[1]

Sack L, Buckley TN. 2020. Trait multi-functionality in plant stress response. Integrative and Comparative Biology 60:98−112

doi: 10.1093/icb/icz152
[2]

Zhang H, Zhu J, Gong Z, Zhu JK. 2021. Abiotic stress responses in plants. Nature Reviews Genetics 23:104−119

doi: 10.1038/s41576-021-00413-0
[3]

Qiu R, Katul GG. 2020. Maximizing leaf carbon gain in varying saline conditions: an optimization model with dynamic mesophyll conductance. The Plant Journal 101:543−554

doi: 10.1111/tpj.14553
[4]

Fan P, Feng J, Jiang P, Chen X, Bao H, et al. 2011. Coordination of carbon fixation and nitrogen metabolism in Salicornia europaea under salinity: comparative proteomic analysis on chloroplast proteins. Proteomics 11:4346−4367

doi: 10.1002/pmic.201100054
[5]

Li N, Chen M, Gao X, Long X, Shao H, et al. 2016. Carbon sequestration and Jerusalem artichoke biomass under nitrogen applications in coastal saline zone in the northern region of Jiangsu, China. Science of the Total Environment 568:885−890

doi: 10.1016/j.scitotenv.2016.06.074
[6]

Chen Z, Dayananda B, Fu B, Li Z, Jia Z, et al. 2022. Research on the potential of forestry's carbon-neutral contribution in China from 2021 to 2060. Sustainability 14(9):5444

doi: 10.3390/su14095444
[7]

Zhao S, Shi W, Qiao F, Wang C, An Y, et al. 2023. Temporal and spatial changes and trend predictions of forest carbon sequestration efficiency in China based on the carbon neutrality goal. Forests 14(12):2387

doi: 10.3390/f14122387
[8]

Ma Z, Cheah WY, Ng IS, Chang JS, Zhao M, et al. 2022. Microalgae-based biotechnological sequestration of carbon dioxide for net zero emissions. Trends in Biotechnology 40:1439−1453

doi: 10.1016/j.tibtech.2022.09.002
[9]

Dröge-Laser W, Snoek BL, Snel B, Weiste C. 2018. The Arabidopsis bZIP transcription factor family — an update. Current Opinion in Plant Biology 45:36−49

doi: 10.1016/j.pbi.2018.05.001
[10]

Guo Z, Dzinyela R, Yang L, Hwarari D. 2024. bZIP transcription factors: structure, modification, abiotic stress responses and application in plant improvement. Plants 13(15):2058

doi: 10.3390/plants13152058
[11]

Choi J, Lim CW, Lee SC. 2025. Role of pepper bZIP transcription factor CaADBZ1 in abscisic acid signalling and drought stress response. Physiologia Plantarum 177(2):e70159

doi: 10.1111/ppl.70159
[12]

Li P, Zheng T, Li L, Wang J, Cheng T, et al. 2022. Genome-wide investigation of the bZIP transcription factor gene family in Prunus mume: classification, evolution, expression profile and low-temperature stress responses. Horticultural Plant Journal 8:230−242

doi: 10.1016/j.hpj.2021.01.009
[13]

Xu ZY, Kim SY, Hyeon DY, Kim DH, Dong T, et al. 2013. The Arabidopsis NAC transcription factor ANAC096 cooperates with bZIP-type transcription factors in dehydration and osmotic stress responses. The Plant Cell 25:4708−4724

doi: 10.1105/tpc.113.119099
[14]

Zhao K, Chen S, Yao W, Cheng Z, Zhou B, et al. 2021. Genome-wide analysis and expression profile of the bZIP gene family in poplar. BMC Plant Biology 21(1):122

doi: 10.1186/s12870-021-02879-w
[15]

Hu J, Nan S, Zhou L, Yu C, Li Y, et al. 2024. PagbZIP75 decreases the ROS accumulation to enhance salt tolerance of poplar via the ABA signaling. Environmental and Experimental Botany 228:106051

doi: 10.1016/j.envexpbot.2024.106051
[16]

Henriquez-Valencia C, Moreno AA, Sandoval-Ibañez O, Mitina I, Blanco‐Herrera F, et al. 2015. bZIP17 and bZIP60 regulate the expression of BiP3 and other salt stress responsive genes in an UPR-independent manner in Arabidopsis thaliana. Journal of Cellular Biochemistry 116:1638−1645

doi: 10.1002/jcb.25121
[17]

Zhao K, Dang H, Nan S, Yu C, Li Y, et al. 2025. PagHSF4 mediates the biosynthesis of jasmonic acid and plant hormone signal transduction to regulate the growth and development as well as salt stress tolerance of poplar. Industrial Crops and Products 234:121582

doi: 10.1016/j.indcrop.2025.121582
[18]

Wu Y, Hou J, Xiao H, Ye S, Tu D, et al. 2025. OsHDAC1 deacetylates the aldehyde dehydrogenase OsALDH2B1, repressing OsGR3 and decreasing salt tolerance in rice. Plant Physiology 198:kiaf149

doi: 10.1093/plphys/kiaf149
[19]

Livak KJ, Schmittgen TD. 2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCᴛ method. Methods 25:402−408

doi: 10.1006/meth.2001.1262
[20]

Shcherbo D, Murphy CS, Ermakova GV, Solovieva EA, Chepurnykh TV, et al. 2009. Far-red fluorescent tags for protein imaging in living tissues. Biochemical Journal 418:567−574

doi: 10.1042/BJ20081949
[21]

He F, Wang HL, Li HG, Su Y, Li S, et al. 2018. PeCHYR1, a ubiquitin E3 ligase from Populus euphratica, enhances drought tolerance via ABA-induced stomatal closure by ROS production in Populus. Plant Biotechnology Journal 16:1514−1528

doi: 10.1111/pbi.12893
[22]

Wang S, Fan Y, Du S, Zhao K, Liu Q, et al. 2022. PtaERF194 inhibits plant growth and enhances drought tolerance in poplar. Tree Physiology 42:1678−1692

doi: 10.1093/treephys/tpac026
[23]

Ismail MS, Nawaz F, Shehzad MA. 2025. Contributions of nitrogen metabolic enzymes in storage protein assimilation and mineral accumulation regulated by nitrogen and selenium in Triticum aestivum L. Plant Physiology and Biochemistry 221:109597

doi: 10.1016/j.plaphy.2025.109597
[24]

Huang R, Lan T, Song X, Li J, Ling J, et al. 2021. Soil labile organic carbon impacts C:N:P stoichiometry in urban park green spaces depending on vegetation types and time after planting. Applied Soil Ecology 163:103926

doi: 10.1016/j.apsoil.2021.103926
[25]

Xia Y, Han Q, Shu J, Jiang S, Kang X. 2024. Stomatal density suppressor PagSDD1 is a 'generalist' gene that promotes plant growth and improves water use efficiency. International Journal of Biological Macromolecules 262:129721

doi: 10.1016/j.ijbiomac.2024.129721
[26]

Rueden CT, Eliceiri KW. 2017. The ImageJ ecosystem: an open and extensible platform for biomedical image analysis. Microscopy and Microanalysis 23:226−227

doi: 10.1017/S1431927617001817
[27]

Song X, Zhao Y, Wang J, Lu MZ. 2021. The transcription factor KNAT2/6b mediates changes in plant architecture in response to drought via downregulating GA20ox1 in Populus alba × P. glandulosa. Journal of experimental botany 72:5625−5637

doi: 10.1093/jxb/erab201
[28]

Wang K, Shen X, Williams R. 2021. Sequencing BGI: the evolution of expertise and research organisation in the world's leading gene sequencing facility. New Genetics and Society 40:305−330

doi: 10.1080/14636778.2020.1843148
[29]

Kim D, Langmead B, Salzberg SL. 2015. HISAT: a fast spliced aligner with low memory requirements. Nature Methods 12(4):357−360

doi: 10.1038/nmeth.3317
[30]

Love MI, Huber W, Anders S. 2014. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biology 15(12):550

doi: 10.1186/s13059-014-0550-8
[31]

Young MD, Wakefield MJ, Smyth GK, Oshlack A. 2010. Gene ontology analysis for RNA-seq: accounting for selection bias. Genome Biology 11(2):R14

doi: 10.1186/gb-2010-11-2-r14
[32]

Wang P, Yang X, Sun S, Wang J, Wang J, et al. 2025. The SCARECROW-LIKE transcription factor from Populus davidiana × P. bolleana simultaneously improved drought tolerance and plant growth through acetylation‐dependent mechanisms. Plant Biotechnology Journal 23(9):3650−3666

doi: 10.1111/pbi.70185
[33]

Chen H, Wu W, Du K, Ling A, Kang X. 2024. The interplay of growth-regulating factor 5 and BZR1 in coregulating chlorophyll degradation in poplar. Plant, Cell & Environment 47:3766−3779

doi: 10.1111/pce.14958
[34]

Iwata Y, Fedoroff NV, Koizumi N. 2008. Arabidopsis bZIP60 is a proteolysis-activated transcription factor involved in the endoplasmic reticulum stress response. The Plant Cell 20:3107−3121

doi: 10.1105/tpc.108.061002
[35]

Wang P, Guo Q, Wang Q, Zhou XR, Wang SM. 2015. PtAKT1 maintains selective absorption capacity for K+ over Na+ in halophyte Puccinellia tenuiflora under salt stress. Acta Physiologiae Plantarum 37(5):100

doi: 10.1007/s11738-015-1846-3
[36]

Zorov DB, Juhaszova M, Sollott SJ. 2014. Mitochondrial reactive oxygen species (ROS) and ROS-induced ROS release. Physiological Reviews 94:909−950

doi: 10.1152/physrev.00026.2013
[37]

Takahashi S, Murata N. 2008. How do environmental stresses accelerate photoinhibition? Trends in Plant Science 13:178−182

doi: 10.1016/j.tplants.2008.01.005
[38]

Fukazawa J, Sakai T, Ishida S, Yamaguchi I, Kamiya Y, et al. 2000. REPRESSION OF SHOOT GROWTH, a bZIP transcriptional activator, regulates cell elongation by controlling the level of gibberellins. The Plant Cell 12:901−915

doi: 10.2307/3871218
[39]

Mittler R, Vanderauwera S, Gollery M, Van Breusegem F. 2004. Reactive oxygen gene network of plants. Trends in Plant Science 9:490−498

doi: 10.1016/j.tplants.2004.08.009
[40]

Van den Ende W, El-Esawe SK. 2014. Sucrose signaling pathways leading to fructan and anthocyanin accumulation: a dual function in abiotic and biotic stress responses? Environmental and Experimental Botany 108:4−13

doi: 10.1016/j.envexpbot.2013.09.017
[41]

Wang J, Lian W, Cao Y, Wang X, Wang G, et al. 2018. Overexpression of BoNAC019, a NAC transcription factor from Brassica oleracea, negatively regulates the dehydration response and anthocyanin biosynthesis in Arabidopsis. Scientific Reports 8:13349

doi: 10.1038/s41598-018-31690-1
[42]

Baxter A, Mittler R, Suzuki N. 2014. ROS as key players in plant stress signalling. Journal of Experimental Botany 65:1229−1240

doi: 10.1093/jxb/ert375
[43]

Huang GT, Ma SL, Bai LP, Zhang L, Ma H, et al. 2012. Signal transduction during cold, salt, and drought stresses in plants. Molecular Biology Reports 39:969−987

doi: 10.1007/s11033-011-0823-1
[44]

Dai W, Wang M, Gong X, Liu JH. 2018. The transcription factor FcWRKY40 of Fortunella crassifolia functions positively in salt tolerance through modulation of ion homeostasis and proline biosynthesis by directly regulating SOS2 and P5CS1 homologs. New Phytologist 219:972−989

doi: 10.1111/nph.15240
[45]

Rolly NK, Imran QM, Lee IJ, Yun BW. 2020. Salinity stress-mediated suppression of expression of salt overly sensitive signaling pathway genes suggests negative regulation by AtbZIP62 transcription factor in Arabidopsis thaliana. International Journal of Molecular Sciences 21(5):1726

doi: 10.3390/ijms21051726
[46]

Tian Q, Shen L, Luan J, Zhou Z, Guo D, et al. 2021. Rice shaker potassium channel OsAKT2 positively regulates salt tolerance and grain yield by mediating K+ redistribution. Plant, Cell & Environment 44:2951−2965

doi: 10.1111/pce.14101
[47]

Wang Z, Hong Y, Zhu G, Li Y, Niu Q, et al. 2020. Loss of salt tolerance during tomato domestication conferred by variation in a Na+/K+ transporter. The EMBO Journal 39(10):EMBJ2019103256

doi: 10.15252/embj.2019103256
[48]

Huang J, Hammerbacher A, Gershenzon J, van Dam NM, Sala A, et al. 2021. Storage of carbon reserves in spruce trees is prioritized over growth in the face of carbon limitation. Proceedings of the National Academy of Sciences of the United States of America 118(33):e2023297118

doi: 10.1073/pnas.2023297118
[49]

Gang H, Li R, Zhao Y, Liu G, Chen S, et al. 2019. Loss of GLK1 transcription factor function reveals new insights in chlorophyll biosynthesis and chloroplast development. Journal of Experimental Botany 70:3125−3138

doi: 10.1093/jxb/erz128
[50]

Sierla M, Waszczak C, Vahisalu T, Kangasjärvi J. 2016. Reactive oxygen species in the regulation of stomatal movements. Plant Physiology 171:1569−1580

doi: 10.1104/pp.16.00328
[51]

Marten H, Konrad KR, Dietrich P, Roelfsema MRG, Hedrich R. 2007. Ca2+-dependent and -independent abscisic acid activation of plasma membrane anion channels in guard cells of Nicotiana tabacum. Plant Physiology 143:28−37

doi: 10.1104/pp.106.092643
[52]

Qi J, Song CP, Wang B, Zhou J, Kangasjärvi J, et al. 2018. Reactive oxygen species signaling and stomatal movement in plant responses to drought stress and pathogen attack. Journal of Integrative Plant Biology 60:805−826

doi: 10.1111/jipb.12654
[53]

Lawson T, Blatt MR. 2014. Stomatal size, speed, and responsiveness impact on photosynthesis and water use efficiency. Plant Physiology 164:1556−1570

doi: 10.1104/pp.114.237107
[54]

Chater C, Peng K, Movahedi M, Dunn JA, Walker HJ, et al. 2015. Elevated CO2-induced responses in stomata require ABA and ABA signaling. Current Biology 25:2709−2716

doi: 10.1016/j.cub.2015.09.013
[55]

Simon C, Langlois-Meurinne M, Didierlaurent L, Chaouch S, Bellvert F, et al. 2014. The secondary metabolism glycosyltransferases UGT73B3 and UGT73B5 are components of redox status in resistance of Arabidopsis to Pseudomonas syringae pv. tomato. Plant, Cell & Environment 37:1114−1129

doi: 10.1111/pce.12221
[56]

Han Y, Vimolmangkang S, Soria-Guerra RE, Rosales-Mendoza S, Zheng D, et al. 2010. Ectopic expression of apple F3'H genes contributes to anthocyanin accumulation in the Arabidopsis tt7 mutant grown under nitrogen stress. Plant Physiology 153:806−820

doi: 10.1104/pp.109.152801
[57]

Röckel N, Wolf S, Kost B, Rausch T, Greiner S. 2008. Elaborate spatial patterning of cell-wall PME and PMEI at the pollen tube tip involves PMEI endocytosis, and reflects the distribution of esterified and de-esterified pectins. The Plant Journal 53:133−143

doi: 10.3410/f.721659452.793503414
[58]

Ruperti B, Bonghi C, Ziliotto F, Pagni S, Rasori A, et al. 2002. Characterization of a major latex protein (MLP) gene down-regulated by ethylene during peach fruitlet abscission. Plant Science 163:265−272

doi: 10.1016/S0168-9452(02)00094-8
[59]

Ren H, Gray WM. 2015. SAUR proteins as effectors of hormonal and environmental signals in plant growth. Molecular Plant 8:1153−1164

doi: 10.1016/j.molp.2015.05.003
[60]

Shen YY, Wang XF, Wu FQ, Du SY, Cao Z, et al. 2006. The Mg-chelatase H subunit is an abscisic acid receptor. Nature 443:823−826

doi: 10.1038/nature05176