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FIG. 6 in Caribou hunting and utilization in West Greenland: Past and present variants

FIG. 6. — Caribou utilization in Angujâartorfiup Nunâ after 2000 AD. (Rangifer tarandus after Beauval & Coutureau © 2003, Archeozoo.org)

opencc-by-4.0Jun 2013View details →
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Figure 7 in Ultrastructure of the pseudocnidae of the palaeonemerteans Cephalothrix cf. rufifrons and Carinomella lactea and an assessment of their phylogenetic utility

Figure 7. Molecular phylogenies of nemerteans. (A) Phylogeny inferred from 18S rDNA sequences. (B) Phylogeny inferred from a simultaneous analysis of partial 28S rRNA, H3, 16S rRNA and COI gene sequences. Phylogeny ''A'' implies that pseudocnidae were present in the common ancestor of nemerteans and subsequently lost in two lineages Phylogeny ''B'' implies independent evolution of pseudocnidae. Open boxes represent character losses and solid boxes represent character acquisitions.

opencc-by-4.0Aug 2006View details →
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Figure 3 in Ultrastructure of the pseudocnidae of the palaeonemerteans Cephalothrix cf. rufifrons and Carinomella lactea and an assessment of their phylogenetic utility

Figure 3. Transmission electron micrographs of Cephalothrix cf. rufifrons pseudocnidae and pseudocnida-forming cells. (A) Longitudinal section of a mature pseudocnida. Note the filament core (fc) and the lateral process (lp). (B) Cross-section of a pseudocnida. Note the Golgi complex in the cell cytoplasm and the putative pseudocnida precursor material (arrows). (C) RER (re) containing flocculent material in a pseudocnida-forming cell. Abbreviations: co, cortex; fc, filament core; go, Golgi complex; lp, lateral process; me, medulla; re, rough endoplasmic reticulum (RER).

opencc-by-4.0Aug 2006View details →
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Figure 6 in Ultrastructure of the pseudocnidae of the palaeonemerteans Cephalothrix cf. rufifrons and Carinomella lactea and an assessment of their phylogenetic utility

Figure 6. Schematic longitudinal TEM sections of nemertean pseudocnidae. (A) Cephalothrix cf. rufifrons. (B) Tubulanus cf. pellucidus. (C) Carinomella lactea. (D) Zygeupolia rubens. (A) and (C) drawn from data presented herein. (B) and (D) drawn from micrographs in Turbeville (1991) and unpublished data. Scale is approximate.

opencc-by-4.0Aug 2006View details →
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Figure 5 in Ultrastructure of the pseudocnidae of the palaeonemerteans Cephalothrix cf. rufifrons and Carinomella lactea and an assessment of their phylogenetic utility

Figure 5. Transmission electron micrographs of Carinomella lactea pseudocnidae and pseudocnida-forming cells. (A) Longitudinal section of pseudocnidae. Note the medulla (me) cortex (co) and filament core (fc). (B) Cross section of a pseudocnida. Putative pseudocnida precursors are present in the cell cytoplasm (*). (C) Pseudocnidaforming cell revealing Gogli complex (go) and pseudocnida precursor material (*). Abbreviations: co, cortex; fc, filament core; go, Golgi complex; me, medulla; ps, pseudocnida.

opencc-by-4.0Aug 2006View details →
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Figure 4 in Ultrastructure of the pseudocnidae of the palaeonemerteans Cephalothrix cf. rufifrons and Carinomella lactea and an assessment of their phylogenetic utility

Figure 4. Cross-sections of the proboscis of Carinomella lactea. (A) Survey transmission electron micrograph of the proboscis. Note the pseudocnida-forming cell containing pseudocnidae (arrow). (B) Low-power micrograph revealing two groups of pseudocnidae (arrows) resting on secretions (*) of underlying gland cells. (C) Cross section of a group of pseudocnidae (ps) and a sensory bristle of an adjacent sensory cell. (D) Low-power micrograph of longitudinal sections of pseudocnidae. Note the filament core (fc). Abbreviations: cm, circular muscle; em, extracellular matrix; fc, filament core; gc, gland cell; lm, longitudinal muscle; pc, pseudocnidaforming cell; pe, proboscis peritoneum; pn, proboscis nerve; ps, pseudocnida; sc, sensory cell cilium.

opencc-by-4.0Aug 2006View details →
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Figure 2 in Ultrastructure of the pseudocnidae of the palaeonemerteans Cephalothrix cf. rufifrons and Carinomella lactea and an assessment of their phylogenetic utility

Figure 2. Transmission electron micrographs of the middle proboscis of Cephalothrix cf. rufifrons. (A) Survey micrograph of a cross section of the middle proboscis. Asterisk (*) indicates a pseudocnida-forming cell. (B) Pseudocnida-forming cell revealing the nucleus, RER and several pseudocnidae. (C) Longitudinal section of pseudocnida. Arrow indicates the filament core. (D) Cross-section of a pseudocnida. Arrow indicates core. (E) Section of an everted proboscis. Apices of the pseudocnidae extend into the lumen. (F) Cross-sections of bases of pseudocnidae. Arrowheads indicate the lateral processes. Also note the sensory cilium of the adjacent sensory cell (sc). Abbreviations: cm, circular muscle; co, cortex; lm, longitudinal muscle; lp, lateral process; me, medulla; pe, proboscis peritoneum; pn, proboscis nerve; rd, fusiform rhabdoid; sc, sensory cell.

opencc-by-4.0Aug 2006View details →
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Figure 1 in Ultrastructure of the pseudocnidae of the palaeonemerteans Cephalothrix cf. rufifrons and Carinomella lactea and an assessment of their phylogenetic utility

Figure 1. Light micrograph of the everted proboscis of Cephalothrix cf. rufifrons revealing apices of pseudocnidae (arrow). Note also the sensory bristles (sb).

opencc-by-4.0Aug 2006View details →
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Fig. 6 in Utilization of the fish ladder at the Engenheiro Sergio Motta Dam, Brazil, by long distance migrating potamodromous species

Fig. 6. Number of individuals for species captured in Protocol II (assessment of ascending and descending movements). Migratory species are in bold.

opencc-by-4.0Dec 2007View details →
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Fig. 3 in Utilization of the fish ladder at the Engenheiro Sergio Motta Dam, Brazil, by long distance migrating potamodromous species

Fig. 3. Number of individuals of the main species and proportions of the life strategies (LDMI: long distance migratory species; SNPC: sedentary species that do not develop parental care; SPC: sedentary species that develop parental care; SIFI: sedentary species with internal fertilization and internal development) sampled in both protocols conducted in the fish ladder located at Engenheiro Sergio Motta Dam (Migratory species are in bold).

opencc-by-4.0Dec 2007View details →
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Fig. 5 in Utilization of the fish ladder at the Engenheiro Sergio Motta Dam, Brazil, by long distance migrating potamodromous species

Fig. 5. Percentage of individuals of migratory species in the pools sampled in the ladder located at Engenheiro Sergio Motta Dam.

opencc-by-4.0Dec 2007View details →
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Fig. 1 in Utilization of the fish ladder at the Engenheiro Sergio Motta Dam, Brazil, by long distance migrating potamodromous species

Fig. 1. Location of the Engenheiro Sergio Motta (Porto Primavera) Hydroelectric power plant in the Paraná River, Brazil.

opencc-by-4.0Dec 2007View details →
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Fig. 4 in Utilization of the fish ladder at the Engenheiro Sergio Motta Dam, Brazil, by long distance migrating potamodromous species

Fig. 4. Monthly averages of the total number of individuals (± standard error) (a) and of migratory species (b), captured at intervals of 8h in the different pools sampled in the fish ladder located at Engenheiro Sergio Motta Dam (N: total number of individuals).

opencc-by-4.0Dec 2007View details →
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Abb. 3 in Tribu des brevipennes. Famille des aleochariens. Septieme branche: Myrmedoniaires. Annales de la Societe d'Agriculture Histoire Naturelle et Arts Utiles de Lyon (ser.

Abb. 3: Nadelwald mit Rhododendron-Unterwuchs bei Dagcanglhamo in der Umgebung des Typenfundortes von Trigonurus ruzickai. Foto: J. RĤžiþka.

opencc-by-4.0Dec 1874View details →
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Abb. 2a-g in Tribu des brevipennes. Famille des aleochariens. Septieme branche: Myrmedoniaires. Annales de la Societe d'Agriculture Histoire Naturelle et Arts Utiles de Lyon (ser.

Abb. 2a-g: Trigonurus ruzickai: -Sternit VIII (a); -Tergit VIII (b); -Sternit IX (c); Aedoeagus, lateral (d); Aedoeagus, dorsal (e); Aedoeagus, ventral (f); Distal-Gonocoxit, Stylus und Hinterrand von -Tergit X (g). -Paratypus (a-f); -Paratypus (g).

opencc-by-4.0Dec 1874View details →
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Abb. 1a-k in Tribu des brevipennes. Famille des aleochariens. Septieme branche: Myrmedoniaires. Annales de la Societe d'Agriculture Histoire Naturelle et Arts Utiles de Lyon (ser.

Abb. 1a-k: Trigonurus ruzickai: Habitus (a); Kopf (b); Kopf, Unterseite (c); Pronotum (d); Elytre (e); Prosternum (f); Mitte von Sternit III (g); Mikroskulptur auf Scutellum (h); Elytren (i) und Abdomen (k). -Holotypus (a, b, d, e, h-k), -Paratypus (c, f, g).

opencc-by-4.0Dec 1874View details →
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Figure 1 in The potential utility of postnatal skeletal developmental patterns in squamate phylogenetics

Figure 1. Simplified hypothesis of squamate relationships showing species investigated. Modified from Estes et al. (1988) with iguanian nomenclature of Frost & Etheridge (1989).

opencc-by-4.0Oct 2002View details →
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Figure 5 in The potential utility of postnatal skeletal developmental patterns in squamate phylogenetics

Figure 5. Strict consensus of seven equally parsimonious trees that result from analysis of discrete data. Tree length = 127 steps, CI = 0.39, RI = 0.57. Node 1, Scleroglossa; node 2, Autarchoglossa; node 3, Scincomorpha; node 4, Gekkota.

opencc-by-4.0Oct 2002View details →
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Figure 3 in The potential utility of postnatal skeletal developmental patterns in squamate phylogenetics

Figure 3. Results of sequence unit analysis with polymorphisms coded by the frequency method of Prober et al. (1990) and Wiens (1993). A, strict consensus of two equally parsimonious trees that result when Bipes biporus is included. B, single most parsimonious tree that results when B. biporus is excluded. Tree length = 2901 steps, CI = 0.40, RI = 0.51. Node 1, Gekkota; node 2, Scincidae; node 3, Xantusiidae.

opencc-by-4.0Oct 2002View details →
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Figure 2 in The potential utility of postnatal skeletal developmental patterns in squamate phylogenetics

Figure 2. Hypothetical example of disparity estimate calculation. Specimens are in columns, postnatal skeletal events are in rows. An X indicates that an event is present in a given specimen.

opencc-by-4.0Oct 2002View 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