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Psychophysical comparison of vertical and angular vibrations.

Three psychophysical matching experiments were conducted to compare the perceived intensity of angular vibrations, in roll, pitch or yaw, with the perceived intensity of Z-axis translational vibrations. Seated subjects matched their perceptions of the intensity of Z-axis stimulus vibrations--at six frequencies from 2.5-8 Hz, at each of three intensity levels--by adjusting the intensity of angular response vibrations at the same frequencies. The results showed that the acceleration of the angular matching responses increased significantly as a function of both the frequency and the intensity of the stimulus vibrations. Since the stimuli were chosen from existing Z-axis equal intensity contours, the mean matching responses define equivalent contours for angular vibrations. Determination of relationships between translational and angular vibration is essential for the development of improved vibration exposure criteria applicable to complex vibration environments.

Humans↗

Vibration syndrome and autonomic nervous system.

It is well known that hand-arm vibration affects the hand and arm which are directly exposed to vibration. However, through the sympathetic nervous system, hand-arm vibration can affect the foot which is not directly exposed to vibration. Hand-arm vibration activates the sympathetic nervous system, and induces vasoconstriction in the four extremities. And patients with vibration syndrome have circulatory disturbances of the foot as well; some patients had Raynaud's phenomenon of both fingers and toes, those with VWF were likely to complain of coldness in the feet as well as the hands, and had low skin temperature of the fingers and toes. In addition, arterial pathological changes like medial muscular hypertrophy have been observed in both fingers and toes of the patients. Prolonged repeated vasoconstriction of the foot induced by hand-arm vibration through the sympathetic nervous system is supposed to result in arterial changes like medial muscular hypertrophy in the foot and eventually circulatory disturbances of the feet. Hyperactivity of the sympathetic nervous system to cold, which is shown in patients with VWF, also probably contributes to the foot disturbances. The effect of hand-arm vibration through the sympathetic nervous system should be considered in hand-arm vibration syndrome.

Cumulative Trauma Disorders↗

The multi-axis vibration environment and man.

Many investigations into the effects of vibration on man have been performed since Mallock's first study of London Underground vibrations in 1902. The vibration research has tended to be confined to the vertical (heave) axis, yet recent experiments have indicated that low frequency vibration along the lateral (sway) axis has a greater adverse effect upon comfort and performance. Measurements of the vibration environments in current forms of transport including motor vehicles, hovercraft and aircraft etc have shown that appreciable quantities of vibration along all three axes exist. Further vibration research should consider the effects of multi-axis vibrations upon man rather than limit tests to single axis vibration.

Journal Article↗

Configurations of high-frequency ultrasonics complex vibration systems for packaging in microelectronics.

Ultrasonic high-frequency complex vibrations are effective for various ultrasonic high-power applications. Three types of ultrasonic complex vibration system with a welding tip vibrating elliptical to circular locus for packaging in microelectronics were studied. The complex vibration sources are using (1) a longitudinal-torsional vibration converter with diagonal slits that is driven only by a longitudinal vibration source, (2) a complex transverse vibration rod with several stepped parts that is driven by two longitudinal vibration source crossed at a right angle and (3) a longitudinal vibration circular disk and three longitudinal transducers that are installed at the circumference of the disk.

Journal Article↗

Spectroscopic and theoretical investigations of vibrational frequencies in binary unsaturated transition-metal carbonyl cations, neutrals, and anions.

Figure 18 presents the C-O stretching vibrational frequencies of the first-row transition-metal monocarbonyl cations, neutrals, and anions in solid neon; similar diagrams have been reported for neutral MCO species in solid argon, but three of the early assignments have been changed by recent work and one new assignment added. The laser-ablation method produces mostly neutral atoms with a few percent cations and electrons for capture to make anions; in contrast, thermal evaporation gives only neutral species. Hence, the very recent neon matrix investigations in our laboratory provide carbonyl cations and anions for comparison to neutrals on a level playing field. Several trends are very interesting. First, for all metals, the C-O stretching frequencies follow the order cations > neutrals > anions with large diagnostic 100-200 cm-1 separations, which is consistent with the magnitude of the metal d to CO pi * donation. Second, for a given charge, there is a general increase in C-O stretching vibrational frequencies with increasing metal atomic number, which demonstrates the expected decrease in the metal to CO pi * donation with increasing metal ionization potential. Some of the structure in this plot arises from the extra stability of the filled and half-filled d shell and from the electron pairing that occurs at the middle of the TM row; the plot resembles the "double-humped" graph found for the variation in properties across a row of transition metals. For the anions, the variation with metal atom is the smallest since all of the metals can easily donate charge to the CO ligand. Third, for the early transition-metal Ti, V, and Cr families, the C-O stretching frequencies decrease when going down the family, but the reverse relationship is observed for the late transition-metal Fe, Co, and Ni families. In most of the present discussion, we have referred to neon matrix frequencies; however, the argon matrix frequencies are complementary, and useful information can be obtained from comparison of the two matrix hosts. In most cases, the neon-to-argon red shift for neutral carbonyls is from 11 to 26 cm-1, but a few (CrCO) lie outside of this range. In the case of FeCO and Fe(CO)2, it appears that neon and argon trap different low-lying electronic states. In general, the carbonyl neutrals and anions have similar shifts but carbonyl cations have larger matrix shifts. For example, the FeCO+ fundamental is at 2123.0 cm-1 in neon and 2081.5 cm-1 in argon, a 42.5 cm-1 shift, which is larger than those found for FeCO- (11.7 cm-1) and FeCO (11.7 cm-1). It is unusual for different low-lying electronic states to be trapped in different matrices, but CUO provides another example. The linear singlet state (1047.3, 872.2 cm-1) is trapped in solid neon, and a calculated 1.2 kcal/mol higher triplet state is trapped in solid argon (852.5, 804.3 cm-1) and stabilized by a specific interaction with argon. The bonding trends are well described by theoretical calculations of vibrational frequencies. Table 5 compares the scale factors (observed neon matrix/calculated) for the C-O stretching modes of the monocarbonyl cations, neutrals, and anions of the first-row transition metals observed in a neon matrix using the B3LYP and BP86 density functionals. Most of the calculated carbonyl harmonic stretching frequencies are within 1% of the experimental fundamentals at the BP86 level of theory, while calculations using the B3LYP functional give frequencies that are 3-4% higher as expected for these density functionals and calculations on saturated TM-carbonyls. For second- and third-row carbonyls using the BP86 density functional and the LANL effective core potential in conjunction with the DZ basis set, the agreement between theory and experiment is just as good. For example, the 16 M(CO)1-4 neutral and anion and 2 MCO+ cation (M = Ru, Os) carbonyl frequencies are fit within 1.5%. The 16 species (M = Rh, Ir) are fit within 1%, but the Rh(CO)1-4+ calculations are 2-3% too low and Ir(CO)1-4+ computations are 1-2% too low. In addition to predicting the vibrational frequencies, DFT can be used to calculate different isotopic frequencies, and isotopic frequency ratios can be computed as a measure of the normal vibrational mode in the molecule for an additional diagnostic. For diatomic CO, the 12CO/13CO ratio 1.0225 and C16O/C18O ratio 1.0244 characterize a pure C-O stretching mode. In a series of molecules such as RhCO+, RhCO, and RhCO-, where the metal-CO bonding varies, the Rh-C, C-O vibrational interaction is different and the unique isotopic ratios for the carbonyl vibration are characteristic of that particular molecule. Table 6 summarizes the isotopic ratios observed and calculated for the RhCO+,0,- species. Note that RhCO+ exhibits slightly more carbon-13 and less oxygen-18 involvement in the C-O vibration than CO itself and that this trend increases to RhCO and to RhCO- as the Rh-C bond becomes shorter and stronger. Note also how closely the calculated and observed ratios both follow this trend. In a molecule with two C-O stretching modes, for example, bent Ni(CO)2 exhibits a strong b2 mode at 1978.9 cm-1 and a weak a1 mode at 2089.7 cm-1 in solid neon, and these two modes involve different C and O participations. The symmetric mode shows substantially more C (1.0242) and less O (1.0217) participation than does the antisymmetric mode with C (1.0228) and O (1.0238) involvement, based on the given isotopic frequency ratios, which are nicely matched by DFT calculations (a1 1.0244, 1.0224 and b2 1.0232, 1.0241, respectively). These investigations of vibrational frequencies in unsaturated transition-metal carbonyl cations, neutrals, and anions clearly demonstrate the value of a close working relationship between experiment and theory to identify and characterize new molecular species.

Journal Article↗

Quasiclassical trajectory simulations of OH(v) + NO2 --> HONO2* --> OH(v') + NO2: capture and vibrational deactivation rate constants.

Quasiclassical trajectory calculations are used to investigate the dynamics of the OH(v) + NO(2) --> HONO(2) --> OH(v') + NO(2) recombination/dissociation reaction on an analytic potential energy surface (PES) that gives good agreement with the known structure and vibrational frequencies of nitric acid. The calculated recombination rate constants depend only weakly on temperature and on the initial vibrational energy level of OH(v). The magnitude of the recombination rate constant is sensitive to the potential function describing the newly formed bond and to the switching functions in the PES that attenuate inter-mode interactions at long range. The lifetime of the nascent excited HONO(2) depends strongly not only on its internal energy but also on the identity of the initial state, in disagreement with statistical theory. This disagreement is probably due to the effects of slow intramolecular vibrational energy redistribution (IVR) from the initially excited OH stretching mode. The vibrational energy distribution of product OH(v') radicals is different from statistical distributions, a result consistent with the effects of slow IVR. Nonetheless, the trajectory results predict that vibrational deactivation of OH(v) via the HONO(2) transient complex is approximately 90% efficient, almost independent of initial OH(v) vibrational level, in qualitative agreement with recent experiments. Tests are also carried out using the HONO(2) PES, but assuming the weaker O-O bond strength found in HOONO (peroxynitrous acid). In this case, the predicted vibrational deactivation efficiencies are significantly lower and depend strongly on the initial vibrational state of OH(v), in disagreement with experiments. This disagreement suggests that the actual HOONO PES may contain more inter-mode coupling than found in the present model PES, which is based on HONO(2). For nitric acid, the measured vibrational deactivation rate constant is a useful proxy for the recombination rate, but IVR randomization of energy is not complete, suggesting that the efficacy of the proxy method must be evaluated on a case-by-case basis.

Journal Article↗

Vibrational energy relaxation of azulene studied by the transient grating method. I. Supercritical fluids.

The vibrational energy dissipation process of the ground-state azulene in supercritical xenon, carbon dioxide, and ethane has been studied by the transient grating spectroscopy. In this method, azulene in these fluids was photoexcited by two counterpropagating subpicosecond laser pulses at 570 nm, which created a sinusoidal pattern of vibrationally hot ground-state azulene inside the fluids. The photoacoustic signal produced by the temperature rise of the solvent due to the vibrational energy relaxation of azulene was monitored by the diffraction of a probe pulse. The temperature-rise time constants of the solvents were determined at 383 and 298 K from 0.7 to 2.4 in rho(r), where rho(r) is the reduced density by the critical density of the fluids, by the fitting of the acoustic signal based on a theoretical model equation. In xenon, the temperature-rise time constant was almost similar to the vibrational energy-relaxation time constant of the photoexcited solute determined by the transient absorption measurement [D. Schwarzer, J. Troe, M. Votsmeier, and M. Zerezke, J. Chem. Phys. 105, 3121 (1996)] at the same reduced density irrespective of the solvent temperature. On the other hand, the temperature-rise time constants in ethane were larger than the vibrational energy-relaxation time constants by a factor of about 2. In carbon dioxide, the difference was small. From these results, the larger time constants of the solvent temperature rise than those of the vibrational energy relaxation in ethane and carbon dioxide were interpreted in terms of the vibrational-vibrational (V-V) energy transfer between azulene and solvent molecules and the vibrational-translational (V-T) energy transfer between solvent molecules. The contribution of the V-V energy transfer process against the V-T energy transfer process has been discussed.

Journal Article↗

[Analytical description of electron-vibrational protein spectra].

Electron-vibrational spectra of phosphorescence and fluorescence of tryptophan residues in proteins at 77 K are best approximated by theoretical curves computed according to a model which suggests the existence of two independent series of Gaussian vibrational components. Each series contains one type of vibrations. Phosphorescence and fluorescence spectra of proteins with various localizations of their single tryptophan residue were fitted by a curve computed according to this model. The results obtained show that the phosphorescence band of tryptophan residues in proteins seems to contain two types of vibrations with frequencies 650-800 cm-1 and 1350-1500 cm-1. Since the substitution of H2O by D2O does not change the frequencies of both vibrations in the phosphorescence spectra of human serum albumin, melittin and tryptophan in 1 M KCl, it is reasonable to suggest that the 1350-1500 cm-1 series corresponds to the W5 type vibrations (B19a type of vibrations of benzene ring). The 650-800 cm-1 series"can be identified with W18 type of vibrations (breathing vibrations of indole ring). Phosphorescence parameters of tryptophan residues in proteins correlate with their fluorescence parameters.

Animals↗

The effect of muscle vibration on human position sense during movements controlled by lengthening muscle contraction.

Muscle vibration studies suggest that during voluntary movement limb position is coded by muscle spindle information derived from the lengthening, antagonist muscle. However, these investigations have been limited to movements controlled by shortening contractions. This study further examined this property of kinesthesia during movements controlled by lengthening contraction. Subjects performed a horizontal flexion of the right forearm to a mechanical stop randomly positioned at 30, 50 and 70 degrees from the starting position. The movement was performed against a flexor load (1 kg) requiring contraction of the triceps muscle. Vision was occluded and movements were performed under three conditions: no vibration, vibration of the right biceps and vibration of the right triceps. The perceived position of the right forearm was assessed by instructing subjects to simultaneously match the right limb position with the left limb. Vibration of the shortening biceps muscle had no effect on limb matching accuracy. However, triceps vibration resulted in significant overestimation of the vibrated limb position (10-13 degrees). The variability in movement distance was uninfluenced by muscle vibration. During movements controlled by lengthening contraction, there is a concurrent gamma dynamic fusimotor input that would enhance primary afferent discharge. Despite this additional regulating input to the muscle spindle, it appears that muscle spindle information from the lengthening muscle is important for the accurate perception of limb movement and/or position.

Adult↗

Vibration aftereffects on vasoconstrictor response to cold in the normal finger.

The acute effects of unilateral 30 min exposure to hand-arm vibration on the vasoconstrictor response to cold in a finger from both hands were investigated in 12 healthy men (age 18-38 years) who had never worked with vibrating tools. One hand was exposed to accelerations of 4.0 and 16.0 m.s-2 on 2 different days. The vasoconstrictor response to cold (R%) was expressed as the relative decrease in finger systolic blood pressure, measured using cuff and strain gauge techniques, when the finger was cooled from 30 to 10 degrees C. The R% of both third fingers were measured simultaneously before unilateral vibration exposure and 15, 60 and 120 min after the end of each exposure. The R% of both fingers were not affected by the low acceleration vibration (P > 0.10). Exposure to the high acceleration vibration was followed by an unchanged R% of the exposed finger but an increased R% of the non-exposed finger after 15 min (P < 0.05); there was an equal increase of 30%-40% in R% of both fingers after 60 min (P < 0.05). The R% of both fingers had returned to normal after 120 min (P > 0.10). The results would indicate that short-term exposure to vibration induces a transitory hyperreactive central vasoconstrictor drive to the central sympathetic nervous system or circulating agents, which initially was locally counteracted by an induced hyporeactive vasoconstrictor function of local vasomotor mechanisms of the vibration exposed digital arteries. The hyperreactive vasoconstrictor effect demonstrated may contribute to the development of vibration-induced white finger if cumulative exposure time were to be considerably increased.

Adolescent↗

Perceptual and motor effects of agonist-antagonist muscle vibration in man.

Perceptual and motor effects of vibration applied simultaneously to the distal tendons of the Biceps and Triceps muscles, in isometric conditions and without sight of the stimulated arm, have been studied in human volunteers. Motor effects, measured by surface EMG, are inexistent when the flexor and extensor muscles are simultaneously vibrated at the same frequency. However, EMG activity appears in the muscle being vibrated at the lower frequency when simultaneous vibration is applied at different frequencies. The sensations felt by the subjects were reproduced by the nonvibrated arm and recorded by a goniometer. The studies show that the velocity and the amplitude of the ilusory movement is related to the difference in vibration frequency applied to the two muscles. The direction of movement felt (flexion or extension) is that produced by shortening of the muscle being vibrated at the lower frequency. When the two vibration frequencies are the same, there is either no sensation of movement, or a sensation of very slow movement. These results support the notion that the sensation of movement at a joint may be derived from a central processing of the proprioceptive inflow data obtained from flexor and extensor muscles. This interpretation may also be valid for the results obtained earlier by vibration of a single muscle. Furthermore, it is coherent with data on spindle afferent fibres obtained by microneurography in man during passive or active movements.

Adult↗

Combined effects of noise, vibration and visual field stimulation on electrical brain activity and optomotor responses.

Eye movements and electroencephalographs (EEG) were recorded in intact rabbits during an optokinetic test. The animals were exposed to pure tone noise (85 dB at 4000 Hz), impulse noise (159 dB), and vibration directed at the abdomen (amplitude 0.9 mm at frequencies of 40, 80, and 120 Hz). The velocity of optokinetic nystagmus (OKN) significantly increased with these stimuli. The increase seen with vibration was greater than the noise-induced increase. The response was strongest when noise and vibration were combined. The increase in OKN induced by vibration was successive and dependent on frequency. The increase was weakest during exposure to vibration at 40 Hz and strongest at 120 Hz. EEGs of the dorsal hippocampus, amygdaloid complex, midbrain reticular formation, and frontal motor cortex were all activated during noise and vibration exposure, but activation of the hippocampal EEG was the most closely related to the increase in OKN. Combination of the different stimuli indicated that their interaction could not be predicted on the basis of responses to single stimuli, and, in most cases, the result was indifference due to the high alerting effect of vibration alone. The findings can be related to the non-specific dizziness found in aerospace workers exposed to excessive noise and vibration.

Animals↗

Cardiovascular changes and hearing threshold shifts in men under complex exposures to noise, whole body vibrations, temperatures and competition-type psychic load.

This study deals with changes in the temporary hearing threshold (TTS2), heart rate (HR), R-wave amplitude (RWA), diastolic blood pressure (DBP), systolic blood pressure (SBP), pulse pressure (PP) and reaction time (RT) in subjects (n = 108) who, while working on a choice reaction apparatus, were exposed in an exposure chamber to combinations of noise and vibration at dry bulb temperatures of 20 degrees and 30 degrees C. The study was carried out as a type 2-3-3 factorial experiment, the number of the exposure combinations thus being 18. To find out the effects of competition-type psychic stress, some of the subjects were placed in a competitive group and some in a non-competitive group. The members of the competitive group were given financial encouragement and information on their progress during the test, whereas those in the non-competitive group worked at the rate they considered best without any monetary rewards or interim information. The noise classes were: no noise, a stable broadband (bandwidth 0.2-16.0 kHz) A-weighted noise of 90 dB not related to competition, and a stable broadband A-weighted noise of 90 dB related to competition about the fastest reaction time. The vibration classes were: no vibration, sinusoidal whole body vibration (Z-axis) at a frequency of 5 Hz, and stochastic broadband (bandwidth 2.8-11.2 Hz) whole body vibration (Z-axis). The acceleration (rms) of both vibrations was 2.12 m/s2. One experiment consisted of a control period of 30 min, three consecutive exposure periods of 16 min with an interval of 4 min, and a 15-min recovery period. The variance analysis model best explained the variation in TTS2 values at 4 kHz and second best the variation in TTS2 values at 6 kHz; it explained the variation in HR values third best, the variation in SBP values fourth best and the variation in PP values fifth best. On the other hand, the model explained least well the variation in DBP and RWA values. In general, the explanatory power of the model increased together with the number of exposures. The psychic stress caused by competition accelerated the growth of the TTS2 values, HR values and SBP values, when the subjects were simultaneously exposed to noise or to a combination of noise and vibration. An interesting finding for the continuation of the research project was that sinusoidal and stochastic vibration affected the cardiovascular changes, temporary hearing threshold and reaction times in different ways.

Adolescent↗

Combined effects of vibration and noise on palmar sweating in healthy subjects.

The combined effects of vibration and noise on palmar sweating were studied experimentally in healthy subjects. Ten subjects were exposed to vibration at an acceleration of 100 m.sec-2 root mean square at a frequency of 125 Hz, a noise level of 105 dB(A) at a frequency of 1000 Hz and both stimuli together. Vibration was applied to the right hand and noise to both ears from headphones. Palmar sweating was measured by the ventilated capsule method. Vibration caused a marked increase in palmar sweating of the right hand directly exposed to vibration and also of the left hand not exposed to vibration. Simultaneous vibration and noise caused a greater increase in palmar sweating than by each of the factors separately. The combined effects tended to be greater in subjects who were more susceptible to vibration or noise.

Adult↗

The effect of agonist/antagonist muscle vibration on human position sense.

During voluntary movement, muscle spindles of both the agonist and antagonist muscles potentially can supply information about position of the limb. Muscle vibration is known to increase muscle spindle discharge and cause systematic distortions of limb position sense in humans. The following two experiments attempted to examine these contributions by separately vibrating over the triceps and biceps muscles during forearm positioning. In the first experiment, subjects performed a horizontal flexion or extension of the right arm to a mechanical stop randomly positioned at 20, 40 or 60 degrees. Vision was occluded and vibration was applied to the right arm. The perceived position of the right limb was assessed by instructing subjects to simultaneously match the right arm position with the left limb. Vibration of the shortening, agonist muscle had no effect on limb matching accuracy. However, antagonist muscle vibration resulted in a significant overestimation of the vibrated limb position by 6-13 degrees. The procedures for the second experiment were similar to the first, except that movements of the right limb were self-terminated and only flexion movements were performed. A screen was mounted over the arms and subjects were instructed to move the right arm until it was positioned beneath a marker on the screen. Vibration of the shortening agonist muscle had no effect on either the positioning accuracy of the right limb or matching accuracy of the left limb. However, antagonist muscle vibration resulted in significantly shorter movements (6-10 degrees) by the right limb and an overestimation of right limb position by the left, matching limb.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗

Temporary threshold shift of vibratory sensation induced by a vibrating handle and its gripping force.

OBJECTIVE: This study examines the effect of the force with which a vibrating handle is gripped on the temporary threshold shift of vibratory sensation (TTSv) induced by hand-arm vibration. METHODS: Six healthy subjects gripped a handle vibrating with a 1.3 octave-band vibration, with a central frequency of 200 Hz and an intensity of 39.2 m/s2. Exposure was for 1 min and 10 min, respectively. Gripping forces for the 1-min exposure were 5 N, 10 N, 40 N and 80 N, respectively, with 0 N push-pull force. Gripping forces for the 10-min exposure were the same as for the 1-min exposure but omitting 80 N. The vibratory sensation threshold at 125 Hz was measured before and after exposure of an exposed fingertip to vibration. The differences measured determine TTSv.t at time t. TTSv.t determines TTSv.0, that is, the temporary threshold shift of vibratory sensation immediately after exposure to vibration according to the estimate made on the basis of the preceding study. The same experimental conditions were repeated 3 times on different days in a soundproof and thermoregulated room. RESULTS: Our findings show that TTSv increases significantly with increasing gripping force. We also determined the quantitative relationships between TTSv.0 and gripping force as described by the equation TTSv.0 = exp(kf x F + Cf). where kt and Cf are constants and F is gripping force. CONCLUSION: This study revealed the importance of ergonomic design in reducing the force with which a vibrating handle is gripped to prevent an adverse effect of local vibration. The equation devised may help in the quantitative assessment of the effect of reduced gripping force.

Adult↗

Vibrating the food receivers: a direct way of signal transmission in stingless bees (Melipona seminigra).

An element common to the recruitment communication of eusocial bees (honey bees, stingless bees and bumble bees) are pulsed thorax vibrations generated by successful foragers within the nest. In stingless bees, foragers vibrate during the unloading of the collected food. In the present study on Melipona seminigra we demonstrate that during trophallactic contacts, the food receivers are directly vibrated by the foragers. As a consequence, both the temporal structure and the main frequency component of the forager's vibrations are directly passed on to the receiver. The vibrations are attenuated by about 17 dB on their way from the forager's thorax (velocity amplitude of the vibrations: approximately 70 mm/s) to the receiver's thorax (approximately 10 mm/s), the main amount of attenuation (about 12 dB) occurring during transmission from the head of the forager to that of the receiver. Vibrations conducted through the substrate between the forager and food receiver are comparatively small with velocity amplitudes of 0.3 mm/s. Possible ways of perception and the advantages of vibration transmission by direct contact within the recruitment context are discussed.

Animal Communication↗

Directionality in the mechanical response to substrate vibration in a treehopper (Hemiptera: Membracidae: Umbonia crassicornis).

The use of substrate vibrations in communication and predator-prey interactions is widespread in arthropods. In many contexts, localization of the vibration source plays an important role. For small species on solid substrates, time and amplitude differences between receptors in different legs may be extremely small, and the mechanisms of vibration localization are unclear. Here we ask whether directional information is contained in the mechanical response of an insect's body to substrate vibration. Our study species was a membracid treehopper (Umbonia crassicornis) that communicates using bending waves in plant stems. We used a bending-wave simulator that allows precise control of the frequency, intensity and direction of the vibrational stimulus. With laser-Doppler vibrometry, we measured points on the substrate and on the insect's thorax and middle leg. Transfer functions showing the response of the body relative to the substrate revealed resonance at lower frequencies and attenuation at higher frequencies. There were two modes of vibration along the body's long axis, a translational and a rotational mode. Furthermore, the transfer functions measured on the body differed substantially depending on whether the stimulus originated in front of or behind the insect. Directional information is thus available in the mechanical response of the body of these insects to substrate vibration. These results suggest a vibration localization mechanism that could function at very small spatial scales.

Acoustic Stimulation↗