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226 results for “Pantanal”
Figs. 11A-H. A-D in PLântuLAs e sementes de mAcrófitAs AquáticAs de LAGoAs do PAntAnAL SuL-MAto-Grossense
Figs. 11A-H. A-D. Victoria amazônica. A. planta; B. plântula, b. limbo com espinhos; C, c. diásporo; D. semente com arilo gelatinoso; d. semente. E-H. Oxycaryum cubense. E. planta; F. plântula; G. inflorescência; H. semente. Barras: Figs. B, b, C, c, D, d = 1 cm; Fig. H = 1 mm.
Figs. 4A-H. A-D. Polygonum punctatum. A in PLântuLAs e sementes de mAcrófitAs AquáticAs de LAGoAs do PAntAnAL SuL-MAto-Grossense
Figs. 4A-H. A-D. Polygonum punctatum. A. planta; B. plântula; C. botão floral com pontuações; D. semente. E-H. Pontederia parviflora. E. planta; F. plântula; G. diásporo; H. semente. Barras: Figs. B, F = 1 cm; Figs. D, G. = 2 mm; Fig. H = 1 mm.
Figs. 7A-H. A-D. Sagittaria guayanensis. A in PLântuLAs e sementes de mAcrófitAs AquáticAs de LAGoAs do PAntAnAL SuL-MAto-Grossense
Figs. 7A-H. A-D. Sagittaria guayanensis. A. planta; B, b. plântula; C. diásporo; D. semente. E-H. Limnobium laevigatum. E. planta com estolões unindo vários indivíduos; F, f. plântula; G, g. diásporo; H, h. semente. Barras: Figs. B, F, f = 1cm; Figs. C, H = 1 mm; Fig. D = 500 μm; Fig. G = 5 mm; Fig. h = 2 mm.
Figs. 1A-H. A-D. Pistia stratiotes. A in PLântuLAs e sementes de mAcrófitAs AquáticAs de LAGoAs do PAntAnAL SuL-MAto-Grossense
Figs. 1A-H. A-D. Pistia stratiotes. A. planta com estolão ligado à plântula, a. flor; B. plântula; C. diásporo; D. semente. E-H. Bacopa australis. E. planta; F. plântula; G. sementes dentro do diásporo, g. diásporo; H. semente. Barras: Figs. A, a, B, C, E, F = 1 cm; Fig. D = 1 mm; Figs. G, g = 2 mm; Fig. H = 200 μm.
Figure 1 in First record of leucism in Megaceryle torquata (Coraciiformes: Alcedinidae) in Pantanal, Brazil
Figure 1. Leucistic individual of Megaceryle torquata recorded on the banks of the São Lourenço river, Poconé - MT. Photo: Diego Velloso do Carmo, 2019. Partial leucistic (left) and normal (rigth) for comparison.
Figure 6. Response curve showing how each environmental variable affected the Maxent prediction. Variables A, B in PhylOgeOgraphy and pOtential distributiOn OF Sturnira lilium and S. giannae (ChirOptera: PhyllOstOmidae) With range eXtensiOn FOr S. giannae in the CerradO and Pantanal biOmes
Figure 6. Response curve showing how each environmental variable affected the Maxent prediction. Variables A, B, and C were the ones that most affected the potential distribution of S. giannae, and D, E, and F most affected the potential distribution of S. lilium. The curves show the average response of the 10 replicate Maxent runs (red) and the standard deviation (blue).
Figure 2 in PhylOgeOgraphy and pOtential distributiOn OF Sturnira lilium and S. giannae (ChirOptera: PhyllOstOmidae) With range eXtensiOn FOr S. giannae in the CerradO and Pantanal biOmes
Figure 2. Detail of the teeth in S. lilium (A and D – MN 82228) and S. giannae (B and E – MN 84766, C and F – MN 82217). The shape of the upper internal incisor unicuspid in S. lilium (A) and unicuspid or bicuspid in S. giannae (respectively B, C). Metaconid of first inferior molar (m1) wide mesodistally and short cervico-occlusal (D, E, and F). Metaconid of second inferior molar (m2) large mesodistally in S. lilium (D) and in S. giannae (F), or short mesodistally and long cervico-occlusally (E) in S. giannae. Scale bars: 1 mm.
Figure 4 in PhylOgeOgraphy and pOtential distributiOn OF Sturnira lilium and S. giannae (ChirOptera: PhyllOstOmidae) With range eXtensiOn FOr S. giannae in the CerradO and Pantanal biOmes
Figure 4. Map showing the distribution and location of analyzed samples of S. giannae in gray circles and blue boundaries, and of S. lilium in black circles and green boundaries. The blue star is the type locality of S. giannae, and the green star is the type locality of S. lilium. The dotted black line marks the extent of S. giannae 's territory in Brazil: Mato Grosso State (1) Barão de Melgaço, and Maranhão State (2) Alto Parnaíba. Other localities are in the Appendix 1.
Figs. 1–10 in Two new species of Trichomyia Haliday 1839 (Diptera, Psychodidae, Trichomyiinae) from the Pantanal of Mato Grosso, Brazil
Figs. 1–10. Trichomyia lamasi sp. nov. 1. Head; 2. Left wing; 3. Palpus; 4. Arm of gonocoxite; 5. Male terminalia, lateral; 6. Scape, pedicel and basal flagellomeres; 7. Aedeagus and parameres, dorsal; 8. Parameres, ventral view; 9. Male terminalia, dorsal; 10. Cerci, epandrium and hypropoct (abbreviations: aed = aedeagus, ag = arm of gonocoxite, bri = gonocoxal bridge, cer = cercus, gst = gonostylus, hyp = hypoproct, pm = paramere, she = parameral sheath).
Figs. 11–19 in Two new species of Trichomyia Haliday 1839 (Diptera, Psychodidae, Trichomyiinae) from the Pantanal of Mato Grosso, Brazil
Figs. 11–19. Trichomyia pantanensis sp. nov. 11. Head; 12. Left wing; 13. Last flagellomeres, 14. Palpus; 15. Male terminalia, lateral; 16. Parameres and aedeagus; 17. Scape, pedicel and basal flagellomeres; 18. Cerci, epandrium and hypropoct; 19. Male terminalia, dorsal (abbreviations:aed = aedeagus, cer = cercus, gst = gonostylus, hyp = hypoproct, il = internal lobe, pm = paramere).
Figure 10 in The SISBIOTA-Diptera Brazilian Network: A long-term survey of Diptera from unexplored Brazilian Western Arc of Amazon, Cerrado, and Pantanal
Figure 10 Comparison of species richness rankings of the top 10 families collected and identified of Mato Grosso, Mato Grosso do Sul, Rondônia, the three states combined, and Brazil. Horizontal lines and bars represent equal ranking; each family is represented by a different color.
Figure 7 in The SISBIOTA-Diptera Brazilian Network: A long-term survey of Diptera from unexplored Brazilian Western Arc of Amazon, Cerrado, and Pantanal
Figure 7 Diversity of genera in each Diptera family in the material collected and identified of the three states combined (Mato Grosso, Mato Grosso do Sul, and Rondônia) in the SISBIOTA-Diptera.
Figure 13 in The SISBIOTA-Diptera Brazilian Network: A long-term survey of Diptera from unexplored Brazilian Western Arc of Amazon, Cerrado, and Pantanal
Figure 13 Number of articles resulting from the SISBIOTA-Diptera published between 2012 and 2022 (2023 is still in course, so it was not included in the graph).
Figure 12 in The SISBIOTA-Diptera Brazilian Network: A long-term survey of Diptera from unexplored Brazilian Western Arc of Amazon, Cerrado, and Pantanal
Figure 12 Number of articles per Diptera families resulting from the SISBIOTA-Diptera published between the first publication in 2012 and 2022.
Figure 4 in The SISBIOTA-Diptera Brazilian Network: A long-term survey of Diptera from unexplored Brazilian Western Arc of Amazon, Cerrado, and Pantanal
Figure 4 Mist net for trapping and examining bats for collecting bat flies (Streblidae). (a) setting up a mist net in a flooded area in the Pantanal, in Poconé, Mato Grosso; (b) mist net set on the flooded area, indicated with red arrows, in Poconé, Mato Grosso; (c) mist net set on drier area, in the Pantanal, in Corumbá, Mato Grosso do Sul; (d) Noctilio albiventris Desmarest, 1818 (Chiroptera: Noctilionidae) trapped with mist net and examined for bat flies, in Corumbá, Mato Grosso do Sul.
Figure 3 in The SISBIOTA-Diptera Brazilian Network: A long-term survey of Diptera from unexplored Brazilian Western Arc of Amazon, Cerrado, and Pantanal
Figure 3 Different types of Malaise traps installed in various sampling sites. (a) in a dry, open area of vegetation in Poconé, Mato Grosso; (b) in a shaded area in open vegetation in Porto Murtinho, Mato Grosso; (c) in a shaded area of forest along a stream in Cacaulândia, Rondônia; (d) in a shaded area of forest in Cacaulândia, Rondônia; (e) classic Malaise trap supported by a metallic structure set up in rocky formation with shrubby vegetation in Chapada dos Guimarães, Mato Grosso; (f) six-meter-long Malaise trap in open vegetation in Poconé, Mato Grosso; (g) six-meter-long Malaise trap in open vegetation in Porto Murtinho, Mato Grosso do Sul.
Figure 2 in The SISBIOTA-Diptera Brazilian Network: A long-term survey of Diptera from unexplored Brazilian Western Arc of Amazon, Cerrado, and Pantanal
Figure 2 Collecting techniques used in the SISBIOTA-Diptera long-term survey. (a) CDC light trap; (b) manual collecting of cecidomyiid galls; (c) drift net; (d–e) classic light trap, with a white vertical sheet and different types of lights; (f–g) McPhail trap, filled with fermented fruit; (h) yellow and white pan traps near temporary ponds; (i) Pennsylvania light trap; (j) Shannon trap, baited with pieces of rotten fish or chicken; (k–m) three different types of Van Sommeren-Rydon (also known as Nymphalidae butterfly trap), modified to collect flies, baited with fermented fruit or decomposing fish; (n) net sweeping of vegetation.
Figure 14 in The SISBIOTA-Diptera Brazilian Network: A long-term survey of Diptera from unexplored Brazilian Western Arc of Amazon, Cerrado, and Pantanal
Figure 14 Outreach pamphlet of the SISBIOTA-Diptera, produced in 2015, highlighting the main results of 11 out of over 60 families reported from the material collected during the project.
Figure 8 in The SISBIOTA-Diptera Brazilian Network: A long-term survey of Diptera from unexplored Brazilian Western Arc of Amazon, Cerrado, and Pantanal
Figure 8 Diversity of species in each Diptera family in the material collected and identified of the three states combined (Mato Grosso, Mato Grosso do Sul, and Rondônia) in the SISBIOTA-Diptera.
Figure 6 in The SISBIOTA-Diptera Brazilian Network: A long-term survey of Diptera from unexplored Brazilian Western Arc of Amazon, Cerrado, and Pantanal
Figure 6 Diptera collected in the SISBIOTA-Diptera,habitus. (a) Tabanus importunus Wiedemann, 1828 (Tabanidae), female, Bodoquena, MS; (b) Rachicerus carrerai Pujol-Luz, 2019 (Xylophagidae), male, Bodoquena, MS; (c) Chrysotus sp. (Dolichopodidae), male, Corumbá, MS; (d) Empidini (Empididae), male, Corumbá, MS; (e) Eudorylas sp. (Pipunculidae), male, Corguinho, MS; (f) Palpada scutellaris (Fabricius, 1805) (Syrphidae), female, Porto Velho, RO; (g) Gaurax sp. (Chloropidae), male, Chapada dos Guimarães, MT; (h) Physegenua sp. (Lauxaniidae), male, Aquidauana, MS; (i) Glyphidops etele Aczél, 1961 (Neriidae), female, Cacaulândia, RO; (j) Phytobia cacaulandia Sousa & Couri, 2018 (Agromyzidae), male, Cacaulândia, RO; (k) Ropalomera sp. (Ropalomeridae), female, Chapada dos Guimarães, MT; (l) Pterocalla sp. (Ulidiidae), male, Porto Murtinho, MS; (m) Senopterina macularis (Fabricius, 1805) (Platystomatidae), male, Bodoquena, MS; (n) Trupanea bonariensis (Brèthes, 1908) (Tephritidae), female, Aquidauana, MS; (o) Noctiliostrebla morena Alcantara, Graciolli & Nihei, 2019 (Streblidae), male, Corumbá, MS; (p) Fannia heydenii (Wiedemann, 1830) (Fanniidae), female, Bodoquena, MS; (q) Polietina prima (Couri & Machado, 1990) (Muscidae), female, Cacaulândia, RO; (r) Chloroprocta idioidea (Robineau-Desvoidy, 1830) (Calliphoridae), male, Cacaulândia, RO; (s) Mesembrinella randa (Walker, 1849) (Mesembrinellidae), male, Monte Negro, RO; (t) Helicobia chapadensis Tibana & Lopes, 1984 (Sarcophagidae), male, Chapada dos Guimarães, MT; (u) Euepalpus flavicauda Townsend, 1908 (Tachinidae), male, Aquidauna, MS. Scale bar = 1 mm.
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