001     58850
005     20180211170127.0
024 7 _ |2 pmid
|a pmid:18761499
024 7 _ |2 DOI
|a 10.1111/j.1438-8677.2008.00062.x
024 7 _ |2 WOS
|a WOS:000258288200009
037 _ _ |a PreJuSER-58850
041 _ _ |a eng
082 _ _ |a 580
084 _ _ |2 WoS
|a Plant Sciences
100 1 _ |a Westhoff, M.
|b 0
|0 P:(DE-HGF)0
245 _ _ |a The mechanisms of refilling of the xylem conduits and bleeding of tall birch during spring
260 _ _ |a Oxford [u.a.] :Wiley- Blackwell
|b Wiley-Blackwell - STM
|c 2008
300 _ _ |a 604 - 623
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|0 0
|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a Plant Biology
|x 1435-8603
|0 10981
|y 5
|v 10
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a Seasonal variations in osmolality and components of xylem sap in tall birch trees were determined using several techniques. Xylem sap was extracted from branch and trunk sections of 58 trees using the very rapid gas bubble-based jet-discharge method. The 5-cm long wood pieces were taken at short intervals over the entire tree height. The data show that large biphasic osmolality gradients temporarily exist within the conducting xylem conduits during leaf emergence (up to 272 mosmol x kg(-1) at the apex). These gradients (arising mainly from glucose and fructose) were clearly held within the xylem conduit as demonstrated by (1)H NMR imaging of intact twigs. Refilling experiments with benzene, sucrose infusion, electron and light microscopy, as well as (1)H NMR chemical shift microimaging provided evidence that the xylem of birch represents a compartment confined by solute-reflecting barriers (radial: lipid linings/lipid bodies; axial: presumably air-filled spaces). These features allow transformation of osmolality gradients into osmotic pressure gradients. Refilling of the xylem occurs by a dual mechanism: from the base (by root pressure) and from the top (by hydrostatic pressure generated by xylem-bound osmotic pressure). The generation of osmotic pressure gradients was accompanied by bleeding. Bleeding could be observed at a height of up to 21 m. Bleeding rates measured at a given height decreased exponentially with time. Evidence is presented that the driving force for bleeding is the weight of the static water columns above the bleeding point. The pressure exerted by the water columns and the bleeding volume depend on the water-filling status of (communicating) vessels.
536 _ _ |a Terrestrische Umwelt
|c P24
|2 G:(DE-HGF)
|0 G:(DE-Juel1)FUEK407
|x 0
588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Betula: physiology
650 _ 2 |2 MeSH
|a Carbohydrate Metabolism
650 _ 2 |2 MeSH
|a Electrolytes: metabolism
650 _ 2 |2 MeSH
|a Magnetic Resonance Spectroscopy
650 _ 2 |2 MeSH
|a Osmolar Concentration
650 _ 2 |2 MeSH
|a Osmotic Pressure
650 _ 2 |2 MeSH
|a Plant Roots: physiology
650 _ 2 |2 MeSH
|a Seasons
650 _ 2 |2 MeSH
|a Trees: physiology
650 _ 2 |2 MeSH
|a Water: physiology
650 _ 2 |2 MeSH
|a Xylem: physiology
650 _ 7 |0 0
|2 NLM Chemicals
|a Electrolytes
650 _ 7 |0 7732-18-5
|2 NLM Chemicals
|a Water
650 _ 7 |a J
|2 WoSType
653 2 0 |2 Author
|a Betula pendula (birch)
653 2 0 |2 Author
|a lipids
653 2 0 |2 Author
|a osmotic pressure gradients
653 2 0 |2 Author
|a root pressure
653 2 0 |2 Author
|a sap bleeding
653 2 0 |2 Author
|a sugars
653 2 0 |2 Author
|a xylem refilling
700 1 _ |a Schneider, H.
|b 1
|u FZJ
|0 P:(DE-Juel1)129397
700 1 _ |a Zimmermann, D.
|b 2
|0 P:(DE-HGF)0
700 1 _ |a Mimietz, S.
|b 3
|0 P:(DE-HGF)0
700 1 _ |a Stinzing, A.
|b 4
|0 P:(DE-HGF)0
700 1 _ |a Wegner, L. H.
|b 5
|0 P:(DE-HGF)0
700 1 _ |a Kaiser, W.
|b 6
|0 P:(DE-HGF)0
700 1 _ |a Krohne, G.
|b 7
|0 P:(DE-HGF)0
700 1 _ |a Shirley, St.
|b 8
|0 P:(DE-HGF)0
700 1 _ |a Jakob, P.
|b 9
|0 P:(DE-HGF)0
700 1 _ |a Bamberg, E.
|b 10
|0 P:(DE-HGF)0
700 1 _ |a Bentrup, F.-W.
|b 11
|0 P:(DE-HGF)0
700 1 _ |a Zimmermann, U.
|b 12
|0 P:(DE-HGF)0
773 _ _ |a 10.1111/j.1438-8677.2008.00062.x
|g Vol. 10, p. 604 - 623
|p 604 - 623
|q 10<604 - 623
|0 PERI:(DE-600)2026390-9
|t Plant biology
|v 10
|y 2008
|x 1435-8603
856 7 _ |u http://dx.doi.org/10.1111/j.1438-8677.2008.00062.x
909 C O |o oai:juser.fz-juelich.de:58850
|p VDB
913 1 _ |k P24
|v Terrestrische Umwelt
|l Terrestrische Umwelt
|b Erde und Umwelt
|0 G:(DE-Juel1)FUEK407
|x 0
914 1 _ |y 2008
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |k ICG-3
|l Phytosphäre
|d 31.10.2010
|g ICG
|0 I:(DE-Juel1)ICG-3-20090406
|x 1
970 _ _ |a VDB:(DE-Juel1)92733
980 _ _ |a VDB
980 _ _ |a ConvertedRecord
980 _ _ |a journal
980 _ _ |a I:(DE-Juel1)IBG-2-20101118
980 _ _ |a UNRESTRICTED
981 _ _ |a I:(DE-Juel1)IBG-2-20101118
981 _ _ |a I:(DE-Juel1)ICG-3-20090406


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