scholarly journals Complexity and coordination of root growth at low water potentials: recent advances from transcriptomic and proteomic analyses

2010 ◽  
Vol 33 (4) ◽  
pp. 590-603 ◽  
Author(s):  
MINEO YAMAGUCHI ◽  
ROBERT E. SHARP
2005 ◽  
Vol 33 (4) ◽  
pp. 697-704 ◽  
Author(s):  
Adriana Sánchez-Urdaneta ◽  
Cecilia Peña-Valdivia ◽  
Carlos Trejo ◽  
J. Aguirre R. ◽  
Elizabeth Cárdenas S.

HortScience ◽  
2005 ◽  
Vol 40 (3) ◽  
pp. 795-798 ◽  
Author(s):  
Dana L. Baumann ◽  
Beth Ann Workmaster ◽  
Kevin R. Kosola

Wisconsin cranberry growers report that fruit production by the cranberry cultivar `Ben Lear' (Vaccinium macrocarpon Ait.) is low in beds with poor drainage, while the cultivar `Stevens' is less sensitive to these conditions. We hypothesized that `Ben Lear' and `Stevens' would differ in their root growth and mortality response to variation in soil water potential. Rooted cuttings of each cultivar were grown in a green-house in sand-filled pots with three different soil water potentials which were regulated by a hanging water column below a fritted ceramic plate. A minirhizotron camera was used to record root growth and mortality weekly for five weeks. Root mortality was negligible (2% to 6%). Whole plant relative growth rates were greatest for both cultivars under the wettest conditions. Rooting depth was shallowest under the wettest conditions. Whole-plant relative growth rates of `Ben Lear' were higher than `Stevens' at all soil water potentials. `Stevens' plants had significantly higher root to shoot ratios and lower leaf area ratios than `Ben Lear' plants, and produced more total root length than `Ben Lear' at all soil water potentials. Shallow rooting, high leaf area ratio, and low allocation to root production by `Ben Lear' plants may lead to greater susceptibility to drought stress than `Stevens' plants in poorly drained cranberry beds.


1988 ◽  
Vol 18 (6) ◽  
pp. 728-732 ◽  
Author(s):  
G. L. Simmons ◽  
P. E. Pope

A root growth model was developed to graphically simulate predicted root responses of yellow-poplar and sweetgum seedlings to changes in soil physical properties. Data for the model were collected in greenhouse and laboratory experiments. Newly germinated yellow-poplar (Liriodendrontulipifera L.) and sweetgum (Liquidambarstyraciflua L.) seedlings were transplanted into pots containing silt loam soil compacted to bulk densities of 1.25, 1.40, or 1.55 Mg m−3 and grown under greenhouse conditions for 3 months. Minimum water potentials were maintained at −10 or −300 kPa. At harvest, root systems were excavated, divided into orders of lateral roots, and length, number, and branching frequency of each order were determined. Air-filled porosity and mechanical resistance were determined for soil samples equilibrated at the same bulk densities and water potentials as those used in the greenhouse study. Based on root and soil parameters, the model ROOTSIM graphically depicts the root distribution of each tree species at different levels of bulk density, mechanical resistance, and air-filled porosity. The model accurately predicts lateral root length and distribution for the range of soil properties used in the greenhouse study but has not been validated for these or other soil conditions.


1991 ◽  
Vol 96 (2) ◽  
pp. 438-443 ◽  
Author(s):  
William G. Spollen ◽  
Robert E. Sharp

1978 ◽  
Vol 58 (2) ◽  
pp. 275-278
Author(s):  
D. T. MORRIS ◽  
T. B. DAYNARD

Corn plants were grown in growth rooms at 1.2 and 1.4 g cm−3 soil bulk density. Leaf water potentials (LWP) of paired plants of similar leaf area were monitored during 3-day drying cycles. With denser soil, LWP declined more rapidly during light, and increased more slowly during dark intervals because of restricted root growth.


1988 ◽  
Vol 18 (11) ◽  
pp. 1392-1396 ◽  
Author(s):  
G. L. Simmons ◽  
P. E. Pope

A greenhouse study was conducted to determine the influence of soil water potential and endomycorrhizal fungi on root growth of yellow-poplar (Liriodendrontulipifera L.) and sweet gum (Liquidambarstyraciflua L.) seedlings grown at three soil bulk densities. Silt loam soil was compacted in PVC pots to bulk densities of 1.25 (low), 1.40 (medium), or 1.55 (high) Mg • m−3, and equilibrated at −10 kPa soil water potential. Newly germinated seedlings were transplanted into the pots, inoculated with fungal chlamydospores of Glomusmacrocarpum or Glomusfasciculaturn, or distilled water (control), and grown for 3 months at −10 or −300 kPa soil water potential. Total porosity, air-filled porosity, water content, and mechanical resistance of the soil were determined for samples compacted to the same bulk densities and equilibrated at the same soil water potentials as were used in the greenhouse study. Root growth was reduced by the high mechanical resistance caused by bulk densities of 1.40 and 1.55 Mg • m−3 at −300 kPa water potential. At both water potentials, total length of lateral roots and fibrosity of the root system of both tree species decreased significantly when bulk density increased from 1.40 to 1.55 Mg • m−3. Air-filled porosity less than 0.12 m3 • m−3 limited root growth when water potential was −10 kPa, and mechanical resistance greater than 3438 kPa restricted growth at −300 kPa. At −10 kPa, root length and fibrosity were greatest for inoculated sweet gum seedlings at each bulk density. At −300 kPa, sweet gum seedlings inoculated with G. fasciculatum had the greatest root length and fibrosity at the low and medium bulk densities. Mycorrhizal effects on root length of yellow-poplar were variable, and fibrosity was not significantly affected by mycorrhizal treatment.


2018 ◽  
Vol 244 (5) ◽  
pp. 628-637 ◽  
Author(s):  
Nicholas W Bateman ◽  
Thomas P Conrads

HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 571b-571
Author(s):  
Robert E. Shar

Plant water deficits usually result in severe inhibition of shoot growth, while root growth is less inhibited or even promoted. Recent advances in understanding the physiology of the differential responses of root and shoot growth to low water potentials will be reviewed. While it might be readily accepted that hormones arc important in transducing environmental conditions into growth responses, there is surprisingly little definitive evidence for the role of any hormone in regulating plant growth in soils of low water potential. Using maize seedlings as a model system, the increase in ABA that accompanies plant water deficits has been shown to be required for root growth maintenance, and also to play a role in shoot growth inhibition. The action of ABA in root growth maintenance appears to involve regulation of ethylene synthesis and/or sensitivity, while the mechanism of shoot growth inhibition is not known. Evidence that ABA acts as a root `signal controlling shoot growth in drying soil will also be considered. The importance of osmotic adjustment as a mechanism of growth maintenance at low water potentials has been questioned by suggestions that solute accumulation may be merely a consequence of stress-induced growth inhibition. Recent studies will be discussed which do not support this idea, and suggest that the response may be useful for crop improvement.


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