4 research outputs found

    Continuous lactate-driven dark fermentation of restaurant food waste: Process characterization and new insights on transient feast/famine perturbations

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    Producción CientíficaThe effect of hydraulic retention time (HRT) on the continuous lactate-driven dark fermentation (LD-DF) of food waste (FW) was investigated. The robustness of the bioprocess against feast/famine perturbations was also explored. The stepwise HRT decrease from 24 to 16 and 12 h in a continuously stirred tank fermenter fed with simulated restaurant FW impacted on hydrogen production rate (HPR). The optimal HRT of 16 h supported a HPR of 4.2 L H2/L-d. Feast/famine perturbations caused by 12-h feeding interruptions led to a remarkable peak in HPR up to 19.2 L H2/L-d, albeit the process became stable at 4.3 L H2/L-d following perturbation. The occurrence of LD-DF throughout the operation was endorsed by metabolites analysis. Particularly, hydrogen production positively correlated with lactate consumption and butyrate production. Overall, the FW LD-DF process was highly sensitive but resilient against transient feast/famine perturbations, supporting high-rate HPRs under optimal HRTs.European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No. 894515MCIN/AEI /10.13039/501100011033 - Unión Europea NextGenerationEU/PRTR (Grant RYC2021‐034559‐I)Junta de Castilla y León - EU-FEDER (CLU 2017-09, CL-EI-2021-07 y UIC 315

    Elucidating the role of pH and total solids content in the co-production of biohydrogen and carboxylic acids from food waste via lactate-driven dark fermentation

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    Producción CientíficaNotwithstanding lactate-driven dark fermentation (LD-DF) can cope with inhibition issues associated with the over-proliferation of lactate producers, there is still a knowledge gap about the role of key operational parameters. In this study, the effect of pH and total solids (TS) content on the co-production of hydrogen and carboxylic acids, including medium-chain carboxylic acids (MCCAs), from food waste (FW) via LD-DF was investigated. A series of batch fermentations was conducted, first, without pH control, and then at fixed pH values of 5.5, 6.0 and 6.5, while maintaining constant the TS content at 5 %. It was observed that the higher the operational pH, the lower the accumulation of lactate and the higher the extent and rate of hydrogen production, sustaining a maximum hydrogen production yield and rate of 81 NmL/g VS fed and 9 NL/L-d, respectively, at pH 6.5. In a second series of batch tests, the TS content was adjusted to 5, 7.5 and 10 % while pH was set at 6.5. The highest hydrogen production performance (103 NmL/g-VS fed and 13.3 NL/L-d) was achieved at 7.5 % TS, which also resulted in the highest accumulation of MCCAs, particularly of caproate, with an associated titer of 8.7 g/L. Hydrogen production plateaued with the exhaustion of lactate regardless of the condition tested. Further assessment through biochemical methane potential tests showed that LD-DF effluents can be alternatively valorised into biogas. Overall, the results obtained confirmed the key role of pH and TS content in the LD-DF of FW and suggested that this non-conventional route may be an alternative approach to cope with lactate flux diverted toward undesirable non-hydrogen-producing metabolic pathways.European Commission-H2020-MSCA-IF-2019 project UP-GRAD (894515)Junta de Castilla y León y EU-FEDER (program CLU 2017-09, CL-EI-2021-07, and UIC 315

    Biotic and abiotic insights into the storage of food waste and its effect on biohydrogen and methane production potential

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    Producción CientíficaThe present study investigated the physicochemical and microbiological changes occurring during the storage of simulated restaurant food waste (FW) and how such changes affected its biohydrogen and biogas production potential. FW was stored for 72 h in a closed atmosphere under two different scenarios: i) without and ii) with inoculation of a mixed microbial culture harboring lactic acid bacteria (LAB). Both storage scenarios resulted in similar biotic and abiotic changes in FW. Particularly, FW was pre-acidified and pre-hydrolyzed to some extent during the storage, resulting in a feedstock enriched in LAB (≈ 95 % total relative abundance) and lactate (10.5–12.3 g/L, 87.0–90.5 % selectivity). Biochemical hydrogen potential tests revealed that the use of stored FW resulted in similar or even higher hydrogen production efficiencies compared to that of non-stored FW, achieving up to 60 NmL H2/g VS added and a maximum volumetric hydrogen production rate of 9.7 NL H2/L-d. Metabolically, the conversion of lactate into hydrogen was crucial regardless of the use of non-stored or stored FW, albeit the presence of fermentable carbohydrates in the substrate was also essential either to produce lactate or to co-produce extra hydrogen. On the contrary, biochemical methane potential tests showed that the biogas production potential of FW was not affected by storage, yielding on average 400 NmL CH4/g VS added and revealing that lactate oxidation to methane precursors represented an important step in FW biomethanization.European Union's Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No. 894515Ministerio de Ciencia e Innovación - AEI and European Union NextGenerationEU/PRTR (RYC2021-034559-I)Junta de Castilla y León and the European FEDER Programme (CLU 2017-09, CL-EI-2021-07 y UIC 315

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

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