Filling the “vertical gap” between canopy tree species and understory shrub species: biomass allometric equations for subcanopy tree species
Subcanopy tree species are an important component of temperate secondary forests. However, their biomass equations are rarely reported, which forms a “vertical gap” between canopy tree species and understory shrub species. In this study, we destructively sampled six common subcanopy species ( Syring...
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description | Subcanopy tree species are an important component of temperate secondary forests. However, their biomass equations are rarely reported, which forms a “vertical gap” between canopy tree species and understory shrub species. In this study, we destructively sampled six common subcanopy species (
Syringa reticulate
var.
amurensis
(Rupr.) Pringle,
Padus racemosa
(Lam.) Gilib.,
Acer ginnala
Maxim.,
Malus baccata
(Linn.) Borkh.,
Rhamnus davurica
Pall., and
Maackia amurensis
Rupr. et Maxim.) to establish biomass equations in a temperate forest of Northeast China. The mixed-species and species-specific biomass allometric equations were well fitted against diameter at breast height (DBH). Adding tree height (H) as the second predictor increased the
R
2
of the models compared with the
DBH-only
models by –1% to + 3%. The
R
2
of
DBH-only
and
DBH-H
equations for the total biomass of mixed-species were 0.985 and 0.986, respectively. On average, the biomass allocation proportions for the six species were in the order of stem (45.5%) > branch (30.1%) > belowground (19.5%) > foliage (4.9%), with a mean root: shoot ratio of 0.24. Biomass allocation to each specific component differed among species, which affected the performance of the mixed-species model for particular biomass component. When estimating the biomass of subcanopy species using the equations for canopy species (e.g.,
Betula platyphylla
Suk.,
Ulmus davidiana
var.
japonica
(Rehd.) Nakai, and
Acer mono
Maxim.), the errors in individual biomass estimation increased with tree size (up to 68.8% at 30 cm DBH), and the errors in stand biomass estimation (up to 19.2%) increased with increasing percentage of basal area shared by subcanopy species. The errors caused by selecting such inappropriate models could be removed by multiplying adjustment factors, which were usually power functions of DBH for biomass components. These results provide methodological support for accurate biomass estimation in temperate China and useful guidelines for biomass estimation for subcanopy species in other regions, which can help to improve estimates of forest biomass and carbon stocks. |
doi_str_mv | 10.1007/s11676-022-01568-0 |
format | Article |
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Syringa reticulate
var.
amurensis
(Rupr.) Pringle,
Padus racemosa
(Lam.) Gilib.,
Acer ginnala
Maxim.,
Malus baccata
(Linn.) Borkh.,
Rhamnus davurica
Pall., and
Maackia amurensis
Rupr. et Maxim.) to establish biomass equations in a temperate forest of Northeast China. The mixed-species and species-specific biomass allometric equations were well fitted against diameter at breast height (DBH). Adding tree height (H) as the second predictor increased the
R
2
of the models compared with the
DBH-only
models by –1% to + 3%. The
R
2
of
DBH-only
and
DBH-H
equations for the total biomass of mixed-species were 0.985 and 0.986, respectively. On average, the biomass allocation proportions for the six species were in the order of stem (45.5%) > branch (30.1%) > belowground (19.5%) > foliage (4.9%), with a mean root: shoot ratio of 0.24. Biomass allocation to each specific component differed among species, which affected the performance of the mixed-species model for particular biomass component. When estimating the biomass of subcanopy species using the equations for canopy species (e.g.,
Betula platyphylla
Suk.,
Ulmus davidiana
var.
japonica
(Rehd.) Nakai, and
Acer mono
Maxim.), the errors in individual biomass estimation increased with tree size (up to 68.8% at 30 cm DBH), and the errors in stand biomass estimation (up to 19.2%) increased with increasing percentage of basal area shared by subcanopy species. The errors caused by selecting such inappropriate models could be removed by multiplying adjustment factors, which were usually power functions of DBH for biomass components. These results provide methodological support for accurate biomass estimation in temperate China and useful guidelines for biomass estimation for subcanopy species in other regions, which can help to improve estimates of forest biomass and carbon stocks.</description><identifier>ISSN: 1007-662X</identifier><identifier>EISSN: 1993-0607</identifier><identifier>DOI: 10.1007/s11676-022-01568-0</identifier><language>eng</language><publisher>Singapore: Springer Nature Singapore</publisher><subject>Biomass ; Biomedical and Life Sciences ; Canopies ; Errors ; Estimation ; Foliage ; Forest biomass ; Forestry ; Height ; Life Sciences ; Mathematical models ; Original Paper ; Plant species ; Species ; Temperate forests ; Trees ; Understory</subject><ispartof>Journal of forestry research, 2023-08, Vol.34 (4), p.903-913</ispartof><rights>Northeast Forestry University 2022. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>COPYRIGHT 2023 Springer</rights><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-96f12c85a020085f20d75663e27d9f52b3e89145456aec4e4d0c1ebc86c5e7b83</citedby><cites>FETCH-LOGICAL-c416t-96f12c85a020085f20d75663e27d9f52b3e89145456aec4e4d0c1ebc86c5e7b83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.wanfangdata.com.cn/images/PeriodicalImages/lyyj/lyyj.jpg</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11676-022-01568-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11676-022-01568-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Sun, Xue</creatorcontrib><creatorcontrib>Wang, Xingchang</creatorcontrib><creatorcontrib>Wang, Chuankuan</creatorcontrib><creatorcontrib>Zhang, Quanzhi</creatorcontrib><creatorcontrib>Guo, Qingxi</creatorcontrib><title>Filling the “vertical gap” between canopy tree species and understory shrub species: biomass allometric equations for subcanopy tree species</title><title>Journal of forestry research</title><addtitle>J. For. Res</addtitle><description>Subcanopy tree species are an important component of temperate secondary forests. However, their biomass equations are rarely reported, which forms a “vertical gap” between canopy tree species and understory shrub species. In this study, we destructively sampled six common subcanopy species (
Syringa reticulate
var.
amurensis
(Rupr.) Pringle,
Padus racemosa
(Lam.) Gilib.,
Acer ginnala
Maxim.,
Malus baccata
(Linn.) Borkh.,
Rhamnus davurica
Pall., and
Maackia amurensis
Rupr. et Maxim.) to establish biomass equations in a temperate forest of Northeast China. The mixed-species and species-specific biomass allometric equations were well fitted against diameter at breast height (DBH). Adding tree height (H) as the second predictor increased the
R
2
of the models compared with the
DBH-only
models by –1% to + 3%. The
R
2
of
DBH-only
and
DBH-H
equations for the total biomass of mixed-species were 0.985 and 0.986, respectively. On average, the biomass allocation proportions for the six species were in the order of stem (45.5%) > branch (30.1%) > belowground (19.5%) > foliage (4.9%), with a mean root: shoot ratio of 0.24. Biomass allocation to each specific component differed among species, which affected the performance of the mixed-species model for particular biomass component. When estimating the biomass of subcanopy species using the equations for canopy species (e.g.,
Betula platyphylla
Suk.,
Ulmus davidiana
var.
japonica
(Rehd.) Nakai, and
Acer mono
Maxim.), the errors in individual biomass estimation increased with tree size (up to 68.8% at 30 cm DBH), and the errors in stand biomass estimation (up to 19.2%) increased with increasing percentage of basal area shared by subcanopy species. The errors caused by selecting such inappropriate models could be removed by multiplying adjustment factors, which were usually power functions of DBH for biomass components. These results provide methodological support for accurate biomass estimation in temperate China and useful guidelines for biomass estimation for subcanopy species in other regions, which can help to improve estimates of forest biomass and carbon stocks.</description><subject>Biomass</subject><subject>Biomedical and Life Sciences</subject><subject>Canopies</subject><subject>Errors</subject><subject>Estimation</subject><subject>Foliage</subject><subject>Forest biomass</subject><subject>Forestry</subject><subject>Height</subject><subject>Life Sciences</subject><subject>Mathematical models</subject><subject>Original Paper</subject><subject>Plant species</subject><subject>Species</subject><subject>Temperate forests</subject><subject>Trees</subject><subject>Understory</subject><issn>1007-662X</issn><issn>1993-0607</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kd9q1zAUx4soOKcv4FVAvOw8-dO09W4Mp8JgNwrehTQ97fKjTbokdfzu9gh7AH25PYmZnQ5hSC4Sks_n5HC-RfGawhEFqN9FSmUtS2CsBFrJpoQnxQFtW16ChPppPmeqlJJ9e168iHEHUAnOxUFxc2qnybqRpAskt9c_vmNI1uiJjHq5vf5JOkxXiI4Y7fyyJykgkrigsRiJdj1ZXY8hJh_2JF6Etfvz-J501s86Zmqa_IwpWEPwctXJehfJ4AOJa_dI1ZfFs0FPEV_d74fF19MPX04-lWfnHz-fHJ-VRlCZylYOlJmm0sAAmmpg0NeVlBxZ3bdDxTqOTUtFJSqp0QgUPRiKnWmkqbDuGn5YvN3qXmk3aDeqnV-Dyz-qab_fMWAcBADP3JuNW4K_XDGmB5A1XNA8xzzmv9SoJ1TWDT4FbWYbjTrOfTHRCnlHHT1C5dXjbI13ONh8_4_ANsEEH2PAQS3BzjrsFQV1F6naglc5ePU7eAVZ4psUM-xGDA8d_8f6BcuBs0w</recordid><startdate>20230801</startdate><enddate>20230801</enddate><creator>Sun, Xue</creator><creator>Wang, Xingchang</creator><creator>Wang, Chuankuan</creator><creator>Zhang, Quanzhi</creator><creator>Guo, Qingxi</creator><general>Springer Nature Singapore</general><general>Springer</general><general>Springer Nature B.V</general><general>Center for Ecological Research,Northeast Forestry University,Harbin 150040,People's Republic of China</general><general>Key Laboratory of Sustainable Forest Ecosystem Management-Ministry of Education,Northeast Forestry University,Harbin 150040,People's Republic of China</general><scope>AAYXX</scope><scope>CITATION</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20230801</creationdate><title>Filling the “vertical gap” between canopy tree species and understory shrub species: biomass allometric equations for subcanopy tree species</title><author>Sun, Xue ; Wang, Xingchang ; Wang, Chuankuan ; Zhang, Quanzhi ; Guo, Qingxi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c416t-96f12c85a020085f20d75663e27d9f52b3e89145456aec4e4d0c1ebc86c5e7b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Biomass</topic><topic>Biomedical and Life Sciences</topic><topic>Canopies</topic><topic>Errors</topic><topic>Estimation</topic><topic>Foliage</topic><topic>Forest biomass</topic><topic>Forestry</topic><topic>Height</topic><topic>Life Sciences</topic><topic>Mathematical models</topic><topic>Original Paper</topic><topic>Plant species</topic><topic>Species</topic><topic>Temperate forests</topic><topic>Trees</topic><topic>Understory</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sun, Xue</creatorcontrib><creatorcontrib>Wang, Xingchang</creatorcontrib><creatorcontrib>Wang, Chuankuan</creatorcontrib><creatorcontrib>Zhang, Quanzhi</creatorcontrib><creatorcontrib>Guo, Qingxi</creatorcontrib><collection>CrossRef</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Journal of forestry research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sun, Xue</au><au>Wang, Xingchang</au><au>Wang, Chuankuan</au><au>Zhang, Quanzhi</au><au>Guo, Qingxi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Filling the “vertical gap” between canopy tree species and understory shrub species: biomass allometric equations for subcanopy tree species</atitle><jtitle>Journal of forestry research</jtitle><stitle>J. For. Res</stitle><date>2023-08-01</date><risdate>2023</risdate><volume>34</volume><issue>4</issue><spage>903</spage><epage>913</epage><pages>903-913</pages><issn>1007-662X</issn><eissn>1993-0607</eissn><abstract>Subcanopy tree species are an important component of temperate secondary forests. However, their biomass equations are rarely reported, which forms a “vertical gap” between canopy tree species and understory shrub species. In this study, we destructively sampled six common subcanopy species (
Syringa reticulate
var.
amurensis
(Rupr.) Pringle,
Padus racemosa
(Lam.) Gilib.,
Acer ginnala
Maxim.,
Malus baccata
(Linn.) Borkh.,
Rhamnus davurica
Pall., and
Maackia amurensis
Rupr. et Maxim.) to establish biomass equations in a temperate forest of Northeast China. The mixed-species and species-specific biomass allometric equations were well fitted against diameter at breast height (DBH). Adding tree height (H) as the second predictor increased the
R
2
of the models compared with the
DBH-only
models by –1% to + 3%. The
R
2
of
DBH-only
and
DBH-H
equations for the total biomass of mixed-species were 0.985 and 0.986, respectively. On average, the biomass allocation proportions for the six species were in the order of stem (45.5%) > branch (30.1%) > belowground (19.5%) > foliage (4.9%), with a mean root: shoot ratio of 0.24. Biomass allocation to each specific component differed among species, which affected the performance of the mixed-species model for particular biomass component. When estimating the biomass of subcanopy species using the equations for canopy species (e.g.,
Betula platyphylla
Suk.,
Ulmus davidiana
var.
japonica
(Rehd.) Nakai, and
Acer mono
Maxim.), the errors in individual biomass estimation increased with tree size (up to 68.8% at 30 cm DBH), and the errors in stand biomass estimation (up to 19.2%) increased with increasing percentage of basal area shared by subcanopy species. The errors caused by selecting such inappropriate models could be removed by multiplying adjustment factors, which were usually power functions of DBH for biomass components. These results provide methodological support for accurate biomass estimation in temperate China and useful guidelines for biomass estimation for subcanopy species in other regions, which can help to improve estimates of forest biomass and carbon stocks.</abstract><cop>Singapore</cop><pub>Springer Nature Singapore</pub><doi>10.1007/s11676-022-01568-0</doi><tpages>11</tpages></addata></record> |
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language | eng |
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source | Alma/SFX Local Collection; SpringerLink Journals - AutoHoldings |
subjects | Biomass Biomedical and Life Sciences Canopies Errors Estimation Foliage Forest biomass Forestry Height Life Sciences Mathematical models Original Paper Plant species Species Temperate forests Trees Understory |
title | Filling the “vertical gap” between canopy tree species and understory shrub species: biomass allometric equations for subcanopy tree species |
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