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133 results for “lamprey”

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zenodo32/100

FIGURE 4. Lampetra soljani, FSJF 3650 in Lampetra soljani, a new brook lamprey from the southern Adriatic Sea basin (Petromyzontiformes: Petromyzontidae)

FIGURE 4. Lampetra soljani, FSJF 3650, paratypes, pre-spawning adults, from the top, 124 mm TL, 128 mm TL; Bosnia and Herzegovina: side-arm of Neretva River east of Čapljina; 16–17 Jan. 2015.

opennotspecifiedDec 2017View details →
zenodo32/100

Supplementary Data Files from: A lamprey neural cell type atlas illuminates the origins of the vertebrate brain

<p><strong>Supplementary Data </strong><strong>1</strong></p> <p>Lamprey genome custom annotation files.</p> <p>&nbsp;</p> <p><strong>Supplementary Data 2</strong></p> <p><em>In situ</em> images produced in this study.</p>

opencc-by-4.0Jan 2023View details →
zenodo32/100

FIGURE 1 in Validity of Lampetra pacifica (Petromyzontiformes: Petromyzontidae), a brook lamprey described from the lower Columbia River Basin

FIGURE 1. Map of localities discussed in text. Type localities are indicated by species labels, and numbers correspond with identifiers in Table 1. Stars are localities for populations of L. pacifica; dots are localities for populations of L. richardsoni. The Tualatin River (4) includes three sampling sites, including McKay Creek.

opennotspecifiedNov 2011View details →
zenodo32/100

FIGURE 3 in Validity of Lampetra pacifica (Petromyzontiformes: Petromyzontidae), a brook lamprey described from the lower Columbia River Basin

FIGURE 3. Percent sequence divergence (Kimura 2-parameter, K2P) in 1191 bp cyt b within and between Lampetra richardsoni and L. pacifica populations, including type localities (with*). All populations except the type locality of L. richardsoni (Smith Creek, Cultus Lake, BC) are in the Columbia Basin (see Map, Fig. 1). Tualatin specimens were from McKay Creek. Numbers of specimens in parentheses.

opennotspecifiedNov 2011View details →
zenodo32/100

FIGURE 7 in Lethenteron ninae, a new nonparasitic lamprey species from the north-eastern Black Sea basin (Petromyzontiformes: Petromyzontidae)

FIGURE 7. Tongue precursor in ammocoete. a, Lethenteron ninae (paratype); b, Eudontomyzon mariae (ZISP 29159). 1, bulb; 2, cirri.

opennotspecifiedAug 2009View details →
zenodo32/100

FIGURE 6 in Lethenteron ninae, a new nonparasitic lamprey species from the north-eastern Black Sea basin (Petromyzontiformes: Petromyzontidae)

FIGURE 6. Lethenteron ninae, holotype (photo made from live specimen, ZISP 54431, TL (measured after preservation) 163.8 mm, Shakhe River).

opennotspecifiedAug 2009View details →
zenodo32/100

FIGURE 3. Oral disc. a in Lethenteron ninae, a new nonparasitic lamprey species from the north-eastern Black Sea basin (Petromyzontiformes: Petromyzontidae)

FIGURE 3. Oral disc. a, Lethenteron ninae, holotype (photo made from live specimen, ZISP 54431, TL (after preservation) 163.8 mm, Shakhe River); b, Eudontomyzon mariae (from Berg 1931: Pl. 4, FIGURE 2, syntype, TL 192 mm). 1, supraoral lamina; 2, infraoral lamina; 3, posterial teeth (one incomplete row in L. ninae and three rows in E. mariae); 4, anterior endolateral bicuspid tooth; 5, row of marginal teeth; 6, fimbriae; 7, ventral pigmented neuromast; 8, exolateral teeth; 9, transverse lingual lamina.

opennotspecifiedAug 2009View details →
zenodo32/100

FIGURE 4. Transverse lingual lamina. a in Lethenteron ninae, a new nonparasitic lamprey species from the north-eastern Black Sea basin (Petromyzontiformes: Petromyzontidae)

FIGURE 4. Transverse lingual lamina. a, Lethenteron ninae, paratype (formula 6u-I-5u); b, Eudontomyzon mariae, syntype (formula 1u-I-2u). Scale bar: 1 mm. Arrows show the differences.

opennotspecifiedAug 2009View details →
dryad32/100

Data from: A simple, cost-effective emitter for controlled release of fish pheromones: development, testing, and application to management of the invasive sea lamprey

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publicMay 2019View details →
dryad32/100

Data from: Riverscape genetics in brook lamprey: genetic diversity is less influenced by river fragmentation than by gene flow with the anadromous ecotype

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publicSep 2020View details →
dryad32/100

The Pacific lamprey genomic divergence, association mapping, temporal Willamette Falls, spatial rangewide datasets

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publicAug 2020View details →
dryad32/100

Data from: Identifying spawning sites and other critical habitat in lotic systems using eDNA “snapshots”: a case study using the sea lamprey Petromyzon marinus L.

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publicDec 2018View details →
dryad32/100

Data from: Population genomics of Pacific lamprey: adaptive variation in a highly dispersive species

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publicOct 2012View details →
dryad32/100

Data from: Use of genotyping-by-sequencing data to develop a high-throughput and multi-functional SNP panel for conservation applications in Pacific lamprey

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publicMay 2014View details →
dryad32/100

Chromosome‐level genome assembly of Lethenteron reissneri provides insights into lamprey evolution

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publicDec 2020View details →
dryad32/100

Data from: Genes predict long distance migration and large body size in a migratory fish, Pacific lamprey

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publicAug 2014View details →
dryad32/100

Data from: Contrasting population genetic structure among freshwater-resident and anadromous lampreys: the role of demographic history, differential dispersal, and anthropogenic barriers to movement.

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publicFeb 2015View details →
dryad28/100

Evidence that male sea lamprey increase pheromone release after perceiving a competitor: raw data, R-code, R analyses

<p class="CxSpFirst">Sexual signals evolve via selective pressures arising from male-male competition and female choice, including those originating from unintended receivers that detect the signal. For example, males can acquire information from other males signaling to females and alter their own signal. Relative to visual and acoustic signals, less is known about how such communication networks influence chemical signaling among animals. In sea lamprey (<i>Petromyzon marinus</i>), chemical communication system is essential for reproduction, offering a useful system to study a pheromone communication network that includes signalers and both intended and unintended receivers. Male sea lamprey aggregate on spawning grounds where individuals build nests and signal to females using sex pheromones. We examined how exposure to a major component of the male pheromone, 3keto-petromyzonol sulfate (3kPZS), influenced male pheromone signaling, and whether females had a preference for males that altered their signal. Exposure to 3kPZS, at a concentration of 5x10<sup>-10 </sup>M, simulated the presence of other male(s) and led to increased 3kPZS release rates within 10 min, followed by a return to baseline levels within 30 min. Exposure also led to increases in hepatic synthesis and circulatory transport of pheromone components. In behavioral assays, females preferred the odor of males that had been exposed to 3kPZS; therefore, males likely benefit from upregulating 3kPZS release after detecting competition for mates. Here, we define how a specific pheromone component influences chemical signaling during intrasexual competition, and show a rare example of how changes in chemical signaling strategies resulting from male competition may influence mate choice.</p>

opencc-zeroJul 2020View details →
zenodo28/100

Figure 6 from: Naseka AM, Renaud CB (2020) Morphology-based taxonomic re-assessment of the Arctic lamprey, Lethenteron camtschaticum (Tilesius, 1811) and taxonomic position of other members of the genus. ZooKeys 991: 1-67. https://doi.org/10.3897/zookeys.991.54938

Figure 6 Oral disc of syntype of Lampetra morii, CMNFI 1986–757 (formerly part of ZIN 23145), 171 mm TL. Photograph by George Ben-Tchavtchavadze, University of Ottawa, pre–1982.

opencc-by-4.0Nov 2020View details →
zenodo28/100

Figure 5 from: Naseka AM, Renaud CB (2020) Morphology-based taxonomic re-assessment of the Arctic lamprey, Lethenteron camtschaticum (Tilesius, 1811) and taxonomic position of other members of the genus. ZooKeys 991: 1-67. https://doi.org/10.3897/zookeys.991.54938

Figure 5 Oral disc of Lethenteron reissneri, ZIN 25204, 146 mm TL with two rows of posterials from Tym' River, Sakhalin Island, Russia.

opencc-by-4.0Nov 2020View 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