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81 results for “morphological measurements”
Data from: How do morphological sharpness measures relate to puncture performance in viperid snake fangs?
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Morphological measurements of arm loss for eight octopus species
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METHODS. Bovine ilia were used in the simulations because their histological structure (a fibrolamellar cortex overlying cancellous bone26) was found to match that of the Triceratops ilium. Bone sections 10 x 50 x 縠 3.0 cm with cortices ranging from 0.5 to 5.5 mm in depth (the range of initial cortical-thickness estimates based on gross morphology) were mounted on a servohydraulic mechanical loading frame (MTS Bionix, Minneapolis) and penetrated with an aluminium-bronze T. rex tooth replica. The replica was cast from an actual adult T. rex maxillary tooth, after casts made from some ofthe deeper bite marks revealed the size and shape of the teeth that had impacted the pelvis8 • The replica was penetrated into the ilia sections at 1 mm s-1 to a depth of 11.5 mm, equivalent to the maximum depth of the deepest ilium bite mark8 • Forces were measured with an MTS 25 N strain-gauge-based axial load cell accurate to 0.2%. The forces increased with increasing penetration depth even after the cortical layer had been perforated and the underlying cancellous bone was being crushed. The increase in force with penetration depth is attributed to a greater cortical surface area coming into contact with the semi-conical penetrator tooth as it descended through the ilia. in Bite-force estimation for Tyrannosaurus rex from tooth-marked bones
METHODS. Bovine ilia were used in the simulations because their histological structure (a fibrolamellar cortex overlying cancellous bone26) was found to match that of the Triceratops ilium. Bone sections 10 x 50 x 縠 3.0 cm with cortices ranging from 0.5 to 5.5 mm in depth (the range of initial cortical-thickness estimates based on gross morphology) were mounted on a servohydraulic mechanical loading frame (MTS Bionix, Minneapolis) and penetrated with an aluminium-bronze T. rex tooth replica. The replica was cast from an actual adult T. rex maxillary tooth, after casts made from some ofthe deeper bite marks revealed the size and shape of the teeth that had impacted the pelvis8 • The replica was penetrated into the ilia sections at 1 mm s-1 to a depth of 11.5 mm, equivalent to the maximum depth of the deepest ilium bite mark8 • Forces were measured with an MTS 25 N strain-gauge-based axial load cell accurate to 0.2%. The forces increased with increasing penetration depth even after the cortical layer had been perforated and the underlying cancellous bone was being crushed. The increase in force with penetration depth is attributed to a greater cortical surface area coming into contact with the semi-conical penetrator tooth as it descended through the ilia.
Phylogeographic analysis of character displacement in feeding phenotypes of snail-feeding Acoptolabrus ground beetles: Morphological measurements
<p>Ecological character displacement predicts that interspecific resource competition results in greater trait divergence between species in sympatry than in allopatry. In this study, we characterize character displacement in 8 species of snail-feeding <i>Acoptolabrus</i> ground beetles (Coleoptera, Carabidae, genus <em>Carabus</em>) in the Far East. <i>Acoptolabrus</i> exhibit divergent feeding phenotypes, including species with a slender forebody for intruding large shells and species with stout heads and mandibles for crushing small shells. Distance measurements (in mm) deposited here are for evaluating body shape variation among 8 <em>Acoptolabrus</em> species.</p>
Data from: Morphological and moisture availability controls of the leaf area-to-sapwood area ratio: analysis of measurements on Australian trees
1. The leaf area-to-sapwood area ratio (LA:SA) is a key plant trait that links photosynthesis to transpiration. The pipe model theory states that the sapwood cross-sectional area of a stem or branch at any point should scale isometrically with the area of leaves distal to that point. Optimization theory further suggests that LA:SA should decrease toward drier climates. Although acclimation of LA:SA to climate has been reported within species, much less is known about the scaling of this trait with climate among species. 2. We compiled LA:SA measurements from 184 species of Australian evergreen angiosperm trees. The pipe model was broadly confirmed, based on measurements on branches and trunks of trees from one to 27 years old. Despite considerable scatter in LA:SA among species, quantile regression showed strong (0.2 < R1 < 0.65) positive relationships between two climatic moisture indices and the lowermost (5%) and uppermost (5–15%) quantiles of log LA:SA, suggesting that moisture availability constrains the envelope of minimum and maximum values of LA:SA typical for any given climate. 3. Interspecific differences in plant hydraulic conductivity are probably responsible for the large scatter of values in the mid-quantile range and may be an important determinant of tree morphology.
APPENDIX III. Morphological measurements taken for the right side of the head. in Revised taxonomy and distributions of Costa Rican moss salamanders (Caudata: Plethodontidae: Nototriton), with descriptions of new taxa
APPENDIX III. Morphological measurements taken for the right side of the head.
Growth and morphological measurements of the coccolithophore Emiliania huxleyi under three salinity conditions
<p>Three datasets presenting results from laboratory culture experiments with the coccolithophore <em>Emiliania huxleyi</em> (Norwegian coastal strain PLYB11 and Mediterranean Sea strain RCC1232) grown for a duration of 156 h under salinity 25 (hyposaline/low salinity), salinity 35 (control) and salinity 45 (hypersaline/high salinity) conditions.<br><br>Cell concentrations and cell size (mean and standard deviation of triplicate counts) were measured using a CASY automated cell counter. Morphometric measurements of coccolith length, coccosphere size and number of coccoliths per cell were measured on scanning electron microscopy images. </p> <p>Supplementary Fig. S1 shows scanning electron microscopy (SEM) images of E. huxleyi coccosphere from strains PLYB11 and RCC1232 under salinity 25, 35, 45 conditions during the early (first 48 h), middle (76-100 h), and end (last 48 h) of each 156-h experiment. A full caption is included within the image file.</p> <p><br><br>These datasets are associated with the following manuscript:</p> <p>Sheward, R. M., Gebühr, C., Bollmann, J. and Herrle, J. O. Short-term response of <em>Emiliania huxleyi</em> growth and morphology to abrupt salinity stress. EGUsphere (preprint), https://doi.org/10.5194/egusphere-2024-349.</p> <p> </p> <p>Correspondence to: Rosie M. Sheward (sheward@em.uni-frankfurt.de)</p>
TABLE 3. Means and standard deviations for 16 morphometric characters measured from males representing 12 in A revision of Anadolua (Orthoptera: Tettigoniidae: Tettigoniinae) based on morphological and bioacoustic characters: Newly confirmed data suggesting a new synonym and two new species
<p><b>TABLE 3</b>. Means and standard deviations for 16 morphometric characters measured from males representing 12 populations belonging to <i>Anadolua</i> genus.</p><table><tbody><tr><th><b>Localities</b></th><th></th><th></th><th></th><th></th><th></th><th></th><th></th><th><b>Characters</b></th><th></th><th></th><th></th><th></th><th></th><th></th><th></th></tr></tbody><tbody><tr><th></th><td></td><td></td><td></td><td></td><td></td><td></td><td>(m ± sd, except NSF)</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr><th></th><td>TLB</td><td>TL</td><td>TLP</td><td>MIDLC</td><td>MADLC</td><td>LHF</td><td>MWHF</td><td>MWFS</td><td>MLS</td><td>MWS</td><td>MWBE</td><td>MLAT</td><td>MWAT</td><td>MLC</td><td>LCMIT</td><td>NSF</td></tr><tr><th><i>A. schwarzi</i> (Muğla-Sandras) N=4</th><td>26.40 ±0.59</td><td>5.26 ±0.11</td><td>7.09 ±0.09</td><td>1.72 ±0.13</td><td>4.79 ±0.09</td><td>18.90 ±0.67</td><td>4.05 ±0.13</td><td>1.06 ±0.01</td><td>0.99 ±0.04</td><td>0.84 ±0.00</td><td>2.41 ±0.05</td><td>1.44 ±0.11</td><td>1.06 ±0.02</td><td>1.80 ±0.02</td><td>0.64 ±0.03</td><td>66.75 ±3.09</td></tr><tr><th><i>A. schwarzi</i> (Denizli-Babadağ) N=10</th><td>23.47 ±1.46</td><td>5.50 ±0.13</td><td>6.30 ±0.10</td><td>1.60 ±0.12</td><td>4.93 ±0.19</td><td>18.57 ±0.40</td><td>3.87 ±0.16</td><td>1.04 ±0.05</td><td>1.04 ±0.01</td><td>0.91 ±0.06</td><td>2.28 ±0.05</td><td>1.42 ±0.09</td><td>0.88 ±0.04</td><td>1.69 ±0.08</td><td>0.52 ±0.02</td><td>65.00 ±2.71</td></tr><tr><th><i>A. schwarzi</i> (İzmir-Bozdağ) N=5</th><td>20.84 ±0.71</td><td>5.37 ±0.14</td><td>6.84 ±0.18</td><td>1.83 ±0.12</td><td>5.08 ±0.08</td><td>18.50 ±0.38</td><td>3.96 ±0.11</td><td>1.00 ±0.08</td><td>1.10 ±0.05</td><td>0.83 ±0.02</td><td>2.43 ±0.07</td><td>1.40 ±0.12</td><td>0.85 ±0.85</td><td>1.63 ±0.09</td><td>0.65 ±0.07</td><td>65.60 ±3.21</td></tr><tr><th><i>A. schwarzi</i> (Antalya-Gömbe_I) N=3</th><td>22.33 ±1.04</td><td>4.76 ±0.09</td><td>6.18 ±0.13</td><td>1.53 ±0.05</td><td>4.72 ±0.13</td><td>18.60 ±0.96</td><td>3.60 ±0.20</td><td>0.91 ±0.06</td><td>1.00 ±0.05</td><td>0.84 ±0.05</td><td>2.19 ±0.08</td><td>1.34 ±0.07</td><td>0.74 ±0.09</td><td>1.74 ±0.07</td><td>0.54 ±0.04</td><td>70.00 ±3.60</td></tr><tr><th><i>A. schwarzi</i> (Antalya-Gömbe_II) N=4</th><td>20.92 ±1.11</td><td>4.82 ±0.10</td><td>6.34 ±0.09</td><td>1.65 ±0.19</td><td>4.89 ±0.16</td><td>18.62 ±0.29</td><td>3.95 ±0.19</td><td>0.93 ±0.03</td><td>1.01 ±0.05</td><td>0.90 ±0.03</td><td>2.22 ±0.07</td><td>1.35 ±0.03</td><td>0.85 ±0.03</td><td>1.71 ±0.03</td><td>0.48 ±0.01</td><td>67.75 ±4.35</td></tr><tr><th><i>A. schwarzi</i> (Antalya-Tahtalıdağ) N=1</th><td>24.40</td><td>5.14</td><td>6.84</td><td>1.84</td><td>4.84</td><td>18.30</td><td>3.90</td><td>1.06</td><td>0.96</td><td>0.84</td><td>2.37</td><td>1.57</td><td>1.00</td><td>1.92</td><td>0.56</td><td>74.00</td></tr><tr><th><i>A. schwarzi</i> (UŞak-Şaphane) N=6</th><td>19.87 ±1.48</td><td>4.81 ±0.14</td><td>6.26 ±0.24</td><td>1.79 ±0.07</td><td>4.79 ±0.19</td><td>18.83 ±0.40</td><td>3.63 ±0.10</td><td>0.97 ±0.02</td><td>1.14 ±0.06</td><td>0.84 ±0.04</td><td>2.10 ±0.06</td><td>1.41 ±0.12</td><td>0.98 ±0.08</td><td>1.77 ±0.10</td><td>0.59 ±0.04</td><td>64.00 ±3.16</td></tr><tr><th><i>A. schwarzi</i> (Kütahya-Civanağa) N=4</th><td>21.17 ±0.89</td><td>5.35 ±0.14</td><td>6.36 ±0.16</td><td>1.72 ±0.11</td><td>4.94 ±0.10</td><td>18.00 ±0.82</td><td>3.42 ±0.15</td><td>0.96 ±0.02</td><td>1.07 ±0.05</td><td>0.71 ±0.03</td><td>2.17 ±0.09</td><td>1.37 ±0.03</td><td>1.02 ±0.09</td><td>1.65 ±0.05</td><td>0.57 ±0.01</td><td>62.2 ±2.22</td></tr><tr><th><i>A. schwarzi</i> (Denizli Çameli) N=5</th><td>22.32 ±4.16</td><td>5.44 ±0.12</td><td>6.81 ±0.15</td><td>1.63 ±0.03</td><td>5.12 ±0.13</td><td>18.98 ±1.24</td><td>4.00 ±0.19</td><td>0.98 ±0.03</td><td>1.13 ±0.03</td><td>0.79 ±0.03</td><td>2.28 ±0.03</td><td>1.45 ±0.06</td><td>0.88 ±0.04</td><td>1.62 ±0.04</td><td>0.57 ±0.01</td><td>64.00 ±3.67</td></tr><tr><th><i>A. bergeri</i> <b>sp. nov.</b> (Konya-Rezebeli) N=4</th><td>22.62 ±1.11</td><td>5.36 ±0.30</td><td>6.43 ±0.30</td><td>2.20 ±0.09</td><td>4.84 ±0.27</td><td>17.27 ±0.48</td><td>4.00 ±0.09</td><td>1.04 ±0.07</td><td>1.13 ±0.07</td><td>0.89 ±0.10</td><td>2.43 ±0.05</td><td>1.33 ±0.11</td><td>1.44 ±0.05</td><td>2.22 ±0.16</td><td>0.87 ±0.06</td><td>46.00 ±1.82</td></tr><tr><th><i>A. bergeri</i> <b>sp. nov.</b> (Antalya-GündoğmuŞ) N=1</th><td>24.00</td><td>5.32</td><td>6.63</td><td>2.21</td><td>4.89</td><td>16.60</td><td>4.00</td><td>0.95</td><td>1.05</td><td>0.84</td><td>2.58</td><td>1.28</td><td>1.19</td><td>2.31</td><td>0.97</td><td>49.00</td></tr><tr><th><i>A. moli</i> <b>sp. nov.</b> (Konya-Sultandağ) N=5</th><td>21.90 ±1.51</td><td>4.72 ±0.08</td><td>6.28 ±0.09</td><td>1.81 ±0.04</td><td>4.59 ±0.10</td><td>17.80 ±0.45</td><td>3.74 ±0.17</td><td>0.93 ±0.05</td><td>1.12 ±0.06</td><td>0.87 ±0.05</td><td>2.24 ±.06</td><td>1.71 ±0.16</td><td>1.14 ±0.05</td><td>1.33 ±0.11</td><td>0.65 ±0.03</td><td>51.80 ±2.39</td></tr></tbody></table><p>m—Mean; sd—Standard deviation; N—individuals</p>
TABLE 5. Means and standard deviations for 15 morphometric characters measured from females representing 10 in A revision of Anadolua (Orthoptera: Tettigoniidae: Tettigoniinae) based on morphological and bioacoustic characters: Newly confirmed data suggesting a new synonym and two new species
<p><b>TABLE 5</b>. Means and standard deviations for 15 morphometric characters measured from females representing 10 populations belonging to <i>Anadolua</i> species.</p><table><tbody><tr><th><b>Characters</b> (mm ± sd)</th></tr></tbody><tbody><tr><th><b>Localities</b></th><td>TLB</td><td>TLP</td><td>MIDLC</td><td>MADLC</td><td>MLHF</td><td>MWHF</td><td>MWFS</td><td>MLS</td><td>MWS</td><td>MWBE</td><td>MLAT</td><td>MWAT</td><td>MLC</td><td>MLO</td><td>MWO</td></tr><tr><th><i>A. schwarzi</i> (Muğla-Sandras) N=3</th><td>25.66 ±1.52</td><td>7.37 ±0.19</td><td>1.96 ±0.08</td><td>5.40 ±0.16</td><td>24.00 ±3.00</td><td>4.33 ±0.15</td><td>1.16 ±0.05</td><td>1.14 ±0.02</td><td>0.89 ±0.05</td><td>2.66 ±0.08</td><td>1.08 ±0.05</td><td>0.27 ±0.02</td><td>1.63 ±0.04</td><td>21.06 ±0.40</td><td>1.90 ±0.10</td></tr><tr><th><i>A. schwarzi</i> (Denizli-Babadağ) N=6</th><td>25.00 ±2.61</td><td>6.96 ±0.25</td><td>2.06 ±0.13</td><td>5.29 ±0.21</td><td>19.83 ±1.25</td><td>4.15 ±0.26</td><td>1.08 ±0.03</td><td>1.30 ±0.09</td><td>0.92 ±0.03</td><td>2.46 ±0.12</td><td>1.15 ±0.07</td><td>0.26 ±0.02</td><td>1.43 ±0.04</td><td>19.80 ±1.58</td><td>1.96 ±0.08</td></tr><tr><th><i>A. schwarzi</i> (İzmir-Bozdağ) N=8</th><td>24.90 ±1.15</td><td>7.89 ±0.31</td><td>2.08 ±0.10</td><td>5.54 ±0.15</td><td>22.00 ±1.00</td><td>4.76 ±0.39</td><td>1.16 ±0.06</td><td>1.13 ±0.09</td><td>0.88 ±0.03</td><td>2.72 ±0.14</td><td>1.06 ±0.07</td><td>0.29 ±0.06</td><td>1.50 ±0.06</td><td>21.81 ±0.55</td><td>2.20 ±0.29</td></tr><tr><th><i>A. schwarzi</i> (Antalya-Gömbe_I) N=2</th><td>23.75 ±0.64</td><td>6.45 ±0.41</td><td>2.00 ±0.07</td><td>5.37 ±0.30</td><td>18.50 ±0.71</td><td>3.90 ±0.00</td><td>1.08 ±0.04</td><td>1.29 ±0.04</td><td>0.84 ±0.07</td><td>2.31 ±0.08</td><td>0.92 ±0.00</td><td>0.32 ±0.01</td><td>1.44 ±0.00</td><td>20.20 ±0.00</td><td>2.00 ±0.00</td></tr><tr><th>A. schwarzi (Antalya-Gömbe_II) N=6</th><td>21.07 ±3.37</td><td>6.28 ±0.41</td><td>1.73 ±0.20</td><td>4.62 ±0.22</td><td>17.67 ±0.42</td><td>3.90 ±0.18</td><td>0.98 ±0.05</td><td>1.09 ±0.04</td><td>0.83 ±0.04</td><td>2.27 ±0.17</td><td>0.94 ±0.06</td><td>0.37 ±0.04</td><td>1.28 ±0.08</td><td>18.41 ±0.58</td><td>2.03 ±0.05</td></tr><tr><th><i>A. schwarzi</i> (UŞak-Şaphane) N=4</th><td>21.70 ±0.57</td><td>6.60 ±0.21</td><td>1.89 ±0.04</td><td>5.14 ±0.20</td><td>20.60 ±0.36</td><td>3.85 ±0.06</td><td>1.06 ±0.03</td><td>1.28 ±0.09</td><td>0.92 ±0.03</td><td>2.43 ±0.03</td><td>1.09 ±0.07</td><td>0.36 ±0.07</td><td>1.22 ±0.03</td><td>22.02 ±0.83</td><td>2.17 ±0.09</td></tr><tr><th><i>A. schwarzi</i> (Kütahya-Civanağa) N=3</th><td>22.33 ±1.15</td><td>6.82 ±0.29</td><td>2.16 ±0.19</td><td>5.04 ±0.28</td><td>18.17 ±0.80</td><td>3.63 ±0.35</td><td>1.05 ±0.00</td><td>1.26 ±0.05</td><td>0.91 ±0.03</td><td>2.45 ±0.03</td><td>0.93 ±0.04</td><td>0.48 ±0.03</td><td>1.28 ±0.05</td><td>19.47 ±0.47</td><td>2.13 ±0.06</td></tr><tr><th><i>A. schwarzi</i> (Denizli Çameli) N=5</th><td>23.04 ±1.51</td><td>7.50 ±0.30</td><td>2.16 ±0.20</td><td>5.61 ±0.11</td><td>21.54 ±0.93</td><td>4.54 ±0.29</td><td>1.09 ±0.03</td><td>1.33 ±0.04</td><td>0.95 ±0.05</td><td>2.62 ±0.09</td><td>1.19 ±0.06</td><td>0.19 ±0.04</td><td>1.40 ±0.02</td><td>22.04 ±1.65</td><td>2.06 ±0.11</td></tr><tr><th><i>A. bergeri</i> <b>sp. nov.</b> (Konya-Rezebeli) N=3</th><td>22.73 ±0.64</td><td>5.80 ±0.16</td><td>1.60 ±0.06</td><td>4.19 ±0.08</td><td>15.97 ±0.15</td><td>3.97 ±0.06</td><td>0.89 ±0.00</td><td>1.09 ±0.03</td><td>0.79 ±0.00</td><td>2.24 ±0.03</td><td>0.80 ±0.04</td><td>0.28 ±0.03</td><td>1.22 ±0.05</td><td>13.97 ±0.15</td><td>1.80 ±0.10</td></tr><tr><th><i>A. moli</i> <b>sp. nov.</b> (Konya-Sultandağ) N=6</th><td>22.25 ±1.17</td><td>6.98 ±0.22</td><td>2.22 ±0.14</td><td>5.22 ±0.16</td><td>20.95 ±0.83</td><td>4.02 ±0.19</td><td>1.10 ±0.06</td><td>1.28 ±0.03</td><td>0.81 ±0.04</td><td>2.49 ±0.07</td><td>1.12 ±0.05</td><td>0.43 ±0.03</td><td>1.45 ±0.07</td><td>21.59 ±1.11</td><td>2.08 ±0.10</td></tr></tbody></table><p>m—Mean; sd—Standard deviation; N—individuals</p>
Phylogeographic analysis of character displacement in feeding phenotypes of snail-feeding Acoptolabrus ground beetles: Morphological measurements
Open the record for dataset details and reuse information.
Data from: Morphological and moisture availability controls of the leaf area-to-sapwood area ratio: analysis of measurements on Australian trees
Open the record for dataset details and reuse information.
Correlation Between Visual Acuity Measurements, Quality of Life and Morphological Parameters in Wet AMD Patients
ClinicalTrials.gov study NCT03438669. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Measuring the Influence of Maxillary Obturator Prosthesis on Facial Morphology in Patient With Unilateral Maxillary Defects Using Stereophotogrammetry
ClinicalTrials.gov study NCT05310149. IPD Sharing: Not stated. Countries: 1. Publications: 0.
A Retrospective, Multicenter, Controlled Clinical Trail: to Evaluate the Clinical Efficiency of Intracranial Aneurysm Assistive Software in the Morphological Measurement
ClinicalTrials.gov study NCT05804474. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Analysis and Measurement of Nail Morphology
ClinicalTrials.gov study NCT06520813. IPD Sharing: UNDECIDED. Countries: 1. Publications: 0.
Pilot Study of Measurement Agreement Between Morphological and Diffusion Tensor Imaging MRI for Pelvic Nerve Cartography
ClinicalTrials.gov study NCT03320343. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Comparisons of Morphological Measurement Between Coronary Computed Tomography and Optical Coherence Tomography
ClinicalTrials.gov study NCT03021382. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Explained variation of the untransformed measurements, the size related ratios, and the ratios defined by the literature for the first two components of the principal component analyses. Abbreviations are explained in table 1. in Morphological variation of the widely distributed genus Stenocorse Marsh, 1968 (Hymenoptera: Braconidae: Doryctinae)
Explained variation of the untransformed measurements, the size related ratios, and the ratios defined by the literature for the first two components of the principal component analyses. Abbreviations are explained in table 1.
Utility of micro-CT for dating post-cranial fractures of known post-traumatic ages through 3D measurements of the trabecular inner morphology
<p>Dataset for the study</p>
Fig. 4 in Towards a standardisation of morphological measurements in the phylum Kinorhyncha
Fig. 4. Schematic representation of the total trunk length and cumulative length. Abbreviations: CL, cumulative length; SL, segment length, including the number of ∑11 the segment; TL, total trunk length; formula: i=1SiL = S1L + S2L + … + S11 L
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