Revealing the transfer pathways of cyanobacterial-fixed N into the boreal forest through the feather-moss microbiome
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In: Frontiers in Plant Science, Vol. 13, 1036258, 09.12.2022.
Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Revealing the transfer pathways of cyanobacterial-fixed N into the boreal forest through the feather-moss microbiome
AU - Arróniz-Crespo, María
AU - Bougoure, Jeremy
AU - Murphy, Daniel V
AU - Cutler, Nick A
AU - Souza-Egipsy, Virginia
AU - Chaput, Dominique L
AU - Jones, Davey L
AU - Ostle, Nicholas
AU - Wade, Stephen C
AU - Clode, Peta L
AU - DeLuca, Thomas H
N1 - Copyright © 2022 Arróniz-Crespo, Bougoure, Murphy, Cutler, Souza-Egipsy, Chaput, Jones, Ostle, Wade, Clode and DeLuca.
PY - 2022/12/9
Y1 - 2022/12/9
N2 - Biological N fixation in feather-mosses is one of the largest inputs of new nitrogen (N) to boreal forest ecosystems; however, revealing the fate of newly fixed N within the bryosphere (i.e. bryophytes and their associated organisms) remains uncertain. Herein, we combined N tracers, high resolution secondary ion mass-spectrometry (NanoSIMS) and a molecular survey of bacterial, fungal and diazotrophic communities, to determine the origin and transfer pathways of newly fixed N within feather-moss ( ) and its associated microbiome. NanoSIMS images reveal that newly fixed N , derived from cyanobacteria, is incorporated into moss tissues and associated bacteria, fungi and micro-algae. These images demonstrate that previous assumptions that newly fixed N is sequestered into moss tissue and only released by decomposition are not correct. We provide the first empirical evidence of new pathways for N fixed in feather-mosses to enter the boreal forest ecosystem (i.e. through its microbiome) and discuss the implications for wider ecosystem function. [Abstract copyright: Copyright © 2022 Arróniz-Crespo, Bougoure, Murphy, Cutler, Souza-Egipsy, Chaput, Jones, Ostle, Wade, Clode and DeLuca.]
AB - Biological N fixation in feather-mosses is one of the largest inputs of new nitrogen (N) to boreal forest ecosystems; however, revealing the fate of newly fixed N within the bryosphere (i.e. bryophytes and their associated organisms) remains uncertain. Herein, we combined N tracers, high resolution secondary ion mass-spectrometry (NanoSIMS) and a molecular survey of bacterial, fungal and diazotrophic communities, to determine the origin and transfer pathways of newly fixed N within feather-moss ( ) and its associated microbiome. NanoSIMS images reveal that newly fixed N , derived from cyanobacteria, is incorporated into moss tissues and associated bacteria, fungi and micro-algae. These images demonstrate that previous assumptions that newly fixed N is sequestered into moss tissue and only released by decomposition are not correct. We provide the first empirical evidence of new pathways for N fixed in feather-mosses to enter the boreal forest ecosystem (i.e. through its microbiome) and discuss the implications for wider ecosystem function. [Abstract copyright: Copyright © 2022 Arróniz-Crespo, Bougoure, Murphy, Cutler, Souza-Egipsy, Chaput, Jones, Ostle, Wade, Clode and DeLuca.]
KW - NanoSIMS
KW - Pleurozium schreberi
KW - biological N2 fixation
KW - boreal forest
KW - moss microbiome
KW - moss-cyanobacteria associations
KW - nitrogen cycling
U2 - 10.3389/fpls.2022.1036258
DO - 10.3389/fpls.2022.1036258
M3 - Article
C2 - 36570951
VL - 13
JO - Frontiers in Plant Science
JF - Frontiers in Plant Science
SN - 1664-462X
M1 - 1036258
ER -