Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
48
datasets available to search
ShareScore release 0.9.0
Dataset results
48 results for “salticids”
Figure 1. Hypothetical salticid archetype for a in A salticid archetype for salticid spiders
Figure 1. Hypothetical salticid archetype for a salticid spider (1) and representatives of five lepidopteran genera that share these archetypal features (2-6), apparently the result of convergent evolution. Attribution and ©: 1, David E. Hill; 2, Ian McMillan; 3, Christian Schwartz; 4, Arnold Wijker; 5, CheongWeei Gan; 6, Eric Carpenter.
Figure 24 in A salticid archetype for salticid spiders
Figure 24. Olethreutes arcuella. Olethreutes is part of a very large tortricid subfamily (Olethreutinae) with many small, hightly, ornamented species, very few of which come close to displaying any features of the hypothetical salticid archetype (Figure 29). Extra "eyes" of O. arcuella may induce a supernormal response by salticids. Attribution and ©: 1, Kostas Zontanos; 2, Felix Riegel; 3, sabine-g; 4, Mirko Tomasi; 5, Marie Lou Legrand; 6, oe5hm; 7, Andrei; 9, 15, Paolo Mazzei; 8, Franziska Bauer; 10, Joey Bom; 11, Xavier Mas; 12, Vojtek Pavel; 13-14, Ryszard.
Figure 28 in A salticid archetype for salticid spiders
Figure 28. Developmental stages of Phidippus princeps from Greenville County, South Carolina. 1, The first emergent or freeliving stage (instar II) is black, with pedipalps and legs that fluoresce (emit bright yellow-green) in near-UV light. 2, The pedipalps and proximal segments of the legs of early instars like this one also fluoresce, but the face now has a cover of setae, including a darker band through the anterior eye row, typical of later instars through the penultimate stage. 3, At the prepenultimate stage males and females are similar. 4, Penultimate male, with distinct enlargement of the pedipalps but otherwise coloration like that of the female. 5, Penultimate female. 6, Adult female, with bright white setae covering the face, highlighting the anterior eyes. Attribution and ©: 1-6, David E. Hill.
Sanger sequences of marpissoid salticids for Kelawakaju placement
<p><span>The genus <em>Kelawakaju</em> Maddison & Ruiz, gen. nov., is described for a lineage of bark-dwelling Asian marpissine jumping spiders that represent a dispersal to Eurasia separate from that of the <em>Marpissa</em>-<em>Mendoza</em> lineage, according to the phylogeny recovered from analysis of four gene regions. All of the species of Kelawakaju are new except <em>K</em>. <em>frenata </em>(Simon, 1901), comb. nov., which is here transferred from <em>Ocrisiona</em> Simon, 1901. <em>K</em>. <em>frenata</em> is known from Hong Kong, Guangdong, Guangxi, and likely Taiwan. The five new species are <em>Kelawakaju</em> <em>mulu</em> Maddison & Ruiz (type species of Kelawakaju, from Sarawak, Malaysia, ♂♀), <em>K</em>. <em>intexta</em> Maddison & Ruiz (from Sarawak, ♂), <em>K</em>. <em>leucomelas</em> Maddison & Ng (Singapore and Johor Bahru, ♂♀), <em>K</em>. <em>sahyadri</em> Vishnudas, Maddison, & Sudhikumar (India, ♂♀), and <em>K</em>. <em>singapura</em> Maddison & Ng (Singapore, ♂♀), all sp. nov.</span></p>
Figure 5 in Studies of salticid behavior by Karl Hubert Heil (1936)
Figure 5. Apparatus for measuring the maximum jumping distance. UB base, S metal rails, W carriage, Z
Sanger sequences of marpissoid salticids for Kelawakaju placement
Open the record for dataset details and reuse information.
FIGURES 15–18 in A basal phylogenetic placement for the salticid spider Eupoa, with descriptions of two new species (Araneae: Salticidae)
FIGURES 15–18. Analyses using all genes for both small sample of salticoids (28S + 18S + 16S-ND1 + CO1) and large sample (28S + 16S-ND1 + CO1). The salticoid taxa in the large sample are unnamed; they are those used by Maddison & Needham (2006). 15 Small sample, majority rule consensus tree of 9900 trees sampled from 10 million generation Bayesian analysis; shown are estimated posterior probabilities; 16 Small sample, single most parsimonious tree found (treelength 7375 steps); shown are bootstrap values (Felsenstein 1985), 1000 replicates; 17 Large sample, majority rule consensus tree of 9900 trees sampled from 10 million generation Bayesian analysis, with estimated posterior probabilities; 18 Large sample, strict consensus of 2 most parsimonious trees found (treelength 22326 steps).
FIGURES 8–14 in A basal phylogenetic placement for the salticid spider Eupoa, with descriptions of two new species (Araneae: Salticidae)
FIGURES 8–14. Eupoa jingwei Maddison & Zhang, new species. 8–10 Palp of male holotype (8 ventral-prolateral view, 9 retrolateral, 10 ventral-retrolateral; 11–12 Male holotype; 13 epigynum of female paratype, ventral view; 14 palpus of female paratype. Scale bars 0.2mm.
FIGURES 1–7 in A basal phylogenetic placement for the salticid spider Eupoa, with descriptions of two new species (Araneae: Salticidae)
FIGURES 1–7. Eupoa nezha Maddison & Zhang, new species. 1–4 Palp of male holotype (1 ventral-prolateral view, 2 retrolateral, 3 ventral-retrolateral, 4 view as Figure 3, but highlighting path of embolus. Arrows show exit path of sperm, first into embolus then out of embolus opening); 5–6 Male paratype; 7 epigynum of paratype female, ventral view. e = embolus; ma = median apophysis; t? = tegulum?; ta = tegular apophysis. Scale bars 0.2mm.
FIGURES 19–20 in A basal phylogenetic placement for the salticid spider Eupoa, with descriptions of two new species (Araneae: Salticidae)
FIGURES 19–20. Results from analyses on separate data partitions. Each is the majority rule consensus tree from sampled trees from Bayesian analysis, with posterior probabilities at nodes. Filled spots on nodes indicate clade was recovered also in parsimony analysis. 19 Ribosomal genes 28S, 18S and 16S plus the non-coding region between 16S and ND1; 20 Mitochondrial protein coding genes ND1 and CO1, analyzed after translating to amino acids.
FIGURES 11–12 in Lapsiines and hisponines as phylogenetically basal salticid spiders (Araneae: Salticidae)
FIGURES 11–12. Ventral view of epigyna of hisponine females used. 11, Hispo cf. frenata; 12, Massagris cf. honesta.
FIGURE 10 in Lapsiines and hisponines as phylogenetically basal salticid spiders (Araneae: Salticidae)
FIGURE 10. Results from Bayesian analysis of large taxon sample, all genes combined. Shown is the majority rules consensus tree of 9900 sampled trees. Among the salticoids, only taxa also used in the small taxon sample are named; the unnamed taxa are those in Maddison & Hedin (2003). Circled numbers mark clades from Figure 1. Estimated posterior probabilities (last 9900000 of 10 million generations) marked for clades outside of the Salticoida. Maximum likelihood tree identical outside the Salticoida except it placed the corinnid/thomisid/Goleba group more basally. Black spots on nodes indicate clade was recovered also in parsimony analysis; hatched spots for nodes 2 and 3 indicate Hispo was placed within the salticoids by parsimony (as a heliophanine).
FIGURES 4–9 in Lapsiines and hisponines as phylogenetically basal salticid spiders (Araneae: Salticidae)
FIGURES 4–9. Results from analyses on separate data partitions. Circled numbers mark clades from Figure 1. Figures 4–8 show majority rule consensus trees from sampled trees from Bayesian analysis, with posterior probabilities at nodes. Spots on nodes indicate clade was recovered also in parsimony analysis. Figure 9 shows strict consensus of nine most parsimonious trees (treelength 602) for ND1CO1 amino acid matrix, with bootstrap values (1000 replicates).
FIGURES 2–3 in Lapsiines and hisponines as phylogenetically basal salticid spiders (Araneae: Salticidae)
FIGURES 2–3. Summary of analyses using All Genes (28S + 18S + H3 + 16SND1 + CO1). Circled numbers mark clades from Figure 1. 2, Majority rule consensus tree of 9900 trees sampled from Bayesian analysis; shown are estimated posterior probabilities (from last 9900000 of 10 million generations). 3, Strict consensus of three most parsimonious trees (treelength 6871 steps); shown are bootstrap values, 1000 replicates.
FIGURE 1 in Lapsiines and hisponines as phylogenetically basal salticid spiders (Araneae: Salticidae)
FIGURE 1. Summary of phylogenetic analyses. Filled ovals indicate support from different data partitions and analytical methods. Bayesian analyses: black indicates posterior probability (p.p.) = 0.75; checkered indicates p.p. 0.51–0.75. Other analyses: black indicates the clade appears in the most parsimonious or highest likelihood trees; striped indicates the clade was supported but with one taxon excluded, as explained in the following notes. Notes concerning numbered clades: (1) 28S+18S p.p. = 0.74; 18S p.p. = 0.58. (2) CO1 p.p. = 0.56; clade by CO1 likelihood and parsimony excludes Orthrus. (3) 18S p.p. = 0.71. (4) H3+16SND1+CO1 p.p. = 0.69; CO1 p.p. = 0.67; clade by 16SND1 Bayesian and parsimony excludes Tomocyrba; clade by CO1 parsimony excludes Thrandina; clade by All Genes parsimony includes Hispo. (5) Clade by 28S parsimony excludes Thrandina. (6) 18S p.p. = 0.57. (7) 16SND1 sequence not obtained for Galianora sacha. (8) 18S p.p. = 0.56. (9) 18S sequences obtained only for Portia s. in this clade. (10) 28S+18S p.p. = 0.63; CO1 sequences not obtained for any hisponine. (11) 28S p.p. = 0.53.
Figure 2. Habitus, dorsal view. A, Female Breda lubomirskii. B in First report of Eustiromastix spinipes (Taczanowski 1872) (Araneae: Salticidae: Saltafresia) from Colombia, with new salticid records for the Department of Córdoba
Figure 2. Habitus, dorsal view. A, Female Breda lubomirskii. B, Male Tanybelus
Supplementary material 1 from: Courtial C, Picard L, Ysnel F, Petillon J (2014) Validation of Eustiromastix guianae (Caporiacco, 1954) (Araneae, Salticidae) with a first description of the female, and additions to the salticid fauna of French Guiana. ZooKeys 420: 11-18. https://doi.org/10.3897/zookeys.420.6977
Electronic supplementary material: Explanation note: Table 1. Detailed records of all salticid species in the National Nature Reserve Trinité. Figure 1. Map showing localities of NNR Trinité and Charvein.
FIGURE 11 in Salticid spider phylogeny revisited, with the discovery of a large Australasian clade (Araneae: Salticidae)
FIGURE 11. Phylogenetic analyses of 16S–ND1sequences. Tree shown is majority rules consensus of trees sampled from the Bayesian analysis of 24–6 aligned data. Spots show strength of support with 24–6 and 8–4 alignments. Darkness of spot shows estimated posterior probability of clade. Footnotes: 1 Tomocyrba excluded from clade. 2 Naphrys and Myrmarachne excluded from clade. 3 Hispo included in clade.
FIGURE 10 in Salticid spider phylogeny revisited, with the discovery of a large Australasian clade (Araneae: Salticidae)
FIGURE 10. Phylogenetic analyses of 28S sequences. Tree shown is majority rules consensus of trees sampled from the Bayesian analysis of 24–6 aligned data. Spots show strength of support with 24–6 and 8–4 alignments. Darkness of spot shows estimated posterior probability of clade. Footnotes: 1 Orthrus included in clade. 2 Mantisatta included in clade. 3 Carrhotus sp. (Phil.) excluded from clade.
FIGURES 1–7 in Salticid spider phylogeny revisited, with the discovery of a large Australasian clade (Araneae: Salticidae)
FIGURES 1–7. Genitalia of some of the more poorly identified taxa sequenced. 1 Left palp of cf. Lystrocteissa sp. (voucher d054), which is small and narrow-bodied. 2 Left palp of Penionomus sp. (d122), medium sized, fairly robust, and bronze. 3 Left palp of cf. Rogmocrypta sp. (d205), small, with body form reminiscent of Sitticus. 4 Left palp of cf. Nimbarus sp. (d218), whose long tibial apophysis extends dorsally over the cymbium. 5 Left palp of Pochyta cf. pannosa Simon (d217), whose tegulum appears to be twisted so as to expose the basal hematadocha. 6 Left palp of Ghana indet. d193. 7 Epigynum of Ghana indet. d196, with two anteriolateral epigynal pockets.
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.