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Fig. 16 in Systematic Reviews Of New Guinea Coccymys And ''Melomys'' Albidens (Muridae, Murinae) With Descriptions Of New Taxa

Fig. 16. View up the valley of the Bele River above the camp at 2200 m showing the combination of primary forest on hillsides, secondary growth (forest regrowth), and anthropogenic grassland. This is the lowest altitude at which Coccymys ruemmleri was recorded on the northern slopes of the Snow Mountains. November–December 1938.

Fig. 15 in Systematic Reviews Of New Guinea Coccymys And ''Melomys'' Albidens (Muridae, Murinae) With Descriptions Of New Taxa

Fig. 15. Specimen scores representing two species of Coccymys projected on first and second components extracted from principal components analyses. Graph A: Comparison among samples of C. ruemmleri from Bele River valley at 2200 m (filled square) and 2800 m (square), Lake Habbema (filled circle), and Mt. Wilhelmina (circle) in the Snow Mountains (N 5 33). Graph B: Samples of C. ruemmleri from the Star Mountains (filled inverted triangle; N 5 13), Lake Habbema (the type locality; filled circle; N 5 13), and Bele River valley at 2200 m (filled square; N 5 4) and 2800 m (square; N 5 2) in the Snow Mountains compared to those of C. shawmayeri from the Telefomin area (filled diamond; N 5 5) and Mt. Wilhelm (filled triangle; N 5 12) in Papua New Guinea. The star identifies the holotype of C. ruemmleri, the filled pentagon indicates the holotype of C. shawmayeri. See table 11 for correlations and percent variances.

Fig. 17. A in Systematic Reviews Of New Guinea Coccymys And ''Melomys'' Albidens (Muridae, Murinae) With Descriptions Of New Taxa

Fig. 17. A garden in beech (Nothofagus) forest at 2480 m in the Bele River valley. The trees were felled with stone axes and by burning; others were girdled but still living. This was the highest altitude at the Bele River camp where gardens were found (see text). The scene is a view of both the primary forest and its human modification at this altitude. November–December 1938.

Fig. 14 in Systematic Reviews Of New Guinea Coccymys And ''Melomys'' Albidens (Muridae, Murinae) With Descriptions Of New Taxa

Fig. 14. Specimen scores representing two species of Coccymys projected on first and second components extracted from principal components analyses. Graph A: the sample of C. ruemmleri from the Star Mountains (inverted filled triangle; N 5 13) contrasted with that of C. shawmayeri from the Telefomin area (filled diamond; N 5 5). Graph B: samples of C. ruemmleri from the Star Mountains (inverted filled triangle; N 5 13) and Lake Habbema (the type locality) in the Snow Mountains (filled circle; N 5 13) compared to samples of C. shawmayeri from the Telefomin area (filled diamond; N 5 5) and Mt. Wilhelm (filled triangle; N 5 12). A star identifies the holotype of C. ruemmleri, a filled pentagon indicates the holotype of C. shawmayeri. See table 10 for correlations and percent variances.

Fig. 9 in Systematic Reviews Of New Guinea Coccymys And ''Melomys'' Albidens (Muridae, Murinae) With Descriptions Of New Taxa

Fig. 9. The cranium and dentary of the holotype of Coccymys ruemmleri (AMNH 150669), an adult male from the northern slopes of the Snow Mountains at Lake Habbema, 3225 m, X3. Measurements are listed in table 7.

Fig. 5 in Systematic Reviews Of New Guinea Coccymys And ''Melomys'' Albidens (Muridae, Murinae) With Descriptions Of New Taxa

Fig. 5. UPGMA clustering of six population samples representing Coccymys ruemmleri, C. shawmayeri, and C. kirrhos generated from Mahalanobis distances (D2) among group centroids (means). Size of samples, mean values of measurements for variables, and specimens measured are listed in tables 4–6.

Fig. 12 in Systematic Reviews Of New Guinea Coccymys And ''Melomys'' Albidens (Muridae, Murinae) With Descriptions Of New Taxa

Fig. 12. Occlusal views of right mandibular molar rows of the specimens illustrated in figure 11. Left: Brassomys albidens (clm1–3 5 5.4 mm). Middle: Coccymys ruemmleri (clm1–3 5 4.4 mm). Right: Coccymys kirrhos (clm1–3 5 4.1 mm). Abbreviations: alab, anterolabial cusp; aling, anterolingual cusp; hd, hypoconid; md, metaconid; ed, entoconid; pc, posterior cingulum; pd, protoconid; plc, posterior labial cusplet.

Fig. 4 in Systematic Reviews Of New Guinea Coccymys And ''Melomys'' Albidens (Muridae, Murinae) With Descriptions Of New Taxa

Fig. 4. Results of discriminant function analysis. Lower left: Individual specimen scores based on logtransformed values of 16 cranial and 2 dental variables and projected onto the first and second canonical variates extracted from discriminant function analysis of six population samples representing Coccymys ruemmleri, C. shawmayeri, and C. kirrhos. Lower right: Plot of group centroids (population sample means) on first two canonical variates derived from discriminant function analysis of the six population samples. Upper right: Vectors of 18 cranial and dental variables corresponding to the magnitude and direction of their loadings on first and second canonical variates (also see table 2).

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Figure 32 in New data on the distribution of Cteipolia murina (Ménétriés, 1848) (Lepidoptera: Noctuidae: Noctuinae: Xylenini)

Figure 32. Habitat of Cteipolia murina: West Kazakhstan, Irgiz River basin, Aiyrkyzyl Sands, 8.IV.2019 (photo by P. Gorbunov).

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Figure 28 in New data on the distribution of Cteipolia murina (Ménétriés, 1848) (Lepidoptera: Noctuidae: Noctuinae: Xylenini)

Figure 28. Habitat of Cteipolia murina: Central Kazakhstan, Karaganda Province, 70 km N of Balkhash town, Central Kazakh Upland, Konyrkulzha Mt., 7.X.2014 (photo by P. Gorbunov).

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Table 1 in Complete mitochondrial genome of the terrestrial isopod Cubaris murina Brandt, 1833: new family gene order and novel tRNA secondary structures

<p><b>Table 1.</b> Arrangement and annotation of the mitochondrial genome of Cubaris murina.</p><table><tbody><tr><th></th><th></th><th></th><th></th><th></th><th>Length</th><th></th><th></th><th></th><th></th></tr></tbody><tbody><tr><th>Name</th><td>Type</td><td>Start</td><td>Stop</td><td>Strand</td><td>(bp)</td><td>Start</td><td>Stop</td><td>Inter-genic space</td><td>Overlap</td></tr><tr><th>Cox1</th><td>Coding</td><td>1</td><td>1536</td><td>+</td><td>1536</td><td>ATG</td><td>TAA</td><td>1</td><td></td></tr><tr><th>trnL2(tta)</th><td>tRNA</td><td>1538</td><td>1598</td><td>+</td><td>61</td><td></td><td></td><td>48</td><td></td></tr><tr><th>Cox2</th><td>Coding</td><td>1647</td><td>2282</td><td>+</td><td>636</td><td>ATA</td><td>TAG</td><td></td><td>2</td></tr><tr><th>trnK(aaa)</th><td>tRNA</td><td>2281</td><td>2336</td><td>+</td><td>56</td><td></td><td></td><td></td><td>8</td></tr><tr><th>trnD(gac)</th><td>tRNA</td><td>2329</td><td>2403</td><td>+</td><td>75</td><td></td><td></td><td></td><td>17</td></tr><tr><th>atp8</th><td>Coding</td><td>2387</td><td>2533</td><td>+</td><td>147</td><td>ATA</td><td>TAA</td><td></td><td>4</td></tr><tr><th>atp6</th><td>Coding</td><td>2530</td><td>3192</td><td>+</td><td>663</td><td>ATA</td><td>TAA</td><td>2</td><td></td></tr><tr><th>Cox3</th><td>Coding</td><td>3195</td><td>3989</td><td>+</td><td>795</td><td>ATG</td><td>TAG</td><td></td><td>2</td></tr><tr><th>trnR(cga)</th><td>tRNA</td><td>3988</td><td>4055</td><td>+</td><td>68</td><td></td><td></td><td>55</td><td></td></tr><tr><th>nad3</th><td>Coding</td><td>4111</td><td>4407</td><td>+</td><td>297</td><td>ATA</td><td>TAA</td><td></td><td>9</td></tr><tr><th>trnA(gca)</th><td>tRNA</td><td>4399</td><td>4446</td><td>+</td><td>48</td><td></td><td></td><td></td><td>8</td></tr><tr><th>nad1 CR putative</th><td>Coding</td><td>4439 5219</td><td>5218 5360</td><td>−</td><td>780 142</td><td>ATG</td><td>TAG</td><td></td><td>14</td></tr><tr><th>NCR1</th><td>tRNA</td><td>5361</td><td>5429</td><td>+</td><td>69</td><td></td><td></td><td></td><td>17</td></tr><tr><th>rrnS</th><td>rRNA</td><td>5413</td><td>6139</td><td>+</td><td>727</td><td></td><td></td><td>48</td><td></td></tr><tr><th>trnW(tga)</th><td>tRNA</td><td>6188</td><td>6244</td><td>+</td><td>57</td><td></td><td></td><td></td><td>7</td></tr><tr><th>trnS1(aga)</th><td>tRNA</td><td>6238</td><td>6296</td><td>−</td><td>59</td><td></td><td></td><td></td><td></td></tr><tr><th>NCR2</th><td></td><td>6297</td><td>6666</td><td></td><td>370</td><td></td><td></td><td></td><td></td></tr><tr><th>trnL1(cta)</th><td>tRNA</td><td>6667</td><td>6731</td><td>−</td><td>65</td><td></td><td></td><td>29</td><td></td></tr><tr><th>cob</th><td>Coding</td><td>6759</td><td>7907</td><td>−</td><td>1,149</td><td>ATA</td><td>TAG</td><td>38</td><td></td></tr><tr><th>trnT(aca)</th><td>tRNA</td><td>7946</td><td>8017</td><td>−</td><td>72</td><td></td><td></td><td>29</td><td></td></tr><tr><th>nad5</th><td>Coding</td><td>8047</td><td>9648</td><td>+</td><td>1,602</td><td>ATG</td><td>TAG</td><td></td><td>3</td></tr><tr><th>trnF(ttc)</th><td>tRNA</td><td>9646</td><td>9707</td><td>+</td><td>62</td><td></td><td></td><td></td><td>15</td></tr><tr><th>trnH(cac)</th><td>tRNA</td><td>9693</td><td>9758</td><td>−</td><td>66</td><td></td><td></td><td></td><td>23</td></tr><tr><th>nad4</th><td>Coding</td><td>9736</td><td>11,082</td><td>−</td><td>1,312</td><td>ATA</td><td>TAA</td><td>13</td><td></td></tr><tr><th>nad4L</th><td>Coding</td><td>11,096</td><td>11,374</td><td>−</td><td>279</td><td>ATA</td><td>TAA</td><td></td><td>13</td></tr><tr><th>trnP(cca)</th><td>tRNA</td><td>11,362</td><td>11,422</td><td>−</td><td>61</td><td></td><td></td><td>25</td><td></td></tr><tr><th>nad6</th><td>Coding</td><td>11,448</td><td>11,903</td><td>+</td><td>456</td><td>ATA</td><td>TAG</td><td></td><td>2</td></tr><tr><th>trnS2(tca)</th><td>tRNA</td><td>11,902</td><td>11,962</td><td>+</td><td>61</td><td></td><td></td><td>17</td><td></td></tr><tr><th>rrnL</th><td>rRNA</td><td>11,980</td><td>12,549</td><td>−</td><td>570</td><td></td><td></td><td></td><td></td></tr><tr><th>NCR3</th><td></td><td>12,550</td><td>12,753</td><td></td><td>204</td><td></td><td></td><td></td><td></td></tr><tr><th>trnE(gaa)</th><td>tRNA</td><td>12,754</td><td>12,812</td><td>−</td><td>59</td><td></td><td></td><td></td><td></td></tr><tr><th>NCR4</th><td></td><td>12,813</td><td>12,950</td><td></td><td>138</td><td></td><td></td><td></td><td></td></tr><tr><th>trnV(gta)</th><td>tRNA</td><td>12,951</td><td>13,019</td><td>−</td><td>69</td><td></td><td></td><td></td><td>5</td></tr><tr><th>trnQ(caa)</th><td>tRNA</td><td>13,015</td><td>13,077</td><td>−</td><td>63</td><td></td><td></td><td></td><td>6</td></tr><tr><th>trnM(atg)</th><td>tRNA</td><td>13,072</td><td>13,141</td><td>+</td><td>70</td><td></td><td></td><td>25</td><td></td></tr><tr><th>nad2</th><td>Coding</td><td>13,167</td><td>14,123</td><td>+</td><td>978</td><td>ATA</td><td>TAG</td><td></td><td>15</td></tr><tr><th>trnC(tgc)</th><td>tRNA</td><td>14,109</td><td>14,158</td><td>−</td><td>50</td><td></td><td></td><td></td><td></td></tr><tr><th>trnY(tac)</th><td>tRNA</td><td>14,159</td><td>14,205</td><td>−</td><td>47</td><td></td><td></td><td>7</td><td></td></tr></tbody></table>

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Table 2 in Complete mitochondrial genome of the terrestrial isopod Cubaris murina Brandt, 1833: new family gene order and novel tRNA secondary structures

<p><b>Table 2.</b> Base composition (%) of nucleotide, AT content, and AT- and GC-skew of the mitochondrial genome of <i>Cubaris murina.</i> Values in bold indicate positive AT-skew.</p><table><tbody><tr><th></th><th></th><th></th><th>Base composition (%)</th><th></th><th></th><th></th><th></th></tr></tbody><tbody><tr><th>Total</th><td></td><td>A</td><td>C</td><td>G</td><td>T</td><td>%AT</td><td>AT skew</td><td>GC skew</td></tr><tr><th>14,212 bp</th><td>28.90%</td><td>15.80%</td><td>23.40%</td><td>31.90%</td><td>60.80%</td><td>−0.049</td><td>0.194</td></tr><tr><th></th><td></td><td></td><td>Base composition (%)</td><td></td><td></td><td></td><td></td></tr><tr><th>Gene Strand</th><td>A</td><td>C</td><td>G</td><td>T</td><td>%AT</td><td>AT skew</td><td>GC skew</td></tr><tr><th><i>cox1</i></th><td>(+)</td><td>22.4%</td><td>18.6%</td><td>24.2%</td><td>34.8%</td><td>57.2%</td><td>−0.217</td><td>0.131</td></tr><tr><th><i>cox2</i></th><td>(+)</td><td>20.6%</td><td>21.7%</td><td>27.7%</td><td>30.0%</td><td>50.6%</td><td>−0.186</td><td>0.121</td></tr><tr><th><i>atp8</i></th><td>(+)</td><td>21.1%</td><td>15.0%</td><td>34.7%</td><td>29.3%</td><td>50.4%</td><td>−0.163</td><td>0.396</td></tr><tr><th><i>atp6</i></th><td>(+)</td><td>20.4%</td><td>19.8%</td><td>29.1%</td><td>30.8%</td><td>51.2%</td><td>−0.203</td><td>0.190</td></tr><tr><th><i>cox3</i></th><td>(+)</td><td>17.2%</td><td>23.6%</td><td>28.6%</td><td>30.6%</td><td>47.8%</td><td>−0.280</td><td>0.096</td></tr><tr><th><i>nad3</i></th><td>(+)</td><td>20.2%</td><td>16.2%</td><td>32.3%</td><td>31.3%</td><td>51.5%</td><td>−0.216</td><td>0.332</td></tr><tr><th><i>nad1</i></th><td>(−)</td><td>31.7%</td><td>22.2%</td><td>27.6%</td><td>18.6%</td><td>50.3%</td><td><b>0.260</b></td><td>0.108</td></tr><tr><th><i>NCR1</i></th><td></td><td>28.9%</td><td>27.5%</td><td>19.7%</td><td>23.9%</td><td>52.8%</td><td>0.095</td><td>−0.165</td></tr><tr><th><i>NCR2</i></th><td></td><td>27.0%</td><td>22.2%</td><td>18.1%</td><td>32.7%</td><td>59.7%</td><td>−0.095</td><td>−0.102</td></tr><tr><th><i>cob</i></th><td>(−)</td><td>36.0%</td><td>12.0%</td><td>23.5%</td><td>28.5%</td><td>64.5%</td><td><b>0.116</b></td><td>0.324</td></tr><tr><th><i>nad5</i></th><td>(+)</td><td>28.5%</td><td>10.5%</td><td>21.7%</td><td>39.3%</td><td>67.8%</td><td>−0.159</td><td>0.348</td></tr><tr><th><i>nad4</i></th><td>(−)</td><td>38.4%</td><td>11.9%</td><td>22.8%</td><td>26.9%</td><td>65.3%</td><td><b>0.176</b></td><td>0.314</td></tr><tr><th><i>nad4L</i></th><td>(−)</td><td>41.9%</td><td>12.2%</td><td>17.6%</td><td>28.3%</td><td>70.2%</td><td><b>0.194</b></td><td>0.181</td></tr><tr><th><i>nad6</i></th><td>(+)</td><td>25.7%</td><td>10.5%</td><td>17.8%</td><td>46.1%</td><td>71.8%</td><td>−0.284</td><td>0.258</td></tr><tr><th><i>NCR3</i></th><td></td><td>36.8%</td><td>9.8%</td><td>19.1%</td><td>34.3%</td><td>71.1%</td><td>0.035</td><td>0.322</td></tr><tr><th><i>NCR4</i></th><td></td><td>35.5%</td><td>13.0%</td><td>15.2%</td><td>36.2%</td><td>71.7%</td><td>−0.010</td><td>0.078</td></tr><tr><th><i>nad2</i></th><td>(+)</td><td>28.9%</td><td>12.4%</td><td>22.6%</td><td>36.1%</td><td>65.0%</td><td>−0.111</td><td>0.291</td></tr></tbody></table>

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Fig. 5 in A Review of Microhydromys (Rodentia: Murinae), with Description of a New Species from Southern New Guinea

Fig. 5. Skull of the holotype and only known specimen of Pseudohydromys musseri (Flannery, 1989) (BBM-NG 101737, Mt. Somoro, Torricelli Mountains), originally described as a species of Microhydromys (Flannery, 1989; Helgen and Helgen, 2009). Scale bar 5 1 cm.

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Fig. 6 in A Review of Microhydromys (Rodentia: Murinae), with Description of a New Species from Southern New Guinea

Fig. 6. ''Expedition camp in flood plain rain-forest at 850 m. on Araucaria Creek, four kilometers southwest of Bernhard Camp'' (Brass, 1941: 342). The holotype of M. richardsoni was collected while the 1938–1939 Archbold Expedition was stationed at this camp. Photograph previously figured by Brass (1941: pl. 6, fig. 1) and Archbold et al. (1942: pl. 11, fig. 2) and reproduced from the Archbold archives.

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Figs. 16–22 in Last Larval Instar and Mature Oocytes of the Old World Cleptoparasitic Bee Stelis murina, Including a Review of Stelis Biology (Apoidea: Megachilidae: Megachilinae: Anthidiini)

Figs. 16–22. SEM micrographs of postdefecating larva of Stelis murina. 16. Head, frontal view. 17. Salivary lips (with right labial palpus broken), showing internal diverging ridges on lower surface of dorsal lip, frontal view from below. 18. Right antenna (with one of three sensilla broken), semilateral view. 19. Right labial palpus, semilateral view, at same magnification as fig. 18 to show that palpus is about twice as long as antennal papilla. 20. Maxillary palpus, lateral view. 21. Close-up of body setae on pleural swelling of abdominal segment 8, showing swollen setal bases and long, tapering shafts. 22. Spiracle, showing narrow peritreme and concentrically directed atrial spines.

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FIG. 7. The tree resulting from a in Archboldomys (Muridae: Murinae) Reconsidered: A New Genus and Three New Species of Shrew Mice from Luzon Island, Philippines

FIG. 7. The tree resulting from a maximum-likelihood analysis of the cytochrome b from Chrotomys Division species under the best-fitting model (GTR + I + Γ4). Numbers at nodes indicate maximum-likelihood (above the line) or parsimony (below the line) bootstrap support. Terminal taxa are identified by species name and a unique alphanumeric identifier (either DNA number or Genbank accession number; table 6). Trees are rooted with Phloeomys cumingi and Batomys granti as outgroups (not shown).

Fig. 95 in A Systematic Review Of Sulawesi Bunomys (Muridae, Murinae) With The Description Of Two New Species

Fig. 95. Ratio diagram illustrating some proportional relationships in cranial and dental dimensions between the sample of Bunomys karokophilus (N 5 17) and all population samples of B. penitus (the standard, N 5 185). Data were derived from values for mean, standard deviation, and sample size of variables listed in table 42. How these diagrams were constructed and how to read them are explained in Material and Methods.

Fig. 88 in A Systematic Review Of Sulawesi Bunomys (Muridae, Murinae) With The Description Of Two New Species

Fig. 88. Occlusal views of right mandibular molar rows from the same examples of Bunomys karokophilus that are portrayed in figure 86. The coronal patterns are uncomplicated and with age the cusp rows wear to dentine basins rimmed by enamel. Left, AMNH 257190 (clm1–3 5 7.0 mm); Middle, AMNH 223072 (clm1–3 5 7.3 mm), Right, AMNH 225027 (clm1–3 5 7.2 mm).

Fig. 94 in A Systematic Review Of Sulawesi Bunomys (Muridae, Murinae) With The Description Of Two New Species

Fig. 94. Specimen scores representing Bunomys karokophilus from Sungai Sadaunta and the Danau Lindu Valley (empty triangles; N 5 17) and population samples of B. penitus (filled inverted triangles; N 5 174) from the west-central mountain block (Gunung Kanino, Gunung Nokilalaki, Rano Rano, Gunung Lehio, Mamasa Area, and Pegunungan Latimojong) projected onto first and second principal components extracted from principal-components analysis of 16 cranial and two dental log-transformed variables. Ellipses outline 95% confidence limits for each group centroid. Equations for the regression lines are: B. karokophilus, Y 5 ‾0.701× ‾3.309 (F 5 16.04, P 5 0.001); B. penitus, Y 5 ‾0.564× 0.279 (F 5 68.86, P 5 0.000). See table 71 for correlations (loadings) of variables with extracted components and for percent variance explained.

Fig. 71 in A Systematic Review Of Sulawesi Bunomys (Muridae, Murinae) With The Description Of Two New Species

Fig. 71. Subfossil mandibular fragments of Bunomys andrewsi. Upper image: right dentary (×3) and first molar (×10) of AMNH 265014. Middle: left dentary (×3) and intact molar row (×10) of AMNH 265013. Both specimens were excavated from Batu Ejaya II, a cave at the southern tip of the southwestern peninsula of Sulawesi (see gazetteer and the map in fig. 50). Lower image: the right dentary (AMNH 266974; ×3) from Ulu Leang I, a cave about 40 km northeast of Ujung Pandang in the Maros region near the tip of Sulawesi's southwestern peninsula (see gazetteer and the map in fig. 50). Measurements and descriptive information are provided in the text and tables 56 and 57.