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    Academic Journal

    Πηγή: Vegetable crops of Russia; № 5 (2024); 84-90 ; Овощи России; № 5 (2024); 84-90 ; 2618-7132 ; 2072-9146

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Annals of Botany. 2017;119(5):681-687. https://doi.org/10.1093/aob/mcw284; Doughari J.H. An Overview of Plant Immunity. J. Plant Pathol. Microbiol. 2015;6(11): 322. DOI:10.4172/2157-7471.1000322; Pélissier R., Cyrille V., Morel J.-B. Plant immunity: Good fences make good neighbors? Curr. Opin. Plant Biol. 2021;62:102045. https://doi.org/10.1016/j.pbi.2021.102045; Jones J., Dangl J. The plant immune system. Nature. 2006;444(7117):323-329. https://doi.org/10.1038/nature05286; Vavilov N.I. Study on plant immunity to infectious diseases. Мoscow, Leningrad: Sel'khozgiz; 1935. 100 p. (In Russ.); Rubin B.A., Artsikhovskaya E.A. Biochemistry and physiology of plant immunity. Moscow: Vysshaya shkola; 1968. 416 p. (In Russ.); Pascutti Simão T.M, Silva F.C, Guerreiro Ju.C., Boiça Junior A.L. Antixenosis in Constitutive Resistance in Maize Genotypes to the Stink Bug Diceraeus melacanthus. Journal of Agricultural Science. 2023;15(11):57. https://doi.org/10.5539/jas.v15n11p57; Shapiro I.D., Vilkova N.A., Slepyan E.I. Plant immunity to pests and diseases. L.: Agropromizdat; 1986. 188 p. (In Russ.); Masters G.J., Brown V.K. Plant-mediated interactions between two spatially separated insects. Funct Ecol. 1992;6:175–179.; Shpirnaya I.A., Ibragimov R.I., Umarov I.A. Suppression of Activity Hydrolytic Enzymes the Larvaes the Potato Beetles of Protein from Plants. Bull. Bashkir Univ. 2006;11:49-52. (In Russ.); Chandel R.S., Sharma P.C., Verma K.S., Mehta P.K., Vinod K. Insect pests of potato – III: Leaf eating and defoliating insects. Pestology. 2011;35:60-66.; Chandel R.S. Chandla V.K., Verma K.S., Pathania M. Insect Pests of Potato Global Perspectives on Biology and Management. In: Insect pests of potato in India: biology and management. Eds: Giordanengo P., Vincent C., Alyokhin A. Waltham, MA: Academic Press; 2013. pp. 227-268.; Chandel R.S., Chandla V.K. Managing tuber damaging pests of potato. Indian Horticulture. 2003;48:15-17.; Courtney S. Coevolution of pierid butterflies and their cruciferous foodplants. III. Anthocharis cardamines (L.) survival, development and oviposition on different plants. Oecologia. 1981;51:91-96. https://doi.org/10.1007/BF00344658; Andrew N.R., Roberts I.R., Hill S.J. Insect herbivory along environmental gradients. Open Journal of Ecology. 2012;2:202-213; Marchin R., Zeng H., Hoffmann W. Drought-deciduous behavior reduces nutrient losses from temperate deciduous trees under severe drought. Oecologia. 2010;163(4):845-854. https://doi.org/10.1007/s00442-010-1614-4; Grostal P., O’Dowd D.J. Plants, mites and mutualism: Leaf domatia and the abundance and reproduction of mites Viburnum tinus. Oecologia. 1994; 97(3): 308-315. DOI:10.1007/BF00317319; Joern A., Provin T., Behmer S.T. Not just the usual suspects: Insect herbivore populations and communities are associated with multiple plant nutrients. Ecology. 2012;93(5):1002-1015.; Schoonhoven L.M., van Loon J.J.A., Dicke M. Insect-plant Biology. Oxford, UK: Oxford University Press; 2005. 421 p.; Read J., Stokes A. Plant biomechanics in an ecological context. American Journal of Botany. 2006;93(10): 1546-1565. DOI:10.3732/ajb.93.10.1546; Howe G.A., Jander G. Plant immunity to insect herbivores. Annu. Rev. Plant Biol. 2008;59:41-66. https://doi.org/10.1146/annurev.arplant.59.032607.092825; Verhage A., van Wees S.C.M., Pieterse C.M.J. Plant immunity: it’s the hormones talking, but what do they say? Plant Physiol. 2010;154(2):536-540. https://doi.org/10.1104/pp.110.161570; Hare J.D. Ecological role of volatiles produced by plants in response to damage by herbivorous insects. Annu. Rev. Entomol. 2011;56:161-180. https://doi.org/10.1146/annurev-ento-120709-144753; Dudareva N., Negre F., Nagegowda D.A., Orlova I. Plant volatiles: recent advances and future perspectives. Crit. Rev. Plant Sci. 2006;25(5):417-440. https://doi.org/10.1080/07352680600899973; Arimura G.I., Matsui K., Takabayashi J.Chemical and molecular ecology of herbivore-induced plant volatiles: proximate factors and their ultimate functions. Plant and Cell Physiology. 2009;50(5):911-923. https://doi.org/10.1093/pcp/pcp030; Agrawal A.A., Janssen A., Bruin J., Posthumus M.A., Sabelis M.W. An ecological cost of plant defence: attractiveness of bitter cucumber plants to natural enemies of herbivores. Ecology Letters. 2002;5:377-385.; War A.R., Paulraj M.G., War M.Y., Ignacimuthu S. Herbivoreand elicitor-induced resistance in groundnut to Asian armyworm, Spodoptera litura (Fab.) (Lepidoptera: Noctuidae). Plant Signal. Behav. 2011;6(11):1769-1777. https://doi.org/10.4161/psb.6.11.17323; Karban R. The ecology and evolution of induced resistance against herbivores. Functional Ecology. 2011;25(2): 339-347. DOI:10.1111/j.1365-2435.2010.01789.x; Sharma H.C., Ortiz R. Host plant resistance to insects: An eco-friendly approach for pest management and environment conservation. J. Environ. Biol. 2002;23(2):111135.; Simmonds M.S.J. Flavonoid-insect interactions:.recent advances in our knowledge. Phytochemistry. 2003;64(1):21-30. https://doi.org/10.1016/s0031-9422(03)00293-0; Duffey S.S., Stout M.J. Antinutritive and toxic components of plant defense against insects. Arch. Insect. Biochem. Physiol. 1996;32:3-37; Steppuhn A., Baldwin I.T. Resistance management in a native plant: nicotine prevents herbivores from compensating for plant protease inhibitors. Ecol. Lett. 2007;10(6):499-511. https://doi.org/10.1111/j.1461-0248.2007.01045.x; Simpson S.J., Simpson C.L. The mechanisms of nutritional compensation by phytophagous insects. In: Insect-Plant Interactions. Ed: E.A. Bemays. 2nd ed. Boca Raton, Fl: CRC Press; 1990. pp 111-160.; Bernays E.A. Evolution of feeding behavior in insect herbivores. BioScience. 1998;48(1):35-44. https://doi.org/10.2307/1313226; Bernays E.A. Phytophagous insects. In: Encyclopedia of Insects. Eds: Resh V.H., Cardé R.T. 2nd ed. San Diego, CA, USA: Academic Press; 2009. pp. 798-800.; Waldbauer G.P., Friedman S. Self-selection of optimal diets by insects. Annu. Rev. Entomol. 1991;36:43-63. https://doi.org/10.1146/annurev.en.36.010191.000355; Moran N., Hamilton W.D. Low nutritive quality as a defence against herbivores. J. Theor. Biol. 1980;86(2):247-254. https://doi.org/10.1016/0022-5193(80)90004-1; Lundberg P., Astrom M. Low nutritive quality as a defense against optimally foraging herbivores. The American Naturalist. 1990;135(4):547-562.; Abe T., Higashi M. Cellulose centered perspective on terrestrial community structure. Oikos. 1991;60(1):127-133. https://doi.org/10.2307/3545003; Hochuli D.F. The ecology of plant/insect interactions: implications of digestive strategy for feeding by phytophagous insects. Oikos. 1996;75(1):133-141. https://doi.org/10.2307/3546331; Choong M.F., Lucas W., Ong J.S.Y., Pereira B., Tan H.T.W., Turner I.M. Leaf fracture-toughness and sclerophylly – their correlations and ecological implications. New Phytologist. 1992;121:597-610. https://doi.org/10.1111/j.1469-8137.1992.tb01131.x; Williams W.P., Davis F.M., Buckley P.M., Hedin P.A., Baker G.T., Luthe D.S. Factors associated with resistance to fall armyworm (Lepidoptera: Noctuidae) and southwestern corn borer (Lepidoptera: Crambidae) in corn at different vegetative stages. J. Econ. Ent. 1998;91(6):1471-1480. https://doi.org/10.1093/jee/91.6.1471; Sands D.P.A., Brancatini V.A. A portable penetrometer for measuring leaf toughness in insect herbivory studies. Proc. Ent. Soc. Wash. 1991;93:786-788.; Slansky F., Feeny P.P. Stabilization of the rate of nitrogen accumulation by larvae of the cabbage butterfly on wild and cultivated food plants. Ecol. Monogr. 1977; 47:209-228.; Simpson S.J., Clissold F.J., Lihoreau M., Ponton F., Wilder,S.M., Raubenheimer D. Recent advances in the integrative nutrition of arthropods. Annu. Rev. Entomol. 2015;60:293-311. https://doi.org/10.1146/annurev-ento-010814-020917; Jarau S., Hrncir M. Food Exploitation by Social Insects: Ecological, Behavioral and Theoretical Approaches. Boca Raton, FL, USA: Taylor & Francis Group; 2009. 360 p; Kaluza B.F., Wallace H.M., Keller A., Heard T.A., Jeffers B., Drescher N., Blüthgen N., Leonhardt S.D. Generalist social bees maximize diversity intake in plant species-rich and resource-abundant environments. Ecosphere. 2017;8:e01758. https://doi.org/10.1002/ecs2.1758; Irwin R.E., Cook D., Richardson L.L., Manson J.S., Gardner D.R. Secondary compounds in floral rewards of toxic rangeland plants: Impacts on pollinators. J. Agric. Food Chem. 2014;62(30):7335-7344. https://doi.org/10.1021/jf500521w; Eckhardt M., Haider M., Dorn S., Müller A. Pollen mixing in pollen generalist solitary bees: A possible strategy to complement or mitigate unfavourable pollen properties? J. Anim. Ecol. 2014;83(3):588-597. https://doi.org/10.1111/1365-2656.12168; Kaluza B.F., Wallace H.M., Heard T.A., Minden V., Klein A.M., Leonhardt S.D. Social bees are fitter in more biodiverse environments. Scientific Reports. 2018;8(3):12353. https://doi.org/10.1002/ecs2.1758; Trinkl M., Kaluza B.F., Wallace H.M., Heard T., Keller A., Leonhardt S.D. Floral species richness correlates with changes in the nutritional quality of larval diets in a stingless bee. Insects. 2020;11(2):125. https://doi.org/10.3390/insects11020125; Grund-Mueller N., Ruedenauer F.A., Spaethe J., Leonhardt S.D. Adding amino acids to a sucrose diet is not sufficient to support longevity of adult bumble bees. Insects. 2020;11(4):247. https://doi.org/10.3390/insects11040247; Ruedenauer F.A., Raubenheimer D., Kessner-Beierlein D., Grund-Mueller N., Noack L., Spaethe J., Leonhardt S.D. Best be(e) on low fat: Linking nutrient perception, regulation and fitness. Ecol. Lett. 2020;23(3):545-554. https://doi.org/10.1111/ele.13454; Vaudo A.D., Patch H.M., Mortensen D.A., Tooker J.F., Grozinger C.M. Macronutrient ratios in pollen shape bumble bee (Bombus impatiens) foraging strategies and floral preferences. Proc. Natl. Acad. Sci. USA. 2016;113:e4035-e4042. https://doi.org/10.1073/pnas.1606101113; Morimoto J., Lihoreau M. Open data for open questions in comparative nutrition. Insects. 2020;11(4): 236. DOI:10.3390/insects11040236; Crumière A.J.J. Stephenson C.J., Nagel M., Shik J.Z. Using nutritional geometry to explore how social insects navigate nutritional landscapes. Insects. 2020;11(1): 53. DOI:10.3390/insects11010053; Simpson S.J., Raubenheimer D. The central role of the haemolymph in the regulation of nutrient intake in insects. Physiol. Entomol. 1993;18:395-403.; Nicholls E., Hempel de Ibarra N. Assessment of pollen rewards by foraging bees. Funct. Ecol. 2017;31(1):76-87. https://doi.org/10.1111/1365-2435.12778; Ruedenauer F.A., Leonhardt S.D., Lunau K., Spaethe J. Bumblebees are able to perceive amino acids via chemotactile antennal stimulation. J. Comp. Physiol. A Neuroethol Sens Neural Behav Physiol. 2019;205(3):321-331. https://doi.org/10.1007/s00359-019-01321-9; Vaudo A.D., Tooker J.F., Patch H.M., Biddinger D.J., Coccia M., Crone M.K., Fiely M., Francis J.S, Hines H.M., Hodges M., Jackson S.W., Michez, D., Mu J., Russo L., Safari M., Treanore E.D., Vanderplanck M., Yip E., Leonard A.S., Grozinger C.M. Pollen protein: Lipid macronutrient ratios may guide broad patterns of bee species floral preferences. Insects. 2020;11(2):132. https://doi.org/10.3390/insects11020132; Cohen A.C. Insect diets: Science and technology. Boca Raton, Florida: CRC Press; 2015. 344 p.; Burov V.N., Petrova M.O., Stepanycheva E.A., Chermenskaya T.D., Shchenikova A.V. Plant defense responses of a direct and indirect effect in a tritrophic system. Plant Protection News. 2002;3:69-70. (In Russ.); Slepyana Eh.I. Problems of plant oncology and teratology: proceedings of the 1st National seminar on the problem of pathological neoplasms in plants. Leningrad: Nauka; 1975. 493 p.; Vilkova N.A., Nefedova L.I., Frolov A.N. Immunity of seed plants and its phytosanitary value in agroecosystems. Plant protection and quarantine. 2015;8:3-9. (In Russ.) https://www.elibrary.ru/uarjwv; Pavlyushin V.A., Vilkova N.A., Sukhoruchenko G.I., Fasulati S.R., Nefedova L.I. Phytosanitary consequences of anthropogenic transformation of agricultural ecosystems. Plant Protection News. 2008;3:3-26. (In Russ.); Vilkova N.A., Sukhoruchenko G.I., Fasulati, S.R. Anthropological factors and microevolution of phytophagous insects in agroecosystems including transgenic potato varieties. Transgenic plants are a new direction in the biological protection of plants. Proceedings of the International Scientific Conference. Krasnodar, 2003. p. 170-179. (In Russ.); Fasulati S.R. Microevolutionary aspects of the influence of potato varieties on the population structure of the Colorado potato beetle. In: Variation of insect pests under the conditions of scientific and technical progress in agriculture: Scientific papers of the All-Soviet Institute of Plant Protection. Leningrad; 1988. 71-84 p. (In Russ.); Burov V.N. Petrova M.O., Selitskaya O.G., Stepanycheva E.A., Chermenskaya T.D., Shamshev I.V. Induced plant resistance to phytophages. Мoscow: Publishing House KMK; 2012. 182 p. (In Russ.) https://www.elibrary.ru/uazocx; Shepelev M.A. Agroecology. Kostanai, 2016. 46 p. (In Russ.); Chernyshev V.B. Ecology of insects. Moscow: Lomonosov Moscow State University; 1996. 304 p. (In Russ.); Chernyshev V.B. Ehkologicheskaya zashchita rastenii: Chlenistonogie v agroehkosisteme [Ecological protection of plants: Arthropods in an agroecosystem]. Moscow: Lomonosov Moscow State University; 2001. 136 p. (In Russ.); Chulkina V.A., Toropova E.Yu., Stetsov G.Ya. Epiphytology bases of integrated plant management (IPM) In: Epiphytology (ecological basics of plant protection). Ed: Zhuchenko A.A. Novosibirsk; 1998. 226 p. (In Russ.) https://www.elibrary.ru/jxrhrv; Vilkova N.A., Nefedova L.I., Asyakin B.P., Konarev Al.V., Vereshchagina A.B., Ivanova O.V., Razdoburdin V.A., Fasulati S.R., Yusupov T.M. Principles and methods of the identification of group and complex resistance of the main agricultural crops. Saint Petersburg: RASKhN; 2009. 88 p.; Bolter C.J. Jongsma M.A. Colorado potato beetles (Leptinotarsa decemlineata) adapt to proteinase inhibitors induced in potato leaves by methyl jasmonate. Journal of Insect Physiology. 1995;41:1071-1078.; Baldwin A.J. Further biological observations on Subcoccinella vigintiquatuorpunctata. Entomologist's Monthly Magazine. 1990;126(1516-1519):223-229.; Cabrera-Brandt M.A., Contreras E.F., Figueroa C.C. Differences in the detoxification metabolism between two clonal lineages of the aphid Myzus persicae (Sulzer) (Hemiptera:Aphididae) reared on tobacco (Nicotiana tabacum L.). Chilean Journal of Agricultural Research. 2010;70(4):567-575.; Ghumare S.S., Mukherjee S.N. Performance of Spodoptera litura Fabricius on different host plants: influence of nitrogen and total phenolics of plants and mid-gut esterase activity of the insect. Indian J. Experiment. Biol. 2003;41(8):895-899.; Gil M.A. Insect resistance in tomato (Solanum spp.). Cultivos Tropicales. 2015;36(2):100-110. https://doi.org/10.13140/RG.2.2.34979.04640; Musser R.O., Cipollini D.F., Hum-Musser S.M., Williams S.A., Brown J.K., Felton G.W. Evidence that the caterpillar salivary enzyme glucose oxidase provides herbivore offense in solanaceous plants. Archives of Insect Biochemistry and Physiology. 2005;58(2):128-137.; Mujica N. Alcázar J., Kroschel J. Interacción del nematode entomopatogénico Heterorhabditis indica (Rhabditida: Heterorhabditidae) y el ectoparasitoide Diglyphus begini (Hymenoptera: Eulophidae) en el control de la mosca minadora Liriomyza huidobrensis (Diptera: Agromyzidae). LV Convencion Nacional de Entomologia, 4-7 November, 2013. La Molina, Lima-Perú.; Matsishina N.V., Fisenko P.V., Ermak M.V., Sobko O.A., Volkov D.I., Boginskaya N.G. Traditional Selection Potato Varieties and Their Resistance to the 28-punctata Potato Ladybug Henosepilachna vigintioctomaculata (Coleoptera: Coccinellidae) in the Southern Russian Far East. Indian Journal of Agricultural Research. 2022;56(4):456-462. https://doi.org/10.18805/IJARe.AF-694; Matsishina N.V., Ermak M.V., Kim I.V., Fisenko P.V., Sobko O.A., Klykov A,G,, Emel'yanov A,N. Allelochemical Interactions in the Trophic System "Henosepilachna vigintioctomaculata Motschulsky Solanum tuberosum Linneus". Insects. 2023;14(5):459. https://doi.org/10.3390/insects14050459; Kondrat'ev M.N., Larikova Yu.S. Allelopathy as a mechanism of interaction plants and plants, plants and insects, plants and microorganisms. Agrarian science. 2019;2:57-61. https://doi.org/10.32634/0869-8155-2019-326-2-57-61 (In Russ.); Jabran K., Mahajan G., Sardana V., Chauhan B. Allelopathy for weed control in agricultural systems. Crop Protection. 2015;72:57-65. https://doi.org/10.1016/j.cropro.2015.03.004; Kong C., Xu T., Hu F. Study on interactions among allelochemicals of Ageratum conyzoides. Acta Phytoecologica Sinica. 1998;22(5):403-408.; Vorontsova E.S. Describing the methods based on allelopathy and allelochemical compounds in agriculture. Scientific Electronic Journal Meridian. 2020;6(40):261-263. (In Russ.); Inderjit, Wardle D.A., Karban R., Callaway R. The ecosystem and evolutionary contexts of allelopathy. Trends Ecol. Evol. 2011;26(12): 655-662. DOI:10.1016/j.tree.2011.08.003; Pickett J.A. Rasmussen H., Woodcock C., Matthest M., Napier J. Plant stress signalling: understanding and exploiting plant-plant interactions. Biochem. Soc. Trans. 2003;31(1):123-127. https://doi.org/10.1042/bst0310123; Konaryov A.V. Molecular aspects of plant immunity and their coevolution with insects. Biosfera. 2017;9(1):79-99. https://doi.org/10.24855/biosfera.v9i1.325 (In Russ.); Vasil'ev A.G., Vasil'eva I.A. Epigenetic changes in a population as a probable mechanism of an ecosystemic crisis. Vestnik of Lobachevsky University of Nizhni Novgorod. Biology. 2005;1:27-38. (In Russ.); https://www.vegetables.su/jour/article/view/2499

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    Academic Journal

    Πηγή: Вестник Бурятской государственной сельскохозяйственной академии имени В. Р. Филиппова. :74-80

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    Academic Journal

    Πηγή: Материалы XVII Всероссийской (национальной) научно-технической конференции студентов и аспирантов

    Περιγραφή αρχείου: application/pdf

    Relation: Научное творчество молодежи – лесному комплексу России : материалы XVII Всероссийской (национальной) научно-технической конференции студентов и аспирантов. – Екатеринбург, 2021; https://elar.usfeu.ru/handle/123456789/10455

    Διαθεσιμότητα: https://elar.usfeu.ru/handle/123456789/10455

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    Academic Journal

    Πηγή: Сборник статей

    Περιγραφή αρχείου: application/pdf

    Relation: Актуальные вопросы современной медицинской науки и здравоохранения: Материалы VI Международной научно-практической конференции молодых учёных и студентов, посвященной году науки и технологий, (Екатеринбург, 8-9 апреля 2021): в 3-х т.; http://elib.usma.ru/handle/usma/6828

    Διαθεσιμότητα: http://elib.usma.ru/handle/usma/6828

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    Academic Journal

    Πηγή: Материалы XVII Всероссийской (национальной) научно-технической конференции студентов и аспирантов

    Περιγραφή αρχείου: application/pdf

    Σύνδεσμος πρόσβασης: https://elar.usfeu.ru/handle/123456789/10455

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    Academic Journal

    Πηγή: Животноводство России.

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    Academic Journal

    Συγγραφείς: Solovyev, M., Gisbert, E.

    Συνεισφορές: Producció Animal, Aqüicultura

    Πηγή: IRTA Pubpro. Open Digital Archive
    Institut de Recerca i Tecnologia Agroalimentàries (IRTA)
    Comparative biochemistry and physiology. Part A: Molecular & integrative physiology. 2022. Vol. 264. P. 111116 (1-10)

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