Coupling Fine Root Dynamics with Ecosystem Carbon Cycling in Black Spruce Forests of Interior Alaska

Fine root processes play a prominent role in the carbon and nutrient cycling of boreal ecosystems due to the high proportion of biomass allocated belowground and the rapid decomposition of fine roots relative to aboveground tissues. To examine these issues in detail, major components of ecosystem ca...

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Veröffentlicht in:Ecological monographs 2003-11, Vol.73 (4), p.643-662
Hauptverfasser: Ruess, Roger W., Hendrick, Ronald L., Burton, Andrew J., Pregitzer, Kurt S., Sveinbjornssön, Bjartmar, Michael E. Allen, Gregory E. Maurer
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container_issue 4
container_start_page 643
container_title Ecological monographs
container_volume 73
creator Ruess, Roger W.
Hendrick, Ronald L.
Burton, Andrew J.
Pregitzer, Kurt S.
Sveinbjornssön, Bjartmar
Michael E. Allen
Gregory E. Maurer
description Fine root processes play a prominent role in the carbon and nutrient cycling of boreal ecosystems due to the high proportion of biomass allocated belowground and the rapid decomposition of fine roots relative to aboveground tissues. To examine these issues in detail, major components of ecosystem carbon flux were studied in three mature black spruce forests in interior Alaska, where fine root production, respiration, mortality and decomposition, and aboveground production of trees, shrubs, and mosses were measured relative to soil CO2fluxes. Fine root production, measured over a two-year period using minirhizotrons, varied from$0.004 \pm 0.001 ram\cdotcm^{-2}\cdot d^{-1}$over winter, to$0.051 \pm 0.015 mm\cdot cm^{-2}d^{-1}$during July, with peak growing season values comparable to those reported for many temperate forests using similar methods. On average, 84% of this production occurred within 20 cm of the moss surface, although the proportion occurring in deeper profiles increased as soils gradually warmed throughout the summer. Monthly rates of production and mortality were somewhat asynchronous because mortality tended to peak during fall and be minimal during periods of peak production. Production and mortality were, however, positively correlated across all tubes and time periods. Annual fine root production averaged$2.45 \pm 0.31$,$8.01 \pm 1.39$, and$2.53 \pm 0.27 mm\cdot cm^{-2}\cdot yr{-1}$($means \pm 1 se$) among the three sites, when averaged across years. Fine root survival and decomposition were measured by tracking and analyzing the fate of individual fine roots using mark-recapture techniques. Fine root survival was greatest during periods of peak root growth, and least over winter ($\phi_{time}$). Roots first appearing in the middle of the growing season had higher survival rates than those first appearing early or late in the growing season, or over winter ($\phi _{cohort}$), and risk of mortality decreased with root age ($\phi_{age}$). Survival estimates translate to mean life spans of$108 \pm 4 d$during the growing season. While these values are in striking contrast to needle longevity and rates of aboveground litter decomposition, they are similar to many values found for temperate systems, supporting the notion that there are basic morphological and physiological traits of first-order roots that are common to most woody plant root systems. During the growing season, monthly fine root decomposition rates averaged$0.46 \pm 0.01$per mon
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Allen ; Gregory E. Maurer</creator><creatorcontrib>Ruess, Roger W. ; Hendrick, Ronald L. ; Burton, Andrew J. ; Pregitzer, Kurt S. ; Sveinbjornssön, Bjartmar ; Michael E. Allen ; Gregory E. Maurer</creatorcontrib><description>Fine root processes play a prominent role in the carbon and nutrient cycling of boreal ecosystems due to the high proportion of biomass allocated belowground and the rapid decomposition of fine roots relative to aboveground tissues. To examine these issues in detail, major components of ecosystem carbon flux were studied in three mature black spruce forests in interior Alaska, where fine root production, respiration, mortality and decomposition, and aboveground production of trees, shrubs, and mosses were measured relative to soil CO2fluxes. Fine root production, measured over a two-year period using minirhizotrons, varied from$0.004 \pm 0.001 ram\cdotcm^{-2}\cdot d^{-1}$over winter, to$0.051 \pm 0.015 mm\cdot cm^{-2}d^{-1}$during July, with peak growing season values comparable to those reported for many temperate forests using similar methods. On average, 84% of this production occurred within 20 cm of the moss surface, although the proportion occurring in deeper profiles increased as soils gradually warmed throughout the summer. Monthly rates of production and mortality were somewhat asynchronous because mortality tended to peak during fall and be minimal during periods of peak production. Production and mortality were, however, positively correlated across all tubes and time periods. Annual fine root production averaged$2.45 \pm 0.31$,$8.01 \pm 1.39$, and$2.53 \pm 0.27 mm\cdot cm^{-2}\cdot yr{-1}$($means \pm 1 se$) among the three sites, when averaged across years. Fine root survival and decomposition were measured by tracking and analyzing the fate of individual fine roots using mark-recapture techniques. Fine root survival was greatest during periods of peak root growth, and least over winter ($\phi_{time}$). Roots first appearing in the middle of the growing season had higher survival rates than those first appearing early or late in the growing season, or over winter ($\phi _{cohort}$), and risk of mortality decreased with root age ($\phi_{age}$). Survival estimates translate to mean life spans of$108 \pm 4 d$during the growing season. While these values are in striking contrast to needle longevity and rates of aboveground litter decomposition, they are similar to many values found for temperate systems, supporting the notion that there are basic morphological and physiological traits of first-order roots that are common to most woody plant root systems. During the growing season, monthly fine root decomposition rates averaged$0.46 \pm 0.01$per month, while decomposition rates over winter averaged$0.73 \pm$0.01 per winter. These growing season estimates translate to$49 \pm 2 d$from the time a root was first observed as dead, to the time it disappeared. For roots that decomposed during the growing season, those with longer life spans decomposed more slowly after death. Comparing these results with other minirhizotron studies suggests that life-history traits of black spruce first-order roots are similar to those from temperate (and perhaps most) forest ecosystems. Annual production of fine roots averaged$228 \pm 75 g biomassm\cdot m^{-2}\cdot yr^{-1}$, constituting ~56% of total stand production. Aboveground production of trees ($50 \pm 14 g biomass\cdot m^{-2}yr^{-1}$, 13%) and shrubs ($40 \pm 2 g biomass\cdot m^{-2}yr^{-1}$, 11%) contributed similarly to total production, while mosses ($73 \pm 14 g biomass\cdot m^{-2}yr^{-1}$, 20%) accounted for the largest component of aboveground production. Soil temperature had a strong control over both soil respiration ($Q_{10} = 2.21 \pm 0.31$) and root respiration ($Q_{10} = 2.30 \pm 0.37$). During the growing season (15 May to 15 September), ~56% of soil$CO_2 efflux$($580 \pm 40 g C/m^2$) was derived from fine root respiration ($329 \pm 54 g C/m^2$). Although apparent rates of heterotrophic respiration (May through September) and total production did not differ, definitive estimates of net ecosystem production are impossible given the potentially large, unmeasured components of NPP (net primary production), such as root exudation and mycorrhizal production. Nevertheless, rates of fine root production, mortality, and decomposition indicate that in these black spruce ecosystems, fine roots are much more dynamic than would be predicted from patterns of aboveground processes, and that carbon, and presumably nutrients, are cycling through fine roots at rates several orders of magnitude faster than through aboveground tissues.</description><identifier>ISSN: 0012-9615</identifier><identifier>EISSN: 1557-7015</identifier><identifier>DOI: 10.1890/02-4032</identifier><identifier>CODEN: ECMOAQ</identifier><language>eng</language><publisher>Washington, DC: Ecological Society of America</publisher><subject>Animal and plant ecology ; Animal, plant and microbial ecology ; belowground allocation ; Biological and medical sciences ; boreal forest ; Boreal forests ; decomposition ; Ecology ; fine roots ; Forest ecology ; Forest ecosystems ; Forest soils ; Forests ; Fundamental and applied biological sciences. Psychology ; Growing seasons ; longevity ; Mortality ; NPP ; Permafrost ; Plant growth ; Plant roots ; Soil ecology ; Soil respiration ; Synecology ; Terrestrial ecosystems ; Trees</subject><ispartof>Ecological monographs, 2003-11, Vol.73 (4), p.643-662</ispartof><rights>Copyright 2003 Ecological Society of America</rights><rights>2003 by the Ecological Society of America</rights><rights>2004 INIST-CNRS</rights><rights>Copyright Ecological Society of America Nov 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3753-60cf4e852367984a62cb9f711809711240944262eea416ebbda7a0ec17c6fda13</citedby><cites>FETCH-LOGICAL-c3753-60cf4e852367984a62cb9f711809711240944262eea416ebbda7a0ec17c6fda13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4134791$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4134791$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,1411,27901,27902,45550,45551,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=15342399$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Ruess, Roger W.</creatorcontrib><creatorcontrib>Hendrick, Ronald L.</creatorcontrib><creatorcontrib>Burton, Andrew J.</creatorcontrib><creatorcontrib>Pregitzer, Kurt S.</creatorcontrib><creatorcontrib>Sveinbjornssön, Bjartmar</creatorcontrib><creatorcontrib>Michael E. Allen</creatorcontrib><creatorcontrib>Gregory E. Maurer</creatorcontrib><title>Coupling Fine Root Dynamics with Ecosystem Carbon Cycling in Black Spruce Forests of Interior Alaska</title><title>Ecological monographs</title><description>Fine root processes play a prominent role in the carbon and nutrient cycling of boreal ecosystems due to the high proportion of biomass allocated belowground and the rapid decomposition of fine roots relative to aboveground tissues. To examine these issues in detail, major components of ecosystem carbon flux were studied in three mature black spruce forests in interior Alaska, where fine root production, respiration, mortality and decomposition, and aboveground production of trees, shrubs, and mosses were measured relative to soil CO2fluxes. Fine root production, measured over a two-year period using minirhizotrons, varied from$0.004 \pm 0.001 ram\cdotcm^{-2}\cdot d^{-1}$over winter, to$0.051 \pm 0.015 mm\cdot cm^{-2}d^{-1}$during July, with peak growing season values comparable to those reported for many temperate forests using similar methods. On average, 84% of this production occurred within 20 cm of the moss surface, although the proportion occurring in deeper profiles increased as soils gradually warmed throughout the summer. Monthly rates of production and mortality were somewhat asynchronous because mortality tended to peak during fall and be minimal during periods of peak production. Production and mortality were, however, positively correlated across all tubes and time periods. Annual fine root production averaged$2.45 \pm 0.31$,$8.01 \pm 1.39$, and$2.53 \pm 0.27 mm\cdot cm^{-2}\cdot yr{-1}$($means \pm 1 se$) among the three sites, when averaged across years. Fine root survival and decomposition were measured by tracking and analyzing the fate of individual fine roots using mark-recapture techniques. Fine root survival was greatest during periods of peak root growth, and least over winter ($\phi_{time}$). Roots first appearing in the middle of the growing season had higher survival rates than those first appearing early or late in the growing season, or over winter ($\phi _{cohort}$), and risk of mortality decreased with root age ($\phi_{age}$). Survival estimates translate to mean life spans of$108 \pm 4 d$during the growing season. While these values are in striking contrast to needle longevity and rates of aboveground litter decomposition, they are similar to many values found for temperate systems, supporting the notion that there are basic morphological and physiological traits of first-order roots that are common to most woody plant root systems. During the growing season, monthly fine root decomposition rates averaged$0.46 \pm 0.01$per month, while decomposition rates over winter averaged$0.73 \pm$0.01 per winter. These growing season estimates translate to$49 \pm 2 d$from the time a root was first observed as dead, to the time it disappeared. For roots that decomposed during the growing season, those with longer life spans decomposed more slowly after death. Comparing these results with other minirhizotron studies suggests that life-history traits of black spruce first-order roots are similar to those from temperate (and perhaps most) forest ecosystems. Annual production of fine roots averaged$228 \pm 75 g biomassm\cdot m^{-2}\cdot yr^{-1}$, constituting ~56% of total stand production. Aboveground production of trees ($50 \pm 14 g biomass\cdot m^{-2}yr^{-1}$, 13%) and shrubs ($40 \pm 2 g biomass\cdot m^{-2}yr^{-1}$, 11%) contributed similarly to total production, while mosses ($73 \pm 14 g biomass\cdot m^{-2}yr^{-1}$, 20%) accounted for the largest component of aboveground production. Soil temperature had a strong control over both soil respiration ($Q_{10} = 2.21 \pm 0.31$) and root respiration ($Q_{10} = 2.30 \pm 0.37$). During the growing season (15 May to 15 September), ~56% of soil$CO_2 efflux$($580 \pm 40 g C/m^2$) was derived from fine root respiration ($329 \pm 54 g C/m^2$). Although apparent rates of heterotrophic respiration (May through September) and total production did not differ, definitive estimates of net ecosystem production are impossible given the potentially large, unmeasured components of NPP (net primary production), such as root exudation and mycorrhizal production. Nevertheless, rates of fine root production, mortality, and decomposition indicate that in these black spruce ecosystems, fine roots are much more dynamic than would be predicted from patterns of aboveground processes, and that carbon, and presumably nutrients, are cycling through fine roots at rates several orders of magnitude faster than through aboveground tissues.</description><subject>Animal and plant ecology</subject><subject>Animal, plant and microbial ecology</subject><subject>belowground allocation</subject><subject>Biological and medical sciences</subject><subject>boreal forest</subject><subject>Boreal forests</subject><subject>decomposition</subject><subject>Ecology</subject><subject>fine roots</subject><subject>Forest ecology</subject><subject>Forest ecosystems</subject><subject>Forest soils</subject><subject>Forests</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Growing seasons</subject><subject>longevity</subject><subject>Mortality</subject><subject>NPP</subject><subject>Permafrost</subject><subject>Plant growth</subject><subject>Plant roots</subject><subject>Soil ecology</subject><subject>Soil respiration</subject><subject>Synecology</subject><subject>Terrestrial ecosystems</subject><subject>Trees</subject><issn>0012-9615</issn><issn>1557-7015</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNp1kE9rGzEQxUVIoY5b-gVyEIU2p21Hf1ayjs7WTgwugbQ9C1nWJrLXkiPtEvbbZx2HBAK9zDDwe28eD6EvBH6QiYKfQAsOjJ6gESlLWUgg5SkaARBaKEHKj-gs5w0cbqVGaF3Fbt_4cIfnPjh8G2OLf_XB7LzN-NG393hmY-5z63a4MmkVA656-yzwAV82xm7xn33qrMPzmFxuM441XoTWJR8TnjYmb80n9KE2TXafX_YY_ZvP_lbXxfLmalFNl4VlsmSFAFtzNykpE1JNuBHUrlQtCZmAGibloDingjpnOBFutVobacBZIq2o14awMfp-9N2n-NANYfTOZ-uaxgQXu6yJokyBYAP49R24iV0KQzZNGSMUyiHPGF0cIZtizsnVep_8zqReE9CHqjVQfah6IL-92JlsTVMnE6zPb3jJ-PBYDRw9co--cf3_7PSs-k0BmGRc8EPW86Nok9uYXkWcMC4VYU9rxJNg</recordid><startdate>200311</startdate><enddate>200311</enddate><creator>Ruess, Roger W.</creator><creator>Hendrick, Ronald L.</creator><creator>Burton, Andrew J.</creator><creator>Pregitzer, Kurt S.</creator><creator>Sveinbjornssön, Bjartmar</creator><creator>Michael E. Allen</creator><creator>Gregory E. Maurer</creator><general>Ecological Society of America</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7SN</scope><scope>7SS</scope><scope>C1K</scope><scope>M7N</scope></search><sort><creationdate>200311</creationdate><title>Coupling Fine Root Dynamics with Ecosystem Carbon Cycling in Black Spruce Forests of Interior Alaska</title><author>Ruess, Roger W. ; Hendrick, Ronald L. ; Burton, Andrew J. ; Pregitzer, Kurt S. ; Sveinbjornssön, Bjartmar ; Michael E. Allen ; Gregory E. Maurer</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3753-60cf4e852367984a62cb9f711809711240944262eea416ebbda7a0ec17c6fda13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animal and plant ecology</topic><topic>Animal, plant and microbial ecology</topic><topic>belowground allocation</topic><topic>Biological and medical sciences</topic><topic>boreal forest</topic><topic>Boreal forests</topic><topic>decomposition</topic><topic>Ecology</topic><topic>fine roots</topic><topic>Forest ecology</topic><topic>Forest ecosystems</topic><topic>Forest soils</topic><topic>Forests</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Growing seasons</topic><topic>longevity</topic><topic>Mortality</topic><topic>NPP</topic><topic>Permafrost</topic><topic>Plant growth</topic><topic>Plant roots</topic><topic>Soil ecology</topic><topic>Soil respiration</topic><topic>Synecology</topic><topic>Terrestrial ecosystems</topic><topic>Trees</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ruess, Roger W.</creatorcontrib><creatorcontrib>Hendrick, Ronald L.</creatorcontrib><creatorcontrib>Burton, Andrew J.</creatorcontrib><creatorcontrib>Pregitzer, Kurt S.</creatorcontrib><creatorcontrib>Sveinbjornssön, Bjartmar</creatorcontrib><creatorcontrib>Michael E. Allen</creatorcontrib><creatorcontrib>Gregory E. Maurer</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Ecological monographs</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ruess, Roger W.</au><au>Hendrick, Ronald L.</au><au>Burton, Andrew J.</au><au>Pregitzer, Kurt S.</au><au>Sveinbjornssön, Bjartmar</au><au>Michael E. Allen</au><au>Gregory E. Maurer</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coupling Fine Root Dynamics with Ecosystem Carbon Cycling in Black Spruce Forests of Interior Alaska</atitle><jtitle>Ecological monographs</jtitle><date>2003-11</date><risdate>2003</risdate><volume>73</volume><issue>4</issue><spage>643</spage><epage>662</epage><pages>643-662</pages><issn>0012-9615</issn><eissn>1557-7015</eissn><coden>ECMOAQ</coden><abstract>Fine root processes play a prominent role in the carbon and nutrient cycling of boreal ecosystems due to the high proportion of biomass allocated belowground and the rapid decomposition of fine roots relative to aboveground tissues. To examine these issues in detail, major components of ecosystem carbon flux were studied in three mature black spruce forests in interior Alaska, where fine root production, respiration, mortality and decomposition, and aboveground production of trees, shrubs, and mosses were measured relative to soil CO2fluxes. Fine root production, measured over a two-year period using minirhizotrons, varied from$0.004 \pm 0.001 ram\cdotcm^{-2}\cdot d^{-1}$over winter, to$0.051 \pm 0.015 mm\cdot cm^{-2}d^{-1}$during July, with peak growing season values comparable to those reported for many temperate forests using similar methods. On average, 84% of this production occurred within 20 cm of the moss surface, although the proportion occurring in deeper profiles increased as soils gradually warmed throughout the summer. Monthly rates of production and mortality were somewhat asynchronous because mortality tended to peak during fall and be minimal during periods of peak production. Production and mortality were, however, positively correlated across all tubes and time periods. Annual fine root production averaged$2.45 \pm 0.31$,$8.01 \pm 1.39$, and$2.53 \pm 0.27 mm\cdot cm^{-2}\cdot yr{-1}$($means \pm 1 se$) among the three sites, when averaged across years. Fine root survival and decomposition were measured by tracking and analyzing the fate of individual fine roots using mark-recapture techniques. Fine root survival was greatest during periods of peak root growth, and least over winter ($\phi_{time}$). Roots first appearing in the middle of the growing season had higher survival rates than those first appearing early or late in the growing season, or over winter ($\phi _{cohort}$), and risk of mortality decreased with root age ($\phi_{age}$). Survival estimates translate to mean life spans of$108 \pm 4 d$during the growing season. While these values are in striking contrast to needle longevity and rates of aboveground litter decomposition, they are similar to many values found for temperate systems, supporting the notion that there are basic morphological and physiological traits of first-order roots that are common to most woody plant root systems. During the growing season, monthly fine root decomposition rates averaged$0.46 \pm 0.01$per month, while decomposition rates over winter averaged$0.73 \pm$0.01 per winter. These growing season estimates translate to$49 \pm 2 d$from the time a root was first observed as dead, to the time it disappeared. For roots that decomposed during the growing season, those with longer life spans decomposed more slowly after death. Comparing these results with other minirhizotron studies suggests that life-history traits of black spruce first-order roots are similar to those from temperate (and perhaps most) forest ecosystems. Annual production of fine roots averaged$228 \pm 75 g biomassm\cdot m^{-2}\cdot yr^{-1}$, constituting ~56% of total stand production. Aboveground production of trees ($50 \pm 14 g biomass\cdot m^{-2}yr^{-1}$, 13%) and shrubs ($40 \pm 2 g biomass\cdot m^{-2}yr^{-1}$, 11%) contributed similarly to total production, while mosses ($73 \pm 14 g biomass\cdot m^{-2}yr^{-1}$, 20%) accounted for the largest component of aboveground production. Soil temperature had a strong control over both soil respiration ($Q_{10} = 2.21 \pm 0.31$) and root respiration ($Q_{10} = 2.30 \pm 0.37$). During the growing season (15 May to 15 September), ~56% of soil$CO_2 efflux$($580 \pm 40 g C/m^2$) was derived from fine root respiration ($329 \pm 54 g C/m^2$). Although apparent rates of heterotrophic respiration (May through September) and total production did not differ, definitive estimates of net ecosystem production are impossible given the potentially large, unmeasured components of NPP (net primary production), such as root exudation and mycorrhizal production. Nevertheless, rates of fine root production, mortality, and decomposition indicate that in these black spruce ecosystems, fine roots are much more dynamic than would be predicted from patterns of aboveground processes, and that carbon, and presumably nutrients, are cycling through fine roots at rates several orders of magnitude faster than through aboveground tissues.</abstract><cop>Washington, DC</cop><pub>Ecological Society of America</pub><doi>10.1890/02-4032</doi><tpages>20</tpages></addata></record>
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source Jstor Complete Legacy; Wiley Online Library Journals Frontfile Complete
subjects Animal and plant ecology
Animal, plant and microbial ecology
belowground allocation
Biological and medical sciences
boreal forest
Boreal forests
decomposition
Ecology
fine roots
Forest ecology
Forest ecosystems
Forest soils
Forests
Fundamental and applied biological sciences. Psychology
Growing seasons
longevity
Mortality
NPP
Permafrost
Plant growth
Plant roots
Soil ecology
Soil respiration
Synecology
Terrestrial ecosystems
Trees
title Coupling Fine Root Dynamics with Ecosystem Carbon Cycling in Black Spruce Forests of Interior Alaska
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