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FIGURES 28–31 in Rearrangements in some species groups of Amblycerus Thunberg, 1815 (Coleoptera: Chrysomelidae: Bruchinae) including keys, description of a new species, new host plant and distributional records
FIGURES 28–31. Head, group spondiae: 28. A. alternatus, 29. A. cuernavacensis, 30. A. spondiae, 31. A. vitis. Scale bars = 1.0 mm.
FIGURES 22–27 in Rearrangements in some species groups of Amblycerus Thunberg, 1815 (Coleoptera: Chrysomelidae: Bruchinae) including keys, description of a new species, new host plant and distributional records
FIGURES 22–27. Head, group dispar: 22. Amblycerus crassipunctatus, 23. A. dispar, 24. A. insuturatus, 25. A. schwarzi, 26. A. taeniopygus, 27. Amblycerus goianiensis Santos & Ribeiro-Costa, sp. n. Scale bars = 1.0 mm.
FIGURES 19–21 in Rearrangements in some species groups of Amblycerus Thunberg, 1815 (Coleoptera: Chrysomelidae: Bruchinae) including keys, description of a new species, new host plant and distributional records
FIGURES 19–21. Species reallocated: 19. A. eustrophoides, 20. A. serieguttatus, 21. A. simulator. Scale bars = 1.0 mm.
FIGURES 9–14 in Rearrangements in some species groups of Amblycerus Thunberg, 1815 (Coleoptera: Chrysomelidae: Bruchinae) including keys, description of a new species, new host plant and distributional records
FIGURES 9–14. Dorsal, group dispar: 9. Amblycerus crassipunctatus, 10. A. dispar, 11. A. insuturatus, 12. A. schwarzi, 13. A. taeniopygus and 14. Amblycerus goianiensis Santos & Ribeiro-Costa, sp. n. Scale bars = 1.0 mm.
FIGURES 1–8 in Rearrangements in some species groups of Amblycerus Thunberg, 1815 (Coleoptera: Chrysomelidae: Bruchinae) including keys, description of a new species, new host plant and distributional records
FIGURES 1–8. Amblycerus dispar: 1. dorsal; 2. scutellum. A. taeniopygus: 3. head, A. insuturatus: 4. lateral. A. alternatus: 5. detail of coarse punctures on median region of pronotum; 6. detail of coarse punctures on median region of pygidium. A. crassipunctatus: 7–8. Male genitalia: 7. Median lobe; 8. Tegmen. Scale bars = 1.0 mm (Figs 5, 7, 8) and 0.25 mm (Fig. 12).
FIGURES 117–118. FIGURE 117 in Rearrangements in some species groups of Amblycerus Thunberg, 1815 (Coleoptera: Chrysomelidae: Bruchinae) including keys, description of a new species, new host plant and distributional records
FIGURES 117–118. FIGURE 117. Map with the geographical distribution of A. crassipunctatus and A. dispar. Leaked symbols refer to bibliography data. FIGURE 118. Map with the geographical distribution of A. insuturatus and A. schwarzi. Leaked symbols refer to bibliography data.
FIGURES 35–40 in Rearrangements in some species groups of Amblycerus Thunberg, 1815 (Coleoptera: Chrysomelidae: Bruchinae) including keys, description of a new species, new host plant and distributional records
FIGURES 35–40. Lateral. group dispar: 35. Amblycerus crassipunctatus, 36. A. dispar, 37. A. insuturatus, 38. A. schwarzi, 39. A. taeniopygus and 40. Amblycerus goianiensis Santos & Ribeiro-Costa, sp. n. Scale bars = 1.0 mm.
Fig. 2 in Absence of co-phylogeny indicates repeated diatom capture in dinophytes hosting a tertiary endosymbiont
Fig. 2 Polyphyletic endosymbionts of Durinskia, Galeidinium and Kryptoperidinium with closest relatives among free-ranging diatoms. Maximum likelihood (ML) tree (−ln = 14,945) of all 77 Bacillariaceae operational taxonomic units available, derived from the comparison of concatenated rRNA and plastid sequences. Highlighted endosymbiont taxa were scattered along up to ten only distantly related lineages over the Bacillariaceae phylogeny. Note that accessions of neither Durinskia nor Kryptoperidinium constituted monophyletic groups. Within such lineages, endosymbionts were usually closer related to free-ranging diatoms than to other endosymbionts (though statistical support was not always high). Some endosymbionts were phylogenetically isolated from free-living diatoms exhibiting long branches (e.g. D. kwazulunatalensis N.Yamada, Sym & T.Horig., D. oculata and G. rugatum Tam. & T.Horig.). Branch lengths are drawn to scale, with the scale bar indicating the number of nt substitutions per site. The numbers on the branches are statistical support values (ML bootstrap values, values <50 are not shown, posterior probabilities below branches, values <90 are not shown; asterisks indicate maximal support)
Fig. 1 in Absence of co-phylogeny indicates repeated diatom capture in dinophytes hosting a tertiary endosymbiont
Fig. 1 Polyphyletic endosymbionts of freshwater Unruhdinium with closest relatives among free-ranging diatoms. Maximum likelihood (ML) tree (−ln = 21,700) of all 37 Stephanodiscaceae operational taxonomic units available, derived from the comparison of concatenated rRNA and plastid sequences. Endosymbiont taxa are highlighted. Note that we did not observe any contradictory tree topologies between separated analyses of nuclear and plastid loci (not shown). Endosymbionts of Unruhdinium segregated into two distinct lineages. Four identical sequences of different U. penardii (Lemmerm.) Gottschling strains clustered together (94LBS, .98BPP) and built a well-supported (99LBS, 1.00BPP) sister group relationship with free-living Discostella nipponica (Skvortzov) A.Tuji & D.M.Williams (strain TNS:AL-5776). A second lineage (100LBS, 1.00BPP) did not include endosymbiont sequences of U. cf. kevei (G.X.Liu & Z.Y.Hu) Gottschling and U. jiulongense (H. Gu) Gottschling only, but also those of the free-living strains L435 and LO4-2. All sequences of this lineage were nearly identical. Branch lengths are drawn to scale, with the scale bar indicating the number of nt substitutions per site. The numbers on the branches are statistical support values (ML bootstrap values, values <50 are not shown, posterior probabilities below branches, values <90 are not shown; asterisks indicate maximal support)
Fig. 2 in Inferring host-cleptoparasite complexes of South American Centridine bees (Hymenoptera: Apidae) using macroecological perspectives
Fig. 2 Potential distribution of Epiclopus and Centris bees considering both MaxEnt and SVM algorithms. Full red lines represent known hostcleptoparasite relationships, while the red dashed lines represent
Fig. 4 in Inferring host-cleptoparasite complexes of South American Centridine bees (Hymenoptera: Apidae) using macroecological perspectives
Fig. 4 Multivariate space used by all host and cleptoparasite species of South American Centridine bees. The solid and the dashed lines illustrate, respectively, 100% and 50% of the available (background) climate for each considered species in its natural range. For the inset corresponding to all species, the solid line represents 10% of the occurrence density and the
Figs 15–20 in Redescription of the parasitic wasp Melittobia sosui Dahms, 1984 (Hymenoptera: Eulophidae), with records on its new hosts in Vietnam
Figs 15–20. Melittobia sosui Dahms, male: 15 — head, frontal view; 16 — mandible; 17 — antenna, ventral view; 18 — mesosoma and metasoma, dorsal view; 19 — mid leg; 20 — habitus, lateral view. Рис. 15–20. Melittobia sosui Dahms, самец: 15 — голова, вид спереди; 16 — нижнЯЯ челюсть; 17 — антенна, вид сниЗу; 18 — меЗосома и метасома, вид сверху; 19 — среднЯЯ ножка; 20 — габитус, вид сбоку.
Fig. 5 in Niche overlap and host specificity in parasitic Maculinea butterflies (Lepidoptera: Lycaenidae) as a measure for potential extinction risks under climate change
Fig. 5 Niche identity tests of Maculinea/Myrmica host associations under the A2a climate change scenario for 2080. The red arrow indicates the measured niche overlap between hosts and parasites
Fig. 3 in Niche overlap and host specificity in parasitic Maculinea butterflies (Lepidoptera: Lycaenidae) as a measure for potential extinction risks under climate change
Fig. 3 Niche identity tests of Maculinea/Myrmica host associations under current climate. The red arrow indicates the measured niche overlap between hosts and parasites derived from ENMs generated
Fig. 2 in Niche overlap and host specificity in parasitic Maculinea butterflies (Lepidoptera: Lycaenidae) as a measure for potential extinction risks under climate change
Fig. 2 Estimated potential distributions of Maculinea butterflies (light grey) and Myrmica ants (dark grey) under current climatic conditions show large geographic overlaps of the butterfly species with their respective main (red) and secondary hosts (orange)
Fig. 1 in Are copepods secondary hosts of Cycliophora?
Fig. 1 Cycliophoran life cycle stages attached to harpacticoid copepods; light micrographs. a Two Symbion sp. feeding stages (fs1–2) attached, respectively, to the metasome and the urosome of a copepod host. The anterior region of the copepod (co) is facing left. The insert figure shows a close up of the trunk of one of the feeding stages with several wrinkles (arrowheads) on the cuticle. b Undetermined cycliophoran stage (ucs) settled on the urosome of a copepod host (co). The anterior of the copepod is facing right. c Same cycliophoran life cycle stage as shown in b, but detached from the copepod host. Note the folded cuticle on its most posterior region. The insert figure shows a close up of the attachment disk that characterizes the most anterior region of this cycliophoran stage. an antennule, as anal somite, ce cephalothorax, cr caudal rami, ds double-somite, ey eye, pc posterior folded cuticle, sl swimming legs
Fig. 3 Parasyllidea humesi Pettibone 1961. Relationships between width and length. a in The symbiotic hesionid Parasyllidea humesi Pettibone, 1961 (Annelida: Polychaeta) hosted by Scrobicularia plana (da Costa, 1778) (Mollusca: Bivalvia: Semelidade) in European waters
Fig. 3 Parasyllidea humesi Pettibone 1961. Relationships between width and length. a Length in mm. b Length as number of setigers
Fig. 8 in High species diversity of fish tapeworms in congeneric hosts in Africa: revision of Monobothrioides (Cestoda: Caryophyllidea), including description of two new species and molecular phylogeny
Fig. 8 Scanning electron micrographs of Monobothrioides species. a, b M. cunningtoni Fuhrmann and Baer, 1925 (type species) from Auchenoglanis occidentalis, Democratic Republic of the Congo; c, d M. chalmersius (Woodland, 1924) from Clarias sp., Sudan; e–h M.
Fig. 7 Monobothrioides zuheiri n in High species diversity of fish tapeworms in congeneric hosts in Africa: revision of Monobothrioides (Cestoda: Caryophyllidea), including description of two new species and molecular phylogeny
Fig. 7 Monobothrioides zuheiri n. sp. from Auchenoglanis occidentalis, White Nile at Kostí, Sudan. a total view, ventrally; b, c anterior end with first testes and vitelline follicles; d region of gonopores, laterally; e posterior part, ventrally; note posterior extent of vitelline follicles reaching ovary; f scolex; g cross section at testicular level; note tightly packed testes in two layers and longitudinal musculature formed by separated muscle fibres
Fig. 4 Monobothrioides tchadensis Troncy, 1978 in High species diversity of fish tapeworms in congeneric hosts in Africa: revision of Monobothrioides (Cestoda: Caryophyllidea), including description of two new species and molecular phylogeny
Fig. 4 Monobothrioides tchadensis Troncy, 1978 from Auchenoglanis occidentalis, Lower Congo River at Bulu, Democratic Repulic of the Congo. a Total view, ventrally; b, e anterior end with first testes and vitelline follicles; c scolex; d posteriod end, ventrally; note large, elongate cirrus-sac; f cross section at testicular level; note outer and inner longitudinal musculature formed by isolated muscle fibres
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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.