Spatial patterns nitrogen transfer models of ectomycorrhizal networks in a Mongolian scotch pine plantation

Yanbin Liu , Hongmei Chen , Pu Mou

Journal of Forestry Research ›› 2017, Vol. 29 ›› Issue (2) : 339 -346.

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Journal of Forestry Research ›› 2017, Vol. 29 ›› Issue (2) : 339 -346. DOI: 10.1007/s11676-017-0454-z
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Spatial patterns nitrogen transfer models of ectomycorrhizal networks in a Mongolian scotch pine plantation

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Abstract

Ectomycorrhizal (EM) networks provide a variety of services to plants and ecosystems include nutrient uptake and transfer, seedling survival, internal cycling of nutrients, plant competition, and so on. To deeply their structure and function in ecosystems, we investigated the spatial patterns and nitrogen (N) transfer of EM networks using 15N labelling technique in a Mongolian scotch pine (Pinus sylvestris var. mongolica Litv.) plantation in Northeastern China. In August 2011, four plots (20 × 20 m) were set up in the plantation. 125 ml 5 at.% 0.15 mol/L 15NH4 15NO3 solution was injected into soil at the center of each plot. Before and 2, 6, 30 and 215 days after the 15N application, needles (current year) of each pine were sampled along four 12 m sampling lines. Needle total N and 15N concentrations were analyzed. We observed needle N and 15N concentrations increased significantly over time after 15N application, up to 31 and 0.42%, respectively. There was no correlation between needle N concentration and 15N/14N ratio (R2 = 0.40, n = 5, P = 0.156), while excess needle N concentration and excess needle 15N/14N ratio were positively correlated across different time intervals (R2 = 0.89, n = 4, P < 0.05), but deceased with time interval lengthening. Needle 15N/14N ratio increased with time, but it was not correlated with distance. Needle 15N/14N ratio was negative with distance before and 6th day and 30th day, positive with distance at 2nd day, but the trend was considerably weaker, their slop were close to zero. These results demonstrated that EM networks were ubiquitous and uniformly distributed in the Mongolian scotch pine plantation and a random network. We found N transfer efficiency was very high, absorbed N by EM network was transferred as wide as possible, we observed N uptake of plant had strong bias for 14N and 15N, namely N fractionation. Understanding the structure and function of EM networks in ecosystems may lead to a deeper understanding of ecological stability and evolution, and thus provide new theoretical approaches to improve conservation practices for the management of the Earth’s ecosystems.

Keywords

Ectomycorrhizal networks / Spatial patterns / Nitrogen transfer / Mongolian scotch pine plantation / Stable isotope 15N labelling

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Yanbin Liu, Hongmei Chen, Pu Mou. Spatial patterns nitrogen transfer models of ectomycorrhizal networks in a Mongolian scotch pine plantation. Journal of Forestry Research, 2017, 29(2): 339-346 DOI:10.1007/s11676-017-0454-z

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References

[1]

Albarracín MV, Six J, Houlton BZ, Bledsoe CS. A nitrogen fertilization field study of carbon-13 and nitrogen-15 transfers in ectomycorrhizas of Pinus sabiniana. Oecologia, 2013, 173: 1439-1450.

[2]

Bahram M, Harend H, Tedersoo L. Network perspectives of ectomycorrhizal associations. Fungal Ecol, 2014, 7: 70-77.

[3]

Barto EK, Monika H, Frank M, Mohney BK, Weidenhamer JD, Rillig MC. The fungal fast lane: common mycorrhizal networks extend bioactive zones of allelochemicals in soils. PLoS ONE, 2011, 6: e27195.

[4]

Barto EK, Weidenhamer JD, Cipollini D, Rillig MC. Fungal superhighways: do common mycorrhizal networks enhance below ground communication?. Trends Plant Sci, 2012, 17: 633-637.

[5]

Beiler KJ, Durall DM, Simard SW, Maxwell SA, Kretzer AM. Architecture of the wood-wide web: Rhizopogon spp. genets link multiple Douglas-fir cohorts. New Phytol, 2010, 185: 543-553.

[6]

Beiler KJ, Simard SW, Durall DM. Topology of tree–mycorrhizal fungus interaction networks in xeric and mesic Douglas-fir forests. J Ecol, 2015, 103: 616-628.

[7]

Bledsoe C, Allen MF, Southworth D. Lüttge U, Beyschlag W, Cushman J. Beyond Mutualism: Complex Mycorrhizal Interactions. Progress in Botany, 2014, Berlin: Springer 311 334

[8]

Booth MG. Mycorrhizal networks mediate overstorey-understorey competition in a temperate forest. Ecol Lett, 2004, 7: 538-546.

[9]

Brady NC, Weil RR. The nature and properties of soils, 2002 13 Upper Saddle River: Prentice Hall.

[10]

Callesen I, Nilsson L, Schmidt I, Vesterdal L, Ambus P, Christiansen J, HögbergP Gundersen P. The natural abundance of 15N in litter and soil profiles under six temperate tree species: N cycling depends on tree species traits and site fertility. Plant Soil, 2013, 368: 375-392.

[11]

Cheng CX, Li J, Sun PF. Analyses of the climate change tendency and abrupt climate change in Wuying, Xiaoxing’an Mountain in recent 49 years. Heilongjiang Meteotol, 2010, 4: 9-12.

[12]

Corrêa A, Strasser RJ, Martins-Loução MA. Response of plants to ectomycorrhizae in N-limited conditions: which factors determine its variation?. Mycorrhiza, 2008, 18: 413-427.

[13]

Dawson TE, Mambelli S, Plamboeck AH, Templer PH, Tu KP. Stable isotopes in plant ecology. Annu Rev Ecol Syst, 2002, 33: 507-559.

[14]

Fry B. Stable isotope ecology, 2006, New York: Springer

[15]

He XH, Critchley C, Bledsoe CS. Nitrogen transfer within and between plants through common mycorrhizal networks (CMNs). Crit Rev Plant Sci, 2003, 22: 531-567.

[16]

He XH, Critchley C, Ng H, Bledsoe CS. Nodulated N2-fixing Casuarina cunninghamiana is the sink for net N transfer from non-N2-fixing Eucalyptus maculata via an ectomycorrhizal fungus Pisolithus sp. using 15NH4 + or 15NO3 supplied as ammonium nitrate. New Phytol, 2005, 167: 897-912.

[17]

He XH, Horwath WR, Zasoski RJ, Aanderud Z, Bledsoe CS. Nitrogen sink strength of ectomycorrhizal morphotypes of Quercus douglasii, Q. garryana, and Q. agrifolia seedlings grown in a northern California oak woodland. Mycorrhiza, 2007, 18: 33-41.

[18]

Heaton LLM, López E, Maini PK, Fricker MD, Jones NS. Advection, diffusion and delivery over a network. Phys Rev E Stat Nonlinear Soft Matter Phys, 2012, 86: 021905-021905.

[19]

Heijden MGAVD, Horton TR. Socialism in soil? The importance of mycorrhizal fungal networks for facilitation in natural ecosystems. J Ecol, 2009, 97: 1139-1150.

[20]

Hobbie EA, Colpaert JV. Nitrogen availability and colonization by mycorrhizal fungi correlate with nitrogen isotope patterns in plants. New Phytol, 2003, 157: 115-126.

[21]

Hobbie E, Colpaert J, White M, Ouimette A, Macko S. Nitrogen form, availability, and mycorrhizal colonization affect biomass and nitrogen isotope patterns in Pinus sylvestris. Plant Soil, 2008, 310: 121-136.

[22]

Hobbie EA, van Diepen LTA, Lilleskov EA, Ouimette AP, Finzi AC, Hofmockel KS. Fungal functioning in a pine forest: evidence from a 15N-labeled global change experiment. New Phytol, 2014, 201: 1431-1439.

[23]

Högberg P, Högberg MN, Quist ME, Ekblad ALF, Näsholm T. Nitrogen isotope fractionation during nitrogen uptake by ectomycorrhizal and non-mycorrhizal Pinus sylvestris. New Phytol, 1999, 142: 569-576.

[24]

Högberg P, Johannisson C, Yarwood S, Callesen I, Näsholm T, Myrold DD, Högberg MN. Recovery of ectomycorrhiza after ‘nitrogen saturation’ of a conifer forest. New Phytol, 2011, 189: 515-525.

[25]

Knowles RR, Blackburn TH. Nitrogen isotope techniques, 1993, San Diego: Academic Press.

[26]

Koide RT, Fernandez C, Malcolm G. Determining place and process: functional traits of ectomycorrhizal fungi that affect both community structure and ecosystem function. New Phytol, 2014, 201: 433-439.

[27]

Kranabetter JM, Hawkins BJ, Jones MD, Robbins S, Dyer T, Li T. Species turnover (β-diversity) in ectomycorrhizal fungi linked to NH4 + uptake capacity. Mol Ecol, 2015, 24: 5992-6005.

[28]

Lang C, Finkeldey R, Polle A. Spatial patterns of ectomycorrhizal assemblages in a monospecific forest in relation to host tree genotype. Front Plant Sci, 2013, 4: 103.

[29]

Leake JR, Johnson D, Donnelly DP, Muckle GE, Boddy L, Read DJ. Networks of power and influence: the role of mycorrhizal mycelium in controlling plant communities and agroecosystem functioning. Can J Bot, 2004, 82: 1016-1045.

[30]

Mayor J, Schuur EG, Mack M, Hollingsworth T, Bååth E. Nitrogen isotope patterns in Alaskan black spruce reflect organic nitrogen sources and the activity of ectomycorrhizal fungi. Ecosystems, 2012, 15: 819-831.

[31]

Mayor JR, Mack MC, Schuur EAG. Decoupled stoichiometric, isotopic, and fungal responses of an ectomycorrhizal black spruce forest to nitrogen and phosphorus additions. Soil Biol Biochem, 2015, 88: 247-256.

[32]

Mayor J, Bahram M, Henkel T, Buegger F, Pritsch K, Tedersoo L. Ectomycorrhizal impacts on plant nitrogen nutrition: emerging isotopic patterns, latitudinal variation and hidden mechanisms. Ecol Lett, 2015, 18: 96-107.

[33]

McGuire KL. Common ectomycorrhizal networks may maintain monodominance in a tropical rain forest. Ecology, 2007, 88: 567-574.

[34]

Moyer-Henry KA, Burton JW, Israel DW, Rufty TW. Nitrogen transfer between plants: A 15N natural abundance study with crop and weed species. Plant Soil, 2006, 282: 7-20.

[35]

Nara K. Ectomycorrhizal networks and seedling establishment during early primary succession. New Phytol, 2006, 169: 169-178.

[36]

Nave LE, Nadelhoffer KJ, Moine JM, Diepen LTA, Cooch JK, Dyke NJ. Nitrogen uptake by trees and mycorrhizal fungi in a successional northern temperate forest: insights from multiple isotopic methods. Ecosystems, 2013, 16: 590-603.

[37]

Pena R, Polle A. Attributing functions to ectomycorrhizal fungal identities in assemblages for nitrogen acquisition under stress. ISME J, 2014, 8: 321-330.

[38]

Pickles BJ, Genney DR, Anderson IC, Alexander IJ. Spatial analysis of ectomycorrhizal fungi reveals that root tip communities are structured by competitive interactions. Mol Ecol, 2012, 21: 5110-5123.

[39]

Selosse MA, Richard F, He XH, Simard SW. Mycorrhizal networks: des liaisons dangereuses?. Trends Ecol Evol, 2006, 21: 621-628.

[40]

Simard SW, Beiler KJ, Bingham MA, Deslippe JR, Philip LJ, Teste FP. Mycorrhizal networks: mechanisms, ecology and modelling. Fungal Biol Rev, 2012, 26: 39-60.

[41]

Simard S, Asay A, Beiler K, Bingham M, Deslippe J, He XH, Philip L, Song YY, Teste F. Horton RT. Resource transfer between plants through ectomycorrhizal fungal networks. Mycorrhizal networks, 2015, Dordrecht: Springer 133 176

[42]

Southworth D, He XH, Swenson W, Bledsoe CS, Horwath WR. Application of network theory to potential mycorrhizal networks. Mycorrhiza, 2005, 15: 589-595.

[43]

Teste FP, Simard SW, Durall DM, Guy RD, Jones MD, Schoonmaker AL. Access to mycorrhizal networks and roots of trees: importance for seedling survival and resource transfer. Ecology, 2009, 90: 2808-2822.

[44]

Toju H, Yamamoto S, Tanabe AS, Hayakawa T, Ishii HS. Network modules and hubs in plant-root fungal biomes. J R Soc Interface, 2016 13 116 20151097

[45]

Wu BY, Nara K, Hogetsu T. Spatiotemporal transfer of carbon-14-labelled photosynthate from ectomycorrhizal Pinus densiflora seedlings to extraradical mycelia. Mycorrhiza, 2002, 12: 83-88.

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