2019
DOI: 10.1186/s12870-019-2017-2
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Gas exchange, biomass and non-structural carbohydrates dynamics in vines under combined drought and biotic stress

Abstract: Background Intensity of drought stress and pest attacks is forecasted to increase in the near future posing a serious threat to natural and agricultural ecosystems. Knowledge on potential effects of a combined abiotic-biotic stress on whole-plant physiology is lacking. We monitored the water status and carbon metabolism of a vine rootstock with or without scion subjected to water shortening and/or infestation with the sucking insect phylloxera (Daktulosphaira vitifoliae Fitch). We measured non-… Show more

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Cited by 19 publications
(22 citation statements)
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References 42 publications
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“…Similar to that study, P. ficus caused stress at the leaf-level and reduced the LMA, suggesting that infested grapevines invest less carbon per unit leaf area compared to the uninfested controls and the low-density treatment. Surprisingly, despite the reduced LMA, phylloxerated grapevines did not show a decline in leaf or stem biomass (Savi et al, 2019), while in our study the reduced LMA translated into reduced leaf biomass. Lower biomass allocation to leaves and stems might be a direct consequence of 1) the carbon export towards the P. ficus population, affecting stems at lower infestation levels than leaves, 2) a reallocation of carbohydrates from the stems to the leaves, 3) the redirection of energy to secondary metabolic pathways (defence, repair, signalling, phytohormonal networks) (Timm and Reineke, 2014), or 4) a reduced source availability due to reduced photosynthetic capacity.…”
Section: Growth Ratios Lar and Lmacontrasting
confidence: 86%
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“…Similar to that study, P. ficus caused stress at the leaf-level and reduced the LMA, suggesting that infested grapevines invest less carbon per unit leaf area compared to the uninfested controls and the low-density treatment. Surprisingly, despite the reduced LMA, phylloxerated grapevines did not show a decline in leaf or stem biomass (Savi et al, 2019), while in our study the reduced LMA translated into reduced leaf biomass. Lower biomass allocation to leaves and stems might be a direct consequence of 1) the carbon export towards the P. ficus population, affecting stems at lower infestation levels than leaves, 2) a reallocation of carbohydrates from the stems to the leaves, 3) the redirection of energy to secondary metabolic pathways (defence, repair, signalling, phytohormonal networks) (Timm and Reineke, 2014), or 4) a reduced source availability due to reduced photosynthetic capacity.…”
Section: Growth Ratios Lar and Lmacontrasting
confidence: 86%
“…The LMA of grapevine plants in the present study varied between 3.16 and 4.03 mg/cm 2 for the high-density and the control treatment respectively; this is somewhat lower than the LMA of Riesling grapevines, which showed a reduction from 6.1 to 5.6 mg/cm 2 when leaves were infested with phylloxera (Savi et al, 2019). Similar to that study, P. ficus caused stress at the leaf-level and reduced the LMA, suggesting that infested grapevines invest less carbon per unit leaf area compared to the uninfested controls and the low-density treatment.…”
Section: Growth Ratios Lar and Lmacontrasting
confidence: 75%
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“…The accumulation of these carbohydrates also improved the water stress tolerance in several plants, such as Arabidopsis thaliana [ 74 76 ], Medicago sativa [ 77 ], Xerophyta viscosa [ 78 ], Zea mays [ 79 ], Coffea [ 80 ] and Malus domestica [ 81 ]. Grapevines subjected to drought generally show an overall reduction of sugars [ 82 ], probably due to a decreased carbon fixation, except for galactinol and raffinose, which accumulate upon water deficit conditions [ 17 ], suggesting, therefore, that their biosynthesis is strictly related to stress. Furthermore, the concentration of osmolytes like raffinose in guard cells has a role in the regulation of stomata aperture [ 83 , 84 ].…”
Section: Discussionmentioning
confidence: 99%
“…host plants by imbibing the cellular content retrieved from the nutritive organoid root or histoid leaf galls [ 8 , 9 , 10 ]. Grape phylloxera root infestation manipulates the host vine physiology by modulating the water, mineral, and assimilate transport pathways [ 11 , 12 , 13 ], interfering with host plant defense mechanisms [ 14 , 15 , 16 , 17 , 18 ] and facilitating secondary root infections by phytopathogenic soil-borne microorganisms [ 19 ], altogether leading to host plant damage or even vine death depending on concomitant biotic and abiotic environmental factors [ 20 , 21 ]. Motile grape phylloxera L1 larvae move and probe Vitis spp.…”
Section: Introductionmentioning
confidence: 99%