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82 results for “Yunga”
Subspecies and Distribution. N. n. nasua Linnaeus, 1766 — French Guiana S through NE Brazil to N Bahia. N. n. dorsalis Gray, 1866 — Amazonian Brazil, Peru, and Ecuador. N. n. arcana Vieira, 1945 — Brazil (Mato Grosso), Bolivia (Santa Cruz), Paraguay, and N Argentina. N. n. boliviensis Cabrera, 1956 — Bolivia (Cochabamba, the Yungas). N. n. candace Thomas, 1912 — Colombia. N. n. anerascens Lonnberg, 1921 — N Argentina (Chaco). N. n. manium Thomas, 1912 — Ecuador W of the Andes. N. n. montana Tschudi, 1844 — Peru. N. n. quichua Thomas, 1901 — S Ecuadorian Andes (Azuay). N. n. solitaria Schinz, 1821 — SE Brazil (Minas Gerais, S. Bahia), NE Argentina (Misiones). N. n. spadicea Olfers, 1818 — S Brazil and Uruguay. N. n. vittata Tschudi, 1844 — Venezuela, the Guianas. in Procyonidae
Subspecies and Distribution. N. n. nasua Linnaeus, 1766 — French Guiana S through NE Brazil to N Bahia. N. n. dorsalis Gray, 1866 — Amazonian Brazil, Peru, and Ecuador. N. n. arcana Vieira, 1945 — Brazil (Mato Grosso), Bolivia (Santa Cruz), Paraguay, and N Argentina. N. n. boliviensis Cabrera, 1956 — Bolivia (Cochabamba, the Yungas). N. n. candace Thomas, 1912 — Colombia. N. n. anerascens Lonnberg, 1921 — N Argentina (Chaco). N. n. manium Thomas, 1912 — Ecuador W of the Andes. N. n. montana Tschudi, 1844 — Peru. N. n. quichua Thomas, 1901 — S Ecuadorian Andes (Azuay). N. n. solitaria Schinz, 1821 — SE Brazil (Minas Gerais, S. Bahia), NE Argentina (Misiones). N. n. spadicea Olfers, 1818 — S Brazil and Uruguay. N. n. vittata Tschudi, 1844 — Venezuela, the Guianas.
FIGURE 2 in Paraboeremia yungensis sp. nov., a new fungal species isolated from Las Yungas, South America, with promising tyrosinase production potential
FIGURE 2. Paraboeremia yungensis (LY 38.7). a. Colony on OA (front and reverse). b. Colony on MEA (front and reverse). c. Colony on PDA (front and reverse). d. Scanning electron micrograph of mature pycnidium with subtending mycelium developed on OA. e. Scanning electron micrograph of conidia covered with a mucilaginous sheath. f. Pycnidium. g. Conidiogenous cells and conidia. h. Conidia with polar guttules. Scale bars (d,f) 25 μm, (g,h) 2 μm, (e) 1 μm.
FIGURE 1 in Paraboeremia yungensis sp. nov., a new fungal species isolated from Las Yungas, South America, with promising tyrosinase production potential
FIGURE 1. Cladogram obtained using RAxML to analyse the concatenated DNA sequence data of ITS, LSU, RPB2, and TUB2. The phylogenetic position of Paraboeremia yungensis is shown in blocks. Group support values are presented above the branches (ML bootstrap values/Bayesian posterior probabilities). Vacuiphoma bulgarica (CBS 357.84) was used as outgroup for rooting the tree in all the analyses.
Distribution. Known only from upper montane forests of Manu National Park and Biosphere Reserve, Cusco Depart ment, S Peru; it could also occur in Yungas of Bolivia. in Phyllostomidae
Distribution. Known only from upper montane forests of Manu National Park and Biosphere Reserve, Cusco Depart ment, S Peru; it could also occur in Yungas of Bolivia.
Distribution. SE Bolivia (departments of Tarija and Santa Cruz), N Argentina (provinces of Jujuy, Salta, Formosa, and Chaco), Brazil (W of the Rio Parana— through the N of Mato Grosso State into SW Goias, and Mato Grosso do Sul states), and Paraguay (E of the Rio Paraguay as far as the mouth of the Rio Parana). Its range to the west in Bolivia is poorly known; it would seem that it is absent from the Bolivian Chaco as it is from the adjacent Paraguayan Chaco west of the Rio Paraguay. There is no evidence to date that the Yungas populations in SE Bolivia and NW Argentina are continuous with the population in Brazil and Paraguay to the E. in Cebidae
Distribution. SE Bolivia (departments of Tarija and Santa Cruz), N Argentina (provinces of Jujuy, Salta, Formosa, and Chaco), Brazil (W of the Rio Parana— through the N of Mato Grosso State into SW Goias, and Mato Grosso do Sul states), and Paraguay (E of the Rio Paraguay as far as the mouth of the Rio Parana). Its range to the west in Bolivia is poorly known; it would seem that it is absent from the Bolivian Chaco as it is from the adjacent Paraguayan Chaco west of the Rio Paraguay. There is no evidence to date that the Yungas populations in SE Bolivia and NW Argentina are continuous with the population in Brazil and Paraguay to the E.
On following pages: 4. Brazilian Lesser Long-nosed Armadillo (Dasypus septemcinctus); 5. Hairy Long-nosed Armadillo Armadillo (Dasypus hybridus). (Dasypus pilosus); 6. Yungas Lesser Long-nosed Armadillo (Dasypus mazzai); 7. Southern Long-nosed in Dasypodidae
On following pages: 4. Brazilian Lesser Long-nosed Armadillo (Dasypus septemcinctus); 5. Hairy Long-nosed Armadillo Armadillo (Dasypus hybridus). (Dasypus pilosus); 6. Yungas Lesser Long-nosed Armadillo (Dasypus mazzai); 7. Southern Long-nosed
On following pages: 526. Spy Hocicudo (Oxymycterus delator); 527. Atlantic Forest Hocicudo (Oxymycterus dosytrichos); 528. Quaestor Hocicudo (Oxymycterus quaeston; 529. Inca Hocicudo (Oxymyecterus inca); 530. Paramo Hocicudo (Oxymycterus paramensis); 531. Elfin Forest Hocicudo (Oxymycterus nigrifrons); 532. Upper Yungas Inca Hocicudo (Oxymycterus juliacae); 533. Small Yungas Hocicudo (Oxymycterus hiska); 534. Quechuan Hocicudo (Oxymycterus hucucha); 535. Mount Caparao Hocicudo (Oxymycterus caparoae); 536. Red Hocicudo (Oxymycterus rufus); 537. Darwin's Hocicudo (Oxymycterus nasutus); 538. Ravine Hocicudo (Oxymycterus wayku); 539. Cook's Hocicudo (Oxymycterus josel); 540. Common Cerrado Mouse (Thalpomys cerradensis); 541. Hairy-eared Cerrado Mouse (Thalpomys lasiotis); 542. Roraima Mouse (Podoxymys roraimae); 543. Blackish Grass Mouse (Thaptomys nigrita); 544. Ecuadorean Akodont (Necromys punctulatus); 545. Northern Akodont (Necromys urichi); 546. Hairy-tailed Akodont (Necromys lasiurus); 547. Pleasant Akodont (Necromys amoenus); 548. White-chinned Akodont (Necromys lactens), 549. Lillo's Akodont (Necromys lilloi); 550. Dark-furred Akodont (Necromys obscurus); 551. Kemp's Grass Mouse (Deltamys kempi); 552. Araucaria Grass Mouse (Deltamys araucaria); 553. Serra do Mar Grass Mouse (Castoria angustidens). in Cricetidae
On following pages: 526. Spy Hocicudo (Oxymycterus delator); 527. Atlantic Forest Hocicudo (Oxymycterus dosytrichos); 528. Quaestor Hocicudo (Oxymycterus quaeston; 529. Inca Hocicudo (Oxymyecterus inca); 530. Paramo Hocicudo (Oxymycterus paramensis); 531. Elfin Forest Hocicudo (Oxymycterus nigrifrons); 532. Upper Yungas Inca Hocicudo (Oxymycterus juliacae); 533. Small Yungas Hocicudo (Oxymycterus hiska); 534. Quechuan Hocicudo (Oxymycterus hucucha); 535. Mount Caparao Hocicudo (Oxymycterus caparoae); 536. Red Hocicudo (Oxymycterus rufus); 537. Darwin's Hocicudo (Oxymycterus nasutus); 538. Ravine Hocicudo (Oxymycterus wayku); 539. Cook's Hocicudo (Oxymycterus josel); 540. Common Cerrado Mouse (Thalpomys cerradensis); 541. Hairy-eared Cerrado Mouse (Thalpomys lasiotis); 542. Roraima Mouse (Podoxymys roraimae); 543. Blackish Grass Mouse (Thaptomys nigrita); 544. Ecuadorean Akodont (Necromys punctulatus); 545. Northern Akodont (Necromys urichi); 546. Hairy-tailed Akodont (Necromys lasiurus); 547. Pleasant Akodont (Necromys amoenus); 548. White-chinned Akodont (Necromys lactens), 549. Lillo's Akodont (Necromys lilloi); 550. Dark-furred Akodont (Necromys obscurus); 551. Kemp's Grass Mouse (Deltamys kempi); 552. Araucaria Grass Mouse (Deltamys araucaria); 553. Serra do Mar Grass Mouse (Castoria angustidens).
FIGURE 3 in Pholiota oblita, new species in sect. Adiposae stirps Subflammans (Strophariaceae, Agaricomycetes), from the Argentinean Yungas
FIGURE 3: A-Pholiota oblita [Niveiro 976b (CTES)]. Material designated as type, B-Pholiota subflammans [Singer M 180 (LIL)]: Material designated as neotype. Bar = 1 cm
FIGURE 4 in Pholiota oblita, new species in sect. Adiposae stirps Subflammans (Strophariaceae, Agaricomycetes), from the Argentinean Yungas
FIGURE 4: Distribution of P. oblita, P. subflammans, and P. baeosperma in Argentina. P. baeosperma is considered synonymous with P. subflammans. They have been shown separately only to exhibit that they share the same area of distribution.
FIGURE 1 in Pholiota oblita, new species in sect. Adiposae stirps Subflammans (Strophariaceae, Agaricomycetes), from the Argentinean Yungas
FIGURE 1: Pholiota oblita [Niveiro 976b (CTES)]: Microscopic characters: A —spores, B —basidia, C—pleurocystidia (chrysocystidia type), D—cheilocystidia. Bar = 10 µm.
Figure 4 in Vocal repertoire of two species of Oreobates Jiménez de la Espada, 1872 (Anura: Strabomantidae) of the Yungas Andean Forest, NW Argentina
Figure 4. Oscillogram and sound spectrogram of the encounter call of Oreobates barituensis from Arroyo La Loza, Jujuy province, Argentina. Recorded on 29 November 2008; air temperature during recording was 18.0◦C.
Figure 2 in Vocal repertoire of two species of Oreobates Jiménez de la Espada, 1872 (Anura: Strabomantidae) of the Yungas Andean Forest, NW Argentina
Figure 2. Oscillogram and sound spectrogram of the encounter call of Oreobates discoidalis from Jaire, Jujuy province, Argentina. Recorded on 14 November 2009; air temperature during recording was 17.4◦C.
Figure 1 in Vocal repertoire of two species of Oreobates Jiménez de la Espada, 1872 (Anura: Strabomantidae) of the Yungas Andean Forest, NW Argentina
Figure 1. Oscillogram and sound spectrogram of the advertisement call and territorial call of Oreobates discoidalis from Jaire, Jujuy province, Argentina. Recorded on 8 November 2009; air temperature during recording was 13.6◦C.
Figure 3 in Vocal repertoire of two species of Oreobates Jiménez de la Espada, 1872 (Anura: Strabomantidae) of the Yungas Andean Forest, NW Argentina
Figure 3. Oscillogram and sound spectrogram of the advertisement call and territorial call of Oreobates barituensis from Río Yerba Buena, Jujuy province, Argentina. Recorded on 1 December 2009; air temperature during recording was 21.1◦C.
FIGURE 4 in New records and distribution modeling of Gryne orensis (Sørensen) (Opiliones: Cosmetidae) support the Mesopotamian-Yungas disjunction in subtropical Argentina
FIGURE 4. Overlay of two binary MAXENT models, one built with the default dataset (45 points, AUC: 0.975), the second with record at Caimancito (a) deleted (44 points, AUC: 0.977); shared areas by the two models (overlap) are displayed in light red; areas lost with the smallest dataset are shown in dark red. Blue dots: training records, yellow dots in province of Chaco: tentative records at El Impenetrable (not used in this model).
FIGURE 3 in New records and distribution modeling of Gryne orensis (Sørensen) (Opiliones: Cosmetidae) support the Mesopotamian-Yungas disjunction in subtropical Argentina
FIGURE 3. Binary distribution models built with BIOCLIM (A) and MAXENT (B), showing the region around the Semiarid Chaco. Maps are overlaid to display changes of the default model (intense red) when points at El Impenetrable are added in the dataset (one at a time): light red, area added with Villa Río Bermejito (1); orange, area added with Las Hacheras (2); yellow, area added with Fuerte Esperanza (3). White dots: localities of the default dataset; blue dots: tentative records at El Impenetrable (numbers as referred to above). Crosses in 3A: localities sampled in the dry Chaco that yielded negative results for Mesopotamian harvestmen.
FIGURE 2 in New records and distribution modeling of Gryne orensis (Sørensen) (Opiliones: Cosmetidae) support the Mesopotamian-Yungas disjunction in subtropical Argentina
FIGURE 2. Potential distribution model of Gryne orensis: median values of the 20-replicates run with MAXENT (default dataset, random test percentage 20%); thresholds displayed are the average of the 20 replicates (average training AUC 0.9762). In the random selection of training points, Caimancito was used in 17/20 runs, Carandazinho in 14/20 runs. Suitability levels: green: 0.15–0.36; yellow: 0.36–0.58; orange: 0.58–0.72; red: above 0.72. Grey: areas below the default threshold (equal training sensitivity plus specificity); darker grey: suitability above 0.112 (maximum training sensitivity plus specificity); medium grey: above 0.0801 (minimum training presence). Blue dots: training records; red dots in province of Chaco: tentative records at El Impenetrable (not used in this model).
FIGURE 1 in New records and distribution modeling of Gryne orensis (Sørensen) (Opiliones: Cosmetidae) support the Mesopotamian-Yungas disjunction in subtropical Argentina
FIGURE 1. Locality records (red dots) and predicted distribution of Gryne orensis built with the default dataset (n=45). Map displays the overlay of models obtained with BIOCLIM (green; true-false, full extension) and MAXENT (light blue; single run, binary), overlapping areas in dark blue. White outline: Humid Chaco and Paraná flooded savanna; grey outline: Pantanal (ecoregions according to Olson et al. 2001). Selected localities: a. Caimancito, b. Carandazinho, c. Posadas, d. Vuelta de Obligado, e. Villa Constitución-Villa del Medio-San Nicolás, f. Santa Fe (2 points)-Madrejón Don Felipe, g. Riacho de Oro (type locality), h. El Colorado, i. Pirané. Yellow dots in province of Chaco indicate the three tentative localities for El Impenetrable: Villa Río Bermejito (1), Las Hacheras (2) and Fuerte Esperanza (3).
FIGURE 8 in A new species of long-tailed mouse, genus Oligoryzomys Bangs, 1900 (Rodentia: Cricetidae), from the Bolivian Yungas
FIGURE 8. Dorsal and ventral, views of the skin of Oligoryzomys pachecoi n. sp. (Holotype, MSB 67304). Scale bar 5 cm.
FIGURE 7 in A new species of long-tailed mouse, genus Oligoryzomys Bangs, 1900 (Rodentia: Cricetidae), from the Bolivian Yungas
FIGURE 7. Dorsal, ventral, and lateral views of the skull, and lateral view of the mandible of Oligoryzomys pachecoi n. sp. (Holotype, MSB 67304). Scale bar 10 mm.
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