{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,21]],"date-time":"2026-10-21T18:01:43Z","timestamp":1792605703701,"version":"4.5.0"},"publisher-location":"New York, NY","reference-count":44,"publisher":"Springer US","isbn-type":[{"value":"9781071639726","type":"print"},{"value":"9781071639733","type":"electronic"}],"license":[{"start":{"date-parts":[[2024,1,1]],"date-time":"2024-01-01T00:00:00Z","timestamp":1704067200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"},{"start":{"date-parts":[[2024,1,1]],"date-time":"2024-01-01T00:00:00Z","timestamp":1704067200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024]]},"DOI":"10.1007\/978-1-0716-3973-3_13","type":"book-chapter","created":{"date-parts":[[2024,6,13]],"date-time":"2024-06-13T09:02:05Z","timestamp":1718269325000},"page":"183-203","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Measurement of Reactive Oxygen Species and Nitric Oxide from Tomato Plants in Response to Abiotic and Biotic Stresses"],"prefix":"10.1007","author":[{"given":"Sanjib Bal","family":"Samant","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"family":"Manbir","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"family":"Rekha","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jagannath","family":"Swain","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pooja","family":"Singh","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Aprajita","family":"Kumari","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kapuganti Jagadis","family":"Gupta","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2024,6,14]]},"reference":[{"key":"13_CR1","doi-asserted-by":"publisher","first-page":"5401","DOI":"10.1038\/ncomms6401","volume":"5","author":"L Frungillo","year":"2014","unstructured":"Frungillo L, Skelly MJ, Loake GJ et al (2014) S-nitrosothiols regulate nitric oxide production and storage in plants through the nitrogen assimilation pathway. Nat Commun 5:5401. https:\/\/doi.org\/10.1038\/ncomms6401","journal-title":"Nat Commun"},{"key":"13_CR2","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1007\/978-3-319-10079-1","volume-title":"Reactive oxygen and nitrogen species signaling and communication in plants","author":"KJ Gupta","year":"2015","unstructured":"Gupta KJ, Igamberdiev AU (2015) Compartmentalization of reactive oxygen species and nitric oxide production in plant cells: an overview. In: Gupta KJ, Igamberdiev AU (eds) Reactive oxygen and nitrogen species signaling and communication in plants. Springer, Cham, pp 1\u201314"},{"key":"13_CR3","doi-asserted-by":"publisher","first-page":"86","DOI":"10.1016\/j.envexpbot.2018.11.010","volume":"161","author":"AA Saddhe","year":"2019","unstructured":"Saddhe AA, Malvankar MR, Karle SB, Kumar K (2019) Reactive nitrogen species: paradigms of cellular signaling and regulation of salt stress in plants. Environ Exp Bot 161:86\u201397. https:\/\/doi.org\/10.1016\/j.envexpbot.2018.11.010","journal-title":"Environ Exp Bot"},{"key":"13_CR4","doi-asserted-by":"publisher","first-page":"136","DOI":"10.1111\/j.1749-6632.2000.tb06182.x","volume":"899","author":"JMC Gutteridge","year":"2000","unstructured":"Gutteridge JMC, Halliwell B (2000) Free radicals and antioxidants in the year 2000. A historical look to the future. Ann N Y Acad Sci 899:136\u2013147. https:\/\/doi.org\/10.1111\/j.1749-6632.2000.tb06182.x","journal-title":"Ann N Y Acad Sci"},{"key":"13_CR5","doi-asserted-by":"publisher","first-page":"10","DOI":"10.3389\/fpls.2018.00296","volume":"9","author":"S Signorelli","year":"2018","unstructured":"Signorelli S, Considine MJ (2018) Nitric oxide enables germination by a four-pronged attack on ABA-induced seed dormancy. Front Plant Sci 9:10\u201313. https:\/\/doi.org\/10.3389\/fpls.2018.00296","journal-title":"Front Plant Sci"},{"key":"13_CR6","doi-asserted-by":"publisher","first-page":"178","DOI":"10.1111\/pce.14198","volume":"45","author":"A Kumari","year":"2022","unstructured":"Kumari A, Singh P, Kaladhar VC et al (2022) Phytoglobin-NO cycle and AOX pathway play a role in anaerobic germination and growth of deepwater rice. Plant Cell Environ 45:178\u2013190. https:\/\/doi.org\/10.1111\/pce.14198","journal-title":"Plant Cell Environ"},{"key":"13_CR7","doi-asserted-by":"publisher","first-page":"4539","DOI":"10.1093\/jxb\/erz185","volume":"70","author":"S Pandey","year":"2019","unstructured":"Pandey S, Kumari A, Shree M et al (2019) Nitric oxide accelerates germination via the regulation of respiration in chickpea. J Exp Bot 70:4539\u20134555. https:\/\/doi.org\/10.1093\/jxb\/erz185","journal-title":"J Exp Bot"},{"key":"13_CR8","doi-asserted-by":"publisher","first-page":"228","DOI":"10.1016\/j.molp.2021.12.012","volume":"15","author":"KJ Gupta","year":"2022","unstructured":"Gupta KJ, Kaladhar VC, Fitzpatrick TB et al (2022) Nitric oxide regulation of plant metabolism. Mol Plant 15:228\u2013242. https:\/\/doi.org\/10.1016\/j.molp.2021.12.012","journal-title":"Mol Plant"},{"key":"13_CR9","doi-asserted-by":"publisher","first-page":"1","DOI":"10.3389\/fpls.2016.00369","volume":"7","author":"KJ Gupta","year":"2016","unstructured":"Gupta KJ, Igamberdiev AU (2016) Reactive nitrogen species in mitochondria and their implications in plant energy status and hypoxic stress tolerance. Front Plant Sci 7:1\u20136. https:\/\/doi.org\/10.3389\/fpls.2016.00369","journal-title":"Front Plant Sci"},{"key":"13_CR10","doi-asserted-by":"publisher","first-page":"113","DOI":"10.1093\/oxfordjournals.pcp.a028908","volume":"37","author":"T Noritake","year":"1996","unstructured":"Noritake T, Kawakita K, Doke N (1996) Nitric oxide induces phytoalexin accumulation in potato tuber tissues. Plant Cell Physiol 37:113\u2013116. https:\/\/doi.org\/10.1093\/oxfordjournals.pcp.a028908","journal-title":"Plant Cell Physiol"},{"key":"13_CR11","doi-asserted-by":"publisher","first-page":"2827","DOI":"10.1093\/jxb\/erv099","volume":"66","author":"LA Del R\u00edo","year":"2015","unstructured":"Del R\u00edo LA (2015) ROS and RNS in plant physiology: an overview. J Exp Bot 66:2827\u20132837. https:\/\/doi.org\/10.1093\/jxb\/erv099","journal-title":"J Exp Bot"},{"key":"13_CR12","doi-asserted-by":"publisher","first-page":"258","DOI":"10.1016\/S0176-1617(96)80251-3","volume":"148","author":"YY Leshem","year":"1996","unstructured":"Leshem YY, Haramaty E (1996) The characterization and contrasting effects of the nitric oxide free radical in vegetative stress and senescence of Pisum sativum Linn. foliage. J Plant Physiol 148:258\u2013263. https:\/\/doi.org\/10.1016\/S0176-1617(96)80251-3","journal-title":"J Plant Physiol"},{"key":"13_CR13","doi-asserted-by":"publisher","first-page":"30","DOI":"10.1016\/j.scienta.2013.03.005","volume":"155","author":"WB Liao","year":"2013","unstructured":"Liao WB, Zhang ML, Yu JH (2013) Role of nitric oxide in delaying senescence of cut rose flowers and its interaction with ethylene. Sci Hortic (Amsterdam) 155:30\u201338. https:\/\/doi.org\/10.1016\/j.scienta.2013.03.005","journal-title":"Sci Hortic (Amsterdam)"},{"key":"13_CR14","doi-asserted-by":"publisher","first-page":"468","DOI":"10.1016\/j.plaphy.2016.08.009","volume":"108","author":"J Floryszak-Wieczorek","year":"2016","unstructured":"Floryszak-Wieczorek J, Arasimowicz-Jelonek M, Izbia\u0144ska K (2016) The combined nitrate reductase and nitrite-dependent route of NO synthesis in potato immunity to Phytophthora infestans. Plant Physiol Biochem 108:468\u2013477. https:\/\/doi.org\/10.1016\/j.plaphy.2016.08.009","journal-title":"Plant Physiol Biochem"},{"key":"13_CR15","doi-asserted-by":"publisher","first-page":"1","DOI":"10.3389\/fpls.2018.00474","volume":"9","author":"YF Fu","year":"2018","unstructured":"Fu YF, Zhang ZW, Yuan S (2018) Putative connections between nitrate reductase S-nitrosylation and NO synthesis under pathogen attacks and abiotic stresses. Front Plant Sci 9:1\u20136. https:\/\/doi.org\/10.3389\/fpls.2018.00474","journal-title":"Front Plant Sci"},{"key":"13_CR16","doi-asserted-by":"publisher","first-page":"1143","DOI":"10.1111\/nph.15969","volume":"225","author":"KJ Gupta","year":"2020","unstructured":"Gupta KJ, Mur LAJ, Wany A et al (2020) The role of nitrite and nitric oxide under low oxygen conditions in plants. New Phytol 225:1143\u20131151. https:\/\/doi.org\/10.1111\/nph.15969","journal-title":"New Phytol"},{"key":"13_CR17","doi-asserted-by":"publisher","first-page":"118","DOI":"10.1016\/j.plaphy.2013.04.004","volume":"68","author":"V Ziogas","year":"2013","unstructured":"Ziogas V, Tanou G, Filippou P et al (2013) Nitrosative responses in citrus plants exposed to six abiotic stress conditions. Plant Physiol Biochem 68:118\u2013126. https:\/\/doi.org\/10.1016\/j.plaphy.2013.04.004","journal-title":"Plant Physiol Biochem"},{"key":"13_CR18","doi-asserted-by":"publisher","first-page":"87","DOI":"10.1016\/j.jprot.2012.12.003","volume":"79","author":"D Camejo","year":"2013","unstructured":"Camejo D, Romero-Puertas M d C, Rodr\u00edguez-Serrano M et al (2013) Salinity-induced changes in S-nitrosylation of pea mitochondrial proteins. J Proteome 79:87\u201399. https:\/\/doi.org\/10.1016\/j.jprot.2012.12.003","journal-title":"J Proteome"},{"key":"13_CR19","doi-asserted-by":"publisher","first-page":"163","DOI":"10.1016\/j.tplants.2016.12.001","volume":"22","author":"A Chamizo-Ampudia","year":"2017","unstructured":"Chamizo-Ampudia A, Sanz-Luque E, Llamas A et al (2017) Nitrate reductase regulates plant nitric oxide homeostasis. Trends Plant Sci 22:163\u2013174. https:\/\/doi.org\/10.1016\/j.tplants.2016.12.001","journal-title":"Trends Plant Sci"},{"key":"13_CR20","doi-asserted-by":"publisher","first-page":"34796","DOI":"10.1074\/jbc.M607697200","volume":"281","author":"A Havemeyer","year":"2006","unstructured":"Havemeyer A, Bittner F, Wollers S et al (2006) Identification of the missing component in the mitochondrial benzamidoxime prodrug-converting system as a novel molybdenum enzyme. J Biol Chem 281:34796\u201334802. https:\/\/doi.org\/10.1074\/jbc.M607697200","journal-title":"J Biol Chem"},{"key":"13_CR21","doi-asserted-by":"publisher","first-page":"576","DOI":"10.1093\/pcp\/pcq022","volume":"51","author":"KJ Gupta","year":"2010","unstructured":"Gupta KJ, Kaiser WM (2010) Production and scavenging of nitric oxide by barley root mitochondria. Plant Cell Physiol 51:576\u2013584. https:\/\/doi.org\/10.1093\/pcp\/pcq022","journal-title":"Plant Cell Physiol"},{"key":"13_CR22","doi-asserted-by":"publisher","first-page":"3401","DOI":"10.1093\/jxb\/erx420","volume":"69","author":"J Astier","year":"2018","unstructured":"Astier J, Gross I, Durner J (2018) Nitric oxide production in plants: an update. J Exp Bot 69:3401\u20133411. https:\/\/doi.org\/10.1093\/jxb\/erx420","journal-title":"J Exp Bot"},{"key":"13_CR23","doi-asserted-by":"publisher","first-page":"534","DOI":"10.1016\/j.plantsci.2011.05.002","volume":"181","author":"E Vandelle","year":"2011","unstructured":"Vandelle E, Delledonne M (2011) Peroxynitrite formation and function in plants. Plant Sci 181:534\u2013539. https:\/\/doi.org\/10.1016\/j.plantsci.2011.05.002","journal-title":"Plant Sci"},{"key":"13_CR24","doi-asserted-by":"publisher","first-page":"332","DOI":"10.1016\/j.tem.2009.04.001","volume":"20","author":"RO Poyton","year":"2009","unstructured":"Poyton RO, Ball KA, Castello PR (2009) Mitochondrial generation of free radicals and hypoxic signaling. Trends Endocrinol Metab 20:332\u2013340. https:\/\/doi.org\/10.1016\/j.tem.2009.04.001","journal-title":"Trends Endocrinol Metab"},{"key":"13_CR25","doi-asserted-by":"publisher","first-page":"E7768","DOI":"10.1073\/pnas.1806239115","volume":"115","author":"AL Hansen","year":"2018","unstructured":"Hansen AL, Buchan GJ, R\u00fchl M et al (2018) Nitro-fatty acids are formed in response to virus infection and are potent inhibitors of STING palmitoylation and signaling. Proc Natl Acad Sci USA 115:E7768\u2013E7775. https:\/\/doi.org\/10.1073\/pnas.1806239115","journal-title":"Proc Natl Acad Sci USA"},{"key":"13_CR26","doi-asserted-by":"publisher","first-page":"82","DOI":"10.3390\/plants8040082","volume":"8","author":"L Aranda-Ca\u00f1o","year":"2019","unstructured":"Aranda-Ca\u00f1o L, S\u00e1nchez-Calvo B, Begara-Morales JC et al (2019) Post-translational modification of proteins mediated by nitro-fatty acids in plants: Nitroalkylation. Plan Theory 8:82. https:\/\/doi.org\/10.3390\/plants8040082","journal-title":"Plan Theory"},{"key":"13_CR27","doi-asserted-by":"publisher","first-page":"26","DOI":"10.1016\/j.niox.2022.07.002","volume":"127","author":"S Chakraborty","year":"2022","unstructured":"Chakraborty S, Mukherjee P, Sengupta R (2022) Ribonucleotide reductase: implications of thiol S-nitrosylation and tyrosine nitration for different subunits. Nitric Oxide 127:26\u201343. https:\/\/doi.org\/10.1016\/j.niox.2022.07.002","journal-title":"Nitric Oxide"},{"key":"13_CR28","doi-asserted-by":"publisher","first-page":"618","DOI":"10.1016\/j.redox.2017.09.009","volume":"14","author":"S Bartesaghi","year":"2018","unstructured":"Bartesaghi S, Radi R (2018) Fundamentals on the biochemistry of peroxynitrite and protein tyrosine nitration. Redox Biol 14:618\u2013625. https:\/\/doi.org\/10.1016\/j.redox.2017.09.009","journal-title":"Redox Biol"},{"key":"13_CR29","doi-asserted-by":"publisher","unstructured":"Arasimowicz-Jelonek M, Jagodzik P, P\u0142\u00f3ciennik A et al (2022) Dynamics of nitration phenomenon during dark-induced leaf senescence in Arabidopsis reveals proteins modified by tryptophan nitration. J Exp Bot erac341. https:\/\/doi.org\/10.1093\/jxb\/erac341","DOI":"10.1093\/jxb\/erac341"},{"key":"13_CR30","doi-asserted-by":"publisher","first-page":"207","DOI":"10.1016\/0014-5793(95)01281-6","volume":"376","author":"V Yermilov","year":"1995","unstructured":"Yermilov V, Rubio J, Ohshima H (1995) Formation of 8-nitroguanine in DNA treated with peroxynitrite in vitro and its rapid removal from DNA by depurination. FEBS Lett 376:207\u2013210. https:\/\/doi.org\/10.1016\/0014-5793(95)01281-6","journal-title":"FEBS Lett"},{"key":"13_CR31","doi-asserted-by":"publisher","first-page":"1777","DOI":"10.1093\/jxb\/erj211","volume":"57","author":"Y Wang","year":"2006","unstructured":"Wang Y, Yun BW, Kwon EJ et al (2006) S-nitrosylation: an emerging redox-based post-translational modification in plants. J Exp Bot 57:1777\u20131784. https:\/\/doi.org\/10.1093\/jxb\/erj211","journal-title":"J Exp Bot"},{"key":"13_CR32","doi-asserted-by":"publisher","first-page":"1206","DOI":"10.1111\/jipb.12780","volume":"61","author":"J Feng","year":"2019","unstructured":"Feng J, Chen L, Zuo J (2019) Protein S-Nitrosylation in plants: current progresses and challenges. J Integr Plant Biol 61:1206\u20131223. https:\/\/doi.org\/10.1111\/jipb.12780","journal-title":"J Integr Plant Biol"},{"key":"13_CR33","doi-asserted-by":"publisher","first-page":"1319","DOI":"10.1111\/nph.16622","volume":"227","author":"KJ Gupta","year":"2020","unstructured":"Gupta KJ, Kolbert Z, Durner J et al (2020) Regulating the regulator: nitric oxide control of post-translational modifications. New Phytol 227:1319\u20131325. https:\/\/doi.org\/10.1111\/nph.16622","journal-title":"New Phytol"},{"key":"13_CR34","doi-asserted-by":"publisher","first-page":"1","DOI":"10.3390\/ijms19071912","volume":"19","author":"G Zhao","year":"2018","unstructured":"Zhao G, Zhao Y, Yu X et al (2018) Nitric oxide is required for melatonin-enhanced tolerance against salinity stress in rapeseed (Brassica napus L.) seedlings. Int J Mol Sci 19:1\u201322. https:\/\/doi.org\/10.3390\/ijms19071912","journal-title":"Int J Mol Sci"},{"key":"13_CR35","doi-asserted-by":"publisher","first-page":"e13649","DOI":"10.1111\/ppl.13649","volume":"174","author":"SP Manbir","year":"2022","unstructured":"Manbir SP, Kumari A, Gupta KJ (2022) Alternative oxidase plays a role in minimizing ROS and RNS produced under salinity stress in Arabidopsis thaliana. Physiol Plant 174:e13649. https:\/\/doi.org\/10.1111\/ppl.13649","journal-title":"Physiol Plant"},{"key":"13_CR36","doi-asserted-by":"publisher","first-page":"261","DOI":"10.1016\/j.sajb.2016.11.003","volume":"108","author":"X Nxele","year":"2017","unstructured":"Nxele X, Klein A, Ndimba BK (2017) Drought and salinity stress alters ROS accumulation, water retention, and osmolyte content in sorghum plants. S Afr J Bot 108:261\u2013266. https:\/\/doi.org\/10.1016\/j.sajb.2016.11.003","journal-title":"S Afr J Bot"},{"key":"13_CR37","doi-asserted-by":"publisher","first-page":"837","DOI":"10.1007\/s12298-017-0477-0","volume":"23","author":"S Basu","year":"2017","unstructured":"Basu S, Giri RK, Benazir I et al (2017) Comprehensive physiological analyses and reactive oxygen species profiling in drought tolerant rice genotypes under salinity stress. Physiol Mol Biol Plants 23:837\u2013850. https:\/\/doi.org\/10.1007\/s12298-017-0477-0","journal-title":"Physiol Mol Biol Plants"},{"key":"13_CR38","doi-asserted-by":"publisher","first-page":"422","DOI":"10.1111\/ppl.13031","volume":"168","author":"S Kataria","year":"2020","unstructured":"Kataria S, Jain M, Tripathi DK, Singh VP (2020) Involvement of nitrate reductase-dependent nitric oxide production in magnetopriming-induced salt tolerance in soybean. Physiol Plant 168:422\u2013436. https:\/\/doi.org\/10.1111\/ppl.13031","journal-title":"Physiol Plant"},{"key":"13_CR39","doi-asserted-by":"publisher","first-page":"128","DOI":"10.1016\/j.envexpbot.2018.01.010","volume":"148","author":"QM Imran","year":"2018","unstructured":"Imran QM, Hussain A, Mun BG et al (2018) Transcriptome wide identification and characterization of NO-responsive WRKY transcription factors in Arabidopsis thaliana L. Environ Exp Bot 148:128\u2013143. https:\/\/doi.org\/10.1016\/j.envexpbot.2018.01.010","journal-title":"Environ Exp Bot"},{"key":"13_CR40","doi-asserted-by":"publisher","first-page":"56","DOI":"10.1016\/j.plaphy.2017.01.028","volume":"113","author":"Z Kolbert","year":"2017","unstructured":"Kolbert Z, Feigl G, Bord\u00e9 \u00c1 et al (2017) Protein tyrosine nitration in plants: present knowledge, computational prediction and future perspectives. Plant Physiol Biochem 113:56\u201363. https:\/\/doi.org\/10.1016\/j.plaphy.2017.01.028","journal-title":"Plant Physiol Biochem"},{"key":"13_CR41","doi-asserted-by":"publisher","first-page":"1","DOI":"10.3390\/plants9070902","volume":"9","author":"G Feigl","year":"2020","unstructured":"Feigl G, Czifra \u00c1, Moln\u00e1r \u00c1 et al (2020) Reorganization of protein tyrosine nitration pattern indicates the relative tolerance of brassica napus (L.) over helianthus annuus (L.) to combined heavy metal treatment. Plan Theory 9:1\u201314. https:\/\/doi.org\/10.3390\/plants9070902","journal-title":"Plan Theory"},{"key":"13_CR42","doi-asserted-by":"publisher","first-page":"137","DOI":"10.1016\/j.plantsci.2012.12.004","volume":"201\u2013202","author":"S Signorelli","year":"2013","unstructured":"Signorelli S, Corpas FJ, Borsani O et al (2013) Water stress induces a differential and spatially distributed nitro-oxidative stress response in roots and leaves of Lotus japonicus. Plant Sci 201\u2013202:137\u2013146. https:\/\/doi.org\/10.1016\/j.plantsci.2012.12.004","journal-title":"Plant Sci"},{"key":"13_CR43","doi-asserted-by":"publisher","first-page":"2460","DOI":"10.1002\/elps.200800826","volume":"30","author":"D Cecconi","year":"2009","unstructured":"Cecconi D, Orzetti S, Vandelle E et al (2009) Protein nitration during defense response in Arabidopsis thaliana. Electrophoresis 30:2460\u20132468. https:\/\/doi.org\/10.1002\/elps.200800826","journal-title":"Electrophoresis"},{"key":"13_CR44","doi-asserted-by":"publisher","first-page":"2665","DOI":"10.1093\/jxb\/erz097","volume":"70","author":"H B\u00e8gue","year":"2019","unstructured":"B\u00e8gue H, Besson-Bard A, Blanchard C et al (2019) The chaperone-like protein CDC48 regulates ascorbate peroxidase in tobacco. J Exp Bot 70:2665\u20132681. https:\/\/doi.org\/10.1093\/jxb\/erz097","journal-title":"J Exp Bot"}],"container-title":["Methods in Molecular Biology","Plant Stress Tolerance"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/978-1-0716-3973-3_13","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,6,13]],"date-time":"2024-06-13T09:03:47Z","timestamp":1718269427000},"score":1,"resource":{"primary":{"URL":"https:\/\/link.springer.com\/10.1007\/978-1-0716-3973-3_13"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024]]},"ISBN":["9781071639726","9781071639733"],"references-count":44,"URL":"https:\/\/doi.org\/10.1007\/978-1-0716-3973-3_13","relation":{},"ISSN":["1064-3745","1940-6029"],"issn-type":[{"value":"1064-3745","type":"print"},{"value":"1940-6029","type":"electronic"}],"subject":[],"published":{"date-parts":[[2024]]},"assertion":[{"value":"14 June 2024","order":1,"name":"first_online","label":"First Online","group":{"name":"ChapterHistory","label":"Chapter History"}}]}}