Terrestrial ecosystem carbon storage (TECS) could significantly affect the concentration of atmospheric CO₂, which is critical for climate change prediction. Along these lines, the Integrated Valuation of Ecosystem Services and Trade-offs model was employed to determine the TECS of Hainan Island (HN) from 2015 to 2050 accurately. Besides, the Future Land-use Simulation model combined with natural and anthropogenic factors was used to forecast the land-use types from 2025 to 2050 in HN by considering different Shared-socioeconomic pathway-Rrepresentative concentration pathway (SSP-RCP) scenarios. Finally, the geographical detector explored the influence mechanism concerning the TECS. Under the SSP1-RCP1.9 scenario, the TECS of HN will be gradually increased to 388.10 million tons in 2050, mainly due to the increase in forest areas and the fact that the majority of grassland in the western part of HN is being converted into forest. Under different SSP-RCP scenarios except for SSP1-RCP1.9, HN's TECS is expected to gradually decrease from 2015 to 2050, mainly due to the loss of grassland and forest in coastal low-altitude areas. From the single/pair factor perspective influenced mechanism concerning the TECS, the elevation (DEM) and DEM∩Slope were found to be the dominant single/pair factor under the SSP1-RCP1.9, SSP1-RCP2.6 and SSP2-RCP4.5 scenarios. The least distance to residential area (LDP) and LDP∩LDR (i.e. LDP and least distance to roads or railways) were found to be the dominant factors under the SSP3-RCP7.0, SSP4-RCP3.4, SSP4-RCP6.0, SSP5-RCP3.4 and SSP5-RCP8.5 scenarios. Besides, the pair factors provided a higher determinant power for TECS than a single factor. Given the results of the TECS and the influence mechanism concerning the TECS under different SSP-RCP scenarios, we suggest reasonably planning the transportation network and limiting the disorderly expansion of construction land.

Drought and high-temperature stress are the main abiotic stresses that alone or simultaneously affect the yield and quality of pears worldwide. However, studies on the mechanisms of drought or high-temperature resistance in pears remain elusive. Therefore, the molecular responses of Pyrus betuleafolia, the widely used rootstock in pear production, to drought and high temperatures require further study. Here, drought- or high-temperature-resistant seedlings were selected from many Pyrus betuleafolia seedlings. The leaf samples collected before and after drought or high-temperature treatment were used to perform RNA sequencing analysis. For drought treatment, a total of 11,731 differentially expressed genes (DEGs) were identified, including 4444 drought-induced genes and 7287 drought-inhibited genes. Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis revealed that these DEGs were more significantly enriched in plant hormone signal transduction, flavonoid biosynthesis, and glutathione metabolism. For high-temperature treatment, 9639 DEGs were identified, including 5493 significantly upregulated genes and 4146 significantly downregulated genes due to high-temperature stress. KEGG analysis showed that brassinosteroid biosynthesis, arginine metabolism, and proline metabolism were the most enriched pathways for high-temperature response. Meanwhile, the common genes that respond to both drought and high-temperature stress were subsequently identified, with a focus on responsive transcription factors, such as MYB, HSF, bZIP, and WRKY. These results reveal potential genes that function in drought or high-temperature resistance. This study provides a theoretical basis and gene resources for the genetic improvement and molecular breeding of pears.

Iron is an essential trace element for plants; however, low bioactive Fe in soil continuously places plants in an Fe-deficient environment, triggering oxidative damage. To cope with this, plants make a series of alterations to increase Fe acquisition; however, this regulatory network needs further investigation. In this study, we found notably decreased indoleacetic acid (IAA) content in chlorotic pear (Pyrus bretschneideri Rehd.) leaves caused by Fe deficiency. Furthermore, IAA treatment slightly induced regreening by increasing chlorophyll synthesis and Fe²⁺ accumulation. At that point, we identified PbrSAUR72 as a key negative effector output of auxin signaling and established its close relationship to Fe deficiency. Furthermore, the transient PbrSAUR72 overexpression could form regreening spots with increased IAA and Fe²⁺ content in chlorotic pear leaves, whereas its transient silencing does the opposite in normal pear leaves. In addition, cytoplasm-localized PbrSAUR72 exhibits root expression preferences and displays high homology to AtSAUR40/72. This promotes salt tolerance in plants, indicating a putative role for PbrSAUR72 in abiotic stress responses. Indeed, transgenic plants of Solanum lycopersicum and Arabidopsis thaliana overexpressing PbrSAUR72 displayed less sensitivity to Fe deficiency, accompanied by substantially elevated expression of Fe-induced genes, such as FER/FIT, HA, and bHLH39/100. These result in higher ferric chelate reductase and root pH acidification activities, thereby hastening Fe absorption in transgenic plants under an Fe-deficient condition. Moreover, the ectopic overexpression of PbrSAUR72 inhibited reactive oxygen species production in response to Fe deficiency. These findings contribute to a new understanding of PbrSAURs and its involvement in Fe deficiency, providing new insights for the further study of the regulatory mechanisms underlying the Fe deficiency response.

Iron (Fe) deficiency is a general stress for many horticulture crops, causing leaf chlorosis and stunted growth. The basic-helix-loop-helix (bHLH) transcription factor (TF) was reported to function in Fe absorption; however, the regulatory mechanism of bHLH genes on iron absorption remains largely unclear in pear. In this study, we found that PbbHLH155 was significantly induced by Fe deficiency. Overexpression of PbbHLH155 in Arabidopsis thaliana and pear calli significantly increases resistance to Fe deficiency. The PbbHLH155-overexpressed Arabidopsis lines exhibited greener leaf color, higher Fe content, stronger Fe chelate reductase (FCR) and root acidification activity. The PbbHLH155 knockout pear calli showed lower Fe content and weaker FCR activity. Interestingly, PbbHLH155 inhibited the expressions of PbFRO2 and PbbHLH38, which were positive regulators in Fe-deficiency responses (FDR). Furthermore, yeast one-hybrid (Y1H) and Dual-Luciferase Reporter (DLR) assays revealed that PbbHLH155 directly binds to the promoters of PbFRO2 and PbbHLH38, thus activating their expression. Overall, our results showed that PbbHLH155 directly promote the expression of PbFRO2 and PbbHLH38 to activate FCR activity for iron absorption. This study provided valuable information for pear breeding.

Iron (Fe) is an essential micronutrient for plant photosynthesis and human health. Pear represents a widely consumed fruit for human Fe intake, yet its yield and quality are frequently challenged by Fe deficiency (FD) stress. Despite the prevalence of FD stress in agricultural production under generally alkaline and calcareous conditions, pear plants implement a series of adaptive responses to maintain Fe homeostasis, which remains poorly understood. In this study, key time points for RNA‐seq analysis were determined by examining FD‐related physiological indicators in pear seedlings ( Pyrus betulaefolia ) under short‐term FD stress. The results revealed that FD stress enhanced root rhizosphere acidification (peaking at 24 h post‐treatment) and caused a gradual decrease in leaf SPAD value and Fe content, while no obvious aboveground chlorosis phenotype was observed. By comparing RNA‐seq data of root samples at 3, 6, 12, and 24 h post‐FD stress with the control (0 h), a total of 8369 differentially expressed genes (DEGs) were generated, and 1423 DEGs were identified throughout the stress period. Functional annotation indicated that DEGs were enriched in transcriptional regulation, signal transduction, and secondary metabolism, while KEGG enrichment implied that DEGs are involved in sugar, proline, γ‐aminobutyric acid (GABA), galactose, raffinose, and polyamines metabolism, as well as hormone signaling. In addition, 18 PbHAs , 18 PbFROs , and 19 PbIRTs were identified, where Chr13.g22071 ( PbHA ), Chr7.g31823 ( PbFRO ), and Chr11.g10287 and Chr11.g10606 ( PbIRTs ) may be responsible for Fe homeostasis in FD‐stressed pear plants. Moreover, 490 transcription factors (TFs) were screened from the DEGs, with ERF, MYB, WRKY, bHLH, and NAC TFs accounting for the majority. Notably, 21 from 36 bHLHs were FD‐induced, among which Chr3.g19682 , Chr5.g08031 , Chr2.g44023 , and Chr8.g558833 might be the core FD regulators. Furthermore, based on the results of the gene coexpression analysis, an intricate regulatory network showing synergistic or antagonistic interactions between these TFs and core Fe uptake‐related genes has been established. Overall, this study identifies prospective genes for maintaining Fe homeostasis under FD stress, offering a theoretical foundation for further research into the molecular mechanisms of pear adaptation to FD stress, and potentially guiding the development of FD‐tolerant pear varieties.

Iron (Fe) deficiency poses a major threat to pear (Pyrus spp.) fruit yield and quality. The Gretchen Hagen 3 (GH3) plays a vital part in plant stress responses. However, the GH3 gene family is yet to be characterized, and little focus has been given to the function of the GH3 gene in Fe deficiency responses. Here, we identified 15 GH3 proteins from the proteome of Chinese white pear (Pyrus bretschneideri) and analyzed their features using bioinformatics approaches. Structure domain and motif analyses showed that these PbrGH3s were relatively conserved, and phylogenetic investigation displayed that they were clustered into two groups (GH3 I and GH3 II). Meanwhile, cis-acting regulatory element searches of the corresponding promoters revealed that these PbrGH3s might be involved in ABA- and drought-mediated responses. Moreover, the analysis of gene expression patterns exhibited that most of the PbrGH3s were highly expressed in the calyxes, ovaries, and stems of pear plants, and some genes were significantly differentially expressed in normal and Fe-deficient pear leaves, especially for PbrGH3.5. Subsequently, the sequence of PbrGH3.5 was isolated from the pear, and the transgenic tomato plants with PbrGH3.5 overexpression (OE) were generated to investigate its role in Fe deficiency responses. It was found that the OE plants were more sensitive to Fe deficiency stress. Compared with wild-type (WT) plants, the rhizosphere acidification and ferric reductase activities were markedly weakened, and the capacity to scavenge reactive oxygen species was prominently impaired in OE plants under Fe starvation conditions. Moreover, the expressions of Fe-acquisition-associated genes, such as SlAHA4, SlFRO1, SlIRT1, and SlFER, were all greatly repressed in OE leaves under Fe depravation stress, and the free IAA level was dramatically reduced, while the conjugated IAA contents were notably escalated. Combined, our findings suggest that pear PbrGH3.5 negatively regulates Fe deficiency responses in tomato plants, and might help enrich the molecular basis of Fe deficiency responses in woody plants.