Skip to main content

Rhizosphere Carbon Turnover from Cradle to Grave: The Role of Microbe–Plant Interactions

  • Chapter
  • First Online:
Rhizosphere Biology: Interactions Between Microbes and Plants

Abstract

Plant roots are the primary source of organic materials that become stabilized in soil. While most root carbon is decomposed into carbon dioxide (CO2), the remainder typically undergoes multiple microbial transformations before it forms longer-term associations with soil minerals. However, the mechanisms by which roots affect microbial utilization of organic materials and subsequent mineral stabilization processes are poorly understood. It is well known that living roots increase the biomass of nearby microbial communities, and shape their population dynamics, diversity, and interactions. Community assembly and metabolic potential of these rhizosphere-enriched microorganisms are strongly influenced by the chemical composition of the exudates released by the host plant. The root exudate pools of plants undergo compositional changes as they grow, reproduce, and senesce. In the well-studied annual grasses Avena barbata and Avena fatua, this changing rhizosphere substrate pool and the “bloom” of organisms that respond are phylogenetically coherent; Acidobacteria and Actinobacteria are consistently depleted, whereas Alpha and Betaproteobacteria and Bacteroidetes are reliably enriched. When compared to non-root-influenced bulk soils, the responsive community is predictably less taxon-rich, yet forms more complex networks. These rhizosphere dynamics have significant downstream effects on the colonization of nearby soil minerals, degradation of prior season’s root litters, and the balance of stabilized versus lost soil carbon.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 149.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 199.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 199.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  • Austin EE, Wickings K, McDaniel MD, Robertson GP, Grandy AS (2017) Cover crop root contributions to soil carbon in a no-till corn bioenergy cropping system. GCB Bioenergy 9:1252–1263

    Article  CAS  Google Scholar 

  • Baetz U, Martinoia E (2014) Root exudates: the hidden part of plant defense. Trends Plant Sci 19:90–98

    Article  PubMed  CAS  Google Scholar 

  • Barnard RL, Osborne CA, Firestone MK (2013) Responses of soil bacterial and fungal communities to extreme desiccation and rewetting. ISME J 7:2229

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • Berg G (2009) Plant–microbe interactions promoting plant growth and health: perspectives for controlled use of microorganisms in agriculture. Appl Microbiol Biotechnol 84:11–18

    Article  PubMed  CAS  Google Scholar 

  • Bird JA, Herman DJ, Firestone MK (2011) Rhizosphere priming of soil organic matter by bacterial groups in a grassland soil. Soil Biol Biochem 43:718–725

    Article  CAS  Google Scholar 

  • Blagodatskaya E, Blagodatsky S, Anderson T-H, Kuzyakov Y (2014) Microbial growth and carbon use efficiency in the rhizosphere and root-free soil. PLoS One 9:e93282

    Article  PubMed  PubMed Central  Google Scholar 

  • Broeckling CD, Broz AK, Bergelson J, Manter DK, Vivanco JM (2008) Root exudates regulate soil fungal community composition and diversity. Appl Environ Microbiol 74:738–744

    Article  PubMed  CAS  Google Scholar 

  • Bulgarelli D, Garrido-Oter R, Münch PC, Weiman A, Dröge J, Pan Y, McHardy AC, Schulze-Lefert P (2015) Structure and function of the bacterial root microbiota in wild and domesticated barley. Cell Host Microbe 17:392–403

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • Canals RM, Herman DJ, Firestone MK (2003) How disturbance by fossorial mammals alters N cycling in a California annual grassland. Ecology 84:875–881

    Article  Google Scholar 

  • Carney KM, Hungate BA, Drake BG, Megonigal JP (2007) Altered soil microbial community at elevated CO2 leads to loss of soil carbon. Proc Natl Acad Sci 104:4990–4995

    Article  PubMed  CAS  Google Scholar 

  • Castanha C, Zhu B, Pries CEH, Georgiou K, Torn MS (2018) The effects of heating, rhizosphere, and depth on root litter decomposition are mediated by soil moisture. Biogeochemistry 137:267–279

    Article  Google Scholar 

  • Chaparro JM, Badri DV, Vivanco JM (2014) Rhizosphere microbiome assemblage is affected by plant development. ISME J 8:790–803

    Article  PubMed  CAS  Google Scholar 

  • Cheng W, Johnson DW (1998) Elevated CO2, rhizosphere processes, and soil organic matter decomposition. Plant Soil 202:167–174

    Article  CAS  Google Scholar 

  • Cheng L, Booker FL, Tu C, Burkey KO, Zhou L, Shew HD, Rufty TW, Hu S (2012) Arbuscular mycorrhizal fungi increase organic carbon decomposition under elevated CO2. Science 337:1084–1087

    Article  PubMed  CAS  Google Scholar 

  • Chenu C, Stotzky G (2002) Interactions between microorganisms and soil particles: an overview. In: Huang PM, Bollag JM, Senesi N (eds) Interactions between soil particles and microorganisms and the impact on the terrestrial environment. Wiley, West Sussex, pp 161–179

    Google Scholar 

  • Clarholm M, Skyllberg U, Rosling A (2015) Organic acid induced release of nutrients from metal-stabilized soil organic matter–the unbutton model. Soil Biol Biochem 84:168–176

    Article  CAS  Google Scholar 

  • Clemmensen KE, Bahr A, Ovaskainen O, Dahlberg A, Ekblad A, Wallander H, Stenlid J, Finlay RD, Wardle DA, Lindahl BD (2013) Roots and associated fungi drive long-term carbon sequestration in boreal forest. Science 339:1615–1618

    Article  PubMed  CAS  Google Scholar 

  • Colombo C, Palumbo G, He JZ, Pinton R, Cesco S (2014) Review on iron availability in soil: interaction of Fe minerals, plants, and microbes. J Soils Sediments 14:538–548

    Article  CAS  Google Scholar 

  • Davidson EA, Ishida FY, Nepstad DC (2004) Effects of an experimental drought on soil emissions of carbon dioxide, methane, nitrous oxide, and nitric oxide in a moist tropical forest. Glob Chang Biol 10:718–730

    Article  Google Scholar 

  • DeAngelis KM, Ji P, Firestone MK, Lindow SE (2005) Two novel bacterial biosensors for detection of nitrate availability in the rhizosphere. Appl Environ Microbiol 71:8537–8547

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • DeAngelis KM, Firestone MK, Lindow SE (2007) Sensitive whole-cell biosensor suitable for detecting a variety of N-Acyl homoserine lactones in intact rhizosphere microbial communities. Appl Environ Microbiol 73:3724–3727

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • DeAngelis KM, Lindow SE, Firestone MK (2008) Bacterial quorum sensing and nitrogen cycling in rhizosphere soil. FEMS Microbiol Ecol 66:197–207

    Article  PubMed  CAS  Google Scholar 

  • DeAngelis KM, Brodie EL, DeSantis T, Andersen G, Lindow S, Firestone MK (2009) Selective progressive response of soil microbial community to wild oat. ISME J 3:168–178

    Article  PubMed  CAS  Google Scholar 

  • Dignac MF, Bahri H, Rumpel C, Rasse DP, Bardoux G, Balesdent J, Girardin C, Chenu C, Mariotti A (2005) Carbon-13 natural abundance as a tool to study the dynamics of lignin monomers in soil: an appraisal at the Closeaux experimental field (France). Geoderma 128:3–17

    Article  CAS  Google Scholar 

  • Donn S, Kirkegaard JA, Perera G, Richardson AE, Watt M (2015) Evolution of bacterial communities in the wheat crop rhizosphere. Environ Microbiol 17:610–621

    Article  PubMed  Google Scholar 

  • Drigo B, Kowalchuk G, Veen J (2008) Climate change goes underground: effects of elevated atmospheric CO2 on microbial community structure and activities in the rhizosphere. Biol Fertil Soils 44:667–679

    Article  Google Scholar 

  • Drigo B, van Veen JA, Kowalchuk GA (2009) Specific rhizosphere bacterial and fungal groups respond differently to elevated atmospheric CO2. ISME J 3:1204–1217

    Article  PubMed  CAS  Google Scholar 

  • Drigo B, Pijl AS, Duyts H, Kielak AM, Gamper HA, Houtekamer MJ, Boschker HTS, Bodelier PLE, Whiteley AS, van Veen JA, Kowalchuk GA (2010) Shifting carbon flow from roots into associated microbial communities in response to elevated atmospheric CO2. Proc Natl Acad Sci 107:10938–10942

    Article  PubMed  CAS  Google Scholar 

  • Drigo B, Kowalchuk GA, Knapp BA, Pijl AS, Boschker HTS, van Veen JA (2013) Impacts of 3 years of elevated atmospheric CO2 on rhizosphere carbon flow and microbial community dynamics. Glob Chang Biol 19:621–636

    Article  PubMed  Google Scholar 

  • Edwards J, Johnson C, Santos-Medellín C, Lurie E, Podishetty NK, Bhatnagar S, Eisen JA, Sundaresan V (2015) Structure, variation, and assembly of the root-associated microbiomes of rice. Proc Natl Acad Sci 112:E911–E920

    Article  PubMed  CAS  Google Scholar 

  • Estera K (2017) The characterization of Avena barbata exudates. M.S. thesis, Range Management Group, University of California, Berkeley

    Google Scholar 

  • Eviner VT, Firestone MK (2007) Mechanisms determining patterns of nutrient dynamics, in California Grasslands. In: Stromberg M, Corbin J, D'Antonio C (eds) California grasslands: ecology and management. University of California Press, Berkeley, CA, pp 94–106

    Google Scholar 

  • Finzi AC, Abramoff RZ, Spiller KS, Brzostek ER, Darby BA, Kramer MA, Phillips RP (2015) Rhizosphere processes are quantitatively important components of terrestrial carbon and nutrient cycles. Glob Chang Biol 21:2082–2094

    Article  PubMed  Google Scholar 

  • Fontaine S, Barot S, Barre P, Bdioui N, Mary B, Rumpel C (2007) Stability of organic carbon in deep soil layers controlled by fresh carbon supply. Nature 450:277–280

    Article  PubMed  CAS  Google Scholar 

  • Gleixner G, Poirier N, Bol R, Balesdent J (2002) Molecular dynamics of organic matter in a cultivated soil. Org Geochem 33:357–366

    Article  CAS  Google Scholar 

  • Golchin A, Oades JM, Skjemstad JO, Clarke P (1994) Study of free and occluded particulate organic matter in soils by solid state 13C Cp/MAS NMR spectroscopy and scanning electron microscopy. Aust J Soil Res 32:285–309

    Article  CAS  Google Scholar 

  • Grayston SJ, Vaughan D, Jones D (1996) Rhizosphere carbon flow in trees, in comparison with annual plants: the importance of root exudation and its impact on microbial activity and nutrient availability. Appl Soil Ecol 5:29–56

    Article  Google Scholar 

  • Haichar F e Z, Marol C, Berge O, Rangel-Castro JI, Prosser JI, Balesdent J, Heulin T, Achouak W (2008) Plant host habitat and root exudates shape soil bacterial community structure. ISME J 2:1221

    Article  PubMed  CAS  Google Scholar 

  • Hartman K, van der Heijden MG, Roussely-Provent V, Walser J-C, Schlaeppi K (2017) Deciphering composition and function of the root microbiome of a legume plant. Microbiome 5:2

    Article  PubMed  PubMed Central  Google Scholar 

  • Hawkes CV, Wren IF, Herman DJ, Firestone MK (2005) Plant invasion alters nitrogen cycling by modifying the soil nitrifying community. Ecol Lett 8:976–985

    Article  Google Scholar 

  • Hawkes C, Belnap J, D’Antonio C, Firestone M (2006) Arbuscular mycorrhizal assemblages in native plant roots change in the presence of invasive exotic grasses. Plant Soil 281:369–380

    Article  CAS  Google Scholar 

  • Hawkes C, DeAngelis K, Firestone M (2007) Root interactions with soil microbial communities and processes. In: Cardon Z, Whitbeck J (eds) The rhizosphere: an ecological perspective. Academic Press, San Diego, pp 1–30

    Google Scholar 

  • He Z, Gentry TJ, Schadt CW, Wu L, Liebich J, Chong SC, Huang Z, Wu W, Gu B, Jardine P, Criddle C, Zhou J (2007) GeoChip: a comprehensive microarray for investigating biogeochemical, ecological and environmental processes. ISME J 1:67–77

    Article  PubMed  CAS  Google Scholar 

  • Herman D, Johnson KK, Jaeger CH, Schwartz E, Firestone MK (2006) Root influence on nitrogen mineralization and nitrification in Avena barbata rhizosphere soil. Soil Sci Soc Am J 70:1504–1511

    Article  CAS  Google Scholar 

  • Hu S, Firestone MK, Chapin FS (1999) Soil microbial feedbacks to atmospheric CO2 enrichment. Trends Ecol Evol 14:433–437

    Article  PubMed  CAS  Google Scholar 

  • Hu S, Chapin Iii FS, Firestone MK, Field CB, Chiariello NR (2001) Nitrogen limitation of microbial decomposition in a grassland under elevated CO2. Nature 409:188

    Article  PubMed  CAS  Google Scholar 

  • Hungate BA (1999) Ecosystem responses to rising atmospheric CO2: feedbacks through the nitrogen cycle. In: Luo Y, Mooney H (eds) Carbon dioxide and environmental stress. Academic Press, San Diego, pp 265–285

    Chapter  Google Scholar 

  • Hungate BA, Lund CP, Pearson HL, Chapin FS (1997) Elevated CO2 and nutrient addition after soil N cycling and N trace gas fluxes with early season wet-up in a California annual grassland. Biogeochemistry 37:89–109

    Article  CAS  Google Scholar 

  • Iannucci A, Fragasso M, Platani C, Narducci A, Miullo V, Papa R (2012) Dynamics of release of allelochemical compounds from roots of wild oat (Avena fatua L.). Agrochimica 6:185–192

    Google Scholar 

  • Jackson RB, Lajtha K, Crow SE, Hugelius G, Kramer MG, Piñeiro G (2017) The ecology of soil carbon: pools, vulnerabilities, and biotic and abiotic controls. Annu Rev Ecol Evol Syst 48:419–445

    Article  Google Scholar 

  • Jain SK, Marshall DR (1967) Population studies in predominantly self-pollinating species. X. variation in natural populations of Avena fatua and A. barbata. Am Nat 101:19–33

    Article  Google Scholar 

  • Jones DL (1998) Organic acids in the rhizosphere–a critical review. Plant Soil 205:25–44

    Article  CAS  Google Scholar 

  • Jones JD, Dangl JL (2006) The plant immune system. Nature 444:323

    Article  PubMed  CAS  Google Scholar 

  • Keiluweit M, Bougoure JJ, Nico PS, Pett-Ridge J, Weber PK, Kleber M (2015) Mineral protection of soil carbon counteracted by root exudates. Nat Clim Chang 5:588–595

    Article  CAS  Google Scholar 

  • Kembel SW, Cowan PD, Helmus MR, Cornwell WK, Morlon H, Ackerly DD, Blomberg SP, Webb CO (2010) Picante: R tools for integrating phylogenies and ecology. Bioinformatics 26:1463–1464

    Article  PubMed  CAS  Google Scholar 

  • Khorassani R, Hettwer U, Ratzinger A, Steingrobe B, Karlovsky P, Claassen N (2011) Citramalic acid and salicylic acid in sugar beet root exudates solubilize soil phosphorus. BMC Plant Biol 11:121

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • Kiem R, Kögel-Knabner I (2003) Contribution of lignin and polysaccharides to the refractory carbon pool in C-depleted arable soils. Soil Biol Biochem 35:101–118

    Article  CAS  Google Scholar 

  • Kögel-Knabner I (2002) The macromolecular organic composition of plant and microbial residues as inputs to soil organic matter. Soil Biol Biochem 34:139–162

    Article  Google Scholar 

  • Kolton M, Green SJ, Harel YM, Sela N, Elad Y, Cytryn E (2012) Draft genome sequence of Flavobacterium sp. strain F52, isolated from the rhizosphere of bell pepper (Capsicum annuum L. cv. Maccabi). J Bacteriol 194:5462–5463

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • Kuzyakov Y, Domanski G (2000) Carbon input by plants into the soil. Review. J Plant Nutr Soil Sci 163:421–431

    Article  CAS  Google Scholar 

  • Kuzyakov Y, Friedel J, Stahr K (2000) Review of mechanisms and quantification of priming effects. Soil Biol Biochem 32:1485–1498

    Article  CAS  Google Scholar 

  • Letunic I, Bork P (2011) Interactive tree of life v2: online annotation and display of phylogenetic trees made easy. Nucleic Acids Res 39:W475–W478

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • Li X, Rui J, Mao Y, Yannarell A, Mackie R (2014) Dynamics of the bacterial community structure in the rhizosphere of a maize cultivar. Soil Biol Biochem 68:392–401

    Article  CAS  Google Scholar 

  • Liu L, King JS, Booker FL, Giardina CP, Lee Allen H, Hu S (2009) Enhanced litter input rather than changes in litter chemistry drive soil carbon and nitrogen cycles under elevated CO2: a microcosm study. Glob Chang Biol 15:441–453

    Article  Google Scholar 

  • Luo Y, Hui D, Zhang D (2006) Elevated CO2 stimulates net accumulations of carbon and nitrogen in land ecosystems: a meta-analysis. Ecology 87:53–63

    Article  PubMed  Google Scholar 

  • Lynch JM, Whipps JM (1990) Substrate flow in the rhizosphere. Plant Soil 129:1–10

    Article  CAS  Google Scholar 

  • Madigan MT, Clark DP, Stahl D, Martinko JM (2010) Brock biology of microorganisms, 13th edn. Benjamin Cummings, San Francisco

    Google Scholar 

  • Manzoni S, Schimel JP, Porporato A (2012) Responses of soil microbial communities to water stress: results from a meta-analysis. Ecology 93:930–938

    Article  PubMed  Google Scholar 

  • Nuccio EE, Anderson-Furgeson J, Estera KY, Pett-Ridge J, Valpine P, Brodie EL, Firestone MK (2016) Climate and edaphic controllers influence rhizosphere community assembly for a wild annual grass. Ecology 97:1307–1318

    Article  PubMed  Google Scholar 

  • Nuccio EE, Starr E, Karaoz U, Brodie EL, Zhou J, Tringe S, Malstrom RR, Woyke T, Banfield J, Firestone MK, Pett-Ridge J (2020) Niche differentiation is spatially and temporally regulated in the rhizosphere. ISME J 14:999–1014

    Google Scholar 

  • Pérez-Jaramillo JE, Carrión VJ, Bosse M, Ferrão LF, de Hollander M, Garcia AA, Ramírez CA, Mendes R, Raaijmakers JM (2017) Linking rhizosphere microbiome composition of wild and domesticated Phaseolus vulgaris to genotypic and root phenotypic traits. ISME J 11:2244

    Article  PubMed  PubMed Central  Google Scholar 

  • Pett-Ridge J, Firestone MK (2017) Using stable isotopes to explore root-microbe-mineral interactions in soil. Rhizosphere 3:244–253

    Article  Google Scholar 

  • Phillips RP, Finzi AC, Bernhardt ES (2011) Enhanced root exudation induces microbial feedbacks to N cycling in a pine forest under long-term CO2 fumigation. Ecol Lett 14:187–194

    Article  PubMed  Google Scholar 

  • Phillips RP, Meier IC, Bernhardt ES, Grandy AS, Wickings K, Finzi AC (2012) Roots and fungi accelerate carbon and nitrogen cycling in forests exposed to elevated CO2. Ecol Lett 15:1042–1049

    Article  PubMed  Google Scholar 

  • Pii Y, Mimmo T, Tomasi N, Terzano R, Cesco S, Crecchio C (2015) Microbial interactions in the rhizosphere: beneficial influences of plant growth-promoting rhizobacteria on nutrient acquisition process. A review. Biol Fertil Soils 51:403–415

    Article  CAS  Google Scholar 

  • Price MN, Dehal PS, Arkin AP (2010) FastTree 2 - approximately maximum-likelihood trees for large alignments. PLoS One 5:e9490

    Article  PubMed  PubMed Central  Google Scholar 

  • Rasse D, Rumpel C, Dignac M-F (2005) Is soil carbon mostly root carbon? Mechanisms for a specific stabilisation. Plant Soil 269:341–356

    Article  CAS  Google Scholar 

  • Schlaeppi K, Dombrowski N, Oter RG, van Themaat EVL, Schulze-Lefert P (2014) Quantitative divergence of the bacterial root microbiota in Arabidopsis thaliana relatives. Proc Natl Acad Sci 111:585–592

    Article  PubMed  CAS  Google Scholar 

  • Shi S, Richardson AE, O'Callaghan M, DeAngelis KM, Jones EE, Stewart A, Firestone MK, Condron LM (2011) Effects of selected root exudate components on soil bacterial communities. FEMS Microbiol Ecol 77:600–610

    Article  PubMed  CAS  Google Scholar 

  • Shi S, Nuccio E, Herman DJ, Rijkers R, Estera K, Li J, da Rocha UN, He Z, Pett-Ridge J, Brodie EL, Zhou J, Firestone M (2015) Successional trajectories of rhizosphere bacterial communities over consecutive seasons. MBio 6:e00746-00715

    Article  Google Scholar 

  • Shi S, Nuccio EE, He Z, Zhou J, Firestone MK (2016) The interconnected rhizosphere: high network complexity dominates rhizosphere assemblages. Ecol Lett 19:926–936

    Article  PubMed  Google Scholar 

  • Shi S, Herman DJ, He Z, Pett-Ridge J, Wu L, Zhou J, Firestone MK (2018) Plant roots alter microbial functional genes supporting root litter decomposition. Soil Biol Biochem 127:90–99

    Article  CAS  Google Scholar 

  • Sokol NW, Kuebbing SE, Karlsen-Ayala E, Bradford MA (2018) Evidence for the primacy of living root inputs, not root or shoot litter, in forming soil organic carbon. New Phytol 221:233–246

    Article  PubMed  Google Scholar 

  • Starr EP, Nuccio EE, Pett-Ridge J, Banfield JF, Firestone MK (2019) Metatranscriptomic reconstruction reveals RNA viruses with the potential to shape carbon cycling in soil. Proc Natl Acad Sci 116(51):25900–25908

    Article  PubMed  CAS  Google Scholar 

  • Steinweg JM, Plante AF, Conant RT, Paul EA, Tanaka DL (2008) Patterns of substrate utilization during long-term incubations at different temperatures. Soil Biol Biochem 40:2722–2728

    Article  CAS  Google Scholar 

  • Swarbreck SM, Lindquist EA, Ackerly DD, Andersen GL (2011a) Analysis of leaf and root transcriptomes of soil-grown Avena barbata plants. Plant Cell Physiol 52:317–332

    Article  PubMed  CAS  Google Scholar 

  • Swarbreck SM, Sudderth EA, Clair SBS, Salve R, Castanha C, Torn MS, Ackerly DD, Andersen GL (2011b) Linking leaf transcript levels to whole plant analyses provides mechanistic insights to the impact of warming and altered water availability in an annual grass. Glob Chang Biol 17:1577–1594

    Article  Google Scholar 

  • Sylvia DM, Fuhrmann JJ, Hartel PG, Zuberer DA (2004) Principles and applications of soil microbiology, 2nd edn. Prentice Hall, Upper Saddle River

    Google Scholar 

  • Throckmorton HM, Bird JA, Dane L, Firestone MK, Horwath WR (2012) The source of microbial C has little impact on soil organic matter stabilisation in forest ecosystems. Ecol Lett 15:1257–1265

    Article  PubMed  Google Scholar 

  • Vamosi SM, Heard SB, Vamosi JC, Webb CO (2009) Emerging patterns in the comparative analysis of phylogenetic community structure. Mol Ecol 18:572–592

    Article  PubMed  CAS  Google Scholar 

  • van Dam NM, Bouwmeester HJ (2016) Metabolomics in the Rhizosphere: tapping into belowground chemical communication. Trends Plant Sci 21:256–265

    Article  PubMed  Google Scholar 

  • Waldrop M, Firestone M (2004) Microbial community utilization of recalcitrant and simple carbon compounds: impact of oak-woodland plant communities. Oecologia 138:275–284

    Article  PubMed  Google Scholar 

  • Waldrop MP, Firestone MK (2006a) Response of microbial community composition and function to soil climate change. Microb Ecol 52:716–724

    Article  PubMed  CAS  Google Scholar 

  • Waldrop MP, Firestone MK (2006b) Seasonal dynamics of microbial community composition and function in oak canopy and open grassland soils. Microb Ecol 52:470–479

    Article  PubMed  CAS  Google Scholar 

  • Webb C, Ackerly D, McPeek M, Donoghue M (2002) Phylogenies and community ecology. Annu Rev Ecol Syst 33:475–505

    Article  Google Scholar 

  • Whitman T, Neurath R, Perera A, Chu-Jacoby I, Ning D, Zhou J, Nico P, Pett-Ridge J, Firestone M (2018) Microbial community assembly differs across minerals in a rhizosphere microcosm. Environ Microbiol 20:4444–4460

    Article  PubMed  CAS  Google Scholar 

  • Yergeau E, Tremblay J, Joly S, Labrecque M, Maynard C, Pitre FE, St-Arnaud M, Greer CW (2018) Soil contamination alters the willow root and rhizosphere metatranscriptome and the root–rhizosphere interactome. ISME J 12:869–884

    Article  PubMed  PubMed Central  Google Scholar 

  • Yin C, Hulbert SH, Schroeder KL, Mavrodi O, Mavrodi D, Dhingra A, Schillinger WF, Paulitz TC (2013) The role of bacterial communities in the natural suppression of Rhizoctonia bare patch of wheat (Triticum aestivum L.). Appl Environ Microbiol 10:01610–01613

    Google Scholar 

  • Zachow C, Müller H, Tilcher R, Berg G (2014) Differences between the rhizosphere microbiome of Beta vulgaris ssp. maritima—ancestor of all beet crops—and modern sugar beets. Front Microbiology 5:415

    Article  Google Scholar 

  • Zhalnina K, Louie KB, Hao Z, Mansoori N, da Rocha UN, Shi S, Cho H, Karaoz U, Loqué D, Bowen BP, Firestone MK, Northen TR, Brodie, EL (2018) Dynamic root exudate chemistry and microbial substrate preferences drive patterns in rhizosphere microbial community assembly. Nat Microbiol 3:470–480

    Google Scholar 

Download references

Acknowledgments

This study is based on research supported by the US Department of Energy, Office of Science, Office of Biological and Environmental Research Genomic Science Program under Award Numbers DE-SC0014079, DE-SC0010570, and DE-SC0016247 to MKF. Part of this work was performed at the University of Oklahoma, funded by the DOE under UC-subcontract number 00008322. J. Pett-Ridge and E. Nuccio contributed under the auspices of the US Department of Energy at LLNL under Contract DE-AC52-07NA27344 and US DOE Genomics Science program awards SCW1039, SCW 1632, SCW1589, and SCW1421. The study performed at the Lawrence Berkeley National Laboratory was supported by the DOE, Office of Science, Office of Biological and Environmental Research through Contract No. DE-AC02-05CH11231. We thank the current and past members of the DOE Genomic Science Carbon Cycling “Cradle to Grave” research team for their support on the multiple projects conducted as part of this research.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jennifer Pett-Ridge .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2021 Springer Nature Singapore Pte Ltd.

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Pett-Ridge, J. et al. (2021). Rhizosphere Carbon Turnover from Cradle to Grave: The Role of Microbe–Plant Interactions. In: Gupta, V.V.S.R., Sharma, A.K. (eds) Rhizosphere Biology: Interactions Between Microbes and Plants. Rhizosphere Biology. Springer, Singapore. https://doi.org/10.1007/978-981-15-6125-2_2

Download citation

Publish with us

Policies and ethics