Micronutrient variation within cotton leaf tissue as related to variety and soil location

1970 ◽  
Vol 1 (3) ◽  
pp. 163-172 ◽  
Author(s):  
O. E. Anderson ◽  
R. M. Harrison
Keyword(s):  
BMC Genomics ◽  
2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Luyao Wang ◽  
Jin Han ◽  
Kening Lu ◽  
Menglin Li ◽  
Mengtao Gao ◽  
...  

Abstract Background An evolutionary model using diploid and allotetraploid cotton species identified 80 % of non-coding transcripts in allotetraploid cotton as being uniquely activated in comparison with its diploid ancestors. The function of the lncRNAs activated in allotetraploid cotton remain largely unknown. Results We employed transcriptome analysis to examine the relationship between the lncRNAs and mRNAs of protein coding genes (PCGs) in cotton leaf tissue under abiotic stresses. LncRNA expression was preferentially associated with that of the flanking PCGs. Selected highly-expressed lncRNA candidates (n = 111) were subjected to a functional screening pilot test in which virus-induced gene silencing was integrated with abiotic stress treatment. From this low-throughput screen, we obtained candidate lncRNAs relating to plant height and tolerance to drought and other abiotic stresses. Conclusions Low-throughput screen is an effective method to find functional lncRNA for further study. LncRNAs were more active in abiotic stresses than PCG expression, especially temperature stress. LncRNA XLOC107738 may take a cis-regulatory role in response to environmental stimuli. The degree to which lncRNAs are constitutively expressed may impact expression patterns and functions on the individual gene level rather than in genome-wide aggregate.


Weed Science ◽  
1968 ◽  
Vol 16 (4) ◽  
pp. 481-484 ◽  
Author(s):  
C. R. Swanson ◽  
H. R. Swanson

Simultaneous treatment with certain carbamate insecticides inhibited degradation of 3-(p-chlorophenyl)-1,1-dimethyrurea (monuron) in cotton (Gossypium hirsutumL.) leaf discs. Monuron degradation was strongly inhibited by 1-naphthyl methylcarbamate (carbaryl) and 4-benzothiophene-N-methylcarbamate, but 2,3-dihydro-2,2-dimethyl-7-benzofuranyl methylcarbamate was ineffective. Effective carbamates did not prevent the metabolism of monuron to 1-(p-chlorophenyl)-3-methylurea (hereinafter referred to as monomethylmonuron), but they inhibited subsequent degradation of monomethylmonuron.


2009 ◽  
Vol 102 (4) ◽  
pp. 1497-1505 ◽  
Author(s):  
K. V. Tindall ◽  
M. Willrich Siebert ◽  
B. R. Leonard ◽  
J. All ◽  
F. J. Haile

1985 ◽  
Vol 63 (12) ◽  
pp. 2470-2472
Author(s):  
H. J. Zeringue Jr. ◽  
E. J. Conkerton ◽  
D. C. Chapital

When initial true leaves of 1-month postemergence Acala SJ-2 cotton plants were wounded by gentle abrasion, accumulations of ferulic acid (4-hydroxy-3-methoxycinnamic acid) were detected on the 3rd and 4th days after treatment. When similar wounds were immediately treated with cell-free extracts of Aspergillus flavus mycelia, elevated levels of scopoletin (6-methoxy-7-hydroxycoumarin) were produced, beginning 1 day after treatment and continuing for 7 days. Elevated levels of scopoletin were not detected in leaves that were only wounded, and enhanced quantities of ferulic acid were not observed in leaf tissue after wounding and exposure to the fungal extract. Accumulations of these compounds were not apparent in nonwounded controls. The results demonstrate a wound response distinct from the wound – fungal extract reaction.


2020 ◽  
Vol 45 (3) ◽  
Author(s):  
Nathan S. Little ◽  
R. Michelle Mullen ◽  
Blake H. Elkins ◽  
Katherine A. Parys ◽  
K. Clint Allen
Keyword(s):  

Author(s):  
O. E. Bradfute ◽  
R. E. Whitmoyer ◽  
L. R. Nault

A pathogen transmitted by the eriophyid mite, Aceria tulipae, infects a number of Gramineae producing symptoms similar to wheat spot mosaic virus (1). An electron microscope study of leaf ultrastructure from systemically infected Zea mays, Hordeum vulgare, and Triticum aestivum showed the presence of ovoid, double membrane bodies (0.1 - 0.2 microns) in the cytoplasm of parenchyma, phloem and epidermis cells (Fig. 1 ).


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