Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Scientific Reports
  • View all journals
  • Search
  • My Account Login
  • Content Explore content
  • About the journal
  • Publish with us
  • Sign up for alerts
  • RSS feed
  1. nature
  2. scientific reports
  3. articles
  4. article
Supplementary filling seedlings in secondary Pinus massoniana forests changed the structure of soil bacterial communities
Download PDF
Download PDF
  • Article
  • Open access
  • Published: 26 March 2026

Supplementary filling seedlings in secondary Pinus massoniana forests changed the structure of soil bacterial communities

  • Ning Pan1,
  • Yun-Long Zhang1,
  • Peng Jia2,
  • Wen-Tao Qiao1,
  • Dao-Lin Du3,
  • Wei Han4,
  • Xiang-Zhen Li5 &
  • …
  • Yong-Feng Wang1 

Scientific Reports , Article number:  (2026) Cite this article

  • 265 Accesses

  • Metrics details

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Ecology
  • Environmental sciences
  • Microbiology
  • Plant sciences

Abstract

Forest reformation can improve productivity and ecological service functions of forest resources. Nonetheless, the influence of different ways of forest reformation on soil microbial communities is still a complex and controversial issue. In this study, we investigated the effects of supplementary seedling planting (hereafter referred to as “filling seedlings”) in secondary Pinus massoniana forests on soil bacterial community. We collected soil samples from original secondary P. massoniana forest and the forests filled with P. massoniana seedlings for 2, 4, and 6 years, respectively. We found that filling seedlings in the secondary P. massoniana forests changed the bacterial community structure compared to the original secondary forests. Filling seedlings in secondary P. massoniana forest significantly decreased soil bacterial abundance from 2.12 × 107 copies g−1 soil to 8.91 × 106 copies g−1 soil (n = 3) after six years of reformation, a decrease by 58.0%. Acidobacteriota (34.96% averagely) was the dominant phylum and Xiphinematobacteraceae (5.76% averagely) was the dominant family in all P. massoniana forests in this study. Soil parameters such as soil pH, soil organic matter, NH4+, NO3-, and total and soluble P were significantly correlated with the structure of bacterial communities (p < 0.05). Moreover, the bacterial community structure and diversity changed over time during forest recovery. Our study demonstrated that filling seedlings in secondary P. massoniana forests could change soil bacterial community, which might in turn affect the nutrient cycling. This study provides scientific basis for managing low quality P. massoniana forests.

Similar content being viewed by others

Bacteria-soil–plant linkages underlie the mosaic structure of the soil bacterial communities in near-natural stands of Białowieża Primeval Forest

Article Open access 13 March 2026

Tree species determine soil microbial diversity: variation in fungal and bacterial communities in temperate forests

Article Open access 25 February 2026

Dynamics and functional roles of fungal communities in Pseudostellaria heterophylla soil under continuous cropping

Article Open access 21 October 2025

Data availability

Raw sequence data from the 16S rRNA genes analyzed in this study were uploaded to the Sequence Read Archive on the NCBI website under the BioProject accession number PRJNA1212573.

References

  1. Liu, X.-Y. et al. The introduction of woody plants for freshwater wetland restoration alters the archaeal community structure in soil. Land Degrad. Dev. 28, 1933–1942. https://doi.org/10.1002/ldr.2713 (2017).

    Google Scholar 

  2. Hua, F. et al. The biodiversity and ecosystem service contributions and trade-offs of forest restoration approaches. Science 376, 839–844. https://doi.org/10.1126/science.abl4649 (2022).

    Google Scholar 

  3. Referowska-Chodak, E. & Kornatowska, B. Effects of forestry transformation on the ecosystem level of biodiversity in Poland’s forests. Forests 14, 1739. https://doi.org/10.3390/f14091739 (2023).

    Google Scholar 

  4. Hou, X.-Y. et al. Reforestation of Cunninghamia lanceolata changes the relative abundances of important prokaryotic families in soil. Front. Microbiol. https://doi.org/10.3389/fmicb.2024.1312286 (2024).

    Google Scholar 

  5. Qu, Z. L., Liu, B., Ma, Y., Xu, J. & Sun, H. The response of the soil bacterial community and function to forest succession caused by forest disease. Funct. Ecol. 34, 2548–2559. https://doi.org/10.1111/1365-2435.13665 (2020).

    Google Scholar 

  6. Zhu, L. et al. Community assembly of organisms regulates soil microbial functional potential through dual mechanisms. Glob. Chang. Biol. 30, e17160. https://doi.org/10.1111/gcb.17160 (2024).

    Google Scholar 

  7. Deng, W. et al. Chemical composition of soil carbon is governed by microbial diversity during understory fern removal in subtropical pine forests. Sci. Total Environ. 914, 169904. https://doi.org/10.1016/j.scitotenv.2024.169904 (2024).

    Google Scholar 

  8. Adomako, M. O., Xue, W., Du, D.-L. & Yu, F.-H. Soil biota and soil substrates influence responses of the rhizomatous clonal grass Leymus chinensis to nutrient heterogeneity. Plant Soil 465, 19–29. https://doi.org/10.1007/s11104-021-04967-0 (2021).

    Google Scholar 

  9. Masse, J., Prescott, C. E., Renaut, S., Terrat, Y. & Grayston, S. J. Plant community and nitrogen deposition as drivers of alpha and beta diversities of prokaryotes in reconstructed oil sand soils and natural boreal forest soils. Appl. Environ. Microbiol. 83, e03319-e13316. https://doi.org/10.1128/AEM.03319-16 (2017).

    Google Scholar 

  10. Zhang, H., Zhou, G., Wang, Y., Tang, C. & Cai, Y. Clear-cut and forest regeneration increase soil N2O emission in Cunninghamia lanceolata plantations. Geoderma 401, 115238. https://doi.org/10.1016/j.geoderma.2021.115238 (2021).

    Google Scholar 

  11. Zhang, Y.-L. et al. Shifts in soil prokaryotic community structure due to clear-cutting secondary Acacia mangium forests and replacing with Eucalyptus urophylla. J. Environ. Manag. 386, 125742. https://doi.org/10.1016/j.jenvman.2025.125742 (2025).

    Google Scholar 

  12. Guignabert, A. et al. Combining partial cutting and direct seeding to overcome regeneration failures in dune forests. For. Ecol. Manag. 476, 118466. https://doi.org/10.1016/j.foreco.2020.118466 (2020).

    Google Scholar 

  13. Khan, A. A. et al. Halotolerant Staphylococcus epidermidis DS2 enhances growth, stress resilience, and ion homeostasis in wheat under saline conditions. World J. Microbiol. Biotechnol. 41, 433. https://doi.org/10.1007/s11274-025-04641-y (2025).

    Google Scholar 

  14. Khan, A. A., Wang, Y.-F., Akbar, R. & Alhoqail, W. A. Mechanistic insights and future perspectives of drought stress management in staple crops. Front. Plant Sci. https://doi.org/10.3389/fpls.2025.1547452 (2025).

    Google Scholar 

  15. d. Quadros, P. D. et al. Coal mining practices reduce the microbial biomass, richness and diversity of soil. Appl. Soil Ecol. 98, 195–203. https://doi.org/10.1016/j.apsoil.2015.10.016 (2016).

    Google Scholar 

  16. Zhang, L., Lai, G., Zeng, W., Zou, W. & Yi, S. Effect of climate on carbon storage growth models for three major coniferous plantations in China based on national forest inventory data. Forests 13, 882. https://doi.org/10.3390/f13060882 (2022).

    Google Scholar 

  17. Wang, D. et al. Identification and expression patterns of WOX transcription factors under abiotic stresses in Pinus massoniana. Int. J. Mol. Sci. 25, 1627. https://doi.org/10.3390/ijms25031627 (2024).

    Google Scholar 

  18. Wen, X. et al. Assessing the impact of pine wilt disease on aboveground carbon storage in planted Pinus massoniana Lamb. forests via remote sensing. Sci. Total Environ. 914, 169906. https://doi.org/10.1016/j.scitotenv.2024.169906 (2024).

    Google Scholar 

  19. Zhang, T. et al. Metal-non-tolerant ecotypes of ectomycorrhizal fungi can protect plants from cadmium pollution. Front. Plant Sci. https://doi.org/10.3389/fpls.2023.1301791 (2023).

    Google Scholar 

  20. Feng, Y. et al. Bursaphelenchus xylophilus venom allergen-like protein BxVAP1, triggering plant defense-related programmed cell death, plays an important role in regulating Pinus massoniana terpene defense responses. Phytopathology 114, 2331–2340. https://doi.org/10.1094/PHYTO-01-24-0026-R (2024).

    Google Scholar 

  21. Zhu, J. et al. Unraveling Pinus massoniana’s defense mechanisms against Bursaphelenchus xylophilus under aseptic conditions: A transcriptomic analysis. Phytopathology 114, 2525–2535. https://doi.org/10.1094/phyto-06-24-0180-r (2024).

    Google Scholar 

  22. Chen, L. et al. Modeling the distribution of pine wilt disease in China using the ensemble models MaxEnt and CLIMEX. Ecol. Evol. 14, e70277. https://doi.org/10.1002/ece3.70277 (2024).

    Google Scholar 

  23. Rushen, L. Methods of Agriculture Chemical Analysis. (China Agriculture Scientech Press, 2000).

  24. Quince, C., Haas, B. J., Clemente, J. C., Knight, R. & Edgar, R. C. UCHIME improves sensitivity and speed of chimera detection(Article). Bioinformatics 27, 2194–2200. https://doi.org/10.1093/bioinformatics/btr381 (2011).

    Google Scholar 

  25. Wang, Q., Garrity, G. M., Tiedje, J. M. & Cole, J. R. Naive Bayesian classifier for rapid assignment of rRNA sequences into the new bacterial taxonomy. Appl. Environ. Microbiol. 73, 5261–5267. https://doi.org/10.1128/aem.00062-07 (2007).

    Google Scholar 

  26. Huang, L. et al. Microbiota recovery in a chronosquences of impoverished Cerrado soils with biosolids applications. Sci. Total Environ. 931, 172958. https://doi.org/10.1016/j.scitotenv.2024.172958 (2024).

    Google Scholar 

  27. Banning, N. C. et al. Soil microbial community successional patterns during forest ecosystem restoration. Appl. Environ. Microbiol. 77, 6158–6164. https://doi.org/10.1128/aem.00764-11 (2011).

    Google Scholar 

  28. Kalam, S. et al. Recent understanding of soil acidobacteria and their ecological significance: A critical review. Front. Microbiol. https://doi.org/10.3389/fmicb.2020.580024 (2020).

    Google Scholar 

  29. Qiao, W.-T. et al. Soil comammox Nitrospira dominates over ammonia-oxidizing archaea and bacteria in the invasion of Solidago canadensis. Plant Soil 513, 2417–2431. https://doi.org/10.1007/s11104-025-07326-5 (2025).

    Google Scholar 

  30. Jiao, F. et al. Diversity and composition of soil acidobacterial communities in different temperate forest types of Northeast China. Microorganisms 12, 963. https://doi.org/10.3390/microorganisms12050963 (2024).

    Google Scholar 

  31. Naether, A. et al. Environmental factors affect Acidobacterial communities below the subgroup level in grassland and forest soils. Appl. Environ. Microbiol. 78, 7398–7406. https://doi.org/10.1128/aem.01325-12 (2012).

    Google Scholar 

  32. DeBruyn, J. M., Nixon, L. T., Fawaz, M., Johnson, A. & Radosevich, M. Global biogeography and quantitative seasonal dynamics of Gemmatimonadetes in soil. Appl. Environ. Microbiol. 77, 6295–6300. https://doi.org/10.1128/aem.05005-11 (2011).

    Google Scholar 

  33. Mujakić, I., Piwosz, K. & Koblížek, M. Phylum Gemmatimonadota and its role in the environment. Microorganisms https://doi.org/10.3390/microorganisms10010151 (2022).

    Google Scholar 

  34. Lei, C., Lu, T., Qian, H. & Liu, Y. Machine learning models reveal how biochar amendment affects soil microbial communities. Biochar 5, 1–15. https://doi.org/10.1007/s42773-023-00291-1 (2023).

    Google Scholar 

  35. Pedrinho, A. et al. Impacts of deforestation and forest regeneration on soil bacterial communities associated with phosphorus transformation processes in the Brazilian Amazon region. Ecol. Indic. 146, 109779. https://doi.org/10.1016/j.ecolind.2022.109779 (2023).

    Google Scholar 

  36. Jiang, Q. et al. Cold seeps are potential hotspots of deep-sea nitrogen loss driven by microorganisms across 21 phyla. Nat. Commun. 16, 1646. https://doi.org/10.1038/s41467-025-56774-1 (2025).

    Google Scholar 

  37. Fuerst, J. A. & Sagulenko, E. Beyond the bacterium: Planctomycetes challenge our concepts of microbial structure and function. Nat. Rev. Microbiol. 9, 403–413. https://doi.org/10.1038/nrmicro2578 (2011).

    Google Scholar 

  38. Schmidt, M. W. I. et al. Persistence of soil organic matter as an ecosystem property. Nature 478, 49–56. https://doi.org/10.1038/nature10386 (2011).

    Google Scholar 

  39. Lan, J. et al. The shift of soil bacterial community after afforestation influence soil organic carbon and aggregate stability in Karst Region. Front. Microbiol. https://doi.org/10.3389/fmicb.2022.901126 (2022).

    Google Scholar 

  40. Ren, C. et al. Differential soil microbial community responses to the linkage of soil organic carbon fractions with respiration across land-use changes. Forest Ecol. Manage. 409, 170–178. https://doi.org/10.1016/j.foreco.2017.11.011 (2018).

    Google Scholar 

  41. Karhu, K. et al. Temperature sensitivity of soil respiration rates enhanced by microbial community response. Nature 513, 81–84. https://doi.org/10.1038/nature13604 (2014).

    Google Scholar 

  42. Duan, P. et al. Tree species diversity increases soil microbial carbon use efficiency in a subtropical forest. Glob. Change Biol. 29, 7131–7144. https://doi.org/10.1111/gcb.16971 (2023).

    Google Scholar 

  43. Wong, M. T. F. & Nortcliff, S. (ed N. Ahmad) 13–26 (Springer Netherlands, 1996).

  44. Philippot, L., Griffiths Bryan, S. & Langenheder, S. Microbial community resilience across ecosystems and multiple disturbances. Microbiol. Mol. Biol. Rev. 85, 10.1128/mmbr.00026-00020. https://doi.org/10.1128/mmbr.00026-20 (2021).

    Google Scholar 

  45. Hong, S. et al. Afforestation neutralizes soil pH. Nat. Commun. 9, 520. https://doi.org/10.1038/s41467-018-02970-1 (2018).

    Google Scholar 

  46. Lan, J., Long, Q., Huang, M., Jiang, Y. & Hu, N. Afforestation-induced large macroaggregate formation promotes soil organic carbon accumulation in degraded karst area. Forest Ecol. Manag. 505, 119884. https://doi.org/10.1016/j.foreco.2021.119884 (2022).

    Google Scholar 

  47. Hu, P. et al. Linking bacterial life strategies with soil organic matter accrual by karst vegetation restoration. Soil Biol. Biochem. 177, 108925. https://doi.org/10.1016/j.soilbio.2022.108925 (2023).

    Google Scholar 

  48. Guo, Y. et al. A systematic analysis and review of the impacts of afforestation on soil quality indicators as modified by climate zone, forest type and age. Sci. Total Environ. 757, 143824. https://doi.org/10.1016/j.scitotenv.2020.143824 (2021).

    Google Scholar 

  49. Wang, Y.-F. et al. Solidago canadensis alters rhizosphere bacterial communities of Artemisia argyi under warming and nitrogen deposition—Invaded rhizospheres become similar to the invader’s. Plant Soil https://doi.org/10.1007/s11104-026-08350-9 (2026).

    Google Scholar 

  50. Wang, Y.-F., Khan, A. A., Iqbal, B. & Du, D. The silent cleanup arsenal: Microbial biofertilizers and their enzymatic pathways for arsenic decontamination in agricultural soils. Eng. Environ. 20, 70. https://doi.org/10.1007/s11783-026-2170-4 (2026).

    Google Scholar 

  51. Vargas, L. K. et al. Soil fertility level is the main modulator of prokaryotic communities in a meta-analysis of 197 soil samples from the Americas and Europe. Appl. Soil Ecol. 186, 104811. https://doi.org/10.1016/j.apsoil.2023.104811 (2023).

    Google Scholar 

  52. Li, W. et al. Effects of long-term warming on soil prokaryotic communities in shrub and alpine meadows on the eastern edge of the Qinghai-Tibetan Plateau. Appl. Soil Ecol. 188, 104871. https://doi.org/10.1016/j.apsoil.2023.104871 (2023).

    Google Scholar 

  53. Jia, W. et al. Zonation of bulk and rhizosphere soil bacterial communities and their covariation patterns along the elevation gradient in riparian zones of Three Gorges Reservoir, China. Environ. Res. 249, 118383. https://doi.org/10.1016/j.envres.2024.118383 (2024).

    Google Scholar 

  54. Zhang, E. et al. Effects of increasing soil moisture on Antarctic desert microbial ecosystems. Conserv. Biol. 38(4), e14268. https://doi.org/10.1111/cobi.14268 (2023).

    Google Scholar 

  55. Lladó, S., López-Mondéjar, R. & Baldrian, P. Drivers of microbial community structure in forest soils. Appl. Microbiol. Biotechnol. 102, 4331–4338 (2018).

    Google Scholar 

  56. Luo, D. et al. Consortium of phosphorus-solubilizing bacteria promotes maize growth and changes the microbial community composition of rhizosphere soil. Agronomy 14, 1535. https://doi.org/10.3390/agronomy14071535 (2024).

    Google Scholar 

  57. Wang, C.-y et al. Soil pH is the primary factor driving the distribution and function of microorganisms in farmland soils in northeastern China. Ann. Microbiol. 69, 1461–1473. https://doi.org/10.1007/s13213-019-01529-9 (2019).

    Google Scholar 

  58. Zhou, X. et al. Global analysis of soil bacterial genera and diversity in response to pH. Soil Biol. Biochem. 198, 109552. https://doi.org/10.1016/j.soilbio.2024.109552 (2024).

    Google Scholar 

  59. Houlton, B. Z., Wang, Y.-P., Vitousek, P. M. & Field, C. B. A unifying framework for dinitrogen fixation in the terrestrial biosphere. Nature 454, 327–330. https://doi.org/10.1038/nature07028 (2008).

    Google Scholar 

  60. Wang, Q. et al. Effects of nitrogen and phosphorus inputs on soil bacterial abundance, diversity, and community composition in Chinese fir plantations. Front. Microbiol. https://doi.org/10.3389/fmicb.2018.01543 (2018).

    Google Scholar 

  61. Wang, P. et al. Correlation of bacterial community with phosphorus fraction drives discovery of Actinobacteria involved soil phosphorus transformation during the trichlorfon degradation. Environ. Pollut. 302, 119043. https://doi.org/10.1016/j.envpol.2022.119043 (2022).

    Google Scholar 

  62. Cui, M. et al. Warming significantly inhibited the competitive advantage of native plants in interspecific competition under phosphorus deposition. Plant. Soil. 486, 503–518. https://doi.org/10.1007/s11104-023-05887-x (2023).

    Google Scholar 

  63. Lopes, Ld. S. et al. Distinct bacterial community structure and composition along different cowpea producing ecoregions in Northeastern Brazil. Sci. Rep. 11, 831. https://doi.org/10.1038/s41598-020-80840-x (2021).

    Google Scholar 

  64. Philippot, L., Chenu, C., Kappler, A., Rillig, M. C. & Fierer, N. The interplay between microbial communities and soil properties. Nat. Rev. Microbiol. 22, 226–239. https://doi.org/10.1038/s41579-023-00980-5 (2024).

    Google Scholar 

  65. Fickling, N. W. et al. Light-dark cycles may influence in situ soil bacterial networks and diurnally-sensitive taxa. Ecol. Evol. 14, e11018. https://doi.org/10.1002/ece3.11018 (2024).

    Google Scholar 

  66. Lai, Z. et al. Distinct microbial communities under different rock-associated microhabitats in the Qaidam Desert. Environ. Res. https://doi.org/10.1016/j.envres.2024.118462 (2024).

    Google Scholar 

  67. Kong, D., Ye, Z., Dai, M., Ma, B. & Tan, X. Light intensity modulates the functional composition of leaf metabolite groups and phyllosphere prokaryotic community in garden lettuce (Lactuca sativa L.) plants at the vegetative stage. Int. J. Mol. Sci. 25, 1451. https://doi.org/10.3390/ijms25031451 (2024).

    Google Scholar 

  68. Han, S. H., Kim, S., Chang, H., Li, G. & Son, Y. Increased soil temperature stimulates changes in carbon, nitrogen, and mass loss in the fine roots of Pinus koraiensis under experimental warming and drought. Turk. J. Agric. For. 43, 80–87. https://doi.org/10.3906/tar-1807-162 (2019).

    Google Scholar 

  69. Li, G. et al. Precipitation affects soil microbial and extracellular enzymatic responses to warming. Soil Biol. Biochem. 120, 212–221 (2018).

    Google Scholar 

  70. Wang, Y.-F. et al. Key factors shaping prokaryotic communities in subtropical forest soils. Appl. Soil Ecol. 169, 104162. https://doi.org/10.1016/j.apsoil.2021.104162 (2022).

    Google Scholar 

  71. Bastida, F. et al. Soil microbial diversity–biomass relationships are driven by soil carbon content across global biomes. ISME J. 15, 2081–2091. https://doi.org/10.1038/s41396-021-00906-0 (2021).

    Google Scholar 

Download references

Funding

The funding for this study was provided by the National Natural Science Foundation of China (32171760), National Key Research and Development Program of China (Grant number: 2023YFD2303100 and 2025YFD2300300) and the Jiangsu University Talents Initiating Fund (22JDG057).

Author information

Authors and Affiliations

  1. School of Environment and Safety Engineering, Jiangsu University, 301 Xuefu Road, Zhenjiang, 212013, People’s Republic of China

    Ning Pan, Yun-Long Zhang, Wen-Tao Qiao & Yong-Feng Wang

  2. Guangzhou Institute of Forestry and Landscape Architecture, 428 Guangyuan Road, Guangzhou, 510420, People’s Republic of China

    Peng Jia

  3. Jingjiang College, Jiangsu University, Zhenjiang, 212013, People’s Republic of China

    Dao-Lin Du

  4. Shandong Agro-Tech Extension Center, Jinan, 250013, People’s Republic of China

    Wei Han

  5. College of Resources and Environment, Fujian Agriculture and Forestry University, Fuzhou, 350002, People’s Republic of China

    Xiang-Zhen Li

Authors
  1. Ning Pan
    View author publications

    Search author on:PubMed Google Scholar

  2. Yun-Long Zhang
    View author publications

    Search author on:PubMed Google Scholar

  3. Peng Jia
    View author publications

    Search author on:PubMed Google Scholar

  4. Wen-Tao Qiao
    View author publications

    Search author on:PubMed Google Scholar

  5. Dao-Lin Du
    View author publications

    Search author on:PubMed Google Scholar

  6. Wei Han
    View author publications

    Search author on:PubMed Google Scholar

  7. Xiang-Zhen Li
    View author publications

    Search author on:PubMed Google Scholar

  8. Yong-Feng Wang
    View author publications

    Search author on:PubMed Google Scholar

Contributions

Ning Pan analyzed the data and wrote the original paper; Yong-Feng Wang conceived and conducted the experiment and revised the paper; Peng Jia participated in field experiment; Yun-Long Zhang, Wen-Tao Qiao, Dao-Lin Du, Xiang-Zhen Li and Wei Han revised the paper.

Corresponding author

Correspondence to Yong-Feng Wang.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Supplementary Information. (download DOCX )

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Pan, N., Zhang, YL., Jia, P. et al. Supplementary filling seedlings in secondary Pinus massoniana forests changed the structure of soil bacterial communities. Sci Rep (2026). https://doi.org/10.1038/s41598-026-45370-y

Download citation

  • Received: 12 December 2025

  • Accepted: 18 March 2026

  • Published: 26 March 2026

  • DOI: https://doi.org/10.1038/s41598-026-45370-y

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

Keywords

  • Pinus massoniana
  • Secondary forests
  • Supplementary seedling planting
  • Forest reformation
  • Soil microorganisms
Download PDF

Advertisement

Explore content

  • Research articles
  • News & Comment
  • Collections
  • Subjects
  • Follow us on Facebook
  • Follow us on X
  • Sign up for alerts
  • RSS feed

About the journal

  • About Scientific Reports
  • Contact
  • Journal policies
  • Guide to referees
  • Calls for Papers
  • Editor's Choice
  • Journal highlights
  • Open Access Fees and Funding

Publish with us

  • For authors
  • Language editing services
  • Open access funding
  • Submit manuscript

Search

Advanced search

Quick links

  • Explore articles by subject
  • Find a job
  • Guide to authors
  • Editorial policies

Scientific Reports (Sci Rep)

ISSN 2045-2322 (online)

nature.com footer links

About Nature Portfolio

  • About us
  • Press releases
  • Press office
  • Contact us

Discover content

  • Journals A-Z
  • Articles by subject
  • protocols.io
  • Nature Index

Publishing policies

  • Nature portfolio policies
  • Open access

Author & Researcher services

  • Reprints & permissions
  • Research data
  • Language editing
  • Scientific editing
  • Nature Masterclasses
  • Research Solutions

Libraries & institutions

  • Librarian service & tools
  • Librarian portal
  • Open research
  • Recommend to library

Advertising & partnerships

  • Advertising
  • Partnerships & Services
  • Media kits
  • Branded content

Professional development

  • Nature Awards
  • Nature Careers
  • Nature Conferences

Regional websites

  • Nature Africa
  • Nature China
  • Nature India
  • Nature Japan
  • Nature Middle East
  • Privacy Policy
  • Use of cookies
  • Legal notice
  • Accessibility statement
  • Terms & Conditions
  • Your US state privacy rights
Springer Nature

© 2026 Springer Nature Limited

Nature Briefing Microbiology

Sign up for the Nature Briefing: Microbiology newsletter — what matters in microbiology research, free to your inbox weekly.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing: Microbiology