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Figure 16 in The phylogenetic relationships of Chalcosiinae (Lepidoptera, Zygaenoidea, Zygaenidae)
Figure 16. Chaetosemata of different zygaenid subfamilies. A, E, F, Aglaope infausta. B, Cyclosia midama. C, Agalope trimacula. D, Adscita statices. G, Elcysma westwoodi. H, Histia flabellicornis ultima. Chalcosiinae: A–C, G–H; Procridinae: D.
Figure 11 in The phylogenetic relationships of Chalcosiinae (Lepidoptera, Zygaenoidea, Zygaenidae)
Figure 11. Characters of frontoclypeus, vertex and prothorax. A, Cyclosia midama. B, Cadphises sp. cf. moorei. C, Campylotes histrionicus taliensis. D, Phlebohecta fuscescens. E, Eterusia vitessa. F, Aglaope infausta. G, Agalope harutai. H, Elcysma dohertyi. I, Amesia aliris.
Figure 20 in The phylogenetic relationships of Chalcosiinae (Lepidoptera, Zygaenoidea, Zygaenidae)
Figure 20. Wing venation of Chalcosiinae. A, Chalcophaedra zuleika. B, Pseudoscaptesyle bicolor. C, Barbaroscia amabilis. D, Psaphis euschemoides. E, Clematoessa virgata. F, Chalcosia zehma, male. G, Ditto, female.
Figure 1 in The phylogenetic relationships of Chalcosiinae (Lepidoptera, Zygaenoidea, Zygaenidae)
Figure 1. Schematic classifications and phylogenetic concepts of Zygaenoidea and Zygaenidae proposed by different authors. In each of the hypotheses, members of Zygaenidae are in bold and non-zygaenoid groups are in italic. A, Alberti (1954). B, Minet (1986, 1991, 1994). C, Common (1970) and Nielsen & Common (1991). D, Scoble (1992). E, Epstein (1996). F, Heppner (1998). G, Fänger et al. (1999). H, Epstein et al. (1999). I, Holloway et al. (2001).
Figure 6 in The phylogenetic relationships of Chalcosiinae (Lepidoptera, Zygaenoidea, Zygaenidae)
Figure 6. In the Zygaenidae biosynthesis of the cyanoglucosides linamarin and lotaustralin begins with the universally available amino acids valine and isoleucine, respectively. The cyanoglucosides found in the tissues of most developmental stages of the Zygaenidae are derived from a de novo biosynthesis. Only a relatively small proportion of cyanoglucosides may be plant-derived in species living on cyanogenic hostplants, usually species of Fabaceae (after Witthohn & Naumann, 1987a).
Figure 5 in The phylogenetic relationships of Chalcosiinae (Lepidoptera, Zygaenoidea, Zygaenidae)
Figure 5. The two chemically related cyanoglucosides linamarin and lotaustralin are found in comparatively high concentrations in zygaenid moths and form the chemical basis for the evolution of the aposematic and mimicry patterns of this family. The release of hydrocyanic acid (hcn) by chemical decomposition of linamarin or lotaustralin depends on the presence of highly specialized glucosidases and is also ph–dependent (after Naumann et al., 1999).
Figure 14. Antennae. A, Agalope trimacula. B, Rhodopsona rutila. C, D, Eterusia aedea formosana. E, Cyclosia midama. F, Heteropan scintillans. G, H, Callizygaena glacon. I, Adscita statices. J, Inouela formosensis. K, Zygaena filipendulae. L, Phauda mimica. M, N, Lactura dives. O, Anomoeotis levis. P, Himantopteus fuscinervis. Q, R in The phylogenetic relationships of Chalcosiinae (Lepidoptera, Zygaenoidea, Zygaenidae)
Figure 14. Antennae. A, Agalope trimacula. B, Rhodopsona rutila. C, D, Eterusia aedea formosana. E, Cyclosia midama. F, Heteropan scintillans. G, H, Callizygaena glacon. I, Adscita statices. J, Inouela formosensis. K, Zygaena filipendulae. L, Phauda mimica. M, N, Lactura dives. O, Anomoeotis levis. P, Himantopteus fuscinervis. Q, R, Chalcosiopsis variata.
Figure 12 in The phylogenetic relationships of Chalcosiinae (Lepidoptera, Zygaenoidea, Zygaenidae)
Figure 12. Stylized drawings of selected characters of adult head. See Appendixes 2 and 3 for character descriptions and their distributions. A–E, frontal view. F–I, dorsal view. J–M, lateral view. N–P, labial palpus. Q–V, dorsal view of chaetosemata. W–Z-5, mandibular lobes.
Figure 9 in The phylogenetic relationships of Chalcosiinae (Lepidoptera, Zygaenoidea, Zygaenidae)
Figure 9. Ingroup (part) and outgroups. From top to bottom, left to right. Row I: (Ingroup) Chalcosiopsis variata, Heteropan sp. (left), Heteropan appendiculata (right), Inouela sp., Doclea syntomoides, (outgroups from here) Callizygaena ada (Callizygaeninae). Row II: Artona gracilis, Clelea formosana, Theresimima ampellophaga (Procridinae), Dianeura jacksoni (Anomoeotidae). Row III: Himantopterus fuscinervis (Himatopteridae), Janseola titaea (placed in Heterogynidae by Scoble, 1992), Burlacena sp. (Zygaenidae, subfamily unassigned), Saliunca sp. (Procridinae). Row IV: Harrisina sp., Pollanisus viridipulverulenta, Adscita statices, Illiberis pruni (Procridinae), Staphylinochrous sp. (Anomoeotidae). Row V: Pryeria sinica, Zygaena fausta (Zygaeninae), Heterogynis sp. (Heterogynidae), Lactura dives (Lacturidae), Phauda sp. (Phaudinae).
Figure 4 in The phylogenetic relationships of Chalcosiinae (Lepidoptera, Zygaenoidea, Zygaenidae)
Figure 4. Distribution of some zygaenid subfamilies: Chalcosiinae s.l. (dark green), Callizygaeninae (light green) and Zygaeninae (yellow).
Figure 19 in The phylogenetic relationships of Chalcosiinae (Lepidoptera, Zygaenoidea, Zygaenidae)
Figure 19. Wing venation of Chalcosiinae. A, Cyclosia pagenstecheri. B, Corma maculata. C, Corma zenotia. D, Docleomorpha boholica. E, Neoherpa nevosa. F, Aglaope infausta. G, Agalope trimacula. H, I, Agalope immaculata (I shows variation of R veins).
Figure 17 in The phylogenetic relationships of Chalcosiinae (Lepidoptera, Zygaenoidea, Zygaenidae)
Figure 17. Stylized drawings of selected characters of adult thorax. A, generalized diagram of prothorax and mesothorax. B, tegula and subtegula. C, D, dorsal view of pronotum. E–O, various combinations of patagia and parapatagia.
Figure 8 in The phylogenetic relationships of Chalcosiinae (Lepidoptera, Zygaenoidea, Zygaenidae)
Figure 8. Zonation (right), wing maculation and wing areas (left) defined for morphological analysis of wing patterns of Chalcosiinae.
Figure 13 in The phylogenetic relationships of Chalcosiinae (Lepidoptera, Zygaenoidea, Zygaenidae)
Figure 13. Heads of adults. A, Soritia strandi. B, Agalope trimacula. C, Inouela formosensis. D, Heteropan sp. E, Chalcosiopsis variata. F, Lactura dives. G, Erasmia pulchella hobisoni. H, Aglaope infausta. Abbreviations: atp, anterior tentorial pit; clsm, chaetosemata; fc, frontoclypeus; gl, galea; lbm, labrum; lp, labial palpus; md, mandible; sgp, subgenal process.
Figure 19. Phylogenetic relationship between basal mesotheriids. A in Late Oligocene mesotheriids (Mammalia, Notoungulata) from Salla and Lacayani (Bolivia): implications for basal mesotheriid phylogeny and distribution
Figure 19. Phylogenetic relationship between basal mesotheriids. A, strict consensus (26 steps, CI = 0.731, RI = 0.731; Bremer indices: Mesotheriidae = 2, Mesotheriinae = 1). B, majority-rule consensus, with percentages of nodes with less than 100% indicated (21 steps, CI = 0.905, RI = 0.923). C, Adams consensus (23 steps, CI = 0.826, RI = 0.846).
Figure 10 in Morphology and phylogenetic relationships of a new eschrichtiid genus (Cetacea: Mysticeti) from the Early Pliocene of northern Italy
Figure 10. Phylogenetic relationships of Eschrichtioides gastaldii gen. nov., comb. nov.. Strict consensus tree from nine equally most-parsimonious trees. Tree statistics: tree length, 503 steps; Consistency Index (CI), 0.5447; Retention Index (RI), 0.8115; Homoplasy Index (HI), 0.4553; Rescaled CI, 0.4421.
Figure 9 in Morphology and phylogenetic relationships of a new eschrichtiid genus (Cetacea: Mysticeti) from the Early Pliocene of northern Italy
Figure 9. Eschrichtioides gastaldii gen. nov., comb. nov.: forelimb (redrawn from Portis, 1885). A, lateral and medial views of humerus. B, lateral and medial views of ulna (lateral view). Scale bar = 100 mm. Horizontal lines indicate shark bite marks discussed by Bianucci et al. (2002).
Figure 7 in Morphology and phylogenetic relationships of a new eschrichtiid genus (Cetacea: Mysticeti) from the Early Pliocene of northern Italy
Figure 7. Eschrichtioides gastaldii gen. nov., comb. nov.: cross-sections of dentary. Selected cross-sections of the left dentary. Numbers over the sections are mm from the anterior end of the dentary. Scale bar = 100 mm. Explanation of abbreviations: a, coronoid process; b, groove between coronoid and satellite process; c, satellite process; mdf, mandibular foramen; *, groove for mental ligament. Broken line indicates missing portion of dentary.
Figure 6 in Morphology and phylogenetic relationships of a new eschrichtiid genus (Cetacea: Mysticeti) from the Early Pliocene of northern Italy
Figure 6. Eschrichtioides gastaldii gen. nov., comb. nov.. A, left dentary, medial view. B, left dentary, lateral view. C, right dentary, dorsal view. D, close-up of the left dentary showing the condyle and coronoid region in medial view. Scale bar = 15 cm in A, B and C, and 5 cm in D.
Figure 8 in Morphology and phylogenetic relationships of a new eschrichtiid genus (Cetacea: Mysticeti) from the Early Pliocene of northern Italy
Figure 8. Eschrichtioides gastaldii gen. nov., comb. nov.: postcrania. A, atlas (rostral view). B, axis (caudal view). C, lumbar vertebra (rostral view). D, caudal vertebra (lateral view). E, ribs of the right side (note double-headed rib shown by arrowhead). Scale bars = 100 mm.
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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)
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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.