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A review of research progress on continuous cropping obstacles |
Kunguang WANG1, Qiaofang LU1, Zhechao DOU1, Zhiguang CHI1, Dongming CUI1, Jing MA1, Guowei WANG2, Jialing KUANG3, Nanqi WANG1, Yuanmei ZUO1( ) |
1. College of Resources and Environmental Sciences, State Key Laboratory of Nutrient Use and Management, National Academy of Agriculture Green Development, China Agricultural University, Beijing 100193, China 2. College of Resources and Environmental Sciences, Southwest University, Chongqing 400715, China 3. Yunnan ICL YTH Phosphate Research and Technology Co., Ltd., Kunming 650228, China |
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Abstract ● Continuous cropping obstacles (CCOs) cause, on average, 22% reduction in crop production, seriously threatening sustainable agricultural development. ● Changes in the soil ecological environment are an essential and easily overlooked cause of CCOs. ● Studying CCOs from the perspective of the soil microbial food web may provide new approaches for explaining the formation mechanism of CCOs and controlling soilborne pathogens. ● Not all continuous cropping systems have CCOs, and some systems may enrich beneficial microorganisms to form healthy and disease-suppressive soil. Due to the increasing global population and limited land resources, continuous cropping has become common. However, after a few years of continuous cropping, obstacles often arise that cause soil degeneration, decreased crop yield and quality, and increased disease incidence, resulting in significant economic losses. It is essential to understand the causes and mitigation mechanisms of continuous cropping obstacles (CCOs) and then develop appropriate methods to overcome them. This review systematically summarizes the causes and mitigation measures of soil degradation in continuous cropping through a meta-analysis. It was concluded that not all continuous cropping systems are prone to CCOs. Therefore, it is necessary to grasp the principles governing the occurrence of diseases caused by soilborne pathogens in different cropping systems, consider plant–soil-organisms interactions as a system, scientifically regulate the physical and chemical properties of soils from a systems perspective, and then regulate the structure of microbial food webs in the soil to achieve a reduction in diseases caused by soilborne pathogens and increase crop yield ultimately. This review provides reference data and guidance for addressing this fundamental problem.
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Continuous cropping obstacles
rhizosphere regulation
soil microecological environment
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Corresponding Author(s):
Yuanmei ZUO
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Just Accepted Date: 25 January 2024
Online First Date: 28 February 2024
Issue Date: 13 June 2024
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|
| 1 |
Y, Chen J, Du Y, Li H, Tang Z, Yin L, Yang X Ding . Evolutions and managements of soil microbial community structure drove by continuous cropping. Frontiers in Microbiology, 2022, 13: 839494
https://doi.org/10.3389/fmicb.2022.839494
|
| 2 |
Z H, Pervaiz J, Iqbal Q, Zhang D, Chen H, Wei M Saleem . Continuous cropping alters multiple biotic and abiotic indicators of soil health. Soil Systems, 2020, 4(4): 59
https://doi.org/10.3390/soilsystems4040059
|
| 3 |
D L Sparks . Advances in Agronomy. Elsevier, 2023
|
| 4 |
Ul Haq M, Zeeshan J, Yu G, Yao H, Yang H A, Iqbal H, Tahir H, Cui Y, Liu Y Wu . A systematic review on the continuous cropping obstacles and control strategies in medicinal plants. International Journal of Molecular Sciences, 2023, 24(15): 12470
https://doi.org/10.3390/ijms241512470
|
| 5 |
M, Xia W, Zhong L S, Ouyang Z, Zhang Z Zhang . Research status of continuous cropping obstacles in China from 1989 to 2018: based on bibliometric analysis and knowledge mapping of CNKI. Journal of Agriculture, 2021, 11(3): 46−54 (in Chinese)
|
| 6 |
Neemisha. Role of soil organisms in maintaining soil health, ecosystem functioning, and sustaining agricultural production. In: Giri B, Varma A, eds. Soil Health. Springer, 2020, 313–335
|
| 7 |
J, Milkereit D, Geisseler P, Lazicki M L, Settles B P, Durbin-Johnson A Hodson . Interactions between nitrogen availability, bacterial communities, and nematode indicators of soil food web function in response to organic amendments. Applied Soil Ecology, 2021, 157: 103767
https://doi.org/10.1016/j.apsoil.2020.103767
|
| 8 |
J, Wang L, Wu H, Tantai M U, Khan P, Letuma H, Wu S, Zhang T, Chen S, Lin W Lin . Properties of bacterial community in the rhizosphere soils of Achyranthes bidentata tolerant to consecutive monoculture. Plant Growth Regulation, 2019, 89(2): 167–178
https://doi.org/10.1007/s10725-019-00523-0
|
| 9 |
J M, Raaijmakers M Mazzola . Soil immune responses. Science, 2016, 352(6292): 1392–1393
https://doi.org/10.1126/science.aaf3252
|
| 10 |
Z, Liu J, Liu Z, Yu Y, Li X, Hu H, Gu L, Li J, Jin X, Liu G Wang . Archaeal communities perform an important role in maintaining microbial stability under long term continuous cropping systems. Science of the Total Environment, 2022, 838: 156413
https://doi.org/10.1016/j.scitotenv.2022.156413
|
| 11 |
C, Yin Vargas J M, Casa D C, Schlatter C H, Hagerty S H, Hulbert T C Paulitz . Rhizosphere community selection reveals bacteria associated with reduced root disease. Microbiome, 2021, 9(1): 86
https://doi.org/10.1186/s40168-020-00997-5
|
| 12 |
M I, Hamid M, Hussain Y, Wu X, Zhang M, Xiang X Liu . Successive soybean-monoculture cropping assembles rhizosphere microbial communities for the soil suppression of soybean cyst nematode. FEMS Microbiology Ecology, 2017, 93(1): fiw222
https://doi.org/10.1093/femsec/fiw222
|
| 13 |
L V, Hedges J, Gurevitch P S Curtis . The meta-analysis of response ratios in experimental ecology. Ecology, 1999, 80(4): 1150–1156
https://doi.org/10.1890/0012-9658(1999)080[1150:TMAORR]2.0.CO;2
|
| 14 |
W Viechtbauer . Conducting meta-analyses in R with the metafor package. Journal of Statistical Software, 2010, 36(3): 1–43
https://doi.org/10.18637/jss.v036.i03
|
| 15 |
Z, Zhang Y, Liu L, Yuan W, Ewald Kleunen M van . Effect of allelopathy on plant performance: a meta-analysis. Ecology Letters, 2021, 24(2): 348–362
https://doi.org/10.1111/ele.13627
|
| 16 |
S, Balduzzi G, Rücker G Schwarzer . How to perform a meta-analysis with R: a practical tutorial. Evidence-Based Mental Health, 2019, 22(4): 153–160
https://doi.org/10.1136/ebmental-2019-300117
|
| 17 |
R A M, Villanueva Z J Chen . ggplot2—Elegant graphics for data analysis (2nd edition). Measurement: Interdisciplinary Research and Perspectives, 2019, 17(3): 160–167
|
| 18 |
Z, Zhou C, Wang Y Luo . Meta-analysis of the impacts of global change factors on soil microbial diversity and functionality. Nature Communications, 2020, 11(1): 3072
https://doi.org/10.1038/s41467-020-16881-7
|
| 19 |
J M Perkel . The software that powers scientific illustration. Nature, 2020, 582(7810): 137–138
https://doi.org/10.1038/d41586-020-01404-7
|
| 20 |
TLi T, Yang L. Overcoming continuous cropping obstacles—The difficult problem. Scientia Agricultura Sinica, 2016, 49(05): 916−918 (in Chinese)
|
| 21 |
J H, Guo X J, Liu Y, Zhang J L, Shen W X, Han W F, Zhang P, Christie K W T, Goulding P M, Vitousek F S Zhang . Significant acidification in major chinese croplands. Science, 2010, 327(5968): 1008–1010
https://doi.org/10.1126/science.1182570
|
| 22 |
H, Zhu C, Chen C, Xu Q, Zhu D Huang . Effects of soil acidification and liming on the phytoavailability of cadmium in paddy soils of central subtropical China. Environmental Pollution, 2016, 219: 99–106
https://doi.org/10.1016/j.envpol.2016.10.043
|
| 23 |
A, Kunhikrishnan R, Thangarajan N S, Bolan Y, Xu S, Mandal D B, Gleeson B, Seshadri M, Zaman L, Barton C, Tang J, Luo R, Dalal W, Ding M B, Kirkham R Naidu . Functional relationships of soil acidification, liming, and greenhouse gas flux. In: Sparks D L, ed. Advances in Agronomy. Elsevier, 2016, 139: 1–71
|
| 24 |
R Y, Shi N, Ni J N, Nkoh Y, Dong W R, Zhao X Y, Pan J Y, Li R K, Xu W Qian . Biochar retards Al toxicity to maize (Zea mays L.) during soil acidification: the effects and mechanisms. Science of the Total Environment, 2020, 719: 137448
https://doi.org/10.1016/j.scitotenv.2020.137448
|
| 25 |
C, Meng D, Tian H, Zeng Z, Li C, Yi S Niu . Global soil acidification impacts on belowground processes. Environmental Research Letters, 2019, 14(7): 074003
https://doi.org/10.1088/1748-9326/ab239c
|
| 26 |
D S, Yadav B, Jaiswal M, Gautam M Agrawal . Soil acidification and its impact on plants//plant responses to soil pollution. In: Singh P, Singh S K, Prasad S M, eds. Plant Responses to Soil Pollution. Springer, 2020, 1–26
|
| 27 |
T, Han A, Cai K, Liu J, Huang B, Wang D, Li M, Qaswar G, Feng H Zhang . The links between potassium availability and soil exchangeable calcium, magnesium, and aluminum are mediated by lime in acidic soil. Journal of Soils and Sediments, 2019, 19(3): 1382–1392
https://doi.org/10.1007/s11368-018-2145-6
|
| 28 |
S, Tyagi R Paudel . Effect of different pH on the growth and sporulation of Fusarium oxysporum: the causal organism of wilt disease of tomato. In: International Congress on “Agriculture, Forestry, Horticulture, Aquaculture, Animal Sciences, Food Technology, Biodiversity and Climate Change Sustainable Approaches” (AFHAFBC-2014), New Delhi. International Journal of Basic and Applied Biology, 2014, 2(1): 103–106
|
| 29 |
C, Hua C, Li Y, Jiang M, Huang V M, Williamson C Wang . Response of soybean cyst nematode (Heterodera glycines) and root-knot nematodes (Meloidogyne spp.) to gradients of pH and inorganic salts. Plant and Soil, 2020, 455(1–2): 305–318
https://doi.org/10.1007/s11104-020-04677-z
|
| 30 |
Molin S J, Dal P R, Ernani J M Gerber . Soil acidification and nitrogen release following application of nitrogen fertilizers. Communications in Soil Science and Plant Analysis, 2020, 51(20): 2551–2558
https://doi.org/10.1080/00103624.2020.1845347
|
| 31 |
Z, Weng G, Li P, Sale C Tang . Application of calcium nitrate with phosphorus promotes rhizosphere alkalization in acid subsoil. European Journal of Soil Science, 2022, 73(1): e13153
https://doi.org/10.1111/ejss.13153
|
| 32 |
S, Kulkarni A Goswami . Effect of Excess Fertilizers and Nutrients: A Review on Impact on Plants and Human Population. In: International Conference on Sustainable Computing in Science, Technology and Management, Jaipur. Elsevier Social Science Research Network, 2019, 2094–2099
|
| 33 |
Bhatt M, Kumar R, Labanya H C Joshi . Influence of long-term chemical fertilizers and organic manures on soil fertility—A review. Universal Journal of Agricultural Research, 2019, 7(5): 177–188
https://doi.org/10.13189/ujar.2019.070502
|
| 34 |
Y, Xu J, Li X Yin . Continuous cropping affects gross nitrogen transformations in subtropical acidic soils under greenhouse cultivation. Journal of Soil Science and Plant Nutrition, 2020, 20(4): 1596–1604
https://doi.org/10.1007/s42729-020-00231-z
|
| 35 |
W, Ma S, Tang Z, Dengzeng D, Zhang T, Zhang X Ma . Root exudates contribute to belowground ecosystem hotspots: a review. Frontiers in Microbiology, 2022, 13: 937940
https://doi.org/10.3389/fmicb.2022.937940
|
| 36 |
I, Bouhaouel A, Gfeller M L, Fauconnier S, Rezgui H S, Amara P Jardin . Allelopathic and autotoxicity effects of barley (Hordeum vulgare L. ssp. vulgare) root exudates. BioControl, 2015, 60(3): 425–436
https://doi.org/10.1007/s10526-014-9634-3
|
| 37 |
N, Serra R, Shanmuganathan C Becker . Allelopathy in rice: a story of momilactones, kin recognition, and weed management. Journal of Experimental Botany, 2021, 72(11): 4022–4037
https://doi.org/10.1093/jxb/erab084
|
| 38 |
N X, Wan J C, Yuan W, He W J, Long Q, Zhang S M, Zhou S L Zheng . Autotoxicity of water extracts from different organs of potato. Journal of Zhejiang University (Agriculture and Life Sciences), 2016, 42(4): 411–418
|
| 39 |
C H, Kong S Z, Zhang Y H, Li Z C, Xia X F, Yang S J, Meiners P Wang . Plant neighbor detection and allelochemical response are driven by root-secreted signaling chemicals. Nature Communications, 2018, 9(1): 3867
https://doi.org/10.1038/s41467-018-06429-1
|
| 40 |
N, Wang C, Kong P, Wang S J Meiners . Root exudate signals in plant-plant interactions. Plant, Cell & Environment, 2021, 44(4): 1044–1058
https://doi.org/10.1111/pce.13892
|
| 41 |
X, Li C, Ding K, Hua T, Zhang Y, Zhang L, Zhao Y, Yang J, Liu X Wang . Soil sickness of peanuts is attributable to modifications in soil microbes induced by peanut root exudates rather than to direct allelopathy. Soil Biology & Biochemistry, 2014, 78: 149–159
https://doi.org/10.1016/j.soilbio.2014.07.019
|
| 42 |
Y Q, Huang X R, Han J F, Yang C H, Liang X M Zhan . Autotoxicity of peanut and identification of phytotoxic substances in rhizosphere soil. Allelopathy Journal, 2013, 31(2): 297–308
|
| 43 |
X, Ren X, He Z, Zhang Z, Yan H, Jin X, Li B Qin . Isolation, identification, and autotoxicity effect of allelochemicals from rhizosphere soils of flue-cured tobacco. Journal of Agricultural and Food Chemistry, 2015, 63(41): 8975–8980
https://doi.org/10.1021/acs.jafc.5b03086
|
| 44 |
F, Cheng M, Ali C, Liu R, Deng Z Cheng . Garlic allelochemical diallyl disulfide alleviates autotoxicity in the root exudates caused by long-term continuous cropping of tomato. Journal of Agricultural and Food Chemistry, 2020, 68(42): 11684–11693
https://doi.org/10.1021/acs.jafc.0c03894
|
| 45 |
X, Huang Z, Bie Y Huang . Identification of autotoxins in rhizosphere soils under the continuous cropping of cowpea. Allelopathy Journal, 2010, 25(2): 383–392
|
| 46 |
P, Chen Y, Wang Q, Liu Y, Zhang X, Li H, Li W Li . Phase changes of continuous cropping obstacles in strawberry (Fragaria × ananassa Duch.) production. Applied Soil Ecology, 2020, 155: 103626
https://doi.org/10.1016/j.apsoil.2020.103626
|
| 47 |
Y, Zhang Z, Xie F, Wang Z, Cheng Y, Liu Z, Li G, Wang Z Zhang . Genome-wide identification and characteristics analysis of melon (Cucumis melo L.) MYB transcription factors and their responses to autotoxicity and saline-alkali stress. Tropical Plant Biology, 2022, 15(1): 93–109
https://doi.org/10.1007/s12042-021-09306-2
|
| 48 |
H, Wu L, Wu Q, Zhu J, Wang X, Qin J, Xu L, Kong J, Chen S, Lin Khan M, Umar H, Amjad W Lin . The role of organic acids on microbial deterioration in the Radix pseudostellariae rhizosphere under continuous monoculture regimes. Scientific Reports, 2017, 7(1): 3497
https://doi.org/10.1038/s41598-017-03793-8
|
| 49 |
L, Bao Y, Liu Y, Ding J, Shang Y, Wei Y, Tan F Zi . Interactions between phenolic acids and microorganisms in rhizospheric soil from continuous cropping of Panax notoginseng. Frontiers in Microbiology, 2022, 13: 791603
|
| 50 |
R, Wang J, Liu W, Jiang P, Ji Y Li . Metabolomics and Microbiomics Reveal Impacts of Rhizosphere Metabolites on Alfalfa Continuous Cropping. Frontiers in Microbiology, 2022, 13: 833968
https://doi.org/10.3389/fmicb.2022.833968
|
| 51 |
X Y, Zhang S L, Shi X L, Li C N, Li C M, Zhang A, Yun W J, Kang G L Yin . Effects of autotoxicity on alfalfa (Medicago sativa): seed germination, oxidative damage and lipid peroxidation of seedlings. Agronomy, 2021, 11(6): 1027
https://doi.org/10.3390/agronomy11061027
|
| 52 |
F, Golzardi N Aghamollaei . Seed treatment to overcome autotoxicity of forage Rape. Environmental and Agricultural Sciences, 2017, 2: 17–24
|
| 53 |
Y, Yuan J, Zuo H, Zhang M, Zu S Liu . The Chinese medicinal plants rhizosphere: metabolites, microorganisms, and interaction. Rhizosphere, 2022, 22: 100540
https://doi.org/10.1016/j.rhisph.2022.100540
|
| 54 |
P, Li X, Wang Y, Li H, Wang F, Liang C Dai . The contents of phenolic acids in continuous cropping peanut and their allelopathy. Acta Ecologica Sinica, 2010, 30(8): 2128−2134 (in Chinese)
|
| 55 |
S, Chen B, Zhou S, Lin X, Li X Ye . Accumulation of cinnamic acid and vanillin in eggplant root exudates and the relationship with continuous cropping obstacle. African Journal of Biotechnology, 2011, 10(14): 2659–2665
https://doi.org/10.5897/AJB10.1338
|
| 56 |
S, Zhang Y, Li C, Kong X Xu . Interference of allelopathic wheat with different weeds. Pest Management Science, 2016, 72(1): 172–178
https://doi.org/10.1002/ps.3985
|
| 57 |
Y, Li Z, Xia C Kong . Allelobiosis in the interference of allelopathic wheat with weeds. Pest Management Science, 2016, 72(11): 2146–2153
https://doi.org/10.1002/ps.4246
|
| 58 |
Y, Feng H, Zhang X, Song T, Ge J, Zhu C, Zhou K, Cobb X, Yan R, Ruan P Cheng . Microalgae as a potential conditioner for continuous cropping obstacles for taro (Colocasia esculenta L. Schott) production. Journal of Cleaner Production, 2022, 369: 133356
https://doi.org/10.1016/j.jclepro.2022.133356
|
| 59 |
X, Gu N, Yang Y, Zhao W, Liu T Li . Long-term watermelon continuous cropping leads to drastic shifts in soil bacterial and fungal community composition across gravel mulch fields. BMC Microbiology, 2022, 22(1): 189
https://doi.org/10.1186/s12866-022-02601-2
|
| 60 |
F, Wang X, Wang N Song . Biochar and vermicompost improve the soil properties and the yield and quality of cucumber (Cucumis sativus L.) grown in plastic shed soil continuously cropped for different years. Agriculture, Ecosystems & Environment, 2021, 315: 107425
https://doi.org/10.1016/j.agee.2021.107425
|
| 61 |
W, Xiong Q, Zhao J, Zhao W, Xun R, Li R, Zhang H, Wu Q Shen . Different continuous cropping spans significantly affect microbial community membership and structure in a vanilla-grown soil as revealed by deep pyrosequencing. Microbial Ecology, 2015, 70(1): 209–218
https://doi.org/10.1007/s00248-014-0516-0
|
| 62 |
Y, Zhao W, Fu C, Hu G, Chen Z, Xiao Y, Chen Z, Wang H Cheng . Variation of rhizosphere microbial community in continuous mono-maize seed production. Scientific Reports, 2021, 11(1): 1544
https://doi.org/10.1038/s41598-021-81228-1
|
| 63 |
Z, Pang F, Dong Q, Liu W, Lin C, Hu Z Yuan . Soil metagenomics reveals effects of continuous sugarcane cropping on the structure and functional pathway of rhizospheric microbial community. Frontiers in Microbiology, 2021, 12: 627569
https://doi.org/10.3389/fmicb.2021.627569
|
| 64 |
N, Liu C, Shao H, Sun Z, Liu Y, Guan L, Wu L, Zhang X, Pan Z, Zhang Y, Zhang B Zhang . Arbuscular mycorrhizal fungi biofertilizer improves American ginseng (Panax quinquefolius L.) growth under the continuous cropping regime. Geoderma, 2020, 363: 114155
https://doi.org/10.1016/j.geoderma.2019.114155
|
| 65 |
L, Dong J, Xu G, Feng X, Li S Chen . Soil bacterial and fungal community dynamics in relation to Panax notoginseng death rate in a continuous cropping system. Scientific Reports, 2016, 6(1): 31802
https://doi.org/10.1038/srep31802
|
| 66 |
F, Xia L, Wang J, Chen M, Fu G, Wang Y, Yan L Cui . Variations of microbial community in Aconitum carmichaeli Debx. rhizosphere soilin a short-term continuous cropping system. Journal of Microbiology, 2021, 59(5): 481–490
https://doi.org/10.1007/s12275-021-0515-z
|
| 67 |
W, Wei Y, Xu S, Li L, Zhu J Song . Developing suppressive soil for root diseases of soybean with continuous long-term cropping of soybean in black soil of Northeast China. Acta Agriculturæ Scandinavica. Section B: Soil and Plant Science, 2015, 65(3): 279–285
https://doi.org/10.1080/09064710.2014.992941
|
| 68 |
Allende-Molar R. Role of 2,4-Diacetylphloroglucinol Producing Pseudomonas fluorescens in the Suppression of Take-all and Pythium Root Rot of Wheat. Dissertation for the Doctoral Degree. Pullman: Washington State University, 2006
|
| 69 |
Y S, Kwak D M Weller . Take-all of wheat and natural disease suppression: a review. Plant Pathology Journal, 2013, 29(2): 125–135
https://doi.org/10.5423/PPJ.SI.07.2012.0112
|
| 70 |
S, Chng M G, Cromey S L, Dodd A, Stewart R C, Butler M V Jaspers . Take-all decline in New Zealand wheat soils and the microorganisms associated with the potential mechanisms of disease suppression. Plant and Soil, 2015, 397(1–2): 239–259
https://doi.org/10.1007/s11104-015-2620-4
|
| 71 |
Y, Pan X, Ji F, Zhou X, Li X, Zhang Q, Peng J Zhang . Long Term monocropping effects tobacco yield by regulating rhizosphere allelochemicals and microbial community. Journal of Biobased Materials and Bioenergy, 2023, 17(1): 65–78
https://doi.org/10.1166/jbmb.2023.2244
|
| 72 |
W F, Schillinger T C Paulitz . Natural suppression of Rhizoctonia bare patch in a long-term no-till cropping systems experiment. Plant Disease, 2014, 98(3): 389–394
https://doi.org/10.1094/PDIS-04-13-0420-RE
|
| 73 |
Z, Shen C R, Penton N, Lv C, Xue Y, Ruan R, Li Q Shen . Banana Fusarium wilt disease incidence is influenced by shifts of soil microbial communities under different monoculture spans. Microbial Ecology, 2018, 75(3): 739–750
https://doi.org/10.1007/s00248-017-1052-5
|
| 74 |
Z, Wei D Yu . Analysis of the succession of structure of the bacteria community in soil from long-term continuous cotton cropping in Xinjiang using high-throughput sequencing. Archives of Microbiology, 2018, 200(4): 653–662
https://doi.org/10.1007/s00203-018-1476-4
|
| 75 |
D M, Weller J M, Raaijmakers B B M, Gardener L S Thomashow . Microbial populations responsible for specific soil suppressiveness to plant pathogens. Annual Review of Phytopathology, 2002, 40(1): 309–348
https://doi.org/10.1146/annurev.phyto.40.030402.110010
|
| 76 |
J D G, Jones J L Dangl . The plant immune system. Nature, 2006, 444(7117): 323–329
https://doi.org/10.1038/nature05286
|
| 77 |
A, Onet L C, Dincă P, Grenni V, Laslo A C, Teusdea D L, Vasile R E, Enescu V E Crisan . Biological indicators for evaluating soil quality improvement in a soil degraded by erosion processes. Journal of Soils and Sediments, 2019, 19(5): 2393–2404
https://doi.org/10.1007/s11368-018-02236-9
|
| 78 |
W, Geng Y, Ma Y, Zhang F Zhu . Research progress in soil health regulation technology for protected agriculture. Chinese Journal of Eco-Agriculture, 2022, 30(12): 1973−1984 (in Chinese)
|
| 79 |
Bruggen A H C, Van K, Sharma E, Kaku S, Karfopoulos V V, Zelenev W J Blok . Soil health indicators and Fusarium wilt suppression in organically and conventionally managed greenhouse soils. Applied Soil Ecology, 2015, 86: 192–201
https://doi.org/10.1016/j.apsoil.2014.10.014
|
| 80 |
F, Pan X, Han N, Li J, Yan Y Xu . Effect of organic amendment amount on soil nematode community structure and metabolic footprints in soybean phase of a soybean-maize rotation on Mollisols. Pedosphere, 2020, 30(4): 544–554
https://doi.org/10.1016/S1002-0160(17)60432-6
|
| 81 |
S L, Cappelli L A, Domeignoz-Horta V, Loaiza A L Laine . Plant biodiversity promotes sustainable agriculture directly and via belowground effects. Trends in Plant Science, 2022, 27(7): 674–687
https://doi.org/10.1016/j.tplants.2022.02.003
|
| 82 |
X, Yuan S, Hong W, Xiong W, Raza Z, Shen B, Wang R, Li Y, Ruan Q, Shen F Dini-Andreote . Development of fungal-mediated soil suppressiveness against Fusarium wilt disease via plant residue manipulation. Microbiome, 2021, 9(1): 200
https://doi.org/10.1186/s40168-021-01133-7
|
| 83 |
Y, Cao C, Wu L, Wang M, Chen H, Zhao X, Bian Y, Chen L Xia . Rotation of broad bean improves the soil quality of facility green house. Legume Research, 2017, 40(4): 710–715
https://doi.org/10.18805/lr.v0i0.8412
|
| 84 |
J, Dai W, Qiu N, Wang T, Wang H, Nakanishi Y Zuo . From Leguminosae/Gramineae intercropping systems to see benefits of intercropping on iron nutrition. Frontiers in Plant Science, 2019, 10: 605
https://doi.org/10.3389/fpls.2019.00605
|
| 85 |
Y, Zuo F, Zhang X, Li Y Cao . Studies on the improvement in iron nutrition of peanut by intercropping with maize on a calcareous soil. Plant and Soil, 2000, 220(1/2): 13–25
https://doi.org/10.1023/A:1004724219988
|
| 86 |
Medeiros E V, de Alcantara Notaro K, de Barros J A, de G P, Duda Cássia Henriques dos Santos Moraes M, de Queiroz Ambrósio M M, de A M P, Negreiros Júnior R Sales . Soils from intercropped fields have a higher capacity to suppress black root rot in cassava, caused by Scytalidium lignicola. Journal of Phytopathology, 2019, 167(4): 209−217
|
| 87 |
Y, Chen M, Bonkowski Y, Shen B S, Griffiths Y, Jiang X, Wang B Sun . Root ethylene mediates rhizosphere microbial community reconstruction when chemically detecting cyanide produced by neighbouring plants. Microbiome, 2020, 8(1): 4
https://doi.org/10.1186/s40168-019-0775-6
|
| 88 |
P P Reddy . Sustainable Intensification of Crop Production. Singapore: Springer, 2016
|
| 89 |
C, He J, Niu C, Xu S, Han W, Bai Q, Song Y P, Dang H Zhang . Effect of conservation tillage on crop yield and soil organic carbon in Northeast China: a meta-analysis. Soil Use and Management, 2022, 38(2): 1146–1161
https://doi.org/10.1111/sum.12784
|
| 90 |
X, Shen L, Wang Y, Wang M, Wang D, Yang J, Zhao G, Li Q, Xuan L Wang . Progress on the effects of conservation tillage on soil aggregates, microbes, and nematode communities. Journal of Agricultural Resources and Environment, 2020, 37(3): 361–370
|
| 91 |
X, Sun Z, Xu J, Xie V, Hesselberg-Thomsen T, Tan D, Zheng M L, Strube A, Dragoš Q, Shen R, Zhang Á T Kovács . Bacillus velezensis stimulates resident rhizosphere Pseudomonas stutzeri for plant health through metabolic interactions. ISME Journal, 2022, 16(3): 774–787
https://doi.org/10.1038/s41396-021-01125-3
|
| 92 |
P, Hedden V Sponsel . A century of Gibberellin research. Journal of Plant Growth Regulation, 2015, 34(4): 740–760
https://doi.org/10.1007/s00344-015-9546-1
|
| 93 |
N, Khan A, Bano J A Curá . Role of beneficial microorganisms and salicylic acid in improving rainfed agriculture and future food safety. Microorganisms, 2020, 8(7): 1018
https://doi.org/10.3390/microorganisms8071018
|
| 94 |
C, Zamioudis C M J Pieterse . Modulation of host immunity by beneficial microbes. Molecular Plant-Microbe Interactions, 2012, 25(2): 139–150
https://doi.org/10.1094/MPMI-06-11-0179
|
| 95 |
C, Tao R, Li W, Xiong Z, Shen S, Liu B, Wang Y, Ruan S, Geisen Q, Shen G A Kowalchuk . Bio-organic fertilizers stimulate indigenous soil Pseudomonas populations to enhance plant disease suppression. Microbiome, 2020, 8(1): 137
https://doi.org/10.1186/s40168-020-00892-z
|
| 96 |
Z, Wei X, Yang S, Yin Q, Shen W, Ran Y Xu . Efficacy of Bacillus-fortified organic fertiliser in controlling bacterial wilt of tomato in the field. Applied Soil Ecology, 2011, 48(2): 152–159
https://doi.org/10.1016/j.apsoil.2011.03.013
|
| 97 |
S, Yuan L, Wang K, Wu J, Shi M, Wang X, Yang Q, Shen B Shen . Evaluation of Bacillus-fortified organic fertilizer for controlling tobacco bacterial wilt in greenhouse and field experiments. Applied Soil Ecology, 2014, 75: 86–94
https://doi.org/10.1016/j.apsoil.2013.11.004
|
| 98 |
S F, Bender F, Conen Der Heijden M G A Van . Mycorrhizal effects on nutrient cycling, nutrient leaching and N2O production in experimental grassland. Soil Biology & Biochemistry, 2015, 80: 283–292
https://doi.org/10.1016/j.soilbio.2014.10.016
|
| 99 |
Wang H, Hao Z, Zhang X, Xie W, Chen B. Effect, mechanisms and application of arbuscular mycorrhizal fungi for biological control of Fusarium oxysporum-caused wilt: a review. Microbiology China, 2022, 49(7): 2819−2837 (in Chinese)
|
| 100 |
L, Dong X, Li C, Huang Q, Lu B, Li Y, Yao T, Liu Y Zuo . Reduced Meloidogyne incognita infection of tomato in the presence of castor and the involvement of fatty acids. Scientia Horticulturae, 2018, 237: 169–175
https://doi.org/10.1016/j.scienta.2018.03.066
|
| 101 |
Q, Lu T, Liu N, Wang Z, Dou K, Wang Y Zuo . Nematicidal effect of methyl palmitate and methyl stearate against Meloidogyne incognita in bananas. Journal of Agricultural and Food Chemistry, 2020, 68(24): 6502–6510
https://doi.org/10.1021/acs.jafc.0c00218
|
| 102 |
Q, Lu K, Wang Z, Dou T, Wang Y Zuo . Agro-industrial waste and a nematicidal substance therein (triethyl phosphate) are effective against Meloidogyne incognita of bananas. Industrial Crops and Products, 2023, 202: 117003
https://doi.org/10.1016/j.indcrop.2023.117003
|
| 103 |
Shen J, Bai Y, Wei Z, Chu C, Yuan L, Zhang L, Cui Z, Cong W, Zhang F. Rhizobiont: an interdisciplinary innovation and perspective for harmonizing resources, environment, and food security. Acta Pedologica Sinica, 2021, 58(4): 805−813 (in Chinese)
|
| 104 |
O, Topalović M, Hussain H Heuer . Plants and associated doil microbiota cooperatively suppress plant-parasitic nematodes. Frontiers in Microbiology, 2020, 11: 313
https://doi.org/10.3389/fmicb.2020.00313
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