Clonal architecture of Salix setchelliana (gravel bar willow) in Alaska

1991 ◽  
Vol 69 (3) ◽  
pp. 590-596 ◽  
Author(s):  
D. A. Douglas

Clones of Salix setchelliana were excavated to describe the architecture of this prostrate clonal species and to determine if there are architectural parameters or clonal growth forms that vary with clonal age. The species' gravel-bar habitat, a mosaic of previous river channels, is unpredictable in time and variable in space. Clones are composed of vertical shoots connected by horizontal roots. Because clones expand by peripheral growth of their root systems, the six studied clones could be placed in order of apparent increasing age, primarily on the basis of size. Substrate was removed by hand and the horizontal root systems mapped. Data on shoots, root branch angles, and root peripheral growing points were recorded. Several density parameters were calculated and examined for trends along the sequence of apparent increasing clonal age. Most measures of shoot density increased along this sequence, as did horizontal root system density and the linear density of horizontal root system branching points. Clones appear to change in time from a "guerrilla" growth form of environmental exploration to more of a "battalion" growth form with increased branching of the underground system. Key words: willow, clonal, architecture, Alaska, Salix.

1975 ◽  
Vol 5 (4) ◽  
pp. 608-625 ◽  
Author(s):  
D. C. F. Fayle

The patterns of ring width throughout the root systems and stems of several 32- to 36-year-old, plantation-grown red pine were analyzed. All root systems showed a basic similarity in their radial sequences of ring width. Within a root system, individual sequences ranged from those similar to the radial sequence at the stem base to ones apparently dissimilar. At the stem–root base, the increasing distance to the tree crown with time and changes in mechanical stresses with increasing tree size appeared to play major roles in the development of the basic pattern. The position and type of root, the environment of its apices, and changes in the transportation pathways in the xylem and phloem at branching points may all have influenced the pattern in individual roots. The pattern of deposition of xylem at branching points was visualized as an interaction between the stream of growth regulators and assimilates towards the root tips and the stream of xylem water (and (or) dissolved substances) towards the root base. Discontinuities in the growth layers did not occur in the stem but increased with time in the roots, particularly in the surface horizontal roots. Moisture availability modified the radial sequence patterns and probably influenced the shifts in longitudinal distribution of radial increment from year to year within and between the stem and the root system. The maximum current annual increment in root wood volume occurred before that in the stem.


2021 ◽  
Vol 31 (3) ◽  
Author(s):  
Pierre-Philippe Dechant

AbstractRecent work has shown that every 3D root system allows the construction of a corresponding 4D root system via an ‘induction theorem’. In this paper, we look at the icosahedral case of $$H_3\rightarrow H_4$$ H 3 → H 4 in detail and perform the calculations explicitly. Clifford algebra is used to perform group theoretic calculations based on the versor theorem and the Cartan–Dieudonné theorem, giving a simple construction of the $${\mathrm {Pin}}$$ Pin and $${\mathrm {Spin}}$$ Spin covers. Using this connection with $$H_3$$ H 3 via the induction theorem sheds light on geometric aspects of the $$H_4$$ H 4 root system (the 600-cell) as well as other related polytopes and their symmetries, such as the famous Grand Antiprism and the snub 24-cell. The uniform construction of root systems from 3D and the uniform procedure of splitting root systems with respect to subrootsystems into separate invariant sets allows further systematic insight into the underlying geometry. All calculations are performed in the even subalgebra of $${\mathrm {Cl}}(3)$$ Cl ( 3 ) , including the construction of the Coxeter plane, which is used for visualising the complementary pairs of invariant polytopes, and are shared as supplementary computational work sheets. This approach therefore constitutes a more systematic and general way of performing calculations concerning groups, in particular reflection groups and root systems, in a Clifford algebraic framework.


1994 ◽  
Vol 37 (3) ◽  
pp. 338-345 ◽  
Author(s):  
D. Ž. Doković ◽  
P. Check ◽  
J.-Y. Hée

AbstractLet R be a root system (in the sense of Bourbaki) in a finite dimensional real inner product space V. A subset P ⊂ R is closed if α, β ∊ P and α + β ∊ R imply that α + β ∊ P. In this paper we shall classify, up to conjugacy by the Weyl group W of R, all closed sets P ⊂ R such that R\P is also closed. We also show that if θ:R —> R′ is a bijection between two root systems such that both θ and θ-1 preserve closed sets, and if R has at most one irreducible component of type A1, then θ is an isomorphism of root systems.


1975 ◽  
Vol 5 (1) ◽  
pp. 109-121 ◽  
Author(s):  
D. C. F. Fayle

Extension of the root system and stem during the first 30 years of growth of plantation-grown red pine (Pinusresinosa Ait.) on four sites was deduced by root and stem analyses. Maximum rooting depth was reached in the first decade and maximum horizontal extension of roots was virtually complete between years 15 and 20. The main horizontal roots of red pine seldom exceed 11 m in length. Elongation of vertical and horizontal roots was examined in relation to moisture availability and some physical soil conditions. The changing relations within the tree in lineal dimensions and annual elongation of the roots and stem are illustrated. The development of intertree competition above and below ground is considered.


1975 ◽  
Vol 5 (2) ◽  
pp. 171-175 ◽  
Author(s):  
Hugh E. Wilcox ◽  
Ruth Ganmore-Neumann

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.


2010 ◽  
Vol 36 (4) ◽  
pp. 149-159
Author(s):  
Susan Day ◽  
P. Eric Wiseman ◽  
Sarah Dickinson ◽  
J. Roger Harris

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.


Weed Science ◽  
1999 ◽  
Vol 47 (1) ◽  
pp. 28-36
Author(s):  
Hwei-Yiing Li ◽  
Chester L. Foy

The mode of action of BAS 517 in a susceptible plant species, corn, was investigated using an excised root system and14C-tracer techniques. The root system of a tolerant species, soybean, was used for comparison. When UL-14C- glucose was used as a precursor,14C incorporation into lipids was reduced in BAS 517-treated corn roots, although14C incorporation from UL-14C-glucose into lipids was relatively low. Inhibition of14C incorporation into water-soluble compounds was not definite because of a high degree of variability. Using14C-acetate as a precursor, 49, 43, and 34% of the recovered radioactivity was found in the lipid fractions of root tips treated with 0, 1.0, and 10 μM BAS 517, respectively. In nontreated soybean root tips, 47% of the recovered radioactivity was found in the lipid fraction compared to 49% in root tips treated with 10 μM BAS 517. Further analysis of lipids showed that BAS 517 inhibited the incorporation of14C from14C-acetate into phosphatidylethanolamine, a phospholipid, whereas the labeling of sterols in treated corn roots was not adversely affected. Acetyl CoA carboxylase extracted from root systems of corn and soybean showed different sensitivity to BAS 517, suggesting its role as the herbicide target site and as a basis for the selectivity.


2019 ◽  
Vol 2 (1) ◽  
Author(s):  
Félicien Meunier ◽  
Adrien Heymans ◽  
Xavier Draye ◽  
Valentin Couvreur ◽  
Mathieu Javaux ◽  
...  

Abstract Functional-structural root system models combine functional and structural root traits to represent the growth and development of root systems. In general, they are characterized by a large number of growth, architectural and functional root parameters, generating contrasted root systems evolving in a highly non-linear environment (soil, atmosphere), which makes the link between local traits and functioning unclear. On the other end of the root system modelling continuum, macroscopic root system models associate to each root system a set of plant-scale, easily interpretable parameters. However, as of today, it is unclear how these macroscopic parameters relate to root-scale traits and whether the upscaling of local root traits is compatible with macroscopic parameter measurements. The aim of this study was to bridge the gap between these two modelling approaches. We describe here the MAize Root System Hydraulic Architecture soLver (MARSHAL), a new efficient and user-friendly computational tool that couples a root architecture model (CRootBox) with fast and accurate algorithms of water flow through hydraulic architectures and plant-scale parameter calculations. To illustrate the tool’s potential, we generated contrasted maize hydraulic architectures that we compared with root system architectural and hydraulic observations. Observed variability of these traits was well captured by model ensemble runs. We also analysed the multivariate sensitivity of mature root system conductance, mean depth of uptake, root system volume and convex hull to the input parameters to highlight the key model parameters to vary for virtual breeding. It is available as an R package, an RMarkdown pipeline and a web application.


2018 ◽  
Vol 28 (5) ◽  
pp. 629-636 ◽  
Author(s):  
Matthew B. Bertucci ◽  
David H. Suchoff ◽  
Katherine M. Jennings ◽  
David W. Monks ◽  
Christopher C. Gunter ◽  
...  

Grafting of watermelon (Citrullus lanatus) is an established production practice that provides resistance to soilborne diseases or tolerance to abiotic stresses. Watermelon may be grafted on several cucurbit species (interspecific grafting); however, little research exists to describe root systems of these diverse rootstocks. A greenhouse study was conducted to compare root system morphology of nine commercially available cucurbit rootstocks, representing four species: pumpkin (Cucurbita maxima), squash (Cucurbita pepo), bottle gourd (Lagenaria siceraria), and an interspecific hybrid squash (C. maxima × C. moschata). Rootstocks were grafted with a triploid watermelon scion (‘Exclamation’), and root systems were compared with nongrafted (NG) and self-grafted (SG) ‘Exclamation’. Plants were harvested destructively at 1, 2, and 3 weeks after transplant (WAT), and data were collected on scion dry weight, total root length (TRL), average root diameter, root surface area, root:shoot dry-weight ratio, root diameter class proportions, and specific root length. For all response variables, the main effect of rootstock and rootstock species was significant (P < 0.05). The main effect of harvest was significant (P < 0.05) for all response variables, with the exception of TRL proportion in diameter class 2. ‘Ferro’ rootstock produced the largest TRL and root surface area, with observed values 122% and 120% greater than the smallest root system (‘Exclamation’ SG), respectively. Among rootstock species, pumpkin produced the largest TRL and root surface area, with observed values 100% and 82% greater than those of watermelon, respectively. These results demonstrate that substantial differences exist during the initial 3 WAT in root system morphology of rootstocks and rootstock species available for watermelon grafting and that morphologic differences of root systems can be characterized using image analysis.


2007 ◽  
Vol 55 (7) ◽  
pp. 749 ◽  
Author(s):  
Alexandre Antonio Alonso ◽  
Silvia Rodrigues Machado

Brazilian cerrado, a neotropical savanna, is characterised by a strongly seasonal climate with distinctive wet and dry seasons, and deep and well drained soils that are acidic and with high aluminium content. Recurrent fires in the dry season place additional stress on the survival of plants, which exhibit an array of strategies of survival. The purpose of this work was to study the underground system of Erythroxylum nanum A.St-Hil. and E. campestre A.St-Hil., two sub-shrubby species, and E. tortuosum Mart., a shrubby species, verifying the possible relationship between the morphology of the underground organs and the resprouting ability of these plants. Anatomical analyses followed the usual techniques of plant anatomy. The cotyledons of the three species were green, foliaceous and photosynthesising. The two sub-shrubby species (Erythroxylum nanum and E. campestre) showed slow development of the aerial shoot system and extensive growth of the primary root in the initial stage of development. E. tortuosum presented the most pronounced development of the aerial system and a poorly developed primary root compared with the sub-shrubby species. The sub-shrubby species occurred in clumps and had underground systems interlinked, consisting of a deep axial primary root system besides soboles in E. nanum and xylopodium in E. campestre. Plants of the E. tortuosum were isolated, highly branched and their underground system consisted of a superficial primary root system. Abundance of reserves and the bud-forming potential of the soboles, xylopodium and roots resulted in production of vigorous branches that are highly valuable in the regeneration of the aerial biomass following fire or seasonal dry in cerrado.


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