A response of biomass and nutrient allocation to the combined effects of soil nutrient, arbuscular mycorrhizal, and root-knot nematode in cherry tomato

Introduction The biomass and nutrient allocation strategies in plants are fundamental for predicting carbon storage and mineral and nutrient cycles in terrestrial ecosystems. However, our knowledge regarding the effects of multiple environmental factors on biomass and nutrient allocation remains limited. Methods Here we manipulated soil composition (three levels), arbuscular mycorrhizal fungi inoculation (AMF, five levels), and root-knot nematode inoculation (RKN, two levels) using random block design to reveal the effects of these factors on biomass and nutrient allocation strategies of cherry tomato. Results and Discussion Our results showed that biomass and nutrient allocation were affected by soil composition, AMF and RKN individually or interactively. The biomass and nutrient allocation in cherry tomato shows different adaptation strategies responded to the joint action of three factors. The reduction of soil nutrients increased belowground biomass allocation, and aboveground nitrogen and phosphorus concentration. AMF colonization increased aboveground biomass allocation and reproductive investment and promoted aboveground nitrogen and phosphorus inputs. Cherry tomato can mitigate the stress of RKN infection by investing more biomass and nutrients into belowground organs. Our study showed that plants can adjust their survival strategies by changing biomass and nutrient allocation to adapt to variation in soil abiotic and biotic factors. These findings contribute to our understanding of the adaptive processes of plant biomass and nutrient allocation strategies under multiple environmental factors.

[1]  Xuhui Zhou,et al.  Global systematic review with meta-analysis shows that warming effects on terrestrial plant biomass allocation are influenced by precipitation and mycorrhizal association , 2022, Nature Communications.

[2]  L. Aragão,et al.  Direct evidence for phosphorus limitation on Amazon forest productivity , 2022, Nature.

[3]  D. Kleijn,et al.  Potential tradeoffs between effects of arbuscular mycorrhizal fungi inoculation, soil organic matter content and fertilizer application in raspberry production , 2022, PloS one.

[4]  S. Branco,et al.  Mechanisms of stress tolerance and their effects on the ecology and evolution of mycorrhizal fungi. , 2022, The New phytologist.

[5]  R. Standish,et al.  Ecological interactions among microbial functional guilds in the plant-soil system and implications for ecosystem function , 2022, Plant and Soil.

[6]  Zhanhui Tang,et al.  Nutrients Regulate the Effects of Arbuscular Mycorrhizal Fungi on the Growth and Reproduction of Cherry Tomato , 2022, Frontiers in Microbiology.

[7]  Yongfei Bai,et al.  Contrasting effects of arbuscular mycorrhizal fungi on nitrogen uptake in Leymus chinensis and Cleistogenes squarrosa grasses, dominants of the Inner Mongolian steppe , 2022, Plant and Soil.

[8]  A. Kaur,et al.  Potential of vermicompost extract in enhancing the biomass and bioactive components along with mitigation of Meloidogyne incognita-induced stress in tomato , 2022, Environmental Science and Pollution Research.

[9]  F. Dijkstra,et al.  Carbon efficiency for nutrient acquisition (CENA) by plants: role of nutrient availability and microbial symbionts , 2022, Plant and Soil.

[10]  Fiona V. Jevon,et al.  Tree biomass allocation differs by mycorrhizal association. , 2022, Ecology.

[11]  T. Thomas,et al.  Arbuscular Mycorrhizal Fungi Contribute to Phosphorous Uptake and Allocation Strategies of Solidago canadensis in a Phosphorous-Deficient Environment , 2022, Frontiers in Plant Science.

[12]  Y. Yao,et al.  Soil N enrichment mediates carbon allocation through respiration in a dominant grass during drought , 2022, Functional Ecology.

[13]  Qing‐Lin Chen,et al.  Calling for comprehensive explorations between soil invertebrates and arbuscular mycorrhizas. , 2022, Trends in plant science.

[14]  Muhammad Zeeshan,et al.  Mycorrhizal symbiosis promotes the nutrient content accumulation and affects the root exudates in maize , 2022, BMC plant biology.

[15]  A. Gojon Nitrogen acquisition in arbuscular mycorrhizal symbioses: A step into the real world. , 2022, Journal of plant physiology.

[16]  I. Bebre,et al.  Biomass Allocation and Leaf Morphology of Saplings Grown under Various Conditions of Light Availability and Competition Types , 2022, Plants.

[17]  T. Minkina,et al.  Plant Nutrition under Climate Change and Soil Carbon Sequestration , 2022, Sustainability.

[18]  P. Urwin,et al.  Disruption of carbon for nutrient exchange between potato and arbuscular mycorrhizal fungi enhanced cyst nematode fitness and host pest tolerance , 2022, The New phytologist.

[19]  S. J. Watts‐Williams,et al.  Arbuscular mycorrhizas increased tomato biomass and nutrition but did not affect local soil P availability or 16S bacterial community in the field. , 2022, Science of The Total Environment.

[20]  M. Pozo,et al.  An Updated Review on the Modulation of Carbon Partitioning and Allocation in Arbuscular Mycorrhizal Plants , 2021, Microorganisms.

[21]  Louis J Irving,et al.  Effects of Light, N and Defoliation on Biomass Allocation in Poa annua , 2021, Plants.

[22]  J. Garnier,et al.  Co-inoculation with arbuscular mycorrhizal fungi differing in carbon sink strength induces a synergistic effect in plant growth. , 2021, Journal of theoretical biology.

[23]  Wei Yan,et al.  Regulation of climate, soil and hydrological factors on macrophyte biomass allocation for coastal and inland wetlands in China , 2021 .

[24]  Jianping Tao,et al.  Reproductive strategies involving biomass allocation, reproductive phenology and seed production in two Asteraceae herbs growing in karst soil varying in depth and water availability , 2021, Plant Ecology.

[25]  D. Kleijn,et al.  Additive and synergistic effects of arbuscular mycorrhizal fungi, insect pollination and nutrient availability in a perennial fruit crop , 2021, bioRxiv.

[26]  Yusheng Yang,et al.  Nitrogen addition affects plant biomass allocation but not allometric relationships among different organs across the globe , 2020, Journal of Plant Ecology.

[27]  Wei Huang,et al.  Phenotypic plasticity in resource allocation to sexual trait of alligatorweed in wetland and terrestrial habitats. , 2020, The Science of the total environment.

[28]  Zhenqing Li,et al.  Effects of Water Addition on Reproductive Allocation of Dominant Plant Species in Inner Mongolia Steppe , 2020, Frontiers in Plant Science.

[29]  Yongfei Bai,et al.  Nitrogen‐induced acidification, not N‐nutrient, dominates suppressive N effects on arbuscular mycorrhizal fungi , 2020, Global Change Biology.

[30]  J. Cornelissen,et al.  AM Fungi Alleviate Phosphorus Limitation and Enhance Nutrient Competitiveness of Invasive Plants via Mycorrhizal Networks in Karst Areas , 2020, Frontiers in Ecology and Evolution.

[31]  J. Helder,et al.  Shifts in the Active Rhizobiome Paralleling Low Meloidogyne chitwoodi Densities in Fields Under Prolonged Organic Soil Management , 2020, Frontiers in Plant Science.

[32]  G. P. Cheplick Life-history variation in a native perennial grass (Tridens flavus): reproductive allocation, biomass partitioning, and allometry , 2020, Plant Ecology.

[33]  Min Liu,et al.  Nitrogen addition alters photosynthetic carbon fixation, allocation of photoassimilates, and carbon partitioning of Leymus chinensis in a temperate grassland of Inner Mongolia , 2019 .

[34]  I. Nou,et al.  Differential Expression Pattern of Lignin Biosynthetic Genes in Dwarf Cherry Tomato (Solanum lycopersicum var. cerasiforme) , 2019, Plant Breeding and Biotechnology.

[35]  R. Rellán-Álvarez,et al.  Inoculation with the mycorrhizal fungus Rhizophagus irregularis modulates the relationship between root growth and nutrient content in maize (Zea mays ssp. mays L.) , 2019, bioRxiv.

[36]  G. Glauser,et al.  Mycorrhizal fungi enhance nutrient uptake but disarm defences in plant roots, promoting plant-parasitic nematode populations , 2018, Soil Biology and Biochemistry.

[37]  E. Khaembah,et al.  Modelling Carbon Fluxes as an Aid to Understanding Perennial Ryegrass (Lolium perenne) Root Dynamics , 2018, Agronomy.

[38]  A. Sharma,et al.  Mycorrhizal colonization and phosphorus uptake in presence of PGPRs along with nematode infection , 2018, Symbiosis.

[39]  Benjamin L Turner,et al.  Responses of arbuscular mycorrhizal fungi to long-term inorganic and organic nutrient addition in a lowland tropical forest , 2018, The ISME Journal.

[40]  M. Westoby,et al.  Costs of acquiring phosphorus by vascular land plants: patterns and implications for plant coexistence. , 2018, The New phytologist.

[41]  M. Bagavathiannan,et al.  Impact of Combined Abiotic and Biotic Stresses on Plant Growth and Avenues for Crop Improvement by Exploiting Physio-morphological Traits , 2017, Front. Plant Sci..

[42]  Xuemei Wang,et al.  Plants adapted to nutrient limitation allocate less biomass into stems in an arid-hot grassland. , 2016, The New phytologist.

[43]  B. Panis,et al.  Arbuscular Mycorrhizal Fungi for the Biocontrol of Plant-Parasitic Nematodes: A Review of the Mechanisms Involved , 2015, Front. Microbiol..

[44]  William R. Wieder,et al.  Future productivity and carbon storage limited by terrestrial nutrient availability , 2015 .

[45]  M. Oesterheld,et al.  Screening of biomass production of cultivated forage grasses in response to mycorrhizal symbiosis under nutritional deficit conditions , 2014 .

[46]  P. D. Ruiter,et al.  Low investment in sexual reproduction threatens plants adapted to phosphorus limitation , 2013, Nature.

[47]  W. Parton,et al.  Patterns of new versus recycled primary production in the terrestrial biosphere , 2013, Proceedings of the National Academy of Sciences.

[48]  Jiangbo Xie,et al.  Distinguishing the Biomass Allocation Variance Resulting from Ontogenetic Drift or Acclimation to Soil Texture , 2012, PloS one.

[49]  D. Robinson,et al.  Root-shoot growth responses during interspecific competition quantified using allometric modelling. , 2010, Annals of botany.

[50]  S. Marhan,et al.  Low amounts of herbivory by root-knot nematodes affect microbial community dynamics and carbon allocation in the rhizosphere. , 2007, FEMS microbiology ecology.

[51]  Ü. Niinemets,et al.  Structural and physiological plasticity in response to light and nutrients in five temperate deciduous woody species of contrasting shade tolerance , 2007 .

[52]  I. Jakobsen,et al.  Functional diversity in arbuscular mycorrhizal (AM) symbioses: the contribution of the mycorrhizal P uptake pathway is not correlated with mycorrhizal responses in growth or total P uptake , 2004 .

[53]  H. Vierheilig,et al.  Variable carbon-sink strength of different Glomus mosseae strains colonizing barley roots , 2003 .

[54]  S. Gleeson,et al.  Root allocation and multiple nutrient limitation in the New Jersey Pinelands , 2003 .

[55]  D. Read,et al.  Mycorrhizal sink strength influences whole plant carbon balance of Trifolium repens L , 1998 .

[56]  D. Camen,et al.  Arbuscular mycorrhizal fungi in terms of symbiosis-parasitism continuum. , 2011, Communications in agricultural and applied biological sciences.

[57]  M. Walters,et al.  Optimal partitioning theory revisited: nonstructural carbohydrates dominate root mass responses to nitrogen. , 2010, Ecology.

[58]  J. Bever,et al.  Preferential allocation to beneficial symbiont with spatial structure maintains mycorrhizal mutualism. , 2009, Ecology letters.

[59]  H. Kesba,et al.  Interactions of three species of plant-parasitic nematodes with arbuscular mycorrhizal fungus, Glomus macrocarpus , and their effect on grape biochemistry , 2005 .