Effects of Irrigation Rate and Media on Growth of Acer rubrum L. in Large Containers

1989 ◽  
Vol 7 (1) ◽  
pp. 38-40
Author(s):  
Chris A. Martin ◽  
Harry G. Ponder ◽  
Charles H. Gilliam
Keyword(s):  
Root Growth ◽  
Root System ◽  
Irrigation System ◽  
Acer Rubrum ◽  
Height Growth ◽  
Sand Content ◽  
Secondary Root ◽  
Irrigation Rate ◽  
Media Types ◽  
Second Year

Abstract Acer rubrum L. seedlings were grown in 38 1 (# 10) containers with 4 irrigation rates of 50%, 100%, 200%, 400% replacement of net evaporation and 3 media types of 100% pine bark; pine bark:sand (4:1 by vol); pine bark:sand (3:2 by vol). A spray stake irrigation system was used to irrigate. Height growth was not affected by irrigation rate. Caliper growth increased cubicly and linearly with increased irrigation rate during the first and second years, respectively. Media affected height and caliper growth the second year only. Height and caliper growth increased linearly with increased sand content. An increase in irrigation rate produced a larger root system, while an increase in sand content increased primary and secondary root growth.

scholarly journals Root and Shoot Growth Periodicity of Pot-in-Pot Red and Sugar Maple

1999 ◽  
Vol 17 (2) ◽  
pp. 80-83 ◽  
Author(s):  
J. Roger Harris ◽  
Jody Fanelli
Keyword(s):  
Root Growth ◽  
Acer Saccharum ◽  
Sugar Maple ◽  
Acer Rubrum ◽  
Shoot Elongation ◽  
Red Maple ◽  
Sugar Maples ◽  
Root And Shoot Growth ◽  
Second Year ◽  
Substrate Temperatures

Abstract Red maple (Acer rubrum L. ‘Franksred’) and sugar maple (Acer saccharum Marsh. ‘Green Mountain’) trees were grown in a 56 liter (15 gal) pot-in-pot system for two years. During the second year of production, root growth was observed through observation plates fitted into the container sidewalls, and shoot extension was periodically measured. Root growth began in early March, approximately one month before budbreak for both species. Root growth dramatically slowed down at the onset of budbreak, but quickly resumed and was concurrent with shoot elongation. Root growth slowed dramatically in the fall when substrate temperatures dropped to 5–7C (40–45F). Root growth stopped during the winter for red maple, but some nominal root growth continued throughout the winter for sugar maple. Red maples had over 5 times more total root length against observation plates at the end of the experiment than sugar maples.

scholarly journals Seasonal Effects of Transplanting on Growth and Pre-bud Break Root System Regeneration of Northern Red Oak and Willow Oak

HortScience ◽  
2004 ◽  
Vol 39 (4) ◽  
pp. 884C-884
Author(s):  
Lisa Richardson-Calfee ◽  
J. Roger Harris* ◽  
Jody Fanelli
Keyword(s):  
Root Growth ◽  
Root System ◽  
Early Spring ◽  
Height Growth ◽  
Seasonal Effects ◽  
Late Winter ◽  
Red Oak ◽  
Bud Break ◽  
Northern Red Oak ◽  
Trunk Diameter

Seasonal effects on transplant establishment of balled-and-burlapped (B&B) shade trees are not well documented. Early post-transplant root growth and above-ground growth over 3 years were therefore documented for November- and March-transplanted northern red oak (Quercus rubra L.) and willow oak (Q. phellos L.). Survival of red oak was 100% for both treatments. Survival of November- and March-transplanted willow oak was 67% and 83%, respectively. No new root growth was observed outside or within the root balls of either species upon excavation in January. However, new root growth was evident when subsamples were excavated the following April for November-transplanted trees of both species, indicating that root system regeneration of November-transplanted trees occurs in late winter and/or early spring, not late fall and/or early winter. November-transplanted red oak, but not willow oak, had grown more roots by spring bud break than March-transplanted trees. While height growth of willow oak was nearly identical between treatments after 3 years, November-transplants exhibited greater trunk diameter increase for all 3 years. Overall, season of transplant had little effect on height and trunk diameter increase of red oak, even though November-transplanted trees grew more roots prior to the first bud break following transplant. Among the willow oaks that survived, season of transplanting had little effect on height growth, but November transplanting resulted in greater trunk diameter increase. However, considering the mortality rate of November-transplanted willow oak, March may be a better time to transplant willow oak in climates similar to southwest Virginia.

Root System Fibrosity of Sitka Spruce Transplants: Relationship with Root Growth Potential

1990 ◽  
Vol 63 (1) ◽  
pp. 1-7 ◽  
Author(s):  
J. D. DEANS ◽  
C. LUNDBERG ◽  
M. G. R. CANNELL ◽  
M. B. MURRAY ◽  
L. J. SHEPPARD
Keyword(s):  
Root Growth ◽  
Root System ◽  
Sitka Spruce ◽  
Growth Potential ◽  
Root Growth Potential

Effects of Temperature on Root Morphology and Ectendomycorrhizal Development in Pinusresinosa Ait.

1975 ◽  
Vol 5 (2) ◽  
pp. 171-175 ◽  
Author(s):  
Hugh E. Wilcox ◽  
Ruth Ganmore-Neumann
Keyword(s):  
Root Growth ◽  
Root System ◽  
Root Morphology ◽  
Root Systems ◽  
Second Order ◽  
Root Temperature ◽  
First Order ◽  
Effects Of Temperature

Seedlings of Pinusresinosa were grown at root temperatures of 16, 21 and 27 °C, both aseptically and after inoculation with the ectendomycorrhizal fungus BDG-58. Growth after 3 months was significantly influenced by the presence of the fungus at all 3 temperatures. The influence of the fungus on root growth was obscured by the effects of root temperature on morphology. The root system at 16 and at 21 °C possessed many first-order laterals with numerous, well developed second-order branches, but those at 27 °C had only a few, relatively long, unbranched first-order laterals. Although the root systems of infected seedlings were larger, the fungus increased root growth in the same pattern as determined by the temperature.

scholarly journals Regulation of lateral root development by shoot-sensed far-red light via HY5 is nitrate-dependent and involves the NRT2.1 nitrate transporter

2021 ◽  
Author(s):  
Kasper van Gelderen ◽  
Chiakai Kang ◽  
Peijin Li ◽  
Ronald Pierik
Keyword(s):  
Root Growth ◽  
Root System ◽  
Lateral Root ◽  
Environmental Changes ◽  
Red Light ◽  
Agar Plate ◽  
Nitrate Transporter ◽  
Loss Of Function ◽  
Lateral Root Development ◽  
Nitrate Signaling

AbstractPlants are very effective in responding to environmental changes during competition for light and nutrients. Low Red:Far-Red (low R:FR)-mediated neighbor detection allows plants to compete successfully with other plants for available light. This above-ground signal can also reduce lateral root growth by inhibiting lateral root emergence, a process that might help the plant invest resources in shoot growth. Nitrate is an essential nutrient for plant growth and Arabidopsis thaliana responds to low nitrate conditions by enhancing nutrient uptake and reducing lateral and main root growth. There are indications that low R:FR signaling and low nitrate signaling can affect each other. It is unknown which response is prioritized when low R:FR light- and low nitrate signaling co-occur. We investigated the effect of low nitrate conditions on the low R:FR response of the A. thaliana root system in agar plate media, combined with the application of supplemental Far-Red (FR) light to the shoot. We observed that under low nitrate conditions main and lateral root growth was reduced, but more importantly, that the response of the root system to low R:FR was suppressed. Consistently, a loss-of-function mutant of a nitrate transporter gene NRT2.1 lacked low R:FR-induced lateral root reduction and its root growth was hypersensitive to low nitrate. ELONGATED HYPOCOTYL5 (HY5) plays an important role in the root response to low R:FR and we found that it was less sensitive to low nitrate conditions with regards to lateral root growth. In addition, we found that low R:FR increases NRT2.1 expression and that low nitrate enhances HY5 expression. HY5 also affects NRT2.1 expression, however, it depended on the presence of ammonium in which direction this effect was. Replacing part of the nitrogen source with ammonium also removed the effect of low R:FR on the root system, showing that changes in nitrogen sources can be crucial for root plasticity. Together our results show that nitrate signaling can repress low R:FR responses and that this involves signaling via HY5 and NRT2.1.

scholarly journals Contemporary Concepts of Root System Architecture of Urban Trees

2010 ◽  
Vol 36 (4) ◽  
pp. 149-159
Author(s):  
Susan Day ◽  
P. Eric Wiseman ◽  
Sarah Dickinson ◽  
J. Roger Harris
Keyword(s):  
Built Environment ◽  
Root Growth ◽  
Root System ◽  
Root Architecture ◽  
Root Systems ◽  
Growth Patterns ◽  
Urban Trees ◽  
Rooting Depth ◽  
Similar Species ◽  
Urban Settings

Knowledge of the extent and distribution of tree root systems is essential for managing trees in the built environment. Despite recent advances in root detection tools, published research on tree root architecture in urban settings has been limited and only partially synthesized. Root growth patterns of urban trees may differ considerably from similar species in forested or agricultural environments. This paper reviews literature documenting tree root growth in urban settings as well as literature addressing root architecture in nonurban settings that may contribute to present understanding of tree roots in built environments. Although tree species may have the genetic potential for generating deep root systems (>2 m), rooting depth in urban situations is frequently restricted by impenetrable or inhospitable soil layers or by underground infrastructure. Lateral root extent is likewise subject to restriction by dense soils under hardscape or by absence of irrigation in dry areas. By combining results of numerous studies, the authors of this paper estimated the radius of an unrestricted root system initially increases at a rate of approximately 38 to 1, compared to trunk diameter; however, this ratio likely considerably declines as trees mature. Roots are often irregularly distributed around the tree and may be influenced by cardinal direction, terrain, tree lean, or obstacles in the built environment. Buttress roots, tap roots, and other root types are also discussed.

scholarly journals Preliminary Evaluation of Olive (Olea europaea L.) Cultivars under Hot and Arid Environment of Mexico

2019 ◽  
pp. 1-7
Author(s):  
Raúl Leonel Grijalva-Contreras ◽  
Rubén Macías-Duarte ◽  
Arturo López-Carvajal ◽  
Fabián Robles-Contreras ◽  
Manuel De Jesús Valenzuela-Ruiz ◽  
...  
Keyword(s):  
Oil Content ◽  
Irrigation System ◽  
Block Design ◽  
Arid Environment ◽  
Preliminary Evaluation ◽  
National Research Institute ◽  
Agronomic Management ◽  
Randomized Complete Block Design ◽  
Olive Cultivars ◽  
Second Year

Currently in Mexico there are few studies on agronomic management in olive production. The objective of this experiment was to evaluate eleven olive cultivars for table and oil production (Arbequina, Koroneiki, Arbosana, Kalamata, Barnea, Pendolino, Empeltre, Manzanilla of Sevilla, Carboncella, Frantoio and Cassaliva) under hot and arid environment of Mexico. The experiment was carried out during two consecutive years in 2015 and 2016 at National Research Institute for Forestry, Agriculture and Livestock (INIFAP) in the Experimental Station of Caborca, Sonora, Mexico. The plantation was done on March, 2012 using a density of 100 trees ha-1 (10 x 10 m) under drip irrigation system. The parameters evaluated were vegetative parameters, yield, fruit quality and oil content. The experiment was analyzed using a randomized complete block design and five replications. The results showed statistical differences for all parameters evaluated. Arbequina obtained the highest olive yield with 34.5 and 70.3 kg per tree for the first and second year production, respectively and Barnea recorded the highest oil content with 19.2%. Finally, Manzanilla of Sevilla and Barnea varieties represent a good option as double-purpose varieties.   

scholarly journals Imaging local soil kinematics during the first days of maize root growth in sand

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Floriana Anselmucci ◽  
Edward Andò ◽  
Gioacchino Viggiani ◽  
Nicolas Lenoir ◽  
Chloé Arson ◽  
...  
Keyword(s):  
Plant Growth ◽  
Root Growth ◽  
Shear Strain ◽  
Root System ◽  
Capillary Rise ◽  
Image Correlation ◽  
Root Tip ◽  
Soil System ◽  
Local Soil ◽  
Initial Soil

AbstractMaize seedlings are grown in Hostun sand with two different gradings and two different densities. The root-soil system is imaged daily for the first 8 days of plant growth with X-ray computed tomography. Segmentation, skeletonisation and digital image correlation techniques are used to analyse the evolution of the root system architecture, the displacement fields and the local strain fields due to plant growth in the soil. It is found that root thickness and root length density do not depend on the initial soil configuration. However, the depth of the root tip is strongly influenced by the initial soil density, and the number of laterals is impacted by grain size, which controls pore size, capillary rise and thus root access to water. Consequently, shorter root axes are observed in denser sand and fewer second order roots are observed in coarser sands. In all soil configurations tested, root growth induces shear strain in the soil around the root system, and locally, in the vicinity of the first order roots axis. Root-induced shear is accompanied by dilative volumetric strain close to the root body. Further away, the soil experiences dilation in denser sand and compaction in looser sand. These results suggest that the increase of porosity close to the roots can be caused by a mix of shear strain and steric exclusion.

Root Morphology and Secretion of two subtropical tree species to NH4+-N and NO3–-N Deposition

2020 ◽  
Author(s):  
Rui Zhang ◽  
Yi Wang ◽  
Zhichun Zhou
Keyword(s):  
Root Growth ◽  
Root System ◽  
Root Morphology ◽  
Tree Species ◽  
Southern China ◽  
N Deposition ◽  
Fibrous Root ◽  
Nitrogen And Phosphorus ◽  
Root Absorption ◽  
Tap Root

Abstract Background: Both NH4+ and NO3– are capable of greatly influencing plants’ growth and biomass. However, the belowground responses of subtropical trees to either NH4+ or NO3– deposition remain poorly understood. Here, we discuss how these two forms of N deposition can affect root development, and experimentally analyzed how they could impact nitrogen and phosphorus absorption in two types (broadleaved with a fibrous root system vs. conifer with a tap root system) of subtropical tree species. Results: In a greenhouse in southern China, 1-year-old S. superba and P. massoniana seedlings grown on P-limited and P-normal soil were treated with NaNO3 and NH4Cl solutions of 0, 80, and 200 kg N ha–1 year–1, corresponding to the control, N80, and N200 groups, respectively. Root phenotype characteristics and metabolism ability were measured after 8 months of growth. The results showed that the root morphology and physiology variables differed significantly between the two species under different N and P treatments. Although S. superba had a larger quantity of roots than P. massoniana, both its root growth rate and root absorption were respectively lower and weaker. N addition differentially affected root growth and activity as follows: (1) NO3–-N80 and NH4+-N80 increased root growth and activity of the two species, but NH4+-N80 led to thicker roots in S. superba; (2) NO3–-N200 and NH4+-N200 had inhibitory effects on the roots of P. massoniana, for which NH4+-N200 led to thinner and longer roots and even the death of some roots; and (3) NH4+-N could promote metabolic activity in thicker roots (> 1.5 mm) and the NO3–-N was found to stimulate activity in thinner roots (0.5–1.5 mm) in the fibrous root system having a larger quantity of roots, namely S. superba. By contrast, NO3–-N and NH4+-N had an opposite influence upon functioning in the tap root system with a slender root, namely P. massoniana. Conclusion: We conclude P. massoniana has a much higher root absorption efficiency; however, nitrogen deposition is more beneficial to the root growth of S. superba.

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