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15,460 results for “Neotrops”

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Fig. 3 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 3. (a) Canonical analysis of principal coordinates for 30 standardized morphology measurements based on Euclidean distance. Letters A, B, and WA indicate the mean canonical value of the WIO IIA, WIO IIB, and WA groups, respectively. Error bars around the mean present one standard error. (b) Contributions of different measurements (measurement scores, proportional to the eigenvalues) on the constrained ordination plot. The measurement abbreviations refer to appendix 1.

opencc-by-4.0Jun 2019View details →
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Fig. 1 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 1. (a) Full phylogenetic tree of the genus Otolithes with specimens from the Indo-Pacific, Western Arabian Gulf, and South Africa by Kimura- 2P distance and maximum-likelihood distance using the GTR + G nucleotide substitution model and Protonibea diacanthus as the outgroup; (b) subtree showing three clades: the Otolithes cuvieri complex, the Otolithes ruber Western Indo Pacific clade, and the Otolithes sp. Arabian Gulf/South Africa clade. The black numbers at nodes are bootstrap supporting values (%). Only values larger than 80% are shown. Grey numbers in italics on the branches represent branch length, with only those longer than 3% plotted.

opencc-by-4.0Jun 2019View details →
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Fig. 6 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 6. Fresh specimen of the holotype of Otolithes arabicus sp. nov. The scale bar represents 5 cm, and each block represents 1 cm.

opencc-by-4.0Jun 2019View details →
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Fig. 3 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 3. Asymptotic analysis of the diversity (Hill numbers, q = 0, 1 and 2) of phyllostomid bats in neotropical temperate forests (MCF: montane cloud forest, POF: pine-oak forest) and agricultural areas (AGR) in southern Mexico. Shadded areas are confidence intervals at 0.95%.

opencc-by-4.0Jun 2019View details →
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Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 4. (a) Illustration of 17 landmarks on the Otolithes sp. 1: tip of snout, 2: termination of maxilla, 3: ventral margin of interopercle, 4: anterior margin of eye orbit, 5: posterior margin of eye orbit, 6: dorsal termination of cranium, 7: origin of lateral line, 8: origin of pectoral fin, 9: origin of pelvic fin, 10: anterior insertion of spinous dorsal fin, 11: origin of soft dorsal fin, 12: origin of anal fin; 13: termination of anal fin, 14: termination of second dorsal fin, 15: insertion of dorsal-most caudal fin ray, 16: termination of lateral line, and 17: insertion of ventral-most caudal fin ray. Procrustes superimposition showing the pair-wise differences in shapes between (b) Western Arabian Gulf group (WA) vs. West Indian Ocean II group, and (c) West Indian Ocean II group type A vs. B. Arrows indicate the difference vector, which is amplified four times for clarity.

opencc-by-4.0Jun 2019View details →
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Fig. 4 in Fig. 4 in Fig. 4 in Responses of Phyllostomid Bats to Traditional Agriculture in Neotropical Montane Forests of Southern Mexico.

Fig. 4. Floors of orbit of male Austruca variegata (Heller, 1862) (a–d), A. bengali (Crane, 1975) (e, f) and A. triangularis (A. Milne-Edwards, 1873) (g, h). (a, b) CW 18.6 mm (ZRC 2018.1375; right-handed; Tamil Nadu, India); (c, d) CW 14.5 mm (ZRC 2017.0917; left-handed; West Bengal, India); (e, f) CW 14.5 mm (NCHUZOOL 14345; right-handed; Selangor, Malaysia); (g, h) CW 14.8 mm (NCHUZOOL 13574; left-handed; Cebu, Philippines). Scale bars = 5.0 mm.

opencc-by-4.0Jul 2019View details →
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Fig. 2 in Temporal and demographic blood parasite dynamics in two free-ranging neotropical primates

Fig. 2. Individual infection status by parasite by year. Strength and thickness of lines are scaled to the number of individuals that took a given infection trajectory from one year to the next. Two diagonal lines span 2012‾2014 because those individuals were not sampled in 2013. The + symbols represent every infection or non-infection found across all individuals in the study.

opencc-by-4.0Aug 2017View details →
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Fig. 3 in Temporal and demographic blood parasite dynamics in two free-ranging neotropical primates

Fig. 3. Parasite species richness by species, age class and sex. Colors represent females (black) and males (gray).

opencc-by-4.0Aug 2017View details →
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Fig. 1. A in Seasonality, richness and prevalence of intestinal parasites of three neotropical primates (Alouatta seniculus, Ateles hybridus and Cebus versicolor) in a fragmented forest in Colombia

Fig. 1. A. Trichuris sp., B. Oxyuridae, C. Ancylostomatidae, D. Strongyloides sp. (larva), E. Ascarididae, F. Gnathostomatidae, G. Trichostrongylidae, H-I. Trematodes, J. Entamoeba sp. (cyst), K. Acanthocephala, L. Balantidiidae.

opencc-by-4.0Dec 2017View details →
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Fig. 1 in Temporal and demographic blood parasite dynamics in two free-ranging neotropical primates

Fig. 1. Annual prevalence of single- and co-infections by species. Prevalence indicated for each parasite (dark gray), and each pairwise combination of parasites (light gray). Numbers near the top of each bar show the exact prevalence; black lines indicate 95% confidence intervals; dots indicate expected levels of co-infection (refer to Section 3.2). M-D is co-occurrence of M. mariae and Dipetalonema spp., D-T is Dipetalonema spp. and T. minasense, and M-T is M. mariae and T. minasense.

opencc-by-4.0Aug 2017View details →
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Fig. 5 in Ectoparasitic copepod infestation on a wild population of Neotropical catfish Sciades herzbergii Bloch, 1794: Histological evidences of lesions on host

Fig. 5. Transverse section of S. herzbergii skin parasitized by copepods. (Hematoxylineosin staining). a. Detail of the outer and middle layer of the epidermis (hyperplasia and hypertrophy) (100X). b. Sacciforme cell (400X).

opencc-by-4.0Dec 2017View details →
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Fig. 4 in Ectoparasitic copepod infestation on a wild population of Neotropical catfish Sciades herzbergii Bloch, 1794: Histological evidences of lesions on host

Fig. 4. Cross section of healthy skin of S. herzbergii. Detail of the epidermis and dermis (staining with hematoxylin-eosin) (400X).

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Fig. 2 in Ectoparasitic copepod infestation on a wild population of Neotropical catfish Sciades herzbergii Bloch, 1794: Histological evidences of lesions on host

Fig. 2. Hemorrhagic cutaneous lesions caused by the infestation of copepods on S. herzbergii. a. Ventral view. b. Pectoral fins and mouth.

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Fig. 3 in Ectoparasitic copepod infestation on a wild population of Neotropical catfish Sciades herzbergii Bloch, 1794: Histological evidences of lesions on host

Fig. 3. Cross section of healthy skin of S. herzbergii, showing the different layers that make it up (Hematoxylin-eosin staining) (100X).

opencc-by-4.0Dec 2017View details →
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Fig. 8 in Description of four new species of the Neotropical genus Scione Walker, 1850 (Diptera: Tabanidae)

Fig. 8. Scione merianae sp. nov., ♂, paratype (MECN). A. Habitus, dorsal view. B. Head, frontal view. C. Wing, dorsal view. D. Habitus, lateral view. E. Head, side view. F. Labels.

opencc-by-4.0Jul 2024View details →
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Fig. 7 in Description of four new species of the Neotropical genus Scione Walker, 1850 (Diptera: Tabanidae)

Fig. 7. Scione merianae sp. nov., ♀, holotype (MECN). A. Habitus, dorsal view. B. Head, frontal view. C. Head, side view. D. Wing, dorsal view. E. Habitus, lateral view. F. Labels.

opencc-by-4.0Jul 2024View details →
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Fig. 6 in Description of four new species of the Neotropical genus Scione Walker, 1850 (Diptera: Tabanidae)

Fig. 6. Scione kroeberi sp. nov. ♀, holotype (CAS). A. Habitus, dorsal view. B. Head, frontal view. C. Head, side view. D. Habitus, lateral view. E. Labels.

opencc-by-4.0Jul 2024View details →
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Fig. 5 in Description of four new species of the Neotropical genus Scione Walker, 1850 (Diptera: Tabanidae)

Fig. 5. Scione gertrudeae sp. nov., ♂, paratype (NHMUK). A. Habitus, dorsal view. B. Habitus, lateral view. C. Head, frontal view. D. Head, lateral view. E. Labels.

opencc-by-4.0Jul 2024View details →
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Fig. 3 in Description of four new species of the Neotropical genus Scione Walker, 1850 (Diptera: Tabanidae)

Fig. 3. Scione cooperi sp. nov., ♂, paratype (NHMUK). A. Habitus, dorsal view. B. Habitus, lateral view. C. Head, frontal view. D. head, side view. E. Wing, dorsal view. F. Labels.

opencc-by-4.0Jul 2024View details →
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Fig. 2 in Description of four new species of the Neotropical genus Scione Walker, 1850 (Diptera: Tabanidae)

Fig. 2. Scione cooperi sp. nov., ♀, holotype (NHMUK). A. Habitus, dorsal view. B. Habitus, lateral view. C. Head, frontal view. D. Head, side view. E. Wing, dorsal view. F. Labels.

opencc-by-4.0Jul 2024View details →

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International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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OpenNeuro

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