Enhanced root system C-sink activity, water relations and aspects of nutrient acquisition in mycotrophic Bouteloua gracilis subjected to CO2 enrichment

Author(s):  
J. A. Morgan ◽  
W. G. Knight ◽  
L. M. Dudley ◽  
H. W. Hunt
2018 ◽  
Author(s):  
Sixtine Passot ◽  
Valentin Couvreur ◽  
Félicien Meunier ◽  
Xavier Draye ◽  
Mathieu Javaux ◽  
...  

AbstractIn the recent years, many computational tools, such as image analysis, data management, process-based simulation and upscaling tools, were developed to help quantify and understand water flow in the soil-root system, at multiple scales (tissue, organ, plant and population). Several of these tools work together or, at least, are compatible. However, for the un-informed researcher, they might seem disconnected, forming a unclear and disorganised succession of tools.In this article, we present how different pieces of work can be further developed by connecting them to analyse soil-root-water relations in a comprehensive and structured network. This “explicit network of soil-root computational tools” informs the reader about existing tools and help them understand how their data (past and future) might fit within the network. We also demonstrate the novel possibilities of scale-consistent parameterizations made possible by the network with a set of case studies from the literature. Finally, we discuss existing gaps in the network and how we can move forward to fill them.HighlightsMany computational tools exist to quantify water flow in the soil-root system. These tools can be arranged in a comprehensive network that can be leveraged to better interpret experimental data.


Oecologia ◽  
1998 ◽  
Vol 114 (4) ◽  
pp. 483-493 ◽  
Author(s):  
J. A. Morgan ◽  
D. R. LeCain ◽  
J. J. Read ◽  
H. W. Hunt ◽  
W. G. Knight

2009 ◽  
Vol 66 (4) ◽  
pp. 436-446 ◽  
Author(s):  
Claudia Rita de Souza ◽  
Luís Henrique Bassoi ◽  
José Moacir Pinheiro Lima Filho ◽  
Fabrício Francisco Santos da Silva ◽  
Leandro Hespanhol Viana ◽  
...  

There is an increased demand for high quality winegrapes in the São Francisco Valley, a new wine producing area in Brazil. As the grape quality is closely linked to the soil water status, understanding the effects of rootstock and irrigation management on grapevine water relations is essential to optimize yield and quality. This study was carried out to investigate the effects of irrigation strategies and rootstocks on water relations and scion vigour of field-grown grapevines in Petrolina, Pernambuco state, Brazil. The cultivars used as scions are Moscato Canelli and Syrah, both grafted onto IAC 572 and 1103 Paulsen rootstocks. The following water treatments were used: deficit irrigation, with holding water after veraison; and partial root-zone drying, supplying (100% of crop evapotranspiration) of the water loss to only one side of the root system after fruit set, alternating the sides periodically (about 24 days). In general, all treatments had values of pre-dawn leaf water potential higher than -0.2 MPa, suggesting absence of water stress. The vine water status was more affected by rootstock type than irrigation strategies. Both cultivars grafted on IAC 572 had the highest values of midday leaf water potential and stem water potential, measured on non-transpiring leaves, which were bagged with both plastic sheet and aluminum foil at least 1 h before measurements. For both cultivars, the stomatal conductance (g s), transpiration (E) and leaf area index (LAI) were also more affected by roostsotck type than by irrigation strategies. The IAC 572 rootstock presented higher g s, E and LAI than the 1103 Paulsen. Differences in vegetative vigor of the scion grafted onto IAC 572 rootstocks were related to its higher leaf specific hydraulic conductance and deeper root system as compared to the 1103 Paulsen, which increased the water-extraction capability, resulting in a better vine water status.


2015 ◽  
Vol 29 ◽  
pp. 203-204 ◽  
Author(s):  
F.M. del Amor ◽  
M.C. Piñero ◽  
G. Otálora-Alcón ◽  
M. Pérez-Jimenez ◽  
M. Marín-Miñano

2014 ◽  
Vol 32 (12) ◽  
pp. 597-598 ◽  
Author(s):  
Xiangpei Kong ◽  
Maolin Zhang ◽  
Ive De Smet ◽  
Zhaojun Ding

2021 ◽  
Author(s):  
Helena Jorda Guerra ◽  
Mutez Ahmed ◽  
Anke Coolens ◽  
Mathieu Javaux ◽  
Doris Vetterlein ◽  
...  

<p>Sustaining world food production under a changing climate and a growing population demands for higher optimization of agricultural resources including water. This requires an accurate understanding and prediction of root water uptake from soils, which depends on several root traits. The role of root hairs in root water uptake is still under debate, with experimental data that both prove and reject the hypothesis that root hairs can facilitate root water uptake, especially under drought conditions. Our objective was to investigate the effect of root hairs in maize at the field scale. A wildtype maize variety (with root hairs) and a hairless mutant were grown in two substrates (loam and sand) at a field site near Halle, Germany (Vetterlein et al., 2020, JPLN). Transpiration, leaf water potential, soil water content and potentials were monitored during 2019 and 2020. Root length density and leaf area were measured at four different plant development stages. A version of Hydrus 1D coupled with Couvreur’s macroscopic root water uptake model (Couvreur et al., 2012, HESS) was parameterized and used to further investigate soil-water relations in this field experiment. In both years, plants emptied the available water in the profile by July, and relied on rain and irrigation afterwards. Non-significant differences in cumulative water losses from the soil, estimated from soil water content measurements, were observed among the four treatments in both years. These results are in agreement with simulated water losses, which also showed small differences in cumulative transpiration among treatments. Mutant plants developed significantly smaller shoots while transpiring similar water volumes as wildtype plants, indicating lower water use efficiency. While there was no visible effect of the genotype in the soil-water relations, a clear effect of the soil type was observed. Simulated collar water potentials and field observations of rolled leaves indicated water stress occurred first in the loam compared to the sand treatments. Plants grew faster in the loam, leading to earlier onset of water stress. Even though plants in the loam produced less roots than in the sand, the onset of stress was not caused by the smaller root system since simulations presuming a larger root system did not predict a later onset of stress. Similarly, a simulation run using a smaller root system in the sandy soil did not predict a significantly earlier onset of stress. Finally, although our model simulations considered only differences in root density among treatments and did not consider different root or rhizosphere properties of the different soils and genotypes, it simulated the observed water dynamics well. Water depletion in the loamy soil was simulated earlier than it was measured. We hypothesize that this is caused by changing root hydraulic properties when roots develop and mature, and suggest that young roots do not start taking up water immediately. Nevertheless, the data quantity and quality obtained in this field experiment exposes the difficulties and challenges we face to monitor water potentials and fluxes in the soil-plant continuum in annual grasses at the field scale.</p>


Ecology ◽  
2013 ◽  
Author(s):  
Angela Hodge

Soils are physically the most complex of all environments, comprising solid, liquid, and gas phases, and vary considerably in their ability to supply nutrients. Plant roots acquire nutrients from the solution (liquid) phase but the equilibrium among these different phases controls the nutrients available, which also depends on the nutrient in question. Consequently, nutrients in soil are distributed in a non-uniform or heterogeneous manner. This heterogeneity occurs at a range of scales including those relevant to plant roots. Roots therefore have to respond to this heterogeneity or “patchiness” in resource supply in order to acquire nutrients essential for growth and normal metabolic function. This is aided by the modular structure of the root system, which enables flexibility in the spatial configuration of the root system (i.e., root system architecture) and plasticity in physiological and morphological responses. Most early studies focused on measuring the type and size of the observed response to nutrient heterogeneity with little consideration as to what this meant in terms of actual nutrient acquisition. Consequently, there is a vast literature on the various root responses by different plant species conducted under a wide range of environmental conditions but from which comparisons are difficult to make and the importance of the response obscure. More recently, investigative studies have moved toward more emphasis being placed upon the functional importance of the root response in terms of nutrient acquisition and, importantly, the environmental context in which that response is produced. This is an important shift in emphasis, as responses observed under ideal and often controlled conditions may not necessarily relate to those that actually occur in the natural environment. The majority of plant species also have additional means to forage their environment for resources including the formation of mycorrhizal symbiotic associations, while a smaller number of plant species can form symbiotic associations with nitrogen-fixing prokaryotes. Roots can also release substances into the soil that have a specific role to play in nutrient acquisition. Although plants can also forage for resources aboveground, resulting in plasticity in aboveground structures, the majority of plants acquire their nutrients from the soil environment: hence, this is the main focus of the text and resulting bibliography.


1978 ◽  
Vol 91 (1) ◽  
pp. 91-102 ◽  
Author(s):  
P. J. Gregory ◽  
M. McGowan ◽  
P. V. Biscoe ◽  
B. Hunter

SummaryThe production of root axes and the growth of the root system are reported for a commercially grown crop of Maris Huntsman winter wheat. Soil cores were extracted on 17 occasions during the growing season permitting a detailed study of root length and root dry weight with depth and time.Production of seminal root axes was complete by the beginning of March when all plants possessed six (occasionally seven) axes which persisted throughout the life of the crop. Nodal axes were produced continuously from mid-February until late May and finally numbered approximately 20 stem nodal axes per main stem. Total root dry weight increased exponentially until the beginning of April and then almost linearly to reach a maximum of 105 g root/m2 field in mid-June (anthesis). After anthesis, total root dry weight decreased but root growth continued below 80 cm. From April onwards, approximately 65% of the total root dry weight was in the 0–30 cm layer.


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