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1  animal traits that do not primarily rely on acoustics.
2 g high-powered comparative analyses of vocal acoustics.
3  vocalizer which they perceived in the voice acoustics.
4  circular cross-sectional microchannel under acoustic actuation.
5 is challenge, and experimentally realize the acoustic analogue of a quantized octupole topological in
6                                              Acoustic analyses and evolutionary reconstructions show
7 electrical stimulation that are analogous to acoustic and cellular stimulation in the natural cochlea
8 part of the effort to realize flat lenses in acoustic and elastic regimes.
9 ale morphs and females with a focus on vocal-acoustic and neuroendocrine networks.
10 truction of an entire manifold of low-energy acoustic and optic branches across a structural transiti
11  we evidence phonon anti-crossings involving acoustic and optical branches, yielding significant tran
12 larity between tones with the predictions of acoustic and perceptual models, we observed a temporal e
13 lanation for the behavioural dissociation of acoustic and visual speech comprehension and suggest tha
14 ng and communication degradation in terms of acoustic attenuation, dispersion and temporal decorrelat
15 uses shell-stabilized gas bubbles to provide acoustic backscatter in vasculature.
16 al applications for soft tissue imaging, the acoustic beams can also be used for sensing and actuatio
17 ales and provides novel information on their acoustic behaviour in a mid-Atlantic region.
18 present an analytical study on generation of acoustic-Brownian noise in nuclear magnetic resonance (N
19        This study investigates the nature of acoustic category representations, their emergence in an
20 gh yields using an innovative and proficient acoustic cavitation technology and well characterized us
21                                 By combining acoustic-cavitation-sensitive liposomes with radiopharma
22  of a microwave-frequency, nanoscale silicon acoustic cavity incorporating a phononic bandgap acousti
23 associations between response likelihood and acoustic characteristics.
24 idence for serotonin as a modulator of vocal-acoustic circuitry and behavior in midshipman fish, cons
25                      We show that origins of acoustic communication are significantly associated with
26              However, how species relying on acoustic communication differ in their adjustments to an
27                                 We find that acoustic communication does not increase diversification
28                        Finally, we find that acoustic communication evolved independently in most maj
29 l fundamental questions about the origins of acoustic communication in terrestrial vertebrates (tetra
30 iced sound production is the primary form of acoustic communication in terrestrial vertebrates, parti
31                                              Acoustic communication in the form of courtship and mati
32     We also demonstrate that the presence of acoustic communication is strongly conserved over time.
33                             In many species, acoustic communication plays a crucial role to maintain
34  and hormonal mechanisms of vertebrate vocal-acoustic communication, to redefine raphe subgroups base
35 ification rates in those lineages with known acoustic communication.
36                           The tight vertical acoustic confinement releases the lateral design of free
37 higher frequencies by overcoming coupling to acoustic contour modes of the chip.
38 n response to achieve coherent and low-power acoustic control of a single SiV spin, and perform acous
39               Type I males mate using either acoustic courtship to attract females to enter a nest th
40 sal evidence that the functional role of the acoustic cues in the listener's native language affects
41 ng are determined by the functional roles of acoustic cues in the listener's native language.SIGNIFIC
42 ng of speech sounds is affected by low-level acoustic cues, but also by their linguistic function.
43 izations) indicate that increases in social (acoustic) cues of density in the absence of additional f
44 ts to unlock previously hidden insights from acoustic data and offers promise as a backbone technolog
45                                              Acoustic data demonstrate that small dolphins consistent
46  song types was examined over decades, using acoustic data from several different sources in the east
47 ating of automated detections from extensive acoustic datasets.
48 eby reducing group temporal availability for acoustic detection by killer whales to <25%.
49     Past reports have hypothesized a role of acoustic detection in backward strike behavior [4, 5, 8]
50           This study offers new prospects in acoustic detection with potential use in real-world diag
51 d be addressed through the use of a magnetic-acoustic device (MAD) combining a magnetic array and ult
52  in graded materials, and the development of acoustic devices.
53                      We reveal how different acoustic dimensions, specifically echo intensity and son
54 oupled with high temporal resolution in situ acoustic doppler current profile measurements at seven s
55 ombined to modulate fusiform cell output and acoustic-driven responses.
56 interface (OPI) was combined with a modified acoustic droplet ejection (ADE) system.
57 nalysis of polar compounds using a prototype acoustic ejection mass spectrometer (AEMS) platform.
58                                We present an acoustic ejection mass spectrometry (AEMS) setup for con
59                                              Acoustic ejection mass spectrometry is a recently develo
60 onant system, and hence store a (mechanical, acoustic, electronic, optical, or of any other nature) w
61 unicative behavior that consists of discrete acoustic elements ("syllables") that are sequenced in a
62 s (1045/1071) reached a pre-defined level of acoustic emission, while the probability of wideband emi
63 With feedback control based on recordings of acoustic emissions, 98% of the sonication targets (1045/
64 d with respect to their ability to dissipate acoustic energy at the level of a single molecule/partic
65 g (AL) occurs by exposing mosquito larvae to acoustic energy that ruptures their dorsal tracheal trun
66 poradically reoccurring structure within the acoustic environment.
67 intrinsic firing patterns in response to the acoustic environment.
68 ), to separating different sounds in complex acoustic environments, and to music enjoyment.
69 ls modify short-term depression in different acoustic environments, which raises the question of what
70 ure waveforms, and power spectra within each acoustic event.
71  In primary auditory cortex, slowly repeated acoustic events are represented temporally by the stimul
72        The ability to visualize and annotate acoustic events efficiently can enhance scientific insig
73 ogy to detect and to identify highly similar acoustic events with high spatial resolution and high ac
74  low-frequency phase, predicts the timing of acoustic events.
75                                    They lack acoustic-evoked behavioral responses, vestibular-induced
76 e MSO are similarly affected by the onset of acoustic experience is unresolved.
77          We demonstrate with both theory and acoustic experiments an "exceptional nexus" (EX), which
78 ocially-relevant signals via detection of an acoustic feature that is ubiquitous in vocalizations.
79 atch socially appropriate vocal responses to acoustic features of male and female calls.
80 s suggests that the auditory cortex recovers acoustic features that are masked in the mixture, even i
81 mation, they produce calls with intermediate acoustic features, suggesting a more generic alarm signa
82 on and prosody, which are mainly captured by acoustic features.
83 e translated into force profiles and thereby acoustic features.
84 e translated into force profiles and thereby acoustic features.
85 rical membership of sounds rather than their acoustic features.
86 nd effectively coupled into remote meta-skin acoustic fibers from free space, which is technologicall
87 ic expressions provide the statistics of the acoustic field after forward propagating through an ocea
88 h exhibit a stronger response to the applied acoustic field and are also used for ultrasound-triggere
89 robubbles and activation with an independent acoustic field to trigger the release of the nanoparticl
90 igning the channel that results in a desired acoustic field, however, is a non-trivial task.
91 tructive effects on cells due to the applied acoustic field, in addition to other produced secondary
92                 To rapidly generate designed acoustic fields from microchannel elements we utilize a
93 oustic waves can generate spatially variable acoustic fields, opening the possibility that the channe
94 ork we utilize this approach to create novel acoustic fields.
95 DNN) that is trained on images of pre-solved acoustic fields.
96                    Music is characterized by acoustic forms that are predictive of its behavioural fu
97 ibrary generation uses enzymatic rather than acoustic fragmentation to generate WGA-free whole-genome
98 g to cochlear amplification at the very high acoustic frequencies processed by some mammals.
99 lve two objects down to 2.1lambda within the acoustic Fresnel zone.
100 sonator, we realized single, nanometer-scale acoustic graphene plasmon cavities, reaching mode volume
101 mation alone (N = 2), but not with visual or acoustic information alone (N = 1).
102 tor in the brain, influences the encoding of acoustic information by the medial nucleus of trapezoid
103 ut with differential sensitivity to specific acoustic information contained in the speech signal.
104 eptors of the mammalian cochlea, transducing acoustic information into electrical signals that are re
105                                              Acoustic information is conveyed to MNTB neurons through
106 cumulative exposure bias the encoding of the acoustic information, but do so distinctly.
107 rocess within honeybee colonies, using vibro-acoustic information.
108        This work illuminates the fundamental acoustic infrastructure-both architecture and function-f
109 ttenuation potential outperforms the perfect acoustic insulation provided by a fully shut single-glaz
110 in auditory and lateral line areas and vocal-acoustic integration sites in the preoptic area and vent
111                                              Acoustics is the primary means of sensing and communicat
112 al., 2018), and are known to be modulated by acoustic landmarks and speech intelligibility (Doelling
113                                              Acoustic larviciding (AL) occurs by exposing mosquito la
114    In this paper, a newly designed composite acoustic lens that can achieve wave convergence is propo
115       Recently, focusing systems composed of acoustic lenses have been found to offer high controllab
116  upon the focusing capability of traditional acoustic lenses while retaining their advantages in term
117 tion, multiunit coherence, phased arrays and acoustic lenses, can be used to manipulate and focus sou
118          The simplest and most commonly used acoustic levitator is comprised of a transmitter and an
119 chemically distinct droplets suspended in an acoustic levitator is reported.
120 um levels recorded by two land-based passive acoustic listening stations (PALS) deployed in Sarasota
121 erpreted on the basis of a steep increase in acoustic loss immediately below the the Pc-P1 transition
122 cal predictions are confirmed with available acoustic measurements in several continental-shelf envir
123 is work, we show how a customised reflective acoustic metamaterial enables the levitation of multiple
124 ncept is demonstrated for a holey-structured acoustic metamaterial in water at 200-300 kHz, via both
125 ological implementation seen in this evolved acoustic metamaterial reveals enticing ways to design hi
126 amaterials are rare in nature and no natural acoustic metamaterials are known.
127                                              Acoustic metamaterials constructed from conventional bas
128 ve-manufacturing for realising polymer-based acoustic metamaterials in water at ultrasonic frequencie
129                                              Acoustic metamaterials with artificial microstructures a
130                     Here, a superhydrophobic acoustic metasurface of microstructured poly(vinylidene
131                                      Passive acoustic methods provide continuous monitoring of sonife
132 d elastic lift force, arising from symmetric acoustic microstreaming flows around each pillar uniform
133 s new processing technique employed resonant acoustic mixing to coat an equiatomic NiCoCr powder with
134 killed at listening to one speaker out of an acoustic mixture of several speech sources.
135 hanical cavity, simultaneously isolating the acoustic mode of interest in the bandgap while allowing
136                                 Longitudinal acoustic mode Raman spectroscopy provides a complementar
137 We trace these disparities to the underlying acoustic models used by the ASR systems as the race gap
138 oupling of the low energy optical modes with acoustic modes causes damping of heat carrying acoustic
139  50 y ago, of the hybridization of polar and acoustic modes in quantum paraelectrics, in contrast to
140                                 However, the acoustic modulations required to do this are extremely b
141 pulation-level acoustic presence via passive acoustic monitoring [11], detection of the life history
142                                      Passive acoustic monitoring has become an important data collect
143                                      Passive acoustic monitoring is an efficient tool to study tempor
144 dividual behavior and continuous broad-scale acoustic monitoring of regional song production (Figure
145           In this study, we utilized passive acoustic monitoring to characterize the response of bott
146 has recently been modified and coupled to an acoustic nanoliter dispenser to enable high-speed direct
147 irements for power and cooling, and reducing acoustic noise.
148 ion of fibers, especially in brainstem vocal-acoustic nuclei and other sensory integration sites that
149                                  A decade of acoustic observations have shown important distributiona
150      Similar to NARWs, sei whales had higher acoustic occurrence in mid-Atlantic regions after 2010.
151 ce of low energy optical phonons, and strong acoustic-optical phonon coupling results in an intrinsic
152             Fibers with optical, electrical, acoustic, or optoelectronic functionalities can be produ
153 nthetic monopoles, achievable in mechanical, acoustic, or ultracold atomic systems, and even with ele
154                                              Acoustic orientation and bunching methods, which include
155                                              Acoustic overexposure, such as listening to loud music t
156                           Moderate levels of acoustic overstimulation associated with tinnitus and im
157                                      Varying acoustic parameters (pulse repetition frequency, duty cy
158 logical validity, especially when the target acoustic parameters vary naturally with other parameters
159 to investigate the origins of wave velocity, acoustic paths, dispersion, and attenuation.
160         This simulation involving the use of acoustic patterns was performed with a neural network th
161 s of memory formation for rarely reoccurring acoustic patterns.
162                               The space-time acoustic phased array enables unprecedented control over
163  of syntactic information but not to sustain acoustic/phonemic processing.
164 om a QCL device, whereby optically-generated acoustic phonon pulses are used to perturb the QCL bands
165 formation storage and processing by coupling acoustic phonon sources with superconducting or spin qub
166                         Since the transverse acoustic phonons are almost fully scattered by the compo
167 p-probe method that uses optically generated acoustic phonons is expanding standard optical character
168 oustic modes causes damping of heat carrying acoustic phonons to ultrasoft frequency (maximum ~37 cm(
169 at is mainly transported by the longitudinal acoustic phonons.
170              By digital regulation of pulsed acoustic power from a low level to high levels, the hund
171 s a striking similarity with the increase in acoustic power observed prior to laboratory slow slip ev
172                   Overall, using exclusively acoustic powering to position and actuate microbubbles p
173 ARs) to investigate the temporal patterns in acoustic presence and foraging activity of oceanic dolph
174  Sei whales showed a bimodal distribution of acoustic presence in spring and autumn, corresponding to
175                      This study assesses the acoustic presence of humpback (Megaptera novaeangliae),
176 via bio-logging [9, 10] and population-level acoustic presence via passive acoustic monitoring [11],
177 ason." With the exception of 2009-2010, when acoustic presence was unusually low, the mean percent of
178 for transmitting vibrations originating from acoustic pressure and active outer hair cell force to th
179                                  Keeping the acoustic pressure at levels where no such sign of microb
180                  The external stimulation is acoustic pressures mediated by the scala fluids, whereas
181 finity microbubble concentrations at various acoustic pressures.
182 (Optimum Duration and Dose of r-tPA With the Acoustic Pulse Thrombolysis Procedure for Intermediate-R
183     We show that the human voice has complex acoustic qualities that are directly coupled to peripher
184 is an elasticity imaging technique that uses acoustic radiation force to evaluate the localized mecha
185                         Given the scaling of acoustic radiation forces and acoustic streaming flow ve
186        A number of physical arrangements for acoustic rainbow sensors have been suggested, where the
187                      In the inner ear, these acoustic receptors are primarily attached to an overlyin
188 inear phased array is no longer bound by the acoustic reciprocity, and supports asymmetric transmissi
189         We deployed bottom-moored Ecological Acoustic Recorders (EARs) to investigate the temporal pa
190  critical paraelectric, and hybridized polar-acoustic regimes.
191 e probed nicotinic cholinergic influences on acoustic responses of MNTB neurons from adult gerbils (M
192 quantitative results is presented to address acoustic ringing that is often associated with high-sens
193             The TOs appear necessary for the acoustic rupture of DTTs; this constriction prevents the
194 on a multi-method approach based on optical, acoustic, satellite remote sensing, and simulations, to
195 ference (ITD) statistics inherent in natural acoustic scenes are parameters determining spatial discr
196       The mammalian cochlea possesses unique acoustic sensitivity due to a mechanoelectrical 'amplifi
197 source, at or above 60 dB SPL, and that this acoustic sensitivity is sufficient to trigger backward s
198                                         MEMS acoustic sensors have been developed to mimic the highly
199 s are incorporated as the active material in acoustic sensors.
200 stic cavity incorporating a phononic bandgap acoustic shield.
201 pid, context-dependent changes in visual and acoustic signal design.
202                                         This acoustic signal is processed in the frequency-domain to
203 uously-varying spectrotemporal cues from the acoustic signal to perceive discrete phonetic categories
204 erstanding how signals are generated and how acoustic signals are perceived is key to understanding t
205                          We quantify how the acoustic signals decorrelate over timescales determined
206                 Ph. argentipes males produce acoustic signals during copulation and two types of song
207 the breast and water tank to investigate the acoustic signals generated by disk-shaped implants when
208  Sexual selection appears to have shaped the acoustic signals of diverse species, including humans.
209  grain dissolves, the pockets burst and emit acoustic signals that are detected by distributed sets o
210  we quantified differences in adjustments of acoustic signals to anthropogenic noise among species.
211 -controlled body functions through visual or acoustic signals to manage conditions like anxiety and h
212 s exploit social defences or produce cryptic acoustic signals, deep-diving beaked whales, well known
213 ch for the continuous measurement of mechano-acoustic signals, from subtle vibrations of the skin at
214                     During these encounters, acoustic signals, used at both short and long ranges, pl
215 tify people and specific events that produce acoustic signals.
216 on for which subjects could discriminate the acoustic signals.
217  relationships by exchanging information via acoustic signals.
218 ognizing events and human identities through acoustic signals.
219 l song production (Figure 1A) to identify an acoustic signature of the transition from foraging to mi
220 rties vary among birds in lawful relation to acoustic similarity of the birds' songs, with adult sibl
221 at the echolocating big brown bat integrates acoustic snapshots over time to build prediction models
222 us perception of sound in the absence of any acoustic source.
223 alisation time intervals and distances in an acoustic space defined by mean pitch and mean amplitude,
224 ted the hypothesis that infants search in an acoustic space for vocalisations that elicit adult utter
225 ongbird responsively exploited newly emptied acoustic space.
226 g of drumming structure within a constrained acoustic space.
227 et, it remains unclear in how far visual and acoustic speech comprehension are mediated by the same b
228 tion are those that are used to generate the acoustic speech signal.
229                                              Acoustic standing wave devices offer excellent potential
230  a startling stimulus), and the effect of an acoustic startle cue on MEPs elicited by cervicomedullar
231  evidence for a conserved neural pathway for acoustic startle modulation between humans and rodents.
232  dysregulated inhibition in vitro as well as acoustic startle reflex and social interaction in vivo o
233  Moreover, we conducted behavioral assays of acoustic stimulation that confirm acoustic triggering of
234                                     However, acoustic stimulation using higher frequency sounds did n
235 neurophysiological recordings in response to acoustic stimulation, both from sound-sensitive areas in
236 ostatic changes with increased and decreased acoustic stimulation.
237 trical responses of the mammalian cochlea to acoustic stimuli are nonlinear and highly tuned in frequ
238  activity in 435 neuronal clusters evoked by acoustic stimuli in the perirhinal cortex (PRC) and in A
239  responses to the temporal fine structure of acoustic stimuli is important for many aspects of hearin
240 uild internal prediction models from dynamic acoustic stimuli to anticipate the future location of mo
241               IHCs are involved in conveying acoustic stimuli to the CNS, while OHCs are implicated i
242  responses to the temporal fine structure of acoustic stimuli, a hallmark of the auditory system's te
243 ture deficits, and a failure to habituate to acoustic stimuli, are replicated by short-term treatment
244 uding abnormal evoked responses to light and acoustic stimuli, prey-capture deficits, and a failure t
245 cochlear mechanics to modulate perception of acoustic stimuli.
246 d selectivity of neural responses to complex acoustic stimuli.
247  can generate complementary neural codes for acoustic stimuli.
248 n of multiple robots in response to a common acoustic stimulus is developed.
249 illiseconds following the termination of the acoustic stimulus.
250 tion of different frequency components of an acoustic stimulus.
251                                    Providing acoustic streaming electrolyte flow during charging, the
252 the scaling of acoustic radiation forces and acoustic streaming flow velocities with increasing frequ
253 enon is attributed to a collective effect of acoustic streaming induced drag force and non-Newtonian
254 the heat-carrying long-wavelength transverse acoustic (TA) phonons coexist with the ultrafast diffusi
255 chlings were actively tracked with miniature acoustic tags off the east coast of Costa Rica for 83.15
256  compensate for these changes to achieve its acoustic targets.
257  the inhomogeneities' motion further reduces acoustic temporal coherence, and becomes important at th
258      While introduced here in the context of acoustics, this approach can also be extended to optical
259  use audiovisual correlations rooted in oral acoustics to extract detailed spectrotemporal informatio
260        We show that the non-linearity in the acoustic transformation plays a critical role in feature
261 antify and separate the contributions of the acoustic transformations and the neuromorphic hardware t
262 rically quantify the impact of the different acoustic transformations for neuromorphic hardware based
263                           This task requires acoustic transformations from sound waveforms with varyi
264                           We presented short acoustic transients to noninvasively estimate the dynami
265 validated by the absolute calibration of the acoustic trapping force and the direct spatial mapping o
266             However, the unique potential of acoustic trapping to be applied in biomedical settings r
267                                          The acoustic trauma also reduced capillary density and incre
268                                              Acoustic trauma disrupts cochlear blood flow and damages
269   Damage and regression of capillaries after acoustic trauma have long been observed, but the underly
270 improves sound discrimination, and mitigates acoustic trauma.
271  frequency tuning, and protects the ear from acoustic trauma.
272 nterpoint to this view, we present a general acoustic treatment of the horn-like geometry of the coch
273  assays of acoustic stimulation that confirm acoustic triggering of backward net-casting by frequenci
274 al studies provide no information about what acoustic variables indicate about the speaker-that is, w
275    We assessed the relative contributions of acoustic versus melodic components of the music to the n
276 e quantified startle behavior in response to acoustic/vibrational stimuli.
277 ls (the outer hair cells) in response to the acoustic vibrations.
278 r relatively low frequency phenomena such as acoustics, water waves and microwaves.
279  carried in a potential minimum of a surface acoustic wave (SAW) and is transported to a region of ho
280 ogies is based on the development of surface acoustic wave (SAW) flexible biosensors, which are highl
281         Mixing is provided by way of surface acoustic wave excitation; this high-frequency vibration
282                             We show that the acoustic wave generated by FOC can directly activate ind
283 t corona discharge (CD) coupled to a surface acoustic wave nebulization (SAWN) device enhanced sampli
284 n is realized by exciting high-overtone bulk acoustic wave resonances (HBAR) in the photonic stack.
285  The multi-mode composite high-overtone bulk acoustic wave resonator (HBAR) is a popular phonon sourc
286 understood about how the brain transforms an acoustic waveform into the complex perceptual structure
287                   In tonal music, continuous acoustic waveforms are mapped onto discrete, hierarchica
288 n be readily realized in an air environment, acoustic waveguiding in an underwater environment remain
289 roparticles and cells in paper using surface acoustic waves (SAW).
290 ical and/or electrical cable communications, acoustic waves can be simply and effectively coupled int
291                                              Acoustic waves can be used to accurately position cells
292 fluidic channel walls and travelling surface acoustic waves can generate spatially variable acoustic
293 ta-skin" insulator, which is able to confine acoustic waves in an all-angle and wide spectrum range d
294   The critical keyhole instability generates acoustic waves in the melt pool that provide additional
295 re has good focusing intensity and can focus acoustic waves over a wide range of incidence angles wit
296 erapy (PDT) by the use of highly penetrating acoustic waves to activate a class of sound-responsive m
297 bits that couple to short-wavelength surface acoustic waves(4-10), probing the properties of the atom
298 for valley states, robust routing of surface acoustic waves, and spatial modulation of group velociti
299                   We also show that the same acoustic waves, used to create the nanolenses, can mitig
300  by combining paper-based microfluidics with acoustics, we present a rapid and powerful method to siz

 
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