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87 results for “campo rupestre”
FIGURE 13 in New species of Marcetia and Microlicia (Melastomataceae) endemic to the campo rupestre of Chapada Diamantina, Bahia, Brazil
FIGURE 13. Microlicia barbata, photos of living plants. A. Flower close up. B. Branches terminating in floral buds. Photos by R.Pacifico. Voucher: R. Pacifico et al. 619.
FIGURE. 3. A. Brazil with Bahia state highlighted. B in New species of Marcetia and Microlicia (Melastomataceae) endemic to the campo rupestre of Chapada Diamantina, Bahia, Brazil
FIGURE. 3. A. Brazil with Bahia state highlighted. B. Bahia with the study area outlined (dashed line). C. Distributions of Marcetia auricularia, Marcetia santosiae and Marcetia unguiculata in the Chapada Diamantina, Bahia, Brazil.
FIGURE 2. Stigmatodon enigmaticus. A. Habit. B. Leaf. C. Peduncle bract. D. Floral bract, adaxial surface. E. Floral bract, abaxial surface. F. Flower. G. Sepal. H in Stigmatodon enigmaticus (Bromeliaceae, Tillandsioideae), a new lithophytic species from the Campos Rupestres within the Brazilian Atlantic Forest
FIGURE 2. Stigmatodon enigmaticus. A. Habit. B. Leaf. C. Peduncle bract. D. Floral bract, adaxial surface. E. Floral bract, abaxial surface. F. Flower. G. Sepal. H. Petals, stamens and appendages at the base. I. Details of basal petal appendages. J. Filament and anther. K. Pistil. Drawing by Joelcio Freitas based on the holotype P.M. Gonella 2965 (MBML).
FIGURE 1. Stigmatodon enigmaticus. A in Stigmatodon enigmaticus (Bromeliaceae, Tillandsioideae), a new lithophytic species from the Campos Rupestres within the Brazilian Atlantic Forest
FIGURE 1. Stigmatodon enigmaticus. A. General view of the landscape of campos rupestres and forests at type locality at Serra do Pinh"o, part of Serra do Padre Ângelo (Conselheiro Pena, MG). B. Quartzitic rocky outcrops, habitat of S. enigmaticus. C. Habit of S. enigmaticus. D. Flowering specimen of S. enigmaticus (specimen Couto et al. 6625, paratype). E. Detail of leaves and bracts of the base of the inflorescence. F. Side view of the inflorescence of a cultivated specimen (specimen Gonella et al. 2965, holotype), showing the red bracts and yellow perianth. G. Lateral view of the flower. H. Front view of the flower, showing the position of stamens and stigma. (Photos: A–C, E, G, H by PMG; F by DRC; D by Lucian Medeiros).
FIGURE 7. Microlicia pumila. A. Fruiting branches. B in Microlicia delicata and Microlicia pumila (Melastomataceae), two new species from unprotected mountains with campo rupestr vegetation in eastern Brazil
FIGURE 7. Microlicia pumila. A. Fruiting branches. B. Branchlet terminating in a floral bud. C. Type locality, Serra da Formosa, Monte Azul, Minas Gerais, Brazil. Photos by R. Pacifico. Voucher: R. Pacifico et al. & V.E. Bressan 725.
FIGURE 8. A in Microlicia delicata and Microlicia pumila (Melastomataceae), two new species from unprotected mountains with campo rupestr vegetation in eastern Brazil
FIGURE 8. A. Map of Brazil with Minas Gerais state highlighted in black. B. Minas Gerais with distributions of Microlicia karinae, M. nervosa, M. naudiniana, M. obovatifolia and M. pumila. C. Satellite image of Serra do Cipó with distributions of M. karinae, M. nervosa, M. naudiniana and M. obovatifolia. D. Satellite image of Serra da Formosa with the distribution record of M. pumila.
FIGURE 1. A in Microlicia delicata and Microlicia pumila (Melastomataceae), two new species from unprotected mountains with campo rupestr vegetation in eastern Brazil
FIGURE 1. A summary of the elliptic Fourier analysis of leaf shape. A. Two main PC axes associated with variation in leaf shape. Each row represents variation in shape explained by each of the first two PC axes, whereas the columns correspond to the mean shape ± 1.5 standard deviations on each side. B. PCA ordination of the elliptical Fourier analysis showing ranges of variation in leaf shape associated with each species. C–G. Photos of representatives leaves of species sampled in the elliptic Fourier analysis. C. Microlicia pumila (R. Pacifico 725 & V.E. Bressan). D. Microlicia obovatifolia (F. Almeda et al. 8899). E. Microlicia karinae (F. Almeda et al. 9705). F. Microlicia naudiniana (R. Pacifico 321). G. Microlicia nervosa (F. Almeda et al. 9124). H. Heatmap highlighting regions that differ in mean leaf shape between M. pumila (outlined in red) and M. karinae (outlined in light blue). Scale bars: 2 mm.
FIGURE 4. A in Microlicia delicata and Microlicia pumila (Melastomataceae), two new species from unprotected mountains with campo rupestr vegetation in eastern Brazil
FIGURE 4. A. Map of Brazil with Bahia state highlighted in black. B. Bahia with distributions of Microlicia coronata, M. delicata, and M. plumosa. C. Satellite image of southwestern Chapada Diamanatina with distributions of M. coronata, M. delicata, and M. plumosa.
FIGURE 6. Microlicia pumila. A. Habit. B in Microlicia delicata and Microlicia pumila (Melastomataceae), two new species from unprotected mountains with campo rupestr vegetation in eastern Brazil
FIGURE 6. Microlicia pumila. A. Habit. B. Detail of the verrucose internodes. C. Apical vegetative branch. D. Leaf (abaxial surface). E. Leaf (adaxial surface). F. Floral bud. G. Antesepalous stamen. H. Antepetalous stamen. I. Capsule enveloped by the hypanthium. J. Capsule. K. Seed in lateral view. Voucher: R. Pacifico 725 & V.E. Bressan. Scale bars: A, 2 cm; B, 1 mm; C, 4 mm; D–J, 2 mm; K, 0.4 mm.
FIGURE 5 in Microlicia delicata and Microlicia pumila (Melastomataceae), two new species from unprotected mountains with campo rupestr vegetation in eastern Brazil
FIGURE 5. Photos of selected species compared to new taxa described in this study. A–D Microlicia plumosa. A. Population on the Pico do Barbado, Abaíra, Bahia, Brazil. B. Habit. C. Branchlet in lateral view, showing the "feather-like" foliage typical of this species. D. Branchlet in upper view showing the decussate cruciate leaf arrangement as seen from above. E. Microlicia coronata, fruiting branches. F. Microlicia naudiniana, flower close up (R. Pacifico et al. 403). G. Microlicia obovatifolia, flower close up (F. Almeda et al. 8899). Photos A–F by R. Pacifico, and G by F. Almeda.
FIGURE 2. A–B in Microlicia delicata and Microlicia pumila (Melastomataceae), two new species from unprotected mountains with campo rupestr vegetation in eastern Brazil
FIGURE 2. A–B. Comparative boxplots of leaf and calyx lobe length between Microlicia plumosa and M. delicata. A. Leaf length boxplot. B. Calyx lobe length boxplot. C–D. Photos of branches of M. delicata and M. plumosa, showing the general aspect of the foliage of each species when dry. C. Microlicia delicata (H.P. Bautista 2897). D. Microlicia plumosa (W. Ganev 2265).
FIGURE 3. Microlicia delicata. A. Habit. B in Microlicia delicata and Microlicia pumila (Melastomataceae), two new species from unprotected mountains with campo rupestr vegetation in eastern Brazil
FIGURE 3. Microlicia delicata. A. Habit. B. Cluster of trichomes above a node. C. Leaf in lateral view (left), abaxial view (middle) and adaxial view (right). D. Close up of a leaf in lateral view showing cilia on the margin. E. Detail of leaf trichome. F. Branchlet terminating in a flower. G. Antesepalous stamen. H. Antepetalous stamen. I. Capsule enveloped by the hypanthium, after calyx lobes fell away. J. Capsule. Voucher: Bautista 2897. Scale bars. A, 2 cm; B, D and E, 0.5 mm; C, G, H, I and J, 2 mm; F, 4 mm.
FIGURE 3 in Chionanthus monteazulensis (Oleaceae), a new species from the campo rupestre of Espinhaço Range, Brazil
FIGURE 3. Elevation map indicating the known occurrence of Chionanthus monteazulensis, north of Serra do Espinhaço Biosphere Reserve, in Minas Gerais, Brazil.
FIGURE 2. Chionanthus monteazulensis Zavatin & Lombardi. A. Branch with Inflorescence, B in Chionanthus monteazulensis (Oleaceae), a new species from the campo rupestre of Espinhaço Range, Brazil
FIGURE 2. Chionanthus monteazulensis Zavatin & Lombardi. A. Branch with Inflorescence, B. Magnification of the leaf showing domatium, C. Flowers in anthesis, D. Magnification of the flower showing two stamens, E. Lenticels, F. Branch with fruits, G. Magnification of the fruits, H. Immature fruit, I. Mature fruit, J. Seed. Photos by D.A. Zavatin taken on the site of the "D.A. Zavatin et al. 1015" specimen.
FIGURE 1. Chionanthus monteazulensis Zavatin & Lombardi. A. Branch with Inflorescence, B in Chionanthus monteazulensis (Oleaceae), a new species from the campo rupestre of Espinhaço Range, Brazil
FIGURE 1. Chionanthus monteazulensis Zavatin & Lombardi. A. Branch with Inflorescence, B. Magnification of the branch showing lenticels, C. Leaf, D. Magnification of the leaf showing domatias, E. Flower, F. Flower showing gynoecium and androecium. Illustration by Klei Souza using the specimen "D.A. Zavatin et al. 1015" as reference.
Data from: Soil types select for plants with matching nutrient‐acquisition and ‐use traits in hyperdiverse and severely nutrient‐impoverished campos rupestres and cerrado in Central Brazil
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Figure 5 in Endophytic fungi in roots of native orchids of rupestrian grasslands (campos rupestres) in Serra do Cipó, Brazil
Figure 5. Phylogenetic inference of the endophytic fungal genus Tulasnella generated by Bayesian analysis of ITS sequences. A posteriori probabilities are indicated on the nodes. Bold codes and respective NCBI access numbers for isolates obtained from roots of the five native orchids (Cattleya brevipedunculata, Epidendrum saxatile, E. secundum, Grobya cipoensis and Pleurothallis teres) sampled in a rupestrian grasslands of Serra do Cipó, Brazil. Identification and accession number for NCBI and UNITE platform are provided to reference sequences.
Figure 3 in Endophytic fungi in roots of native orchids of rupestrian grasslands (campos rupestres) in Serra do Cipó, Brazil
Figure 3. Fungal genera occurring as endophytic in roots of the five native orchids (Cattleya brevipedunculata, Epidendrum saxatile, E. secundum, Grobya cipoensis and Pleurothallis teres) sampled in a rupestrian grasslands of Serra do Cipó, Brazil.
Figure 2 in Endophytic fungi in roots of native orchids of rupestrian grasslands (campos rupestres) in Serra do Cipó, Brazil
Figure 2. Number of fungal isolates at the levels of phylum and order obtained from roots of the five native orchids (Cattleya brevipedunculata, Epidendrum saxatile, E. secundum, Grobya cipoensis and Pleurothallis teres) sampled in an area of rupestrian grasslands at Serra do Cipó/ Brazil.
Figure 1 in Endophytic fungi in roots of native orchids of rupestrian grasslands (campos rupestres) in Serra do Cipó, Brazil
Figure 1. Number of isolates and species of endophytic fungi obtained from roots of the five native orchids (Cattleya brevipedunculata, Epidendrum saxatile, E. secundum, Grobya cipoensis and Pleurothallis teres) sampled in a rupestrian grasslands of Serra do Cipó, Brazil. Species definition was based on ITS sequence analysis, considering isolates with greater than 97% similarity as belonging to the same fungal species.
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Allen Brain Atlas
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International Brain Laboratory public data
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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.