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157 results for “wax”
FIGURE 6 in Morphology of the immature female stages and the wax test of ten species of Ceroplastes (Hemiptera: Coccomorpha: Coccidae: Ceroplastinae) from Brazil
FIGURE 6. Glassy wax tests on first-instar nymphs: A) Ceroplastes formosus Hempel; B) C. lucidus Hempel; C) C. diospyros Hempel; D) C. flosculoides Matile-Ferrero; E) C. iheringi Cockerell.
FIGURE 8 in Morphology of the immature female stages and the wax test of ten species of Ceroplastes (Hemiptera: Coccomorpha: Coccidae: Ceroplastinae) from Brazil
FIGURE 8. Wax tests on early third-instar nymphs: A) Ceroplastes formosus Hempel; B) C. lucidus Hempel; C) C. diospyros Hempel; D) C. flosculoides Matile-Ferrero; E) C. iheringi Cockerell.
Distribution. Bahamas, only known from the type locality in East Plana Cay. Introduced into Little Wax Cay in 1973 and on Warderick Wells Cay in 1981, also in Bahamas. in Echimyidae
Distribution. Bahamas, only known from the type locality in East Plana Cay. Introduced into Little Wax Cay in 1973 and on Warderick Wells Cay in 1981, also in Bahamas.
Leaf wax δD record from the Shuizhuyang (SZY) peat deposit in Southeast China
<p>In May 2018, a 2.73-m-long peat core (abbr. SZY18; 26°46′27″N, 119°2′41″E; 990 m above sea level; Figure 1 and S1) was collected from the SZY peat deposit and sliced at 1 cm interval in the field. The lithology of the SZY18 core is as below: 0-30 cm: cultivated soil; 30-195 cm: brown-black peat with visible plant debris; 195-200 cm: gray black peat; 200-220 cm: light brown black peat and 220-273 cm: brown-black to gray black peat.</p>
Jojoba (Simmondsia chinensis) LDAP1 facilitates the efficient packaging of wax esters into lipid droplets
<p>Input structures for a manuscript, along with selected output data and structures. This directory structure contains a cut-down copy of the directories used to generate the simulation data and the analysis. In order to make this fit into the 50GB Zenodo limit, it was constructed with the following tar command: <br><code>tar -zcvf LDAP1.tar.gz --exclude="*BAK" --exclude="*#" --exclude="*log" --exclude="*xsc" --exclude="*coor" --exclude="*vel" --exclude="*[0-9].out" --exclude="*old" --exclude="*dcd" --exclude="*tmp" --exclude="*ppm" --exclude="*png" --exclude="*pdf" --exclude="*catchy*" --exclude="*svg" --exclude="*restart*" --exclude="*history" --exclude="core.*" --exclude="FFTW_NAMD*" --exclude="*avi" --exclude="*mp4" --exclude="*dimer*" --exclude="models" LDAP1</code><br><br></p> <p>The data is split into two directories initially "<strong>build</strong>" and "<strong>Simulations</strong>"</p> <ul> <li>"<strong>build</strong>" directory is the part where initial system for bilayer and lipid droplet simulation were build.</li> <li>"<strong>Simulations</strong>" directory has the different namd files for running simulation, and a sub folder of "<strong>Analysis"</strong> contains script for analysis of the simulation trajectory.</li> </ul>
Data from: Nuclear DNA based species delineations of Coccus scale insects in symbiosis with plants and ants, and the role of plant epicuticular wax in structuring associations
We undertook phylogenetic analysis of nuclear DNA to elucidate species boundaries in the symbiotic Coccus scale insects associated with mutualistic Crematogaster ants and Macaranga plants occurring in the ever-wet forests of Southeast Asia. The coccid specimens clustered into ten lineages, each corresponding to a morphospecies assignment. The lineage identified as C. secretus was separated from the Main Clade by an outgroup. We also examined all pairwise associations among the three symbiont guilds to understand how patterns of association were structured. The analyses revealed that each ant, plant or coccid operational (taxonomic) unit often associated with multiple O(T)Us of each of the other two guilds. However, where testing was feasible, a 'preference' for one or sometimes two partner O(T)Us of each guild was often detected. Mutual 'preferences' or 'avoidances' were relatively common among the symbionts, and no conflicts of interest were apparent. The network of preferred partners among all three guilds showed compartmentalization structured by the presence/absence of plant epicuticular wax, suggesting that this feature plays a fundamental role in how the symbionts select partners that best serve their needs. To a lesser degree, the network was also structured by whether the host plant stems were ant-excavated or hollowed naturally.
Leaf wax data from the Yanjiang peat deposit in Southwest China
<p>The peat sequence was retrieved from the Yanjiang peatland in May 2019. The topmost 8 cm is mainly composed of abundant plant debris. The layer of 8-50 cm consists of brown-black peat. The underlined layer of 50-74 cm is dark brown peat. It transitions to brown-black peat from 74 to 120 cm.</p>
Fig. 3 in Classification of sugarcane genotypes susceptible and resistant to the initial attack of sugarcane borer Diatraea saccharalis using epicuticular wax composition
Fig. 3. Graph with the importance of each selected compound by OPSDA. A) Resistant class – before infestation; B) Susceptible class – before infestation; C) Resistant class – after infestation; and D) Susceptible class – after infestation.
Fig. 2 in Classification of sugarcane genotypes susceptible and resistant to the initial attack of sugarcane borer Diatraea saccharalis using epicuticular wax composition
Fig. 2. Classification of GC-MS dataset before (A–D) and after (E–H) infestation for PLS-DA, LDA, OPSDA, and GA-LDA models. Filled red circles (●) and empty red circles (○) are samples of resistant class. Filled black squares (■) and empty black squares (□) are samples of susceptible class. Filled and empty shapes refer respectively to training and test sets. AI: after infestation; BI: before infestation; Res: resistant; Sus: susceptible. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Classification of sugarcane genotypes susceptible and resistant to the initial attack of sugarcane borer Diatraea saccharalis using epicuticular wax composition
Fig. 1. Chromatogram obtained from refined wax after derivatization of genotypes IM76-228 (resistant) and RB047016 (susceptible) highlights important peaks. AI: after infestation; BI: before infestation; Res: resistant; Sus: susceptible. Peak number identification was listed in Table 2.
Fig. 4 in Cuticular wax composition contributes to different strategies of foliar water uptake in six plant species from foggy rupestrian grassland in tropical mountains
Fig. 4. Chain-length distribution of the very-long-chain (VLC) aliphatic compounds of leaf cuticular waxes of each of the six plant species with two different strategies of foliar water uptake. Data are shown as mean ± SD (n = 3). Bars stand for the contribution of a single chain-length to the total of VLC aliphatic wax load. Dark and grey bars represent plants with fast and slow FWU strategies, respectively. ACL: average-chain-length of the aliphatic wax fraction.
Fig. 5 in Cuticular wax composition contributes to different strategies of foliar water uptake in six plant species from foggy rupestrian grassland in tropical mountains
Fig. 5. NMDS plot of leaf cuticular wax composition of each of the six plant species and (A) leaf water uptake speed (parameter k) and (B) maximum leaf water absorption (parameter Cmax).
Fig. 3 in Cuticular wax composition contributes to different strategies of foliar water uptake in six plant species from foggy rupestrian grassland in tropical mountains
Fig. 3. Gas chromatographic analysis of cuticular waxes of the six plant species with two different strategies of foliar water uptake (FWU). Data are shown as mean ± SD (n = 3). Different letters indicate significant differences among plant species (P ≤ 0.05, One-Way ANOVA). Note that the x-axis scale is modified after the break.
Fig. 2 in Cuticular wax composition contributes to different strategies of foliar water uptake in six plant species from foggy rupestrian grassland in tropical mountains
Fig. 2. Leaf surfaces of the three plant species with fast foliar water uptake strategy under scanning electron microscopy. (A–C) Leandra australis (B) adaxial and (C) abaxial surfaces. (D–F) Byrsonima variabilis (E) adaxial and (F) abaxial surfaces. (G–I) Ocotea pulchella (H) adaxial and (I) abaxial surfaces. St: stomata; T: trichomes. Bars = 10 μm.
Fig. 1 in Cuticular wax composition contributes to different strategies of foliar water uptake in six plant species from foggy rupestrian grassland in tropical mountains
Fig. 1. Leaf surfaces of the three plant species with slow foliar water uptake strategy under scanning electron microscopy. (A–C) Pleroma heteromallum (B) adaxial and (C) abaxial surfaces. (D–F) Trembleya laniflora (E) adaxial and (F) abaxial surfaces. (G–I) Senna reniformis (H) adaxial and (I) abaxial surfaces. Em: emergence; St: stomata; T: trichomes; GT: glandular trichomes. Bars = 10 μm.
Comparison of Effect of Prolotherapy and Paraffin Waxes for Hand Osteoarthritis
ClinicalTrials.gov study NCT03839108. IPD Sharing: NO. Countries: 1. Publications: 2.
Effects of Paraffin Wax Therapy vs METs in Post Burn Hand Contractures
ClinicalTrials.gov study NCT06198062. IPD Sharing: NO. Countries: 1. Publications: 1.
Use of Bee Wax Mammary Areolae to Improve Breastfeeding
ClinicalTrials.gov study NCT03676608. IPD Sharing: NO. Countries: 3. Publications: 2.
Paraffin Wax Bath With Joint Mobilization Technique in Post-traumatic Stiff Knee
ClinicalTrials.gov study NCT06049303. IPD Sharing: NO. Countries: 1. Publications: 9.
Evaluation of the Efficacy and Safety of Absorbable vs Traditional Bone Wax for Facet Fusion After Lumbar Fusion Surgery
ClinicalTrials.gov study NCT07040293. IPD Sharing: YES. Countries: 1. Publications: 17.
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