Browse Subject Areas

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Tremulatory and Abdomen Vibration Signals Enable Communication through Air in the Stink Bug Euschistus heros

Tremulatory and Abdomen Vibration Signals Enable Communication through Air in the Stink Bug Euschistus heros

  • Andreja Kavčič, 
  • Andrej Čokl, 
  • Raúl A. Laumann, 
  • Maria Carolina Blassioli-Moraes, 
  • Miguel Borges


Communication by substrate-borne mechanical signals is widespread among animals but remains one of their least understood communication channels. Past studies of vibrational communication in insects have been oriented predominantly to communication during mating, showing that species- and sex-specific vibrational signals enable recognition and localization of potential mates on continuous solid substrates. No special attention has been paid to vibrational signals with less obvious specificity as well as to the possibility of vibrational communication across substrates that are not in physical contact. We aimed to reinvestigate emission of the aforementioned vibrational signals transmitted through a plant in the stink bug Euschistus heros (Pentatomidae: Pentatominae) and to check whether individuals are able to communicate across adjecent, physically separated substrates. We used laser vibrometry for registration of substrate-borne vibrational signals on a bean plant. Using two bean plants separated for 3 to 7 cm between two most adjacent leaves, we investigated the possibility of transmission of these signals through air. Our study showed that males and females of E. heros communicate using tremulatory, percussion and buzzing signals in addition to the previously described signals produced by vibrations of the abdomen. Contrary to the latter, the first three signal types did not differ between sexes or between pentatomid species. Experiments with two physically separated plants showed significant searching behaviour and localization of vibrational signals of an E. heros male or a female, in response to abdominal vibration produced signals of a pair duetting on the neighbouring plant, in comparison to control where no animals were on the neighbouring plant. We also confirmed that transmission through air causes amplitude and frequency decay of vibrational signals, which suggests high-amplitude, low-frequency tremulatory signals of these stink bugs their most plausible way of communication across discontinuous substrates.


Substrate-borne sound communication is the most widely used insect way of information exchange with mechanical signals [1], [2]. Although their small body size prevents efficient emission of low frequency airborne sound [3], [4] Eriksson and co-authors [5] recently demonstrated airborne inter-plant communication with low frequency signals in the less than 5 mm body sized leafhopper Scaphoideus titanus Ball (Hemiptera: Cicadellidae). Despite of high attenuation during transmission through air, females standing on a leaf replied steadily to male calls emitted from another leaf separated by 6 cm air gap.

Nezara viridula L. (Hemiptera: Pentatomidae) and many other plant-dwelling species of the stink bug subfamily Pentatominae emit species-specific male pheromones with long range action [6], [7], [8] to attract mates on common places on plants. Once animals are closer together and on the same substrate, medium and short range signalling cues become prominent, namely substrate-borne vibrational signals, visual and tactile signals. Use of airborne component of substrate-borne vibrational signals could represent a potentially important suplementary mechanism for information exchange in mating behaviour [9], [10], [11] when use of other communications mechanisms is impossible or inefficient. This new communication channel could represent a shortcut not only for substrate-borne vibrational signals to reach the intended receiver, but also for the receiver to find the emitter of vibrational signals. What is more, airborne component of substrate-borne vibrational signals could enable communication between animals on substrates that are not in physical contact and communication by chemical, vibrational and visual signals is impossible or inefficient. The possibility for airborne sound communication remained completely ignored in Pentatomidae and other plant-dwelling Heteroptera, and the role of group characteristic vibrational signal frequency and velocity for efficient transmission through air has not been studied yet. Leafhoppers [5] and pentatominae stink bugs [12], [13] produce vibrational signals of similar velocity at the source but of different frequency characteristics: compared to leafhoppers’ vibrational signals, which contain also high frequency components (author’s personal communication), all until now investigated pentatominae stink bugs produce signals of lower frequencies tuned with the mechanical properties of plants [14], [15]. A broader repertoire of vibration producing mechanisms has been described in predatory stink bugs of the pentatomid subfamily Asopinae that emit high amplitude tremulatory signals [16], [17], [18], which have been ignored until now in Pentatominae. The role of different time parameters of pentatominae abdomen produced signals for mate recognition and location in the field is well understood [19][23] but communication distance with substrate- and/or airborne high amplitude and species less specific signals may be significantly increased.

The aim of the present study was to get answers to the following questions. (A) Do stink bugs of the subfamily Pentatominae produce vibrational signals also with mechanisms other than abdomen vibration? (B) If so, what are characteristics of such signals and in what behavioural context are they emitted? (C) Can pentatominae stink bugs communicate with airborne component of narrow-band low frequency signals produced by different mechanisms? (D) If so, what is the velocity and frequency relation between naturally emitted signals recorded simultaneously from plants of which parts are not in a contact. To get the answers to these questions we investigated in natural conditions, insects placed on bean plants, different aspects of vibrational communication in the stink bug species Euschistus heros whose abdomen vibration produced signals have been first described by Blassioli-Moraes and co-workers [24] from vibrations recorded on a non-resonant substrate.


E. heros males and females emitted in our experimental conditions species-specific vibrational signals produced by abdomen vibration as described by Blassioli-Moraes and co-authors [24]. On the plant we recorded as first among Pentatominae also signals produced by tremulation (vigorous vibration of the whole body), percussion (tapping with forelegs on the ground) and buzzing (vibration of lifted wings) (Figures 1, 2; Table 1).

Figure 1. Spectral characteristics of tremulatory, buzzing, percussion and abdomen vibration produced signals.

(Above) Vibrational signals produced by tremulation (TR), buzzing (BZ), percussion (PER) and by vibrating the abdomen (AV) on the leaf and recorded on the stem 14–16 cm from the source. Sequence shown is 1 minute long. (Below) Frequency spectra of single tremulatory, buzzing and abdomen vibration produced pulses, and of a 10 s sequence of percussion signals.

Figure 2. Oscillograms of tremulatory, percussion and buzzing signals.

Signals were emitted by E. heros on the leaf of a bean plant and recorded on the stem 14–16 cm from the source.

Table 1. Parameters of vibrational signals produced by mechanisms other than abdomen vibration.

Characteristics of Tremulatory, Percussion and Buzzing Signals

Males and females produced tremulatory signals (Figures 1, 2; Table 1) vigorously shaking the body with legs firmly standing on the plant substrate. Pulses were produced with irregular repetition rate. Frequency spectrum shows a broad peak below 200 Hz and another peak around 260 Hz at 30 dB lower amplitude (Figure 1, TR). Tremulatory signals recorded on the plant stem have a characteristic high frequency onset with a tail of prolonged low frequency vibration (Figure 2) and have been recorded on a plant in the calling phase of mating behaviour. A searching mate emitted these signals in the absence or presence of vibrational signals produced by signalling bugs on the neighbouring plant. We did not record this type of signals when bugs touched each other or refused to copulate as typical for investigated predatory bugs [16].

Percussion signals (Figures 1, 2) also were emitted by males and females, and were recorded during searching phase of a single insect on the plant or together with the exchange of male and female signals produced by abdomen vibration. Percussion signals were emitted as sequences of regularly repeated pulses as a response to other vibrational signals produced by the mate or were emitted as independent sequences. Percussion pulse duration was statistically significantly different when signals were emitted as a response to other vibrational signals compared to when they were emitted as independent sequences. Statistical differences between signals emitted as a response to other vibrational signals and those emitted in independent sequences were also recorded for signal velocity (Table 1). Frequency spectrum of percussion signals (Figure 1, PER) shows similar general characteristics as the one of tremulatory signals: a broad peak below 200 Hz and a peak of lower amplitude around 260 Hz.

In two males we observed vigorous vibration of lifted wings that produced high amplitude plant vibrations (Figures 1, 2; Table 1). Buzzing signals were repeated randomly with repetition time between 5 and 12 s. Their spectra show basic characteristics of abdomen vibration signals. Buzzing signals are characterized by narrow dominant frequency peak at 117.1±10.3 Hz (n = 11, N = 2) and regularly repeated higher harmonic peaks up to 1000 Hz with peak amplitude not falling more than 60 dB below that of the dominant frequency (Figure 1, BZ). The behavioural context of buzzing signal production is not clear and shows no connection to vibrational emissions of other bugs.

Airborne Inter-plant Communication

A single male or female placed on a plant exhibited different activities when the plant was not vibrated (control) or when vibrated with signals emitted naturally on a neighbouring plant in contact or non-contact conditions (Table 2). In control conditions no searching and/or directional movement to the closest leaf of the neighbouring plant could be observed. Moreover, significantly (Fisher’s exact test for count data, p<0.05) less bugs stayed on the plant until the end of the test and lower number of tremulatory signals was emitted. On the other hand, normal communication between individuals on different plants with signals produced by abdomen vibration, tremulation and percussion (Figure 3) was recorded on a plant when in contact with another plant on which E. heros couples were singing: single males and females searched the source of vibration and moved directionally to the leaf in contact with neighbouring plant eventually moving on it over leaves in contact with their tips.

Figure 3. Vibrational responses to abdominal vibration produced signals on a neighbouring plant.

Tremulatory (A), percussion (B) and abdomen vibration produced signals (C and D) emitted by a male as a response to abdomen vibrational signals (asterisks) produced on a neighbouring plant. Plants were in contact with the tips of the two closest leaves (A, B and C) or were separated by a 3–7 cm wide gap of air (D).

Table 2. Comparison of animal activity on a non-vibrated and on a vibrated plant.

When plants were separated by 3 to 7 cm air gap significantly (Fisher’s exact test for count data, p<0.05) less bugs left the plant before the end of the test and higher percent of them searched and reached the point on the leaf that was closest to the leaf of the neighbouring plant. The number of tremulatory signals emitted per minute was 10.5±7.7 (n = 34, N = 4), which was higher compared to 4.4±1.9 (n = 16, N = 2) tremulatory signals emitted per minute in control conditions, where there were no animals on the neighbouring plant. The main difference observed between conditions when plants were in contact and conditions with no mechanical contact, was in the type of the song emitted: in non-contact conditions (and in control) single males or females produced mainly tremulatory signals while in contact conditions they predominantly emitted signals produced by abdomen vibration.

Frequency spectra of naturally emitted E. heros vibrational signals differ when recorded simultaneously on two plants separated by an air gap of approximately 3 or 6 cm (Figure 4). Transmission over the air from one to another plant shows low-pass filtering with increasing cut-off of frequencies above 300 Hz with increasing distance between both plants. The velocity difference between simultaneously recorded signals on two plants separated by an air gap of approximately 3 cm varied in three bugs between 22.5±7.8 (n = 11) and 29.3±5.6 (n = 11) dB for abdomen vibration produced signals and between 24.7±6.7 (n = 7) and 32.2±5.7 (n = 11) dB for tremulatory signals emitted naturally. At approximately 6 cm air distance the velocity difference was measured only for one animal. For simultaneously recorded signals it was 26.6±7.6 (n = 11) dB for abdomen vibrations and 34.3±2.6 (n = 11) dB for tremulatory signals.

Figure 4. Spectral characteristics of vibrational signals before and after transmission through air.

Frequency spectra (A) (one pulse), sonograms (B) (10 s sequence) and oscillograms (C) (10 s sequence) of abdomen vibration produced signals, recorded simultaneously from the plant where insects were singing (lower traces) and from the neighbouring plant (upper traces). The two plants were separated by an approximately 3 (left) or 6 (right) cm air gap.


This study first demonstrated that stink bugs of the subfamily Pentatominae emit vibrational signals produced by tremulation, percussion and buzzing in addition to the previously described abdominal vibrational signals [24]. The emission of high amplitude tremulatory and buzzing signals with low species specificity is an advantage in long range inter-plant communication, but on the other hand increases the risk of erroneous decisions in mate recognition and of attracting predators.

The role of tremulatory signals has been described in the Neotropical katydid Docidocercus gigliotosi Griffini (Orthoptera: Tettigoniidae) in a cost-benefit analysis of public and private communication [25], and in meadow katydids during courtship as an important parameter for female preference for large male vibrations [26]. Tremulatory signals have been first described in Pentatomidae in the predatory stink bug species Podisus maculiventris [16] and Picromerus bidens [18]. Males produced sequences of regularly repeated pulse trains composed of a tremulatory signal followed by an abdominal vibration produced pulse [16]. Tremulatory signals were recorded on a loudspeaker in male and female P. bidens when touching each other, when repelling a mate trying to copulate and as a response to female song signals [18].

Results of the present study on the pentatominae stink bug E. heros on a plant indicate that tremulatory signals have an important function in the calling phase of mating behaviour. A combination of long range oriented tremulatory signal with the shorter range species-specific signal produced by abdomen vibration has not been previously observed. Percussion signals have been recorded in P. maculiventris in connection with abdominal vibrations in the pause between pulses or as longer sequences following them [16]. We have recorded tremulatory signals in E. heros males and females either when they were alone or singing in a duet on a plant, as well as when responding to airborne signals. The role of E. heros’ percussion and buzzing signals in communication needs further behavioural studies.

Results of the present study showed inter-plant communication with airborne vibrational signals in the stink bug E. heros and opened a new modality of information exchange in Heteroptera plant-dwelling insects on the same and on different plants. Two sensory systems are able to detect airborne signals involved in E. heros communication. The first includes leg vibrational receptors detecting vibrations of the plant substrate that were induced by airborne component of substrate-borne signals emitted on another plant. Simultaneous recording of naturally emitted E. heros vibrations on one plant and vibrations induced by its airborne component on the other shows 20–40 dB velocity decay at the air gap of 3 to 7 cm. Velocity values of plant recorded E. heros signals range between 1 and 10 mm/s for tremulatory and buzzing signals, between 0.1 and 1 mm/s for abdomen vibration signals and between 0.01 and 0.1 mm/s for percussion signals. At velocity decay of vibrational signals transmitted from one plant to the other through an air gap, as measured in our experimental conditions, we can expect that only values of percussion signals fall below the threshold of the low and high frequency leg vibrational receptor organs described in the related pentatomid species N. viridula [27].

Highly sensitive hair sensilla situated on the insect’s body represent the second sensory input for direct detection of airborne sound. Amputation of antennae did not decrease female S. titanus leafhopper response to conspecific airborne male calling song signals [5], indicating that sensilla on other parts of the body may be involved. Stink bug N. viridula has trichobothria at the edge of abdomen [28] and high sensitivity of these sensilla has been determined in the Heteroptera species Pyrrhocoris apterus [29]. Barth and Höller [30] demonstrated that spider’s trichobothria of 0.5 mm length detect airflow produced by a fly at a horizontal distance of 30 cm. Spectra of airflow signals produced by a fly show low frequency characteristics similar to those of E. heros tremulatory and buzzing signals, and their frequency rapidly decreases below 100 Hz at distances above 15 cm. Direct measurements of air particle movements around the tremulating, buzzing or abdomen vibrating stink bug have not been conducted yet but we can hypothesize that their airborne component is high enough to involve this sensory input both at the close and long range airborne sound communication.

Frequency decay with distance of airborne signals as shown in a spider-fly model [30] was confirmed in our study when comparing spectra of simultaneously recorded signals induced naturally on one and by airborne signals on another plant. We can conclude that the use of low frequency and narrow band vibrational signals had an advantage in evolution of communication in plant-dwelling insects not only because of their tuning with mechanical properties of herbaceous plants [31], [23] but also because of their better transmission through the air. Frequency increase of airborne signals with increasing distance as documented in S. titanus [5] was not measured in E. heros. This difference may be caused by different frequency properties of vibrational signals and/or by different way of test plant vibration.

Responsiveness of small plant-dwelling insects like leafhoppers and pentatominae stink bugs to vibrations transmitted through air does not coincide with the hypothesis that insects’ small body size prevents efficient emission of low-frequency airborne sound [3], [4]. Low-frequency and narrow-band vibrational signals induce vibrations of leaves of dimensions much larger compared to the insect. Moreover, it was shown that the amplitude of naturally emitted vibrational signals of Nezara viridula is significantly higher on leaves than on the stem [32]. If the amplitude of leaf induced low-frequency vibrations is high enough, we can assume that the airborne component of this substrate-borne vibrational signal may induce vibrations of the leaf with which it is not in physical contact. With the amplitude not falling below the sensitivity threshold of insect’s vibrational receptors, these signals can be detected by the animal on the adjacent leaf.

In conclusion, we showed that pentatominae stink bugs E. heros in addition to species- and sex-specific vibrational signals produced by abdomen vibrations communicate also with substrate-borne vibrational signals produced by other mechanisms, and that information exchange can take place between individuals on physically separated substrates. Our behavioural observations together with measurements of frequency and velocity decay of vibrational signals when transmitted through air suggest that high-amplitude low-frequency tremulatory signals propagate particularly well in the signaling medium/context examined.

Materials and Methods

Experimental Animals and Plants

Males and females from a colony reared Euschistus heros (Heteroptera: Pentatomidae), following the methodologies described by Borges et al. [33], were separated two days after the final moult and reared in the environmental room (26±1°C, 60±10% RH, 14∶10 h LD photoperiod under fluorescent lights of 40W) in plastic cages of 26 cm height and 22 cm diameter on raw peanut seeds (Arachis hypogaea L.), green beans (Phaseolus vulgaris L.) and sunflower seeds (Helianthus annuus L.). Vibrational signals were recorded between 9.00 and 17.00 h under laboratory conditions (26±1°C, 65±10% RH, laboratory light) in a sound insulated room at Embrapa Genetic Resources and Biotechnology in Brasilia (Brazil). Virgin males and females were used in the experiments 15–25 days after the final moult to ensure their sexual maturity [34], [35]. Phaseolus vulgaris L. test plants, grown in sterilized soil in plastic pots of 20 cm height and 15 cm width, were placed on a shock-proved table to reduce environmental sound and vibration noise (Figure 5).

Figure 5. Architecture of bean plants (Phaseolus vulgaris L.) and experimental setup.

Structure and dimensions of bean plants used, and experimental setup in airborne inter-plant communication experiments (below). See text for detailed description of experimental procedures.

Registration of Vibrational Signals

The experimental setup for registration of E. heros vibrational signals consisted of a single P. vulgaris plant potted in a plastic pot and placed on a rubber base to exclude unwanted substrate borne vibrations. The test started by placing a male on a leaf of a plant and waiting for 3 minutes to record spontaneous vibration emissions. After three minutes we put a female on the same plant and their behaviour was observed for 15 minutes. Vibrations were registered by a laser vibrometer (PDV-100, Polytec, Waldbronn, Germany) with the beam oriented perpendicularly at the surface of the plant’s stem at a distance 14–16 cm from the point where the bugs was singing. To get better laser beam reflection a small piece of reflecting tape (> 1 mm2 surface) was glued on the recording point on the plant. The analysis of signal characteristic was conducted by the Sound Forge software, version 6.0 (Sonic Foundry Inc., Madison, WI), the signals were digitized and stored via a sound card (24-bit, 96-kHz, 100-dB signal-to-noise ratio, Sound Blaster Extigy, Creative Laboratories Inc., Milpitas, CA) on a computer by the aid of the Cool Edit Pro software version 2.0 (Adobe Systems Inc., San Jose, CA).

Pulses defined as unitary homogenous parcels of vibrations of finite duration [36] were described by their duration (time between signal onset and its end determined by the amplitude of the cycle that decreased to the level of the noise range), repetition time (time between onsets of the two sequential signals) and by frequency spectra and sonagrams. Frequency spectra and sonograms have been constructed by the Sound Forge software (32768 FFT, 99% FFT overlap, Blackman-Harris smoothing window, slices displayed 1 and 9000 sonogram resolution). Velocity as vector quantity specifying the time rate of displacement was measured with the laser vibrometer at 5 mm/s/V sensitivity at the maximum amplitude of the pulse.

Airborne Inter-plant Communication

The experimental setup in airborne inter-plant communication experiments consisted of two P. vulgaris plants placed in pots on separate rubber bases in order to exclude interplant transmission of substrate-borne vibrations (Figure 5). Plants were either in contact or separated by the air gap, defined in our experiments as the distance between two most adjacent leaves of the two neighbouring plants.

Experiments were conducted at different gap distances, ranging from 3 to 11 cm in successive steps of approximately 2 cm. Initial gap widths were 3, 5, 7, 9 and 11 cm. Because of the leaf architecture and animals moving on the plats, the initial distance between the two most adjacent leaves changed significantly during the experiments. What is more, at gap distances up to 7 cm bugs’ responses did not differ, while at distances above 7 cm no response was observed. For this reasons, we did not distinguish in the text between individual gap widths but focused on the range of gap distances where animals’ responses were recorded.

Signals were recorded from the plant with a single bug using one laser vibrometer or simultaneously from both plants using two identical laser vibrometers. Recording points are shown in Figure 5.

The test started by placing a male on a leaf of one plant for 3 minutes to record spontaneous vibration emissions. After three minutes we put a female on the same plant, but on a different part of it so that the mates could not see each other, and when they started singing we placed a male or a female on the neighbouring plant. Vibrational signals were recorded from a plant with a single bug using one laser or simultaneously from both plants using two identical laser vibrometers.

A single male or a female on one plant and no animals on the neighbouring plant presented control conditions, and a single male or a female on one plant and a male-female pair of E. heros signalling on the neighbouring plant presented test conditions. In both cases the neighbouring plants were separated by a gap of air. Insects were observed during a 15 min interval.

The choice of aspects of insects’ behaviour that were recorded in control and test conditions stems from the fact that successful communication in the stink bug E. heros during mating involves emission of species- and sex-specific vibrational signals and directional movement of a male toward the singing female, known as searching behaviour. This behavioural pattern, common to some other pentatomidae species, is in nature triggered by the species-specific male pheromone with long-range action. This enables distant mates to meet on the same plant substrate where middle- and short-range substrate-borne vibrational communication can take place. If communication is successful, it leads to copulation.

In the experiment we recorded the number of animals staying on the plant throughout the experiment, the emission of vibrational signals, searching behaviour and directional movement towards the neighbouring plant. To check whether the number of tremulatory signals emitted is different between control and test conditions, which would indicate that these signals could be involved in E. heros’s vibrational communication, as was reported for some Asopinae species, we compared the tremulation rate between control and test conditions.

We hypothesised that substrate-borne vibrational signals could be transmitted over the gap to the neighbouring plant, which would result in inter-plant communication indicated by a higher number of animals exhibiting the recorded behaviour and by higher tremulation rate in test conditions compared to control conditions.

In order to test how transmission through air of substrate-borne vibrational signals affects their characteristics, we measured velocity and frequency changes of the signals by simultaneously recording vibrations from both neighbouring plants.

Our assumption was that after transmission through air substrate-borne vibrational signals would retain their low frequency characteristics, typical of Pentatomidae stink bugs’ vibrational signals, and that the amplitude of high-amplitude vibrational signals would not fall below the threshold of the bugs’ sensory organs.

Data are represented as means ± SD (n- the number of signals analysed, N- the number of individuals) when there were no statistically significant differences between groups of values, and as minimum and maximum values when statistically significant differences existed between groups of values.

Assuming normal distribution and homogeneity of variances 2-tailed Student’s t-test and one-way ANOVA were used. Fisher’s exact test for count data was used to compare animal activity in inter-plant communication experiments.


We thank Warley Dias Oliveira Barbosa and Priscila Shaene Sousa Silva for helping with laboratory rearing of the insects, and Prof Dr Andrej Blejec for help with statistics.

Author Contributions

Conceived and designed the experiments: AČ AK RAL. Performed the experiments: AČ AK. Analyzed the data: AČ AK RAL. Contributed reagents/materials/analysis tools: MCBM RAL MB. Wrote the paper: AK AČ RAL.


  1. 1. Hill PSM (2008) Vibrational Communication in Animals. Cambridge, MA: Harvard University Press.
  2. 2. Cocroft RG, Rodriguez RL (2005) The behavioral ecology of insect vibrational communication. Bio Science 55: 323–334.
  3. 3. Markl H (1983) Vibrational communication. In: Huber F, Markl H, editors. Neuroethology and behavioural physiology: roots ad growing points. Heidelberg: Springer-Verlag. 332–353.
  4. 4. Bennet-Clark HC (1998) Size and scale effects as constraints in insect sound communication. Philos T R Soc B 353: 407–419.
  5. 5. Eriksson A, Anfora G, Lucchi A, Virant-Doberlet M, Mazzoni V (2011) Inter-plant vibrational communication in a leafhopper insect. PLoS ONE 6(5): e19692 .
  6. 6. Aldrich JR (1995) Chemical communication in the true bugs and parasitoid exploitation. In: Carde RT, Bell WJ, editors. Chemical ecology of insects 2. New York: Chapman and Hall. 318–363.
  7. 7. Aldrich JR, Oliver JE, Kochansky JP, Lockwood JA (1987) Pheromone strains of the cosmopolitan pest, Nezara viridula (Heteroptera: Pentatomidae). J Exp Zool 244: 171–175.
  8. 8. McBrien HL, Millar JG (1999) Phytophagous bugs. In: Hardie J, Minks AK, editors. Pheromones of non-lepidopteran insects associated with agricultural plants. Wallingford: CABI Publishing. 277–304.
  9. 9. Borges M, Jepson PC, Howse PE (1987) Long range mate location and close-range courtship behaviour of the green stink bug, Nezara viridula and its mediation by sex pheromone. Entomol Exper Appl 44: 205–212.
  10. 10. Ota D, Čokl A (1991) Mate location in the southern green stink bug Nezara viridula (Heteroptera: Pentatomidae) mediated through substrate-borne signals on ivy. J Insect Behav 4: 441–447.
  11. 11. Čokl A, Virant-Doberlet M, McDowell A (1999) Vibrational directionality in the southern green stink bug Nezara viridula (L.) is mediated by female song. Anim Behav 58: 1277–1283.
  12. 12. Čokl A, Virant-Doberlet M (2003) Communication with substrate-borne signals in small plant-dwelling insects. Annu Rev Entomol 48: 29–50.
  13. 13. Čokl A (2008) Stink bug interaction with host plants during communication. J Insect Physiol 54: 1113–1124.
  14. 14. Čokl A, Zorović M, Žunič A, Virant-Doberlet M (2005) Tuning of host plants with vibratory songs of Nezara viridula L (Heteroptera: Pentatomidae). J Exp Biol 208: 1481–1488.
  15. 15. Polajnar J, Svenšek D, Čokl A (2012) Resonance in herbaceous plant stems as a factor in vibrational communication of pentatomid bugs (Heteroptera: Pentatomidae). J Roy Soc Interface doi:
  16. 16. Žunič A, Čokl A, Virant-Doberlet M, Millar JG (2008) Communication with signals produced by abdominal vibration, tremulation, and percussion in Podisus maculiventris (Heteroptera: Pentatomidae). Ann Entomol Soc Am 101: 1169–1178.
  17. 17. Čokl A, Žunič A, Millar JG (2009) Transmission of Podisus maculiventris tremulatory signals through plants. Centr Eur J Biol 4: 585–594.
  18. 18. Čokl A, Žunič A, Virant-Doberlet M (2011) Predatory bug Picromerus bidens communicates at different frequency levels. Centr Eur J Biol 6: 431–439.
  19. 19. Čokl A (2008) Stink bug interaction with host plants during communication. J Insect Physiol 54: 1113–1124.
  20. 20. de Groot M, Čokl A, Virant-Doberlet M (2010) Effects of heterospecific and conspecific vibrational signal overlap and signal-to-noise ratio on male responsiveness in Nezara viridula (L.). J Exp Biol 213: 3213–3222.
  21. 21. de Groot M, Čokl A, Virant-Doberlet M (2011a) Species identity cues: possibilities for errors during vibrational communication on plant stems. Behav Ecol 22: 1209–1217.
  22. 22. de Groot M, Čokl A, Virant-Doberlet M (2011b) Search behaviour of two hemipteran species using vibrational communication. Centr Eur J Biol 6: 756–769.
  23. 23. Žunič A, Virant-Doberlet M, Čokl A (2011) Species recognition during substrate-borne communication in Nezara viridula (L.) (Pentatomidae: Heteroptera). J Insect Behav 24: 468–487.
  24. 24. Blassioli-Moraes MC, Laumann RA, Čokl A, Borges M (2005) Vibratory signals of four Neotropical stink bug species. Physiol Entomol 30: 175–188.
  25. 25. Roemer H, Land A, Hartbauer M (2010) The signaller’s dilemma: A cost-benefit analysis of public and private communication. PLoS ONE 5(10): e13325 .
  26. 26. De Luca P, Morris GK (1998) Courtship communication in meadow katydids: female preference for large male vibrations. Behaviour 135: 777–793.
  27. 27. Čokl A (1983) Functional properties of vibroreceptors in the legs of Nezara viridula (L.) (Heteroptera, Pentatomidae). J Comp Physiol A 150: 261–269.
  28. 28. Staddon BW, Ahmad I (1994) A further study of the sternal patches of Heteroptera-Pentatomidae with considerations of their function and value for classification. J Nat Hist 28: 353–364.
  29. 29. Drašlar K (1973) Functional properties of trichobothria in the bug Pyrrhocoris apterus (L.). J Comp Physiol 84: 175–184.
  30. 30. Barth FG, Höller A (1999) Dynamics of arthropod filiform hairs. V. The response of spider trichobothria to natural stimuli. Philos Trans R Soc Lond Ser B 354: 183–192.
  31. 31. Čokl A, Nardi C, Bento JMS, Hirose E, Panizzi AR (2006) Transmission of stridulatory signals of the burrower bugs, Scaptocoris castanea and Scaptocoris carvalhoi (Heteroptera: Cydnidae) through the soil and soybean. Physiol Entomol 31: 371–381.
  32. 32. Amon T, Čokl A (1999) Transmission of the vibratory song of the bug Nezara viridula (Pentatomidae, Heteroptera) on the Hedera helix plant. Scopolia Suppl 1: 133–141.
  33. 33. Borges M, Laumann RA, Silva CC, Moraes MCB, Santos HM, et al. (2006) Metodologias de criação e manejo de colônias de percevejos de soja (Hemiptera: Pentatomidae) para estudos de comportamento e ecologia química. Brasilia-DF: Embrapa Resursos Genéticos e Biotecnologia (Documentos No. 182).
  34. 34. Brennan BM, Chang F, Mitchell WC (1977) Physiological effects on sex pheromone communication in the southern green stink bug, Nezara viridula. Environ Entomol 6: 169–172.
  35. 35. Costa MLM, Borges M, Vilela EF (1998) Biologia reprodutiva de Euschistus heros (F.) (Heteroptera: Pentatomidae). An Soc Entomol Bras 27: 559–568.
  36. 36. Broughton WB (1963) Methods in bioacoustic terminology. In: Busnel RG, editor. Acoustic behaviour of animals. Amsterdam: Elsevier. 3–24.