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78 results for “endemic bird”

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zenodo40/100

High MHC gene copy number maintains diversity despite homozygosity in a Critically Endangered single-island endemic bird, but no evidence of MHC-based mate choice

<p>Raw sequence data from two amplicon libraries of MHC class I exon 3 of Raso Lark&nbsp;<em>Alauda razae</em>, sequenced on an Illumina Miseq. The two different libraries (two different Illumina runs) are collected in separat tar archive (.tar). Within each of those are individual sequence reads as gzipped fastq files (.fastq.gz). Each sample has two files, one for read 1 (R1) and one for read 2 (R2), with file names&nbsp;structured as&nbsp;follows. Delimited by underscore (_) are:</p> <ol> <li>sample name as referred to in the data and paper (&ldquo;RingNo&rdquo; in the Supporting data table);</li> <li>formal ID (also referred to in data table, often corresponding to full ring number);</li> <li>Illumina sample number (i.e. based on the order that samples are listed in the sample sheet);</li> <li>Illumina lane number (static as&nbsp;L001, as Miseq instruments have a single lane on their flow cells);</li> <li>read number (R1 [forward] or R2 [reverse]);</li> <li>static identifier from Illumina (001).</li> </ol> <p>Thus, the file 83304_TJ83304_S163_L001_R2_001.fastq.gz is the reverse (read 2) MHC class I exon 3 sequence of individual 83304 (ring number TJ83304).</p>

opencc-by-4.0Jan 2020View details →
dryad40/100

Habitat-linked genetic variation supports microgeographic adaptive divergence in an island-endemic bird species

<p>We present evidence for and investigate potential mechanisms driving habitat-linked genetic divergence within a bird species endemic to a single 250 km<sup>2</sup> island. The island scrub-jay (<em>Aphelocoma insularis</em>) exhibits microgeographic divergence in bill morphology across pine-oak ecotones on Santa Cruz Island, California (USA) similar to adaptive differences described in mainland congeners over much larger geographic scales. To test whether individuals exhibit genetic differentiation related to habitat type and divergence in bill length, we genotyped over 3,000 single nucleotide polymorphisms (SNPs) in 123 adult island scrub-jay males from across Santa Cruz Island using restriction site-associated DNA sequencing (RADseq). Neutral landscape genomic analyses revealed that genome-wide genetic differentiation was primarily related to geographic distance and differences in habitat composition. We also found 168 putatively adaptive loci associated with habitat type using multivariate redundancy analysis (RDA) while controlling for spatial effects. Finally, two genome-wide association analyses revealed a polygenic basis to variation in bill length with multiple loci detected in or near genes known to affect bill morphology in other birds. Our findings support the hypothesis that divergent selection at microgeographic scales can cause adaptive divergence in the presence of ongoing gene flow.</p>

opencc-zeroApr 2022View details →
zenodo40/100

Figure 3 in Avifauna of the Adelbert Mountains, New Guinea: why is Fire-maned Bowerbird Sericulus bakeri the mountains' only endemic bird species?

Figure 3. Terrain map of north-east New Guinea. Areas above 500 m are coloured grey; areas between 300 and 500 m blue; and areas below 300 m green. 1 = the Gogol River valley, between the Adelbert Mts. to the north and the Finisterre Mts. of the Huon Peninsula to the south. 2 = the Ramu River valley, between the Adelberts to the north-east and the Central Range to the south-west. 3 = the upper Ramu River valley and its headwaters, between the Finisterre Mts. of the Huon Peninsula to the north and the Central Range to the south. 4 = the Sepik River basin, between the Adelbert Mts. to the east and Prince Alexander Mts. of the North Coastal Range to the west. Map kindly produced by Iain Woxvold.

opencc-by-4.0Mar 2021View details →
zenodo40/100

Figure 2 in Avifauna of the Adelbert Mountains, New Guinea: why is Fire-maned Bowerbird Sericulus bakeri the mountains' only endemic bird species?

Figure 2. Presence and absence of Sericulus bowerbirdsȱonȱNewȱGuinea'sȱnorthernȱwatershed,ȱmodifiedȱfromȱ Diamondȱ(1969).ȱEachȱfilledȱdotȱrepresentsȱrecordsȱbyȱoneȱobserver.ȱThereȱareȱonlyȱsevenȱdocumentedȱareasȱ of occurrence of the allospecies Masked Bowerbird S. aureus, numbered from west to east, with observer names in parentheses: 1 = Tamrau Mts. (E. T. Gilliard and B. M. Beehler) and Arfak Mts. (many observers) of the Vogelkop. 2 = Wandammen Mts. (E. Mayr). 3 = Weyland Mts. (F. Shaw-Mayer). 4 = Bernhard Camp (A. Rand). 5 = Foja Mts. (B. M. Beehler and J. Diamond). 6 = Mt. Nibo (J. Diamond). 7 = Mt. Turu (J. Diamond). The asterisk depicts the range of the allospecies Fire-maned Bowerbird S. bakeri in the Adelberts. X = areas surveyedȱintensivelyȱwithoutȱfindingȱanyȱSericulus.? = an undocumented report of S. aureus from the Jimi River.ȱExceptȱforȱtheȱlatter,ȱS. aureus is known mainly from outlying ranges (locations 1, 2, 5, 6 and 7). There are only two documented localities for it in the Central Range (3–4), and there is a large gap between the easternmost record of S. aureus (7) and the range of S. bakeri. The remaining Sericulus allospecies in New Guinea is Flame Bowerbird S. ardens of the southern watershed.

opencc-by-4.0Mar 2021View details →
zenodo40/100

Figure 1 in Avifauna of the Adelbert Mountains, New Guinea: why is Fire-maned Bowerbird Sericulus bakeri the mountains' only endemic bird species?

Figure 1. New Guinea's principal mountain ranges: the Central Range forming New Guinea's backbone; and the ten outlying ranges along the north and north-west coasts, from Huon and Adelbert in the east, to Fakfak and Kumawa in the west.

opencc-by-4.0Mar 2021View details →
zenodo40/100

Fig. 4 in Patterns of Bird Diversity and Endemism Along an Elevational Gradient in the Southern Mexican Highlands.

Fig. 4. Rank-abundance curves for bird species at each of the four elevation sites in the Sierra Madre del Sur in southern Mexico. Bird species code: Aphelocoma sumichrasti (Asu), Catharus aurantiirostris (Cau), Cyanocitta coronata (Cco), Icterus pustulatus (Ipu), Junco phaeonotus (Jph), Melanerpes formicivorus (Mfo), Myadestes occidentalis (Moc), Myioborus miniatus (Mmi), Peucaea acuminata (Pac), Setophaga nigrescens (Sni), Tyrannus verticalis (Tve).

opencc-by-4.0Dec 2020View details →
zenodo40/100

Fig. 5 in Patterns of Bird Diversity and Endemism Along an Elevational Gradient in the Southern Mexican Highlands.

Fig. 5. Differences in the abundance and composition of bird species per sampling point along an elevational gradient in the Sierra Madre del Sur in southern Mexico ordered by a non-metric multidimensional scaling based on the Bray-Curtis similarity index. Ellipses indicate 95% significance.

opencc-by-4.0Dec 2020View details →
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Fig. 2 in Patterns of Bird Diversity and Endemism Along an Elevational Gradient in the Southern Mexican Highlands.

Fig. 2. Bird species richness (q0) and diversity (q1 and q2) along an elevational gradient in the Sierra Madre del Sur in southern Mexico.

opencc-by-4.0Dec 2020View details →
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Fig. 1 in Patterns of Bird Diversity and Endemism Along an Elevational Gradient in the Southern Mexican Highlands.

Fig. 1. Geographic location of the (a) state of Guerrero in southern Mexico and (b) sampling sites (white triangles) within the Sierra Madre del Sur (red polygon). The nearest human settlements to each study site are shown as green stars.

opencc-by-4.0Dec 2020View details →
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Fig. 3 in Patterns of Bird Diversity and Endemism Along an Elevational Gradient in the Southern Mexican Highlands.

Fig. 3. Endemic bird species richness (q0) along an elevational gradient in the Sierra Madre del Sur in southern Mexico.

opencc-by-4.0Dec 2020View details →
zenodo40/100

Fig. 6 in Patterns of Bird Diversity and Endemism Along an Elevational Gradient in the Southern Mexican Highlands.

Fig. 6. Faunal congruence curves for endemic bird species along an elevational gradient in the Sierra Madre del Sur in southern Mexico.

opencc-by-4.0Dec 2020View details →
zenodo40/100

Fig. 1 in Haemoparasites in endemic and non-endemic passerine birds from central Mexico highlands

Fig. 1. Location of study sites. (A) Location of the State of Mexico, (B) Location of Nevado de Toluca Natural Protected Area (NTNPA), and Valle de Bravo Natural Protected Area (VBNPA), (C) Parque Ecológico Ejidal de Cacalomacán (PEEC) and (D) Parque Ecoturístico Corral de Piedra (PECP). Datum WGS_1984_UTM Zone 14.

opencc-by-4.0Apr 2020View details →
zenodo40/100

Figure 19 in Are some of the birds endemic to the Tres Marías Islands (Mexico) species?

Figure 19. Mainland Rufous-backed Robin Turdus rufopalliatus far from the Tres Marías, with an anomalous grey breast-band resembling T. r. graysoni and note the prominent throat streaks and warm-coloured back, wing-coverts and flanks, Cuernavaca, Morelos, Mexico, June 2017 (Juan Manuel Ramos Merino)

opencc-by-4.0Mar 2020View details →
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Figure 20. Presumed Rufousbacked Robin Turdus rufopalliatus graysoni with mainly narrow throat streaks, a in Are some of the birds endemic to the Tres Marías Islands (Mexico) species?

Figure 20. Presumed Rufousbacked Robin Turdus rufopalliatus graysoni with mainly narrow throat streaks, a strong salmon wash on the breast, and wing-coverts and back colours close to those of non-graysoni T. rufopalliatus, Isla María Cleofas, November 2015 (Javier Cruz Nieto)

opencc-by-4.0Mar 2020View details →
zenodo40/100

Figure 15 in Are some of the birds endemic to the Tres Marías Islands (Mexico) species?

Figure 15. Back patern, size and intensity of orange in Streak-backed Oriole Icterus pustulatus specimens from Nayarit, from left to right: two typical microstictus / yaegeri, two presumed hybrids (with Phillips' specimen at right) and a typical graysoni; note the similar overall size of graysoni and Phillips' specimen, which is, however, more orange overall (especially the head), while the other presumed hybrid (which appears almost as long due to specimen preparation) has back streaks intermediate between graysoni and typical mainland Nayarit orioles (Héctor Gómez de Silva)

opencc-by-4.0Mar 2020View details →
zenodo40/100

Figure 11 in Are some of the birds endemic to the Tres Marías Islands (Mexico) species?

Figure 11. Pair of Mexican Parrotlets Forpus cyanopygius insularis copulating, Isla María Cleofas, May 2016; note the male's pale malachite-green underparts, neck-sides and postocular region contrasting with the yellower green cheeks, throat, forehead and forecrown, and that the male's undertail-coverts are not concolorous with the breast and belly (contra Grant 1965a) (Javier Cruz Nieto)

opencc-by-4.0Mar 2020View details →
zenodo40/100

Figure 12 in Are some of the birds endemic to the Tres Marías Islands (Mexico) species?

Figure 12. Instituto de Biología, Universidad Nacional Autónoma de México specimens of Mexican Parrotlet Forpus cyanopygius from Nayarit; the two specimens on the right are adult male insularis, their malachitegreen breast and belly contrasts strongly with the throat, unlike in cyanopygius specimens (Héctor Gómez de Silva)

opencc-by-4.0Mar 2020View details →
zenodo40/100

Figure 8 in Are some of the birds endemic to the Tres Marías Islands (Mexico) species?

Figure 8. Presumed hybrid Broad-billed Hummingbird Cynanthus lawrencei × magicus specimen, Isla María Cleofas, April 2016 (Héctor Gómez de Silva)

opencc-by-4.0Mar 2020View details →
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Figure 7 in Are some of the birds endemic to the Tres Marías Islands (Mexico) species?

Figure 7. Presumed hybrid Broad-billed Hummingbird Cynanthus lawrencei × magicus specimen in the Instituto de Biología, Universidad Nacional Autónoma de México collection; note magicus-like blue throat and lawrencei-like white-edged grey undertail-coverts (Héctor Gómez de Silva)

opencc-by-4.0Mar 2020View details →
zenodo40/100

Figure 5 in Are some of the birds endemic to the Tres Marías Islands (Mexico) species?

Figure 5. Two specimens of male Broad-billed Hummingbirds Cynanthus latirostris with similarly grey anterior undertailcoverts and white or whitish posterior undertail-coverts; above C. l. magicus, below, C. l. lawrencei (Héctor Gómez de Silva)

opencc-by-4.0Mar 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