scholarly journals Mini-rhizotrons transparents pour l'étude du système racinaire de jeunes plantes. Application à la caractérisation du développement racinaire de jeunes chênes (Quercus robur)

1992 ◽  
Vol 70 (9) ◽  
pp. 1840-1847 ◽  
Author(s):  
Loïc Pages

A new type of root-observation box is described, which allows continuous observations on entire growing root systems of young plants. Each root-observation box consists of two transparent plastic plates separated by a few millimetres. On the internal face of each plate, a sheet of transparent filter paper is fixed, which allows absorption and distribution of water and nutrients to the root system. The root system can grow between these two plates, the roots growing on either one face or the other. Thus, the entire root system can be observed continuously. It is easy to manipulate it experimentally. The root-observation boxes are placed away from the light into a container. As an example, and to show the suitability of the method, we studied the development of the root system of young oak seedlings (Quercus robur L.). We compared their architectural characteristics with those described by different authors who have used other methods. The specific interests of this new method are emphasized. Key words: root, morphogenesis, rhizotron, root observation box, growth, development, Quercus robur.

1996 ◽  
Vol 74 (12) ◽  
pp. 1910-1918 ◽  
Author(s):  
Yannick Le Roux ◽  
Loïc Pagès

To describe the different types of geotropic reactions of hevea (Hevea brasiliensis), young seedlings were cultivated in root observation boxes and submitted to a double gravistimulation (90° rotation of the minirhizotrons in the vertical plane). It was demonstrated that the taproot is a strongly orthogeotropie organ since it resumed rapidly its prestimulation vertical position. Morphological and morphogenetic modifications were associated with the geotropic response: reduced speed of growth coupled with a reduction of the apical diameter as well as an alteration of ramification density in the curving zone and the following one. Early secondary roots showed a somewhat reduced orthogeotropism that was weaker as the growth direction before gravistimulation was more distant from the vertical. Secondary roots of the acropetal sequence were semiplagiotropic, that is only those roots oriented upward after the gravistimulation resumed, more or less, the original direction. Tertiary roots didn't respond to the gravistimulation and therefore were ageotropic. Complementary observations conducted in large laboratory rhizotrons showed that late forming secondary roots were plagiotropic in their younger stages, thereafter loosing most of their sensitivity to gravity. Quaternary roots were ageotropic. On the basis of these data, a geotropic gradient was defined within the hevea root system, where the strongly responding taproot and late secondary roots are opposed to the weakly or nonresponding tertiary and quaternary roots. Functional significations of these differential geotropic reactions in different hevea root types are discussed. Keywords: geotropism, gravistimulation, root system, growth, development, morphogenesis, root observation box, Hevea brasiliensis. [Journal translation]


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.


Mycorrhiza ◽  
2021 ◽  
Author(s):  
P. W. Thomas

AbstractVery little is known about the impact of flooding and ground saturation on ectomycorrhizal fungi (EcM) and increasing flood events are expected with predicted climate change. To explore this, seedlings inoculated with the EcM species Tuber aestivum were exposed to a range of flood durations. Oak seedlings inoculated with T. aestivum were submerged for between 7 and 65 days. After a minimum of 114-day recovery, seedling growth measurements were recorded, and root systems were destructively sampled to measure the number of existing mycorrhizae in different zones. Number of mycorrhizae did not display correlation with seedling growth measurements. Seven days of submersion resulted in a significant reduction in mycorrhizae numbers and numbers reduced most drastically in the upper zones. Increases in duration of submersion further impacted mycorrhizae numbers in the lowest soil zone only. T. aestivum mycorrhizae can survive flood durations of at least 65 days. After flooding, mycorrhizae occur in higher numbers in the lowest soil zone, suggesting a mix of resilience and recovery. The results will aid in furthering our understanding of EcM but also may aid in conservation initiatives as well as providing insight for those whose livelihoods revolve around the collection of EcM fruiting bodies or cropping of the plant partners.


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.


2008 ◽  
Vol 255 (3-4) ◽  
pp. 495-505 ◽  
Author(s):  
Fyodor Tatarinov ◽  
Josef Urban ◽  
Jan Čermák

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.


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