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Article

Container Type and Substrate Affect Root Zone Temperature and Growth of ‘Green Giant’ Arborvitae

by
Anthony L. Witcher
1,*,
Jeremy M. Pickens
2 and
Eugene K. Blythe
3
1
Department of Agricultural and Environmental Sciences, Otis L. Floyd Nursery Research Center, Tennessee State University, McMinnville, TN 37110, USA
2
Department of Horticulture, Auburn University, Auburn, AL 36849, USA
3
College of Agriculture, Auburn University, Auburn, AL 36849, USA
*
Author to whom correspondence should be addressed.
Horticulturae 2020, 6(2), 22; https://doi.org/10.3390/horticulturae6020022
Submission received: 20 December 2019 / Revised: 14 February 2020 / Accepted: 25 March 2020 / Published: 7 April 2020

Abstract

:
Root zone temperature (RZT) in nursery containers commonly exceeds ambient temperature during the growing season, negatively impacting crop growth and quality. Black nursery containers absorb radiant heat resulting in excessive RZT, yet other types of containers and different substrates can moderate RZT. We conducted studies in Tennessee and Alabama to evaluate the effects of container type and substrate on RZT and growth of ‘Green Giant’ arborvitae (Thuja standishii × plicata ‘Green Giant’). Trade gallon arborvitae were transplanted into black, white, or air pruning containers filled with pine bark (PB) or 4 PB: 1 peatmoss (v:v) (PB:PM). Plants grown in PB:PM were larger and had greater shoot and root biomass than plants grown in PB, likely due to increased volumetric water content. Plant growth response to container type varied by location, but white containers with PB:PM produced larger plants and greater biomass compared with the other container types. Root zone temperature was greatest in black containers and remained above 38 °C and 46 °C for 15% and 17% longer than white and air pruning containers, respectively. Utilizing light color containers in combination with substrates containing peatmoss can reduce RZT and increase substrate moisture content thus improving crop growth and quality.

1. Introduction

Container-grown nursery crops are subjected to extended periods of root zone heat stress throughout the growing season, negatively impacting crop growth and quality. The deleterious effects of high root zone temperature (RZT) have been observed historically in commercial container production. Self and Ward [1] observed less root growth of loquat (Eriobotrya japonica) on the south side of black metal cans where substrate temperature was 10 °C to 15 °C greater than ambient temperature (30 °C). In nursery containers, maximum RZT can reach 54 °C which can damage crops even when exposed for short periods [2,3]. At RZTs above 46 °C, direct injury to plants including immediate root cell damage can occur even with an exposure time under 30 min. Indirect injury to plants can occur at RZTs above 38 °C, including interruption of physiological mechanisms which may not present visible signs of damage but lead to reduced growth [4,5].
Many factors contribute to high RZT in container production. Nursery containers have a high surface-to-volume ratio, allowing excessive heat to be absorbed by the container and exchanged between the substrate through conduction [4]. Root zone temperature will vary within the container, with greater temperatures occurring in the region with direct exposure to the sun which will change throughout the growing season [3,4].
Container color, composition, or porosity can also affect RZT and plant growth. Dark-colored containers absorb more solar radiation than light-colored containers leading to excessive heat buildup in the substrate. Containers with a more porous exterior facilitate evaporation from the substrate and reduce heat exchange between the container wall and the substrate [6,7]. Markham et al. [3] evaluated the growth of red maple (Acer rubrum) and redbud (Cercis canadensis) along with RZT in conventional black containers and white painted containers. They reported RZT was 7.7 °C greater in black containers compared with white containers and that red maple had 2.5 times greater root density in white containers. In the same study, they noted white containers had little effect on redbud growth suggesting sensitivity to supraoptimal RZT varies by plant species.
Another alternative to conventional containers is air pruning containers which are available from several manufacturers and are designed with circular openings or long open slots to prevent root circling and improve root branching. Arnold and McDonald [8] evaluated the growth of five tree species in air pruning and conventional black containers. Although results were species specific, plant height, trunk diameter, and root and shoot biomass were similar or improved in the air pruning container compared to the conventional container. In the same study, it was also reported RZT near the exterior edges was 5 °C cooler in the air pruning container.
Container substrate porosity and moisture content are also factors in the rate of heat buildup or dissipation. Substrates with low air-filled porosity may improve heat energy diffusion through the substrate due to the physical connectivity of substrate particles. Water is an effective thermal conductor; thus, heat builds up more slowly in substrates with greater water content and minimizing temperature fluctuations in the substrate [4]. Pine bark (PB) is the most widely used substrate for nursery crops in the eastern United States and can be used alone or in combination with other components such as peatmoss (PM) or sand [9,10]. Pine bark typically has a high proportion of drainable air space, whereas PM has greater water holding capacity. Nevertheless, PB physical properties can vary by region and source due to processing methods and aging which could affect crop growth [11]. The combination of PM with PB would increase substrate water holding capacity and possibly reduce RZT.
Plant species vary in response to RZT and duration of exposure. Eastern arborvitae (Thuja occidentalis) is sensitive to high RZT and performs best in the United States Department of Agriculture (USDA) plant hardiness zones two to seven where summer temperatures are more moderate [5,12]. In a similar species such as ‘Green Giant’ arborvitae (Thuja standishii × plicata ‘Green Giant’), root temperature sensitivity has not been reported but it is more heat tolerant and adapted to various soil types and climates including areas with long durations of high summer temperatures [13].
Although the benefits of light-colored containers and air pruning containers have been well documented, commercial adoption of these products remains low. Substrates with increased water retention properties can improve crop growth, yet most nursery producers continue to use PB as the sole substrate component (personal observation). Previous research has focused on differences among container type or among substrates, but the combined effects of container type and substrate have not been reported. Determining which factors (container or substrate) or combination of factors have the greatest impact on crop growth could increase adoption of these practices.
The objective of this research was to evaluate the combined effects of container type and substrate on RZT and growth of ‘Green Giant’ arborvitae.

2. Materials and Methods

Two separate studies were conducted concurrently at the Tennessee State University Otis L. Floyd Nursery Research Center, McMinnville, TN (USDA Plant Hardiness Zone 7a) and the Auburn University Ornamental Horticulture Research Center, Mobile, AL, USA (USDA Plant Hardiness Zone 8b). The studies were conducted at two locations due to potential differences in environmental conditions which may affect plant growth including temperature and rainfall. The average daily temperature in Tennessee (TN) ranged from 20.8 °C (September) to 26.7 °C (July) and ranged from 24 °C (May) to 27.3 °C (July) in Alabama (AL). Rainfall totaled 75.4 cm (TN) and 103.6 cm (AL) over the duration of each study.
Three different container types included black or white solid wall containers (11.3 L; PF1200; Nursery Supplies Inc., Kissimmee, FL, USA) and an air pruning container (10.5 L; #5 Rediroot; Nursery Source Inc., Boring, OR, USA). Two substrates were evaluated in combination with each container type (for a total of six treatments) and included PB and 4 PB: 1 peatmoss (v:v) (PB:PM). Pine bark was obtained from Morton’s Horticultural Products (McMinnville, TN, USA) and from Longleaf Mulch (Semmes, AL, USA) for the TN and AL studies, respectively. Both substrates were amended (per 1 m3) with 5.9 kg 18N-2.6P-6.6K controlled-release fertilizer (18-6-8 Nutricote® Total Type 180; Florikan USA, Sarasota, FL, USA), 3.6 kg dolomitic limestone, and 0.9 kg micronutrient granules (Micromax; ICL Specialty Fertilizers, Summerville, SC, USA). Trade gallon (2.4 L) ‘Green Giant’ arborvitae were transplanted on 19 April 2017 (AL) or 27 April 2017 (TN) into each treatment with 12 replicates (for a total of 72 individual experimental units) and plants were arranged on a gravel container pad in a randomized complete block design. To provide maximum container surface area to sunlight, plants were spaced 0.9 m apart.
Separate irrigation zones were used for each treatment to monitor and adjust irrigation application rates. Plants were irrigated daily using a modified dribble ring (15.2 cm diameter; Dramm Corp., Manitowoc, WI) fitted with a pressure-compensating emitter (8 L h–1; Netafim USA, Fresno, CA). Irrigation application volume for each treatment was adjusted every two weeks to a target leaching fraction of 10% to 20%. Decagon 5TE (AL) and 5TM (TN) sensors and EM50 data loggers (Decagon Devices Inc., Pullman, WA) were used to measure and record RZT and volumetric water content (VWC; m3·m–3) every 15 min throughout both studies. Sensors (1 per container; n = 3) were positioned vertically approximately 4.3 cm from the south-facing container sidewall and placed midway between the substrate surface and bottom of the container. Plant height and diameter were measured at 0, 59, 138, and 166 days after planting (DAP) in AL and 0, 69, 95, 120, and 173 DAP in TN. Growth index was calculated [(height + width at widest point + perpendicular width) / 3] and increase in plant height and growth index was also reported (increase = final – initial). The studies were terminated at 166 (AL) and 173 (TN) DAP and plants were destructively harvested. Shoot dry weight (n = 12) and root dry weight (n = 4) were measured after samples were oven-dried at 70 °C for approximately 7 days. Substrate pH and electrical conductivity (EC) were recorded using the pour-through method [14] at 52, 97, 146, and 166 DAP (AL) and at 60, 95, and 120 DAP (TN). The percentage of time roots were exposed to temperatures above critical thresholds (38 °C and 46 °C) mentioned by Ingram et al. (2015) was calculated using the total number of data recordings during daylight hours. Substrate physical properties (n = 3) including air space, container capacity, total porosity, and bulk density were determined using porometer analysis [15].
Multi-factor data were analyzed with linear mixed models using the GLIMMIX procedure of SAS (Version 9.3; SAS Institute, Inc., Cary, NC, USA) by first testing for an interaction between treatment factors (container type and substrate). When there was an interaction between treatment factors, levels of container type were compared within each substrate. Porometer data were analyzed with linear models using the GLIMMIX procedure of SAS. P-values for all simultaneous comparisons were adjusted using the Tukey method to maintain an overall significance level of α = 0.05.

3. Results

3.1. Plant Growth

In the TN study, there was an interaction between container type and substrate for final plant height and height increase (Table 1). Both height and height increase were greatest for plants in the white container for PB:PM. White containers with PB:PM also produced plants with the greatest growth index (final and increase) (Table 2). Overall, plants grown in PB:PM produced more shoot and root dry weight (biomass) compared with plants grown in PB. White and black containers had similar shoot and root dry weight in PB but shoot dry weight was greatest in white containers for PB:PM. In the white container, shoot dry weight and root dry weight were 56% and 68% greater, respectively, for PB:PM compared with PB. In PB, final growth index and increase were similar for plants in black and white containers. Regardless of substrate, however, plants were shortest in the air pruning container.
In the AL study after approximately two months of growth, plant height was similar between the two substrates and among the three types of containers (Table 1). At the end of the study, plant height was greater in PB:PM compared to PB and greatest in the white container (by over 18%). The plant height increase was also greatest in white containers and PB:PM. Plant growth index followed a similar trend with white containers and PB:PM producing larger plants throughout the study and the greatest growth index increase (Table 2). Although the white container with PB:PM tended to produce taller plants, shoot dry weight was similar among all container types in PB:PM and similar between black and white containers in PB. Container type did not have an effect on root dry weight, but root dry weight was 12% greater in PB:PM compared to PB.

3.2. Substrate Chemical and Physical Properties

Substrate pH ranged from 5.3 to 6.4 (TN) and from 5.4 to 6.7 (AL) for all treatments in each study (data not shown), remaining within the recommended range of 4.5 to 6.5 [16] except at 52 DAP in AL. Substrate pH was only 0.3 units lower in PB:PM at 95 and 120 DAP in TN and the addition of PM had no effect on substrate pH in the AL study. Substrate EC varied among treatments in the TN study but no clear trend was observed (data not shown). Conversely, substrate and container type had no effect on substrate EC in the AL study except at 146 DAP with substrate EC being greatest in the black container.
Substrate container capacity increased 12% (TN) and 7% (AL) with the addition of PM compared to PB (Table 3). Substrate air space was greater for PB in the TN study, being reduced by 8% in PB:PM. Substrate air space was similar for substrates in the AL study, and air space was overall lower in PB from AL compared with TN.

3.3. Root Zone Temperature and Volumetric Water Content

Substrate did not have an effect on the percentage of time at or above specific threshold temperatures (38 °C and 46 °C) in either study, but black containers produced the greatest RZT and remained above the critical thresholds far longer than the other container types (Table 4). In TN, RZT in the black container remained above 38° C for over 19% of the time which was 15% and 17% longer than white and air pruning containers, respectively. Although RZT in black containers only remained at or above 46 °C for 0.1% of the time, RZT in air pruning and white containers remained below 46° C throughout the study. In AL, there was an interaction between container type and substrate for a percentage of time at or above 38 °C. Root zone temperature in the black container remained above 38 °C for over 21% of the time (regardless of substrate), over 13% longer than the other container types. Root zone temperature in air pruning and white containers did not reach the 46 °C threshold but RZT in black containers remained at this threshold for nearly 2% of the time.
Volumetric water content was lowest in the air pruning container throughout most of the TN study (Table 5). Volumetric water content was similar for black and white containers in June and July, but black containers had the greatest VWC compared with the other container types in August and September. Substrate also affected VWC, with PB:PM maintaining greater VWC throughout the study. Similar trends were observed for VWC in the AL study, with VWC greater in black containers compared to the air pruning containers and VWC was also greater in PB:PM throughout the study (data not shown).

4. Discussion

Overall, arborvitae grew taller and produced more biomass in white containers with PB:PM. Plants in air pruning containers were smaller than those grown in black or white containers (regardless of substrate), but more growth occurred when PB:PM was used. The air pruning and white containers provided a lower RZT for plants throughout both studies, minimizing heat-related stress which likely led to reduced plant growth in the black container. Maximum RZT (data not shown) was reduced from 5 °C to 8 °C in the air pruning and white containers. Root zone temperature in the black container reached 46 °C (TN) and 51 °C (AL), while RZT in the air pruning and white containers reached a maximum of 41 °C (TN) and 43 °C (AL). These results support previous research documenting increased growth in white containers due to the deleterious effects of supraoptimal RZT. Root zone temperatures can commonly exceed 54 °C in container-grown crops, but RZT near 38 °C can cause indirect injury to plants leading to reduced shoot and root growth, increased water stress, interruption of physiological mechanisms (photosynthesis and respiration, and increased susceptibility to pathogens [3,4,7]. In our study, fewer roots were observed on the south-facing side of the solid wall containers, regardless of container color, suggesting supraoptimal RZT prevents root growth and development near the container sidewall even in light color containers.
Although air pruning containers had lower RZT, plant growth and biomass were consistently lower than plants in white containers. These results contradict previous work by Arnold and McDonald [8] where tree growth of several tree species was similar or superior in the air pruning container compared to the black container. In the present study, black and white containers had a 7% larger volume than the air pruning container which could have attributed to some of the reduced plant growth observed in the air pruning container. The physical design of the air pruning container likely also contributed to the reduced growth. The air pruning container was designed with open slots, aligned longitudinally around the container side wall, to prevent root circling and improve root branching and growth. The slots increase aeration which prevents buildup of heat, resulting in moderated RZT closer to ambient conditions. In air pruning containers, a larger portion of substrate surface is exposed to the outside environment resulting in more rapid drying out due to increased evaporation through solar radiation and air flow. Arnold and McDonald [8] also noted the air pruning container moderated RZT and that plants in the air pruning container dried out sooner. In the present study, VWC was lowest in the air pruning container which limited the amount of plant-available water and likely led to the reduced plant growth. Irrigation volume was calculated based on leaching fraction and applied once daily, thus the substrate in air pruning containers dried more rapidly after irrigation compared with the solid wall containers and likely never reached container capacity. Overall, black and white containers received more irrigation volume (13% and 38%, respectively; data not shown) compared to the air pruning containers corresponding to the observed differences in arborvitae growth. Therefore, growers using air pruning containers should utilize more frequent (cyclic) irrigation to maximize VWC throughout the day and reduce water-related stress especially in substrates with high air-filled porosity and lower water holding capacity.
Peatmoss increased substrate container capacity by up to 12% compared to PB alone resulting in PB:PM having at least 7% greater VWC throughout both studies. On average, plants grown in PB:PM received 90% more irrigation volume compared PB. The combined benefits of greater water retention and irrigation volume corresponded to superior plant growth in PB:PM. Peatmoss has greater container capacity and easily available water compared to PB, likely due to a higher proportion of macropores and a lower proportion of fine particles in PB [17]. The PB and PM for each study were obtained from different sources which led to slight differences in physical properties for each study. Pine bark physical properties can vary due to a number of factors including source, age, and processing method [11]. Nevertheless, the addition of PM provided PB:PM with more plant-available water resulting in overall improved plant growth at both locations.
Peatmoss typically has a lower inherent pH compared to PB. It has been shown that increasing the percentage of PM in PB does not increase cation exchange capacity (and thus nutrient retention) on a volumetric basis [9,18]. Johnson et al. [18] reported an increase in soluble salt level with an increasing proportion of PM in PB substrates despite no increase in CEC. In our studies, PB:PM was composed of 20% PM but substrate pH was not negatively affected and differences in EC between substrates were not observed. However, EC was generally lower for PB:PM in both studies and a lack of significance might be due to sample variation and small sample size (n = 4).
Root zone temperature was not affected by substrate in the present studies, yet substrate porosity and VWC may contribute to the rate of heat buildup and dissipation in a substrate. Amoroso et al. [19] reported RZT was greater in substrates irrigated to 100% container capacity compared to 30% container capacity. In their study, the substrate was composed of 80% PM which typically has smaller particle size and lower air space compared to PB. Martin and Ingram [20] suggested substrates with lower pore space combined with greater VWC (25% to 40%) could dissipate heat more effectively. As a result, substrate temperature would increase at a slower rate and maintain a lower RZT overall. Although PB:PM had greater VWC, there was very little difference in substrate total porosity compared to PB alone which may have minimized thermal dissipation in this study. Plants were irrigated once daily at 12 pm, thus VWC may have been too low during the hottest portion of the day for heat to effectively dissipate. Applying irrigation multiple times throughout the afternoon would increase VWC over a longer period and possibly improve heat dissipation from the substrate.
All the arborvitae plants grown in these studies were marketable, but plants grown in PB:PM grew significantly larger and were visually superior in quality (Figure 1). Plants in PB:PM benefited from overall greater VWC and which remained higher throughout the day compared with PB. Peatmoss is more expensive than PB and requires additional equipment for mixing into the substrate, but the added benefits (water retention and availability) could result in higher quality crops that reach a finished size more quickly. For example, plants in PB:PM were on average larger (height and growth index) than plants in PB that had been grown for 30 additional days (data not shown).
White containers provided lower RZT that likely reduced plant stress resulting in slightly larger and potentially healthier plants. White plastic containers are commercially available from a number of manufacturers in a variety of sizes (up to 11 or 19 L). Modern white containers are high quality and typically manufactured with co-extruded black (interior) and white (exterior) plastic to prevent light diffusion through the container which was a problem with earlier products. Plants grown in air pruning containers tend to have better branched and more vigorous root systems that can improve transplant establishment and subsequent crop quality, but to prevent drying out they will require more frequent irrigation and possibly higher application rates compared with crops in traditional black containers.
The impact of abiotic factors on crop growth has been well documented and developing methods for reducing root zone stress would improve root development, crop quality, and transplant success [21]. The interaction of factors such as container type, substrate, and moisture content must be considered when evaluating alternative production practices. Growers typically use a single substrate/container type for all the different crop species in production. Light-colored containers can effectively reduce RZT which may be especially important in temperature-sensitive species, but we found that using substrates with higher VWC had a greater effect on overall crop growth especially when used in white containers. Although ‘Green Giant’ arborvitae is highly adaptable to soil type and is considered a heat-tolerant plant, we demonstrated increased growth by modifying the substrate and container type. Growers should consider conducting small-scale evaluations to determine if a particular substrate/container combination works in their production system. When conducting small trials, growers should place each substrate/container combination in separate irrigation zones and adjust irrigation volume based on plant needs to ensure moisture is not a limiting factor.

Author Contributions

Conceptualization, A.L.W. and J.M.P.; methodology, A.L.W. and J.M.P.; formal analysis, A.L.W. and E.K.B.; investigation, A.L.W. and J.M.P.; writing—original draft preparation, A.L.W.; writing—review and editing, A.L.W., J.M.P., and E.K.B.; funding acquisition, A.L.W. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported the National Institute of Food and Agriculture (NIFA), United States Department of Agriculture (USDA) Evans-Allen grant, under award number TENX-1519-CCOCP.

Acknowledgments

The authors wish to thank Terry Kirby for assistance with data collection and project maintenance.

Conflicts of Interest

The authors declare no conflicts of interest.

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Figure 1. Representative ‘Green Giant’ arborvitae plants 173 days after planting (in Tennessee) in 100% pine bark (three plants on left) and 4 pine bark: 1 peatmoss (v:v; three plants on right) in standard black, standard white, and air pruning containers (left to right within each substrate).
Figure 1. Representative ‘Green Giant’ arborvitae plants 173 days after planting (in Tennessee) in 100% pine bark (three plants on left) and 4 pine bark: 1 peatmoss (v:v; three plants on right) in standard black, standard white, and air pruning containers (left to right within each substrate).
Horticulturae 06 00022 g001
Table 1. Plant height and height increase (n = 12) of ‘Green Giant’ arborvitae grown in different types of containers and substrates in Tennessee and Alabama.
Table 1. Plant height and height increase (n = 12) of ‘Green Giant’ arborvitae grown in different types of containers and substrates in Tennessee and Alabama.
Plant Height (cm)Plant Height (cm)
69 DAP x173 DAPIncrease w59 DAP166 DAPIncrease
TennesseeAlabama
Significance of treatment factors
Container (C) z 0.0055<0.0001<0.00010.1523<0.0001<0.0001
Substrate (S) y 0.8889<0.0001<0.00010.73280.02670.0053
C by S 0.18170.00060.00030.47440.95440.9757
Least squares means for main effects
SubstrateContainer
Black69.3 ab v--72.1 a78.2 b16.1 b
White71.8 a--72.9 a92.7 a31.3 a
Air66.9 b--69.3 a75.1 b14.0 b
PB 69.4 a--71.2 a79.6 b17.6 b
PB:PM 69.3 a--71.7 a84.4 a23.3 a
Treatment least squares means grouped by substrate
SubstrateContainer
PBBlack67.885.8 a27.3 a70.975.813.4
White72.383.3 a21.8 ab73.990.728.6
Air68.275.0 b14.9 b68.772.310.8
PB:PMBlack70.799.2 b41.0 b73.380.718.8
White71.4114.8 a56.0 a71.894.734.1
Air65.788.2 c32.5 c7077.917.2
z Container type: Black and White—standard solid wall (11.3 L; PF1200; Nursery Supplies Inc., Kissimmee, FL, USA); Air—air pruning (10.5 L; #5 Rediroot; NurserySource Inc., Boring, OR, USA). y Substrate: Pine bark alone (PB) or combined (v:v) with peatmoss (PB:PM; 4 pine bark: 1 peatmoss). x DAP = days after planting. w Increase = final plant height—initial plant height. v When the interaction term in the model is not significant (P > 0.10), main effects means for levels within each treatment factor followed by the same lower-case letter are not significantly different using the Tukey method for multiple comparisons (α = 0.05). When the interaction term in the model is significant (P ≤ 0.10), simple effects means (treatment means for container grouped within substrate) followed by the same lower-case letter are not significantly different using the Tukey method for multiple comparisons (α = 0.05); otherwise, the treatment means are presented without letter groupings for informational purposes.
Table 2. Plant growth index (n = 12), growth index increase and dry weight (shoot and root) of ‘Green Giant’ arborvitae grown in different types of containers and substrates in Tennessee and Alabama.
Table 2. Plant growth index (n = 12), growth index increase and dry weight (shoot and root) of ‘Green Giant’ arborvitae grown in different types of containers and substrates in Tennessee and Alabama.
Growth Index xShoot Dry wt (g)Root Dry wt (g)Growth IndexShoot Dry wt (g)Root Dry wt (g)
69 DAP w173 DAPIncrease v 59 DAP166 DAPIncrease
TennesseeAlabama
Significance of treatment factors
Container (C) z 0.005<0.0001<0.0001<0.00010.00840.55<0.0001<0.00010.00020.3203
Substrate (S) y 0.6342<0.0001<0.0001<0.0001<0.00010.02190.00020.0025<0.00010.0452
C by S 0.43620.0002<0.0001<0.00010.03320.76460.62230.74240.04970.2689
Least squares means for main effects
SubstrateContainer
Black56.5 abu----52.3 a56.9 b15.2 b-507 a
White58.1 a----53.0 a63.3 a22.4 a-560 a
Air54.4 b----51.7 a55.2 b13.8 b-534 a
PB 56.1 a----51.3 b56.3 b15.3 b-503 b
PB:PM 56.5 a----53.4 a60.7 a19.0 a-564 a
Treatment least squares means grouped by substrate
SubstrateContainer
PBBlack56.568.9 a26.6 a330 a629 a51.355.112.8162 a508.5
White58.468.4 a25.1 a299 a487 ab52.361.521170 a506.5
Air53.461.9 b21.4 b191 b366 b50.252.212120 b494
PB:PMBlack56.474.9 b33.5 b383 b698 a53.458.817.7195 a504.5
White57.883.8 a42.2 a466 a820 a53.765.123.7201 a614
Air55.472.6 b31.8 b361 b653 a53.358.115.5186 a574
z Container type: Black and White—standard solid wall (11.3 L; PF1200; Nursery Supplies Inc., Kissimmee, FL); Air—air pruning (10.5 L; #5 Rediroot; NurserySource Inc., Boring, OR). y Substrate: Pine bark alone (PB) or combined (v:v) with peatmoss (PB:PM; 4 pine bark: 1 peatmoss). x Growth index = (height + width at widest point + perpendicular width) / 3. w DAP = days after planting. v Increase = final growth index—initial growth index. u When the interaction term in the model is not significant (P > 0.10), main effects means for levels within each treatment factor followed by the same lower-case letter are not significantly different using the Tukey method for multiple comparisons (α = 0.05). When the interaction term in the model is significant (P ≤ 0.10), simple effects means (treatment means for container grouped within substrate) followed by the same lower-case letter are not significantly different using the Tukey method for multiple comparisons (α = 0.05); otherwise, the treatment means are presented without letter groupings for informational purposes.
Table 3. Physical properties (n = 3) of substrates for production of ‘Green Giant’ arborvitae in Tennessee and Alabama.
Table 3. Physical properties (n = 3) of substrates for production of ‘Green Giant’ arborvitae in Tennessee and Alabama.
Substrate zAir Space yContainer CapacityTotal PorosityBulk Density
(% volume)(g·cm−3)
Tennessee
PB30.4 a x42.8 b73.2 a0.233 a
PB:PM21.8 b54.7 a76.5 a0.226 a
Alabama
PB25.4 a41.1 b66.6 a0.267 a
PB:PM21.7 a48.9 a70.6 a0.259 a
z Substrate: Pine bark alone (PB) or combined (v:v) with peatmoss (PB:PM; 4 pine bark: 1 peatmoss). y Data obtained using the North Carolina State University porometer method (Fonteno and Harden, 2010). x Means followed by the same letter within a location are not significantly different (α = 0.05).
Table 4. Percent of time (n = 3) substrate temperature remained at or above critical thresholds (38 °C and 46 °C) during daylight hours for ‘Green Giant’ arborvitae grown in different types of containers and substrates in Tennessee and Alabama.
Table 4. Percent of time (n = 3) substrate temperature remained at or above critical thresholds (38 °C and 46 °C) during daylight hours for ‘Green Giant’ arborvitae grown in different types of containers and substrates in Tennessee and Alabama.
38 °C (%)46 °C (%)38 °C (%)46 °C (%)
TennesseeAlabama
Significance of treatment factors
Container (C) z <0.00010.0221<0.0001<0.0001
Substrate (S) y 0.52290.51440.71820.6128
C by S 0.3970.58640.0470.6464
Least squares means for main effects
SubstrateContainer
Black19.4 a x0.1 a-1.93 a
White4.2 b0.0 b-0.00 b
Air2.7 b0.0 b-0.00 b
PB 7.9 a0.0 a-0.85 a
PB:PM 8.3 a0.0 a-0.43 a
Treatment least squares means grouped by substrate
SubstrateContainer
PBBlack20.20.024.2 a2.5
White5.10.08.4 b0.0
Air2.50.05.5 c0.0
PB:PMBlack18.80.121.6 a1.3
White3.20.07.2 b0.0
Air2.90.07.8 b0.0
z Container type: Black and White—standard solid wall (11.3 L; PF1200; Nursery Supplies Inc., Kissimmee, FL); Air—air pruning (10.5 L; #5 Rediroot; NurserySource Inc., Boring, OR). y Substrate: Pine bark alone (PB) or combined (v:v) with peatmoss (PB:PM; 4 pine bark: 1 peatmoss). x When the interaction term in the model is not significant (P > 0.10), main effects means for levels within each treatment factor followed by the same lower-case letter are not significantly different using the Tukey method for multiple comparisons (α = 0.05). When the interaction term in the model is significant (P ≤ 0.10), simple effects means (treatment means for container grouped within substrate) followed by the same lower-case letter are not significantly different using the Tukey method for multiple comparisons (α = 0.05); otherwise, the treatment means are presented without letter groupings for informational purposes.
Table 5. Average daytime volumetric water content (n = 3) over a four-month period for ‘Green Giant’ arborvitae grown in different types of containers and substrates in Tennessee.
Table 5. Average daytime volumetric water content (n = 3) over a four-month period for ‘Green Giant’ arborvitae grown in different types of containers and substrates in Tennessee.
Volumetric Water Content (m3·m−3)
JuneJulyAugustSeptember
Significance of treatment factors
Container (C)z 0.02740.00440.00060.0007
Substrate (S)y 0.00210.02260.01760.0183
C by S 0.01750.24210.74090.2288
Least squares means for main effects
SubstrateContainer
Black-0.314 a x0.320 a0.312 a
White-0.274 a0.220 b0.201 b
Air-0.178 b0.131 c0.139 c
PB -0.214 b0.180 b0.176 b
PB:PM -0.283 a0.247 a0.240 a
Treatment least squares means grouped by substrate
SubstrateContainer
PBBlack0.270 a0.2830.30.307
White0.319 a0.2660.1870.159
Air0.152 b0.1170.0930.105
PB:PMBlack0.367 a0.3460.3410.316
White0.323 a0.2860.2690.265
Air0.342 a0.2380.1690.173
z Container type: Black and White—standard solid wall (11.3 L; PF1200; Nursery Supplies Inc., Kissimmee, FL, USA); Air—air pruning (10.5 L; #5 Rediroot; NurserySource Inc., Boring, OR, USA). y Substrate: Pine bark alone (PB) or combined (v:v) with peatmoss (PB:PM; 4 pine bark: 1 peatmoss). x When the interaction term in the model is not significant (P > 0.10), main effects means for levels within each treatment factor followed by the same lower-case letter are not significantly different using the Tukey method for multiple comparisons (α = 0.05). When the interaction term in the model is significant (P ≤ 0.10), simple effects means (treatment means for container grouped within substrate) followed by the same lower-case letter are not significantly different using the Tukey method for multiple comparisons (α = 0.05); otherwise, the treatment means are presented without letter groupings for informational purposes.

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MDPI and ACS Style

Witcher, A.L.; Pickens, J.M.; Blythe, E.K. Container Type and Substrate Affect Root Zone Temperature and Growth of ‘Green Giant’ Arborvitae. Horticulturae 2020, 6, 22. https://doi.org/10.3390/horticulturae6020022

AMA Style

Witcher AL, Pickens JM, Blythe EK. Container Type and Substrate Affect Root Zone Temperature and Growth of ‘Green Giant’ Arborvitae. Horticulturae. 2020; 6(2):22. https://doi.org/10.3390/horticulturae6020022

Chicago/Turabian Style

Witcher, Anthony L., Jeremy M. Pickens, and Eugene K. Blythe. 2020. "Container Type and Substrate Affect Root Zone Temperature and Growth of ‘Green Giant’ Arborvitae" Horticulturae 6, no. 2: 22. https://doi.org/10.3390/horticulturae6020022

APA Style

Witcher, A. L., Pickens, J. M., & Blythe, E. K. (2020). Container Type and Substrate Affect Root Zone Temperature and Growth of ‘Green Giant’ Arborvitae. Horticulturae, 6(2), 22. https://doi.org/10.3390/horticulturae6020022

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