WA 38 Fruiting Habit, Pruning, Training Systems, Rootstocks, and Replanting (WA 38: Best Management Practices)

Description

Intended for Washington WA 38 growers, orchard managers, and researchers, this publication covers pruning, training systems, rootstocks, and replanting practices to improve orchard performance and fruit quality.
SKU:
EM137E
Published:
August 2026

Table of Contents

WA 38 apples in orchard
Photo: S. Musacchi.

Abbreviations

ARD = apple replant disease
B = brindilla
DAFB = days after full bloom
DM = dry matter
GS = Granny Smith
ha = hectare
HDP = high-density planting
IAD = index of absorbance difference
M = month
RM = ramo misto
S = spur
SSC = soluble solid content
SNK = Student–Newman–Keuls test
SRO = Sunrise Research Orchard
TA = titratable acidity
VHDP = very high-density planting

Introduction

New orchards in Washington State are characterized by high-density plantings (HDP) and dwarfing or semi-dwarfing rootstocks. The concept of HDP in apple orchards originated with the introduction of the M.9 rootstock by Hatton (1917) at the East Malling Research Station in the UK, marking a significant shift in modern orchard management.

One of the most significant effects of dwarfing rootstocks is the reduction in tree height and overall size (Wertheim 1998), which enabled the adoption of diverse training systems and facilitated early bearing, typically by the second or third growing season. A significant advantage of HDP using dwarfing rootstocks is the early return on initial investment, which significantly improves orchard profitability (Musacchi and Greene 2017). These systems often reach full production by year five, achieving maximum yield potential much earlier than traditional lower density orchard systems.

High-density orchards enable production to occur alongside canopy development, thanks to more efficient light interception and distribution within the canopy (Jackson 1980; Jackson and Palmer 1980; Robinson et al. 1991; Robinson and Lakso, 1991; Tustin et al. 2001a, 2001b; Hampson et al. 2002). Dwarfing rootstocks have also transformed key orchard management practices, including establishment, pruning, irrigation, and nutrition.

This publication outlines standard production practices for the WA 38 apple cultivar, focusing on planting distances, rootstocks, and training systems tailored to the cultivar’s growth and productivity characteristics, and provides guidance based on firsthand cultivar management. A reliable production protocol for new cultivars, such as WA 38, has been developed over time. Understanding how the cultivar performs during the initial training phase (one- to three-year-old trees) and after reaching the adult stage (four years and beyond) is crucial for optimizing orchard performance.

WA 38 Habit and Blind Wood

Apple Growth Habit

Defining appropriate pruning techniques and orchard planting systems is impossible without reference to the four cropping models originally proposed by Lespinasse (1977, 1980). Each apple cultivar requires a specific pruning strategy (Lespinasse 1977; Sansavini and Corelli-Grappadelli 1990; Lauri et al. 1995; Lauri and Laurens 2005). A clear understanding of where mixed buds develop on different types of bearing wood is critical, as this determines the approach to adopt in pruning and training the trees. This section describes the growth habit of common cultivars in comparison to the growth habit of WA 38.

Lespinasse (1977, 1980) identified four main tree habits based on branching behavior, bud positioning, and fruiting patterns.

Type 1: Spur-Type Red Delicious

These cultivars exhibit basitonic growth, with branches forming primarily in the lower part of the trunk. Leader dominance is weak and varies among cultivars. Most fruiting spurs (S) are found on branches that are at least two years old. Effective pruning requires careful thinning and the removal of small or poorly positioned mixed buds, particularly those located at the bottom of the branches (Lespinasse 1977, 1980; Sansavini and Corelli-Grappadelli 1990).

Type 2: Red Delicious, Reine des Reinettes, Stayman, and Gloster

These cultivars are well-suited for a free-growing form, with major branches inserted at wide angles into the trunk. The central leader is more dominant than in spur types, although basitonic tendencies persist, mainly when grown on vigorous rootstocks. Fruiting spurs are commonly found on two- to four-year-old wood, and brindilla (B) (short shoots, flowering at the tip) are more frequent. Branch bending is required to promote flowering and fruit set (Lespinasse 1977, 1980; Sansavini and Corelli-Grappadelli 1990).

Type 3: Golden Delicious, Elstar, Jonagold, Royal Gala, Braeburn, and Cripps Pink

These cultivars are ideal for vertical axis or spindle systems. Fruiting branches arise directly from the trunk at wide angles (60°–90°). Most fruiting spurs are borne on young wood (one-year-old). Brindilla (also known as brindles) are abundant, and the fruiting zone moves quickly away from the tree center, often resulting in branch bending. Some cultivars in this group are prone to biennial bearing when overcropped (Lespinasse 1977, 1980; Sansavini and Corelli-Grappadelli 1990).

Type 4: Rome Beauty, Granny Smith, Cortland, Fuji, and WA 38

These cultivars typically exhibit strong acrotonic growth, producing few lateral shoots on the lower trunk. On the contrary, WA 38 does not exhibit an acrotonic tendency, and branching in the nursery is relatively easy; however, it shows a strong tendency to crop centrifugally or outward to the canopy periphery. Branching is concentrated in the upper third of the tree, giving the canopy a cylindrical shape. Fruiting spurs typically develop on one- to two-year-old wood, and the fruiting zone tends to move toward the periphery of the canopy, especially in cultivars like Granny Smith and WA 38 (Lespinasse 1977, 1980; Sansavini and Corelli-Grappadelli 1990), causing the onset or formation of nonproductive blind wood. This group includes cultivars that have a genetic tendency to bear fruit at the tip of the brindilla (tip bearers).

Tree Habit of WA 38 (Cosmic Crisp®)

WA 38 is classified as a Type 4 tree, similar to Granny Smith, characterized by long branches and a tendency to develop blind wood (unproductive wood) near the trunk (Anthony et al. 2019, 2020). It is a moderately vigorous variety, with vigor that can be effectively managed through cropping. While young trees may initially exhibit high vigor, a noticeable reduction typically occurs once fruiting begins.

  • Growth Type: Type 4.
  • Branching: Tends to develop long branches with blind wood near the trunk (areas lacking fruitful buds) (Figure 1).
  • Vigor (can be manipulated by the choice of rootstock).
  • Naturally vigorous, especially in young trees.
  • Vigor reduces once cropping begins, which helps with management.
  • Management: Vigor can be effectively managed through appropriate pruning, training, and cropping practices.

Fruiting Characteristics of WA 38

WA 38 exhibits a unique fruiting pattern. Apples can develop from three distinct types of bearing wood. Specifically, fruit can originate from spurs (S) on two- to three-year-old wood (Figure 2), from ramo misto (RM) on one-year-old shoots bearing lateral buds in its second year of development (Figure 3), and from brindilla (B) at the tips of bearing shoots (Figure 4).

WA 38 Fruiting Woods

Spur (S): Short and compact fruiting formation found on branches two years old or older (Figure 2).

A WA 38 apple tree shoot exhibiting blind wood formation. Along the length of the shoot, multiple internode sections lack visible lateral buds or spur development, creating extended segments of non-fruiting wood. In contrast, areas with normal bud development are visible near the shoot base and tip. The image illustrates how blind wood interrupts regular bud distribution along the branch, reducing potential fruiting sites and affecting canopy structure and productivity in WA 38 apple trees.
Figure 1. WA 38 blind wood formation. Photo: S. Musacchi.
  • Characterized by stacked rings of wood.
  • Spur leaf growth is completed at the end of June (Flore et al. 1984).
  • Traditional fruiting structure showing a zig-zag growth pattern (Flore et al. 1984).
Figure 2 consists of two photographs comparing flower cluster origin in apple trees. The left photograph shows a flower cluster developing from a single spur (S), characterized by a compact structure with a single point of attachment to the branch. The right photograph shows a flower cluster originating from a spur complex, in which multiple closely spaced spurs contribute to the cluster, resulting in a more branched, compact floral structure. Together, the images illustrate structural differences between flower clusters arising from individual spurs versus spur complexes.
Figure 2. A flower cluster originating from a spur (S) (left) and a spur complex (right). Photos: S. Musacchi.
This photograph shows a ramo misto (RM), defined as a one-year-old shoot bearing lateral mixed buds as it enters its second year of growth (yellow circle). Flower clusters developing from lateral mixed buds are visibly at an earlier bloom stage compared with flower clusters originating from spurs (yellow rectangle). The image highlights the asynchronous flowering pattern within the ramo misto, with delayed bloom in lateral positions relative to the more advanced spurs on the axis, illustrating differences in developmental timing within the same shoot structure.
Figure 3. A Ramo misto (RM) one-year-old shoot with later, mixed buds entering its second year (yellow circle). The picture highlights the delayed bloom of flower clusters in the lateral positions of the ramo misto (yellow circle) compared to the spurs on the axis (yellow rectangle). Photo: S. Musacchi.

Ramo misto (RM): A spur-like, one-year-old shoot bearing on lateral buds and on tip bud in its second year of development (Figure 3).

  • Fruit also develops from lateral buds along the shoot.

Brindilla (B): Tip bearing one-year-old shoot with vegetative lateral buds entering its second year of development (also known as brindle).

  • Apples are produced on the terminal bud of the brindilla shoot, with a variable set of one to three apples (more frequently a single one).

Key Points on Fruiting Characteristics

  • WA 38 is a Type 4 variety similar in its habit to Granny Smith.
  • Depending on the rootstock, the variety can modulate its natural vigor.
  • This variety sets fruit mainly on spurs, ramo misto, and brindilla.
  • Bloom sequence from first to last is S (spur), then B (brindilla), then RM (ramo misto).
This photograph shows a brindilla (B), defined as a one-year-old shoot bearing a terminal mixed bud that has developed into a flower cluster. The image represents the developmental stage approximately two weeks after full bloom, before the onset of natural fruitlet abscission. At this stage, the flower cluster is fully formed and attached at the terminal position of the shoot, illustrating the reproductive role of brindilla shoots and their contribution to early fruit set before thinning processes begin.
Figure 4. Example of a brindilla (B) one-year-old shoot with a terminal mixed bud generating a flower cluster. The pictured stage corresponds to two weeks after full bloom, before the beginning of the natural abscission. Photo: S. Musacchi.

Investigation of WA 38 Fruiting Habit, Cluster Occupancy, and Quality in the Different Types of Wood

WA 38 is a self-thinning cultivar that exhibits a bloom gradient within each cluster, with king flower opening first and lateral blooms following 48–72 hours later. Under favorable conditions, the king flower is most likely to set fruit, while laterals act as a backup if the king fails. Under typical Washington State spring conditions, bloom within a cluster spans about five to eight days, with petal fall beginning as early as two days after king bloom and lasting eight to ten days (Serra et al. 2025). For this reason, chemical thinning is not necessary and could pose a problem due to the high risk of overthinning the fruit. Manual thinning can be adopted only in specific years with high fruit set.

To provide an analytical determination of the fruiting habit of WA 38 for two consecutive years, 2021 and 2022, samples from different sites were collected at harvest, keeping crop separated by the different bearing woods (S = spur [fruiting two- to three-year-old wood], RM = ramo misto [one-year-old shoot bearing on lateral buds], B = brindilla [tip bearing shoot]) and fruit type based on total occupancy within a cluster (S = single, D = double, T = triple, Q = quadruple, similarly to what reported in Serra et al. 2024).

Results of 2021 Studies and Observations

In 2021, we conducted a study on flower bud formation and potential differences in fruit set across five distinct apple cultivation scenarios in the Wenatchee and Columbia Basin regions of Washington State. These scenarios will be referred to as “combinations” (Table 1). At harvest, apples were collected from three trees per scenario and location, for a total of 15 trees. Each harvested apple was labeled based on its bearing wood type—spur (S), ramo misto (RM), or Brindilla (B)—and its fruit type, classified by the number of fruits per cluster—single (S), double (D), triple (T), or quadruple (Q). This resulted in up to 12 potential bearing wood–fruit combinations per tree (Musacchi et al. 2022).

Table 1. WA 38 combinations investigated in the 2021 survey on fruiting wood. All locations are commercial or research orchards in Washington State. GS = Granny Smith as interstem in the top graft scenario.
CombinationLocationYear of PlantingDensity (trees/acre)Training SystemRootstocks
WA 38/M.9-NIC29_SpindleQuincy20181,584SpindleM.9-NIC29
WA 38/G.935_V_systemRoyal City20181,980V systemG.935
WA 38/M.9-T337 -GS_SpindleRock Island (SRO)2009 (top-worked 2016)1,499SpindleGS/M.9-T337
WA 38/M.9-T337 -GS_2-axisRock Island (SRO)2009 (top-worked 2016)1,4992-axisGS/M.9-T337
WA 38/M.9-T337 -GS_3-axisRock Island (SRO)2009 (top-worked 2016)1,4993-axisGS/M.9-T337

For each tree, total yield (both number of fruits and weight in kg) was recorded. The harvested apples were then boxed and stored at 33°F in regular air. Seven weeks postharvest, apples were sorted and graded using an Aweta Cupsizer TV-HS 2–4 (2019) line, which grouped fruit by color and size. A customized program categorized fruit into four size classes (Serra et al. 2024):

  • Small (≤ 215 g)—equivalent to ≥ 88 apples per box.
  • Medium (216–263 g)—approximately 80 apples per box.
  • Large (264–339 g)—approximately 72 to 64 apples per box.
  • Extra-Large (≥ 340 g)—≤ 56 apples per box.

Table 2 presents the yield parameters from the 2021 harvest for each WA 38 training system and rootstock combination. On average (N = three trees per combination), the number of apples per tree ranged from 57 in the WA 38/M.9-T337 -GS_3-axis_SRO system to 159 in the WA 38/M.9-NIC29_Spindle_Quincy system. Corresponding fruit production ranged between 15.1 kg and 29.3 kg per tree (Table 3). As expected, the combination with the highest crop load (WA 38/M.9-NIC29_Spindle_Quincy) produced the lowest average fruit weight, at 184 g per apple (equivalent to approximately 110–113 apples per 40 lb box). In contrast, the WA 38/M.9-T337 -GS_3-axis_SRO combination yielded the highest average fruit weight, at 271 g per apple (large size, approximately 72 apples per box), as shown in Table 2.

Table 2. Productivity data for the WA 38 combinations evaluated at harvest 2021 are presented as the number of apples per tree, net yield (kg per tree; 1 kg = 2,205 lb), and average fruit weight (g). Values represent the average of three trees per combination. Statistical significance is indicated in the table as ** = p < 0.01 and *** = p < 0.001, and letters separating means were assigned using the SNK test.
Combination (2021)No. Apples/Tree (***)Yield (kg/tree) (**)Yield (Mtons/acre) (**)Avg. Apple Weight (g) (**)
WA 38/M.9-NIC29_Spindle_Quincy159 a29 a46 a184 b
WA 38/G.935_V_system_Royal_City71 b16 b31 b226 ab
WA 38/M.9-T337 -GS_Spindle_SRO64 b17 b25 b254 a
WA 38/M.9-T337 -GS_2-axis_SRO71 b19 b29 b267 a
WA 38/M.9-T337 -GS_3-axis_SRO57 b15 b23 b271 a

Working on orchards of different ages provided a broad range of information on the bearing wood characteristics of WA 38. We analyzed the types of apple set, determined by occupancy patterns within a cluster at harvest (S, D, T, Q/cluster), and the proportion of apples harvested from each bearing wood combination in the trial as a function of the aforementioned descriptors for each WA 38 cultivation scenario. This survey may have wide practical value, including generating knowledge to support targeted pruning that encourages fruiting on specific wood types or to adjust the training system (e.g., number of axes per tree) to achieve more uniform apple size. Overall, across the five combinations, the proportion of culled apples in 2021 ranged from 1% in WA 38/G.935_V system_Royal City to 16% in WA 38/M.9-T337 -GS_3-axis_SRO (Figure 5). In Figure 6, we present the yield distribution at harvest for each of the five combinations, based on fruit set occupancy within a cluster. Most WA 38 fruit was harvested as one fruit per cluster (single), accounting for 57% to 80% of the total fruit per tree, followed by two fruits per cluster (double), which represented 14% to 34% of the total yield per tree. The proportion of yield from triple clusters (three apples within the same cluster) was generally very low, as observed for WA 38/G.935_V_system_Royal_City and WA 38/M.9-T337 -GS_3-axis_SRO (Figure 6). The peculiar tendency of WA 38 to set a single fruit per cluster was already reported by Serra et al. (2024) and is further confirmed by these datasets.

Figure 7 illustrates the proportion of apples harvested from each bearing wood type within each combination. In most cases (four out of five), 72% to 80% of the apples were produced on spurs (S), followed by 10% to 15% on brindilla (B), and 8% to 13% on ramo misto (RM). However, one combination—WA 38/M.9-NIC29_Spindle_Quincy—showed a different pattern, with 81% of the apples harvested from ramo misto (lateral buds on one-year-old shoots). In comparison, only 11% and 8% of the harvested fruit came from spurs and brindilla, respectively (Figure 7). The peculiar distribution of bearing wood in that block can be explained by the targeted pruning carried out in the orchard the year before the survey (2020). The specific pruning consisted of a moderate click-pruning approach (Anthony et al. 2019; Serra et al. 2025), with the preservation of young fruiting structures, such as brindilla and ramo misto.

Merging data from all five combinations to evaluate overall variability in apple size, we found that apples produced on brindilla were distributed across small, medium, and large categories, with no clear tendency toward a specific size class. In contrast, apples borne on lateral buds of one-year-old shoots (RM) tended to be predominantly small (Figure 8). The tendency for fruit on ramo misto to produce smaller apples may be attributed to several factors. Lateral buds on one-year-old shoots are generally smaller, which implies a lower initial cell number. Additionally, these flowers typically bloom later than those on spurs or terminal buds (Figure 3); in some years, we have observed a five-to-seven-day delay, depending on the season. Spurs produced most of the WA 38 apples, with fruit sizes ranging from small to extra-large, and with a greater proportion in the medium and large size classes, corresponding to 80 and 72–64 apples per box, respectively (Figure 8). The fruit size distribution by wood type shown in Figure 8 reflects cumulative data across all five orchards.

For this reason, the graphs shown in Figure 9 (A–E) provide a more realistic representation of each combination evaluated in this trial. The combination WA 38/M.9-NIC29_Spindle_Quincy, illustrated in Figure 9A as the proportion of apples produced per tree by bearing wood type and fruit size, demonstrates the predominance of fruit harvested from RM (lateral buds on one-year-old shoots) compared with the other two wood types and its tendency to set smaller WA 38 apples rather than medium or large ones. In contrast, all four size classes were represented among apples harvested from spur structures (S), with most fruit falling into the medium and large categories, accounting for 55% to 65% of production in fully cropping mature trees, such as those in the Sunrise block top-grafted in 2016 (Figure 9C, 9D, 9E), with the exception of the two younger orchards (Figure 9A and 9B). At the SRO site, we compared three training systems (Figure 9C, 9D, 9E)—a one-axis (spindle), a two-axis (bi-axis), and a three-axis (multi-leader) system—highlighting how the number of leaders per tree and overall architecture influence the distribution of apples by wood type and size. WA 38/M.9-T337 -GS_2-axis_SRO showed a tendency to produce up to 72% of its fruit on spurs and primarily in the medium to extra-large size classes (Figure 9D), with a lower proportion of small fruit compared to WA 38/M.9-T337 -GS_1-axis_SRO (Figure 9C). This observation supports previous studies in the literature, which have shown that spurs are the primary bearing wood in bi-axis (Musacchi et al. 2014) and exhibit greater uniformity of production in 2D canopies (Musacchi 2008; Sazo 2018).

Results of 2022 Studies and Observations

The 2022 survey focused on three WA 38 orchard sites, each varying in rootstock, planting density, planting year, and location (Table 3), to further explore the role of different bearing wood types in WA 38 production under diverse conditions. Unlike in 2021, the 2022 analysis excluded the two-axis and three-axis systems. Two sites, WA 38/M.9-NIC29_Spindle_Quincy and WA 38/G.935_V system_Royal City (both planted in 2018) demonstrated consistent productivity across both years (Tables 2 and 3). Among the sites, WA 38/M.9-NIC29_Spindle_Quincy recorded the highest apple count per tree (161), while WA 38/G.935_V system_Royal City had the lowest (66). This difference in crop load significantly influenced average fruit weight, which was 179 g (equivalent to approximately 113–100 apples per box) and 242 g (equivalent to approximately 80 apples per box), respectively (Table 3). A notable change occurred at the WA 38/M.9-NIC29_Spindle_Quincy site: in 2021, 81% of apples were borne on ramo misto shoots, but by 2022 this proportion dropped to 22% (Figure 10). This shift reflects the natural aging of fruiting structures, as many ramo misto from 2021 had transitioned into spur-bearing wood by 2022.

Figure 5 presents a graphical representation of WA 38 apple packout across five management or treatment combinations evaluated in 2021 at three sites. For each combination, the chart shows the proportions of apples classified as culls and as marketable fruit. Cull apples are indicated in black and range from 1 to 16 %, while marketable apples are shown in red and range from 84% to 98%. The proportions were determined by visual assessment before grading on a commercial sorting line. Across combinations, the relative balance between cull and marketable fruit varies, illustrating differences in fruit quality outcomes among the surveyed treatments and sites.
Figure 5. WA 38 packout across the five combinations surveyed in 2021 (three sites). The proportion of cull apples (in black) versus marketable apples (in red) was determined by visual rating before grading on a sorting line. The number within the bars indicates the percentage of marketable fruit.
Figure 6 displays a graphic summarizing WA 38 apple yield classified by cluster occupancy at harvest across five combinations evaluated in the 2021 survey at three sites. Yield is categorized by the number of fruit per cluster: single, double, triple, or quadruple. Single-cluster fruits are represented in green, double in pink, triple in pale yellow, and quadruple in black. The chart compares how different cluster-occupancy types contribute to total yield across each combination, highlighting variability in fruit distribution and crop structure among the surveyed treatments. Single fruit percentage ranges from 57 to 85, double percentage ranges from 14 to 34. Triple and quadruple are minimal amounts.
Figure 6. WA 38 yield classified by type of cluster occupancy at harvest as single (green), double (pink), triple (pale yellow), quadruple (black) per cluster for each of the five combinations in the 2021 survey (three sites). The numbers within the bars indicate the percentage of single-cluster fruit.
Figure 7 presents a graphic showing the proportion of WA 38 apples harvested from different bearing wood types across combinations surveyed in 2021. Data are based on three trees per scenario across three sites. Bearing wood is categorized as spur, ramo misto, and brindilla. Spurs are represented in green, ramo misto in yellow, and brindilla in fuchsia. The chart compares how each bearing wood type contributes to total harvested fruit within each combination, illustrating differences in crop distribution and bearing habit among the evaluated scenarios. Fruit on spur ranges from 11 to 80. Fruit on ramo misto from 8% to 81%. Fruit on brindilla ranged from 8% to 15%.
Figure 7. WA 38 proportion (%) of apples harvested by bearing woods for each combination surveyed in 2021 (N = three trees/scenario and three sites). Bearing wood is presented as spur (in green), ramo misto (in yellow), and brindilla (in fuchsia). The numbers within each colored bar indicate the percentage of the fruit crop on each fruiting structure.
Figure 8 presents a graphic illustrating the distribution of WA 38 apple yield by bearing wood type and fruit size class, based on grading conducted with an Aweta sorting line. The proportions shown represent the total number of apples produced per tree in 2021 when combined. Data are averaged across 15 trees, and individual treatment combinations are not shown in order to emphasize differences among bearing wood types. A total of 1,239 apples were graded across three sites. Fruit size classes are categorized as small (blue), medium (white), large (red), and extra-large (black). The figure highlights how fruit size distribution varies among bearing wood types. Spur produces larger fruit, followed by ramo misto. Brindilla, in general, produces small fruit.
Figure 8. WA 38 apple yield distribution by bearing wood type and size class, sorted using the Aweta sorting line. When combined, these proportions represent the total number of apples produced per tree in 2021. An average of 15 trees were evaluated, and individual combinations were not included in order to emphasize differences among bearing wood types. A total of 1,239 apples were graded across three sites. Size classes are reported as small (blue), medium (white), large (red), and extra-large (black). The numbers within the bars indicate the percentage of fruit of each size category for each fruiting structure.
Figure 9 presents a multi-panel graphic (panels A through E) showing the distribution of WA 38 apple yield by bearing wood type and fruit size class for five individual combinations evaluated in 2021. The combinations include: (A) WA 38/M.9-NIC29, one-axis system, Quincy; (B) WA 38/G.935, V-system, Royal City; (C) WA 38/M.9-T337 -GS, one-axis system, SRO; (D) WA 38/M.9-T337 -GS, two-axis system, SRO; and (E) WA 38/M.9-T337 -GS, three-axis system, SRO. For each panel, the proportions shown represent the total number of apples produced per tree in 2021. An average of three trees was evaluated per combination. The total number of apples graded per combination was 477 for A, 213 for B, 184 for C, 209 for D, and 156 for E. Fruit size classes are categorized as small (blue), medium (white), large (red), and extra-large (black). The figure allows comparison of fruit-size distributions among bearing wood types within each management combination.
Figure 9. WA 38 apple yield distribution by bearing wood type and size class is shown for each combination: (A) WA 38/M.9-NIC29_1-axis_Quincy, (B) WA 38/G.935_V_system_Royal_City, (C) WA 38/M.9-T337 -GS_1-axis_SRO, (D) WA 38/M.9-T337 -GS_2-axis_SRO, and (E) WA 38/M.9-T337 -GS_3-axis_SRO. When combined, these proportions represent the total number of apples produced per tree in 2021. The average number of trees evaluated per combination was three. The total number of apples graded per combination was: (A) 477, (B) 213, (C) 184, (D) 209, and (E) 156. Size classes are reported as small (blue), medium (white), large (red), and extra-large (black). The numbers within the bars indicate the percentage of fruit of each size category for each fruiting structure.
Table 3. Productivity data for the WA 38 combinations evaluated at harvest 2022 are presented as the number of apples per tree, net yield (kg per tree and Mton/acre), and average fruit weight (g) (N = 3). Statistical significance is indicated in the table as * = p < 0.05 and NS = not significant, and letters separating means were assigned using the SNK test.
Combination (2022)No. Apples per TreeYield (kg/tree)Yield (Mtons/acre)Apple Weight (g)
WA 38/M.9M.9-NIC29_Spindle_Quincy161 a2845179 b
WA 38/G.935_V_system_Royal_City66 b1631242 a
WA 38/M.9-T337 -GS_Spindle_SRO109 ab2233202 ab
Significance*NSNS*

To picture the overall variability in apple size based on bearing wood, we averaged the three combinations and observed that apples from brindilla and ramo misto were mainly small (≥ 88 apples per box) in 2022; while spur-borne apples showed higher proportions in medium (80 apples per box) and large size (72–64 apples per box), despite 34% of the apples belonging to the small size category (Figure 11).

Due to WA 38’s natural self-thinning trait, the majority of clusters self-singularize (57% to 73% of apples harvested as single in a cluster), followed by doubles (Figure 12). This two-year survey confirmed previously published data (Serra et al. 2022; Serra et al. 2025).

Fruit Quality Analysis by Bearing Wood (2021–2022)

This study examined the impact of bearing wood on WA 38 fruit quality. Apples (crop 2021) from two combinations in two locations (WA 38/M.9-NIC29_Spindle_Quincy and WA 38/M.9-T337 -GS_Spindle_SRO, where the trees were trained as a spindle) were compared among the three bearing woods. The quality analysis was performed after six months of storage (1°C ± 1°C) on single (S) apples in the cluster, with the best overcolor, no defects, and a size of 65–90 mm (Table 4). Apples harvested in SRO—regardless of the bearing wood—were larger, heavier, and riper (lower IAD) (Ziosi et al. 2008), with higher firmness, soluble solid content (SSC), and dry matter (DM) than apples from Quincy (Table 4). This can likely be attributed to differences in crop load recorded in 2021, with the Quincy combination yielding 29 kg per tree and the SRO combination yielding just 17 kg per tree (Table 2). However, in 2022, the yield per tree was not different (Table 3). There were no significant differences among sites in the number of mature, healthy seeds per apple or in titratable acidity (TA). However, when comparing the three bearing wood types—a primary focus of this analysis—some differences were observed. Apples produced on ramo misto (RM) had a larger diameter and higher SSC and DM than those produced on brindilla (Table 4). No significant difference in maturity (IAD) emerged between apples of different woods after six months of storage, but differences can be expected at earlier postharvest durations. Parameters such as apple maximum diameter, apple mass, and SSC showed a significant location-by-wood interaction (Table 4), suggesting that differences in fruit quality may also reflect the influence of crop load.

In 2022, only IAD, firmness, and TA differed between the two locations (Table 5). Significant differences have been observed among the bearing types, with fruit from brindilla appearing smaller and less ripe than those from ramo misto and spur. Notably, WA 38 apples from spurs were larger and heavier and had a higher number of healthy, viable seeds, compared to apples from lateral shoots of ramo misto (Table 5). Some of the flower clusters in the lateral positions of ramo misto often bloom several days later than the majority of clusters on spurs; therefore, it is too late to have synchrony with ideal pollen donor trees (most likely at petal fall). In 2022, the TA of WA 38 apples from spurs was higher than that of apples from the other two bearing types, suggesting better postharvest storage potential. The recommended click-pruning practice to manage the blind wood in this variety can also help reduce variability in quality by limiting the proportion of one-year-old wood used for branch renewal, thereby increasing the proportion of high-quality fruit.

Figure 10 presents a graphic illustrating the proportion of WA 38 apples harvested from three bearing wood types—spur, ramo misto, and brindilla—across combinations evaluated in 2022. Data are based on three trees per combination across three sites. Spurs are represented in green, ramo misto in yellow, and brindilla in fuchsia. When comparisons are made horizontally among combinations within the same bearing wood type, no statistically significant differences are observed, as indicated by “NS.” However, when comparisons are made vertically within individual sites, significant differences among bearing wood types are observed for two of the three combinations. Fruit on spur ranges from 51% to 71%. Fruit on ramo misto ranges from 5% to 22%. Fruit on Brindilla from 19% to 36%. Lowercase letters indicate statistically significant differences among bearing wood types at the Royal City site, while uppercase letters indicate significant differences at the SRO site, based on the Student–Newman–Keuls (SNK) test at p = 0.05.
Figure 10. Proportion of WA 38 apples harvested from each bearing wood type—spur (green), ramo misto (yellow), and brindilla (fuchsia)—is shown for each combination evaluated in 2022 (N = three trees across three sites). There were no significant differences (NS) among the three combinations within each bearing wood type when comparisons were made horizontally. However, within each site, significant differences between bearing wood types were observed for two of the three combinations. When reading vertically, lowercase letters indicate statistically different proportions in Royal City, and uppercase letters indicate differences in SRO, based on the SNK test at p = 0.05. The numbers within the colored bars indicate the percentage of fruit borne on the different fruiting structures.
Figure 11 presents a graphic illustrating the distribution of WA 38 apples by bearing wood type and fruit size class following the 2022 harvest. The proportions shown represent the total number of apples produced and graded per tree in 2022, averaged across nine trees evaluated at three sites. A total of 1,007 apples were graded. Fruit size classes are categorized as small (blue), medium (white), large (red), and extra-large (black). The figure highlights differences in fruit size distribution among bearing wood types during the 2022 season, mirroring the 2021 trend.
Figure 11. WA 38 apple distribution by bearing wood type and size class after the 2022 harvest is shown in this figure. These proportions represent the total number of apples produced and graded per tree in 2022 (N = 9 trees across three sites). The proportions of apples by size and wood type presented here are averages across the nine trees evaluated. A total of 1,007 apples were graded. Size classes are reported as small (blue), medium (white), large (red), and extra-large (black). The numbers within the bars indicate the percentage of fruit of each size category for each fruiting structure.
Figure 12 presents a graphic illustrating WA 38 apple yield classified by cluster occupancy type at harvest across three combinations trained to a single leader and evaluated in the 2022 survey at three sites. Yield is categorized by the number of fruit per cluster: single, double, triple, or quadruple. Single clusters are represented in green, double clusters in pink, triple clusters in pale yellow, and quadruple clusters in black. Comparisons among combinations within each cluster occupancy category show no statistically significant differences, indicating similar yield distribution patterns across the evaluated single-leader systems.
Figure 12. WA 38 yield was classified by cluster occupancy type at harvest as single (green), double (pink), triple (pale yellow), or quadruple (black) per cluster for each of the three combinations trained as a single leader in the 2022 survey across three sites. Not significant across combinations within each cluster occupancy scenario. The numbers within the bars indicate the percentage of fruit that, at harvest, resulted in single, double, triple, or quadruple in a cluster.

Table 4. WA 38 quality was evaluated after six months (6M) of regular air storage following harvest 2021 for the locations WA 38/M.9-NIC29_Spindle_Quincy and WA 38/M.9-T337 -GS_Spindle_SRO included in the 2021 survey. Statistical significance is reported as follows: * = p ≤ 0.05, ** = p ≤ 0.01, *** = p ≤ 0.001, and NS = not significant; letters separating means within each treatment were assigned using the SNK test. The index of absorbance difference (IAD) is a nondestructive measure of chlorophyll degreening beneath the skin and is used as a proxy for fruit maturity, with values ranging from zero (fully ripe) to 2.25 (fully unripe). DM percentage and TA were assessed with a different number of replications, which did not correspond to the N apples reported here.
WA 38Diameter (mm)Weight (g)IAD at 6MFirmness (lb)SSC (%)DM (%)TA (% malic acid)
Quincy75.1b198b0.92a14.0b13.5b13.9b0.38
SRO79.8a243a0.13b14.8a14.2a14.6a0.38
Significance******************NS
Brindilla76.0b2120.5714.3ab13.6b14.0b0.38
Ramo misto78.2a2240.6713.9b14.0a14.4a0.37
Spur77.1ab2160.5414.7a13.8b14.4a0.39
Wood Significance*NSNS****NS
Significance Location × Wood**NSNSNSNSNSNS

Table 5. WA 38 quality was evaluated after 3.5 months (3.5M) of regular air storage following harvest in 2022 for the locations WA 38/M.9-NIC29_Spindle_Quincy and WA 38/M.9-T337 -GS_Spindle_SRO, which were included in the 2021–2022 survey. Apples were selected using the following sorting criteria: only single (S) fruit per cluster, all with the best color, free of defects, and within a size range of 216–339 g (80–64 apples per box). Statistical significance is indicated as follows: * = p ≤ 0.05, ** = p ≤ 0.01, *** = p ≤ 0.001, and NS = not significant; letters separating means within each treatment were assigned using the SNK test. DM percentage and TA were evaluated with a different number of replications, which did not correspond to the N apples reported here.
WA 38Diameter (mm)Weight (g)IAD at 3.5MFirmness (lb)SSC (%)DM (%)TA (% malic acid)
Quincy75.95090.75a15.5a12.913.50.41a
SRO76.32180.36b14.6b12.913.40.35b
SignificanceNSNS******NSNS***
Brindilla73.8c194c0.67a15.112.813.20.36b
Ramo misto75.9b212b0.54b15.013.113.40.36b
Spur78.4a233a0.50b15.012.813.60.40a
Wood Significance*********NSNSNS**
Significance Location × WoodNSNSNSNSNSNS***

Key Points on Fruit Quality Analysis

  • The majority of WA 38 production occurs with one apple per cluster (65%–75%), followed by two apples per cluster, and a minimal number of clusters have three or more apples per cluster.
  • If the blocks are managed with click-pruning from the beginning, 60%–77% of the apples are produced on spurs, followed by brindilla and by one-year-old shoot lateral buds (ramo misto).
  • Apples from one-year-old shoots (ramo misto) were smaller, while spurs produced apples with more variable sizes, ranging from small to extra-large.
  • Apples borne on brindilla and ramo misto are smaller in size than apples cropped on spurs.

“Spur Extinction” and Blind Wood Development in WA 38

WA 38 commonly develops blind wood because of natural spur extinction. Lateral flower clusters on the ramo misto often exhibit weak floral development, particularly at the base of the shoot (proximal portion of the ramo misto, near the main leader). In many instances, the flower cluster is incomplete, consisting of fewer flowers lacking a vegetative meristem, leading to the extinction of the bearing spur. Additionally, young spurs (those in the second year of shoot development in a lateral direction) located in the basal to mid-section of the ramo misto often fail to set fruit or experience early fruit drop, leaving behind blind buds (Figures 13 and 14).

Figure 13 consists of five photographs (panels A–E) illustrating spur extinction and blind wood formation on a WA 38 ramo misto at the end of the June drop period in Washington State. Panel A shows a dormant bud that did not initiate visible growth. Panel B shows a bud that developed a fruit, but did not produce a lateral shoot. Panel C shows a spur that is already extinct, indicating loss of future bearing potential. Panel D shows a bud that developed only a vegetative shoot; visible bourse fruitlet scars indicate where fruitlets were lost through natural abscission. Panel E shows a bud that developed both a fruit and a shoot, which will form a two-year-old spur in the following season. The figure also highlights differences in fruit size between positions B and E. Fruitlets originating from position B are smaller, primarily due to the initially smaller bud size, and are more likely to drop or remain undersized compared with fruit developed from well-formed buds such as those in position E. Together, the panels illustrate how early bud development influences fruit retention, spur survival, and future bearing structure.
Figure 13. Spur extinction and blind wood formation in a WA 38 ramo misto at the end of June drop in Washington. Dormant bud (A); bud developing only fruit, with no lateral shoot (B); spur already extinct (C); bud that developed only a shoot (note the visible bourse fruitlet scars from natural abscission) (D); bud developing both a fruit and shoot (next year, a two-year-old spur) (E). Note the difference in fruit size between positions B and E, primarily due to the initial difference in bud size. The fruitlets in position B are more likely to drop or remain smaller than those developed from better-formed buds (E). Photo: S. Musacchi.
Figure 14 consists of multiple photographs (panels A, B, C, and Et) illustrating spur extinction and the progression of blind wood formation in a WA 38 ramo misto at harvest in Washington State. Panel A shows a dormant bud that did not develop during the growing season. Panel B shows a bud that developed only a fruit, with no accompanying lateral shoot. Panel C shows a spur that is already extinct, indicating permanent loss of bearing capacity. Panel Et shows an apical, or tip-bearing (“t”), bud that developed both a fruit in the current season and a spur that will bear in the following season. The figure highlights a clear difference in fruit size between positions B and Et. Fruit originating from position B is smaller, primarily due to the originally smaller bud size, whereas fruit from the apical mixed bud (Et) developed from a better-formed bud and exhibits greater size and bearing potential. White letters shown in red squares correspond to and mirror the classification used in Figure 13, allowing direct comparison of developmental outcomes between stages.
Figure 14. Spur extinction and the evolution of blind wood formation in a WA 38 ramo misto at harvest in Washington. Dormant bud (A); bud developing only fruit, with no lateral shoot (B); spur already extinct (C); bud developing both a fruit and shoot is not represented in Figure 14 (D); apical (or tip-bearing “t”) bud developing both a fruit (current season) and a spur (next season) (Et). Note the difference in fruit size between positions B and Et, primarily due to the original difference in bud size. Letters in the red squares are mirroring the classification in Figure 13. Photos: S. Musacchi.

Spur extinction presents several cultural issues:

  • Reduction in flower clusters: The annual number of flower clusters per tree is naturally diminished due to failed spur renewal and floral inhibition.
  • Overreliance on one-year-old wood: A large portion of fruiting occurs on one-year-old shoots, which typically produce smaller fruit compared to older, well-established spurs (Tables 4 and 5).
  • Shoot weeping: Fruit set predominantly at the distal end of the shoot (see the fruit indicated with Et in Figure 14), resulting in excessive bending or “weeping” of branches, negatively affecting canopy structure, blind wood, and light penetration.

The weak flower clusters often have small leaves, reduced floral numbers, and reduced flower quality, contributing to poor fruit set and increasing the likelihood of spur abortion. Over time, this leads to widespread blind wood development, characterized by short stumps and the absence of viable buds for renewal, ultimately compromising both yield potential and fruit quality (Figure 15).

A similar pattern of spur degeneration and blind wood formation was documented in Scifresh (Jazz) by Palmer et al. (2008), suggesting a potentially broader issue among certain modern cultivars with similar architectural traits.

Figure 15 consists of two images (panels A and B) illustrating the developmental progression of a shoot into a ramo misto. Panel A shows a current-season shoot during its first year of development. Panel B shows the same shoot type in its second year of development, approximately five to six weeks after bloom of the lateral flower clusters. In panel B, the basal lateral buds, indicated by red arrows, are no longer viable. These buds show evidence of flower abscission and a lack of vegetative shoot development. In contrast, the bud located in the more central portion of the shoot in panel A may still develop into a new shoot, as observed in the central region of panel B, and may occasionally set fruit. The distal bud near the shoot tip in panel A is typically the most productive, often generating a new shoot and setting at least one fruit in panel B. Together, the panels illustrate a centrifugal or outward shift in the cropping zone along the shoot, with fruiting potential progressively moving outward toward the shoot tip. This developmental pattern is consistent with the Type 4 fruiting habit described by Lespinasse in 1977 and 1980.
Figure 15. Development of (A) a current season shoot into (B) ramo misto (in its second year of development, five to six weeks after bloom of the lateral clusters). In sample B, the lateral basal buds (indicated by red arrows) are no longer viable and exhibit signs of abscised flowers and a lack of shoot development. The bud more central in sample A may still produce a new shoot (see central portion of sample B) and occasionally set fruit, while the distal bud near the shoot tip in sample A is typically more productive—often generating a new shoot and setting at least one fruit. This pattern reflects a centrifugal shift in the cropping zone, with fruiting potential gradually moving outward toward the tip, as described in the Type 4 fruiting habit by Lespinasse (1977, 1980). Photo: S. Musacchi.

Key Points on “Spur Extinction” and Blind Wood

  • Natural spur extinction and blind wood are commonly observed in the basal buds of one-year-old fruiting shoots in their second year of development.
  • The variety shows a centrifugal or outward shift in the cropping zone, with the onset of blind wood at the base of the branch near its insertion into the trunk.

General Pruning Principles

Pruning plays a critical role in modern orchard management by influencing tree architecture, canopy porosity, crop load, and fruit quality. It also affects key physiological processes, including flowering, root-to-shoot growth ratio, and nutrient uptake (Ferree and Schupp 2003). Pruning techniques must be adapted over time to align with the tree’s training system, cultivar, and orchard age. As trees mature, pruning helps guide their natural bearing habits to optimize productivity during the commercial fruiting stage. Pruning should be considered the first tool for adjusting crop load in the new season.

In high-density (HDP) and very high-density (VHDP) orchard systems, pruning regimes have evolved to include innovative practices such as green (or summer) pruning, bending, and heading back (Li and Lakso 2004; Bhusal et al. 2017; Musacchi and Greene 2017; Dominguez and Robinson 2025). These techniques, used in conjunction with traditional winter pruning, promote efficient canopy management and sustained fruit quality.

Many of the cultivars suited to HDP and VHDP systems fall into Type 3 or Type 4 architectural categories, as defined by the Lespinasse model (1977, 1980). For these cultivars, two key pruning techniques are commonly applied: bending (Dominguez and Robinson 2025) to regulate vigor and encourage lateral development, and click-pruning (Musacchi and Greene 2017; Anthony et al. 2020) to renovate fruiting wood and reduce blind wood. Research by Mohammadi et al. (2013) found that click-pruning significantly enhances flower bud formation in apple trees. Click-pruning has been shown to reduce the biennial bearing index compared to bending (Anthony et al. 2020). To maintain fruit quality, 20%–25% of the branches should be renewed annually (Anthony et al. 2020).

Bending and Long Pruning

Bending is a traditional method used by horticulturists to open the crotch angle of shoots, reducing vigor and altering the vegetative-to-reproductive balance (Grisvard 1957; Giulivo 1990). Lespinasse and Delort (1986) showed that bending increases flower bud formation and carbohydrate accumulation while reducing shoot size:

  • Bending at 30 degrees to 90 degrees (where zero degrees is the tree leader) increases flower buds by 64%.
  • Bending to 120 degrees results in 2.2 times more flower buds than at 30 degrees.
This photograph shows a WA 38 apple shoot entering its second year of development at Rock Island, Washington. The one-year-old shoot has set fruit near the terminal position, and the weight of the developing fruit causes the shoot to bend downward. At the basal portion of the shoot, extended sections lacking active buds or spur development are visible, indicating the formation of blind wood. The image illustrates the relationship between fruit load, shoot bending, and the loss of bearing potential in basal portions of the shoot during the transition from the first to the second year of development.
Figure 16. WA 38 one-year-old shoots enter their second year of development. They often set fruit at the tip and bend under the weight of the developing fruit. Note the formation of blind wood at the basal portion of the shoot (Rock Island, Washington). Photo: S. Musacchi.

Bending can occur in spring or summer to slow shoot growth and increase flower bud formation (Baldini 1990). The bending stress can stimulate ethylene production in the shoot’s internal air space (Ferree and Schupp 2003).

This principle underlies the long pruning technique, initially developed by Lespinasse and later by the Mafcot (1999, 2000) research group at the National Institute for Agricultural Research (INRA) in France (“Maitrise de la fructification, concepts et techniques”). In this method, shoots and leaders are bent horizontally without cutting or shortening the shoots. Fruiting density is adjusted through “extinction” (flower bud thinning) to enhance light penetration (Diemoz 2005). This is the basis for the Solaxe training system (Lauri and Lespinasse 1998). Bending has been widely adopted in spindles and other training systems to reduce vigor and increase flowering (Lauri et al. 2004).

The Mafcot research group developed a tool called Equilifruit, designed to determine the optimal number of fruiting units per branch by measuring branch diameter (Diemoz et al. 2002; Diemoz 2005). During the first two years, this method requires approximately 150 labor hours per hectare per year, but this decreases significantly once the tree structure is established (Diemoz et al. 2002). Our experience with bending branches in WA 38 showed more blind wood at the shoot base, which negatively impacted the trees in subsequent years.

For WA 38, specific modifications to standard apple pruning are necessary. Feathers often need trimming to prevent blind wood, a common issue in this variety. In some cases, removing the apical portion of shoots with flower buds helps prevent excessive arching under the weight of developing apples. Leaving branches too long frequently results in spur extinction and blind wood formation, as illustrated in Figure 16.

Click-Pruning

Click-pruning is ideal for Type 4 cultivars, which tend to produce terminal-bearing shoots and blind wood at the branch base (Lauri and Lespinasse 1998). Originating in northern Europe to improve light penetration (Dallabetta 2014), click-pruning involves:

  • Stubbing feathers at planting (Figure 17 [before stubbing]—Figure 18 [after stubbing]).
  • WA 38 requires a long stub under Washington climatic conditions to prevent stub dieback (Figure 19).
  • Bending new, developing feathers 40 degrees to 45 degrees.
  • Heading the tip of the one-year-old shoot growing from the previous year’s branches.
  • Removing apical dominance to encourage lateral bud breaking closer to the trunk.

This rejuvenates branches, improves structure, and enhances flower bud development (Mohammadi et al. 2013; Musacchi and Green 2017). Since 20%–25% of branches must be renewed annually, trees should have 25–30 short branches to maintain yield.

This photograph shows one-year-old apple shoots at the beginning of their second growing season. Along the shoot axis, both vegetative buds and floral buds are visible, indicating mixed developmental potential within the same shoot. Vegetative buds are positioned to produce new shoot growth, while floral buds are differentiated and capable of developing into flower clusters. The image illustrates the coexistence of vegetative and reproductive structures during early-season development and highlights the structural basis for future canopy growth and fruit production.
Figure 17. One-year-old shoots exhibiting both vegetative and floral buds at the beginning of their second growing season. Photo: S. Musacchi.
This photograph shows a shoot that has been stubbed to retain a minimum of three viable buds. The retained buds are positioned along the remaining portion of the shoot and can develop into new vegetative growth the following season. The image illustrates a pruning practice designed to preserve shoot renewal potential and maintain future canopy structure by ensuring sufficient viable buds remain after cutting.
Figure 18. Each shoot was stubbed to retain a minimum of three viable buds, ensuring the potential for new shoot development. Photo: S. Musacchi.
Figure 19 consists of two photographs comparing the outcome of different stub lengths following pruning. The left photograph shows a short stub that exhibits dieback, with no evidence of new shoot development, indicating loss of renewal potential. The right photograph shows a longer stub that has successfully produced one or more new shoots, demonstrating maintained bud viability and effective shoot regeneration. Together, the images illustrate how retaining a longer stub length supports successful shoot renewal, whereas excessively short stubs increase the risk of dieback.
Figure 19. Short stubs exhibit dieback (left), whereas long stubs successfully produce new shoots (right). Photos: S. Musacchi.

If click-pruning is adopted, feathers are shortened to two to four inches (5–10 cm) with the possibility of leafing out from several growing points, as shown in Figures 18 and 19 (right). Under Washington’s environmental conditions, the WA 38 branch collar rarely produces new shoots from latent buds, making proper stub length critical for successful renewal (Figure 19).

From each long stub, two or three shoots may develop (Figure 20). One or two of these shoots can be overly vigorous, but the shoot growing from the vegetative bud at the base of the stub will have a favorable crotch angle. This particular shoot will be used to build the branch, while the others will be stubbed again to reduce their vigor (Schupp et al. 2019).

This photograph shows the effect of stubbing on shoot development in WA 38 apple branches. Following the cut, typically three shoots—labeled as shoots 1, 2, and 3—develop from the stub, demonstrating the branch’s capacity for renewal growth after pruning. The image also illustrates potential cutting positions used in a click-pruning style; these positions are indicated by yellow lines. The figure highlights how the location of the cut influences shoot emergence and future branch structure.
Figure 20. Effect of the stub in WA 38 branches. Typically, three shoots (1, 2, and 3) develop from the cut (or stub). Yellow lines indicate possible cutting positions in a click-pruning style. Photo: S. Musacchi.

Overly vigorous branches should be removed to maintain the vegetative balance of the tree. When removing these branches, leaving a stub approximately two to four inches (5–10 cm) long is recommended to encourage the formation of a new shoot. Shorter stubs often die back, failing to regenerate growth (Figure 19, left).

For WA 38, it is recommended that the branches be trained at a 40- to 45-degree angle. The scaffold branches should be 1 to 1.5 feet (30 cm to 45 cm) above the ground. It is essential to maintain a good crotch angle of around 40 to 45 degrees between the branches and the main trunk to ensure structural integrity. Click-pruning with adequate vigor can improve bud swelling and minimize blind wood (Figure 21).

This photograph illustrates the effect of a heading cut applied to a one-year-old WA 38 shoot entering its second growing season. The shoot is oriented at approximately 45 degrees relative to the trunk. Following the heading cut, buds located near the point of insertion on the trunk show increased swelling, indicating enhanced bud activation and potential for new shoot development. The image demonstrates how heading cuts influence the distribution of growth vigor along the shoot, particularly promoting bud growth in proximal positions close to the trunk.
Figure 21. Effect of the heading cut on a 45 degree one-year-old shoot (entering its second season) on bud swelling in proximity to the insertion on the trunk. Photos: S. Musacchi.

Management of the Central Leader and Development of Fruiting Wood

The central axis should be left free to grow, allowing for the development of short, one-year-old laterals. Over time, these will become productive branches through appropriate pruning, depending on the adopted training system. If vigorous shoots begin to compete with the central leader, they should be pruned (Figures 22 and 23) or snapped off (Figure 24) once or twice during the summer, depending on the tree’s vigor. Trees trained as a spindle can take various shapes depending on the spacing between trees within the row and the tree height, which is influenced by the row-to-row distance. As planting density increases, the tree shape becomes more cylindrical rather than conical. These trees are typically called slender spindle and are characterized by short branches that can be periodically renewed.

WA 38 requires specific adjustments in pruning and managing the tree during the growing season. Key points are:

  • Excessive bending increases blind wood risk.
  • Feather trimming and apical shoot removal help reduce spur extinction and manage branch structure.
  • Shoots that develop from the base of long stubs exhibit favorable crotch angles.
  • Overly vigorous or supernumerary shoots should be stubbed or removed, leaving stubs to encourage regrowth.
Figure 22 consists of two photographs illustrating the management of vigorous competing shoots at the top of a WA 38 apple tree. The left photograph shows multiple strong shoots competing with the central leader, which can reduce leader dominance and disrupt tree structure. The right photograph shows the same area after these competing shoots have been shortened through pruning. This intervention reduces competition and allows the central leader to grow uninterrupted. The figure demonstrates how selective shortening of vigorous shoots helps maintain proper tree architecture and apical dominance.
Figure 22. Vigorous competing shoots (left) on the top of the tree must be shortened (right) to allow the leader to grow. Photos: S. Musacchi.
This photograph shows the top of a WA 38 apple tree after vigorous competing shoots have been shortened through pruning. The competing shoots, which would otherwise interfere with the growth and dominance of the central leader, have been shortened to minimize competition. This pruning practice allows the leader to grow uninterrupted, supporting proper tree structure, height control, and long-term canopy development.
Figure 23. Vigorous competing shoots at the tree top were shortened to allow the leader to grow. Photos: S. Musacchi.
This photograph shows the top of a WA 38 apple tree where vigorous competing shoots have been manually snapped off by hand to promote uninterrupted growth of the central leader. Among the remaining shoots, the straightest and most vertically oriented shoot is selected as the leader tip. This selected leader is then tied to a bamboo support on the trellis system to maintain proper orientation and structural stability. The image illustrates a manual canopy management practice aimed at reinforcing apical dominance and guiding tree architecture.
Figure 24. Vigorous competing shoots are snapped off by hand to allow the leader to grow. Usually, the straightest shoot is chosen as the leader tip and tied to the bamboo trellis. Photos: S. Musacchi.

Key Points Specific for WA 38 Management

  • Pruning is essential for managing tree architecture, canopy porosity, crop load, fruit quality, and physiological processes, like flowering and nutrient uptake.
  • Techniques should match the training system, cultivar, and tree age and serve as a primary method to adjust crop load before the season.
  • In HDP and VHDP systems, pruning practices include green or summer pruning, heading back, bending (to regulate vigor and encourage lateral growth), and click-pruning (to reduce blind wood and renew fruiting wood).
  • Click-pruning involves stubbing feathers at planting (WA 38 requires longer stubs: 2–4 inches [5–10 cm]), orienting new shoots to 40 to 45 degrees, and heading one-year-old shoot tips to remove apical dominance.
  • Click-pruning benefits include improved lateral bud development, flowering, and overall branch rejuvenation.

Techniques to Minimize Blind Wood

Scoring and Girdling

Scoring and girdling are horticultural techniques used to manipulate plant growth by temporarily disrupting phloem transport. Scoring involves severing the phloem without removing the bark, whereas girdling entails removing a strip of bark that includes the phloem layer (Ferree and Schupp 2003). Both methods alter the plant’s carbohydrate and hormone distribution, often stimulating localized vegetative growth and bud break. These practices are typically performed with a knife, a double-bladed shearer, or a small saw. The resulting wounds from light scoring generally heal within a couple of weeks.

In contrast, more aggressive girdling, such as that done with a scoring knife in grape production, removes a broader band of bark and takes longer to heal. Scoring or girdling is best performed in the spring at the green tip stage, either during the first year of growth (Figure 25A) or in the second year (Figure 25B), once the root system is well-established. At this stage, the plant’s response to the cut is often more vigorous, resulting in numerous new shoots and strong regrowth (Figure 25B). To minimize the risk of the trees snapping in high-wind conditions, orient the blades at a 45 degree angle to avoid completely incising the trunk circumference in the affected area.

Dutch Cut Stubbing to Increase Fruit Structure Formation

For training systems based on vertical axes with short fruiting shoots extending laterally from the trunk, if shoot renewal is lacking or a vigorous upright bud regrowth is present, an angled cut can be used to promote new growth. This can be remedied with a so-called “Dutch cut” (Musacchi and Greene 2017), which involves cutting horizontally rather than at an angle (Schupp et al. 2019; Einhorn 2022).

The horizontal cut often stimulates bud growth just below the cut, which emerges at a wider angle relative to the trunk. This results in the development of two new shoots that are typically less vigorous than the original shoot and have wider insertion angles, characteristics desirable for managing canopy structure and promoting fruiting. In WA 38, the response from the collar buds is relatively low. For this reason, it is better to leave a longer stub (2–4 inches [5–10 cm]) to ensure that at least one shoot is growing (Figures 18 and 26) (Schupp et al. 2019; Einhorn 2022).

Figure 25 consists of two photographs illustrating the effect of scoring on blind wood development in WA 38 apple trees. Panel A shows a scored cut through the trunk, disrupting normal phloem continuity. Panel B shows the resulting response below the cut, where new leaves or shoots are emerging. This response is attributed to the interruption of auxin flow in the phloem caused by scoring, which reduces apical dominance and promotes bud activation in previously blind wood areas. The figure demonstrates how scoring can stimulate vegetative growth below the cut and partially mitigate blind wood formation.
Figure 25. Scoring (A) effects on blind wood is evident as (B) new leaves or shoots are emerging below the cut (interruption of auxin flow in the phloem). Photos: S. Musacchi.
Figure 26 consists of three photographs (panels A–C) illustrating the effect of stub length on shoot regeneration in WA 38 apple branches. Panel A shows short stubs that have become extinct, highlighted within a yellow circle, indicating loss of bud viability and no new shoot development. Panel B shows longer stubs that have successfully produced at least one new shoot, demonstrating maintained renewal potential. Panel C shows branches uniformly stubbed to approximately four inches in length, a pruning practice that promotes consistent shoot formation across branches. Together, the panels illustrate how retaining sufficient stub length supports bud survival and shoot regeneration, whereas excessively short stubs increase the risk of extinction.
Figure 26. Extinct short stubs (A) in the yellow circle and the longer (B) that produce at least one new shoot. Stubbing all branches to four inches (C) promotes shoot formation. Photos: S. Musacchi.

Key Points for Minimizing Blind Wood in WA 38

  • Temporarily, phloem disruption from scoring and girdling can allow bud break of latent buds beneath the cut.
  • Depth and intensity of scoring and girdling practices should be adjusted to account for wind effects to preserve tree integrity.
  • A “Dutch cut” can stimulate a latent bud that can generate a new shoot at a wider crotch angle.
  • This type of cut requires a stub length of two to four inches to ensure renewal underneath the cut.

Summer Pruning and Mechanical Hedging

Summer pruning can be effectively used in WA 38 to manage excessive vigor, increase fruiting wood, and promote light and color distribution. During the summer, fully developed leaves become the source of carbohydrates and sugars for the developing fruit, buds, and root system. Pruning branches during the summer thus reduces the source of carbohydrates and the buildup of reserves for the next season, while helping to improve light and color distribution, air flow, water demand, and other hormonal regulation (Ferree and Schupp 2003).

This photograph shows vegetative regrowth on WA 38 apple trees following summer pruning carried out on June 26 in Prosser, Washington. New shoots and leaves are visible emerging from pruned areas, indicating an active vegetative response to pruning during the growing season. The image illustrates how summer pruning can stimulate regrowth and influence canopy development by promoting new vegetative growth later in the season.
Figure 27. Vegetative regrowth after the 4th week of June’s summer pruning in Prosser, Washington. Photos: B. Sallato.

In WA 38, summer pruning for vigor control and to promote fruiting buds has been adopted by many Washington growers who utilize different techniques and timings. For example, pruning during spring (May–June) removes remobilized carbohydrates and nutrients, reducing vigor. According to Ferree and Schupp (2003), pruning shortly after bloom time inhibits growth and may interfere with the initiation of flower buds. Summer pruning after the end of shoot growth (July–September) removes a portion of the leaf canopy, thereby affecting carbohydrate redistribution (Saure 1987).

In the WA 38 experimental orchard in Prosser, spring pruning (May) led to reduced regrowth vigor (Figure 27), higher fruit set, but small fruit size (Sallato and Khot 2024). In some years, spring pruning also stimulated autumn flowering (Figure 28). Summer pruning after the end of shoot elongation (July–August) was more devigorating, with reduced regrowth, improved light distribution, and fruit coloring, particularly at the base of the trees. Summer pruning, accompanied by reduced irrigation in vigorous trees, helped balance the fruit-to-shoot ratio, yield, and fruit quality. Similar conclusions were reported by Quinlan and Preston (1971).

Figure 28 consists of three photographs (panels A–C) illustrating possible negative effects of summer pruning in WA 38 apple trees. Panel A shows secondary bloom occurring after summer pruning, indicating a disruption of expected reproductive timing. Panel B shows vegetative regrowth, which is more susceptible to aphid infestation, highlighting the increased pest vulnerability of newly formed tissues. Panel C shows leaf damage caused by sudden exposure to direct sunlight; the affected leaves were not acclimated to high-light conditions following pruning, resulting in visible injury. Together, the panels illustrate how summer pruning, while useful for canopy management, can also lead to unintended physiological, pest-related, and environmental stress responses.
Figure 28. Possible negative effects of summer pruning: secondary bloom (A); regrowth more susceptible to aphids (B); unacclimated leaves damaged by sudden exposure to sunlight (C). Photos: B. Sallato.

Summer-pruned regrowth can be more susceptible to pests like aphids (Figure 28B) or sunburn of unacclimated organs, such as leaves and fruit (Figure 28C). Avoiding hot weeks and applying sunburn protectants after summer pruning can reduce sunburn.

WA 38 Mechanical Hedging Experience

Mechanical pruning has been evaluated at the WSU Roza Farm in Prosser, Washington, and the Sunrise Research Orchard, in Rock Island, Washington, using spindle, bi-axis, and angled canopy systems. The horticultural response to mechanical pruning is directly correlated with the timing of the operation and the amount of wood accessible to the hedging blade.

Three timing options have been tested:

  • Dormant (February)
  • 12-leaf stage (early June)
  • 22-leaf stage (mid July)

Dormant hedging reduces canopy depth and helps define the space assigned to the canopy. Pruning at the 12-leaf stage breaks apical dominance. It promotes latent bud break closer to the trunk and increases general bud activity in the portions of the branches usually more prone to blind wood (Figure 29). No significant positive or negative effects have been observed from pruning at the 22-leaf stage. Dormant mechanical pruning followed by selective hand removal of limbs produces a narrow, well-defined canopy. Mechanical summer pruning done in early June promotes the development of the flower bud below the cut (Figures 30 and 31). Pruning at 8 to 12 inches in length of current season growth led to vegetative regrowth of one or two shoots with lower vigor and less spur development at the base (Figure 30).

Figure 29 consists of three photographs (panels A–C) documenting mechanical summer pruning of third-leaf WA 38 top-worked apple trees in Rock Island, Washington. Panel A shows the trees before summer pruning, with fully developed canopies. Panel B shows the pruning process in progress, with a hedge machine actively cutting the canopy during summer pruning. Panel C shows the trees after mechanical pruning, illustrating the resulting canopy structure following removal of excess vegetative growth. Together, the panels illustrate the sequence and immediate structural effects of mechanical summer pruning on young, top-worked WA 38 trees.
Figure 29. Third leaf WA 38 top-worked trees (Rock Island, Washington) before summer pruning (A), during summer pruning with hedge machine (B), and after mechanical pruning (C). Photo: K. Lewis.
This photograph illustrates the effect of mechanical summer pruning performed in early July on flower bud response in WA 38 apple trees. Following pruning, flower buds along the shoots show a visible response in their development, indicating that mechanical removal of vegetative growth during mid-summer can influence floral differentiation or bud status for the subsequent season. The image highlights the relationship between pruning timing and flower bud behavior in WA 38.
Figure 30. Effect of mechanical summer pruning performed in early July on WA 38 flower bud response. Photo: S. Musacchi.
This photograph illustrates the effect of mechanical summer pruning on flower bud formation in WA 38 apple trees. Following summer pruning, differences in flower bud presence and development are visible along the shoots, indicating that mechanical removal of vegetative growth can influence floral initiation and bud formation for the subsequent growing season. The image emphasizes the role of summer pruning practices in shaping reproductive potential and return bloom in WA 38.
Figure 31. Effect of mechanical summer pruning on flower bud formation. Photo: S. Musacchi.

Key Points for Managing Summer Pruning in WA 38

  • Summer pruning in WA 38 can be used to manage vigor, promote fruiting wood, and improve color.
  • Spring (May–June) pruning removes stored nutrients, while summer (July–September) pruning removes leaf-based carbohydrates, reducing vigor and stimulating bud development.
  • Mechanical pruning at the dormant and 12-leaf stages improves canopy structure and bud activity. Pruning after growth ends (August–September) enhances fruit color but may increase sunburn risk for newly exposed fruit.
  • Potential drawbacks include aphid-susceptible regrowth, sunburn on exposed tissues, and a risk of fall bloom from early pruning of older wood. These can be mitigated with proper timing and protective strategies (e.g., netting, sunburn protectants).

Training Systems and Planting Distance for High-Density Apple Production in Washington

The primary training systems adopted for high-density apple orchards (HDP) in Washington include the spindle, angled canopy (V-system, Y-system), and, more recently, the bi-axis (Zhang et al. 2023). Among these, the spindle system has proven effective in optimizing light interception and canopy light availability, particularly in low-vigor sites. However, spindle trees are not ideal for high-vigor conditions, as excessive growth in the upper canopy often leads to shading of the lower canopy, resulting in poor light distribution (Tustin et al. 1998). Similar light distribution challenges in the slender spindle system were reported by Robinson and Lakso (1991) and Robinson et al. (1991).

Several alternative training systems have been developed since the 1980s to improve light interception, enhance light distribution, and control tree vigor, thereby addressing these limitations. These include the vertical axis (Lespinasse and Delort 1986), Y- and V-trellis systems (Robinson 1998), HYTEC system (Barritt 1998), Solaxe (Lauri and Lespinasse 1998), super spindle (Weber 2001), and slender pyramid (Tustin et al. 2001b). Despite these innovations, many systems still struggled to ensure uniform light distribution throughout the canopy (Lakso et al. 1989; Robinson et al. 1991). In response, more planar and two-dimensional (2D) canopy systems have been introduced and evaluated. Examples include the Washington V- trellis (Robinson 1998), Mur Fruitier in France (Masseron 2002), and the bi-axis system (Bibaum) in Italy (Musacchi 2006, 2008; Dorigoni et al. 2011). These systems aim to improve light penetration and promote balanced growth by creating narrow, vertically structured canopies.

A further evolution of these systems is evident in multi-leader training, which originated in European fruit gardens during the 15th and 18th centuries (Robinson 1878). Louis Lorette provided a detailed description of this system in 1925, highlighting its suitability for continuous fruiting rows (Lorette 1925). These systems typically consist of two (bi-axis) to six or more vertical, parallel leaders, aligned flat to the trellis and bearing numerous short, lateral limbs, resulting in a narrow 2D canopy (Musacchi 2006, 2008; Dorigoni et al. 2009).

More recent developments include the planar cordon (Tustin et al. 2018) and Guyot system (Dorigoni and Micheli 2019), which features up to ten unbranched vertical fruiting stems on a bi-cordon framework. These designs have gained popularity due to the increasing availability of preformed, split-branch nursery trees, which eliminate the need for post-planting topping and reduce delays in canopy formation (Musacchi 2006, 2008; Musacchi and Neri 2019) (Table 6).

Table 6. Between-row by in-row planting distances for WA 38 trees by rootstock and training system.
RootstocksSpindle Spacing (ft)Bi-Axis Spacing (ft)Y System Spacing (2-leader tree) (ft)V System Spacing (single tree) (ft)
G.4112 × 3–412 × 3–412 × 1.5–210–12 × 1.5–2
M.9-NIC2911–12 × 311–12 × 312 × 1.5–210–11 × 1.5–2
M.9-T33712 × 311–12 × 312 × 1.5–211–12 × 1.5
G.93512 × 3–412 × 412 × 1.5–212 × 1.5
Pajam 212 × 312 × 312 × 1.5–212 × 2.0
G.1112 × 311–12 × 312 × 1.5–212 × 1.5
Bud 911–12 × 2–311–12 × 2–3Not recommended10 × 1.5
G.89012–13 × 412 × 4–512 × 1.5–212 × 2.5
Bud 1012–13 × 3–412 × 4–512 × 1.5–212 × 1.5
G.96911–12 × 3–411–12 × 3–412 × 1.5–212 × 2

Spindle

The spindle training system is the most widely adopted training system for medium- to high-density apple orchards globally, typically planted at 809–1,336 trees per acre (2,000–3,300 trees/ha). Its ability to maximize planting density while maintaining relatively low labor requirements makes it popular (Musacchi and Greene 2017). A critical component of spindle training is using well-feathered trees at planting. These feathers—preformed lateral shoots from the nursery—help establish the first scaffold of branches (Figure 32), enabling fruit production as early as the second year (Figures 32–34), often reaching 2.8–3.2 Mton/acre (7–8 Mton/ha) when paired with dwarfing rootstocks (Musacchi and Greene 2017).

The spindle system features a dominant central leader with lateral fruiting branches. Typically, five to seven branches are distributed around the trunk in a loose spiral or whorl without strict positioning rules, but care is taken to avoid overlap and shading between them. Starting with high-quality, well-feathered nursery trees is essential for efficient canopy development. However, if the tree lacks feathers or is poorly formed, it can be headed back two to three feet (60–90 cm) above the ground to stimulate shoot development.

This photograph shows first-leaf WA 38 apple trees grafted on M.9-T337 rootstock, trained to a spindle system and subjected to summer pruning. The young trees exhibit early canopy structure shaped by both training and pruning practices during their establishment year. The image illustrates how summer pruning is applied in first-leaf spindle-trained trees to guide shoot distribution, manage vigor, and support the development of a well-structured canopy early in orchard establishment.
Figure 32. First-leaf WA 38/M.9-T337 trees trained as a spindle and pruned in summer. Photo: S. Musacchi.
This photograph shows fifth-leaf WA 38 apple trees grafted on M.9-NIC29 rootstock and trained to a slender spindle system during the bloom period in 2017 at Prosser, Washington. The trees exhibit a well-developed canopy structure with flowering distributed along the central leader and lateral branches, reflecting the cumulative effects of training and pruning practices over multiple growing seasons. The image illustrates the mature expression of the slender spindle architecture and its associated flowering pattern in established WA 38 orchards.
Figure 33. Fifth-leaf WA 38/M.9-NIC29 trees trained as a slender spindle during bloom (2017, Prosser, Washington). Photo: S. Musacchi.
This photograph shows fifth-leaf WA 38 apple trees grafted on M.9-NIC29 rootstock and trained to a slender spindle system at harvest in 2017 at Rock Island, Washington. The trees display a fully developed canopy with fruit distributed along the central leader and lateral branches, reflecting the mature orchard structure achieved through consistent training and pruning practices. The image illustrates fruit load, canopy balance, and overall tree architecture at harvest, highlighting the production characteristics of established WA 38 slender spindle systems.
Figure 34. Fifth-leaf WA 38/M.9-NIC29 trees trained to a slender spindle system at harvest (2017, Rock Island, Washington). Photo: S. Musacchi.

Bi-Axis

This photograph shows fifth-leaf WA 38 apple trees grafted on M.9-NIC29 rootstock and trained to a bi-axis system during the bloom period in 2017 at Prosser, Washington. The trees exhibit two primary vertical axes with flowering distributed along both leaders, illustrating the structural characteristics of the bi-axis training system. The image highlights how this training approach influences canopy architecture, branch arrangement, and flowering distribution in mature WA 38 orchards.
Figure 35. Fifth-leaf WA 38/M.9-NIC29 trees trained as bi-axis (during bloom 2017, Prosser, Washington). Photo: S. Musacchi.

This training system modulates vegetative vigor and can be initiated in the nursery using double budding or a side grafting technique. A nursery company has patented this process, and the resulting trees are known as Bibaum (Musacchi 2006, 2008).

Alternatively, a single leader tree can be headed back in the field after planting and then two shoots are selected to produce a double-stem (or bi-axis) tree. Dividing the vigor offers several clear advantages, including improved control over vegetative growth. The bi-axis system is ideal for creating a fruiting wall or a thin canopy. Recommended planting distances range from 11 to 12 feet (3.4–3.7 m) between rows and 3 to 4 feet (90–120 cm) between trees, which support the development of short branches 9 to 12 inches (23–30 cm) in length (Figures 35 and 36). This system also requires click-pruning, which helps minimize the formation of blind wood, a common issue with WA 38. Large limbs should be removed, leaving a two-inch (5 cm) stub to reduce blind wood and encourage new branch growth.

This photograph shows detailed views of branch structure and pruning stubs in fifth-leaf WA 38 apple trees grafted on M.9-NIC29 rootstock and trained to a bi-axis system during bloom in 2017 at Prosser, Washington. The image highlights the arrangement of lateral branches along the two primary axes and the presence of pruning stubs resulting from renewal and canopy management practices. These structural features illustrate how pruning and training decisions shape branch distribution, spur development, and overall canopy architecture in mature bi-axis systems.
Figure 36. Fifth-leaf WA 38/M.9-NIC29 trained as bi-axis, showing branch structure and stubs at bloom (2017, Prosser, Washington). Photo: S. Musacchi.

Angled Canopy (V-Shape and Y-Shape)

In addition to spindle training systems, oblique tree training systems have gained popularity in Washington for their high yields. However, these training systems require substantial investment in support structures, trellises, and wiring, particularly for creating tree walls, resulting in a mirrored, symmetrical tree structure on both sides of each orchard row.

The principle behind these oblique forms is to split the tree structure of a single row into two separate fruit walls. These fruit walls can be arranged in various shapes: one option is a transverse Y-shape, where the branches diverge dichotomously at a height of 1.5–2 feet (40–60 cm) from the ground, or a V-shape, which is formed by planting two trees close together with a diverging angle between 15 degrees and 20 degrees (Figure 37). This results in a canopy structured on two inclined planes. The Y-shape is more difficult and slower to form than the V-shape, but it requires only half as many trees for the same skeletal structure (Musacchi and Greene 2017).

This photograph shows an example of an angled canopy system created by alternately tilting trees at an angle of approximately 15 to 20 degrees from vertical. Adjacent trees are inclined in opposite directions, resulting in a staggered canopy architecture. This alternating inclination modifies canopy geometry and light interception compared with vertically trained trees, illustrating how deliberate tree tilting can be used as a training strategy to influence canopy structure and orchard spatial arrangement.
Figure 37. An example of an angled canopy, where trees are tilted alternately at a 15- to 20-degree angle from vertical. Photo: S. Musacchi.

V-Shape

This photograph shows fourth-leaf WA 38 apple trees planted in 2013 and trained to a V-system in 2017 at Prosser, Washington. The trees are arranged in a high-density planting configuration with a spacing of 1.5 feet (0.45 meters) between trees within the row and 12 feet (3.7 meters) between rows. This planting design corresponds to a density of 2,323 trees per acre, equivalent to 5,740 trees per hectare. The image illustrates the canopy structure and spatial arrangement characteristic of V-system training under high-density orchard conditions at bloom.
Figure 38. Fourth-leaf WA 38 trees (planted 2013) and trained to a V-system in Prosser, Washington, 2017. Planting distances are: 1.5 ft (0.45 m) between trees along the row by 12 ft (3.7 m) between rows (2,323 trees/acre=5,740 trees/ha). Photo: S. Musacchi.

These training systems have been developed to increase planting density while maintaining a single row (instead of double or triple rows, as used in northern European countries), splitting the fruiting wall into two distinct units. The V-shape, created by tilting the trees alternately toward each other at a 15-degree angle from vertical, is well suited to the trees’ vegetative and productive habits. It has the advantage of double-wall production, which maximizes light interception. However, it entails higher support structure costs and is more labor-intensive to prune than a single-row system (Robinson 1998; Musacchi and Greene 2017).

This farming method allows for planting densities of over 2,000 trees per acre (5,000 trees per hectare) (Figure 38). By reducing planting distances, it is possible to grow trees with permanent branches near the base, with branch size decreasing as the tree height increases. Vegetative activity is controlled by strong competition for water and nutrients between the root systems.

Y-Shape

The Y-shaped system has been successfully tested in many countries. A notable example is the “Tatura Trellis” system developed in Australia, which requires a complex and expensive structure with more than ten wires (five per side) compared to simpler ones like the palmette. The main advantage of these systems is that they double the irradiated surface area of the fruiting wall while reducing the wall thickness (Sansavini and Corelli-Grappadelli 1997).

The method for achieving a double fruiting wall within a single Y-system is to obtain two axes that develop transversally at 1.5–2 feet (40–60 cm) from the ground. In contrast to the V-system, where the two distinct walls are formed by planting two trees with an inclination of 25 to 30 degrees, the Y-system takes longer and is more challenging to grow; however, the V-system requires about twice as many trees. Both systems require an expensive trellis structure with posts and wires for support.

This photograph shows WA 38 apple trees trained to a Y-shaped canopy system. In this training approach, the Y structure was not created by having the main leader head; instead, a second leader was developed from an existing lateral branch. As a result, the two axes differ in vigor and structure. This asymmetry persists throughout the orchard's life, influencing canopy balance and long-term tree architecture. The image illustrates both the feasibility and the structural limitations of forming a Y-shaped system through secondary leader development rather than symmetrical leader establishment.
Figure 39. WA 38 trees trained to a Y-shaped system. The tree’s structure was created not by heading the main leader but by growing a second leader from an existing branch. This can be a possible solution, but the difference between the two axes will last the whole life of the orchard. Photo: S. Musacchi.

An alternative approach to creating Y-shaped training systems for WA 38 is to designate a secondary leader by promoting an existing lateral branch rather than appointing the primary leader (Figure 39). Although this method is operationally viable, it inherently results in structural asymmetry between the two axes. This disparity in vigor, orientation, and developmental timing is likely to persist throughout the tree’s productive life, potentially affecting canopy balance and long-term management.

Key Points for WA 38 Tree Training

Spindle

  • Most widely used globally in HDP (809–1,336 trees/acre).
  • Requires well-feathered nursery trees for rapid scaffold development.
  • Dominating central leader with five to seven lateral branches in a loose spiral.
  • Poorly feathered trees may be headed back 2–3 ft (60–90 cm) to stimulate lateral growth.
  • Works best with dwarfing rootstocks, yielding early crops (2.8–3.2 Mtons/acre by year 2).

Bi-Axis

  • Developed from double-budded nursery stock (Bibaum) or from headed trees post-planting.
  • Produces two leaders for better vigor distribution and canopy flattening.
  • Ideal for creating fruit walls with narrow branch architecture.
  • Requires click-pruning and 2–4 in. stub cuts to prevent blind wood.
  • Recommended spacing: 11–12 ft (3.4–3.7 m) between rows, 3–4 ft (0.9–1.2 m) between trees.

Angled Canopy Systems (V- and Y-Shape)

  • Designed to split a single row into two oblique canopy units or fruiting walls.
  • Y-shape: from a single tree, branches diverge at 1.5–2 ft (40–60 cm) height.
  • V-shape: two trees planted closely at a 15- to 20-degree outward angle (diverging from the vertical).
  • Y-shape is slower to establish but requires fewer trees.
  • Support structure costs are high due to wiring and anchor systems.
  • Enables planting densities of over 2,000 trees/acre (approximately 5,000 trees/ha).
  • Improves light interception and canopy structure but increases pruning labor.

Rootstocks Commonly Used in WA 38 Orchard Establishment

In modern apple orchards, rootstock choice focuses on dwarfing genotypes with vigor levels similar to M.9 (Basile and DeJong 2019). These orchards are typically planted at a density of around 1,300 trees/acre (~3,200 trees/ha), requiring precise vigor control to manage tree growth within the limited space (Musacchi and Greene 2017). One of the most prominent rootstock breeding programs is based at Cornell University in New York, where the Geneva C.G. series was developed (Robinson et al. 1997). Several Geneva rootstocks have been released in the US, and many are now predominantly used in Washington State. The most commonly used rootstock for WA 38 in the Geneva series is G.41, followed by G.935 and G.11. G.41 is similar in size to the more vigorous M.9 clones, such as M.9-NIC29 or Pajam 2, and has a positive effect on fruit size (Figure 40). Additionally, it is highly resistant to fire blight and offers resistance to replanting and woolly apple aphids (Fazio et al. 2013; Cornell 2024).

Figure 40 presents a chart illustrating the percentage distribution of WA 38 apple trees produced by rootstock combinations between 2017 and 2024. The chart summarizes relative production volumes across multiple rootstocks based on Proprietary Variety Management (PVM) data collected in 2024. In addition to the primary rootstock combinations shown, several other combinations produced between 14,000 and 117,000 trees, including WA 38 grafted on Bud 118, M.26, G.210, MM.106, G.214, MM.111, and G.202. Rootstock combinations producing fewer than 6,000 trees include WA 38 with G.30, G.222, M.7, M.26, G.2406, G.4814, G.2034, and additional minor combinations. The figure provides an overview of how WA 38 tree production has been distributed among different rootstocks over time, highlighting the relative adoption of major versus minor rootstock combinations in commercial propagation. G.41, with 23.2% is the most utilized, followed by M.9-T337 with 19.1% and M.9-NIC29 with 11.8%.
Figure 40. Percentage of WA 38 trees produced divided by rootstock combinations (2017–2024). Other combinations between 14,000 and 117,000 trees include combinations of WA 38 with Bud 118, M.26, G.210, MM.106, G.214, MM.111, and G.202. Other rootstocks below 6,000 include WA 38 with G.30, G.222, M.7, M.26, G.2406, M.9, G.4814, G.2034, G.2406, and G.4814. Chart made with Proprietary Variety Management (PVM) data (2024).

Of the total WA 38 trees planted by 2024 in Washington, 23% were on G.41, 19.1% on M.9-T337, and 11.8% on M.9-NIC29. At lower percentages, G.935, Pajam 2, and G.11 were planted, with values ranging from 6.7% to 5.7% (Figure 40). Interestingly, 17.9% of trees are unknown and have probably been top-worked with other cultivars that are no longer profitable.

In fertile soils with no limitations to root growth, G.41 can grow for longer periods and exhibits higher root growth rates and total root growth volume than M.9-NIC29 under the same conditions. In the seven-year trial described above, on sandy soil in Washington State, G.41 showed higher green spot incidence in only one of the five years in which fruit data were collected. Greater root growth was directly correlated with increased shoot growth, higher uptake of nitrogen, potassium, and magnesium, and a higher green spot incidence (Sallato et al. 2021). Under some conditions, G.41 also produces larger fruit than other rootstocks but may exacerbate green spot development (Sheick et al. 2022; Sheick et al. 2023).

WA 38 (commercialized as Cosmic Crisp®) can be a vigorous variety and requires careful rootstock selection to balance vegetative growth and optimize fruit quality and precocity.

Commonly adopted rootstocks:

M.9 (Various Clones, like T337, NIC29)

  • Still used as a dwarfing rootstock in Washington.
  • Controls vigor effectively, especially in high-fertility soils.
  • Promotes early bearing and high fruit quality.
  • Requires support structures due to limited anchorage.
  • Fire blight susceptible.

G.41 (Geneva Series)

  • Dwarfing capacity is similar to M.9, but under certain conditions, it can be 10%–20% more vigorous.
  • Improved fire blight resistance.
  • Better replant tolerance and root anchorage.
  • Woolly aphid resistant.

G.935

  • Semi-dwarf rootstock with good vigor control.
  • Often used in replant situations or marginal soils.
  • Better anchorage than M.9 but slightly more vigorous.
  • Sensitive to latent viruses (Cornell 2024). Requires certified virus-free scionwood.

Bud.9 (Budagovsky Series)

  • Dwarfing rootstock with excellent cold hardiness.
  • Used in colder sites and very fertile soil in Washington.
  • May be too nonvigorous for low-vigor sites and soils, and should not be used for some training systems, such as the two-leader Y-system.

Evaluation of New Rootstock Accessions in Washington State

From 2017 to 2023, rootstocks were evaluated for WA 38 on several Geneva rootstocks, with G.41 as the industry-standard control. Trees were planted in 2017 at a density of 3,010 trees/ha with a row spacing of 12 feet (3.6 m) and tree spacing of 3 feet (0.9 m). Cumulative yields for five cropping years (2019–2023) for all rootstocks ranged from 317 to 432 Mtons/ha (Table 7). Most rootstocks were similar, except for G.4288, which yielded less than G.5030, G.4292, G.4809, G.41, and G.5087. This was mainly due to a tendency to produce smaller fruit than the other rootstocks. Green spot incidence was 10.8% in 2020, then below 3% in the other four cropping years, and was not significantly different among rootstocks (Table 8). Rootstocks also varied in their tendency for biennial bearing. G.4809 was a stable bearing rootstock with consistently high yields (Table 9). Other rootstocks like G.41 and G.4292 also had high cumulative yields but were more inconsistent year to year.

Table 7. Mean cumulative yields for 2019–2023 for WA 38 apple grown on eight rootstocks.
RootstocksCumulative Yield (Mtons/ha)Statistical DifferencesMean Annual (Mtons/ha)Statistical Differences
CG.5030432a86a
CG.4292427ab85ab
CG.4809416a83a
G.41393ab79ab
CG.5087385ab77ab
CG.6040358bc72bc
CG.4010327bc65bc
CG.4288317c63c
Table 8. Mean green spot incidence (%) among eight different rootstocks from 2019–2023 for WA 38 apple.
Rootstocks20192020202120222023
CG.40100.007.3ab1.00.06.2
CG.42880.004.2b0.00.00.0
CG.42920.009.4ab1.00.04.2
CG.48092.0818.8ab0.00.06.2
CG.50300.0010.4ab2.10.02.1
CG.50874.170.0b1.00.04.2
CG.60400.008.3ab0.00.04.2
G.410.0024.0a1.00.02.1
Table 9. Mean biennial bearing tendency for WA 38 on eight rootstocks. Values closer to one indicate greater stability. Values greater than two indicate that yields more than double or halve each subsequent year.
RootstocksBiennial Bearing Tendency (1–2)Statistical Differences
CG.50301.74bc
CG.42922.40a
CG.48091.51c
G.412.42a
CG.50872.07ab
CG.60401.34c
CG.40101.80bc
CG.42881.69bc

Key Points for WA 38 Rootstocks

  • G.41 is the most utilized WA38 rootstock and induces larger apple size.
  • Green spot can be higher on G.41 in some years under conditions of excessive vegetative vigor that promote rapid fruit growth.
  • M.9 rootstocks promote early bearing and high fruit quality.
  • Bi-axis on Bud 9 is not recommended in low vigor and sandy soil conditions.
  • G.890 is suitable for replant sites and poor soil conditions.

Top-Working an Apple Orchard and Apogee Application

Over 60 apple cultivars are grown in Washington State, and the continual release of new cultivars can quickly shift consumer demand. To respond to these changes, growers frequently use the top-working technique (Schupp 2023) to replace older cultivars with newer, more marketable ones. In addition to variety replacement, top-working enables the conversion of existing training systems into new ones—for example, transforming a single-leader tree into a multi-leader structure (Figure 41) (Schupp 2023).

However, top-working often stimulates excessive canopy growth, which may require additional summer pruning (Saure 1987) or the use of plant growth regulators to manage vigor effectively (Rademacher 2016).

Of the 22.2 million WA 38 apple trees that were planted in Washington State by 2024, an estimated 18% (approximately four million trees) were established through top-working. The most common approach involves converting a single-axis tree into a multi-leader system. The number of leaders typically depends on the trunk size of the original tree; large-diameter trunks are often restructured into multi-leader trees with six to eight new axes (Figure 42), frequently using a Y-transversal system.

This photograph shows an example of an older orchard tree that has been top-worked and converted into a multi-leader tree system. The original canopy has been modified through top-working, resulting in the development of multiple leaders originating from the main framework of the tree. The image illustrates how top-working can be used to restructure mature trees, allowing the establishment of a multi-leader architecture that supports renewed productivity, improved canopy balance, and extended orchard lifespan.
Figure 41. Example of an old orchard tree top-worked and converted into a multi-leader tree. Photo: S. Musacchi.
This photograph shows an example of an old orchard that has been top-worked and retrained to a multi-leader system. Following top-working, multiple leaders have been established from the existing tree framework, replacing the original canopy structure. The image illustrates how multi-leader training can be implemented in mature orchards to rejuvenate trees, redistribute vigor, and create a more balanced and productive canopy structure over time.
Figure 42. Example of an old orchard top-worked into multi-leader system. Photo: S. Musacchi.

Managing excessive vegetative growth is essential to reduce competition between shoots and fruit (Meintjes et al. 2005), prevent internal canopy shading, enhance light interception, and ultimately improve fruit quality (Rademacher et al. 2004; Rademacher 2016; Musacchi and Serra 2018). Numerous studies have demonstrated that unmanaged vegetative growth has a negative impact on fruit quality, yield, and pest management (Greene 1999; Miller and Tworkoski 2003). Tree vigor is typically managed through a combination of pruning strategies, including hand, chemical, and mechanical methods, with manual methods remaining the most labor-intensive and costly (Carra et al. 2016).

WA 38 Top-Working Trial in Washington

To support Washington growers with practical data, a top-working trial was established in March 2016 at the Washington State University Sunrise Research Orchard (Rock Island, Washington). An existing eight-year-old Granny Smith block on M.9-T337 rootstock was top-grafted with WA 38 budsticks. For experimental purposes, four bud sticks were grafted onto each Granny Smith interstem. By June 2016, successful grafts within each plot were trained to one of three systems: a single-leader (spindle), two-leader (bi-axis), or three-leader (candelabra) architecture (Figure 43). Surplus bud sticks were removed accordingly (Figure 43A–C). Trees were spaced 11 ft (3 m) between rows by 3 ft (0.9 m) within rows, resulting in a planting density of 1,500 trees per acre (3,703 trees per hectare) (Musacchi et al. 2023).

Figure 43 consists of three photographs (panels A–C) showing an example of a Granny Smith/M.9-T337 orchard that has been top-worked and converted to WA 38 in Rock Island, Washington, and trained using three different canopy architectures. Panel A shows trees trained to a single-leader spindle system, characterized by one dominant central leader. Panel B shows trees trained to a two-leader, or bi-axis, system, with two primary vertical axes developing from the tree framework. Panel C shows trees trained to a three-leader, or candelabra, system, where three main leaders form the primary canopy structure. The figure illustrates how the same top-worked orchard can be managed using different leader configurations, resulting in distinct canopy architectures that influence tree balance, light distribution, and long-term orchard management.
Figure 43. Example of a top-worked Granny Smith/M.9-T337 orchard, converted to a WA 38 block and trained to three systems: single-leader (spindle) (A), two-leader (bi-axis) (B), and three-leader (candelabra) (C) (Rock Island, Washington). Photo: S. Musacchi.

Apogee Applications to Control the Vigor

In 2016, to control vigor, all trees were mechanically hedged in July and stub-pruned during the winter of 2016–17. In addition to stubbing the branches at four inches (approximately 10 cm) in spring 2017, scoring and notching were executed on the leaders to promote bud swelling.

In 2018 and 2019, Apogee (3-oxido-4-propionyl-5-oxo-3-cyclohexenecarboxylate; prohexadione-calcium, or Pro-Ca; BASF Corp., Ludwigshafen, Germany) was sprayed three times at a concentration of 12 oz/acre/100 gal (247 mg/L) (approximately 250 ppm per application) using an air-blast sprayer. Each year, treatments were applied on three dates in the weeks following bloom (Musacchi et al. 2023). In 2018, the first Apogee spray was applied approximately seven days after first bloom (DAFB), followed by the other two at 15 DAFB and 26 DAFB. Whereas, in 2019, the three applications were performed at 9 DAFB, 16 DAFB, and 23 DAFB. In 2018, applications occurred on May 3, May 11, and May 22, with king bloom around April 26. In 2019, applications were made on May 9, May 16, and May 23, following the full bloom, which occurred approximately on April 30. In both years, the first application coincided with an average shoot length of roughly 4.7 inches (12 cm), which was around seven leaves. This relatively late timing, compared to Rothwell and Schwallier (2016), was chosen to minimize Apogee impact on the spur shoots formed from lateral buds on one-year-old wood.

In 2018, trees treated with Apogee had significantly shorter one-year-old shoots at the end of the growing season, averaging 29.5 cm (11.6 inches) compared to 50.9 cm (20.0 inches) in untreated control trees. Apogee treated trees also exhibited reduced internode length relative to controls (−44%). However, no significant differences were observed among training systems in terms of shoot length, leaf number per shoot, or internode length (Musacchi et al. 2023).

Key Points for Managing Top-Worked WA 38

  • Top-work reduces unproductive time and quickly rebuilds a productive canopy.
  • By top-working, it is possible to modify the training system of the new orchard, utilizing a multi-axis planar canopy.
  • Unfortunately, if a virus infects the original tree, it can be transmitted to a new variety. Virus-infected rootstocks will reduce the performance of Washington top-worked trees. Likewise, virus-infected scionwood may reduce rootstock performance or delay death in some stocks.
  • Scion budsticks must originate from a nursery and be certified virus-free.
  • Applications of Apogee help control tree vigor and growth.
  • Apogee did not negatively impact WA 38 productivity.

Avoiding Replant Problems

Apple replant disease (ARD) is a soilborne syndrome that occurs when new orchards are planted on sites previously planted to the same or closely related tree fruit species. Replant disease causes tree stunting and reduced yields (Mai and Abawi 1981). In Washington State, fungi, including Ilyonectria robusta, Rhizoctonia solani, multiple species of oomycetes in the genera Phytophthora and Pythium, as well as the lesion nematode Pratylenchus penetrans, are known components of the replant complex (Mazzola and Mullinix 2005).

If replanting in previously planted soil, whether for apples, pears, or cherries and regardless of the root’s ability to withstand replant disease, the ground should be deeply tilled and fumigated prior to planting. In Washington, the general practice is to fumigate with 1-3 dichloropropene plus chloropicrin (e.g., Telone C-35). 1,3-dichloropropene is nematicidal, while chloropicrin is fungicidal. Remember that when fumigating, it is essential to remove crowns and roots that can harbor nematodes. Rip to break up compaction layers that can also limit root growth of young trees. Adequate soil moisture and temperature is critical for the fumigant to move properly through the soil. Make sure you allot enough time for fumigation chemicals to fully dissipate from the soil before planting. Check this by digging test holes throughout the orchard and checking for fumigation odor. Follow fumigation labels.

Reducing replant pressure before planting is critical. For example, recent studies found that growth of WA 38 trees on M.9 rootstock was significantly lower in non-fumigated soil than in soil fumigated with 1-3 dichloroprene plus chloropicrin or treated with a brassica seed meal bioremediation at a site in Rock Island (DuPont et al. 2021). “In the first three harvest years, trees in non-fumigated soils averaged four to six bins fewer per acre on G.41 and four to eight bins fewer per acre on M.9 rootstock than soil treated with fumigation, brassica seed meal biorenovation, or anaerobic soil disinfestation” (p < 0.05; directly reported from DuPont et al. [2026]).

Key Points for Managing WA 38 Orchard Replant Problems

  • It is critical to prevent apple replant disease (ARD) in new plantings, as it can stunt trees and reduce yield.
  • The most common practice to mitigate apple replant disease (ARD) in Washington is to fumigate the orchard with 1-3 dichloroprene plus chloropicrin before planting.
  • Brassica seed meal biorenovation is a promising new alternative to fumigation and may be suitable for organic systems.

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Stefano Musacchi, Professor and Endowed Chair of Tree Fruit Physiology and Management, Department of Horticulture, Wenatchee Tree Fruit & Extension Center, Washington State University
Karen Lewis, Extension Regional Specialist, Grant County, Washington State University
Bernardita Sallato, Associate Professor and Tree Fruit Extension Specialist, Prosser Irrigated Agriculture Research and Extension Center, Washington State University
S. Tianna DuPont, Associate Professor and Tree Fruit Extension Specialist, Wenatchee Tree Fruit Research & Extension Center, Washington State University
Lee Kalcsits, Professor and Endowed Chair of Environmental Tree Fruit Physiology and Management, and Wenatchee Tree Fruit Programmatic Lead, Department of Horticulture, Wenatchee Tree Fruit Research & Extension Center, Washington State University
Sara Serra, Research Associate Professor, Department of Horticulture, Wenatchee Tree Fruit & Extension Center, Washington State University*

*Sara Serra is now an Assistant Professor at Pennsylvania State University, Department of Plant Science, University Park, PA 16802, and is affiliated with Fruit Research and Extension Center, Pennsylvania State University, Biglerville, PA, USA.

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