34 research outputs found

    ETo estandarizada en el sur de España ¿Cuál debe ser la referencia?

    Get PDF
    La evapotranspiración de referencia (ETo) cuantifica la demanda evaporativa del aire y es necesaria para el cálculo del uso consuntivo de agua de los cultivos. Las redes de estaciones agrometeorológicas proporcionan esta información, utilizando diferentes versiones de la ecuación de Penman-Monteith, realizando cálculos horarios o diarios. Este trabajo pretende arrojar luz sobre la controversia que existe en la utilización de ambos tiempos de cálculo, realizando una comparación a escala local y regional entre las versiones FAO56 y ASCE de esta ecuación. La comparación se realizó en 31 localizaciones de Andalucía, calculando los valores diarios mediante suma de horarios. Además, se comparó la estimación diaria de ETo de la ecuación FAO56-PM con la medida en un lisímetro de pesada en Córdoba. Los resultados de la comparación entre valores medidos y estimados usando ambas ecuaciones estandarizadas indican que los métodos más precisos para estimar los valores diarios de la ETo fueron FAO56-PM en base diaria y ASCE-PM en base horaria. Ambos mostraron una precisión similar cuando se compararon con los valores medidos en un lisímetro de pesada. La ecuación FAO56-PM en base horaria mostró una menor precisión, con subestimaciones del 5%. A escala regional, la ecuación FAO56-PM en base horaria subestimó los valores diarios de ETo calculados mediante la misma ecuación estandarizada en su versión ASCE hasta un 6%, produciéndose una subestimación media del 4%. Esta diferencia fue debida al uso de un mayor valor de rc (70 s m-1) en la ecuación FAO56-PM, en relación con el valor de 50 s m-1 aplicado en la ecuación estandarizada ASCE durante las horas diurnas.The most practical way to quantify water consumption by the crops is by using the concept of reference crop evapotranspiration (ETo). Agrometeorological networks provide daily ETo values using the Penman-Monteith equation on a daily or hourly basis. Up till now, the ETo methods are being used mainly for computation with a 24-h timestep because hourly meteorological data are not readily accessible for the users to apply ETo procedures on an hourly basis. This work quantifies the differences associated with using two different timesteps (hourly and daily basis) for computing ETo using two standardized Penman– Monteith equations (ASCE and FAO56) under different climatic conditions in Andalusia. Hourly ETo was measured in Córdoba, southern Spain, using a precision weighing lysimeter. Close to the lysimeter, an automatic weather station was located to register hourly meteorological variables. Penman-Monteith equation to estimate ETo was evaluated for hourly and daily estimates. ASCE and FAO-56 standardized ETo equations were also compared using data from 31 meteorological stations in Andalusia. Comparisons were made between daily ETo obtained by summing hourly standardized ASCE–Penman–Monteith estimations and calculated from the addition of hourly FAO56–Penman–Monteith estimations and daily ETo estimated on a daily basis. On an hourly basis, the FAO-56 version estimated lower than the ASCE version as 6% in some locations, with a difference of 4% on the average, mainly due to the higher surface resistance (70 s m−1) used in the FAO-56 version during daytime periods, as opposed to the 50 s m−1 value used by the ASCE version. The level of agreement improved when the two computational time steps (hourly and daily) were compared, because differences were lower (2% on the average)

    Lipopolysacharide-induced neuroinflammation leads to the accumulation of ubiquitinated proteins and increases susceptibility to neurodegeneration induced by proteasome inhibition in rat hippocampus

    Get PDF
    BACKGROUND: Neuroinflammation and protein accumulation are characteristic hallmarks of both normal aging and age-related neurodegenerative diseases. However, the relationship between these factors in neurodegenerative processes is poorly understood. We have previously shown that proteasome inhibition produced higher neurodegeneration in aged than in young rats, suggesting that other additional age-related events could be involved in neurodegeneration. We evaluated the role of lipopolysaccharide (LPS)-induced neuroinflammation as a potential synergic risk factor for hippocampal neurodegeneration induced by proteasome inhibition. METHODS: Young male Wistar rats were injected with 1 μL of saline or LPS (5 mg/mL) into the hippocampus to evaluate the effect of LPS-induced neuroinflammation on protein homeostasis. The synergic effect of LPS and proteasome inhibition was analyzed in young rats that first received 1 μL of LPS and 24 h later 1 μL (5 mg/mL) of the proteasome inhibitor lactacystin. Animals were sacrificed at different times post-injection and hippocampi isolated and processed for gene expression analysis by real-time polymerase chain reaction; protein expression analysis by western blots; proteasome activity by fluorescence spectroscopy; immunofluorescence analysis by confocal microscopy; and degeneration assay by Fluoro-Jade B staining. RESULTS: LPS injection produced the accumulation of ubiquitinated proteins in hippocampal neurons, increased expression of the E2 ubiquitin-conjugating enzyme UB2L6, decreased proteasome activity and increased immunoproteasome content. However, LPS injection was not sufficient to produce neurodegeneration. The combination of neuroinflammation and proteasome inhibition leads to higher neuronal accumulation of ubiquitinated proteins, predominant expression of pro-apoptotic markers and increased neurodegeneration, when compared with LPS or lactacystin (LT) injection alone. CONCLUSIONS: Our results identify neuroinflammation as a risk factor that increases susceptibility to neurodegeneration induced by proteasome inhibition. These results highlight the modulation of neuroinflammation as a mechanism for neuronal protection that could be relevant in situations where both factors are present, such as aging and neurodegenerative diseases

    Alpha-catenin-Dependent Recruitment of the Centrosomal Protein CAP350 to Adherens Junctions Allows Epithelial Cells to Acquire a Columnar Shape

    Get PDF
    Epithelial morphogenesis involves a dramatic reorganisation of the microtubule cytoskeleton. How this complex process is controlled at the molecular level is still largely unknown. Here, we report that the centrosomal microtubule (MT)-binding protein CAP350 localises at adherens junctions in epithelial cells. By two-hybrid screening, we identified a direct interaction of CAP350 with the adhesion protein α-catenin that was further confirmed by co-immunoprecipitation experiments. Block of epithelial cadherin (E-cadherin)-mediated cell-cell adhesion or α-catenin depletion prevented CAP350 localisation at cell-cell junctions. Knocking down junction-located CAP350 inhibited the establishment of an apico-basal array of microtubules and impaired the acquisition of columnar shape in Madin-Darby canine kidney II (MDCKII) cells grown as polarised epithelia. Furthermore, MDCKII cystogenesis was also defective in junctional CAP350-depleted cells. CAP350-depleted MDCKII cysts were smaller and contained either multiple lumens or no lumen. Membrane polarity was not affected, but cortical microtubule bundles did not properly form. Our results indicate that CAP350 may act as an adaptor between adherens junctions and microtubules, thus regulating epithelial differentiation and contributing to the definition of cell architecture. We also uncover a central role of α-catenin in global cytoskeleton remodelling, in which it acts not only on actin but also on MT reorganisation during epithelial morphogenesis.This work was supported by Ministerio de Economia y Competitividad, Spain (BFU2012-36717 and CSD2009-00016 to RMR and BFU2011-22916 to JRM) and by Junta de Andalucia (CVI-7256 and CTS-2071), and by a funding GenHomme Network 02490-6088 to Hybrigenics and the Institut Curie. MA and AZ were supported by MEC–FPI Grants.Peer Reviewe

    CartoCell, a high-content pipeline for 3D image analysis, unveils cell morphology patterns in epithelia

    Get PDF
    Decades of research have not yet fully explained the mechanisms of epithelial self-organization and 3D packing. Single-cell analysis of large 3D epithelial libraries is crucial for understanding the assembly and function of whole tissues. Combining 3D epithelial imaging with advanced deep-learning segmentation methods is essential for enabling this high-content analysis. We introduce CartoCell, a deep-learning-based pipeline that uses small datasets to generate accurate labels for hundreds of whole 3D epithelial cysts. Our method detects the realistic morphology of epithelial cells and their contacts in the 3D structure of the tissue. CartoCell enables the quantification of geometric and packing features at the cellular level. Our single-cell cartography approach then maps the distribution of these features on 2D plots and 3D surface maps, revealing cell morphology patterns in epithelial cysts. Additionally, we show that CartoCell can be adapted to other types of epithelial tissues

    Objective and subjective measures of physical functioning in women with fibromyalgia: what type of measure is associated most clearly with subjective well-being?

    Get PDF
    Purpose: To find modifiable factors that are related to subjective well-being would be valuable for improving interventions in fibromyalgia. Physical activity, sedentary behaviour, and physical fitness may represent potential areas to optimize treatment regimens. In fibromyalgia, there is a discordance between clinical observations and patient-reported outcomes (objective and subjective assessments). Therefore, the present study aims at analyzing the associations of objective and subjective evaluations of physical activity, sedentary behaviour, and physical fitness with subjective well-being and determine if and how objective and subjective associations differ. Methods: In this population-based cross-sectional study participated 375 women with fibromyalgia from the al-Ándalus project (Spain). Physical activity, sedentary behaviour, and physical fitness were objectively (accelerometers and performance testing) and subjectively (questionnaires) measured. Participants self-reported their levels of positive affect, negative affect, and life satisfaction. Results: In the most conservative multivariate analysis, we found independent associations of the objective measures of physical activity with positive affect and life satisfaction and sedentary behaviour with positive affect. No such relationship was seen with subjective measures of the same behaviours. Moreover, we observed that objective and subjective physical fitness evaluations were independent of each other related to subjective well-being. Conclusions: Independent associations of the objective measures (but not the subjective assessments) of physical activity with positive affect and life satisfaction, and of sedentary behaviour with positive affect were observed. However, objective measures and subjective appraisals of physical fitness appear to be independently related to well-being, which should be considered when developing physical exercise interventions for fibromyalgia.Implications for rehabilitation The analysis of concurrent associations of objective and subjective evaluations of physical functioning with subjective well-being offers indications for modifiable targets in rehabilitation that can improve well-being in fibromyalgia. Exercise-based rehabilitation may help women with fibromyalgia to improve subjective well-being, particularly positive affect. Rehabilitation should focus on both the objective physical performance of women with fibromyalgia and on their perceptions of what they can do physically. When rehabilitation aims at enhancing positive affect or life satisfaction by changing the lifestyle of women with fibromyalgia, physical activity and sedentary behaviour should be objectively monitored

    Post-glacial determinants of regional species pools in alpine grasslands

    Get PDF
    [Aim] Alpine habitats support unique biodiversity confined to high-elevation areas in the current interglacial. Plant diversity in these habitats may respond to area, environment, connectivity and isolation, yet these factors have been rarely evaluated in concert. Here we investigate major determinants of regional species pools in alpine grasslands, and the responses of their constituent species groups.[Location] European mountains below 50° N.[Time period] Between 1928 and 2019.[Major taxa studied] Vascular plants.[Methods] We compiled species pools from alpine grasslands in 23 regions, including 794 alpine species and 2,094 non-alpines. We used species–area relationships to test the influence of the extent of alpine areas on regional richness, and mixed-effects models to compare the effects of 12 spatial and environmental predictors. Variation in species composition was addressed by generalized dissimilarity models and by a coefficient of dispersal direction to assess historical links among regions.[Results] Pool sizes were partially explained by current alpine areas, but the other predictors largely contributed to regional differences. The number of alpine species was influenced by area, calcareous bedrock, topographic heterogeneity and regional isolation, while non-alpines responded better to connectivity and climate. Regional dissimilarity of alpine species was explained by isolation and precipitation, but non-alpines only responded to isolation. Past dispersal routes were correlated with latitude, with alpine species showing stronger connections among regions.[Main conclusions] Besides area effects, edaphic, topographic and spatio-temporal determinants are important to understand the organization of regional species pools in alpine habitats. The number of alpine species is especially linked to refugia and isolation, but their composition is explained by past dispersal and post-glacial environmental filtering, while non-alpines are generally influenced by regional floras. New research on the dynamics of alpine biodiversity should contextualize the determinants of regional species pools and the responses of species with different ecological profiles.The authors thank Daniela Gaspar for support in GIS analyses. B.J.-A. thanks the Marie Curie Clarín-COFUND program of the Principality of Asturias-EU (ACB17-26), the regional grant IDI/2018/000151, and the Spanish Research Agency grant AEI/ 10.13039/501100011033. J.V.R.-D. was supported by the ACA17-02FP7 Marie Curie COFUND-Clarín grant. G.P.M. was funded by US National Science Foundation award 1853665. C.M. was funded by grant no. 19-28491 of the Czech Science Foundation.Peer reviewe

    GrassPlot - a database of multi-scale plant diversity in Palaearctic grasslands

    Get PDF
    GrassPlot is a collaborative vegetation-plot database organised by the Eurasian Dry Grassland Group (EDGG) and listed in the Global Index of Vegetation-Plot Databases (GIVD ID EU-00-003). GrassPlot collects plot records (releves) from grasslands and other open habitats of the Palaearctic biogeographic realm. It focuses on precisely delimited plots of eight standard grain sizes (0.0001; 0.001;... 1,000 m(2)) and on nested-plot series with at least four different grain sizes. The usage of GrassPlot is regulated through Bylaws that intend to balance the interests of data contributors and data users. The current version (v. 1.00) contains data for approximately 170,000 plots of different sizes and 2,800 nested-plot series. The key components are richness data and metadata. However, most included datasets also encompass compositional data. About 14,000 plots have near-complete records of terricolous bryophytes and lichens in addition to vascular plants. At present, GrassPlot contains data from 36 countries throughout the Palaearctic, spread across elevational gradients and major grassland types. GrassPlot with its multi-scale and multi-taxon focus complements the larger international vegetationplot databases, such as the European Vegetation Archive (EVA) and the global database " sPlot". Its main aim is to facilitate studies on the scale-and taxon-dependency of biodiversity patterns and drivers along macroecological gradients. GrassPlot is a dynamic database and will expand through new data collection coordinated by the elected Governing Board. We invite researchers with suitable data to join GrassPlot. Researchers with project ideas addressable with GrassPlot data are welcome to submit proposals to the Governing Board

    Time to Switch to Second-line Antiretroviral Therapy in Children With Human Immunodeficiency Virus in Europe and Thailand.

    Get PDF
    Background: Data on durability of first-line antiretroviral therapy (ART) in children with human immunodeficiency virus (HIV) are limited. We assessed time to switch to second-line therapy in 16 European countries and Thailand. Methods: Children aged <18 years initiating combination ART (≥2 nucleoside reverse transcriptase inhibitors [NRTIs] plus nonnucleoside reverse transcriptase inhibitor [NNRTI] or boosted protease inhibitor [PI]) were included. Switch to second-line was defined as (i) change across drug class (PI to NNRTI or vice versa) or within PI class plus change of ≥1 NRTI; (ii) change from single to dual PI; or (iii) addition of a new drug class. Cumulative incidence of switch was calculated with death and loss to follow-up as competing risks. Results: Of 3668 children included, median age at ART initiation was 6.1 (interquartile range (IQR), 1.7-10.5) years. Initial regimens were 32% PI based, 34% nevirapine (NVP) based, and 33% efavirenz based. Median duration of follow-up was 5.4 (IQR, 2.9-8.3) years. Cumulative incidence of switch at 5 years was 21% (95% confidence interval, 20%-23%), with significant regional variations. Median time to switch was 30 (IQR, 16-58) months; two-thirds of switches were related to treatment failure. In multivariable analysis, older age, severe immunosuppression and higher viral load (VL) at ART start, and NVP-based initial regimens were associated with increased risk of switch. Conclusions: One in 5 children switched to a second-line regimen by 5 years of ART, with two-thirds failure related. Advanced HIV, older age, and NVP-based regimens were associated with increased risk of switch

    Spatiotemporal organization of Aurora-B by APC/CCdh1 after mitosis coordinates cell spreading through FHOD1

    Get PDF
    Floyd, Suzanne et al.Spatiotemporal regulation of mitotic kinase activity underlies the extensive rearrangement of cellular components required for cell division. One highly dynamic mitotic kinase is Aurora-B (AurB), which has multiple roles defined by the changing localisation of the chromosome passenger complex (CPC) as cells progress through mitosis, including regulation of cytokinesis and abscission. Like other mitotic kinases, AurB is a target of the anaphase-promoting complex (APC/C) ubiquitin ligase during mitotic exit, but it is not known if APC/C-mediated destruction plays any specific role in controlling AurB activity. We have examined the contribution of the Cdh1 coactivator-associated APC/CCdh1 to the organization of AurB activity as cells exit mitosis and re-enter interphase. We report that APC/ CCdh1-dependent proteolysis restricts a cell-cortex-associated pool of active AurB in space and time. In early G1 phase this pool of AurB is found at protrusions associated with cell spreading. AurB retention at the cortex depends on a formin, FHOD1, critically required to organize the cytoskeleton after division. We identify AurB phosphorylation sites in FHOD1 and show that phosphomutant FHOD1 is impaired in post-mitotic assembly of oriented actin cables. We propose that Cdh1 contributes to spatiotemporal organization of AurB activity and that organization of FHOD1 activity by AurB contributes to daughter cell spreading after mitosis. © 2013 Published by The Company of Biologists Ltd.This work was supported by a Medical Research Council Career Development Award [grant number G120/892 to C.L.]; the Deutsche Forschungsgemeinschaft [grant numbers FA 378/6-2 to O.T.F., GRK1188 fellowship to S.K.]; the Isaac Newton Trust. (to C.L.); a Biochemical Society Summer Studentship (to N.W.); Consolider [grant number CSD2009-00016 to M.P.G.]; and Ministerio de Ciencia e Innovación, Spain, through JdC and Jose Castillejo programs.Peer Reviewe
    corecore