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Fig. 10 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 10. Photographs and line drawings of the interorbital region in M-2968 (A) and M-2983 (B). Note differences in the breadth of contact of the prefrontal (PF) and palatine (PAL) above the foramen orbitonasale (fon).

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Fig. 20 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 20. Photographs and line drawings of the caudal margin of the left orbital floor and rostral margin of the cavum cranii as viewed through the left orbit of M-2966. A rostral opening of the vidian canal (acnv) lies in the caudal margin of the foramen palatinum posterior. The foramen arteriae anteriovidianae (faa) is a second rostral opening of a vidian canal that transmits a branch of the vidian nerve and vein onto the dorsal surface of the palate.

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Fig. 9 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 9. Photographs and line drawings of the rostral view of M-2995 (A), an immature female, and M-2987 (B), an adult male exhibiting teratological variation in the rostral portion of the skull. This variation is most clearly expressed in the shape of the apertura narium externa, fissura ethmoidalis, premaxillae, and vomer.

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Fig. 13 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 13. Photographs and line drawings of the left lateral surface of the skull showing the presence (A, M-2984) and absence (B, M-2983) of a contribution from the jugal to the rostral rim of the upper temporal fenestra.

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Fig. 33 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 33. Scree plot showing the distribution of eigenvalue scores for each principal component derived from the analysis of 25 continuous characters from the skull and lower jaws of Sternotherus odoratus from the SMRS. PC1, which generally represents size, constitutes a large percentage (over 80%) of the total sample variance. The first three principal components account for more than 90% of the total sample variance.

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Fig. 7 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 7. Photographs and line drawings of the left lateral view of the skull of Sternotherus odoratus based on the least mature (M-2980, A) and most mature (M-2983, B) specimens from the SMRS.

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Fig. 6 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 6. Photographs and line drawings of the dorsal and ventral views of the skull of Sternotherus odoratus based on the most mature specimen from the SMRS (M-2983).

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Fig. 3 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 3. Continuous characters included in morphometric and growth analyses. Numbers refer to character descriptions in text. Dorsal view of skull (A), ventral view of skull (B), left lateral view of skull (C), rostral view of skull (D), dorsal view of lower jaw (E), and left lateral view of lower jaw (F).

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Fig. 32 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 32. Photographs and line drawings of the dorsal surface of the parabasisphenoid in M-2990 (A), M-2978 (B), and M-2982 (C), and a caudal view of the parabasisphenoid in articulation with the prootic and pterygoid in M-2982 (D). Note the variable development of the rostrum basisphenoidale (rb), trabeculae (tr), and the caudolateral concavities that contribute to the ventral margin of the cavum labyrinthicum (cl).

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Fig. 2 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 2. Relationship between carapace length and plastron length (A), condylobasal length (B), and greatest length of the skull (C) for Sternotherus odoratus from the SMRS.

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Fig. 1 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 1. Phylogenetic hypotheses regarding the systematic position of Sternotherus odoratus. The sister taxon to Kinosternoidea within Cryptodira is currently a point of contention (Meylan and Gaffney, 1989; Krenz et al., 2005; Near et al., 2005). Kinosternoidea here is considered to reflect the crown-clade of Kinosternidae + Dermatemys. This usage follows Joyce et al. (2004) and reflects the unresolved position of Emarginachelys (Shaffer et al., 1997). Asterisks (*) denote extinct lineages.

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Fig. 15 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 15. Photograph and line drawing of the rostroventral surface of the left quadrate and basicranium of M-2981. Note the relatively close approximation of the laterally positioned quadratojugal to the articular surface of the quadrate, and contact between the quadrate ramus of pterygoid and the articular surface of quadrate.

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Fig. 28 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 28. Photographs and line drawings of the left basicranial region in posterolateral view through the fenestra postotica in M-2983 (A) and M-2995 (B). Note the increased ossification in M-2983 (a large, mature male) relative to M-2995 (an immature male). This increased ossification is especially apparent around the fenestra ovalis (fo) and the lateral margin of the foramen jugular posterius (fjp). The columella auris is absent in both specimens.

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Fig. 29 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 29. Photographs and line drawings of the left basicranial region in M-2969 (A), the exoccipital and basioccipital in left lateral view in M-2960 (B), and the medial view of the prootic and opisthotic in M-2964 (C). The floor of the recessus scalae tympani is formed by a caudal shelf of the opisthotic and a rostral extension of the exoccipital. X in M-2960 marks a concavity in the basioccipital that accepts the distal end of the cochlear duct (cochlear recess). X in M-2964 marks the notch in the processus interfenestralis of the opisthotic through which the cochlear duct extends caudomedially.

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Fig. 23 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 23. Photographs and line drawings of the dorsal surface of the pterygoid in M-2960 (A, left) and M-2990 (B, right). The foramen caroticum laterale, which transmits the palatine artery rostrally, was closed dorsally in M-2960 by the overlying prootic, whereas in M-2990 the dorsal margin of this foramen is formed by the pterygoid. The pterygoid falls just short of forming the entire medial margin of the foramen caroticum laterale in M-2990. This margin would have been closed medially by the parabasisphenoid. Arrows show path of internal carotid artery.

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Fig. 4 in Postnatal Ontogeny Of The Skull In Th E Ex Tant North Am Eric An Turtle Sternotherus Odoratus (Crypto Dir A: Kinosterni Dae) G A B E S. B E V Er

Fig. 4. Illustrations of three skeletal characters often used to estimate maturity in turtles and their graphical relationship with greatest length of the carapace for Sternotherus odoratus from the SMRS. These characters include closure of the costoperipheral fontanelles (A), closure of the ectepicondylar foramen in the humerus (B), and closure of the otic fontanelle (C). Shaded squares represent juvenile males, clear squares represent juvenile females. Shaded circles represent adult males, clear circles represent adult females. The transformation of these features during postnatal ontogeny has a variable relationship with the average carapace length at which specimens become sexually mature in southern populations of S. odoratus (dashed lines; Tinkle, 1961).

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00887 LII. Woche II. 9. Br. Johannis Rede in der Abend-Versammlung ... d. 26. Dec. über die Loosung: Der Herr wird ausgehen aus seinem Ort und herab fahren. So fuhr Er aus der Ewigkeit in diese abgemeßne Zeit u. ward im Leib eines Jungfräuleins, der sterbenden Gebeine eins. Und den Text: Auf daß Seine Herrschaft groß werde und des Friedes kein Ende auf dem Stuhl David und seinen König reiche. Daß Er zurichte und stärcke mit Gericht und Gerechtigkeit, von nun an bis in Ewigkeit

<p>Mit den&nbsp;<em><strong>Gemein-Nachrichten</strong></em>&nbsp;stellt das Unit&auml;tsarchiv Herrnhut der weltweiten Evangelischen Br&uuml;der-Unit&auml;t - Herrnhuter Br&uuml;dergemeine (Unitas Fratrum / Moravian Church) das &auml;lteste und umfangreichste Mitteilungsblatt der Br&uuml;dergemeine digital zur Verf&uuml;gung. Es enth&auml;lt Berichte aus Gemeinden sowie dem Missions- und Diasporawerk der Br&uuml;dergemeine sowie Reden und Lebensl&auml;ufe. Die&nbsp;<em>Gemein-Nachrichten</em>&nbsp;wurden ab 1765 in Fortsetzung des&nbsp;<em>J&uuml;ngerhaus-Diariums</em>&nbsp;(1747-1764) ausschlie&szlig;lich handschriftlich vervielf&auml;ltigt. In Druck gingen 1817 und 1818 die <em>Beytr&auml;ge aus der Br&uuml;der-Gemeine</em> und zwischen 1819 und 1894 die&nbsp;<em>Nachrichten aus der Br&uuml;der-Gemeine</em>. Das Nachrichtenblatt fand in den&nbsp;<em>Mitteilungen aus der Br&uuml;der-Gemeine zur F&ouml;rderung christlicher Gemeinschaft</em>&nbsp;ab 1895 bis 1941 seine Fortsetzung.</p> <p>Das hier <strong>vorliegende Datenset</strong> umfasst Transkriptionen nach XML-TEI in verschiedenen Versionierungen und einen normalisierten Text. Die ID bezieht sich auf den <strong>Index</strong> der handschriftlichen Gemein-Nachrichten (<a href="../doi/10.5281/zenodo.8228849">DOI</a>). Metadaten werden nach einem standardisierten <strong>XML-Schema</strong> angelegt (<a href="../doi/10.5281/zenodo.10375427">DOI</a>). Die Dateinamen sind sprechend:<br><br>[ID]_01.xml: Export (XML-TEI) nach Transkription vom Prim&auml;rdigitalisat</p> <p>[ID]_02.xml: um Metadaten angereichtertes Transkript (XML-TEI)&nbsp;</p> <p>[ID]_03.txt: normalisierter Text zur weiteren Nutzung (z.B. f&uuml;r maschinelle Analysen)</p> <p>[ID]_04.xml: angereichertes Transkript (XML-TEI) mit Metadaten und Glossarannotation</p>

opencc-by-4.0Jan 2024View details →
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Fig.ç4.Ec hinoderes ohtsukai sp. nov., paratype, female (ZIHU 3983), scanning electron micrographs. A, Mouth cone, lateral view; B, introvert, lateral view. Abbreviations: oo, outer oral styles; sc, scalids; sp, spinoscalids; tr, trichoscalids. Digits a er the labels refer to introvert ring numbers. in A New Brackish-water Species of Echinoderes (Kinorhyncha: Cyclorhagida) from the Seto Inland Sea, Japan

Fig.ç4.Ec hinoderes ohtsukai sp. nov., paratype, female (ZIHU 3983), scanning electron micrographs. A, Mouth cone, lateral view; B, introvert, lateral view. Abbreviations: oo, outer oral styles; sc, scalids; sp, spinoscalids; tr, trichoscalids. Digits a er the labels refer to introvert ring numbers.

opencc-by-4.0May 2012View details →
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Native MS dataset for: "Caldendrin and myosin V regulate synaptic spine apparatus localization via ER stabilization in dendritic spines."

<p>Native mass spectrometry dataset used in: <strong>Caldendrin and myosin V regulate synaptic spine apparatus localization via ER stabilization in dendritic spines.</strong> Anja Konietzny, Jasper Grendel, Alan Kadek, Michael Bucher, Yuhao Han, Nathalie Hertrich, Dick H. W. Dekkers, Jeroen A. A. Demmers, Kay Grünewald, Charlotte Uetrecht and Marina Mikhaylova. <i>The EMBO Journal</i> (2021) e106523. doi:<a href="https://doi.org/10.15252/embj.2020106523">10.15252/embj.2020106523</a></p><p>&nbsp;</p><p><strong>Description:</strong></p><p>Native mass spectrometry (MS) analysis of the stoichiometry and ion occupancy of recombinant human calmodulin (CaM) and recombinant rat caldendrin (CaD) complex with synthetic mouse myosinV IQ1 (myoIQ) motif in the presence / absence of excess Ca2+ and Mg2+ ions.</p><p><strong>Sample processing:</strong></p><p>Full-length CaD and CaM as well as the synthetic myoVa peptide were buffer exchanged into 150 mM aqueous ammonium acetate solution (pH&nbsp;7.4). CaM was twice passed through a Bio-Spin P-6 gel filtration spin column (6 kDa cut-off, <i>Bio-Rad</i>), CaD and the myoVa peptide were buffer exchanged through five cycles of tenfold dilution and re-concentration using centrifugal concentrators Vivaspin 500 (10 kDa cut-off, <i>Sartorius</i>) or Amicon Ultra 0.5mL (3 kDa cut-off, <i>Merck/Millipore</i>), respectively. Desalted proteins were introduced into an Orbitrap Q Exactive UHMR mass spectrometer (<i>Thermo Scientific</i>) via static nanoelectrospray ionization from in-house prepared gold-coated borosilicate glass capillaries Kwik-Fil 1B120F-4 (<i>World Precision Instruments</i>). Proteins were sprayed and analysed at 8.5 µM concentration in ammonium acetate alone or supplemented with 200 µM calcium acetate and 100 µM magnesium acetate (both for trace metal analysis, <i>Sigma-Aldrich</i>). For interaction analysis, CaM and/or caldendrin were mixed with myoVa peptide which had final concentration of 8.5 µM (low concentration) or 34 µM (high concentration). The mass spectrometer was tuned for best signal quality and intensity, keeping ion activation and unfolding minimal. Namely, electrospray voltage was kept at 1.3 kV, source desolvation temperature 250°C, in-source desolvation -50 V, ion transfer profile "high m/z", analyzer profile "low m/z", analyzer target resolution 12500 acquiring in mass range 500 – 9000 m/z. Nitrogen was used as collision gas in HCD cell at relative gas pressure setting 7.0 with gentle collisional activation by 10 V HCD voltage gradient.</p><p><strong>Data processing:</strong></p><p>Raw spectra were averaged over at least 50 scans for mass deconvolution and peak assignment in UniDec 4.4.1 package (<i>Marty et al., 2015</i>). The averaged spectra were exported for ZENODO deposition using <i>Thermo Scientific</i> FreeStyle 1.5.93.34 as single-scan Thermo .raw files (including instrumental parameters metadata) as well as in plain m/z vs intensity .txt files.</p>

opencc-by-4.0Dec 2021View details →
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(Cot)Er(Cnt)

<p>This contains the dataset for&nbsp;(Cot)Er(Cnt)</p>

opencc-by-4.0Dec 2021View details →

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Allen Brain Atlas

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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.

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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