Developmental changes in shoot N dynamics of lucerne (Medicago sativa L.) in relation to leaf growth dynamics as a function of plant density and hierarchical position within the canopy. [Erratum: 2005 May, v. 56, no. 415, p. 1437.]
Shoot N concentration in plants decreases as they get bigger, due to the fact that N accumulates less rapidly than dry matter in plants during the plant growth process, leading to an allometric relationship between shoot N content (N[subscript sh]) and shoot mass (W[subscript sh]): N[subscript sh]=a...
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description | Shoot N concentration in plants decreases as they get bigger, due to the fact that N accumulates less rapidly than dry matter in plants during the plant growth process, leading to an allometric relationship between shoot N content (N[subscript sh]) and shoot mass (W[subscript sh]): N[subscript sh]=a(W[subscript sh])[superscript b]. The results obtained on lucerne plants growing either under controlled low density conditions or in dense stands under field conditions show that the value of the allometric coefficient b that represents the ratio between the relative N accumulation rate in shoots [dN[subscript sh]/(N[subscript sh]dt)] and the relative growth rate [dW[subscript sh]/(W[subscript sh]dt)], decreases from 0.88 for a low plant density to 0.72 for a dense stand. Therefore, the fractional increase of shoot N per unit of shoot dry matter is lower when plants are in competition for light in dense canopies. This decrease can be entirely explained by the parallel decline in the leaf area per unit of shoot mass. Thus, a remarkably constant linear relationship can be established between N[subscript sh] and leaf area (LA): N[subscript sh]=1.7 g m⁻² LA, regardless of the conditions (low versus high density, controlled versus field conditions). Moreover, in a field dense stand, the comparison of plants with contrasting positions between the top and the bottom of the canopy (dominant, intermediate or suppressed plants), also shows that the difference in N[subscript sh] at similar shoot mass is explained by the proportion of leaf mass to shoot mass. These data support the idea that leaf growth drives the dynamics of shoot N accumulation. These results also indicate that competition for light among individual plants within a dense canopy induces developmental changes in plant morphology (leaf:stem ratio) that explain the differences observed in shoot N concentration. This last observation could be extrapolated to multispecific plant stands. Therefore, the sharing of N resources among plant species could partially be the result of the sharing of light within the canopy. |
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[Erratum: 2005 May, v. 56, no. 415, p. 1437.]</title><source>MEDLINE</source><source>Oxford Academic Journals (OUP)</source><source>Alma/SFX Local Collection</source><source>JSTOR</source><source>EZB Electronic Journals Library</source><creator>Lemaire, G ; Avice, J-C ; Kim, T-H ; Ourry, A</creator><creatorcontrib>Lemaire, G ; Avice, J-C ; Kim, T-H ; Ourry, A</creatorcontrib><description>Shoot N concentration in plants decreases as they get bigger, due to the fact that N accumulates less rapidly than dry matter in plants during the plant growth process, leading to an allometric relationship between shoot N content (N[subscript sh]) and shoot mass (W[subscript sh]): N[subscript sh]=a(W[subscript sh])[superscript b]. The results obtained on lucerne plants growing either under controlled low density conditions or in dense stands under field conditions show that the value of the allometric coefficient b that represents the ratio between the relative N accumulation rate in shoots [dN[subscript sh]/(N[subscript sh]dt)] and the relative growth rate [dW[subscript sh]/(W[subscript sh]dt)], decreases from 0.88 for a low plant density to 0.72 for a dense stand. Therefore, the fractional increase of shoot N per unit of shoot dry matter is lower when plants are in competition for light in dense canopies. This decrease can be entirely explained by the parallel decline in the leaf area per unit of shoot mass. Thus, a remarkably constant linear relationship can be established between N[subscript sh] and leaf area (LA): N[subscript sh]=1.7 g m⁻² LA, regardless of the conditions (low versus high density, controlled versus field conditions). Moreover, in a field dense stand, the comparison of plants with contrasting positions between the top and the bottom of the canopy (dominant, intermediate or suppressed plants), also shows that the difference in N[subscript sh] at similar shoot mass is explained by the proportion of leaf mass to shoot mass. These data support the idea that leaf growth drives the dynamics of shoot N accumulation. These results also indicate that competition for light among individual plants within a dense canopy induces developmental changes in plant morphology (leaf:stem ratio) that explain the differences observed in shoot N concentration. This last observation could be extrapolated to multispecific plant stands. Therefore, the sharing of N resources among plant species could partially be the result of the sharing of light within the canopy.</description><identifier>ISSN: 0022-0957</identifier><identifier>ISSN: 1460-2431</identifier><identifier>EISSN: 1460-2431</identifier><identifier>DOI: 10.1093/jxb/eri084</identifier><identifier>PMID: 15710638</identifier><identifier>CODEN: JEBOA6</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Average linear density ; Biological and medical sciences ; Botanics ; canopy ; Coefficients ; forage crops ; forage legumes ; Fundamental and applied biological sciences. Psychology ; Leaf area ; leaf:stem ratio ; Leaves ; Life Sciences ; Light ; Medicago sativa ; Medicago sativa L ; Medicago truncatula - growth & development ; N dilution ; Nitrogen ; Nitrogen - physiology ; nitrogen content ; nutrient uptake ; Plant density ; plant development ; Plant growth ; Plant growth. Development of the storage organs ; Plant Leaves - growth & development ; plant nutrition ; Plant physiology and development ; Plant Shoots - physiology ; Plants ; Population Density ; Regrowth ; RESEARCH PAPER ; shoot N accumulation ; shoots ; Vegetal Biology ; Vegetation canopies ; Vegetative apparatus, growth and morphogenesis. Senescence</subject><ispartof>Journal of experimental botany, 2005-03, Vol.56 (413), p.935-943</ispartof><rights>Society for Experimental Biology 2005</rights><rights>2005 INIST-CNRS</rights><rights>Copyright Oxford University Press(England) Mar 15, 2005</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c496t-e73e2347854b7f9a50b5bf3a8891f87f6ac75975835e5a5d770b09643665461a3</citedby><orcidid>0000-0003-3676-8364</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/24031054$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/24031054$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,315,781,785,804,886,27929,27930,58022,58255</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16642780$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15710638$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-02678576$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Lemaire, G</creatorcontrib><creatorcontrib>Avice, J-C</creatorcontrib><creatorcontrib>Kim, T-H</creatorcontrib><creatorcontrib>Ourry, A</creatorcontrib><title>Developmental changes in shoot N dynamics of lucerne (Medicago sativa L.) in relation to leaf growth dynamics as a function of plant density and hierarchical position within the canopy. [Erratum: 2005 May, v. 56, no. 415, p. 1437.]</title><title>Journal of experimental botany</title><addtitle>J. Exp. Bot</addtitle><description>Shoot N concentration in plants decreases as they get bigger, due to the fact that N accumulates less rapidly than dry matter in plants during the plant growth process, leading to an allometric relationship between shoot N content (N[subscript sh]) and shoot mass (W[subscript sh]): N[subscript sh]=a(W[subscript sh])[superscript b]. The results obtained on lucerne plants growing either under controlled low density conditions or in dense stands under field conditions show that the value of the allometric coefficient b that represents the ratio between the relative N accumulation rate in shoots [dN[subscript sh]/(N[subscript sh]dt)] and the relative growth rate [dW[subscript sh]/(W[subscript sh]dt)], decreases from 0.88 for a low plant density to 0.72 for a dense stand. Therefore, the fractional increase of shoot N per unit of shoot dry matter is lower when plants are in competition for light in dense canopies. This decrease can be entirely explained by the parallel decline in the leaf area per unit of shoot mass. Thus, a remarkably constant linear relationship can be established between N[subscript sh] and leaf area (LA): N[subscript sh]=1.7 g m⁻² LA, regardless of the conditions (low versus high density, controlled versus field conditions). Moreover, in a field dense stand, the comparison of plants with contrasting positions between the top and the bottom of the canopy (dominant, intermediate or suppressed plants), also shows that the difference in N[subscript sh] at similar shoot mass is explained by the proportion of leaf mass to shoot mass. These data support the idea that leaf growth drives the dynamics of shoot N accumulation. These results also indicate that competition for light among individual plants within a dense canopy induces developmental changes in plant morphology (leaf:stem ratio) that explain the differences observed in shoot N concentration. This last observation could be extrapolated to multispecific plant stands. Therefore, the sharing of N resources among plant species could partially be the result of the sharing of light within the canopy.</description><subject>Average linear density</subject><subject>Biological and medical sciences</subject><subject>Botanics</subject><subject>canopy</subject><subject>Coefficients</subject><subject>forage crops</subject><subject>forage legumes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Leaf area</subject><subject>leaf:stem ratio</subject><subject>Leaves</subject><subject>Life Sciences</subject><subject>Light</subject><subject>Medicago sativa</subject><subject>Medicago sativa L</subject><subject>Medicago truncatula - growth & development</subject><subject>N dilution</subject><subject>Nitrogen</subject><subject>Nitrogen - physiology</subject><subject>nitrogen content</subject><subject>nutrient uptake</subject><subject>Plant density</subject><subject>plant development</subject><subject>Plant growth</subject><subject>Plant growth. Development of the storage organs</subject><subject>Plant Leaves - growth & development</subject><subject>plant nutrition</subject><subject>Plant physiology and development</subject><subject>Plant Shoots - physiology</subject><subject>Plants</subject><subject>Population Density</subject><subject>Regrowth</subject><subject>RESEARCH PAPER</subject><subject>shoot N accumulation</subject><subject>shoots</subject><subject>Vegetal Biology</subject><subject>Vegetation canopies</subject><subject>Vegetative apparatus, growth and morphogenesis. Senescence</subject><issn>0022-0957</issn><issn>1460-2431</issn><issn>1460-2431</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkl1rFDEUhgdRbK3eeK8GQbHSnSaTrxnvaq1W2fpBLYgi4exsZmfW2WRMMtvuL_ZvmHGWFoRAyDlP3peTvEnykOCU4IIeLq9mh9o1OGe3kl3CBJ5kjJLbyS7GWTbBBZc7yT3vlxhjjjm_m-wQLgkWNN9N_rzRa93abqVNgBaVNZiF9qgxyNfWBvQRzTcGVk3pka1Q25faGY1enOl5U8LCIg-hWQOapvvDHafbeLYGBYtaDRVaOHsZ6hsNiAtVvSn_UVGxa8EENNfGN2GDwMxR3WgHrqyjfos6G-sDetmEOhqEWqMSjO02Kfpx4hyEfvUKZXEwdAabA7ROERcHyNgUMcIPUJciwqhMf95P7lTQev1gu-8lF29Pvh6fTqaf3r0_PppOSlaIMNGS6owymXM2k1UBHM_4rKKQ5wWpclkJKCUvJM8p1xz4XEo8w4VgVAjOBAG6l-yPujW0qnPNCtxGWWjU6dFUDTWciaguxZpE9vnIds7-7rUPatX4UrfxSbTtvRKSFZLxAXz6H7i0vTNxDpVRjocf5hF6OUKls947XV3bE6yGnKiYEzXmJMKPt4r9bKXnN-g2GBF4tgXAx4-oHJiy8TecECyTOY7co5Fb-mDddT9jmBLMB6PJ2G980FfXfXC_4nhUcnX67bv68nlKP7DXVJ1H_snIV2AVLFz0vDjPMKFxykIQjulf-ZDlVQ</recordid><startdate>20050301</startdate><enddate>20050301</enddate><creator>Lemaire, G</creator><creator>Avice, J-C</creator><creator>Kim, T-H</creator><creator>Ourry, A</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><general>Oxford University Press (OUP)</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7QP</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-3676-8364</orcidid></search><sort><creationdate>20050301</creationdate><title>Developmental changes in shoot N dynamics of lucerne (Medicago sativa L.) in relation to leaf growth dynamics as a function of plant density and hierarchical position within the canopy. [Erratum: 2005 May, v. 56, no. 415, p. 1437.]</title><author>Lemaire, G ; Avice, J-C ; Kim, T-H ; Ourry, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c496t-e73e2347854b7f9a50b5bf3a8891f87f6ac75975835e5a5d770b09643665461a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Average linear density</topic><topic>Biological and medical sciences</topic><topic>Botanics</topic><topic>canopy</topic><topic>Coefficients</topic><topic>forage crops</topic><topic>forage legumes</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Leaf area</topic><topic>leaf:stem ratio</topic><topic>Leaves</topic><topic>Life Sciences</topic><topic>Light</topic><topic>Medicago sativa</topic><topic>Medicago sativa L</topic><topic>Medicago truncatula - growth & development</topic><topic>N dilution</topic><topic>Nitrogen</topic><topic>Nitrogen - physiology</topic><topic>nitrogen content</topic><topic>nutrient uptake</topic><topic>Plant density</topic><topic>plant development</topic><topic>Plant growth</topic><topic>Plant growth. Development of the storage organs</topic><topic>Plant Leaves - growth & development</topic><topic>plant nutrition</topic><topic>Plant physiology and development</topic><topic>Plant Shoots - physiology</topic><topic>Plants</topic><topic>Population Density</topic><topic>Regrowth</topic><topic>RESEARCH PAPER</topic><topic>shoot N accumulation</topic><topic>shoots</topic><topic>Vegetal Biology</topic><topic>Vegetation canopies</topic><topic>Vegetative apparatus, growth and morphogenesis. Senescence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lemaire, G</creatorcontrib><creatorcontrib>Avice, J-C</creatorcontrib><creatorcontrib>Kim, T-H</creatorcontrib><creatorcontrib>Ourry, A</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of experimental botany</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lemaire, G</au><au>Avice, J-C</au><au>Kim, T-H</au><au>Ourry, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Developmental changes in shoot N dynamics of lucerne (Medicago sativa L.) in relation to leaf growth dynamics as a function of plant density and hierarchical position within the canopy. [Erratum: 2005 May, v. 56, no. 415, p. 1437.]</atitle><jtitle>Journal of experimental botany</jtitle><addtitle>J. Exp. Bot</addtitle><date>2005-03-01</date><risdate>2005</risdate><volume>56</volume><issue>413</issue><spage>935</spage><epage>943</epage><pages>935-943</pages><issn>0022-0957</issn><issn>1460-2431</issn><eissn>1460-2431</eissn><coden>JEBOA6</coden><abstract>Shoot N concentration in plants decreases as they get bigger, due to the fact that N accumulates less rapidly than dry matter in plants during the plant growth process, leading to an allometric relationship between shoot N content (N[subscript sh]) and shoot mass (W[subscript sh]): N[subscript sh]=a(W[subscript sh])[superscript b]. The results obtained on lucerne plants growing either under controlled low density conditions or in dense stands under field conditions show that the value of the allometric coefficient b that represents the ratio between the relative N accumulation rate in shoots [dN[subscript sh]/(N[subscript sh]dt)] and the relative growth rate [dW[subscript sh]/(W[subscript sh]dt)], decreases from 0.88 for a low plant density to 0.72 for a dense stand. Therefore, the fractional increase of shoot N per unit of shoot dry matter is lower when plants are in competition for light in dense canopies. This decrease can be entirely explained by the parallel decline in the leaf area per unit of shoot mass. Thus, a remarkably constant linear relationship can be established between N[subscript sh] and leaf area (LA): N[subscript sh]=1.7 g m⁻² LA, regardless of the conditions (low versus high density, controlled versus field conditions). Moreover, in a field dense stand, the comparison of plants with contrasting positions between the top and the bottom of the canopy (dominant, intermediate or suppressed plants), also shows that the difference in N[subscript sh] at similar shoot mass is explained by the proportion of leaf mass to shoot mass. These data support the idea that leaf growth drives the dynamics of shoot N accumulation. These results also indicate that competition for light among individual plants within a dense canopy induces developmental changes in plant morphology (leaf:stem ratio) that explain the differences observed in shoot N concentration. This last observation could be extrapolated to multispecific plant stands. Therefore, the sharing of N resources among plant species could partially be the result of the sharing of light within the canopy.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>15710638</pmid><doi>10.1093/jxb/eri084</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-3676-8364</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Average linear density Biological and medical sciences Botanics canopy Coefficients forage crops forage legumes Fundamental and applied biological sciences. Psychology Leaf area leaf:stem ratio Leaves Life Sciences Light Medicago sativa Medicago sativa L Medicago truncatula - growth & development N dilution Nitrogen Nitrogen - physiology nitrogen content nutrient uptake Plant density plant development Plant growth Plant growth. Development of the storage organs Plant Leaves - growth & development plant nutrition Plant physiology and development Plant Shoots - physiology Plants Population Density Regrowth RESEARCH PAPER shoot N accumulation shoots Vegetal Biology Vegetation canopies Vegetative apparatus, growth and morphogenesis. Senescence |
title | Developmental changes in shoot N dynamics of lucerne (Medicago sativa L.) in relation to leaf growth dynamics as a function of plant density and hierarchical position within the canopy. [Erratum: 2005 May, v. 56, no. 415, p. 1437.] |
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