Paper · 2008 · Charles Sturt University Research Output (CRO)

Studying root development in soil using DNA technology: idea to impact

A. McKay; I. T. Riley; Diana Hartley; et al.

2
claims
3
verbatim quotes
2
citations
1
research areas
✓
Open access · other-oa

Abstract

Quantitative DNA assays for measuring root distribution and seed banks in soil are under development for wheat, barley, ryegrass, subterranean clover, phalaris and lucerne. These assays have potential to determine root distributions in soil profiles in either monoculture or mixed sward systems. The assays quantify DNA from live cells only and many of these cells will be in fine roots, prone to loss during soil washing with conventional root assessment procedures. In pot experiments the ryegrass DNA assay showed a rapid decline in soil root DNA over 10 days following plants being either defoliated or sprayed with glyphosate. This response is most likely due to DNA degrading in dying root cells. DNA assays for wheat and barley have also been used to assess genetic differences in root architecture under drought conditions and at field sites with hostile subsoils. The assays for pasture species have been used to measure differences in root distribution of pasture species in lime amended plots at the MASTER site (NSW DPI, Wagga Wagga). Results from the above studies show that quantitative DNA assays combined with high throughput DNA extraction systems are potentially useful to determine distribution of root systems under field conditions. This paves the way for high-throughput root phenotyping and incorporation of root architecture traits into breeding programs to improve drought tolerance as one possible role for the technology. In pasture trials the assays have the capacity to measure the impact of different management systems on specific species in mixed swards.

Abstract from the paper’s OpenAlex record; open copy licensed other-oa. Read at the source ↗

The text the model read, with the source record’s inline markup (italics, sub- and superscripts) rendered and its character entities decoded; quote offsets refer to the raw text.

Claims 2

Intervention effectobservedoriginal resultmeasured

Claim · model-written summary

In pot experiments, ryegrass soil root DNA declined rapidly over 10 days after defoliation or glyphosate spraying.

Taxon
ryegrassLoliume1
Treatment
defoliated or sprayed with glyphosatee1
Outcome
soil root DNAe1
Direction
declinee1
Qualifier
over 10 dayse1
Setting
pot experimentse1

Not reportedComparator

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Lolium
Lolium · Taxon · picture of the genus (one of its species)Forest & Kim Starr · CC BY 3.0 · Wikimedia Commons ↗

Verbatim

e1

“In pot experiments the ryegrass DNA assay showed a rapid decline in soil root DNA over 10 days following plants being either defoliated or sprayed with glyphosate”

✓ located verbatim in the source · abstract, characters 468–630 · show in text ↑
Mechanismauthor interpretationoriginal resultbasis n/a

Claim · model-written summary

The rapid decline in ryegrass soil root DNA is most likely due to DNA degrading in dying root cells.

Taxon
ryegrassLoliume1
Outcome
rapid decline in soil root DNAe1
Qualifier
DNA degrading in dying root cellse2

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Lolium
Lolium · Taxon · picture of the genus (one of its species)Forest & Kim Starr · CC BY 3.0 · Wikimedia Commons ↗

Verbatim

e1

“In pot experiments the ryegrass DNA assay showed a rapid decline in soil root DNA over 10 days following plants being either defoliated or sprayed with glyphosate”

✓ located verbatim in the source · abstract, characters 468–630 · show in text ↑
e2

“This response is most likely due to DNA degrading in dying root cells”

✓ located verbatim in the source · abstract, characters 632–701 · show in text ↑