Resultados totales (Incluyendo duplicados): 35638
Encontrada(s) 3564 página(s)
Encontrada(s) 3564 página(s)
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359067
Dataset. 2021
SUPPLEMENTARY MATERIAL STRUCTURE AND TROPHIC NICHES IN MOBILE EPIFAUNA ASSEMBLAGES ASSOCIATED WITH SEAWEEDS AND HABITATS OF SYNGNATHID FISHES IN CÍES ARCHIPELAGO (ATLANTIC ISLANDS MARINE NATIONAL PARK, NORTH WEST IBERIA)
- Piñeiro-Corbeira, Cristina
- Iglesias, Laura
- Nogueira, Raquel
- Campos, Sara
- Jiménez, Arturo
- Regueira, Marcos
- Barreiro, Rodolfo
- Planas, Miguel
5 tables, 3 figures, Supplementary Table 1. Conversion factors applied to δ15N and δ13C for lipid normalization in taxa associated to seaweeds on Cíes Archipelago. (-) normalization not required.-- Supplementary Table 2. Relative abundances (%) in epifauna identified in 2017-2018 (spring, summer and autumn) on canopy-forming seaweeds in Cíes Archipelago. * indicates <0.01%.-- Supplementary Table 3. Summary table for Multipatt results (p-value) showing taxa significantly associated to Year (2017 – 2018) and Season (Sp – Spring; Su – Summer; Au – Autumn).-- Supplementary Table 4. Taxa richness (S), Shannon diversity (H’), Simpson dominance (D’), and Pielou’s evenness (J’) in epifaunal assemblages associated to Codium spp. and Gongolaria baccata.-- Supplementary Table 5. Summary table for Multipatt results (p-value) showing taxa significantly associated to seaweed (Codium spp and G. baccata) assemblages seasonally sampled from Summer-2017 (Su17) to Autumn-2018 (Au18).-- Supplementary Table 6. Syngnathid specimens (recaptured specimens not included) collected in 2017 and 2018 (spring, summer and autumn) by UVC on Cíes Archipelago.-- Supplementary Figure 1. Two-dimensional non-metric multidimensional scaling (NMDS; Bray–Curtis similarities) plot of the variation in stable isotopes (δ13C and δ15N) in syngnathids (H. guttulatus, E. aequoreus and S. acus) collected in spring, summer and autumn (2017 and 2018).-- Supplementary Figure 2. Two-dimensional convex hulls of the variation in δ13C and δ15N in epifauna community and syngnathids, considering Year (2017 – 2018), functional groups (FG), and main taxa (Taxa).-- Supplementary Figure 3. Seasonal fluctuations of epifaunal taxa (bars; relative abundance in taxa contributing to syngnathid feeding regimes) in canopy-forming assemblages (Codium spp. and Gongolaria baccata), and syngnathids abundance (dotted lines) on Cíes Archipelago in surveys carried out in 2017 – 2018, Peer reviewed
Proyecto: //
DOI: http://hdl.handle.net/10261/359067
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359067
HANDLE: http://hdl.handle.net/10261/359067
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359067
PMID: http://hdl.handle.net/10261/359067
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359067
Ver en: http://hdl.handle.net/10261/359067
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359067
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359154
Dataset. 2021
SEA TEMPERATURE EFFECTS ON DEPTH USE AND HABITAT SELECTION IN A MARINE FISH COMMUNITY [DATASET]
- Freitas, Carla
- Villegas-Ríos, David
- Moland, Even
- Olsen, Esben Moland
4 files, 1. Understanding the responses of aquatic animals to temperature variability is essential to predict impacts of future climate change and to inform conservation and management. Most ectotherms such as fish are expected to adjust their behaviour to avoid extreme temperatures and minimize acute changes in body temperature. In coastal Skagerrak, Norway, sea surface temperature (SST) ranges seasonally from 0 to over 20 °C, representing a challenge to the fish community which includes both cold-, cool- and warm-water affinity species.
2. By acoustically tracking 111 individuals of Atlantic cod (Gadus morhua), pollack (Pollachius pollachius) and ballan wrasse (Labrus bergylta) in 2015 - 2018, we examined how coexisting species within a fish community adjusted their behaviour (i.e. vertical distribution in the water column and habitat selection) to cope with the thermal variation.
3. Mixed-effect models showed that thermal preference was a main driver of behaviour and habitat use of the fish community in a southern Norwegian fjord. Cod used colder waters, compared with pollack and ballan wrasse. Increases in SST during summer were associated with the use of deeper, colder waters by cod, especially by larger individuals, and conversely with the occupancy of shallower areas by pollack and ballan wrasse. During winter, when SST dropped and the thermal stratification reversed, pollack and ballan wrasse moved to deeper, relatively warmer areas, while cod selected shallower, colder habitats. Though habitat selection was affected by temperature, species-specific habitat selection was observed even when temperature was similar throughout habitats.
4. This study shows how cohabiting fish species respond to thermal heterogeneity, suggesting that i) temperature regulates the access to the different depths and habitats and ii) behavioural plasticity may be an important factor for coping with temperature variability and potentially for adaptation to climate change, The Research Council of Norway, Award: 294926; European Union’s Horizon 2020, Award: 793627; Regionale forskningsfond Oslofjordfondet, Award: 272090, Peer reviewed
Proyecto: EC/H2020/793627
DOI: http://hdl.handle.net/10261/359154
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359154
HANDLE: http://hdl.handle.net/10261/359154
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359154
PMID: http://hdl.handle.net/10261/359154
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359154
Ver en: http://hdl.handle.net/10261/359154
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359154
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359192
Dataset. 2024
PUSHING THE LIMITS OF C3 INTRINSIC WATER USE EFFICIENCY IN MEDITERRANEAN SEMIARID STEPPES: RESPONSES OF A DROUGHT-AVOIDER PERENNIAL GRASS TO CLIMATE ARIDIFICATION [DATASET]
- Ren, Wei
- García-Palacios, Pablo
- Soliveres, Santiago
- Prieto Aguilar, Iván
- Maestre, Fernando T.
- Querejeta Mercader, José Ignacio
We investigated the variations in multiple plant traits in the perennial tussock grass Stipa tenacissima along an aridity gradient in Spain. Traits measured include leaf stable isotopes (δ18O, δ13C, δ15N), nutrient concentrations (N, P, K), and culm water content and isotopic composition (δ18O, δ2H) of paired pure-grass and shrub-encroached S. tenacissima steppes along a 350 km aridity gradient in Spain (10 sites, 160 individuals). Here, we provide a summary of mean (± SE), minimum and maximum values of S. tenacissima traits for pure grass and shrub-encroached steppes at ten sampling locations. The blank cells for the variable "Plant cover" indicate that there are no maximum or minimum values per study plot, just a single overall value for each study plot., [Methods] We selected 10 locations along a ~350 km transect from Central to Southeastern Spain (Fig. S1) representing an increasing climatic aridity gradient encompassing much of the geographical distribution of S. tenacissima in the Iberian Peninsula, including areas with MAP ranging from 346 to 464 mm and mean annual temperature (MAT) from 12.6 to 16.3℃ (Supporting Information Table S1, S2). The climate is semiarid Mediterranean, with asynchronous wet and warm seasons, as maximum and minimum precipitation fall in winter and summer, respectively. The soils are classified as Calcisols and are weakly developed and thin, with sandy loam texture and high pH values (>7–8) (Maestre et al. 2009). Transpiration fluxes and primary productivity in semiarid S. tenacissima steppes are rather low, with peak plant ecophysiological activity occurring shortly after the irregular rainfall pulses (Domingo et al. 2011).
Using the geographical coordinates of each location, we obtained the elevation and available climatic information from Worldclim (http://www.worldclim.org; Hijmans et al. 2005), and measured the minimum distance to the Mediterranean Sea (DTMS) using Google Earth. Climate variables included temperature and precipitation (mean annual, average of the wettest and coldest quarter and month, average of the driest and warmest quarter and month). We calculated the Aridity for each location as A= 1- (annual precipitation/annual potential evapotranspiration). Mean annual vapor pressure deficit (VPD) for each location was obtained from TerraClimate data (Abatzoglou et al. 2018). Several geographic and climatic variables showed substantial multi-collinearity along the aridity gradient (Table S3)., [Field surveys] Field sampling was conducted during May 2008, and no permissions were needed for fieldwork. At each sampling location, we selected two paired sites with contrasting woody shrub cover (i.e. pure S. tenacissima grass steppes vs. nearby shrub-encroached steppes with 26.4% shrub cover; see Maestre et al. 2009), totaling 20 sites. The encroaching shrub species were Quercus coccifera, Pistacia lentiscus, Rhamnus lycioides, Juniperus phoenicea and Juniperus oxycedrus. Plant cover at each site was measured using the point-intercept methodology in four 30-m transects separated 8 m from each other.
At each of the 20 sites, we sampled 8 adult S. tenacissima individuals (replicates) resulting in 160 individuals. The canopy size of each tussock individual was measured using two diameters (parallel and perpendicular to the steepest slope) and calculated using the formula for the area of an ellipse. At sites undergoing woody shrub encroachment, we sampled tussock individuals located at a fixed distance (5-m) from the canopy edge of woody shrubs to exclude direct, immediate competition effects between shrubs and S. tenacissima at close range. Our assessment of how woody shrub encroachment impacts on the water and nutrient status of S. tenacissima focuses on diffuse competitive effects of encroaching shrubs, and therefore excludes the effects of direct, interspecific shrub-grass interactions at close range., [Isotopic and nutrient analyses] Fully expanded and healthy-looking leaves with their corresponding basal culms were collected for isotopic and nutrient analyses. Green leaf samples were oven-dried (60℃, 24h) and finely ground using a ball mill. Leaf δ13C and δ15N were measured by continuous flow dual isotopic analysis using an IsoPrime 100 IRMS (IsoPrime, UK) interfaced to a CHNOS C/N Elemental Analyzer. Leaf δ18O was measured in continuous flow using an Elementar PYRO Cube interfaced to a Thermo Finnigan Delta V IRMS (Thermo Finnigan, Germany). The analytical precision was ±0.1‰ for leaf δ13C and ±0.2‰ for leaf δ18O and δ15N. Ground leaves were digested with HNO3:HClO4 (2:1, v:v) and P and K concentrations were measured in the digested solution by a Perkin Elmer Inductively Coupled Plasma 5500 atomic absorption spectrometer.
Time-integrated WUEi at leaf level was estimated based on foliar δ13C values (Cernusak et al., 2013) as determined by the atmospheric CO2 concentration (385.97 ppm in 2008) and the ratio of atmospheric [CO2] to intracellular [CO2] (ci/ca) as follows:
WUEi = A/gs = ca [1-(ci/ca)]×0.625 Eqn (1)
d13Cleaf = d13Catm – a - (b-a)×(ci/ca) Eqn (2)
where δ13Cleaf is the foliar isotope ratio, δ13Catm is isotopic ratio of atmospheric CO2 (-8.321‰ in 2008) and a and b are isotopic fractionation factors associated with CO2 diffusion (4.4‰) and Rubisco discrimination (27‰), respectively.
Non-transpiring basal culms (5-6) from the base of the perennial tussock grasses near ground level were collected from each target individual as a proxy of the isotopic signature of source water used by S. tenacissima at the peak of the growing season. The basal culms were quickly placed in capped glass vials, sealed with parafilm, transported in coolers, and stored in the freezer (-20℃) until water extraction. Water extractions were performed using cryogenic vacuum distillation and lasted 2-4 h at 105 ºC until culm water was extracted completely. Culm water content (CWC) was calculated as:
CWC=(Wwet-Wdry)/Wwet·100% Eqn (3)
where Wwet is the weight of fresh culm sample and Wdry is the weight of culm sample after water extraction. The culm water δ18O and δ2H values of half of the samples (n=80) were determined by continuous flow using a Thermo Gas Bench II interfaced to a Thermo Finnigan Delta plus XL IRMS (Thermo Finnigan, Germany). The analytical precision was ±0.12‰ for δ18O and ±0.6‰ for δ2H. Water extracted from non-transpiring tissues in grasses inevitably includes some phloem water mixed with xylem water, which may cause some isotopic fractionation issues (Barnard et al., 2006; Jiang et al., 2022)., 1. Intrinsic water use efficiency (WUEi) reflects the trade-off between photosynthetic carbon gain and water loss through stomatal conductance and is key for understanding dryland plant responses to climate change. Stipa tenacissima is a perennial tussock C3 grass with an opportunistic, drought-avoiding water use strategy that dominates arid and semiarid steppes across the western Mediterranean region. However, its ecophysiological responses to aridification and woody shrub encroachment, a major land-use change in drylands worldwide, are not well understood., 2. We investigated the variations in leaf stable isotopes (δ18O, δ13C, δ15N), nutrient concentrations (N, P, K), and culm water content and isotopic composition (δ18O, δ2H) of paired pure-grass and shrub-encroached S. tenacissima steppes along a 350 km aridity gradient in Spain (10 sites, 160 individuals)., 3. Culm water isotopes revealed that S. tenacissima is a shallow-rooted grass that depends heavily on recent rainwater for water uptake, which may render it vulnerable to increasingly irregular rainfall combined with faster topsoil drying under climate warming and aridification. With increasing aridity, S. tenacissima enhanced leaf-level WUEi through more stringent stomatal regulation of plant water flux and carbon assimilation (higher δ13C and δ18O), reaching exceptionally high δ13C values (-23 to -21‰) at the most arid steppes. Foliar N concentration was remarkably low across sites regardless of woody shrub encroachment, evidencing severe water and N co-limitation of photosynthesis and productivity. Shrub encroachment decreased leaf P and K but did not affect S. tenacissima water status. Perennial grass cover decreased markedly with both declining winter rainfall and shrub encroachment suggesting population- rather than individual-level responses of S. tenacissima to these changes., 4. The fundamental physiological constraints of photosynthetic C3 metabolism combined with low foliar N content may hamper the ability of S. tenacissima and other drought-avoider species with shallow roots to achieve further adaptive improvements in WUEi under increasing climatic stress. A drought-avoiding water use strategy based on early stomatal closure and photosynthesis suppression during prolonged rainless periods may thus compromise the capacity of S. tenacissima steppes to maintain perennial grass cover, sustain productivity and cope with ongoing climate aridification at the drier parts of their current distribution., Ministerio de Ciencia e Innovación, Award: AGL-2006-11234, Ministerio de Ciencia e Innovación, Award: CGL2010-21064, Ministerio de Ciencia e Innovación, Award: CGL2013-48753-R, Ministerio de Ciencia e Innovación, Award: PID2019-107382RB-I00, Ministerio de Ciencia e Innovación, Award: PRX19/00301, Ministerio de Ciencia e Innovación, Award: EUR2022-134048, European Research Council, Award: 647038 [BIODESERT], Fundación BBVA, Award: BIOCON06 ⁄ 105, Generalitat Valenciana, Award: CIDEGENT/2018/041, Peer reviewed
DOI: http://hdl.handle.net/10261/359192
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359192
HANDLE: http://hdl.handle.net/10261/359192
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359192
PMID: http://hdl.handle.net/10261/359192
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359192
Ver en: http://hdl.handle.net/10261/359192
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359192
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359198
Dataset. 2024
FUNCTIONAL ECOLOGY SUPPLEMENTARY INFORMATION: PUSHING THE LIMITS OF C3 INTRINSIC WATER USE EFFICIENCY IN MEDITERRANEAN SEMIARID STEPPES: RESPONSES OF A DROUGHT-AVOIDER PERENNIAL GRASS TO CLIMATE ARIDIFICATION
- Ren, Wei
- García-Palacios, Pablo
- Soliveres, Santiago
- Prieto Aguilar, Iván
- Maestre, Fernando T.
- Querejeta Mercader, José Ignacio
The following Supporting Information is available for this article:
Fig. S1 Map showing the ten sampling locations (denoted by two letter codes) along a 350 km aridity gradient in the Iberian Peninsula.
Fig. S2 Relationship between leaf δ18O and K concentration for S. tenacissima individuals at ten sampling locations along the studied aridity gradient.
Fig. S3 Culm water δ18O plotted against δ2H values for S. tenacissima individuals at ten sampling locations along the studied aridity gradient.
Table S1 Geographic and climatic characteristics of ten sampling locations along the aridity gradient from Central to Southeastern Spain
Table S2 Summary of mean (± SE), minimum and maximum values of S. tenacissima traits for pure grass and shrub-encroached steppes at ten sampling locations.
Table S3 Pearson’s correlation coefficients between geographic and climatic variables of sampling locations along the studied aridity gradient (n=10).
Table S4 Results from linear mixed regression models for relationships of S. tenacissima traits and PCAaxis1 scores with key geographic and mean annual mean climatic variables across individuals along the studied aridity gradient.
Table S5 Results from linear mixed regression models for relationships of S. tenacissima traits and PCAaxis1 scores with key mean seasonal climatic variables across individuals along the studied aridity gradient., Peer reviewed
Proyecto: //
DOI: http://hdl.handle.net/10261/359198, https://doi.org/10.1111/1365-2435.14518
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359198
HANDLE: http://hdl.handle.net/10261/359198, https://doi.org/10.1111/1365-2435.14518
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359198
PMID: http://hdl.handle.net/10261/359198, https://doi.org/10.1111/1365-2435.14518
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359198
Ver en: http://hdl.handle.net/10261/359198, https://doi.org/10.1111/1365-2435.14518
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359198
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359207
Dataset. 2023
SUPPLEMENTARY MATERIALS FOR A MULTI-SPECIFIC, MULTI-AFFINITY ANTIBODY PLATFORM NEUTRALIZES SARBECOVIRUSES AND CONFERS PROTECTION AGAINST SARS-COV-2 IN VIVO
- Burn Aschner, Clare
- Muthuraman, Krithika
- Kucharska, Iga
- Cui, Hong
- Prieto, Katherine
- Nair, Manoj S.
- Wang, Maple
- Huang, Yaoxing
- Christie-Holmes, Natasha
- Poon, Betty
- Lam, Jessica
- Sultana, Azmiri
- Kozak, Robert
- Mubareka, Samira
- Rubinstein, John L.
- Rujas, Edurne
- Treanor, Bebhinn
- Ho, David D.
- Jetha, Arif
- Julien, Jean-Philippe
All data associated with this study are present in the paper or the Supplementary Materials. The electron microscopy maps have been deposited in the Electron Microscopy Data Bank (EMDB) with accession codes EMD-28067 (tri-specific MB, refinement with no symmetry) and EMD-28068 (tri-specific MB, octahedral symmetry). The crystal structure of 80 Fab–RBD has been deposited in the Protein Data Bank (PDB ID: 8DNN). Materials will be made available to the scientific community by contacting the corresponding author and completion of a materials transfer agreement. This work is licensed under a Creative Commons Attribution 4.0 International (CC BY 4.0) license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. This license does not apply to figures/photos/artwork or other content included in the article that is credited to a third party; obtain authorization from the rights holder before using this material., The PDF file includes:
Supplementary Materials and Methods
Figs. S1 to S10
Tables S1 to S3
Legend for data file S1
References (72–92)
Other Supplementary Material for this manuscript includes the following:
Data file S1
MDAR Reproducibility Checklist, Peer reviewed
Proyecto: //
DOI: http://hdl.handle.net/10261/359207
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359207
HANDLE: http://hdl.handle.net/10261/359207
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359207
PMID: http://hdl.handle.net/10261/359207
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359207
Ver en: http://hdl.handle.net/10261/359207
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359207
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359208
Dataset. 2024
SUPPLEMENTARY MATERIAL FOR LIFE CYCLE ASSESSMENT OF WHEAT STRAW PYROLYSIS WITH VOLATILE FRACTIONS CHEMICAL LOOPING COMBUSTION [DATASET]
- Mendiara, Teresa
- Navajas, A.
- Abad Secades, Alberto
- Pröll, Tobias
- Munárriz, Mikel
- Gandía, L. M.
- García Labiano, Francisco
- Diego Poza, Luis F. de
Under a Creative Commons license CC BY 4.0., Table S1: Numerical values of the EIIs for the processes of Case I. Table S2: Numerical values of the EIIs for the processes of Case II. Table S3: Numerical values of the EIIs for the processes of Case III., Peer reviewed
Proyecto: //
DOI: http://hdl.handle.net/10261/359208
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359208
HANDLE: http://hdl.handle.net/10261/359208
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359208
PMID: http://hdl.handle.net/10261/359208
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359208
Ver en: http://hdl.handle.net/10261/359208
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359208
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359221
Dataset. 2023
SUPPLEMENTARY MATERIAL AROMATIC PLANTS AND THEIR ASSOCIATED ARBUSCULAR MYCORRHIZAL FUNGI OUTCOMPETE TUBER MELANOSPORUM IN COMPATIBILITY ASSAYS WITH TRUFFLE-OAKS
- Barou, Vasiliki
- Rincón, Ana
- Calvet, Cinta
- Camprubí, Amelia
- Parladé, Javier
Supplementary Material contains: Figures S1-S3, Tables S1-S6 and References. Figure S1: Stereomicroscope photographs of arbuscular mycorrhizal fungi (AMF) structures; Figure S2. Amplification plot of fungal ITS1 multicopy gene; Figure S3: Quercus ilex roots colonized by (a) Tuber melanosporum and (b) arbuscular mycorrhizal fungi, from co-cultured plants collected at the end of the experiment; Table S1: Physical-chemical properties of the soil used in the compatibility assays; Table S2: Primer pairs tested in this work; Table S3: Truffle-oak’s growth variables; Table S4: Medicinal and aromatic plants’ (MAPs) growth variables; Table S5: Quantification of arbuscular mycorrhizal (AM) extraradical mycelium in soils with truffle-oak growing together with AM lavender, sage, or thyme; Table S6: Percentage of arbuscular mycorrhizas (AM) in roots of MAPs growing alone or with truffle-oaks. References [66,67,68] are cited in here., Peer reviewed
Proyecto: //
DOI: http://hdl.handle.net/10261/359221
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359221
HANDLE: http://hdl.handle.net/10261/359221
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359221
PMID: http://hdl.handle.net/10261/359221
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359221
Ver en: http://hdl.handle.net/10261/359221
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359221
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359226
Dataset. 2023
SUPPLEMENTARY MATERIAL ANTI‐TRYPANOSOMATIDAE ACTIVITY OF ESSENTIAL OILS AND THEIR MAIN COMPONENTS FROM SELECTED MEDICINAL PLANT
- Bailén, María
- Illescas, Cristina
- Quijada, Mónica
- Martínez-Díaz, Rafael A.
- Ochoa, Eneko
- Gómez-Muñoz, María Teresa
- Navarro-Rocha, Juliana
- González-Coloma, Azucena
Table S1. Plant species selected, localization, coordinates, and voucher numbers. Table S2. Chemical composition of the EOs from the most active species: L. luisieri (1 and 2) (Ll1 and Ll2), M. suaveolens (Ms); S. hybrid (Sh), S. montana (Sm), T. vulgaris (Tv), and T. zygis (Tz). RI, Retention index; RT, Retention time; HD, EOs obtained by hydrodistillation; SD, EOs obtained by steam distillation. Figure S1. Percentage of antiprotozoal activity of EOs obtained by hydrodistillation (HD) and steam distillation (SD) from L. x intermedia “Abrial” (Lab), L. x intermedia “Grosso” (Lg), L. x intermedia “Super” (Lsu), L. lanata (Ll), L. angustifolia (La), L. mallete (Lm), T. mastichina (Tm), O. virens (Ov), S. blancoana (Sb), S. officinalis (So), S. sclarea (Ss), R. officinalis (Ro), S. chamaecyparissus (Sc), T. vulgare (Tav), D. graveolens (Dg). A. Anti-Leishmania activity. B. Anti-Phytomonas activity of EOs. Figure S2. Chromatograms of the most active species EOs: L. luisieri (1 and 2) (Ll1 and Ll2), M. suaveolens (Ms); S. hybrid (Sh), S. montana (Sm), T. vulgaris (Tv), and T. zygis (Tz); HD, EOs obtained by hydrodistillation; SD, EOs obtained by steam distillation., Peer reviewed
Proyecto: //
DOI: http://hdl.handle.net/10261/359226
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359226
HANDLE: http://hdl.handle.net/10261/359226
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359226
PMID: http://hdl.handle.net/10261/359226
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359226
Ver en: http://hdl.handle.net/10261/359226
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359226
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359229
Dataset. 2023
ADDITIONAL FILE 1 BIOCHAR FROM GRAPE POMACE, A WASTE OF VITIVINICULTURAL ORIGIN, IS EFFECTIVE FOR ROOT-KNOT NEMATODE CONTROL
- Martínez-Gómez, Ángela
- Andrés, María Fé
- Barón-Sola, Ángel
- Díaz-Manzano, Fernando E.
- Yousef, Ibraheem
- Mena, Ismael F.
- Díaz, Elena
- Gómez-Torres, Óscar
- González-Coloma, Azucena
- Hernández, Luis E.
- Escobar, Carolina
pH values of different dilutions of the aqueous extracts (BC350AE and BC700AE) obtained from washing BC350 and BC700 (3% (w/v) with distilled water), respectively, for 24 h. Figure S1. SR-FTIR spectroscopy of grape pomace (GP) and biochars prepared at 350 °C and 700 °C (BC350, BC700, respectively). Full 2nd derivative spectra (wavenumber range between 3100 and 900 cm−1) along with the first two main principal components (PC-1 and PC-2) for different wavenumber ranges, which explain the largest contributions of signal shifts between samples. Numbers in red indicate the wavenumber values of the most representative peaks. Figure S2. SR-FTIR spectroscopy of grape pomace (GP), washed (BC350W) and unwashed (BC350) biochar prepared at 350 °C, and BC350 aqueous extract (BC350AE). Full 2nd derivative spectra (wavenumber range between 3100 and 900 cm−1) along with the first two main principal components (PC-1 and PC-2) for different wavenumber ranges, which explain the largest contributions of signal shifts between samples. Numbers in red indicate the wavenumber values of the most representative peaks. Figure S3. SR-FTIR spectroscopy of grape pomace (GP), washed (BC700W) and unwashed (BC700) biochar prepared at 700 °C, and BC700 aqueous extract (BC700AE). Full 2nd derivative spectra (wavenumber range between 3100 and 900 cm−1) and along with the first two main principal components (PC-1 and PC-2) for different wavenumber ranges, which explain the largest contributions of signal shifts between samples. Numbers in red indicate the wavenumber values of the most representative peaks. Figure S4. Effect of different concentrations (3%, 1.5% and 0.75%) of the unwashed biochar obtained at 700 °C (BC700) on 3-week old tomato plants 24 h and 6 days after its transplantation into biochar-amended sandy soils. Figure S5. Effect of different concentrations (3%, 1.5% and 0.75%) of the unwashed biochar obtained at 350 °C (BC350) on roots and shoots of tomato plants 3 weeks after its transplantation into biochar-amended sandy soils. Figure S6. Effect of different concentrations of BC350W on the percentage of seed germination (a), number of leaves (b), shoot length (c), relative water content (RCW) (d) and total fresh biomass (f) of 6-week-old tomato plants. Means ± standard errors (n ≥ 8). Significant differences with respect to the control according to Mann–Whitney U test. ***p < 0.001; **p < 0.01., Peer reviewed
Proyecto: //
DOI: http://hdl.handle.net/10261/359229
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359229
HANDLE: http://hdl.handle.net/10261/359229
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359229
PMID: http://hdl.handle.net/10261/359229
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359229
Ver en: http://hdl.handle.net/10261/359229
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359229
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359238
Dataset. 2023
INSECT ANTIFEEDANT BENZOFURANS FROM PERICALLIS SPECIE [DATASET]
- Díaz, Carmen E.
- Fraga, Braulio M.
- Portero, Adriana G.
- Brito, Iván
- López-Balboa, Carmen
- Ruiz-Vásquez, Liliana
- González-Coloma, Azucena
Figures S1–S2: 1H-NMR and 13C-NMR of compound 1a; Figure S3: 13C-NMR of compound 2; Figures S4–S5: 13C-NMR of compounds 4–5; Figures S6–S7: 1H-NMR an 13C-NMR of compound 7a; Figures S8–S10: 13C-NMR of compounds 8–10; Figures S11–S20: 1H-NMR and 13C-NMR of compounds 11–14 and 15–16; Figure S21: 1H-NMR of compound 17; Figures S22–S27: 1H-NMR and 13C-NMR of compounds 18,18a and 19., Peer reviewed
Proyecto: //
DOI: http://hdl.handle.net/10261/359238
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359238
HANDLE: http://hdl.handle.net/10261/359238
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359238
PMID: http://hdl.handle.net/10261/359238
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359238
Ver en: http://hdl.handle.net/10261/359238
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/359238
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