Nitrogen isotopes, carbon isotopes, and pyrolysis products in wood decay fungi, woody tissues, and cellulose from a long-term log decomposition experiment at H.J. Andrews Experimental Forest, Oregon, USA

Main Author: Hobbie, Erik A.
Other Authors: Grandy, A. Stuart, Harmon, Mark
Format: Dataset
Terbitan: Mendeley , 2019
Subjects:
Online Access: https:/data.mendeley.com/datasets/hwtz5j2k7c
ctrlnum 0.17632-hwtz5j2k7c.1
fullrecord <?xml version="1.0"?> <dc><creator>Hobbie, Erik A.</creator><title>Nitrogen isotopes, carbon isotopes, and pyrolysis products in wood decay fungi, woody tissues, and cellulose from a long-term log decomposition experiment at H.J. Andrews Experimental Forest, Oregon, USA</title><publisher>Mendeley</publisher><description>We combined elemental, isotopic, and compositional patterns in wood, cellulose, and sporocarps to investigate functional and isotopic differences in six taxa of decay fungi during log decomposition. Fungal protein was 4-5&#x2030; higher in &#x3B4;15N and 3-4&#x2030; higher in &#x3B4;13C than non-protein. Fungal &#x3B4;15N correlated with the proportion of protein in N-containing pyrolysis products. 15N partitioning between protein and non-protein pools in mycelia prior to sporocarp formation controlled sporocarp &#x3B4;15N relative to N sources. Radiocarbon measurements separated fungi into heartwood colonizers (Fomitopsis and Hericium, ~30+-year-old carbon) and sapwood colonizers (Mycena, Hypholoma, and Trametes, 1-12-year-old carbon). Sporocarps were 0-2.5&#x2030; higher in &#x3B4;13C than wood cellulose; this was attributed to compositional differences, assimilation of some 13C-enriched hemicellulose or sucrose, and 13C discrimination during metabolism. Research highlights included: (1) Strategies of carbon and nitrogen acquisition differ among wood decay fungi, (2) Fungal taxa varied widely in chemical composition as assessed by pyrolysis GC-MS, (3) Fungal carbon was from one (Mycena) to 30+ years (Fomitopsis, Hericium) old, (4) Hericium preferentially assimilated 13C-enriched hemicellulose, (5) The removal of 13C-depleted C6 atoms in pentoses causes high &#xF064;13C in hemicellulose, (6) taxa varied in N partitioning among sporocarps, mycelia, protein, and non-protein. From these measurements, we improved the quantitative and conceptual understanding of how sources, composition and metabolic processing determined isotopic composition of fungi. </description><subject>Forest Ecology</subject><contributor>Grandy, A. Stuart</contributor><contributor>Harmon, Mark</contributor><type>Other:Dataset</type><identifier>10.17632/hwtz5j2k7c.1</identifier><rights>Creative Commons Attribution 4.0 International</rights><rights>http://creativecommons.org/licenses/by/4.0</rights><relation>https:/data.mendeley.com/datasets/hwtz5j2k7c</relation><date>2019-02-20T02:23:39Z</date><recordID>0.17632-hwtz5j2k7c.1</recordID></dc>
format Other:Dataset
Other
author Hobbie, Erik A.
author2 Grandy, A. Stuart
Harmon, Mark
title Nitrogen isotopes, carbon isotopes, and pyrolysis products in wood decay fungi, woody tissues, and cellulose from a long-term log decomposition experiment at H.J. Andrews Experimental Forest, Oregon, USA
publisher Mendeley
publishDate 2019
topic Forest Ecology
url https:/data.mendeley.com/datasets/hwtz5j2k7c
contents We combined elemental, isotopic, and compositional patterns in wood, cellulose, and sporocarps to investigate functional and isotopic differences in six taxa of decay fungi during log decomposition. Fungal protein was 4-5‰ higher in δ15N and 3-4‰ higher in δ13C than non-protein. Fungal δ15N correlated with the proportion of protein in N-containing pyrolysis products. 15N partitioning between protein and non-protein pools in mycelia prior to sporocarp formation controlled sporocarp δ15N relative to N sources. Radiocarbon measurements separated fungi into heartwood colonizers (Fomitopsis and Hericium, ~30+-year-old carbon) and sapwood colonizers (Mycena, Hypholoma, and Trametes, 1-12-year-old carbon). Sporocarps were 0-2.5‰ higher in δ13C than wood cellulose; this was attributed to compositional differences, assimilation of some 13C-enriched hemicellulose or sucrose, and 13C discrimination during metabolism. Research highlights included: (1) Strategies of carbon and nitrogen acquisition differ among wood decay fungi, (2) Fungal taxa varied widely in chemical composition as assessed by pyrolysis GC-MS, (3) Fungal carbon was from one (Mycena) to 30+ years (Fomitopsis, Hericium) old, (4) Hericium preferentially assimilated 13C-enriched hemicellulose, (5) The removal of 13C-depleted C6 atoms in pentoses causes high 13C in hemicellulose, (6) taxa varied in N partitioning among sporocarps, mycelia, protein, and non-protein. From these measurements, we improved the quantitative and conceptual understanding of how sources, composition and metabolic processing determined isotopic composition of fungi.
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