Pub Date : 2026-04-01Epub Date: 2025-12-28DOI: 10.1111/pce.70352
Lian Chen, Changyu Qiu, Gaocong Li, Qiang Lin, Jiehua Chen, Lingyun Sun, Dan Liu, Sen Lin, Dan Wang, Jianan Wu, Zhiyi Li, Yuan Wang, Zhenjiang Wang
This study investigated the mechanisms of cadmium (Cd) tolerance and root exudate-mediated soil activation in mulberry (Morus alba L.), a promising species for phytoremediation. Hydroponic experiments with Cd-tolerant seedlings exposed to 5 and 50 mg/L Cd revealed a biphasic concentration-dependent response. Low Cd induced negligible biological effects, whereas high Cd triggered substantial disturbances across multiple biological levels, including morphological alterations, physiological dysregulation and disrupted elemental accumulation patterns. Metabolomic profiling indicated that Cd stress significantly altered the secretion patterns of 17 root exudate metabolites in mulberry, exemplified by the upregulation of sucrose, lactose and 4-acetylbutyric acid, and the downregulation of β-alanine and myo-inositol. Further pathway enrichment analysis linked these differential metabolites to 17 metabolic pathways, with carbohydrate and amino acid metabolism as the main Cd-responsive pathways, suggesting their core role in mediating mulberry's Cd resistance. Root exudates enhanced soil Cd mobilisation in a positive concentration-dependent yet negative time-dependent manner. Consequently, mulberry adapts to Cd stress via metabolic reprogramming of root exudates-a strategic trade-off that serves a dual role by enhancing plant tolerance while simultaneously increasing Cd bioavailability in the soil. This insight provides a foundational framework for phytoremediation, centred on exudate management and the selection of stress-tolerant varieties.
研究了桑树(Morus alba L.)对镉(Cd)的耐受性和根系分泌物介导的土壤活化机制。对5和50 mg/L Cd的耐Cd幼苗进行水培试验,结果显示出双相浓度依赖性。低Cd诱导的生物效应可以忽略不计,而高Cd则在多个生物水平上引发了实质性的干扰,包括形态改变、生理失调和元素积累模式的破坏。代谢组学分析表明,Cd胁迫显著改变了桑树17种根分泌物代谢物的分泌模式,表现为蔗糖、乳糖和4-乙酰丁酸的分泌上调,β-丙氨酸和肌醇的分泌下调。进一步的途径富集分析将这些差异代谢物与17条代谢途径联系起来,其中碳水化合物和氨基酸代谢是主要的Cd响应途径,表明它们在介导桑树抗Cd的核心作用。根系分泌物对土壤镉的动员具有正向浓度依赖性和负时间依赖性。因此,桑树通过根分泌物的代谢重编程来适应Cd胁迫,这是一种战略性的权衡,在增强植物耐受性的同时增加了土壤中Cd的生物利用度。这一见解为植物修复提供了一个基本框架,以渗出物管理和耐应力品种的选择为中心。
{"title":"Morphological, Physiological and Metabolomic Responses of Mulberry to Cadmium Exposure: Unveiling Dose-Dependent Tolerance and Activation Mechanism.","authors":"Lian Chen, Changyu Qiu, Gaocong Li, Qiang Lin, Jiehua Chen, Lingyun Sun, Dan Liu, Sen Lin, Dan Wang, Jianan Wu, Zhiyi Li, Yuan Wang, Zhenjiang Wang","doi":"10.1111/pce.70352","DOIUrl":"10.1111/pce.70352","url":null,"abstract":"<p><p>This study investigated the mechanisms of cadmium (Cd) tolerance and root exudate-mediated soil activation in mulberry (Morus alba L.), a promising species for phytoremediation. Hydroponic experiments with Cd-tolerant seedlings exposed to 5 and 50 mg/L Cd revealed a biphasic concentration-dependent response. Low Cd induced negligible biological effects, whereas high Cd triggered substantial disturbances across multiple biological levels, including morphological alterations, physiological dysregulation and disrupted elemental accumulation patterns. Metabolomic profiling indicated that Cd stress significantly altered the secretion patterns of 17 root exudate metabolites in mulberry, exemplified by the upregulation of sucrose, lactose and 4-acetylbutyric acid, and the downregulation of β-alanine and myo-inositol. Further pathway enrichment analysis linked these differential metabolites to 17 metabolic pathways, with carbohydrate and amino acid metabolism as the main Cd-responsive pathways, suggesting their core role in mediating mulberry's Cd resistance. Root exudates enhanced soil Cd mobilisation in a positive concentration-dependent yet negative time-dependent manner. Consequently, mulberry adapts to Cd stress via metabolic reprogramming of root exudates-a strategic trade-off that serves a dual role by enhancing plant tolerance while simultaneously increasing Cd bioavailability in the soil. This insight provides a foundational framework for phytoremediation, centred on exudate management and the selection of stress-tolerant varieties.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":"1884-1898"},"PeriodicalIF":6.3,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145848439","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-04-01Epub Date: 2026-01-06DOI: 10.1111/pce.70373
Subhasis Karmakar, S P Avinash, Sabarinathan Selvaraj
{"title":"Breaking the Yield-Immunity Trade-Off: OsPIL1 Integrates Light Signals to Coordinate Rice Growth and Blast Resistance, and Its Breeding Implications.","authors":"Subhasis Karmakar, S P Avinash, Sabarinathan Selvaraj","doi":"10.1111/pce.70373","DOIUrl":"10.1111/pce.70373","url":null,"abstract":"","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":"2095-2097"},"PeriodicalIF":6.3,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145909743","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-04-01Epub Date: 2026-01-05DOI: 10.1111/pce.70359
Shaobo Cheng, Lihong Su, Wei Yan, Zhili Chen, Xiaoting Zhou, Qingming Li, Chaoxing He, Zhiqing Zhang, Hejun Wu, Zhongqun He
Fruit peel colour is a critical quality trait in chayote, directly influencing its commercial value. However, the molecular mechanisms underlying peel colour variation remain poorly understood. In this study, we observed higher chlorophyll content in deep green peel (DGP), green peel (GP), and light green peel (LGP) compared to white peel (WP). Additionally, WP exhibited reduced chloroplast number and structural disorganisation, with metabolomics confirming the reduction of galactolipids (DGDG and MGDG) essential for membrane stability. Integrated transcriptomic, resequencing, and WGCNA analyses identified SeAPRR2 as a candidate gene controlling peel colour, with a ~ 13-kb deletion in WP responsible for the white phenotype. This deletion triggered downregulation of DEGs related to chlorophyll biosynthesis and photosynthesis pathways. DAP-Seq revealed that SeAPRR2 binds to the cis-element (AAT(G/C)ATT) in promoters. Through Y1H, DLR, GUS activity, EMSA, and molecular docking assays, we confirmed that SeAPRR2 activates the transcription of SeHEMA1 and SeLHCB4 via promoter binding. Heterologous overexpression of SeAPRR2, SeHEMA1, and SeLHCB4 in tomato significantly elevated chlorophyll content and increased chloroplast number. Collectively, this study establishes SeAPRR2 as a master regulator of peel colour through the SeAPRR2-SeHEMA1/SeLHCB4 module. The large-fragment deletion mechanism provides novel genetic insights for breeding colour traits in cucurbit crops.
{"title":"A 13-kb Deletion in SeAPRR2 Disrupts Chloroplast Development by Dual-Targeting SeHEMA1/SeLHCB4 for White Peel Formation in Chayote.","authors":"Shaobo Cheng, Lihong Su, Wei Yan, Zhili Chen, Xiaoting Zhou, Qingming Li, Chaoxing He, Zhiqing Zhang, Hejun Wu, Zhongqun He","doi":"10.1111/pce.70359","DOIUrl":"10.1111/pce.70359","url":null,"abstract":"<p><p>Fruit peel colour is a critical quality trait in chayote, directly influencing its commercial value. However, the molecular mechanisms underlying peel colour variation remain poorly understood. In this study, we observed higher chlorophyll content in deep green peel (DGP), green peel (GP), and light green peel (LGP) compared to white peel (WP). Additionally, WP exhibited reduced chloroplast number and structural disorganisation, with metabolomics confirming the reduction of galactolipids (DGDG and MGDG) essential for membrane stability. Integrated transcriptomic, resequencing, and WGCNA analyses identified SeAPRR2 as a candidate gene controlling peel colour, with a ~ 13-kb deletion in WP responsible for the white phenotype. This deletion triggered downregulation of DEGs related to chlorophyll biosynthesis and photosynthesis pathways. DAP-Seq revealed that SeAPRR2 binds to the cis-element (AAT(G/C)ATT) in promoters. Through Y1H, DLR, GUS activity, EMSA, and molecular docking assays, we confirmed that SeAPRR2 activates the transcription of SeHEMA1 and SeLHCB4 via promoter binding. Heterologous overexpression of SeAPRR2, SeHEMA1, and SeLHCB4 in tomato significantly elevated chlorophyll content and increased chloroplast number. Collectively, this study establishes SeAPRR2 as a master regulator of peel colour through the SeAPRR2-SeHEMA1/SeLHCB4 module. The large-fragment deletion mechanism provides novel genetic insights for breeding colour traits in cucurbit crops.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":"2028-2044"},"PeriodicalIF":6.3,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145898937","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-04-01Epub Date: 2025-12-28DOI: 10.1111/pce.70356
Liu Li, Hewen Li, Qinghua Liu, Chaoqun Chen, Shulan Wu, Lin Luo, Xueyong Pang, Chunying Yin
The mechanisms of selenium (Se) oxyanion transformation in endophytic bacteria remain poorly understood, which limits their application in biofortification and phytoremediation. Here, we investigated these mechanisms using the plant-growth-promoting (PGP) endophyte Erwinia sp. PSI-03. Under 2 mM selenite stress, the strain intracellularly and extracellularly produced spherical selenium nanoparticles (SeNPs; ab57 nm average diameter). Multi-omics analyses revealed that these SeNPs were formed through parallel enzymatic (mediated by sulfite reductase, cysI) and non-enzymatic (via glutathione and l-cysteine) reduction pathways. Additionally, γ-glutamyl-Se-methylselenocysteine was identified as a key organo-selenium metabolite. Selenite exposure induced extensive reprogramming of the metabolome and transcriptome, highlighting key roles for glutathione metabolism and stress response systems related to cell wall/membrane maintenance, oxidative phosphorylation, two-component signaling systems, and DNA repair. Intriguingly, selenite stress concurrently stimulated bacterial synthesis of PGP compounds, including the auxin precursor indole-3-pyruvate, the defense hormone salicylic acid, and acetate. Consistent with this, under selenite-free and high-selenite (12 mg kg-1 Se) conditions, inoculation with Erwinia sp. PSI-03 significantly promoted tea plant growth. Compared to uninoculated controls, the leaf biomass increased by 52.8% and 51.7%, and the total biomass by 82.9% and 49.6%, respectively. These findings establish a paradigm where endophytic bacteria simultaneously detoxify Se and promote plant health, offering a robust strategy for agricultural and environmental Se management.
{"title":"Erwinia sp. PSI-03 Promotes Plant Growth and Detoxifies Selenite Through Selenium Nanoparticles Biosynthesis.","authors":"Liu Li, Hewen Li, Qinghua Liu, Chaoqun Chen, Shulan Wu, Lin Luo, Xueyong Pang, Chunying Yin","doi":"10.1111/pce.70356","DOIUrl":"10.1111/pce.70356","url":null,"abstract":"<p><p>The mechanisms of selenium (Se) oxyanion transformation in endophytic bacteria remain poorly understood, which limits their application in biofortification and phytoremediation. Here, we investigated these mechanisms using the plant-growth-promoting (PGP) endophyte Erwinia sp. PSI-03. Under 2 mM selenite stress, the strain intracellularly and extracellularly produced spherical selenium nanoparticles (SeNPs; ab57 nm average diameter). Multi-omics analyses revealed that these SeNPs were formed through parallel enzymatic (mediated by sulfite reductase, cysI) and non-enzymatic (via glutathione and l-cysteine) reduction pathways. Additionally, γ-glutamyl-Se-methylselenocysteine was identified as a key organo-selenium metabolite. Selenite exposure induced extensive reprogramming of the metabolome and transcriptome, highlighting key roles for glutathione metabolism and stress response systems related to cell wall/membrane maintenance, oxidative phosphorylation, two-component signaling systems, and DNA repair. Intriguingly, selenite stress concurrently stimulated bacterial synthesis of PGP compounds, including the auxin precursor indole-3-pyruvate, the defense hormone salicylic acid, and acetate. Consistent with this, under selenite-free and high-selenite (12 mg kg<sup>-1</sup> Se) conditions, inoculation with Erwinia sp. PSI-03 significantly promoted tea plant growth. Compared to uninoculated controls, the leaf biomass increased by 52.8% and 51.7%, and the total biomass by 82.9% and 49.6%, respectively. These findings establish a paradigm where endophytic bacteria simultaneously detoxify Se and promote plant health, offering a robust strategy for agricultural and environmental Se management.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":"1899-1912"},"PeriodicalIF":6.3,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145848505","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Global climate warming has significantly increased plant diseases prevalence. In subtropical regions, high temperature frequently co-occurs with bacterial wilt caused by Ralstonia solanacearum, creating compound stress conditions that severely compromise eggplant productivity. However, the molecular mechanisms governing eggplant's response to combined heat and pathogen stress remain poorly characterized. In this study, we conducted the temperature analyses of Guangzhou, China, and isolated a thermotolerant strain PSS219-GZ under high temperatures in eggplant. Phenotypic analysis of eggplants inoculated with PSS219-GZ at different temperature, indicated that PSS219-GZ have maximal pathogenicity at 37°C. SmWRKY6 is a WRKY transcription factor activated by both high temperatures and Ralstonia solanacearum infection. Genetic evidence from silencing of SmWRKY6 via VIGS in eggplants and overexpression of SmWRKY6 in tomato demonstrated that SmWRKY6 is essential for enhancing resistance to Ralstonia solanacearum under high-temperature stress. SmWRKY6 directly binds to and transcriptionally activates the SmPR1b promoter, forming a key regulatory node in bacterial wilt resistance pathways. This study provides novel insights into plant responses to combined heat and R. solanacearum stress and highlights potential resistance genes for mitigating compound stress effects.
{"title":"SmWRKY6 Mediates Thermo-Enhanced Resistance to Ralstonia solanacearum in Eggplant by Activating SmPR1b.","authors":"Yonggui Liang, Bingwei Yu, Renjian Liu, Zhilei Xia, Liping Chen, Zhengkun Qiu, Shuangshuang Yan, Bihao Cao","doi":"10.1111/pce.70360","DOIUrl":"10.1111/pce.70360","url":null,"abstract":"<p><p>Global climate warming has significantly increased plant diseases prevalence. In subtropical regions, high temperature frequently co-occurs with bacterial wilt caused by Ralstonia solanacearum, creating compound stress conditions that severely compromise eggplant productivity. However, the molecular mechanisms governing eggplant's response to combined heat and pathogen stress remain poorly characterized. In this study, we conducted the temperature analyses of Guangzhou, China, and isolated a thermotolerant strain PSS219-GZ under high temperatures in eggplant. Phenotypic analysis of eggplants inoculated with PSS219-GZ at different temperature, indicated that PSS219-GZ have maximal pathogenicity at 37°C. SmWRKY6 is a WRKY transcription factor activated by both high temperatures and Ralstonia solanacearum infection. Genetic evidence from silencing of SmWRKY6 via VIGS in eggplants and overexpression of SmWRKY6 in tomato demonstrated that SmWRKY6 is essential for enhancing resistance to Ralstonia solanacearum under high-temperature stress. SmWRKY6 directly binds to and transcriptionally activates the SmPR1b promoter, forming a key regulatory node in bacterial wilt resistance pathways. This study provides novel insights into plant responses to combined heat and R. solanacearum stress and highlights potential resistance genes for mitigating compound stress effects.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":"1943-1957"},"PeriodicalIF":6.3,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145852712","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Rice (Oryza sativa L.) features a unique inflorescence organ known as the spikelet, comprising floret, lemma/palea, sterile lemmas, and rudimentary glumes, of which the molecular regulation underlying sterile lemma identity remains elusive. Here, we isolated the G1 locus for sterile lemma specification using an F2 population developed by crossing between Nipponbare and LG7, a variety with a lemma-like-sterile lemma (lsl). An SNP (+323 G/A) in G1 alleles causes a serine to asparagine (S108N) substitution, leading to the lsl phenotype. Mechanistically, we found that G1 transactivates the expressions of both OsMADS34 and TGW2, two genes known to regulate sterile lemma identity and grain size, through binding to the YACTGTW and CArG-box motifs within their promoters, respectively. Subsequently, we reveal that the transactivation activity of G1NIP (allele from Nipponbare) is further enhanced through interactions with either OsMADS34 or TGW2. Furthermore, we demonstrated that G1 specifies sterile lemma identity via OsMADS34 and controls grain size through TGW2. Our results reveal two transcriptional circuits (G1-OsMADS34 and G1-TGW2) that are crucial for determining sterile lemma identity and grain size of rice, providing insights into genetic improvement for breeding programs.
{"title":"Dual Transcriptional Circuits: G1-OsMADS34 and G1-TGW2 Cooperatively Regulate Sterile Lemma Identity and Grain Size in Rice.","authors":"Xuemei Qin, Ping Gan, Jinliang Sun, Di Wu, Ru Li, Tianmin Ouyang, Kaichong Teng, Weijian Cen, Baoxiang Qin, Fang Liu, Rongbai Li, Jijing Luo","doi":"10.1111/pce.70364","DOIUrl":"10.1111/pce.70364","url":null,"abstract":"<p><p>Rice (Oryza sativa L.) features a unique inflorescence organ known as the spikelet, comprising floret, lemma/palea, sterile lemmas, and rudimentary glumes, of which the molecular regulation underlying sterile lemma identity remains elusive. Here, we isolated the G1 locus for sterile lemma specification using an F<sub>2</sub> population developed by crossing between Nipponbare and LG7, a variety with a lemma-like-sterile lemma (lsl). An SNP (+323 G/A) in G1 alleles causes a serine to asparagine (S108N) substitution, leading to the lsl phenotype. Mechanistically, we found that G1 transactivates the expressions of both OsMADS34 and TGW2, two genes known to regulate sterile lemma identity and grain size, through binding to the YACTGTW and CArG-box motifs within their promoters, respectively. Subsequently, we reveal that the transactivation activity of G1<sup>NIP</sup> (allele from Nipponbare) is further enhanced through interactions with either OsMADS34 or TGW2. Furthermore, we demonstrated that G1 specifies sterile lemma identity via OsMADS34 and controls grain size through TGW2. Our results reveal two transcriptional circuits (G1-OsMADS34 and G1-TGW2) that are crucial for determining sterile lemma identity and grain size of rice, providing insights into genetic improvement for breeding programs.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":"2008-2023"},"PeriodicalIF":6.3,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145898901","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-04-01Epub Date: 2025-12-21DOI: 10.1111/pce.70334
Hirotsuna Yamada, Clément E Gille, Pallavi, Li Yan, Gareth Nealon, Jun Wasaki, Erik J Veneklaas, Hans Lambers
Most Proteaceae and some Fabaceae species produce specialised cluster roots (CRs), and are abundant in severely phosphorus (P)-impoverished soils in southwest Australia. Two types of CRs, compound and simple, have been identified. However, the difference in their P-mining strategies remains unclear. Therefore, we conducted glasshouse and field experiments to compare the P-acquisition strategies among 18 CR-producing species in Proteaceae and Fabaceae. Proteaceae produced a significantly larger mass of CRs than Fabaceae. Particularly, Banksia species produced the largest mass of compound CRs and exhibited the greatest net plant-absorbed P in pots and consistently higher mature leaf manganese concentration in the field. In contrast, Hakea and Grevillea species produced less mass of simple CRs but three times as much soil adhered to their CRs per CR dry weight, resulting in greater absorbed P per CR weight. All plants depleted similar P compounds from soil and accessed c. 52% of P that was not extracted by a NaOH-EDTA solution, suggesting that both CRs shared a common physiological function for mining scarcely available P. This study highlights two divergent P-acquisition strategies: greater biomass investment in compound CRs versus greater P-acquisition efficiency in simple CRs.
{"title":"Divergent Phosphorus-Mining Strategies in Simple and Compound Cluster Roots in Extremely Phosphorus-Impoverished Soils in Southwest Australia.","authors":"Hirotsuna Yamada, Clément E Gille, Pallavi, Li Yan, Gareth Nealon, Jun Wasaki, Erik J Veneklaas, Hans Lambers","doi":"10.1111/pce.70334","DOIUrl":"10.1111/pce.70334","url":null,"abstract":"<p><p>Most Proteaceae and some Fabaceae species produce specialised cluster roots (CRs), and are abundant in severely phosphorus (P)-impoverished soils in southwest Australia. Two types of CRs, compound and simple, have been identified. However, the difference in their P-mining strategies remains unclear. Therefore, we conducted glasshouse and field experiments to compare the P-acquisition strategies among 18 CR-producing species in Proteaceae and Fabaceae. Proteaceae produced a significantly larger mass of CRs than Fabaceae. Particularly, Banksia species produced the largest mass of compound CRs and exhibited the greatest net plant-absorbed P in pots and consistently higher mature leaf manganese concentration in the field. In contrast, Hakea and Grevillea species produced less mass of simple CRs but three times as much soil adhered to their CRs per CR dry weight, resulting in greater absorbed P per CR weight. All plants depleted similar P compounds from soil and accessed c. 52% of P that was not extracted by a NaOH-EDTA solution, suggesting that both CRs shared a common physiological function for mining scarcely available P. This study highlights two divergent P-acquisition strategies: greater biomass investment in compound CRs versus greater P-acquisition efficiency in simple CRs.</p>","PeriodicalId":222,"journal":{"name":"Plant, Cell & Environment","volume":" ","pages":"1833-1847"},"PeriodicalIF":6.3,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12976584/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145802787","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}