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FIGURE 10 in The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) - taxonomy and palaeobiological implications
FIGURE 10. Two-dimensional plot Lsn (standardised length form apex to the protoconch) vs. AV (ventral aspect) of guards of Bln. kazimiroviensis and Bln. skolozdrownae from the Kazimierz Opoka (Kongiel Collection) from different localities (Kazimierz, Bochotnica and Nasilów), all except one from levels x and y sensu Pożaryski (1938).
FIGURE 12 in The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) - taxonomy and palaeobiological implications
FIGURE 12. Two-dimensional plot Lsn (standardised length form apex to the protoconch) vs. AV (ventral aspect) of guards of Bln. kazimiroviensis and Bln. skolozdrownae from the glauconitic sandstone at Nasilów quarry. The dashed line indicates the variability of both species in the stratigraphically older Kazimierz Opoka.
FIGURE 5 in Telychian (Llandovery, Silurian) conodonts from the LaPorte City Formation of eastern Iowa, USA (East-Central Iowa Basin) and their implications for global Telychian conodont biostratigraphic correlation
FIGURE 5. Stratigraphic column and conodont range chart for the LPC in the Garrison Core. Dashed lines indicate uncertainty in range. M = mudstone, W = Wackestone, P = Packstone, F = Floatstone for carbonate lithologies. L.H. = Lower Hopkinton. Log colors represent the color of the rock. Correlation of conodont biozonation to chronostratigraphic units from Cramer et al. (2011).
FIGURE 6 in The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) - taxonomy and palaeobiological implications
FIGURE 6. Diagram illustrating morphological features of the belemnite guard (lateral view of a longitudinally split guard on the left, ventral view on the right). AA = alveolar angle; FA = fissure angle; SD = Schatzky distance; Ls = length from apex to protoconch; Ds, Dp, Dc = dorso-ventral diameters at different part of the rostrum; Bs, Bp, Bc = lateral diameters at different part of the rostrum (after Keutgen, 1997; Keutgen et al., 2012).
FIGURE 5 in The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) - taxonomy and palaeobiological implications
FIGURE 5. Age, lithostratigraphy, general lithology and subdivision into lithostratigraphical horizons and units (IVe-1 to Va-4) of the section formerly exposed at the Curfs-Ankerpoort quarry (Geulhem), with indication (arrow) of the KPg boundary, equating with the Berg en Terblijt Horizon at the top of subunit IVf-6 (modified after Jagt and JagtYazykova, 2012). The range of belemnite species shown is that for the entire Maastricht area. R = remanié specimens.
FIGURE 3. 1, Generalised K in The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) - taxonomy and palaeobiological implications
FIGURE 3. 1, Generalised K-Pg section at Nasiłów; 2, Details of the boundary interval and the position of the K-Pg boundary placed at the top of the Kazimierz Opoka; according to Machalski (1998).
FIGURE 4. 1 in The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) - taxonomy and palaeobiological implications
FIGURE 4. 1, Schematic map of southern Limburg (the Netherlands) showing the formerly available outcrops of the Meerssen Member (red stars) (after Jagt et al., 1996) that yielded representatives of the Belemnella kazimiroviensis group; black dots are smaller towns in the area; 2, Position of the Netherlands within Europe (red star).
FIGURE 10 in Telychian (Llandovery, Silurian) conodonts from the LaPorte City Formation of eastern Iowa, USA (East-Central Iowa Basin) and their implications for global Telychian conodont biostratigraphic correlation
FIGURE 10. Conodonts from the Garrison Core and DX5 outcrop. 1-7, Pterospathodus amorphognathoides angulatus, Sc1 element, posterior view, GC 115.51–115.76 m, SUI 142304 (1); Pb1? element, lateral view, GC 115.51– 115.76 m, SUI 142305 (2); Pb2 element, GC 111.38–111.63 m, SUI 142306 (3); Pb1 element, inner lateral, and oral views, GC 115.51–115.76 m, SUI 132410 (4 and 5); Pa element, oral view, DX5 3.49–3.59 m, SUI 142307 (6); and Pa element, lateral view, DX5 4.59–4.61 m, SUI 142308 (7). 8-19, Pterospathodus eopennatus ssp. n. 2 sensu Männik (1998), Sb2 element, posterior, and lateral views, GC 130.79–131.09 m, SUI 142309 (8 and 9); Sc1 element, lateral view, GC 130.79–131.09 m, SUI 142310 (10); M element, GC 130.79–131.09 m, SUI 142311 (11); Pb1 element, lateral view, GC 128.85–129.11 m, SUI 142312 (12); Pc element, lateral view, GC 130.20–130.48 m, SUI 142313 (13); Pb1 element, lateral view, GC 130.20–130.48 m, SUI 142314 (14); Pa element, lateral view, GC 128.85–129.11 m, SUI 142315 (15); Pb1 element, lateral view, GC 130.20–130.48 m, SUI 142316 (16); Pa element, lateral, and oral views, GC 130.79–131.09 m, SUI 142317 (17 and 18); and Pa element fragment, oral view, GC 130.20–130.48 m, SUI 142318 (19). 20-21, Aulacognathus sp., juvenile P1 element, oral, and lateral-anterior views, GC 135.65–136.10 m, SUI 142319. 22-23, Kockelella cf. K. abrupta, P1 element, oral, and lateral views, DX5 0.67–0.74 m, SUI 142320.
FIGURE 13 in The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) - taxonomy and palaeobiological implications
FIGURE 13. Two-dimensional plot Lsn (standardised length form apex to the protoconch) vs. AV (ventral aspect) of guards of Bln. kazimiroviensis from the basal Siwak at Nasilów quarry. The dashed lines indicate the variability of Bln. kazimiroviensis and Bln. skolozdrownae from the stratigraphically older glauconitic sandstone.
FIGURE 1 in The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) - taxonomy and palaeobiological implications
FIGURE 1. Map of Europe and Central Asia, illustrating the general distribution of representatives of the Belemnella kazimiroviensis group as a whole, without differentiation into particular species of the group. The origin of holotype specimens of representatives of this group recorded in the literature are as follows: Belemnella kazimiroviensis – Vistula section; Belemnella skolozdrownae – Stevns Klint; Belemnella pensaensis – Saratov/Penza; Belemnella arkhangelskii – Turgay Plateau.
FIGURE 16 in The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) - taxonomy and palaeobiological implications
FIGURE 16. Two-dimensional plot Lsn (standardised length form apex to the protoconch) vs. AV (ventral aspect) of guards of Bln. kazimiroviensis and Bln. skolozdrownae from Denmark mentioned in the scientific literature. The holotypes of Bln. kazimiroviensis, proposed by Jeletzky (1951) and Kongiel (1962), are also indicated (blank squares), in addition to the holotype of Bln. skolozdrownae from Denmark. The dashed lines indicate the variability of Bln. kazimiroviensis and Bln. skolozdrownae from the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium).
FIGURE 2. 1 in Telychian (Llandovery, Silurian) conodonts from the LaPorte City Formation of eastern Iowa, USA (East-Central Iowa Basin) and their implications for global Telychian conodont biostratigraphic correlation
FIGURE 2. 1, Paleogeographic map showing the locations of the continents during the lower to middle Silurian. Black box indicates approximate location of the Illinois Basin. From Torsvik et al. (1996, figure 13). 2, Map showing the deepest part of the Illinois and East-Central Iowa basins, and trans-Iowa sag in Iowa and nearby states during the Silurian. Shading indicates extent of basins. Modified from Cramer et al. (2006, figure 1).
FIGURE 22 in The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) - taxonomy and palaeobiological implications
FIGURE 22. Estimation of percentage of belemnites of the kazimiroviensis group remaining in the habitat, calculated from size-group distribution at Nasiłów (Poland) and the Maastricht area (the Netherlands, Belgium).
FIGURE 21 in The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) - taxonomy and palaeobiological implications
FIGURE 21. An excellently preserved specimen of Bln. kazimiroviensis (left) retaining part of the proostracum, together with a normally preserved guard (right) in the glauconitic sandstone at Nasiłów (field photograph; specimen with proostracum could not be collected completely).
FIGURE 19 in The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) - taxonomy and palaeobiological implications
FIGURE 19. Belemnella (Neobelemnella) skolozdrownae (Kongiel 1962). 1-4, NHMM MK 2815, Albert Canal near Vroenhoven (61F-19), uppermost Meerssen Member; 5-8, NHMM JJ 8759, ENCI-HeidelbergCement Group quarry, Maastricht, Meerssen Member, IVf-4 or IVf-5; 9-12, MWGUW ZI/69/70, and 13-16, ZI/69/86 – from the glauconitic sandstone below the "phosphatic layer" at Nasiłów; 17-20, MWGUW ZI/69/60 and 21-24, ZI/69/61 – from the "phosphatic layer" at Nasiłów quarry. All specimens are in natural size in following views: dorsal (1, 5, 9, 13, 17, 21), lateral (2, 6, 10, 14, 18, 22), longitudinally split specimen showing internal features (3, 7, 11, 15, 19, 23), and close-up of alveolar part [x2] with the course of the bottom of ventral fissure – dashed line (4, 8, 12, 16, 20, 24).
FIGURE 4 in Telychian (Llandovery, Silurian) conodonts from the LaPorte City Formation of eastern Iowa, USA (East-Central Iowa Basin) and their implications for global Telychian conodont biostratigraphic correlation
FIGURE 4. Specimens reported from the DX5 outcrop section in Metzger (2005). All specimens in lateral view. 1-3, 5, Pterospathodus eopennatus ssp. n. 2 sensu Männik (1998), Pa element, DLH 4, SUI 132418 (1); Pa element, DLH 6, SUI 132420 (2); Pb element, DLH 6, SUI 132420 (3); and Pa element, DLH 9, SUI 132423 (5). 4, 6-9, Pterospathodus amorphognathoides angulatus, Pa element, DLH 6, SUI 132420 (4); Pb element, DLH 6, SUI 132420 (6); Pa element, DLH 6, SUI 132420 (7); Pb element, DLH 6, SUI 132420 (8); and Pa element, DLH 11, SUI 132425 (9). 10, Aulacognathus bullatus? Pb element, DLH 11, SUI 132425.
FIGURE 2. 1 in The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) - taxonomy and palaeobiological implications
FIGURE 2. 1, location of the Middle Vistula River valley section in the Europe; 2, location in Poland together with the schematic extension of the Cretaceous and pre-Cretaceous deposits in Poland (without the Cenozoic cover); 3, position of Nasiłów along the Vistula River between the villages of Solec nad Wisłą and Kazimierz.
FIGURE 18 in The late Maastrichtian Belemnella kazimiroviensis group (Cephalopoda, Coleoidea) in the Middle Vistula valley (Poland) and the Maastricht area (the Netherlands, Belgium) - taxonomy and palaeobiological implications
FIGURE 18. Relationship of BI (Birkelund Index) vs Dp (dorso ventral diameter at the protoconch) (BI = Ls/Dp; compare with Figure 6) of guards of Bln. kazimiroviensis from the Middle Vistula valley and the Maastricht area. The growth relationship is best described by a logarithmic curve.
FIGURE 9 in Telychian (Llandovery, Silurian) conodonts from the LaPorte City Formation of eastern Iowa, USA (East-Central Iowa Basin) and their implications for global Telychian conodont biostratigraphic correlation
FIGURE 9. Conodonts from the Garrison Core and DX5 outcrop. 1-8, Wurmiella? polinclinata polinclinata, S0 element, anterior view, GC 130.79–131.09 m, SUI 142286 (1); S1/2 element, posterior view, GC 115.51–115.79 m, SUI 142287 (2); S3/4 element, lateral view, GC 115.51–115.76 m, SUI 142288 (3); M element, lateral view, GC 130.20– 130.48 m, SUI 142289 (4); P2 element, lateral view, GC 130.20–130.48 m, SUI 142290 (5); P2 element, GC 130.79– 131.09 m, SUI 142291 (6); P1 element, lateral view, DX5 4.59–4.61 m, SUI 142292 (7); and P1 element, lateral view, DX5 3.49–3.59 m, SUI 142293 (8). 9-10, Aulacognathus angulatus, P1 element, oral view, GC 135.65–136.10 m, SUI 142294 (9) and S1/2? element, posterior view, GC 135.65–136.10 m, SUI 142295 (10). 11-14, Aulacognathus bullatus, P2 element, lateral view, DX5 1.34–1.54 m, SUI 142296 (11); P1 element, oral view, DX5 4.59–4.61 m, SUI 142297 (12); P1 element, oral view, DX5 0.67–0.74 m, SUI 142298 (13); and P1 element, oral view, GC 120.88– 121.13 m, SUI 142299 (14). 15-16, Aulacognathus kuehni, P1 element, oral view, GC 131.95–132.23 m, SUI 142300 (15) and juvenile P1 element, oral view, GC 131.95–132.23 m, SUI 142301 (16). 17, Astrolecignathus cf. milleri, Pa element, oral view, GC 121.92–121.88 m, SUI 142302. 18, Apsidognathus tuberculatus, Pa element, oral view, DX5 1.34–1.54 m, SUI 142303.
FIGURE 8. Conodonts from the Garrison Core. 1-12, 19 in Telychian (Llandovery, Silurian) conodonts from the LaPorte City Formation of eastern Iowa, USA (East-Central Iowa Basin) and their implications for global Telychian conodont biostratigraphic correlation
FIGURE 8. Conodonts from the Garrison Core. 1-12, 19, Psuedolonchodina sp. n., Sa element, posterior view, GC 115.51–115.76 m, SUI 152266 (1); Sa element, posterior-aboral view, GC 121.62–121.88 m, SUI 142267 (2); Sb element, anterior view, GC 134.06–134.31 m, SUI 142268 (3); Sc element, lateral view, GC 130.20–130.48, SUI 142269 (4); Sc/M? element fragment, lateral view, GC 128.85–129.11 m, SUI 142270 (5); M element, lateral-posterior view, GC 131.95–132.23 m, SUI 142271 (6); M element, anterior-lateral view, GC 134.06–134.31 m, SUI 142272 (7); Pa element, oral view, GC 134.06–134.31 m, SUI 142273 (8); Pa element, oral view, GC 130.79–131.09m, SUI 142274 (9); Sc element, lateral view, GC 135.65–136.10 m, SUI 142259 (10); Pb element, lateral, and lateral-aboral views, GC 115.51–115.76 m, SUI 142275 (11 and 12); and Pb element, lateral view, GC 130.79-131.09 m, SUI 142276 (19). 13, 15, Oulodus sp. indet., Sa element, anterior-lateral view, GC 137.12–137.40 m, SUI 142277 (13) and Pa element, posterior view, GC 135.65–136.10 m, SUI 142278 (15). 14, 16-17, Oulodus cf. Ou. petilus pacificus, Sc element, lateral view, GC 134.06–134.31 m, SUI 142279 (14); Sb element, posterior-oral view, GC 130.20–130.48 m, SUI 142280 (16); and Pb element, anterior-lateral view, GC 130.79–131.09 m, SUI 142281 (17). 18, 21-22, Distomodus staurognathoides, Sb element, posterior view, GC 134.06–134.31 m, SUI 142282 (18); Pa element, oral view, GC 135.65– 136.10 m, SUI 142283 (21); and Pa element, oral view, GC 135.65–136.10 m, SUI 142282 (22). 20, Aulacognathus angulatus, P2 element, lateral view, GC 135.65–136.10 m, SUI 142285.
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Allen Brain Atlas
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International Brain Laboratory public data
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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.