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Frontiers of Agricultural Science and Engineering

ISSN 2095-7505

ISSN 2095-977X(Online)

CN 10-1204/S

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Front. Agr. Sci. Eng.    2024, Vol. 11 Issue (2) : 253-270    https://doi.org/10.15302/J-FASE-2024543
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.

Keywords Continuous cropping obstacles      rhizosphere regulation      soil microecological environment     
Corresponding Author(s): Yuanmei ZUO   
Just Accepted Date: 25 January 2024   Online First Date: 28 February 2024    Issue Date: 13 June 2024
 Cite this article:   
Kunguang WANG,Qiaofang LU,Zhechao DOU, et al. A review of research progress on continuous cropping obstacles[J]. Front. Agr. Sci. Eng. , 2024, 11(2): 253-270.
 URL:  
https://academic.hep.com.cn/fase/EN/10.15302/J-FASE-2024543
https://academic.hep.com.cn/fase/EN/Y2024/V11/I2/253
Fig.1  Overview of research on CCOs: (a) numbers of articles and citations related to CCOs published over time; (b) main research fields related to continuous cropping; and (c) proportion of studies on continuous cropping in different countries.
Fig.2  Distribution of the database on different crops. (a) National distribution of study sites included in the meta-analysis; (b) proportions of crop types in the continuous cropping database; (c) proportions of various crops in the continuous cropping database; (d) proportions of different causes of continuous cropping obstacles.
Fig.3  Effects of continuous cropping on the physicochemical properties of soils. (a) Response ratio (RR) of physicochemical properties; (b) RR of acidification or alkalization; (c) meta-regression analysis of acidification degree in different continuous cropping years. TN, total nitrogen; AN, available nitrogen; NH4+, ammonia nitrogen; NO3, nitrate nitrogen; TP, total phosphorus; AP, available phosphorus; TK, total potassium; AK, available potassium; OM, organic matter; TC, total carbon; C:N, carbon-to-nitrogen ratio; EC, cation exchange capacity; pH–, observations of acidified soil under continuous cropping; and pH+, observations on alkalized soil under continuous cropping. Red and green dots indicate studies on acidification and soil alkalinization caused by continuous cropping. The dashed line indicates mean RR = 0. Error bars represent 95% confidence intervals (CIs); numbers at the top and bottom of the CI are the numbers of observations. If a 95% CI did not overlap zero, the effect of continuous cropping on the variable was considered significant at various levels (?P < 0.1; *P < 0.05; **P < 0.001; and ***P < 0.0001).
Crop typesCropsAllelochemicals and performanceSources
Food cropsBarleyBarley root exudates inhibit root development in barley seedlings and weeds[36]
RiceSome specialized metabolites found in rice straw have been proposed to be autotoxic: phenolic acids (e.g., ferulic acid (FA), o-hydroxy phenylacetic acid and p-coumaric acid), flavonoids, and terpenoids[37]
PotatoWater extracts from different organs of the potato exhibited an apparent inhibitory effect on the growth of the potato, and the extracts from the stem and leaves had a significant inhibitory effect on the height of the potato; the root extracts significantly inhibited the number of branches and stem diameter[38]
WheatDIMBOA is a specific allelopathic substance of wheat and other grass plants and plays a vital role in antibacterial, insect-resistant, and weed suppression[39,40]
Economic cropsPeanutContinuous cropping for 5 years; accumulation of phenolic acids in peanut rhizosphere; destruction of soil microbial community. Continuous cropping for four years; substances in peanut root exudates (e.g., myristic acid, palmitic acid, stearic acid, p-hydroxybenzoic acid, vanillic acid and coumaric acid) inhibited peanut growth[41,42]
Tobaccoβ-cembrenediol, di-n-hexyl phthalate, and bis(2-propylheptyl) phthalate showed observable autotoxic activities on tobacco[43]
Vegetable cropsTomatoContinuous cropping for 7 years; accumulation of root exudate fatty acids in soil; tomato growth inhibition[44]
CowpeaContinuous cropping for 8 years; accumulation of organic acids (e.g., cinnamic and phenylacetic acid) in soil inhibited cowpea growth[45]
Fruit cropsStrawberryContinuous cropping for 12 years; accumulation of phenolic acids such as p-hydroxybenzoic acid in soil[46]
MelonThe content of chlorophyll and carotenoid, photosynthetic rate, stomatal conductance, water-use efficiency, and transpiration rate decreased significantly in melon seedlings under autotoxicity[47]
Medicinal cropsPseudostellaria heterophyllaContinuous cropping for 3 years; accumulation of soil tartaric acid, succinic acid, and other organic acids; imbalance of soil microbial community[48]
Panax notoginsengContinuous cropping for 3 years; accumulation of soil phenolic acids; imbalance of microbial community[49]
Forage cropsAlfalfaRoot exudates and plant extracts negatively affect several traits related to germination and plant growth in the model legume Medicargo truncatula. Autotoxicity caused different oxidative stress strategies for the two alfalfa cultivars[50,51]
Forage rapeThe residues of cultivated rape leave adverse effects on future crops; the observed effects are a reduction in plant dry weight, height, number of tillers per plant, and grain yield[52]
Tab.1  Allelochemicals of different plants and their harmful effects on plants
Fig.4  Current status of research on the causes of continuous cropping obstacles. (a)The proportion of research on different biological communities in continuous cropping obstacles; (b) the number of studies on different numbers of biological communities (1 means studying only one community, 2 means studying the interaction of 2 communities, 3 means studying the interaction of 3 communities, and so forth); (c) microbial diversity index and community structure of bacteria and fungi in bulk soil and rhizosphere soil under continuous cropping. The dashed line indicates mean RR = 0. Error bars represent 95% CIs; numbers at the top and bottom of the CIs are the numbers of observations. If a 95% CI did not overlap zero, the effect of continuous cropping on the variable was considered significant at various levels (?P < 0.1; *P < 0.05; **P < 0.001; and ***P < 0.0001).
Fig.5  Effects of continuous cropping on crop growth and disease index. (a) Response ratio (RR) of crop growth-related indicators; (b) RR of crop yield; (c) RR of the disease index for different soilborne pathogens. The dashed line indicates mean RR = 0. Error bars represent 95% CIs; numbers close to the CI are the numbers of observations. If a 95% CI did not overlap zero, the effect of continuous cropping on the variable was considered significant at various levels (?P < 0.1; *P < 0.05; **P < 0.001; and ***P < 0.0001).
Incidence patternCropDiseaseContinuous cropping period and performanceSource
Persistent severeWatermelonUnknown21 years of continuous cropping changes soil physical and chemical properties and microbial community composition, thereby reducing watermelon yields[59]
CucumberUnknownDuring 20 years of continuous cropping, soil degradation caused cucumber yield and quality to continue to decrease[60]
VanillaStem rotDuring the 21 years of continuous cropping, stem rot became more serious yearly. Soil weakness and vanilla stem wilt disease after long-term continuous cropping can be attributed to the alteration of the soil microbial community membership and structure, i.e., the reduction of the beneficial microbes and the accumulation of the fungal pathogen[61]
MaizeBlightEar rotThe highest disease incidence of seedling blight and ear rot was 8.2% in 20 years of continuous cropping and 13% in 30 years, respectively[62]
SugarcaneUnknownContinuous cropping for 30 years changes microbial communities by changing soil physical and chemical properties, thereby causing crop yield reductions[63]
American ginsengPanax notoginsengAconitum carmichaeliRoot rotSevere diseases occur in short-term continuous cropping of such medicinal crops, but the impact of long-term continuous cropping on diseases is unknown[6466]
SoybeanRoot rotDuring 20 years of continuous cropping, harmful microorganisms decreased, beneficial microorganisms increased, and diseases were reduced[67]
Reduced in later stagesWheatTake-allWheat take-all disease is reduced in the late stage of continuous cropping. Pseudomonas fluorescens that produce the antibiotic 2,4-diacetylphloroglucinol are the major determinant of the suppressiveness of take-all[6870]
SoybeanUnknownDuring 13 years of continuous cropping, the abundance of archaea increased, and the abundance of harmful microorganisms decreased. Archaeal communities perform an important role in maintaining microbial stability under long-term continuous cropping systems[10]
SoybeanCyst nematodeContinuous cropping reduces the abundance of soil cyst nematodes by increasing the abundance of beneficial soil microorganisms[12]
TobaccoUnknownThe continuous cropping obstacles were severe in the first 5 years; however, after 15 years, the yield gradually recovered, and the soilborne pathogens were significantly inhibited[71]
WheatBare patchIn the 5th to 7th year of continuous cropping, the area of bare patches reaches a peak, starts to decrease in the 8th year, and approaches 0 in the 11th year[72]
Continuous fluctuationBananaWiltThe disease occurred seriously after 6 and 11 years of continuous cropping but was milder after 1 and 10 years[73]
CottonUnknownCropping is the leading cause of changes in the structure of the bacteria community; however, the new structure formed under the continued duress of long-term cotton cultivation, and the associated farming methods gradually stabilized after 10 years of repeated fluctuations[74]
Tab.2  Incidence patterns of disease caused by soilborne pathogens in continuous cropping soils
Fig.6  Effects of continuous cropping years on crop yield reduction. Blue dots indicate the effect value corresponding to each observation point; point size is proportional to its weight. The red line represents the fitting curve, and the shading represents the 95% CI.
Fig.7  Conceptual model of the effects and the regulation mechanisms of continuous cropping on plant growth, soil physical and chemical properties, and soil microbial communities and their interactions.
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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