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Fig. 4 in Phylogeography of the Ibero-Maghrebian red-eyed grass snake (Natrix astreptophora)
Fig. 4 Principal Component Analysis (PCA) for microsatellite data. Samples are coloured according to mitochondrial lineages. The oval outlines represent 95% confidential intervals. For axes 1–2 (left), the x
Fig. 1 in Phylogeography of the Ibero-Maghrebian red-eyed grass snake (Natrix astreptophora)
Fig. 1 Sampling sites and mitochondrial identity of studied red-eyed grass snakes (n = 56). Olive green areas indicate distribution of Natrix astreptophora in Northern Africa according to Bons and Geniez (1996), Schleich et al. (1996) and Sindaco et al. (2013). Two questionable localities in North Africa are not shown (Atlantic coast of Morocco, Schleich et al. 1996; southern Algeria, Hecht 1930). Colours of sampling sites correspond to Figs. 2, 3, 4. Inset: N. astreptophora from Morocco; photo: Salvador Carranza
Fig. 2 in Polyphyly of the grass tribe Hainardieae (Poaceae: Pooideae): identification of its different lineages based on molecular phylogenetics, including morphological and cytogenetic characteristics
Fig. 2 Bayesian phylogenetic tree obtained from nuclear ITS DNA sequences. Branches collapsed in the strict consensus tree based on maximum parsimony analysis are in bold. Posterior probabilities ≥0.95
Fig. 4 in Mitochondrial DNA sequences suggest unexpected phylogenetic position of Corso-Sardinian grass snakes (Natrix cetti) and do not support their species status, with notes on phylogeography and subspecies delineation of grass snakes
Fig. 4 Geographic distribution of mitochondrial clades in grass snakes. Symbols correspond to Fig. 1
Fig. 1 in Mitochondrial DNA sequences suggest unexpected phylogenetic position of Corso-Sardinian grass snakes (Natrix cetti) and do not support their species status, with notes on phylogeography and subspecies delineation of grass snakes
Fig. 1 Maximum likelihood (ML) tree for Natrix sequences calculated with RAxML based on 3,806 bp of mtDNA (ND1, ND2, ND4, cyt b). Numbers above nodes are thorough bootstrap values (RAxML); below nodes, Bayesian posterior probabilities and bootstrap values obtained under maximum parsimony (MP; not shown for some terminal clades with short branch lengths). For new samples, voucher codes (Table 1)
Fig. 3 in Mitochondrial DNA sequences suggest unexpected phylogenetic position of Corso-Sardinian grass snakes (Natrix cetti) and do not support their species status, with notes on phylogeography and subspecies delineation of grass snakes
Fig. 3 Estimated split ages of grass snake clades and their 95% HPD intervals (grey bars). Narrow grey bars are derived from the dating approach using the post-Messinian reopening of the Strait of Gibraltar as age constraint (calibration point I); wide grey bars, using the Sardinian fossil node constraint (calibration point II). Numbers along nodes refer to Table 2; see there for exact values. The depicted nodal ages are based on calibration point I
Fig. 2 in Mitochondrial DNA sequences suggest unexpected phylogenetic position of Corso-Sardinian grass snakes (Natrix cetti) and do not support their species status, with notes on phylogeography and subspecies delineation of grass snakes
Fig. 2 Parsimony networks for haplotypes of Natrix natrix helvetica, N. n. lanzai, a N. n. helvetica x natrix hybrid (left) and Corso-Sardinian grass snakes (right) based on 3,806 bp of mtDNA (ND1, ND2, ND4, cyt b). The large symbol for N. n. helvetica indicates that this haplotype was found twice; small black circles, missing node haplotypes. Connections between haplotypes show number of mutation steps. Connection of haplotypes in left network enforced; 95% connection limit: 27 steps
FIGURE 3 in Nomenclature review on grasses (Poaceae) published in the Bombay Flora
FIGURE 3. Lectotype of Isachne elegans Dalzell, K (barcode K000245419) [© The Board of Trustees of the RBG, Kew. Reproduced with the consent of the Royal Botanic Gardens, Kew]
Effects of different grass distribution patterns and coverage combinations on overland flow resistance mechanisms
<p>To clarify the relationship between grass cover and water flow resistance, laboratory-simulated rainfall experiments were conducted. Five rainfall intensities and three degrees of slope were applied to six degrees of grass cover and six distribution patterns to elucidate the response of overland resistance to the experimental design factors and hydrodynamic parameters and to establish a predictive model. The results indicated that as grass coverage increases, the resistance coefficient also increases; however, with increases in the rainfall intensity and slope, the resistance coefficient decreases, with no apparent critical slope or rainfall intensity. Overland resistance was higher for the horizontal vegetation pattern than the vertical pattern. The flow Reynolds and Froude numbers were negatively correlated with the resistance coefficient. The water flow path index was useful for characterizing overland resistance, reflecting the influence of different grass cover types, and was positively correlated with the resistance coefficient. Based on a dimensional analysis and the π theorem, a model of overland flow resistance was developed. This model effectively predicted overland resistance and quantified the contribution of each factor to the resistance coefficient. The contributions of the slope, rainfall Reynolds number, flow Reynolds number, Froude number, and water flow path index to overland resistance were 12.78%, 6.02%, 34 9.77%, 15.04%, and 56.39%, respectively, with grass cover playing a key role. Simulated rainfall experiments with different degrees of grass coverage and distribution patterns revealed the dynamic mechanisms of overland hydraulic erosion.</p>
Table 4 in The grass root endophytic fungus Flavomyces fulophazii: An abundant source of tetramic acid and chlorinated azaphilone derivatives
<p><b>Table 4</b> NMR spectroscopic data of <i>E</i> and <i>Z</i> diastereoisomers of 11-hydroxyvermelhotin (compound <b>2</b>) in DMSO <i>d</i> 6 and methanol- <i>d</i> 4.</p><table><tbody><tr><th>No. a</th><th>DMSO <i>d</i> 6</th><th></th><th>methanol- <i>d</i> b 4</th><th></th><th></th><th></th></tr></tbody><tbody><tr><th></th><td><i>δ</i> H (<i>E</i> -)</td><td><i>δ</i> C (<i>E</i> -)</td><td><i>δ</i> H (<i>Z</i> -)</td><td><i>δ</i> C (<i>Z</i> -)</td><td><i>δ</i> H</td><td><i>δ</i> C</td></tr><tr><th>1 (NH)</th><td>7.50, brs, 1H</td><td></td><td>7.60, brs, 1H</td><td></td><td>–</td><td>–</td></tr><tr><th>2</th><td></td><td>170.4</td><td></td><td>169.7</td><td>–</td><td>175.9</td></tr><tr><th>3</th><td></td><td>97.9</td><td></td><td>97.7</td><td>–</td><td>98.9</td></tr><tr><th>4</th><td></td><td>192.4</td><td></td><td>193.9</td><td></td><td>194.5</td></tr><tr><th>5</th><td>3.53, s, 2H</td><td>51.3</td><td>3.59, s, 2H</td><td>51.8</td><td>3.80, s, 2H</td><td>54.9</td></tr><tr><th>6</th><td></td><td>163.5</td><td></td><td>164.8</td><td>–</td><td>164.4</td></tr><tr><th>7</th><td>8.07, d, (9.4), 1H</td><td>115.1</td><td>8.05 d, (9.4), 1H</td><td>114.9</td><td>8.17, br, 1H</td><td>116.0</td></tr><tr><th>8</th><td>7.62, dd (9.4, 7.2),1H</td><td>142.0</td><td>7.65, dd (9.4, 7.2), 1H</td><td>142.5</td><td>7.67, dd (9.2, 7.0), 1H</td><td>144.7</td></tr><tr><th>9</th><td>6.64 d (7.2), 1H</td><td>109.0</td><td>6.62 d (7.2), 1H</td><td>108.7</td><td>6.68, d (7.0), 1H</td><td>110.1</td></tr><tr><th>10</th><td>–</td><td>157.6</td><td>–</td><td>157.5</td><td>–</td><td>160.9</td></tr><tr><th>11</th><td>2.74 m, 2H</td><td>40.4</td><td>2.69, m, 2H</td><td>39.9</td><td>2.85,m, 2H</td><td>41.4</td></tr><tr><th>12</th><td>4.19, m, 1H</td><td>61.3</td><td>4.14, m, 1H</td><td>60.7</td><td>4.29, m, 1H</td><td>61.7</td></tr><tr><th>13</th><td>1.14, d (6.0), 3H</td><td>21.9</td><td>1.13, d (6.0), 3H</td><td>21.8</td><td>1.25 d (6.0), 3H</td><td>22.4</td></tr></tbody></table><p><sup>a</sup> Corresponding numbered molecular structure is found in Fig. 2.</p><p><sup>b</sup> Diastereoisomers <i>E</i> and <i>Z</i> hydroxyvermelhotin could not be separately detected in methanol- <i>d</i>.</p>
Table 3 in The grass root endophytic fungus Flavomyces fulophazii: An abundant source of tetramic acid and chlorinated azaphilone derivatives
<p><b>Table 3</b> NMR spectroscopic data of <i>E</i> and <i>Z</i> diastereoisomers of vermelhotin (compound <b>5</b>) in chloroform- <i>d</i>, DMSO <i>d</i> 6 and methanol- <i>d</i> 4.</p><table><tbody><tr><th>No. a</th><th>chloroform- <i>d</i></th><th></th><th></th><th></th><th>DMSO <i>d</i> 6</th><th></th><th></th><th></th><th>methanol- <i>d</i> b 4</th><th></th></tr></tbody><tbody><tr><th></th><td><i>δ</i> H (<i>E-</i>)</td><td><i>δ</i> C (<i>E-</i>)</td><td><i>δ</i> H (<i>Z-</i>)</td><td><i>δ</i> C (<i>Z-</i>)</td><td><i>δ</i> H (<i>E-</i>)</td><td><i>δ</i> C (<i>E-</i>)</td><td><i>δ</i> H (<i>Z-</i>)</td><td><i>δ</i> C (<i>Z-</i>)</td><td><i>δ</i> H</td><td><i>δ</i> C</td></tr><tr><th>1 (N)</th><td>5.62, 1H, brs</td><td>–</td><td>5.50, 1H, brs</td><td>–</td><td>7.45 brs, 1H</td><td>–</td><td>7.65 brs, 1H</td><td>–</td><td>–</td><td>–</td></tr><tr><th>2</th><td>–</td><td>171.4</td><td>–</td><td>172.4</td><td>–</td><td>170.9</td><td>–</td><td>170.0</td><td>–</td><td>175.5</td></tr><tr><th>3</th><td>–</td><td>98.1</td><td>–</td><td>97.9</td><td>–</td><td>97.8</td><td>–</td><td>97.7</td><td>–</td><td>98.7</td></tr><tr><th>4</th><td></td><td>192.5</td><td></td><td>194.6</td><td>–</td><td>192.4</td><td>–</td><td>194.8</td><td>–</td><td>195.8</td></tr><tr><th>5</th><td>3.79, s, 2H</td><td>50.4</td><td>3.82, s, 2H</td><td>50.9</td><td>3.58, s, 2H</td><td>49.9</td><td>3.63, s, 2H</td><td>50.4</td><td>3.74, s, 2H</td><td>54.8</td></tr><tr><th>6</th><td>–</td><td>165.4</td><td>–</td><td>166.7</td><td>–</td><td>163.9</td><td>–</td><td>165.3</td><td>–</td><td>162.3</td></tr><tr><th>7</th><td>8.17, d (9.2), 1H</td><td>116.0</td><td>8.18, d (9.2), 1H</td><td>116.5</td><td>8.03, d (9.0), 1H</td><td>115.3</td><td>8.00, d (9.0), 1H</td><td>115.1</td><td>8.10, br, 1H</td><td>116.5</td></tr><tr><th>8</th><td>7.40, dd (9.2, 7.0),</td><td>141.5</td><td>7.41, dd (9.2, 7.0),</td><td>142.0</td><td>7.63, dd (9.0, 7.2),</td><td>142.1</td><td>7.65, dd (9.0, 7.2),</td><td>142.8</td><td>7.67 dd (9.4, 7.2),</td><td>144.7</td></tr><tr><th></th><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td></tr><tr><th>9</th><td>6.29, d (7.0), 1H</td><td>107.5</td><td>6.28, d (7.0), 1H</td><td>107.5</td><td>6.63, d (7.2), 1H</td><td>108.1</td><td>6.63 d, (7.2), 1H</td><td>108.0</td><td>6.60 d (7.2), 1H</td><td>109.9</td></tr><tr><th>10</th><td>–</td><td>158.7</td><td>–</td><td>158.8</td><td>–</td><td>157.3</td><td>–</td><td>157.4</td><td>–</td><td>160.8</td></tr><tr><th>11</th><td>6.17, dq (15.3, 1.5),</td><td>122.1</td><td>6.16, dq (15.3, 1.5),</td><td>122.1</td><td>6.38, dq (15.5, 1.5),</td><td>122.7</td><td>6.38, dq (15.5, 1.5),</td><td>122.8</td><td>6.35 dq (15.5, 1.5),</td><td>123.5</td></tr><tr><th></th><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td></tr><tr><th>12</th><td>7.42, dq (15.3, 7.1),</td><td>138.6</td><td>7.39, dq (15.3, 7.1),</td><td>139.3</td><td>7.18, dq (15.5, 7.0),</td><td>136.1</td><td>7.17 dq (15.5, 7.0),</td><td>136.5</td><td>7.35, br, 1H</td><td>139.5</td></tr><tr><th></th><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td><td>1H</td><td></td><td></td><td></td></tr><tr><th>13</th><td>2.01, dd (7.1, 1.5),</td><td>19.0</td><td>1.99, dd (7.1, 1.5),</td><td>18.9</td><td>1.97, dd (7.0, 1.5),</td><td>18.3</td><td>1.95, dd (7.0, 1.5),</td><td>18.4</td><td>1.99 dd (7.2, 1.5),</td><td>18.8</td></tr><tr><th></th><td>3H</td><td></td><td>3H</td><td></td><td>3H</td><td></td><td>3H</td><td></td><td>3H</td><td></td></tr></tbody></table><p><sup>a</sup> Corresponding numbered molecular structure is found in Fig. 2.</p><p><sup>b</sup> Diastereoisomers <i>E</i> and <i>Z</i> vermelhotin could not be separately detected in methanol- <i>d</i>.</p>
FIGURES 8–9 in Taxonomic notes on subgenus Steneotarsonemoides (Acari: Tarsonemidae) with description of a new species of Steneotarsonemus from Tiger grass in the northern hill zone of West Bengal, India
FIGURES 8–9. Steneotarsonemus (Steneotarsonemoides) amlisoae n. sp., (male). 8. Dorsal surface. 9. Ventral surface.
FIGURE 2 in Checklist of Kilimanjaro grasses shows that both plot and herbarium methods are necessary to record diversity
FIGURE 2. Collection history of the Mount Kilimanjaro grass specimens by collection year. Hemp's plot collections (blue) are plotted separately from the specimens generated by general botanical surveys (red).
Figure 5 in Aloe liliputana, a new grass aloe from Pondoland, Eastern Cape, Republic of South Africa
Figure 5. The basal portion of the rosette showing the base of the leaves. Photograph: Adam Harrower
Efficacy and Safety of Levocetirizine 8 Weeks Prior and After the Onset of the Grass Pollen Season in Subjects With SAR
ClinicalTrials.gov study NCT00521040. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Efficacy and Safety From a High-dosed Sublingual Grass Pollen Preparation
ClinicalTrials.gov study NCT00623701. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Evaluation of Safety and Efficacy of Specific Immunotherapy With Recombinant Major Allergens of Timothy Grass Pollen Adsorbed Onto Aluminium-hydroxide in Patients With IgE-mediated Allergic Rhinoconju
ClinicalTrials.gov study NCT00671268. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Clinical Efficacy and Safety of Subcutaneous Immunotherapy With gpASIT+™ in Patients With Grass Pollen-induced Allergic Rhinoconjunctivitis
ClinicalTrials.gov study NCT03724240. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Study of Specific Allergen Immunotherapy in Grass Pollen Allergic Subjects by Epicutaneous Allergen Administration
ClinicalTrials.gov study NCT00719511. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Super-fast generation of all-X sperm grass carp by female germline stem cell transplantation
GEO Series GSE261835. Danio rerio; Ctenopharyngodon idella. 13 samples. Type: Expression profiling by high throughput sequencing.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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