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Figs 6–9 in Description of a new species of Loxosceles Heineken & Lowe (Araneae, Sicariidae) recluse spiders from Hidalgo, Mexico, under integrative taxonomy: morphological and DNA barcoding data (CO1 + ITS2)
Figs 6–9. Live female paratype (CNAN-T01321) of Loxosceles tolantongo sp. nov. from the type locality: Tourist Center Grutas de Tolantongo Municipality of Cardonal, Hidalgo, Mexico. Photos 6–7 by Alejandro Valdez-Mondragón (2019); photos 8–9 by Claudia Isabel Navarro-Rodríguez (2019).
Figs 1–5 in Description of a new species of Loxosceles Heineken & Lowe (Araneae, Sicariidae) recluse spiders from Hidalgo, Mexico, under integrative taxonomy: morphological and DNA barcoding data (CO1 + ITS2)
Figs 1–5. Live male holotype (CNAN-T01317) of Loxosceles tolantongo sp. nov. from the type locality: Tourist Center Grutas de Tolantongo, Municipality of Cardonal, Hidalgo, Mexico. Photos 1–4 by Alejandro Valdez-Mondragón (2019); photo 5 by Claudia Isabel Navarro-Rodríguez (2019).
Fig. 53 in Description of a new species of Loxosceles Heineken & Lowe (Araneae, Sicariidae) recluse spiders from Hidalgo, Mexico, under integrative taxonomy: morphological and DNA barcoding data (CO1 + ITS2)
Fig. 53. Neighbor joining tree of ITS2 data of nine species of Loxosceles Heineken & Lowe, 1832 from Mexico. Colors of branches indicate different species. Numbers at nodes represent bootstrap support values. Red circle at node represent Loxosceles tolantongo sp. nov.
Fig. 57 in Description of a new species of Loxosceles Heineken & Lowe (Araneae, Sicariidae) recluse spiders from Hidalgo, Mexico, under integrative taxonomy: morphological and DNA barcoding data (CO1 + ITS2)
Fig. 57. Haplotype network from the CO1 data obtained with TCS using PopArt. Each circle represents the haplotypes found in nine species of Loxosceles Heineken & Lowe, 1832 from Mexico. Numbers on branches indicate the number of mutations between haplotypes.
Figs 36–43 in Description of a new species of Loxosceles Heineken & Lowe (Araneae, Sicariidae) recluse spiders from Hidalgo, Mexico, under integrative taxonomy: morphological and DNA barcoding data (CO1 + ITS2)
Figs 36–43. Variation of the seminal receptacles of females, dorsal view. 36–39. Loxosceles tolantongo sp. nov. 36, 39. Tourist Center Grutas de Tolantongo, Municipality of Cardonal. 37–38. 500 m west of the entrance No. 5 to the Tourist Center Grutas de Tolantongo, Municipality of Cardonal. 40–43. Loxosceles jaca Gertsch & Ennik, 1983. 2.5 km north of Jacala de Ledezma, Municipality of Jacala de Ledezma, Hidalgo. Scale bars = 0.2 mm.
Data from: Discovery of a new ant species of the elusive termitophilous genus Metapone in Singapore (Hymenoptera: Formicidae: Myrmicinae), with first detailed description of male genitalia of the genus
A new species of the rare ant genus Metapone – Metapone murphyi – is described based on aged museum material: a single nest series (workers, queens and males) collected from a decayed coconut (tree) stump on Pulau Sakra – previously an offshore island south of mainland Singapore. Workers can be distinguished from other named congeners mainly by the following characters: 1) subpetiolar lamella subrectangular; 2) short subpetiolar edge and roundly obtuse subpetiolar angle; 3) outer margin of posterior subpetiolar face forming a continuous, U-shaped, translucent, laminate carina; 4) subtrapezoidal petiole in dorsal view with extended blunt tooth-like posterolateral corners. Detailed description and illustrations of the male genitalia are given for the first time in the genus. The key to Asian species of Metapone is updated to include the new species.
Data from: Dispersal barriers and opportunities drive multiple levels of phylogeographic concordance in the Southern Alps of New Zealand
<p>Phylogeographic concordance, or the sharing of phylogeographic patterns among co-distributed species, suggests similar responses to topography or climatic history. While the orientation and timing of breaks between lineages are routinely compared, spatial dynamics within regions occupied by individual lineages provide a second opportunity for comparing responses to past events. In environments with complex topography and glacial history, such as New Zealand's South Island, geographically nested comparisons can identify the processes leading to phylogeographic concordance between and within regional genomic clusters. Here, we used single nucleotide polymorphisms (obtained via ddRADseq) for two co-distributed forest beetle species, <i>Agyrtodes labralis</i> (Leiodidae) and <i>Brachynopus scutellaris</i> (Staphylinidae), to evaluate <a name="_Hlk34399639">the role of climate change and topography in shaping phylogeographic concordance at two, nested spatial scales: do species diverge over the same geographic barriers, with similar divergence times? And within regions delimited by these breaks</a>, do species share similar spatial dynamics of directional expansion or isolation-by-distance? We found greater congruence of phylogeographic breaks between regions divided by the strongest dispersal barriers (i.e., the Southern Alps). However, these shared breaks were not indicative of shared spatial dynamics within the regions they delimit, and the most similar spatial dynamics between species occurred within regions with the strongest gradients in historical climatic stability. Our results indicate that <span>lack of concordance as traditionally detected by lineage turnover does not rule out the possibility of shared histories, and variation in the presence and type of concordance may provide insights into the different processes shaping phylogeographic patterns across geologically dynamic regions. </span> </p>
Fig. 19 in The Indo-Pacific Amalda (Neogastropoda, Olivoidea, Ancillariidae) revisited with molecular data, with special emphasis on New Caledonia
Fig. 19. Sequenced species of Amalda H. Adams & A. Adams, 1853. A–B. Amalda sp., MNHN IM-2013-63891, SL 20 mm. C–D. A. contusa (Reeve, 1864), MNHN IM-2009-22263, SL 24.9 mm. E. A. optima (G.B. Sowerby III, 1897), MNHN IM-2007-38287. F–G. A. monilifera (Reeve, 1864), MNHN IM-2013-63898, SL 11.7 mm. H–I. A. hinomotoensis (Yokoyama, 1922), MNHN IM-2019-618, SL 41.4 mm. J–K. A. hayashii Ninomiya, 1988, MNHN IM-2013-44413, SL 38.4 mm. L–M. A. bellonarum Kilburn & Bouchet, 1988, MNHN IM-2007-33273. Shells not to scale.
Fig. 15 in The Indo-Pacific Amalda (Neogastropoda, Olivoidea, Ancillariidae) revisited with molecular data, with special emphasis on New Caledonia
Fig. 15. Amalda alabaster sp. nov. A–B. Holotype, MNHN IM-2007-43627, SL 26.7 mm. C-D. MNHN IM-2007-43583, SL 24.8 mm. E. MNHN IM-2007-43621, SL 27.1 mm. F. MNHN IM-2007-43626, SL 22.2 mm, specimen not sequenced. G. MNHN IM-2007-43633, SL 22 mm, specimen not sequenced. H–I. A. cf. alabaster, MNHN IM-2013-63897, SL 18.1 mm. Shells at the same scale, all specimens except F–G sequenced.
Fig. 16. A–F. Amalda allaryi Bozzetti, 2007. A–B in The Indo-Pacific Amalda (Neogastropoda, Olivoidea, Ancillariidae) revisited with molecular data, with special emphasis on New Caledonia
Fig. 16. A–F. Amalda allaryi Bozzetti, 2007. A–B. Holotype, MNHN IM-2000-20532, SL 29.4 mm. C–D. MNHN IM-2007-43630, SL 27.2 mm. E. MNHN IM-2007-43628, SL 24.4 mm. F. KANACONO, stn CP4656, 22°40′ S, 167°12′ E, 219–244 m, W of Île des Pins, SL 64.5 mm. G–H. A. maritzae Bozzetti, 2007, holotype, MNHN IM-2000-24475, SL 54.4 mm. A–E = at the same scale; F–H = at the same scale; C–E = sequenced specimens.
Fig. 14. A–B in The Indo-Pacific Amalda (Neogastropoda, Olivoidea, Ancillariidae) revisited with molecular data, with special emphasis on New Caledonia
Fig. 14. A–B. Live specimens of Amalda montrouzieri (Souverbie, 1860), Nouméa, 8 m. C–E. Shell and live specimen of A. herberti Cossignani, 2013, Nouméa, South Lagoon, about 250 m. Photos courtesy of David Massemin.
Fig. 13 in The Indo-Pacific Amalda (Neogastropoda, Olivoidea, Ancillariidae) revisited with molecular data, with special emphasis on New Caledonia
Fig. 13. Radulae of species of Amalda H. Adams & A. Adams, 1853. A–C. A. montrouzieri (Souverbie, 1860). A–B. Île Ouen – Baie du Prony, LAGON, stn DW239, 22°24.3′ S, 166°57.8′ E, 42–43 m, SL 20.2 mm. C. Grand Récif Sud, LAGON, stn DW544, 22°50.8′ S, 166°48.5′ E, 25 m, SL 25.4 mm (shell on Fig. 12I). D–E. A. alabaster sp. nov. D. Holotype, MNHN IM-2007-43627, SL 26.7 mm (shell on Fig. 15A–B). E. MNHN IM-2007-43636, SL 17.6 mm. F. A. cf. alabaster, MNHN IM-2013-63897, SL 18.1 mm (shell on Fig. 15H–I). G. A. allaryi Bozzetti, 2007, MNHN IM-2013- 68272 (shell on Fig. 17A). H. A. coriolis Kilburn & Bouchet, 1988, MNHN IM-2013-63899 (shell on Fig. 18H–I).
Fig. 10 in The Indo-Pacific Amalda (Neogastropoda, Olivoidea, Ancillariidae) revisited with molecular data, with special emphasis on New Caledonia
Fig. 10. Amalda miriky sp. nov., Madagascar. A–E. Holotype, MNHN IM-2007-36868, SL 39.6 mm (D–E = enlarged lateral and apical views of the protoconch). F. MNHN IM-2007-38073, SL 35.8 mm (specimen not sequenced). G. MNHN IM-2007-36842, SL 35.7 mm. H. MNHN IM-2007-36866, SL 37.9 mm. I. MNHN IM-2007-38064, SL 30 mm. J. Miriky, stn DW3215, between Nosy-Be and Banc du Leven, 12°32′ S, 47°54′ E, 316–433 m, SL 38.9 mm (specimen not sequenced, radula on Fig. 7J). Scale bars: A–C, F–J= 2 cm; D–E = 1 mm.
Fig. 8. A–H in The Indo-Pacific Amalda (Neogastropoda, Olivoidea, Ancillariidae) revisited with molecular data, with special emphasis on New Caledonia
Fig. 8. A–H. Amalda aureomarginata Kilburn & Bouchet, 1988, southern New Caledonia. A–C. Holotype, MNHN IM-2000-1345, SL 34.1 mm. D. MNHN IM-2007-43644, SL 26.6 mm. E. MNHN IM-2007- 43655, SL 31.5 mm. F. MNHN IM-2007-43551, SL 30.5 mm. G–H. MNHN IM-2007-43654, SL 28.2 mm. I–J. A. hilgendorfi (von Martens, 1897), MNHN IM-2009-11968, northern New Caledonia, SL 31.6 mm. Shells at the same scale; H, J = enlarged upper part of the shell. Arrow on H points at dark brown line, bordering secondary spire callus.
Fig. 7 in The Indo-Pacific Amalda (Neogastropoda, Olivoidea, Ancillariidae) revisited with molecular data, with special emphasis on New Caledonia
Fig. 7. Radulae of species of Amalda H. Adams & A. Adams, 1853. A–G. A. hilgendorfi (von Martens, 1897). A–B. MNHN IM-2019-621 (shell on Fig. 4D). C. MNHN IM-2009-11961 (shell on Fig. 4J). D. MNHN IM-2013-58045, Papua New Guinea. E. MNHN IM-2013-19909, Papua New Guinea. F. MNHN IM-2013-63430, southern New Caledonia. G. MNHN IM-2007-33312 (shell on Fig. 5F). H. A. aureomarginata Kilburn & Bouchet, 1988, MNHN IM-2013-63421, specimen not sequenced, southern New Caledonia. I–J. A. miriky sp. nov. I. Miriky, stn CP3210, specimen not sequenced, Madagascar. J. Miriky, stn DW3215 (shell on Fig. 10J). K–L. A. cacao sp. nov., holotype, MNHN IM-2000-35296 (shell on Fig. 11A–E).
Fig. 9 in The Indo-Pacific Amalda (Neogastropoda, Olivoidea, Ancillariidae) revisited with molecular data, with special emphasis on New Caledonia
Fig. 9. Distribution map of Amalda aureomarginata Kilburn & Bouchet, 1988 (A) and A. fuscolingua Kilburn & Bouchet, 1988 (B) off southern New Caledonia. Red circles = the type localities; stars = indicate stations where the species were recovered.
Fig. 5 in The Indo-Pacific Amalda (Neogastropoda, Olivoidea, Ancillariidae) revisited with molecular data, with special emphasis on New Caledonia
Fig. 5. Amalda hilgendorfi (von Martens, 1897). A–F. Coral Sea morph. A-B. MNHN IM-2007- 33313, SL 66 mm. C. MNHN IM-2007-33289, SL 51.3 mm. D. MNHN IM-2007-33288, SL 60.3 mm. E. MNHN IM-2013-63901, SL 27-3 mm. F. MNHN IM-2007-33312, SL 25.9 mm. G–K. Northern New Caledonia morph = A. hilgendorfi richeri Kilburn & Bouchet, 1988. G. Holotype, MNHN IM-2000- 1378, SL 66.9 mm. H. MNHN IM-2009-11916, SL 65 mm. I. MNHN IM-2009-11918, SL 43.2 mm. J. MNHN IM-2007-42675, SL 48.7 mm. K. MNHN IM-2009-11966, SL 29 mm. Shells at the same scale.
Fig. 4 in The Indo-Pacific Amalda (Neogastropoda, Olivoidea, Ancillariidae) revisited with molecular data, with special emphasis on New Caledonia
Fig. 4. Amalda hilgendorfi (von Martens, 1897). A–D. Typical morph, Japan. A–C. MNHN IM-2019- 616, SL 53.1 mm. D. MNHN IM-2019-621, SL 50.0 mm. E–G. Philippine morph. E. MNHN IM-2007- 31950, SL 38.7 mm. F–G. MNHN IM-2007-33427, SL 40.3 mm. H–L. Solomon Islands and Papua New Guinea (PNG) morph. H. Solomons, MNHN IM-2007-33286, SL 52.6 mm. I. PNG, MNHN IM-2013- 44995, SL 51.3 mm. J. Solomons, MNHN IM-2009-11961, SL 32.9 mm. K. PNG, MNHN IM-2009- 22244, SL 63.1 mm. L. PNG, MNHN IM-2009-23330, SL 69.3 mm. M. Amalda tankervillii (Swainson, 1825), Venezuela, Isla de Margarita, 30–35 m, collection of Ron Voskuil, RV 0175, SL 80 mm. Photo by Ron Voskuil et al. (2011) (http://olivirv.myspecies.info/en/taxon-pages/ancillaria-tankervillii). Shells (except M, reduced) at the same scale.
Fig. 3 in The Indo-Pacific Amalda (Neogastropoda, Olivoidea, Ancillariidae) revisited with molecular data, with special emphasis on New Caledonia
Fig. 3. Median-joining haplotype network based on Cox1 sequences of Amalda hilgendorfi (von Martens, 1897). Circles are colour coded by general location reported on the map and sized according to each haplotype's relative abundance. Lengths of the lines connecting haplotype circles are proportional to the number of nucleotide differences among haplotypes. Green rectangle and oval encircle assemblages of haplotypes from New Caledonia (each including a specimen from Papua New Guinea).
Fig. 1 in The Indo-Pacific Amalda (Neogastropoda, Olivoidea, Ancillariidae) revisited with molecular data, with special emphasis on New Caledonia
Fig. 1. Bayesian tree (MrBayes) for the Cox1 gene. Bootstrap supports (± 70) and posterior probabilities (> 0.90) values are shown for each supported node. The unit for the scale is "substitutions/site". The clades of Amalda hayashii Ninomiya, 1988, A. fuscolingua Kilburn & Bouchet, 1988 and A. aureomarginata Kilburn & Bouchet, 1988 containing multiple specimens with minimal genetic distances are collapsed. The clade of A. hilgendorfi (von Martens, 1897) is collapsed and shown on Fig. 2.
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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.