114 research outputs found

    The development of an experimental approach for the generation of a usability hypothesis about the academic use of geo-information

    Get PDF
    Very little attention has been given to understanding how academics obtain and use geo-information to support their tasks of teaching and research. Considering usability, fewer methods have been developed for determining the potential use of geoinformation. This paper describes our efforts to develop an experimental approach to generate a usability hypothesis on the academic use of geo-information. This approach is based on a step-wise process that includes the identification of a usability premise, the performance of a user survey, the analysis of the results, and finally, the inference of a usability hypothesis. Towards a consistent identification of a usability premise, a web questionnaire was designed and distributed to academics from 25 Spanish Universities, covering several scientific and technological fields. Three usability elements have been considered in the questionnaire: purpose of use, trust and accessibility of geoinformation. More than 100 answers have been received showing how the academics strongly welcomed the questionnaire and how involved they are in using geoinformation for both education and research activities. Very little attention has been given to understanding how academics obtain and use geo-information to support their tasks of teaching and research. Considering usability, fewer methods have been developed for determining the potential use of geoinformation. This paper describes our efforts to develop an experimental approach to generate a usability hypothesis on the academic use of geo-information. This approach is based on a step-wise process that includes the identification of a usability premise, the performance of a user survey, the analysis of the results, and finally, the inference of a usability hypothesis. Towards a consistent identification of a usability premise, a web questionnaire was designed and distributed to academics from 25 Spanish Universities, covering several scientific and technological fields. Three usability elements have been considered in the questionnaire: purpose of use, trust and accessibility of geoinformation. More than 100 answers have been received showing how the academics strongly welcomed the questionnaire and how involved they are in using geoinformation for both education and research activities. In fact, only 6% of the answers reveal the lack of use of geo-information. The results show a high level of trust in the quality of geo-information, and that there are less difficulties of accessing geoinformation than previously expected. However, the existing accessibility issues are mainly related to the lack of knowledge and use of metadata (formats) and Spatial Data Infrastructures (interoperability). The main findings confirm the important role of identifying a usability premise based on explicit users input that will support a usability hypothesis

    Adaptability of invasive plants to climate change

    Full text link
    [EN] Climate change represents one of the greatest environmental challenges of the 21st century, accentuated by deforestation and the degradation of habitats. Changes in vital aspects such as temperature, the amount and distribution of rainfall or the frequency of extreme meteorological phenomena will probably negatively affect ecosystems. The possibilities of invasion will predictably increase, being endemic species especially vulnerable to the effects of climate change. Invasive species are extremely adaptable to climate variability, as evidenced by their current large latitudinal ranges. Generally, invasive plants also have rapid dispersal characteristics, allowing them to vary their ranges in response to changing climatic conditions rapidly. As a result, these species could become more dominant in many areas under changing climatic conditions. In many situations, the environmental stress generated by climate change and invasive plants are synergistic: invasive species can exacerbate the impacts of climate change on ecosystems, and in the same way, climate change can allow new invasions.S.G-O acknowledges a 'Margarita Salas' postdoctoral contract from Universitat Politècnica de València and the Spanish Ministry of Universities, supported by the European Union - Next Generation fundsGonzález-Orenga, S.; Boscaiu, M.; Verdeguer Sancho, MM.; Sánchez-Moreiras, AM.; González, L.; Vicente, O. (2022). Adaptability of invasive plants to climate change. AgroLife Scientific Journal (Online). 11(2):58-65. https://doi.org/10.17930/AGL202227586511

    Autologous stem-cell transplantation as consolidation of first-line chemotherapy in patients with peripheral T-cell lymphoma: a multicenter GELTAMO/FIL study

    Get PDF
    Autologous stem-cell transplantation; Chemotherapy; T-cell lymphomaTrasplante autólogo de células madre; Quimioterapia; Linfoma de células TTrasplantament autòleg de cèl·lules mare; Quimioteràpia; Limfoma de cèl·lules TPeripheral T-cell lymphomas (PTCL) are a heterogeneous group of rare lymphoid malignancies that mostly have poor prognoses with currently available treatments. Upfront consolidation with autologous stem cell transplantation (ASCT) is frequently carried out, but its efficacy has never been investigated in randomized trials. We designed a multicenter, international, retrospective study with the main objective of comparing progression-free survival and overall survival of patients with PTCL who underwent ASCT in complete remission (CR) after first-line chemotherapy with a control group who did not undergo ASCT. From the initial population of 286 registered patients, 174 patients with PTCL other than anaplastic large cell lymphoma, ALK-positive, deemed fit for ASCT at the time of diagnosis, and who were in CR or uncertain CR after induction therapy (CR1) were included in our analysis. one hundred and three patients underwent ASCT, whereas 71 did not, in most cases (n=53) because the physician decided against it. With a median follow-up of 65.5 months, progression-free survival was significantly better in the transplanted patients than in the non-transplanted group: 63% versus 48% at 5 years (P=0.042). Overall survival was significantly longer for ASCT patients in the subgroup with advanced stage at diagnosis (5-year overall survival: 70% vs. 50%, P=0.028). In the multivariate analysis, first-line ASCT was associated with significantly prolonged progression-free survival (HR=0.57, 95% CI: 0.35-0.93) and overall survival (HR=0.57, 95% CI: 0.33-0.99). In conclusion, our study supports the use of ASCT as a consolidation strategy for patients with PTCL in CR1. These results should be confirmed in a prospective randomized study

    Physiological and Biochemical Responses to Water Stress and Salinity of the Invasive Moth Plant, Araujia sericifera Brot., during Seed Germination and Vegetative Growth

    Full text link
    [EN] Araujia sericifera is an invasive plant with an increasing presence in South East Spain, where it produces damage to native trees and shrubs and citric orchards. As the climatic conditions in the study area are becoming harsher due to the climate change, the stress tolerance of this species has been studied during germination and vegetative growth. Growth parameters, photosynthetic pigments, ion accumulation, and antioxidant mechanisms were analysed in plants that were subjected to water deficit and salt stress. Seed germination was reduced by salinity but 50% of the seeds still germinated at 50 mM NaCl. The ungerminated seeds did not lose their germination capacity as shown in `recovery¿ germination assays in distilled water. Germination was less affected by osmotic stress that was induced by polyethylene glycol (PEG), and germination velocity increased in the recovery treatments after exposure to NaCl or PEG. Plant growth was practically unaffected by 150 mM NaCl but inhibited by higher NaCl concentrations or severe drought stress. Nevertheless, all the plants survived throughout the experiment, even under high salinity (600 mM NaCl). A. sericifera relative stress tolerance relies, at least to some extent, on effective antioxidant mechanisms that are based on flavonoid biosynthesis and the activation of antioxidant enzymes such as superoxide dismutase, ascorbate peroxidase, and glutathione reductase.Bellache, M.; Moltó, N.; Allal Benfekih, L.; Torres-Pagán, N.; Mir Moreno, R.; Verdeguer Sancho, MM.; Boscaiu, M.... (2022). Physiological and Biochemical Responses to Water Stress and Salinity of the Invasive Moth Plant, Araujia sericifera Brot., during Seed Germination and Vegetative Growth. Agronomy. 11(2):1-20. https://doi.org/10.3390/agronomy1202036112011

    Essential Oils of Three Aromatic Plant Species as Natural Herbicides for Environmentally Friendly Agriculture

    Full text link
    [EN] Natural herbicides based on essential oils (EOs) extracted from aromatic plants are gaining relevance in contemporary agriculture. Due to their allelopathic properties, they have an inhibitory effect on the germination and growth of different species, having, in general, the advantage of high specificity. For this reason, the analysis of the effects of these natural compounds on noxious weeds is continuously increasing. In the present study, three commercial EOs extracted from Mentha piperita L., Thymbra capitata (L.) Cav. and Santolina chamaecyparissus L. were tested on two invasive weeds with an increasing presence in southern Europe, Erigeron bonariensis L. and Araujia sericifera Brot. Five concentrations (0.125, 0.25, 0.50, 1 and 2 mu L mL(-1)) were tested in a randomized manner for each essential oil and five replicates with 20 seeds each for E. bonariensis and 10 replicates with 10 seeds each for A. sericifera. Two higher concentrations of 4 and 8 mu L mL(-1) of the three EOs were applied with irrigation on the plants of the two species at the vegetative growth stage. The number of replicas for each treatment and species was 7. The results obtained confirmed the significant inhibitory effects on seed germination and early seedling development, especially in E. bonariensis; of the three EOs, peppermint had the strongest effect, completely preventing germination in both species. Multivariate analysis, performed on several morphological traits scored after one month of treatment in young plants, showed a different pattern: the highest inhibition was recorded in A. sericifera and the greatest reduction in growth in the treatment with the highest dose of Santolina EO. The results obtained revealed the efficacy of these natural compounds and the specificity of their toxicity according to the species and stage of development.Bellache, M.; Torres-Pagan, N.; Verdeguer Sancho, MM.; Benfekih, LA.; Vicente, O.; Sestras, RE.; Sestras, AF.... (2022). Essential Oils of Three Aromatic Plant Species as Natural Herbicides for Environmentally Friendly Agriculture. Sustainability. 14(6):1-22. https://doi.org/10.3390/su1406359612214

    Qualitative and Quantitative Dierences in Osmolytes Accumulation and Antioxidant Activities in Response to Water Deficit in Four Mediterranean Limonium Species

    Full text link
    [EN] Limonium is a genus represented in the Iberian Peninsula by numerous halophytic species that are a ected in nature by salinity, and often by prolonged drought episodes. Responses to water deficit have been studied in four Mediterranean Limonium species, previously investigated regarding salt tolerance mechanisms. The levels of biochemical markers, associated with specific responses¿photosynthetic pigments, mono- and divalent ions, osmolytes, antioxidant compounds and enzymes¿were determined in the control and water-stressed plants, and correlated with their relative degree of stress-induced growth inhibition. All the tested Limonium taxa are relatively resistant to drought on the basis of both the constitutive presence of high leaf ion levels that contribute to osmotic adjustment, and the stress-induced accumulation of osmolytes and increased activity of antioxidant enzymes, albeit with di erent qualitative and quantitative induction patterns. Limonium santapolense activated the strongest responses and clearly di ered from Limonium virgatum, Limonium girardianum, and Limonium narbonense, as indicated by cluster and principal component analysis (PCA) analyses in agreement with its drier natural habitat, and compared to that of the other plants. Somewhat surprisingly, however, L. santapolense was the species most a ected by water deficit in growth inhibition terms, which suggests the existence of additional mechanisms of defense operating in the field that cannot be mimicked in greenhouses.This research was partially funded by Project AICO/2017/039 from the Generalitat Valenciana, granted to M. Boscaiu.González-Orenga, S.; Al Hassan, M.; Llinares Palacios, JV.; Lisón, P.; López-Gresa, MP.; Verdeguer Sancho, MM.; Vicente, O.... (2019). Qualitative and Quantitative Dierences in Osmolytes Accumulation and Antioxidant Activities in Response to Water Deficit in Four Mediterranean Limonium Species. Plants. 8(11):1-21. https://doi.org/10.3390/plants8110506S121811Hoerling, M., Eischeid, J., Perlwitz, J., Quan, X., Zhang, T., & Pegion, P. (2012). On the Increased Frequency of Mediterranean Drought. Journal of Climate, 25(6), 2146-2161. doi:10.1175/jcli-d-11-00296.1Munns, R. (2002). Comparative physiology of salt and water stress. Plant, Cell & Environment, 25(2), 239-250. doi:10.1046/j.0016-8025.2001.00808.xVan Breusegem, F., & Dat, J. F. (2006). Reactive Oxygen Species in Plant Cell Death. Plant Physiology, 141(2), 384-390. doi:10.1104/pp.106.078295Li, Z., Wakao, S., Fischer, B. B., & Niyogi, K. K. (2009). Sensing and Responding to Excess Light. Annual Review of Plant Biology, 60(1), 239-260. doi:10.1146/annurev.arplant.58.032806.103844Shabala, S., Bose, J., Fuglsang, A. T., & Pottosin, I. (2015). On a quest for stress tolerance genes: membrane transporters in sensing and adapting to hostile soils. Journal of Experimental Botany, 67(4), 1015-1031. doi:10.1093/jxb/erv465Schachtman, D. P., & Goodger, J. Q. D. (2008). Chemical root to shoot signaling under drought. Trends in Plant Science, 13(6), 281-287. doi:10.1016/j.tplants.2008.04.003Fang, Y., & Xiong, L. (2014). General mechanisms of drought response and their application in drought resistance improvement in plants. Cellular and Molecular Life Sciences, 72(4), 673-689. doi:10.1007/s00018-014-1767-0Martìnez, J. P., Ledent, J. F., Bajji, M., Kinet, J. M., & Lutts, S. (2003). Plant Growth Regulation, 41(1), 63-73. doi:10.1023/a:1027359613325Xi, J.-J., Chen, H.-Y., Bai, W.-P., Yang, R.-C., Yang, P.-Z., Chen, R.-J., … Wang, S.-M. (2018). Sodium-Related Adaptations to Drought: New Insights From the Xerophyte Plant Zygophyllum xanthoxylum. Frontiers in Plant Science, 9. doi:10.3389/fpls.2018.01678MILLER, G., SUZUKI, N., CIFTCI-YILMAZ, S., & MITTLER, R. (2010). Reactive oxygen species homeostasis and signalling during drought and salinity stresses. Plant, Cell & Environment, 33(4), 453-467. doi:10.1111/j.1365-3040.2009.02041.xSharma, P., Jha, A. B., Dubey, R. S., & Pessarakli, M. (2012). Reactive Oxygen Species, Oxidative Damage, and Antioxidative Defense Mechanism in Plants under Stressful Conditions. Journal of Botany, 2012, 1-26. doi:10.1155/2012/217037Kar, R. K. (2011). Plant responses to water stress: Role of reactive oxygen species. Plant Signaling & Behavior, 6(11), 1741-1745. doi:10.4161/psb.6.11.17729Golldack, D., Li, C., Mohan, H., & Probst, N. (2014). Tolerance to drought and salt stress in plants: Unraveling the signaling networks. Frontiers in Plant Science, 5. doi:10.3389/fpls.2014.00151Gagneul, D., Aïnouche, A., Duhazé, C., Lugan, R., Larher, F. R., & Bouchereau, A. (2007). A Reassessment of the Function of the So-Called Compatible Solutes in the Halophytic Plumbaginaceae Limonium latifolium  . Plant Physiology, 144(3), 1598-1611. doi:10.1104/pp.107.099820Al Hassan, M., Estrelles, E., Soriano, P., López-Gresa, M. P., Bellés, J. M., Boscaiu, M., & Vicente, O. (2017). Unraveling Salt Tolerance Mechanisms in Halophytes: A Comparative Study on Four Mediterranean Limonium Species with Different Geographic Distribution Patterns. Frontiers in Plant Science, 8. doi:10.3389/fpls.2017.01438Galmés, J., Cifre, J., Medrano, H., & Flexas, J. (2005). Modulation of relative growth rate and its components by water stress in Mediterranean species with different growth forms. Oecologia, 145(1), 21-31. doi:10.1007/s00442-005-0106-4Galmés, J., Molins, A., Flexas, J., & Conesa, M. À. (2017). Coordination between leaf CO2diffusion and Rubisco properties allows maximizing photosynthetic efficiency inLimoniumspecies. Plant, Cell & Environment, 40(10), 2081-2094. doi:10.1111/pce.13004Guerin, G. R., Wen, H., & Lowe, A. J. (2012). Leaf morphology shift linked to climate change. Biology Letters, 8(5), 882-886. doi:10.1098/rsbl.2012.0458Kumar, D., Al Hassan, M., Naranjo, M. A., Agrawal, V., Boscaiu, M., & Vicente, O. (2017). Effects of salinity and drought on growth, ionic relations, compatible solutes and activation of antioxidant systems in oleander (Nerium oleander L.). PLOS ONE, 12(9), e0185017. doi:10.1371/journal.pone.0185017Marček, T., Hamow, K. Á., Végh, B., Janda, T., & Darko, E. (2019). Metabolic response to drought in six winter wheat genotypes. PLOS ONE, 14(2), e0212411. doi:10.1371/journal.pone.0212411Silva, E. N., Ferreira-Silva, S. L., Viégas, R. A., & Silveira, J. A. G. (2010). The role of organic and inorganic solutes in the osmotic adjustment of drought-stressed Jatropha curcas plants. Environmental and Experimental Botany, 69(3), 279-285. doi:10.1016/j.envexpbot.2010.05.001Gámez, A. L., Soba, D., Zamarreño, Á. M., García-Mina, J. M., Aranjuelo, I., & Morales, F. (2019). Effect of Water Stress during Grain Filling on Yield, Quality and Physiological Traits of Illpa and Rainbow Quinoa (Chenopodium quinoa Willd.) Cultivars. Plants, 8(6), 173. doi:10.3390/plants8060173Van der Weijde, T., Huxley, L. M., Hawkins, S., Sembiring, E. H., Farrar, K., Dolstra, O., … Trindade, L. M. (2016). Impact of drought stress on growth and quality of miscanthus for biofuel production. GCB Bioenergy, 9(4), 770-782. doi:10.1111/gcbb.12382Tabot, P. T., & Adams, J. B. (2014). Salt secretion, proline accumulation and increased branching confer tolerance to drought and salinity in the endemic halophyte Limonium linifolium. South African Journal of Botany, 94, 64-73. doi:10.1016/j.sajb.2014.05.009Hanson, A. D., Rathinasabapathi, B., Chamberlin, B., & Gage, D. A. (1991). Comparative Physiological Evidence that β-Alanine Betaine and Choline-O-Sulfate Act as Compatible Osmolytes in Halophytic Limonium Species. Plant Physiology, 97(3), 1199-1205. doi:10.1104/pp.97.3.1199Rhodes, D., & Hanson, A. D. (1993). Quaternary Ammonium and Tertiary Sulfonium Compounds in Higher Plants. Annual Review of Plant Physiology and Plant Molecular Biology, 44(1), 357-384. doi:10.1146/annurev.pp.44.060193.002041Murakeözy, É. P., Nagy, Z., Duhazé, C., Bouchereau, A., & Tuba, Z. (2003). Seasonal changes in the levels of compatible osmolytes in three halophytic species of inland saline vegetation in Hungary. Journal of Plant Physiology, 160(4), 395-401. doi:10.1078/0176-1617-00790GIL, R., LULL, C., BOSCAIU, M., BAUTISTA, I., LIDÓN, A., & VICENTE, O. (2011). Soluble Carbohydrates as Osmolytes in Several Halophytes from a Mediterranean Salt Marsh. Notulae Botanicae Horti Agrobotanici Cluj-Napoca, 39(2), 09. doi:10.15835/nbha3927176Halliwell, B. (2006). Reactive Species and Antioxidants. Redox Biology Is a Fundamental Theme of Aerobic Life. Plant Physiology, 141(2), 312-322. doi:10.1104/pp.106.077073Sofo, A., Scopa, A., Nuzzaci, M., & Vitti, A. (2015). Ascorbate Peroxidase and Catalase Activities and Their Genetic Regulation in Plants Subjected to Drought and Salinity Stresses. International Journal of Molecular Sciences, 16(12), 13561-13578. doi:10.3390/ijms160613561Del Rio, L. A., Palma, J. M., Sandalio, L. M., Corpas, F. J., Pastori, G. M., Bueno, P., & López-Huertas, E. (1996). Peroxisomes as a source of superoxide and hydrogen peroxide in stressed plants. Biochemical Society Transactions, 24(2), 434-438. doi:10.1042/bst0240434Kedare, S. B., & Singh, R. P. (2011). Genesis and development of DPPH method of antioxidant assay. Journal of Food Science and Technology, 48(4), 412-422. doi:10.1007/s13197-011-0251-1Gil, R., Bautista, I., Boscaiu, M., Lidon, A., Wankhade, S., Sanchez, H., … Vicente, O. (2014). Responses of five Mediterranean halophytes to seasonal changes in environmental conditions. AoB PLANTS, 6(0), plu049-plu049. doi:10.1093/aobpla/plu049Bose, J., Rodrigo-Moreno, A., & Shabala, S. (2013). ROS homeostasis in halophytes in the context of salinity stress tolerance. Journal of Experimental Botany, 65(5), 1241-1257. doi:10.1093/jxb/ert430Fini, A., Brunetti, C., Di Ferdinando, M., Ferrini, F., & Tattini, M. (2011). Stress-induced flavonoid biosynthesis and the antioxidant machinery of plants. Plant Signaling & Behavior, 6(5), 709-711. doi:10.4161/psb.6.5.15069Souid, A., Bellani, L., Magné, C., Zorrig, W., Smaoui, A., Abdelly, C., … Ben Hamed, K. (2018). Physiological and antioxidant responses of the sabkha biotope halophyte Limonium delicatulum to seasonal changes in environmental conditions. Plant Physiology and Biochemistry, 123, 180-191. doi:10.1016/j.plaphy.2017.12.008Alscher, R. G. (2002). Role of superoxide dismutases (SODs) in controlling oxidative stress in plants. Journal of Experimental Botany, 53(372), 1331-1341. doi:10.1093/jexbot/53.372.1331Caverzan, A., Casassola, A., & Brammer, S. P. (2016). Antioxidant responses of wheat plants under stress. Genetics and Molecular Biology, 39(1), 1-6. doi:10.1590/1678-4685-gmb-2015-0109Gunes, A., Pilbeam, D. J., Inal, A., Bagci, E. G., & Coban, S. (2007). Influence of silicon on antioxidant mechanisms and lipid peroxidation in chickpea (Cicer arietinumL.) cultivars under drought stress. Journal of Plant Interactions, 2(2), 105-113. doi:10.1080/17429140701529399Hameed, A., Gulzar, S., Aziz, I., Hussain, T., Gul, B., & Khan, M. A. (2015). Effects of salinity and ascorbic acid on growth, water status and antioxidant system in a perennial halophyte. AoB PLANTS, 7. doi:10.1093/aobpla/plv004LICHTENTHALER, H. K., & WELLBURN, A. R. (1983). Determinations of total carotenoids and chlorophylls a and b of leaf extracts in different solvents. Biochemical Society Transactions, 11(5), 591-592. doi:10.1042/bst0110591Weimberg, R. (1987). Solute adjustments in leaves of two species of wheat at two different stages of growth in response to salinity. Physiologia Plantarum, 70(3), 381-388. doi:10.1111/j.1399-3054.1987.tb02832.xBates, L. S., Waldren, R. P., & Teare, I. D. (1973). Rapid determination of free proline for water-stress studies. Plant and Soil, 39(1), 205-207. doi:10.1007/bf00018060Grieve, C. M., & Grattan, S. R. (1983). Rapid assay for determination of water soluble quaternary ammonium compounds. Plant and Soil, 70(2), 303-307. doi:10.1007/bf02374789Nawaz, K., & Ashraf, M. (2010). Exogenous Application of Glycinebetaine Modulates Activities of Antioxidants in Maize Plants Subjected to Salt Stress. Journal of Agronomy and Crop Science, 196(1), 28-37. doi:10.1111/j.1439-037x.2009.00385.xDuBois, M., Gilles, K. A., Hamilton, J. K., Rebers, P. A., & Smith, F. (1956). Colorimetric Method for Determination of Sugars and Related Substances. Analytical Chemistry, 28(3), 350-356. doi:10.1021/ac60111a017Al Hassan, M., Chaura, J., López-Gresa, M. P., Borsai, O., Daniso, E., Donat-Torres, M. P., … Boscaiu, M. (2016). Native-Invasive Plants vs. Halophytes in Mediterranean Salt Marshes: Stress Tolerance Mechanisms in Two Related Species. Frontiers in Plant Science, 7. doi:10.3389/fpls.2016.00473Hodges, D. M., DeLong, J. M., Forney, C. F., & Prange, R. K. (1999). Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds. Planta, 207(4), 604-611. doi:10.1007/s004250050524Taulavuori, E., Hellström, E., Taulavuori, K., & Laine, K. (2001). Comparison of two methods used to analyse lipid peroxidation from Vaccinium myrtillus (L.) during snow removal, reacclimation and cold acclimation. Journal of Experimental Botany, 52(365), 2375-2380. doi:10.1093/jexbot/52.365.2375Loreto, F., & Velikova, V. (2001). Isoprene Produced by Leaves Protects the Photosynthetic Apparatus against Ozone Damage, Quenches Ozone Products, and Reduces Lipid Peroxidation of Cellular Membranes. Plant Physiology, 127(4), 1781-1787. doi:10.1104/pp.010497Blainski, A., Lopes, G., & de Mello, J. (2013). Application and Analysis of the Folin Ciocalteu Method for the Determination of the Total Phenolic Content from Limonium Brasiliense L. Molecules, 18(6), 6852-6865. doi:10.3390/molecules18066852Zhishen, J., Mengcheng, T., & Jianming, W. (1999). The determination of flavonoid contents in mulberry and their scavenging effects on superoxide radicals. Food Chemistry, 64(4), 555-559. doi:10.1016/s0308-8146(98)00102-2Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 72(1-2), 248-254. doi:10.1016/0003-2697(76)90527-3Beyer, W. F., & Fridovich, I. (1987). Assaying for superoxide dismutase activity: Some large consequences of minor changes in conditions. Analytical Biochemistry, 161(2), 559-566. doi:10.1016/0003-2697(87)90489-1Aebi, H. (1984). [13] Catalase in vitro. Oxygen Radicals in Biological Systems, 121-126. doi:10.1016/s0076-6879(84)05016-3Connell, J. P., & Mullet, J. E. (1986). Pea Chloroplast Glutathione Reductase: Purification and Characterization. Plant Physiology, 82(2), 351-356. doi:10.1104/pp.82.2.35

    Insights on Salt Tolerance of Two Endemic Limonium Species from Spain

    Full text link
    [EN] We have analysed the salt tolerance of two endemic halophytes of the genus Limonium, with high conservation value. In the present study, seed germination and growth parameters as well as different biomarkers-photosynthetic pigments, mono and divalent ion contents-associated to salt stress were evaluated in response to high levels of NaCl. The study was completed with an untargeted metabolomics analysis of the primary compounds including carbohydrates, phosphoric and organic acids, and amino acids, identified by using a gas chromatography and mass spectrometry platform. Limonium albuferae proved to be more salt-tolerant than L. doufourii, both at the germination stage and during vegetative growth. The degradation of photosynthetic pigments and the increase of Na+/K+ ratio under salt stress were more accentuated in the less tolerant second species. The metabolomics analysis unravelled several differences between the two species. The higher salt tolerance of L. albuferae may rely on its specific accumulation of fructose and glucose under high salinity conditions, the first considered as a major osmolyte in this genus. In addition, L. albuferae showed steady levels of citric and malic acids, whereas the glutamate family pathway was strongly activated under stress in both species, leading to the accumulation of proline (Pro) and gamma-aminobutyric acid (GABA).This research was funded by GENERALITAT VALENCIANA, grant number AICO/2017/039, to M. Boscaiu.González-Orenga, S.; Ferrer-Gallego, PP.; Laguna, E.; López-Gresa, MP.; Donat-Torres, MP.; Verdeguer Sancho, MM.; Vicente, O.... (2019). Insights on Salt Tolerance of Two Endemic Limonium Species from Spain. Metabolites. 9(12):1-22. https://doi.org/10.3390/metabo9120294S12291

    Herbicidal Activity of Thymbra capitata (L.) Cav. Essential Oil

    Get PDF
    [EN] The bioherbicidal potential ofThymbra capitata(L.) Cav. essential oil (EO) and its main compound carvacrol was investigated. In in vitro assays, the EO blocked the germination and seedling growth ofErigeron canadensisL.,Sonchus oleraceus(L.) L., andChenopodium albumL. at 0.125 mu L/mL, ofSetaria verticillata(L.) P.Beauv.,Avena fatuaL., andSolanum nigrumL. at 0.5 mu L/mL, ofAmaranthus retroflexusL. at 1 mu L/mL and ofPortulaca oleraceaL., andEchinochloa crus-galli(L.) P.Beauv. at 2 mu L/mL. Under greenhouse conditions,T. capitataEO was tested towards the emergent weeds from a soil seedbank in pre and post emergence, showing strong herbicidal potential in both assays at 4 mu L/mL. In addition,T. capitataEO, applied by spraying, was tested againstP. oleracea,A. fatuaandE. crus-galli. The species showed different sensibility to the EO, beingE. crus-gallithe most resistant. Experiments were performed againstA. fatuatestingT. capitataEO and carvacrol applied by spraying or by irrigation. It was verified that the EO was more active at the same doses in monocotyledons applied by irrigation and in dicotyledons applied by spraying. Carvacrol effects onArabidopsisroot morphology were also studied.This research was supported by the Universitat Politècnica de València [project number: SP20120543], by Generalitat Valenciana [project number GV/2014/039], and by the Spanish Ministry of Science, Innovation and Universities [project number: RTI2018¿094716¿B¿I00]. Thanks to Jovano Erris Nugroho and Muhamad Iqbal who collaborate to carry out in vivo experiment 4 during their internship in the Plant Health in Sustainable Cropping Systems Erasmus+ Programme. This research work has been developed as a result of a mobility stay funded by the Erasmus+-KA1 Erasmus Mundus Joint Master Degrees Programme of the European Commission under the PLANT HEALTH Project. Thanks to Xeda Italia S.r.l. for providing us Fitoil always when we need it. Thanks to Vicente Estornell Campos and the Library staff from Polytechnic University of Valencia that assisted us to get some helpful references.Verdeguer Sancho, MM.; Torres-Pagan, N.; Muñoz, M.; Jouini, A.; García-Plasencia, S.; Chinchilla, P.; Berbegal Martinez, M.... (2020). Herbicidal Activity of Thymbra capitata (L.) Cav. Essential Oil. Molecules. 25(12):1-31. https://doi.org/10.3390/molecules25122832S1312512Barros, L., Heleno, S. A., Carvalho, A. M., & Ferreira, I. C. F. R. (2010). Lamiaceae often used in Portuguese folk medicine as a source of powerful antioxidants: Vitamins and phenolics. LWT - Food Science and Technology, 43(3), 544-550. doi:10.1016/j.lwt.2009.09.024Goudjil, M. B., Zighmi, S., Hamada, D., Mahcene, Z., Bencheikh, S. E., & Ladjel, S. (2020). Biological activities of essential oils extracted from Thymus capitatus (Lamiaceae). South African Journal of Botany, 128, 274-282. doi:10.1016/j.sajb.2019.11.020Gagliano Candela, R., Maggi, F., Lazzara, G., Rosselli, S., & Bruno, M. (2019). The Essential Oil of Thymbra capitata and its Application as A Biocide on Stone and Derived Surfaces. Plants, 8(9), 300. doi:10.3390/plants8090300Tohidi, B., Rahimmalek, M., Arzani, A., & Sabzalian, M. R. (2020). Thymol, carvacrol, and antioxidant accumulation in Thymus species in response to different light spectra emitted by light-emitting diodes. Food Chemistry, 307, 125521. doi:10.1016/j.foodchem.2019.125521Vladimir-Knežević, S., Blažeković, B., Kindl, M., Vladić, J., Lower-Nedza, A., & Brantner, A. (2014). Acetylcholinesterase Inhibitory, Antioxidant and Phytochemical Properties of Selected Medicinal Plants of the Lamiaceae Family. Molecules, 19(1), 767-782. doi:10.3390/molecules19010767BRÄUCHLER, C. (2018). Delimitation and revision of the genus Thymbra (Lamiaceae). Phytotaxa, 369(1), 15. doi:10.11646/phytotaxa.369.1.2Paton, A. J., Springate, D., Suddee, S., Otieno, D., Grayer, R. J., Harley, M. M., … Savolainen, V. (2004). Phylogeny and evolution of basils and allies (Ocimeae, Labiatae) based on three plastid DNA regions. Molecular Phylogenetics and Evolution, 31(1), 277-299. doi:10.1016/j.ympev.2003.08.002Pastore, J. F. B., Harley, R. M., Forest, F., Paton, A., & van den Berg, C. (2011). Phylogeny of the subtribe Hyptidinae (Lamiaceae tribe Ocimeae) as inferred from nuclear and plastid DNA. TAXON, 60(5), 1317-1329. doi:10.1002/tax.605008Salmaki, Y., Zarre, S., Ryding, O., Lindqvist, C., Bräuchler, C., Heubl, G., … Bendiksby, M. (2013). Molecular phylogeny of tribe Stachydeae (Lamiaceae subfamily Lamioideae). Molecular Phylogenetics and Evolution, 69(3), 535-551. doi:10.1016/j.ympev.2013.07.024Salmaki, Y., Kattari, S., Heubl, G., & Bräuchler, C. (2016). Phylogeny of non-monophyletic Teucrium (Lamiaceae: Ajugoideae): Implications for character evolution and taxonomy. Taxon, 65(4), 805-822. doi:10.12705/654.8LI, B., & OLMSTEAD, R. G. (2017). Two new subfamilies in Lamiaceae. Phytotaxa, 313(2), 222. doi:10.11646/phytotaxa.313.2.9Bräuchler, C., Meimberg, H., & Heubl, G. (2010). Molecular phylogeny of Menthinae (Lamiaceae, Nepetoideae, Mentheae) – Taxonomy, biogeography and conflicts. Molecular Phylogenetics and Evolution, 55(2), 501-523. doi:10.1016/j.ympev.2010.01.016World Checklist of Lamiaceae. Facilitated by the Royal Botanic Gardens, Kewhttp://wcsp.science.kew.orgHarley, R. M., Atkins, S., Budantsev, A. L., Cantino, P. D., Conn, B. J., Grayer, R., … Upson, T. (2004). Labiatae. Flowering Plants · Dicotyledons, 167-275. doi:10.1007/978-3-642-18617-2_11Miceli, A., Negro, C., & Tommasi, L. (2006). Essential oil variability in Thymbra capitata (L.) Cav. growing wild in Southern Apulia (Italy). Biochemical Systematics and Ecology, 34(6), 528-535. doi:10.1016/j.bse.2005.12.010Delgado-Adámez, J., Garrido, M., Bote, M. E., Fuentes-Pérez, M. C., Espino, J., & Martín-Vertedor, D. (2017). Chemical composition and bioactivity of essential oils from flower and fruit of Thymbra capitata and Thymus species. Journal of Food Science and Technology, 54(7), 1857-1865. doi:10.1007/s13197-017-2617-5Alves, T. M. de A., Silva, A. F., Brandão, M., Grandi, T. S. M., Smânia, E. de F. A., Smânia Júnior, A., & Zani, C. L. (2000). Biological screening of Brazilian medicinal plants. Memórias do Instituto Oswaldo Cruz, 95(3), 367-373. doi:10.1590/s0074-02762000000300012BOUNATIROU, S., SMITI, S., MIGUEL, M., FALEIRO, L., REJEB, M., NEFFATI, M., … PEDRO, L. (2007). Chemical composition, antioxidant and antibacterial activities of the essential oils isolated from Tunisian Thymus capitatus Hoff. et Link. Food Chemistry, 105(1), 146-155. doi:10.1016/j.foodchem.2007.03.059Nejad Ebrahimi, S., Hadian, J., Mirjalili, M. H., Sonboli, A., & Yousefzadi, M. (2008). Essential oil composition and antibacterial activity of Thymus caramanicus at different phenological stages. Food Chemistry, 110(4), 927-931. doi:10.1016/j.foodchem.2008.02.083Casiglia, S., Bruno, M., Scandolera, E., Senatore, F., & Senatore, F. (2019). Influence of harvesting time on composition of the essential oil of Thymus capitatus (L.) Hoffmanns. & Link. growing wild in northern Sicily and its activity on microorganisms affecting historical art crafts. Arabian Journal of Chemistry, 12(8), 2704-2712. doi:10.1016/j.arabjc.2015.05.017Grayer, R. J., & Harborne, J. B. (1994). A survey of antifungal compounds from higher plants, 1982–1993. Phytochemistry, 37(1), 19-42. doi:10.1016/0031-9422(94)85005-4Kalemba, D., & Kunicka, A. (2003). Antibacterial and Antifungal Properties of Essential Oils. Current Medicinal Chemistry, 10(10), 813-829. doi:10.2174/0929867033457719Ricci, D., Fraternale, D., Giamperi, L., Bucchini, A., Epifano, F., Burini, G., & Curini, M. (2005). Chemical composition, antimicrobial and antioxidant activity of the essential oil of Teucrium marum (Lamiaceae). Journal of Ethnopharmacology, 98(1-2), 195-200. doi:10.1016/j.jep.2005.01.022Al-Mustafa, A. H., & Al-Thuniba, O. Y. (2008). Antioxidant Activity of Some Jordanian Medicinal Plants Used Traditionally for Treatment of Diabetes. Pakistan Journal of Biological Sciences, 11(3), 351-358. doi:10.3923/pjbs.2008.351.358Dhifi, W., Bellili, S., Jazi, S., Bahloul, N., & Mnif, W. (2016). Essential Oils’ Chemical Characterization and Investigation of Some Biological Activities: A Critical Review. Medicines, 3(4), 25. doi:10.3390/medicines3040025Ruberto, G., Biondi, D., & Piattelli, M. (1992). The Essential Oil of SicilianThymus capitatus(L.) Hoffmanns, et Link. Journal of Essential Oil Research, 4(4), 417-418. doi:10.1080/10412905.1992.9698094Saija, A., Speciale, A., Trombetta, D., Leto, C., Tuttolomondo, T., La Bella, S., … Ruberto, G. (2016). Phytochemical, Ecological and Antioxidant Evaluation of Wild Sicilian Thyme: Thymbra capitata (L.) Cav . Chemistry & Biodiversity, 13(12), 1641-1655. doi:10.1002/cbdv.201600072Arras, G., & Grella, G. E. (1992). Wild thyme,Thymus capitatus, essential oil seasonal changes and antimycotic activity. Journal of Horticultural Science, 67(2), 197-202. doi:10.1080/00221589.1992.11516237Tommasi, L., Negro, C., Cerfeda, A., Nutricati, E., Zuccarello, V., De Bellis, L., & Miceli, A. (2007). Influence of Environmental Factors on Essential Oil Variability inThymbra capitata(L.) Cav. Growing Wild in Southern Puglia (Italy). Journal of Essential Oil Research, 19(6), 572-580. doi:10.1080/10412905.2007.9699335Salas, J. B., Téllez, T. R., Alonso, M. J. P., Pardo, F. M. V., de los Ángeles Cases Capdevila, M., & Rodríguez, C. G. (2010). Chemical composition and antioxidant activity of the essential oil ofThymbra capitata(L.) Cav. in Spain. Acta Botanica Gallica, 157(1), 55-63. doi:10.1080/12538078.2010.10516189Rodrigues, L. S., Monteiro, P., Maldoa-Martins, M., Monteiro, A., Povoa, O., & Teixeira, G. (2006). BIODIVERSITY STUDIES ON PORTUGUESE THYMBRA CAPITATA. Acta Horticulturae, (723), 127-132. doi:10.17660/actahortic.2006.723.13El Hadj Ali, I. B., Guetat, A., & Boussaid, M. (2012). Variation of Volatiles in Tunisian Populations of Thymbra capitata (L.) Cav. (Lamiaceae). Chemistry & Biodiversity, 9(7), 1272-1285. doi:10.1002/cbdv.201100344Katz, D. A., Sneh, B., & Friedman, J. (1987). The allelopathic potential ofCoridothymus capitatus L. (Labiatae). Preliminary studies on the roles of the shrub in the inhibition of annuals germination and/or to promote allelopathically active actinomycetes. Plant and Soil, 98(1), 53-66. doi:10.1007/bf02381727Dudai, N., Poljakoff-Mayber, A., Mayer, A. M., Putievsky, E., & Lerner, H. R. (1999). Journal of Chemical Ecology, 25(5), 1079-1089. doi:10.1023/a:1020881825669Saoud, I., Hamrouni, L., Gargouri, S., Amri, I., Hanana, M., Fezzani, T., … Jamoussi, B. (2013). Chemical composition, weed killer and antifungal activities of Tunisian thyme (Thymus capitatusHoff. et Link.) essential oils. Acta Alimentaria, 42(3), 417-427. doi:10.1556/aalim.42.2013.3.15Chaimovitsh, D., Shachter, A., Abu-Abied, M., Rubin, B., Sadot, E., & Dudai, N. (2016). Herbicidal Activity of Monoterpenes Is Associated with Disruption of Microtubule Functionality and Membrane Integrity. Weed Science, 65(1), 19-30. doi:10.1614/ws-d-16-00044.1Verdeguer, M., Castañeda, L. G., Torres-Pagan, N., Llorens-Molina, J. A., & Carrubba, A. (2020). Control of Erigeron bonariensis with Thymbra capitata, Mentha piperita, Eucalyptus camaldulensis, and Santolina chamaecyparissus Essential Oils. Molecules, 25(3), 562. doi:10.3390/molecules25030562Cordeau, S., Triolet, M., Wayman, S., Steinberg, C., & Guillemin, J.-P. (2016). Bioherbicides: Dead in the water? A review of the existing products for integrated weed management. Crop Protection, 87, 44-49. doi:10.1016/j.cropro.2016.04.016Mahmood, I., Imadi, S. R., Shazadi, K., Gul, A., & Hakeem, K. R. (2016). Effects of Pesticides on Environment. Plant, Soil and Microbes, 253-269. doi:10.1007/978-3-319-27455-3_13Harker, K. N., & O’Donovan, J. T. (2013). Recent Weed Control, Weed Management, and Integrated Weed Management. Weed Technology, 27(1), 1-11. doi:10.1614/wt-d-12-00109.1Olson, S. (2015). An Analysis of the Biopesticide Market Now and Where it is Going. Outlooks on Pest Management, 26(5), 203-206. doi:10.1564/v26_oct_04Santamarina, M., Ibáñez, M., Marqués, M., Roselló, J., Giménez, S., & Blázquez, M. (2017). Bioactivity of essential oils in phytopathogenic and post-harvest fungi control. Natural Product Research, 31(22), 2675-2679. doi:10.1080/14786419.2017.1286479Tuttolomondo, T., Dugo, G., Leto, C., Cicero, N., Tropea, A., Virga, G., … La Bella, S. (2015). Agronomical and chemical characterisation ofThymbra capitata(L.) Cav. biotypes from Sicily, Italy. Natural Product Research, 29(14), 1289-1299. doi:10.1080/14786419.2014.997726Miguel, M. G., Gago, C., Antunes, M. D., Megías, C., Cortés-Giraldo, I., Vioque, J., … Figueiredo, A. C. (2015). Antioxidant and Antiproliferative Activities of the Essential Oils fromThymbra capitataandThymusSpecies Grown in Portugal. Evidence-Based Complementary and Alternative Medicine, 2015, 1-8. doi:10.1155/2015/851721Karousou, R., Koureas, D. N., & Kokkini, S. (2005). Essential oil composition is related to the natural habitats: Coridothymus capitatus and Satureja thymbra in NATURA 2000 sites of Crete. Phytochemistry, 66(22), 2668-2673. doi:10.1016/j.phytochem.2005.09.020Vasilakoglou, I., Dhima, K., Paschalidis, K., & Ritzoulis, C. (2013). Herbicidal potential onLolium rigidumof nineteen major essential oil components and their synergy. Journal of Essential Oil Research, 25(1), 1-10. doi:10.1080/10412905.2012.751054Hazrati, H., Saharkhiz, M. J., Niakousari, M., & Moein, M. (2017). Natural herbicide activity of Satureja hortensis L. essential oil nanoemulsion on the seed germination and morphophysiological features of two important weed species. Ecotoxicology and Environmental Safety, 142, 423-430. doi:10.1016/j.ecoenv.2017.04.041Pinheiro, P. F., Costa, A. V., Alves, T. de A., Galter, I. N., Pinheiro, C. A., Pereira, A. F., … Fontes, M. M. P. (2015). Phytotoxicity and Cytotoxicity of Essential Oil from Leaves of Plectranthus amboinicus, Carvacrol, and Thymol in Plant Bioassays. Journal of Agricultural and Food Chemistry, 63(41), 8981-8990. doi:10.1021/acs.jafc.5b03049Tworkoski, T. (2002). Herbicide effects of essential oils. Weed Science, 50(4), 425-431. doi:10.1614/0043-1745(2002)050[0425:heoeo]2.0.co;2Benvenuti, S., Cioni, P. L., Flamini, G., & Pardossi, A. (2017). Weeds for weed control: Asteraceae essential oils as natural herbicides. Weed Research, 57(5), 342-353. doi:10.1111/wre.12266N. MALPASSI, R. (2006). Herbicide effects on cuticle ultrastructure in Eleusine indica and Portulaca oleracea. BIOCELL, 30(1), 51-56. doi:10.32604/biocell.2006.30.051Schreiber, L. (1995). A mechanistic approach towards surfactant/wax interactions: Effects of octaethyleneglycolmonododecylether on sorption and diffusion of organic chemicals in reconstituted cuticular wax of barley leaves. Pesticide Science, 45(1), 1-11. doi:10.1002/ps.2780450102Hull, H. M., Morton, H. L., & Wharrie, J. R. (1975). Environmental influences on cuticle development and resultant foliar penetration. The Botanical Review, 41(4), 421-452. doi:10.1007/bf02860832Kern, A. J., Jackson, L. L., & Dyer, W. E. (1997). Fatty acid and wax biosynthesis in susceptible and triallate-resistantAvena fatuaL. Pesticide Science, 51(1), 21-26. doi:10.1002/(sici)1096-9063(199709)51:13.0.co;2-9SANYAL, D., BHOWMIK, P. C., & REDDY, K. N. (2008). Effects of surfactants on primisulfuron activity in barnyardgrass (Echinochloa crus-galli [L.] Beauv.) and green foxtail (Setaria viridis [L.] Beauv.). Weed Biology and Management, 8(1), 46-53. doi:10.1111/j.1445-6664.2007.00273.xPrinciples of Soil and Plant Water Relations. (2014). doi:10.1016/c2013-0-12871-1Kim, H. K., Park, J., & Hwang, I. (2014). Investigating water transport through the xylem network in vascular plants. Journal of Experimental Botany, 65(7), 1895-1904. doi:10.1093/jxb/eru075Norris, R. F. (1974). PENETRATION OF 2,4-D IN RELATION TO CUTICLE THICKNESS. American Journal of Botany, 61(1), 74-79. doi:10.1002/j.1537-2197.1974.tb06029.xSchönherr, J., & Riederer, M. (1989). Foliar Penetration and Accumulation of Organic Chemicals in Plant Cuticles. Reviews of Environmental Contamination and Toxicology, 1-70. doi:10.1007/978-1-4613-8850-0_1GOURET, E., ROHR, R., & CHAMEL, A. (1993). Ultrastructure and chemical composition of some isolated plant cuticles in relation to their permeability to the herbicide, diuron. New Phytologist, 124(3), 423-431. doi:10.1111/j.1469-8137.1993.tb03832.xRiederer, M., & Schönherr, J. (1985). Accumulation and transport of (2,4-dichlorophenoxy)acetic acid in plant cuticles. Ecotoxicology and Environmental Safety, 9(2), 196-208. doi:10.1016/0147-6513(85)90022-3Melo, C. R., Picanço, M. C., Santos, A. A., Santos, I. B., Pimentel, M. F., Santos, A. C. C., … Bacci, L. (2018). Toxicity of essential oils of Lippia gracilis chemotypes and their major compounds on Diaphania hyalinata and non-target species. Crop Protection, 104, 47-51. doi:10.1016/j.cropro.2017.10.013Araniti, F., Graña, E., Krasuska, U., Bogatek, R., Reigosa, M. J., Abenavoli, M. R., & Sánchez-Moreiras, A. M. (2016). Loss of Gravitropism in Farnesene-Treated Arabidopsis Is Due to Microtubule Malformations Related to Hormonal and ROS Unbalance. PLOS ONE, 11(8), e0160202. doi:10.1371/journal.pone.0160202Smyth, D. R. (2016). Helical growth in plant organs: mechanisms and significance. Development, 143(18), 3272-3282. doi:10.1242/dev.134064Graña, E., Costas-Gil, A., Longueira, S., Celeiro, M., Teijeira, M., Reigosa, M. J., & Sánchez-Moreiras, A. M. (2017). Auxin-like effects of the natural coumarin scopoletin on Arabidopsis cell structure and morphology. Journal of Plant Physiology, 218, 45-55. doi:10.1016/j.jplph.2017.07.007Verbelen, J.-P., Le, J., Vissenberg, K., De Cnodder, T., Vandenbussche, F., Sugimoto, K., & Van Der Straeten, D. (2008). Microtubules And The Control Of Cell Elongation In Arabidopsis Roots. NATO Science for Peace and Security Series C: Environmental Security, 73-90. doi:10.1007/978-1-4020-8843-8_4Blume, Y. B., Krasylenko, Y. A., & Yemets, A. I. (2012). Effects of phytohormones on the cytoskeleton of the plant cell. Russian Journal of Plant Physiology, 59(4), 515-529. doi:10.1134/s1021443712040036López-González, D., Costas-Gil, A., Reigosa, M. J., Araniti, F., & Sánchez-Moreiras, A. M. (2020). A natural indole alkaloid, norharmane, affects PIN expression patterns and compromises root growth in Arabidopsis thaliana. Plant Physiology and Biochemistry, 151, 378-390. doi:10.1016/j.plaphy.2020.03.047The International Herbicide-Resistant Weed Databasewww.weedscience.orgAngelini, L. G., Carpanese, G., Cioni, P. L., Morelli, I., Macchia, M., & Flamini, G. (2003). Essential Oils from Mediterranean Lamiaceae as Weed Germination Inhibitors. Journal of Agricultural and Food Chemistry, 51(21), 6158-6164. doi:10.1021/jf0210728DÍAZ-TIELAS, C., GRAÑA, E., SOTELO, T., REIGOSA, M. J., & SÁNCHEZ-MOREIRAS, A. M. (2012). The natural compound trans-chalcone induces programmed cell death in Arabidopsis thaliana roots. Plant, Cell & Environment, 35(8), 1500-1517. doi:10.1111/j.1365-3040.2012.02506.

    Autologous stem-cell transplantation as consolidation of first-line chemotherapy in patients with peripheral T-cell lymphoma : a multicenter GELTAMO/FIL study

    Get PDF
    Peripheral T-cell lymphomas (PTCL) are a heterogeneous group of rare lymphoid malignancies that mostly have poor prognoses with currently available treatments. Upfront consolidation with autologous stem cell transplantation (ASCT) is frequently carried out, but its efficacy has never been investigated in randomized trials. We designed a multicenter, international, retrospective study with the main objective of comparing progression-free survival and overall survival of patients with PTCL who underwent ASCT in complete remission (CR) after first-line chemotherapy with a control group who did not undergo ASCT. From the initial population of 286 registered patients, 174 patients with PTCL other than anaplastic large cell lymphoma, ALK-positive, deemed fit for ASCT at the time of diagnosis, and who were in CR or uncertain CR after induction therapy (CR1) were included in our analysis. one hundred and three patients underwent ASCT, whereas 71 did not, in most cases (n=53) because the physician decided against it. With a median follow-up of 65.5 months, progression-free survival was significantly better in the transplanted patients than in the non-transplanted group: 63% versus 48% at 5 years (P =0.042). Overall survival was significantly longer for ASCT patients in the subgroup with advanced stage at diagnosis (5-year overall survival: 70% vs. 50%, P =0.028). In the multivariate analysis, first-line ASCT was associated with significantly prolonged progression-free survival (HR=0.57, 95% CI: 0.35-0.93) and overall survival (HR=0.57, 95% CI: 0.33-0.99). In conclusion, our study supports the use of ASCT as a consolidation strategy for patients with PTCL in CR1. These results should be confirmed in a prospective randomized study
    corecore