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FIGURES 64–67 in Revision of the Ephippiochthonius complex in the Iberian Peninsula, Balearic Islands and Macaronesia, with proposed changes to the status of the Chthonius subgenera (Pseudoscorpiones, Chthoniidae)
FIGURES 64–67. Habitus of living specimens of Ephippiochthonius and Occidenchthonius species from Spain. 64, Ephippiochthonius mahnerti (Zaragoza, 1984) n. comb., Cova del Bolumini, Beniarbeig, Alicante province; 65, Occidenchthonius bullonorum (Carabajal Márquez, García Carrillo & Rodríguez Fernández, 2012) n. comb., Cueva de la Pileta, Benaojan, Málaga province; 66, Occidenchthonius ventalloi (Beier, 1939) n. comb., Cova de les Gralles, Tous, Valencia province; 67, Occidenchthonius cazorlensis (Carabajal Márquez, García Carrillo & Rodríguez Fernández, 2012) n. comb., Cueva Secreta del Sagreo, La Iruela, Jaén province. Photographs: Ximo Baixeras (Fig. 64), Adrià Miralles (Figs 65, 67), Sergio Montagud (Fig. 66).
FIGURES 105–110. Ephippiochthonius castellonensis n in Revision of the Ephippiochthonius complex in the Iberian Peninsula, Balearic Islands and Macaronesia, with proposed changes to the status of the Chthonius subgenera (Pseudoscorpiones, Chthoniidae)
FIGURES 105–110. Ephippiochthonius castellonensis n. sp., male holotype (105–109) and female paratype (110). 105, anterior margin of carapace, partial view; 106, carapace; 107, left chelicera; 108, fingers of left chelicera, partial view; 109, left chela, antiaxial view; 110, movable cheliceral finger, partial view.
FIGURES 130–135. Ephippiochthonius galcerani n in Revision of the Ephippiochthonius complex in the Iberian Peninsula, Balearic Islands and Macaronesia, with proposed changes to the status of the Chthonius subgenera (Pseudoscorpiones, Chthoniidae)
FIGURES 130–135. Ephippiochthonius galcerani n. sp., male holotype. 130, anterior margin of carapace, partial view; 131, carapace; 132, tip of fixed chelal finger, dorsal view; 133, left chelicera; 134, fingers of left chelicera, partial view; 135, left chela, antiaxial view.
FIGURES 169–173. Ephippiochthonius portugalensis n in Revision of the Ephippiochthonius complex in the Iberian Peninsula, Balearic Islands and Macaronesia, with proposed changes to the status of the Chthonius subgenera (Pseudoscorpiones, Chthoniidae)
FIGURES 169–173. Ephippiochthonius portugalensis n. sp., female holotype. 169, anterior margin of carapace, partial view; 170, carapace; 171, left chelicera; 172, fingers of left chelicera, partial view; 173, right chela, antiaxial view.
Figs. 24-38. Figs. 24-26 in On the spider species described by L. Koch in 1882 from the Balearic Islands (Araneae)
Figs. 24-38. Figs. 24-26: Ozyptila furcula L. Koch, 1882. 24. Male palp of Ozyptila furcula in KOCH (1882); 25. Male palp, ventral view; 26. Idem, lateral view. Figs. 27-28. Haplo- drassus parvicorpus (Roewer, 1951). 27. Male palp of Drassus parvulus in KOCH (1882). 28. Male palp of Haplodrassus parvicorpus, specimen from Tarifa. Figs. 29-35. Zelotes callidus (Simon, 1878). 29. Epigyne of Zelotes semirufus in KOCH (1882); 30. Epigyne of Zelotes callidus, specimen from Talavan; 31. Vulva; 32. Male palp of Zelotes callidus in SIMON (1914, fig. 298); 33. Male palp, detail; 34. Male palp, ventral view; 35. Male palp, lateral view; Fig. 36. Male palp of Zelotes plumiger L. Koch, 1882 in L. KOCH (1882). Figs. 37-38 Phlegra bresnieri (Lucas, 1846). 37. Male palp of Phlegra simoni in L. KOCH (1882); 38. Male palp of Phlegra bresnieri in METZNER (1999).
Figs. 1-10 in On the spider species described by L. Koch in 1882 from the Balearic Islands (Araneae)
Figs. 1-10: Fig. 1. Male palp of Dysdera mordax L. Koch, 1882 in L. KOCH (1882). Figs. 2-3: Enoplognatha diversa (Blackwall, 1859) 2. Epigyne of Theridion elimatum in KOCH (1882); 3. Epigyne of Enoplognatha diversa in BOSMANS & VAN KEER (1999). Figs. 4-5. Oedothorax fuscus (Blackwall, 1834). 4. Epigyne of Erigone marina in KOCH (1882). 5. Epigyne of Oedothorax fuscus in LOCKET & MILLIE (1953). Figs. 6-7: Liocranum inornatum (L. Koch, 1882). 6. Epigyne of Zora inornata in KOCH (1882); 7. Epigyne of Liocranum variabilis in WUNERLICH (2008). Figs. 8-10: Cheiracanthium occidentale L. Koch, 1882. 8. Epigyne of Cheiracanthium occidentale in KOCH (1882). 9. Vulva, ventral view; 10. Idem, dorsal view.
Figs. 24 - 38. Figs. 24 - 26 in On the spider species described by L. Koch in 1882 from the Balearic Islands (Araneae)
Figs. 24 - 38. Figs. 24 - 26: Ozyptila furcula L. Koch, 1882. 24. Male palp of Ozyptila furcula in Koch (1882); 25. Male palp, ventral view; 26. Idem, lateral view. Figs. 27 - 28. Haplo- drassus parvicorpus (Roewer, 1951). 27. Male palp of Drassus parvulus in Koch (1882). 28. Male palp of Haplodrassus parvicorpus, specimen from Tarifa. Figs. 29 - 35. Zelotes callidus (Simon, 1878). 29. Epigyne of Zelotes semirufus in Koch (1882); 30. Epigyne of Zelotes callidus, specimen from Talavan; 31. Vulva; 32. Male palp of Zelotes callidus in simon (1914, fig. 298); 33. Male palp, detail; 34. Male palp, ventral view; 35. Male palp, lateral view; Fig. 36. Male palp of Zelotes plumiger L. Koch, 1882 in L. Koch (1882). Figs. 37 - 38 Phlegra bresnieri (Lucas, 1846). 37. Male palp of Phlegra simoni in L. Koch (1882); 38. Male palp of Phlegra bresnieri in metzner (1999).
Figs. 11-23. Figs. 11-12 in On the spider species described by L. Koch in 1882 from the Balearic Islands (Araneae)
Figs. 11-23. Figs. 11-12: Arctosa fulvolineata (Lucas, 1846). 11. Epigyne of Lycosa perspicax in KOCH (1882); 12. Epigyne of Arctosa fulvolineata in KNÜLLE (1959). Figs 13-16. Arctosa lacustris (Simon, 1876). 13. Male palp of Lycosa subhirsuta in KOCH (1882); 14. Male palp of Arctosa lacustris in KNÜLLE (1959); 15. Epigyne of Lycosa subhirsuta in KOCH (1882); 16. Epigyne of Arctosa lacustris in KNÜLLE (1959). Fig. 17. Epigyne of Lycosa conspersa in KOCH (1882). Fig. 18. Epigyne of Lycosa fraisei in KOCH (1882). Fig. 19. Epigyne of Lycosa insulana in KOCH (1882). Fig. 20. Epigyne of Lycosa simplex in KOCH (1882). Fig. 21. Male palp of Pardosa tenuipes in KOCH (1882). Figs 22-23. Thanatus vulgaris Simon, 1870. 22. Epigyne of Philodromus vegetus in KOCH (1882). 23. Epigyne of Thanatus vulgaris in SZITA & SAMU (2000).
Figs. 11 - 23. Figs. 11 - 12 in On the spider species described by L. Koch in 1882 from the Balearic Islands (Araneae)
Figs. 11 - 23. Figs. 11 - 12: Arctosa fulvolineata (Lucas, 1846). 11. Epigyne of Lycosa perspicax in Koch (1882); 12. Epigyne of Arctosa fulvolineata in KnüLLe (1959). Figs 13 - 16. Arctosa lacustris (Simon, 1876). 13. Male palp of Lycosa subhirsuta in Koch (1882); 14. Male palp of Arctosa lacustris in KnüLLe (1959); 15. Epigyne of Lycosa subhirsuta in Koch (1882); 16. Epigyne of Arctosa lacustris in KnüLLe (1959). Fig. 17. Epigyne of Lycosa conspersa in Koch (1882). Fig. 18. Epigyne of Lycosa fraisei in Koch (1882). Fig. 19. Epigyne of Lycosa insulana in Koch (1882). Fig. 20. Epigyne of Lycosa simplex in Koch (1882). Fig. 21. Male palp of Pardosa tenuipes in Koch (1882). Figs 22 - 23. Thanatus vulgaris Simon, 1870. 22. Epigyne of Philodromus vegetus in Koch (1882). 23. Epigyne of Thanatus vulgaris in szita & samu (2000).
Figs. 1 - 10 in On the spider species described by L. Koch in 1882 from the Balearic Islands (Araneae)
Figs. 1 - 10: Fig. 1. Male palp of Dysdera mordax L. Koch, 1882 in L. Koch (1882). Figs. 2 - 3: Enoplognatha diversa (Blackwall, 1859) 2. Epigyne of Theridion elimatum in Koch (1882); 3. Epigyne of Enoplognatha diversa in Bosmans & Van Keer (1999). Figs. 4 - 5. Oedothorax fuscus (Blackwall, 1834). 4. Epigyne of Erigone marina in Koch (1882). 5. Epigyne of Oedothorax fuscus in LocKet & miLLidge (1953). Figs. 6 - 7: Liocranum inornatum (L. Koch, 1882). 6. Epigyne of Zora inornata in Koch (1882); 7. Epigyne of Liocranum variabilis in WunderLich (2008). Figs. 8 - 10: Cheiracanthium occidentale L. Koch, 1882. 8. Epigyne of Cheiracanthium occidentale in Koch (1882). 9. Vulva, ventral view; 10. Idem, dorsal view.
Fig. 1 in A redescription of Harpactea dufouri (Thorell, 1873) (Araneae, Dysderidae), its occurrence outside the Balearic Islands, and some notes on the corticalis group of the genus
Fig. 1. Harpactea dufouri (Thorell, 1873), Mont Ras specimens. A. Male palp, prolateral view. B. Tip of male embolus and conductor, retrolateral view. C. Endogyne, external ventral view, uncleared. D. Cleared vulva, ventral view. E. Leg spination scheme, legend. F. Leg spination scheme of male. White dots are spines present on one leg and absent on the other. G. Leg spination scheme of female. White dots are spines present on one leg and absent on the other. Scale bars: A, C = 0.5 mm; B, D = 100 µm.
Fig. 2. A – G in A redescription of Harpactea dufouri (Thorell, 1873) (Araneae, Dysderidae), its occurrence outside the Balearic Islands, and some notes on the corticalis group of the genus
Fig. 2. A – G. Harpactea dufouri (Thorell, 1873), Mont Ras specimens, except F – G. A. ♂, dorsal view. B. ♀, dorsal view. C. Tip of male embolus and conductor, retrolateral view, Nomarski interference contrast. D. Tip of male embolus and conductor, retrolateral view, bright Feld. E. Cleared vulva, ventral view. Left: bright Feld, middle: phase contrast, right: Nomarski interference contrast. F. Tip of male embolus and conductor, Banyalbufar specimen. G. Endogyne, external ventral view, Banyalbufar specimen. — H. Map showing the Mont Ras site of Harpactea dufouri (red square), the Gavarres are delimited by a black line. Scale bars: A – B = 1 mm; C – F = 100 µm; G = 0.5 mm; H = 5 km.
Figures 2–10 in A new species of Oxalis section Corniculatae (Oxalidaceae) from the Balearic islands
Figures 2–10. SEM pictures of Oxalis ferae sp. nov. Collection details. Fig. 2. Glabrescent floral peduncle. Scale bar = 100 Mm. Fig. 3. Undersurface of leaflet. Scale bar = 1 mm. Figs 4–5. Petiolule. Scale bars: Fig. 4 = 1 mm; Fig. 5 = 200 Mm. Fig. 6. Midrib of undersurface of leaflet. Scale bar = 500 Mm. Figs 7–10. Seeds. Scale bars = 500 Mm.
Figure 1 in A new species of Oxalis section Corniculatae (Oxalidaceae) from the Balearic islands
Figure 1. Oxalis ferae sp. nov. Collection details. A, habit. B, pedicel with fresh fruit. C, dry fruit. D, dehiscent fruit with seeds. Scale bar = 2 cm.
Subspecies and Distribution. L.g.granatensisRosenhauer,1856—IberianPeninsulaexceptN&NE. L.g.gallaeciusMiller,1907—Galicia,andWAsturias(NWSpain). L. g. solisi Palacios & Fernandez, 1992 — Mallorca (Balearic Is), but this population may have been introduced by early settlers on the islands. in Leporidae
Subspecies and Distribution. L.g.granatensisRosenhauer,1856—IberianPeninsulaexceptN&NE. L.g.gallaeciusMiller,1907—Galicia,andWAsturias(NWSpain). L. g. solisi Palacios & Fernandez, 1992 — Mallorca (Balearic Is), but this population may have been introduced by early settlers on the islands.
Subspecies and Distribution. O.c.cuniculusLinnaeus,1758—N,NE&EIberianPeninsula(Spain). O.c.algirusLoche,1858—S,SW&WIberianPeninsula(Spain,Portugal),NMorocco,NAlgeria(includingHabibasI). O.c.brachyotusTrouessart,1917—SFrance. O.c.cnossiusBate,1906—CreteI. O.c.habetensisCabrera,1923—Tanger-Tetouan-AlHoceimaRegion(NMorocco). O. c. huxleyi Haeckel, 1874 — Mediterranean Is (Balearic Is, Corsica, Sardinia, Sicily and Macaronesia (Azores, Madeira, and Canary Is). Original distribution after last Ice Age restricted to Iberian Peninsula, W France, and N Africa. Ancient introductions of the nominate subspecies probably during the Ro- man period have spread it throughout Europe, and now it is present in most of W, C & E Europe and the Mediterranean and Macaronesian Is (these mostly old introductions are also shaded on the map). During the 20" century it has been released into the steppes of the Black Sea in Ukraine and Russia (N Caucasus); introduced into Australia in 1788 and again in 1859 where it is now widespread; it is found on many Pacific Is, islands off the coast of South Africa and Namibia, and in New Zealand; successfully introduced only since 1936 into South America, nowadays with a limited range in Chile, Argentina, and Falkland Is, it is also present in the Caribbean Is (all these modern introductions not shaded in the map). Worldwide as domesticated forms. in Leporidae
Subspecies and Distribution. O.c.cuniculusLinnaeus,1758—N,NE&EIberianPeninsula(Spain). O.c.algirusLoche,1858—S,SW&WIberianPeninsula(Spain,Portugal),NMorocco,NAlgeria(includingHabibasI). O.c.brachyotusTrouessart,1917—SFrance. O.c.cnossiusBate,1906—CreteI. O.c.habetensisCabrera,1923—Tanger-Tetouan-AlHoceimaRegion(NMorocco). O. c. huxleyi Haeckel, 1874 — Mediterranean Is (Balearic Is, Corsica, Sardinia, Sicily and Macaronesia (Azores, Madeira, and Canary Is). Original distribution after last Ice Age restricted to Iberian Peninsula, W France, and N Africa. Ancient introductions of the nominate subspecies probably during the Ro- man period have spread it throughout Europe, and now it is present in most of W, C & E Europe and the Mediterranean and Macaronesian Is (these mostly old introductions are also shaded on the map). During the 20" century it has been released into the steppes of the Black Sea in Ukraine and Russia (N Caucasus); introduced into Australia in 1788 and again in 1859 where it is now widespread; it is found on many Pacific Is, islands off the coast of South Africa and Namibia, and in New Zealand; successfully introduced only since 1936 into South America, nowadays with a limited range in Chile, Argentina, and Falkland Is, it is also present in the Caribbean Is (all these modern introductions not shaded in the map). Worldwide as domesticated forms.
Figure 8 in Discovery of a new scale worm (Annelida: Polynoidae) with presumed deep-sea affinities from an anchialine cave in the Balearic Islands (western Mediterranean)
Figure 8. Pollentia perezi gen. & sp. nov. (paratype MNCN 16.01/18956), parapodia. A, anterior parapodia, showing arrangement of elytrophores and cirrophores. B, dorsal view of parapodia of segments 13–15. C, detail of cirrophores, segment 14. D, micrograph of midbody parapodium, anterior view, showing neuroacicula by transparency. E, midbody parapodium, anterior view, scanning electron micrograph, showing chaetal bundles and tapering neuroacicular lobe. F, scanning electron micrograph of midbody parapodium with dorsal cirrus, posterior view. G, midbody parapodium ventral view, with elytrophore and a low, inconspicuous dorsal tubercle. H, detail of papilla on dorsal cirrus. I, anterior parapodia, ventral view. J, detail of papillae ventral cirrus segment 3. K, ventral cirri, smooth from segment 4. L, midbody ventral cirrus. M, ventral papilla. Abbreviations: al, acicular lobe; ci, cirrophore; dc, dorsal cirrus; el, elytrophore; nea, neuroacicular lobe; nei, interior neurochaetae; nes, superior neurochaetae; no, notochaetae; noa, notoacicular lobe; vc, ventral cirrus; 1–15,
Figure 9 in Discovery of a new scale worm (Annelida: Polynoidae) with presumed deep-sea affinities from an anchialine cave in the Balearic Islands (western Mediterranean)
Figure 9. Pollentia perezi gen. & sp. nov. (paratype MNCN 16.01/18956), chaetae. A, notochaetae tentacular segment (segment 1). B, notochaetae bundle. C, detail of tip of notochaetae. D, E, detail of superior neurochaetae, mid length. F, detail of distal end of superior neurochaetae. G, inferior neurochaetae. H, detail of distal end of inferior neurochaeta.
Figure 7 in Discovery of a new scale worm (Annelida: Polynoidae) with presumed deep-sea affinities from an anchialine cave in the Balearic Islands (western Mediterranean)
Figure 7. Pollentia perezi gen. & sp. nov. (paratype MNCN 16.01/18956), elytra. A, outer edge, with microtubercles. B, same, scanning electron micrograph. C, D, detail of microtubercles, scanning electron micrograph. E, light micrograph of tubercles on outer surface. F, smooth inner edge, scanning electron micrograph.
Figure 6 in Discovery of a new scale worm (Annelida: Polynoidae) with presumed deep-sea affinities from an anchialine cave in the Balearic Islands (western Mediterranean)
Figure 6. Pollentia perezi gen. & sp. nov. (paratype MNCN 16.01/18956). A, head with dissected appendages except for lateral antennae. B, head and anterior parapodia, side view (tentacular cirri with removed styles). C, lateral antenna. D, detail of lateral antenna, with internal papillae. E, detail of wrinkled palp, with longitudinal rows of papillae. F, papilla on palp. G, upper lip, without facial tubercle. H, second segment, with wide neuropodial acicular lobe. I, ventral cirrus of second segment. J, detail of papilla of first ventral cirrus. K, transverse rows of cilia on midbody dorsal sides. L, detail of dorsal rows of cilia. M, pharyngeal papillae. N, detail of jaw. Abbreviations: la, lateral antenna; ma, median antenna; mo, mouth; nea, neuroacicular lobe; noa, notoacicular lobe; pa, palp; ph, pharyx; tc, tentacular cirrus; ti, inferior tentacular cirrus; ts, superior tentacular cirrus; vc, ventral cirrus; 1–4, segment number; stars, rows of cilia.
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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)
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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.