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FIGURE 23 in Some new data on tropical western Pacific Ascidians
FIGURE 23. Polycarpa mytiligera: A: body, B: branchial sac, sacle bar=1cm.
FIGURE 16. A in Some new data on tropical western Pacific Ascidians
FIGURE 16. A: Eudistoma amplum. B: Eudistoma globosum. C: Eudistoma vulgare. D: Perophora namei.
FIGURE 17 in Some new data on tropical western Pacific Ascidians
FIGURE 17. Eudistoma vulgare: digestive loop, scale bar: 0.5mm.
Text-fig. 4. Fern remains from Remigiusberg Formation. A) pecopterid remain belonging to Pecopteris arborescens/cyathea group, Inv.-Nr. PB 2016/5033 LS (LS-RLP), scalebar = 2 cm; B) pecopterid remain belonging to Pecopteris arborescens/cyathea group, Inv.-Nr. PB 2016/5029a+b LS (LS-RLP), scalebar = 2 cm; C) Pecopteris sp., Inv.-Nr. PB 2010/5809 LS (LS-RLP), scalebar = 2.5 cm; D) Pecopteris sp., Inv.-Nr. PB 2016/5029b LS (LS-RLP), scalebar = 2 cm; E) Asterotheca sp., Inv.-Nr. PB 2010/5812 LS (LS-RLP), scalebar = 2 mm. in New Data On The Macroflora Of The Basal Rotliegend Group (Remigiusberg Formation; Gzhelian) In The Saar-Nahe Basin (Sw-Germany)
Text-fig. 4. Fern remains from Remigiusberg Formation. A) pecopterid remain belonging to Pecopteris arborescens/cyathea group, Inv.-Nr. PB 2016/5033 LS (LS-RLP), scalebar = 2 cm; B) pecopterid remain belonging to Pecopteris arborescens/cyathea group, Inv.-Nr. PB 2016/5029a+b LS (LS-RLP), scalebar = 2 cm; C) Pecopteris sp., Inv.-Nr. PB 2010/5809 LS (LS-RLP), scalebar = 2.5 cm; D) Pecopteris sp., Inv.-Nr. PB 2016/5029b LS (LS-RLP), scalebar = 2 cm; E) Asterotheca sp., Inv.-Nr. PB 2010/5812 LS (LS-RLP), scalebar = 2 mm.
Fig. 5 in New Stratigraphic Data from the Erlian Basin: Implications for the Division, Correlation, and Definition of Paleogene Lithological Units in Nei Mongol (Inner Mongolia)
Fig. 5. Stratigraphic correlations of the Nuhetingboerhe-Huheboerhe area (NHA). See Fig. 1B for the locations of the sections.
Fig. 1 in First Precise Locality Data for Onthophagus atriglabrus Howden and Gill and New State Record for Onthophagus anewtoni Howden and Génier (Coleoptera: Scarabaeidae: Scarabaeinae) in Mexico
Fig. 1. Dorsal habitus of a) Onthophagus atriglabrus and b) Onthophagus anewtoni.
Figure 3 a–b in Mideopsis milankovici sp. nov. a new water mite from Montenegro based on morphological and molecular data (Acariformes, Hydrachnidia, Mideopsidae)
Figure 3 a–b Mideopsis milankovici sp. nov., ♀ paratype, Međurječka rijeka stream, Montenegro. a – ventral shield; b – palp; c–e, ejaculatory complex (c–d, from Biesiadka and Kowalik 1979; e – from Pešić and Saboori 2015): c – M. orbicularis (Müller, 1776); d – M. roztoczensis Biesiadka & Kowalik, 1979; e – M. persicus Pešić & Saboori, 2015. Scale bar = 100 µm.
FIGURE 3 in Cymbidium weishanense (Orchidaceae; Epidendroideae), a new species from China: evidence from morphological and molecular data
FIGURE 3. Cymbidium weishanense (A), C. concinnum (B) and C. insigne (C).
Figure 8 in The differentiation of bunodont Listriodontinae (Mammalia, Suidae) of Africa: new data from Kalodirr and Moruorot, Kenya
Figure 8. Postcranial remains of Listriodon jeanneli (KNM MO 18127). A, atlas in view: a, dorsal; b, posterior; c, anterior; d, ventral; e, lateral; B, proximal right ulna in view: a, anterior; b, lateral; c, posterior; d, medial. Scale bars = 50 mm.
Figure 1 in The differentiation of bunodont Listriodontinae (Mammalia, Suidae) of Africa: new data from Kalodirr and Moruorot, Kenya
Figure 1. Stratigraphical and regional distribution of the listriodont taxa mentioned in the present article. Miocene subdivisions are from Berggren et al. (1995); European mammalian Neogene zones (MN zones) given are from (A) Van der Made (1996) and (B) Pickford & Morales (2003). Correlations between European mammalian zones and African and Siwaliks faunal zones are respectively from Pickford & Senut (1997) and Welcome et al. (2001); correlations between mammalian Neogene zones and time scale are given by Van der Made (1997) and Pickford & Morales (2003). Most common synonymies are: Turkey + Asia, Listriodon jeanneli = Libycochoerus fategadensis (Prasad, 1967); Listriodon splendens = Listriodon xinanensis Chen, 1986; Listriodon lockharti = Listriodon intermedius Liu & Lee, 1963; Kubanochoerus gigas = Kubanochoerus robustus Gabunia, 1960 = Listriodon lantiensis Liu & Lee, 1963; Africa, Lopholistriodon moruoroti = Namachoerus moruoroti.
Figure 5 in New data on the braincase of the aetosaurian archosaur (Reptilia: Diapsida) Stagonolepis robertsoni Agassiz
Figure 5. Alternative hypotheses of phylogenetic relationships of aetosaurians to other major clades of Crurotarsan archosaurs. (A) Currently orthodox hypothesis based on the five most recent numerical cladistic analyses (see Gower & Wilkinson, 1996; Benton, 1999) in which aetosaurians are more distantly related to Crocodylomorpha than are at least some rauisuchians. (B) Currently unorthodox hypothesis forwarded here for further consideration, in which aetosaurians are the major archosaurian clade most closely related to Crocodylomorpha. Sphenosuchia may not be monophyletic (e.g. Clark et al., 2001). Some taxa of uncertain affinity are not shown here including Ornithosuchia and Gracilisuchus stipanicicorum. Labelled nodes: (1) Archosauria (2) crown-group archosaurs = Avesuchia (Benton, 1999) (3) Crurotarsi (4) Suchia (5) Crocodylomorpha.
Figure 2 in New data on the braincase of the aetosaurian archosaur (Reptilia: Diapsida) Stagonolepis robertsoni Agassiz
Figure 2. Stagonolepis robertsoni Agassiz. External view of left otic region of braincase of MCZD 2-4 in ventral (A) and posterolateroventral (B) views. Anterior is to the bottom of the figure. For scale see Fig. 1. bk = break in specimen; bpt = basipterygoid process; bs-pr = parabasisphenoid-prootic suture; btbo = basal tuber of basioccipital; btbs = basal tuber of parabasisphenoid; cpr = crista prootica; op = opisthotic; op-pr = opisthotic-prootic suture; uc = unossified channel/cleft; VII = foramen for facial nerve.
Figure 3. Plesiomeryx cadurcensis. A & B, occlusal view. A, left P2 in New data on the Cainotheriidae (Mammalia, Artiodactyla) from the early Oligocene of south-western France
Figure 3. Plesiomeryx cadurcensis. A & B, occlusal view. A, left P2/-M3/ (ABL1 1452). B, right C-M/3 (MGT 104). P. huerzeleri. C & D, occlusal view. C, right P2/-M3/ (MGT 3209). D, left P/2-M/3 (MGT 3187). Scale bar = 1 mm.
Figure 4 in Avian brain evolution: new data from Palaeogene birds (Lower Eocene) from England
Figure 4. Virtual endocranial cast of Odontopteryx toliapica. A, expanded view of the dorsal surface of the telencephalon, showing the shape and extent of the poorly developed eminentia sagittalis. B, ventral view of virtual endocast. See text for list of anatomical abbreviations.
Figure 7 in Avian brain evolution: new data from Palaeogene birds (Lower Eocene) from England
Figure 7. Virtual endocranial cast of Prophaethon shrubsolei. A, expanded view of the dorsal surface of the telencephalon, showing the shape and extent of the eminentia sagittalis. The eminentia sagittalis of this species is similar to living birds, but is not well developed dorsally. B, ventral view of virtual endocast. See text for list of anatomical abbreviations.
Figure 11 in Avian brain evolution: new data from Palaeogene birds (Lower Eocene) from England
Figure 11. Fossil endocast of 'Numenius' gypsorum from the Upper Eocene of the Paris Basin (MNHN AC7992). A, endocast in dorsal view showing the poor lateral development of the rostrally positioned eminentia sagittalis. B, line trace of the endocast in caudal view showing the poor dorsal development of the eminentia sagittalis. See text for abbreviations.
Figure 1 in Avian brain evolution: new data from Palaeogene birds (Lower Eocene) from England
Figure 1. Recent phylogenetic hypotheses of the relationships of A, Odontopteryx toliapica (after Bourdon, 2005) and B, Prophaethon shrubsolei (after Bourdon et al., 2005).
FIGURES 12–15. Lasioseius foliatisetus n in A new species of Lasioseius (Acari: Blattisociidae) from Brazil with morphological and DNA barcode data
FIGURES 12–15. Lasioseius foliatisetus n. sp., adult female. Legs I-IV, dorsal view.
Supplementary material 1 from: Ingala MR, Werner IE, Fitzgerald AM, Naro-Maciel E (2021) 18S rRNA amplicon sequence data (V1–V3) of the Bronx river estuary, New York. Metabarcoding and Metagenomics 5: e69691. https://doi.org/10.3897/mbmg.5.69691
Scripts used for metabarcoding analysis
Supplementary material 2 from: Ingala MR, Werner IE, Fitzgerald AM, Naro-Maciel E (2021) 18S rRNA amplicon sequence data (V1–V3) of the Bronx river estuary, New York. Metabarcoding and Metagenomics 5: e69691. https://doi.org/10.3897/mbmg.5.69691
Figure S1, Tables S1, S2
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.