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Figure 27. Postclymenia calceola n in A morphometric approach to conch ontogeny of Cymaclymenia and related genera (Ammonoidea, Late Devonian)
Figure 27. Postclymenia calceola n. sp. from Lalla Mimouna (Anti-Atlas of Morocco); all × 1.0. (A) Paratype MB.C.22662.2 (Ebbighausen 2005 Coll.). (B) Holotype MB.C.22662.1 (Ebbighausen 2005 Coll.). (C) Paratype MB.C.22662.3 (Ebbighausen 2005 Coll.). (D) Paratype MB.C.22663.1 (Korn 2005 Coll.). (E) Paratype MB.C.22663.2 (Korn 2005 Coll.).
Figure 19 in A morphometric approach to conch ontogeny of Cymaclymenia and related genera (Ammonoidea, Late Devonian)
Figure 19. Cross sections (A–D; all × 1.5) and ontogenetic trajectories (E–H) of Cymaclymenia costellata (Münster, 1832) from the Rhenish Mountains of Germany. (A) Specimen MB.C.22693 (Korn 1975 Coll.) from Reigern. (B) Specimen MB.C.22694 (Korn 1974 Coll.) from Reigern. (C) Specimen MB.C.22695.2 (Korn 1977 Coll.) from Oberrödinghausen. (D) Specimen MB.C.22695.3 (Korn 1977 Coll.) from Oberrödinghausen. (E) Conch width index (ww / dm). (F) Umbilical width index (ww / wh). (G) Whorl width index (uw / dm). (H) Whorl expansion rate (WER).
Figure 18 in A morphometric approach to conch ontogeny of Cymaclymenia and related genera (Ammonoidea, Late Devonian)
Figure 18. Cymaclymenia costellata (Münster, 1832) from the Rhenish Mountains (Germany); all × 1.0. (A) Specimen MB.C.22692 (Korn 1974 Coll.) from Reigern. (B) Specimen MB.C.4179 (Denckmann 1900 Coll.) from Wettmarsen. (C) Specimen MB.C.22695.1 (Korn 1977 Coll.) from Oberrödinghausen. (D) Specimen MB.C.22700 (Schindewolf 1931 Coll.) from Hauern near Braunau. (E) Specimen MB.C.22697 (Korn 1987 Coll.) from Effenberg. (F) Specimen MB.C.4185 (Lotz and Denckmann 1900 Coll.) from Langenholthausen. (G) Specimen MB.C.22701 (Denckmann 1895 Coll.) from Hauern. (H) Specimen MB.C.4202.2 (purchased 1903) from Hauern. (I) Specimen MB.C.4202.1 (purchased 1903) from Hauern.
Figure 15. Cymaclymenia formosa n in A morphometric approach to conch ontogeny of Cymaclymenia and related genera (Ammonoidea, Late Devonian)
Figure 15. Cymaclymenia formosa n. sp. from the Anti-Atlas of Morocco; all × 1.0. (A) Holotype MB.C.22609.1 (Korn 1995 Coll.) from Erfoud. (B) Paratype MB.C.22669.1 (Wendt Coll.) from Hamar Laghdad. (C) Paratype MB.C.22669.2 (Wendt Coll.) from Hamar Laghdad. (D) Paratype MB.C.22669.3 (Wendt Coll.) from Hamar Laghdad. (E) Paratype MB.C.22649.1 (Korn 2009 Coll.) from Lambidia (Aguelmous). (F) Paratype MB.C.22649.2 (Korn 2009 Coll.) from Lambidia (Aguelmous). (G) Paratype MB.C.22669.4 (Wendt Coll.) from Hamar Laghdad.
Figure 1 in A morphometric approach to conch ontogeny of Cymaclymenia and related genera (Ammonoidea, Late Devonian)
Figure 1. Modes of allometry expressed in ammonoid conchs, exemplified in the conch width index (CWI) of modelled and real ammonoids (Korn, 2012). (A) Isometry (stable allometry coefficient α = 1). (B) Monophasic linear allometry (stable α; α <1). (C) Monophasic nonlinear allometry (decreasing α). (D) Biphasic linear allometry (succession of two different allometry coefficients α). (E) Triphasic linear allometry (succession of three different allometry coefficients α). (F) Triphasic non-linear allometry in the Early Carboniferous example Cravenoceras leion Bisat, 1930 (ontogenetically variable allometry coefficient α).
Figure 11. Procymaclymenia ebbighauseni n in A morphometric approach to conch ontogeny of Cymaclymenia and related genera (Ammonoidea, Late Devonian)
Figure 11. Procymaclymenia ebbighauseni n. sp. from the Anti-Atlas of Morocco; all × 1.0. (A) Paratype MB.C.22619.1 (Ebbighausen and Korn 2009 Coll.) from Madène el Mrakib. (B) MB.C.22621.1 (Ebbighausen and Korn 2009 Coll.) from Madène el Mrakib. (C) Paratype MB.C.22665.1 (Korn 1995 Coll.) from El Atrous. (D) Paratype MB.C.22665.2 (Korn 1995 Coll.) from El Atrous. (E) Paratype MB.C.22620.2 (Ebbighausen and Korn 2009 Coll.) from Madène el Mrakib. (F) Paratype MB.C.22620.1 (Ebbighausen and Korn 2009 Coll.) from Madène el Mrakib. (G) Paratype MB.C.22622.1 (Ebbighausen and Korn 2009 Coll.) from Madène el Mrakib.
Figure 14 in A morphometric approach to conch ontogeny of Cymaclymenia and related genera (Ammonoidea, Late Devonian)
Figure 14. Cross sections (A–I; all × 1.5) and ontogenetic trajectories (J–M) of Cymaclymenia subvexa n. sp. from the Anti-Atlas of Morocco. (A) Paratype MB.C.22647.1 (Korn 2009 Coll.) from Madène el Mrakib. (B) Paratype MB.C.22686.1 (Wendt Coll.) from Khorb et Attil. (C) Paratype MB.C.22675 (Wendt Coll.) from Bou Ifarherioun. (D) Paratype MB.C.22636.2 (Korn 1998 Coll.) from Madène el Mrakib. (E) Paratype MB.C.22682 (Wendt Coll.) from Taourirt. (F) Paratype MB.C.22686.2 (Wendt Coll.) from Khorb et Attil. (G) Paratype MB.C.22683.1 (Wendt Coll.) from Taourirt. (H) Paratype MB.C.22684.1 (Wendt Coll.) from Taourirt. (I) Paratype MB.C.22636.3 (Korn 1998 Coll.) from Madène el Mrakib. (J) Conch width index (ww / dm). (K) Umbilical width index (ww / wh). (L) Whorl width index (uw / dm). (M) Whorl expansion rate (WER).
Figure 26 in A morphometric approach to conch ontogeny of Cymaclymenia and related genera (Ammonoidea, Late Devonian)
Figure 26. Cross sections (A, C; all × 1.5), photograph (B; × 1.0) and ontogenetic trajectories (D–G) of Cymaclymenia carnata n. sp. from the Anti-Atlas of Morocco. (A, B) Holotype MB.C.22654 (Kullmann Coll.) from Aguelmous. (C) Paratype MB.C.22645 (Korn 2009 Coll.) from Madène el Mrakib. (D) Conch width index (ww / dm). (E) Umbilical width index (ww / wh). (F) Whorl width index (uw / dm). (G) Whorl expansion rate (WER).
Fig. 7 in Certesella larai (Amoebozoa: Arcellinida: Hyalospheniformes) a new soil testate amoeba species from the Dominican Republic and Chile challenges the definition of genera Certesella and Porosia
Fig. 7. Maximum range of shell length and width of the three known Certesella and Porosia species showing a lack of overlap between C. larai n.sp. and all other species from the two genera in this two-dimensional space. Each species is illustrated (images not exactly to scale).
Fig. 6 in Certesella larai (Amoebozoa: Arcellinida: Hyalospheniformes) a new soil testate amoeba species from the Dominican Republic and Chile challenges the definition of genera Certesella and Porosia
Fig. 6. Comparative overview of the morphology of all known species of genera Certesella and Porosia species. A: Certesella larai n. sp., B: C. certesi, C: C. australis, D: C. murrayi, E: C. martiali, F: Porosia paracarinata, G: P. bigibbbosa. Images are not to scale as some early images lacked a scale.
Fig. 5 in Certesella larai (Amoebozoa: Arcellinida: Hyalospheniformes) a new soil testate amoeba species from the Dominican Republic and Chile challenges the definition of genera Certesella and Porosia
Fig. 5. Biplot of length vs. width of two populations of Certesella larai n.sp. from Dominican Republic and Chile.
Fig. 3 in Certesella larai (Amoebozoa: Arcellinida: Hyalospheniformes) a new soil testate amoeba species from the Dominican Republic and Chile challenges the definition of genera Certesella and Porosia
Fig. 3. Light microscopy images of Certesella larai n.sp. from Parque Nacional Alerce Costero, Los Ríos Region, Chile, showing the detail of the pseudostome. The right image shows internal teeth fully visible on the flank of the neck (solid arrow and visible only in transparency (empty arrow). Such structures are only visible in ca. 10% of the specimens. Scale bar 10 µm.
Fig. 1 in Certesella larai (Amoebozoa: Arcellinida: Hyalospheniformes) a new soil testate amoeba species from the Dominican Republic and Chile challenges the definition of genera Certesella and Porosia
Fig. 1. General shape of Certesella larai n.sp. and indication of the morphometrical measurements. 1 – shell length, 2 – shell breadth, 3 – shell length / breadth ratio (not illustrated), 4 – aperture (long axis), 5 – distance from fundus to the pores, 6 – distance from fundus to base of neck, 7 – distance between the pores, 8 – width of the neck at narrowest point, 9 – pore length, 10 – pore width.
Fig. 2 in Certesella larai (Amoebozoa: Arcellinida: Hyalospheniformes) a new soil testate amoeba species from the Dominican Republic and Chile challenges the definition of genera Certesella and Porosia
Fig. 2. Light microscopy images of Certesella larai n.sp. from Parque Nacional Alerce Costero, Los Ríos Region, Chile. Left: DIC image of the type specimen deposited at the Natural History Museum of Neuchâtel (slide 95–2). Centre and right: brightfield images of specimens from the same sample. Scale bar 20 µm.
Figure 9 in A morphometric approach to conch ontogeny of Cymaclymenia and related genera (Ammonoidea, Late Devonian)
Figure 9. Ontogenetic pathways of six cymaclymeniid species in the morphospace calculated with morphometric data: (A) Procymaclymenia ebbighauseni n. sp., (B) Cymaclymenia subvexa n. sp., (C) Cymaclymenia formosa n. sp., (D) Cymaclymenia lambidia n. sp., (E) Cymaclymenia carnata n. sp. and (F) Postclymenia calceola n. sp.
Fig. 18 in New genera of stiletto flies endemic to Madagascar (Therevidae: Therevinae)
Fig. 18. Distribution of species of Rinhatiana gen. nov. with eco-regions indicated. Inset image of adult ♀ of R. latifestuca gen. et sp. nov. (photograph copyright: Len de Beer).
Fig. 17 in New genera of stiletto flies endemic to Madagascar (Therevidae: Therevinae)
Fig. 17. Collecting localities in Madagascar. A. Ambohimahavelona, Andoharano stunted spiny forest. B. Coastal dune, Toliara (photograph copyright: M. Hauser). C. Andohaela National Park, Parcel II – Tsimela spiny forest. D. Anja Community Reserve, dry evergreen forest. E. Andohaela National Park, Parcel III – Ihazofotsy, transitional forest. F. Tsimanampetsotsa National Park, Mitoho dry deciduous forest (habitat of T. goodmani gen. et sp. nov.). G. Monambo, Mikea spiny forest (habitat of R. latifestuca gen. et sp. nov.). H. Cape St Marie Special Reserve, coastal spiny bush (habitat of T. goodmani).
Fig. 14 in New genera of stiletto flies endemic to Madagascar (Therevidae: Therevinae)
Fig. 14. Tianarinha spp., heads, anterior view. A. Tianarinha goodmani gen. et sp. nov., ♂, paratype (CASC). B. Same, ♀, paratype (CASC). C. Tianarinha micet gen. et sp. nov., ♂, paratype (CASC). D. Same, ♀, paratype (CASC).
Fig. 10 in New genera of stiletto flies endemic to Madagascar (Therevidae: Therevinae)
Fig. 10. Tianarinha goodmani gen. et sp. nov., ♂, holotype (CASC). A. Lateral view. B. Oblique view.
Fig. 9 in New genera of stiletto flies endemic to Madagascar (Therevidae: Therevinae)
Fig. 9. Rinhatiana spp., heads, anterior view. A. Rinhatiana arctifestuca gen. et sp. nov., ♂ (CSCA). B. Same, ♀ (CSCA). C. Rinhatiana cracentis gen. et sp. nov., ♂ (CSCA). D. Same, ♀ (CSCA). E. Rinhatiana distincta (Lyneborg, 1976) comb. nov., ♂ (CSCA). F. Same, ♀ (CSCA). G. Rinhatiana latifestuca gen. et sp. nov., ♂ (CSCA). H. Same, ♀ (CSCA).
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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.
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.
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.
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.
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.