scholarly journals Chromosomal Changes in Prosopis glandulosa var. torreyana (Honey Mesquite) Species Widely Distributed in North America

CYTOLOGIA ◽  
2021 ◽  
Vol 86 (3) ◽  
pp. 235-239
Author(s):  
Fernando Tapia-Pastrana
Weed Science ◽  
1986 ◽  
Vol 34 (1) ◽  
pp. 88-93 ◽  
Author(s):  
G. Allen Rasmussen ◽  
Roger P. Smith ◽  
Charles J. Scifres

Tebuthiuron {N-[5-(1,1-dimethylethyl)-1,3,4-thiadiazol-2-yl]-N,N′-dimethylurea} at 2 or 4 ppmw placed 0 to 3, 8 to 11, or 15 to 18 cm deep in soil columns reduced root and shoot weights of buffelgrass [Pennisetum ciliare(L.) Link # PESCI] 30 days after emergence. Plains bristlegrass (Setaria macrostachyaH.B.K.) seedling shoot weights were not reduced when 2 ppmw tebuthiuron was placed 8 to 11 cm deep or deeper. Effects of tebuthiuron at 0.13 to 0.50 ppmw on buffelgrass shoot and net tiller production were not moderated by the presence of honey mesquite (Prosopis glandulosa# PRCJG) in the pots. However, regardless of tebuthiuron dosage, average height and shoot weight of buffelgrass seedlings were greater when seedlings were grown in soil collected from beneath honey mesquite canopies compared to growth in soil from interspaces. Therefore, spatial variations in buffelgrass response to applications of tebuthiuron for control of invading shrubs may largely be attributed to soil changes induced by woody plants rather than to presence of shrubs.


Weed Science ◽  
1986 ◽  
Vol 34 (2) ◽  
pp. 211-217 ◽  
Author(s):  
Rodney W. Bovey ◽  
Hugo Hein ◽  
Robert E. Meyer

Triclopyr {[(3,5,6-trichloro-2-pyridinyl)oxy] acetic acid}, 2,4,5-T [(2,4,5-trichlorophenoxy)acetic acid], picloram (4-amino-3,5,6-trichloro-2-pyridinecarboxylic acid), and clopyralid (3,6-dichloro-2-pyridinecarboxylic acid) were applied to honey mesquite (Prosopis glandulosaTorr. # PRCJG) on seven different dates about every 3 weeks from May to September in 1980 and 1981. Concentrations of 2,4,5-T or triclopyr in stem tissue were usually less than 2 μg/g fresh weight regardless of date of application. Concentrations of picloram and clopyralid were as high as 11 and 22 μg/g fresh weight, respectively, in upper stem phloem at some dates of application. Higher concentrations of all herbicides were detected in upper stem phloem than in the upper stem xylem or basal stem phloem or xylem. More herbicide tended to be detected in stems when herbicides were applied early (May and June) than late (August and September) in the season. Concentrations of triclopyr and picloram recovered from honey mesquite stems were about 25% greater at 3 than at 30 days after treatment, whereas concentrations of 2,4,5-T and clopyralid were about 50% greater at 3 than at 30 days after application.


Weed Science ◽  
1989 ◽  
Vol 37 (1) ◽  
pp. 19-22 ◽  
Author(s):  
Rodney W. Bovey ◽  
Hugo Hein ◽  
F. Nelson Keeney

Foliar sprays of the monoethanolamine salt, potassium salt, free acid, and 1-decyl ester of clopyralid were more effective in killing greenhouse-grown honey mesquite than the 2-ethylhexyl ester at rates of 0.28 ae/ha or less. More clopyralid was transported to the lower canopy from application of the monoethanolamine salt and potassium salt than the 2-ethylhexyl ester of clopyralid at 4 h or 1, 3, or 8 days after treatment. Application of the monoethanolamine salt and the 2-ethylhexyl ester to leaves with a pipet indicated that about twice as much clopyralid was absorbed within 15 min from the ester form (26%) than from the amine form (12%) of the total recovered. However, after 24 h, absorption of the ester was less than the amine. More than twice as much clopyralid was transported from the treated leaf after application of amine than the ester. Only the acid form of clopyralid was transported away from the site of application of either ester or amine.


1996 ◽  
Vol 16 (10) ◽  
pp. 817-823 ◽  
Author(s):  
H. W. Polley ◽  
H. B. Johnson ◽  
H. S. Mayeux ◽  
C. R. Tischler ◽  
D. A. Brown

1990 ◽  
Vol 4 (1) ◽  
pp. 26-30 ◽  
Author(s):  
Rodney W. Bovey ◽  
Robert E. Meyer ◽  
Steven G. Whisenant

Greenhouse and field experiments were conducted in east-central Texas to evaluate the influence of simulated rainfall on the availability of foliar-applied herbicides for huisache and honey mesquite control. The foliar activity of the amine salts of glyphosate, dicamba, picloram, clopyralid, and triclopyr was decreased on greenhouse-grown huisache when simulated rainfall was applied up to 240 min after herbicide treatment. The effectiveness of the butoxyethyl ester of triclopyr or 2,4,5-T was not reduced by rainfall washoff within 15 min after application. In natural huisache stands, injury from the ester of triclopyr or amine salts of picloram or clopyralid was not reduced by simulated rainfall at 60 min after herbicide treatment. In the greenhouse and field, honey mesquite leaves rapidly absorbed most herbicides, and triclopyr, 2,4,5-T, picloram, and clopyralid were highly phytotoxic even when simulated rainfall was applied within 15 min after herbicide treatment.


Ecology ◽  
1983 ◽  
Vol 64 (6) ◽  
pp. 1381-1393 ◽  
Author(s):  
Erika Tallak Nilsen ◽  
M. Rasoul Sharifi ◽  
Philip W. Rundel ◽  
Wesley M. Jarrell ◽  
Ross A. Virginia

Weed Science ◽  
1987 ◽  
Vol 35 (2) ◽  
pp. 253-258 ◽  
Author(s):  
Rodney W. Bovey ◽  
Hugo Hein ◽  
Robert E. Meyer ◽  
L. Fred Bouse

The addition of surfactant (trimethylnonylpolyethoxyethanol) at 0.5% (v/v) of the spray solution caused a twofold increase in the deposit of clopyralid (3,6-dichloro-2-pyridinecarboxylic acid) applied at 0.14 or 0.28 kg ae/ha on greenhouse-grown honey mesquite (Prosopis glandulosaTorr. # PRCJG) and increased transport into the plants compared to clopyralid applied alone. Application of equal rates of benazolin [4-chloro-2-oxo-3(2H)-benzothiazoleacetic acid] with clopyralid at 0.28 + 0.28 kg/ha enhanced transport of clopyralid into honey mesquite. Spray deposit, absorption, and translocation of clopyralid was unaffected by addition of 0.5% (v/v) of d'limonene (4-isopropenyl-1-methyl-cyclohexane). Greater spray deposit of clopyralid on plant surfaces after addition of surfactant was associated with reduced liquid surface tension and greater percentage of spray volume in small droplets (<204-μm diam).


2008 ◽  
Vol 3 (1) ◽  
pp. 1934578X0800300
Author(s):  
Volodymyr Samoylenko ◽  
D. Chuck Dunbar ◽  
Melissa R. Jacob ◽  
Vaishali C. Joshi ◽  
Mohammad K. Ashfaq ◽  
...  

Prosopis glandulosa Torr. var. torreyana (L. Benson) M. C. Johnston root bark, collected in Texas, yielded two new alkylated piperidine alkaloids, namely 3-isocassine (1) and N-methyl-3-isocassine (2), together with the previously reported N-methylcassine (3). In addition, the alkylated piperidinyl indolizidine alkaloid juliprosopine (4) was isolated from the leaves of the same plant. The structures and stereochemistry of compounds 1–4 were determined from 1D and 2D NMR data, including COSY, HMQC, HMBC and NOESY experiments, and ESI-HRMS. Juliprosopine (4) demonstrated antimicrobial activities against a panel of microorganisms, including potent antifungal activities against Aspergillus fumigatus.


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