107 research outputs found

    Responses of five Mediterranean halophytes to seasonal changes in environmental conditions

    Full text link
    In their natural habitats, different mechanisms may contribute to the tolerance of halophytes to high soil salinity and other abiotic stresses, but their relative contribution and ecological relevance, for a given species, remain largely unknown. We studied the responses to changing environmental conditions of five halophytes (Sarcocornia fruticosa, Inula crithmoides, Plantago crassifolia, Juncus maritimus and J. acutus) in a Mediterranean salt marsh, from summer 2009 to autumn 2010. A principal component analysis was used to correlate soil and climatic data with changes in the plants contents of chemical markers associated with stress responses: ions, osmolytes, malondialdehyde (MDA, a marker of oxidative stress) and antioxidant systems. Stress tolerance in S. fruticosa, I. crithmoides and P. crassifolia (all succulent dicots) seemed to depend mostly on the transport of ions to aerial parts and the biosynthesis of specific osmolytes, whereas both Juncus species (monocots)were able to avoid accumulation of toxic ions, maintaining relatively high K+/Na+ ratios. For the most salt-tolerant taxa (S. fruticosa and I. crithmoides), seasonal variations of Na+, Cl2, K+ and glycine betaine, their major osmolyte, did not correlate with environmental parameters associated with salt or water stress, suggesting that their tolerance mechanisms are constitutive and relatively independent of external conditions, although they could be mediated by changes in the subcellular compartmentalization of ions and compatible osmolytes. Proline levels were too low in all the species to possibly have any effect on osmotic adjustment. However except for P. crassifolia proline may play a role in stress tolerance based on its osmoprotectant functions. No correlation was observed between the degree of environmental stress and the levels of MDA or enzymatic and non-enzymatic antioxidants, indicating that the investigated halophytes are not subjected to oxidative stress under natural conditions and do not, therefore, need to activate antioxidant defence mechanismsThis work was funded by a grant to O.V. from the Spanish Ministry of Science and Innovation (Project CGL2008-00438/BOS), with contribution from the European Regional Development Fund.Gil Ortiz, R.; Bautista Carrascosa, I.; Boscaiu Neagu, MT.; Lidón Cerezuela, AL.; Wankhade, SD.; Sánchez Rodríguez, H.; Llinares Palacios, JV.... (2014). Responses of five Mediterranean halophytes to seasonal changes in environmental conditions. AoB PLANTS. 6:1-18. https://doi.org/10.1093/aobpla/plu049S1186Adrian-Romero, M., Wilson, S. J., Blunden, G., Yang, M.-H., Carabot-Cuervo, A., & Bashir, A. K. (1998). Betaines in coastal plants. Biochemical Systematics and Ecology, 26(5), 535-543. doi:10.1016/s0305-1978(98)00013-1Aebi, H. (1984). [13] Catalase in vitro. Oxygen Radicals in Biological Systems, 121-126. doi:10.1016/s0076-6879(84)05016-3Aghaleh, M., Niknam, V., Ebrahimzadeh, H., & Razavi, K. (2009). Salt stress effects on growth, pigments, proteins and lipid peroxidation in Salicornia persica and S. europaea. Biologia Plantarum, 53(2), 243-248. doi:10.1007/s10535-009-0046-7Aghaleh, M., Niknam, V., Ebrahimzadeh, H., & Razavi, K. (2010). Effect of salt stress on physiological and antioxidative responses in two species of Salicornia (S. persica and S. europaea). Acta Physiologiae Plantarum, 33(4), 1261-1270. doi:10.1007/s11738-010-0656-xAlbert, A., Yenush, L., Gil-Mascarell, M. ., Rodriguez, P. ., Patel, S., Martı́nez-Ripoll, M., … Serrano, R. (2000). X-ray structure of yeast hal2p, a major target of lithium and sodium toxicity, and identification of framework interactions determining cation sensitivity. Journal of Molecular Biology, 295(4), 927-938. doi:10.1006/jmbi.1999.3408Albert, R., & Popp, M. (1977). Chemical composition of halophytes from the Neusiedler Lake region in Austria. Oecologia, 27(2), 157-170. doi:10.1007/bf00345820Apel, K., & Hirt, H. (2004). REACTIVE OXYGEN SPECIES: Metabolism, Oxidative Stress, and Signal Transduction. Annual Review of Plant Biology, 55(1), 373-399. doi:10.1146/annurev.arplant.55.031903.141701Ashraf, M. (2009). Biotechnological approach of improving plant salt tolerance using antioxidants as markers. Biotechnology Advances, 27(1), 84-93. doi:10.1016/j.biotechadv.2008.09.003Ashraf, M., & Foolad, M. R. (2007). Roles of glycine betaine and proline in improving plant abiotic stress resistance. Environmental and Experimental Botany, 59(2), 206-216. doi:10.1016/j.envexpbot.2005.12.006Bartels, D., & Sunkar, R. (2005). Drought and Salt Tolerance in Plants. Critical Reviews in Plant Sciences, 24(1), 23-58. doi:10.1080/07352680590910410Bates, 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/bf00018060Bazihizina, N., Barrett-Lennard, E. G., & Colmer, T. D. (2012). Plant growth and physiology under heterogeneous salinity. Plant and Soil, 354(1-2), 1-19. doi:10.1007/s11104-012-1193-8Amor, N. B., Jimenez, A., Megdiche, W., Lundqvist, M., Sevilla, F., & Abdelly, C. (2006). Response of antioxidant systems to NaCl stress in the halophyte Cakile maritima. Physiologia Plantarum, 126(3), 446-457. doi:10.1111/j.1399-3054.2006.00620.xHamed, K. B., Ellouzi, H., Talbi, O. Z., Hessini, K., Slama, I., Ghnaya, T., … Abdelly, C. (2013). Physiological response of halophytes to multiple stresses. Functional Plant Biology, 40(9), 883. doi:10.1071/fp13074Beyer, 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)90489-1Boscaiu, M., Ballesteros, G., Naranjo, M. A., Vicente, O., & Boira, H. (2011). Responses to salt stress in Juncus acutus and J. maritimus during seed germination and vegetative plant growth. Plant Biosystems - An International Journal Dealing with all Aspects of Plant Biology, 145(4), 770-777. doi:10.1080/11263504.2011.628446Boscaiu, M., Lull, C., Llinares, J., Vicente, O., & Boira, H. (2012). Proline as a biochemical marker in relation to the ecology of two halophytic Juncus species. Journal of Plant Ecology, 6(2), 177-186. doi:10.1093/jpe/rts017Boyer, J. S. (1982). Plant Productivity and Environment. Science, 218(4571), 443-448. doi:10.1126/science.218.4571.443Bradford, 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)90527-3Bressan, R. A., Hasegawa, P. M., & Pardo, J. M. (1998). Plants use calcium to resolve salt stress. Trends in Plant Science, 3(11), 411-412. doi:10.1016/s1360-1385(98)01331-4Cavalieri, A. J. (1983). Proline and glycinebetaine accumulation by Spartina alterniflora Loisel. in response to NaCl and nitrogen in a controlled environment. Oecologia, 57(1-2), 20-24. doi:10.1007/bf00379556Chen, T. H. H., & Murata, N. (2008). Glycinebetaine: an effective protectant against abiotic stress in plants. Trends in Plant Science, 13(9), 499-505. doi:10.1016/j.tplants.2008.06.007Connell, J. P., & Mullet, J. E. (1986). Pea Chloroplast Glutathione Reductase: Purification and Characterization. Plant Physiology, 82(2), 351-356. doi:10.1104/pp.82.2.351Del Rio, D., Stewart, A. J., & Pellegrini, N. (2005). A review of recent studies on malondialdehyde as toxic molecule and biological marker of oxidative stress. Nutrition, Metabolism and Cardiovascular Diseases, 15(4), 316-328. doi:10.1016/j.numecd.2005.05.003Demiral, T., & Türkan, I. (2004). Does exogenous glycinebetaine affect antioxidative system of rice seedlings under NaCl treatment? Journal of Plant Physiology, 161(10), 1089-1100. doi:10.1016/j.jplph.2004.03.009Doddema, H., Saad Eddin, R., & Mahasneh, A. (1986). Effects of seasonal changes of soil salinity and soil nitrogen on the N-metabolism of the halophyteArthrocnemum fruticosum (L.) Moq. Plant and Soil, 92(2), 279-293. doi:10.1007/bf02372641FEDOROFF, N. (2006). Redox Regulatory Mechanisms in Cellular Stress Responses. Annals of Botany, 98(2), 289-300. doi:10.1093/aob/mcl128Flowers, T. J., & Colmer, T. D. (2008). Salinity tolerance in halophytes*. New Phytologist, 179(4), 945-963. doi:10.1111/j.1469-8137.2008.02531.xFlowers, T. J., Troke, P. F., & Yeo, A. R. (1977). The Mechanism of Salt Tolerance in Halophytes. Annual Review of Plant Physiology, 28(1), 89-121. doi:10.1146/annurev.pp.28.060177.000513Flowers, T. J., Galal, H. K., & Bromham, L. (2010). Evolution of halophytes: multiple origins of salt tolerance in land plants. Functional Plant Biology, 37(7), 604. doi:10.1071/fp09269Gagneul, 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.107.099820Gil, R., Boscaiu, M., Lull, C., Bautista, I., Lidón, A., & Vicente, O. (2013). Are soluble carbohydrates ecologically relevant for salt tolerance in halophytes? Functional Plant Biology, 40(9), 805. doi:10.1071/fp12359Glenn, E. (1999). Salt Tolerance and Crop Potential of Halophytes. Critical Reviews in Plant Sciences, 18(2), 227-255. doi:10.1016/s0735-2689(99)00388-3Grieve, 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/bf02374789Halliwell, 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.106.077073HAUSER, F., & HORIE, T. (2010). A conserved primary salt tolerance mechanism mediated by HKT transporters: a mechanism for sodium exclusion and maintenance of high K+/Na+ratio in leaves during salinity stress. Plant, Cell & Environment, 33(4), 552-565. doi:10.1111/j.1365-3040.2009.02056.xHodges, 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/s004250050524Horie, T., Hauser, F., & Schroeder, J. I. (2009). HKT transporter-mediated salinity resistance mechanisms in Arabidopsis and monocot crop plants. Trends in Plant Science, 14(12), 660-668. doi:10.1016/j.tplants.2009.08.009Katschnig, D., Broekman, R., & Rozema, J. (2013). Salt tolerance in the halophyte Salicornia dolichostachya Moss: Growth, morphology and physiology. Environmental and Experimental Botany, 92, 32-42. doi:10.1016/j.envexpbot.2012.04.002Ajmal Khan, M., Ungar, I. A., & Showalter, A. M. (2000). The effect of salinity on the growth, water status, and ion content of a leaf succulent perennial halophyte, Suaeda fruticosa (L.) Forssk. Journal of Arid Environments, 45(1), 73-84. doi:10.1006/jare.1999.0617Koiwa, H., Bressan, R. A., & Hasegawa, P. M. (2006). Identification of plant stress-responsive determinants in arabidopsis by large-scale forward genetic screens. Journal of Experimental Botany, 57(5), 1119-1128. doi:10.1093/jxb/erj093Krasensky, J., & Jonak, C. (2012). Drought, salt, and temperature stress-induced metabolic rearrangements and regulatory networks. Journal of Experimental Botany, 63(4), 1593-1608. doi:10.1093/jxb/err460Kronzucker, H. J., & Britto, D. T. (2010). Sodium transport in plants: a critical review. New Phytologist, 189(1), 54-81. doi:10.1111/j.1469-8137.2010.03540.xLi, G., Wan, S., Zhou, J., Yang, Z., & Qin, P. (2010). Leaf chlorophyll fluorescence, hyperspectral reflectance, pigments content, malondialdehyde and proline accumulation responses of castor bean (Ricinus communis L.) seedlings to salt stress levels. Industrial Crops and Products, 31(1), 13-19. doi:10.1016/j.indcrop.2009.07.015Li, Y. (2008). Kinetics of the antioxidant response to salinity in the halophyte Limonium bicolour. Plant, Soil and Environment, 54(No. 11), 493-497. doi:10.17221/434-pseMiller, G., Shulaev, V., & Mittler, R. (2008). Reactive oxygen signaling and abiotic stress. Physiologia Plantarum, 133(3), 481-489. doi:10.1111/j.1399-3054.2008.01090.xMILLER, 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.xMoghaieb, R. (2004). Effect of salinity on osmotic adjustment, glycinebetaine accumulation and the betaine aldehyde dehydrogenase gene expression in two halophytic plants, Salicornia europaea and Suaeda maritima. Plant Science, 166(5), 1345-1349. doi:10.1016/j.plantsci.2004.01.016Mouri, C., Benhassaini, H., Bendimered, F. Z., & Belkhodja, M. (2012). Variation saisonnière de la teneur en proline et en sucres solubles chez l’oyat (Ammophila arenaria(L.) Link) provenant du milieu naturel de la côte ouest de l’Algérie. Acta Botanica Gallica, 159(1), 127-135. doi:10.1080/12538078.2012.673822Munns, R., & Termaat, A. (1986). Whole-Plant Responses to Salinity. Functional Plant Biology, 13(1), 143. doi:10.1071/pp9860143Munns, R., & Tester, M. (2008). Mechanisms of Salinity Tolerance. Annual Review of Plant Biology, 59(1), 651-681. doi:10.1146/annurev.arplant.59.032607.092911Murakeözy, É. P., Smirnoff, N., Nagy, Z., & Tuba, Z. (2002). Seasonal accumulation pattern of pinitol and other carbohydrates in Limonium gmelini subsp. hungarica. Journal of Plant Physiology, 159(5), 485-490. doi:10.1078/0176-1617-00617Murakeözy, 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:10.1078/0176-1617-00790Nawaz, 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.xNiu, X., Bressan, R. A., Hasegawa, P. M., & Pardo, J. M. (1995). Ion Homeostasis in NaCl Stress Environments. Plant Physiology, 109(3), 735-742. doi:10.1104/pp.109.3.735Ozgur, R., Uzilday, B., Sekmen, A. H., & Turkan, I. (2013). Reactive oxygen species regulation and antioxidant defence in halophytes. Functional Plant Biology, 40(9), 832. doi:10.1071/fp12389Parida, A. K., Das, A. B., & Mohanty, P. (2004). Defense potentials to NaCl in a mangrove, Bruguiera parviflora: Differential changes of isoforms of some antioxidative enzymes. Journal of Plant Physiology, 161(5), 531-542. doi:10.1078/0176-1617-01084Popp, M., & Polania, J. (1989). Compatible solutes in different organs of mangrove trees. Annales des Sciences Forestières, 46(Supplement), 842s-844s. doi:10.1051/forest:198905art0185Redondo-Gómez, S., Wharmby, C., Castillo, J. M., Mateos-Naranjo, E., Luque, C. J., de Cires, A., … Enrique Figueroa, M. (2006). Growth and photosynthetic responses to salinity in an extreme halophyte, Sarcocornia fruticosa. Physiologia Plantarum, 128(1), 116-124. doi:10.1111/j.1399-3054.2006.00719.xRENGEL, Z. (1992). The role of calcium in salt toxicity. Plant, Cell and Environment, 15(6), 625-632. doi:10.1111/j.1365-3040.1992.tb01004.xRodríguez-Navarro, A., & Rubio, F. (2006). High-affinity potassium and sodium transport systems in plants. Journal of Experimental Botany, 57(5), 1149-1160. doi:10.1093/jxb/erj068Hediye Sekmen, A., Türkan, İ., & Takio, S. (2007). Differential responses of antioxidative enzymes and lipid peroxidation to salt stress in salt-tolerant Plantago maritima and salt-sensitive Plantago media. Physiologia Plantarum, 131(3), 399-411. doi:10.1111/j.1399-3054.2007.00970.xSHORT, D. (1999). Salt Tolerance in the HalophyteHalosarcia pergranulatasubsp.pergranulata. Annals of Botany, 83(3), 207-213. doi:10.1006/anbo.1998.0812Szabados, L., & Savouré, A. (2010). Proline: a multifunctional amino acid. Trends in Plant Science, 15(2), 89-97. doi:10.1016/j.tplants.2009.11.009Tipirdamaz, R., Gagneul, D., Duhazé, C., Aïnouche, A., Monnier, C., Özkum, D., & Larher, F. (2006). Clustering of halophytes from an inland salt marsh in Turkey according to their ability to accumulate sodium and nitrogenous osmolytes. Environmental and Experimental Botany, 57(1-2), 139-153. doi:10.1016/j.envexpbot.2005.05.007Türkan, I., & Demiral, T. (2009). Recent developments in understanding salinity tolerance. Environmental and Experimental Botany, 67(1), 2-9. doi:10.1016/j.envexpbot.2009.05.008Vicente, O., Boscaiu, M., Naranjo, M. Á., Estrelles, E., Bellés, J. M., & Soriano, P. (2004). Responses to salt stress in the halophyte Plantago crassifolia (Plantaginaceae). Journal of Arid Environments, 58(4), 463-481. doi:10.1016/j.jaridenv.2003.12.003Walker, D. J., Romero, P., de Hoyos, A., & Correal, E. (2008). Seasonal changes in cold tolerance, water relations and accumulation of cations and compatible solutes in Atriplex halimus L. Environmental and Experimental Botany, 64(3), 217-224. doi:10.1016/j.envexpbot.2008.05.012Watson, E. B., & Byrne, R. (2009). Abundance and diversity of tidal marsh plants along the salinity gradient of the San Francisco Estuary: implications for global change ecology. Plant Ecology, 205(1), 113-128. doi:10.1007/s11258-009-9602-7Weimberg, 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.xZhishen, 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)00102-2Zhu, J.-K. (2000). Genetic Analysis of Plant Salt Tolerance Using Arabidopsis: Fig. 1. Plant Physiology, 124(3), 941-948. doi:10.1104/pp.124.3.941Zhu, J.-K. (2001). Plant salt tolerance. Trends in Plant Science, 6(2), 66-71. doi:10.1016/s1360-1385(00)01838-0Zhu, J.-K. (2002). SALT ANDDROUGHTSTRESSSIGNALTRANSDUCTION INPLANTS. Annual Review of Plant Biology, 53(1), 247-273. doi:10.1146/annurev.arplant.53.091401.14332

    Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project

    Get PDF
    INTRODUCTION: Large variability among Alzheimer's disease (AD) cases might impact genetic discoveries and complicate dissection of underlying biological pathways. METHODS: Genome Research at Fundacio ACE (GR@ACE) is a genome-wide study of dementia and its clinical endophenotypes, defined based on AD's clinical certainty and vascular burden. We assessed the impact of known AD loci across endophenotypes to generate loci categories. We incorporated gene coexpression data and conducted pathway analysis per category. Finally, to evaluate the effect of heterogeneity in genetic studies, GR@ACE series were meta-analyzed with additional genome-wide association study data sets. RESULTS: We classified known AD loci into three categories, which might reflect the disease clinical heterogeneity. Vascular processes were only detected as a causal mechanism in probable AD. The meta-analysis strategy revealed the ANKRD31-rs4704171 and NDUFAF6-rs10098778 and confirmed SCIMP-rs7225151 and CD33-rs3865444. DISCUSSION: The regulation of vasculature is a prominent causal component of probable AD. GR@ACE meta-analysis revealed novel AD genetic signals, strongly driven by the presence of clinical heterogeneity in the AD series

    Association between convalescent plasma treatment and mortality in COVID-19: a collaborative systematic review and meta-analysis of randomized clinical trials.

    Get PDF
    Funder: laura and john arnold foundationBACKGROUND: Convalescent plasma has been widely used to treat COVID-19 and is under investigation in numerous randomized clinical trials, but results are publicly available only for a small number of trials. The objective of this study was to assess the benefits of convalescent plasma treatment compared to placebo or no treatment and all-cause mortality in patients with COVID-19, using data from all available randomized clinical trials, including unpublished and ongoing trials (Open Science Framework, https://doi.org/10.17605/OSF.IO/GEHFX ). METHODS: In this collaborative systematic review and meta-analysis, clinical trial registries (ClinicalTrials.gov, WHO International Clinical Trials Registry Platform), the Cochrane COVID-19 register, the LOVE database, and PubMed were searched until April 8, 2021. Investigators of trials registered by March 1, 2021, without published results were contacted via email. Eligible were ongoing, discontinued and completed randomized clinical trials that compared convalescent plasma with placebo or no treatment in COVID-19 patients, regardless of setting or treatment schedule. Aggregated mortality data were extracted from publications or provided by investigators of unpublished trials and combined using the Hartung-Knapp-Sidik-Jonkman random effects model. We investigated the contribution of unpublished trials to the overall evidence. RESULTS: A total of 16,477 patients were included in 33 trials (20 unpublished with 3190 patients, 13 published with 13,287 patients). 32 trials enrolled only hospitalized patients (including 3 with only intensive care unit patients). Risk of bias was low for 29/33 trials. Of 8495 patients who received convalescent plasma, 1997 died (23%), and of 7982 control patients, 1952 died (24%). The combined risk ratio for all-cause mortality was 0.97 (95% confidence interval: 0.92; 1.02) with between-study heterogeneity not beyond chance (I2 = 0%). The RECOVERY trial had 69.8% and the unpublished evidence 25.3% of the weight in the meta-analysis. CONCLUSIONS: Convalescent plasma treatment of patients with COVID-19 did not reduce all-cause mortality. These results provide strong evidence that convalescent plasma treatment for patients with COVID-19 should not be used outside of randomized trials. Evidence synthesis from collaborations among trial investigators can inform both evidence generation and evidence application in patient care

    Inclusive and multiplicity dependent production of electrons from heavy-flavour hadron decays in pp and p-Pb collisions

    Get PDF
    Measurements of the production of electrons from heavy-flavour hadron decays in pp collisions at root s = 13 TeV at midrapidity with the ALICE detector are presented down to a transverse momentum (p(T)) of 0.2 GeV/c and up to p(T) = 35 GeV/c, which is the largest momentum range probed for inclusive electron measurements in ALICE. In p-Pb collisions, the production cross section and the nuclear modification factor of electrons from heavy-flavour hadron decays are measured in the p(T) range 0.5 < p(T) < 26 GeV/c at root s(NN) = 8.16 TeV. The nuclear modification factor is found to be consistent with unity within the statistical and systematic uncertainties. In both collision systems, first measurements of the yields of electrons from heavy-flavour hadron decays in different multiplicity intervals normalised to the multiplicity-integrated yield (self-normalised yield) at midrapidity are reported as a function of the self-normalised charged-particle multiplicity estimated at midrapidity. The self-normalised yields in pp and p-Pb collisions grow faster than linear with the self-normalised multiplicity. A strong p(T) dependence is observed in pp collisions, where the yield of high-p(T) electrons increases faster as a function of multiplicity than the one of low-p(T) electrons. The measurement in p-Pb collisions shows no p(T) dependence within uncertainties. The self-normalised yields in pp and p-Pb collisions are compared with measurements of other heavy-flavour, light-flavour, and strange particles, and with Monte Carlo simulations

    Hypertriton Production in p-Pb Collisions at √sNN = 5.02 TeV

    Get PDF
    The study of nuclei and antinuclei production has proven to be a powerful tool to investigate the formation mechanism of loosely bound states in high-energy hadronic collisions. The first measurement of the production of Λ3H{\rm ^{3}_{\Lambda}\rm H} in p-Pb collisions at sNN\sqrt{s_{\rm{NN}}} = 5.02 TeV is presented in this Letter. Its production yield measured in the rapidity interval -1 < y < 0 for the 40% highest multiplicity p-Pb collisions is dN/dy=[6.3±1.8(stat.)±1.2(syst.)]×107{\rm d} N /{\rm d} y =[\mathrm{6.3 \pm 1.8 (stat.) \pm 1.2 (syst.) ] \times 10^{-7}}. The measurement is compared with the expectations of statistical hadronisation and coalescence models, which describe the nucleosynthesis in hadronic collisions. These two models predict very different yields of the hypertriton in small collision systems such as p-Pb and therefore the measurement of dN/dy{\rm d} N /{\rm d} y is crucial to distinguish between them. The precision of this measurement leads to the exclusion with a significance larger than 6σ\sigma of some configurations of the statistical hadronisation, thus constraining the production mechanism of loosely bound states

    Measurement of the non-prompt D-meson fraction as a function of multiplicity in proton-proton collisions at s \sqrt{s} = 13 TeV

    Get PDF
    The fractions of non-prompt (i.e. originating from beauty-hadron decays) D0 and D+ mesons with respect to the inclusive yield are measured as a function of the charged-particle multiplicity in proton-proton collisions at a centre-of-mass energy of √s = 13 TeV with the ALICE detector at the LHC. The results are reported in intervals of transverse momentum (pT) and integrated in the range 1 < pT < 24 GeV/c. The fraction of non-prompt D0 and D+ mesons is found to increase slightly as a function of pT in all the measured multiplicity intervals, while no significant dependence on the charged- particle multiplicity is observed. In order to investigate the production and hadronisation mechanisms of charm and beauty quarks, the results are compared to PYTHIA 8 as well as EPOS 3 and EPOS 4 Monte Carlo simulations, and to calculations based on the colour glass condensate including three-pomeron fusion

    General balance functions of identified charged hadron pairs of (pi,K,p) in Pb-Pb collisions at 2.76 TeV

    Get PDF
    First measurements of balance functions (BFs) of all combinations of identified charged hadron ( π , K, p) pairs in Pb–Pb collisions at √sNN = 2.76 TeV recorded by the ALICE detector are presented. The BF measurements are carried out as two-dimensional differential correlators versus the relative rapidity (delta-y) and azimuthal angle (delta-φ) of hadron pairs, and studied as a function of collision centrality. The delta-φ dependence of BFs is expected to be sensitive to the light quark diffusivity in the quark–gluon plasma. While the BF azimuthal widths of all pairs substantially decrease from peripheral to central collisions, the longitudinal widths exhibit mixed behaviors: BFs of π π and cross-species pairs narrow significantly in more central collisions, whereas those of KK and pp are found to be independent of collision centrality. This dichotomy is qualitatively consistent with the presence of strong radial flow effects and the existence of two stages of quark production in relativistic heavy-ion collisions. Finally, the first measurements of the collision centrality evolution of BF integrals are presented, with the observation that charge balancing fractions are nearly independent of collision centrality in Pb–Pb collisions. Overall, the results presented provide new and challenging constraints for theoretical models of hadron production and transport in relativistic heavy-ion collisions

    K∗(892)0 and φ(1020) production in p-Pb collisions at √s NN = 8.16 TeV

    Get PDF
    The production of K*(892)(0) and phi(1020) resonances has been measured in p-Pb collisions at root s(NN) = 8.16 TeV using the ALICE detector. Resonances are reconstructed via their hadronic decay channels in the rapidity interval -0.5 8 GeV/c), the R-pPb values of all hadrons are consistent with unity within uncertainties. The R-pPb of K*(892)(0) and phi(1020) at root s(NN) = 8.16 and 5.02 TeV show no significant energy dependence

    Characterizing the initial conditions of heavy-ion collisions at the LHC with mean transverse momentum and anisotropic flow correlations

    Get PDF
    Correlations between mean transverse momentum and anisotropic flow coefficients or are measured as a function of centrality in Pb–Pb and Xe–Xe collisions at sqrt(sNN) = 5.02 TeV and 5.44 TeV, respectively, with ALICE. In addition, the recently proposed higher-order correlation between [pt], v2, and v3 is measured for the first time, which shows an anticorrelation for the presented centrality ranges. These measurements are compared with hydrodynamic calculations using IP-Glasma and TRENTO initial-state shapes, the former based on the Color Glass Condensate effective theory with gluon saturation, and the latter a parameterized model with nucleons as the relevant degrees of freedom. The data are better described by the IP-Glasma rather than the TRENTO based calculations. In particular, Trajectum and JETSCAPE predictions, both based on the TRENTO initial state model but with different parameter settings, fail to describe the measurements. As the correlations between [pt] and vn are mainly driven by the correlations of the size and the shape of the system in the initial state, these new studies pave a novel way to characterize the initial state and help pin down the uncertainty of the extracted properties of the quark–gluon plasma recreated in relativistic heavy-ion collisions
    corecore