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Appendix List of samples of deep frozen frog legs with purchase date, collection number, haplotype number, taxonomic identification, tibia length (TL) and estimated snout vent length (SVL). in Which frog's legs do froggies eat? The use of DNA barcoding for identification of deep frozen frog legs (Dicroglossidae, Amphibia) commercialized in France
Appendix List of samples of deep frozen frog legs with purchase date, collection number, haplotype number, taxonomic identification, tibia length (TL) and estimated snout vent length (SVL).
Fig. 8 in An assessment of the taxonomic status of the Mediterranean endemic genus Acrodiscus Zanardini (Halymeniales, Rhodophyta)
Fig. 8. ML phylogram inferred from the combined LSU-rbcL data by PhyML. Supports at nodes indicate bootstrap values (from PhyML and RaxML) and posterior probabilities inferred from Bayesian analysis. Generitype species are indicated in bold; concatenate sequences obtained from different samples for LSU and rbcL are indicated by "*".
Fig. 2. Analine-blue stained vegetative features. A. A in An assessment of the taxonomic status of the Mediterranean endemic genus Acrodiscus Zanardini (Halymeniales, Rhodophyta)
Fig. 2. Analine-blue stained vegetative features. A. A transapical longitudinal section indicative of its multiaxial structure. B. The anticlinal orientation of pseudo-dichotomous cortical filaments. C. Mostly paired cortical cells in surface view. D. Longitudinally aligned, peripherally inverwoven medullary filaments. Scale bars: A, D = 20 μm; B–C = 10 μm.
Fig. 1. A–B in An assessment of the taxonomic status of the Mediterranean endemic genus Acrodiscus Zanardini (Halymeniales, Rhodophyta)
Fig. 1. A–B. Herbarium sheets MS35027-1 and MS35027-14, respectively, both from Sicily. C–D. Herbarium sheets PC0152091 (LLG0393) and PC0152089 (LLG0394), respectively, both from Vis Island, Croatia. Scale bars: A–B = 2 cm; C–D = 1 cm.
Fig. 5. A in An assessment of the taxonomic status of the Mediterranean endemic genus Acrodiscus Zanardini (Halymeniales, Rhodophyta)
Fig. 5. A. Detail of front page of Meneghini's 1841 manuscript "Alghe Dalmate, Enumerate ed Illustrate dal Professor Giuseppe Meneghini". B. Detail of protologue page of Chondrus? vidovichii (Menegh.) Zanardini.
Fig. 4 in An assessment of the taxonomic status of the Mediterranean endemic genus Acrodiscus Zanardini (Halymeniales, Rhodophyta)
Fig. 4. Recorded sites of Acrodiscus vidovichii (Menegh.) Zanardini along the shores of the Mediterranean Sea.
Fig. 6 in An assessment of the taxonomic status of the Mediterranean endemic genus Acrodiscus Zanardini (Halymeniales, Rhodophyta)
Fig. 6. Plate and caption of Chondrus? vidovichii (Menegh.) Zanardini from Meneghini's manuscript "Alghe Dalmate, Enumerate ed Illustrate dal Professor Giuseppe Meneghini".
Fig. 7 in An assessment of the taxonomic status of the Mediterranean endemic genus Acrodiscus Zanardini (Halymeniales, Rhodophyta)
Fig. 7. Two fragments (B–C, arrows) of the specimen (A) of Chondrus? vidovichii (Menegh.) Zanardini illustrated in Meneghini's protologue manuscript. The sheets are currently filed in folder 742.4, labelled "Euhymenia dichotoma Kg." at the Herbarium Orti Botanici Pisani (PI). Scale bars = 1 cm.
Fig. 3. A in An assessment of the taxonomic status of the Mediterranean endemic genus Acrodiscus Zanardini (Halymeniales, Rhodophyta)
Fig. 3. A. Elliptical outline of a subapical nemathecial sorus. B. Lugol-stained l.s. of a tetrasporangial nemathecium. C. Schematic drawing of terminal tetrasporangia and jacketing nemathecial filaments. D. Horizontally aligned cruciate and decussate-cruciate tetrasporangia within the palisade of nemathecial filaments. Scale bars: A = 200 μm; B, D = 20 μm.
Fig. 46. A in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 46. A. Canthon cobosi (Pereira & Martínez, 1960) stat. et comb. nov., holotype. B–C. Canthon machadoi (Martínez & Pereira, 1967) comb. nov. B. Paratype 2. C. Paratype 4.
Fig. 43 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 43. The three Amazonian species of the furvus subgroup. A, D. Sylvicanthon furvus (Schmidt, 1920). A. Dorsal view. D. Ventral view. B, E. S. monnei sp. nov. B. Dorsal view. E. Ventral view. C, F. S. mayri sp. nov. C. Dorsal view. F. Ventral view.
Fig. 44 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 44. Differences on the parameres of Sylvicanthon mayri sp. nov. and S. monnei sp. nov. (grayish zones represent original membraneous areas). A–B. S. mayri sp. nov. C–D. S. monnei sp. nov. Note that both branches of the apical bifurcation of the parameres of S. mayri sp. nov. are much more divergent than those of S. monnei sp. nov., which makes the internal angle between them more open in the first species (~110º) than in the second (~78º). In the same way, as the inferior branch is much more projected in S. mayri sp. nov. than in S. monnei sp. nov., the angle between the posterior region of that branch and the rest of the paramere is more open in S. monnei sp. nov. (~147º) than in S. mayri sp. nov. (~137º), species that seems to have a strong excavation at this point of the paramere (indicated by red arrow in A).
Fig. 42 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 42. Sylvicanthon obscurus (Schmidt, 1920). A. Dorsal view of the purplish form. B. Dorsal view of the yellowish form. C. Ventral view.
Fig. 41 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 41. Distribution of Sylvicanthon securus (Schmidt, 1920) comb. nov. and the four species of the furvus subgroup.
Fig. 35 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 35. Variation on the pilosity at the centre of the hypomeral cavity among members of the bridarollii subgroup. A. Sylvicanthon seag sp. nov. B. S. attenboroughi sp. nov. C–D. S. bridarollii (Martínez, 1949). Note the first two species have the hypomeral cavity entirely glabrous or with setae limited to its periphery (centre always glabrous), whereas S. bridarollii possesses long and dense setae throughout the tegument of the hypomeral cavity.
Fig. 32 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 32. Sylvicanthon bridarollii (Martínez, 1949). A–B. Individual from southern Bolivia. A. Dorsal view. B. Ventral view. C–D. Individual from Ecuador. C. Dorsal view. D. Ventral view.
Fig. 36 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 36. Clinal morphological variation in S. bridarollii (Martínez, 1949). Note that, from south to north, the colouration of metafemora gradually fades from dark brown to reddish brown and orange with a light-brown base in populations of northern Peru, Ecuador, and Colombia, and that the internal margin of protibiae (indicated by the red arrows) becomes progressively much subtler. Other features varying along this north-south cline are the presence of coarse elongate punctures at the base of metafemora (present in southern populations and absent in the northern ones) and of a fine transverse line on the posterior edge of pronotum (absent in the southern populations). See the text for more details.
Fig. 21 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 21. Sylvicanthon enkerlini (Martínez et al., 1964) comb. nov. A. Dorsal view. B. Ventral view. C. Holotype and its labels.
Fig. 16 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 16. Abdominal lateral foveae of females (arrows). A. Sylvicanthon furvus (Schmidt, 1920). B. S. mayri sp. nov. C. S. obscurus (Schmidt, 1920). D. S. foveiventris (Schmidt, 1920).
Fig. 15 in A monographic revision of the Neotropical dung beetle genus Sylvicanthon Halffter & Martínez, 1977 (Coleoptera: Scarabaeidae: Scarabaeinae: Deltochilini), including a reappraisal of the taxonomic history of 'Canthon sensu lato'
Fig. 15. Morphological variation and sexual dimorphism in the protibial spur of Sylvicanthon. A. S. enkerlini (Martínez et al., 1964) comb. nov., ♂. B. S. foveiventris (Schmidt, 1920), ♂. C. S. candezei (Harold, 1869), ♂. D. S. genieri sp. nov., ♂. E. S. aequinoctialis (Harold, 1868), ♂. F. S. aequinoctialis comb. nov., ♀. G. S. proseni (Martínez, 1949) stat. et comb. nov., ♂. H. S. proseni stat. et comb. nov., ♀. I. S. bridarollii (Martínez, 1949), ♂. J. S. seag sp. nov., ♂. K. S. edmondsi sp. nov., ♂. L. S. attenboroughi sp. nov., ♂. M. S. obscurus (Schmidt, 1920), ♂. N. S. furvus (Schmidt, 1920), ♂. O. S. securus (Schmidt, 1920) comb. nov., ♂.
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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.