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9 results for “acoustic occurrence”

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zenodo44/100

Diverse baleen whale acoustic occurrence around two sub-Antarctic Islands: A tale of residents and visitors

<p>This dataset contains the acoustic .wav file of all exemplar calls illustrated by the spectrograms in the manuscript figure, MS Excel Spreadsheet file with baleen whale call occurrence and environmental data, and the R code used for fitting the RF models. R codes must be run in the following manner:</p> <p>1. 01_tune_occ_enviro_rf_model_balance_baleen_whales</p> <p>2. 02_process_occ_enviro_rf_model_balance_baleen_whales</p> <p>The codes are self-explanatory given the comments contained therein, and the source code for fitting the codes is provided as 000_source_all.</p>

opencc-by-4.0Mar 2024View details →
dryad32/100

Summer circumpolar acoustic occurrence and call rates of Ross (Ommatophoca rossii) and leopard (Hydrurga leptonyx) seals in the Southern Ocean

<p>Two of the Antarctic pack ice seals, Ross, Ommatophoca rossii, and leopard, Hydrurga leptonyx, seals, are extremely dificult to study via traditional visual survey techniques, yet are ideal for an acoustic survey as they are highly vociferous and produce an array of underwater sounds during the austral summer. To determine their acoustic occurrence in the Antarctic pack ice, we use their calls, detected within 680 acoustic recordings made between 1999 and 2009 as part of two multinational programmes. Siren calls of Ross seals were detected mainly in January, and 9.88 calls per minute from low siren calls was the highest call rate for this species. High numbers of Ross seal calls were detected close to the ice edge in areas between 0° and 20° E and 60° and 130° E, suggesting these are important summer habitats. Leopard seal calls were detected mainly in December and January, and December had the highest percentage of calls. Call rate of 11.93 calls per minute from low double trills was the highest call rate for leopard seals. Leopard seal calls were detected throughout the Southern Ocean with more calls detected throughout the pack ice. There was little spatio-temporal overlap in call occurrence of Ross and leopard seals, but both species were more vocally active during the day. Longitude and latitude were the most important predictors of Ross seal occurrence, and month of the year highly predicted leopard seal occurrence. This is the irst study to examine the circumpolar acoustic occurrence of Ross and leopard seals in the Southern Ocean pack ice.</p>

opencc-zeroJan 2021View details →
zenodo32/100

Fig. 3 in Temporal occurrence of three blue whale populations in New Zealand waters from passive acoustic monitoring

Fig. 3.—Temporal occurrence pattern of New Zealand (dark blue), Antarctic (red), and Australian (yellow) blue whale song detections at each of the five hydrophones. The y-axis represents the number of hours per day that blue whale song was detected, and the x-axis represents the recording period. Grayed out sections represent gaps in recording due to hydrophone refurbishment.

opennotspecifiedDec 2022View details →
zenodo32/100

Fig. 2 in Temporal occurrence of three blue whale populations in New Zealand waters from passive acoustic monitoring

Fig. 2.—Example spectrograms of the three song types recorded in New Zealand waters. (A) New Zealand song on 31 May 2016, (B) Antarctic song on 26 August 2017, and (C) Australian song on 22 January 2017. Spectrograms are configured with a 2048-point fast Fourier transform, Hann window, 50% overlap.

opennotspecifiedDec 2022View details →
zenodo32/100

Fig. 4 in Temporal occurrence of three blue whale populations in New Zealand waters from passive acoustic monitoring

Fig. 4.—Conceptual map illustrating the current understanding of the approximate typical range of each blue whale population. Colors indicate the song type, and patterns represent inferred ecological use of each region. Distribution and occurrence patterns are synthesized from acoustic research published in the literature (e.g., Stafford et al. 2004; Balcazar et al. 2015, 2017; Tripovich et al. 2015; McCauley et al. 2018; Warren et al. 2021), and findings presented in this study.

opennotspecifiedDec 2022View details →
zenodo32/100

Fig. 1 in Temporal occurrence of three blue whale populations in New Zealand waters from passive acoustic monitoring

Fig. 1.—Map of the study area in the South Taranaki Bight region, with hydrophone locations denoted by the stars. Gray lines show bathymetry contours at 50-m depth increments, from 0 to 500 m. Location of the study area within New Zealand is indicated by the inset map.

opennotspecifiedDec 2022View details →
dryad32/100

Data from: Integrating passive acoustic and visual data to model spatial patterns of occurrence in coastal dolphins

Open the record for dataset details and reuse information.

publicMay 2015View details →
dryad32/100

Summer circumpolar acoustic occurrence and call rates of Ross (Ommatophoca rossii) and leopard (Hydrurga leptonyx) seals in the Southern Ocean

Open the record for dataset details and reuse information.

publicJan 2021View details →
zenodo20/100

Fig. 5 in Temporal occurrence of three blue whale populations in New Zealand waters from passive acoustic monitoring

Fig. 5.—Temporal occurrence pattern of the Antarctic blue whale song at each of the five hydrophones during the seasonal periods when the song was recorded in the South Taranaki Bight in New Zealand during 2016 (left panels) and 2017 (right panels). The y-axis represents the number of hours per day during which blue whale song was detected, and the x-axis represents the date. Grayed out sections represent gaps in recording due to hydrophone refurbishment. Synchronous peaks in occurrence between hydrophones and the overlapping detection ranges of the hydrophones (MARU1–5) indicate calls are detected simultaneously at multiple locations.

opennotspecifiedDec 2022View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record