Effect of top excision and replacement by 1-naphthylacetic acid on partition and flow of potassium in tobacco plants

The effect of removal of the shoot apex of 92-d-old tobacco plants and its replacement by 1-naphthylacetic acid (NAA) on sink-source relationships and on the flows and partitioning of potassium and water has been studied over a short-term period of 7 d (intact control plants) or 8 d (decapitated and...

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Publié dans:Journal of experimental botany. - 1985. - 52(2001), 364 vom: 15. Nov., Seite 2143-50
Auteur principal: Jiang, F (Auteur)
Autres auteurs: Li, C, Jeschke, W D, Zhang, F
Format: Article
Langue:English
Publié: 2001
Accès à la collection:Journal of experimental botany
Sujets:Journal Article Research Support, Non-U.S. Gov't Naphthaleneacetic Acids 1-naphthaleneacetic acid 33T7G7757C Potassium RWP5GA015D
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520 |a The effect of removal of the shoot apex of 92-d-old tobacco plants and its replacement by 1-naphthylacetic acid (NAA) on sink-source relationships and on the flows and partitioning of potassium and water has been studied over a short-term period of 7 d (intact control plants) or 8 d (decapitated and NAA-treated plants). For determining flows an upper, middle and lower stratum of three leaves each were analysed. Within the study period three new leaves were formed in control plants and 57.7% of the total dry matter increment during the experimental period was allocated to the apex and these newly formed leaves. An even higher proportion of the K+ taken up (93.8%) was deposited in these organs and this was imported via xylem (72%) and phloem (28%). Only 18.7% and 9.8% of the total dry matter increment were found in the previously present upper leaves and the roots, respectively, and substantial net K+ export occurred from middle and lower leaves and roots. Decapitation removed the dominant phloem sink and caused marked changes in sink-source relationships. After decapitation the net increase in root dry matter was twice that of control plants. 56.2% of the total net increments in dry matter and 70% of the absorbed K+ were deposited in upper leaves (below the excised apex). There was only slight net K+ export from the middle leaves. Application of NAA on the cut surface of the stem stump did not change the growth of plants that much, apart from a substantial increase in stem growth, correspondingly it stimulated the partitioning of K+ into the upper leaves and most dramatically into the stem, which deposited 64.5% or 27% of the K+ uptake, respectively. In these plants K+ uptake was increased and the K+ concentrations in upper, middle and lower leaves were increased from 4.7, 5.4 and 5.6 to 5.1, 6.1 and 6.1% of dry matter, respectively. Possible mechanisms of this effect of NAA on the improvement of K+ concentration in tobacco leaves are discussed in detail 
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