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INTRODUCTION
Glufosinateis a nonselective postemergenceherbicide
used for weed control in orchards,vineyards, and prior
to no-till planting. Glufosinate inhibits glutamine synthetase (GS) enzyme in susceptible plants (Bellinder et
al. 1985; Logusch et al. 1991; Sauer et al. 1987; Wild
et al. 1987; Wild and Wendler 1993). The GS enzyme
catalyzes an essential reaction for nitrogen metabolism
in plants, the conversion of glutamate plus ammonia to
glutamine. Only 1 d after a glufosinate application, the
ammonia levels in treated leaves may increase as much
as 100-fold over the level in nontreatedtissue (Shelp et
al. 1991; Wild et al. 1987). The accumulation of ammonia is enhanced greatly in the presence of light and
ultimately results in membranedisruption,inhibition of
photosynthesis, and plant death (Bellinder et al. 1987;
Wendleret al. 1990).
Although glufosinate is considered a nonselective her' Received for publication June 13, 1996, and in revised form March 17,
1997.
2Graduate Research Assistant, Department of Crop Science, Research
Agronomist,USDA-ARS, Crop ProtectionResearch,Departmentof Crop Science, Associate Professor, Department of Natural Resources and Environmental Science, Research Specialist, Departmentof Crop Science, University
of Illinois, 1102 South Goodwin Avenue, Urbana, IL 61801.
3 Letters following this symbol are a WSSA-approvedcomputercode from
Composite List of Weeds, Revised 1989. Available from WSSA.
bicide, differentialresponse to glufosinate has been observed, even in sensitive species. Ridley and McNally
(1985) found greaterthan a 70-fold differencein the susceptibility of seven plant species to glufosinate, possibly
due to different ratios of the two isoenzymes of glutamine synthetase that can occur in plants. Mersey et al.
(1990) found that glufosinate absorptionand translocation differences accountedfor greatersensitivity in green
foxtail [Setaria viridis (L.) Beauv.] than in barley (Hordeum vulgare L.), while very little metabolicdegradation
of glufosinate was detected in either of the species.
Environmentalconditions such as air temperatureand
relative humidityat applicationcan influencethe activity
of many postemergence herbicides (Prasad et al. 1967;
Ritter and Coble 1981; Wills 1984). Low relative humidity prior to, during, and after treatmentmay cause
the cuticle to be dehydrated,thus possibly reducing absorptionof water soluble herbicides such as glufosinate.
For example, the toleranceof green foxtail and barley to
glufosinate was significantly higher when relative humidity was maintainedat 40% comparedwith 95% (Anderson et al. 1993a). Air temperaturemay change the
permeabilityof both the cutin matrix and soluble membranesin some species. Activity of glyphosate [N-(phosphonomethyl)glycine] on johnsongrass [Sorghum hale-
484
WEED TECHNOLOGY
5a
10
1994
15
10
Before application
1995
15
10
15
2
4
3
3
3
6
4
4
4
8
5
7
No. of leaves
Giant foxtail
Common lambsquarters
Common cocklebur
Pennsylvania smartweed
2
2
2
2
4
4
3
4
5
5
4
5
3
2
3
3
4
5
4
4
5
6
4
5
Air temperatureb
Weed
heighta 1993 1994 1995
cm
5
10
15
Relative humidityc
Rainfalld
1993 1994 1995 1993 1994 1995
C
20
15
17
16
15
20
%
11
17
22
65
51
59
77
61
59
mm
74
71
73
10
0
14
45
4
42
130
46
12
After application
cm
mm
485
STECKELET AL.: GLUFOSINATEEFFICACYON ANNUAL WEEDS IS INFLUENCEDBY RATE AND GROWTH STAGE
100 90
1993
100
90 - 1993
80 70 60 -
80HA
60
50_ -.403020 10 10
50 -_
40 30-
20 - =_
20
10]- 1994
90 -1
80 -
60 50
40
30 20
100
90 199
80
70 -1
60-1
40 20
5
303 -
1995
.-19
90
80 A
(g/ha)
_4
10 -v
100-kA
20
40
30140950
302010
200
r -
20
10
100-
60 A
100
100 - 1994
90 199
80 70 -
60
50
40j
3020
10
300
400
500
600
Glufosinate(glha)
Figure 1. Linearregressionand predictedvalues of mean giant foxtail control
at four rates of glufosinate,each appliedat weed heights of 5 (@), 10 (U) and
15 cm (A). Regression models and r2 are for each line where significanceis
representedby * and # for 5 and 10% level, respectively. The models fitted
were for 1993: 5 cm, y = 13 + O.lOx,r2 = 0.63; 10 cm, y = 14 + 0.15x, r2
= 0.81#; and 15 cm, y = 46 + 0.09x, r2 = 0.96*. For 1994: 5 cm, y = 18 +
0.15x, r2 = 0.81*; 10 cm, y = 34 + 0.12x, r2 = 0.77*;and 15 cm, y = 31 +
0.12x, r2 = 0.77*. For 1995: 5 cm, y = 44 + 0.09x, r2 = 0.84*; 10 cm, y =
73 + 0.05x, r2 = 0.98*; and 15 cm, y = 25 + 0.12x, r2 = 0.96*.
The experiment was established as a randomized complete block design with three blocks in a four by three
factorial arrangementof four glufosinate rates and three
application timings. Data were subjected to analysis of
variance (ANOVA) at the 5% level to determine significance of any interactions among main effects. The
ANOVA revealed a significant year by treatmentinteraction, resulting in a regression analysis conducted for
each year. The mean control data were regressed over
herbiciderate for each growth stage. Regressionlines are
presented with symbols representingpredictedvalues at
the three treatmentrates. Correlationanalyses were conducted on rainfall and control ratings at the 10% level.
While some correlations were significant, no overall
trends were apparent.
100
200
300
400
500
600
Glufosinate(glha)
Figure 2. Linear regression and predicted values of mean common lambsquarterscontrol at four rates of glufosinate, each applied at weed heights of
5 (@), 10 (U) and 15 cm (A). Regression models and r2 are for each line
where significance is representedby * and * for 5 and 10%level, respectively.
The models fitted were for 1993: 5 cm, y = -14 + O.lIx, r2 = 0.98*; 10
cm, y = 1.0 + O.lix, r2 = 0.94*; and 15 cm, y = 7.0 + 0.05x, r2 = 0.82#.
For 1994: 5 cm, y = -1.7 + 0.llx, r2 = 0.79#; 10 cm, y = 9.0 + 0.llx,
r2 = 0.76#; and 15 cm, y = 8.0 + 0.08x, r2 = 0.46. For 1995: 5 cm, y =
4.2 + O.lIx, r2 = 0.84*; 10 cm, y = 11 + 0.16x, r2 = 0.94*; and 15 cm,
y = 2.0 + O.lIx, r2 = 0.99*.
RESULTSAND DISCUSSION
486
WEED TECHNOLOGY
1oo
100
90 - 1993
80 70 60- 50 403020 10
90 - 1993
80 70 60 40 30 20 10 -
[~
0-
100
1900- 1994
80 A
100
10090
1994
80 7
3060 10 -
60 -
-40
40
30 l0O-20
10
40
-4
,01,3020-
100
100 -
100199
90 1995
90 - 1995
80 A
80 70 60 50 4030 20 10 -
10 60 -i
40 30
120-
kA
0 -
100
200
300
400
500
600
Glufosinate(g/ha)
100
200
300
400
500
600
Glufosinate(glha)
Figure 4. Linearregressionand predictedvalues of mean Pennsylvaniasmartweed control at four rates of glufosinate, each applied at weed heights of 5
(0), 10 (U) and 15 cm (A). Regression models and r2are for each line where
significance is representedby * and for 5 and 10% level, respectively. The
models fitted were for 1993: 5 cm, y = 3.0 + 0.14x, r2 = 0.99*; 10 cm, y
= 14 + l.Olx, r2 = 0.77#; and 15 cm, y = 22 + 0.06x, r2 = 0.89*. For
1994: 5 cm, y = 17 + 0.14x, r2 = 0.88#; 10 cm, y = 29 + 0.12x, r2 =
0.99*; and 15 cm, y = 25 + 0.14x, r2 = 0.90*. For 1995: 5 cm, y = 13 +
O.lix, r2 = 0.79#; 10 cm, y = 9.0 + 0.14x, r2 = 0.93*; and 15 cm, y = 27
+ 0.09x, r2 = 0.97*.
of Higgins et al. (1991), who found that glufosinate applied to common lambsquartersplants as tall as 60 cm
resulted in very good control. Often, early researchwith
glufosinate evaluatedrates of 600 g/ha and higher.These
elevated rates may explain the enhanced control of
weeds such as common lambsquarters.In this study, all
rates at all plant heights but one resulted in less than
70% control. Only at the 10-cm plant height in 1995 did
the 420 and 560 g/ha rates give control that was approximately 80% or greater.In 1995, favorable environmental conditions before and after the 10-cm height application could have resulted in this enhanced control of
common lambsquarters. Adequate soil moisture and
good growing conditions prior to treatment are often
found to enhance herbicidecontrol, as stressedplants are
usually difficult to control. When plants are water
stressed, the reduced efficacy has been found to be the
result of reduced uptake and translocationof other herbicides such as glyphosate (Ahmadi et al. 1980).
487
STECKELET AL.: GLUFOSINATEEFFICACYON ANNUAL WEEDS IS INFLUENCEDBY RATE AND GROWTH STAGE
(July-September) 1997