Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
919
datasets available to search
ShareScore release 0.9.0
Dataset results
919 results for “Hearing”
FIGS. 77–84 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 77–84. Chaetotaxy and middle bladder: 77, slender hook of Oligotoma saundersi (Oligotomidae); 78, slender hook of Archembia lacombea (Archembiidae); 79, middle bladder with sculpture on Archembia lacombea (Archembiidae); 80, middle bladder with few microtrichia of Gibocercus chaco (Archembiidae); 81, middle bladder without sculpture or michrotrichia Pachylembia unicincta (Archembiidae); 82, small middle bladder with microtrichia Pararhagadochir trachelia (Archembiidae); 83, mechanoreceptor on middle bladder Antipaluria urichi (Clothodidae); 84, detail of mechanoreceptor (circle in fig. 83) on middle bladder of Antipaluria urichi (Clothodidae).
FIGS. 85–90 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 85–90. Apical bladder of hind tarsus midsegment: 85, Clothoda longicauda (Clothodidae) left leg; 86, Notoligotoma hardyi (Notoligotomidae) right leg; 87, Gibocercus chaco (Archembiidae) left leg; 88, Dihybocercus femorata (Embiidae) right leg; 89, Oligotoma saundersii (Oligotomidae) left leg; 90, Teratembia geniculata (Teratembiidae) right leg.
FIGS. 71–76 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 71–76. Chaetotaxy of hind basitarsus: 71, broad setae of Antipaluria urichi (Clothodidae); 72, broad setae of Clothoda longicauda (Clothodidae); 73, jagged setae of Chelicerca barbara (Anisembiidae); 74, jagged setae of Saussurembia calypso (Anisembiidae); 75, serrate hairs on lateroapical surface of Clothoda longicauda (Clothodidae); 76, three-pronged setae on lateroapical surface of Dihybocercus femorata (Embiidae); an enlarged section of this type of setae is shown in the adjacent circle.
FIGS. 63–70 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 63–70. Hind tarsus, ventral view: 63, broad setae in Antipaluria caribbeana (Clothodidae) left leg; 64, broad setae in Australembia incompta (Australembiidae) left leg; 65, jagged setae in Chelicerca barbara (Anisembiidae) left leg: an enlarged section of this seta is shown in the adjacent circle; 66, broad setae in Notoligotoma hardy (Notoligotomidae) right leg; 67, broad setae in Dihybocercus femorata (Embiidae) right leg; 68, broad setae in Gibocercus chaco (Archembiidae) left leg; 69, broad setae in Oligotoma saundersii (Oligotomidae) left leg; 70, jagged setae in Teratembia geniculata (Teratembiidae) right leg.
FIGS. 57–62 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 57–62. Comb setae on ventral surface of foretarsus basal segment: 57, Clothoda longicauda (Clothodidae); 58, Haploembia solieri (Oligotomidae); 59, Oligotoma saundersii (Oligotomidae); 60, Pararhagadochir trachelia (Archembiidae); 61, Saussurembia calypso (Anisembiidae); 62, Gibocercus chaco (Archembiidae).
FIG. 52 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIG. 52. Optimization of the silk ejectors length: state 0, short as in Embiidae (less than 80 μm); state 1, long (more than 100 μm).
FIGS. 45–50 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 45–50. Ventral view of basal segment of foretarsus: 45, Australembia incompta (Australembiidae) left leg; 46, Saussurembia calypso (Anisembiidae) left leg; 47, Notoligotoma hardy (Notoligotomidae) right leg; 48, Pararhagadochir trachelia (Archembiidae) right leg; 49, Embia ramburi (Embiidae) right leg; 50, Teratembia geniculata (Teratembiidae) right leg.
FIGS. 30–32 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 30–32. Silk ejectors and combs on basal segment of foretarsus: 30, detail of ventral left margin view of Gibocercurs chaco (Archembiidae): A, silk ejector Type I, B, silk ejector Type II, C, comb setae; 31, silk ejector Type I of Oligotoma saundersii (Oligotomidae), slightly curved; 32, silk ejector Type I of Gibocercus chaco, erect and slender.
FIGS. 39-44 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 39-44. Ventral view of basal segment of foretarsus: 39, Haploembia solieri (Oligotomidae), left leg; 40, Clothoda longicauda (Clothodidae), right leg; 41, Antipaluria caribbeana (Clothodidae), left leg; 42, Oligotoma saundersii (Oligotomidae), left leg; 43, Dihybocercus femorata (Embiidae), right leg; 44, Chelicerca barbara (Anisembiidae), left leg.
FIGS. 14–23 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 14–23. Shapes of auditory organ on middle femur: 14, Chelicerca wheeleri (Anisembiidae) right leg; 15, Mesembia chamulae (Anisembiidae) right leg; 16, Teratembia geniculata (Teratembiidae) left leg; 17, Clothoda longicauda (Clothodidae) right leg; 18, Chelicerca barbara (Anisembiidae) left leg; 19, Australembia nodosa (Australembiidae) left leg; 20, Biguembia copo (Archembiidae) left leg; 21, Machadoembia angolica (Embiidae) right leg; 22, Dihybocercus femorata (Embiidae) right leg; 23, Aposthonia indica (Oligotomidae) right leg.
FIG. 29 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIG. 29. Optimization of the shape of tympanal organ in the hind femur: state 0, small and semicircular; state 1, small disk depressed area; state 2, absent.
FIGS. 33–38 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 33–38. Ventral view of midsegment of foretarsus: 33, Saussurembia calypso (Anisembiidae) left leg: A, silk ejector Type I, B, comb setae, C, serrate hairs; 34, Haploembia solieri (Oligotomidae); 35, Notoligotoma nitens (Notoligotomidae); 36, Australembia incompta (Australembiidae) left leg; 37, Pararhagadochir trachelia (Archembiidae); 38, Teratembia geniculata (Teratembiidae).
FIGS. 6–12 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIGS. 6–12. Shapes of auditory organ on forefemur: 6, Chelicerca barbara (Anisembiidae) right leg; 7, C. wheeleri right leg; 8, Machadoembia angolica (Embiidae) right leg; 9, Teratembia geniculata (Teratembiidae) left leg; 10, Australembia nodosa (Australembiidae) right leg; 11, Clothoda longicauda (Clotodidae) left leg; 12, Aposthonia indica (Oligotomidae) right leg.
FIG. 13 in Implications of the tympanal hearing organ and ultrastructure of chaetotaxy for the higher classification of Embioptera
FIG. 13. Optimization of the shape of the forefemora tympanal organ: state 0, semicircular with well-defined edges; state 1, a curved, slender band, elongated along the femoral axis; state 2, a tiny triangle. Arrows (>>>) in some parts of the cladogram represent higher groups, with several species included in the dataset, but the internal resolution of which is not relevant for this level of analysis (hence, for clarity, the groups are collapsed and replaced by the corresponding name).
Perceived sound quality of hearing aids with varying placements of microphone and receiver
<p>This is the raw data for the paper published by the above authors in the American Journal of Audiology in 2022.</p>
Dataset for Personalizing Over-the-Counter Hearing Aids using Pairwise Comparisons
<p>This is the initial release of the dataset.</p>
Bilateral hearing impaired children assessment of horizontal auditory localization accuracy in a virtual visual environment with free head movement
<p>Twenty-two hearing-impaired children (13 males and 9 females, mean age: 10.45 years, standard deviation 3.13 years) participated in an auditory localization experiment in a virtual visual environment. We investigated the contribution of head movements to localization along the interaural plane in absence of motor constraints and visual cues on a virtual scene, experienced by individuals wearing a head-mounted display while listening to stimuli coming from a circular loudspeaker array. Each session included multiple test conditions. In each condition, the stimulus was presented from loudspeaker positions that were randomly balanced across a sequence of 13 x 5 = 65 trials. Each participant performed the task first with both devices turned on ("On-On"), then with one device (either the left or right one) turned on and one off ("On-Off"), and finally with both devices turned off ("Off-Off"). The On-On condition was presented first during each test session because it provided an everyday listening context participants were accustomed to, and consequently confident with. The third condition was omitted if a patient's pure tone average threshold was above the stimulus level used for the test in the frequency range [0.5-4] kHz. Depending on this threshold, nine Bi HA listeners attended also the Off-Off condition. Two Bi HA listeners were unable to attend the On-Off test condition either, since their session had to be stopped as early as they reported annoyance or fatigue to the experimenter. Children were affected by non-syndromic hearing loss ("GEN NO SDR") in 8 cases (6 GJB2 gene mutations, 2 other gene mutations), syndromic hearing loss ("SDR") in 4 (2 Usher syndromes, 1 chromosomal instability, 1 Waardenburg syndrome), and 1 enlarged vestibular aqueduct (inner ear malformation, "IEM"). Other causes of hearing loss ("Other") were congenital cytomegalovirus infection in 2 cases, chemotherapy with platinum derivatives for neuroblastoma in 2, preterm delivery in 1, and prolonged neonatal intensive care unit stay in 1 case. The cause was not identified ("ND") in 3 cases. All participants were right-handed and had no diagnosis of motor impairment. Reported are: the participant's anonymous id ("Participant"), the age ("Age"), the cause of hearing impairment ("MacroCause"), the years of experience with each device ("Experience DX", "Experience SX"), the left and right pure-tone individual hearing thresholds at 500 Hz, 1000 Hz, 2000 Hz, and 4000 Hz, without and with devices ("Threshold w/o 500 DX" is the right threshold at 500 Hz without devices, and the others are named accordingly), the group ("Group", an example is "Bi CI On-Off" identifying the group of listeners with two cochlear implants, one turned on and the other turned off, and the others are named accordingly), the test condition ("Condition", an example is "NOICSX_ICDX", identifying the listening condition with the left cochlear implant turned off and the right cochlear implant turned on, and the others are named accordingly), the target ("Target", angle in sexagesimal degrees), the signed error ("Signed_error", the difference between the target angle and the pointed angle in sexagesimal degrees), the unsigned error ("Unsigned_error", the absolute difference between the target angle and the pointed angle in sexagesimal degrees), the difference between the target and head orientation angle in the moment when the target was hit ("Head_rotation", in sexagesimal degrees), the head covered distance during a single trial ("Head_distance", in meters). Here are presented only sessions including the complete set of 65 trials, except seven sessions attended by Bi-CI listeners, each missing one trial (six in the On-Off condition and one in the On-On condition) that was not recorded due to a technical problem.</p>
Towards a real-world technical test battery for remote microphone systems used with hearing prostheses
<p>Wav format audio files of both source and response for 5 different wireless remote microphone systems under various test conditions, as reported in the paper :</p> <p>Stone M.A., Lough M., Whiston H., Wilbraham K., Dillon H. (2023) Towards a real-world technical test battery for remote microphone systems used with hearing prostheses. Trends in Hearing DOI: 10.1177/23312165231182518</p> <p>Also includes the MATLAB script used to analyse the recordings.</p>
Market Analysis for the creation of an NGO for professional qualification of People with Hearing Impairment
<p>The data set is part of the TCC of the MBA course at USP - University of São Paulo. This paper studied the creation of an NGO to train people with hearing impairments. The research was carried out with people with hearing impairment in the city of Londrina, in the state of Paraná, Brazil.<br> Participants were asked about their degree of deafness, educational context and their knowledge of the main skills that are being sought by employers nowadays; such skills were based on the Future of Jobs 2023 report, published by the World Economic Forum in May, 2023.</p>
"I made the recording because Iam an amateur recording engineer and also work for a radio station. At the time, Iwas researching for a religious programme, for the radio and by pure chance and good luck, Iwas in the centre of York at the time the street preacher was there. Iam building up a personal library of 'ambient sounds' to use on various radio shows as 'sound effects'. The recording was taken outside St Helen's Church in St Helen's Square, in the centre of York. There was a fairly large crowd walking about, shopping. It was a Saturday. Some people were standing and listening to the man, some were mocking him, others didn't even notice. It was a sunny day, with a slight wind. St Helen's square is a large 'meeting place' for people with seats, flowers and usually musicians. I live in the centre of York and hear a lot of very interesting sounds there, everything from busking musicians, to many foreign languages, church bells, animals and much more. Ireally liked the recording of the preacher as it is quite clear that he passionately believes what he is saying. He was unaware that Iwas recording him. Iwish Ihad captured his whole sermon. He, and other members of his church visit the centre of York quite often, and preach there. Idon't know the name of his church." [Jools/vedas]19 in Collecting Sounds. Online Sharing of Field Recordings as Cultural Practice
"I made the recording because Iam an amateur recording engineer and also work for a radio station. At the time, Iwas researching for a religious programme, for the radio and by pure chance and good luck, Iwas in the centre of York at the time the street preacher was there. Iam building up a personal library of 'ambient sounds' to use on various radio shows as 'sound effects'. The recording was taken outside St Helen's Church in St Helen's Square, in the centre of York. There was a fairly large crowd walking about, shopping. It was a Saturday. Some people were standing and listening to the man, some were mocking him, others didn't even notice. It was a sunny day, with a slight wind. St Helen's square is a large 'meeting place' for people with seats, flowers and usually musicians. I live in the centre of York and hear a lot of very interesting sounds there, everything from busking musicians, to many foreign languages, church bells, animals and much more. Ireally liked the recording of the preacher as it is quite clear that he passionately believes what he is saying. He was unaware that Iwas recording him. Iwish Ihad captured his whole sermon. He, and other members of his church visit the centre of York quite often, and preach there. Idon't know the name of his church." [Jools/vedas]19
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.