Identification and Mechanism of <i>Echinochloa crus-galli</i> Resistance to Fenoxaprop-p-ethyl with respect to Physiological and Anatomical Differences

Hamza, Amany; Derbalah, Aly; El-Nady, Mohamed

doi:https://doi.org/10.1100/2012/893204

The Scientific World Journal

On this page

Abstract Introduction Materials and Methods Results Discussion Conclusions References Copyright Related Articles

Research Article | Open Access

Volume 2012 | Article ID 893204 | https://doi.org/10.1100/2012/893204

Identification and Mechanism of Echinochloa crus-galli Resistance to Fenoxaprop-p-ethyl with respect to Physiological and Anatomical Differences

Amany Hamza,¹Aly Derbalah,¹and Mohamed El-Nady^2,3

Academic Editor: R. Sarkar, S. Y. Morozov

Received11 Oct 2011

Accepted30 Nov 2011

Published19 Apr 2012

Abstract

Identification and mechanism of Echinochloa crus-galli (L.) resistance to fenoxaprop-p-ethyl via physiological and anatomical differences between susceptible and resistant were investigated. The physiological and anatomical differences that were take into account were growth reduction, chlorophyll content reduction, lamina thickness, and xylem vessel diameter in both susceptible and resistant biotypes of E. crus-galli. The results showed that the growth reduction fifty (GR₅₀) of resistant biotype was 12.07-times higher than that of the susceptible biotype of E. crus-galli treated with fenoxaprop-p-ethyl. The chlorophyll content was highly reduced in the susceptible biotype relative to the resistant one of E. crus-galli treated with fenoxaprop-p-ethyl. An anatomical test showed significant differences in the cytology of susceptible and resistant biotypes of E. crus-galli treated with fenoxaprop-p-ethyl with respect to lamina thickness and xylem vessel diameter. The resistance of E. crus-galli to fenoxaprop-p-ethyl may be due to the faster metabolism of fenoxaprop-p-ethyl below the physiologically active concentration or the insensitivity of its target enzyme (Acetyl-CoA carboxylase).

1. Introduction

E. crus-galli (L.) Beauv is a type of wild grass originating from tropical Asia that was formerly classified as a type of panicum grass. Considered as one of the world’s worst weeds, it reduces crop yields and causes forage crops to fail by removing up to 80% of the available soil nitrogen. The high levels of nitrates it accumulates can poison livestock. It acts as a host for several mosaic virus diseases. Heavy infestations can interfere with mechanical harvesting. Individual plants can produce up to 40,000 seeds per year. Water, birds, insects, machinery, and animal feet disperse it, but contaminated seed is probably the most common dispersal method. More than 35% of grain yield in seeded rice was reduced by infestation with E. crus-galli [1].

Due to the great risk of this weed infestation in Egypt and worldwide, herbicide is becoming the most popular method of weed control in rice. However, while herbicide application certainly controls the weeds, experience shows, however, that although herbicide use alleviates the problem of labor for weeding, incorrect use of herbicides may bring about other environmental problems such as selecting for resistance to herbicides. Weed resistance to herbicides concerns many sectors of the agricultural community: farmers, advisors, researchers, and the agrochemical industry in Egypt and worldwide. The fear exists that in an extreme case of resistance, farmers might lose a valuable chemical tool that had previously provided effective control of yield-reducing weeds. Resistance is often seen as a problem caused by a particular active ingredient. This is an over-simplification and a misconception. Resistance results from agronomic systems which have been developed to rely too heavily on herbicides as the sole method of weed control [2]. Without monitoring and rapid detection of the resistance evolution, interpretation of its mechanism and trying to find sustainable management strategies, the future usefulness of herbicides as a tool for weed control might be seriously jeopardized. Furthermore, the identification of resistance mechanism to herbicides is considered the key step toward developing appropriate solutions to overcome this phenomenon.

Resistance mechanism through evaluation of the activity of target site enzymes has been reported before [3–5]; however, characterizing the resistance mechanisms of weeds to herbicides via investigating the anatomical and physiological differences in susceptible and resistant biotypes considered a source of major concern and has not been studied before.

Therefore, this study attempted to identify the occurrence and mechanism of E. crus-galli-resistant biotype against fenoxaprop-p-ethyl via investigation of the physiological (chlorophyll content and growth reduction) and anatomical differences between the susceptible and resistant biotypes of E. crus-galli (barnyardgrass) treated with fenoxaprop-p-ethyl.

2. Materials and Methods

2.1. The Used Herbicide

Fenoxaprop-p-ethyl with the trade name of Whip-super EW 7.5% was obtained from Rice Weeds Research Department, Rice Research and Training Center, Sakah, and Kafr el-Sheikh, Egypt. This herbicide was applied at the filed rate of 49.5 gm a.i/hectare.

2.2. The Tested Weed

The susceptible biotype (SBT) of the Echinochloa crus-galli to fenoxaprop-p-ethyl (obtained from Rice Weeds Research Department, Rice Research and Training Centre, Sakah, Kafr El-Sheikh). The resistant biotype (RBT) of Echinochloa crus-galli used in this study was previously treated for several years with the tested herbicide by selection pressure and recorded resistance [6].

2.3. Whole Plant Bioassay

Dose-response experiments were conducted at the greenhouse of the Agricultural Botany Department, Faculty of Agriculture, Kafr El-Sheikh University, Egypt. The soil used in this experiment was fertilized with nitrogen at a rate of 360 kg/h of urea fertilizer (containing 46% nitrogen). Super phosphate fertilizer (phosphorus 15%) was added at a rate of 240 kg/ha before planting. Potassium was not added because the Egyptian soil is rich in this element. Seeds of susceptible and resistant biotypes of Echinochloa crus-galli were planted in 30 × 30 cm plastic pots filled with soil. Emerged seedlings were thinned to four uniform and equally distant-spaced plants per pot. These experiments were conducted at average daily temperatures ranging from 22 to 31°C and at a 16-h day length. Pots were immersed with water up to 4 cm above the soil surface. The tested herbicide, fenoxaprop-p-ethyl, was applied as a single application using a hand sprayer at the 4-leaf to 1-tiller stage of growth of the tested weed. The concentration levels used were 0.1, 0.5, 1, and 2 folds of fenoxaprop-p-ethyl recommended dose. After forty-eight hours of treatment, the plants were irrigated and water was raised up to 4 cm above the soil surface [4]. Experiments were done in a completely randomized design with six replicates. Fresh weight of treated and untreated plant was determined after 14 days of fenoxaprop-p-ethyl application. Data were pooled and fitted to a log-logistic regression model [7, 8] as shown in (1) where is the fresh weight of germinated seedling aboveground expressed as percentage of the untreated control, and are the coefficients corresponding to the lower and upper asymptotes, is the slope of the line, (GR₅₀) is the herbicide rate at the point of inflection halfway between the upper () and lower () asymptotes, and (independent variable) is the herbicide dose.

Regression analysis was conducted using the Sigma Plot statistical software version 10.0 [4]. The herbicide rate used to reduce plant growth by 50% relative to the untreated control (GR₅₀) was calculated for resistant and susceptible biotypes of E. crus-galli. R/S ratios were calculated as the GR₅₀ of the resistant (R) biotype divided by the GR₅₀ of the susceptible (S) biotype.

2.4. Chlorophyll Measurements

Plant leaves differ from that used in fresh weight determination were used to determine the chlorophyll content of resistant and sensitive biotypes of E. crus-galli after 14 days of treatment with fenoxaprop-p-ethyl at the level applied in the real field conditions. Chlorophyll content of untreated controls was measured after 14 days also. Moreover, chlorophyll content of resistant treated and untreated biotypes were remeasured after 21 days of treatment with fenoxaprop-p-ethyl (treated leaves were regrown again and chlorophyll content increased). No chlorophyll data was taken for the suscipble biotype after 21 days due to the plant is completely dead. Chlorophyll A, B, and total were determined in E. crus-galli lamina using the method described by Moran and Porath [9]. Data were subjected to statistical analysis of variance according to the method described by K. A. Gomez and A. A. Gomez [10].

2.5. Anatomical Test

The leaf specimens which included the midrib collected from plants differ from that used in fresh weight and chlorophyll determination were taken after 14 days of treatment from the second leaf of the resistant and susceptible biotypes of E. crus-galli treated with fenoxaprop-p-ethyl at the recommended dose level (1 fold). Moreover, leaf specimens of resistant treated and untreated biotypes were measured again after 21 days of treatment with fenoxaprop-p-ethyl (treated leaves were recovered again and chlorophyll content increased). No leaf specimens were taken for the susceptible biotype after 21 days due to the plant is completely dead. Specimens were fixed in a formalin, ethyl alcohol, and acetic acid mixture (1 : 18 : 1 v/v). Then specimens were washed and dehydrated in an alcohol series. The dehydrated specimens were infiltrated and embedded in paraffin wax (52–54°C m.p.). The embedded specimens were sectioned using a rotary microtome (Leica RM 2125) to a thickness of 8–10 μm. Sections were mounted on slides and deparaffinized. Staining was accomplished with safranine and azur II [11], cleared in xylol, and mounted in Canada balsam [12]. Ten readings from 3 slides from different leaves of the same plant were examined with electric microscope (Lieca DM LS) with digital camera (Lieca DC 300) and then photographed. The anatomical manifestation was calculated using Lieca IM 1000 image manager software. Lieca software was calibrated using 1 cm stage micrometer scaled at 100 μm increment (Leitz Wetzler, Germany 604364) at a 4 and 10x magnifications.

2.6. Statistical Analysis

Data from the experiments were statistically analyzed using one-way repeated measurement analysis of variance according to the method described by K. A. Gomez and A. A. Gomez [10]. Duncan’s multiple range test was used to separate means using SAS software (version 6.12, SAS Institute Inc., and Cary, USA).

3. Results

3.1. E. crus-galli Resistance to Fenoxaprop-p-ethyl by Means of Fresh Weight Reduction of Treated Plants

A dose-response experiment was conducted on whole plants of E. crus-galli treated with fenoxaprop-p-ethyl to detect its resistance against this herbicide. The response of the tested susceptible and resistant biotypes against this herbicide was determined as reduction in the fresh weight of the treated plants relative to the control after 14 days of fenoxaprop-p-ethyl application. The results showed that the rates of fenoxaprop-p-ethyl required for 50% growth reduction were 3 and 36.2 gm a.i./ha for the susceptible and resistant biotypes of E. crus-galli, respectively (Table 1). Table 1 revealed that the GR₅₀ of E. crus-galli-resistant biotype was 12.07-times higher than that required to obtain the same effect on the susceptible biotype.

3.2. Effect of Tested Herbicide on Chlorophyll Content of Susceptible and Resistant Biotypes of E. crus-galli

The chlorophyll content of E. crus-galli was measured after 14 days of herbicide application to evaluate the physiological conditions of the tested weed. Table 2 showed that the chlorophyll content after fenoxaprop-p-ethyl application was decreased either in the resistant or susceptible biotypes. The rate of reduction in chlorophyll content was higher in susceptible biotype than the resistant one of E. crus-galli. The chlorophyll content was higher in the untreated susceptible biotype of E. crus-galli relative to the treated one. The chlorophyll content was slightly higher in the untreated resistant biotype of E. crus-galli relative to the treated one. A very important action took place. Chlorophyll content of the resistant biotype treated with fenoxaprop-p-ethyl increased again relative to the untreated resistant plants after 21 days of treatment. This action was due to the re-growth of E. crus-galli leaves as shown in Table 3.

3.3. Anatomical Differences between Susceptible and Resistant Biotypes of E. crus-galli against Fenoxaprop-p-ethyl

The anatomical differences between the susceptible and resistant biotypes of E. crus-galli treated with fenoxaprop-p-ethyl with respect to lamina thickness and xylem vessel diameter are presented in Table 4 and Figure 1. The results showed that susceptible biotype (SBT) treated with fenoxaprop-p-ethyl had less laminal thickness and tissues intensively stained with azur II compared with the untreated plants. The normal internal leaf structure of treated SBT is more difficult to be identified, which may be due to cell death compared with untreated plants. Laminal thickness and xylem vessel diameter of treated biotypes were reduced compared with the untreated plants, but the lowest value was caused by treated SBT. In contrast, leaf tissues in treated resistant biotype (RBT) seem to be normal and easily identified. Intensively stained cells with azur II, though, were noticed in some local lesions (areas), which may be due to cell death.

(a)

(b)

(c)

(d)

(e)

(f)

(g)

(h)

Concerning of recovery in RBT of E. crus-galli treated with fenoxaprop-p-ethyl, relative to the untreated one, data in Table 5 and Figure 2 indicated that lamina thickness was increased up to untreated RBT. Furthermore, no differences in xylem vessel diameter were found between treated and untreated RBT.

(a)

(b)

(c)

(d)

4. Discussion

The resistance of E. crus-galli to fenoxaprop-p-ethyl (ACCase inhibitor) was identified in this study and confirmed the occurrence of E. crus-galli resistance to fenoxaprop-p-ethyl in Egypt. This finding had been reported previously outside Egypt [3, 13–17]. The results of this study also implied that the physiological and anatomical dereferences as well as growth reduction help to identify the occurrence of resistant weed.

Chlorophyll content has been known as a typical parameter for evaluating the physiological conditions in common sense. The reduction in chlorophyll content of E. crus-galli resistant and susceptible biotypes after foliar application of fenoxaprop-p-ethyl in this study is in agreement with the findings of [18, 19] who reported that the application of fenoxaprop-p-ethyl as ACCase-inhibitor leads to injury symptoms in the form of chlorosis (reduction in the chlorophyll content). The reduction in chlorophyll content after foliar application of fenoxaprop-p-ethyl is likely to be due to its incorporation into the cell membrane function through physiological processes, such as depolarization of membrane potential [20] which is not clarified yet. Subsequently, this makes the translocation of fenoxaprop-p-ethyl become more difficult and thus, relatively large amount of the herbicide retained in the treated leaf tissue and reduce the chlorophyll content [21]. Moreover, this reduction may be due to the enhanced activity of chlorophyll degrading enzyme chlorophyllase and/or disruption of the fine structure of chloroplast and instability of chloroplast or pigment-protein complex, which leads to oxidation of chlorophyll and decreased its concentration.

The results also showed that the reduction in chlorophyll content in resistant biotype treated with fenoxaprop-p-ethyl was lower than that of susceptible biotype of E. crus-galli. Furthermore, the results indicated that the chlorophyll content of the treated resistant biotype of E. crus-galli again increased more than the untreated one after 21 days of fenoxaprop-p-ethyl application. The possible mechanism of lower reduction or reincrease of chlorophyll content in the resistant biotype of E. crus-galli relative to the susceptible one, may be due to the relatively faster metabolism of fenoxaprop-p-ethyl through glycosylation [22] which occurs relatively high in the resistant biotype. That is, relatively small amount of the compound was retained in the treated leaf tissue and, thus, photosynthesis in the treated leaf was able to occur continuously [21]. The accumulation of carbohydrates that has been found in the leaves treated with ACCase inhibitors [23, 24] support, this point of view. Therefore, even if the plant is treated with a rate close to the lethal dose, the treated plants are still alive and likely to regrow when the phytotoxic compound is degraded below the physiologically active concentration [21].

In this study, there were anatomical differences between resistant and susceptible biotypes of E. crus-galli treated with fenoxaprop-p-ethyl with respect to leaf lamina thickness and xylem vessel diameter. Moreover, lamina thickness of treated RBT was increased up to untreated RBT. Moreover, no differences in xylem vessel diameter were found between treated and untreated RBT of E. crus-galli. Reduction in leaf lamina thickness in sensitive biotype of E. crus-galli treated with fenoxaprop-p-ethyl was a reflection of the decrease in mesophyll cells. The decrease in mesophyll cells may be attributed to inhibition of cell division and/or cell enlargement which subsequently may be due to the disruption in plasma membrane that mainly consists of phospholipids. Therefore, any reduction in fatty acids biosynthesis due to fenoxaprop-p-ethyl application that is known as fatty acids synthesis inhibitor [25–27] will affect the membrane formation and subsequently its functions such as cell division and/or cell enlargement. The inhibition in cell division and/or ell enlargement resulted in reduction in mesophyll cells and subsequently in leaf laminal thickness.

From all previous data, fatty acids are critical components of cell membranes, therefore, reduction or inhibition of fatty acids biosynthesis will affect chlorophyll content and plasma membrane functions. Since that fenoxaprop-p-ethyl is known as fatty acids biosynthesis inhibitor [25–28], its foliar application lead to reduction in chlorophyll content and disruption in plasma membrane functions and subsequently the photosynthesis, number of mesophyll cells, and growth indicators such as growth reduction fifty. All of these parameters were recorded in this study for the treated sensitive biotype of E. crus-galli with fenoxaprop-p-ethyl. However, for the resistant biotype of E. crus-galli a slight reduction was recorded relative to the sensitive one and this may be due to the fact that the reduction in fatty acids biosynthesis was much lower than that of sensitive biotype.

Therefore, the resistance mechanism of E. crus-galli to the fenoxaprop-p-ethyl may be conferred by two proposed mechanisms. Firstly, the mechanism may be due to an alteration in the gene(s) of target site enzyme (ACCase) protein likely the mechanism that confers resistance of E. crus-galli to the fenoxaprop-p-ethyl herbicide. The alteration or changes in the protein of ACCase enzyme (the target of fenoxaprop-p-ethyl) in the resistant biotype compared to the susceptible one, induced low affinity of fenoxaprop-p-ethyl herbicide to bind with the target enzyme and the enzyme became insensitive to the herbicide. Moreover, it is apparent that the altered sensitivity of ACCase of the resistant Echinochloa sp. to fenoxaprop-p-ethyl may be due to a mutation of the target site enzyme which does not affect equally the bending of the other aryloxyphenoxypropionate [26]. Similarly, the relatively high growth reduction dose of the resistant E. crus-galli biotype in this study to the herbicide, chlorophyll content and anatomical differences of the two E. crus-galli biotypes provides additional support to this proposed mechanism of resistance.

The second mechanism of E. crus-galli resistant to fenoxaprop-p-ethyl may be due to the relatively faster metabolism of fenoxaprop-p-ethyl through glycosylation [22] occurs relatively high in the resistant biotype. That is which relatively small amount of the compound was retained in the treated leaf tissue and, thus, photosynthesis in the treated leaf was able to occur continuously [21]. There are some reports that revealed that an accumulation of carbohydrates has been found in the leaves treated with ACCase inhibitors [23, 24]. Therefore, even if the plant is treated with a rate close to the lethal dose, the treated plants are still alive and likely to re-grow when the phytotoxic compound is degraded below the physiologically active concentration which may be due to the faster metabolism of fenoxaprop-p-ethyl. This proposed mechanism was in agreement with chlorophyll data in this study. Both proposed mechanisms to fenoxaprop-p-ethyl and other ACCase inhibitors had been reported before for another weed [28]; however, against E. crus-galli based on physioanatomical differences, this is considered to be the first report.

5. Conclusions

There were significant differences between susceptible and resistant biotypes of E. crus-galli treated with fenoxaprop-p-ethyl with respect to chlorophyll content, growth reduction, and anatomical test. These differences concluded the ability to identify the occurrence of E. crus-galli resistant to fenoxaprop-p-ethyl and assumed that the resistance mechanism was explained either by target site insensitivity or by an enhanced rate of metabolism.

References

M. L. Naples and P. J. A. Kessler, Weeds of rain fed lowland rice fields of Laos & Cambodia, M.S. thesis, University of Leiden, Cambodia, 2005.
Weed Science Society oF America, Herbicide Handbook, 9th edition, 2007.
A. J. Fischer, C. M. Ateh, D. E. Bayer, and J. E. Hill, “Herbicide-resistant Echinochloa oryzoides and E. phyllopogon in California Oryza sativa fields,” Weed Science, vol. 48, no. 2, pp. 225–230, 2000.
View at: Google Scholar
M. D. Osuna, F. Vidotto, A. J. Fischer, D. E. Bayer, R. De Prado, and A. Ferrero, “Cross-resistance to bispyribac-sodium and bensulfuron-methyl in Echinochloa phyllopogon and Cyperus difformis,” Pesticide Biochemistry and Physiology, vol. 73, no. 1, pp. 9–17, 2002.
View at: Publisher Site | Google Scholar
R. Busi, F. Vidotto, and A. Ferrero, “Resistance patterns to ALS-inhibitors in Cyperus difformis and Schoenoplectus mucronatus (abstract),” in Abstract Book of the 4th International Weed Science Congress, 2004.
View at: Google Scholar
A. M. Hamza, Evoloution and resistance mechanism of some rice weeds against some herbicides, Doctoral thesis, Faculty of Agriculture, Kafr-El Sheikh University, Kafrelsheikh, Egypt, 2009.
J. C. Streibig, M. Rudemo, and J. E. Jensen, “Dose response curves and statistical models,” in Herbicides Bioassays, J. C. Streibig and P. Kudsk, Eds., pp. 30–55, CRC, Boca Raton, Fla, USA, 1993.
View at: Google Scholar
S. S. Seefeldt, J. E. Jensen, and E. P. Feurst, “Log-logistic analysis of herbicide dose-response relationships,” Weed Technology, vol. 9, no. 2, pp. 218–227, 1995.
View at: Google Scholar
R. Moran and D. Porath, “Chlorophyll determination in intact tissues using N, N-Dimethyl formamide,” Plant Physiology, vol. 69, pp. 1370–1381, 1980.
View at: Google Scholar
K. A. Gomez and A. A. Gomez, Statistical procedures for agricultural research, John Wiley & Sons, New York, NY, USA, 2nd edition, 1984.
M. Gutmann, “Improved staining procedures for photographic documentation of phenolic deposits in semithin sections of giant tissue,” Journal of Microscopy, vol. 179, no. 3, pp. 277–281, 1995.
View at: Google Scholar
S. E. Ruzin, Plant Microtechniques and Microscopy, Oxford University Press, New York, NY, USA, 1st edition, 1999.
J. Gressel, “More non-target site herbicide cross-resistance in Echinochloa spp. in rice,” Residential Pest Management, vol. 11, pp. 6–7, 2000.
View at: Google Scholar
J. P. Ruiz-Santaella, Y. Bakkali, A. J. Fischer, and R. De Prado, “Is it possible to detect Echinochloa spp. tolerance to ACCase-inhibiting herbicides using a simple quick tolerance test?” Communications in Agricultural and Applied Biological Sciences, vol. 68, no. 4, pp. 331–334, 2003.
View at: Google Scholar
J. P. Ruiz-Santaella, A. J. Fisher, and R. De Prado, “Alternative control of two biotypes of Echinochloa phyllopogon susceptible and resistant to fenoxaprop-ethyl,” Communications in Agricultural and Applied Biological Sciences, vol. 68, no. 4, pp. 403–407, 2003.
View at: Google Scholar
D. S. Kim, J. C. Caseley, P. Brain, C. R. Riches, and B. E. Valverde, “Rapid detection of propanil and fenoxaprop resistance in Echinochloa colona,” Weed Science, vol. 48, no. 6, pp. 695–700, 2000.
View at: Google Scholar
B. E. Valverde and K. Itoh, “World rice and herbicide resistance,” in Herbicide Resistance and World Grains, S. B. Powles and D. L. Shaner, Eds., pp. 195–249, CRC Press, Boca Raton, Fla, USA, 2001.
View at: Google Scholar
D. W. Lycan and S. E. Hart, “Cool-season turfgrass response to bispyribac-sodium,” HortScience, vol. 40, no. 5, pp. 1552–1555, 2005.
View at: Google Scholar
W. P. Anderson, Weed Sciences: Principles and Application, West Publishing, Minneapolis, Minn, USA, 3rd edition, 1996.
J. P. Wright, “Use of membrane potential measurements to study mode of action of diclofop-methyl,” Weed Science, vol. 42, pp. 285–292, 1994.
View at: Google Scholar
J. S. Kim, J. I. Oh, T. J. Kim, Y. P. Jong, and Y. C. Kwang, “Physiological basis of differential phytotoxic activity between fenoxaprop-P-ethyl and cyhalofop-butyl-treated barnyardgrass,” Weed Biology and Management, vol. 5, no. 2, pp. 39–45, 2005.
View at: Publisher Site | Google Scholar
H. Hosaka, H. Inaba, A. Satoh, and H. Ishikawa, “Morphological and histological effects of sethoxydim on corn (Zea mays) seedlings,” Weed Science, vol. 32, pp. 711–721, 1984.
View at: Google Scholar
H. Hosaka and M. Takagi, “Effects and absorption of sethoxydim in cell cycle progression of corn (Zea mays) and pea (Pisum sativum),” Plant Physiology, vol. 99, no. 4, pp. 1650–1656, 1992.
View at: Google Scholar
A. Tal, M. L. Romano, G. R. Stephenson, A. L. Schwan, and J. C. Hall, “Glutathione conjuction: a detoxification pathway for fenoxaprop-p-ethyl in barley ,crabgrass , oat and wheat,” Pesticide Biochemistry and Physiology, vol. 46, pp. 190–199, 1993.
View at: Google Scholar
Y. I. Kuk, J. Wu, J. F. Derr, and K. K. Hatzios, “Mechanism of fenoxaprop resistance in an accession of smooth crabgrass (Digitaria ischaemum),” Pesticide Biochemistry and Physiology, vol. 64, no. 2, pp. 112–123, 1999.
View at: Publisher Site | Google Scholar
Y. I. Kuk, J. Wu, J. F. Derr, and K. K. Hatzios, “Mechanism of fenoxaprop resistance in an accession of smooth crabgrass (Digitaria ischaemum),” Pesticide Biochemistry and Physiology, vol. 64, no. 2, pp. 112–123, 1999.
View at: Publisher Site | Google Scholar
D. S. Volenberg and D. E. Stoltenberg, “Giant foxtail (Setaria faberi) outcrossing and inheritance of resistance to acetyl-coenzyme A carboxylase inhibitors,” Weed Science, vol. 50, no. 5, pp. 622–627, 2002.
View at: Publisher Site | Google Scholar
M. S. Yun, Y. Yogo, R. Miura, Y. Yamasue, and A. J. Fischer, “Cytochrome P-450 monooxygenase activity in herbicide-resistant and -susceptible late watergrass (Echinochloa phyllopogon),” Pesticide Biochemistry and Physiology, vol. 83, no. 2-3, pp. 107–114, 2005.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2012 Amany Hamza et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PDF Download Citation

Download other formats

Order printed copies

Views

2054

Downloads

1287

Citations