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FIGURE 2. C. aemulus and C. graomogolensis. A–E. C in Croton aemulus and C. graomogolensis (Euphorbiaceae): Two new species from Minas Gerais, Brazil, based on distinct lines of evidence and their relation to C. muscicapa and C. longibracteatus
FIGURE 2. C. aemulus and C. graomogolensis. A–E. C. aemulus (Barbosa et al. 19, HUEFS). A. Habit; B. Stipules, glandular, lanceolate; C. Bracts; D. Staminate flower; E. Pistillate flower. F–L. C. graomogolensis (Barbosa et al. 17, HUEFS). F. Habit; G. Glandular stipules, resembling a bunch of grapes; H. Bracts in frontal view; I. Bracts in lateral view; J. Staminate flower; K. Pistillate flower; L. Ovary and styles. Drawing by Natanael Nascimento.
FIGURE 11 in A new infrageneric classification for Amorimia (Malpighiaceae) based on morphological, phytochemical and molecular evidence
FIGURE 11. Distribution map of species from Amorimia subg. Uncinae R.F.Almeida: ●—A. septentrionalis; ○—A. amazonica; ▲—A. pubiflora; Δ—A. tumida; ■—A. kariniana; □—A. camporum; *—A. concinna. South American phytogeographical domains: Amazon rainforest—light green, Chaco/Pantanal—yellow, cerrado—orange, caatinga—white, Atlantic Forest—dark green, and Pampas—blue.
FIGURE 5 in A new infrageneric classification for Amorimia (Malpighiaceae) based on morphological, phytochemical and molecular evidence
FIGURE 5. Reconstruction of morphological characters (texture of lateral wings, size of dorsal wing, shape of dorsal wing, conation of lateral wings, shape of lateral wings, and seed texture) on the Bayesian tree (Fig. 3).
FIGURE 6 in A new infrageneric classification for Amorimia (Malpighiaceae) based on morphological, phytochemical and molecular evidence
FIGURE 6. Reconstruction of morphological characters (shape of the apex of reduced leaves in the inflorescence, shape of bracteoles, shape of sepal apex, posture of the sepal apex, adaxial indumentum of sepals and posture of sepals) on the Bayesian tree (Fig. 3).
FIGURE 10 in A new infrageneric classification for Amorimia (Malpighiaceae) based on morphological, phytochemical and molecular evidence
FIGURE 10. Distribution map of species from Amorimia subg. Amorimia: ●—A. exotropica; ○—A. rigida; ▲—A. coriacea; Δ—A. candidae; ■—A. velutina; □—A. maritima; *—A. pellegrinii; A—A. andersonii. South American phytogeographical domains: Amazon rainforest—light green, Chaco/Pantanal—yellow, cerrado—orange, caatinga—white, Atlantic Forest—dark green, and Pampas—blue.
FIGURE 1 in A new infrageneric classification for Amorimia (Malpighiaceae) based on morphological, phytochemical and molecular evidence
FIGURE 1. Some species of Amorimia sampled in this study. A. Amorimia amazonica (photograph by D. Daly). B. Amorimia andersonii (photograph by A.M.A. Amorim). C. Amorimia candidae (photograph by R.F. Almeida). D. Amorimia coriacea (photograph by M.O.O. Pellegrini). E. Amorimia exotropica (photograph by A. Gava). F. Amorimia maritima (photograph by F. Flores). G. Amorimia pellegrinii (photograph by R.F. Almeida). H. Amorimia pubiflora (photograph by E. Moleta) I. Amorimia rigida (photograph by R.F. Almeida). J. Amorimia septentrionalis (photograph by M.O.O. Pellegrini). K. Amorimia tumida (photograph by M.N. Coelho). L. Amorimia velutina (photograph by L.C. Marinho).
FIGURE 9 in A new infrageneric classification for Amorimia (Malpighiaceae) based on morphological, phytochemical and molecular evidence
FIGURE 9. Synapomorphies of Amorimia (clade A): bracts glandular, petals pubescent on both sides, samaras with the two lateral wings larger than the dorsal wing and presence of monofluoracetate. Synapomorphies of Amorimia subg. Uncinae (clade B): sepals acute at apex and glabrous abaxially, elaiophores green turning yellow, petals yellow never turning orange or red with age and cuneate at base, styles uncinate at apex and pollen grains spherical. Synapomorphies of Amorimia subg. Amorimia (clade C): sepals rounded at apex and pubescent abaxially, elaiophores yellow turning red to ochre, petals yellow turning orange to red with age and truncate at base, styles truncate at apex and pollen grains polygonal. Synapomorphies of Mascagnia: elaiophores pink turning ochre with age, petals keeled and samaras with lateral wings larger than dorsal wing, and fused into an orbicular wing. Synapomorphies of Ectopopterys: sepals eglandular, deflexed, anther with enlarged connectives, apex of foliate styles and samaras with the dorsal wing larger than the lateral wings thickened on the lower side.
FIGURE 8 in A new infrageneric classification for Amorimia (Malpighiaceae) based on morphological, phytochemical and molecular evidence
FIGURE 8. Pollen morphology of eleven species of Amorimia sampled in this study. Amorimia subg. Uncinae. A. A. amazonica; B. A. concinna; C. A. kariniana; D. A. pubiflora; E. A. septentrionalis. Amorimia subg. Amorimia - F. A. candidae; G. A. coriacea; H. A. exotropica; I. A. maritima; J. A. pellegrinii; K. A. rigida.
FIGURE 4 in A new infrageneric classification for Amorimia (Malpighiaceae) based on morphological, phytochemical and molecular evidence
FIGURE 4. Reconstruction of morphological characters (connation of stipules, occurrence of glands on bracts, occurrence of elaiophores, abaxial indumentum of petals and position of stigmas) and chemical traits (monofluoracetate) on the Bayesian tree (Fig. 3).
FIGURE 3 in A new infrageneric classification for Amorimia (Malpighiaceae) based on morphological, phytochemical and molecular evidence
FIGURE 3. Bayesian inference and maximum parsimony tree based on the combined dataset. Clade support above 50% bootstrap and 0.50 Bayesian posterior probabilities are indicated above/below branches.
FIGURE 7 in A new infrageneric classification for Amorimia (Malpighiaceae) based on morphological, phytochemical and molecular evidence
FIGURE 7. Reconstruction of morphological (colour of elaiophores, shape of petals at base, shape of petals, adaxial indumentum of petals, stamens symmetry and shape of the style apex) on the Bayesian tree (Fig. 3).
FIGURE 2 in A new infrageneric classification for Amorimia (Malpighiaceae) based on morphological, phytochemical and molecular evidence
FIGURE 2. Bayesian inference and maximum parsimony trees based on the ETS and ndhF datasets. Clade support above 50% bootstrap and 0.50 Bayesian posterior probabilities are indicated above/below branches.
FIGURE 2 in New insights on Trametopsis Tomšovský (Polyporales Gäum) based on phylogenetic evidences and morphological analyses of neotropical species
FIGURE 2. Macroscopic features of Trametospis species. Trametopsis aborigena A–D [HOLOTYPE FCOS41, CORD(C 00005352], A) Pileus, B) Context, C) Reddish veins pileal surface, D) Pores. Trametopsis cervina E–G (FCOS-39), E) Pileus, F) Context, G) Pores. Trametopsis brasiliensis H–J (HOLOTYPE, HF C3637), H) Pileus, I) Context, J) Pores. Trametopsis luteocontexta K–M (HOLOTYPE, MBM 180795), K) Pileus, L) Context, M) Pores. Bars = 0.5 cm. Photos by: Nataly Gómez-Montoya and Gerardo Robledo
FIGURE 1 in New insights on Trametopsis Tomšovský (Polyporales Gäum) based on phylogenetic evidences and morphological analyses of neotropical species
FIGURE 1. Best-scored tree representing the phylogenetic relationships based on ITS and LSU rDNA. Bayesian Inference, Maximum Parsimony and Maximum Likelihood support values are given above the branches.
FIGURE 3 in New insights on Trametopsis Tomšovský (Polyporales Gäum) based on phylogenetic evidences and morphological analyses of neotropical species
FIGURE 3. Microscopic characters of Trametopsis aborigena A–C, F [HOLOTYPE FCOS41, CORD(C) 00005352]. A–C) Clamped generative hyphae, F) Basidiospores. Trametopsis cervina D–E, G (FCOS39) D) Generative hyphae clamped, E) Metachromatic, clamped generative hyphae, G) Basidiospores. Trametopsis.brasiliensis (HOLOTYPE, HF C3637) H) Basidiospores. Trametopsis luteocontexta (HOLOTYPE, MBM 180795) I) Basidiospores. Bars = 5 μm. Photos by: Nataly Gómez-Montoya
FIGURE 4 in New insights on Trametopsis Tomšovský (Polyporales Gäum) based on phylogenetic evidences and morphological analyses of neotropical species
FIGURE 4. Microscopic features of Trametopsis aborigena [HOLOTYPE FCOS41, CORD(C) 00005352]. A) Sporogram from the basidiospores in equatorial and polar view, (el = equatorial lateral view; ead = equatorial adaxial view; eab = equatorial abaxial view; dp = distal polar view and pp = proximal polar view). B) Basidia, C) Thick and thin-walled generative hyphae from the context, D) Skeletal hyphae in the trama of the tubes. Drawings by Nataly Gómez-Montoya.
FIGURE 1 in Two new combinations in Iberian Santolina (Compositae) based on morphology and molecular evidences
FIGURE 1. Strict consensus tree obtained with parsimony analysis from ongoin molecular studies (Carbajal et al., unpublished). Bootstrap values over 60% are shown above branches.
FIGURE 2 in Two new combinations in Iberian Santolina (Compositae) based on morphology and molecular evidences
FIGURE 2. Holotype of Santolina vedranensis (O. Bolòs & Vigo) L. Sáez, M. Serrano, S. Ortiz & R. Carbajal.
FIGURE 1 in Three novel species of Russula from southern China based on morphological and molecular evidence
FIGURE 1. Phylogram generated from Maximum Likelihood (ML) method based on rDNA ITS sequences performed by RAxML. One thousand bootstrap replicates followed by a heuristic ML tree search was adopted and bootstrap values higher than 70% are shown on the left of "/" and Bayesian posterior probabilities (PP) values> 0.95 are shown on the right. Three novel taxa are shown in bold.
FIGURE 6 in Three novel species of Russula from southern China based on morphological and molecular evidence
FIGURE 6. Russula subatropurpurea. (Holotype GDGM70634). a. Basidia; b. Cheilocystidia; c. Pleurocystidia; d. Pileipellis; e. Pileocystidia; f. Caulocystidia. Scale bars= 10 μm.
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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.