0.01 to 7 m/s2 until a freezing response appeared. From an intact beetle, the threshold of the freezing response was determined as described in Experiment 1. After each behavioral test on intact beetles, the acceleration on the surface of the rod at 15 cm from the exciter was measured. Differences in the response at the same frequency were determined by Fisher’s exact probability test and Ryan’s multiple comparison test. The thresholds among different frequencies were tested by the Kruskal-Wallis test.
Although the exciter generated airborne sounds at frequencies above 500 Hz, the beetles did not exhibit any behavioral responses to sounds with similar frequencies and amplitudes broadcast from a speaker.
The FCOs and other chordotonal organs were stained by backfills from the main leg nerve (n = 12). The beetle was briefly anesthetized with carbon dioxide and then fixed ventral-side-up on a beeswax plate using insect pins. To stain peripheral nerves in the leg, the main leg nerve was cut at the terminus of the thoracic ganglion and its peripheral cut end placed into the tip of a tapered glass capillary tube filled with a 1 % micro-Ruby solution (MW = 3000; Invitrogen, Carlsbad, CA, USA). After fixation in 4 % paraformaldehyde solution for 6 h, specimens were dehydrated through an ethanol series, cleared in methyl salicylate, and viewed under a confocal microscope (LSM510; Zeiss, Jena, Germany). The stained chordotonal organs are shown in a false color (green). Optical sections (1.2 μm thick) were reconstructed two-dimensionally using commercial software (Amira ver. 3.1; FEI Visualization Sciences Group, Burlington, VT, USA) linked to the LSM510.
For FCO surgery, cell clusters (scoloparia) attached to the apodemes of all six femora of anesthetized beetles were carefully removed with microscissors immediately after opening a flap of the overlaying cuticle. The flaps were replaced to minimize damage to the surrounding muscles and tracheae. FCO-operated beetles were capable of walking although they exhibited deficits in the righting response (after turning them onto their backs) , which was slower than in intact beetles (6.8 s and 1.2 s, respectively; means of three measurements on two operated and two intact beetles) (Additional file 1: Video S1).
Monochamus alternatus showed startle responses and stridulation from a standstill, when subjected to a broad range of vibrations below 1 kHz. In addition, the beetles froze or walked in response to vibrations at 100 Hz. Beetles with operated FCOs did not show freezing behavior, suggesting that the FCOs detect low-frequency vibrations and mediate this behavior. This finding is in accordance with a report that the cricket Gryllus bimaculatus with all FCOs operated tended not to exhibit long-lasting freezing behavior . Freezing behavior mediated by excitation of sensory neurons in FCOs seems widespread across insects.
Monochamus alternatus showed different thresholds for the behavioral responses. Low-frequency vibrations of amplitudes 3.5–23.5 m/s2 induced the startle response and stridulation, whereas lower amplitudes of 0.3–0.4 m/s2 induced the freezing response. Similar differences in the stimuli needed to trigger the startle and freezing responses have been reported in P. fortunei . Although the threshold was unclear, walking from a standstill was evoked by continuous vibrations with a low amplitude at 0.03 m/s2 in M. alternatus. Repeated exposures to vibrations above the threshold allow M. alternatus to walk, after initially showing the startle response.
What is the behavioral significance of the vibrational responses in M. alternatus? Some of the responses may be associated with anti-predator behavior. Approaching predators (e.g., birds ) cause low-frequency vibrations through a tree, which may elicit the startle and freezing responses mediated by the FCO of M. alternatus. For example, the cerambycid beetle Hylotrupes bajulus  and other insects [5, 9, 11] exhibit these responses, presumably as a defense against predators. Freezing and motionless insects are capable of hiding without emitting vibrational and/or other cues to predators [10, 11]. In addition, M. alternatus stridulates in response to vibrations. In cerambycids and other beetles, stridulation is regarded as a defensive, disturbance, or warning signal to potential predators [25, 29]. Startle and freezing responses may also serve for conspecific recognition in M. alternatus. Detection of approaching conspecifics by their vibrations could allow insects to prepare for subsequent behaviors, e.g., escaping or mating . P. fortunei are able to detect vibrations from conspecifics landing and walking on the host leaf . In addition to vibrations, contact sex pheromones and visual cues play important roles in conspecific recognition in cerambycids [31, 32]. Hence, vibrations may play an important role in both inter- and intraspecific interactions in concert with other sensory cues.
We identified for the first time the femoral chordotonal organ of a coleopteran species as a sensory organ detecting vibrations. In the absence of any specialized vibration detectors such as subgenual organs, the FCO, the largest leg chordotonal organ in M. alternatus, is suggested to play a pivotal role in the detection of low-frequency vibrations below 1 kHz. The FCO of M. alternatus possesses only a single scoloparium, which morphologically resembles the distal scoloparium in a locust [19, 20]. Considering that the distal scoloparia are sensitive to tibial movements and mediate reflexes in the leg muscles of a locust  and a stick insect , the FCOs of M. alternatus are likely to be bifunctional sensory organs that detect: i) small, fast small movements, e.g., accelerations through the tibia; and ii) large, slow movements, e.g., displacements of tibia. In fact, M. alternatus with operated FCOs took more time to right themselves (after turning them onto their backs) (Additional file 1: Video S1), an action that requires coordination of leg muscles. Possibly, pairs of neurons within a sensillum of the M. alternatus FCO have different physiological properties, as reported in the paired neurons of the antennal chordotonal organ in a cockroach . Furthermore, the shorter apodeme of the metathoracic FCOs compared with the pro- and mesothoracic FCOs might be related to physiological properties (e.g., vibration detection, proprioception) in M. alternatus. Further studies are needed to determine the relationships between function and structure in M. alternatus FCOs.
Our findings revealed that a cerambycid beetle showed behavioral responses, such as startle and freezing, when subjected to vibrations. For the first time, the internal mechanoreceptors, ‘chordotonal organs’, responsible detecting vibrations in a coleopteran species was identified. Micro-ablation of the femoral chordotonal organs in all legs completely abolished vibration-mediated freezing behavior. Freezing behavior may be associated with defense against predators.
Femoral chordotonal organ
Standard error of mean
We thank M. Jinkawa and Y. Suzuki (Forestry and Forest Products Research Institute) for the loan of the instruments. This work was supported in part by the Ministry of Education, Culture, Sports, Science and Technology KAKENHI Grant Nos. 80332477 (TT, HN), 24580075 (MF, TT), and 15 K07327 (MF), Council for Science, Technology and Innovation, Cross-ministerial Strategic Innovation Promotion Program (TT), and the FFPRI Encouragement Model in Support of Researchers with Family Responsibilities (TT).
This work was partly supported by Ministry of Education, Culture, Sports, Science and Technology KAKENHI Grant Nos. 80332477 (TT, HN), 24580075 (MF, TT), and 15 K07327 (MF), Council for Science, Technology and Innovation, Cross-ministerial Strategic Innovation Promotion Program (TT), and the FFPRI Encouragement Model in Support of Researchers with Family Responsibilities (TT). The funders had no role in the design of the study and collection, analysis, or interpretation of data, or in the writing of the manuscript.
Availability of data and materials
The datasets supporting the conclusions of this article are included within the article and its additional file.
TT, NS, and HN designed the study. All authors wrote the manuscript. TT and MF carried out the behavioral experiments; HN carried out anatomical experiments; TT and KN collected and reared insects. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
Laboratory-maintained insects were used in all experiments. Ethical approval and consent to participate were not required for this work.
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- Hill PSM. Vibrational Communication in Animals. Cambridge: Harvard University Press; 2008.Google Scholar
- Cocroft RB, Rodríguez RL. The behavioral ecology of insect vibrational communication. Bioscience. 2005;55:323–34.View ArticleGoogle Scholar
- Michelsen A, Fink F, Gogala M, Traue D. Plants as transmission channels for insect vibrational songs. Behav Ecol Sociobiol. 1982;11:269–81.View ArticleGoogle Scholar
- McVean A, Field LH. Communication by substratum vibration in the New Zealand tree weta, Hemideina femorata (Stenopelmatidae: Orthoptera). J Zool. 1996;239:101–22.View ArticleGoogle Scholar
- Friedel T. The vibrational startle response of the desert locust Schistocerca gregaria. J Exp Biol. 1999;202:2151–9.PubMedGoogle Scholar
- Bullock TH. Comparative neuroethology of startle, rapid escape and giant fiber-mediated responses. In: Eaton RC, editor. Neural mechanisms of startle behaviour. New York: Plenum Press; 1984. p. 1–13.View ArticleGoogle Scholar
- Tsubaki R, Hosoda N, Kitajima H, Takanashi T. Substrate-borne vibrations induce behavioral responses of a leaf-dwelling cerambycid Paraglenea fortune. Zool Sci. 2014;31:789–94.View ArticlePubMedGoogle Scholar
- Nishino H, Sakai M. Behaviorally significant immobile state so called of thanatosis in the cricket Gryllus bimaculatus DeGeer: its characterization, sensory mechanism and function. J Comp Physiol A. 1996;179:613–24.View ArticleGoogle Scholar
- Rohrseitz K, Kilpinen O. Vibration transmission characteristics of the legs of freely standing honeybees. Zoology. 1997;100:80–4.Google Scholar
- Miyatake T, Katayama K, Takeda Y, Nakashima A, Sugita A, Mizumoto M. Is death-feigning adaptive? Heritable variation in fitness difference of death-feigning behaviour. Proc R Soc Lond B. 2004;271:2293–6.View ArticleGoogle Scholar
- Kojima W, Ishikawa Y, Takanashi T. Deceptive vibratory communication: pupae of a beetle exploit the freeze response of larvae to protect themselves. Biol Lett. 2012;8:717–20.View ArticlePubMedPubMed CentralGoogle Scholar
- Acheampong S, Mitchell BK. Quiescence in the Colorado potato beetle, Leptinotarsa decemlineta. Entomol Exp Appl. 1997;82:83–9.View ArticleGoogle Scholar
- Hanrahan SA, Kirchener WH. Acoustic orientation and communication in Desert tenebrionid beetles in sand dunes. Ethology. 1994;97:26–32.View ArticleGoogle Scholar
- Goulson D, Birch MC, Wyatt TD. Mate location in the deathwatch beetle, Xestobium rufovillosum De Geer (Anobiidae): orientation to substrate vibrations. Anim Behav. 1993;47:899–907.View ArticleGoogle Scholar
- Kojima W, Takanashi T, Ishikawa Y. Vibratory communication in the soil: pupal signals deter larval intrusion in a group-living beetle Trypoxylus dichotoma. Behav Ecol Sociobiol. 2012;66:171–9.View ArticleGoogle Scholar
- Breidbach O. Studies on the stridulation of Hylotrupes bajulus (L.) (Cerambycidae, Coleoptera): communication through support vibration- morphology and mechanics of the signal. Behav Processes. 1986;12:169–86.View ArticlePubMedGoogle Scholar
- Travassos MA, Pierce NE. Acoustics, context and function of vibrational signalling in a lycaenid butterfly-ant mutualism. Anim Behav. 2000;60:13–26.View ArticlePubMedGoogle Scholar
- Schneider W. Über den Erschütterungssinn von Käfern und Fliegen. Z vergl Physiol. 1950;32:287–302.View ArticleGoogle Scholar
- Field LH, Pflüger HJ. The femoral chordotonal organ: a bifunctional orthopteran (Locusta migratoria) sense organ? Comp Biochem Physiol. 1989;93A:729–43.View ArticleGoogle Scholar
- Field LH, Matheson T. Chordotonal organs in insects. Adv Insect Physiol. 1998;27:1–228.View ArticleGoogle Scholar
- Field LH, Burrows M. Reflex effects of the femoral chordotonal organ upon leg motor neurones of the locust. J Exp Biol. 1982;101:265–85.Google Scholar
- Stein W, Sauer E. Physiology of vibration-sensitive afferents in the femoral chordotonal organ of the stick insect. J Comp Physiol A. 1999;184:253–63.View ArticleGoogle Scholar
- Nishino H, Sakai M, Field LH. Two antagonistic functions of neural groups of the femoral chordotonal organ underlie thanatosis in the cricket Gryllus bimaculatus DeGeer. J Comp Physiol A. 1999;185:143–55.View ArticleGoogle Scholar
- Kobayashi F, Yamane A, Ikeda T. The Japanese pine sawyer beetle as the vector of pine wilt disease. Ann Rev Entomol. 1984;29:115–35.View ArticleGoogle Scholar
- Alexander RD, Moore TE, Woodruff RE. The evolutionary differentiation of stridulatory signals in beetles (Insecta: Coleoptera). Anim Behav. 1963;11:111–2.View ArticleGoogle Scholar
- Frantsevich L. Righting kinematics in beetles (Insecta: Coleoptera). Arthropod Struct Dev. 2004;33:221–35.View ArticlePubMedGoogle Scholar
- Nishino H, Mukai H, Takanashi T. Chordotonal organs in hemipteran insects: unique peripheral structures but conserved central organization revealed by comparative neuroanatomy. Cell Tiss Res. (in press).
- Inoue M. Predation of the Japanese pine sawyer (Monochamus alternatus) by wild birds. Bull Tottori Pre For Exp Stn. 1987;30:47–71 (in Japanese).Google Scholar
- Masters WM. Insect disturbance stridulation: characterization of airborne and vibrational components of the sound. J Comp Physiol A. 1980;135:259–68.View ArticleGoogle Scholar
- Fauziah BA, Hidaka T, Tabata K. The reproductive behaviour of Monochamus alternatus Hope. Appl Entomol Zool. 1987;22:272–85.Google Scholar
- Allison JD, Borden JH, Seybold SJ. A review of the chemical ecology of the Cerambycidae (Coleoptera). Chemoecology. 2004;14:123–50.View ArticleGoogle Scholar
- Fukaya M, Akino T, Yasuda T, Yasui H, Wakamura S. Visual and olfactory cues for mate orientation behaviour in male white-spotted longicorn beetle, Anoplophora malasiaca. Entomol Exp Appl. 2004;111:111–5.View ArticleGoogle Scholar
- Ikeda S, Toh Y, Okamura J, Okada J. Intracellular responses of antennal chordotonal sensilla of the American cockroach. Zool Sci. 2004;21:375–83.View ArticlePubMedGoogle Scholar