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Fig. 1 in A new species of Megacricetodon (Cricetidae, Rodentia, Mammalia) from the Middle Miocene of northern Junggar Basin, China
Fig. 1. SEM images of a left fragmentary maxilla with the M1 and two isolated M1s of Megacricetodon yei n. sp. showing variations. A, ventral view of the maxilla (IVPP V15349.9); B, occlusal view of a right M1 (V15349.3); C, occlusal view of a left M1 (V15349.10). Arrows point to labial spur of the anterolophule in both B and C. Abbreviations: inf, incisive foramen; sm, the oval patch for the superficial masseter; zp, zygomatic plate.
Fig. 8 in A new species of Megacricetodon (Cricetidae, Rodentia, Mammalia) from the Middle Miocene of northern Junggar Basin, China
Fig. 8. Baculum of Megacricetodon yei (IVPP V 15350.1). A, ventral view; B, dorsal view; C, lateral view.
Fig. 12 in A new species of Megacricetodon (Cricetidae, Rodentia, Mammalia) from the Middle Miocene of northern Junggar Basin, China
Fig. 12. Left tibia of Megacricetodon yei (IVPP V15350.22). A, anterior view; B, lateral view; C, posterior view; D, medial view. Abbreviations: fs, flexor sulcus; ltf, lateral tibial fossa; mm, medial malleolus; ptf, posterior tibial fossa; ptp, posterior tibial process; tcr, tibial crest.
Fig. 10 in A new species of Megacricetodon (Cricetidae, Rodentia, Mammalia) from the Middle Miocene of northern Junggar Basin, China
Fig. 10. Right proximal portion (IVPP V15350.7) and left distal portion (V15350.11) of the ulna of Megacricetodon yei. A, lateral view; B, medial view; C, lateral view; D, medial view. Abbreviations: ap, anconeal process; br, brachial ridge; cp, coronoid process; ole, olecranon; rn, radial notch; sp, styloid process; tn, trochlear notch.
Text-fig. 4. Known geographic distribution of Microtscoptini on a modern-day biome map (Arc-GIS feature TNC terrestrial ecoregions). 1 – Ertemte 1 and 2; 2 – Olan Chorea; 3 – Harr Obo 2; 4 – Shala; 5 – Baogeda Ula; 6 – Bilutu; 7 – Kholu (Southern Tuva); 8 – Sarayskoe (Olkhon Island); 9 – Hyargas-nuur; 10 – Petropavlovsk; 11 – Pavlodar; 12 – Akshauli; 13 – Selety 1A; 14 – Kedej 1A; 15 – Makovka; 16 – Cherevychne 3; 17 – Protopopovka 3; 18 – Verkhnya Krynytsa 2; 19 – Vasylivka 1; 20 – Lobkove; 21 – Rome; 22 – Bartlett Mountain; 23 – Bartlett Mountain (General); 24 – Juniper Creek; 25 – Little Valley; 26 – Stroud Claim; 27 – Kelley Road; 28 – Moonstone Formation; 29 – Lemoyne Quarry; 30 – Feltz Ranch; 31 – Cambridge; 32 – Rick Irwin Site; 33 – Rabbit Hole. 1–20, 30–32 – Steppe biomes, 21–29, 33 – xeric shrubland biomes. in Comments On The Age And Dispersal Of Microtoscoptini (Rodentia: Cricetidae)
Text-fig. 4. Known geographic distribution of Microtscoptini on a modern-day biome map (Arc-GIS feature TNC terrestrial ecoregions). 1 – Ertemte 1 and 2; 2 – Olan Chorea; 3 – Harr Obo 2; 4 – Shala; 5 – Baogeda Ula; 6 – Bilutu; 7 – Kholu (Southern Tuva); 8 – Sarayskoe (Olkhon Island); 9 – Hyargas-nuur; 10 – Petropavlovsk; 11 – Pavlodar; 12 – Akshauli; 13 – Selety 1A; 14 – Kedej 1A; 15 – Makovka; 16 – Cherevychne 3; 17 – Protopopovka 3; 18 – Verkhnya Krynytsa 2; 19 – Vasylivka 1; 20 – Lobkove; 21 – Rome; 22 – Bartlett Mountain; 23 – Bartlett Mountain (General); 24 – Juniper Creek; 25 – Little Valley; 26 – Stroud Claim; 27 – Kelley Road; 28 – Moonstone Formation; 29 – Lemoyne Quarry; 30 – Feltz Ranch; 31 – Cambridge; 32 – Rick Irwin Site; 33 – Rabbit Hole. 1–20, 30–32 – Steppe biomes, 21–29, 33 – xeric shrubland biomes.
Text-fig. 3 Comparison of various stratigraphic subdivisions: European (ELMA), North American (NALMA) (Hilgen et al. 2012) and Chinese (CLMA) (Qiu Zhanxiang et al. 2013, Qiu Zhuding et al. 2013) Land Mammal Ages and Eastern Paratethys stages. in Comments On The Age And Dispersal Of Microtoscoptini (Rodentia: Cricetidae)
Text-fig. 3 Comparison of various stratigraphic subdivisions: European (ELMA), North American (NALMA) (Hilgen et al. 2012) and Chinese (CLMA) (Qiu Zhanxiang et al. 2013, Qiu Zhuding et al. 2013) Land Mammal Ages and Eastern Paratethys stages.
Text-fig. 2. Stratigraphic ranges of Microtoscoptini-bearing sites. Correlation of ELMA and NALMA with earth years is according to Hilgen et al. (2012). Localities of very broad stratigraphic range (e.g., the entire Turolian or Hemphillian, as for Vasilivka 1, Lobkove, Little Valley, Cambridge), do not contribute to detail the range, and are omitted in this figure. in Comments On The Age And Dispersal Of Microtoscoptini (Rodentia: Cricetidae)
Text-fig. 2. Stratigraphic ranges of Microtoscoptini-bearing sites. Correlation of ELMA and NALMA with earth years is according to Hilgen et al. (2012). Localities of very broad stratigraphic range (e.g., the entire Turolian or Hemphillian, as for Vasilivka 1, Lobkove, Little Valley, Cambridge), do not contribute to detail the range, and are omitted in this figure.
Text-fig. 1. Known geographic distribution of Microtoscoptini. 1 – Ertemte 1 and 2; 2 – Olan Chorea; 3 – Harr Obo 2; 4 – Shala; 5 – Baogeda Ula; 6 – Bilutu; 7 – Kholu (Southern Tuva); 8 – Sarayskoe (Olkhon Island); 9 – Hyargas-nuur; 10 – Petropavlovsk; 11 – Pavlodar; 12 – Akshauli; 13 – Selety 1A; 14 – Kedej 1A; 15 – Makovka; 16 – Cherevychne 3; 17 – Protopopovka 3; 18 – Verkhnya Krynytsa 2; 19 – Vasylivka 1; 20 – Lobkove; 21 – Rome; 22 – Bartlett Mountain; 23 – Bartlett Mountain (General); 24 – Juniper Creek; 25 – Little Valley; 26 – Stroud Claim; 27 – Kelley Road; 28 – Moonstone Formation; 29 – Lemoyne Quarry; 30 – Feltz Ranch; 31 – Cambridge; 32 – Rick Irwin Site; 33 – Rabbit Hole. in Comments On The Age And Dispersal Of Microtoscoptini (Rodentia: Cricetidae)
Text-fig. 1. Known geographic distribution of Microtoscoptini. 1 – Ertemte 1 and 2; 2 – Olan Chorea; 3 – Harr Obo 2; 4 – Shala; 5 – Baogeda Ula; 6 – Bilutu; 7 – Kholu (Southern Tuva); 8 – Sarayskoe (Olkhon Island); 9 – Hyargas-nuur; 10 – Petropavlovsk; 11 – Pavlodar; 12 – Akshauli; 13 – Selety 1A; 14 – Kedej 1A; 15 – Makovka; 16 – Cherevychne 3; 17 – Protopopovka 3; 18 – Verkhnya Krynytsa 2; 19 – Vasylivka 1; 20 – Lobkove; 21 – Rome; 22 – Bartlett Mountain; 23 – Bartlett Mountain (General); 24 – Juniper Creek; 25 – Little Valley; 26 – Stroud Claim; 27 – Kelley Road; 28 – Moonstone Formation; 29 – Lemoyne Quarry; 30 – Feltz Ranch; 31 – Cambridge; 32 – Rick Irwin Site; 33 – Rabbit Hole.
Fig. 1 in Ten New Genera of Oryzomyine Rodents (Cricetidae: Sigmodontinae)
Fig. 1. Phylogenetic relationships of oryzomyines based on a heuristic parsimony analysis of sequence data from the Interphotoreceptor Retinoid Binding Protein (IRBP, 1266 bp from exon 1) and 99 morphological characters (after Weksler, 2006: fig. 37). Numbers above and below branches represent jackknife support (.50%) and decay indices (.1), respectively. Vertical bars on the right-hand side of the figure indicate taxon membership in clades A–D. See Weksler (2006: 14–17) for methodological details.
Figure 2 in New records of Gigantolaelaps wolffsohni (Mesostigmata: Laelapidae) in Chile, an ectoparasite of Oligoryzomys longicaudatus (Rodentia: Cricetidae): ecological aspects and relation to body size and sex of their host
Figure 2 Larva of Gigantolaelaps wolffsohni from NP Chiloé, Chile. A. Full body of larvaeG. wolffsohni (10x). B. Zoom to gnathosoma of larvae G. wolffsohni (40x).
Figure 1 Localities where G in New records of Gigantolaelaps wolffsohni (Mesostigmata: Laelapidae) in Chile, an ectoparasite of Oligoryzomys longicaudatus (Rodentia: Cricetidae): ecological aspects and relation to body size and sex of their host
Figure 1 Localities where G. wolffsohni were found and ecoregions in Chile. 1. National Park (NP) Bosque Fray Jorge; 2. NP Las Chinchillas; 3. National Reserve (NR) Lago Peñuelas; 4. NP La Campana; 5. Sierras de Bellavista; 6. Termas del Flaco; 7. NR Altos de Lircay; 8. Parque Inglés; 9. Quilmo; 10. NP Nonguén; 11. Santa Elena; 12. NP Laguna del Laja; 13. NP Nahuelbuta; 14. Angol; 15. Bosque San Martín experimental station; 16. Gorbea; 17. Puyehue; 18. Hornopirén; 19. NP Chiloé; 20. NP Patagonia; 21. NP Tamango. All localities represent a new distributional record except the locality number 10 and 19. Yellow: Mediterranean ecoregion, green: Template Forest ecoregion, blue: Magellanic ecoregion.
Fig. 2 in Rediscovery Of The Northern Mole Vole, Ellobius Talpinus (Rodentia, Cricetidae), At The Western Bank Of The Dnipro River, Ukraine
Fig. 2. Localities of Ellobius talpinus to the west of the Dnipro River.
Fig. 1 in Rediscovery Of The Northern Mole Vole, Ellobius Talpinus (Rodentia, Cricetidae), At The Western Bank Of The Dnipro River, Ukraine
Fig. 1. Survey routes to the west of the Dnipro River.
FIGURA 1 in MAMÍFEROS PEQUEÑOS EN LA DIETA DE LA LECHUZA TYTO ALBA (STRIGIFORMES: TYTONIDAE) EN DOS LOCALIDADES DEL OCCIDENTE DE ECUADOR, CON AMPLIACIÓN DISTRIBUCIONAL DE ICHTHYOMYS HYDROBATES (RODENTIA: CRICETIDAE)
FIGURA 1: Ubicación de los dos sitios de estudio en el occidente de Ecuador.
Figure 1 in Microtus guentheri (Danford & Alston, 1880) (Rodentia: Cricetidae) as a biomonitor for radionuclides in Mersin Province of Turkey
Figure 1. The localities of samples collected within Mersin Province.
TABLE 4 in A New Species of the Rodent Genus Oecomys (Cricetidae: Sigmodontinae: Oryzomyini) from Eastern Bolivia, with Emended Definitions of O. concolor (Wagner) and O. mamorae (Thomas)
<p>TABLE 4 <b>External and Craniodental Measurements for the Type Series of <i>O. sydandersoni</i>, New Species, and Samples of <i>O. concolor</i> and <i>O. mamorae</i></b> (Sample statistics include the mean, ± 1 standard deviation, and the observed range).</p><table><thead><tr><th></th><th><i>O. sydandersoni</i> Holotype</th><th><i>O. sydandersoni</i> El Refugio</th><th><i>O. concolor</i> Amazonas, Brazil</th><th><i>O. mamorae</i> Beni, Bolivia</th></tr></thead><tbody><tr><th>Variable</th><td>(MNK 2679)</td><td>(<i>N</i> <b>=</b> 21–23)</td><td>(<i>N</i> <b>=</b> 23, 24)</td><td>(<i>N</i> <b>=</b> 14–16)</td></tr><tr><th>TOTL</th><td>242</td><td>257.9 ± 16.7 233–290</td><td>273.2 ± 11.2 255–296</td><td>296.0 ± 18.3 270–230</td></tr><tr><th>HBL</th><td>118</td><td>125.0 ± 12.2 109–166</td><td>125.4 ± 5.8 115–141</td><td>139.8 ± 13.1 120–170</td></tr><tr><th>TL</th><td>124</td><td>132.8 ± 8.4 115–145</td><td>147.9 ± 6.9 137–160</td><td>158.5 ± 10.7 144–180</td></tr><tr><th>HFL</th><td>23</td><td>24.1 ± 1.7 21–27</td><td>27.4 ± 1.1 26–29</td><td>27.3 ± 1.8 23–30</td></tr><tr><th>EL</th><td>17</td><td>16.4 ± 1.1 15–19</td><td>17.1 ± 1.3 15–20</td><td>18.0 ± 1.2 17–20</td></tr><tr><th>WT</th><td>45</td><td>44.9 ± 7.8 30–57</td><td>57.8 ± 9.5 41–80</td><td>73.9 ± 29.9 48–120</td></tr><tr><th>ONL</th><td>30.7</td><td>29.8 ± 1.2 27.7–32.0</td><td>32.2 ± 0.9 30.2–34.3</td><td>32.5 ± 1.2 30.9–34.5</td></tr><tr><th>ZB</th><td>16.7</td><td>16.5 ± 0.6 15.3–17.6</td><td>17.7 ± 0.6 16.6–19.1</td><td>17.1 ± 0.7 15.6–18.1</td></tr><tr><th>BBC</th><td>11.8</td><td>11.8 ± 0.3 11.3–12.4</td><td>12.5 ± 0.4 11.8–13.3</td><td>12.6 ± 0.3 12.0–13.2</td></tr><tr><th>DBC</th><td>9.5</td><td>9.1 ± 0.3 8.5–9.7</td><td>9.4 ± 0.3 8.8–9.9</td><td>9.3 ± 0.5 7.7–10.0</td></tr><tr><th>BOC</th><td>6.6</td><td>6.5 ± 0.1 6.3–6.8</td><td>6.8 ± 0.2 6.4–7.3</td><td>7.3 ± 0.4 6.6–7.8</td></tr><tr><th>IOB</th><td>5.4</td><td>5.3 ± 0.3 4.8–5.7</td><td>5.5 ± 0.2 5.1–6.0</td><td>4.9 ± 0.2 4.6–5.2</td></tr><tr><th>LR</th><td>8.2</td><td>8.4 ± 0.5 7.5–9.1</td><td>9.1 ± 0.4 8.4–9.9</td><td>9.1 ± 0.4 8.6–10.0</td></tr><tr><th>BR</th><td>5.4</td><td>5.5 ± 0.3 4.7–6.2</td><td>6.1 ± 0.3 5.5–6.7</td><td>5.8 ± 0.3 5.4–6.2</td></tr><tr><th>PPL</th><td>10.4</td><td>10.3 ± 0.5 9.2–11.4</td><td>10.6 ± 0.4 9.9–11.4</td><td>11.3 ± 0.5 10.4–12.0</td></tr><tr><th>BPL</th><td>5.7</td><td>5.6 ± 0.3 4.9–6.0</td><td>6.6 ± 0.3 5.9–7.3</td><td>6.1 ± 0.4 5.4–6.9</td></tr><tr><th>LIF</th><td>5.6</td><td>5.4 ± 0.3 4.9–5.8</td><td>5.3 ± 0.3 4.5–6.2</td><td>5.8 ± 0.3 5.3–6.3</td></tr><tr><th>BIF</th><td>2.6</td><td>2.6 ± 0.2 2.2–2.8</td><td>2.3 ± 0.2 1.8–2.7</td><td>2.5 ± 0.3 2.0–2.9</td></tr><tr><th>LD</th><td>7.4</td><td>7.7 ± 0.5 6.8–8.7</td><td>8.1 ± 0.4 7.6–9.1</td><td>8.0 ± 0.5 7.2–8.7</td></tr><tr><th>BBP</th><td>5.7</td><td>5.7 ± 0.2 5.2–6.2</td><td>6.1 ± 0.2 5.7–6.4</td><td>5.9 ± 0.3 5.4–6.4</td></tr><tr><th>Variable</th><td>(MNK 2679)</td><td>(<i>N</i> <b>=</b> 21–23)</td><td>(<i>N</i> <b>=</b> 23, 24)</td><td>(<i>N</i> <b>=</b> 14–16)</td></tr><tr><th>BZP</th><td>3.2</td><td>2.9 ± 0.2 2.5–3.2</td><td>3.3 ± 0.2 2.9–3.6</td><td>3.4 ± 0.3 2.8–3.9</td></tr><tr><th>CLM</th><td>4.80</td><td>4.57 ± 0.14 4.35–4.90</td><td>4.93 ± 0.13 4.70–5.10</td><td>5.04 ± 0.21 4.70–5.40</td></tr><tr><th>WM1</th><td>1.40</td><td>1.32 ± 0.05 1.25–1.40</td><td>1.40 ± 0.06 1.30–1.50</td><td>1.39 ± 0.09 1.30–1.50</td></tr></tbody></table>
TABLE 6 in A New Species of the Rodent Genus Oecomys (Cricetidae: Sigmodontinae: Oryzomyini) from Eastern Bolivia, with Emended Definitions of O. concolor (Wagner) and O. mamorae (Thomas)
<p>TABLE 6 <b>External and Craniodental Measurements of the Four Species of <i>Oecomys</i> Collected in the Parc Nacional Noel Kempff Mercado, Eastern Bolivia</b> (Sample statistics include the mean, ± 1 standard deviation, and the observed range.)</p><table><thead><tr><th>Variable</th><th><i>O. bicolor</i> a (<i>N</i> <b>=</b> 7, 8)</th><th><i>O. sydandersoni</i> (<i>N</i> <b>=</b> 21–23)</th><th><i>O. roberti</i> b (<i>N</i> <b>=</b> 4, 6)</th><th><i>O. trinitatis</i> c (<i>N</i> <b>=</b> 3, 4)</th></tr></thead><tbody><tr><th>TOTL</th><td>211.8 ± 23.4 172–240</td><td>257.9 ± 16.7 233–290</td><td>273.5 ± 22.3 237–295</td><td>260.7 ± 17.6 241–275</td></tr><tr><th>TL</th><td>103.9 ± 10.8 87–122</td><td>132.8 ± 8.4 115–145</td><td>142.2 ± 13.1 127–160</td><td>135.3 ± 3.8 131–138</td></tr><tr><th>HFL</th><td>19.4 ± 1.0 18–21</td><td>24.1 ± 1.7 21–27</td><td>25.7 ± 1.7 24–28</td><td>26.0 ± 1.1 25–27</td></tr><tr><th>EL</th><td>14.5 ± 0.5 14–15</td><td>16.4 ± 1.1 15–19</td><td>15.8 ± 1.0 14–17</td><td>17.3 ± 1.7 15–19</td></tr><tr><th>WT</th><td>29.9 ± 8.1 20–43</td><td>44.9 ± 7.8 30–57</td><td>50.5 ± 18.1 34–86</td><td>45.8 ± 8.7 33–52</td></tr><tr><th>ONL</th><td>26.8 ± 1.3 24.6–27.8</td><td>29.8 ± 1.2 27.7–32.0</td><td>31.9 ± 1.5 29.6–33.7</td><td>30.7 ± 1.6 28.5–32.0</td></tr><tr><th>ZB</th><td>14.1 ± 0.8 12.9–15.1</td><td>16.5 ± 0.6 15.3–17.6</td><td>16.7 ± 0.9 15.1–17.6</td><td>16.1 ± 0.9 15.1–17.3</td></tr><tr><th>BBC</th><td>11.1 ± 0.4 10.5–11.7</td><td>11.8 ± 0.3 11.3–12.4</td><td>12.1 ± 0.2 11.9–12.4</td><td>11.8 ± 0.4 11.4–12.3</td></tr><tr><th>DBC</th><td>8.4 ± 0.2 8.1–8.7</td><td>9.1 ± 0.3 8.5–9.7</td><td>9.1 ± 0.5 8.3–9.6</td><td>9.0 ± 0.2 8.9–9.3</td></tr><tr><th>BOC</th><td>5.9 ± 0.2 5.7–6.3</td><td>6.5 ± 0.1 6.3–6.8</td><td>6.6 ± 0.1 6.4–6.7</td><td>6.5 ± 0.1 6.4–6.6</td></tr><tr><th>IOB</th><td>4.7 ± 0.2 4.3–4.9</td><td>5.3 ± 0.3 4.8–5.7</td><td>5.5 ± 0.2 5.2–5.7</td><td>5.1 ± 0.3 4.9–5.6</td></tr><tr><th>LR</th><td>7.7 ± 0.6 6.6–8.3</td><td>8.4 ± 0.5 7.5–9.1</td><td>9.7 ± 0.4 9.2–10.3</td><td>9.5 ± 0.6 8.6–9.9</td></tr><tr><th>BR</th><td>4.9 ± 0.3 4.4–5.2</td><td>5.5 ± 0.3 4.7–6.2</td><td>5.9 ± 0.2 5.7–6.1</td><td>5.9 ± 0.5 5.2–6.4</td></tr><tr><th>PPL</th><td>9.4 ± 0.7 8.1–9.9</td><td>10.3 ± 0.5 9.2–11.4</td><td>11.1 ± 1.0 9.6–12.7</td><td>10.4 ± 0.6 9.7–11.0</td></tr><tr><th>BPL</th><td>4.4 ± 0.4 3.8–4.9</td><td>5.6 ± 0.3 4.9–6.0</td><td>6.3 ± 0.2 6.1–6.7</td><td>6.3 ± 0.5 5.7–6.8</td></tr><tr><th>LIF</th><td>4.5 ± 0.3 3.8–4.9</td><td>5.4 ± 0.3 4.9–5.8</td><td>5.2 ± 0.4 4.5–5.7</td><td>5.1 ± 0.3 4.7–5.4</td></tr><tr><th>BIF</th><td>2.1 ± 0.1 1.9–2.2</td><td>2.6 ± 0.2 2.2–2.8</td><td>2.5 ± 0.2 2.3–2.8</td><td>2.3 ± 0.1 2.2–2.4</td></tr><tr><th>LD</th><td>6.7 ± 0.6 5.7–7.3</td><td>7.7 ± 0.5 6.8–8.7</td><td>8.3 ± 0.4 7.7–8.9</td><td>7.6 ± 0.6 6.9–8.2</td></tr><tr><th>BBP</th><td>4.9 ± 0.3 4.5–5.2</td><td>5.7 ± 0.2 5.2–6.2</td><td>5.8 ± 0.2 5.6–6.1</td><td>5.9 ± 0.3 5.5–6.1</td></tr><tr><th>BZP</th><td>2.2 ± 0.3 1.8–2.7</td><td>2.9 ± 0.2 2.5–3.2</td><td>2.8 ± 0.4 2.1–3.3</td><td>3.3 ± 0.3 3.0–3.7</td></tr><tr><th>CLM</th><td>3.75 ± 0.14 3.57–3.93</td><td>4.57 ± 0.14 4.35–4.90</td><td>4.76 ± 0.23 4.48–5.15</td><td>4.80 ± 0.18 4.64–5.05</td></tr><tr><th></th><td><i>O. bicolor</i> a</td><td><i>O. sydandersoni</i></td><td><i>O. roberti</i> b</td><td><i>O. trinitatis</i> c</td></tr><tr><th>Variable</th><td>(<i>N</i> <b>=</b> 7, 8)</td><td>(<i>N</i> <b>=</b> 21–23)</td><td>(<i>N</i> <b>=</b> 4, 6)</td><td>(<i>N</i> <b>=</b> 3, 4)</td></tr><tr><th>WM1</th><td>1.09 ± 0.04</td><td>1.32 ± 0.05</td><td>1.36 ± 0.06</td><td>1.41 ± 0.08</td></tr><tr><th></th><td>1.05–1.17</td><td>1.25–1.40</td><td>1.28–1.46</td><td>1.35–1.53</td></tr></tbody></table><p><sup>a</sup> Bolivia, Santa Cruz, Parque Nacional Noel Kempff Mercado, 2.5 km NE El Refugio (MNK-LHE 1561; MNK-VCC 13, 20, 132; USNM 584546–584549).</p><p><sup>b</sup> Bolivia, Santa Cruz, Parque Nacional Noel Kempff Mercado, 2.5 km NE El Refugio (MNK-LHE 1658, 1669, 1681, 1685; MNK-VCC 9; USNM 584550, 584551).</p><p><sup>c</sup> Bolivia, Santa Cruz, Parque Nacional Noel Kempff Mercado, Los Fierros (MNK-LHE 1565, 1682; USNM 584552, 584553).</p>
TABLE 2 in A New Species of the Rodent Genus Oecomys (Cricetidae: Sigmodontinae: Oryzomyini) from Eastern Bolivia, with Emended Definitions of O. concolor (Wagner) and O. mamorae (Thomas)
<p>TABLE 2 <b>Results of Principal Components Analyses Comparing Adult <i>Oecomys</i> sp. novum with <i>O. concolor</i> and <i>O. mamorae</i></b> (Based on 17 log-transformed craniodental variables; see Materials and Methods and fig. 2.)</p><table><thead><tr><th></th><th colspan="2"><i>O. sp. novum</i> + <i>O. concolor</i></th><th colspan="2"><i>O. sp. novum</i> + <i>O. mamorae</i></th></tr></thead><tbody><tr><th></th><td colspan="2">Correlations</td><td colspan="2">Correlations</td></tr><tr><th>Variable</th><td>PC I</td><td>PC II</td><td>PC I</td><td>PC II</td></tr><tr><th>ONL</th><td>0.96***</td><td>0.10</td><td>0.97***</td><td><b>-</b> 0.07</td></tr><tr><th>ZB</th><td>0.86***</td><td>0.13</td><td>0.83***</td><td>0.29</td></tr><tr><th>BBC</th><td>0.80***</td><td>0.02</td><td>0.74***</td><td><b>-</b> 0.15</td></tr><tr><th>DBC</th><td>0.53***</td><td>0.15</td><td>0.32</td><td>0.26</td></tr><tr><th>BOC</th><td>0.63***</td><td><b>-</b> 0.24</td><td>0.75***</td><td><b>-</b> 0.28</td></tr><tr><th>IOB</th><td>0.54***</td><td>0.13</td><td><b>-</b> 0.17</td><td>0.76***</td></tr><tr><th>LR</th><td>0.82***</td><td>0.26</td><td>0.84***</td><td><b>-</b> 0.05</td></tr><tr><th>BR</th><td>0.84***</td><td><b>-</b> 0.04</td><td>0.74***</td><td>0.06</td></tr><tr><th>BZP</th><td>0.76***</td><td>0.11</td><td>0.88***</td><td><b>-</b> 0.03</td></tr><tr><th>PPL</th><td>0.73***</td><td>0.41**</td><td>0.91***</td><td><b>-</b> 0.06</td></tr><tr><th>BPL</th><td>0.87***</td><td><b>-</b> 0.29*</td><td>0.71***</td><td><b>-</b> 0.14</td></tr><tr><th>LD</th><td>0.84***</td><td>0.35**</td><td>0.85***</td><td>0.41**</td></tr><tr><th>LIF</th><td>0.35**</td><td>0.72***</td><td>0.81***</td><td><b>-</b> 0.09</td></tr><tr><th>BIF</th><td><b>-</b> 0.18</td><td>0.91***</td><td>0.36</td><td>0.82***</td></tr><tr><th>BBP</th><td>0.82***</td><td>0.11</td><td>0.78***</td><td>0.07</td></tr><tr><th>CLM</th><td>0.72***</td><td><b>-</b> 0.40**</td><td>0.59***</td><td><b>-</b> 0.69***</td></tr><tr><th>WM1</th><td>0.64***</td><td><b>-</b> 0.37**</td><td>0.38</td><td><b>-</b> 0.58***</td></tr><tr><th>Eigenvalue</th><td>0.033</td><td>0.011</td><td>0.045</td><td>0.012</td></tr><tr><th>% Variance</th><td>53.5</td><td>17.5</td><td>55.8</td><td>14.9</td></tr></tbody></table><p>* <b>=</b> P <b>#</b> 0.05; ** <b>=</b> P <b>#</b> 0.01; *** <b>=</b> P <b>#</b> 0.001.</p>
TABLE 5 in A New Species of the Rodent Genus Oecomys (Cricetidae: Sigmodontinae: Oryzomyini) from Eastern Bolivia, with Emended Definitions of O. concolor (Wagner) and O. mamorae (Thomas)
<p>TABLE 5 <b>Occurrence of Alisphenoid Struts</b> (<b>-</b> / <b>- =</b> struts absent both sides; <b>-</b> /+ <b>=</b> strut present on one side; +/+ <b>=</b> struts present both sides.)</p><table><thead><tr><th></th><th colspan="3">Alisphenoid Struts</th></tr></thead><tbody><tr><th>Species and Country</th><td><b>-</b> / <b>-</b></td><td><b>-</b> /+</td><td>+/+</td></tr><tr><th colspan="4"><i>O. concolor</i></th></tr><tr><th>Brazil Colombia Venezuela Totals</th><td>1 0 0 1</td><td>0 1 0 1</td><td>25 0 18 43</td></tr><tr><th colspan="4"><i>O. mamorae</i></th></tr><tr><th>Bolivia Brazil Paraguay Totals</th><td>29 1 7 37</td><td>1 0 0 1</td><td>0 0 0 0</td></tr><tr><th colspan="4"><i>O. sydandersoni</i></th></tr><tr><th>Bolivia</th><td>1</td><td>2</td><td>23</td></tr></tbody></table>
Natterer collected this species at the Curicuriari River in northwestern Brazil. in A New Species of the Rodent Genus Oecomys (Cricetidae: Sigmodontinae: Oryzomyini) from Eastern Bolivia, with Emended Definitions of O. concolor (Wagner) and O. mamorae (Thomas)
<p>Natterer collected this species at the Curicuriari River in northwestern Brazil.</p><table><thead><tr><th></th><th><i>H. concolor</i></th><th></th><th><i>H. Anguya</i></th></tr></thead><tbody><tr><th>Body</th><td>4 <b>"</b> 10 <b>"</b></td><td>|</td><td>5 <b>"</b> 8 <b>"</b></td></tr><tr><th>Tail</th><td>4 9</td><td>|</td><td>5 6</td></tr><tr><th>Ear</th><td>0 6 2/2 [sic]</td><td>|</td><td>0 8</td></tr><tr><th>Hindfoot</th><td>1 0</td><td>|</td><td>1 3</td></tr></tbody></table><p>Natterer collected this species at the Curicuriari River in northwestern Brazil.</p>
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