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Figure 4 from: da Costa e Silva G, Roxo F, Britzke R, Oliveira C (2014) New species of the Pseudancistrus barbatus group (Siluriformes, Loricariidae) with comments on its biogeography and dispersal routes. ZooKeys 406: 1-23. https://doi.org/10.3897/zookeys.406.7011
Figure 4 - Map showing the type locality (red square) of Pseudancistrus zawadzkii at rio Tapajós, 04°33'09.7"S, 56°17'59.6"W, and paratype locality (black circle) at rio Tracuá, Tapajós river basin, 04°28'11.2"S, 56°17'01.1"W.
Figure 3 from: da Costa e Silva G, Roxo F, Britzke R, Oliveira C (2014) New species of the Pseudancistrus barbatus group (Siluriformes, Loricariidae) with comments on its biogeography and dispersal routes. ZooKeys 406: 1-23. https://doi.org/10.3897/zookeys.406.7011
Figure 3 - Pseudancistrus zawadzkii, live specimen, LBP 15045, paratype, female, 128.7 mm SL, Tapajós river, Pará State, Brazil.
Figure 1 from: da Costa e Silva G, Roxo F, Britzke R, Oliveira C (2014) New species of the Pseudancistrus barbatus group (Siluriformes, Loricariidae) with comments on its biogeography and dispersal routes. ZooKeys 406: 1-23. https://doi.org/10.3897/zookeys.406.7011
Figure 1 - Pseudancistrus zawadzkii, MZUSP 115056, holotype, male, 116.4 mm SL; Pará State, Tapajós river basin, Brazil.
Figure 4 from: Mar SS, Saunders RMK (2015) Thismia hongkongensis (Thismiaceae): a new mycoheterotrophic species from Hong Kong, China, with observations on floral visitors and seed dispersal. PhytoKeys 46: 21-33. https://doi.org/10.3897/phytokeys.46.8963
Figure 4 - Thismia hongkongensis sp. nov. (S.S. Mar 2, HK). A Entire flower. B Flower with proximal part of perianth tube removed, showing pendent stamens. C Apex of the perianth tube, showing annulus (a) and pendent stamens, with filament (f), thecae (th), lateral appendage (la), and aperture (ap) between filaments. D Longitudinal section through fused carpels. Scale bars: A, B, D = 2 mm; C = 1 mm. Drawings by Caren Pearl Shin.
Figure 2 from: Mar SS, Saunders RMK (2015) Thismia hongkongensis (Thismiaceae): a new mycoheterotrophic species from Hong Kong, China, with observations on floral visitors and seed dispersal. PhytoKeys 46: 21-33. https://doi.org/10.3897/phytokeys.46.8963
Figure 2 - Flower structure in Thismia hongkongensis sp. nov. A Mature flower, showing outer tepals (ot), inner tepals (it) and abscission zone (ab) at the base of the perianth tube. B Entire plant (S.S. Mar 1, HK). C Perianth tube with annulus (a), following removal of the proximal face of the tube, exposing pendent stamens with filament (f), thecae (th), connective (c) and lateral appendage (la) (S.S. Mar 2, HK). D Inner face of perianth tube, showing network patterning and putative nectaries (arrowed) (S.S. Mar 2, HK). Scale bars: A, D = 2 mm; B = 5 mm; C = 1 mm. Photos: A, B S.S. Mar; C, D R.M.K. Saunders.
Figure 1 from: Mar SS, Saunders RMK (2015) Thismia hongkongensis (Thismiaceae): a new mycoheterotrophic species from Hong Kong, China, with observations on floral visitors and seed dispersal. PhytoKeys 46: 21-33. https://doi.org/10.3897/phytokeys.46.8963
Figure 1 - Flower development in Thismia hongkongensis sp. nov. A, B Root system, with young flowering stalk developing (arrowed). C–H Developing flower, photographed over a 17-day period (10th, 14th, 16th, 19th, 23rd and 27th May, respectively) (S.S. Mar 1, HK). I, J Post-fertilization flower, showing abscission of perianth tube. Photos by S.S. Mar.
Figure 3 from: Mar SS, Saunders RMK (2015) Thismia hongkongensis (Thismiaceae): a new mycoheterotrophic species from Hong Kong, China, with observations on floral visitors and seed dispersal. PhytoKeys 46: 21-33. https://doi.org/10.3897/phytokeys.46.8963
Figure 3 - Fruit structure in Thismia hongkongensis sp. nov. A Flower (rear right), immature fruit, shortly after fertilization (left), and mature fruit with exposed seeds (front). B Two fruiting individuals, each with three fruits. C Lateral view of fruiting specimen, illustrating elongated fruit stalk. D Mature fruit with exposed seeds. E Dehydrated fruit. F Rehydrated fruit, after rainfall. Photos by S.S. Mar.
Figure 4 from: Roxo FF, Ochoa LE, Silva GSC, Oliveira C (2015) Rhinolekos capetinga: a new cascudinho species (Loricariidae, Otothyrinae) from the rio Tocantins basin and comments on its ancestral dispersal route. ZooKeys 481: 109-130. https://doi.org/10.3897/zookeys.481.8755
Figure 4 - a Map showing the distribution of Rhinolekos capetinga. Type locality at córrego da Branca, green star – 14°53'47.2"S, 47°34'58.4"W. Paratype localities at córrego da Branca, red star – 14°57'01.6"S, 47°35'57.0"W, and at córrego Roncador, pink star – 14°43'51.3"S, 47°32'34.0"W b Habitat and submerged vegetation where the specimens were found in type locality of córrego da Branca, 14°53'47.2"S, 47°34'58.4"W. Photo: LH Roxo.
Figure 3 from: Roxo FF, Ochoa LE, Silva GSC, Oliveira C (2015) Rhinolekos capetinga: a new cascudinho species (Loricariidae, Otothyrinae) from the rio Tocantins basin and comments on its ancestral dispersal route. ZooKeys 481: 109-130. https://doi.org/10.3897/zookeys.481.8755
Figure 3 - Rhinolekos capetinga, live specimen, MZUSP 116102, holotype, male, 37.5 mm SL, rio Tocantins basin, Goiás State, Brazil. Photo: FF Roxo.
Figure 5 from: Roxo FF, Ochoa LE, Silva GSC, Oliveira C (2015) Rhinolekos capetinga: a new cascudinho species (Loricariidae, Otothyrinae) from the rio Tocantins basin and comments on its ancestral dispersal route. ZooKeys 481: 109-130. https://doi.org/10.3897/zookeys.481.8755
Figure 5 - Biogeographic distribution and time-calibrated phylogenetic tree of Microlepidogaster and Rhinolekos species, based on three mitochondrial (16SrRNA, COI, Cytb) and one nuclear marker (F-reticulon 4), modified from figure 7 of Roxo et al. (2014a). The map colorations indicate distinct biogeographic regions according to classification available in Roxo et al. (2014a): Green – Coastal drainages (A); Red – upper rio Paraná basin (B); Purple – Paraguay, Lower Paraná and Uruguay basins (C); Blue – Amazon basin (D); Yellow – São Francisco basin (E).
Figure 2 from: Roxo FF, Ochoa LE, Silva GSC, Oliveira C (2015) Rhinolekos capetinga: a new cascudinho species (Loricariidae, Otothyrinae) from the rio Tocantins basin and comments on its ancestral dispersal route. ZooKeys 481: 109-130. https://doi.org/10.3897/zookeys.481.8755
Figure 2 - Rhinolekos capetinga, LBP 19001, paratype, 34.5 mm SL. a Anterior portion of axial skeleton and dorsal-fin supports (left side, lateral view). Vertebrae counts included five vertebrae of the Weberian apparatus. np nucal plate; rv6 rib of sixth vertebrae; px2 compound proximal and medial radial 2; sn+px1 compound supraneural first dorsal-fin proximal radial; sp1 first dorsal-fin spinelet; sp2 second dorsal-fin spine; v6−12 vertebrae 6−12 b Skull of Rhinolekos capetinga; f frontal; soc supraoccipital; cpt parieto-supraoccipital; op opercle; io1−5 infraorbitals; pop preopercle; cp 1−2 cheek plates; pr 1−3 postrostral plates; pf prefrontal plates; le lateral ethmoid; n nasal; lpn lateronasal plate; r rostral plate; pn prenasal; sp sphenotic.
Figure 1 from: Roxo FF, Ochoa LE, Silva GSC, Oliveira C (2015) Rhinolekos capetinga: a new cascudinho species (Loricariidae, Otothyrinae) from the rio Tocantins basin and comments on its ancestral dispersal route. ZooKeys 481: 109-130. https://doi.org/10.3897/zookeys.481.8755
Figure 1 - Rhinolekos capetinga MZUSP 116102, holotype, male, 37.5 mm SL, Goiás State, rio Tocantins basin, Brazil.
Figure 1 from: Martine CT, Cantley JT, Frawley ES, Butler AR, Jordon-Thaden IE (2016) New functionally dioecious bush tomato from northwestern Australia, Solanum ossicruentum, may utilize "trample burr" dispersal. PhytoKeys 63: 19-29. https://doi.org/10.3897/phytokeys.63.7743
Figure 1 - Solanum ossicruentum sp. nov. A Typical habitat, Mirima National Park, WA B Leaf morphology C Female individual, Mirima NP D Close-up of functionally female (morphologically hermaphrodite) flower E Abaxial side of functionally female flower showing elongated calyx lobes F Male individual, Mirima NP G Male flower, abaxial view H Developing fruit within calyx I Immature fruits showing blood-red staining at 2 minutes (lower) and 5 minutes (above) after cutting J Mature bony fruits removed from calyces and (lower right) as collected from ground beneath plant. Yellow scale bars as follows: 3 cm (B, C, F); 1 cm (D); 2 cm (E, G, H, J); 0.75 cm (I). Photos A, C, F, and J by C.T. Martine; all others by J.T. Cantley.
Figure 3 from: Martine CT, Cantley JT, Frawley ES, Butler AR, Jordon-Thaden IE (2016) New functionally dioecious bush tomato from northwestern Australia, Solanum ossicruentum, may utilize "trample burr" dispersal. PhytoKeys 63: 19-29. https://doi.org/10.3897/phytokeys.63.7743
Figure 3 - Map showing distribution of Solanum ossicruentum sp. nov. accessions held at the Northern Territory Herbarium, Palmerston (DNA) and examined for this description. Map base layer generated from ArcGIS.
Figure 2 from: Martine CT, Cantley JT, Frawley ES, Butler AR, Jordon-Thaden IE (2016) New functionally dioecious bush tomato from northwestern Australia, Solanum ossicruentum, may utilize "trample burr" dispersal. PhytoKeys 63: 19-29. https://doi.org/10.3897/phytokeys.63.7743
Figure 2 - SEM images of Solanum ossicruentum sp. nov. pollen grains. A Functional pollen produced by male flowers, and B Inaperturate pollen produced by morphologically hermaphrodite, yet functionally female, flowers. Images by A. Butler.
Figure 5 from: Agnarsson I, LeQuier SM, Kuntner M, Cheng R-C, Coddington JA, Binford G (2016) Phylogeography of a good Caribbean disperser: Argiope argentata (Araneae, Araneidae) and a new 'cryptic' species from Cuba. ZooKeys 625: 25-44. https://doi.org/10.3897/zookeys.625.8729
Figure 5 - Comparative morphology of the male palpal organ of the widespread Argiope argentata and the new Argiope butchko. No clearly diagnostic features were identified in the new species, though slight differences in the terminal parts of the median apophysis and the embolus are observed and merit further comparative investigation.
Figure 4 from: Agnarsson I, LeQuier SM, Kuntner M, Cheng R-C, Coddington JA, Binford G (2016) Phylogeography of a good Caribbean disperser: Argiope argentata (Araneae, Araneidae) and a new 'cryptic' species from Cuba. ZooKeys 625: 25-44. https://doi.org/10.3897/zookeys.625.8729
Figure 4 - Female holotype Argiope butchko sp. n. a dorsal b lateral c ventral; Male paratype Argiope butchko sp. n. d dorsal e lateral f ventral g external epigynum h external epigynum illustration showing spermatheca and spiraling ducts i internal epigynum illustration dorsal m palp lateral n palp ventral; Argiope argentata j external epigynum k external epigynum illustration showing spermatheca and spiraling ducts l internal epigynum illustration dorsal o palp lateral p palp ventral.
Figure 1 from: Agnarsson I, LeQuier SM, Kuntner M, Cheng R-C, Coddington JA, Binford G (2016) Phylogeography of a good Caribbean disperser: Argiope argentata (Araneae, Araneidae) and a new 'cryptic' species from Cuba. ZooKeys 625: 25-44. https://doi.org/10.3897/zookeys.625.8729
Figure 1 - A dated phylogeny of Argiope argentata in the Caribbean, and other Argiope relatives. Shown are the results of tree based species delimitation analyses (GMYC method) on a BEAST phylogeny (node ages in million years) and the location of spiders used in this study (inset picture). Asterisk denotes posterior probability support >95%. The OTUs (operational taxonomic units) correspond to a cryptic species, Argiope butchko sp. n., from Cuba (argentataCU) and populations from other Caribbean islands (argentataCAR) plus mainland (argentataUS) treated as conspecific (Argiope argentata).
Figure 3 from: Agnarsson I, LeQuier SM, Kuntner M, Cheng R-C, Coddington JA, Binford G (2016) Phylogeography of a good Caribbean disperser: Argiope argentata (Araneae, Araneidae) and a new 'cryptic' species from Cuba. ZooKeys 625: 25-44. https://doi.org/10.3897/zookeys.625.8729
Figure 3 - A haplotype network of Caribbean Argiope argentata and Argiope butchko sp. n. Haplotypes are colored by locality as indicated, circle size reflects number of individuals carrying that haplotype from 1-7 in total, open circles represent unobserved haplotypes. Hash marks indicate mutational differences among haplotypes. Inset photograph is of a female Argiope butchko.
Figure 2 from: Agnarsson I, LeQuier SM, Kuntner M, Cheng R-C, Coddington JA, Binford G (2016) Phylogeography of a good Caribbean disperser: Argiope argentata (Araneae, Araneidae) and a new 'cryptic' species from Cuba. ZooKeys 625: 25-44. https://doi.org/10.3897/zookeys.625.8729
Figure 2 - Regression analysis between geographic and genetic distances among all specimens of Argiope argiope s.l. included here. Blue dots and line represent within species comparisons and red dots and line those among the two species as here defined. Black line is regression across all data. Geographical distances well explain genetic distances within species, but not between the species, as expected.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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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.