Abstract
Root pruning by shaving 12 L container root balls when shifting to 51 L containers did not impact Acer rubrum L. or Quercus virginiana Mill. root architecture within the top 12 cm of planted 51 L root balls five years later, despite marked differences at planting, and had no impact on tree height or trunk diameter increase. Root pruning in the nursery did not affect bending stress required to tilt Acer trunks up to five degrees (anchorage) either one, two, or three years after landscape planting. In contrast, anchorage was greater the second year after planting Quercus that were root pruned. Rotating trees 180 degrees at planting from their orientation in the nursery had no impact on Acer or Quercus anchorage, tree height, or trunk diameter. Rotating oak (not maple) trees 180 degrees at planting increased root cross-sectional area growing from the hot (south) side of the root ball when trees were rotated at planting.
- Acer rubrum
- Anchorage
- Bending Stress
- Maple
- Oak
- Quercus virginiana
- Root Ball Shaving
- Root Morphology
- Root Pruning
- Winching
Trees grown in containers develop root systems that are different from trees grown by other nursery production methods. Instead of spreading to their natural distance (Stout 1956; Watson and Himelick 1982), roots on shade trees are deflected up, down, or around by container walls (Harris and Gilman 1991), and this can affect post-landscape planting root architecture (Marshall and Gilman 1998). Roots growing away from the trunk can also be deflected 180 degrees and grow back to and close to the trunk (Fare 2005). Root systems of container-grown seedlings can develop poor symmetry with fewer main lateral roots after 12 years; naturally regenerated seedlings often have greater sinker root development, and can possess self-grafted roots (Halter et al. 1993).
Container dimensions, size, and container-wall porosity can change root architecture (Struve 1993; Arnold 1996; Marshall and Gilman 1998). Seedlings in porous-walled 5 cm diameter containers had fewer packed roots, fewer spiraling roots, and fewer L-shaped roots than those grown in solid-walled containers (Ortega et al. 2006). Root elongation on the periphery of the root ball can be stalled, at least for a time, by growing trees in containers coated with copper (Burdett 1978; Struve 1993; Gilman and Beeson 1995). Rooted cuttings in copper-treated containers had a greater percentage (40%) of roots emerging from the top one-third of the plug, compared to trees grown in containers not treated with copper (18%); there were also more roots on the interior of the root ball and fewer on the outside, forming a cage or imprint (Smith and McCubbin 1992). In contrast, Gilman and Beeson (1995) found no increase in root tips on the root ball interior for Ilex cassine L.
Lateral roots were more evenly distributed throughout the root ball in mechanically pruned Pinus contorta (Dougl. Ex Loud) than in the solid-walled, untreated control (Krasowski 2003). The same was true for at least seven other temperate and tropical hardwood trees (Gilman et al. 2010b). Roots that emerged in the non-pruned, non-treated control after seedlings were installed in the field were located primarily at the bottom of the original plug; this was considered a defective root system, resulting in a less stable tree following planting into the field (Lindgren and Örlander 1978).
Root deformations caused by deflection in the propagation container can lead to poor rooting out, which results in unstable trees (Lindgren and Örlander 1978). For example, Scots pine (Pinus sylvestris L.) trees developed spiraling roots when in 75 ml propagation containers, causing them to be less stable in the soil seven to nine years after planting compared to naturally regenerated trees (Lindström et al. 2005). Other root defects, such as downward-deflected roots, were later recognized as causing problems with stability following planting jack pine (Pinus banksiana Lamb. (Chapman and Colombo 2006). Many studies on conifer seedlings show that root deflection in propagation containers can contribute to long-term growth problems after planting in the forest (Krasowski 2003). Roots on shade trees in larger containers also deflect around or downward and proliferate at the bottom of containers (Gilman and Paz 2014)—probably because of suitable air, nutrition, and water at the bottom—but the impacts on health and anchorage are poorly documented.
Because straight, non-deflected roots appear to be associated with well-anchored trees planted into field soil from propagation (Salonius et al. 2000) and larger nursery (Gilman and Harchick 2014) containers, the main goal of the present study was to determine influence of root form in a container root ball on growth, root architecture, and anchorage, several growing seasons after planting into landscape soil. Specifically, the study authors wanted to determine the influence of shaving the periphery of a 12 L root ball when shifting into a 51 L nursery container on growth and anchorage several years after planting the 51 L root ball into the landscape. The secondary objective was to determine the importance of planting the imprinted (Gilman et al. 2010b) north side of the tree as it stood in the nursery toward the north in the landscape. Acer and Quercus were chosen due to their popularity as urban landscape trees in many temperate climates.
MATERIALS AND METHODS
Trees and Landscape Planting
On 29–30 April 2008, forty 12 L (30 cm tall × 26 cm top diameter) cutting-propagated, container-grown (Airpot™, Caledonian Tree Company, Ltd., Scotland) ‘Florida Flame’ red maples (Acer rubrum L.) and 40 Cathedral Oak® live oaks (Quercus virginiana Mill. ‘SDLN’), selected for trunk diameter uniformity from Cherry Lake Tree Farm in Groveland, Florida, U.S., were shifted into 51 L solid-walled containers (35 cm tall × 44 cm top diameter, Nursery Supplies, Inc., Chambersburg, Pennsylvania, U.S.) 112 km north in Gainesville, Florida, U.S. Trunk diameter averaged 16.8 mm (SD = 1.8) for maples and 14.0 mm (SD = 1.5) for oaks, placing them well within standard size (American Association of Nurserymen 2014). Twenty trees of each taxa were root pruned by shaving (removing, Gilman et al. 2010a) about 3 cm from the root ball periphery and bottom before shifting. The other 20 trees were shifted without disturbing the root ball, acting as controls. After shifting into 51 L containers, the north side of the trunk was marked and always maintained toward the north while trees were in 51 L containers. Trees of each taxon were arranged on black woven nursery ground cloth in separate randomized complete block designs with one tree per treatment combination in each of 20 blocks. Each was irrigated three times daily, pruned to one leader, and staked in June 2008. In October (maples) 2008 and January 2009 (oaks), ten of the twenty blocks chosen at random (2 root pruning × 10 replicates = 20 trees) of each taxon were destructively harvested to measure root system attributes described in Gilman et al. (2010a).
Twenty trees remaining of each taxon (2 root pruning × 10 replicate blocks = 20) were planted into landscape soil in a field [Millhopper fine sand (loamy, siliceous, hyperthermic Grossarenic Paleudults)] with less than 2% organic matter and a bulk density of 1.51 g/cc in USDA hardiness zone 8b in Gainesville, on 25–26 November 2008 (maples) and 6–7 January 2009 (oaks). Trunk diameter was 37 mm (SD = 2.6) for maples and 27 mm (SD = 1.9) for oaks, placing them well within standard size. The north mark on the trunk was placed either north or rotated 180 degrees south when field planting. This provided for two tree orientations: north in the nursery to north in the landscape, and north rotated to the south. Trees were in four rows 3.4 m apart. Holes 10 to 15 cm wider than the root balls were dug with straight sides and flat bottoms with height adjustment so the top of the undisturbed root ball was about even with the landscape soil surface. One person packed the bottom of holes by foot in an effort to standardize settling. No trees were root pruned when planted into the landscape. Once the root ball was placed in the planting hole a 15 cm wide volume of undisturbed soil at the edge of hole was pushed into the hole. The rest of the void around the root ball was filled with soil from the planting hole. Water was added to settle backfill soil and soil was lightly tamped by foot to standardize compaction of backfill soil. No berm or water ring was constructed around the root ball.
Chipped, whole branches and leaves from utility line clearance operations were applied as mulch 12 cm thick (before settling) 1.8 m wide within each of four rows. Trees were irrigated on the root ball three times a week and were fertilized under the crown with 200 g of 16-4-8 (N-P2 O5-K2O) in March and June 2009, and 400 g of 20-0-8 (N-P2 O5-K2O) in March and May 2010, and March and June 2011 and 2012. Weeds were controlled in the mulch with periodic (three to four) annual applications of glyphosate (isopropylamine salt, 41%); vegetation between rows was periodically mowed.
Evaluating Post-Planting Anchorage and Growth
To evaluate lateral tree stability (anchorage), trunks were pulled laterally with a winch in late August/early September 2009, 2010, and 2011 for maples, and October 2009, 2010, and 2011 for oaks. All trees were pulled (one or two blocks each rain-free day) with a steel cable and electric winch (Model 40764; Chicago Electric Power Tools, Inc., Camarillo, California, U.S.) in the 350 degree azimuth (from north) direction. There was no prevailing wind direction at the site. The winch attached to a cable about 1.2 m from the ground remained parallel to ground. A 3,629 kg capacity load cell (SSM-AF-8000; Interface Inc., Scottsdale, Arizona, U.S.) was placed in-line with the winching cable. An inclinometer (model N4; Rieker Inc., Aston, Pennsylvania, U.S.) was mounted to a fabricated steel plate (5.1 cm × 7.6 cm). The plate was secured to the trunk 15 cm from soil surface, which was just above the swollen flare. The cable was winched at 2 cm•sec−1 until the inclinometer tilted five degrees from vertical start position; then the cable was released.
Data from load cell and inclinometer were collected at 2 Hz by Data Acquisition System (National Instruments Corporation, Austin, Texas, U.S.). Data from pulling tests were displayed in real time on a laptop running LabView software (v: 7.0; National Instruments, Austin, Texas, U.S.). Trunk bending stress was calculated according to Equation 1:
1
where
σ = bending stress
F = pulling force
d = distance from pulling point to inclinometer
R = trunk radius (calculated as halving diameter measured with a diameter tape)
Trunk diameters at 15 cm from ground and tree height were measured at planting and in September of each year through 2013. In May 2014, soil was removed with high-speed air in a 40 cm radius around the trunk to expose the top 12 cm of the original 51 L root ball. Measurements included diameter of the five largest roots 10 cm beyond edge of the 51 L container in the top 12 cm of soil profile on the north and south 180 degree circumference of the tree (total 10 roots on each tree). Root diameter was measured from the top of the root to the bottom and perpendicular to that, and these were averaged to calculate the cross-sectional area (CSA) of a circle on the ten roots on each tree. Visual root system imprint (1 = little imprint with mostly straight roots; 5 = strong imprint, many roots deflected by and retaining the shape of the container) caused by roots deflected by the 12 L or 51 L container walls was rated for each tree.
Experimental Design and Statistical Analysis
Trees in 51 L containers were placed on nursery ground cloth in a randomized complete block design described in Gilman et al. (2010b). Trees of both taxa were planted into landscape soil in a randomized complete block design with 2 taxa × 2 root prunings × 2 tree orientations × 5 blocks = 40 trees. Taxa were statistically analyzed separately. Main effects on trunk tilt from root pruning and tree orientation were analyzed in the GLM procedure of SAS (1992) with repeated measures two-way analysis of variance (ANOVA); main effects on root CSA from root pruning, tree orientation, and side of the trunk (north or south) were analyzed with three-way ANOVA. Means were separated with Tukey’s multiple range test; interaction means were compared using LSD. Stepwise procedure in SAS (1992) calculated regression coefficients.
RESULTS AND DISCUSSION
Root pruning 12 L container root balls as they were shifted to 51 L containers in the nursery did not impact mean trunk diameter (37 mm, maple; 27 mm, oak) or tree height (3.4 m, maple; 2.4 m, oak) at landscape planting (Gilman et al. 2010b). This also held true after planting into the landscape (data not shown). For example, nursery root pruning had no effect on mean tree height increase (4.6 m, P = 0.69, maple; 5.0 m, P = 0.93, oak) through 2012 (four years after planting) or mean trunk diameter increase (121 mm, P = 0.27, maple; 132 mm, P = 0.73, oak) through 2013 (five years after planting). Changing tree orientation at planting—by rotating trees 180 degrees compared to their orientation in the nursery—also had no influence on tree height or trunk diameter increase for either taxon in any year after landscape planting (P > 0.73). There was no trunk bark damage evident on any trees at any time.
There was no impact (P > 0.42) of root pruning in nursery containers or tree orientation when planting into the landscape on root system imprint rating (from 12 L or 51 L containers) five years later on either taxon (data not shown). This occurred despite significant root architecture differences at planting—due to root pruning during nursery production (Gilman et al. 2010b)—and appears to suggest that deflections from container walls occurring five years previously did not persist and did not result in the potential, long-term health issues caused by roots circling the trunk. This might be attributed to the short duration in 12 L (14 months) and 51 L containers (seven months) prior to landscape planting; whereas trees are often retained for much longer by many growers (personal observation) even as they remain in conformance with industry standard sizes (American Association of Nurserymen 2014). A longer retention time for these and other taxa would likely have resulted in a greater container imprint on the root system as others found (Salonius et al. 2000; Gilman et al. 2012). Moreover, the type of 12 L container used in this study has been shown to reduce root system imprint and length of roots circling the container compared to smooth-sided containers (Gilman et al. 2010a). In addition, both taxa were propagated from cuttings, and there is evidence that each taxa continues forming new roots from the root collar when planted from 12 L into larger containers (Gilman and Harchick 2008, oaks; Gilman et al. 2013, maples). Continued new root production within the 51 L container may have allowed both to mostly outgrow the 12 L container imprint by generating new roots that became larger than those deflected by the smaller container. Results would likely be different for species that cease producing new roots from the root collar soon after seed germination, such as Tabebuia spp. (Gilman et al. 2010b).
Arborists and other practitioners report that stem-girdling roots in the landscape are a direct result of roots circling in nursery containers, and these can cause trees to become physiologically stressed or worse in the landscape (Giblin et al. 2005). Perhaps surprisingly, there is sparse documentation in the scientific literature of container-induced root deflections causing health issues in the landscape, although there is ample evidence that conifers planted from propagation containers in reforestation efforts can perform poorly when planted with root defects (Burdett 1978; Salonius et al. 2000). In related work, Tate (1980) and Giblin et al. (2005) showed that encircling roots in the landscape—typically attributed to planting too deeply—can cause a decline in health as long as three decades later. However, these roots could have been generated after planting and been the result of site conditions or other factors not inherent to the nursery stock. Arborists also report poor anchorage on trees with severe circling roots and other root defects from the nursery (Johnson and Hauer 2002); Gilman and Masters (2010) documented that some of the reported instability is directly attributed to root architecture created in the nursery and other factors.
Root pruning during production did not impact bending stress required to tilt maple trunks one to five degrees in either one (P > 0.19), two (P > 0.84), or three (P > 0.84) years after landscape planting (Table 1). Tree orientation at planting also had no impact on maple bending stress in the first three years after landscape planting—the only years tested (Table 1, P > 0.17). Lack of impact on post-planting maple anchorage from either main effect came despite significant pruning-induced changes in root architecture (i.e., smaller container imprint) within the root ball at planting five years earlier (Gilman et al. 2010b). No main effects (root pruning, tree orientation, side of tree) influenced maple root CSA; however, root pruning inexplicably reduced root CSA in the five largest roots when maple trees were rotated 180 degrees at planting but had no impact when trees were planted in their nursery orientation (Table 2).
Similarity in maple anchorage between treatments in the current study could have been due to the relatively small size of the trees (16 mm trunk diameter) in the 12 L containers prior to shifting into 51 L containers compared to a recent study on slightly older trees of the same maple (20 mm trunk diameter in 12 L container, Gilman et al. 2016) that showed better anchorage after planting of nursery stock that was root pruned when shifted to larger containers. Trees retained in containers for a longer period have more root defects with a greater root system imprint than those retained for a shorter period, leading to a smaller amount of roots growing into substrate or soil after planting (Salonius et al. 2000). Root pruning by shaving older propagation container root balls that were more imprinted had a greater impact on root architecture within 12 L root balls than shaving less pot-bound trees (Gilman et al. 2012).
Like maples, root pruning during nursery production did not impact bending stress required to tilt oak trunks one to three degrees at the end of the first or third year after planting (P > 0.75, Table 3). Unlike maples, at the end of the second growing season, there was a significant root pruning effect on bending stress required to winch oaks to all angles (P < 0.03; Table 3 and Figure 1). Specifically, shaving 12 L container root balls as they were shifted into 51 L containers resulted in about a 28% increase in bending stress required to tilt oaks five degrees (Figure 1); this indicated better anchorage. There are few other studies evaluating post-planting anchorage of trees root pruned during nursery production. Gilman et al. (2016) found that planting 57 L (similar size as current study) or 170 L red maple root balls that were shaved in the nursery improved anchorage in the landscape by 20%–25% compared to trees not shaved. Improved anchorage in that study was attributed to an abundance of straight roots in the root ball. This has been accomplished by shaving when shifting to a larger container size in the nursery, or by growing in certain porous-walled containers (Gilman and Paz 2014).
In slight contrast to maples, oak tree orientation at planting affected (P = 0.06) bending stress required to tilt trunks at the end of the first year after planting, but only to four and five degrees (Table 3) and not in the second and third growing seasons. Specifically, rotating the north side of oaks 180 degrees to the south when planting into the landscape resulted in about a 15% decrease in anchorage when winched north to four and five degrees trunk tilt, compared to maintaining trees in the same orientation as in the nursery at planting (Table 4). Oak trees rotated at planting had nearly five times the root CSA (3,485 mm2, averaged across root pruning) on the north side of the tree measured five growing seasons after planting than those not rotated at planting (776 mm2; Table 5). Although this indicated more growth from the hot (south) side of the container, trees not rotated at planting failed to show this response. This makes definitive conclusions on the impact of orientation in the nursery container on post-planting root growth difficult. There is evidence of reduced root growth on the periphery of the hot side of nursery containers (Ruter 1993), resulting in smaller diameter and fewer roots (Gilman et al. 2016) that can position more root tips within the root ball (Smith and McCubbin 1992) capable of growing out into landscape soil. An increase in root CSA outside the root ball could eventually contribute to anchorage by entrapping a larger volume—and therefore mass—of soil in the root plate to resist overturning (Fourcaud et al. 2007; Gilman and Masters 2010).
Stability in forest plantations has been associated with shallow roots in the windward direction (Stokes 1999), lateral roots positioned symmetrically around the trunk (Coutts et al. 1999), tap and sinker root mass (Danjon et al. 2005), leeward sinker root length (Hayfa et al. 2007), and combinations of these. There is far less known about the anchorage of trees planted from landscape-sized root balls, and results vary even for similar taxa. For example, root CSA measured toward the pulling winch three years after landscape planting of four-year-old Quercus virginiana Cathedral Oak from 170 L containers (Gilman and Masters 2010) has been associated with anchorage; whereas root CSA on the opposite side of the tree was most correlated with anchorage for a different cultivar of the same species (Q. virginiana Highrise®) planted from 57 L containers (Gilman and Weise 2012). Experimental design did not allow roots to be measured when trees were winched, making direct relationships between root attributes and anchorage difficult; however, there were some correlations. Maple and oak bending stress to tilt trunks three years after planting was positively correlated with root CSA in the largest five roots in the north and south sides of the tree measured five years after planting (Equation 2; Equation 3). Only about 20% of the variability in trunk tilt could be explained by root CSA. This significant but weak relationship suggests that although the CSA of the largest roots bridging the interface of container substrate and landscape soil play a role in anchoring trees in the first few years after planting, there are other factors involved. Future studies should excavate and characterize entire root systems—not just the top 12 cm, as in the current study—in an effort more comprehensively quantify anchorage. Results could have been different if trees were retained in containers longer, if porous-walled containers were used, or if trees were planted in a different season.
2
3
CONCLUSIONS
Oak and maple trunk diameter and tree height growth in the five growing seasons after planting were not impacted by rotating trees 180 degrees from their orientation in the nursery. Rotating trees 180 degrees at planting also had little impact on anchorage for either taxa the first three years after planting. Root pruning by mechanically shaving the periphery of the root ball as 12 L containers were shifted to 51 L containers reduced occurrence of root defects at the 12 L container position on finished 51 L nursery stock of both taxa (Gilman et al. 2010b) without impacting trunk or height growth (one to five growing seasons) or tree anchorage (one to three growing seasons) after planting into the landscape. Root pruning in the nursery improved oak anchorage only in the second growing season after landscape planting (not in the first or third). Oak (not maple) roots measured in the top 12 cm of soil grew substantially more in the five growing seasons after landscape planting from the side of the container that faced south in the nursery than from the side facing the north, but only on trees rotated 180 degrees at planting from their orientation in the nursery.
Acknowledgments
Thanks to innumerable nurseries in Florida, U.S., for provided financial support for this research.
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