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14 results for “Tonatia”
On following pages: 26. Striped Hairy-nosed Bat (Gardnerycteris crenulatum); 27. Keenan's Hairy-nosed Bat (Gardnerycteris keenani); 28. Koepcke's Hairy-nosed Bat (Gardnerycteris koepckeae); 29. Kalko's Round-eared Bat (Lophostoma kalkoae); 30. Pygmy Round-eared Bat (Lophostoma brasiliense); 31. Carriker's Round-eared Bat (Lophostoma carrikeri); 32. Schulz's Round-eared Bat (Lophostoma schulzi); 33. Western Round-eared Bat (Lophostoma occidentale); 34. Davis's Round-eared Bat (Lophostoma evotis); 35. White-throated Round-eared Bat (Lophostoma silvicola); 36. Greater Round-eared Bat (Tonatia bidens); 37. Stripe-headed Round-eared Bat (Tonatia saurophila); 38. Pale-faced Bat (Phylloderma stenops); 39. Pale Spearnosed Bat (Phyllostomus discolon; 40. Lesser Spearnosed Bat (Phyllostomus elongatus); 41. Greater Spearnosed Bat (Phyllostomus hastatus); 42. Guianan Spearnosed Bat (Phyllostomuslatifolius); 43. Woolly False Vampire Bat (Chrotopterus auritus); 44. Southern Golden Bat (Mimon bennett); 45. Cozumelan Golden Bat (Mimon cozumelae); 46. Spectral Bat (Vampyrum spectrum). in Phyllostomidae
On following pages: 26. Striped Hairy-nosed Bat (Gardnerycteris crenulatum); 27. Keenan's Hairy-nosed Bat (Gardnerycteris keenani); 28. Koepcke's Hairy-nosed Bat (Gardnerycteris koepckeae); 29. Kalko's Round-eared Bat (Lophostoma kalkoae); 30. Pygmy Round-eared Bat (Lophostoma brasiliense); 31. Carriker's Round-eared Bat (Lophostoma carrikeri); 32. Schulz's Round-eared Bat (Lophostoma schulzi); 33. Western Round-eared Bat (Lophostoma occidentale); 34. Davis's Round-eared Bat (Lophostoma evotis); 35. White-throated Round-eared Bat (Lophostoma silvicola); 36. Greater Round-eared Bat (Tonatia bidens); 37. Stripe-headed Round-eared Bat (Tonatia saurophila); 38. Pale-faced Bat (Phylloderma stenops); 39. Pale Spearnosed Bat (Phyllostomus discolon; 40. Lesser Spearnosed Bat (Phyllostomus elongatus); 41. Greater Spearnosed Bat (Phyllostomus hastatus); 42. Guianan Spearnosed Bat (Phyllostomuslatifolius); 43. Woolly False Vampire Bat (Chrotopterus auritus); 44. Southern Golden Bat (Mimon bennett); 45. Cozumelan Golden Bat (Mimon cozumelae); 46. Spectral Bat (Vampyrum spectrum).
Figure 3 in The bat Tonatia bidens (Phyllostomidae) as an insect pest predator in the Brazilian Caatinga
Figure 3: Temporal distribution of insect remains preyed upon by Tonatia bidens in the Brazilian Caatinga. (A) Richness, number of insect remains, and monthly rainfall recorded in each sampled month. (B) Richness and number of insect remains in the dry (September and October 2016, March and August 2017) and rainy (May and November 2022) seasons, considering all data gathered. Rainfall data from https://www.apac.pe.gov. br.
Figure 1 in The bat Tonatia bidens (Phyllostomidae) as an insect pest predator in the Brazilian Caatinga
Figure 1: Abundance of remains of different lepidopteran taxa sampled under feeding perches of the bat Tonatia bidens, in the Brazilian Caatinga. Data collected in September and October 2016, March and August 2017, and May and November 2022. Undet. = undetermined. Lepidopteran silhouettes were used under CC0 1.0 license (www.phylopic.org).
Figure 2 in The bat Tonatia bidens (Phyllostomidae) as an insect pest predator in the Brazilian Caatinga
Figure 2: Abundance of remains of different coleopteran taxa sampled under feeding perches of the bat Tonatia bidens, in the Brazilian Caatinga. Data collected in September and October 2016, March and August 2017, and May and November 2022. Coleopteran silhouettes were used under CC0 1.0 license (www.phylopic.org).
Figure 7 from: Basantes M, Tinoco N, Velazco PM, Hofmann MJ, Rodríguez-Posada ME, Camacho MA (2020) Systematics and Taxonomy of Tonatia saurophila Koopman & Williams, 1951 (Chiroptera, Phyllostomidae). ZooKeys 915: 59-86. https://doi.org/10.3897/zookeys.915.46995
Figure 7 Geographic distribution of Tonatia saurophila†, T. bakeri, and T. maresi. Map of Central and South America showing the geographical distribution of T. saurophila† (subfossil records, Jamaica, type locality), T. bakeri, and T. maresi. Modified from Williams and Genoways (2008), and based on the localities of the specimens included in this study.
Figure 6 from: Basantes M, Tinoco N, Velazco PM, Hofmann MJ, Rodríguez-Posada ME, Camacho MA (2020) Systematics and Taxonomy of Tonatia saurophila Koopman & Williams, 1951 (Chiroptera, Phyllostomidae). ZooKeys 915: 59-86. https://doi.org/10.3897/zookeys.915.46995
Figure 6 Phylogenetic relationships within Tonatia based on Maximum-likelihood derived from the analyses of the RAG2 exon (top) and Cyt-b gene (below). Both consensus trees depict three strongly supported clades: T. bidens, T. s. bakeri, and T. s. maresi. The support of each node is represented by the values of posterior probability (PP) and bootstrap (BS), in the phylogeny only the values of PP < 0.90 and BS < 70 are presented. Nodal support is represented by posterior probabilities (<0.90), and bootstrap values (<70).
Figure 5 from: Basantes M, Tinoco N, Velazco PM, Hofmann MJ, Rodríguez-Posada ME, Camacho MA (2020) Systematics and Taxonomy of Tonatia saurophila Koopman & Williams, 1951 (Chiroptera, Phyllostomidae). ZooKeys 915: 59-86. https://doi.org/10.3897/zookeys.915.46995
Figure 5 Differences in the dorsal pelage between Tonatia bakeri and T. maresi. Dorsal view of the body in aT. bakeri (QCAZ 9234) showing lighter and uniform colored pelage, and bT. maresi (QCAZ 15498) showing darker pelage and patches of hair with reddish tips.
Figure 3 from: Basantes M, Tinoco N, Velazco PM, Hofmann MJ, Rodríguez-Posada ME, Camacho MA (2020) Systematics and Taxonomy of Tonatia saurophila Koopman & Williams, 1951 (Chiroptera, Phyllostomidae). ZooKeys 915: 59-86. https://doi.org/10.3897/zookeys.915.46995
Figure 3 Illustrations showing the differences of the posterior edge of the cranium and the mandibular condyle between Tonatia bakeri and T. maresi. In the dorsal view of the skull, arrows point to the posterior border of the cranium in aT. bakeri and bT. maresi. In the occlusal view of the mandible, arrows point the mandibular condyle of cT. bakeri and dT. maresi.
Figure 2 from: Basantes M, Tinoco N, Velazco PM, Hofmann MJ, Rodríguez-Posada ME, Camacho MA (2020) Systematics and Taxonomy of Tonatia saurophila Koopman & Williams, 1951 (Chiroptera, Phyllostomidae). ZooKeys 915: 59-86. https://doi.org/10.3897/zookeys.915.46995
Figure 2 Discriminant Function Analysis of six morphometric groups. Projection of 137 specimens of Tonatia saurophila, assembled in six groups according to their localities of origin: western Colombia and Ecuador (squares); eastern Colombia, Ecuador, and Peru (diamonds); Caribbean of Colombia and Venezuela (circles); Guyana, French Guiana, and northeastern Brazil (ovals); Central America (crosses); and Trinidad and Tobago (triangles), on DF1 and DF2 of a Discriminant Function Analysis with 21 morphometric cranio-dental and external variables.
Figure 4 from: Basantes M, Tinoco N, Velazco PM, Hofmann MJ, Rodríguez-Posada ME, Camacho MA (2020) Systematics and Taxonomy of Tonatia saurophila Koopman & Williams, 1951 (Chiroptera, Phyllostomidae). ZooKeys 915: 59-86. https://doi.org/10.3897/zookeys.915.46995
Figure 4 Differences in the separation of the canine with respect to the first premolar, and the development of the clinoid process between Tonatia bakeri and T. maresi. Illustrations of the lateral view of the mandible, arrows indicate the separation between the canine and the first premolar in aT. bakeri and bT. maresi. In the posterior basioccipital view, arrows indicate the clinoid process in cT. bakeri (QCAZ 9754) and dT. maresi (QCAZ 4972).
Figure 1 from: Basantes M, Tinoco N, Velazco PM, Hofmann MJ, Rodríguez-Posada ME, Camacho MA (2020) Systematics and Taxonomy of Tonatia saurophila Koopman & Williams, 1951 (Chiroptera, Phyllostomidae). ZooKeys 915: 59-86. https://doi.org/10.3897/zookeys.915.46995
Figure 1 Principal Component Analysis (PCA) of two morphometric groups. Projection of 137 specimens of Tonatia saurophila from western (squares) and eastern (rhombuses) localities with respect to the Andes on PC1 and PC2 of a Principal Component Analysis with 21 morphometric cranio-dental and external variables.
Figure 3 from: Carvalho F, Bôlla DAS, Mottin V, Kiem SZ, Zocche JJ, Passos FC (2020) Chilling to the bone: Lower temperatures increase vertebrate predation by Tonatia bidens (Chiroptera: Phyllostomidae). Zoologia 37: 1-5. https://doi.org/10.3897/zoologia.37.e37682
Figure 3 Relation of mean temperature (°C) per month and the number of records of invertebrate (black dots) and vertebrates (grey dots). Dashed line represents the vertebrate model.
Figure 2 from: Carvalho F, Bôlla DAS, Mottin V, Kiem SZ, Zocche JJ, Passos FC (2020) Chilling to the bone: Lower temperatures increase vertebrate predation by Tonatia bidens (Chiroptera: Phyllostomidae). Zoologia 37: 1-5. https://doi.org/10.3897/zoologia.37.e37682
Figure 2 Variation in the precipitation and average temperature from March to November 2013, obtained in a meteorological station, installed in the RNSM area, on the northern coast of Paraná state. Samplings were carried between March 2013 and July 2014.
Figure 1 from: Carvalho F, Bôlla DAS, Mottin V, Kiem SZ, Zocche JJ, Passos FC (2020) Chilling to the bone: Lower temperatures increase vertebrate predation by Tonatia bidens (Chiroptera: Phyllostomidae). Zoologia 37: 1-5. https://doi.org/10.3897/zoologia.37.e37682
Figure 1 Localization of Reserva Particular do Patrimônio Natural (RPPN) Salto Morato (black star) in the municipality of Guaraqueçaba, northern coast of Paraná state, southern Brazil.
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