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zenodo44/100

Ancillary files for "Reinterpreting the ATLAS bounds on heavy neutral leptons in a realistic neutrino oscillation model [arXiv: 2107.12980]"

<p><em>(Description copied from Appendix A &quot;Ancillary files&quot; of the companion paper)</em></p> <p>In order to simplify the interpretation of experimental results within realistic HNL models, we are including a number of data files along with the present publication. They can be used to generate the relevant signal samples, or to implement the extrapolation method presented in section 3.2.</p> <p><strong>Card files for the Monte-Carlo event generation</strong></p> <p>The /attachments/card_files folder contains the MadGraph card files (ending in .dat) and scripts (ending in .txt) for generating the signal samples used in this analysis, as well as for computing the total HNL width. Due to the OSSF veto, only processes with no opposite-charge same-flavor lepton pairs have been included. Additional relevant processes can easily be added by modifying the <em>generate</em> and <em>add process</em> lines in the *.txt files. All samples (except the ones used to compute the HNL width, which are generated at parton level) are generated at leading order, include up to two hard jets, and are showered and hadronized using Pythia 8. This is essential for obtaining a realistic W spectrum. The shower parameters could probably benefit from further tuning, and further improvements in the W spectrum accuracy are expected at NLO (using a suitable model). To allow computing the signal efficiencies, all cuts have been disabled in the run card (with the exception of the maximum <span class="math-tex">\(|\eta_{\mathrm{jet}}|\)</span> which needs to be set to 5 for correct matching).</p> <p><strong>Signal cross sections</strong></p> <p>The cross sections for the various processes considered in this analysis, as well as the total HNL width (both computed using MadGraph as described in section 3.2), are provided as JSON files in the /attachments/cross_sections folder.</p> <p>The file total_hnl_width.json contains the total HNL width&nbsp;<span class="math-tex">\(\hat{\Gamma}_{\alpha}(M_N)\)</span> (expressed in GeV), computed for the 5 mass points used in this analysis, and under the assumption of unit mixing with a single flavor <span class="math-tex">\(\alpha\)</span>, for each flavor. The total HNL width can then be computed for any combinations of mixing angles using eq. (3.2). The file is organized as two nested dictionaries, with the first key denoting the HNL mass <span class="math-tex">\(M_N\)</span>, and the second one the flavor&nbsp;<span class="math-tex">\(\alpha\)</span> for which the total width&nbsp;<span class="math-tex">\(\hat{\Gamma}_{\alpha}(M_N)\)</span> has been computed for a unit mixing angle&nbsp;<span class="math-tex">\(|\Theta_{\alpha}|^2 = 1\)</span> (with <em>Wtot_e</em> for <span class="math-tex">\(\alpha=e\)</span>, <em>Wtot_mu</em> for <span class="math-tex">\(\mu\)</span> and <em>Wtot_tau</em> for <span class="math-tex">\(\tau\)</span>).</p> <p>The file cross_sections.json contains the reference cross sections&nbsp;<span class="math-tex">\(\sigma_P^{\mathrm{ref}}\)</span> (in pb) for all the processes <em>P</em> considered in this analysis, expressed for&nbsp;<span class="math-tex">\(|\Theta|_{\mathrm{ref}}^2 = 1\)</span> and <span class="math-tex">\(\Gamma_{\mathrm{ref}} = 10^{-5}\,\mathrm{GeV}\)</span>. The file is organized as two nested dictionaries, with the first key denoting the HNL mass <span class="math-tex">\(M_N \)</span> and the second the process <em>P</em>. The correspondence between the key and the physical process can be found in table 7.</p> <p><strong>Signal efficiencies</strong></p> <p>The efficiencies resulting from the event selection described in section 3.1, as well as their parametrization according to eq. (3.6) (as discussed in section 3.3) can respectively be found in the files efficiencies.json and fitted_efficiencies.json in the /attachments/efficiencies folder.</p> <p>The file efficiencies.json is organized as follows. The data is located in a triply nested dictionary under the data key: the first level corresponds to the HNL mass hypothesis <span class="math-tex">\(M_N\)</span>, the second to the process key (cf. table 7) and the third to the&nbsp;<span class="math-tex">\(M(l_{\mathrm{sublead}},l')\)</span> bin for which the efficiency is computed. The values of the bottom-most dictionary are lists containing the efficiencies for a number of HNL lifetimes, as listed in meters in levels/lifetime.</p> <p>Finally, the file fitted_efficiencies.json is also organized as a triply nested dictionary, with the first level corresponding to the HNL mass <span class="math-tex">\(M_N\)</span>, the second to the process key, and where the third level denotes the fit parameter from eq. (3.6). tau0 is for <span class="math-tex">\(\tau_0\)</span>, epsilon0_total for&nbsp;<span class="math-tex">\(\epsilon_0\)</span> (the unbinned prompt efficiency), and epsilon0_binned is a list containing the prompt efficiencies&nbsp;<span class="math-tex">\(\epsilon_{0,b}\)</span> for the five&nbsp;<span class="math-tex">\(M(l_{\mathrm{sublead}},l')\)</span> bins <em>b</em> (in the same order as in efficiencies.json). The layout described here (or a similar one) can be used by experiments to report their signal efficiencies in a way that allows theorists to compute the expected signal for arbitrary choices of mixing angles.</p>

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FIG. 8 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets

FIG. 8. — Hypotheses of primary venation homology of forewing of A, †Angarogryllus angaricus (Sharov 1968) (PIN 1873-16, †Protogryllidae, cf fig. 6A); B, Gryllotalpa sp. (MNHN-EO-ENSIF3938, Gryllotalpidae); C, Scapteriscus sp. (MNHN-EO-ENSIF3068, Gryllotalpidae). Abbreviations and colour code: see text. Scale bars: 1 mm.

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FIG. 5 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets

FIG. 5. — Hypothesis of primary venation homology in male Grylloidea with particular forewing venation: A, B, species with 'shortened' wings; B, C, species with 'reduced' stridulatory apparatus. A, Landreva sp. (MNHN-EO-ENSIF9775, Gryllidae); B, Nemobius sylvestris (Bosc, 1792) (MNHN-EO-ENSIF9786, Trigonidiidae); C, Tafalisca lineatipes Bruner, 1916 (MNHN-EO-ENSIF9760, Oecanthidae); D, Aphonomorphus sp. (MNHN-EO-ENSIF9764, Oecanthidae). Abbreviations: 'ha', distally opened harp; 'mi' distally opened mirror; others and colour code: see text. Grey dash lines represent folds. Scale bars: 1 mm.

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FIG. 1 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets

FIG. 1. — Theoretical pattern of venation of a gryllidean forewing (terminology after Béthoux &amp; Nel [2002], modified after Schubnel et al. [2020]). Abbreviations and colour code: see text.

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FIG. 7 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets

FIG. 7. — Hypothesis of primary venation homology of forewing of male Scapteriscus sp. MNHN-EO-ENSIF3069 (Gryllotalpidae). Abbreviations and colour code: see text. Grey dash lines represent folds. Scale bar: 1 mm.

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APPENDIX 1 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets

<p>APPENDIX 1. &mdash; List of specimens observed in the MNHN Orthoptera collections. Supplementary figures gathered in Appendix 3.</p><table><thead><tr><th>Family, subfamily</th><th><b>Tribe</b></th><th><b>Genus Species</b></th><th><b>Identified</b></th><th>Sex</th><th><b>Inventory number</b></th><th><b>Origin</b></th><th><b>Figures</b></th></tr><tr><th colspan="8">OECANTHIDAE</th></tr></thead><tbody><tr><th>Oecanthinae</th><td>Oecanthini</td><td><i>Oecanthus rufescens</i> Serville, 1838</td><td>L. Desutter</td><td>&male;</td><td>MNHN-EO-ENSIF9765</td><td>New Caledonia</td><td></td></tr><tr><th>Tafaliscinae</th><td>Tafaliscini</td><td><i>Tafalisca lineatipes</i> Bruner, 1916</td><td rowspan="2">L. Denadai de Campos</td><td>&male;</td><td>MNHN-EO-ENSIF9760</td><td>Jamaica</td><td>5C; S3C</td></tr><tr><th></th><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td>Paroecanthini</td><td><i>Paroecanthus simplex</i> Gorochov, 2011</td><td>L. Denadai de Campos</td><td>&male;</td><td>MNHN-EO-ENSIF9782</td><td>Mexique</td><td></td></tr><tr><th></th><td></td><td><i>Angustitrella vicina</i> (Chopard, 1912)</td><td>L. Denadai de Campos</td><td>&male;</td><td>MNHN-EO-ENSIF9783</td><td>French Guiana</td><td></td></tr><tr><th></th><td></td><td><i>Ectotrypa olmeca</i> Saussure, 1874</td><td>L. Denadai de Campos</td><td>&male;</td><td>MNHN-EO-ENSIF12163</td><td>Mexico</td><td>S2C</td></tr><tr><th>Podoscirtinae</th><td>Podoscirtini</td><td><i>Archenopterus bouensis</i> Otte, 1987</td><td>L. Desutter</td><td>&male;</td><td>MNHN-EO-ENSIF3935</td><td>New Caledonia</td><td></td></tr><tr><th></th><td>Aphonomorphini</td><td><i>Aphonomorphus</i> sp.</td><td></td><td>&male;</td><td>MNHN-EO-ENSIF9764</td><td>French Guiana</td><td>5D; S3D</td></tr><tr><th></th><td>Phyllogryllini</td><td><i>Phyllogryllus</i> sp.</td><td></td><td>&male;</td><td>MNHN-EO-ENSIF9768</td><td>Guadeloupe</td><td>4B; S2B</td></tr><tr><th colspan="8">PHALANGOPSIDAE</th></tr><tr><th>Luzarinae</th><td>Luzarini</td><td><i>Luzara obscura</i> Desutter-Grandcolas, 1992</td><td>L. Desutter</td><td>&male;</td><td>MNHN-EO-ENSIF5876</td><td>French Guiana</td><td></td></tr><tr><th></th><td></td><td><i>Lerneca fuscipennis</i> (Saussure, 1874)</td><td>L. Desutter</td><td>&male;/&female;</td><td>MNHN-EO-ENSIF9780, MNHN-EO-ENSIF9781</td><td>French Guiana</td><td>&male;: 3B; S1D / &female;: S4A</td></tr><tr><th>Phalangopsinae</th><td>Phalangopsini</td><td><i>Endecous Itatibensis</i> Rehn, 1918</td><td>L. Desutter</td><td>&male;</td><td>MNHN-EO-ENSIF9761</td><td>Brazil</td><td></td></tr><tr><th></th><td>Homoeogryllini</td><td rowspan="2"><i>Homoeogryllus</i> xanthographus Gu&eacute;rin-M&eacute;nevile, 1844</td><td></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td></td><td>L. Desutter</td><td>&male;</td><td>MNHN-EO-ENSIF9779</td><td><i>Farm strain</i></td><td></td></tr><tr><th></th><td></td><td>orientalis Desutter, 1985</td><td>L. Desutter</td><td>&male;</td><td>MNHN-EO-ENSIF3069</td><td>Mozambique</td><td></td></tr><tr><th></th><td></td><td><i>affinis lyristes</i> Gorochov, 1988</td><td>L. Desutter</td><td>&female;</td><td>MNHN-EO-ENSIF9784</td><td>Rwanda</td><td>Fig. S4B</td></tr><tr><th>Paragryllinae</th><td>Aclodini</td><td><i>Paraclodes guyanensis</i> Desutter-Grandcolas, 1992</td><td>L. Desutter</td><td>&male;</td><td>MNHN-EO-ENSIF9762</td><td>French Guiana</td><td></td></tr><tr><th></th><td>Paragryllini</td><td><i>Aclogryllus</i> sp ..</td><td>L. Desutter</td><td>&male;</td><td>MNHN-EO-ENSIF9785</td><td>Equateur</td><td></td></tr><tr><th>Phaloriinae</th><td></td><td><i>Phaloria</i> sp.</td><td>L. Desutter</td><td>&male;</td><td>MNHN-EO-ENSIF3078</td><td>Philippines</td><td></td></tr><tr><th colspan="8">GRYLLIDAE</th></tr><tr><th>Eneopterinae</th><td>Eneopterini</td><td><i>Eneoptera guyanensis</i> Chopard, 1931</td><td>L. Desutter</td><td>&male;</td><td>MNHN-EO-ENSIF9766</td><td>French Guiana</td><td></td></tr><tr><th></th><td>Lebinthini</td><td><i>Ligypterus fuscus</i> Chopard, 1920</td><td>L. Desutter</td><td>&male;</td><td>MNHN-EO-ENSIF9767</td><td>French Guiana</td><td></td></tr><tr><th></th><td>Lebinthini</td><td><i>Agnotecous</i> sp.</td><td>T. Robillard</td><td>&male;</td><td>MNHN-EO-ENSIF9937</td><td>New Caledonia</td><td></td></tr><tr><th></th><td>Nisitrini</td><td><i>Nisitrus vittatus</i> (Haan, 1844)</td><td>T. Robillard</td><td>&male;</td><td>MNHN-EO-ENSIF9938</td><td>Laboratory strain</td><td></td></tr><tr><th>Pentacentrinae</th><td>Pentacentrini</td><td><i>Pentacentrodes</i> sp.</td><td>L. Desutter</td><td>&male;</td><td>MNHN-EO-ENSIF9776</td><td>Madagascar</td><td></td></tr><tr><th>Gryllinae</th><td>Gryllini</td><td rowspan="2"><i>Brachytrupes</i> (Drury, 1773) <i>membranaceus</i></td><td rowspan="2">L. Desutter</td><td rowspan="2">&male;/&female;</td><td rowspan="2">MNHN-EO-ENSIF9769/ MNHN-EO-ENSIF12162</td><td rowspan="2">Republic of Congo/ Guinea</td><td rowspan="2">&male;: 2A, B; 4A; S2A / &female;: S4C</td></tr><tr><th></th><td></td></tr><tr><th></th><td></td><td><i>Acheta domesticus</i> (Linnaeus, 1758)</td><td></td><td>&male;</td><td>MNHN-EO-ENSIF9777</td><td>Farm strain</td><td></td></tr><tr><th>Landrevinae</th><td>Landrevini</td><td><i>Landreva</i> sp.</td><td>L. Desutter</td><td>&male;</td><td>MNHN-EO-ENSIF9775</td><td>India</td><td>5A; S3A</td></tr><tr><th colspan="8">TRIGONIDIIDAE</th></tr><tr><th>Trigonidiinae</th><td>Trigonidiini</td><td><i>Anaxipha</i> sp.</td><td>L. Desutter</td><td>&male;</td><td>MNHN-EO-ENSIF9770</td><td>French Guiana</td><td></td></tr><tr><th></th><td></td><td><i>Natula longipennis</i> (Serville, 1838)</td><td></td><td>&male;</td><td>MNHN-EO-ENSIF9933</td><td>Indonesia</td><td>3A, B; S1A, B, C</td></tr><tr><th>Nemobiinae</th><td>Nemobiini</td><td>Nemobius sylvestris (Bosc, 1792)</td><td>L. Desutter</td><td>&male;</td><td>MNHN-EO-ENSIF9786</td><td>France</td><td>5B; S3B</td></tr></tbody></table>

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FIG. 6 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets

FIG. 6. — Hypothesis of primary venation homology of male forewing of †Protogryllidae (A, B) and †Baissogryllidae (C-E): A, †Angarogryllus angaricus (Sharov 1968), PIN 1873-16; B, †Falsipseculum karatavicum (Sharov 1968), PIN 3791/1345; C, †Neosharategia paradoxa Gorochov, 1992, PIN 4270-210a; D, †Baissogryllidae sp., CCNH-293; E, †Anglogryllus lyristes Gorochov et al., 2006, MNEMG 2003.46. Abbreviations: "ha", distally opened harp; "mi", distally opened mirror, others and colour code, see text. Grey dash lines represent folds. Scale bars: 1 mm.

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FIG. 9 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets

FIG. 9. — Hypotheses of primary venation homology of forewing of †Liassophyllum caii Gu &amp; Ren, 2012 (CNU-ORT-NN2009008, †Tuphelidae). Modified from Gu et al. (2012). Abbreviations and colour code: see text. Scale bar: 5 mm.

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FIG. 3 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets

FIG. 3. — Hypothesis of primary homology of venation of male Grylloidea: A, Natula longipennis (Serville, 1838) (MNHN-EO-ENSIF9933, Trigonidiidae); B, Lerneca fuscipennis (Saussure, 1874) (MNHN-EO-ENSIF9780, Phalangopsidae). Abbreviations and colour code: see text. Scale bars:1 mm.

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FIG. 4 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets

FIG. 4. — Hypothesis of primary homology of venation of male Grylloidea: A, Brachytrupes membranaceus (Drury, 1773) (MNHN-EO-ENSIF9769, Gryllidae); B, Phyllogryllus sp. (MNHN-EO-ENSIF9768, Oecanthidae). Abbreviations and colour code: see text. Grey dash lines represent folds. Scale bars: 5 mm.

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FIG. 2 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets

FIG. 2. — Main fields (A, C) and functional structures (B, D) of a male grylloid forewing (A, B: Brachytrupes membranaceus (Drury, 1773), MNHN-EO-ENSIF9769) and a male gryllotalpid forewing (C, D: Scapteriscus sp., MNHN-EO-ENSIF3068). Abbreviations: lc, lanceolate cell; ha, harp; mi, mirror. Scale bars: 5 mm.

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FIG. S1 in Reconciliation between neontology and paleontology in the Gryllidea (Orthoptera, Ensifera): reinterpreting the venation of the stridulatory apparatus in crickets

FIG. S1. — Forewings of male Grylloidea with hypothesis of venation: A, B, Natula longipennis (Serville, 1838) (MNHN-EO-ENSIF9933, Trigonidiidae); C, Anaxipha sp. (MNHN-EO-ENSIF9770, Trigonidiidae);D, Lerneca fuscipennis (Saussure,1874) (MNHN-EO-ENSIF9780, Phalangopsidae).Abbreviations:see text. Scale bars:1 mm.

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FIGURE 15. Ultrastenos huberi, rostral fragments. A-B in A reinterpretation and taxonomic revision of Ultrastenos willisi Stein, Hand and Archer, 2016, a short-snouted mekosuchine crocodylian from the Oligocene of northern Australia

FIGURE 15. Ultrastenos huberi, rostral fragments. A-B, QM F31064, fragment of right maxilla. A, ventral view. B, lateral view. C-F, QM F31061, rostral fragment, including right premaxilla and fragment of right maxilla. C, ventral view. D, dorsal view. E, lateral view. F, medial view. Abbreviations: appa, antepenultimate premaxillary alveolus; ect sut, sutural surface for articulation with the ectopterygoid; idp, interdental reception pit; lpal, last premaxillary alveolus; lr, lateral ridge; mal, maxillary alveolus; mn, margin of the naris; mr, medial ridge; msy, articular surface for maxillary symphysis; nar, naris; nc, nasal cavity; nsy, articular surface for nasal symphysis; pm, premaxilla; pmf, premaxillary fenestra; ppal, penultimate premaxillary alveolus; psy, articular surface for premaxillary symphysis; rp, reception pit; sofm, margin of the suborbital fenestra; Vpal, maxillary foramen for palatine ramus of cranial nerve V2 (maxillary division of the trigeminal nerve), note that the margins of this foramen are broken, thus enlarging the apparent size of the foramen. Scale bar equals 20 mm.

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FIGURE 19 in A reinterpretation and taxonomic revision of Ultrastenos willisi Stein, Hand and Archer, 2016, a short-snouted mekosuchine crocodylian from the Oligocene of northern Australia

FIGURE 19. Ultrastenos huberi, reconstructed left mandibular ramus based largely upon QM F61096 and QM F42665, scaled to the size of the former. A, dorsal view. B, medial view (reversed for comparison). C, lateral view. Abbreviations: an, angular; ar, articular; c, coronoid; d, dentary; dal, dentary alveolus; dsy, symphyseal surface of the dentary; emf, external mandibular fenestra; fa, foramen aëreum; fic, foramen intermandibularis caudalis; gl, mandibular glenoid; ms, Meckelian sulcus; rap, retroarticular process; sa, suraqngular; sp, splenial. Scale bar equals 50 mm.

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FIGURE 6 in A reinterpretation and taxonomic revision of Ultrastenos willisi Stein, Hand and Archer, 2016, a short-snouted mekosuchine crocodylian from the Oligocene of northern Australia

FIGURE 6. Comparison of the occipital proportions of various crocodylians. A: Osteolaemus tetraspis NTM unregistered cast, a brevirostrine form. B: Ultrastenos huberi, QM F31075. C. Tomistoma schlegelii, NTM P3142 (cast), a slender longirostrine form. Images are not to scale.

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FIGURE 5 in A reinterpretation and taxonomic revision of Ultrastenos willisi Stein, Hand and Archer, 2016, a short-snouted mekosuchine crocodylian from the Oligocene of northern Australia

FIGURE 5. Ultrastenos huberi QM F31076, White Hunter Cranial Form 1, posterior cranial fragment. A, dorsal view. B, ventral view. C, occipital view. D, right lateral view. Abbreviations: bo, basioccipital; boa, bony otic aperture; cb, caudal bridge of the laterosphenoid; cp, capitate process of the laterosphenoid; cqp, cranioquadrate passage; fa, foramen aereum; fm, foramen magnum; fr, frontal; I, foramen for cranial nerve I (olfactory foramen); II, foramen for cranial nerve II (optic foramen); III+orb, common foramen for cranial nerve III (oculomotor nerve) and the orbital artery and vein; ioc, incisure of the cranioquadrate passage in the otic aperture; IV, foramen for cranial nerve IV (trochlear foramen); lb, lateral bridge of the laterosphenoid; ls, laterosphenoid; mf, metotic foramen; ncr, nuchal crest; oto, otoccipital; ott, olfactory tract trough; pa, parietal; parp, paroccipital process; pbs, parabasisphenoid; pcf, posterior carotid foramen; pfss, sutural surface for articulation with the prefrontal; plp, posterolateral process of the sqamosal; po, postorbital; pob, postorbital bar; pop, postoccipital process of the supraoccipital; ptf, posttemporal fenestra; q, quadrate; qjss, sutural surface for articulation with the quadratougal; so, supraoccipital; sq, squamosal; ss, squamosal sulcus; stf, supratemporal fenestra; V, foramen for cranial nerve V (trigeminal foramen); XIIa, anterior foramen for cranial nerve XII (anterior hypoglossal foramen); XIIp, posterior foramen for cranial nerve XII (posterior hypoglossal foramen). Scale bar equals 50 mm.

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FIGURE 23 in A reinterpretation and taxonomic revision of Ultrastenos willisi Stein, Hand and Archer, 2016, a short-snouted mekosuchine crocodylian from the Oligocene of northern Australia

FIGURE 23. Curvature of the mandible of Ultrastenos huberi compared to Baru iylwenpeny Yates et al. A-C: Ultrastenos huberi, QM F42665, mandibular fragments. A, posterior fragment of the left mandibular ramus. B, right surangular. C, mirror image of the right surangular overlain onto the left mandibular ramus fragment (drawn in red). The left surangular in (A) is filled with white, the other bones are shaded grey. The rectangular bracket in (A) indicates a highly fractured and re-glued zone. Note the offset of the end anterior of the left ramus in (C), which has rotated medially relative to the right surangular (marked with red arrow). D: Baru iylwenpeny, NTM P2787, right mandibular ramus (image reversed). The triangle indicates an inflection point similar to that exhibited in QM F42665. Scale bar equals 50 mm.

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FIGURE 11 in A reinterpretation and taxonomic revision of Ultrastenos willisi Stein, Hand and Archer, 2016, a short-snouted mekosuchine crocodylian from the Oligocene of northern Australia

FIGURE 11. Comparison of the squamosal in right lateral view of Ultrastenos huberi with various species of Baru, showing the angle of descent of the posterolateral process and sculptural elements of the lateral surface. A: Ultrastenos huberi, QM F31075. Note that the lateral squamosal sulcus is both broad and extensive and the posterolateral process descends at a steep angle. B: Baru wickeni, NTM P9464-10 (image reversed for comparison). Note that the lateral surface is largely flat with a short, narrow sulcus and the posterolateral process descends at a shallow angle. C: Juvenile Baru iylwenpeny (NTM P6478). Note the flat lateral surface with a short, narrow sulcus and the shallow angle of descent. D: Adult Baru iylwenpeny (NTM P6515) Note the flat lateral surface with a short, narrow sulcus and the shallow angle of descent shared with other Baru specimens. Note also the presence of a posterolateral boss shared with (B) but not (C). Dashed lines demarcate each posterolateral boss. Hatched areas demarcate lateral sulci. Scale bars equal 20 mm.

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FIGURE 2 in A reinterpretation and taxonomic revision of Ultrastenos willisi Stein, Hand and Archer, 2016, a short-snouted mekosuchine crocodylian from the Oligocene of northern Australia

FIGURE 2. Ultrastenos huberi, QM F42665, significant fragments of the holotype of U. willisi Stein et al. A, B, basicranial fragment with displaced adherent left pterygoid in right lateral (A) and occipital views (B). C, D, right temporal fragment in lateral (C) and dorsal views (D). E, G, I, posterior end of left mandibular ramus in lateral (E), medial (G) and dorsal (I) views. F, H, disarticulated right suranguar and angular in medial (F) and lateral (H) views. J, right surangular in dorsal view (anterior to the left). Scale bar equals 50 mm.

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FIGURE 8 in A reinterpretation and taxonomic revision of Ultrastenos willisi Stein, Hand and Archer, 2016, a short-snouted mekosuchine crocodylian from the Oligocene of northern Australia

FIGURE 8. Dermal bone ornamentation of Baru wickeni and Ultrastenos huberi compared. A: Explanatory drawing of the skull of Baru wickeni in dorsal view with frontal and right squamosal marked in red and the areas shown in (B) and (C) marked by boxes. B: Baru wickeni (NTM P91171-1), frontal in dorsal view showing the ornamentation. C: Baru wickeni (NTM P902-4), right squamosal in dorsal view showing the ornamentation. D: Explanatory drawing of the skull of Ultrastenos huberi in dorsal view with frontal and right squamosal marked in red and the areas shown in (E) and (F) marked by boxes. E: Ultrastenos huberi (QM F F31076), frontal in dorsal view showing the ornamentation. F: Ultrastenos huberi (QM F F31075), right squamosal in dorsal view showing the ornamentation. Scale bars in (B, C, E, F) equal 10 mm. (A, D) are not to scale.

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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