Shading decreases the growth rate of young apple fruit by reducing their phloem import

This study investigates the effects of shading on the biophysical mechanisms of apple (Malus Domestica Bork.) fruit growth by assessing how vascular and transpiration flows to/from the fruit are affected by shading. At 30 days after full bloom, a 90% neutral shading net was applied to four trees of the cv. Gala, for seven days, while four more trees, chemically thinned, were used as control. Fruit vascular and transpiration flows were assessed from two days before, to the end of shading. The daily patterns of fruit relative growth rate (RGR) and of phloem, xylem and transpiration flows were determined by continuous monitoring of fruit diameter by automatic fruit gauges. Before shading application, no differences between the two groups of trees selected were found for any of the parameters measured. Despite shading induced an immediate drop in canopy photosynthesis, both fruit daily RGR and phloem flow decreased gradually, until reaching 20% of the before treatment values after 7 days of shading. Differences in RGR and phloem flow appeared especially during the afternoon and night, i.e. post carbon assimilation by the tree, and fruit growth rates were higher in control trees. In the same period no, or very small differences were found between treatments for transpiration rates, while xylem flow was affected later than phloem and only at specific times during the day. These results suggest that the decrease in fruit growth rate under shading should be attributed to the reduction of canopy photosynthesis, rather than to a direct effect of shading on fruit sink strength.     

The Effects of Manurial Treatments on the Chemical Composition of Gooseberry Bushes.: I. Effects on Dry Matter,Ash and Ash Constituents of Leaves and Stems of Terminal Shoots and of Fruits; and on Total Nitrogen of Fruits.

Summary

The effects of different timings of fruit thinning at the lower nodes (nodes 4 to 7) on fruit growth and abortion at higher nodes were investigated in a gynoecious, parthenocarpic cultivar of cucumber (Cucumis sativus L.), ‘NK x AN8’. Fruits at the lower nodes were removed 0, 5, 10, 15 and 20 d after anthesis of flowers at node 8 (DAA₈).

Total leaf areas and growth patterns of individual fruit were then monitored. When fruits at nodes 4 to 7 were thinned 0 or 5 DAA₈, all fruits at nodes 8 to 12 grew to commercial size, without fruit abortion. When fruits were thinned 10 DAA₈, the fruits at nodes 8 to 12 ceased to grow after anthesis, but growth was restored a few days after fruit thinning. Fruit thinning at 15 or 20 DAA₈ forced most fruits at nodes 8 to 12 to abort, while fruits at node 13 and above ceased to grow for a while, but resumed growth after fruit thinning. In all treatments, total leaf area increased with time throughout the experiment. High fruit load depressed the rate of growth of leaf area slightly, 65 to 75 d after sowing. Fruit load (fresh weight) per leaf area was about 50 mg cm^–2 just before fruits at nodes 4 to7 were thinned at 20 DAA₈.These results suggest that fruit abortion occurs if fruits at the lower nodes persist for a long period, and fruits at the middle nodes senesce before enlargement. Fruit thinning at the lower nodes can restore the growth of fruits in the stagnant growth phase within 10 d.     

Does dry matter partitioning to fruit in early- and late-ripening peach (Prunus persica) cultivars confirm the branch autonomy theory?

Summary

We studied dry matter partitioning to fruit by establishing different patterns of fruit distribution between and within main branch units (scaffolds) on early (cv. ‘Alexandra’) and late (cv. ‘Suncrest’) maturing cultivars of peach (Prunus persica L. Batsch). The desired fruit loads were obtained by differential thinning of scaffolds and the commercial crop-load per tree was maintained. Each tree had four main scaffolds, one of these scaffolds was lightly thinned (High-crop scaffold), another one was heavily thinned (Low-crop scaffold) and the different fruit bearing stems (FBS) were alternately lightly thinned or heavily thinned in two scaffolds (Alternative-scaffold). Growth of fruits and of leafy shoots on all FBS were measured periodically from hand-thinning 30 and 50 days after full-bloom (DAFB) until harvest for cvs. ‘Alexandra’ and Suncrest, respectively. The mean fruit dry weight (DW) per FBS was strongly affected by fruit distribution between and within scaffolds in the late cv. ‘Suncrest’, indicating that branch autonomy was functional at the level of FBS in this case. In the early cv. ‘Alexandra’, mean fruit DW per FBS in each scaffold was similar, suggesting C-transfer between individual FBS. Branch autonomy could not be explained by fruit sink-strength being equal in both cultivars. In contrast to generative growth, vegetative growth was similar between scaffolds in both cultivars suggesting its independence from fruit sink removal.     

Effects of fruit load on flower bud initiation and development in peach

Summary

This study aims to quantify the effects of fruit crop-load on flowering and to determine the relationships between flowering and phloem sap carbohydrate and nitrogen content fractions from budding to dormancy in ‘Zincal 5’ nectarine. Fruit load significantly reduced the number of flowers per tree both indirectly, by reducing the number of shoots per tree and the number of nodes per shoot, and directly, by reducing the number of floral buds per node. The intensity of the response depended on the number of fruits developed per tree. Trees that kept all fruits up to senescence flowered 35% less than trees thinned by hand to 40% of fruits at pit hardening, and 55% less than trees completely thinned in bloom by hand. Trees that kept all fruits had significantly lower glucose and sorbitol contents in the phloem sap of mixed branches up to harvest date and full vegetative growth, respectively, but no significant relationships were found between the concentrations of these carbohydrates and flowering intensity in the following Spring. Sucrose and fructose did not show any significant difference in regard to crop-load. In fibrous roots, starch content was not related to fruit load up to dormancy, indicating that starch content is not associated with flower bud induction and differentiation. The nitrate-nitrogen fraction was significantly higher, and the ammonium-nitrogen fraction was significantly lower, in trees that tended to flower less, suggesting some disturbance in nitrate reduction in these trees.     

Flower thinning method affects mineral composition of `Braeburn' and `Fiesta' apple fruit

Summary

Fruit mineral concentrations measured at harvest can have major effects on apple fruit quality on the tree or during storage. Orchard practices must therefore seek to optimize fruit mineral composition. The purpose of this study was to describe and elucidate the effects of hand thinning on whole trees and individual spurs on apple fruit mineral composition. Two methods of flower and fruitlet thinning were compared with no thinning on `Braeburn' and `Fiesta' apple trees. Alternate whole flower/fruitlet clusters or all but one flower/fruitlet within every cluster were removed at full bloom or 14±21 d after full bloom. Alternate-cluster thinning reduced final fruit numbers per tree and fruit Ca concentrations by up to 22%, while increasing final fruit size by up to 21%, compared with no thinning. These effects on fruit Ca concentrations were also measured across a range of fruit size classes. Within-cluster thinning at full bloom or up to 21 d after full bloom also reduced fruit numbers per tree but increased fruit size substantially, by up to 65% compared with no thinning, this effect being less for later thinning. However, fruit mineral concentrations were not influenced by this treatment. Some fruiting spurs were singled to one fruit 14 d after full bloom on alternately flower cluster thinned trees and on trees that had not been thinned at bloom, and compared with unthinned spurs on the same trees. Fruit Ca concentrations, primary spur leaf areas and primary spur leaf areas per fruit were greater for spurs bearing a single fruit (achieved by thinning manually or through natural abscission) than for multi-fruited spurs on the same trees. Spurs bearing one fruit on unthinned trees had greater fruit Ca concentrations, primary spur leaf areas and primary spur leaf areas per fruit, but lower fruit weight than the same spurs on alternate-cluster thinned trees. However, spurs on unthinned and alternate-cluster thinned trees with the same primary leaf areas per fruit had similar final Ca concentrations. Fruit size and crop loads were found not to be important in explaining fruit Ca concentration differences between thinning methods. However our results suggest that thinning method may affect Ca accumulation in apple fruit by altering the relationship between fruit numbers and leaf areas on individual spurs.     

Effects of different crop loads and thinning times on yield,fruit quality,and return bloom in Malus × domestica Borkh. ‘Elstar’

Summary

‘Elstar’ is the latest-maturing commercial apple cultivar grown in Norway, with high fruit quality when properly managed. In May 2006, an experiment with four different crop loads [2, 4 ,6, or 8 flowers or fruitlets cm^–2 trunk cross-sectional area (TCSA), respectively] was established at two different stages [first bloom (FB), or 20-mm diameter fruitlets] and compared to unthinned control trees. Fruit growth was measured on individual fruit for each treatment throughout the season at weekly intervals. Thinning at FB gave a significantly lower final percentage fruit set than thinning to the same cropping level at the 20-mm fruitlet stage. However, fruit weights and soluble solids contents (SSC) were significantly higher, and the background fruit colour improved when trees were thinned at FB. The final number of fruit at harvest was less than the amount established at FB, or at the 20-mm fruitlet stage. There were significant differences between treatments in final fruit numbers per TCSA, which reflected the different crop loads. Fruit weights and SSC values were highest with the lowest crop load, and decreased with increasing crop loads. There was also a strong crop-load effect on the extent of return bloom per tree in the subsequent year. Trees thinned at FB had significantly more flower clusters than those thinned at the 20-mm fruitlet stage of. Untreated control trees had the lowest number of flower clusters. The amount of return bloom declined with increasing crop load. Second year crop loads and fruit weights were highest when trees were thinned at FB to two or four apples cm^?2 TCSA in the previous year. Trees with the highest crop load had the lowest crop load in the following year. Fruit quality was generally high for all treatments.     

Interaction of Maximum Daily Trunk Shrinkage and Fruit Quality in European Plum

Maximum daily trunk shrinkage (MDS) has been suggested as an appropriate indicator of plant water status because it is closely related to stem water potential. Interaction of MDS and fruit quality was studied in plum (Prunus domestica L. ‘Jojo’/Wavit and ‘Tophit plus’/Wavit) in temperate climate. According to the MDS data, trees were grouped as low MDS (LMDS) and high MDS (HMDS). Fruit quality was analysed during fruit development (95, 103, 117 DAFB for ‘Jojo’ and 99, 112, 121 DAFB for ‘Tophit plus’) before commercial harvest. Fruit picked at commercial harvest (137 DAFB and 140 DAFB for ‘Jojo’ and ‘Tophit plus’, respectively) were stored at 2 ± 0.5?°C (90 ± 2% RH) for 28 days, and 2 days shelf life at 20?°C providing 6 measuring dates postharvest. Results confirmed that MDS was positively correlated with water vapour pressure deficit also in the apparent temperate, semi-humid climate. Transpiration of fruit from high crop load and resulting HMDS trees, which can be assessed as physiologically drought, was low compared to that of fruit from LMDS trees. Furthermore, HMDS tree grown plums had enhanced soluble solids and dry matter contents with a tendency of reduced fruit size.     

Size factors in apple fruit

Eight ‘Golden Delicious’ apple trees on an experimental plot were systematically thinned to give different numbers of fruit per spur, per branch, and per tree. At harvest, fruits were weighed individually and their positions on spurs and branches noted. Trunk and branch girths were measured.Mean fruit weights were not significantly affected by the presence of several fruits on a spur, or by the degree of local crowding on branches, compared with the general mean for the whole tree. However, mean fruit weight varied between trees, depending on the number of fruits carried per unit of trunk girth of cross-sectional area.μ (mean fruit weight) = a — bN (number of fruit per unit trunk dimension)The distribution of fruit weights on each tree can be regarded as normal and on the 8 trees examined, standard deviations did not differ significantly. An equation was derived relating total crop per tree and fruit-size distribution to trunk dimensions and fruit number, both of which were variable from tree to tree, involving 2 coefficients of the mean size equation and the standard deviation of the weight distribution, which seem to be constant for the 8 trees under the prevailing conditions.Using the equations, it could be shown that although fruit thinning would increase the proportion of larger fruit in the crop, in only one case would careful thinning have increased the total weight of larger fruit.     

Pruning Trials With Worcester Pearmain Apple

Three pruning treatments were compared on Worcester Pearmain on M.IV rootstock, viz.: open-centre tree, established-spur pruned; delayed open-centre tree, established-spur pruned; regulated pruned tree. In the fifteenth year secondary treatments were begun, the trees being pruned either annually or in alternate years, with and without fruit thinning by hand. The trees were grubbed after 21 years and scion weights were obtained.

There were no important differences in growth and cropping between open-centre and delayed open-centre trees. Regulated trees had an 11% smaller area of branch spread than established-spur pruned trees at 21 years. At 15 years there was no significant difference between treatments in total weight of prunings, but three times as much old wood as new had been removed from regulated trees compared with two and a half times as much new wood as old from established-spur pruned trees. During a 6-year period, the same weight of wood was removed from alternate-year pruned trees as from those pruned annually.

During the first 10 years regulated trees yielded twice as much fruit as did established-spur pruned ones, and 49% more during the second 10-year period. In many years, in the absence of fruit thinning, regulated trees bore smaller fruits than did established-spur pruned trees. Regulated trees had more red colour on the fruits than established-spur pruned trees, and alternate-year pruning, whether regulated or established-spur, gave more red colour on the fruits than did annual pruning, especially in seasons following no pruning. Alternate-year pruning had no harmful effect upon fruit size. Fruit thinning had no important effect upon red colour but it increased the percentage crop weight in the larger size grades, especially on established-spur pruned trees. The regulated method is well suited to the growth habit of Worcester provided that the fruit is thinned by hand or chemical spray in years of heavy setting.

The relative ratios between total crop : scion weight and crop 15–21 years : scion weight, were similar; scion weights were twice as heavy as weights of prunings.     

Thinning time during stage I and fruit spacing influences fruit size of ‘Contender’ peach

Early peach thinning during stage I was done at 0, 10, 20, 30, and 40 days after full bloom (DAFB). At each thinning time, trees were hand-thinned to achieve different crop loads by spacing flowers or fruits 10, 15, or 25 cm along the shoot on whole tree canopies. In 2001 and 2002, fruit weight decreased quadratically with increasing time to hand-thin and increased linearly with increasing spacing. In both years, fruit diameter decreased linearly with increasing time to thin and increased linearly with increased fruit spacing. In both years, number of fruits harvested and yield per tree decreased linearly with increased spacing. Hand-thinning at 0 or 10 DAFB resulted in fewer fruit and lower yield; therefore, thinning at 20 DAFB was better. The effect of time of thinning on soluble solids was not consistent. In both years spacing (i.e., crop load) did not affect soluble solids.     

Flowering and fruiting in ‘Patterson’ apricot (Prunus armeniaca) in response to postharvest application of gibberellic acid

In July or August of 1988 and 1989 which was approximately 2 or 6 weeks, respectively, after fruit harvest, cultivar ‘Patterson’ apricot (Prunus armeniaca) trees were sprayed with a single spray of either 10, 50 or 100 p.p.m. gibberellic acid (gibberellin A₃, GA). GA sprays of 100 p.p.m. applied in early July reduced flower number per centimeter of limb length in the year following treatment. Flower number per centimeter of limb circumference was reduced by sprays of 50 and 100 p.p.m. GA applied in July. Fruit set was not affected by GA sprays. The yield and fruit number of hand thinned trees was equivalent to that found on trees treated with 50 and 100 p.p.m. GA sprays in July. Individual fruit weight (size) was increased by GA sprays of 50 and 100 p.p.m. in July compared to hand thinned trees. Fruit maturity was advanced when yields were reduced by GA sprays. In July, GA sprays of 10 p.p.m. resulted in increased individual fruit weight without reduced total yields per tree compared to non-thinned control trees. Results showed that the use of GA sprays the year before flowering (July) decreased flower numbers, eliminating the need for chemical or hand fruit thinning of ‘Patterson’ apricot.     

Light distribution in apple orchard systems in relation to production and fruit quality

Summary

The effect of tree density (2000, 2667, and 4000 trees per ha) and the ratio of between to within-row distance (1:1, 2:1, and 3:1) on light interception, fruit production, colour and individual fruit weight was evaluated in a ten-year comparative field study with apple at two sites in The Netherlands (51° 30′ and 52°0′ N) and one site in Denmark (55°30′). For each combination of tree density and rectangularity, trees were pruned at three heights (1.50, 1.88, or 2.25 m). Fruit production over nine years and seasonal incoming radiation between bloom and harvest were 20 and 15% greater in The Netherlands. Climate-based estimates of potential production as provided by a crop-growth model, predicted 18% higher fruit production in The Netherlands. Production was proportional to light interception and increased with tree density, but the amount of well-coloured fruit per ha in later years did not increase with planting density. With more than 70% light interception in later years, a large proportion of shade within the canopy was found. Fruits were smaller and less coloured at the Danish site. Fruits were more coloured in the taller and more open trees, even at the highest tree densities. Plantings with 1:1 and 2:1 between-to within-row distances intercepted more light and had a more uniform light distribution than 3:1 designs. This led to higher fruit production and better fruit colour. Fruit weight was not influenced by tree density, rectangularity, or tree height.     

Performance of some apple cultivars under tropical Zambian conditions

Summary

Ten apple cultivars (Malus domestica Bork) Ein Shemer, Anna, Rome Beauty, Tropical Beauty, Alexander, Orleans, Winter Banana, Black John, Starking Delicious and Red Delicious were evaluated for their suitability for tropical Zambian conditions. Winter Banana, Black John, Starking Delicious and Red Delicious, which were mostly high-chill cultivars, showed poor vegetative development: delayed budbreak, shoot growth and progressive loss of vigour and most of the trees died before maturity. Of the remaining low-chill cultivars, ‘Ein Shemer’ had the highest fruit yield at 49 6 2.3 kg tree²¹ and ‘Alexander’ the lowest (5.3 6 1.0 kg tree²¹). This response was due to the high number of fruits per tree, ‘Ein Shemer’ had up to 907 6 83.7 per tree whereas low yielding cultivars like ‘Rome Beauty’ and ‘Tropical Beauty’ had fewer than 106 6 25.3 fruits per tree. The individual fruit weight was inversely related to the total number of fruits per tree. It ranged from 58 6 5.1 g in Ein Shemer to 191 6 24.8 g in ‘Rome Beauty’.     

The Effects of Fruit Thinning on the Development of Cox’s Orange Pippin Apples in Relation to the Incidence of Storage Disorders

Severe hand thinning of fruitlets on Cox’s Orange Pippin trees five weeks after full blossom led to a doubling of fruit weight by harvest. Although the rate of cell division was stimulated slightly, the larger fruit size was due mainly to an increased rate of cell enlargement.

The respiration rate of whole fruits was slightly higher after thinning and the onset of the climacteric rise was advanced. Respiration per cell was correspondingly higher in the larger cells of the thinned fruit and respiration per unit protein was similar to that of fruit from unthinned trees.

Potassium, magnesium, and phosphorus contents, expressed on a fresh weight basis, were higher in the cortical tissue of the thinned fruits. Calcium per unit fresh weight was unaffected by thinning and the ratio of calcium to cell surface remained relatively constant throughout development in both types of fruit.

Senescent breakdown and bitter pit developed during storage only in the thinned fruit. Slight differences in the incidence of rotting and low temperature breakdown between the two types of fruit are attributed to the effects of maturity rather than of fruit size.     

Einfluss selektiver mechanischer Fruchtbehangsregulierung auf Ethylensynthese als Stressindikator sowie Ertrag und Fruchtqualität bei Kernobst

The overall objective of this work was to improve fruit quality, break alternate bearing and reduce hand thinning using fewer chemicals in fruit crops. A device was constructed for mechanical thinning, which consisted of three independent horizontal rotors with ropes and freely adjustable angles on a frame, mounted on a front three point hitch and powered by the tractor hydraulics. This can be adapted to any fruit tree trained as spindle, Solaxe, (tall) vertical axis or fruit wall (le mur fruitier) irrespective of rootstock employed. Rotor speed varied from 300 to 460?rpm at either 5 or 7.5?km/h tractor speed. Eight-year-old or twelve-old apple trees cvs. ‘Gala’ and ‘Golden Delicious’ were mechanically thinned in 2007 between pink bud and full bloom (flower bud stages 6–8 or F1–F2) near Bonn, Germany; non-thinned and hand-thinned apple trees of the same block and variety served as control. Mechanically thinned flowering branches showed a similar amount of ethylene efflux (0.4–0.6?ppm C₂H₄/branch) as non-thinned flower branches, preventing potentially unexpected subsequent fruit drop, except for those removed by the rotors. The impact of the horizontal rotors on the branches was from the upper side and removed excessive flowers right to the tree trunk viz. the centre of the tree canopy, where fruits of lesser quality are expected leaving 2–3 flowers per cluster. Leaf damage was less than??10%, even at the fast rotor speed of 420?rpm, which was associated with negligible wood injury. Mechanical thinning induced firmer and sweeter fruit, i.e. tastier apples with longer shelf life, relative to control fruit from non-thinned apple trees. The greatest efficacy in terms of final fruit quality in the grading/sorting was achieved by a rotor speed of 360?rpm at a tractor speed of 5?km/h: Fruit mass increased by up to 20?g and the proportion of fruit larger than 70–75?mm by 10–30% compared with the fruit from non-thinned trees. Mechanical thinning with this newly constructed device led to a 10–20% reduction in yield, but increased returns due to better fruit size and colouration in apple with the potential to overcome alternate bearing.     

Evaluating the effectiveness of different strategies for calcium application on the accumulation of calcium in apple (Malus × domestica Borkh. ‘Braeburn’) fruit

Summary

Orchards displaying calcium (Ca) deficiency are a common phenomenon worldwide, despite the presence of sufficient Ca in the soil and the plant. A 3-year trial was conducted between the 2007 – 2008 and 2009 – 2010 growing seasons to evaluate the contributions of soil and foliar Ca applications to Ca concentrations in ‘Braeburn’ apple (Malus × domestica Borkh.) fruit. Ca(NO₃)₂ (Calflo; Yara Africa, Fourways North, South Africa) was applied as six separate foliar sprays until run-off. Applications were made at 1-week intervals between approx. 21 – 70 d after full bloom (DAFB) at 6.75 ml l^–1. Soil applications of Ca (Tropicote^TM; International ASA, Oslo, Norway) at 300 kg ha^–1 were applied at fruit set, or after harvest, according to standard practice. Mineral analysis was conducted to assess the soluble Ca concentrations of whole fruit (without pips and stalks), to quantify the contribution of foliar sprays or soil-applied Ca. Fruit Ca concentrations were maintained at satisfactory levels (4.5 mg Ca 100 g^–1 FW) at harvest by applying a series of six foliar sprays early in the season (for all seasons) during the trial period. Fruit Ca concentrations at 80 DAFB were highest in the treatments with foliar applications of Ca. In 2009 – 2010, Ca concentrations in apple fruit were lowest (8.38 mg 100 g^–1 FW) for soil application of Ca at fruit set. Ca applications to soil after harvest in the previous season, and soil applications shortly after fruit set in the current season, did not significantly increase Ca concentrations in current-season fruit, providing soil Ca levels were above the minimum requirement for apple trees. A possible explanation is that apple trees regulate their uptake of Ca through the roots when soil Ca is available in sufficient quantities. This confirms the importance of active root growth for efficient Ca uptake by apple trees when applying Ca to the soil.     

Fruit thinning in ‘Conference’ pear grown under deficit irrigation: Implications for fruit quality at harvest and after cold storage

Fruit thinning in pear is feasible for mitigation of water stress effects. However, it is not well known how fruit quality at harvest and after cold storage is affected by pre-harvest water stress. Even less is known about the effects of fruit thinning on quality under these circumstances. To elucidate these, we applied deficit irrigation (DI) and fruit thinning treatments to ‘Conference’ pear over the growing seasons of 2008 and 2009. At the onset of Stage II (80 and 67 days before harvest in 2008 and 2009, respectively), two irrigation treatments were applied: full irrigation (FI) and DI. FI trees received 100% of crop evapotranspiration (ETc). DI trees received no irrigation during the first three weeks of Stage II to induce water stress, but then received 20% of ETc to ensure tree survival. From bud-break until the onset of Stage II and during post-harvest, FI and DI trees received 100% of ETc. Each irrigation treatment received two thinning levels: no thinning leaving commercial crop load (∼180 fruits tree⁻¹), and hand-thinning at the onset of Stage II leaving a light crop load (∼85 fruits tree⁻¹). Under commercial crop loads, DI trees were moderately water-stressed and this had some positive effects on fruit quality. DI increased fruit firmness (FF), soluble solids concentrations (SSC) and acidity at harvest while no changes were observed in fruit maturity (based on ethylene production). Differences in FF and acidity at harvest between FI and DI fruit were maintained during cold storage. DI also reduced fruit weight loss during storage. But fruit size was reduced under DI. Fruit thinning under DI resulted in better fruit composition with no detrimental effect on fresh-market yield compared to un-thinned fruit. Fruit size at harvest and SSC values after five months of cold storage were higher in fruit from thinned trees than fruit from un-thinned trees. Fruit thinning increased fruit ethylene production, indicating advanced maturity. This may lead to earlier harvest which is desirable in years with impending drought. Fruit thinning is therefore a useful technique to enhance pear marketability under water shortage.     

Effect of crop load,fruit position and shoot vigour on yield and quality of Annona atemoya × Annona squamosa in India

The effect of crop load, position of the fruit on the shoots and vigour of the shoots on yield and quality of Annona atemoya × A. squamosa hybrid ‘Arka Sahan’ was investigated in India over two years. The trees were hand-pollinated and thinned to 20, 40, 60, 80 or 100 fruit after fruit set. Information was collected on total and marketable yield, yield efficiency, average fruit fresh weight, peel weight, the number of seeds per 100 g of pulp, pulp content in the fruit, total soluble solids (TSS) and total titratable acidity. In other experiments, fruit were harvested from weak, medium or vigrous shoots, or from basal, middle or apical nodes. Total yield increased up to 60 or 80 fruit per tree and marketable yield increased up to 60 fruit per tree. Average fruit weight and peel weight increased as cropping increased. These results suggest that optimum productivity and quality is associated with 60 fruit per tree or 0.17 to 0.19 kg cm² trunk-cross sectional area. The quality of the fruit in different positions on the shoots or on the different types of shoots was highly variable and generally not affected by the various treatments.     

Summer pruning reduces whole-canopy carbon fixation and transpiration in apple trees

Summary

Canopy size control is one of the major purposes of summer pruning. However, reducing canopy size might also result in less light interception, consequently decreasing canopy photosynthetic efficiency and carbohydrate production, which might lead to the imbalance of carbohydrate supply and fruit demand. To document the effectiveness of summer pruning on canopy control and the impact on canopy gas exchange, pruning treatments at four levels of intensity (unpruned, light, moderate, and severe) were carried out on mature ‘Empire’/M.9 slender spindle apple trees (Malus domestica Borkh.) on 30 July 1998 and 4 August 1999. Changes in canopy leaf area after summer pruning were estimated. Canopy net carbon exchange rate (NCER) and canopy transpiration before and after summer pruning were monitored. Canopy growth was suppressed by summer pruning and the post-pruning regrowth was insignificant. Canopy NCER was reduced in proportion to the amount of leaf area removed by summer pruning. The result suggests that commercial pruning intensity similar to the moderate to severe treatments in this study could cause a significant reduction in canopy NCER and carbohydrate production. In addition, canopy transpiration was reduced in proportion to pruning intensity. Lower water consumption and improved water status during the growing season after summer pruning might benefit fruit growth and relieve the potential detriment due to carbohydrate shortage.