| [1] | 刘小京, 郭凯, 封晓辉, 等. 农业高效利用盐碱地资源探讨[J]. 中国生态农业学报(中英文), 2023, 31(3): 345−353. https://doi.org/10.12357/cjea.20220967 doi: 10.12357/cjea.20220967 |
| [2] | 于功霞, 李迎, 刘宏元, 等. 我国盐碱地改良与利用技术研究进展[J]. 黑龙江农业科学, 2025(7): 96−103. https://doi.org/10.11942/j.issn1002-2767.2025.07.0096 doi: 10.11942/j.issn1002-2767.2025.07.0096 |
| [3] | 王遵亲. 中国盐渍土[M]. 北京: 科学出版社, 1993. (查阅网上资料, 未找到本条文献页码信息, 请补充) |
| [4] | 梁淑敏, 许艳萍, 陈裕, 等. 工业大麻对重金属污染土壤的治理研究进展[J]. 生态学报, 2013, 33(5): 1347−1356. https://doi.org/10.5846/stxb201209231342 doi: 10.5846/stxb201209231342 |
| [5] | Chibuike G U, Obiora S C. Heavy metal polluted soils: effect on plants and bioremediation methods [J]. Applied and Environmental Soil Science, 2014, 2014: 752708. https://doi.org/10.1155/2014/752708 doi: 10.1155/2014/752708 |
| [6] | Hou D Y, Jia X Y, Wang L W, et al. Global soil pollution by toxic metals threatens agriculture and human health [J]. Science, 2025, 388(6744): 316−321. https://doi.org/10.1126/science.adr5214 doi: 10.1126/science.adr5214 |
| [7] | Haider F U, Cai L Q, Coulter J A, et al. Cadmium toxicity in plants: impacts and remediation strategies [J]. Ecotoxicology and Environmental Safety, 2021, 211: 111887. https://doi.org/10.1016/j.ecoenv.2020.111887 doi: 10.1016/j.ecoenv.2020.111887 |
| [8] | 王智慧, 牛二利, 高远亮, 等. 浙麦冬HMA基因家族鉴定及镉胁迫响应分析[J]. 生物工程学报, 2025, 41(2): 771−790. https://doi.org/10.13345/j.cjb.240475 doi: 10.13345/j.cjb.240475 |
| [9] | Cobbett C, Goldsbrough P. Phytochelatins and metallothioneins: roles in heavy metal detoxification and homeostasis [J]. Annual Review of Plant Biology, 2002, 53: 159−182. https://doi.org/10.1146/annurev.arplant.53.100301.135154 doi: 10.1146/annurev.arplant.53.100301.135154 |
| [10] | Macfarlane G R, Pulkownik A, Burchett M D. Accumulation and distribution of heavy metals in the grey mangrove, Avicennia marina (Forsk. )Vierh. : biological indication potential [J]. Environmental Pollution, 2003, 123(1): 139−151. https://doi.org/10.1016/S0269-7491(02)00342-1 doi: 10.1016/S0269-7491(02)00342-1 |
| [11] | Wang Y T, Qiu Q, Xin G R, et al. Heavy metal contamination in a vulnerable mangrove swamp in South China [J]. Environmental Monitoring and Assessment, 2013, 185(7): 5775−5787. https://doi.org/10.1007/s10661-012-2983-4 doi: 10.1007/s10661-012-2983-4 |
| [12] | Nikalje G C, Nikam T D, Suprasanna P. Looking at halophytic adaptation to high salinity through genomics landscape [J]. Current Genomics, 2017, 18(6): 542−552. https://doi.org/10.2174/1389202918666170228143007 doi: 10.2174/1389202918666170228143007 |
| [13] | Christofilopoulos S, Syranidou E, Gkavrou G, et al. The role of halophyte Juncus acutus L. in the remediation of mixed contamination in a hydroponic greenhouse experiment [J]. Journal of Chemical Technology & Biotechnology, 2016, 91(6): 1665−1674. https://doi.org/10.1002/jctb.4939 doi: 10.1002/jctb.4939 |
| [14] | Pan X, Chen G P, Shi C, et al. Effects of Zn stress on growth, Zn accumulation, translocation, and subcellular distribution of Spartina alterniflora Loisel [J]. CLEAN-Soil, Air, Water, 2016, 44(5): 579−585. https://doi.org/10.1002/clen.201400288 doi: 10.1002/clen.201400288 |
| [15] | Gill S S, Khan N A, Tuteja N. Differential cadmium stress tolerance in five indian mustard (Brassica juncea L. ) cultivars: an evaluation of the role of antioxidant machinery [J]. Plant Signaling & Behavior, 2011, 6(2): 293−300. https://doi.org/10.4161/psb.6.2.15049 doi: 10.4161/psb.6.2.15049 |
| [16] | Møller I M, Jensen P E, Hansson A. Oxidative modifications to cellular components in plants [J]. Annual Review of Plant Biology, 2007, 58: 459−481. https://doi.org/10.1146/annurev.arplant.58.032806.103946 doi: 10.1146/annurev.arplant.58.032806.103946 |
| [17] | Sharma S S, Dietz K J. The relationship between metal toxicity and cellular redox imbalance [J]. Trends in Plant Science, 2009, 14(1): 43−50. https://doi.org/10.1016/j.tplants.2008.10.007 doi: 10.1016/j.tplants.2008.10.007 |
| [18] | Keunen E, Remans T, Bohler S, et al. Metal-induced oxidative stress and plant mitochondria [J]. International Journal of Molecular Sciences, 2011, 12(10): 6894−6918. https://doi.org/10.3390/ijms12106894 doi: 10.3390/ijms12106894 |
| [19] | Tsukagoshi H, Busch W, Benfey P N. Transcriptional regulation of ROS controls transition from proliferation to differentiation in the root [J]. Cell, 2010, 143(4): 606−616. https://doi.org/10.1016/j.cell.2010.10.020 doi: 10.1016/j.cell.2010.10.020 |
| [20] | Rucińiska-Sobkowiak R. Oxidative stress in plants exposed to heavy metals [J]. Postepy Biochemii, 2010, 56(2): 191−200. https://doi.org/10.1201/9781003022879-7 doi: 10.1201/9781003022879-7 |
| [21] | Miller G, Suzuki N, Ciftci-Yilmaz S, et al. Reactive oxygen species homeostasis and signalling during drought and salinity stresses [J]. Plant, Cell & Environment, 2010, 33(4): 453−467. https://doi.org/10.1111/j.1365-3040.2009.02041.x doi: 10.1111/j.1365-3040.2009.02041.x |
| [22] | 王会方, 於朝广, 王涛, 等. 硅缓解植物重金属毒害机理的研究进展[J]. 云南农业大学学报(自然科学), 2016, 31(3): 528−535. https://doi.org/10.16211/j.issn.1004-390X(n).2016.03.021 doi: 10.16211/j.issn.1004-390X(n).2016.03.021 |
| [23] | 郑昕煜, 王辰雨, 周益峰, 等. 金属伴侣蛋白在植物重金属解毒中的作用[J]. 植物生理学报, 2025, 61(7): 916−925. https://doi.org/10.13592/j.cnki.ppj.300310 doi: 10.13592/j.cnki.ppj.300310 |
| [24] | 陈沁. 氯化血红素通过HO1/CO、Fe2+途径参与缓解水稻幼苗重金属胁迫[D]. 南京: 南京农业大学, 2016. |
| [25] | 卢诗雨, 令建伟, 吴琳, 等. 湿地植物对重金属污染的去除机制研究进展[J]. 湿地科学, 2025, 23(4): 846−857. https://doi.org/10.13248/j.cnki.wetlandsci.20240183 doi: 10.13248/j.cnki.wetlandsci.20240183 |
| [26] | Anjum N A, Hasanuzzaman M, Hossain M A, et al. Jacks of metal/metalloid chelation trade in plants-an overview [J]. Frontiers in Plant Science, 2015, 6: 192. https://doi.org/10.3389/fpls.2015.00192 doi: 10.3389/fpls.2015.00192 |
| [27] | 杨柳. 刚毛藻植物螯合肽对Pb胁迫的响应及吸收[D]. 合肥: 安徽农业大学, 2022. https://doi.org/10.26919/d.cnki.gannu.2022.000791 |
| [28] | Tennstedt P, Peisker D, Böttcher C, et al. Phytochelatin synthesis is essential for the detoxification of excess zinc and contributes significantly to the accumulation of zinc [J]. Plant Physiology, 2009, 149(2): 938−948. https://doi.org/10.1104/pp.108.127472 doi: 10.1104/pp.108.127472 |
| [29] | Gonzalez-Mendoza D, Moreno A Q, Zapata-Perez O. Coordinated responses of phytochelatin synthase and metallothionein genes in black mangrove, Avicennia germinans, exposed to cadmium and copper [J]. Aquatic Toxicology, 2007, 83(4): 306−314. https://doi.org/10.1016/j.aquatox.2007.05.005 doi: 10.1016/j.aquatox.2007.05.005 |
| [30] | Bankaji I, Caçador I, Sleimi N. Physiological and biochemical responses of Suaeda fruticosa to cadmium and copper stresses: growth, nutrient uptake, antioxidant enzymes, phytochelatin, and glutathione levels [J]. Environmental Science and Pollution Research, 2015, 22(17): 13058−13069. https://doi.org/10.1007/s11356-015-4414-x doi: 10.1007/s11356-015-4414-x |
| [31] | Cobbett C, Goldsbrough P. Phytochelatins and metallothioneins: roles in heavy metal detoxification and homeostasis [J]. Annual Review of Plant Biology, 2002, 53: 159−182. (查阅网上资料,本条文献与第9条文献重复,请确认) https://doi.org/10.1146/annurev.arplant.53.100301.135154 |
| [32] | Guo W J, Bundithya W, Goldsbrough P B. Characterization of the Arabidopsis metallothionein gene family: tissue-specific expression and induction during senescence and in response to copper [J]. New Phytologist, 2003, 159(2): 369−381. https://doi.org/10.1046/j.1469-8137.2003.00813.x doi: 10.1046/j.1469-8137.2003.00813.x |
| [33] | Pakdee O, Tshering S, Pokethitiyook P, et al. Examination of the metallothionein gene family in greater duckweed Spirodela polyrhiza [J]. Plants, 2022, 12(1): 125. https://doi.org/10.3390/plants12010125 doi: 10.3390/plants12010125 |
| [34] | Huang G Y, Wang Y S. Expression analysis of type 2 metallothionein gene in mangrove species (Bruguiera gymnorrhiza) under heavy metal stress [J]. Chemosphere, 2009, 77(7): 1026−1029. https://doi.org/10.1016/j.chemosphere.2009.07.073 doi: 10.1016/j.chemosphere.2009.07.073 |
| [35] | Usha B, Venkataraman G, Parida A. Heavy metal and abiotic stress inducible metallothionein isoforms from Prosopis juliflora (SW) D. C. show differences in binding to heavy metals in vitro [J]. Molecular Genetics and Genomics, 2009, 281(1): 99−108. https://doi.org/10.1007/s00438-008-0398-2 doi: 10.1007/s00438-008-0398-2 |
| [36] | 赵之伟, 曹冠华, 李涛. 金属硫蛋白的研究进展[J]. 云南大学学报(自然科学版), 2013, 35(3): 390−398. https://doi.org/10.7540/j.ynu.20130187 doi: 10.7540/j.ynu.20130187 |
| [37] | Yang J L, Wang Y C, Liu G F, et al. Tamarix hispida metallothionein-like ThMT3, a reactive oxygen species scavenger, increases tolerance against Cd2+, Zn2+, Cu2+, and NaCl in transgenic yeast [J]. Molecular Biology Reports, 2011, 38(3): 1567−1574. https://doi.org/10.1007/s11033-010-0265-1 doi: 10.1007/s11033-010-0265-1 |
| [38] | Sun X H, Yu G, Li J T, et al. A heavy metal-associated protein (AcHMA1) from thehalophyte, Atriplex canescens (Pursh) Nutt. , confers tolerance to iron and other abioticstresses when expressed in Saccharomyces cerevisiae [J]. International Journal of Molecular Sciences, 2014, 15(8): 14891-14906. https://doi.org/10.3390/ijms150814891 |
| [39] | Su H, Balderas E, Vera-Estrella R, et al. Expression of the cation transporter McHKT1 in a halophyte [J]. Plant Molecular Biology, 2003, 52(5): 967−980. https://doi.org/10.1023/a:1025445612244 doi: 10.1023/a:1025445612244 |
| [40] | Papoyan A, Kochian L V. Identification of Thlaspi caerulescens genes that may be involved in heavy metal hyperaccumulation and tolerance. Characterization of a novel heavy metal transporting ATPase [J]. Plant Physiology, 2004, 136(3): 3814−3823. https://doi.org/10.1104/pp.104.044503 doi: 10.1104/pp.104.044503 |
| [41] | Belouchi A, Kwan T, Gros P. Cloning and characterization of the OsNramp family from Oryza sativa, a new family of membrane proteins possibly implicated in the transport of metal ions [J]. Plant Molecular Biology, 1997, 33(6): 1085−1092. https://doi.org/10.1023/A:1005723304911 doi: 10.1023/A:1005723304911 |
| [42] | 刘霄霏, 甘锦鑫, 周涛, 等. 千穗谷MTP基因家族生信分析及镉胁迫下的表达特征[J]. 植物科学学报, 2023, 41(4): 467−478. https://doi.org/10.11913/PSJ.2095-0837.22279 doi: 10.11913/PSJ.2095-0837.22279 |
| [43] | Van Der Zaal B J, Neuteboom L W, Pinas J E, et al. Overexpression of a novel Arabidopsis gene related to putative zinc-transporter genes from animals can lead to enhanced zinc resistance and accumulation [J]. Plant Physiology, 1999, 119(3): 1047−1056. https://doi.org/10.1104/pp.119.3.1047 doi: 10.1104/pp.119.3.1047 |
| [44] | Llorens E, González-Hernández A I, Scalschi L, et al. Priming mediated stress and cross-stress tolerance in plants: concepts and opportunities[M]//Hossain M A, Liu F L, Burritt D J, et al. Priming-mediated stress and cross-stress tolerance in crop plants. London: Academic Press, 2020: 1−20. https://doi.org/10.1016/B978-0-12-817892-8.00001-5 |
| [45] | Foyer C H, Rasool B, Davey J W, et al. Cross-tolerance to biotic and abiotic stresses in plants: a focus on resistance to aphid infestation [J]. Journal of Experimental Botany, 2016, 67(7): 2025−2037. https://doi.org/10.1093/jxb/erw079 doi: 10.1093/jxb/erw079 |
| [46] | Dhar R, Sägesser R, Weikert C, et al. Yeast adapts to a changing stressful environment by evolving cross-protection and anticipatory gene regulation [J]. Molecular Biology and Evolution, 2013, 30(3): 573−588. https://doi.org/10.1093/molbev/mss253 doi: 10.1093/molbev/mss253 |
| [47] | Knight H, Knight M R. Abiotic stress signalling pathways: specificity and cross-talk [J]. Trends in Plant Science, 2001, 6(6): 262−267. https://doi.org/10.1016/s1360-1385(01)01946-x doi: 10.1016/s1360-1385(01)01946-x |
| [48] | Capiati D A, País S M, Téllez-Iñón M T. Wounding increases salt tolerance in tomato plants: evidence on the participation of calmodulin-like activities in cross-tolerance signalling [J]. Journal of Experimental Botany, 2006, 57(10): 2391−2400. https://doi.org/10.1093/jxb/erj212 doi: 10.1093/jxb/erj212 |
| [49] | Chinnusamy V, Schumaker K, Zhu J K. Molecular genetic perspectives on cross-talk and specificity in abiotic stress signalling in plants [J]. Journal of Experimental Botany, 2004, 55(395): 225−236. https://doi.org/10.1093/jxb/erh005 doi: 10.1093/jxb/erh005 |
| [50] | Munné-Bosch S, Queval G, Foyer C H. The impact of global change factors on redox signaling underpinning stress tolerance [J]. Plant Physiology, 2013, 161(1): 5−19. https://doi.org/10.1104/pp.112.205690 doi: 10.1104/pp.112.205690 |
| [51] | Amtmann A. Learning from evolution: thellungiella generates new knowledge on essential and critical components of abiotic stress tolerance in plants [J]. Molecular Plant, 2009, 2(1): 3−12. https://doi.org/10.1093/mp/ssn094 doi: 10.1093/mp/ssn094 |
| [52] | 刘岚钰. NaCl缓解盐地碱蓬Cd毒性机制研究[D]. 西安: 陕西科技大学, 2022. https://doi.org/10.27290/d.cnki.gxbqc.2022.000265 |
| [53] | 杨琳. Na+/H+逆向转运蛋白提高浮萍镉胁迫抗性的机制研究[D]. 天津: 天津师范大学, 2017. |
| [54] | Walter J, Jentsch A, Beierkuhnlein C, et al. Ecological stress memory and cross stress tolerance in plants in the face of climate extremes [J]. Environmental and Experimental Botany, 2013, 94: 3−8. https://doi.org/10.1016/j.envexpbot.2012.02.009 doi: 10.1016/j.envexpbot.2012.02.009 |
| [55] | Bruce T J A, Matthes M C, Napier J A, et al. Stressful “memories” of plants: evidence and possible mechanisms [J]. Plant Science, 2007, 173(6): 603−608. https://doi.org/10.1016/j.plantsci.2007.09.002 doi: 10.1016/j.plantsci.2007.09.002 |
| [56] | Ellouzi H, Hamed K B, Cela J, et al. Early effects of salt stress on the physiological and oxidative status of Cakile maritima (halophyte) and Arabidopsis thaliana (glycophyte) [J]. Physiologia Plantarum, 2011, 142(2): 128−143. https://doi.org/10.1111/j.1399-3054.2011.01450.x doi: 10.1111/j.1399-3054.2011.01450.x |
| [57] | Jaskiewicz M, Conrath U, Peterhänsel C. Chromatin modification acts as a memory for systemic acquired resistance in the plant stress response [J]. The EMBO Reports, 2011, 12(1): 50−55. https://doi.org/10.1038/embor.2010.186 doi: 10.1038/embor.2010.186 |
| [58] | Ryals J A, Neuenschwander U H, Willits M G, et al. Systemic acquired resistance [J]. The Plant Cell, 1996, 8(10): 1809−1819. https://doi.org/10.1105/tpc.8.10.1809 doi: 10.1105/tpc.8.10.1809 |
| [59] | Conrath U. Chapter 9 priming of induced plant defense responses [J]. Advances in Botanical Research, 2009, 51: 361−395. https://doi.org/10.1016/S0065-2296(09)51009-9 doi: 10.1016/S0065-2296(09)51009-9 |
| [60] | Wang Z, Gerstein M, Snyder M. RNA-Seq: a revolutionary tool for transcriptomics [J]. Nature Reviews Genetics, 2009, 10(1): 57−63. https://doi.org/10.1038/nrg2484 doi: 10.1038/nrg2484 |
| [61] | Sruthi P, Shackira A M, Puthur J T. Heavy metal detoxification mechanisms in halophytes: an overview [J]. Wetlands Ecology and Management, 2017, 25(2): 129−148. https://doi.org/10.1007/s11273-016-9513-z doi: 10.1007/s11273-016-9513-z |
| [62] | Jam M, Alemzadeh A, Tale A M, et al. Heavy metal regulation of plasma membrane H+-ATPase gene expression in halophyte Aeluropus littoralis [J]. Molecular Biology Research Communications, 2014, 3(2): 129−139. |
| [63] | Chen Y, Chen C M, Tan Z Q, et al. Functional identification and characterization of genes cloned from halophyte seashore paspalum conferring salinity and cadmium tolerance [J]. Frontiers in Plant Science, 2016, 7: 102. https://doi.org/10.3389/fpls.2016.00102 doi: 10.3389/fpls.2016.00102 |
| [64] | Cong M, Lv J S, Liu X L, et al. Gene expression responses in Suaeda salsa after cadmium exposure [J]. SpringerPlus, 2013, 2(1): 232. https://doi.org/10.1186/2193-1801-2-232 doi: 10.1186/2193-1801-2-232 |
| [65] | Xie Q J, Wang D N, Ding Y T, et al. The ethylene response factor gene, ThDRE1A, is involved in abscisic acid- and ethylene-mediated cadmium accumulation in Tamarix hispida [J]. Science of the Total Environment, 2024, 937: 173422. https://doi.org/10.1016/j.scitotenv.2024.173422 doi: 10.1016/j.scitotenv.2024.173422 |
| [66] | Jing C L, Wang M, Lu X L, et al. Transcriptome analysis reveals how cadmium promotes root development and accumulates in Apocynum venetum, a promising plant for greening cadmium-contaminated soil [J]. Ecotoxicology and Environmental Safety, 2024, 270: 115872. https://doi.org/10.1016/j.ecoenv.2023.115872 doi: 10.1016/j.ecoenv.2023.115872 |
| [67] | Zhang X, Liao M S, Chang D, et al. Comparative transcriptome analysis of the Asteraceae halophyte Karelinia caspica under salt stress [J]. BMC Research Notes, 2014, 7: 927. https://doi.org/10.1186/1756-0500-7-927 doi: 10.1186/1756-0500-7-927 |
| [68] | Wang J C, Meng Y X, LI B C, et al. Physiological and proteomic analyses of salt stress response in the halophyte Halogeton glomeratus [J]. Plant, Cell & Environment, 2015, 38(4): 655−669. https://doi.org/10.1111/pce.12428 doi: 10.1111/pce.12428 |
| [69] | Luo Y, Reid R, Freese D, et al. Salt tolerance response revealed by RNA-Seq in a diploid halophytic wild relative of sweet potato [J]. Scientific Reports, 2017, 7(1): 9624. https://doi.org/10.1038/s41598-017-09241-x doi: 10.1038/s41598-017-09241-x |
| [70] | Garg R, Verma M, Agrawal S, et al. Deep transcriptome sequencing of wild halophyte rice, Porteresia coarctata, provides novel insights into the salinity and submergence tolerance factors [J]. DNA Research, 2014, 21(1): 69−84. https://doi.org/10.1093/dnares/dst042 doi: 10.1093/dnares/dst042 |
| [71] | Li S F, Fan C M, Li Y, et al. Effects of drought and salt-stresses on gene expression in Caragana korshinskii seedlings revealed by RNA-seq [J]. BMC Genomics, 2016, 17: 200. https://doi.org/10.1186/s12864-016-2562-0 doi: 10.1186/s12864-016-2562-0 |
| [72] | Krishnamurthy P, Mohanty B, Wijaya E, et al. Transcriptomics analysis of salt stress tolerance in the roots of the mangrove Avicennia officinalis [J]. Scientific Reports, 2017, 7(1): 10031. https://doi.org/10.1038/s41598-017-10730-2 doi: 10.1038/s41598-017-10730-2 |
| [73] | Tsukagoshi H, Suzuki T, Nishikawa K, et al. RNA-Seq analysis of the response of the halophyte, Mesembryanthemum crystallinum (ice plant) to high salinity [J]. PLoS One, 2015, 10(2): e0118339. https://doi.org/10.1371/journal.pone.0118339 doi: 10.1371/journal.pone.0118339 |
| [74] | Dang Z H, Zheng L L, Wang J, et al. Transcriptomic profiling of the salt-stress response in the wild recretohalophyte Reaumuria trigyna [J]. BMC Genomics, 2013, 14: 29. https://doi.org/10.1186/1471-2164-14-29 doi: 10.1186/1471-2164-14-29 |
| [75] | Bedre R, Mangu V R, Srivastava S, et al. Transcriptome analysis of smooth cordgrass (Spartina alterniflora Loisel), a monocot halophyte, reveals candidate genes involved in its adaptation to salinity [J]. BMC Genomics, 2016, 17(1): 657. https://doi.org/10.1186/s12864-016-3017-3 doi: 10.1186/s12864-016-3017-3 |
| [76] | Yamamoto N, Takano T, Tanaka K, et al. Comprehensive analysis of transcriptome response to salinity stress in the halophytic turf grass Sporobolus virginicus [J]. Frontiers in Plant Science, 2015, 6: 241. https://doi.org/10.3389/fpls.2015.00241 doi: 10.3389/fpls.2015.00241 |
| [77] | Diray-Arce J, Clement M, Gul B, et al. Transcriptome assembly, profiling and differential gene expression analysis of the halophyte Suaeda fruticosa provides insights into salt tolerance [J]. BMC Genomics, 2015, 16(1): 353. https://doi.org/10.1186/s12864-015-1553-x doi: 10.1186/s12864-015-1553-x |
| [78] | Gharat S A, Parmar S, Tambat S, et al. Transcriptome analysis of the response to NaCl in Suaeda maritima provides an insight into salt tolerance mechanisms in halophytes [J]. PLoS One, 2016, 11(9): e0163485. https://doi.org/10.1371/journal.pone.0163485 doi: 10.1371/journal.pone.0163485 |
| [79] | Jin H X, Dong D K, Yang Q H, et al. Salt-responsive transcriptome profiling of Suaeda glauca via RNA sequencing [J]. PLoS One, 2016, 11(3): e0150504. https://doi.org/10.1371/journal.pone.0150504 doi: 10.1371/journal.pone.0150504 |
| [80] | Anjum N A, Gill S S, Tuteja N. Enhancing cleanup of environmental pollutants [M]. Cham: Springer, 2017: 275−288. https://doi.org/10.1007/978-3-319-55423-5 |
| [81] | Pan L Y, Ma J J, Li J M, et al. Advances of salt stress-responsive transcription factors in plants [J]. Chinese Journal of Biotechnology, 2022, 38(1): 50−65.(查阅网上资料,本条文献是中文文献,请确认) https://doi.org/10.13345/j.cjb.210135 |
| [82] | Narendrula-Kotha R, Nkongolo K K. Microbial response to soil liming of damaged ecosystems revealed by pyrosequencing and phospholipid fatty acid analyses [J]. PLoS One, 2017, 12(1): e0168497. https://doi.org/10.1371/journal.pone.0168497 doi: 10.1371/journal.pone.0168497 |
| [83] | Khan A G, Kuek C, Chaudhry T M, et al. Role of plants, mycorrhizae and phytochelators in heavy metal contaminated land remediation [J]. Chemosphere, 2000, 41(1/2): 197−207. https://doi.org/10.1016/S0045-6535(99)00412-9 doi: 10.1016/S0045-6535(99)00412-9 |
| [84] | Yu Y, Li Z M, Liu Y H, et al. Roles of plant-associated microorganisms in regulating the fate of Hg in croplands: a perspective on potential pathways in maintaining sustainable agriculture [J]. Science of the Total Environment, 2022, 834: 155204. https://doi.org/10.1016/j.scitotenv.2022.155204 doi: 10.1016/j.scitotenv.2022.155204 |
| [85] | Kong Z Y, Glick B R. The role of plant growth-promoting bacteria in metal phytoremediation [J]. Advances in Microbial Physiology, 2017, 71: 97−132. https://doi.org/10.1016/bs.ampbs.2017.04.001 doi: 10.1016/bs.ampbs.2017.04.001 |
| [86] | Otero X L, Macías F. Spatial and seasonal variation in heavy metals in interstitial water of salt marsh soils [J]. Environmental Pollution, 2002, 120(2): 183−190. https://doi.org/10.1016/S0269-7491(02)00159-8 doi: 10.1016/S0269-7491(02)00159-8 |
| [87] | Otero X L, Macias F. Variation with depth and season in metal sulfides in salt marsh soils [J]. Biogeochemistry, 2002, 61(3): 247−268. https://doi.org/10.1023/A:1020230213864 doi: 10.1023/A:1020230213864 |
| [88] | Reboreda R, Caçador I. Enzymatic activity in the rhizosphere of Spartina maritima: potential contribution for phytoremediation of metals [J]. Marine Environmental Research, 2008, 65(1): 77−84. https://doi.org/10.1016/j.marenvres.2007.09.001 doi: 10.1016/j.marenvres.2007.09.001 |
| [89] | Carbonell A A, Aarabi M A, Delaune R D, et al. Arsenic in wetland vegetation: availability, phytotoxicity, uptake and effects on plant growth and nutrition [J]. Science of the Total Environment, 1998, 217(3): 189−199. https://doi.org/10.1016/S0048-9697(98)00195-8 doi: 10.1016/S0048-9697(98)00195-8 |
| [90] | Lin S Q, He Q, Zhang M X, et al. Effects of cadmium stress on root exudates and soil rhizosphere microorganisms of rice (Oryza sativa L. ) and its ecological regulatory mechanisms [J]. Plants, 2025, 14(11): 1695. https://doi.org/10.3390/plants14111695 doi: 10.3390/plants14111695 |
| [91] | Liu Y, He G D, He T B, et al. Signaling and detoxification strategies in plant-microbes symbiosis under heavy metal stress: a mechanistic understanding [J]. Microorganisms, 2022, 11(1): 69. https://doi.org/10.3390/microorganisms11010069 doi: 10.3390/microorganisms11010069 |
| [92] | Sánchez-Thomas R, Hernández-Garnica M, Granados-Rivas J C, et al. Intertwining of cellular osmotic stress handling mechanisms and heavy metal accumulation [J]. Molecular Biotechnology, 2025, 67(12): 4386−4402. https://doi.org/10.1007/s12033-024-01351-y doi: 10.1007/s12033-024-01351-y |
| [93] | Singh J S, Seneviratne G. Agro-environmental sustainability: volume 2: managing environmental pollution [M]. Cham: Springer, 2017: 147−163. https://doi.org/10.1007/978-3-319-49727-3 |
| [94] | Dighton J, White J F. The fungal community [M]. 4th ed. Boca Raton: CRC Press, 2017: 287−305. https://doi.org/10.1201/9781315119496 |
| [95] | Gadd G M, Bahri-Esfahani J, Li Q W, et al. Oxalate production by fungi: significance in geomycology, biodeterioration and bioremediation [J]. Fungal Biology Reviews, 2014, 28(2/3): 36−55. https://doi.org/10.1016/j.fbr.2014.05.001 doi: 10.1016/j.fbr.2014.05.001 |
| [96] | Saxena B, Sharma K, Kapoor R, et al. Insights into the molecular aspects of salt stress tolerance in mycorrhizal plants [J]. World Journal of Microbiology and Biotechnology, 2022, 38(12): 253. https://doi.org/10.1007/s11274-022-03440-z doi: 10.1007/s11274-022-03440-z |
| [97] | Lu C Y, Zhang Z C, Guo P R, et al. Synergistic mechanisms of bioorganic fertilizer and AMF driving rhizosphere bacterial community to improve phytoremediation efficiency of multiple HMs-contaminated saline soil [J]. Science of the Total Environment, 2023, 883: 163708. https://doi.org/10.1016/j.scitotenv.2023.163708 doi: 10.1016/j.scitotenv.2023.163708 |
| [98] | Nikalje G C, Srivastava A K, Pandey G K, et al. Halophytes in biosaline agriculture: mechanism, utilization, and value addition [J]. Land Degradation & Development, 2018, 29(4): 1081−1095. https://doi.org/10.1002/ldr.2819 doi: 10.1002/ldr.2819 |
| [99] | Lutts S, Qin P, Han R M. Salinity influences biosorption of heavy metals by the roots of the halophyte plant species Kosteletzkya pentacarpos [J]. Ecological Engineering, 2016, 95: 682−689. https://doi.org/10.1016/j.ecoleng.2016.06.009 doi: 10.1016/j.ecoleng.2016.06.009 |
| [100] | Caparrós P G, Ozturk M, Gul A, et al. Halophytes have potential as heavy metal phytoremediators: a comprehensive review [J]. Environmental and Experimental Botany, 2022, 193: 104666. https://doi.org/10.1016/j.envexpbot.2021.104666 doi: 10.1016/j.envexpbot.2021.104666 |
| [101] | Ayyappan D, Sathiyaraj G, Ravindran K C. Phytoextraction of heavy metals by Sesuvium portulacastrum l. a salt marsh halophyte from tannery effluent [J]. International Journal of Phytoremediation, 2016, 18(5): 453−459. https://doi.org/10.1080/15226514.2015.1109606 doi: 10.1080/15226514.2015.1109606 |