001     14158
005     20200423202939.0
024 7 _ |2 DOI
|a 10.1071/FP10156
024 7 _ |2 WOS
|a WOS:000286773600005
037 _ _ |a PreJuSER-14158
041 _ _ |a eng
082 _ _ |a 580
084 _ _ |2 WoS
|a Plant Sciences
100 1 _ |0 P:(DE-Juel1)VDB67249
|a Thorpe, M.R.
|b 0
|u FZJ
245 _ _ |a Modelling phloem transport within a pruned dwarf bean: a 2-source-3-sink system
260 _ _ |a Collingwood, Victoria
|b CSIRO Publ.
|c 2011
300 _ _ |a 127 - 138
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 |0 9141
|a Functional Plant Biology
|x 1445-4408
|y 38
500 _ _ |a The 11C work could not have been done without the very competent technical help from Marco Dautzenberg. PEHM was funded by FRST funding: Contract C06X0706.
520 _ _ |a A mechanistic model of carbon partitioning, based on the Munch hypothesis of phloem transport and implemented with PIAF-Munch modelling platform (Lacointe and Minchin 2008), was tested for an architecture more complex than any tested previously. Using C-11 to label photosynthate, responses in transport of photosynthate within a heavily pruned dwarf bean plant (Phaseolus vulgaris L.) to changes in source and sink activities were compared with model predictions. The observed treatment responses were successfully predicted. However, the observations could not be completely explained if the modelled stem contained only one phloem pathway: tracer from a labelled leaf was always detected in both shoot apex and root, whichever of the two leaves was labelled. This shows that bidirectional flow occurred within the stem, with solute moving simultaneously in both directions. Nevertheless, a model architecture with very little more complexity could incorporate such bidirectional flow. We concluded that the model could explain the observations, and that the PIAF-Munch model platform can be expected to describe partitioning in even more complex architectures.
536 _ _ |0 G:(DE-Juel1)FUEK407
|2 G:(DE-HGF)
|a Terrestrische Umwelt
|c P24
|x 0
588 _ _ |a Dataset connected to Web of Science
650 _ 7 |2 WoSType
|a J
653 2 0 |2 Author
|a C-11
653 2 0 |2 Author
|a carbon-11
653 2 0 |2 Author
|a Munch
653 2 0 |2 Author
|a source sink interactions
700 1 _ |0 P:(DE-HGF)0
|a Lacointe, A.
|b 1
700 1 _ |0 P:(DE-Juel1)VDB97177
|a Minchin, P.W.
|b 2
|u FZJ
773 _ _ |0 PERI:(DE-600)1496158-1
|a 10.1071/FP10156
|g p. 127 - 138
|p 127 - 138
|q 127 - 138
|t Functional plant biology
|x 1445-4408
|y 2011
856 4 _ |u https://juser.fz-juelich.de/record/14158/files/FZJ-14158.pdf
|y Restricted
|z Published final document.
909 C O |o oai:juser.fz-juelich.de:14158
|p VDB
913 1 _ |0 G:(DE-Juel1)FUEK407
|a DE-HGF
|b Erde und Umwelt
|k P24
|l Terrestrische Umwelt
|v Terrestrische Umwelt
|x 0
913 2 _ |0 G:(DE-HGF)POF3-582
|1 G:(DE-HGF)POF3-580
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|a DE-HGF
|b Key Technologies
|l Key Technologies for the Bioeconomy
|v Plant Science
|x 0
914 1 _ |y 2011
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |0 I:(DE-Juel1)IBG-2-20101118
|g IBG
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|l Pflanzenwissenschaften
|x 0
970 _ _ |a VDB:(DE-Juel1)126089
980 _ _ |a VDB
980 _ _ |a ConvertedRecord
980 _ _ |a journal
980 _ _ |a I:(DE-Juel1)IBG-2-20101118
980 _ _ |a UNRESTRICTED


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