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dc.contributor.authorMencuccini, M
dc.contributor.authorRosas, T
dc.contributor.authorRowland, L
dc.contributor.authorChoat, B
dc.contributor.authorCornelissen, H
dc.contributor.authorJansen, S
dc.contributor.authorKramer, K
dc.contributor.authorLapenis, A
dc.contributor.authorManzoni, S
dc.contributor.authorNiinemets, Ü
dc.contributor.authorReich, P
dc.contributor.authorSchrodt, F
dc.contributor.authorSoudzilovskaia, N
dc.contributor.authorWright, IH
dc.contributor.authorMartínez-Vilalta, J
dc.date.accessioned2019-07-23T09:11:33Z
dc.date.issued2019-06-19
dc.description.abstractBiomass and area ratios between leaves, stems and roots regulate many physiological and ecological processes. The Huber value Hv (sapwood area/leaf area ratio) is central to plant water balance and drought responses. However, its coordination with key plant functional traits is poorly understood, which prevents developing trait-based prediction models. Based on theoretical arguments, we hypothesise that global patterns in Hv of terminal woody branches can be predicted from variables related to plant trait spectra, i.e., plant hydraulics and size and leaf economics. Using a global compilation of 1135 species-averaged Hv , we show that Hv varies over 3 orders of magnitude. Higher Hv are seen in short small-leaved low-SLA shrubs with low Ks in arid relative to tall large-leaved high-SLA trees with high Ks in moist environments. All traits depend on climate but climatic correlations are stronger for explanatory traits than Hv . Negative isometry is found between Hv and Ks , suggesting a compensation to maintain hydraulic supply to leaves across species. This work identifies the major global drivers of branch sapwood/leaf area ratios. Our approach based on widely available traits facilitates the development of accurate models of aboveground biomass allocation and helps predict vegetation responses to drought.en_GB
dc.description.sponsorshipSpanish Ministry of Economy and Competitiveness (MINECO)en_GB
dc.description.sponsorshipUniversity of Nottinghamen_GB
dc.description.sponsorshipSwedish Research Council Formasen_GB
dc.identifier.citationPublished online 19 June 2019en_GB
dc.identifier.doi10.1111/nph.15998
dc.identifier.grantnumberCGL2013‐46808‐Ren_GB
dc.identifier.grantnumberCGL2017‐89149‐C2‐1‐Ren_GB
dc.identifier.grantnumber2016–00998en_GB
dc.identifier.urihttp://hdl.handle.net/10871/38082
dc.language.isoenen_GB
dc.publisherWiley for Phytologist Trusten_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/31215647en_GB
dc.rights.embargoreasonUnder embargo until 19 June 2020 in compliance with publisher policyen_GB
dc.rights© 2019 The Authors. New Phytologist © 2019 New Phytologist Trusten_GB
dc.subjectCorner's rulesen_GB
dc.subjectHuber valueen_GB
dc.subjectbiomechanicsen_GB
dc.subjectleaf economics spectrumen_GB
dc.subjectleaf sizeen_GB
dc.subjecttrait tradeoffen_GB
dc.subjectwood densityen_GB
dc.subjectxylem hydraulicsen_GB
dc.titleLeaf economics and plant hydraulics drive leaf : wood area ratiosen_GB
dc.typeArticleen_GB
dc.date.available2019-07-23T09:11:33Z
exeter.place-of-publicationEnglanden_GB
dc.descriptionThis is the author accepted manuscript. The final version is available from Wiley via the DOI in this recorden_GB
dc.descriptionData accessibility: All data are archived and are available from the TRY plant trait data base: www.try-db.org (https://doi.org/10.1111/j.1365-2486.2011.02451.x).en_GB
dc.identifier.eissn1469-8137
dc.identifier.journalNew Phytologisten_GB
dc.rights.urihttp://www.rioxx.net/licenses/all-rights-reserveden_GB
dcterms.dateAccepted2019-06-08
exeter.funder::Natural Environment Research Council (NERC)en_GB
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2019-06-19
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2019-07-23T09:07:04Z
refterms.versionFCDAM
refterms.dateFOA2020-06-18T23:00:00Z
refterms.panelCen_GB


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