13 research outputs found

    A new subspecies of Peucedanum officinale L. subsp. album (Apiaceae) from the eastern part of the Iberian Peninsula

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    [EN] We describe Peucedanum officinale L. subsp. album Martinez-Fort & Donat-Torres subsp. nov., in which we grouped the thermomediterranean populations scattered along the eastern part of the Iberian Peninsula. The characters that differentiate this new subspecies from other infraspecific taxa in Peucedanum officinale are its canaliculated leaflet, the inflorescences much branched and lack of dominant terminal umbels, the umbels are few rayed, sometimes sessile and lateral, the petals are white and the fruit pedicels short, the same or shorter in length than the fruit. We provide here a full description of the new subspecies based on herbarium specimens and field measurements, as well as providing dichotomous keys to the subspecies within P. officinale. In addition, we provide a comparison of the ITS sequences of nrDNA with the most closely related taxons.Martínez-Fort, J.; León Santana, M.; Donat-Torres, MP. (2019). A new subspecies of Peucedanum officinale L. subsp. album (Apiaceae) from the eastern part of the Iberian Peninsula. PhytoKeys (Online). (131):37-55. https://doi.org/10.3897/phytokeys.131.321733755131Altschul, S. F., Gish, W., Miller, W., Myers, E. W., & Lipman, D. J. (1990). Basic local alignment search tool. Journal of Molecular Biology, 215(3), 403-410. doi:10.1016/s0022-2836(05)80360-2Darriba, D., Taboada, G. L., Doallo, R., & Posada, D. (2012). jModelTest 2: more models, new heuristics and parallel computing. Nature Methods, 9(8), 772-772. doi:10.1038/nmeth.2109Downie, S. R., Watson, M. F., Spalik, K., & Katz-Downie, D. S. (2000). Molecular systematics of Old World Apioideae (Apiaceae): relationships among some members of tribe Peucedaneae sensu lato, the placement of several island-endemic species, and resolution within the apioid superclade. Canadian Journal of Botany, 78(4), 506-528. doi:10.1139/b00-029Downie, S. R., Spalik, K., Katz-Downie, D. S., & Reduron, J.-P. (2010). Major clades within Apiaceae subfamily Apioideae as inferred by phylogenetic analysis of nrDNA ITS sequences. Plant Diversity and Evolution, 128(1-2), 111-136. doi:10.1127/1869-6155/2010/0128-0005Engler, A., Krause, K., Pilger, R. K. F., & Prantl, K. A. E. (1887). Die Natürlichen Pflanzenfamilien nebst ihren Gattungen und wichtigeren Arten, insbesondere den Nutzpflanzen, unter Mitwirkung zahlreicher hervorragender Fachgelehrten begründet von A. Engler und K. Prantl, fortgesetzt von A. Engler ... doi:10.5962/bhl.title.4635García Martín, F., & Silvestre, S. (1992). Peucedanum officinale L. subsp. brachyradium García-Martín y Silvestre: nuevo taxon de Umbelliferae. Acta Botanica Malacitana, 17, 119-121. doi:10.24310/abm.v17i.9022Kljuykov, E. V., Liu, M., Ostroumova, T. A., Pimenov, M. G., Tilney, P. M., van Wyk, B.-E., & van Staden, J. (2004). Towards a standardised terminology for taxonomically important morphological characters in the Umbelliferae. South African Journal of Botany, 70(3), 488-496. doi:10.1016/s0254-6299(15)30233-7Kumar, S., Stecher, G., Li, M., Knyaz, C., & Tamura, K. (2018). MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms. Molecular Biology and Evolution, 35(6), 1547-1549. doi:10.1093/molbev/msy096Spalik, K., Reduron, J.-P., & Downie, S. R. (2004). The phylogenetic position of Peucedanum sensu lato and allied genera and their placement in tribe Selineae (Apiaceae, subfamily Apioideae). Plant Systematics and Evolution, 243(3-4), 189-210. doi:10.1007/s00606-003-0066-2White, T. J., Bruns, T., Lee, S., & Taylor, J. (1990). AMPLIFICATION AND DIRECT SEQUENCING OF FUNGAL RIBOSOMAL RNA GENES FOR PHYLOGENETICS. PCR Protocols, 315-322. doi:10.1016/b978-0-12-372180-8.50042-1Magee, A. R., Van Wyk, B.-E., Tilney, P. M., & Downie, S. R. (2007). New generic circumscriptions of Cape peucedanoid species (Apiaceae). South African Journal of Botany, 73(2), 298-299. doi:10.1016/j.sajb.2007.02.07

    Antioxidant responses under salinity and drought in three closely related wild monocots with different ecological optima

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    [EN] Antioxidant enzymes; antioxidant phenolics; ecological adaptation; Juncus; malondialdehyde (MDA); photosynthetic pigments; salt stress; water deficiency stress.This work was financed by internal funds for research support of the Polytechnic University of Valencia to M.P.D.-T., M.B. and O.V.Al Hassan, M.; Chaura, J.; Donat-Torres, MP.; Boscaiu, M.; Vicente, O. (2017). Antioxidant responses under salinity and drought in three closely related wild monocots with different ecological optima. AoB Plants. 9(2):1-20. https://doi.org/10.1093/aobpla/plx009S12092Abogadallah, G. M. (2010). Insights into the significance of antioxidative defense under salt stress. Plant Signaling & Behavior, 5(4), 369-374. doi:10.4161/psb.5.4.10873Aebi, H. (1984). [13] Catalase in vitro. Oxygen Radicals in Biological Systems, 121-126. doi:10.1016/s0076-6879(84)05016-3Al Hassan, M., López-Gresa, M. del P., Boscaiu, M., & Vicente, O. (2016). Stress tolerance mechanisms in Juncus: responses to salinity and drought in three Juncus species adapted to different natural environments. Functional Plant Biology, 43(10), 949. doi:10.1071/fp16007Alscher, R. G., Erturk, N., & Heath, L. S. (2002). Role of superoxide dismutases (SODs) in controlling oxidative stress in plants. Journal of Experimental Botany, 53(372), 1331-1341. doi:10.1093/jxb/53.372.1331Anschütz, U., Becker, D., & Shabala, S. (2014). Going beyond nutrition: Regulation of potassium homoeostasis as a common denominator of plant adaptive responses to environment. Journal of Plant Physiology, 171(9), 670-687. doi:10.1016/j.jplph.2014.01.009Apel, 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.55.031903.141701Asada, K. (2006). Production and Scavenging of Reactive Oxygen Species in Chloroplasts and Their Functions: Figure 1. Plant Physiology, 141(2), 391-396. doi:10.1104/pp.106.082040Bartels, D., & Sunkar, R. (2005). Drought and Salt Tolerance in Plants. Critical Reviews in Plant Sciences, 24(1), 23-58. doi:10.1080/07352680590910410Bautista, I., Boscaiu, M., Lidón, A., Llinares, J. V., Lull, C., Donat, M. P., … Vicente, O. (2015). Environmentally induced changes in antioxidant phenolic compounds levels in wild plants. Acta Physiologiae Plantarum, 38(1). doi:10.1007/s11738-015-2025-2Beyer, 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)90489-1Blainski, 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/molecules18066852Boira, H. (1995). Edaphic characteristics of salt meadow vegetation in the eastern regions of Spain. Ecologia mediterranea, 21(3), 1-11. doi:10.3406/ecmed.1995.1789Boscaiu, 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/rts017Bose, 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/ert430Bradford, 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)90527-3Van Breusegem, F., Vranová, E., Dat, J. F., & Inzé, D. (2001). The role of active oxygen species in plant signal transduction. Plant Science, 161(3), 405-414. doi:10.1016/s0168-9452(01)00452-6Connell, J. P., & Mullet, J. E. (1986). Pea Chloroplast Glutathione Reductase: Purification and Characterization. Plant Physiology, 82(2), 351-356. doi:10.1104/pp.82.2.351Cramer, G., Alberico, G., & Schmidt, C. (1994). Leaf Expansion Limits Dry Matter Accumulation of Salt-Stressed Maize. Functional Plant Biology, 21(5), 663. doi:10.1071/pp9940663Del 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/bst0240434Demidchik, V., Cuin, T. A., Svistunenko, D., Smith, S. J., Miller, A. J., Shabala, S., … Yurin, V. (2010). Arabidopsis root K+-efflux conductance activated by hydroxyl radicals: single-channel properties, genetic basis and involvement in stress-induced cell death. Journal of Cell Science, 123(9), 1468-1479. doi:10.1242/jcs.064352Demidchik, V., & Maathuis, F. J. M. (2007). Physiological roles of nonselective cation channels in plants: from salt stress to signalling and development. New Phytologist, 175(3), 387-404. doi:10.1111/j.1469-8137.2007.02128.xDemidchik, V., Shabala, S. N., & Davies, J. M. (2007). Spatial variation in H2O2 response of Arabidopsis thaliana root epidermal Ca2+ flux and plasma membrane Ca2+ channels. The Plant Journal, 49(3), 377-386. doi:10.1111/j.1365-313x.2006.02971.xDEMIRAL, T., & TURKAN, I. (2005). Comparative lipid peroxidation, antioxidant defense systems and proline content in roots of two rice cultivars differing in salt tolerance. Environmental and Experimental Botany, 53(3), 247-257. doi:10.1016/j.envexpbot.2004.03.017Dunson, W. A., & Travis, J. (1991). The Role of Abiotic Factors in Community Organization. The American Naturalist, 138(5), 1067-1091. doi:10.1086/285270Ellouzi, H., Ben Hamed, K., Cela, J., Munné-Bosch, S., & Abdelly, C. (2011). Early effects of salt stress on the physiological and oxidative status of Cakile maritima (halophyte) and Arabidopsis thaliana (glycophyte). Physiologia Plantarum, 142(2), 128-143. doi:10.1111/j.1399-3054.2011.01450.xFarah, A., & Donangelo, C. M. (2006). Phenolic compounds in coffee. Brazilian Journal of Plant Physiology, 18(1), 23-36. doi:10.1590/s1677-04202006000100003Flowers, T. J., & Colmer, T. D. (2008). Salinity tolerance in halophytes*. New Phytologist, 179(4), 945-963. doi:10.1111/j.1469-8137.2008.02531.xFoyer, C. H., & Noctor, G. (2003). Redox sensing and signalling associated with reactive oxygen in chloroplasts, peroxisomes and mitochondria. Physiologia Plantarum, 119(3), 355-364. doi:10.1034/j.1399-3054.2003.00223.xFoyer, C. H., & Noctor, G. (2005). Redox Homeostasis and Antioxidant Signaling: A Metabolic Interface between Stress Perception and Physiological Responses. The Plant Cell, 17(7), 1866-1875. doi:10.1105/tpc.105.033589Gill, S. S., & Tuteja, N. (2010). Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry, 48(12), 909-930. doi:10.1016/j.plaphy.2010.08.016Gong, Q., Li, P., Ma, S., Indu Rupassara, S., & Bohnert, H. J. (2005). Salinity stress adaptation competence in the extremophile Thellungiella halophila in comparison with its relative Arabidopsis thaliana. The Plant Journal, 44(5), 826-839. doi:10.1111/j.1365-313x.2005.02587.xHarinasut, P., Poonsopa, D., Roengmongkol, K., & Charoensataporn, R. (2003). ScienceAsia, 29(2), 109. doi:10.2306/scienceasia1513-1874.2003.29.109Hasegawa, P. M., Bressan, R. A., Zhu, J.-K., & Bohnert, H. J. (2000). PLANTCELLULAR ANDMOLECULARRESPONSES TOHIGHSALINITY. Annual Review of Plant Physiology and Plant Molecular Biology, 51(1), 463-499. doi:10.1146/annurev.arplant.51.1.463Hodges, 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/s004250050524Horling, F., Lamkemeyer, P., König, J., Finkemeier, I., Kandlbinder, A., Baier, M., & Dietz, K.-J. (2003). Divergent Light-, Ascorbate-, and Oxidative Stress-Dependent Regulation of Expression of the Peroxiredoxin Gene Family in Arabidopsis. Plant Physiology, 131(1), 317-325. doi:10.1104/pp.010017Hummel, I., Pantin, F., Sulpice, R., Piques, M., Rolland, G., Dauzat, M., … Muller, B. (2010). Arabidopsis Plants Acclimate to Water Deficit at Low Cost through Changes of Carbon Usage: An Integrated Perspective Using Growth, Metabolite, Enzyme, and Gene Expression Analysis. Plant Physiology, 154(1), 357-372. doi:10.1104/pp.110.157008Inan, G., Zhang, Q., Li, P., Wang, Z., Cao, Z., Zhang, H., … Zhu, J.-K. (2004). Salt Cress. A Halophyte and Cryophyte Arabidopsis Relative Model System and Its Applicability to Molecular Genetic Analyses of Growth and Development of Extremophiles. Plant Physiology, 135(3), 1718-1737. doi:10.1104/pp.104.041723Jaspers, P., & Kangasjärvi, J. (2010). Reactive oxygen species in abiotic stress signaling. Physiologia Plantarum, 138(4), 405-413. doi:10.1111/j.1399-3054.2009.01321.xKANT, S., KANT, P., RAVEH, E., & BARAK, S. (2006). Evidence that differential gene expression between the halophyte, Thellungiella halophila, and Arabidopsis thaliana is responsible for higher levels of the compatible osmolyte proline and tight control of Na+ uptake in T. halophila. Plant, Cell and Environment, 29(7), 1220-1234. doi:10.1111/j.1365-3040.2006.01502.xKukreja, S., Nandwal, A. S., Kumar, N., Sharma, S. K., Sharma, S. K., Unvi, V., & Sharma, P. K. (2005). Plant water status, H2O2 scavenging enzymes, ethylene evolution and membrane integrity of Cicer arietinum roots as affected by salinity. Biologia plantarum, 49(2), 305-308. doi:10.1007/s10535-005-5308-4Larkindale, J., & Huang, B. (2004). Thermotolerance and antioxidant systems in Agrostis stolonifera: Involvement of salicylic acid, abscisic acid, calcium, hydrogen peroxide, and ethylene. Journal of Plant Physiology, 161(4), 405-413. doi:10.1078/0176-1617-01239Lee, S.-H., Ahsan, N., Lee, K.-W., Kim, D.-H., Lee, D.-G., Kwak, S.-S., … Lee, B.-H. (2007). Simultaneous overexpression of both CuZn superoxide dismutase and ascorbate peroxidase in transgenic tall fescue plants confers increased tolerance to a wide range of abiotic stresses. Journal of Plant Physiology, 164(12), 1626-1638. doi:10.1016/j.jplph.2007.01.003LI, R., GUO, P., Michael, B., Stefania, G., & Salvatore, C. (2006). Evaluation of Chlorophyll Content and Fluorescence Parameters as Indicators of Drought Tolerance in Barley. Agricultural Sciences in China, 5(10), 751-757. doi:10.1016/s1671-2927(06)60120-xLICHTENTHALER, 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/bst0110591MAATHUIS, F. (1999). K+Nutrition and Na+Toxicity: The Basis of Cellular K+/Na+Ratios. Annals of Botany, 84(2), 123-133. doi:10.1006/anbo.1999.0912Martinez, C. A., Loureiro, M. E., Oliva, M. A., & Maestri, M. (2001). Differential responses of superoxide dismutase in freezing resistant Solanum curtilobum and freezing sensitive Solanum tuberosum subjected to oxidative and water stress. Plant Science, 160(3), 505-515. doi:10.1016/s0168-9452(00)00418-0Miller, 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.xMittler, R., Vanderauwera, S., Gollery, M., & Van Breusegem, F. (2004). Reactive oxygen gene network of plants. Trends in Plant Science, 9(10), 490-498. doi:10.1016/j.tplants.2004.08.009Mittler, R. (2002). Oxidative stress, antioxidants and stress tolerance. Trends in Plant Science, 7(9), 405-410. doi:10.1016/s1360-1385(02)02312-9MITTOVA, V., TAL, M., VOLOKITA, M., & GUY, M. (2003). Up-regulation of the leaf mitochondrial and peroxisomal antioxidative systems in response to salt-induced oxidative stress in the wild salt-tolerant tomato species Lycopersicon pennellii. Plant, Cell & Environment, 26(6), 845-856. doi:10.1046/j.1365-3040.2003.01016.xMittova, V., Volokita, M., Guy, M., & Tal, M. (2000). Activities of SOD and the ascorbate-glutathione cycle enzymes in subcellular compartments in leaves and roots of the cultivated tomato and its wild salt-tolerant relative Lycopersicon pennellii. Physiologia Plantarum, 110(1), 42-51. doi:10.1034/j.1399-3054.2000.110106.xMunns, R. (2002). Comparative physiology of salt and water stress. Plant, Cell & Environment, 25(2), 239-250. doi:10.1046/j.0016-8025.2001.00808.xMunns, 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.59.032607.092911Ozgur, 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/fp12389Ozgur, R., Uzilday, B., Sekmen, A. H., & Turkan, I. (2015). The effects of induced production of reactive oxygen species in organelles on endoplasmic reticulum stress and on the unfolded protein response in arabidopsis. Annals of Botany, 116(4), 541-553. doi:10.1093/aob/mcv072Pan, Y., Wu, L. J., & Yu, Z. L. (2006). Effect of salt and drought stress on antioxidant enzymes activities and SOD isoenzymes of liquorice (Glycyrrhiza uralensis Fisch). Plant Growth Regulation, 49(2-3), 157-165. doi:10.1007/s10725-006-9101-yParida, A. K., Das, A. B., Sanada, Y., & Mohanty, P. (2004). Effects of salinity on biochemical components of the mangrove, Aegiceras corniculatum. Aquatic Botany, 80(2), 77-87. doi:10.1016/j.aquabot.2004.07.005Quiles, M. J., & López, N. I. (2004). Photoinhibition of photosystems I and II induced by exposure to high light intensity during oat plant growth. Plant Science, 166(3), 815-823. doi:10.1016/j.plantsci.2003.11.025Richards, S. L., Laohavisit, A., Mortimer, J. C., Shabala, L., Swarbreck, S. M., Shabala, S., & Davies, J. M. (2013). Annexin 1 regulates the H2O2-induced calcium signature inArabidopsis thalianaroots. The Plant Journal, 77(1), 136-145. doi:10.1111/tpj.12372Rossel, J. B. (2002). Global Changes in Gene Expression in Response to High Light in Arabidopsis. PLANT PHYSIOLOGY, 130(3), 1109-1120. doi:10.1104/pp.005595SAI KACHOUT, S., JAFFEL HAMZA, K., KARRAY BOURAOUI, N., LECLERC, J. C., & OUERGHI, Z. (2013). Salt-Induced Changes in Antioxidative Enzyme Activities in Shoot Tissues of Two Atriplex Varieties. Notulae Botanicae Horti Agrobotanici Cluj-Napoca, 41(1), 115. doi:10.15835/nbha4118258Sanders, D. (2000). Plant biology: The salty tale of Arabidopsis. Current Biology, 10(13), R486-R488. doi:10.1016/s0960-9822(00)00554-6Seckin, B., Turkan, I., Sekmen, A. H., & Ozfidan, C. (2010). The role of antioxidant defense systems at differential salt tolerance of Hordeum marinum Huds. (sea barleygrass) and Hordeum vulgare L. (cultivated barley). Environmental and Experimental Botany, 69(1), 76-85. doi:10.1016/j.envexpbot.2010.02.013Hediye 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.xShabala, S. (2009). Salinity and programmed cell death: unravelling mechanisms for ion specific signalling. Journal of Experimental Botany, 60(3), 709-712. doi:10.1093/jxb/erp013Shalata, A., Mittova, V., Volokita, M., Guy, M., & Tal, M. (2001). Response of the cultivated tomato and its wild salt-tolerant relative Lycopersicon pennellii to salt-dependent oxidative stress: The root antioxidative system. Physiologia Plantarum, 112(4), 487-494. doi:10.1034/j.1399-3054.2001.1120405.xSharma, P., & Shanker Dubey, R. (2005). Modulation of nitrate reductase activity in rice seedlings under aluminium toxicity and water stress: role of osmolytes as enzyme protectant. Journal of Plant Physiology, 162(8), 854-864. doi:10.1016/j.jplph.2004.09.011Uchida, A., Jagendorf, A. T., Hibino, T., Takabe, T., & Takabe, T. (2002). Effects of hydrogen peroxide and nitric oxide on both salt and heat stress tolerance in rice. Plant Science, 163(3), 515-523. doi:10.1016/s0168-9452(02)00159-0Chang-Quan, W., & Rui-Chang, L. (2008). Enhancement of superoxide dismutase activity in the leaves of white clover (Trifolium repens L.) in response to polyethylene glycol-induced water stress. Acta Physiologiae Plantarum, 30(6), 841-847. doi:10.1007/s11738-008-0189-8Wang, L., Zhou, Q., Ding, L., & Sun, Y. (2008). Effect of cadmium toxicity on nitrogen metabolism in leaves of Solanum nigrum L. as a newly found cadmium hyperaccumulator. Journal of Hazardous Materials, 154(1-3), 818-825. doi:10.1016/j.jhazmat.2007.10.097Yang, Y., Han, C., Liu, Q., Lin, B., & Wang, J. (2008). Effect of drought and low light on growth and enzymatic antioxidant system of Picea asperata seedlings. Acta Physiologiae Plantarum, 30(4), 433-440. doi:10.1007/s11738-008-0140-zYu, T., Jhun, B. S., & Yoon, Y. (2011). High-Glucose Stimulation Increases Reactive Oxygen Species Production Through the Calcium and Mitogen-Activated Protein Kinase-Mediated Activation of Mitochondrial Fission. Antioxidants & Redox Signaling, 14(3), 425-437. doi:10.1089/ars.2010.3284Zhishen, 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. (2001). Plant salt tolerance. Trends in Plant Science, 6(2), 66-71. doi:10.1016/s1360-1385(00)01838-0Zlatev, Z. S., Lidon, F. C., Ramalho, J. C., & Yordanov, I. T. (2006). Comparison of resistance to drought of three bean cultivars. Biologia plantarum, 50(3), 389-394. doi:10.1007/s10535-006-0054-

    Responses to Increased Salinity and Severe Drought in the Eastern Iberian Endemic Species Thalictrum maritimum (Ranunculaceae), Threatened by Climate Change

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    [EN] Thalictrum maritimum is an endangered, endemic species in East Spain, growing in areas of relatively low salinity in littoral salt marshes. A regression of its populations and the number of individuals has been registered in the last decade. This study aimed at establishing the causes of this reduction using a multidisciplinary approach, including climatic, ecological, physiological and biochemical analyses. The climatic data indicated that there was a direct negative correlation between increased drought, especially during autumn, and the number of individuals censused in the area of study. The susceptibility of this species to water deficit was confirmed by the analysis of growth parameters upon a water deficit treatment applied under controlled greenhouse conditions, with the plants withstanding only 23 days of complete absence of irrigation. On the other hand, increased salinity does not seem to be a risk factor for this species, which behaves as a halophyte, tolerating in controlled treatments salinities much higher than those registered in its natural habitat. The most relevant mechanisms of salt tolerance in T. maritimum appear to be based on the control of ion transport, by (i) the active transport of toxic ions to the aerial parts of the plants at high external salinity¿where they are presumably stored in the leaf vacuoles to avoid their deleterious effects in the cytosol, (ii) the maintenance of K+ concentrations in belowground and aboveground organs, despite the increase of Na+ levels, and (iii) the salt-induced accumulation of Ca2+, particularly in stems and leaves. This study provides useful information for the management of the conservation plans of this rare and endangered species.This research was funded by GENERALITAT VALENCIANA, grant number AICO/2017/039, to M. Boscaiu.González-Orenga, S.; Trif, C.; Donat-Torres, MP.; Llinares Palacios, JV.; Collado, F.; Ferrer-Gallego, PP.; Laguna, E.... (2020). Responses to Increased Salinity and Severe Drought in the Eastern Iberian Endemic Species Thalictrum maritimum (Ranunculaceae), Threatened by Climate Change. Plants. 9(10):1-24. https://doi.org/10.3390/plants9101251S124910Laguna Lumbreras, E., & Ferrer Gallego, P. P. (2015). Global environmental change in the unique flora: Endangered plant communities in the Valencia region. Mètode Revista de difusió de la investigació, 0(6). doi:10.7203/metode.6.4127Gómez Mercado, F., de Haro Lozano, S., & López-Carrique, E. (2017). Impacts of future climate scenarios on hypersaline habitats and their conservation interest. Biodiversity and Conservation, 26(11), 2717-2734. doi:10.1007/s10531-017-1382-0Dufour, M. L. (1860). Diagnoses Et Observations Critiques Sur Quelques Plantes D’Espagne Mal Connues Ou Nouvelles. Bulletin de la Société Botanique de France, 7(4), 221-227. doi:10.1080/00378941.1860.10826242FORTE GIL, J. A., YABOR, L., BELLIDO NADAL, A., COLLADO, F., FERRER-GALLEGO, P., VICENTE, O., & BOSCAIU, M. (2017). A Methodological Approach for Testing the Viability of Seeds Stored in Short-Term Seed Banks. Notulae Scientia Biologicae, 9(4), 563-570. doi:10.15835/nsb9410173Conselleria de Medi Ambient, Aigua, Urbanisme i Habitatge, Generalitat Valenciana, Valencia http://bdb.gva.es/Lionello, P., & Scarascia, L. (2018). The relation between climate change in the Mediterranean region and global warming. Regional Environmental Change, 18(5), 1481-1493. doi:10.1007/s10113-018-1290-1Worldwide Bioclimatic Classification System, 1996−2020, S. Rivas-Martinez & S. Rivas-Saenz, Phytosociological Research Center, Spain http://www.globalbioclimatics.orgThe Agroclimatic Information System for Irrigation (SIAR, Sistema de Información Agroclimática para Regadío), Benifaió, Llíria and Moncada Agro-Meteorological Stations http://eportal.miteco.gob.es/websiar/Inicio.aspxAl 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.2016.00473Kozminska, A., Al Hassan, M., Hanus-Fajerska, E., Naranjo, M. A., Boscaiu, M., & Vicente, O. (2018). Comparative analysis of water deficit and salt tolerance mechanisms in Silene. South African Journal of Botany, 117, 193-206. doi:10.1016/j.sajb.2018.05.022González-Orenga, S., Llinares, J. V., Al Hassan, M., Fita, A., Collado, F., Lisón, P., … Boscaiu, M. (2020). Physiological and morphological characterisation of Limonium species in their natural habitats: Insights into their abiotic stress responses. Plant and Soil, 449(1-2), 267-284. doi:10.1007/s11104-020-04486-4Zheng, Q., Liu, L., Liu, Z., Chen, J., & Zhao, G. (2009). Comparison of the response of ion distribution in the tissues and cells of the succulent plants Aloe vera and Salicornia europaea to saline stress. Journal of Plant Nutrition and Soil Science, 172(6), 875-883. doi:10.1002/jpln.200900122González-Orenga, S., Ferrer-Gallego, P. P., Laguna, E., López-Gresa, M. P., Donat-Torres, M. P., Verdeguer, M., … Boscaiu, M. (2019). Insights on Salt Tolerance of Two Endemic Limonium Species from Spain. Metabolites, 9(12), 294. doi:10.3390/metabo9120294Flowers, 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.28.060177.000513Greenway, H., & Munns, R. (1980). Mechanisms of Salt Tolerance in Nonhalophytes. Annual Review of Plant Physiology, 31(1), 149-190. doi:10.1146/annurev.pp.31.060180.001053Wu, H., Zhang, X., Giraldo, J. P., & Shabala, S. (2018). It is not all about sodium: revealing tissue specificity and signalling roles of potassium in plant responses to salt stress. Plant and Soil, 431(1-2), 1-17. doi:10.1007/s11104-018-3770-yBrenes, M., Solana, A., Boscaiu, M., Fita, A., Vicente, O., Calatayud, Á., … Plazas, M. (2020). Physiological and Biochemical Responses to Salt Stress in Cultivated Eggplant (Solanum melongena L.) and in S. insanum L., a Close Wild Relative. Agronomy, 10(5), 651. doi:10.3390/agronomy10050651RENGEL, 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.xBressan, 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)01331-4Hepler, P. K. (2005). Calcium: A Central Regulator of Plant Growth and Development. The Plant Cell, 17(8), 2142-2155. doi:10.1105/tpc.105.032508Mahajan, S., Pandey, G. K., & Tuteja, N. (2008). Calcium- and salt-stress signaling in plants: Shedding light on SOS pathway. Archives of Biochemistry and Biophysics, 471(2), 146-158. doi:10.1016/j.abb.2008.01.010González-Orenga, S., Al Hassan, M., Llinares, J. V., Lisón, P., López-Gresa, M. P., Verdeguer, M., … Boscaiu, M. (2019). Qualitative and Quantitative Differences in Osmolytes Accumulation and Antioxidant Activities in Response to Water Deficit in Four Mediterranean Limonium Species. Plants, 8(11), 506. doi:10.3390/plants8110506Zhu, J.-K. (2001). Plant salt tolerance. Trends in Plant Science, 6(2), 66-71. doi:10.1016/s1360-1385(00)01838-0Ashraf, 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.2005.12.006CHEN, T. H. H., & MURATA, N. (2010). Glycinebetaine protects plants against abiotic stress: mechanisms and biotechnological applications. Plant, Cell & Environment, 34(1), 1-20. doi:10.1111/j.1365-3040.2010.02232.xSzabados, L., & Savouré, A. (2010). Proline: a multifunctional amino acid. Trends in Plant Science, 15(2), 89-97. doi:10.1016/j.tplants.2009.11.009Apel, 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.55.031903.141701Foyer, C. H., & Noctor, G. (2005). Redox Homeostasis and Antioxidant Signaling: A Metabolic Interface between Stress Perception and Physiological Responses. The Plant Cell, 17(7), 1866-1875. doi:10.1105/tpc.105.033589Asada, K. (2006). Production and Scavenging of Reactive Oxygen Species in Chloroplasts and Their Functions. Plant Physiology, 141(2), 391-396. doi:10.1104/pp.106.082040Gill, S. S., & Tuteja, N. (2010). Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry, 48(12), 909-930. doi:10.1016/j.plaphy.2010.08.016Bose, 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/ert430Shabala, S. (2009). Salinity and programmed cell death: unravelling mechanisms for ion specific signalling. Journal of Experimental Botany, 60(3), 709-712. doi:10.1093/jxb/erp013Demidchik, V., Shabala, S. N., & Davies, J. M. (2007). Spatial variation in H2O2 response of Arabidopsis thaliana root epidermal Ca2+ flux and plasma membrane Ca2+ channels. The Plant Journal, 49(3), 377-386. doi:10.1111/j.1365-313x.2006.02971.xYu, J., Chen, S., Zhao, Q., Wang, T., Yang, C., Diaz, C., … Dai, S. (2011). Physiological and Proteomic Analysis of Salinity Tolerance in Puccinellia tenuiflora. Journal of Proteome Research, 10(9), 3852-3870. doi:10.1021/pr101102pKumari, A., Das, P., Parida, A. K., & Agarwal, P. K. (2015). Proteomics, metabolomics, and ionomics perspectives of salinity tolerance in halophytes. Frontiers in Plant Science, 6. doi:10.3389/fpls.2015.00537Ozgur, 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/fp12389Alscher, 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/53.372.1331Jaleel, C. A., Riadh, K., Gopi, R., Manivannan, P., Inès, J., Al-Juburi, H. J., … Panneerselvam, R. (2009). Antioxidant defense responses: physiological plasticity in higher plants under abiotic constraints. Acta Physiologiae Plantarum, 31(3), 427-436. doi:10.1007/s11738-009-0275-6Del 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.2005.05.003Arbona, V., Flors, V., Jacas, J., García-Agustín, P., & Gómez-Cadenas, A. (2003). Enzymatic and Non-enzymatic Antioxidant Responses of Carrizo citrange, a Salt-Sensitive Citrus Rootstock, to Different Levels of Salinity. Plant and Cell Physiology, 44(4), 388-394. doi:10.1093/pcp/pcg059Al Hassan, M., Chaura, J., Donat-Torres, M. P., Boscaiu, M., & Vicente, O. (2017). Antioxidant responses under salinity and drought in three closely related wild monocots with different ecological optima. AoB PLANTS, 9(2). doi:10.1093/aobpla/plx009Bautista, I., Boscaiu, M., Lidón, A., Llinares, J. V., Lull, C., Donat, M. P., … Vicente, O. (2015). Environmentally induced changes in antioxidant phenolic compounds levels in wild plants. Acta Physiologiae Plantarum, 38(1). doi:10.1007/s11738-015-2025-2Gil, 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/plu049Euro+Med (2006+): Euro+Med PlantBase—The Information Resource for Euro-Mediterranean Plant Diversity http://ww2.bgbm.org/EuroPlusMed/Bouyoucos, G. J. (1962). Hydrometer Method Improved for Making Particle Size Analyses of Soils 1. Agronomy Journal, 54(5), 464-465. doi:10.2134/agronj1962.00021962005400050028xWALKLEY, A., & BLACK, I. A. (1934). AN EXAMINATION OF THE DEGTJAREFF METHOD FOR DETERMINING SOIL ORGANIC MATTER, AND A PROPOSED MODIFICATION OF THE CHROMIC ACID TITRATION METHOD. Soil Science, 37(1), 29-38. doi:10.1097/00010694-193401000-00003LICHTENTHALER, 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/bf00018060DuBois, 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/ac60111a017Hodges, 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/52.365.2375Blainski, 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

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    [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

    Multidisciplinary studies supporting conservation programmes of two rare, endangered Limonium species from Spain

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    [EN] Background and aims Two local threatened endemics from Valencian salt marshes were analysed from a multidisciplinary perspective combining field studies with experiments performed under greenhouse-controlled conditions. The work aimed to investigate the habitat of the two species but also to explore their limits of tolerance to severe drought and salinity and the mechanisms behind their stress responses. Methods The number of individuals in several populations, climatic conditions, soil characteristics and accompanying vegetation in the natural habitats were analysed in the field study. Plants obtained by seed germination were grown in the greenhouse and subjected to one month of water and salt stress treatments. Growth and biochemical parameters were analysed after the treatments were finalised. Results No correlation between climatic parameters and the number of individuals censed of the two Limonium species could be established. Although L. dufourii was found in more saline soils in the natural habitats, under controlled greenhouse conditions, this species was more severely affected by salt treatment than L. albuferae, which is more susceptible to water stress. A common biochemical response was the increase of proline under all stress treatments, but mostly in water-stressed plants. Oxidative stress markers, MDA and H2O2, did not indicate significant differences between the treatments. The differences in the two species¿ responses to the two kinds of stress were correlated with the activation of the antioxidant enzymes, more pronounced in conditions of salt stress in L. albuferae and of water stress in L. dufourii. Conclusions Although L. albuferae is found in sites with lower salinity in the natural habitats, the greenhouse experiment indicated that it tolerates higher concentrations of salt than L. dufouri, which is more resistant to drought. The two species efficiently mitigate oxidative stress by activation of antioxidant enzymes. The results obtained may be helpful for the conservation management of the two species: whereas salinity is not problematic, as the two species tolerated under controlled conditions salinities far beyond those in their natural environments, water scarcity may be a problem for L. albuferae, which proved to be more susceptible to water deficit.This research was supported by the project AICO/2017/039 from Generalitat Valenciana. We are indebted to Dr Inmaculada Bautista (Universitat Politecnica de Valencia, Spain) for her valuable suggestions for improving the manuscript. Thanks to Inmaculada Ferrando Pardo for helping in the study and conservation of the seeds in the Centre for Forest Research and Experimentation of the Valencian Region (CIEF).González-Orenga, S.; Donat-Torres, MP.; Llinares Palacios, JV.; Navarro, A.; Collado, F.; Ferrer-Gallego, PP.; Laguna Lumbreras, E.... (2021). Multidisciplinary studies supporting conservation programmes of two rare, endangered Limonium species from Spain. Plant and Soil. 466(1-2):505-524. https://doi.org/10.1007/s11104-021-05059-95055244661-

    Seasonal variation of Glycine Betaine in Plants from a Littoral Salt-Marsh in SE Spain

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    Supported by the Spanish Ministry of Science and Innovation (project CGL2008-00438/BOS), with contribution from the European Regional Development Fund.Boscaiu Neagu, MT.; Tifrea, M.; Donat-Torres, MP.; Mayoral García-Berlanga, O.; Llinares Palacios, JV.; Bautista Carrascosa, I.; Lidón Cerezuela, AL.... (2011). Seasonal variation of Glycine Betaine in Plants from a Littoral Salt-Marsh in SE Spain. Bulletin of University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca : Horticulture. 68(1):543-544. http://hdl.handle.net/10251/62931S54354468

    Contacts in the last 90,000 years over the Strait of Gibraltar evidenced by genetic analysis of wild boar (Sus scrofa)

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    [EN] Contacts across the Strait of Gibraltar in the Pleistocene have been studied in different research papers, which have demonstrated that this apparent barrier has been permeable to human and fauna movements in both directions. Our study, based on the genetic analysis of wild boar (Sus scrofa), suggests that there has been contact between Africa and Europe through the Strait of Gibraltar in the Late Pleistocene (at least in the last 90,000 years), as shown by the partial analysis of mitochondrial DNA. Cytochrome b and the control region from North African wild boar indicate a close relationship with European wild boar, and even some specimens belong to a common haplotype in Europe. The analyses suggest the transformation of the wild boar phylogeography in North Africa by the emergence of a natural communication route in times when sea levels fell due to climatic changes, and possibly through human action, since contacts coincide with both the Last Glacial period and the increasing human dispersion via the strait.This study was supported by The Emirates Centre for Wildlife Propagation (Morocco). The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.Soria-Boix, C.; Donat-Torres, MP.; Urios, V. (2017). Contacts in the last 90,000 years over the Strait of Gibraltar evidenced by genetic analysis of wild boar (Sus scrofa). PLoS ONE. 12(7). doi:10.1371/journal.pone.0181929S12

    Photography-based taxonomy is inadequate, unnecessary, and potentially harmful for biological sciences

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    The question whether taxonomic descriptions naming new animal species without type specimen(s) deposited in collections should be accepted for publication by scientific journals and allowed by the Code has already been discussed in Zootaxa (Dubois & Nemésio 2007; Donegan 2008, 2009; Nemésio 2009a–b; Dubois 2009; Gentile & Snell 2009; Minelli 2009; Cianferoni & Bartolozzi 2016; Amorim et al. 2016). This question was again raised in a letter supported by 35 signatories published in the journal Nature (Pape et al. 2016) on 15 September 2016. On 25 September 2016, the following rebuttal (strictly limited to 300 words as per the editorial rules of Nature) was submitted to Nature, which on 18 October 2016 refused to publish it. As we think this problem is a very important one for zoological taxonomy, this text is published here exactly as submitted to Nature, followed by the list of the 493 taxonomists and collection-based researchers who signed it in the short time span from 20 September to 6 October 2016

    Evolutionary ecology of hares (Lepus spp.) from northwestern Africa; The problem of cryptic species and the description of a new species (Lepus saharae sp. nov.)

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    [EN] Objective: We examine the different pressures that lead to the occurrence of new species and thus to their phylogenies. From an evolutionary ecology perspective, we examine the phylogenetic relationships of different lineages, as well as the evolutionary pressures that lead to them and, in some cases, mask them. Organisms and locales: Hares (Lepus spp.) in northwest Africa that are morphologically similar, which, superficially, makes it appear that there is only one species. Methods: We describe different populations of hares in northwest Africa. We describe the morphology of a new species and provide photographs of specimens from across the study area. We analyse five mitochondrial DNA fragments. Results: Mitochondrial DNA analysis revealed the presence of three Lepus species which are different from both Lepus capensis and L. victoriae and which have contiguous, partially overlapping geographical ranges. One of the species, found in the western Sahara (Morocco), is new (Lepus saharae sp. nov.). The other two species (Lepus mediterraneus Wagner, 1841 and Lepus schlumbergeri Remy-St. Loup, 1894) inhabit the northern and central regions of Morocco. The distributions of at least two of the three species extend to countries other than Morocco. Various eco-evolutionary pressures have masked this diversity until now. Certainly, the species have had to adapt to different habitats that include mountains and desert; and isolation of populations by distance, or because of climatic or geographical barriers has led - or at least facilitated - them to appear different. Yet some evolutionary pressures have made them converge morphologically, making it appear that there is only one species.Soria-Boix, C.; Donat-Torres, MP.; Rguibi Idrissi, H.; Urios, V. (2019). Evolutionary ecology of hares (Lepus spp.) from northwestern Africa; The problem of cryptic species and the description of a new species (Lepus saharae sp. nov.). Evolutionary Ecology Research (Online). 20(5):537-555. http://hdl.handle.net/10251/167876S53755520

    Median-joining networks based on mtDNA.

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    <p>(A) The cytochrome b network was constructed with 308 wild boar sequences (1,030 bp). (B) The control region network was constructed with 328 wild boar sequences (534 bp).</p
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