Non-structural carbohydrates (NSC) in plant tissue are frequently quantified to make inferences about plant responses to environmental conditions. Laboratories publishing estimates of NSC of woody plants use many different methods to evaluate NSC. We asked whether NSC estimates in the recent literature could be quantitatively compared among studies. We also asked whether any differences among laboratories were related to the extraction and quantification methods used to determine starch and sugar concentrations. These questions were addressed by sending sub-samples collected from five woody plant tissues, which varied in NSC content and chemical composition, to 29 laboratories. Each laboratory analyzed the samples with their laboratory-specific protocols, based on recent publications, to determine concentrations of soluble sugars, starch and their sum, total NSC. Laboratory estimates differed substantially for all samples. For example, estimates for Eucalyptus globulus leaves (EGL) varied from 23 to 116 (mean = 56) mg g(-1) for soluble sugars, 6-533 (mean = 94) mg g(-1) for starch and 53-649 (mean = 153) mg g(-1) for total NSC. Mixed model analysis of variance showed that much of the variability among laboratories was unrelated to the categories we used for extraction and quantification methods (method category R(2) = 0.05-0.12 for soluble sugars, 0.10-0.33 for starch and 0.01-0.09 for total NSC). For EGL, the difference between the highest and lowest least squares means for categories in the mixed model analysis was 33 mg g(-1) for total NSC, compared with the range of laboratory estimates of 596 mg g(-1). Laboratories were reasonably consistent in their ranks of estimates among tissues for starch (r = 0.41-0.91), but less so for total NSC (r = 0.45-0.84) and soluble sugars (r = 0.11-0.83). Our results show that NSC estimates for woody plant tissues cannot be compared among laboratories. The relative changes in NSC between treatments measured within a laboratory may be comparable within and between laboratories, especially for starch. To obtain comparable NSC estimates, we suggest that users can either adopt the reference method given in this publication, or report estimates for a portion of samples using the reference method, and report estimates for a standard reference material. Researchers interested in NSC estimates should work to identify and adopt standard methods.

Eucalyptus species are grown widely outside of their native ranges in plantations on all vegetated continents of the world. We predicted that such a plantation species would show high potential for acclimation of photosynthetic traits across a wide range of growth conditions, including elevated [CO2] and climate warming. To test this prediction, we planted temperate Eucalyptus globulus Labill. seedlings in climate-controlled chambers in the field located >700 km closer to the equator than the nearest natural occurrence of this species. Trees were grown in a complete factorial combination of elevated CO2 concentration (eC; ambient [CO2] +240 ppm) and air warming treatments (eT; ambient +3 °C) for 15 months until they reached ca. 10 m height. There was little acclimation of photosynthetic capacity to eC and hence the CO2-induced photosynthetic enhancement was large (ca. 50%) in this treatment during summer. The warming treatment significantly increased rates of both carboxylation capacity (V(cmax)) and electron transport (Jmax) (measured at a common temperature of 25 °C) during winter, but decreased them significantly by 20-30% in summer. The photosynthetic CO2 compensation point in the absence of dark respiration (Γ*) was relatively less sensitive to temperature in this temperate eucalypt species than for warm-season tobacco. The temperature optima for photosynthesis and Jmax significantly changed by about 6 °C between winter and summer, but without further adjustment from early to late summer. These results suggest that there is an upper limit for the photosynthetic capacity of E. globulus ssp. globulus outside its native range to acclimate to growth temperatures above 25 °C. Limitations to temperature acclimation of photosynthesis in summer may be one factor that defines climate zones where E. globulus plantation productivity can be sustained under anticipated global environmental change.

Increased climatic variability, including extended periods of drought stress, may compromise on the health of forest ecosystems. The effects of defoliating pests on plantations may also impact on forest productivity. Interactions between climate signals and pest activity are poorly understood. In this study, we examined the combined effects of reduced water availability and defoliation on maximum photosynthetic rate (A(sat)), stomatal conductance (g(s)), plant water status and growth of Eucalyptus globulus Labill. Field-grown plants were subjected to two water-availability regimes, rain-fed (W-) and irrigated (W+). In the summer of the second year of growth, leaves from 75% of crown length removed from trees in both watering treatments and physiological responses within the canopies were examined. We hypothesized that defoliation would result in improved plant water status providing a mechanistic insight into leaf- and canopy-scale gas-exchange responses. Defoliated trees in the W+ treatment exhibited higher A(sat) and g(s) compared with non-defoliated trees, but these responses were not observed in the W- treatment. In contrast, at the whole-plant scale, maximum rates of transpiration (E(max)) and canopy conductance (G(Cmax)) and soil-to-leaf hydraulic conductance (K(P)) increased in both treatments following defoliation. As a result, plant water status was unaffected by defoliation and trees in the defoliated treatments exhibited homeostasis in this respect. Whole-plant soil-to-leaf hydraulic conductance was strongly correlated with leaf scale g(s) and A(sat) following the defoliation, providing a mechanistic insight into compensatory up-regulation of photosynthesis. Above-ground height and diameter growth were unaffected by defoliation in both water availability treatments, suggesting that plants use a range of responses to compensate for the impacts of defoliation.

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Abstract• Artificial defoliation is often used to simulate defoliation by herbivory and is usually considered a good indication of a plant's response to a given type of damage. However, the findings of studies directly comparing the two defoliation types are inconsistent.• Here, the short term effects of artificial and insect defoliation by larvae of Paropsisterna agricola on growth, biomass allocation and photosynthetic capacity of Eucalyptus globulus seedlings were compared in a glasshouse experiment. The artificial defoliation was carried out to closely resemble the spatial patterns observed for insect defoliation.• Height and diameter increments were reduced as a result of insect defoliation, whereas artificial defoliation had no significant effect on height. Increased photosynthetic capacity was observed in response to both treatments, but the magnitude of this increase was larger in insect-than in artificially-defoliated seedlings. Significant reductions in foliar carbohydrate content and total biomass were noticeable in artificially-defoliated seedlings. Although the foliar carbohydrate levels also decreased across the crown zones following insect defoliation treatment, seedlings allocated a large amount of their biomass in the branches of the damaged zone.• Despite our best endeavours to simulate insect defoliation in the artificial treatment, the latter may not reflect accurately the full strength of the effects. However, artificial and insect defoliation were similar in their direction of the responses they caused in E. globulus seedlings. Mots-clés :Paropsisterna agricola / croissance / allocation de la biomasse / capacité de la photosynthèse / glucides Résumé -Les défoliations artificielle et naturelle ont-elles des effets similaires sur la physiologie de jeune plants d'Eucalyptus globulus Labill. ?• La défoliation artificielle est couramment employée pour simuler la défoliation par les insectes herbivores et elle est généralement considérée comme un bon indicateur de la réponse des plantes pour un type de dommage donné. Cependant, les résultats d'études comparant directement les deux types de défoliation sont inconsistants.• Ici, les effets court terme des défoliations artificielles et naturelles par la larve de Paropsisterna agricola ont été comparés au plan de la croissance, de l'allocation de la biomasse et de la capacité de photosynthèse dans une expérimentation conduite en serre. La défoliation artificielle a été menée pour ressembler étroitement aux modèles spatiaux observés avec la défoliation par les insectes.• À la suite de la défoliation par les insectes, les accroissements en hauteur et en diamètre ont été ré-duits, alors que la défoliation artificielle n'a eu aucun effet significatif sur la hauteur. L'augmentation de la capacité de photosynthèse a été observée en réponses aux deux traitements, mais l'ampleur de cette augmentation a été plus forte pour les plants défoliés par les insectes que pour les plants artificiellement défoliés. Des réductions significatives de la teneur foliaire en...

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Balanced crop load is key to the production of export-quality cherries. We investigated the level and timing of crop load regulation on fruit quality. Additionally we sought to investigate possible correlation between firmness estimated by compression test or flesh penetrability. Fruit diameter was similar between 1 and 2 bud/spur treatments but was significantly lower in the 4 bud/spur treatment at all thinning times in 'Van' in the 2010/11 season. In contrast 'Sweetheart' fruit diameter was only decreased at 6 and 8 WAFB in the 4 bud/spur treatment in 2010/11. This decrease in 'Sweetheart' was associated with significantly higher soluble solids and starch reserves in leaves, stem, trunk and roots 2-weeks post-harvest in trees thinned at dormancy, relative to trees thinned 8 WAFB. Fruit flesh firmness significantly increased with decreased crop load irrespective of time of thinning in 'Van' in 2010/11. In contrast flesh firmness was significantly higher in the 1 bud/spur treatment and similar between other treatments in 'Sweetheart' in 2010/11. In 2011/12 flesh firmness, soluble solids and colour significantly increased whilst fruit weight and TA significantly decreased 28 days post-harvest relative to at-harvest values. We found strong correlation between values obtained with the FirmTech II and the Guss fruit texture analyser. Sweet cherry fruit quality is optimised through attaining crop load of approximately 10 fruit per cm 2 of limb cross-sectional area through thinning at dormancy or full bloom.