66 research outputs found

    Light clusters in nuclear matter of finite temperature

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    We investigate properties and the distribution of light nuclei (A<4) in symmetric nuclear matter of finite temperature within a microscopic framework. For this purpose we have solved few-body Alt-Grassberger-Sandhas type equations for quasi-nucleons that include self-energy corrections and Pauli blocking in a systematic way. In a statistical model we find a significant influence in the composition of nuclear matter if medium effects are included in the microscopic calculation of nuclei. If multiplicities are frozen out at a certain time (or volume), we expect significant consequences for the formation of light fragments in a heavy ion collision. As a consequence of the systematic inclusion of medium effects the ordering of multiplicities becomes opposite to the law of mass action of ideal components. This is necessary to explain the large abundance of α\alpha-particles in a heavy ion collision that are otherwise largely suppressed in an ideal equilibrium scenario.Comment: 9 pages, 9 figures, epja-style file

    Color-Neutral Superconducting Quark Matter

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    We investigate the consequences of enforcing local color neutrality on the color superconducting phases of quark matter by utilizing the Nambu-Jona-Lasinio model supplemented by diquark and the t'Hooft six-fermion interactions. In neutrino free matter at zero temperature, color neutrality guarantees that the number densities of u, d, and s quarks in the Color-Flavor-Locked (CFL) phase will be equal even with physical current quark masses. Electric charge neutrality follows as a consequence and without the presence of electrons. In contrast, electric charge neutrality in the less symmetric 2-flavor superconducting (2SC) phase with ud pairing requires more electrons than the normal quark phase. The free energy density cost of enforcing color and electric charge neutrality in the CFL phase is lower than that in the 2SC phase, which favors the formation of the CFL phase. With increasing temperature and neutrino content, an unlocking transition occurs from the CFL phase to the 2SC phase with the order of the transition depending on the temperature, the quark and lepton number chemical potentials. The astrophysical implications of this rich structure in the phase diagram, including estimates of the effects from Goldstone bosons in the CFL phase, are discussed.Comment: 20 pages, 4 figures; version to appear in Phys. Rev.

    Thermodynamics of the 3-flavor NJL model : chiral symmetry breaking and color superconductivity

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    Employing an extended three flavor version of the NJL model we discuss in detail the phase diagram of quark matter. The presence of quark as well as of diquark condensates gives raise to a rich structure of the phase diagram. We study in detail the chiral phase transition and the color superconductivity as well as color flavor locking as a function of the temperature and chemical potentials of the system.Comment: 27 pages, 7 figure

    The Origins of Phase Transitions in Small Systems

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    The identification and classification of phases in small systems, e.g. nuclei, social and financial networks, clusters, and biological systems, where the traditional definitions of phase transitions are not applicable, is important to obtain a deeper understanding of the phenomena observed in such systems. Within a simple statistical model we investigate the validity and applicability of different classification schemes for phase transtions in small systems. We show that the whole complex temperature plane contains necessary information in order to give a distinct classification.Comment: 3 pages, 4 figures, revtex 4 beta 5, for further information see http://www.smallsystems.d

    Statistical evolution of isotope composition of nuclear fragments

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    Calculations within the statistical multifragmentation model show that the neutron content of intermediate mass fragments can increase in the region of liquid-gas phase transition in finite nuclei. The model predicts also inhomogeneous distributions of fragments and their isospin in the freeze-out volume caused by an angular momentum and external long-range Coulomb field. These effects can take place in peripheral nucleus-nucleus collisions at intermediate energies and lead to neutron-rich isotopes produced in the midrapidity kinematic region.Comment: 14 pages with 4 figures. GSI preprint, Darmstadt, 200

    A Quasi-Classical Model of Intermediate Velocity Particle Production in Asymmetric Heavy Ion Reactions

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    The particle emission at intermediate velocities in mass asymmetric reactions is studied within the framework of classical molecular dynamics. Two reactions in the Fermi energy domain were modelized, 58^{58}Ni+C and 58^{58}Ni+Au at 34.5 MeV/nucleon. The availability of microscopic correlations at all times allowed a detailed study of the fragment formation process. Special attention was paid to the physical origin of fragments and emission timescales, which allowed us to disentangle the different processes involved in the mid-rapidity particle production. Consequently, a clear distinction between a prompt pre- equilibrium emission and a delayed aligned asymmetric breakup of the heavier partner of the reaction was achieved.Comment: 8 pages, 7 figures. Final version: figures were redesigned, and a new section discussing the role of Coulomb in IMF production was include

    Phosphoglycerate Kinases Are Co-Regulated to Adjust Metabolism and to Optimize Growth

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    [EN] In plants, phosphoglycerate kinase (PGK) converts 1,3-bisphosphoglycerate into 3-phosphoglycerate in glycolysis but also participates in the reverse reaction in gluconeogenesis and the Calvin-Benson cycle. In the databases, we found three genes that encode putative PGKs. Arabidopsis (Arabidopsis thaliana) PGK1 was localized exclusively in the chloroplasts of photosynthetic tissues, while PGK2 was expressed in the chloroplast/plastid of photosynthetic and nonphotosynthetic cells. PGK3 was expressed ubiquitously in the cytosol of all studied cell types. Measurements of carbohydrate content and photosynthetic activities in PGK mutants and silenced lines corroborated that PGK1 was the photosynthetic isoform, while PGK2 and PGK3 were the plastidial and cytosolic glycolytic isoforms, respectively. The pgk1.1 knockdown mutant displayed reduced growth, lower photosynthetic capacity, and starch content. The pgk3.2 knockout mutant was characterized by reduced growth but higher starch levels than the wild type. The pgk1.1 pgk3.2 double mutant was bigger than pgk3.2 and displayed an intermediate phenotype between the two single mutants in all measured biochemical and physiological parameters. Expression studies in PGK mutants showed that PGK1 and PGK3 were down-regulated in pgk3.2 and pgk1.1, respectively. These results indicate that the down-regulation of photosynthetic activity could be a plant strategy when glycolysis is impaired to achieve metabolic adjustment and optimize growth. The double mutants of PGK3 and the triose-phosphate transporter (pgk3.2 tpt3) displayed a drastic growth phenotype, but they were viable. This implies that other enzymes or nonspecific chloroplast transporters could provide 3-phosphoglycerate to the cytosol. Our results highlight both the complexity and the plasticity of the plant primary metabolic network.This work has been funded by the Spanish Government and the European Union: FEDER/ BFU2012-31519 and FEDER/ BFU2015-64204R, FPI fellowship to S.R.-T., and the Valencian Regional Government: PROMETEO II/2014/052.Rosa-Tellez, S.; Anoman, A.; Flores-Tornero, M.; Toujani, W.; Alseek, S.; Fernie, A.; Nebauer, SG.... (2018). Phosphoglycerate Kinases Are Co-Regulated to Adjust Metabolism and to Optimize Growth. PLANT PHYSIOLOGY. 176(2):1182-1198. https://doi.org/10.1104/pp.17.01227S11821198176

    Compatibility of localized wave packets and unrestricted single particle dynamics for cluster formation in nuclear collisions

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    Antisymmetrized molecular dynamics with quantum branching is generalized so as to allow finite time duration of the unrestricted coherent mean field propagation which is followed by the decoherence into wave packets. In this new model, the wave packet shrinking by the mean field propagation is respected as well as the diffusion, so that it predicts a one-body dynamics similar to that in mean field models. The shrinking effect is expected to change the diffusion property of nucleons in nuclear matter and the global one-body dynamics. The central \xenon+\tin collisions at 50 MeV/nucleon are calculated by the models with and without shrinking, and it is shown that the inclusion of the wave packet shrinking has a large effect on the multifragmentation in a big expanding system with a moderate expansion velocity.Comment: 16 pages, 7 figure

    Statistical Multifragmentation of Non-Spherical Expanding Sources in Central Heavy-Ion Collisions

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    We study the anisotropy effects measured with INDRA at GSI in central collisions of Xe+Sn at 50 A.MeV and Au+Au at 60, 80, 100 A.MeV incident energy. The microcanonical multifragmentation model with non-spherical sources is used to simulate an incomplete shape relaxation of the multifragmenting system. This model is employed to interpret observed anisotropic distributions in the fragment size and mean kinetic energy. The data can be well reproduced if an expanding prolate source aligned along the beam direction is assumed. An either non-Hubblean or non-isotropic radial expansion is required to describe the fragment kinetic energies and their anisotropy. The qualitative similarity of the results for the studied reactions suggests that the concept of a longitudinally elongated freeze-out configuration is generally applicable for central collisions of heavy systems. The deformation decreases slightly with increasing beam energy.Comment: 35 pages, 19 figures, submitted to Nuclear Physics

    Protein kinase GCN2 mediates responses to glyphosate in Arabidopsis

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    Background: The increased selection pressure of the herbicide glyphosate has played a role in the evolution of glyphosate-resistance in weedy species, an issue that is becoming a threat to global agriculture. The molecular components involved in the cellular toxicity response to this herbicide at the expression level are still unidentified. Results: In this study, we identify the protein kinase GCN2 as a cellular component that fosters the action of glyphosate in the model plant Arabidopsis thaliana. Comparative studies using wild-type and gcn2 knock-out mutant seedlings show that the molecular programme that the plant deploys after the treatment with the herbicide, is compromised in gcn2. Moreover, gcn2 adult plants show a lower inhibition of photosynthesis, and both seedlings and adult gcn2 plants accumulate less shikimic acid than wild-type after treatment with glyphosate. Conclusions: These results points to an unknown GCN2-dependent factor involved in the cascade of events triggered by glyphosate in plants. Data suggest either that the herbicide does not equally reach the target-enzyme in a gcn2 background, or that a decreased flux in the shikimate pathway in a gcn2 plants minimize the impact of enzyme inhibition.p This work was mainly supported by the Universidad Politecnica de Valencia (PAID2011-16) and the Ministerio Espanol de Ciencia y Tecnologia (BFU2011-22526). The work was partially supported through a grant from the Ministerio Espanol de Ciencia y Tecnologia (AGL-2010-18621).Faus, I.; Zabalza Ostos, AM.; Santiago, J.; GonzĂĄlez Nebauer, S.; Royuela, M.; Serrano, R.; Gadea, J. (2015). Protein kinase GCN2 mediates responses to glyphosate in Arabidopsis. BMC Plant Biology. 15(14). https://doi.org/10.1186/s12870-014-0378-0S1514Basu, C., Halfhill, M. D., Mueller, T. C., & Stewart, C. N. (2004). Weed genomics: new tools to understand weed biology. Trends in Plant Science, 9(8), 391-398. doi:10.1016/j.tplants.2004.06.003DĂ©lye, C. (2012). Unravelling the genetic bases of non-target-site-based resistance (NTSR) to herbicides: a major challenge for weed science in the forthcoming decade. Pest Management Science, 69(2), 176-187. doi:10.1002/ps.3318Powles, S. B., & Yu, Q. (2010). Evolution in Action: Plants Resistant to Herbicides. Annual Review of Plant Biology, 61(1), 317-347. doi:10.1146/annurev-arplant-042809-112119Ge, X., d’ Avignon, D. A., Ackerman, J. J. H., Collavo, A., Sattin, M., Ostrander, E. L., 
 Preston, C. (2012). Vacuolar Glyphosate-Sequestration Correlates with Glyphosate Resistance in Ryegrass (Lolium spp.) from Australia, South America, and Europe: A31P NMR Investigation. Journal of Agricultural and Food Chemistry, 60(5), 1243-1250. doi:10.1021/jf203472sDuke, S. O., & Powles, S. B. (2008). Glyphosate: a once-in-a-century herbicide. Pest Management Science, 64(4), 319-325. doi:10.1002/ps.1518De MarĂ­a, N., Becerril, J. M., GarcĂ­a-Plazaola, J. I., HernĂĄndez, A., de Felipe, M. R., & FernĂĄndez-Pascual, M. (2006). New Insights on Glyphosate Mode of Action in Nodular Metabolism:  Role of Shikimate Accumulation. Journal of Agricultural and Food Chemistry, 54(7), 2621-2628. doi:10.1021/jf058166cZulet, A., Gil-Monreal, M., Villamor, J. G., Zabalza, A., van der Hoorn, R. A. L., & Royuela, M. (2013). Proteolytic Pathways Induced by Herbicides That Inhibit Amino Acid Biosynthesis. PLoS ONE, 8(9), e73847. doi:10.1371/journal.pone.0073847Ahsan, N., Lee, D.-G., Lee, K.-W., Alam, I., Lee, S.-H., Bahk, J. D., & Lee, B.-H. (2008). Glyphosate-induced oxidative stress in rice leaves revealed by proteomic approach. Plant Physiology and Biochemistry, 46(12), 1062-1070. doi:10.1016/j.plaphy.2008.07.002Lu, W., Li, L., Chen, M., Zhou, Z., Zhang, W., Ping, S., 
 Lin, M. (2013). Genome-wide transcriptional responses of Escherichia coli to glyphosate, a potent inhibitor of the shikimate pathway enzyme 5-enolpyruvylshikimate-3-phosphate synthase. Mol. BioSyst., 9(3), 522-530. doi:10.1039/c2mb25374gServaites, J. C., Tucci, M. A., & Geiger, D. R. (1987). Glyphosate Effects on Carbon Assimilation, Ribulose Bisphosphate Carboxylase Activity, and Metabolite Levels in Sugar Beet Leaves. Plant Physiology, 85(2), 370-374. doi:10.1104/pp.85.2.370Zhu, J., Patzoldt, W. L., Shealy, R. T., Vodkin, L. O., Clough, S. J., & Tranel, P. J. (2008). Transcriptome Response to Glyphosate in Sensitive and Resistant Soybean. Journal of Agricultural and Food Chemistry, 56(15), 6355-6363. doi:10.1021/jf801254eMarc, J., Mulner-Lorillon, O., & BellĂ©, R. (2004). Glyphosate-based pesticides affect cell cycle regulation. Biology of the Cell, 96(3), 245-249. doi:10.1016/j.biolcel.2003.11.010Wek, R. C., Jiang, H.-Y., & Anthony, T. G. (2006). Coping with stress: eIF2 kinases and translational control. Biochemical Society Transactions, 34(1), 7-11. doi:10.1042/bst0340007Hinnebusch, A. G. (2005). TRANSLATIONAL REGULATION OFGCN4AND THE GENERAL AMINO ACID CONTROL OF YEAST. Annual Review of Microbiology, 59(1), 407-450. doi:10.1146/annurev.micro.59.031805.133833Zhang, Y., Dickinson, J. R., Paul, M. J., & Halford, N. G. (2003). Molecular cloning of an arabidopsis homologue of GCN2, a protein kinase involved in co-ordinated response to amino acid starvation. Planta, 217(4), 668-675. doi:10.1007/s00425-003-1025-4Zhang, Y., Wang, Y., Kanyuka, K., Parry, M. A. J., Powers, S. J., & Halford, N. G. (2008). GCN2-dependent phosphorylation of eukaryotic translation initiation factor-2α in Arabidopsis. Journal of Experimental Botany, 59(11), 3131-3141. doi:10.1093/jxb/ern169Lageix, S., Lanet, E., Pouch-PĂ©lissier, M.-N., Espagnol, M.-C., Robaglia, C., Deragon, J.-M., & PĂ©lissier, T. (2008). Arabidopsis eIF2α kinase GCN2 is essential for growth in stress conditions and is activated by wounding. BMC Plant Biology, 8(1), 134. doi:10.1186/1471-2229-8-134Shaikhin, S. M., Smailov, S. K., Lee, A. V., Kozhanov, E. V., & Iskakov, B. K. (1992). Interaction of wheat germ translation initiation factor 2 with GDP and GTP. Biochimie, 74(5), 447-454. doi:10.1016/0300-9084(92)90085-sKrishna, V. M., Janaki, N., & Ramaiah, K. V. A. (1997). Wheat Germ Initiation Factor 2 (WG·eIF2) Decreases the Inhibition in Protein Synthesis and eIF2B Activity of Reticulocyte Lysates Mediated by eIF2α Phosphorylation. Archives of Biochemistry and Biophysics, 346(1), 28-36. doi:10.1006/abbi.1997.0263Immanuel, T. M., Greenwood, D. R., & MacDiarmid, R. M. (2012). A critical review of translation initiation factor eIF2α kinases in plants - regulating protein synthesis during stress. Functional Plant Biology, 39(9), 717. doi:10.1071/fp12116Byrne, E. H., Prosser, I., Muttucumaru, N., Curtis, T. Y., Wingler, A., Powers, S., & Halford, N. G. (2011). Overexpression of GCN2-type protein kinase in wheat has profound effects on free amino acid concentration and gene expression. Plant Biotechnology Journal, 10(3), 328-340. doi:10.1111/j.1467-7652.2011.00665.xDas, M., Reichman, J. R., Haberer, G., Welzl, G., Aceituno, F. F., Mader, M. T., 
 Olszyk, D. M. (2009). A composite transcriptional signature differentiates responses towards closely related herbicides in Arabidopsis thaliana and Brassica napus. Plant Molecular Biology, 72(4-5), 545-556. doi:10.1007/s11103-009-9590-yYuan, J. S., Tranel, P. J., & Stewart, C. N. (2007). Non-target-site herbicide resistance: a family business. Trends in Plant Science, 12(1), 6-13. doi:10.1016/j.tplants.2006.11.001Peng, Y., Abercrombie, L. L., Yuan, J. S., Riggins, C. W., Sammons, R. D., Tranel, P. J., & Stewart, C. N. (2010). Characterization of the horseweed (Conyza canadensis) transcriptome using GS-FLX 454 pyrosequencing and its application for expression analysis of candidate non-target herbicide resistance genes. Pest Management Science, 66(10), 1053-1062. doi:10.1002/ps.2004Baena-GonzĂĄlez, E. (2010). Energy Signaling in the Regulation of Gene Expression during Stress. Molecular Plant, 3(2), 300-313. doi:10.1093/mp/ssp113Vivancos, P. D., Driscoll, S. P., Bulman, C. A., Ying, L., Emami, K., Treumann, A., 
 Foyer, C. H. (2011). Perturbations of Amino Acid Metabolism Associated with Glyphosate-Dependent Inhibition of Shikimic Acid Metabolism Affect Cellular Redox Homeostasis and Alter the Abundance of Proteins Involved in Photosynthesis and Photorespiration. Plant Physiology, 157(1), 256-268. doi:10.1104/pp.111.181024Daudi, A., Cheng, Z., O’Brien, J. A., Mammarella, N., Khan, S., Ausubel, F. M., & Bolwell, G. P. (2012). The Apoplastic Oxidative Burst Peroxidase in Arabidopsis Is a Major Component of Pattern-Triggered Immunity. The Plant Cell, 24(1), 275-287. doi:10.1105/tpc.111.093039Denis, M.-H., & Delrot, S. (1993). Carrier-mediated uptake of glyphosate in broad bean (Vicia faba) via a phosphate transporter. Physiologia Plantarum, 87(4), 569-575. doi:10.1111/j.1399-3054.1993.tb02508.xHetherington, P. R., Marshall, G., Kirkwood, R. C., & Warner, J. M. (1998). Absorption and efflux of glyphosate by cell suspensions. Journal of Experimental Botany, 49(320), 527-533. doi:10.1093/jxb/49.320.527Goossens, A., Dever, T. E., Pascual-Ahuir, A., & Serrano, R. (2001). The Protein Kinase Gcn2p Mediates Sodium Toxicity in Yeast. Journal of Biological Chemistry, 276(33), 30753-30760. doi:10.1074/jbc.m102960200Muaddi, H., Majumder, M., Peidis, P., Papadakis, A. I., Holcik, M., Scheuner, D., 
 Koromilas, A. E. (2010). Phosphorylation of eIF2α at Serine 51 Is an Important Determinant of Cell Survival and Adaptation to Glucose Deficiency. Molecular Biology of the Cell, 21(18), 3220-3231. doi:10.1091/mbc.e10-01-0023Geiger, D. R., Kapitan, S. W., & Tucci, M. A. (1986). Glyphosate Inhibits Photosynthesis and Allocation of Carbon to Starch in Sugar Beet Leaves. Plant Physiology, 82(2), 468-472. doi:10.1104/pp.82.2.468Cummins, I., Wortley, D. J., Sabbadin, F., He, Z., Coxon, C. R., Straker, H. E., 
 Edwards, R. (2013). Key role for a glutathione transferase in multiple-herbicide resistance in grass weeds. Proceedings of the National Academy of Sciences, 110(15), 5812-5817. doi:10.1073/pnas.1221179110Orcaray, L., Igal, M., Marino, D., Zabalza, A., & Royuela, M. (2010). The possible role of quinate in the mode of action of glyphosate and acetolactate synthase inhibitors. Pest Management Science, 66(3), 262-269. doi:10.1002/ps.1868Orcaray, L., Zulet, A., Zabalza, A., & Royuela, M. (2012). Impairment of carbon metabolism induced by the herbicide glyphosate. Journal of Plant Physiology, 169(1), 27-33. doi:10.1016/j.jplph.2011.08.009Li, M.-W., AuYeung, W.-K., & Lam, H.-M. (2012). The GCN2 homologue inArabidopsis thalianainteracts with uncharged tRNA and uses Arabidopsis eIF2α molecules as direct substrates. Plant Biology, 15(1), 13-18. doi:10.1111/j.1438-8677.2012.00606.xGe, X., d’ Avignon, D. A., Ackerman, J. J. H., & Sammons, R. D. (2014). In Vivo 31P-Nuclear Magnetic Resonance Studies of Glyphosate Uptake, Vacuolar Sequestration, and Tonoplast Pump Activity in Glyphosate-Resistant Horseweed. PLANT PHYSIOLOGY, 166(3), 1255-1268. doi:10.1104/pp.114.247197Feng, P. C. C., Chiu, T., & Douglas Sammons, R. (2003). Glyphosate efficacy is contributed by its tissue concentration and sensitivity in velvetleaf (Abutilon theophrasti). Pesticide Biochemistry and Physiology, 77(3), 83-91. doi:10.1016/j.pestbp.2003.08.005Koger, C. H., & Reddy, K. N. (2005). Role of absorption and translocation in the mechanism of glyphosate resistance in horseweed (Conyza canadensis). Weed Science, 53(1), 84-89. doi:10.1614/ws-04-102rPerez-Jones, A., Park, K. W., Colquhoun, J., Mallory-Smith, C., & Shaner, D. (2005). Identification of glyphosate-resistant Italian ryegrass (Lolium multiflorum) in Oregon. Weed Science, 53(6), 775-779. doi:10.1614/ws-04-200r.1Morin, F., Vera, V., Nurit, F., Tissut, M., & Marigo, G. (1997). Glyphosate Uptake inCatharanthus roseusCells: Role of a Phosphate Transporter. Pesticide Biochemistry and Physiology, 58(1), 13-22. doi:10.1006/pest.1997.2280Jander, G., Baerson, S. R., Hudak, J. A., Gonzalez, K. A., Gruys, K. J., & Last, R. L. (2003). Ethylmethanesulfonate Saturation Mutagenesis in Arabidopsis to Determine Frequency of Herbicide Resistance. Plant Physiology, 131(1), 139-146. doi:10.1104/pp.102.010397Brotherton, J. E., Jeschke, M. R., Tranel, P. J., & Widholm, J. M. (2007). Identification of Arabidopsis thaliana variants with differential glyphosate responses. Journal of Plant Physiology, 164(10), 1337-1345. doi:10.1016/j.jplph.2006.08.008Forment, J., Gadea, J., Huerta, L., Abizanda, L., Agusti, J., Alamar, S., 
 Beltran, J. P. (2005). Development of a citrus genome-wide EST collection and cDNA microarray as resources for genomic studies. Plant Molecular Biology, 57(3), 375-391. doi:10.1007/s11103-004-7926-1Medina, I., Carbonell, J., Pulido, L., Madeira, S. C., Goetz, S., Conesa, A., 
 Dopazo, J. (2010). Babelomics: an integrative platform for the analysis of transcriptomics, proteomics and genomic data with advanced functional profiling. Nucleic Acids Research, 38(suppl_2), W210-W213. doi:10.1093/nar/gkq388Tusher, V. G., Tibshirani, R., & Chu, G. (2001). Significance analysis of microarrays applied to the ionizing radiation response. Proceedings of the National Academy of Sciences, 98(9), 5116-5121. doi:10.1073/pnas.091062498Koger, C. H., Shaner, D. L., Krutz, L. J., Walker, T. W., Buehring, N., Henry, W. B., 
 Wilcut, J. W. (2005). Rice (Oryza sativa) response to drift rates of glyphosate. Pest Management Science, 61(12), 1161-1167. doi:10.1002/ps.1113Flexas, J., Ortuño, M. F., Ribas-Carbo, M., Diaz-Espejo, A., FlĂłrez-Sarasa, I. D., & Medrano, H. (2007). Mesophyll conductance to CO2in Arabidopsis thaliana. New Phytologist, 175(3), 501-511. doi:10.1111/j.1469-8137.2007.02111.xGenty, B., Briantais, J.-M., & Baker, N. R. (1989). The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochimica et Biophysica Acta (BBA) - General Subjects, 990(1), 87-92. doi:10.1016/s0304-4165(89)80016-
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