Water use efficiency (WUE), measured as the ratio of plant biomass to water consumption, is an essential agronomical trait for enhancing crop production under drought. Measuring water consumption is logistically difficult, especially in field conditions. The general objective of the present Thesis is to respond to three main questions: (i) can WUE be determined by using carbon isotope discrimination (CID), easy to measure?, (ii) how WUE and CID variation analysis can contribute to the genotypic selection of sunflower subjected to drought?, and (iii) can WUE variation be revealed by the variation of plant-water relation traits. Four experiments were carried out in greenhouse across two different years: (i) on two drought scenarios, progressive soil drying and stable water-stress, and (ii) on five levels of soil water content. The main traits that have been measured include WUE, CID, as well as plant-water relation traits, i.e. control of transpiration (FTSWt), water extraction capacity (TTSW), and dehydration tolerance (OA). A highly significant negative correlation was observed between WUE and CID, and a wide phenotypic variability was observed for both WUE and CID. A wide variability was also observed for FTSWt, TTSW and OA. The results provide new insight into the genetic control of WUE and CID related-traits, which, unlike to other crops, genetic control of WUE, CID, and TTSW in sunflower have never been reported in the literature. Further, quantitative trait loci (QTL) mapping for FTSWt was never reported in any plant species. The QTL for WUE and CID were identified across different drought scenarios. The QTL for CID is considered as a ‘‘constitutive’’ QTL, because it is consistently detected across different drought scenarios. The QTL for CID co-localized with the QTL for WUE, biomass and cumulative water transpired. Co-localization was also observed between the QTL for FTSWt and TTSW, between the QTL for TTSW and WUE-CID-biomass, as well as between the QTL for FTSWt-TTSW and biomass. This study highlights that WUE is physiologically and genetically associated with CID. CID is an excellent surrogate for WUE measurement, and can be used to improve WUE by using marker-assisted selection (MAS) to achieve the ultimate goal of plant breeding at genomic level.

The goal of this project was to determine the genetic architecture of water-use efficiency (WUE) for foxtail pine, which included genomic loci, and effect sizes of this trait. Foxtail pine is a subalpine endemic conifer that inhabits two distinct regional populations separated by 500 km in the mountains of California. In order to achieve this goal, a robust linkage map containing thousands of genetic markers was created using four megagametophyte arrays ranging in size from approximately 70 to 95 megagametophytes. Quantitative trait loci (QTL) discovered for WUE were mapped along the linkage map using linear mixed models and five half-sibling families grown in a common garden. Effect sizes of these QTL were tested for differences between the two regional populations of foxtail pine.

Cette thèse visait (i) à quantifier la variabilité de l’efficience d’utilisation de l’eau (WUE) chez le peuplier noir (Populus nigra L.), (ii) à juger de sa plasticité phénotypique en réponse à des contraintes hydrique et thermique et (iii) à juger des liens entre WUE, croissance et survie. A cette fin, des études à partir de semis, en chambre de croissance et en milieu naturel, ainsi qu’à partir de populations installées en dispositifs de pépinière ont été réalisées. Nos travaux ont permis de montrer une importante variabilité et une importante plasticité du caractère ‘efficience d’utilisation de l’eau’ quels que soient l’échelle d’étude, le fond génétique et les conditions de croissance. Une diminution de WUE a été observée en réponse à la contrainte thermique alors qu’une augmentation de WUE a été observée en réponse à un déficit hydrique modéré. Nos travaux démontrent également un lien entre WUE et la survie sous de fortes températures suggérant que sous ces conditions, une faible efficience d’utilisation de l’eau conférerait un avantage pour les individus. De plus in situ, un lien négatif entre WUE et la densité de régénération a été observé démontrant que les plus faibles valeurs de WUE sont observées pour les plus fortes densités. Le caractère ‘efficience d’utilisation de l’eau’ pourrait donc s’avérer un caractère limitant de la régénération de l’espèce dans des conditions d’augmentation de température ; une telle augmentation pourrait alors avoir une conséquence directe sur la structuration génétique des populations futures. Ces travaux suggèrent enfin une structuration géographique de la variabilité de WUE qui reste à confirmer à partir d’un plus grand nombre de populations. Ce travail ouvre des perspectives intéressantes pour l’identification des bases physiologiques à l’origine des variations de WUE, de sa plasticité et de sa structuration géographique. / This work aimed (i) to quantify variability of water-use efficiency (WUE) on black poplar (Populus nigra L.), (ii) to quantify the phenotypic plasticity in response to water deficit and increase of temperature and (iii) to precise the relationships between WUE, growth and leaf survival. Studies on seedlings in growth chambers and in natural conditions, and on populations established in common garden studies were realized. Significant variations and significant plasticity of water-use efficiency were observed on seedlings and adults whatever growth conditions and genetic background. A significant decrease of WUE was observed in response to increase of temperature while an increase of WUE was observed in response to moderate water deficit. Under elevated temperature a significant relationship was observed between WUE and leaf survival suggesting that low WUE confers an advantage for individuals under these conditions. Moreover in situ, a negative relationship between WUE and seedlings density was detected suggesting that low WUE are observed under high seedlings densities. The complex trait ‘water-use efficiency’ should be a limiting character of species establishment under increase of temperatures; this temperature elevation should have consequences on genetic structuration of populations in the future. Our results suggest a geographical structuration of WUE variability but results must be confirmed on several others populations. This present work opens prospects for identification of physiological bases of WUE variations, its plasticity and its geographical structuration.

Perennial ryegrass (Lolium perenne L.) is a cool-season turfgrass susceptible to low temperature injury. Wilt-based (WB) irrigation is a common practice in scheduling turf irrigation as an alternative to well-watered (WW). Moisture stress has been shown to promote cold hardiness but this has not been investigated in response to WB irrigation. Measurements of 13C isotope discrimination (DELTA) are useful predictors of water use efficiency (WUE), drought resistance, evapotranspiration (ET) and salinity tolerance but the relevance to turfgrass cold hardiness has not been determined. DELTA analyses may enable more efficient screening protocols in breeding for improved cold hardiness. Objectives of this study were to examine perennial ryegrass genotypes in relation to cold hardiness, DELTA and WUE in response to WW and WB irrigation schedules, to compare genetic diversity between top-performing (TP) and bottom-performing (BP) perennial ryegrass genotypes, and to assess the predictive value of DELTA of for cold hardiness. Six genotypes were selected based on turf quality from the most northern NTEP location (Orono, ME) and included three TP (‘All Star 2’, ‘Mach I’ and ‘Sunkissed’) and three BP (‘APR-1234’, ‘Buccaneer’ and ‘WVPB-R-82’) genotypes. ET, yield, WUE, shoot water content, rooting potential, wilting tendency, DELTA and median lethal temperatures (LT50) using whole-plant survival were measured from greenhouse samples grown in weighing lysimeters in 2007 and 2008. Plant measurements in both years were based on sampling conducted at the last cycle after 68-d of irrigation with 100% of ET applied at leaf-roll (WB) versus ET replacement every 4-d (WW). Lower LT50 values were generally associated with low yield, low WUE and low shoot water content, whether the result of irrigation treatment or genotypic variation. TP genotypes demonstrated significantly lower LT50 temperatures (greater cold hardiness) in comparison to BP genotypes in both years. Modest cold hardiness enhancement with WB irrigation was highest for TP genotypes. Wilting tendency and DELTA were not reliable predictors of cold hardiness, although individual TP genotypes exhibited responses distinctly different than some BP genotypes. Further research is needed to investigate the physiological mechanisms of enhanced turfgrass cold hardiness in response to moisture stress.

No description available.

Varietal forestry may increase the productivity of loblolly pine (Pinus taeda L.) in the Southern United Sates. However, the effects of these genetic x environment interactions are still poorly understood. In this study we examined the responses in growth, stand uniformity and leaf level physiology of loblolly pine clonal varieties and families to silvicultural intensity and site effects. We also looked for patterns in observed traits that were consistent between crown ideotypes. Two varieties of each crown ideotype (narrow vs broad crowns) and two families (controlled mass pollinated (CMP) and open pollinated (OP) family) were tested on the Virginia Piedmont (VA) and the North Carolina Coastal Plain (NC) under different silvicultural intensities (operational vs intensive), and planting density (617, 1235 and 1852 trees per hectare). Data were collected during the first four growing season after establishment. At NC, intensive silviculture increased crown-width, height and dbh by 33%, 14%, and 23%, respectively. At VA, intensive silviculture increased crown-width, height and dbh by 41%, 10%, and 23%, respectively. Intensive silviculture also increased slightly but significantly the stand uniformity of stem growth. However, the differences in productivity between silvicultural treatments were not explained by differences in leaf-level physiology. Across all treatments and sites the varieties generally grew faster than the OP family, but the differences were higher at VA. Varieties did not differ in stem growth, but the broadest crown variety had greater stand uniformity, photosynthetic rate (Asat), carbon isotope discrimination (∆¹³) and lower fascicle size than the OP family. None of the traits assessed inthis study was consistent within the ideotypes. Varieties classified in the same crown-ideotypes may respond differently to the environmental effects of site and silviculture, which reinforces the need of matching varietal forestry with precision silviculture to achieve gains in productivity. / Ph. D.

No description available.

C4 plants have a biochemical carbon concentrating mechanism (CCM) that increases CO2 concentration around Rubisco in the bundle sheath (BS). Maize CCM has two CO2 delivery pathways to the Bundle Sheath (BS) (respectively via malate, MAL or aspartate, ASP); rates of PGA reduction, carbohydrate synthesis and PEP regeneration vary between BS and Mesophyll (M) cells. For these anatomical and biochemical complexities, C4 plants are highly sensitive to light conditions. Under limiting light, the activity of the CCM generally decreases, causing an increase in leakiness, (Φ), the ratio of CO2 retrodiffusing from the BS relative to C4 carboxylation processes. This increase in Φ had been theoretically associated with a decrease in biochemical operating efficiency (expressed as ATP cost of gross assimilation, ATP / GA) under low light and, because a proportion of canopy photosynthesis is carried out by shaded leaves, to potential productivity losses at field scale. In C4 leaves, because of the concentric anatomy, light reaches M cells before the deeper BS (Evans et al., 2007), and could alter the energetic partitioning balance between BS and M and potentially cause efficiency losses. In this experimental programme I investigated strategies deployed by C4 plants to adjust operating efficiency under different illumination conditions. Firstly, maize plants were grown under high and low light regimes (respectively HL, 600 vs LL, 100 μE m-2 s-1). Short term acclimation of Φ was compared from isotopic discrimination (Δ), gas exchange and photochemistry using an improved modelling approach which does not suffer from elements of circularity. Long term acclimation to low light intensities brought about physiological changes which could potentially increase the operating efficiency under limiting ATP supplies. Secondly, profiles of light penetration across a leaf were used to derive the potential ATP supply for M and BS cells induced by changing light quality. Empirical measurements of net CO2 uptake, ATP production rate and carbon isotope discrimination were made on plants under a low light intensity. The overall conversion efficiency was not affected by light quality. A comprehensive metabolic model highlighted the importance of both CO2 delivery pathways in maize. Further, metabolic plasticity allowed the balancing of ATP and NADPH requirements between BS and M. Finally, I tested the hypothesis that plants can modify their physiology so as to reach a status of higher operating efficiency when exposed to high light and then to low light, so as to mimic the transition which leaves undergo when shaded by newly emerging leaves in a crop canopy. Plants were grown under high light and low light for three weeks, then, HL plants were transferred to low light for a further three weeks. Re-acclimation was very effective in reducing ATP cost of net assimilation under low light intensities. In addition, the hyperbolic leakiness increase observed under low light intensities was not associated to operating efficiency loss. Overall, in the three experimental Chapters I showed compelling theoretical and empirical evidence proving the hypothesis that C4 plants deal with low light conditions and with different light qualities without losing operating efficiency.

L’efficience d’utilisation de l’eau (WUE), rapport entre la biomasse produite et l’eau consommée, est un trait essentiel à étudier en agronomie pour améliorer la production des cultures soumises à la sécheresse. Cependant, mesurer l’eau consommée par un couvert végétal est difficile à réaliser. L’objectif général de ce travail de thèse est de répondre à trois principales questions : (i) peut-on déterminer WUE en utilisant la discrimination isotopique du carbone (CID) facile à mesurer? (ii) comment l’analyse de la variabilité de WUE et CID peut contribuer à sélectionner des génotypes de tournesol soumis à la sécheresse? (iii) et les variations de WUE peuvent-elles être révélées par les variations de relations hydriques? Quatre expériences ont été conduites en serre pendant deux années : (i) avec deux scenario de sécheresse, l’une progressive, l’autre stable, et (ii) avec cinq niveaux de contenu en eau du sol stables. Les principaux traits mesurés sont WUE, CID et d’autres traits représentant les relations hydriques tels que le contrôle de la transpiration (FTSWt), la capacité d’extraction de l’eau (TTSW) et la tolérance à la déshydratation (OA). Une forte corrélation négative a été mise en évidence entre WUE et CID. Une large variabilité a également été observée pour FTSWt, TTSW et OA. Ces résultats permettent de connaitre le contrôle génétique de WUE et CID, ainsi que des traits associés, lesquels n’ont jamais été relatés dans la littérature. De plus, l’analyse QTL pour FTSWt n’a pas non plus été réalisée, chez aucune plante. Des QTL pour WUE et CID ont été identifiés pour différents scenario de sécheresse. Les QTL pour CID sont considérés comme ‘constitutifs’, parce qu’ils sont détectés dans les différents scenarios. Les QTL pour CID co-localisent avec ceux pour WUE, pour la biomasse et pour la transpiration cumulée. Des co-localisations de QTL ont également été observées entre FTSWt et TTSW, entre TTSW et WUE-CID-Biomasse, et entre FTSWt-TTSW et Biomasse. Cette étude met en évidence que WUE est physiologiquement et génétiquement associée à CID. De plus, CID représente un excellent substitue à la mesure de WUE et permet d’améliorer l’efficience d’utilisation de l’eau par sélection assistée par marqueurs. / Water use efficiency (WUE), measured as the ratio of plant biomass to water consumption, is an essential agronomical trait for enhancing crop production under drought. Measuring water consumption is logistically difficult, especially in field conditions. The general objective of the present Thesis is to respond to three main questions: (i) can WUE be determined by using carbon isotope discrimination (CID), easy to measure?, (ii) how WUE and CID variation analysis can contribute to the genotypic selection of sunflower subjected to drought?, and (iii) can WUE variation be revealed by the variation of plant-water relation traits. Four experiments were carried out in greenhouse across two different years: (i) on two drought scenarios, progressive soil drying and stable water-stress, and (ii) on five levels of soil water content. The main traits that have been measured include WUE, CID, as well as plant-water relation traits, i.e. control of transpiration (FTSWt), water extraction capacity (TTSW), and dehydration tolerance (OA). A highly significant negative correlation was observed between WUE and CID, and a wide phenotypic variability was observed for both WUE and CID. A wide variability was also observed for FTSWt, TTSW and OA. The results provide new insight into the genetic control of WUE and CID related-traits, which, unlike to other crops, genetic control of WUE, CID, and TTSW in sunflower have never been reported in the literature. Further, quantitative trait loci (QTL) mapping for FTSWt was never reported in any plant species. The QTL for WUE and CID were identified across different drought scenarios. The QTL for CID is considered as a ‘‘constitutive’’ QTL, because it is consistently detected across different drought scenarios. The QTL for CID co-localized with the QTL for WUE, biomass and cumulative water transpired. Co-localization was also observed between the QTL for FTSWt and TTSW, between the QTL for TTSW and WUE-CID-biomass, as well as between the QTL for FTSWt-TTSW and biomass. This study highlights that WUE is physiologically and genetically associated with CID. CID is an excellent surrogate for WUE measurement, and can be used to improve WUE by using marker-assisted selection (MAS) to achieve the ultimate goal of plant breeding at genomic level.

Thesis (MScAgric (Viticulture and Oenology))--University of Stellenbosch, 2010. / ENGLISH ABSTRACT: Within-vineyard variability in vigour and water status commonly occurs in South African vineyards. Different soil types found over short distances are probably the main cause of vigour variability, while differences in grapevine water status are commonly induced by lateral water flow in the vineyard, blocked irrigation emitters and differences in soil water-holding capacity. These factors can cause heterogeneous ripening and differences in fruit quality between different parts of the vineyard, an aspect that needs to be avoided as far as possible in order to produce quality wines. Measurements of carbon isotope discrimination (CID) have proved to be a tool to assess grapevine physiology in order to study the effects of environmental parameters on leaf carbon dioxide (CO2) gas exchange and stomatal conductance (gs). Grapevine water deficit stress/strain in reaction to these environmental conditions can then be determined by observing the amount of 13C absorbed by plant material after discrimination of 13C has taken place, and this is influenced by the grapevine stress condition and can indicate water-use efficiency. In this study, the variability of grapevine water status and vigour was determined in order to quantify these parameters in different parts of the vineyard. Two separate trials were conducted, the first at Wellington, South Africa, where different irrigation regimes resulted in variability in grapevine water status between plots. The second trial was at Stellenbosch, South Africa, where plots were divided among different vigour classes and irrigation was applied in different quantities for different irrigation treatments. Within-vineyard variability in water status (Wellington and Stellenbosch) and vigour (Stellenbosch) were then quantified and the effects on some grapevine physiological parameters and berry composition were measured. The treatments in the Wellington trial led to differences in grapevine water status, which could be quantified by measurements of stem water potential (SWP) and leaf water potential (LWP). Soil variability also led to differences in grapevine vigour, which were quantified by measurements of pruning mass, leaf area and shoot length. The effect of the variability in grapevine water status on grapevine physiology was assessed by measuring CID, which was the main focus of the study. Other physiological measurements, such as gs and leaf and canopy temperature, were also conducted. The effect of these conditions on grape berry composition was also studied. In the Stellenbosch trial, soil water content, plant water status measurements (SWP, predawn LWP and LWP), physiological measurements (CID and gs) and berry size measurements were used to classify plots into water status treatments (“wet” and “dry” treatments). The effect of vigour differences was analysed separately from these treatments by using pruning mass as a covariate in the statistical analyses. The effect of vigour variability on the measurements was studied by looking at the effect of the covariate on the measurements, while shoot growth rate, shoot length and leaf area measurements were conducted as vegetative growth measurements. Differences in measurements were then studied between the treatments and between the vigour levels of the different plots. In the Wellington trial, plant water status was determined by irrigation, showing increased stress for treatments that received less irrigation. The differences in plant water status then caused differences in grapevine physiology between the treatments, leading to increased gs for increased irrigation. This of course influenced leaf internal CO2 and therefore CID, although CID was also clearly influenced by berry development. Berry size was influenced by irrigation, with larger berries found in wetter treatments, while berry chemical composition was influenced by the irrigation regime, with increased irrigation leading to increased pH and leading to trends showing increased total soluble solids and malic acid, and reduced total and tartaric acid and colour intensity. In the Stellenbosch trial, plots with higher vigour had increased shoot growth rate, longer shoots and increased leaf area, although topping influenced this. Wet treatment vines also showed slightly longer shoots and larger leaf areas. There were differences in soil water content between the wet and dry treatments, and this led to differences in plant water status. Vigour also influenced pre-dawn LWP, especially in the 2007 season, as higher-vigour vines struggled more to rehydrate through the night. Differences in plant water potential led to differences in grapevine physiology, with increased gs for vines from the wet treatment, while higher-vigour vines had slightly increased gs. The differences in gs led to gas exchange differences and therefore differences in CID, meaning that water status and vigour influenced CID. CID measurements illustrated the long term effect of water status on plant physiology, while measurements such as SWP illustrated the short term effects. CID measurements therefore proved to be accumulative over the season, in contrast to SWP measurements that were much more dependent on the current state of grapevine water status. Other physiological measurements showed that wet-treatment vines had higher photosynthetic rates and evapotranspiration and lower leaf temperatures, while higher-vigour vines had slightly increased evapotranspiration and decreased leaf temperatures. Wet-treatment vines had larger berries, while a higher vigour also led to slightly larger berries. Berry composition was influenced by treatment, where wet-treatment vines had increased pH and total soluble solids, while higher-vigour vines had increased juice pH and, in the 2008 season, decreased total soluble solids. Extremely stressed conditions did not show significant effects on plant water potential, but SWP measurements indicated slightly higher stress for the extremely stressed vines and LWP showed slightly less stressed conditions for these vines. Measurements of gs showed slightly lower values for the extremely stressed vines, while measurements of CID showed large significant differences, with the extremely stressed vines having measurements showing high stress. The measurement therefore indicated highly stressed conditions accurately, while other physiological measurements, such as photosynthetic rate, evapotranspiration and leaf temperatures, only showed trends and no significant differences. Measurements of stomatal conductance reacted to plant water status measurements throughout the diurnal measurement days, while CID only reacted slightly with gs changes during these days and was perhaps influenced more by berry chemical composition and development at this early stage of the season. Vigour and water status therefore influenced grapevine physiology, with a more direct effect by water status and an indirect effect by vigour due to microclimatic differences. This also influenced berry composition and therefore quality. In future studies, CID measurements should be done on juice from which organic acids have been removed in order to eliminate the effect of seasonal berry composition on the measurement. Measurements of CID proved to be an integrative, but sensitive, indicator of grapevine stress, especially at the end of the season. It might at best be useful as a post-harvest management tool for producers or grape buyers, especially for irrigation control, as has also been stated by Van Leeuwen et al. (2007). / AFRIKAANSE OPSOMMING: Binne-wingerd variasie in groeikrag en waterstatus is algemeen in Suid-Afrikaanse wingerde. Verskillende grondsoorte wat na aan mekaar voorkom, is seker een van die vernaamste oorsake van variasie in groeikrag, terwyl verskille in wingerdwaterstatus algemeen deur laterale watervloei in die wingerd, verstopte besproeiingspuite en verskille in grond waterhouvermoë geïnduseer word. Hierdie faktore kan aanleiding gee tot heterogene rypwording en verskille in vrugkwaliteit tussen verskillende dele van die wingerd, ‘n aspek wat so ver moontlik vermy moet word om kwaliteitwyne te kan produseer. Die meting van koolstof-isotoopdiskriminasie (KID) is bewys om as gereedskap te kan dien vir die assessering van wingerdfisiologie om die effekte van omgewingsparameters op blaar koolstofdioksied (CO2) - gasuitruiling en stomatale geleiding (gs) te bestudeer. Die stres/stremming as gevolg van ‘n watertekort in die wingerd in reaksie op hierdie omgewingstoestande kan dan bepaal word deur te kyk na hoeveel 13C deur die plantmateriaal geabsorbeer word ná 13C-diskriminasie plaasgevind het, en dít word deur die wingerdstrestoestande beïnvloed en kan ‘n aanduiding verskaf van die doeltreffendheid van waterverbruik. In hierdie studie is die variasie in wingerdwaterstatus en groeikrag bepaal om hierdie parameters in verskillende dele van die wingerd te kwantifiseer. Twee afsonderlike proewe is uitgevoer, die eerste by Wellington, Suid-Afrika, waar verskillende besproeiingsregimes gelei het tot verskille in die wingerdwaterstatus tussen persele. Die tweede proef was by Stellenbosch, Suid-Afrika, waar persele tussen verskillende groeikragklasse verdeel is en besproeiing in verskillende hoeveelhede vir verskillende besproeiingsbehandelings toegepas is. Binne-wingerd variasie in waterstatus (Wellington en Stellenbosch) en groeikrag (Stellenbosch) is toe gekwantifiseer en die effekte op sekere wingerd-fisiologiese parameters en korrelsamestelling is gemeet. Die behandelings in die Wellington-proef het gelei tot verskille in wingerdwaterstatus, wat deur metings van stamwaterpotensiaal (SWP) en blaarwaterpotensiaal (BWP) gekwantifiseer kon word. Grondverskille het ook gelei tot verskille in wingerdgroeikrag, wat deur metings van snoeimassa, blaaroppervlak en lootlengte gekwantifiseer is. Die effek van die variasie in wingerdwaterstatus op wingerdfisiologie is deur metings van KID bepaal wat die hooffokus van hierdie studie was. Ander fisiologiese metings, soos gs en blaar- en lowertemperatuur, is ook gedoen. Die effekte van hierdie toestande op die samestelling van die druiwekorrels is ook bestudeer. In die Stellenbosch-proef is grondwaterinhoud, metings van plantwaterstatus (SWP, voorsonopgang SWP en BWP), fisiologiese metings (KID en gs) en metings van korrelgrootte gebruik om die persele in waterstatusbehandelings (“nat” en “droë” behandelings) te verdeel. Die effek van verskille in groeikrag is apart van hierdie behandelings geanaliseer deur snoeimassa as ‘n kovariaat in die statistiese analises te gebruik. Die effek van groeikragvariasie op die metings is bestudeer deur ondersoek in te stel na die effek van die kovariaat op die metings, terwyl lootgroeitempo-, lootlengte- en blaaroppervlakmetings as metings van vegetatiewe groei uitgevoer is. Verskille in metings tussen die behandelings en tussen die groeikragvlakke van die verskillende persele is toe bestudeer. In die Wellington-proef is plantwaterstatus deur besproeiing bepaal, met verhoogde stres in behandelings waar daar minder besproeiing toegedien is. Die verskille in plantwaterstatus het dan verskille in wingerdfisiologie tussen die behandelings veroorsaak, wat gelei het tot ‘n verhoogde gs in die geval van verhoogde besproeiing. Dit het natuurlik ‘n effek op die interne CO2 van die blaar en dus op KID gehad, hoewel KID ook duidelik deur korrelontwikkeling beïnvloed is. Korrelgrootte is deur besproeiing beïnvloed, met groter korrels in die natter behandelings, terwyl die chemiese samestelling van die korrel deur besproeiingsregime beïnvloed is. Verhoogde besproeiing het pH verhoog en gelei na tendense wat verhoogde totale oplosbare vaste stowwe en appelsuur, en verminderde totale suur, wynsteensuur en kleurintensiteit getoon het. In die Stellenbosch-proef het persele met hoër groeikrag ook verhoogde lootgroeitempo, langer lote en verhoogde blaaroppervlak getoon, hoewel dit deur top beïnvloed is. Wingerdstokke van die nat behandeling het ook effe langer lote en groter blaaroppervlakke getoon. Daar was verskille in grondwaterinhoud tussen die nat en droë behandelings en dit het verskille in plantwaterstatus veroorsaak. Groeikrag is ook deur voor-sonopgang BWP beïnvloed, veral in die 2007-seisoen, aangesien stokke met hoër groeikrag meer gesukkel het om in die nag te rehidreer. Verskille in plantwaterpotensiaal het gelei tot verskille in wingerdfisiologie, met ‘n verhoogde gs vir stokke in die nat behandeling, terwyl stokke met hoër groeikrag ‘n effens verhoogde gs getoon het. Die verskille in gs het gelei tot verskille in gasuitruiling en dus verskille in KID, wat beteken dat waterstatus en groeikrag ‘n invloed op KID het. KID was meer verteenwoordigend van die langtermyneffekte van water status op plantfisiologie, terwyl metings soos SWP die korttermyneffekte weerspieël het. KID metings was dus akkumalatief oor die seisoen, terwyl SWP metings meer ‘n weerspieëling was van die huidige toestand van plantwaterpotensiaal. Ander fisiologiese metings het getoon dat stokke in die nat behandeling ‘n hoër fotosintesetempo en evapotranspirasie sowel as laer blaartemperature ondervind het, terwyl die stokke met hoër groeikrag effe verhoogde evapotranspirasie en verminderde blaartemperature getoon het. Stokke in die nat behandeling het groter korrels gehad, terwyl hoër groeikrag ook effens groter korrels veroorsaak het. Korrelsamestelling is deur die behandelings beïnvloed, met stokke in die nat behandeling wat verhoogde pH en totale oplosbare vaste stowwe getoon het, terwyl stokke met hoër groeikrag verhoogde pH van die sap en verminderde totale oplosbare vaste stowwe (laasgenoemde in die 2008-seisoen) gehad het. Uitermate toestande van stres het geen beduidende effekte op plantwaterpotensiaal getoon nie, hoewel SWP-metings effens hoër stres vir die uitermate gestresde wingerde getoon het en BWP effens minder gestresde toestande vir hierdie stokke getoon het. Metings van gs het effens laer waardes vir die uitermate gestresde stokke getoon, terwyl metings van KID groot noemenswaardige verskille getoon het, met die metings vir die uitermate gestresde wingerde wat hoër stres aangedui het. Dié meting het dus hoogs gestresde toestande akkuraat aangedui, terwyl ander fisiologiese metings, soos tempo van fotosintese, evapotranspirasie en blaartemperature net tendense en nie beduidende verskille aangedui het nie. Metings van stomatale geleiding het dwarsdeur die dae waarop daaglikse metings gedoen is op plantwaterstatusmetings gereageer, terwyl KID net effens met gs-veranderinge op hierdie dae gereageer het en moontlik meer deur die chemiese samestelling en ontwikkeling van die korrel in hierdie vroeë stadium van die seisoen beïnvloed is. Groeikrag en waterstatus het dus wingerdfisiologie beïnvloed, met ‘n meer direkte effek deur waterstatus en ‘n indirekte effek deur groeikrag as gevolg van mikroklimaatsverskille. Dit het ook korrelsamestelling en dus kwaliteit beïnvloed. In toekomstige studies moet KID-metings gedoen word op sap waarvan die organiese sure verwyder is om die effek van seisoenale korrelsamestelling op die meting uit te sluit. Metings van KID is getoon om ‘n integrerende, maar gevoelige, aanduider van wingerdstres te wees, veral aan die einde van die seisoen. Dit is ten beste miskien bruikbaar as naoesbestuursgereedskap vir produsente of druiwekopers, veral vir besproeiingsbeheer, soos ook reeds deur Van Leeuwen et al. (2007) aangedui is.