ライフサイエンスコーパス: playback

1 ssion (closed-loop contingent parental vocal playback).

2 be stimulated to evoke reverse spike pattern playback.

3 ports also respond more aggressively to song playback.

4 but not stressed rats, after exposure to the playback.

5 vented this avoidance reaction evoked by the playback.

6 ons was detrimentally affected by road-noise playback.

7 antly enhanced during speaking compared with playback.

8 those reared with exposure to ambient-noise playback.

9 dstarts than control points that received no playback.

10 disrupted via stimulus inversion or reversed playback.

11 e HVC-RA neurons are also responsive to song playback.

12 s compared with baseline rates or tank noise playbacks.

13 ches and canaries after presentation of song playbacks.

14 ments and social behavior in response to the playbacks.

15 Expression could be further induced by song playbacks 30 days after hatching but not at 20 days nor

16 at CM neurons are active in response to song playback and during singing, indicating their potential

17 ucture of natural scallops during behavioral playback and in vivo electrophysiology experiments to pr

18 respond at markedly different times to song playback and that different syllables activate spatially

19 tors, DA reduced responses in Area X to song playback and to electrical stimulation of its afferent c

20 Birds that heard the playbacks and did not sing in response showed increased

21 ses (Helogale parvula) [4], we combine sound playbacks and faecal presentations to demonstrate that a

22 ng-finned pilot whales to killer whale sound playbacks and two anthropogenic sources of disturbance:

23 banded mongoose groups to scents, 'war cry' playbacks, and live intruders from a rival group.

24 for learned features of song observed during playback arises in HVc or also in structures afferent to

25 The use of video playback as a visual stimulus in this experiment permitt

26 Using playback assays, we show that cries result in a more rap

27 avioral, were most pronounced during initial playback, but then declined rapidly with subsequent pres

28 ator, sperm whales responded to killer whale playbacks by interrupting their foraging or resting dive

29 re not inherently more strongly attracted to playback calls than males.

30 ending more time away from the source of the playback calls.

31 and (4) test whether conspecific social call playback can increase capture success.

32 We found that exposure to boat-noise playback, compared to ambient-noise playback, reduced su

33 e response was the same for the speaking and playback conditions.

34 mesopallium (CMM) in response to father song playback differed between control F2 sons and those with

35 Sampled motion degraded forwards/reversed playback discrimination, indicating observers were sensi

36 pressing ZENK in NCM and cmHV following song playback does not vary with sex or photoperiod in starli

37 nvestigate the effect of repeated boat-noise playback during early life on the development and surviv

38 ere we show that, in juvenile zebra finches, playback during the day of an adult 'tutor' song induced

39 nse of hoary bats to conspecific social call playback during the spring and fall migration to: (1) te

40 d and validated against seven user-specific 'playback' emissions observations.

41 puts of HVC and account for some of the song playback-evoked inhibition in HVC(X) cells.

42 Here we describe a playback experiment conducted on wild female baboons, su

43 A playback experiment confirmed that this illusion was suf

44 We conducted a landscape-scale playback experiment demonstrating that the sound of huma

45 Results of simultaneous observations and a playback experiment indicate that the contact function o

46 Observations and a playback experiment indicated that adult babblers use a

47 A playback experiment shows that females are sexually arou

48 We then used another playback experiment to assess delayed effects of within-

49 Here, we use a playback experiment to quantify how wild female geladas

50 We used an automated playback experiment to simulate two types of social info

51 Avian vocalizations were used in a playback experiment to stimulate begging behavior in cow

52 We tested this in a vocal playback experiment utilizing highly affective vocal seq

53 We conducted a playback experiment with male cuckoos, broadcasting ten

54 Using playback experiments and computational modeling we find

55 In playback experiments and natural observations, gelada ma

56 Playback experiments and quantification of species discr

57 We also conducted playback experiments at the airport and a control popula

58 We conducted song playback experiments between 109 related pairs of mostly

59 Playback experiments conducted in the wild indicate that

60 Auditory playback experiments demonstrated that individual neuron

61 Using playback experiments in the absence of natural rainfall

62 esponse to different classes of threats, and playback experiments in the field confirmed that the ala

63 -production mechanism, we conducted acoustic playback experiments in the frogs' natural habitat.

64 Playback experiments indicate that related species' song

65 Recent evidence from acoustic analysis and playback experiments indicates that adult female rhesus

66 Additionally, playback experiments involving original chants (with a p

67 Using playback experiments on African elephants (Loxodonta afr

68 We carried out a series of field playback experiments on females (N = 6) in a habituated

69 Playback experiments on white-faced capuchins (Cebus cap

70 Follow-up playback experiments revealed an asymmetry between the a

71 Companion playback experiments revealed that chickadees detect thi

72 Our playback experiments revealed that hyrax males tend to r

73 Playback experiments show that the two Siberian forms do

74 These playback experiments showed that female preference indic

75 Using playback experiments simulating territorial intrusions b

76 ral data combined with 40 contemporary sound playback experiments to 14 allied males, recording respo

77 Here, we use playback experiments to examine how social context influ

78 We now use controlled playback experiments to investigate whether family group

79 Here, we used playback experiments to investigate whether wild jackdaw

80 Here we used playback experiments to present free-ranging male koalas

81 used a series of habituation-dishabituation playback experiments to test whether tamarins attend to

82 In playback experiments using a robotic model frog and an e

83 Eight-speaker playback experiments were used to demonstrate that dista

84 Here, we present the results of playback experiments with wild Diana monkeys, a species

85 th of a close relative, and responses during playback experiments), suggesting that females who manif

86 In playback experiments, baboons respond more strongly to c

87 omatic identification of anomalous sounds in playback experiments, providing a potential route for re

88 In 3 field playback experiments, the authors found evidence for 5 r

89 ral observations, and a series of controlled playback experiments, we demonstrate that this species u

90 neous chemical sampling and captive-elephant playback experiments, we have discovered that young, soc

91 Control "playback" experiments demonstrated that differences in n

92 ips played at standard speed as too fast, so playback had to be slowed down in order for it to appear

93 viewing fast-forward videos for 30 seconds, playback had to be speeded up in order to appear natural

94 we examined the intelligibility of auditory playbacks (i.e., "sonifications") of brainstem potential

95 ere both modulated by speaking compared with playback in a subset of STG contacts.

96 sponse, in one of the few examples of direct playback in social insects.

97 y in Area X also decreased responses to song playback in the cortical output nucleus of the BG loop,

98 xperiments, passive acoustic monitoring, and playback in the field.

99 le swarms with artificial female swarm audio playback indicate that frequency differences of approxim

100 did not respond more strongly to infidelity playbacks, indicating that jackdaws may not attend and/o

101 production of imitations by adult males and playback-induced calling by young birds during the sensi

102 ounds during vocalization (talk) and passive playback (listen) were compared to assess the degree of

103 During song playback, local interactions, including inhibition onto

104 reduced the population growth rate (predator playback mean lambda = 0.91, 95% CI = 0.80 to 1.04; nonp

105 Sensory neural responses to song playback mirror motor-related activity recorded during s

106 hanges in the audio component more often led playback mothers to change responses.

107 Thus, playback mothers used vocalizations as cues as the infan

108 Playback mothers' responses to the episodes were consist

109 Playback of 2-stroke engines had the greatest effect on

110 lso show that some of rats' responses to the playback of 44-kHz calls were more akin to that of avers

111 ith multiple microelectrodes during repeated playback of a conspecific song, followed by further play

112 r to recall testing and involved the passive playback of a small number of movements, which were spre

113 red by ventricular sensing mode triggered by playback of an FM tape previously recorded from the righ

114 wered emission rates when hearing artificial playback of another bat's calls.

115 roduced ultrasound to tactile stimulation or playback of bat echolocation attack.

116 across the globe, assaying moth response to playback of bat echolocation.

117 a differential topographic responsiveness to playback of bird's own song, tutor song, conspecific son

118 , HVC-projecting NIf neurons fire throughout playback of BOS as well as non-BOS stimuli.

119 Petrels (Hydrobates pelagicus), attracted to playback of conspecific calls during their northwards mi

120 Playback of electric signaling patterns recorded from fr

121 tammetry, freely moving rats were exposed to playback of four acoustic stimuli via an ultrasonic spea

122 x-week field experiment, we demonstrate that playback of healthy reef sound can increase fish settlem

123 n of digital coronary angiograms facilitates playback of images and decreases cost.

124 We demonstrated that the playback of killer whale sounds to pilot whales induced

125 ease and usually decreased DA release, while playback of mating sequences evoked the opposite neuroch

126 Both playback of motorboat noise and direct disturbance by mo

127 for a neuronal correlate for syntax, we used playback of natural and temporally destructured complex

128 laboratory experiment determined whether the playback of noise from motorboats powered by two- or fou

129 neurons often generate action potentials to playback of only a single song type, even though synapti

130 ic inputs on these cells can be activated by playback of other song types in the bird's repertoire an

131 Fish exposed long-term to playback of pile-driving noise also no longer responded

132 We recorded responses to auditory playback of pseudorandomly sequenced syllables from the

133 h harbours), rather than control conditions (playback of recordings from the same harbours without sh

134 uilla anguilla) exposed to additional noise (playback of recordings of ships passing through harbours

135 epetitions; and neural responses to auditory playback of repeated syllable sequences gradually adapt

136 In male mice, playback of restraint vocalizations increased ACh releas

137 noise also no longer responded to short-term playback of seismic noise.

138 finch sensory-motor area HVC in response to playback of sequences from individuals' songs, and exami

139 ng and structure of activity elicited by the playback of song during sleep matches activity during da

140 Our data highlighted that the playback of sounds produced by sea turtles was associate

141 orally sparse bursts of action potentials to playback of the bird's own song (BOS) but are essentiall

142 g selective, firing more to forward auditory playback of the bird's own song (BOS) than to reverse BO

143 zations as well as excitation were evoked by playback of the bird's own song, a stimulus that potentl

144 of awake birds also responded selectively to playback of the bird's own song, but neural activity dur

145 male zebra finches responded selectively to playback of the bird's own song, like neurons in its ups

146 during singing and auditory activity during playback of the bird's own song.

147 cing in which the pacemaker was triggered by playback of the FM tape recording of the right ventricul

148 recorded when subjects passively listened to playback of their own pitch-shifted vocalizations.

149 compared with when subjects listened to the playback of their own voice.

150 k of a conspecific song, followed by further playback of this test song in different interleaved sequ

151 white shark, Carcharodon carcharias) to the playback of two distinct sound stimuli in the wild: an o

152 Studies using playback of USV sequences have used randomly selected se

153 ynamic bimodal stimuli in which the acoustic playback of vocalizations is coupled with vocal sac puls

154 Earlier research had shown that initial playbacks of a novel song transiently increase the ZENK

155 aring nature of the call combination, we use playbacks of artificially-constructed call combinations

156 non better, we studied zebra finches hearing playbacks of birdsong.

157 eover, elephants differentially responded to playbacks of calls originally addressed to them relative

158 undulatus) were stimulated to vocalize with playbacks of conspecific vocalizations (warbles), and th

159 vior of a native large carnivore, presenting playbacks of dog vocalizations to pumas in central Calif

160 eding seasons by intermittently broadcasting playbacks of either predator or nonpredator vocalization

161 using automated camera-speakers broadcasting playbacks of humans, dogs, or non-predator controls (bir

162 erholes during the dry season that broadcast playbacks of humans, lions, hunting sounds (dogs, gunsho

163 ral regularity and preferentially approached playbacks of intact over rhythmically irregular versions

164 To address this hypothesis, we conducted playbacks of killer whale vocalizations recorded during

165 ded with lower levels of arousal behavior to playbacks of long calls from current mates and from sepa

166 unching and investigative smelling following playbacks of Maasai voices.

167 hat the calls of a predator were followed by playbacks of male or female alarms with a matching or mi

168 towards and spent more time in proximity to playbacks of male vocal sequences containing one of the

169 However, fish exposed to playbacks of pile-driving or seismic noise for 12 weeks

170 , in response to impulsive additional noise (playbacks of recordings of pile-driving and seismic surv

171 o a more continuous additional noise source (playbacks of recordings of ship passes).

172 Scallop larvae exposed to playbacks of seismic pulses showed significant developme

173 Then, we paired playbacks of signature whistles of known animals with ur

174 that landed more often on nest boxes during playbacks of spring song compared to fall song, and the

175 heir natural environment were presented with playbacks of synthetic signals, resembling their species

176 d a novel technique that combines the use of playbacks of territorial vocalizations with traditional

177 thers to high-density cues, accomplished via playbacks of territorial vocalizations, led to increased

178 Playbacks of the jamming call, but not of control sounds

179 model and pupil songs, we discovered that 40 playbacks of the song motif per day, lasting a total of

180 ere presented with 'infidelity simulations': playbacks of their male partner copulating with a neighb

181 t macaques' flight and scanning responses to playbacks of their own alarm vocalizations were compared

182 ations were compared with their responses to playbacks of vocalizations of Nilgiri langurs (Trachypit

183 irds were either tutored using tape-recorded playback or housed with adult conspecific tutors.

184 utilized a pitch shift self-vocalization and playback paradigm to investigate the underlying neural m

185 Using a video playback paradigm, we found that juvenile birds that rec

186 of offspring survival, resulting in predator playback parents producing 53% fewer recruits to the adu

187 es were allowed to hear different numbers of playbacks per day.

188 Modifying AVAS sounds with playback rate and level changes with respect to operatio

189 at-noise playback, compared to ambient-noise playback, reduced successful development of embryos by 2

190 We used a playback regimen to examine the roles of acoustic and no

191 stimulus neural activity induced by sequence playback resembled the neural response to the next sylla

192 s in freely behaving control rats exposed to playback showed enhanced theta activity in the BLA, whic

193 Consistent with this, playbacks showed that maternal care was stronger in resp

194 Males that sang in response to the playbacks showed, in addition to auditory areas, increas

195 rs reacted most strongly to mobbing sequence playbacks, showing a greater attentiveness and a quicker

196 First, we used natural and playback-simulated foraging displacements to demonstrate

197 time bellowing when they were presented with playbacks simulating larger rivals.

198 nt levels of proximal orientation toward the playback speaker.

199 e accelerations were observed in response to playback stimuli involving conspecific vocalizations com

200 ificantly slower to respond to this class of playback stimuli than they were to bellows simulating sm

201 aptive dolphin (Tursiops truncatus) to sound playback stimuli.

202 Here, the authors describe playback studies on the alarm call system of two colobin

203 llidal units were distinctly excited by song playback, suggesting an increase in GABAergic transmissi

204 ay show increased firing in response to song playback, suggesting largely excitatory connections amon

205 nd toward increased aggression during visual playbacks suggests that the visual component of tremulat

206 licits significant dishabituation within the playback, supporting the habituation hypothesis as an ev

207 hnique shows potential to replace the manual playback test, a potentially destructive technique, ulti

208 During playback tests of SDC and INC songs, SD females gave mor

209 Playback tests to young naive birds before they even beg

210 Playback tests were used to assess the effects of substr

211 to control/low treatments, during high noise playbacks the mother's proportion of time resting decrea

212 quantified the neurogenetic response to song playback through immediate early gene (IEG) expression i

213 We used song playback to demonstrate that counter-singing can most ro

214 We used video playback to manipulate social information about novel ap

215 We recorded mating calls and used playback trials to gauge preference for different chorus

216 By using playback trials with the predatory electric eel (Electro

217 cellular physiology, optogenetics, and sound playback, we also found that directly activating M2 axon

218 erimental manipulations with robotic lizard "playbacks," we show that free-living territorial Anolis

219 e magnitudes of these effects during initial playback were significantly correlated.

220 , patterns of ACh and DA release with mating playback were similar to males.

221 Young males heard a brief song playback when they pecked at a key, but different males

222 a method, recordings are put at risk during playback, which is the current method for identifying de

223 Experimental playbacks with a biorobotic squirrel model reveal this s

224 Males and females preferred chorus playbacks with low variance in dominant frequency.

225 By performing playbacks with natural and modified vocalizations, we sh