BUSCADOR RECOLECTA

Mixed gas separation setup: Fig. S1 Single gas separation setup: Time lag method: Fig. S2, Peer reviewed

Contents of this file: Figures S1 to S8 and Table S1. -- Figure S1. CDOM absorption coefficients (aCDOM, in m-1) at UV-B wavelengths 305 nm (top panel), 313 nm (middle panel), and 320 nm (bottom panel) measured during the Malaspina 2010 Expedition. Reported values are depth-weighted averages from surface waters (3 m depth) down to the 20% PAR depth. -- Figure S2. Results of the Dunn’s tests, that were performed after Kruskal-Wallis tests to identify if aCDOM (top row), ap (middle row) and ap as % of anw (bottom row) at 305 nm (left column), 313 nm (middle column) and 320 nm (right column) varied significantly (p<0.05) between Longhurst provinces during the Malaspina 2010 Expedition. For a description of the Longhurst province codes, see Fig. 1. -- Figure S3. Particulate absorption coefficients (ap, in m-1) at UV-B wavelengths 305 nm (top panel), 313 nm (middle panel), and 320 nm (bottom panel) measured during the Malaspina Expedition. Reported values are depth-weighted averages from surface waters (3 m depth) down to the 20% PAR depth. -- Figure S4. Downwelling diffuse attenuation coefficients (Kd, in m-1) for the UV-B wavelengths 305 nm (top panel), 313 nm (middle panel), and 320 nm (bottom panel) measured during the Malaspina 2010 Circumnavigation. -- Figure S5. Downwelling diffuse attenuation coefficients (Kd, in m-1) for the UV-A wavelengths 340 nm (top panel), 380 nm (middle panel), and 395 nm (bottom panel) measured during the Malaspina 2010 Expedition. -- Figure S6. Downwelling diffuse attenuation coefficients (Kd, in m-1) for the integrated PAR spectrum (400–700 nm) measured during the Malaspina 2010 Expedition. -- Figure S7. Results of the Dunn’s tests, that were performed after Kruskal-Wallis tests to identify if the downwelling diffuse attenuation coefficient (Kd) at 305, 313, 320, 340 nm varied significantly (p <0.05) between Longhurst provinces during the Malaspina 2010 Expedition. For a description of the Longhurst provinces code, see Fig. 1. -- Figure S8. Seasonal comparison between cloud fractions in the northern and southern tropics (15.5N to 15.5S) in year 2010. Bars represent monthly averages (mean  SD) of 1 x 1 sector squares between 179.5W and 179.5E (n=5760 per bar). Data were obtained from the publicly available Aqua/MODIS satellite data set curated by NASA’s Earth Observatory (https://earthobservatory.nasa.gov/global-maps/MODAL2_M_CLD_FR). WIN, SPR, SUM and AUT refer to winter, spring, summer and autumn, respectively. WIN1 represents December for the northern latitudes and June for the southern latitudes. Asterisks indicate instances where the non-paired t-test identified significantly different means at level p <0.01. -- Table S1. Slope, correlation, 95% confidence intervals and p-values determined as part of the pairwise correlation analysis with the variables sea surface temperature, Chl-a and Kd(PAR), as well as aCDOM, ap and Kd(λ) at wavelengths 305, 313 and 320 nm. For Chl-a, aCDOM and ap, depth-weighted (3 m to 20% PAR depth) average values were used for the analysis., Peer reviewed

Supplementary data 1. Surveyed vineyards: characterization, management, climatological data, and abiotic factors. • Table S1. Characterization of the 80 vineyards surveyed in early autumn of 2019. • Table S2. Pesticide application schedule for integrated pest management. • Figure S1. Monthly precipitations in DOCa Rioja region in 2019. Supplementary data 2. Development, optimization, and implementation of the qPCR toolkit. • Table S3. Soil organisms identified from sucrose-gradient centrifugation isolates. • Table S4. Steinernematid populations used in cross-amplification tests for Steinernema sp. affine-group. Supplementary data 3. Results • Table S5. Descriptive and statistics of abiotic factors. • Table S6. Bivariate Pearson correlation tests among soil properties and environmental variables. • Figure S2. DNA abundance of soil samples extracted through sucrose-gradient centrifugation. • Figure S3. Frequencies of occurrences of soil organisms isolated through sucrose-gradient centrifugation. • Table S7. Statistics of abundance and frequency of occurrence of soil organisms isolated through sucrose-gradient centrifugation. • Table S8. Statistics of soil activity rates. • Figure S4. Effect of different vineyard managements on the soil activity associated with larval mortality in insect-baits. • Figure S5. Effect of different vineyard managements on soil activities associated with nematode emergences in insect-baits., Peer reviewed

Suplementary information: TABLES: Table S.1. Almond hulls ash composition. Table S.2. Relative influence of the feedstock composition and reaction medium from the analysis of variance (ANOVA) and cause-effect Pareto principle. Table S.3 Detailed biocrude chemical composition (% Area). Table S.4. Hydrothermal treatment experiments: comparation between Actual (Act.) experimental and predicted (Pred.) data obtained with the ANOVA models FIGURES: Figure S.1. FT-IR of disposable FFP2 masks., Peer reviewed

Multimedia component 1: Figures, tables and schemes supplementarys., Peer reviewed

FIGURE S1 Custom FIB pattern for the fabrication of graded ZPPs. (A) Grey-scale coded dwell-time distribution of the applied ‘stream file’ with decreasing dwell times towards the outer diameter of the graded region. (B) The dwell-time line profile along the green-dotted line in A shows the cosinusoidal shape of the dwell-time distribution. TABLE S1 Fabrication parameters (number of passes/magnification) for graded Zernike phase plates with different inner and outer radii. TABLE S2 Parameters for the fabrication of conventional ZPP with different inner radii. FIGURE S2 30 keV STEM images and thickness profile at the aC-film/vacuum interface of a holey carbon film. (A) BF-STEM image and (B) HAADF-STEM image of a holey aC film at the interface between the aC film and vacuum region. (C) Thickness profile along the red arrow in B showing a smooth thickness increase over a width of ∼5 nm., Peer reviewed

Resources available on the publisher's site: http://dx.doi.org/10.1016/j.foodres.2022.111203, Peer reviewed

BVS calculations for complexes 1 and 2, data collection parameters and structure solution and refinement details for complexes 1 and 2, overlay of the metallic cores displayed by complex 1 and the recently reported complex [MnIII12MnII6(O)6(OH)2(OMe)6(L)4(LH)2Br12], (22) packing diagrams for 1 and 2, and powder XRD patterns for 1 and 2., Peer reviewed

Some remarks on the yield of the carbonization and activation processes As summarized in Table S1, the yields of the pyrolysis process of VS is equal to 28.28% at 600ºC and 25.08 % at 900ºC. The fact that the carbonization temperature does not exert any significant influence on the final yield of the process is coherent with the mechanism commonly postulated for the pyrolysis of lignocellulosic materials. Briefly, when these materials are subjected to heat treatments under an inert atmosphere, a remarkable mass loss occurs at temperatures below 660◦C due to the removal of volatile matter. Above this temperature, a progressive aromatization of the remaining carbonaceous solid can be observed. Such an aromatization takes place as a result of the release of a small amount of hydrogen. Hence, the mass loss is scarce and virtually constant regardless of what the thermal treatment temperature is., Peer reviewed

15 pages. -- The file includes tables and figures. -- Table S1. Oligonucleotides used in this study. -- Fig. S1. Sequence alignment of TbLipT with octanoyltransferases. Identical residues are shown highlighted in black and similar residues are highlighted in grey. The conserved lysine residues of PFAM03099 are indicated by an arrow; cysteines involved in catalytic activity are marked with an asterisk. The alignment was created using T-Coffe and BoxShade programs ((Notredame et al., 2000) with the following sequences: Trypanosoma brucei TbLipT (EAN79891); Trypanosoma cruzi TcLipT (EAN92615.1); Leishmania major LmLipT (CAJ09270.1); Arabidopsis thaliana LIP2 (Q9SXP7.1); Saccharomyces cerevisiae ScLip2 (NP_013340.1); Homo sapiens HsLIPT2 (NP_001138341.1); Mycobacterium tuberculosis MtLipB (CCE37687.1); Escherichia coli EcLipB (AKF71110.1); Bacillus subtilis BsLipM (P54511.2). -- Figure S2. Phylogenetic analysis of octanoyltransferases. -- Fig. S3. Sequence alignment of TbLipL with lipoate ligases. -- Fig. S4. Alignment of TbLipL with amidotransferases. -- Fig. S5. Growth of Saccharomyces cerevisiae wild type strain (BY4741, WT), ∆lip2 and ∆lip3 null mutants expressing TbLipT and TbLipL in complex medium containing ethanol as carbon source. -- Fig. S6. Loading controls related to Fig. 2C.-- Fig. S6. Loading controls related to Fig. 2C. -- Fig. S8. Loading controls related to Fig. 4C. -- Fig. S9. Loading controls related to Fig. 5C. -- Fig. S10. A) Original uncropped image related to Fig. 6B. Protein extracts from the indicated strains were analyzed by Western blot with antibodies against LA. Amersham ECL Rainbow Marker (Cytiva) was used as molecular weight marker. B) In parallel, a 12% SDS-PAGE gel was stained with Coomassie blue. MWM: Amersham LMW Calibration kit (GE Healthcare). -- Fig. S11. Loading controls related to Fig. 8C. -- Fig. S12. Overlay of I-tasser generated model of the N-term domain of TbLipL (pink) and the crystal structure of the bovine lipoyltransferase bLT (light green, Protein Data Bank 2E5A), highlighting the similar position of lysine residues K169 of TbLipL (red) and K135 of bLT (green), shown as stick representation., Peer reviewed