Response of Horseweed Biotypes to Foliar Applications of Cloransulam-methyl and Glyphosate

2005 ◽  
Vol 19 (2) ◽  
pp. 231-236 ◽  
Author(s):  
Geoffrey D. Trainer ◽  
Mark M. Loux ◽  
S. Kent Harrison ◽  
Emilie Regnier

Studies were conducted from 2001 through 2003 to determine the extent of resistance to acetolactate synthase (ALS) inhibitors and glyphosate in Ohio horseweed biotypes. The response of 66 horseweed biotypes to cloransulam-methyl and glyphosate was determined in the greenhouse. Application of 0.07 kg ai cloransulam/ha reduced plant biomass by less than 60% for 38 of the 66 biotypes. Application of 3.4 kg ae glyphosate/ha reduced biomass by at least 80% for the 51 biotypes collected in 2001, but biomass was similar to that of nontreated plants for 11 of the 15 populations collected in 2002. A dose–response study was conducted with selected biotypes, and a nonlinear, logistic dose–response curve was fit to the data to calculate the herbicide dose required to reduce fresh weight 50% (GR50). On the basis of GR50values, the resistance ratio (R/S) for two ALS-resistant biotypes was 34 and 943 for chlorimuron-ethyl and 32 and 168 for cloransulam, respectively. The R/S ratio for two glyphosate-resistant biotypes was 33 and 39. Results of these studies indicate that, in 2002, ALS-resistant horseweed was widespread throughout Ohio, whereas resistance to glyphosate occurred primarily in several counties in southwestern Ohio.

1962 ◽  
Vol 13 (6) ◽  
pp. 1030 ◽  
Author(s):  
HL Davies ◽  
D Bennett

The oestrogenic activity of three varieties of subterranean clover (Trifolium subterraneum L.) — Dwalganup, Yarloop, and Mount Barker — was measured by means of the response in fresh weight of uterus + cervix in both ovariectomized virgin and ovariectomized cast-for-age ewes. The standard oestrogen used was diethylstilboestrol, administered intramuscularly. There was no difference between virgin and aged sheep in the slope of the dose-response curve. Thus aged sheep can be used for biological assay of oestrogens. The varieties Yarloop and Dwalganup were highly potent; Mount Barker produced only slight increases in uterine weight. The relevance of these varietal differences in oestrogenic potency is discussed in relation to the sheep infertility problem associated with oestrogenic pastures.


2015 ◽  
Vol 29 (1) ◽  
pp. 82-92 ◽  
Author(s):  
Debalin Sarangi ◽  
Lowell D. Sandell ◽  
Stevan Z. Knezevic ◽  
Jatinder S. Aulakh ◽  
John L. Lindquist ◽  
...  

Glyphosate-resistant common waterhemp is a difficult-to-control annual broadleaf weed that has become a serious management challenge for growers in Nebraska and other states in the United States. The objectives of this study were to confirm glyphosate-resistant common waterhemp in Nebraska by quantifying level of resistance in a dose-response study, and to determine the sensitivity and efficacy of POST soybean herbicides for controlling suspected glyphosate-resistant common waterhemp biotypes. Seeds of suspected glyphosate-resistant common waterhemp biotypes were collected from seven eastern Nebraska counties. Greenhouse dose-response experiments were conducted to evaluate the response of common waterhemp biotypes to nine rates of glyphosate (0 to 16×). Common waterhemp biotypes were 3- to 39-fold resistant to glyphosate depending on the biotype being investigated and the susceptible biotype used for comparison. Results of the POST soybean herbicides efficacy experiment suggested that glyphosate-resistant biotypes, except a biotype from Pawnee County, had reduced sensitivity to acetolactate synthase (ALS)–inhibiting herbicides (chlorimuron-ethyl, imazamox, imazaquin, imazethapyr, and thifensulfuron-methyl). Glufosinate and protoporphyrinogen oxidase (PPO)–inhibiting herbicides (acifluorfen, fluthiacet-methyl, fomesafen, and lactofen) provided ≥ 80% control of glyphosate-resistant common waterhemp at 21 d after treatment (DAT). This study confirmed the first occurrence of glyphosate-resistant common waterhemp in Nebraska, and also revealed reduced sensitivity to ALS-inhibiting herbicides in most of the biotypes tested in this study.


1967 ◽  
Vol 56 (4) ◽  
pp. 619-625 ◽  
Author(s):  
Hans Jacob Koed ◽  
Christian Hamburger

ABSTRACT Comparison of the dose-response curves for LH of ovine origin (NIH-LH-S8) and of human origin (IRP-HMG-2) using the OAAD test showed a small, though statistically significant difference, the dose-response curve for LH of human origin being a little flatter. Two standard curves for ovine LH obtained with 14 months' interval, were parallel but at different levels of ovarian ascorbic acid. When the mean ascorbic acid depletions were calculated as percentages of the control levels, the two curves for NIH-LH-S8 were identical. The use of standards of human origin in the OAAD test for LH activity of human preparations is recommended.


1961 ◽  
Vol 37 (4) ◽  
pp. 565-576 ◽  
Author(s):  
Richard A. Miller

ABSTRACT Four per cent formaldehyde, insulin, or epinephrine in oil was injected for 5 days into pigeons subjected to varying degrees of hypophysectomy alone or together with large lesions in the median eminence and hypothalamus. Adrenals atrophied after the removal of the pars distalis alone or together with the neurohypophysis in untreated pigeons but showed markedly hypertrophic interrenal tissue (cortex in mammals) after treatment with formaldehyde or insulin. The slope of the dose-response curve was similar in operated and unoperated pigeons. The accumulation of bile in the liver parenchyma, which may occur after removal of the pars distalis, is an endogenous stress which was associated regularly with adrenal hypertrophy. After very large lesions of the median eminence and ventral hypothalamus in addition to total hypophysectomy, adrenals hypertrophied rather than atrophied, and the response to formaldehyde paralleled that in intact and »hypohysectomized« pigeons. Interrenal tissue was stimulated regularly; chromaffin tissue was partially degranulated, sometimes showed hyperplasia with colchicine, but only occasionally appeared hypertrophied. Epinephrine in nearly lethal doses caused only minimal adrenal enlargement. After adrenal denervation followed by hypophysectomy, the adrenals were still stimulated by formaldehyde. It appears that the interrenal tissue of the pigeon responds to a humoral stimulus not of hypophyseal origin in the absence of the hypophyseal-hypothalamic system.


1963 ◽  
Vol 42 (2_Suppl) ◽  
pp. S17-S30
Author(s):  
Fred A. Kind ◽  
Ralph I. Dorfman

ABSTRACT Thirty-seven steroids have been studied as orally effective inhibitors of ovulation in the mated oestrus rabbit. Norethisterone served as the reference standard and a dose response curve was established between the 0.31 and 1.25 mg dose levels. Nine highly active anti-ovulatory compounds are described listed in a decreasing order of potency with norethisterone having the arbitrary value of one: 6-chloro-Δ6-dehydro-17α-acetoxyprogesterone (35), 6α-methyl-Δ1-dehydro-17α-acetoxyprogesterone (≥ 10), 6-fluoro-Δ6-dehydro-17α-acetoxyprogesterone(9), 6-methyl-Δ6-dehydro-17α-acetoxyprogesterone (5), Δ6-dehydro-17α-acetoxyprogesterone (≥ 3), 6α-methyl-17α-acetoxyprogesterone (2.6), 6-chloro-Δ1,6-bisdehydro-17α-acetoxyprogesterone (≥ 2), 2-hydroxymethyl-17α-methyl-17β-hydroxyandrostan-3-one (≥ 2), and 6α-fluoro-16α-methyl-17α-acetoxyprogesterone (≥ 1.25). The anti-ovulatory activity of a compound was not related necessarily to the progestational activity of a compound nor to the anti-gonadotrophic activity as measured in parabiotic rats. 6-Chloro-Δ60dehydro-17-acetoxyprogesterone was as effective by gavage as previously shown by subcutaneous injection. 2-Hydroxymethyl-17α-methyl-17β-hydroxyandrostan-3-one was at least 2.5 times more active by gavage than by injection. While 17α-acetoxyprogesterone was a very weak anti-ovulatory steroid, modifications of the structure by addition of methyl or halogen at the 6α position with or without unsaturation greatly increased the activity. 6-Chloro-Δ6-dehydro-27α-acetoxyprogesterone was the most active compound in this series showing a relative potency of 3500 times that of the parent compound 17α-acetoxyprogesterone.


2021 ◽  
Vol 17 ◽  
pp. 174480692199262
Author(s):  
Ken Iwata ◽  
Yukio Takamatsu ◽  
Nagafumi Doi ◽  
Kazutaka Ikeda

Electroconvulsive therapy (ECT) has been applied for chronic pain for decades. The amounts of opioids to treat pain are sometimes reduced after a series of ECT. The effect of ECT on morphine-induced analgesia and its mechanism underlying the reduction of morphine requirement has yet to be clarified. Therefore, we administered electroconvulsive shocks (ECS) to mice and investigated the antinociceptive effect of morphine in a hot plate test. We examined the expression level of µ-opioid receptor in the thalami of mice 25 h after administration of ECS compared to the thalami of mice without ECS administration using western blotting. ECS disturbed the development of a decrease in the percentage of maximal possible effect (%MPE), which was observed 24 h after a morphine injection, when ECS was applied 25, 23, 21, and 12 h before the second administration of morphine. We also examined the effect of ECS on the dose-response curve of %MPE to morphine-antinociception. Twenty-five hours after ECS, the dose-response curve was shifted to the left, and the EC50 of morphine given to ECS-pretreated mice decreased by 30.1% compared to the mice that were not pretreated with ECS. We also found that the expression level of µ-opioid receptors was significantly increased after ECS administration. These results confirm previous clinical reports showing that ECT decreased the required dose of opioids in neuropathic pain patients and suggest the hypothesis that this effect of ECT works through the thalamus.


1981 ◽  
Vol 27 (11) ◽  
pp. 1838-1844 ◽  
Author(s):  
G A Hudson ◽  
R F Ritchie ◽  
J E Haddow

Abstract Antiserum performance in a nephelometric system can be characterized by parameters derived from measuring reaction rates. The characterization process is derived from a series of dose-response curves (elicited nephelometric response vs antigen concentration) generated from various dilutions of the antiserum being tested. Antiserum titer can then be calculated by plotting the antigen concentration found at one-half the maximum nephelometric response (Hmax) of each dose-response curve (C50) vs the corresponding antiserum dilution. Antiserum avidity can be calculated by plotting Hmax against its corresponding antiserum concentration. After general expressions are determined for C50 and Hmax vs antiserum concentration, a single dose-response curve suffices for characterizing antisera with respect to titer and avidity. Direct evidence is provided for the validity of C50 and Hmax as measures of titer and avidity by correlating these parameters with antiserum binding strength and with the number of antibodies eluted from immobilized antigen. This method can be applied to evaluate and compare different antiserum lots having the same specificity, to identify reagent inadequacies by comparing antisera of different specificity, and to predict the optimal antiserum dilution to use in performing an assay.


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