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Fig. 14 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 14. Habitats near the central transect (tables 2, 3; figs. 3, 5; appendix 1), between Road Forks and Lordsburg, Animas Valley, 22 August 1990. Top. Intersection of NM Hwy 338 and Hwy I­10 about halfway between Road Forks and site 29, looking SW at alkali flats. Bottom. Looking NE at alkali flats, with creosote desertscrub in near background, from the same place as the top photograph.

opencc-by-4.0Jan 2000View details →
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Fig. 15 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 15. Habitats near the central transect (tables 2, 3; figs. 3, 5; appendix 1), between Road Forks and Lordsburg, Animas Valley, 22 August 1990. Top. Looking SW along Hwy I­10, just N of site 29 Bottom. Looking NE along Hwy I­10 from the same place as the top photograph (note creosote bushes on right).

opencc-by-4.0Jan 2000View details →
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Fig. 38 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 38. Frequencies of the marmoratus body coloration characters at sites along the southern transect (fig. 5). Site 42 was the center of the southern hybrid zone in genetic characters (fig. 32). Interpretation as in figure 37.

opencc-by-4.0Jan 2000View details →
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Fig. 29 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 29. Banding patterns illustrating the high polymorphism in PEPD and GPI. Left. Gel stained for PEPD, the most polymorphic of the loci examined. The gel shows six combinations of the five PEPD alleles. The a­ and b­alleles had the highest frequencies in punctilinealis; the c­allele was highest in marmoratus. Right. Gel stained for GPI. The a­ and b­alleles had their highest frequencies in marmoratus; the c­allele was most frequent in punctilinealis. As this analysis utilized hemolysates, hemoglobin appears as a cathodally migrating band. Arrows indicate sites of sample application; anode is to the right.

opencc-by-4.0Jan 2000View details →
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Fig. 37 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 37. Frequencies of the marmoratus body coloration characters at sites along the central transect (fig. 5). Site 26 was the center of the central hybrid zone in the genetic characters (fig. 31). Site 27 was not included because of crowding. Interpretation as in figure 36, with black spots representing samples in which all individuals were identical.

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Fig. 31 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 31. Average frequencies of the marmoratus alleles at each of the four diagnostic loci and of the marmoratus mtDNA haplotype at sites along the central transect (fig. 5). The frequency change in the IDDH a­allele, which occurs only in marmoratus, is also shown. The central hybrid zone was about 3.2 km wide, with the midpoint of gene exchange at site 26 (compare with fig. 40).

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Fig. 36 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 36. Frequencies of the marmoratus body coloration characters at sites along the northern transect (fig. 4). Site 3 was the center of the northern hybrid zone in genetic characters (fig. 30). Vertical line represents range of data, thick bar the mean, black rectangle the 95% confidence interval.

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Fig. 13 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 13. Habitats near the central transect (tables 2, 3; figs. 3, 5; appendix 1), between San Simon and Lordsburg, 22 August 1990. Top. Looking W at Steins Pass from the intersection of NM Hwy 80 and Hwy I­10, Road Forks; grassland, with creosote desertscrub visible in the pass. Bottom. Looking NE at grassland and alkali flats in Animas Valley, from the same place as the top photograph.

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Fig. 12 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 12. Habitats in the central transect (table 2; figs. 3, 5; appendix 1), between San Simon and Lordsburg, 22 August 1990. Top. Site 28, looking W at Steins Pass from NM Hwy 80 along the gas pipeline road; creosote desertscrub. Bottom. Looking E from site 28; grassland and alkali flats in near background.

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Fig. 8 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 8. Habitats at collecting sites in the northern transect, Animas Valley, north of Lordsburg (table 2; figs. 3, 4; appendix 1), 22 August 1990. Top. Site 5, looking W from NM Hwy 464; mesquite grassland. Bottom. Site 6, looking W from NM Hwy 464.

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Fig. 5 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 5. Top. The central hybrid zone (enlarged from fig. 3), with collecting sites numbered as in figure 4. Site 26 is the midpoint (50:50 point of gene exchange) in the transect (sites 20–30; table 2 appendix 1). Sites 23–25 are between sites 22 and 26, while site 27 is between sites 26 and 28. Note that site 30 comes before site 29 (reading left to right) in the transect from west to east. Bottom. The southern hybrid zone (enlarged from fig. 3), with collecting sites numbered as in figure 4. Site 42 is the midpoint (50:50 point of gene exchange) in the transect (sites 36–40, 42, 44, 46, and 48; table 2 appendix 1).

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Fig. 10 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 10. Habitats near the northern transect (tables 2, 3; figs. 3, 4; appendix 1), Animas Valley, NW Lordsburg along NM Hwy 70, 2 September 1990. Top. Site 10, looking NNW; creosote desertscrub Bottom. Grassland and abrupt ecotone with creosote desertscrub (in near background), 32.1 km (by road) NW of Lordsburg, looking NNW; site 10 is 0.8 km to the NW.

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Fig. 1 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 1. Geographic range of the western whiptail lizard, Cnemidophorus tigris sensu lato, in the continental southwestern United States and northern Mexico. Rectangle (SE Arizona and SW New Mexico) outlines the contact region (detailed in figs. 3–5) where C. t. punctilinealis interbreeds with C. t. marmoratus. Numbers designate collecting sites (appendix 2) for specimens additional to those obtained within the contact region (fig. 3; appendix 1).

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Fig. 7 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 7. Habitats at collecting sites in the northern transect, Animas Valley, north of Lordsburg (table 2; figs. 3, 4; appendix 1), 22 August 1990. Top. Site 3, midpoint of the northern hybrid zone, looking E from NM Hwy 464. Bottom. Site 4, looking NW from NM Hwy 464; mesquite grassland.

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Fig. 6 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 6. Habitats at collecting sites in the northern transect, Animas Valley, north of Lordsburg (table 2; figs. 3, 4; appendix 1), 22 August 1990. Top. Site 1, looking E from NM Hwy 464; riparian thornscrub. Bottom. Site 2, looking W from NM Hwy 464.

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Fig. 11 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 11. Habitats near the northern transect (tables 2, 3; figs. 3, 4; appendix 1), Animas Valley, NW of Lordsburg along NM Hwy 70, 2 September 1990. Top. Grassland about halfway between sites 10 and 13, at 27.9 km (by road) NW Lordsburg, looking N. Bottom. Site 14, looking WSW.

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Fig. 4 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 4. The northern hybrid zone, with collecting sites numbered (enlarged from fig. 3). Transect sites are numbers within squares (1–7), but the midpoint (50:50 point of gene exchange) is within a diamond (site 3). Associated sites are numbers in circles (table 2; appendix 1).

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Fig. 9 in Hybridization Among Western Whiptail Lizards (Cnemidophorus Tigris) In Southwestern New Mexico: Population Genetics, Morphology, And Ecology In Three Contact Zones

Fig. 9. Habitats at collecting sites in the northern transect and near an associated site, Animas Valley north of Lordsburg (tables 2, 3; figs. 3, 4; appendix 1), 22 August 1990. Top. Site 7, looking W from NM Hwy 464. Bottom. Abrupt ecotone of mesquite grassland and creosote desertscrub (in near background), 5.8 km (by road) W of site 3, looking NW. Site 8 is 0.3 km off the left side of the photo.

opencc-by-4.0Jan 2000View details →
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FIG. 8. — A, contact between facies C in Stratigraphy and sedimentology of Neogene mammal bearing deposits in the Akkașdağı area, Turkey

FIG. 8. — A, contact between facies C (limestone) and D (claystone) beds, hammer is 35 cm for scale; B, thick bedded and travertine-like texture of the limestones, lens cap in the circle is scale; C, horizontal field position of limestones covered by red mudstones of facies A at Killik Tepe (measured section AK-3); D, thin bedded and nodular natures of the limestones, hammer is 35 cm for scale.

opencc-zeroDec 2005View details →
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Text-fig. 16. a) MNHN LBE 007, symphysis with left and right i/1 of Barytherium sp. from Dor el Talha, Libya. (a1 – superior stereo views of the symphysis, a2 – stereo distal view of right i/1 (arrow 1 shows the interstitial contact facet close to the apex caused by abrasion against the right i/2), a3 – section of right i/1 viewed from the radicular end to show the extent of the enamel cover (below the arrows 2) and the dome-shaped dentine mass on the lingual aspect (above the arrows), a4 – stereo occlusal views of right i/1 (note the orientation of the apical wear facet), a5 – stereo mesial view) (scale bar 5 cm); b–c) NHMUK M 82167b, distal stereo views of lower central incisors of Arcanotherium savagei from Dor el Talha, Libya, to show the interstitial wear facets near cervix caused by abrasion against the i/2s (b – left i/1, c – right i/1) (scale bar 10 cm). in Large Mammals From The Rupelian Of Oman - Recent Finds

Text-fig. 16. a) MNHN LBE 007, symphysis with left and right i/1 of Barytherium sp. from Dor el Talha, Libya. (a1 – superior stereo views of the symphysis, a2 – stereo distal view of right i/1 (arrow 1 shows the interstitial contact facet close to the apex caused by abrasion against the right i/2), a3 – section of right i/1 viewed from the radicular end to show the extent of the enamel cover (below the arrows 2) and the dome-shaped dentine mass on the lingual aspect (above the arrows), a4 – stereo occlusal views of right i/1 (note the orientation of the apical wear facet), a5 – stereo mesial view) (scale bar 5 cm); b–c) NHMUK M 82167b, distal stereo views of lower central incisors of Arcanotherium savagei from Dor el Talha, Libya, to show the interstitial wear facets near cervix caused by abrasion against the i/2s (b – left i/1, c – right i/1) (scale bar 10 cm).

opencc-by-4.0Dec 2017View 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