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435 results for “myrmecophilous”

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Figure 7 in Homoplasy and morphological stasis revealed through multilocus phylogeny of new myrmecophilous species in Armadillidiidae (Isopoda: Oniscidea)

Figure 7. Scanning electron photomicrographs showing details of the telson of Iberiarmadillidium psammophilum (A), Iberiarmadillidium pinicola (B), Iberiarmadillidium sakura (C), Cristarmadillidium myrmecophilum (D) and Cristarmadillidium breuili (E).

opennotspecifiedDec 2021View details →
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Figure 6 in Homoplasy and morphological stasis revealed through multilocus phylogeny of new myrmecophilous species in Armadillidiidae (Isopoda: Oniscidea)

Figure 6. Scanning electron photomicrographs showing details of pereonite 1 and 2 epimera of Iberiarmadillidium psammophilum (A), Iberiarmadillidium pinicola (B), Iberiarmadillidium sakura (C), Cristarmadillidium myrmecophilum (D) and Cristarmadillidium muricatum (E) (only epimera 1 is shown).

opennotspecifiedDec 2021View details →
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Figure 3 in Homoplasy and morphological stasis revealed through multilocus phylogeny of new myrmecophilous species in Armadillidiidae (Isopoda: Oniscidea)

Figure 3. *BEAST chronogram of Armadillidiidae. Bars represent, highest posterior densities (95% HPD), and are shown only in highly supported nodes (posterior probabilities values ≥ 0.95).

opennotspecifiedDec 2021View details →
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Figure 4 in Homoplasy and morphological stasis revealed through multilocus phylogeny of new myrmecophilous species in Armadillidiidae (Isopoda: Oniscidea)

Figure 4. Ancestral state reconstruction for the following characters: A, myrmecophily; B, schisma on pereon 1 epimera; and C, head morphology type. Reconstructions are shown on the species tree based on the multispecies coalescent implemented in *BEAST; highly supported nodes (posterior probabilities values ≥ 0.95) are marked with an asterisk.

opennotspecifiedDec 2021View details →
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Figure 5 in Homoplasy and morphological stasis revealed through multilocus phylogeny of new myrmecophilous species in Armadillidiidae (Isopoda: Oniscidea)

Figure 5. Scanning electron photomicrographs showing the general habitus of Iberiarmadillidium psammophilum (A), Iberiarmadillidium pinicola (B), Iberiarmadillidium sakura (C), Cristarmadillidium myrmecophilum (D) and Cristarmadillidium muricatum (E).

opennotspecifiedDec 2021View details →
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Figure 2 in Homoplasy and morphological stasis revealed through multilocus phylogeny of new myrmecophilous species in Armadillidiidae (Isopoda: Oniscidea)

Figure 2. Multilocus Bayesian phylogenetic reconstruction of Armadillidiidae, based on the full dataset and including the new taxa. Numbers at nodes correspond to posterior probabilities/maximum likelihood bootstrap values (values <0.7/50 are not shown). Symbols match those in Figure 1.

opennotspecifiedDec 2021View details →
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Figure 1 in Homoplasy and morphological stasis revealed through multilocus phylogeny of new myrmecophilous species in Armadillidiidae (Isopoda: Oniscidea)

Figure 1. Map showing the sampling localities of Iberiarmadillidium pinicola (black stars), I. psammophilum (purple stars), I. sakura (white star), Cristarmadillidium breuili (black circle), Cristarmadillidium muricatum (red circles) and C. myrmecophilum (yellow circles). Habitus in vivo: A, I. pinicola from Valdemaqueda, Madrid; B, I. psammophilum from El Pardo, Madrid; C, C. myrmecophilum from Casas de Don Antonio, Cáceres; D, C. muricatum from Punta de Benimaquia Cave, Alicante; and E, C. breuili from Bolumini Cave, Alicante.

opennotspecifiedDec 2021View details →
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FIGURES 1–5 in A new myrmecophilous genus of Falagriini from Colorado, USA (Coleoptera: Staphylinidae: Aleocharinae)

FIGURES 1–5. (1) Habitus of Myrmecoagria hoebekei, male holotype. (2) Head and pronotum of Myrmecoagria hoebekei, male holotype. (3) Paratype labels, female. (4) Holotype labels, male. (5) Habitus of host pinned with paratype female.

opennotspecifiedJul 2022View details →
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FIGURE 18 in A new myrmecophilous genus of Falagriini from Colorado, USA (Coleoptera: Staphylinidae: Aleocharinae)

FIGURE 18. Reanalysis of a modified Ahn & Ashe (1995) dataset with bootstrap values. Circles are unambiguous changes; closed circles are unique changes; numbers above circles are character numbers and below are state changes along the branch. Colored branches represent reconstruction of marine and myrmecophilous ecologies.

opennotspecifiedJul 2022View details →
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FIGURES 11–14 in A new myrmecophilous genus of Falagriini from Colorado, USA (Coleoptera: Staphylinidae: Aleocharinae)

FIGURES 11–14. (11) Female tergite VIII, paratype. (12) Female sternite VIII, paratype. (13) Male tergite VIII, holotype. (14) Male sternite VIII, holotype.

opennotspecifiedJul 2022View details →
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FIGURES 7–8 in A new myrmecophilous genus of Falagriini from Colorado, USA (Coleoptera: Staphylinidae: Aleocharinae)

FIGURES 7–8. (7) Right mandible, dorsal, paratype female. (8) Right maxilla, ventral, paratype female.

opennotspecifiedJul 2022View details →
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Fig. 37. A in Faunistic survey of myrmecophilous and other ant-associated beetles and spiders in the Belgian province of Limburg (Araneae, Coleoptera, Hymenoptera: Formicidae)

Fig. 37. A, Nalassus laevioctostriatus (Goeze, 1777) (9.9 mm; range 7.0-11.0 mm). B, Pentaphyllus testaceus (Hellwig, 1792) (2.0 mm; range 1.5-2.0 mm). C, Scaphidema metallicum (Fabricius, 1793) (5.0 mm; range 4.0- 5.0 mm). © U. Schmidt.

opennotspecifiedOct 2023View details →
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Fig. 34. A in Faunistic survey of myrmecophilous and other ant-associated beetles and spiders in the Belgian province of Limburg (Araneae, Coleoptera, Hymenoptera: Formicidae)

Fig. 34. A, Cephennium gallicum Ganglbauer, 1899 (range 1.3-1.5 mm). © U. Schmidt. B, Neuraphes elongatulus (P.J.W. MÜller & Kunze, 1822) (range 1.4-1.5 mm). © U. Schmidt. C, Scydmaenus perrisi (Reitter, 1879) (1.8 mm), © Ignace David. D, Stenichnus godarti (Latreille, 1806) (1.7 mm), © Ignace David.

opennotspecifiedOct 2023View details →
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Fig. 36. A in Faunistic survey of myrmecophilous and other ant-associated beetles and spiders in the Belgian province of Limburg (Araneae, Coleoptera, Hymenoptera: Formicidae)

Fig. 36. A, Sepedophilus testaceus (Fabricius, 1793) (range 3.5-5.0 mm). B, Tachyporus hypnorum (Fabricius, (1775) (3.8 mm; range 3.1-4.0 mm). © U. Schmidt.

opennotspecifiedOct 2023View details →
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Fig. 32. A in Faunistic survey of myrmecophilous and other ant-associated beetles and spiders in the Belgian province of Limburg (Araneae, Coleoptera, Hymenoptera: Formicidae)

Fig. 32. A, Batrisodes venustus (Reichenbach, 1816) (2.0 mm; range 2.0-2.2 mm). B, Bibloporus bicolor (Denny, 1825) (1.2 mm; range 1.2-1.4 mm). C, Bryaxis curtisii (Leach, 1817) (range 1.45-1.65 mm). D, Trichonyx sulcicollis (Reichenbach, 1816) (2.9 mm; range 2.5-3.0 mm). © U. Schmidt.

opennotspecifiedOct 2023View details →
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Fig. 39 in Faunistic survey of myrmecophilous and other ant-associated beetles and spiders in the Belgian province of Limburg (Araneae, Coleoptera, Hymenoptera: Formicidae)

Fig. 39. Myrmarachne formicaria (De Geer, 1778) (range 5.0-6.5 mm). Public domain https://www.inaturalist.org/ photos/76645906

opennotspecifiedOct 2023View details →
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Fig. 29. A in Faunistic survey of myrmecophilous and other ant-associated beetles and spiders in the Belgian province of Limburg (Araneae, Coleoptera, Hymenoptera: Formicidae)

Fig. 29. A, Anthobium unicolor (Marsham, 1802) (3.5 mm; range 3.0-3.5 mm). B, Coryphium angusticolle Stephens, 1834 (3.0 mm; range 2.5-3.0 mm). C, Omalium rivulare (Paykull, 1789) (3.8 mm; range 3.0-4.0 mm). D, Phloeonomus punctipennis Thomson, 1867 (1.9 mm; range 1.7-2.0 mm). E, Phyllodrepa ioptera (Stephens, 1834)) (2.6 mm; range 2.5-3.0 mm). F, Xylodromus affinis (Gerhardt, 1877) (range 3.2-3.7 mm). © U. Schmidt.

opennotspecifiedOct 2023View details →
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Fig.26. A in Faunistic survey of myrmecophilous and other ant-associated beetles and spiders in the Belgian province of Limburg (Araneae, Coleoptera, Hymenoptera: Formicidae)

Fig.26. A, Aloconota gregaria (Erichson, 1839) (range 2.7-3.8 mm). B, Euryusa optabilis Heer, 1839 (2.7 mm; range 2.5-3.0 mm). C, Leptusa pulchella (Mannerheim, 1830) (3.2 mm; range 2.7-3.2 mm). D, Lomechusa emarginata (Paykull, 1789) (4.5 mm; range 3.5-4.5 mm). E, Pella funesta (Gravenhorst, 1806) (5.2 mm; range 5.0-5.5 mm). © U. Schmidt.

opennotspecifiedOct 2023View details →
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Fig. 22. A in Faunistic survey of myrmecophilous and other ant-associated beetles and spiders in the Belgian province of Limburg (Araneae, Coleoptera, Hymenoptera: Formicidae)

Fig. 22. A, Anobium punctatum (De Geer, 1774) (range 2.5-5.0 mm). B, Priobium carpini (Herbst, 1793) (4.8 mm; range 3.0-5.0 mm). C, Ptilinus pectinicornis (Linnaeus, 1758) (3.6 mm; range 3.5-5.5 mm). D, Ptinus fur (Linnaeus, 1758) male) (3.3 mm; range 2.6-4.3 mm). E, Ptinus fur (Linnaeus, 1758) female (3.8 mm; range 2.6-4.3 mm). © U. Schmidt.

opennotspecifiedOct 2023View details →
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Fig. 21. A in Faunistic survey of myrmecophilous and other ant-associated beetles and spiders in the Belgian province of Limburg (Araneae, Coleoptera, Hymenoptera: Formicidae)

Fig. 21. A, Acrotrichis intermedia (Gillmeister, 1845) (range 1.0-1.1 mm). B, Pteryx suturalis (Heer, 1841) (range 0.75-0.85 mm). C, Ptilium myrmecophilum (Alibert, 1844) (range 0.6-0.65 mm). © U. Schmidt.

opennotspecifiedOct 2023View details →

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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.

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OpenNeuro

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