Growth and stability of deep planted red maple and northern red oak trees and the efficacy of root collar excavations

Trees with root systems established well below grade due to deep planting or soil disturbance are common in urban landscapes, yet the long term effects of buried trunks and subsequent remediation strategies, such as root collar excavation are poorly documented. We evaluated the consequences of deep planting over a 10-year period on tree growth and stability, with and without root collar excavation, for red maple [Acer rubrum L. Red Sunset^® (‘Franksred’)] and Northern red oak (Quercus rubra L.) planted at grade or 30-cm below grade. Sleeves to prevent soil-trunk contact were installed around trunks on a subset of deep trees. Root collar excavations were made during the 6th growing season for both species and trees were grown for an additional 4 and 3 growing seasons for red maples and Northern red oaks, respectively. Within two weeks of root collar excavations, pulling tests compared the effect of treatments on stability of red maples. Deep planting generally slowed growth of red maple but had no clear effect on Northern red oak. Root collar excavation had no lasting effect on growth of either species. Approximately 55% of deep red maples and 33% of deep Northern red oaks had roots crossing and in intimate contact with buried trunks, suggesting a potential for future girdling roots. Approximately 25% of deep maples had substantial adventitious rooting. All deep Northern red oaks had new roots emerging just above the first original structural roots but none were clearly adventitious. Trunk sleeves had no effect on growth for either species. Neither deep planting nor root collar excavation resulted in a loss of tree stability compared to trees planted at grade, although failure patterns varied among treatments. Overall, the biggest long term concern for deep-planted trees is the potential for girdling root formation.     

Growth, survival, and root system morphology of deeply planted Corylus colurna 7 years after transplanting and the effects of root collar excavation

Urban trees are frequently planted with their root collars and structural roots buried well below soil grade, either because of planting practices, nursery production practices, or both. These deeply planted structural roots can impair tree establishment and are thought to reduce tree growth, lifespan, and stability, although research has provided few and contradictory results on these questions to date. This study examines container-grown (55 L) Turkish hazel trees (Corylus colurna L.), planted either at grade, 15 cm below grade, or 30 cm below grade into a well-drained silt loam soil, over nearly 8 years. Five years after planting, in 2004, remediation treatments (root collar excavations) were performed on two replicates of each below-ground treatment. Subsequently, all trees were subjected to flooding stress by being irrigated to soil saturation for approximately 6 weeks. In 2006, flooding stress was repeated. Trees root systems were partially excavated in 2007, and root architecture was characterized. Deep planting did not affect trunk diameter growth over 8 years. Survival was 100% for the first 5 years; however, one 30 cm below grade tree died after flooding in 2004 and another died after the 2006 flooding. Photosynthesis was monitored during the 2004 flooding and all trees experienced decline in photosynthetic rates. There was an apparent slight delay in the decline for trees with excavated root collars and those planted at grade. Girdling roots reduced trunk taper and occurred primarily on unremediated trees planted 30 cm below grade.

Selected individual roots were excavated and followed from the root ball and were observed to gradually rise to the upper soil regions. Analysis of roots emerging from excavation trench faces indicated that vertical root distribution at approximately 1.25 m from the tree trunks was the same regardless of planting depth. Longterm consequences of planting below grade are discussed.     

Influence of rate and method of application of superphosphate on the growth and nutrient status of newly planted peach trees

A field experiment was carried out with newly planted peach trees to determine the influence of both rate and method of application of superphosphate on tree growth and nutrient status during the first growing season. Superphosphate was applied at planting at rates ranging from ¼ to 9 lb per tree, and applications were made either to the soil surface, in the planting hole, under tree roots, or in a band around the tree at a depth of 6 inches. Trees were grown under straw mulch and were irrigated as required.

Results showed that, in this soil of low initial ? content, trees receiving 9 lb superphosphate on the soil surface or in a ring band grew significantly larger than trees receiving ¼ lb superphosphate per tree (this applied for butt circumference only on surface-treated trees), but high rates of superphosphate in the planting hole or under tree roots resulted in tree death. No significant differences in growth were recorded at harvest between surface and ring-banded treatments at any phosphate rate, but leaf analysis in midsummer and tree analysis at harvest showed that the phosphate status of surface-treated trees was significantly higher than that of ring-banded trees.

At low rates of superphosphate (¼ and 1 lb per tree), surface treatment tended to give larger trees at the end of the growing season than band treatment, but differences were not significant. It is thought that this differential response occurred because the phosphate-fixing potential of the soil increased sharply with depth and hence band applications were inefficient unless very high rates of superphosphate were used.

The tree damage observed when high rates of superphosphate were applied in the planting hole or under tree roots was probably due to a combination of osmotic stress, acidity damage to the roots and possibly toxic nutrient levels in tree tissues. Hence high rates of superphosphate should not be placed close to tree roots at planting.

Leaf analysis in midsummer and tree analysis at harvest showed that the main effect of superphosphate application was on the ? status of the trees, and maximum tree growth in the surface and band treatments corresponded to a value of approximately 0.28% ? (dry weight basis) in the leaves. The efficiency of uptake of applied superphosphate was very low at all rates of application and was especially so at high rates. However, positive growth responses were recorded to 9 lb superphosphate per tree in surface and banding treatments. It is suggested that, although most of the applied superphosphate could not be utilized, tree growth rate was proportional to the concentration of ? in the soil zone which could be exploited by the roots.     

Trees in planters – Growth,structure and ecosystem services of Platanus x hispanica and Tilia cordata and their reaction to soil drought

Urban environments are often characterized by extensive paved surfaces, exacerbating the urban heat island effect. At the same time, limited root space due to underground infrastructure poses a challenge for planting new trees in these areas. Trees in planters have emerged as popular design elements, offering innovative and sustainable greening solutions, particularly in urban environments with limited rooting space. However, growing conditions in planters may strongly impact tree growth and the provision of environmental ecosystem services (ES). In this 3-year study, we analyzed tree growth and ecosystem services (cooling by shading, CO₂-fixation) of London plane (Platanus x hispanica Münchh.) and small-leaved lime (Tilia cordata Mill.) in four planting treatments: in-ground (G), planters in the ground (PG), non-insulated plastic planters (P), and insulated planters (PI). We also recorded soil temperature throughout the experiment and implemented soil drought conditions by reducing soil irrigation for half of the trees after one year. Our findings revealed higher thermal fluctuations in soil temperature within non-insulated plastic planters (P), reaching a maximum of 45 °C, surpassing the critical temperature threshold for plant growth (>38 °C). In contrast, insulated planters (PI) effectively mitigated soil temperatures, staying below 33.8 °C. When planted in the ground (G), P. x hispanica exhibited a significantly higher stem diameter increment (52–66%) compared to other planting treatments, aligning with the provision of ecosystem services. However, T. cordata trees showed a more moderate response to planting treatments in terms of growth and ecosystem service provision. Furthermore, the implementation of soil drought conditions resulted in a reduction of up to 34% in stem diameter increment for P. x hispanica and up to 25% for T. cordata. Our results underscore the necessity of tree species-specific knowledge about growth responses to different planting treatments for effective urban planning perspectives, as the provision of ecosystem services may be influenced differently.     

苹果中间砧入土深度对根系生长及其激素含量和果实产量品质的影响

 以陕西杨凌试验区大田栽培的3 年生‘长富2 号’苹果为材料,结合凤翔、永寿和蒲城等 试验区的调查,研究比较矮化中间砧（M26）入土深度对富士苹果树基砧根系生长分布、根系激素含量和 果实产量品质的影响。结果表明,矮化中间砧入土深度为15 cm 时,树体细根（＜ 2 mm）主要分布在0 ~ 40 cm 土层,细根数比其他处理多13.6% ~ 41.5%,总根数多18.2% ~ 33.3%,根系干质量多11.2% ~ 68.4%, 果实产量高,单果质量大,可溶性固形物含量高,硬度大,可滴定酸含量少,着色率高,品质较好。矮 化中间砧入土深度为15 cm,树体根系中促进生长的IAA、ZR、GA 含量较高,抑制生长的ABA 含量较 少,（IAA + GA + ZR）/ABA 比值较大,有利于刺激根系的生长。研究表明矮化中间砧入土深度为15 cm 时,根系生长旺盛,细根数量较多,能够为果树生长发育提供较多养分,果实品质较好。     

Effects of nitrogen and phosphorus on root and shoot growth of Cotoneaster divaricata Rehd. & Wils.

Root and shoot growth rates of Cotoneaster divaricata were determined using a growing system of polyvinyl chloride pipe cylinders in which longitudinal sections could be removed for periodic root observations. Plants were fertilized with nitrogen (N), phosphorus (P), and potassium (K). N, as NH₄NO₃, was applied weekly at levels of 0, 250 or 500 mg/l and P, as H₃PO₄, was incorporated in the medium at levels of 0, 5 or 50 mg/l. K, as KCl, was maintained in the medium at a 150 mg/l level by soil tests conducted weekly. Shoot growth was increased after N application. However, no difference was observed between N levels. P increased shoot growth only at the highest N level applied. Although root growth was not increased by either N or P, high N levels inhibited root growth, whereas P stimulated root growth. No correlation (r = 0.19) was observed between shoot and root growth.     

Effects of tree age at planting,root manipulation and trickle irrigation on growth and cropping of apple (Malus pumila) cultivar Queen Cox on M.9 rootstock

Summary

The apple cultivar Queen Cox on M.9 rootstock cropped more precociously when planted as two year old trees than when planted as one year old trees, even though there were no significant differences in the sizes (leader height and branch length) of the trees at the time of planting. However, the two year old trees had larger root systems at planting. As the trees aged, those planted as one year olds grew more vigorously and bore higher cumulative yields than those planted as two year olds. Annual root pruning of the trees, commencing 15 months after planting, reduced extension shoot growth, crown volume and grubbing weights (final fresh weights of scions) severely. In some seasons root pruning increased the number of spur and terminal floral buds produced and also the final sets and yield efficiencies on the treated trees. Planting trees within semi-permeable fabric membranes also reduced extension shoot growth and tree size, but less severely than the root-pruning treatment. Root restriction increased the efficiency of fruit set and yields and also improved the grades of fruits produced. Trickle irrigation treatments increased shoot growth and tree fresh weight at the time of grubbing, but had inconsistent and small effects on fruit set and yields. Interactions between tree age at the time of planting and the root manipulative treatments were significant.     

Responses of morphology and drought tolerance of Sedum lineare to watering regime in green roof system: A root perspective

The presence of drought tolerant vegetation is essential for the longevity of an extensive green roof when irrigation is not installed. Earlier studies have examined performance of green roof plants under contrasting watering regimes and found that higher watering frequency provided better growth and survival rates. The effect of early watering regimes on the subsequent response of plants to persistent drought stress in extensive green roofs, however, has not been extensively studied. In order to evaluate the effects of watering regime during the establishment period of Sedum lineare on its growth and drought tolerance, two greenhouse experiments using simulated green roofs were conducted. It was found in the first experiment that a 2-day-interval watering regimen at the early planting stage produced greater root biomass and root size than those of 6-day- and 13-day-interval watering, indicating that deficit watering tended to induce thinner roots in S. lineare. In the second experiment, the remaining plants were subsequently subjected to a 28-day drought treatment. The roots of plants watered at 13-day-interval maintained the highest respiration activity among all plants during the drought period. Results suggest that an appropriate deficit watering regimen at the early planting stage may lead to smaller root size and higher root:shoot ratios in S. lineare, and thereby improve its drought tolerance performance on extensive green roofs.     

A strain of Bacillus subtilis stimulates sunflower growth (Helianthus annuus L.) temporarily

Preliminary studies showed that a Bacillus subtilis strain stimulates plant growth. We investigated how inoculating seeds of a sunflower cultivar (Helianthus annuus L.) with this strain stimulated plant growth, soil properties and emissions of greenhouse gasses, i.e. carbon dioxide (CO₂) and nitrous oxide (N₂O), when cultivated in a greenhouse. Unfertilized sunflowers or fertilized with urea served as controls. After one month, root length and fresh and dry root weight of the sunflower was significantly higher in the bacteria amended plant than in the urea and unfertilized plants. However, at harvest, no positive effect was observed. The number of seeds per plant and seed weight was not significantly different between the treatments, but total plant N was significantly higher in urea-amended plants than in unfertilized plants. The CO₂ production rate was not affected by treatment, but the N₂O emission rate was significantly higher in soil amended with urea plus bacteria soil compared to the unfertilized treatments. It was found that the B. subtilis strain used in this study had a positive, but only temporarily effect on growth of the sunflower cultivar used.     

Micro-scale heterogeneity in urban forest soils affects fine root foraging by ornamental seedlings of Buddhist pine and Northeast yew

Urban soils are frequently characterized by a strong heterogeneity caused by intense anthropogenic activity and land use changes. Soil heterogeneity is commonly known to affect tree root development, but little has been detected concerning root foraging by ornamental trees in heterogeneous urban soils at micro-scale. In this study, Buddhist pine [Podocarpus macrophyllus (Thunb.) D. Don] and Northeast yew (Taxus cuspidata S. et Z.) were selected as ornamental tree species for a two-year study. In the first-year, seedlings were cultured under contrasting photoperiods to generate different morphologies. In the second year, seedlings were transplanted to pots filled with soils collected from an urban forest. Controlled-release fertilizers (N-P₂O₅-K₂O, 14-13-13) were evenly broadcasted to a half patch of the pot (heterogeneity) or to both halves (homogeneity) on the surface 5 cm beneath the pot-top at the rate of 0.135 g N seedling⁻¹. In the fertilized heterogeneous patch, larger Buddhist pine seedlings had greater dry weight, length, surface area, volume, number of tips, and morphological foraging-precision in fine roots. Compared to Northeast yew seedlings under natural photoperiod in the first year, those under the extended photoperiod had larger size, greater fine root biomass, and length but lower foraging-precision in the second year. N and P concentrations in second-year fine roots mainly increased with the availability of patches generated by fertilization for both species. In conclusion, the ability to forage for nutrients by ornamental tree seedlings in heterogeneous urban forest soils was species-specific. Buddhist pine seedlings had higher foraging precision in heterogeneous urban soils than Northeast yew seedlings due to their response to the extended photoperiod during culture.     

Root system traits of Mahonia aquifolium and its potential use in soil reinforcement in mountain horticultural practices

The structural changes of Hungarian agriculture in 1989 led to many mountain horticultural farms being abandoned. These structural changes have modified land use patterns which often resulted in decreasing slope stability in mountainous farms. Mahonia aquifolium has been cultivated in Hungary for over half a century for ornamental purposes; however its possible application in shallow slope stabilization has not been discussed. This paper presents the first results on the root morphology, and root tensile strength of M. aquifolium and determines its efficiency for soil protection in horticultural farming practice. Measurements were carried out on M. aquifolium seedlings from cultivated (C) and non-cultivated (NC) soil conditions. The C and NC specimens were measured and compared for root area ratio (RAR) and root tensile strength (T_R). These results were then compared with other species for which data was available. Results showed that M. aquifolium plants from C soil conditions had a significantly higher mean RAR with depth than M. aquifolium plants from NC soil conditions. The mean T_R results showed no significant difference between M. aquifolium plants from C and NC environments. The study also showed that M. aquifolium's root structure is comparable as soil protection with the other species although a higher degree of soil reinforcement by roots was obtained with C M. aquifolium specimens. M. aquifolium roots could represent effective soil protection. Moreover the plant is well suited to the demands of small-scale horticultural farm practices under mountainous conditions.     

Porous-permeable pavements promote growth and establishment and modify root depth distribution of Platanus × acerifolia (Aiton) Willd. in simulated urban tree pits

In dense urban areas with heavy pedestrian traffic, current trends favor covering tree pits with porous-permeable pavement over installing grates or leaving the soil exposed. However, pavement cover potentially modifies soil moisture and temperature, altering tree growth and overall resilience, especially when coupled with heat stress and drought in a changing climate. This study evaluated the response of newly planted London plane (Platanus × acerifolia ‘Bloodgood’) trees to porous-permeable resin-bound gravel pavement and associated alterations in soil water distribution and temperature, in two distinct physiographic regions in Virginia, USA. Simulated urban tree pits were either covered with porous-permeable pavement or left unpaved, and root growth and depth, soil water content and temperature, and tree stem diameter measured over two growing seasons. At both sites, trees in paved tree pits grew larger than trees without pavement. Stem diameters were 29% greater at the Mountain site and 51% greater at the Coastal Plain site, as were tree heights (19% and 38% greater), and above ground dry biomass (67% and 185% greater). Roots under pavement developed faster and shallower, with many visible surface roots. In contrast, unpaved tree pits had almost no visible surface roots, and at the Mountain site only occupied an average area of 7 cm² within the 1-m² tree pits, compared with 366 cm² in paved tree pits. Pavement may have extended the root growing season by as much as 14 days, as the average soil temperature for the month of October was 1.1 °C and 1.2 °C higher under pavement than in unpaved pits. Porous-permeable pavement installations in tree pits accelerated establishment and increased growth of transplanted trees, but may result in shallower root systems that can damage pavement and other infrastructure. In addition, shallow root systems may prevent water extraction from deeper soils, compromising drought resilience.     

Vine growth and nitrogen metabolism of ‘Fujiminori’ grapevines in response to root restriction

Two-year-old ‘Fujiminori’ grapevines (Vitis Venifera × V. Labrasca) planted in plastic pots (10 L) were used to evaluate vine growth and nitrogen metabolism in response to root restriction. Results show that root restriction reduced shoot growth and photosynthetic rate, but promoted root growth in vines. NO₃⁻-N concentration in all plant parts, and total N concentrations in brown roots and new leaves were decreased by root restriction, and chlorophyll and carotenoid concentrations in mature leaves were also reduced. Nitrate and nitrite reductase activities in brown roots and mature leaves were significantly reduced in root-restricted vines. The results suggest that the reduction of nitrate and nitrite reductase activities caused the inhibition of nitrogen assimilation, and this might be an important reason for root restriction inhibiting shoot growth.     

Growth of Betula pendula Roth. the first season after transplanting at two phenological stages

The root extension rate of Betula pendula, transplanted at two phenological stages, was studied in a Nordic climate. Landscape-size trees were transplanted from the field into root-study boxes (rhizotron) in early and late spring of 1999 and 2000. In early spring, 6 trees were transplanted when the leaves had just started to unfold; likewise, in late spring, six trees were transplanted when the leaves were fully unfolded and the shoot extension was in progress. Root growth was recorded during the first post-transplant season and the tree roots were finally excavated. Results indicate that the root extension rate of B. pendula follows seasonal soil temperature. The mean root extension rates at ten days intervals varied from 4 to 11 mm/day with a total average for the growing season of 7 mm/day in 1999 and varied from 4 to 9 mm/day with a total average for the growing season of 4 mm/day for 2000. The average length of new roots was 89 cm and there was no significant difference in length, dry weight or number of new roots between the two transplant times. It appears, therefore, that the phenological stage at transplanting during the period from bud break to fully developed leaves has minor effect on landscape establishment of B. pendula, when an adequate amount of water is provided.     

Apple rootstock studies: growth of trees on three clonal rootstocks planted with or without roots

Trees of Cox's Orange Pippin on M.IXa, M.26 and MM. 106 were planted either normally with roots or without roots to simplify the planting operation. Pruning treatments were superimposed, the trees being cut back at planting, left unpruned the first year and cut back the second year, or left entirely unpruned. All trees survived. After two growing seasons the trees were lifted and weighed. Removal of all roots before planting reduced shoot growth, trunk girth increment, final tree weight and incremental weight. However, on all rootstocks, trees planted without roots and left unpruned were similar in size when lifted to those planted with roots and cut back at planting in the orthodox manner.

In a complementary trial lasting one season Cox's Orange Pippin trees on M.26 were planted with or without roots. All trees were cut back at planting, and four times of planting were compared. The mid-April planting included trees that had been stored at 2.8 °C and trees that had been bedded-in outdoors. There were no tree losses attributable to removal of the roots before planting. Removing the roots at planting again reduced growth and weight of tree at lifting. Month of planting had no effect upon shoot growth or trunk girth increment.

The results are discussed, together with their practical implications in relation to mechanical tree planting for high density orchards.     

The Reinvigoration of Apple Trees by the Inarching of Vigorous Rootstocks

Summary

The purpose of this research was to determine if established, orchard-grown apple trees that were con®ned in root-restricting membranes received adequate water for growth when irrigated. Previous data had shown positive effects of root restriction on reducing shoot extension growth in apple. Soil matric potential (Ψ_sm), leaf stomatal conductance (g) and leaf water potentials (Ψ_l) were measured over daily cycles during the period of maximum tree water use (July and August). Measurements were also made of the Ψ_sm and fruit size throughout the growing season. Daily and seasonal Ψ_sm showed that the soil within the root restricting membranes (+R) when irrigated (+I) remained closed to field capacity (<100 HPa), which was not the case for unirrigated soil within the membranes (-I +R). Ψ_l measured before dawn, showed that similar levels of drought stress were evident between irrigated and restricted (+I +R) and unrestricted (+I -R and -I -R) trees. The Ψ_sm, and Ψ_l for trees with roots within restricting membranes were significantly more negative, in the absence of irrigation (-I +R). Measurement of g showed that root restricted trees were transpiring at similar rates in the presence of irrigation (+I +R) as unrestricted trees (+I -R) with or without irrigation. Stomatal closure could not explain the increased Ψ_l observed for the restricted irrigated (+I +R) treatment compared with unrestricted (-R) trees. A reduced stomatal aperture was the most likely explanation for the reduction in growth previously observed with the restricted unirrigated trees. Fruit size was also affected by root restriction and the effect became greater as the roots became more restricted with tree age. Similarly, there was also a negative effect, in one year, of root restriction on fruit size at harvest, even in the presence of irrigation. Data show that reductions in soil water availability, Ψ_l and g, for the root-restricted trees (+I +R), were unlikely to be the causes for the previously observed reductions in shoot growth (tree size). These results imply that other factors were in operation, among which root-synthesized chemical regulators of shoot growth are the most likely candidates.     

Rootstock and pruning effects on first season dry weight distribution in delicious apple trees

Redchief Delicious apple trees on MM. 106 and M.9 rootstocks were left unpruned, dormant headed at planting, or summer headed 12 weeks after planting, to investigate pruning and rootstock effects on dry weight distribution between roots and shoots during the first growing season. Dormant heading stimulated new shoot dry weight and reduced new root dry weight during the first six weeks after planting. However, by 12 weeks differences in new root dry weight and new shoot dry weight were insignificant. Summer heading resulted in a significant increase in new shoot growth and decrease in new root growth. This caused the root/shoot ratio in headed trees to return to the unpruned value within six weeks after summer heading. New root growth was reduced over a longer time by dormant heading trees on MM. 106 than those on M.9. New shoot growth was increased longer in trees on M.9. Allometric constants (K) of new shoot growth relative to new root growth were significantly changed by dormant heading with both rootstocks. Summer heading had the greatest effect on K values by shifting growth heavily toward new shoots. Root/shoot ratios in all treatments for both rootstocks showed no differences 24 weeks after planting.     

The impact of soil compaction on soil aeration and fine root density of Quercus palustris

The soil around Quercus palustris trees, 30 cm (11.8 in) average diameter breast height (DBH) were treated by compaction (C) or C plus clay slurry (CS) treatments in November 1994 and repeated in May 1996. Soil oxygen diffusion rate (ODR), fine root density (FRD), DBH, twig growth, leaf area and dieback were monitored for 4 years beginning in 1996. Both compaction treatments significantly reduced ODR at 15 cm. Early each season, ODR was below the 0.20 g/cm²/min threshold level reported to inhibit root growth in several species [Stolzy, L.H., Letey, J., 1964. Correlation of plant response to soil oxygen diffusion rates. Hilgardia 35, 567–576] for all treatments and depths. In summer each year, ODR was adequate in the shallow soils of all treatments, though often still significantly lower in compacted soils. At 30 cm, there were no consistent differences in ODR between compacted and uncompacted soil. Significant differences in FRD due to compaction treatments were inconsistent and limited to the upper 9 cm of soil in years 2 and 3. Reduced FRD in compacted soils may be a response to the reduced ODR in spring. There were no differences in DBH, twig growth, leaf area or dieback rating. Given the minimal difference in root growth, the lack of differences in top growth are understandable. This controlled study, and others preceding it, have failed to clearly show the underlying causes of tree decline and death commonly associated with soil compaction and addition of fill soil in real landscapes.     

Stability of landscape trees in engineered and conventional urban soil mixes

Urban trees are frequently exposed to unsuitable soil conditions that can hamper root system development, potentially affecting both tree health and stability. Engineered soil designs have been developed to increase soil volume for trees planted in confined spaces, and past research has shown that these designs improve growing conditions. However, tree stability in these engineered soils has received limited attention from researchers. In this study, we evaluated the stability of two tree species of contrasting soil quality tolerance (Prunus serrulata and Ulmus parvifolia) after 3 years growth in two skeletal soil mixes, in a suspended pavement design (uncompacted soil), and in a conventionally prepared soil pit. Tree stability was evaluated by measuring trunk resistance to a lateral deflecting force applied with a rope winch system under both ambient and near-saturated soil conditions. Although heavily irrigating the experimental soils had no effect on tree stability, species-specific responses to soil mixes were observed. P. serrulata grown in the gravel-based skeletal soil showed greater trunk deflection resistance than trees grown in the other soil treatments, yet the stability of U. parvifolia was unaffected by soil type. These species-specific responses were consistent with earlier observations of root development in which P. serrulata grew up to 60 times greater root length in gravel-based skeletal soil whereas U. parvifolia root growth was similar in all soil treatments. This research provides evidence that certain tree species planted in conventional tree pits may be more prone to uprooting due to poor root development and that root anchorage might be improved for these species by utilizing a skeletal soil mix.     

Root shoot interactions in passionfruit (Passiflora sp.) under the influence of changing root volumes and soil temperatures

Summary

Passionfruit are grown in the tropics and subtropics where mean monthly soil temperatures at 15 cm range from about 10° to 30°C. The choice of rootstock can also influence production with most industries exploiting either the purple (Passiflora edulis f. edulis) or golden passionfruit (P. edulis tflavicarpa). We examined the relationship between shoot and root growth in purple x golden hybrid E-23 grafted onto golden passionfruit seedlings. Growth was manipulated by varying the volume of the soil available to the roots or temperature of the root zone. Shoot and root growth increased as root zone volume increased from 0.3, 1.4, 4, 12 to 24 1. Shoot weight (W_s) was correlated with root weight (W_R):W_S = 12.697 + 5.272 W_R + 0.195 W_R² (r² = 91%, P<0.001), with the plants allocating a smaller proportion of dry matter to the roots as root weight increased. Differences in shoot growth with pot volume were not due to changes in water or nutrient status. In the temperature experiment, the two critical root zone temperatures at 90% of maximum growth were about 20° and 35° C for vine extension, leaf area, node and leaf production, and 20° and 30°C for flower production. Leaf and stem dry weight were optimal between about 18° and 34°C, while maximum root growth occurred at 38°C. There was a weak relationship between shoot (W_s) and root dry weight (W_R): W_s = ?19.346 + 24.500 W_R ?1.046 W_R² (r² = 53%, .P<0.001). Apparently, variations in shoot growth at different soil temperatures cannot be explained solely by differences in root growth. Reduced growth at 10°C was associated with lower chlorophyll concentration, stomatal conductance and net CO₂ assimilation, but not lower leaf water potential. The concentration of most nutrients were lower at 10°C than at higher temperatures, but none was outside the range which would be expected to restrict growth. There appears to be a co-ordination of shoot and root growth as the soil volume available for root growth increases, whereas root temperature affects the roots and tops differently. The results of the pot volume experiment demonstrate the importance of rootstock vigour in passionfruit breeding. Productivity would be affected in cool subtropical areas with soil <20°C and in tropical areas with soil >30°C.