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312 results for “bass”
The influence of boating noise on the parental care behaviors of smallmouth bass (Micropterus dolomieu) during the summer of 2024 at Douglas Lake, Michigan, USA.
Anthropogenic noise is on the increase and in aquatic systems one of the major sources of noise is boat traffic. For organisms in lakes, rivers, and oceans that are capable of hearing, anthropogenic noise may alter behavior in a number of different ways. Here we did a combination of field and experimental work by locating smallmouth bass nests that were actively being guarded by males. Using an underwater drone, we monitored nest guarding behavior before and after a boat ran by the nest. In addition, we monitored behavior during this period while simultaneously recording boat motor noise. The results showed that the sequence of behavior performed by bass was altered during and after the boat ran by the nest.
Relative predation rates on juvenile Chinook Salmon in the lower Stanislaus River, California, 2012-2024 by habitat suitability informed by juvenile Chinook Salmon and black bass observations in the lower Stanislaus and Merced rivers, California, 2012-2017
Overview The purpose of this work was to estimate relative predation on juvenile Chinook Salmon rearing in tributaries of the San Joaquin River, California in relation to meso- and microhabitat factors. Predation rates were estimated using predation bioassays. Ranges of depth and velocity targeted by the bioassays were informed by habitat suitability indices developed prior to field efforts. Juvenile Chinook and Bass Habitat Suitability Indices The purpose of this dataset is to develop habitat suitability indices for juvenile Chinook Salmon (<120mm) on the lower Stanislaus River and nonnative black bass ( Micropterus spp.). on the lower Merced River, both tributaries of the San Joaquin. This data was used to identify target ranges of depth and velocity during predation fieldwork. Occupancy data was collected via snorkel surveys on the lower Stanislaus River in 2018 and 2019 and on the Merced River in 2012 and 2014-2017. Predation Tethering Bioassay Study The purpose of this field study was to estimate relative rates of predation of juvenile Chinook Salmon. Predation rates were estimated using assays of tethered hatchery Chinook Salmon deployed across a range of mesohabitats on the lower Stanislaus River. Habitat suitability was expected to vary across mesohabitats and across depths and velocities sampled within habitats. Cameras were deployed with tethers to identify predators for a subset of predation events happening within the first 1-2 hours of deployment. Assays were deployed monthly March-May in 2022 and 2024. A supplemental set of assays were deployed in May 2023 under wet water year conditions that varied strongly from conditions sampled in 2022 and 2024.
Biocomplexity at North Temperate Lakes LTER: Coordinated Field Studies: Large Mouth Bass Growth 2006
Lakeshore residential development is associated with changes in littoral habitat, riparian habitat, and ecosystem function with potential impacts ramifying through aquatic food webs. Effects of these changes on economically important game fishes may vary with fish size. We investigated largemouth bass (Micropterus salmoides) size-specific growth rates across 16 lakes spanning the range of lakeshore residential development in Wisconsin’s Northern Highland Lake District using a longitudinal multilevel model. Growth rates of small fish had a strong positive relationship with lakeshore residential development. The strength of the relationship decreased with length and became increasingly negative for fish longer than 210 mm. This pattern may be driven by a release from density-dependent growth, shifts in available prey sources, reduced macrophyte cover, or angling-induced selection pressures. Regardless of the mechanism, our results indicate, relative to undeveloped lakes, largemouth bass in highly developed lakes take 1.5 growing seasons longer to enter the fishery (356 mm).
REU data set from summer of 2022. Project was designed to understand how crayfish (Faxonius rusticus) respond to chemical cues from largemouth bass predators under different shelter distributions.
Research into predator–prey interactions has focused on the landscape of fear and nonconsumptive effects that result from prey responses. Prey behavior is influenced by predator presence and the location and quality of foraging resources in habitats. These areas have been fruitful, but the role of prey refuges has lagged. We investigated how refuge spatial distribution and quality influence prey behavior. To determine the role of the landscape of safety (LOS) in prey decision-making, we altered spatial relationships between refuges, refuge quality, and predation threats in mesocosms. Mesocosms were constructed such that prey only received predatory chemical cues. We employed a behavioral assay including largemouth bass (Micropterus salmoides (Lacepède, 1802): predator) and virile crayfish (Faxonius rusticus (Girard, 1852): prey). Crayfish shelter use was significantly influenced by quality and spatial relationship of shelters to predatory threats, and the interaction of these two factors. Particularly, crayfish used high-quality shelters more often when located closer to predatory cues than farther away and did not use low-quality shelters more than controls. High-quality shelter usage decreased as threat level (measured by gape ratio) decreased. These results support the idea that prey utilize an LOS, and information contained in these two landscapes may alter behavioral decisions.
Comparing effects of auditory and visual disturbances on smallmouth bass parental care behaviors during the summer of 2025 at Douglas Lake, Michigan, USA
A prevalent source of sensory pollution within aquatic systems is recreational motorboats that can impact aquatic organisms through several exposure mechanisms. Auditory and visual sensory disturbances are particularly important as fish may utilize these cues during critical reproductive behaviors such as parental care. Here, we conducted a field study in Douglas Lake, Michigan, and located wild smallouth bass nests actively guarded by males. We exposed smallmouth bass to two sequential treatments of playback auditory noise and visual disturbances. Using an underwater drone, parental care behaviors of smallmouth bass were monitored before, during, and after both auditory and visual disturbances. The results show that auditory and visual disturbances may alter smallmouth bass parental care behaviors differently.
Water Body Checklists 2019: Bass Strait Species List
Species checklists created using effechecka and modified polygons from IHO. The polygons were reduced in resolution.<p></p>List of species collected from the Bass Strait using effechecka and a modified polygon from the International Hydrographic Association. A filter was applied (based on data from WoRMS) to remove all non-marine taxa.
Water Body Checklists: Bass Strait Species List
Species checklists created using effechecka and modified polygons from IHO. The polygons were reduced in resolution.<p></p>List of species collected from the Bass Strait using effechecka and a modified polygon from the International Hydrographic Association. A filter was applied (based on data from WoRMS) to remove all non-marine taxa.
Bach Chorales Figured Bass (BCFB) dataset
<p>The Bach Chorales Figured Bass (BCFB) dataset includes the complete 139 Johann Sebastian Bach chorales with figured bass encodings in MusicXML, **kern, and MEI formats, based on the Neue Bach Ausgabe (NBA) critical edition. This work was presented at the International Society for Music Information Retrieval (ISMIR) Conference<em> </em>2020. The files can be found within the folder <strong>FB_source</strong>. </p> <p>Within the folders <strong>FB_source/musicXML_master</strong> (.musicxml, ignore the files of the following subfolders: <strong>editorial_ones</strong>, <strong>editorial_FB_only</strong>, <strong>BCMCL</strong>), <strong>FB_source/translated_kern</strong> (.krn), and <strong>FB_source/translated_mei</strong> (.mei), you can find 143 (more than 139) symbolic files with figured bass annotations. This is because BWV 10.07, BWV 161.06, BWV 38.06, and BWV 177.05 have two different versions based on NBA. </p> <p>You can use <a href="https://musescore.org/">MuseScore</a> to open (.musicxml) files, <a href="https://verovio.humdrum.org/">Verovio Humdrum Viewer</a> to open (.krn) file, and <a href="https://www.verovio.org/mei-viewer.xhtml">Verovio</a> to open (.mei) file to view both the music and the figured bass annotations. </p> <p>If you use this version of the files, it will be greatly appreciated if you cite the following <a href="http://www.music.mcgill.ca/~cmckay/papers/musictech/ju20automatic.pdf">paper</a>: </p> <pre><code>@inproceedings{ju_automatic_2020, title = {Automatic {Figured} {Bass} {Annotation} {Using} the {New} {Bach} {Chorales} {Figured} {Bass} {Dataset}}, booktitle = {Proceedings of the 21th {International} {Society} for {Music} {Information} {Retrieval} {Conference}}, author = {Ju, Yaolong and Margot, Sylvain and McKay, Cory and Dahn, Luke and Fujinaga, Ichiro}, year = {2020}, pages = {640--646}, } </code></pre> <p>The metadata of these chorales can be found in <strong>Reference Table.csv </strong>under the root directory.</p> <p>If you have any questions, please email to <strong>yaolong.ju@mail.mcgill.ca</strong>.</p>
Counts of tagged striped bass at forty sites throughout Plum Island estuary conducted July-October 2009 using acoustic telemetry.
Manual survey data was collected to measure striped bass distribution in Plum Island Estuary during the time period that they are in New England during their summer foraging migration. Acoustic telemetry was used to tag and track individual fish and provide measures of abundance at sample sites distributed throughout the estuary.
Daily presence of individual tagged striped bass as measured by stationary receiver detections in Plum Island Estuary in 2009
Stationary receiver data was collected to measure striped bass distribution in Plum Island Estuary during the time period that they are in New England during their summer foraging migration. Acoustic telemetry was used to tag and detect individual fish throughout the estuary.
IG. 6. — A, Trunk vertebra of Alsophis sp. 2 from Pointe du Helleux archaeological site (Square 2 – crab layer) located on Grande-Terre Island; B, trunk vertebra of Erythrolamprus juliae cf. copeae (Parker, 1936) from Sainte-Rose La Ramée archaeological site (US 2058) located on Basse-Terre Island. Abbreviations: cd., condyle; ct., cotyle; di., diapophysis; h. k., hemal keel; m. c., medial constriction; n. a., neural arch; n. s., neural spine; p. c., precondylar constriction; p. d., paracotylar depression; p. n., postero-medial notch of the zygantrum; pa., parapophysis; pz. f., prezygapophyseal facet; pz. p., prezygapophyseal process; s. d., subcentral depression; s. r., subcentral ridge; s. t., sub-cotylar tubercle; zs., zygosphene. Scale bars: 4 mm in Fossil dipsadid snakes from the Guadeloupe Islands (French West-Indies) and their interactions with past human populations
IG. 6. — A, Trunk vertebra of Alsophis sp. 2 from Pointe du Helleux archaeological site (Square 2 – crab layer) located on Grande-Terre Island; B, trunk vertebra of Erythrolamprus juliae cf. copeae (Parker, 1936) from Sainte-Rose La Ramée archaeological site (US 2058) located on Basse-Terre Island. Abbreviations: cd., condyle; ct., cotyle; di., diapophysis; h. k., hemal keel; m. c., medial constriction; n. a., neural arch; n. s., neural spine; p. c., precondylar constriction; p. d., paracotylar depression; p. n., postero-medial notch of the zygantrum; pa., parapophysis; pz. f., prezygapophyseal facet; pz. p., prezygapophyseal process; s. d., subcentral depression; s. r., subcentral ridge; s. t., sub-cotylar tubercle; zs., zygosphene. Scale bars: 4 mm
Data from: Multiple spawning run behavior and population consequences in migratory striped bass Morone saxatilis
<p>Multiple spawning runs cause different contingents within the same population to experience varying demographic fates that can stabilize populations through the portfolio effect. Multiple spawning runs are reported here for the first time for striped bass, an economically important coastal species, which is well known for plastic estuarine and shelf migration behaviors. Adult Hudson River Estuary striped bass (n=66) were tagged and tracked with acoustic transmitters from two known spawning reaches separated by 90 km. Biotelemetry recaptures for two years demonstrated that each reach was associated with separate spawning runs. Time series of spawning run trajectories were examined via nonparametric dynamic time warping and revealed two dominant time series centroids, each associated with the two spawning reaches. In 2017, the lower reach run occurred earlier than the higher reach run, but difference in timing was not observed in 2018. The majority (84%) of returning adults in 2018 showed the same run behaviors exhibited in 2017. The two spawning run may have been cued differently by temperatures, where warming lagged 1-week at the higher reach in comparison to the lower reach. The two spawning runs exhibited similar Atlantic shelf migration patterns with strong summer fidelity to Massachusetts Bay and winter migrations to the southern US Mid-Atlantic Bight. Still, in 2017, differing times of departure from spawning reaches into nearby shelf waters likely caused the early spawning run to experience substantially higher mortality than the later run. Anecdotal evidence suggests that higher fishing effort is exerted on the early-spawning run as it first enters shelf fisheries. Thus, as in salmon, multiple spawning runs by striped bass can lead to differential demographic outcomes, contributing to overall population dynamics.</p>
Figure 61 in Nannastacidae (Crustacea: Cumacea) from eastern Bass Strait, the south-eastern Australian slope, and Antarctica in the collections of Museum Victoria
Figure 61. Styloptocuma poorei sp. nov. female holotype: a, body, lateral view; b, antenna 1; c, maxilliped 3; d, pereopod 1; e, pereopod 2; f, pereopod 3; g, pereopod 4; h, pereopod 5; i, pleonite 6 and left uropod. Scale (in mm): a, 0.5; b, 0.2; c, 0.1; d–i, 0.25.
Figure 66 in Nannastacidae (Crustacea: Cumacea) from eastern Bass Strait, the south-eastern Australian slope, and Antarctica in the collections of Museum Victoria
Figure 66. Vemacumella bacescui sp. nov. female holotype: a, pereopod 2; b, pereopod 3; c, pereopod 4; d, pereopod 5; e, pleonite 6 and left uropod. Scale bar: a–e, 0.2
Figure 60 in Nannastacidae (Crustacea: Cumacea) from eastern Bass Strait, the south-eastern Australian slope, and Antarctica in the collections of Museum Victoria
Figure 60. Styloptocuma nodosum sp. nov. male allotype: a, maxilliped 3; b, pereopod 1; c, pereopod 2; d, pereopod 3; e, pereopod 4; f, pereopod 5; g, pleonite 6 and left uropod. Scale (in mm): a, c–g, 0.5; b, 0.5.
Figure 64 in Nannastacidae (Crustacea: Cumacea) from eastern Bass Strait, the south-eastern Australian slope, and Antarctica in the collections of Museum Victoria
Figure 64. Styloptocumoides australiensis sp. nov. female holotype: a, body, lateral view; b, antenna 1; c, maxilliped 3; d, pereopod 1; e, pereopod 2; f, pereopod 3; g, pereopod 4; h, pereopod 5; I, pleonite 6 and right uropod. Scale (in mm): a, 0.5; b–e, i, 0.2; f–h, 0.25.
Figure 57 in Nannastacidae (Crustacea: Cumacea) from eastern Bass Strait, the south-eastern Australian slope, and Antarctica in the collections of Museum Victoria
Figure 57. Styloptocuma nodosum sp. nov. female holotype: a, body, lateral view; b, antenna 1; c, maxilliped 2; d, maxilliped 3. Scale (in mm): a, 0.5; b, d, 0.5; c, 0.2.
Figure 62 in Nannastacidae (Crustacea: Cumacea) from eastern Bass Strait, the south-eastern Australian slope, and Antarctica in the collections of Museum Victoria
Figure 62. Styloptocuma spinosum sp. nov. female holotype: a, body, lateral view; b, carapace, lateral view, magnified; c, antenna 1; d, maxilliped 3. Scale (in mm): a, 0.5; b, c, 0.5; d, 0.25.
Figure 65 in Nannastacidae (Crustacea: Cumacea) from eastern Bass Strait, the south-eastern Australian slope, and Antarctica in the collections of Museum Victoria
Figure 65. Vemacumella bacescui sp. nov. female holotype: a, body, lateral view; b, body, dorsal view; c, antenna 1; d, maxilliped 3; e, pereopod 1. Scale (in mm): a, 0.5; b, 0.5; c, d, 0.1; e, 0.2.
Figure 63 in Nannastacidae (Crustacea: Cumacea) from eastern Bass Strait, the south-eastern Australian slope, and Antarctica in the collections of Museum Victoria
Figure 63. Styloptocuma spinosum sp. nov. female holotype: a, pereopod 1; b, pereopod 2; c, pereopod 3; d, pereopod 4; e, pereopod 5; f, pleonite 6 and right uropod. Scale (in mm): a–e, 0.25; f, 0.5.
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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.
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.