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Figure 2. Carcinonemertes caissarum n in Three new species of Carcinonemertes (Nemertea, Carcinonemertidae) from the southeastern coast of Brazil
Figure 2. Carcinonemertes caissarum n. sp. (A) Filiform mucus sheath of adult worm; (B) male with rounded posterior end; (C) stylet and basis (arrow) in a male worm; (D) juvenile worm encysted on pleopod setae of Hepatus pudibundus.
Figure 4. Carcinonemertes sebastianensis n in Three new species of Carcinonemertes (Nemertea, Carcinonemertidae) from the southeastern coast of Brazil
Figure 4. Carcinonemertes sebastianensis n. sp. (A) Detail of lapilli of adult mucus sheath. (B) Rounded anterior end of female, showing the great distance from first gonad to tip of head. (C) Stylet and basis (arrow) in a female worm. (D) Anterior end of male. (E) Posterior end of male. Abbreviations: b, proboscis bulb; d, diaphragm; g, gonad.
Figure 1. Carcinonemertes divae n in Three new species of Carcinonemertes (Nemertea, Carcinonemertidae) from the southeastern coast of Brazil
Figure 1. Carcinonemertes divae n. sp. (A) Anterior end of female, (B) proboscis aligned in a straight line, (C) stylet and basis (arrow) in a female worm, (D) male with rounded anterior end, (E) pointed posterior end of male, with seminal vesicle, (F) adult female (arrow) on Libinia spinosa eggs. Abbreviations: b, proboscis bulb; d, diaphragm; p, posterior proboscis chamber.
Figure 3 in Three new species of Carcinonemertes (Nemertea, Carcinonemertidae) from the southeastern coast of Brazil
Figure 3. Scanning electron micrograph of the lapilli of the mucus sheath produced by the adults of Carcinonemertes sebastianensis n. sp.
Figure 3 in Progressive troglomorphism of ambulatory and sensory appendages in three Mexican cave decapods
Figure 3. (A–F) Electron micrographs of segments from antennae (left column) and antennules external branch (right column), respectively, of Procambarus olmecorum (A, B), P. cavernicola (C, D), and P. oaxacae reddelli (E, F); (G–J) electron micrographs of segments of antennae (left column) and tip of antennules (right column), respectively, of M. totonacum (G, H) and M. villalobosi (I, J).
Figure 2 in Progressive troglomorphism of ambulatory and sensory appendages in three Mexican cave decapods
Figure 2. Electron micrographs of carapace surface, magnification of surface, and dactyl of third maxilliped, respectively, of Procambarus olmecorum (A–C), P. oaxacae reddelli (D–F), and P. cavernicola (G–I).
Figures 8–13 in Some bathyal cheilostome Bryozoa (Bryozoa, Cheilostomata) from the Canary Islands (Spain, Eastern Atlantic), with descriptions of three new species, a new genus, and a new family
Figures 8–13. (8) Distansescharella alcicornis (MNCN 25.03/3723). (9–13) Acorania enmediensis gen. et sp. nov.: (9–12) holotype (MNCN 25.03/3726); (13) paratype 1 (MNCN 25.03/3727). (9) Autozooid with ovicell and avicularia, the broken ovicell at right shows the unfused endooecium and ectooecium. (10) Growing tip of a branch. (11) Uniporous chamber, distal side, with pore and limit of the chamber (arrow). (12) Inner side of the frontal wall, with condyles. (13) Ancestrula and first zooids.
Figures 4–7 in Some bathyal cheilostome Bryozoa (Bryozoa, Cheilostomata) from the Canary Islands (Spain, Eastern Atlantic), with descriptions of three new species, a new genus, and a new family
Figures 4–7. Copidozoum magnum sp. n.: (4–6) holotype (MNCN 25.03/3723); (7) paratype (MNCN 25.03/ 3723). (4) Autozooids, ovicells, and avicularia. (5) Avicularium. (6) Broken ovicell, with the basal kenozooid below. (7) Ancestrula (a) and first zooids, the small ancestrula at right (C.a.) belongs to Distansescharella alcicornis.
Figure 1 in Taxonomic affinities of three stalked colonial species of the Ascidiacea (Tunicata) from the central coast of New South Wales and indications of a trans-Tasman connection
Figure 1. Euclavella claviformis (QM G308883): (A) colony; (B) developmental sequence of embryos in the distal part of the oviduct forming a collar around the top of the oesophageal neck. Hypsistozoa distomoides (QM G308880): (C) colony; (D) zooid; (E) zooid (with denticles on the atrial lip); (F) larva (left side with ectotrophic membranes pulled away from the trunk); (G) larva (with ectotrophic membranes intact); (H) larva (right side with ectotrophic membranes pulled away from the trunk). Scale bars: A, B, 10 mm; C–G, 0.2 mm.
Figure 2 in Taxonomic affinities of three stalked colonial species of the Ascidiacea (Tunicata) from the central coast of New South Wales and indications of a trans-Tasman connection
Figure 2. Hypsistozoa distomoides (QM G308880) postero-dorsal vertical section of larval trunk (semidiagramatic): e, endodermal tube; nc, nerve cord; o, section through oesophagus; ec, ectotrophic membrane; s, stomach wall; oe, oesophagus; h, haemocoele; le, larval ectoderm; n, notochord; r, rectum. Scale bar, 0.1 mm.
Figure 3 in Taxonomic affinities of three stalked colonial species of the Ascidiacea (Tunicata) from the central coast of New South Wales and indications of a trans-Tasman connection
Figure 3. In situ colour images: (A) Euclavella claviformis; (B) Hypsistozoa distomoides colony lying flat on the sea floor at low slack tide; (C) Sigillina cyanea from high-energy location, showing tip of colony worn by abrasion on sea floor sediments. The possibly commensal nudibranch Nembrotha sp. is associated with the colony.
Figure 13 in Abundance, reproduction, and feeding of three species of British terrestrial planarians: Observations over 4 years
Figure 13. Microplana scharffi. The numbers of specimens of each colour category. (a) Using 23 colour categories: figure in parentheses indicates the eight-colour category that the colour is assigned to; (b) using eight colour categories (1–8). Data are ranked from highest to lowest totals.
Figure 11 in Abundance, reproduction, and feeding of three species of British terrestrial planarians: Observations over 4 years
Figure 11. Kitchen site: numbers of hatchlings seen each month for 2003 and 2004. (a) Microplana scharffi; (b) Microplana terrestris; (c) khaki Microplana species.
Figure 5 in Abundance, reproduction, and feeding of three species of British terrestrial planarians: Observations over 4 years
Figure 5. Microplana scharffi. (a) Monthly occurrence (corrected numbers) over 48 months from March 2001 to February 2005: 1 to 5 on the x-axis are years 2001 to 2005; (b) mean ¡ SE monthly numbers from January (J) to December (D) over 4 years.
Figure 4 in Abundance, reproduction, and feeding of three species of British terrestrial planarians: Observations over 4 years
Figure 4. Soil temperature (°C) at the kitchen site. (a) Monthly average from March 2001 to February 2005: 1 to 5 on the x-axis are years 2001 to 2005; (b) mean¡SE values from January (J) to December (D) over 4 years.
Figure 6 in Abundance, reproduction, and feeding of three species of British terrestrial planarians: Observations over 4 years
Figure 6. Microplana terrestris. (a) Monthly occurrence (corrected numbers) over 48 months from March 2001 to February 2005: 1 to 5 on the x-axis are years 2001 to 2005; (b) mean¡SE monthly numbers from January (J) to December (D) over 4 years.
Figure 3 in Abundance, reproduction, and feeding of three species of British terrestrial planarians: Observations over 4 years
Figure 3. Rainfall (mm). (a) Monthly totals from March 2001 to February 2005: 1 to 5 on the x-axis are years 2001 to 2005; (b) mean¡SE monthly values from January (J) to December (D) over 4 years.
Figure 1 in Abundance, reproduction, and feeding of three species of British terrestrial planarians: Observations over 4 years
Figure 1. The kitchen site. (a) General view, with one of the authors (J.M.); (b) close-up of traps.
Figure 12 in Abundance, reproduction, and feeding of three species of British terrestrial planarians: Observations over 4 years
Figure 12. Microplana terrestris. Kitchen site. The mean ¡ SE number of flatworms seen feeding per day per calendar month over 4 years.
Figure 10. Microplana terrestris and M in Abundance, reproduction, and feeding of three species of British terrestrial planarians: Observations over 4 years
Figure 10. Microplana terrestris and M. scharffi. The time taken for cocoons to hatch after shedding or collection at different dates. Collected cocoons were within 1 day of being shed so that the maximum error in the time taken to hatch is 1 day.
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.