Postharvest nutrition in stone fruit: the next crop is made in July
Savvas Pastopoulos, Agronomist MSc — Pastopoulos Agricultural Ltd, Neos Mylotopos, Pella
Something happens in sweet cherry and apricot that does not happen in most fruit crops: harvest ends in May or June, and the tree is left in full leaf for another four or five months with no fruit on it. Those months are usually treated as dead time. They are not. They are the period in which the next crop is made — and made twice over: once in the buds and once in the reserves. In this article every recommendation is accompanied by the study that supports it.
spring spur leaves comes
from reserves
flower buds with
autumn urea
hardiness
the pistil is
formed
- Why the period after harvest is the most underestimated
- What happens in the buds: sweet cherry and apricot
- The reserves and their remobilisation
- Nitrogen after harvest
- When autumn fertilisation is pointless
- Boron — the target with the best return
- Zinc
- Water: without it nothing works
- Temperature and doubled fruit in sweet cherry
- Early defoliation cancels everything out
- How foliar sprays are applied correctly
- The programme as a calendar
- Sources
1. Why the period after harvest is the most underestimated
In most fruit crops harvest comes close to leaf fall and the tree has little time afterwards. In sweet cherry and apricot the opposite happens. The canopy works at full intensity through a whole July, August, September and October — and all of that photosynthetic product, together with whatever the root takes up, goes into two things and two only:
- The differentiation of the flower buds from which next spring's bloom will come.
- Loading the reserves in root, trunk, scaffold limbs and buds.
Sources: 1
2. What happens in the buds: sweet cherry and apricot
This is not theory. It has been observed under a scanning electron microscope, bud by bud, from May to November.
Sweet cherry — the timetable
- Differentiation begins at about the same moment in all cultivars, with the first buds visible in mid to late May. No clear relationship was found between harvest date and the date differentiation began.
- The sequence is constant: first a pentagonal ring of sepal primordia, then the petals, then the anthers, and last of all the pistil.
- The rate of progress follows the ripening order: in the early ‘Chelan’ the pistil primordia are visible in early August, whereas in the late ‘Sweetheart’ about three weeks later.
- Overall, the start of pistil development occurs roughly 7 to 9 weeks after harvest.
Observations on ‘Chelan’, ‘Tieton’, ‘Bing’, ‘Skeena’ and ‘Sweetheart’.
Sources: 2
Apricot — the timetable
- The initial phase of differentiation starts in mid to late July, followed by differentiation of the floral organs.
- In deciduous fruit trees generally, initiation, differentiation and organogenesis of the flower bud all take place within the summer–autumn period preceding bloom.
- The abnormalities of the flower buds — the well-known problem of sterile apricot flowers — are linked to precisely this first period of development.
3. The reserves and their remobilisation
During autumn, the nitrogen inside the plant is mobilised and transported to the roots, where it stays in storage until the next season. In spring the reverse journey follows.
How important are those reserves? The cleanest measurement comes from apple, using labelled nitrogen:
| Where the nitrogen ends up next spring | Proportion coming from reserves |
|---|---|
| Nitrogen of the shoots | 50% |
| Nitrogen of the spur leaves | 90% |
| Nitrogen of the fruit | 60% |
The 90% for the spur leaves is the figure to hold on to. The spurs are exactly the positions on which sweet cherry fruits. The spur leaf that will feed the cherry in May is built almost entirely from nitrogen stored the previous September.
4. Nitrogen after harvest
What autumn urea achieves in sweet cherry
Postharvest foliar urea is not a new idea: it had already been tested on pear, with a measurable response from the tree [21]. In experiments with 3.5% foliar urea on sweet cherries on dwarfing rootstocks, over four successive application periods from late August to late October:
- An increase in nitrogen reserves in the flowering spurs of up to 40%.
- Improved cold acclimation, with hardiness up to 4.25 °C better than the control.
- Early defoliation had a negative effect both on the nitrogen reserves and on spur leaf development in spring.
Sources: 3
How much is actually absorbed
- The efficiency of autumn foliar nitrogen ranges from 30% to 80%, depending on the weather conditions.
- With 2% urea, 48% absorption was measured.
- In a comparison of application timings in sweet cherry, uptake efficiency was 65.7% for the spring application against 37.4% for the summer one — but the summer nitrogen was distributed not only to trunk and roots but also to the buds, which is exactly the target here.
In a trial with labelled urea on fruiting limbs of ‘Bing’/‘Gisela 6’ sweet cherry, with four application dates after harvest, the earliest application gave the highest nitrogen use efficiency, while in all treatments the urea was transported from the leaves to the other organs, with the highest values in the fruiting section.
Sources: 12
5. When autumn fertilisation is pointless
The timing of the application and the texture of the soil together determine how much of the nitrogen the tree will actually use [23]. This is the point that separates agronomy from selling fertiliser. Autumn sprays pay off only where there is a real deficiency. They are not tonics.
On mature ‘Burlat’ sweet cherries in central Poland, on a coarse-textured soil with adequate phosphorus, potassium, magnesium, calcium, iron, manganese, zinc and copper — but low boron, autumn sprays of nitrogen, boron and zinc were tested over three years. The result:
- The sprays had no effect at all on flower bud damage from cold, on the nitrogen status of the tree, or on the soluble solids of the fruit.
- Only boron improved the reproductive response. Nitrogen, on trees that did not need it, did nothing.
Sources: 5
When nitrogen is needed — and when it is a mistake
It is needed when:
- There is a documented deficiency. In sweet cherry, a nitrogen concentration in recently matured leaves in midsummer below 2.0% indicates deficiency. The sufficiency range is 1.7–2.5%.
- The orchard has carried a heavy crop and the trees are showing a loss of vigour.
It is a mistake when:
- Levels are adequate and vigour is balanced — the spray is then simply ineffective.
- There is excessive vigour. There the extra nitrogen is counterproductive, and leaf analysis can mislead: in very vigorous tissue the nitrogen concentration is diluted. That is why the assessment has to combine leaf analysis and a visual judgement of vigour.
Sources: 1
6. Boron — the target with the best return
If there is one element for which postharvest application has clearer documentation than spring application, it is boron.
What it does and why in autumn
- Boron is fundamental to pollen germination, pollen tube growth and fruit set. Demand for it peaks at exactly the start of the season.
- In the xylem it has low mobility. In Prunus, Malus and Pyrus, however, it has sufficient phloem mobility — and that is what makes an autumn foliar spray actually reach the buds.
- Autumn application is more effective than spring application in raising boron in the flowers and improving fruit set.
In the Malatya region of Turkey, over four years (2009–2012), on unirrigated apricot trees of cultivar ‘Hacıhaliloğlu’, autumn foliar application of boron, urea, and the combination of the two was tested. The results:
- The proportion of sterile flowers was reduced. That is the classic problem of apricot.
- Yield increased.
- The highest concentrations in the buds were measured in the boron + urea treatment: 16.53 ppm boron and 1.56% nitrogen.
- The combination of boron 1,000 ppm + urea 3% improved flower development and fruit set.
Sources: 4
7. Zinc
Sweet cherry, along with apple, is among the species most sensitive to zinc deficiency. The symptoms are characteristic: small leaves, chlorosis, rosetting and short internodes. Levels below 25 mg/kg in recently matured leaves indicate deficiency.
Deficiency appears mainly on cold, wet, sandy and alkaline soils with a pH above 7.5, where zinc is fixed. Under those conditions the problem is not a shortage of quantity but an inability to take it up — and that is why soil application is ineffective.
8. Water: without it nothing works
Every correct spray can be made and nothing gained, if the tree has no water during the differentiation period. And in apricot this has been measured in the most direct way.
In two-year-old apricot trees of cultivar ‘Portici’ subjected to controlled water stress in June, in July and in October, with irrigation restored afterwards:
- Both summer stress periods caused a temporary halt in flower differentiation.
- Trees stressed in June were able to recover; those stressed in July showed a marked delay.
- All stress treatments caused slower development of the xylem vessels inside the bud, changes in bud size, in flowering intensity, and flower abnormalities.
Sources: 8
Translated to the orchard: July — that is, precisely the month after the apricot harvest — is the worst month for the tree to go thirsty. Irrigation does not stop at harvest.
9. Temperature and doubled fruit in sweet cherry
Doubled fruit — polycarpy, that is more than one pistil in a flower — is one of the leading causes of fruit rejection. And it is created the previous summer, within the period discussed here.
| Finding | Source |
|---|---|
| Exposure to 35 °C day / 25 °C night from June to September increased doubled fruit in ‘Satohnishiki’ | [16] |
| High temperature, and not water stress, is responsible for doubled fruit | [17] |
| 80% shading during differentiation reduced doubles from 47% to 24% | [18] |
| In ‘Bing’, sensitivity extends from late July to early September, peaking in early August. Once pistil development has advanced, the bud is no longer sensitive | [2] |
In a commercial ‘Tieton’ orchard with a natural doubling rate of around 30%, with treatments from mid-July to mid-August:
- Overhead evaporative cooling: a 50% reduction (applied only when the temperature exceeded 34 °C, in cycles of 20 minutes on and 10 minutes off).
- Kaolin: a 45% reduction, with three applications to maintain coverage.
- 20% shading: a 37% reduction.
Overhead cooling dropped tissue temperature by about 5 °C, kaolin and shading by about 2 °C.
And the warning: under-canopy microsprinklers were ineffective and in fact slightly raised canopy temperature, because the increased humidity reduces the vapour pressure deficit and therefore the foliage's own evaporative cooling. Running under-canopy sprinklers with the aim of reducing doubles is not recommended.
Sources: 2
10. Early defoliation cancels everything out
Everything described above presupposes one thing: that the foliage will stay on the tree, healthy and functional, until natural leaf fall.
- Early defoliation had a negative effect on nitrogen reserves and on spur leaf development the following spring in sweet cherry.
- In a separate trial on ‘Selah’ sweet cherry, early defoliation reduced yield and the concentration of nutrients in the buds.
11. How foliar sprays are applied correctly
The application conditions
- Temperature: not below 20 °C and not above 29 °C.
- Wind: strong wind shortens the drying time of the droplet and therefore the absorption.
- Relative humidity: low humidity affects droplet size and how long it stays on the leaf surface.
- Sulphate salts — such as zinc sulphate — are applied only once the temperature has fallen below 27 °C.
Two technical details that matter
- The urea must have a biuret content below 0.25%. Biuret is phytotoxic.
- Mixing the trace elements with urea improves their uptake. It is not a combination of convenience — it is a documented enhancement.
- Urea: 2% on apple [14], 3% on apricot [4], 3.5% on sweet cherry [3].
- Boron: 1,000 ppm combined with 3% urea, on apricot [4].
- Zinc: zinc sulphate; the general recommendation for apple and sweet cherry is a higher rate than for peach and nectarine [1].
These figures are experimental, from particular conditions and cultivars. They do not transfer unchanged to every orchard. The choice of rate is always made on the basis of leaf analysis, the condition of the block and the authorisations in force.
12. The programme as a calendar
| Period | Sweet cherry | Apricot |
|---|---|---|
| Immediately after harvest | Fruiting-wood pruning, irrigation restored to full rate, foliage protection. | Pruning, full irrigation — July is the most critical month. |
| Midsummer | Leaf analysis on recently matured leaves. It is the only basis for deciding whether an autumn treatment is needed and for which element. Targets: N 1.7–2.5%, B 20–80 mg/kg, Zn above 25 mg/kg. | |
| Late July to early September | Window of sensitivity for doubled fruit. In a heatwave, canopy cooling measures. No under-canopy sprinklers. | Differentiation of the floral organs. No water stress. |
| Autumn, before the leaves yellow | Foliar sprays — only for the elements the analysis showed to be deficient. Nitrogen for the reserves and cold hardiness, boron for fruit set, zinc where there is a deficiency. | |
| Until natural leaf fall | The foliage stays on and healthy. Every week of early defoliation is a loss of reserves. | |
- The next crop is made from July to October, not in March.
- 90% of the nitrogen in the spur leaves comes from the previous year's reserves.
- Autumn sprays work only on a real deficiency. Without leaf analysis they are a lottery.
- Boron is the element with the clearest documentation for autumn application — and in apricot it reduces sterile flowers.
- Water and foliage. Without those two, no fertiliser matters.
13. Sources
The numbers in the text refer to the list below.
- [1] Sallato, B. (2024). Fall Nutrient Sprays in Tree Fruit. Washington State University Tree Fruit Extension, Fact Sheet FS365E. The main reference text for the sufficiency thresholds, the application conditions and when a spray is pointless.
- [2] Whiting, M. and Martin, R. (2025). When and How to Reduce Doubling in Sweet Cherry. WSU Tree Fruit. Source for the differentiation timetable in sweet cherry, the window of sensitivity and the results of the cooling measures.
- [3] Ouzounis, T. and Lang, G. (2011). Foliar applications of urea affect nitrogen reserves and cold acclimation of sweet cherries (Prunus avium L.) on dwarfing rootstocks. HortScience 46(7):1015–1021. Source for the 3.5% urea, the 40% increase in spur reserves, the 4.25 °C of hardiness and the effect of early defoliation.
- [4] Karlıdağ, H., Eşitken, A., Turan, M. and Atay, S. (2017). The effects of autumn foliar applications of boron and urea on flower quality, yield, boron and nitrogen reserves of apricot. Journal of Plant Nutrition 40(19):2721–2727. The main study for apricot: reduction of sterile flowers, increase in yield, 16.53 ppm B and 1.56% N in the buds.
- [5] Wójcik, P. and Morgaś, H. (2013). Response of ‘Burlat’ sweet cherry trees to postharvest sprays of nitrogen, boron and zinc. Journal of Plant Nutrition 36(3):503–514. Source for the finding that only boron paid off where the other elements were adequate.
- [6] Wójcik, P. and Morgaś, H. (2015). Impact of postharvest sprays of nitrogen, boron and zinc on nutrition, reproductive response and fruit quality of ‘Schattenmorelle’ tart cherries. Journal of Plant Nutrition 38(9):1456–1468.
- [7] Wójcik, P. and Wójcik, M. (2006). Effect of boron fertilization on sweet cherry tree yield and fruit quality. Journal of Plant Nutrition 29:1755–1766.
- [8] Cirillo, C. and co-workers (2021). Different summer and autumn water deficit affect the floral differentiation and flower bud growth in apricot (Prunus armeniaca L.). Agronomy 11(6):1226. Source for the halt in differentiation caused by water stress and for the severity of July stress.
- [9] Cirillo, C. and co-workers. The effect of summer shading on flower bud morphogenesis in apricot (Prunus armeniaca L.). Central European Journal of Biology. Shading in July and August with histological monitoring of differentiation.
- [10] Flower bud differentiation and development characteristics of Prunus sibirica L. and Prunus armeniaca L. Acta Horticulturae 1450. Source for the start of differentiation in apricot in mid to late July.
- [11] Neilsen, D., Millard, P., Herbert, L.C., Neilsen, G.H. and co-workers (2010). Isotopically-labelled nitrogen uptake and partitioning in sweet cherry as influenced by timing of fertilizer application. Scientia Horticulturae. Source for the uptake efficiency of 65.7% against 37.4%.
- [12] Distribution and recycling of canopy nitrogen storage reserves in sweet cherry (Prunus avium L.) fruiting branches following 15N-urea foliar applications after harvest. Acta Horticulturae 1020; also published in Ciencia e Investigación Agraria 41(1):71–80 (2014). Source for the superiority of the earlier postharvest application.
- [13] Neilsen, G.H. and Neilsen, D. (2003). Nutritional requirements of apple. In: Ferree, D.C. and Warrington, I.J. (eds), Apples: Botany, Production and Uses, CABI Publishing, pp. 267–302. Source for the 50%, 90% and 60% figures.
- [14] Guak, S., Neilsen, D., Millard, P. and Looney, N.E. (2004). Leaf absorption, withdrawal and remobilization of autumn-applied urea-N in apple. Canadian Journal of Plant Science 84:259–264. Source for the 48% absorption with 2% urea.
- [15] Brown, P.H. and Hu, H. (1996). Phloem mobility of boron is species dependent: evidence for phloem mobility in sorbitol-rich species. Annals of Botany 77:497–505. Source for the phloem mobility of boron in Prunus.
- [16] Beppu, K., Ikeda, T. and Kataoka, I. (2001). Effect of high temperature exposure time during flower bud formation on the occurrence of double pistils in ‘Satohnishiki’ sweet cherry. Scientia Horticulturae 87:77–84.
- [17] Beppu, K. and Kataoka, I. (1999). High temperature rather than drought stress is responsible for the occurrence of double pistils in ‘Satohnishiki’ sweet cherry. Scientia Horticulturae 81:125–134.
- [18] Beppu, K. and Kataoka, I. (2000). Artificial shading reduces the occurrence of double pistils in ‘Satohnishiki’ sweet cherry. Scientia Horticulturae 83:241–247.
- [19] Fernández, V., Sotiropoulos, T. and Brown, P. (2013). Foliar Fertilization: Scientific Principles and Field Practices. 1st edition, International Fertilizer Industry Association, Paris.
- [20] Sánchez, E.E. and Righetti, T.L. (2005). Effect of postharvest soil and foliar application of boron fertilizer on the partitioning of boron in apple trees. HortScience 40(7):2115–2117.
- [21] Sánchez, E.E., Righetti, T.L., Sugar, D. and Lombard, P.B. (1990). Responses of ‘Comice’ pear trees to a postharvest urea spray. Journal of Horticultural Science 65:541–546.
- [22] Sallato, B. and Whiting, M.D. (2021). Early defoliation reduced yield and bud nutrient concentration in ‘Selah’ sweet cherry. Acta Horticulturae, IX International Symposium on Mineral Nutrition of Fruit Crops, Tel Aviv.
- [23] Weinbaum, S.A., Klein, I., Broadbent, F.E., Micke, W.C. and Muraoka, T.T. (1984). Effects of time of nitrogen application and soil texture on the availability of isotopically labeled fertilizer nitrogen to reproductive and vegetative growth of mature almond trees. Journal of the American Society for Horticultural Science 109:339–343.
- [24] Faust, M. (1989). Physiology of Temperate Zone Fruit Trees. John Wiley & Sons, New York. Source for the superiority of autumn boron application and for the one spray a year.
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