Effect of ultraviolet-C light on quality and microbial population of fresh-cut watermelon

The influence of ultraviolet (UV-C) light (1.4–13.7 kJ m⁻² at 254 nm) on the quality and microbial populations of fresh-cut watermelon [Citrulus lanatus (Thunb.) Matsum. and Nakai] was investigated and compared to that of common sanitizing solutions used for fresh-cut produce. Dipping cubes in chlorine (40 μL L⁻¹) and ozone (0.4 μL L⁻¹) was not effective in reducing microbial populations and quality was lower in cubes receiving these aqueous treatments compared to UV-irradiated cubes or control. In commercial trials, exposing packaged watermelons cubes to UV-C light at 4.1 kJ m⁻² produced >1 log reduction in microbial populations by the end of the product's shelf life without affecting juice leakage, color and, overall visual quality. In further experimentation, lower UV-C dose (1.4 kJ m⁻²) reduced microbial populations to a lower degree and only when complete surface exposure was ensured. Higher UV-C doses did not show any difference in microbial populations (6.3 kJ m⁻²) or result in quality deterioration (13.7 kJ m⁻²). Spray applications of hydrogen peroxide (2%) and chlorine (40 μL L⁻¹), without subsequent removal of excess water, failed to further decrease microbial load of cubes exposed to UV-C light at 4.1 kJ m⁻². When properly utilized, UV-C light is the only method tested in this study that could potentially be used for sanitizing fresh-cut watermelon.     

Influence of aqueous 1-methylcyclopropene concentration, immersion duration, and solution longevity on the postharvest ripening of breaker-turning tomato (Solanum lycopersicum L.) fruit

The influence of aqueous 1-methylcyclopropene (1-MCP) concentration, immersion duration, and solution longevity on the ripening of early ripening-stage tomato (Solanum lycopersicum L.) has been investigated. Tomato fruit at the breaker-turning stage were fully immersed in aqueous 1-MCP at 50, 200, 400 and 600 μg L⁻¹ for 1 min, quickly dried, and then stored at 20 °C. Ethylene production, respiration, surface color development, and rate of accumulation of lycopene and polygalacturonase (PG) activity were suppressed and/or delayed in fruit exposed to aqueous 1-MCP. Suppression of ripening was concentration dependent, with maximum inhibition in response to 1 min immersion occurring at concentrations of 400 and 600 μg L⁻¹. Climacteric ethylene peaks were delayed approximately 6, 7, and 9 d and respiration was strongly suppressed in fruit treated with aqueous 1-MCP at 200, 400, and 600 μg L⁻¹, respectively, compared with control fruit. Fruit firmness, lycopene content, PG activity, and surface hue of fruit treated at the three higher levels remained strongly suppressed compared with control. Skin hue values and pericarp lycopene content in response to treatment at the subthreshold 50 μg L⁻¹ provided evidence for differential ripening suppression in external versus internal tissues. Maximum delay of softening and surface color development in response to 50 μg L⁻¹ aqueous 1-MCP occurred following immersion periods of between 6 and 12 min. Factors affecting fruit penetration by aqueous 1-MCP and mechanisms contributing to recovery from 1-MCP-induced ripening inhibition are discussed.     

Storage characteristics and relationships between microbial growth parameters and shelf life of MAP sliced onions

Microbial proliferation and sensory quality aspects of sliced onions were tested at different temperatures (−2, 4 and 10 °C) and atmospheric conditions (with or without 40% CO₂ + 59% N₂ + 1% O₂). The relationships among microorganism growth parameters (the initial cell number (N₀), the maximum cell number (N_max), the maximum specific growth rate (μ_max) and lag-phase (λ)) and the microbial or sensory shelf life were determined. The microorganism growth parameters were obtained by fitting the modified Gompertz equation to the microbial counts. The results showed that color intensity (yellowness), sensory scores and microbial counts increased, and firmness decreased during storage. The total plate counts (TPC) provided the best indication of the spoilage organism growth capacity under tested temperatures and atmospheric conditions. The microbial shelf lives of the tested onions in 40% CO₂ + 59% N₂ + 1% O₂, or at −2, 4 and 10 °C, were 12.5, 9.5, 7, 12, 9 and 6 days, respectively, and their sensory shelf lives were 12, 8, 5, 10.5, 7 and 5 days, respectively. The lag time (λ) of the TPC, coliforms, pseudomonads and yeasts correlated well with the microbial and sensory shelf life results. The correlations between microbial and sensory shelf life, and the μ_max of TPC, lactic acid bacteria (LAB) and coliforms were between (−0.61 and −0.85). The initial microbial counts (N₀) of the five microorganisms showed a slight correlation, and the maximum microbial counts (N_max) of this group showed no obvious correlation with onion shelf life, apart from the LAB and yeasts.     

Effect of fruit maturity on efficiency of 1-methylcyclopropene to delay the ripening of bananas

Three bunches of unripe ‘Williams’ banana fruit of different maturity, 173, 156 and 71 days from bunch emergence, were harvested. Fruit from the top, bottom and middle hands from each bunch were fumigated for 24 h with 1-methylcyclopropene (1-MCP) at 0, 5, 50 or 500 nl l⁻¹ at 20^oC. All fruit were then stored at 20^oC in air containing 0.1 μl l⁻¹ ethylene and the time taken for each fruit to ripen (green life) was noted. The green life of fruit treated with 500 nl l⁻¹ 1-MCP varied with fruit maturity. In the two most mature bunches it was 27.9±2.3 days, 4-fold longer than fruit fumigated with 0 nl l⁻¹ 1-MCP (6.7±0.6 days). In the least mature bunch, green life was 39.7±3.0 days, 1.5-fold longer than fruit fumigated with 0 nl l⁻¹ 1-MCP (25.7±2.5 days). Most fruit treated with 500 nl l⁻¹ 1-MCP showed an unacceptable uneven skin colouration when ripe. There was no significant effect on green life of 1-MCP at 50 nl l⁻¹ and 5 nl l⁻¹. Other fruit from these bunches were not exposed to 1-MCP and were held in ethylene-free air until ripe. In the two most mature bunches, these fruit had a significantly shorter green life (11.2±5.6 days in hand 1; 18.9±4.1 days in hands 4 and 6) than fruit that were fumigated with 500 nl l⁻¹ 1-MCP. In the least mature bunch, however, these fruit had a significantly longer green life (56.0±5.9 days) than 1-MCP treated fruit. Since the effectiveness of 1-MCP varied with fruit maturity and in any commercial consignment there is a mixture of fruit maturity, it is concluded that 1-MCP has limited commercial potential for the storage of unripe ‘Williams’ bananas.     

The components of lucerne (Medicago sativa) leaf area index respond to temperature and photoperiod in a temperate environment

Irrigated crops of ‘Grasslands Kaituna’ lucerne were grown for 5 years in a temperate climate at Lincoln University, Canterbury, New Zealand (43°38′S, 172°28′E). From these the response of the components of leaf area index (LAI) to environmental factors was determined. A broken stick temperature threshold with a base temperature (T_b) of 1 °C at air temperatures (T_a) <15 °C and a T_b = 5 °C for T_a ≥ 15 was required to accumulate thermal time (Tt). Using this, the appearance of nodes on the main-stem (phyllochron) was constant in Tt within a re-growth cycle (30–42 days). The phyllochron was 37 ± 7 °Cd but declined from 60 to 37 °Cd as photoperiod decreased from 15.7 to 11.4 h. Branching began at the appearance of the fifth main-stem node with 2.5 secondary nodes produced per main-stem node in spring re-growth cycles but only 1.7 produced in summer. Leaf senescence increased from 0.3 to 1.08 leaves per main-stem node after the appearance of the ninth node. Spring re-growth cycles had a mean individual leaf area of 170 mm² compared with 400 mm² for summer re-growth cycles. These results demonstrate systematic variation in LAI components and suggest they need to be considered separately in response to environmental factors to provide a quantitative framework for crop simulation analyses of lucerne canopy development.     

Photosynthetic responses in spring wheat grown under elevated CO2 concentrations and stress conditions in the European, multiple-site experiment ‘ESPACE-wheat’

Spring wheat cv. Minaret crop stands were grown under ambient and elevated CO₂ concentrations at seven sites in Germany, Ireland, the UK, Belgium and the Netherlands. Six of the sites used open-top chambers and one used a controlled environment mimicking field conditions. The effect of elevated CO₂ for a range of N application regimes, O₃ concentrations, and growth temperatures on flag leaf photosynthesis was studied. Before anthesis, flag leaf photosynthesis was stimulated about 50% by 650 compared with 350 μmol mol⁻¹ CO₂ at all sites, regardless of other treatments. Furthermore, there was no evidence of a decrease in photosynthetic capacity of flag leaves due to growth at elevated CO₂ before anthesis, even for low N treatments. However, photosynthetic capacity, particularly carboxylation capacity, of flag leaves was usually decreased by growth at elevated CO₂ after anthesis, especially in low N treatments. Acclimation of photosynthesis to elevated CO₂ therefore appears to occur only slowly, consistent with a response to changes in sink–source relationships, rather than a direct response. Effect of elevated CO₂ on stomatal conductance was much more variable between sites and treatments, but on average was decreased by ˜10% at 650 compared with 350 μmol mol⁻¹ CO₂. Carboxylation capacity of flag leaves was decreased by growth at elevated O₃ both before and after anthesis, regardless of CO₂ concentration.     

Growth and marketable-yield responses of potato to increased CO2 and ozone

Central to the CHanging climate and potential Impacts on Potato yield and quality project (CHIP) was the consideration of the potential impacts of ozone and CO₂ on growth and yield of future European Potato crops. Potato crops, cv. Bintje, were exposed to ambient or elevated ozone; targeted daily average, 60 nl l⁻¹ for 8 h, and ambient or elevated CO_2; targeted 680 μl l⁻¹ averaged over the full growing season, in open top chambers (OTCs) at six European sites in 1998 and 1999, or to elevated CO₂ (550 μl l⁻¹) in Free Air Carbon dioxide Enrichment facilities (FACE) at two sites in both years. Some OTC experiments included 550 μl l⁻¹. Above and below ground biomass were measured at two destructive harvests; at maximum leaf area (MLA) and at final-harvest. Final-harvest fresh weight yields of marketable-size tubers, >35 mm diameter, from ambient conditions ranged from 1 to 12 kg m⁻². There was no consistent (P>0.1) CO₂×O₃ interaction for growth or yield variables at either harvest. No consistent effects of ozone were detected at the maximum-leaf-area harvest. However, at final harvest, ozone had reduced both above-ground biomass and tuber dry weight (P<0.05), particularly of the largest (>50 mm) size class. These yield losses showed linear relationships both with accumulated ozone exposure; AOT40 expressed as nl l⁻¹ h over 40 nl l⁻¹, and with yields from chambered ambient-ozone treatments (P<0.05) but, because of partial confounding between the treatment AOT40s and the ambient-ozone yields in the data, the two relationships were not completely independent. Yields from ambient-ozone treatments, however, explained a significant (P<0.01) amount of the residual variation in ozone effects unexplained by AOT40. When averaged over all experiments, mean dry weights and tuber numbers from both harvests were increased by elevated CO₂. Only green leaf number at the MLA harvest was reduced. The CO₂ responses varied between sites and years. For marketable-size tubers, this variation was unrelated to variation in ambient-CO₂ treatment yields. Yield increases resulting from the 680 μl l⁻¹ and 550 μl l⁻¹ treatments were similar. Thus elevating [CO₂] from 550 to 680 μl l⁻¹ was less effective than elevating [CO₂] from ambient to 550 μl l⁻¹. On average, CO₂ elevation to 680 μl l⁻¹ increased the dry weight of marketable-size tubers by about 17%, which far exceeded the average ozone-induced yield loss of about 5%. The net effect of raising CO₂ and O₃ concentrations on the European potato crop would be an increase marketable yield.     

Pod photosynthesis and drought adaptation of field grown rape (Brassica napus L.)

In rape (Brassica napus L., cv. Global) seed growth mainly depends on husk CO₂ assimilation. In irrigated plants, the net photosynthetic rate (A_max) was 10–13 μmol CO₂ m⁻² s⁻¹ in non-maturing pods and correlated with nitrogen content. The stomatal conductance of water vapour (g_H2O) was 0.3 mol m⁻² s⁻¹ in non-maturing pods. The photosynthetic nitrogen use efficiency (NUE) was 8.3 μmol CO₂g⁻¹ N s⁻¹, about one-third of that in leaves. The photosynthetic water use efficiency (WUE; A_maxg_H2O⁻¹) was similar in pods and leaves. In severely droughted plants, the photosynthetic rate was reduced to 38%. The seed growth rate, however, was not influenced by intermittent periods of water stress, indicating translocation of assimilates to the seeds. The drought resistant character of the pods was due to low specific area, succulence, low stomatal conductance causing a small decrease of ΔΨ day⁻¹ during soil drying and maintenance of high relative water content during severe drought. A mathematical formulation of the pod water release curve was undertaken. © (1997) Elsevier Science B.V.     

Stomatal conductance and ozone exposure in relation to potato tuber yield—results from the European CHIP programme

Measurements of stomatal conductance on field-grown potato (Solanum tuberosum L.) cv. Bintje from the CHIP programme were combined to study the response to environmental factors. 3274 data points were used. Data were obtained from five sites: Jokioinen in Finland, Östad in Sweden, Giessen in Germany, Tervuren in Belgium and Sutton Bonnington in UK. Measurements were made in open-top chamber treatments with ozone and carbon dioxide exposure and in the ambient air. A typical light response curve was obtained with light saturation at approximately 400 μmol m⁻² s⁻¹ photosynthetically active radiation (PAR). The leaf temperature optimum for stomatal conductance was 29 °C. The stomatal conductance declined strongly at leaf-to-air vapour pressure differences >20 hPa. An elevated carbon dioxide concentration (680 μl l⁻¹) reduced the stomatal conductance by up to approximately 20%. Elevated ozone reduced the stomatal conductance towards the end of the growth period, in addition to the negative effect by ordinary senescence on stomatal conductance. A multiplicative model, based on the boundary line technique, was used to estimate the relationship between stomatal conductance and the environmental variables. Test with the data sets from two sites providing sufficient data, Östad and Giessen, showed that the multiplicative model had R²-values of 0.60 and 0.42, respectively, for the relationship between calculated and observed conductance. Test of the model with an independent data set from an open-top chamber experiment with the potato cultivar Kardal showed an R² of 0.59 between calculated and observed conductance. The conductance model was used to estimate the accumulated ozone uptake (CUO₃) by potato leaves from emergence to harvest. The relationship between CUO₃ and relative yield loss, using a threshold for the ozone uptake rate of 7 nmol m⁻² s⁻¹, provided a higher R²-value (0.45) than CUO₃ without any threshold and relationships based on the accumulated exposure over 40 nmol mol⁻¹ (AOT40) or the sum of all hourly average ozone concentrations exceeding 60 nmol mol⁻¹ (SUM06). All four relationships were however statistically significant.     

Water relations, gas exchange and growth of cool-season grain legumes in a Mediterranean-type environment

The aim of this study was to identify the physiological characteristics which may affect the yield of six cool-season grain legume species grown in a water-limited Mediterranean-type climate in Western Australia. The rate of net photosynthesis, stomatal conductance and water relations were measured from flowering to complete leaf senescence in white lupin, chickpea, faba bean, field pea, grass pea and lentil. In irrigated plants, the midday leaf water potential was about −0.6 MPa in all species, while the maximum rate of leaf photosynthesis was 30 μmol m⁻² s⁻¹ for chickpea and white lupin, and below 20 μmol m⁻² s⁻¹ for the other species. With the development of water deficits, the leaf water potential in rain-fed plants decreased to about −3 MPa in chickpea and lentil and −2 MPa in the other species. Photosynthesis and stomatal conductance decreased markedly as the leaf water potential decreased below −0.9 MPa in all six species, including chickpea and lentil, which showed a high degree of osmotic adjustment. Despite the similarity in water use, restricted to the top 40 cm of soil, and water relations characteristics, yields varied markedly among species. Yields were strongly correlated with early biomass production and early pod development.     

Manganese requirement of sunflower (Helianthus annuus L.), tobacco (Nicotiana tabacum L.) and triticale (x Triticosecale W.) at early stage of growth

Manganese deficiency symptoms are more often observed in crops at early stages of growth since Mn²⁺ can be easily mobilized from the surface soil. The objectives of this study were to evaluate some of the popular rotation crops grown in Hungary for tolerance to low external Mn²⁺ levels and to determine the critical tissue concentration for Mn²⁺ deficiency during early stages of growth. Indicator plants of sunflower (Helianthus annuus L.) were grown with NPKCaMg-fertilization induced of 0.0425–0.0700 g kg⁻¹; of tobacco (Nicotiana tabacum L.) 0.0237–0.0337 g kg⁻¹; of triticale (x Triticosecale W.) 0.0103–0.0327 g NH₄-acetate + EDTA extractable soil Mn²⁺ kg⁻¹; and were grown for 73, 50, and 191 days. The minimum Mn²⁺ concentration required in soil nutrient contents was 0.0425 g kg⁻¹ for sunflower, 0.0243 g kg⁻¹ for tobacco, and 0.0103 g kg⁻¹ for triticale. Sunflower, tobacco and triticale achieved optimum growth from 0.048 to 0.065 g Mn²⁺ kg⁻¹, from 0.0249 to 0.0321 g Mn²⁺ kg⁻¹, and from 0.0287 to 0.0296 g Mn²⁺ kg⁻¹, respectively. Critical ABP's dry weight Mn²⁺ concentration at early stages of growth was 0.0536 g kg⁻¹ in sunflower, 0.458 g kg⁻¹ in tobacco, and 0.1938 g kg⁻¹ in triticale. Our results demonstrate that the tolerance to low external Mn²⁺ (triticale <0.0302 g kg⁻¹; sunflower <0.0562 g kg⁻¹; tobacco <0.0693 g kg⁻¹) and the critical tissue Mn²⁺ levels for deficiency varied significantly among crop species tested.     

Modelling potential growth and yield of olive (Olea europaea L.) canopies

The wide variability and complexity of olive orchards makes it difficult to provide solutions to the numerous management questions using a pure experimental approach. In this paper we calibrate and validate a simple model of olive orchard productivity based on the Radiation-Use Efficiency (RUE) concept of Monteith. A calibration experiment was performed in Cordoba from 1998 to 2001 with drip-irrigated olive trees cv. ‘Arbequina’. Destructive samples of 18 trees and non-destructive measurements on 80 trees were used to determine RUE and dry matter partitioning coefficients. Validation experiments were performed in 18 drip-irrigated orchards of seven locations in Southern Spain, including two cultivars (‘Arbequina’ and ‘Picual’). Average RUE was 0.86 g dry matter (MJ PAR)⁻¹ which is equivalent to 1.56 g glucose (MJ PAR)⁻¹. Aboveground accumulated biomass was allocated equally to fruits and vegetative growth, which in turn was partitioned into 30% for leaves and 70% for stems, branches and trunk. The fraction of oil in fruits was 0.38 which implies that the average ratio oil yield/intercepted PAR, which is an equivalent RUE for oil production (_o), is 0.17 g oil (MJ PAR)⁻¹. The prediction of oil yield as the product of 0.17 and total intercepted PAR was tested successfully in the validation experiments (relative RMSE = 0.26). Errors of this simple model were partly due to alternate bearing and partly to a decrease in _o as canopy size increases, which deserves further research. The concept of _o may be also useful for the evaluation of alternate bearing in olive trees.

Estimated potential carbon sequestration by intensive irrigated olive orchards in Southern Spain was 7 t CO₂ ha⁻¹ year⁻¹ which is much higher than that of other agricultural systems in Europe.

The simple model of growth and yield presented herein is the core of a complete model of olive growth and yield and may be useful not only for evaluating productivity at different scales but also for solving different management problems (nutrient requirements, plant protection, etc.)     

Effects of elevated carbon dioxide and ozone on potato tuber quality in the European multiple-site experiment ‘CHIP-project’

Potato (Solanum tuberosum L cv. Bintje) was exposed to ambient and elevated carbon dioxide (CO₂), to ambient and elevated ozone (O₃) and to elevated levels of both gases during two growing seasons, 1998 and 1999. Experiments in open-top chambers (OTC) were carried out in Finland, Sweden, Ireland, United Kingdom, Germany and Belgium and a FACE (Free Air Carbon dioxide Enrichment) experiment was carried out in Italy. In OTCs the plants were grown under ambient CO₂ concentrations or with 550 and 680 μl l⁻¹ CO₂ alone or in combination with ambient or elevated O₃ concentrations (target seasonal mean of 60 nl l⁻¹ 8 h per day). In the FACE systems the plants were exposed to ambient or 550 μl l⁻¹ CO₂. In the OTC experiments the reducing sugar content of potato tubers decreased significantly with increased concentration of O₃. The starch content of potato tubers decreased, with negative impact on tuber quality, but the ascorbic acid concentration increased as a function of the AOT40 (The sum of the differences between hourly ozone concentration and 40 nl l⁻¹ for each hour when the concentration exceeds 40 nl l⁻¹ during a relevant growing season). However, simultaneous exposure to elevated CO₂ counteracted the ozone effect. With increase in the CO₂ exposure, glycoalkaloid and nitrate concentrations decreased yielding improved quality, while the citric acid concentration decreased causing a higher risk for discoloration after cooking. The amount of dry matter and starch increased significantly in the FACE experiment.     

Extending the postharvest life of carnations with nitric oxide—comparison of fumigation and in vivo delivery

The ability of nitric oxide (NO) to extend the postharvest life at 20 °C of carnations (Dianthus caryophyllus L. cv. White-Sim) was investigated using delivery by gas-based fumigation and in vivo release via a solution containing the NO donor compound 2,2′-(hydroxynitrosohydrazino)-bisethanamine (DETA/NO). Treatment with NO gas in air at 1 and 5 μl l⁻¹ produced about a 30% increase in postharvest life while DETA/NO applied in solution at 10 mg l⁻¹ extended postharvest life by about 50% when dissolved in water. For flowers, use of solid delivery appears to offer a more convenient and more effective method of NO treatment than gaseous fumigation to extend postharvest life.     

Chlorophyll content of spring wheat flag leaves grown under elevated CO2 concentrations and other environmental stresses within the ‘ESPACE-wheat’ project

Spring wheat cv. Minaret was grown in open-top chambers at four sites across Europe. The effect of different treatments (CO₂ enrichment, O₃ fumigation, drought stress and temperature) on the chlorophyll content of the flag leaf was investigated using the MINOLTA SPAD-502 meter. Under optimum growth conditions the maximum chlorophyll content, which was reached at anthesis, was consistent among the sites ranging from 460 to 500 mg chlorophyll m⁻². No significant effect of elevated CO₂ or O₃ was observed at anthesis. Leaf senescence, indicated by the chlorophyll breakdown after anthesis, was relatively constant in the control chambers. Under control conditions, thermal time until 50% chlorophyll loss was reached was 600°C day. Elevated CO₂ caused a faster decline in chlorophyll content (thermal time until 50% chlorophyll loss was reduced to 500–580°C day) indicating a faster rate of plant development at two experimental sites. The effect of ozone on chlorophyll content depended on the time and dose of O₃ exposure. During grain filling, high O₃ concentrations induced premature senescence of the flag leaves (up to −130°C day). This deleterious effect was mitigated by elevated CO₂. Drought stress led to faster chlorophyll breakdown irrespective of CO₂ treatment.     

Interactive effects of elevated atmospheric CO2 concentrations and plant available soil water content on canopy evapotranspiration and conductance of spring wheat

The present study was conducted to investigate the possible interactive effects of rising atmospheric CO₂ concentration [CO₂] and drought stress on water use of wheat. Spring wheat (Triticum aestivum cv. “Minaret”) was grown either in 1 m diameter lysimeters with 0.4 m soil depth (1998) or in the field (1999) in open-top chambers under two CO₂-concentrations (ambient, ambient + 280 ppm) and two watering regimes (well-watered = WW with a plant available water content PAW > 40 mm and drought stressed = DS, 10 mm < PAW < 30 mm) beginning after first node stage. Canopy evapotranspiration (E_C) was measured continuously from first the node stage until the beginning of flag leaf senescence using four open-system canopy chambers (0.78 m³). Seasonal changes of the absorption of photosynthetically active radiation (APAR) of the canopy and root growth (1999) were also measured.

In both growing seasons leaf area index increased in response to elevated [CO₂] in both water treatments. The related effects of [CO₂] on canopy radiation absorption (APAR) were, however, smaller. E_C was linearily related to APAR in both growing seasons. While elevated [CO₂] reduced the slope of this relation under WW conditions by ca. 20% in both growing seasons, it was not reduced (1998) and even increased (1999) under drought. Canopy conductance (G_C) calculated as E_C divided by vapour pressure deficit of air, showed a non-linear relationship to APAR that was best explained by saturation curves. Under WW conditions, elevated [CO₂] reduced the initial slope of G_C versus APAR as well as G_C at saturating light conditions (ca. −30%), while under DS conditions no effect of elevated [CO₂] could be detected. Under high light conditions (PAR > 400 μmol m⁻² s⁻¹) a critical “threshold value” of PAW (T_PAW, ca. 40 mm) could be identified above which G_C did not respond to PAW. While in 1998 G_C did not respond to elevated [CO₂] at PAW < T_PAW, it was slightly increased at low PAW values in the field experiments of 1999. The reduction of T_PAW by elevated [CO₂] may be explained by enhanced root growth (1999) that would have given the plants better access to soil water resources. The present results suggest that below a critical soil water content elevated [CO₂] will not reduce canopy water loss of wheat or may even enhance it.     

Photosynthetic and stomatal responses of potatoes grown under elevated CO2 and/or O3—results from the European CHIP-programme

The physiological effects of elevated CO₂ and/or O₃ on Solanum tuberosum cv. Bintje were examined in Open-Top Chambers during 1998 and 1999 at experimental sites across Europe as part of the EU ‘Changing Climate and Potential Impacts on Potato Yield and Quality’ programme (CHIP). At tuber initiation (≈20 days after emergence, DAE) elevated CO₂ (680 μl l⁻¹) induced a 40% increase in the light saturated photosynthetic rate (A_sat) of fully expanded leaves in the upper canopy. This was 16% less than expected from short-term exposures of plants grown under ambient CO₂ (360 μl l⁻¹) to elevated CO₂, indicating that photosynthetic acclimation began at an early stage of crop growth. This effect resulted from a combination of a 12% reduction in stomatal conductance (g_s) and a decline in photosynthetic capacity, as indicated by the significant reductions in the maximum carboxylation rate of Rubisco (Vc_max) and light-saturated rate of electron transport (J_max) under elevated CO₂. The seasonal decline in the promotion of photosynthesis by elevated CO₂ reflected the concurrent decrease in g_s. Vc_max and J_max were both reduced in plants grown under elevated CO₂ until shortly after maximum leaf area (MLA) was attained. Although non-photorespiratory mitochondrial respiration in the light (R_d) increased during the later stages of the season, net photosynthesis was consistently increased by elevated CO₂ during the main part of the season. Photosynthetic rate declined more rapidly in response to elevated O₃ under ambient CO₂, and the detrimental impact of O₃ was most obvious after MLA was attained (DAE 40–50). Several exposure indices were compared, with the objective of determining the critical ozone level required to induce physiological effects. The critical O₃ exposure above which a 5% reduction in light saturated photosynthetic rate may be expected (expressed in terms of cumulative exposure above 0 nl l⁻¹ O₃ between emergence and specific dates during the season (AOT0-cum)) was 11 μl l⁻¹ h; however this value should only be extrapolated beyond the CHIP dataset with caution. The interaction between O₃ and stomatal behaviour was more complex, as it was influenced by both long-term and daily exposure levels. Elevated CO₂ counteracted the adverse effect of O₃ on photosynthesis, perhaps because the observed reduction in stomatal conductance decreased O₃ fluxes into the leaves. The results are discussed in the context of nitrogen deficiency, carbohydrate accumulation and yield.     

Climatic conditions and concentrations of carbon dioxide and air pollutants during ‘ESPACE—wheat’ experiments

A major objective of the ESPACE—wheat programme was to perform by means of open-top chambers (OTCs) ‘standardised’ experimental investigations of spring wheat responses to increased atmospheric CO₂ and O₃ concentrations and to other environmental stresses at different locations in Europe, representing a broad range of different climatic conditions. From 1994 to 1996 a total number of 25 OTC experiments were carried out. In addition, four growth chamber experiments focusing on key physiological processes of wheat growth in CO₂-enriched air were performed. According to the specific needs for subsequent modelling purposes, environmental data were collected during experiments, i.e. air temperature, global radiation, humidity and trace gas concentrations. In the present paper results of these measurements are summarised. It was shown, that the OTC-experiments covered a considerable range of growing season mean-air-temperatures (13.0–23.4°C) and global irradiances (10.8–18.1 MJ m⁻² d⁻¹), the most important driving variables for crop growth simulation models. Mean concentrations of CO₂ and O₃ in ambient air and in different treatments illustrated the observed variability of trace gas exposures between different experiments. Implications for subsequent analyses of biological response data are discussed.     

不同浸种剂对稻草还田条件下油菜发芽出苗的影响

为了缓解水稻秸秆还田对直播油菜的负面影响,实现水稻秸秆还田下直播油菜全苗、壮苗,本研究以‘沣油737’为试验材料,通过不同浸种剂处理,探究不同浸种剂对水稻秸秆还田下直播油菜发芽出苗的影响。结果表明,C₁（40 mg/L赤霉素+200 mg/L钼酸铵+2000 mg/L磷酸二氢钾+400 mg/L的硼酸）和C₂（100 μmol/L褪黑素+200 mg/L钼酸铵+2000 mg/L磷酸二氢钾+400 mg/L的硼酸）试剂浸种处理后水稻秸秆还田下直播油菜每平方出苗数分别较CK增加23.28%和3.97%;C₁试剂浸种后油菜幼苗根长增加,下胚轴的伸出长度变长,C₂试剂浸种后油菜幼苗的根长变长,下胚轴长度较CK有所降低;C₁、C₂试剂浸种后幼苗干物质积累较CK增加。C₁、C₂试剂浸种一定程度缓解秸秆还田对直播油菜出苗的不利影响,C₂试剂浸种更有利于促进油菜根系发育,促进秸秆还田下直播油菜壮苗。     

Effects on nutrients and on grain quality in spring wheat crops grown under elevated CO2 concentrations and stress conditions in the European, multiple-site experiment ‘ESPACE-wheat’

Nutrient element concentrations and grain quality were assessed in spring wheat grown under elevated CO₂ concentrations and contrasting levels of tropospheric ozone at different nitrogen supply rates at several European sites. Carbon dioxide enrichment proved to affect nutrient concentrations in a complex manner. In green leaves, all elements (with exception of phosphorus and iron) decreased. In contrast, effects on the element composition of grains were restricted to reductions in nitrogen, calcium, sulphur and iron. Ozone exposure resulted in no significant effects on nutrient element concentrations in different tissues in the overall analysis. The nitrogen demand of green tissues was reduced due to CO₂ enrichment as shown by reductions in the critical leaf nitrogen concentration and also enhanced nitrogen use efficiency. Reductions in the content of ribulose-bisphosphate carboxylase/oxygenase and repression of the photorespiratory pathway and reduced nitrogen allocation to enzymes driving the photosynthetic carbon oxidation cycle were chiefly responsible for this effect. Thus, nitrogen acquisition by the crop did not match carbon acquisition under CO₂ enrichment. Since crop nitrogen uptake from the soil was already completed at anthesis, nitrogen allocated to the grain after anthesis originated from vegetative pools—causing grain nitrogen concentrations to decrease under CO₂ enrichment (on average by 15% when CO₂ concentrations increased from 360 to 680 μmol mol⁻¹). Correspondingly, grain quality was reduced by CO₂ enrichment. The Zeleny value, Hagberg value and dry/wet gluten content decreased significantly with increasing [CO₂]. Despite the beneficial impact of CO₂ enrichment on growth and yield of C₃ cereal crops, declines in flour quality due to reduced nitrogen content are likely in a future, [CO₂]-rich world.