scholarly journals Phenotyping cowpea for seedling root architecture reveals root phenes important for breeding phosphorus efficient varieties

Crop Science ◽  
2021 ◽  
Author(s):  
Saba B. Mohammed ◽  
James D. Burridge ◽  
Mohammad F. Ishiyaku ◽  
Ousmane Boukar ◽  
Jonathan P. Lynch
2017 ◽  
Vol 68 (5) ◽  
pp. 965-982 ◽  
Author(s):  
Jiangsan Zhao ◽  
Gernot Bodner ◽  
Boris Rewald ◽  
Daniel Leitner ◽  
Kerstin A. Nagel ◽  
...  

2019 ◽  
Vol 237 ◽  
pp. 53-64 ◽  
Author(s):  
Christopher F. Strock ◽  
James Burridge ◽  
Anica S.F. Massas ◽  
James Beaver ◽  
Stephen Beebe ◽  
...  

2019 ◽  
Vol 37 (2) ◽  
pp. 50-54 ◽  
Author(s):  
Shanon Hankin ◽  
Marvin Lo ◽  
Frank Balestri ◽  
Gary Watson

Abstract Nursery production of strong taprooted woody plants typically includes pruning to interrupt taproot development. To discern the impact this practice could have on seedling root architecture, we quantified changes to root architecture after taproot pruning and restriction separately in Catalpa (Catalpa speciosa) and Kentucky coffee tree (Gymnocladus dioicus). Taproot pruning resulted in a large and significant increase in the number of new, vertically oriented roots from the cut end of the primary root (regenerated taproots) in both species. Catalpa seedlings, which produced many strong laterals on unpruned taproots, showed greater reduction in lateral root number and size after taproot pruning than Kentucky coffee tree (with fewer and smaller natural lateral roots). The two species responded differently to restriction of the single, unpruned taproot by container depth (15, 30, 60 cm). For catalpa, with more shallow laterals naturally, the number of laterals was not significantly changed by restriction of the taproot by air pruning at any container depth, but lateral diameter was reduced by the 15 cm-deep container and biomass was reduced by the 30 cm-deep container, compared to the 60 cm-deep container. For Kentucky coffee tree with fewer natural laterals, restricting the taproot at 15 cm significantly increased the number and diameter of lateral roots compared to the 30 and 60 cm-deep containers, suggesting that restricting the taproot could increase the number of laterals in species that naturally produce fewer. Restricting multiple taproots on root-pruned plants generally did not affect lateral root development for either species, but this may have been due to the low number of lateral roots on those root systems. Index words: root architecture, nursery production, urban soils Species used in this study: Catalpa [Catalpa speciosa (Warder) Warder ex Engelm. ]; Kentucky coffee tree [Gymnocladus dioicus (L.) K. Koch]


2021 ◽  
Vol 120 (6) ◽  
pp. 1050
Author(s):  
Dipika S. Patel ◽  
Bardhan Kirti ◽  
P. Patel Dhiraji ◽  
Parekh Vipulkumar ◽  
Jena Suchismita ◽  
...  

1990 ◽  
Vol 79 (1) ◽  
pp. 78-84 ◽  
Author(s):  
Abha Upadhyaya ◽  
Tim D. Davis ◽  
M. H. Larsen ◽  
R. H. Walser ◽  
N. Sankhla

2009 ◽  
Vol 36 (11) ◽  
pp. 938 ◽  
Author(s):  
Nima Yazdanbakhsh ◽  
Joachim Fisahn

Plant organ phenotyping by non-invasive video imaging techniques provides a powerful tool to assess physiological traits and biomass production. We describe here a range of applications of a recently developed plant root monitoring platform (PlaRoM). PlaRoM consists of an imaging platform and a root extension profiling software application. This platform has been developed for multi parallel recordings of root growth phenotypes of up to 50 individual seedlings over several days, with high spatial and temporal resolution. PlaRoM can investigate root extension profiles of different genotypes in various growth conditions (e.g. light protocol, temperature, growth media). In particular, we present primary root growth kinetics that was collected over several days. Furthermore, addition of 0.01% sucrose to the growth medium provided sufficient carbohydrates to maintain reduced growth rates in extended nights. Further analysis of records obtained from the imaging platform revealed that lateral root development exhibits similar growth kinetics to the primary root, but that root hairs develop in a faster rate. The compatibility of PlaRoM with currently accessible software packages for studying root architecture will be discussed. We are aiming for a global application of our collected root images to analytical tools provided in remote locations.


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