Chemical and Physical Modification of the Rhizosphere

Author(s):  
Peter B. Tinker ◽  
Peter Nye

The term ‘rhizosphere’ tends to mean different things to different people. In discussing how a root affects the soil, it is well to bear in mind the spread of the zone being exploited for a particular solute: if this is wide, there may be no point in emphasizing effects close to the root; but if it is narrow, predictions based on the behaviour of the bulk soil may be wide of the mark. In a moist loam after 10 days, a simple non-adsorbed solute moves about 1 cm, but a strongly adsorbed one will move about 1 mm. In a dry soil, the spread may be an order of magnitude less. The modifications to the soil in the rhizosphere may be physical, chemical or microbiological. In this chapter, we discuss essentially non-living modifications, and in chapter 8 the modifications that involve living organisms and their effects. Roots tend to follow pores and channels that are not much less, and are often larger, in diameter than their own. If the channels are larger, the roots are not randomly arranged in the void (Kooistra et al. 1992), but tend to be held against a soil surface by surface tension, and to follow the channel geotropically on the down-side. If the channels are smaller, good contact is assured, but the roots do not grow freely unless some soil is displaced as the root advances. For example, in winter wheat, Low (1972) cites minimum pore sizes of 390–450 μm for primary seminal roots, 320–370 μm for primary laterals, 300–350 μm for secondary laterals, and 8–12 μm for root hairs, though some figures seem large. Whiteley & Dexter (1984) and Dexter (1986a, b, c) have studied the mechanics of root penetration in detail (section 9.3.5). It may compact and reorient the soil at the root surface. Greacen et al. (1968) found that wheat roots penetrating a uniform fine sand increased the density only from 1.4 to 1.5 close to the root; and a pea radicle, a comparatively large root, raised the density of a loam from 1.5 to 1.55.

2002 ◽  
Vol 29 (5) ◽  
pp. 595 ◽  
Author(s):  
Sergey Shabala ◽  
Andrew Knowles

Oscillatory patterns in H+, K+, Ca2+ and Cl- uptake were observed at different regions of the root surface, including root hairs, using a non-invasive ion flux measuring technique (the MIFE™ technique). To our knowledge, this is the first report of ultradian oscillations in nutrient acquisition in the mature root zone. Oscillations of the largest magnitude were usually measured in the elongation region, 2–4 mm from the root apex. There were usually at least two oscillatory components present for each ion measured: fast, with periods of several minutes; and slow, with periods of 50–80 min. Even within the same functional zone, the periods of ion flux oscillations were significantly different, suggesting that they are driven by some internal mechanisms located in each cell rather than originating from one ‘central clock pacemaker’. There were also significant changes in the oscillatory characteristics (both periods and amplitudes) of fluxes from a single small cluster of cells over time. Analysis of phase shifts between oscillations in different ions suggested that rhythmic activity of a plasma membrane H+-pump may be central to observed rhythmic nutrient acquisition by plant roots. We discuss the possible adaptive significance of such an oscillatory strategy for root nutrient acquisition.


2001 ◽  
Vol 47 (8) ◽  
pp. 741-753 ◽  
Author(s):  
T Yu ◽  
A Nassuth ◽  
R L Peterson

Phialocephala fortinii Wang & Wilcox is a member of root-inhabiting fungi known collectively as dark septate endophytes (DSE). Although very common and distributed worldwide, few studies have documented their interaction with roots on a structural basis. The objective of this study was to determine the early colonization events and formation of microsclerotia of P. fortinii in roots of Asparagus officinalis L., a species known to have DSE. A loose network of hyphae accumulated at the root surface, and coils formed around root hairs and external to epidermal cells overlying short cells of the dimorphic, suberized exodermis. Root penetration occurred via swollen, appressorium-like structures into epidermal cells where coiling of hyphae occurred along the periphery of the cells. Hyphae penetrated from the epidermis into short exodermal cells and from these into cortical cells. Hyphae colonized the cortex up to the endodermis and sometimes entered the vascular cylinder. Some root tips were colonized as well. Microsclerotia in epidermal and exodermal short cells accumulated glycogen, protein, and polyphosphate. Energy-dispersive X-ray spectroscopy on distinct bodies visible in microsclerotial hyphae revealed high levels of phosphorus.Key words: Mycelium radicis atrovirens, Phialocephala fortinii, microsclerotia, DSE.


2014 ◽  
Vol 1 (3) ◽  
pp. 57-61
Author(s):  
E. Kopylov

Aim. To study the specifi cities of complex inoculation of spring wheat roots with the bacteria of Azospirillum genus and Chaetomium cochliodes Palliser 3250, and the isolation of bacteria of Azospirillum genus, capable of fi xing atmospheric nitrogen, from the rhizospheric soil, washed-off roots and histoshere. Materials and meth- ods. The phenotypic features of the selected bacteria were identifi ed according to Bergi key. The molecular the polymerase chain reaction and genetic analysis was used for the identifi cation the bacteria. Results. It has been demonstrated that during the introduction into the root system of spring wheat the strain of A. brasilensе 102 actively colonizes rhizospheric soil, root surface and is capable of penetrating into the inner plant tissues. Conclusions. The soil ascomucete of C. cochliodes 3250 promotes better settling down of Azospirillum cells in spring wheat root zone, especially in plant histosphere which induces the increase in the content of chlorophyll a and b in the leaves and yield of the crop.


1986 ◽  
Vol 64 (10) ◽  
pp. 2216-2226 ◽  
Author(s):  
Yves Prin ◽  
Mireille Rougier

The aim of the present study was to investigate the Alnus root surface using seedlings grown axenically. This study has focused on root zones where infection by the symbiotic actinomycete Frankia takes place. The zones examined extend from the root cap to the emerging root hair zone. The root cap ensheaths the Alnus root apex and extends over the root surface as a layer of highly flattened cells closely appressed to the root epidermal cell wall. These cells contain phenolic compounds as demonstrated by various histochemical tests. They are externally bordered by a thin cell wall coated by a thin mucilage layer. The root cap is ruptured when underlying epidermal cells elongate, and cell remnants are still found in the emerging root hair zone. Young emerging root hairs are bordered externally by a cell wall covered by a thin mucilage layer which reacts positively to the tests used for the detection of polysaccharides, glycoproteins, and anionic sites. The characteristics of the Alnus root surface and the biological function of mucilage and phenols present at the root surface are discussed in relation to the infection process.


1995 ◽  
Vol 117 (2) ◽  
pp. 100-107 ◽  
Author(s):  
M. Krarti ◽  
D. E. Claridge ◽  
J. F. Kreider

This paper presents an analytical model to predict the temperature variation within a multilayered soil. The soil surface temperature is assumed to have a sinusoidal time variation for both daily and annual time scales. The soil thermal properties in each layer are assumed to be uniform. The model is applied to two-layered, three-layered, and to nonhomogeneous soils. In case of two-layered soil, a detailed analysis of the thermal behavior of each layer is presented. It was found that as long as the order of magnitude of the thermal diffusivity of soil surface does not exceed three times that of deep soil; the soil temperature variation with depth can be predicted accurately by a simplified model that assumes that the soil has constant thermal properties.


Author(s):  
A. Sivanesan

Abstract A description is provided for Rosellinia bunodes. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On arrowroot, Artocarpus integer, avocado, banana, cacao, camphor, cassava, Centrosemapubescens, Cinchona, Citrus, coffee, Colocasia antiquorum, Crotalaria, Desmodium gyroides, Dryobalanops aromatica, Erythrina, ginger, Gliricidia, Grevillea robusta, Hibiscus rosa-sinensis, Holigarna longifolia, Indigofera, Inga laurina, Leucaena glauca, Litsea, pepper (black), Petiveria alliacea, Phyllanthus, rattan, rubber, Schleichera trijuga, tea, Tephrosia and yams. DISEASE: Black root rot, mainly of tropical and subtropical woody hosts; plurivorous but described mostly from cacao (Theobroma cacao), quinine (Cinchona spp.), coffee (Coffea spp.), rubber (Hevea brasiliensis) and tea (Camellia sinensis). Wilt and death of the whole plant or single branches may be the first signs of attack. At the collar the mycelial sheet is at first cream-white shading to purplish-black and may extend well above the soil surface in damp conditions. On the root surface the firm, black, branching strands are firmly applied and thicken into irregular knots. In the cortex the strands have a black periphery and white core; in the wood they appear thread-like and black or sometimes as dots in transverse section. In culture the mycelium is white, later buff with black strands. GEOGRAPHICAL DISTRIBUTION: Widespread in tropical America and also in Central African Republic, India (Nilgris, Maharashtra). Indonesia (Java, Sumatra), Malaysia (W.), Philippines. Sri Lanka (Ceylon) and Zaire Republic (CMI Map 358, ed. 2, 1970). Additional records not yet mapped are Honduras, Panama. TRANSMISSION: As mycelium from surface oreanic litter and woody debris.


1990 ◽  
Vol 68 (3) ◽  
pp. 579-593 ◽  
Author(s):  
H. B. Massicotte ◽  
R. L. Peterson ◽  
C. A. Ackerley ◽  
L. H. Melville

The ontogeny and ultrastructure of ectomycorrhizae synthesized between Betula alleghaniensis (yellow birch) and Pisolithus tinctorius, a broad host range fungus, were studied to determine the structural modifications in both symbionts during ectomycorrhiza establishment. A number of stages, including initial contact of hyphae with the root surface, early mantle formation, and mature mantle formation, were distinguished. Interactions between hyphae and root hairs were frequent. As a paraepidermal Hartig net developed, root epidermal cells elongated in a radial direction, but wall ingrowths were not formed. Repeated branching of Hartig net hyphae resulted in extensive fine branches and the compartmentalization of hyphal cytoplasm. Nuclei and elongated mitochondria were frequently located in the narrow cytoplasmic compartments, and [Formula: see text] thickenings developed along walls of cortical cells in primary roots.


2007 ◽  
Vol 19 (4) ◽  
pp. 1-13
Author(s):  
Manaf Ezzldien Al-Sabbagh ◽  
Jasim Khalaf Shallal ◽  
Sabah Hussein Ali

1974 ◽  
Vol 22 (2) ◽  
pp. 82-88
Author(s):  
J.J. Schuurman ◽  
L. Knot

Westerwolds ryegrass was grown in tubes on artificial soil profiles at N rates equivalent to 25, 50 or 100 kg/ha with a water table maintained 70 cm below the soil surface. Average results/plant after 13 weeks at low and high N were: DM yield of tops 5.0 and 14.6 g, water consumption 2660 and 4850 cm2, DM yield of roots 1.4 and 3.4 g, total length of all primary roots 2589 and 3374 cm, number of primary roots 103 and 161, number of secondary roots in topsoil 63 and 83 and in subsoil 71 and 83, and total root surface area 1084 and 1736 cm2. ADDITIONAL ABSTRACT: L. multiflorum plants were grown on sandy soil in asbestos tubes with an inner diameter of 15 cm, and 75 cm high, and supplied with 25, 50 or 100 kg N/ha. The soil water level was maintained at 70 cm below soil level. Top growth 8 and 13 weeks after sowing was progressively enhanced by the 2 higher rates, weight increments amounting to at least 72 and 188 %, respectively. These growth increases were accompanied by augmented water consumption, as well as root growth and numbers. (Abstract retrieved from CAB Abstracts by CABI’s permission)


Author(s):  
Earl B. Alexander ◽  
Roger G. Coleman ◽  
Todd Keeler-Wolfe ◽  
Susan P. Harrison

We walk on soils frequently, but we seldom observe them. Soils are massive, even though they are porous. Soil 1m (40 inches) deep over an area of 1 hectare (2.5 acres) might weigh 10,000–15,000 metric tons. It is teeming with life. There are trillions, or quadrillions, of living organisms (mostly microorganisms), representing thousands of species, in each square meter of soil (Metting 1993). In fact, species diversity, or number of species, may be greater below ground than above ground. We seldom see these organisms because we seldom look below ground or dig into it. The many worms and insects one finds digging in a garden are a small fraction of the species in soils because the greatest diversity of soil-dwelling species exists among microscopic insects, mites, roundworms (or nematodes), and fungi. Even though individual organisms in soils are mostly very small or microscopic, the total mass of living organisms in a hectare of soil, excluding plant roots, may be 1–5 or 10 metric tons. More than one-half of that biomass is bacteria and fungi. Living microorganism biomass generally accounts for about 1%–5% of the organic carbon and about 2%–6% of the nitrogen in soils (Lavelle and Spain 2001). The upper limit of soil is the ground surface of the earth. The lower limit is bedrock for engineers, or the depth of root penetration for edaphologists. Unconsolidated material that engineers call soil can be called “regolith” (Merrill 1897, Jackson 1997) to distinguish it from the soil of pedologists and edaphologists. Regolith may consist of disintegrated bedrock, gravel, sand, clay, or other materials that have not been consolidated to form rock. Pedologists investigate the upper part of regolith, where changes are effected by exchanges of gases between soil and aboveground atmosphere and by biological activity. This soil of pedologists may coincide with that of edaphologists or include more regolith. In fact, the lower limit of soil that pedologists investigate is arbitrary, unless this limit is a contact with bedrock that is practically impenetrable with pick and shovel.


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