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Responses of "Newhall" orange trees to iron deficiency in hydroponics : Effects on leaf chlorophyll, photosynthetic efficiency, and root ferric chelate reductase activity

Identifieur interne : 000838 ( PascalFrancis/Checkpoint ); précédent : 000837; suivant : 000839

Responses of "Newhall" orange trees to iron deficiency in hydroponics : Effects on leaf chlorophyll, photosynthetic efficiency, and root ferric chelate reductase activity

Auteurs : Maribela Pestana [Portugal] ; Manuela David [Portugal] ; Amarilis De Varennes [Portugal] ; Javier Abadia [Espagne] ; Eugénio Araujo Faria [Portugal]

Source :

RBID : Pascal:03-0026028

Descripteurs français

English descriptors

Abstract

Orange (Citrus sinensis L. Osb. cv. 'Newhall') plants grafted on Citrange troyer rootstock were grown in nutrient solution with 0, 5, 10, or 20 μM iron (Fe), with and without calcium carbonate. Calcium carbonate was added in order to mimic the natural conditions in calcareous soils. Leaf chlorophyll concentration was estimated every 3-4 days using the portable instrument SPAD-502 meter. Chlorophyll fluorescence parameters, photosynthetic capacity estimated from oxygen evolution, leaf Fe concentrations, and root tip ferric chelate reductase activity were measured at the end of the experiment. Plants from the 0 and 5 μM Fe treatments showed leaf chlorosis and had decreased leaf chlorophyll concentrations. Leaves of plants grown in the absence of Fe in the solution had smaller rates of oxygen evolution both in the presence and absence of calcium carbonate, compared with plants grown in the presence of 10 μM Fe. In the absence of calcium carbonate the photosystem II efficiency, estimated from fluorescence parameters, was similar in all treatments. A slight decrease in photosystem II efficiency was observed in plants grown without Fe and in the presence of calcium carbonate. A 2.5-fold increase in root tip ferric chelate reductase activity over the control values was found only when plants were grown with low levels of Fe and in the presence of calcium carbonate.


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Pascal:03-0026028

Le document en format XML

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<title xml:lang="en" level="a">Responses of "Newhall" orange trees to iron deficiency in hydroponics : Effects on leaf chlorophyll, photosynthetic efficiency, and root ferric chelate reductase activity</title>
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<term>Ferric-chelate reductase</term>
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<div type="abstract" xml:lang="en">Orange (Citrus sinensis L. Osb. cv. 'Newhall') plants grafted on Citrange troyer rootstock were grown in nutrient solution with 0, 5, 10, or 20 μM iron (Fe), with and without calcium carbonate. Calcium carbonate was added in order to mimic the natural conditions in calcareous soils. Leaf chlorophyll concentration was estimated every 3-4 days using the portable instrument SPAD-502 meter. Chlorophyll fluorescence parameters, photosynthetic capacity estimated from oxygen evolution, leaf Fe concentrations, and root tip ferric chelate reductase activity were measured at the end of the experiment. Plants from the 0 and 5 μM Fe treatments showed leaf chlorosis and had decreased leaf chlorophyll concentrations. Leaves of plants grown in the absence of Fe in the solution had smaller rates of oxygen evolution both in the presence and absence of calcium carbonate, compared with plants grown in the presence of 10 μM Fe. In the absence of calcium carbonate the photosystem II efficiency, estimated from fluorescence parameters, was similar in all treatments. A slight decrease in photosystem II efficiency was observed in plants grown without Fe and in the presence of calcium carbonate. A 2.5-fold increase in root tip ferric chelate reductase activity over the control values was found only when plants were grown with low levels of Fe and in the presence of calcium carbonate.</div>
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<s0>Culture hydroponique</s0>
<s5>28</s5>
</fC03>
<fC03 i1="14" i2="X" l="ENG">
<s0>Hydroponic cultivation</s0>
<s5>28</s5>
</fC03>
<fC03 i1="14" i2="X" l="SPA">
<s0>Cultivo hidropónico</s0>
<s5>28</s5>
</fC03>
<fC03 i1="15" i2="X" l="FRE">
<s0>Absorption</s0>
<s4>INC</s4>
<s5>68</s5>
</fC03>
<fC03 i1="16" i2="X" l="FRE">
<s0>Biodisponibilité</s0>
<s4>INC</s4>
<s5>69</s5>
</fC03>
<fC03 i1="17" i2="X" l="FRE">
<s0>Concentration chimique</s0>
<s4>INC</s4>
<s5>70</s5>
</fC03>
<fC03 i1="18" i2="X" l="FRE">
<s0>Echange gazeux</s0>
<s4>INC</s4>
<s5>71</s5>
</fC03>
<fC03 i1="19" i2="X" l="FRE">
<s0>Fluorescence</s0>
<s4>INC</s4>
<s5>72</s5>
</fC03>
<fC03 i1="20" i2="X" l="FRE">
<s0>Oxydoréduction</s0>
<s4>INC</s4>
<s5>73</s5>
</fC03>
<fC03 i1="21" i2="X" l="FRE">
<s0>Transport membranaire</s0>
<s4>INC</s4>
<s5>74</s5>
</fC03>
<fC03 i1="22" i2="X" l="FRE">
<s0>Trouble nutrition</s0>
<s4>INC</s4>
<s5>75</s5>
</fC03>
<fC03 i1="23" i2="X" l="FRE">
<s0>Membrane plasmique</s0>
<s4>INC</s4>
<s5>76</s5>
</fC03>
<fC03 i1="24" i2="X" l="FRE">
<s0>Photosystème 2</s0>
<s4>INC</s4>
<s5>77</s5>
</fC03>
<fC03 i1="25" i2="X" l="FRE">
<s0>Facteur influence</s0>
<s4>INC</s4>
<s5>78</s5>
</fC03>
<fC03 i1="26" i2="X" l="FRE">
<s0>Facteur milieu</s0>
<s4>INC</s4>
<s5>79</s5>
</fC03>
<fC03 i1="27" i2="X" l="FRE">
<s0>Facteur édaphique</s0>
<s4>INC</s4>
<s5>80</s5>
</fC03>
<fC03 i1="28" i2="X" l="FRE">
<s0>Calcium carbonate</s0>
<s4>INC</s4>
<s5>81</s5>
</fC03>
<fC03 i1="29" i2="X" l="FRE">
<s0>Oxygène?Molécule</s0>
<s4>INC</s4>
<s5>82</s5>
</fC03>
<fC03 i1="30" i2="X" l="FRE">
<s0>Solution nutritive</s0>
<s4>INC</s4>
<s5>83</s5>
</fC03>
<fC03 i1="31" i2="X" l="FRE">
<s0>Sol calcaire</s0>
<s4>INC</s4>
<s5>84</s5>
</fC03>
<fC03 i1="32" i2="X" l="FRE">
<s0>Sol de verger</s0>
<s4>INC</s4>
<s5>85</s5>
</fC03>
<fC03 i1="33" i2="X" l="FRE">
<s0>Simulation physique</s0>
<s4>INC</s4>
<s5>86</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Rutaceae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Rutaceae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Rutaceae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Oxidoreductases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Oxidoreductases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Oxidoreductases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Enzyme</s0>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Enzyme</s0>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Enzima</s0>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Arboriculture</s0>
<s5>33</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Arboriculture</s0>
<s5>33</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Arboricultura</s0>
<s5>33</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Nutrition</s0>
<s5>35</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>Nutrition</s0>
<s5>35</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>Nutrición</s0>
<s5>35</s5>
</fC07>
<fC07 i1="09" i2="X" l="FRE">
<s0>Physiologie</s0>
<s5>36</s5>
</fC07>
<fC07 i1="09" i2="X" l="ENG">
<s0>Physiology</s0>
<s5>36</s5>
</fC07>
<fC07 i1="09" i2="X" l="SPA">
<s0>Fisiología</s0>
<s5>36</s5>
</fC07>
<fC07 i1="10" i2="X" l="FRE">
<s0>Relation sol plante</s0>
<s5>37</s5>
</fC07>
<fC07 i1="10" i2="X" l="ENG">
<s0>Soil plant relation</s0>
<s5>37</s5>
</fC07>
<fC07 i1="10" i2="X" l="SPA">
<s0>Relación suelo planta</s0>
<s5>37</s5>
</fC07>
<fC07 i1="11" i2="X" l="FRE">
<s0>Agrume</s0>
<s5>41</s5>
</fC07>
<fC07 i1="11" i2="X" l="ENG">
<s0>Citrus fruit</s0>
<s5>41</s5>
</fC07>
<fC07 i1="11" i2="X" l="SPA">
<s0>Agrios</s0>
<s5>41</s5>
</fC07>
<fC07 i1="12" i2="X" l="FRE">
<s0>Arbre fruitier</s0>
<s5>42</s5>
</fC07>
<fC07 i1="12" i2="X" l="ENG">
<s0>Fruit tree</s0>
<s5>42</s5>
</fC07>
<fC07 i1="12" i2="X" l="SPA">
<s0>Arbol frutal</s0>
<s5>42</s5>
</fC07>
<fC07 i1="13" i2="X" l="FRE">
<s0>Plante fruitière</s0>
<s5>43</s5>
</fC07>
<fC07 i1="13" i2="X" l="ENG">
<s0>Fruit crop</s0>
<s5>43</s5>
</fC07>
<fC07 i1="13" i2="X" l="SPA">
<s0>Planta frutal</s0>
<s5>43</s5>
</fC07>
<fC07 i1="14" i2="X" l="FRE">
<s0>Elément minéral</s0>
<s5>50</s5>
</fC07>
<fC07 i1="14" i2="X" l="ENG">
<s0>Inorganic element</s0>
<s5>50</s5>
</fC07>
<fC07 i1="14" i2="X" l="SPA">
<s0>Elemento inorgánico</s0>
<s5>50</s5>
</fC07>
<fC07 i1="15" i2="X" l="FRE">
<s0>Oligoélément</s0>
<s5>51</s5>
</fC07>
<fC07 i1="15" i2="X" l="ENG">
<s0>Trace element (nutrient)</s0>
<s5>51</s5>
</fC07>
<fC07 i1="15" i2="X" l="SPA">
<s0>Oligoelemento</s0>
<s5>51</s5>
</fC07>
<fC07 i1="16" i2="X" l="FRE">
<s0>Pigment photosynthétique</s0>
<s5>52</s5>
</fC07>
<fC07 i1="16" i2="X" l="ENG">
<s0>Photosynthetic pigment</s0>
<s5>52</s5>
</fC07>
<fC07 i1="16" i2="X" l="SPA">
<s0>Pigmento fotosintético</s0>
<s5>52</s5>
</fC07>
<fN21>
<s1>013</s1>
</fN21>
</pA>
</standard>
</inist>
<affiliations>
<list>
<country>
<li>Espagne</li>
<li>Portugal</li>
</country>
<region>
<li>Aragon</li>
</region>
</list>
<tree>
<country name="Portugal">
<noRegion>
<name sortKey="Pestana, Maribela" sort="Pestana, Maribela" uniqKey="Pestana M" first="Maribela" last="Pestana">Maribela Pestana</name>
</noRegion>
<name sortKey="Araujo Faria, Eugenio" sort="Araujo Faria, Eugenio" uniqKey="Araujo Faria E" first="Eugénio" last="Araujo Faria">Eugénio Araujo Faria</name>
<name sortKey="David, Manuela" sort="David, Manuela" uniqKey="David M" first="Manuela" last="David">Manuela David</name>
<name sortKey="De Varennes, Amarilis" sort="De Varennes, Amarilis" uniqKey="De Varennes A" first="Amarilis" last="De Varennes">Amarilis De Varennes</name>
</country>
<country name="Espagne">
<region name="Aragon">
<name sortKey="Abadia, Javier" sort="Abadia, Javier" uniqKey="Abadia J" first="Javier" last="Abadia">Javier Abadia</name>
</region>
</country>
</tree>
</affiliations>
</record>

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