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135 results for “Mygalomorph”

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zenodo40/100

Fig. 5 in A Revision Of The Mygalomorph Spider Genus Monodontium Kulczynski (Barychelidae: Araneae)

Fig. 5. Monodontium bukittimah, new species, holotype male: A, spinnerets, showing apical segment of PLS; B, tibia and metatarsus I, prolateral view; C, D, palp, distal tibia, tarsus and bulb, retrolateral view (C), prolateral view (D); E, palpal tibia, dorsal view; F, sternum, maxillae, labium and chelicerae; G, cephalothorax, dorsal view; H, tarsus; I, lateral view. Scale bars = 0.5 mm for F, G; 1 mm for rest.

opencc-by-4.0Feb 2008View details →
zenodo40/100

Fig. 2 in A Revision Of The Mygalomorph Spider Genus Monodontium Kulczynski (Barychelidae: Araneae)

Fig. 2. Monodontium mutabile Kulczynski, holotype female, A–E: A, cephalothorax and abdomen, dorsal view; B, eyes, dorsal view; C, abdomen, ventral view; D, sternum, maxillae, labium and chelicerae; E, spermathecae. F, Monodontium tetrathela Kulczynski, spermathecae. Scale bars = 1 mm for A, C; 0.5 mm for B, D.

opencc-by-4.0Feb 2008View details →
zenodo40/100

Fig. 3 in A Revision Of The Mygalomorph Spider Genus Monodontium Kulczynski (Barychelidae: Araneae)

Fig. 3. Monodontium tetrathela Kulczynski, holotype female, photomicrographs: A, cephalothorax and abdomen, dorsal view; B, eyes, dorsal view; C, spinnerets, showing PMS; D, sternum, maxillae, labium and chelicerae. Scale bar = 1 mm.

opencc-by-4.0Feb 2008View details →
dryad36/100

Data from: Ring species dynamics in California mygalomorph spiders (Nemesiidae, Calisoga)

<p>Idealized ring species, with approximately continuous gene flow around a geographic barrier but singular reproductive isolation at a ring terminus, are rare in nature. A broken ring species model preserves the geographic setting and fundamental features of an idealized model but accommodates varying degrees of gene flow restriction over complex landscapes through evolutionary time. Here we examine broken ring species dynamics in <em>Calisoga </em>spiders, which like classic Ensatina salamanders, are distributed around the Central Valley of California. Using nuclear and mitogenomic data we test key predictions of common ancestry, ring-like biogeography, biogeographic timing, population connectivity and terminal overlap. We show that a ring complex of populations shares a single common ancestor, and from an ancestral area in the Sierra Nevada mountains, two distributional and phylogenomic arms encircle the Central Valley. Isolation by distance occurs along these distributional arms, although gene flow restriction is also evident. Where divergent lineages meet in the South Coast Ranges we find rare lineage sympatry, without evidence for nuclear gene flow, and with clear evidence for morphological and ecological divergence. We discuss general insights provided by broken ring species, and how such a model could be explored and extended in other systems and future studies.</p>

opencc-zeroMar 2024View details →
zenodo36/100

Fig. 12 in Description and Sexual Behavior of Two New Species of Mygalomorph Spiders (Araneae: Theraphosidae, Pycnothelidae), and First Record of (Pycnothelidae) of Corrientes, Argentina.

Fig. 12. Distribution map of Xenonemesia platensis.

opencc-by-4.0Nov 2022View details →
zenodo36/100

Fig. 10 in Description and Sexual Behavior of Two New Species of Mygalomorph Spiders (Araneae: Theraphosidae, Pycnothelidae), and First Record of (Pycnothelidae) of Corrientes, Argentina.

Fig. 10. Distribution map of the known species of Catumiri in Argentina.

opencc-by-4.0Nov 2022View details →
zenodo36/100

Fig. 1 in A Revision Of The Mygalomorph Spider Genus Monodontium Kulczynski (Barychelidae: Araneae)

Fig. 1. Occurrence of Monodontium.

opencc-by-4.0Feb 2008View details →
dryad36/100

Mygalomorph spiders: Discrete data matrix of burrow construction behavior and somatic morphology

<p>Mygalomorph spiders (trapdoor spiders and their kin) have long been associated with high levels of homoplasy, and many convergent features can be intuitively associated with different behavioral niches. This dataset includes two discrete behavioral characters and 55 somatic morphological characters (scored from adult females), for 110 genera of mygalomorph spiders, along with a complete reference list and exemplar list used when constructing the dataset. This dataset was used to reconstruct the evolution of burrowing behavior in the Mygalomorphae, compare the influence of behavior and evolutionary history on somatic morphology, and test hypotheses of correlated evolution between specific morphological features and behavior. The results revealed the simplicity of the mygalomorph adaptive landscape, with opportunistic, web-building taxa at one end, and burrowing/nesting taxa with structurally-modified burrow entrances (e.g., a trapdoor) at the other. Shifts in behavioral niche, in both directions, are common across the evolutionary history of the Mygalomorphae, and several major clades include taxa inhabiting both behavioral extremes. Somatic morphology is heavily influenced by behavior, with taxa inhabiting the same behavioral niche often more similar morphologically than more closely-related but behaviorally-divergent taxa.</p>

opencc-zeroNov 2022View details →
dryad36/100

Mygalomorph spiders: Discrete data matrix of burrow construction behavior and somatic morphology

Open the record for dataset details and reuse information.

publicDec 2022View details →
dryad36/100

Data from: Ring species dynamics in California mygalomorph spiders (Nemesiidae, Calisoga)

Open the record for dataset details and reuse information.

publicMar 2024View details →
zenodo32/100

FIGURE 12 in Records and redescription of a mygalomorph spider genus ignored for over 100 years with a new species: the genus Atmetochilus Simon, 1887 (Araneae Nemesiidae) in Thailand

FIGURE 12. Atmetochilus, type localities of A. songsangchotei sp. nov., A. fossor, A. atriceps, A. A. lehtineni, B. A. sumatranus and C. A. koponeni. (Scale bar = 200 km), modified from Zonstein and Marusik, 2016.

opennotspecifiedJul 2020View details →
zenodo32/100

FIGURE 11 A–D in Records and redescription of a mygalomorph spider genus ignored for over 100 years with a new species: the genus Atmetochilus Simon, 1887 (Araneae Nemesiidae) in Thailand

FIGURE 11 A–D. Atmetochilus, spermathecae: A. A. fossor neotype; B. A. atriceps; C. A. songsangchotei sp. nov. paratype (ARA-2017-117).

opennotspecifiedJul 2020View details →
zenodo32/100

FIGURE 9 A–L in Records and redescription of a mygalomorph spider genus ignored for over 100 years with a new species: the genus Atmetochilus Simon, 1887 (Araneae Nemesiidae) in Thailand

FIGURE 9 A–L. Atmetochilus, prolateral views of patella and femur of palp, legs I and II; A–C. A. songsangchotei sp. nov. male holotype (ARA-2017-116); D–F. A. songsangchotei sp. nov. female paratype (ARA-2017-117); G–I. A. fossor female neotype (ARA-2018-132); J–L. A. atriceps female (ARA-2018-173).

opennotspecifiedJul 2020View details →
zenodo32/100

FIGURE 10 A–F. Atmetochilus, metatarsi I and II, ventral view. A–B in Records and redescription of a mygalomorph spider genus ignored for over 100 years with a new species: the genus Atmetochilus Simon, 1887 (Araneae Nemesiidae) in Thailand

FIGURE 10 A–F. Atmetochilus, metatarsi I and II, ventral view. A–B of A. songsangchotei sp. nov., female paratype (ARA2017-117); C–D. A. fossor female neotype (ARA-2018-132); E–F. A. atriceps female (ARA-2018-173).

opennotspecifiedJul 2020View details →
zenodo32/100

FIGURE 2 A–C in Records and redescription of a mygalomorph spider genus ignored for over 100 years with a new species: the genus Atmetochilus Simon, 1887 (Araneae Nemesiidae) in Thailand

FIGURE 2 A–C. Collecting sites and Atmetochilus habitats; A. A. songsangchotei—Phra Thaen Dong Rang Forest Park; B. A. fossor—Roadside hill, Dawei. 4/5/2018; C. A. atriceps Roadside hill, Tenasserim mountain range, 2/5/2018.

opennotspecifiedJul 2020View details →
zenodo32/100

FIGURE 3 A–D in Records and redescription of a mygalomorph spider genus ignored for over 100 years with a new species: the genus Atmetochilus Simon, 1887 (Araneae Nemesiidae) in Thailand

FIGURE 3 A–D. Atmetochilus songsangchotei sp. nov. male holotype (ARA-2017-116) habitus; A (left). dorsal habitus, A (right). ventral habitus; B. Carapace; C. Eye tubercle; D. Maxillae &amp; labium.

opennotspecifiedJul 2020View details →
zenodo32/100

FIGURE 7 A–D in Records and redescription of a mygalomorph spider genus ignored for over 100 years with a new species: the genus Atmetochilus Simon, 1887 (Araneae Nemesiidae) in Thailand

FIGURE 7 A–D. Atmetochilus atriceps female lectotype (NHMUK 1895.9.21.16). A. Habitus; A dorsal (left), ventral (right); B. Carapace; C. Eye tubercle; D. Maxillae &amp; labium.

opennotspecifiedJul 2020View details →
zenodo32/100

FIGURE 8 A–D in Records and redescription of a mygalomorph spider genus ignored for over 100 years with a new species: the genus Atmetochilus Simon, 1887 (Araneae Nemesiidae) in Thailand

FIGURE 8 A–D. Atmetochilus atriceps female (ARA-2018-173). A. Habitus; A dorsal (left), ventral (right); B. Carapace; C. Eye tubercle; D. Maxillae &amp; labium.

opennotspecifiedJul 2020View details →
zenodo32/100

FIGURE 1 A–F. Atmetochilus and Damarchus bifidus. Sternum. A in Records and redescription of a mygalomorph spider genus ignored for over 100 years with a new species: the genus Atmetochilus Simon, 1887 (Araneae Nemesiidae) in Thailand

FIGURE 1 A–F. Atmetochilus and Damarchus bifidus. Sternum. A. Atmetochilus songsangchotei sp. nov. male holotype (ARA2017-116); B. A. songsangchotei sp. nov. female paratype (ARA-2017-117); C. A. fossor female neotype (ARA-2018-132); D. A. atriceps female (ARA-2018-173); E. A. atriceps female lectotype; F. Damarchus bifidus type specimen.

opennotspecifiedJul 2020View details →
zenodo32/100

FIGURE 5 A–D in Records and redescription of a mygalomorph spider genus ignored for over 100 years with a new species: the genus Atmetochilus Simon, 1887 (Araneae Nemesiidae) in Thailand

FIGURE 5 A–D. Atmetochilus songsangchotei sp. nov. female paratype (ARA-2017-117) habitus; A (left) dorsal habitus, A (right) ventral habitus; B. Carapace; C. Eye tubercle; D. Maxillae &amp; labium.

opennotspecifiedJul 2020View details →

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