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753 results for “Brazilian Atlantic Forest”
FIGURE 2 in Two new species of Myrcia (Myrtaceae) from Brazilian Atlantic Forest
FIGURE 2. Myrcia congestiflora. Flowering branch (C.P. Caliari, M.F. Santos e M. Bünger. 3024—ESA).
FIGURE 2. Aspidogyne caraguatatubensis. A. Habit. B. Inflorescence. C in A new Aspidogyne (Orchidaceae: Goodyerinae) from the Brazilian Atlantic Forest
FIGURE 2. Aspidogyne caraguatatubensis. A. Habit. B. Inflorescence. C. Flower in lateral view.
FIGURE 1 in Rediscovery, considerations about type locality and conservation of Rhipsalis agudoensis (Cactaceae) from the Brazilian Atlantic Forest
FIGURE 1. Distribution map of Rhipsalis agudoensis.
FIGURE 3 in Behuria lumiarensis (Melastomataceae), a new species on a mountaintop of the Brazilian Atlantic Forest
FIGURE 3. Map with the collection locality of Behuria lumiarensis at central Rio de Janeiro (RJ).
FIGURE 2 in Turnera spicata: a new species of Turneraceae (Passifloraceae s.l.) from the Brazilian Atlantic Forest
FIGURE 2. Distribution map of Turnera spicata in the Espírito Santo state (ES).
FIGURE 4 in Re-establishment of Psidium macahense (Myrtaceae, Myrteae), an endemic species from the Brazilian Atlantic Forest
FIGURE 4. Tree for psbA-trnH.
FIGURE 2 in Two new Brazilian Atlantic Forest Eugenia (Myrtaceae)
FIGURE 2. Eugenia sudestis (isotype at HUFSJ; scale: 50 mm).
FIGURE 1 in A new species of Chrysophyllum (Sapotaceae) from the Brazilian Atlantic forest
FIGURE 1. Geographical distribution of Chrysophyllum pubipetalum Sossai & Alves-Araújo sp. nov.
FIGURE 3 in Peperomia calcicola (Piperaceae), a new species from limestone outcrops of the southeastern Brazilian Atlantic Forest
FIGURE 3. Holotypus of Peperomia calcicola (from G.M. Marcusso et al. 1720, HRCB).
TABLE 1 S in A new endemic species of Macropsychanthus (Leguminosae: Papilionoideae) from the Brazilian Atlantic Forest
<p><b>TABLE 1S.</b> Voucher information and GenBank accession numbers for the DNA sequences used in this study.</p><table><tbody><tr><th>Taxon</th><th>Voucher</th><th>Locality</th><th>ITS</th><th>ETS</th><th>trnK/matK</th></tr></tbody><tbody><tr><th><i>Dioclea sericea</i> Kunth</th><td>R. Schultze-Kraft s.n. (CIAT 9578)</td><td>Colombia, Cauca</td><td>KC779715</td><td>KC779823</td><td>KC779588</td></tr><tr><th><i>Macropsychanthus comosus</i> (G. Mey.) L.P. Queiroz & Snak</th><td>C. van den Berg 1796 (HUEFS)</td><td>Venezuela, Bolívar</td><td>KC779706</td><td>KC779856</td><td>KC779583</td></tr><tr><th><i>Macropsychanthus edulis</i> (Kuhlm.) L.P. Queiroz & Snak</th><td>L.P. Queiroz 15226 (HUEFS)</td><td>Brazil, Bahia</td><td>KC779683</td><td>KC779835</td><td>KC779573</td></tr><tr><th><i>Macropsychanthus glaber</i> (Benth.) L.P. Queiroz & Snak</th><td>L.P. Queiroz 10381 (HUEFS)</td><td>Brazil, Mato Grosso</td><td>KC779684</td><td>KC779837</td><td></td></tr><tr><th><i>Macropsychanthus grandiflorus</i> (Mart. ex Benth.) L.P. Queiroz & Snak</th><td>Queiroz 7325 (HUEFS)</td><td>Brazil, Bahia</td><td>KC779686</td><td>KC779839</td><td>KC779574</td></tr><tr><th><i>Macropsychanthus grandistipula</i> (L.P. Queiroz) L.P. Queiroz & Snak</th><td>H.C. Lima 6634 (HUEFS)</td><td>Brazil, Rio de Janeiro</td><td>KC779688</td><td>KC779840</td><td></td></tr><tr><th><i>Macropsychanthus latifolius</i> (Benth.) L.P. Queiroz & Snak</th><td>C. van den Berg 1163 (HUEFS)</td><td>Brazil, Bahia</td><td>KC779696</td><td>KC779843</td><td>KC779579</td></tr><tr><th><i>Macropsychanthus macrocarpus</i> (Ducke) L.P. Queiroz & Snak</th><td>L.P. Queiroz 13910 (HUEFS)</td><td>Brazil, Amazonas</td><td>KC779697</td><td>KC779844</td><td>KC779580</td></tr><tr><th><i>Macropsychanthus lauterbachii</i> Harms var. <i>hirsutus</i></th><td>A.N. Millar NGF13855 (L)</td><td>Papua New Guinea Morobe</td><td>MT565584</td><td>MT565564</td><td></td></tr><tr><th><i>Macropsychanthus lauterbachii</i> var. <i>lauterbachii</i> Verd.</th><td>M. Hopkins 1360 (K)</td><td>Papua New Guinea</td><td>KP262490</td><td></td><td>KP658375</td></tr><tr><th><i>Macropsychanthus malacocarpus</i> (Huber) L.P. Queiroz & Snak</th><td>L.P. Queiroz 13076 (HUEFS)</td><td>Brazil, Pará</td><td>KC779698</td><td>KC779845</td><td></td></tr><tr><th><i>Macropsychanthus marginatus</i> (Benth.) L.P. Queiroz & Snak</th><td>L.P. Queiroz 9136 (HUEFS)</td><td>Brazil, Bahia</td><td>KC779700</td><td>KC779847</td><td>KC779581</td></tr><tr><th><i>Macropsychanthus megacarpus</i> (Rolfe) L.P. Queiroz & Snak</th><td>L.P. Queiroz 10135 (HUEFS)</td><td></td><td>KC779701</td><td></td><td></td></tr><tr><th><i>Macropsychanthus pulcher</i> (Moldenke) L.P. Queiroz & Snak</th><td>M. Sousa 11095 (MEXU)</td><td>Panama, Darién</td><td>MT565575</td><td>MT565557</td><td>MT565542</td></tr><tr><th><i>Macropsychanthus purpureus</i> (Elmer) L.P. Queiroz & Snak</th><td>Soejarto 7967 (F)</td><td>Philippines, Luzon</td><td>MT565583</td><td>MT565563</td><td>KX652152</td></tr><tr><th><i>Macropsychanthus violaceus</i> (Mart. ex Benth.) L.P. Queiroz & Snak</th><td>Cabid s.n. (CTES)</td><td>Argentina, Corrientes</td><td>KC779702</td><td>KC779848</td><td></td></tr><tr><th><i>Macropsychanthus rufescens</i> (Benth.) L.P. Queiroz & Snak</th><td>J. Stehman 4721 (BHCB)</td><td>Brazil, Espírito Santo</td><td>MT565579</td><td>MT565561</td><td></td></tr><tr><th><i>Macropsychanthus ruschii</i> Fonseca-Cortés & Queiroz</th><td>L.P. Queiroz 15254 (HUEFS)</td><td>Brazil, Espírito Santo</td><td>KC779717</td><td>KC779854</td><td>KC779590</td></tr><tr><th><i>Macropsychanthus schottii</i> (Benth.) L.P. Queiroz & Snak</th><td>S. Buzato 28114 (UEC)</td><td>Brazil, São Paulo</td><td>KC779710</td><td>KC779852</td><td></td></tr><tr><th><i>Macropsychanthus sclerocarpus</i> (Ducke) L.P. Queiroz & Snak</th><td>L.P. Queiroz 15911 (HUEFS)</td><td>Brazil, Pará</td><td>MT565577</td><td>MT565558</td><td>MT565543</td></tr><tr><th><i>Macropsychanthus wilsonii</i> (Standl.) L.P. Queiroz & Snak</th><td>L.P. Queiroz 4899 (HUEFS)</td><td>Brazil, São Paulo</td><td>KC779725</td><td>KC779857</td><td>KC779594</td></tr></tbody></table>
TABLE 1. Morphological characteristics for distinguishing M in A new endemic species of Macropsychanthus (Leguminosae: Papilionoideae) from the Brazilian Atlantic Forest
<p><b>TABLE 1.</b> Morphological characteristics for distinguishing <i>M. ruschii</i> of other morphological similar species of the AF, in bold the diagnostic characters of each species.</p><table><tbody><tr><th>Characters</th><th><i>M. edulis</i></th><th><i>M. grandistipula</i></th><th><i>M. rufescens</i></th><th><i>M. ruschii</i></th><th><i>M. schottii</i></th></tr></tbody><tbody><tr><th>Stipule length (mm)</th><td>10–20</td><td><b>15–30</b></td><td>10–20</td><td><b>17–20</b></td><td>10–20</td></tr><tr><th>Stipule width (mm)</th><td>3–6</td><td><b>7–15</b></td><td>3–6</td><td><b>2–3</b></td><td>3–5</td></tr><tr><th>Rachis length</th><td><b>1–2</b></td><td>2–2.5 cm long</td><td><b>To 0.5 cm</b></td><td>0.5–0.7 cm</td><td>0.2–1.5 cm</td></tr><tr><th>leaflet undersurface indumentum</th><td>Strigose to sericeous and fulvous</td><td>Glabrescent</td><td>Strigose to sericeous and fulvous</td><td>Glabrescent</td><td><b>Sericeous and argenteus</b></td></tr><tr><th>bracteoles size (mm)</th><td>3–4 × 3–4</td><td>1–3 × 1–3</td><td>3–4 × 3–4</td><td>2–3 × 1–3</td><td>2–4 × 2–3</td></tr><tr><th>flower length (mm)</th><td>13–16</td><td><b>17–20</b></td><td>13–16</td><td><b>10–12</b></td><td>13–16</td></tr><tr><th>petal color</th><td>White to bright pink</td><td>White with the center with lilac stripes</td><td>White to bright pink</td><td><b>Lilac with white stripes</b></td><td>White to bright pink</td></tr><tr><th>keel petal apex</th><td>Concave</td><td>Rounded</td><td>Concave</td><td>Rounded</td><td>Concave</td></tr><tr><th>keel petal length (mm)</th><td>8–12</td><td><b>14–17</b></td><td>8–12</td><td><b>8–12</b></td><td>9–13</td></tr></tbody></table>
FIGURE 23 in An overview of the Brazilian Atlantic Forest species of Pachythone Bates (Lepidoptera: Riodinidae), with the description of a new species and an updated checklist of Pachythonina
FIGURE 23. Distribution map of the species of Pachythone endemic to the Brazilian Atlantic Forest.
FIGURE 1 in Two new Brazilian Atlantic Forest Eugenia (Myrtaceae)
FIGURE 1. Eugenia mimetica (holotype).
FIGURE 1 in Octomeria lilliputana (Orchidaceae), a new species from Brazilian Atlantic Forest, State of Paraná, Brazil
FIGURE 1. Map of Paraná State, Brazil, showing the known distribution of Octomeria lilliputana.
FIGURE 2 in A new species of Erythroxylum (Erythroxylaceae) from the Brazilian Atlantic Forest
FIGURE 2. Geographic distribution of Erythroxylum umbrosum.
FIGURE 7 in Taxonomic revision of the Brazilian Atlantic Forest Atractus (Reptilia: Serpentes: Dipsadidae) 2364
FIGURE 7. Geographical distribution of Atractus francoi, A. serranus, and A. trihedrurus.
FIGURE 19 in Taxonomic revision of the Brazilian Atlantic Forest Atractus (Reptilia: Serpentes: Dipsadidae) 2364
FIGURE 19. Original plate of the holotype of Rabdosoma zebrinum, modified from Jan (1862).
FIGURE 2 in Rediscovering Rhipsalis hoelleri (Cactaceae), a Critically Endangered species from Brazilian Atlantic Forest
FIGURE 2. Distribution map of the Brazilian endemic Rhipsalis hoelleri.
FIGURE 4 in Vellozia inselbergae (Velloziaceae), a new species from the Brazilian Atlantic Forest inselbergs
FIGURE 4. Distribution of Vellozia inselbergae through two lowland inselbergs in the Bahia state.
A holocenic and dynamic hybrid zone between two cactophilic Drosophila species in a coastal lowland plain of the Brazilian Atlantic Forest
<p>Hybridization and introgression are processes that contribute to shaping biological diversity. The factors promoting the formation of these processes are multiples but poorly explored in a biogeographical and ecological context. In the southeast coastal plain of the Brazilian Atlantic Forest, a hybrid zone was described between two closely related cactophilic species, <i>Drosophila antonietae</i> and <i>D. serido. </i>Here, we revisited and analyzed specimens from this hybrid zone to evaluate its temporal and spatial dynamic. We examined allopatric and sympatric populations of the flies using independent sources of data such as mitochondrial and nuclear sequences, microsatellite loci, morphometrics of wings and male genitalia, and climatic niche models. We also verified the emergence of the flies from necrotic tissues of collected cacti to verify the role of host association for the population dynamics. Our results support the existence of a hybrid zone due to secondary contact and limited to the localities where the two species are currently in contact. Furthermore, we detected asymmetric bidirectional introgression and the maintenance of the species integrity, ecological association, and morphological characters, suggesting selection and limited introgression. Considering our paleomodels, probably this hybrid zone is recent and the contact occurred during the Holocene to the present-day, favored by range expansion of their populations due to expansion of open and dry areas in eastern South America during palaeoclimatic and geomorphological events.</p>
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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.