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Fig. 2 in Investigation of Bartonella spp. in brazilian mammals with emphasis on rodents and bats from the Atlantic Forest
Fig. 2. Phylogenetic relationships within the Bartonella genus based on the groEL gene. The tree was inferred by using the Maximum Likelihood (ML) and Bayesian inference (BI) with the HKY + I + G model. The nodal support is described at the left by bootstrap replicates and at the right by posterior probability to each node represented. The symbol of one asterisk (*) indicates low nodal support in ML or BI, and the symbol of two asterisk (**) indicates incongruence between ML and BI. The sequences detected in the present study are described in red and the sequences of previous studies of Brazilian genotypes in blue. The highlighted clades represented the genotypes described to Brazil. The clade E, F and G represent the genotypes obtained in this study. Brucella abortus and Ca. Tokpelaia hoelldoblerii was used as an outgroup. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3 in Investigation of Bartonella spp. in brazilian mammals with emphasis on rodents and bats from the Atlantic Forest
Fig. 3. Phylogenetic relationships within the Bartonella genus based on the ftsZ gene. The tree was inferred by using the Maximum Likelihood (ML) and Bayesian inference (BI) with the GTR + I + G model. The nodal support is described at the left by bootstrap replicates and at the right by posterior probability to each node represented. The symbol of one asterisk (*) indicates low nodal support in ML or BI, and the symbol of two asterisk (**) indicates incongruence between ML and BI. The sequences detected in the present study are described in red and the sequences of previous studies of Brazilian genotypes in blue. The highlighted clades represented the genotypes described to Brazil. The clade H, I, J, K and L represent the genotypes obtained in this study. Brucella abortus and Ca. Tokpelaia hoelldoblerii was used as an outgroup. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Investigation of Bartonella spp. in brazilian mammals with emphasis on rodents and bats from the Atlantic Forest
Fig. 1. Phylogenetic relationships within the Bartonella genus based on the gltA gene. The tree was inferred by using the Maximum Likelihood (ML) and Bayesian inference (BI) with the GTR + I + G model. The nodal support is described at the left by bootstrap replicates and at the right by posterior probability to each node represented. The symbol of one asterisk (*) indicates low nodal support in ML or BI, and the symbol of two asterisk (**) indicates incongruence between ML and BI. The sequences detected in the present study are described in red and the sequences of previous studies of brazilian genotypes in blue. The highlighted clades represented the genotypes described to Brazil. The clade A, B, C and D represent the genotypes obtained in this study. Brucella abortus and Ca. Tokpelaia hoelldoblerii was used as an outgroup. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Figure 2 in Preliminary study of mosquitoes' diversity (Diptera: Culicidae) in tree holes in an Atlantic Forest reserve in Rio Grande do Norte, Brazil
Figure 2. Detailed steps of the collection. (a) Measurement of circumference with a tape measure. (b) Removal of water with an artisanal siphon. (c) Basin for sorting immatures. / Figura 2. Detalle de las etapas de recolección. (a) Medición de la circunferencia con cinta métrica. (b) Extracción del agua con sifón artesanal. (c) Recipiente para la clasificación de inmaduros.
Figure 1 in Preliminary study of mosquitoes' diversity (Diptera: Culicidae) in tree holes in an Atlantic Forest reserve in Rio Grande do Norte, Brazil
Figure 1. Location of the study area with identification of the states of Rio Grande do Norte and ParaÍba, municipality of Baia Formosa, area of the Mata Estrela Private Natural Heritage Reserve (RPPN) and transects of the investigated hollows. Sentinel-2 images and land use and land cover classes from MapBiomas were used. / Figura 1. Ubicación del área de estudio con la identificación de los estados de Rio Grande do Norte y ParaÍba, el municipio de Baia Formosa, el área de la RPPN Mata Estrela y los transectos de las cavidades investigadas se muestran utilizando imágenes del Sentinel-2 y las clases de uso y cobertura del suelo del MapBiomas.
Fig. 4 in Herpetofauna of Marechal Newton Cavalcanti Instruction Center, a hotspot Atlantic Forest fragment in Pernambuco, north-eastern Brazil
Fig. 4. Testudines, amphisbaenians, and crocodilians found in the Marechal Newton Cavalcanti Instruction Center Atlantic Forest fragment. (A) Phrynops geoffroanus (Schweigger, 1812); (B) Kinosternon scorpioides (Linneaus, 1766); (C) Mesoclemmys tuberculata (Lüederwalt, 1926); (D) Amphisbaena vermiculares (Wagler, 1824); (E) Amphisbaena alba (Liennaeus, 1758); (F) Caiman latirostris (Daudin, 1802); (G) Paleosuchus palpebrosus (Cuvier, 1807). Photos: M.A. Freitas.
Fig. 7 in Herpetofauna of Marechal Newton Cavalcanti Instruction Center, a hotspot Atlantic Forest fragment in Pernambuco, north-eastern Brazil
Fig. 7. Comparative evaluation of the sampling methods for anurans and reptiles recorded at Marechal Newton Cavalcanti Instruction Center (CMNIC) Atlantic Forest fragment, from August 2008 through December 2009.
Fig. 3 in Herpetofauna of Marechal Newton Cavalcanti Instruction Center, a hotspot Atlantic Forest fragment in Pernambuco, north-eastern Brazil
Fig. 3. Additional anuran species found in the Marechal Newton Cavalcanti Instruction Center Atlantic Forest fragment. (A) Boana crepitans (Wied-Neuwied, 1824); (B) Leptodactylus troglodytes (A. Lutz, 1926); (C) Leptodactylus natalensis (A. Lutz, 1930); (D) Dendropsophus branneri (Cochran, 1948); (E) Boana faber (Wied-Neuwied, 1821); (F) Boana raniceps (Cope, 1862); (G) Boana semilineatus (Spix, 1824); (H) Boana albomarginatus (Spix, 1824); (I) Leptodactylus latrans (Linneaus, 1758); (J) Leptodactylus marmoratus (Steindachner, 1867); (K) Leptodactylus mystacinus (Burmeister, 1861); (L) Leptodactylus fuscus (Schneider, 1799); (M) Leptodactylus vastus (A. Lutz, 1930); (N) Physalaemus cuvieri (Cruz and Pimenta, 2004); (O) Dendropsophus haddadi (Bastos and Pombal, 1996); (P) Dendropsophus minutus (Peters, 1872). Photos: M.A. Freitas.
Fig. 2 in Herpetofauna of Marechal Newton Cavalcanti Instruction Center, a hotspot Atlantic Forest fragment in Pernambuco, north-eastern Brazil
Fig. 2. Anuran species found in the Marechal Newton Cavalcanti Instruction Center Atlantic Forest fragment. (A) Phyllodytes gyrinaethes (Peixoto, Caramaschi, and Freire, 2003); (B) Phyllodytes edelmoi (Peixoto, Caramaschi, and Freire, 2003); (C) Phyllodytes luteolus (Wied-Neuwied, 1824); (D) Pristimantis ramagii (Boulenger, 1888); (E) Pithecopus nordestinus (Caramaschi, 2006); (F) Dendropsophus elegans (Wied-Neuwied, 1824); (G) Scinax cretatus (Nunes and Pombal, 2011); (H) Scinax eurydice (Bokermann, 1968); (I) Scinax x-signatus (Spix, 1824); (J) Dermatonotus muelleri (Boettger, 1885); (K) Elachistocleis ovalis (Schneider, 1799); (L) Stereocyclops incrassatus (Cope, 1870). Photos: M.A. Freitas.
Fig. 1 in Herpetofauna of Marechal Newton Cavalcanti Instruction Center, a hotspot Atlantic Forest fragment in Pernambuco, north-eastern Brazil
Fig. 1. Atlantic Forest fragment of Marechal Newton Cavalcanti Instruction Center (CIMNIC), Pernambuco, Northeastern Brazil. A few other Ecological Reserves located in Pernambuco State, as well as other states in Northeastern Brazil, are also shown.
Fig. 6 in Herpetofauna of Marechal Newton Cavalcanti Instruction Center, a hotspot Atlantic Forest fragment in Pernambuco, north-eastern Brazil
Fig. 6. Snakes species found in the Marechal Newton Cavalcanti Instruction Center Atlantic Forest fragment. (A) Boa constrictor (Linneaus, 1758); (B) Epicrates cenchria (Linneaus, 1758); (C) Chironius flavolineatus (Jan, 1863); (D) Dendrophidion atlantica (Freire, Caramaschi, and Gonçalves, 2010); (E) Spilotes pullatus (Linneaus, 1758); (F) Tantilla melanocephala (Linneaus, 1758); (G) Erythrolamprus almadensis (Wagler, 1824); (H) Erythrolamprus poecilogyrus (Wied-Neuwied, 1825); (I) Erythrolamprus viridis (Wagler, 1824); (J) Helicops angulatus (Linneaus, 1758); (K) Oxybelis aeneus (Wagler, 1824); (L) Oxyrhopus petolarius (Linneaus, 1758); (M) Oxyrhopus trigeminus (Duméril, Bibron, and Dumeril, 1854); (N) Philodryas olferssi (Lichtenstein, 1823); (O) Philodryas patagoniensis (Girard, 1825); (P) Sibynomorphus neuwiedi (Ihering, 1911); (Q) Siphlophis compressus (Daundin, 1803); (R) Xenodon merremii (Wagler, 1824); (S) Thamnodynastes pallidus (Linneaus, 1758); (T) Micrurus leminiscatus (Linneaus, 1758); (U) Micrurus ibiboboca (Merrem, 1820); (V) Amerotyphlops brongersmianus (Vanzolini, 1976); (W) Crotalus durissus (Linneaus, 1758); (X) Lachesis muta (Linneaus, 1766). Photos: M.A. Freitas.
Fig. 5 in Herpetofauna of Marechal Newton Cavalcanti Instruction Center, a hotspot Atlantic Forest fragment in Pernambuco, north-eastern Brazil
Fig. 5. Lacertid species found in the Marechal Newton Cavalcanti Instruction Center Atlantic Forest fragment. (A) Enyalius catenatus (Wied-Neuwied, 1821); (B) Gymnodactylus aff. darwinii (Gray, 1845); (C) Norops fuscoauratus (D'Orbigny, 1837); (D) Tropidurus hispidus (Spix, 1825); (E) Tropidurus semitaeniatus (Spix, 1825); (F) Ameiva ameiva (Linneaus, 1758); (G) Ameivula ocellifera (Spix, 1825); (H) Salvator merianae (Dumeril and Bíbron, 1839); (I) Kentropyx calcarata (Spix, 1825); (J) Cercosaura ocellata (Weagler, 1830); (K) Hemidactylus mabouia (Moreau de Jonnés, 1818); (L) Iguana iguana (Linneaus, 1758); (M) Coleodactylus meridionalis (Boulenger, 1888); (N) Polychrus marmoratus (Linneaus, 1758); (O) Strobilurus torquatus (Wiegmann, 1834). Photos: M.A. Freitas.
Fig. 2 in Seasonal parasitism of the leaf-cutting ant Atta sexdens Linnaeus (Hymenoptera: Formicidae) by phorid flies (Diptera: Phoridae) in a Brazilian Cerrado-Atlantic Forest ecotone
Fig. 2. Correlation between temperature and the number of leaf-cutting ants Atta sexdens parasitized by Apocephalus attophilus (r = −0.722; df = 9; P <0.05).
Fig. 1 in Seasonal parasitism of the leaf-cutting ant Atta sexdens Linnaeus (Hymenoptera: Formicidae) by phorid flies (Diptera: Phoridae) in a Brazilian Cerrado-Atlantic Forest ecotone
Fig. 1. Number of leaf-cutting ants Atta sexdens parasitized by Apocephalus attophilus and Eibesfeldtphora tonhascai in a Brazilian Cerrado-Atlantic Forest ecotone. The seasons are as follows: spring (Sep–Nov), summer (Dec–Feb), fall (Mar–May), and winter (Jun–Aug).
Fig. 3 in Composition and structure of the helminth community of rodents in matrix habitat areas of the Atlantic forest of southeastern Brazil
Fig. 3. Bipartite plot of the interactions between the mammal hosts and the helminth parasites identified in the present study.
Fig. 2 in Composition and structure of the helminth community of rodents in matrix habitat areas of the Atlantic forest of southeastern Brazil
Fig. 2. Species accumulation curve of the helminths recorded in each mammalian host: a. Akodon cursor b. Mus musculus c. Necromys lasiurus.
Fig. 1 in Composition and structure of the helminth community of rodents in matrix habitat areas of the Atlantic forest of southeastern Brazil
Fig. 1. Location of the sampling sites within the REBIO Poço das Antas and the APA-BRSJ in Rio de Janeiro state (RJ), southeastern Brazil, showing the distribution of the different vegetation types and the canals that separate the two reserves.
Fig. 5 in Small mammals in high fragmented landscape in Cerrado/ Atlantic Forest ecotone, Southeastern Brazil
Fig. 5. Diagram of ordering of species of small mammals and environmental variables in the 24 small forest fragments in southeastern Brazil, produced by canonical correspondence analysis. The Acronyms represent "uc" to understory closure, "co" to canopy openness, "ep" to epiphytism, "lia" to lianas, "ft" to cattle, "cs" to creeks and streams, "we" to wetlands, "se" to soil exposure, "ro" to rocky outcrop, "lit" to litter, "ab" to arthropod biomass, "vr" to vegetal richness, "va" to vegetal abudance, and "ath" to average tree height.
Fig. 1 in Small mammals in high fragmented landscape in Cerrado/ Atlantic Forest ecotone, Southeastern Brazil
Fig. 1. Location of the forest communities studied in 24 forest fragments located in southeastern Brazil. A description of individual forest fragments can be found in Supplementary Material Tab. A1.
Fig. 4 in Small mammals in high fragmented landscape in Cerrado/ Atlantic Forest ecotone, Southeastern Brazil
Fig. 4. Beta (β) diversity values for small mammals related to nesting (βsne), turnover (βsim) and general dissimilarity (βsor) in the 24 small forest fragments located in southeastern Brazil. The figures on the right represent the final percentage for each index.
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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.