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Fig. 3 in CYP71BL9, the missing link in costunolide synthesis of sunflower
Fig. 3. Two alternative pathways of eupatolide biosynthesis. Comparison of the extracts of transiently transformed N. benthamiana leaves carrying the vector combinations [p19/DXS + HaGAS1 + HaGAO + HaG8H], [p19/DXS + HaGAS1 + HaGAO + HaG8H + HaES] and [p19/DXS + HaGAS1 + HaGAO + HaG8H + CYP71BL9]; A, LC-MS chromatograms; B, UV and (+) MS spectrum of peak d; C, UV and (+) MS spectrum of peak h; D, EIC (C18H27NO5S) [M +H]+ = 370; E, EIC (C H N O S) [M+H]+ = 556; F, scheme, conversion of germacrene A acid to eupatolide by HaG8H and HaES; G, scheme, conversion of 25 37 3 9 germacrene A acid to eupatolide by HaG8H and CYP71BL9
Fig. 4 in CYP71BL9, the missing link in costunolide synthesis of sunflower
Fig. 4. The expression of candidate gene CYP71BL9 in combination with HaG8H in yeast. A, HPLC comparison of extracts from yeast strains [EPY300:Leu2d:GAS/ CR/GAO/HaG8H||Ura:CYP71Bl9] and control [EPY300:Leu2d:GAS/CR/GAO/HaG8H||Ura:empty] peak a: CYP71BL9 enzyme product, peak b: enzyme product of HaG8H and CYP71BL9 at 15.61 min; B, DAD-chromatogram, peak b purified, in comparison with costunolide standard; C UV–Vis spectrum of peak b and costunolide; D, (+) MS2 spectrum of peak b; E, (+) MS2 spectrum of costunolide; F, reaction scheme for the generation of costunolide with HaG8H and CYP71BL9 (not shown: 8βhydroxy-germacrene A acid, 11.50 min)
Fig. 1 in CYP71BL9, the missing link in costunolide synthesis of sunflower
Fig. 1. Phylogeny of cytochrome p450 enzymes. Phylogeny of cytochrome p450 enzymes found in the Asteraceae plant family involved in sesquiterpene lactone biosynthesis. All enzymes shown are members of the CYP71 family. The classification in the subfamilies CYP71AV and CYP71BL is shown on the right side. The numbers at the nodes show bootstrap values from 1000 iterations.
Fig. 2 in CYP71BL9, the missing link in costunolide synthesis of sunflower
Fig. 2. Comparison of the expression of LsCOS and CYP71BL9 in planta. Comparison of extracts from N. benthamiana leaves transiently transformed with the vectors [p19/DXS + HaGAS1 + HaGAO], [p19/DXS + HaGAS1 + HaGAO+ LsCOS] und [p19/DXS + HaGAS1 + HaGAO + CYP71BL9]; A, LC-MS chromatograms; B, UV and (+) MS spectrum von peak a; C, Conversion of germacrene A acid to costunolide by LsCOS and CYP71BL9 as well as addition reaction to costunolide-glutathione (peak b); D, UV and (+) MS spectrum of peak b; peak a: costunolide-cysteine, Peak b: costunolide-glutathione, (*) costunolide-glutathione shown in EIC, (**) Traces of free costunolide shown (peak c); BPC: base peak count, EIC: extracted ion chromatogram
FIGURE 10. Comparison between male and female M in A hidden gem from Northeastern Brazil: A new species of Metaphotina Piza, 1964 (Mantodea, Acontistidae) ecologically linked to the Caatinga
FIGURE 10. Comparison between male and female M. austri sp. n. (A–C) and M. bimaculata (D–F). (A) Head of male M. austri sp. n.; (B) Head of female M. austri sp. n.; (C) Detail of vertex of female M. austri sp. n.; (D) Head of male M. bimaculata; (E) Head of female M. bimaculata; (F) Detail of vertex of female M. bimaculata. Scale bars: 1mm.
FIGURE 9 in A hidden gem from Northeastern Brazil: A new species of Metaphotina Piza, 1964 (Mantodea, Acontistidae) ecologically linked to the Caatinga
FIGURE 9. Comparison between genitalia of known male Metaphotina species. (A) Metaphotina piracicabensis holotype; (B) Metaphotina bimaculata; (C) Metaphotina austri sp. n. holotype. Individual phallomeres out of natural proportion respectively to their matching phallomere and between pairs of phallomeres.
FIGURE 7 in A hidden gem from Northeastern Brazil: A new species of Metaphotina Piza, 1964 (Mantodea, Acontistidae) ecologically linked to the Caatinga
FIGURE 7. Variation in male genitalia in specimens of Metaphotina austri sp. n. in dorsal view (A–B) MNRJ-ENT14-229 [Holotype]; (C–D) MNRJ-ENT14-239; (E–F) MNRJ-ENT14-237; (G–H) MNRJ-ENT14-238. Scale bar: 1mm.
FIGURE 8 in A hidden gem from Northeastern Brazil: A new species of Metaphotina Piza, 1964 (Mantodea, Acontistidae) ecologically linked to the Caatinga
FIGURE 8. Map showing the geographic distribution of Metaphotina austri sp. n. across the Caatinga biome. Specific geographic locality data from Rehn (1916) (as Acontista brevipennis) follows Baker (1913) and Mann (1916).
FIGURE 12 in A hidden gem from Northeastern Brazil: A new species of Metaphotina Piza, 1964 (Mantodea, Acontistidae) ecologically linked to the Caatinga
FIGURE 12. Brazilian Caatinga. (A) Brazilian states encompassing the Caatinga biome, highlighting the location of the 'Depressão Sertaneja Setentrional'; (B) Estação Ecológica de Aiuaba (Ceará), type locality of Metaphotina austri sp. n. (by Nádia Cavalcante); (C–D) Parque Nacional do Catimbau (Pernambuco), where specimens of Metaphotina austri sp. n. were sampled from (by Nathalia Hiluy). Brazilian federal state codes: AL—Alagoas; BA—Bahia; CE—Ceará; MA—Maranh"o; MG—Minas Gerais; PB—Paraíba; PE—Pernambuco; PI—Piauí; RN—Rio Grande do Norte; SE—Sergipe.
FIGURE 4 in A hidden gem from Northeastern Brazil: A new species of Metaphotina Piza, 1964 (Mantodea, Acontistidae) ecologically linked to the Caatinga
FIGURE 4. Colour gradation in the forewing spot of male specimens of Metaphotina austri sp. n. (A) MNRJ-ENT14-232; (B) MNRJ-ENT14-239; (C) MNRJ-ENT14-229 [Holotype]; (D) MNRJ-ENT14-240. Scale bar: 10mm.
FIGURE 1 in A hidden gem from Northeastern Brazil: A new species of Metaphotina Piza, 1964 (Mantodea, Acontistidae) ecologically linked to the Caatinga
FIGURE 1. Representation of Metaphotina austri sp. n. head. (A) Head frontal view; (B) Frons, frontal view, showing the three thirds configuration.
FIGURE 5 in A hidden gem from Northeastern Brazil: A new species of Metaphotina Piza, 1964 (Mantodea, Acontistidae) ecologically linked to the Caatinga
FIGURE 5. Comparison between the wings of Metaphotina austri sp. n. (A) male (wings mirrored) and (B) female and Metaphotina bimaculata (C) male and (D) female. Scale bars: (A, C) 5mm; (B, D) 1mm.
FIGURE 2 in A hidden gem from Northeastern Brazil: A new species of Metaphotina Piza, 1964 (Mantodea, Acontistidae) ecologically linked to the Caatinga
FIGURE 2. Metaphotina austri sp. n. (A) male holotype habitus; (B) Female allotype habitus; (C) Head of male holotype, frontal view; (D) Head of female allotype, frontal view; (E) Allotype ocellar projections; (F) Pronotum of male holotype, dorsal view; (G) Pronotum of female allotype, dorsal view. Scale bars: (A–B) 10mm; (C–G) 1mm.
FIGURE 13 in A hidden gem from Northeastern Brazil: A new species of Metaphotina Piza, 1964 (Mantodea, Acontistidae) ecologically linked to the Caatinga
FIGURE 13. This chart compares the occurrence date of adults (based on collection label data and crowdsourced data from iNaturalist) [green line] with precipitation levels [blue line] between 02°45ꞌS, 34°15ꞌW and 08°45ꞌS, 43°15ꞌW, the geographical range of M. austri sp. n. (data 2019–2020). The chart demonstrates a strong correlation between adult activity and water availability in this specific area of its distribution.
FIGURE 6 in A hidden gem from Northeastern Brazil: A new species of Metaphotina Piza, 1964 (Mantodea, Acontistidae) ecologically linked to the Caatinga
FIGURE 6. (A–E) Genitalia of Metaphotina austri sp. male holotype (A) Left phallomere, dorsal view; (B) Ventral phallomere, dorsal view; (C) Right phallomere, ventral view; (D) Ventral phallomere, oblique view; (E) Ventral phallomere pda and the spine-like projection characteristic of Metaphotina; (F–G) Genitalia of Metaphotina austri sp. n. female allotype (F) Dorsal view; (G) Lateral view. Scale bars: 1mm.
Data of "Towards linking slab window geodynamics with the geophysical and geochemical signature of the upper mantle", Sanhueza et al. EPSL
<p><strong>Description for sanhuezaetal_epsl_ternary.zip</strong><br> These files contain a high resolution figure and a script to reproduce the ternary diagram (Figure 5d) of the paper:</p> <p>Sanhueza et al. Towards linking slab window geodynamics with the geophysical and geochemical signature of the upper mantle, <br> under review in Earth and Planetary Science Letters.</p> <p>A high resolution figure of the ternary diagram is provided (sanhuezaetal_EPSL_ternary.pdf).</p> <p>In addition, the MATLAB script to plot this diagram is included.<br> This script (ternary_plot.m) uses 4 files: temp_RGB.txt, melt_RGB.txt, matrix_RGB.txt, rminmax_RGB.txt</p> <p><br> FILE LIST<br> sanhuezaetal_EPSL_ternary.zip<br> -sanhuezaetal_EPSL_ternary.pdf - High resolution Figure 5d of the manuscript<br> -ternary_plot.m - MATLAB script to generate Figure 5d<br> -temp_RGB.txt - Normalized temperatures in the r-alpha space<br> -melt_RGB.txt - Normalized upward melt flux in the r-alpha space<br> -matrix_RGB.txt - Normalized upward matrix flux in the r-alpha space<br> -rminmax.txt - Envelope of r = rcmin and r = rcmax<br> </p> <p>---------------------------------------------------------------------------------------------------------------------------------------------------------------</p> <p><strong>Description for sanhuezaetal_epsl_3dmodelresults.zip</strong><br> These files contain 3D model results presented in the manuscript:</p> <p>Sanhueza et al. Towards linking slab window geodynamics with the geophysical and geochemical signature of the upper mantle, <br> under review in Earth and Planetary Science Letters.</p> <p>These files were obtained after interpolating the model in a regular grid with cells of 10 km x 10 km x 10 km.</p> <p><br> FILE LIST<br> sanhuezaetal_EPSL_results.zip</p> <p>a0r1_Tvxvyvz.txt, a0r2_Tvxvyvz.txt a0r05_Tvxvyvz.txt<br> a10r1_Tvxvyvz.txt, a10r3_Tvxvyvz.txt, a10r04_Tvxvyvz.txt<br> a20r1_Tvxvyvz.txt, a20r2_Tvxvyvz.txt, a20r05_Tvxvyvz.txt<br> a30r1_Tvxvyvz.txt, a30r07_Tvxvyvz.txt, a30r15_Tvxvyvz.txt<br> a45r1_Tvxvyvz.txt, a45r08_Tvxvyvz.txt, a45r12_Tvxvyvz.txt<br> a60r1_Tvxvyvz.txt, a70r1_Tvxvyvz.txt</p>
Menghubungkan Data Musik dari Spotify dan YouTube dengan Menggunakan Vocabularies Extended dan Linked Data
<p><strong>Menghubungkan Data Musik dari Spotify dan YouTube dengan Menggunakan Vocabularies dan Linked Data. Dataset diambil dari link </strong><a href="https://www.kaggle.com/datasets/salvatorerastelli/spotify-and-youtube">Spotify and Youtube (kaggle.com)</a></p>
Impairments of saccadic and reaching adaptation in Essential Tremor are linked to movement execution - Dataset
<p>Data used for the publication "Impairments of saccadic and reaching adaptation in Essential Tremor are linked to movement execution" https://doi.org/10.1101/2023.04.21.537795</p>
Fig. 5 in An integrated analysis of hyperspectral and morphological data of cicada ovipositors revealed unexplored links to specific oviposition hosts
Fig. 5 Hierarchical cluster cladogram based on 25 morphological characters for each of the 11 cicada species. Ca, Cryptotympana atrata; Hm, Hyalessa maculaticollis; Kc, Karenia caelatata; Kn, Katoa neokanagana; Mm, Meimuna mongolica; Mo, Meimuna opalifera; Ph, Platypleura hilpa; Pk, Platypleura kaempferi; Pl, Pomponia linearis; Sy, Subpsaltria yangi; Tj, Tanna japonensis. Height: the value of the criterion associated with the clustering method for the particular agglomeration
Fig. 4 in An integrated analysis of hyperspectral and morphological data of cicada ovipositors revealed unexplored links to specific oviposition hosts
Fig. 4 Comparison of morphological characters of ovipositors among different species. a Ovipositor length; b ovipositor height; c basal width of ovipositor; d apical width of ovipositor; e subapical width of ovipositor; f curvature. Data are presented as mean ± SE. Ca, Cryptotympana atrata; Hm, Hyalessa maculaticollis; Kc, Karenia caelatata; Kn, Katoa neokanagana; Mm, Meimuna mongolica; Mo, Meimuna opalifera; Ph, Platypleura hilpa; Pk, Platypleura kaempferi; Pl, Pomponia linearis; Sy, Subpsaltria yangi; Tj, Tanna japonensis
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OpenNeuro
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