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FIGURE 5. Call variation between Ameerega bassleri, A. pepperi and A in Complicated histories: three new species of poison frogs of the genus Ameerega (Anura: Dendrobatidae) from north-central Peru
FIGURE 5. Call variation between Ameerega bassleri, A. pepperi and A. yoshina. Box plots show period of silence between notes (L) and the calling rate (notes per minute) of the three species (R).
FIGURE 3 in Complicated histories: three new species of poison frogs of the genus Ameerega (Anura: Dendrobatidae) from north-central Peru
FIGURE 3. Map of study areas. Inset in bottom right shows the two primary regions dealt with in this paper. Box B corresponds to Fig. 8. Box A corresponds to the detailed map shown here. Black dots represent A. bassleri localities, red dots represent A. yoshina localities, and orange dots represent A. pepperi localities. All localities are in Departamento San Martín unless stated otherwise. Ameerega bassleri: (1) Chumia (6° 37' 5.10" S, 76° 10' 12.22" W); (2) Sauce (6° 41' 41.90" S, 76° 14' 11.87" W); (3) Cainarachi Valley (6° 27' 4.54" S, 76° 17' 30.84" W); (4) Huallaga Canyon (6° 34' 18.76" S, 75° 57' 51.12" W, north side of river); (5) Chazuta (6° 33' 30.68" S, 76° 8' 44.88" W); (6) Roque (6° 20' 48.54" S, 76° 43' 38.60" W, type locality of A. bassleri); (7) Saposoa (6° 53' 46.85" S, 76° 49' 41.41" W); (8) Alto Shima (6° 46' 15.85" S, 76° 56' 28.32" W); (9) Sisa (6° 35' 37.10" S, 76° 34' 29.41" W). Ameerega yoshina: (1) Callanayacu (6° 35' 17.61" S, 75° 55' 2.47" W; south side of river); (2) El Unión, Loreto (7° 11' 7.43" S, 74° 57' 13.12" W, type locality of A. yoshina). Ameerega pepperi: (1) Río Abiseo near Huicungo (7° 22' 2.88" S, 76° 48' 42.81" W); (2) Chumanza (7° 34' 7.8" S, 76° 41' 34.4" W); (3) Nuevo San Martín (7° 42' 13.64" S, 76° 40' 3.15" W; (4) San Francisco (8° 18' 30.3" S, 76° 40'40' 37.6" W, type locality of A. pepperi); (5) Campanilla (7° 25' 38.6" S, 76° 39' 53.3" W); (6) Polvora (7° 53' 28.75" S, 76° 40' 21.49" W). Note: Shucushuyacu, Loreto (shown near the top of the map) is the locality of a newly-discovered population of A. pongoensis (Fig. 11 c & d) and represents a substantial northward extension of the known range of this species.
FIGURE 1 in Complicated histories: three new species of poison frogs of the genus Ameerega (Anura: Dendrobatidae) from north-central Peru
FIGURE 1. (a) Holotype of Ameerega ignipedis sp. nov. (MUSM 24948); (b) A. pepperi sp. nov. (uncollected individual from Polvora, San Martín, Peru); (c) Holotype of A. yoshina sp. nov. (MUSM 24945); (d) A. bassleri (MUSM 26965) from type locality (Roque, San Martín, Peru).
FIGURE 8 in Complicated histories: three new species of poison frogs of the genus Ameerega (Anura: Dendrobatidae) from north-central Peru
FIGURE 8. Map of central Peru. Orange circles represent localities of Ameerega petersi, green circles represent A. smaragdina localities. Localities are based on personal observations and Silverstone (1976). Localities labeled with numbers are those which were included in the phylogenetic analysis; localities with letters are those for which individuals have not been sequenced. (1) Miguel Grau, Ucayali (9° 11' 11.47" S, 75° 47' 4.13" W); (2) Aguaytia, Ucayali (9° 0' 54.00" S, 75° 29' 2.40" W); (3) Tournavista, Huánuco (8° 54' 23.50" S, 74° 44' 7.20" W); (4) Codo del Pozuzo, Huánuco (9° 44' 5.22" S, 75° 30' 37.59" W); (5) Puerto Inca, Huánuco (9° 23' 10.39" S, 74° 54' 37.21" W); (6,7) Cordillera El Sira, Huánuco (9° 26' 50.86" S, 74° 48' 1.91" W); (8) Panguana, Huánuco (9° 33' 51.40" S, 74° 52' 16.29" W); (9) Pan de Azucar, Pasco (10° 14' 56.34" S, 75° 13' 32.09" W, type locality of A. smaragdina); (A) Río Iscozacin, Pasco (10° 24' 5.66" S, 75° 3' 47.29" W); (B) Cacazú, Pasco (10° 33' 16.29" S, 75° 5' 4.79" W); (C) Santa Isabel, Pasco (approximate location; type locality of A. petersi); (D) Nevati, Pasco (approximate location); (E) Río Vitoc, Junín (approximate location).
FIGURE 2 in Complicated histories: three new species of poison frogs of the genus Ameerega (Anura: Dendrobatidae) from north-central Peru
FIGURE 2. Advertisement calls of Ameerega ignipedis sp. nov. and A. pongoensis, spectrograms for calls with matching waveforms. (A) A. ignipedis, field recording of a male in type locality, 24 C, 5 May 2007. Dominant frequency 4583 Hz. (B) A. pongoensis, captive recording of a male from type locality (Huallaga Canyon). Dominant frequency 4233 Hz.
FIGURE 10 in Complicated histories: three new species of poison frogs of the genus Ameerega (Anura: Dendrobatidae) from north-central Peru
FIGURE 10. Advertisement calls of species in the Ameerega petersi group. (A) A. petersi, field recording in the Cordillera Azul 20 km NE of Tingo Maria, near the village of Miguel Grau (#1 on Fig. 8), 24.5 C, 27 April 2006. Dominant frequency 3570 Hz. (B) A. smaragdina, field recording from Pan de Azucar, near the town of Iscozacin (#9 on Fig. 8), 24.5 C, 9 August 2007. Dominant frequency 3594 Hz. (C) A. cainarachi, field recording from Chazuta, San Martin, Peru, 25 C, 7 July 2007, Dominant frequency 3590 Hz.
FIGURE 7 in Complicated histories: three new species of poison frogs of the genus Ameerega (Anura: Dendrobatidae) from north-central Peru
FIGURE 7. The biogeography of the bassleri clade is likely the result of multiple disturbance-vicariance events that resulted in periodic connections between the Cordillera Oriental and the Serranía de Contamana, followed by longer periods of isolation. This scenario assumes three periods of connectivity between the Cordillera Oriental and Contamana and would provide a mechanism for allopatric speciation in this group. Each species' distribution (and their ancestors) is depicted by the corresponding color. The bicolored pattern depicts the sympatry of two species.
FIGURE 4 in Complicated histories: three new species of poison frogs of the genus Ameerega (Anura: Dendrobatidae) from north-central Peru
FIGURE 4. Advertisement calls of Ameerega yoshina, A. pepperi, and A. bassleri. (A) A. yoshina standard advertisement call, field recording from 1.6 km SE of Callanayacu, San Martín, 25.5 C, 19 July 2007. Dominant frequency 3244 Hz. (B) A. yoshina short call, same location, temperature, and date as previous. Dominant frequency 3141 Hz. (C) A. pepperi advertisement call, field recording from near Polvora, San Martín, 24.5 C, 8 November 2008. Dominant frequency 2749 Hz. (D) A. bassleri advertisement call, field recording from 5.7 km NE of Roque, San Martín, 26.5 C, 16 June 2007. Dominant frequency 2714 Hz. See Fig. 3 for map of localities.
FIGURE 14. Ameerega yoshina, A in Complicated histories: three new species of poison frogs of the genus Ameerega (Anura: Dendrobatidae) from north-central Peru
FIGURE 14. Ameerega yoshina, A. cainarachi, and A. pepperi. (a-c) A. yoshina from Callanayacu, San Martín, Peru (MUSM 26985-26987); (d-f) A. yoshina from type locality (MUSM 24945, 26953, 26954), (g) A. yoshina (left) and sympatric A. cainarachi (right) from Callanayacu, San Martín, Peru; (h) A. cainarachi from Cainarachi Valley, San Martín, Peru; (i) A. cainarachi from Chazuta, San Martín, Peru; (j,k) A. pepperi from type locality, (l) A. pepperi from Nuevo San Martín, San Martín, Peru.
FIGURE 13 in Complicated histories: three new species of poison frogs of the genus Ameerega (Anura: Dendrobatidae) from north-central Peru
FIGURE 13. Ameerega bassleri. (a,b) Roque, San Martín, Peru (type locality); (c-e) Cainarachi Valley, San Martín, Peru; (f-j) Chazuta, San Martín, Peru; (k) Sauce, San Martín, Peru; (l-m) Cordillera Azul, 14 km SE of Shamboyacu, San Martín, Peru (photo by M. Ramírez Zárate); (n-p) eggs and tadpoles of A. bassleri.
FIGURE 9 in Complicated histories: three new species of poison frogs of the genus Ameerega (Anura: Dendrobatidae) from north-central Peru
FIGURE 9. Speciation and biogeography of the petersi clade. The series of maps depicts the putative ancestral distributions of the petersi clade through time, with (A) being the oldest and (E) being present-day. This hypothetical scenario could explain the discordance between our observed mitochondrial gene tree and the suggested species tree (in which A. petersi and A. smaragdina are the same species). Each species' distribution (and their ancestors' distribution) is depicted by the corresponding color. (F) Depiction of the known localities for each of these species.
FIGURES 8–9 in Taxonomy of the Alloraphes-Stenichnaphes-Parastenichnaphes complex: Stenichnodes complicates the picture (Coleoptera: Staphylinidae: Scydmaeninae)
FIGURES 8–9. Comparison of dorsal habitus of Stenichnodes (Parastenichnaphes) ceylonensis (Franz) (8); Alloraphes peruanus Franz (9) and Stenichnaphes urbanus Franz (10).
FIGURES 3–7 in Taxonomy of the Alloraphes-Stenichnaphes-Parastenichnaphes complex: Stenichnodes complicates the picture (Coleoptera: Staphylinidae: Scydmaeninae)
FIGURES 3–7. Morphological structures of Stenichnodes saheliensis Franz. Head in ventral view (3), prothorax in ventral view (4), pterothorax and abdomen in ventral view (5), aedeagus in ventral (6) and lateral (7) views. Abbreviations: ar, anterior ridge of mesoventrite; bst, basisternal part of prosternum; gal, galea; gp, gular plate; gs, gular suture; hr, hypostomal ridge; hy, hypomeron; hyr, hypomeral ridge; lac, lacinia; lmfa, lateral metafurcal arm; lp3, labial palpomere III; lss, lateral suture of submentum; mcp, mesocoxal projection; md, mandible; mn, mentum; mscc, mesocoxal cavity; mscs, mesocoxal socket; msvp, mesoventral intercoxal process; mtvc, metaventral lateral carina; mtvp, metaventral intercoxal process; mxp, maxillary palpomere; nss, pronotosternal suture; occ, occipital constriction; pcc, procoxal cavity; pcs, procoxal socket; pff, profurcal fovea; pr, procoxal rest; pre, prepectus; psp, prosternal process; smn, submentum; v3, metaventrite.
FIGURES 1–2 in Taxonomy of the Alloraphes-Stenichnaphes-Parastenichnaphes complex: Stenichnodes complicates the picture (Coleoptera: Staphylinidae: Scydmaeninae)
FIGURES 1–2. Doral habitus (1) and original set of labels (2) of the holotype male of Stenichnodes saheliensis Franz.
Malaria disease and grading system dataset from public hospitals reflecting complicated and uncomplicated conditions
<p>Malaria is the leading cause of death in the African region. Data mining can help extract valuable knowledge from available data in the healthcare sector. This makes it possible to train models to predict patient health faster than in clinical trials. Implementations of various machine learning algorithms such as K-Nearest Neighbors, Bayes Theorem, Logistic Regression, Support Vector Machines, and Multinomial Naïve Bayes (MNB), etc., has been applied to malaria datasets in public hospitals, but there are still limitations in modeling using the Naive Bayes multinomial algorithm. This study applies the MNB model to explore the relationship between 15 relevant attributes of public hospitals data. The goal is to examine how the dependency between attributes affects the performance of the classifier. MNB creates transparent and reliable graphical representation between attributes with the ability to predict new situations. The model (MNB) has 97% accuracy. It is concluded that this model outperforms the GNB classifier which has 100% accuracy and the RF which also has 100% accuracy.</p>
Pisgah Complicated Stamped Jar (2021p3113,p3114)
** Pisgah Complicated Stamped jar rim** Location: Garden Creek Mound No. 1 (31Hw1), Haywood County, North Carolina. Period: Mississippian, Pisgah phase (AD 1000-1400) Material: ceramic. Dimensions: length, 255 mm; width, 145 mm; thickness, 7.5 mm. Notes: Catalog no. 2021p3113, p3114, North Carolina Archaeological Collection, Research Laboratories of Archaeology, University of North Carolina at Chapel Hill. Model by Aidan Paul. Source: Objaverse 1.0 / Sketchfab
Cowans Ford Complicated Stamped Jar Rim (1041p)
**Cowans Ford Complicated Stamped Jar Rim** Location: Low site (31Id31), Iredell County, North Carolina. Period: Late Precontact (AD 1400-1600). Material: ceramic. Dimensions: length, 152.9 mm; width, 106.3 mm; thickness, 8.7 mm. Notes: Catalog no. 1041p?. North Carolina Archaeological Collection, Research Laboratories of Archaeology, University of North Carolina at Chapel Hill. Model by Chris LaMack. Source: Objaverse 1.0 / Sketchfab
Qualla Complicated Stamped Jar Rim (2156p19)
**Qualla Complicated Stamped jar rim** Location: Birdtown Mound (31Sw7), Swain County, North Carolina. Period: Mississippian, Qualla phase (AD 1400-1700). Material: ceramic. Dimensions: length, 142.1 mm; width, 71.1 mm; thickness, 7.7 mm. Notes: Catalog no. 2156p19, North Carolina Archaeological Collection, Research Laboratories of Archaeology, University of North Carolina at Chapel Hill. Model by Abigail Gancz. Source: Objaverse 1.0 / Sketchfab
Pisgah Complicated Stamped Jar (2021p812,p900)
**Pisgah Complicated Stamped jar rim** Location: Garden Creek Mound No. 1 (31Hw1), Haywood County, North Carolina. Period: Mississippian, Pisgah phase (AD 1000-1400) Material: ceramic. Dimensions: length, 194 mm; width, 132 mm; thickness, 6.5 mm. Notes: Catalog no. 2021p812, p900, North Carolina Archaeological Collection, Research Laboratories of Archaeology, University of North Carolina at Chapel Hill. Model by Aidan Paul. Source: Objaverse 1.0 / Sketchfab
Qualla Complicated Stamped Jar Rim (2156p39)
**Qualla Complicated Stamped jar rim** Location: Birdtown Mound (31Sw7), Swain County, North Carolina. Period: Mississippian, Qualla phase (AD 1400-1700). Material: ceramic. Dimensions: length, 206.0 mm; width, 100.6 mm; thickness, 8.3 mm. Notes: Catalog no. 2156p39, North Carolina Archaeological Collection, Research Laboratories of Archaeology, University of North Carolina at Chapel Hill. Model by Chris LaMack. Source: Objaverse 1.0 / Sketchfab
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