ABSTRACT
Coconut (Cocos nucifera L.) is an important palm species that serves as the mainstay of several industries and contributes to the livelihoods of millions of smallholder farmers. International exchange of coconut germplasm has been undertaken for several decades to facilitate the conservation of selected varieties within global genebanks and for the distribution to farmers and scientists. In vitro systems are a convenient and an efficient method for the exchange of coconut germplasm. However, it is possible that these tissue culture systems can transfer lethal pathogens causing a threat to the importing countries. In this review, the following topics are discussed: the major disease-causing agents of concern, the various tissues that could be used for coconut germplasm exchange, and the techniques available for the detection and elimination of disease-causing agents from various transmission systems. Additionally, the lack of clear, science-backed guidelines to facilitate the exchange of in vitro coconut materials is raised, along with recommendations for future studies to ensure the safe movement of coconut germplasm without biosecurity risks.
ABSTRACT
Pimelea trichostachya Lindl. is a native Australian forb responsible for livestock poisoning and reducing the productivity and sustainability of grazing enterprises. This study was conducted as a pot trial under controlled conditions to investigate an effective chemical management strategy for P. trichostachya, a method that did not leave standing dead plant material, as such material can also be toxic to grazing cattle. Three herbicides, including one pre-emergence (tebuthiuron) and two post-emergence herbicides (2,4-D and metsulfuron-methyl), were tested in pot trials for their efficacy on P. trichostachya. Results showed that tebuthiuron applied as either a granular (10% active ingredient, a.i.) or pelleted (20% a.i.) form efficiently reduced the emergence of P. trichostachya seedlings. Although some seedlings emerged, they perished within 7 days post treatment, leaving no residual plant matter. Testing now needs to be undertaken under field conditions to validate the findings within vegetation communities where potential non-target impacts need to be accounted for as well. The post-emergence application of 2,4-D and metsulfuron-methyl demonstrated that the highest efficacy and reduced application rates were achieved by treating earlier growth stages (i.e., seedlings) of P. trichostachya plants. In addition, the amount of toxic dead plant material was minimized due to the faster degradation of these small plants. These findings offer practical, cost-effective solutions for sustaining grazing lands from P. trichostachya challenges.
ABSTRACT
Understanding how seed functional traits interact with environmental factors to determine seedling recruitment is critical to assess the impact of climate change on ecosystem restoration. This study focused on the effects of environmental factors on the mother plant during early plant life history stages and during seed development. Desmodium brachypodum A. Gray (large tick trefoil, Fabaceae) was used as a model species. Firstly, this study analyzed seed germination traits in response to temperature and moisture stress. Secondly, it investigated how seed burial depth interacts with temperature and soil moisture to influence seedling emergence traits. Finally, it determined if contrasting levels of post-anthesis soil moisture could result in changes in D. brachypodum reproductive biology and seed and seedling functional traits. The results showed that elevated temperature and moisture stress interacted to significantly reduce the seed germination and seedling emergence (each by >50%), while the seed burial improved the seedling emergence. Post-anthesis soil moisture stress negatively impacted the plant traits, reducing the duration of the reproductive phenology stage (by 9 days) and seed production (by almost 50%). Unexpectedly, soil moisture stress did not affect most seed or seedling traits. In conclusion, elevated temperatures combined with low soil moisture caused significant declines in seed germination and seedling emergence. On the other hand, the reproductive output of D. brachypodum had low seed variability under soil moisture stress, which might be useful when sourcing seeds from climates with high variability. Even so, a reduction in seed quantity under maternal moisture stress can impact the long-term survival of restored plant populations.
ABSTRACT
Pimelea is a genus of about 140 plant species, some of which are well-known for causing animal poisoning resulting in significant economic losses to the Australian livestock industry. The main poisonous species/subspecies include Pimelea simplex (subsp. simplex and subsp. continua), P. trichostachya and P. elongata (generally referred to as Pimelea). These plants contain a diterpenoid orthoester toxin, called simplexin. Pimelea poisoning is known to cause the death of cattle (Bos taurus and B. indicus) or weaken surviving animals. Pimelea species are well-adapted native plants, and their diaspores (single seeded fruits) possess variable degrees of dormancy. Hence, the diaspores do not generally germinate in the same recruitment event, which makes management difficult, necessitating the development of integrated management strategies based on infestation circumstances (e.g., size and density). For example, the integration of herbicides with physical control techniques, competitive pasture establishment and tactical grazing could be effective in some situations. However, such options have not been widely adopted at the field level to mitigate ongoing management challenges. This systematic review provides a valuable synthesis of the current knowledge on the biology, ecology, and management of poisonous Pimelea species with a focus on the Australian livestock industry while identifying potential avenues for future research.
Subject(s)
Diterpenes , Plant Poisoning , Thymelaeaceae , Animals , Cattle , Plants, Toxic , Australia , Livestock , Plant Poisoning/veterinaryABSTRACT
Parthenium hysterophorus L. (Asteraceae), commonly known as parthenium weed, is a highly invasive weed spreading rapidly from northern to southern parts of Pakistan. The persistence of parthenium weed in the hot and dry southern districts suggests that the weed can survive under more extreme conditions than previously thought. The development of a CLIMEX distribution model, which considered this increased tolerance to drier and warmer conditions, predicted that the weed could still spread to many other parts of Pakistan as well as to other regions of south Asia. This CLIMEX model satisfied the present distribution of parthenium weed within Pakistan. When an irrigation scenario was added to the CLIMEX program, more parts of the southern districts of Pakistan (Indus River basin) became suitable for parthenium weed growth, as well as the growth of its biological control agent, Zygogramma bicolorata Pallister. This expansion from the initially predicted range was due to irrigation producing extra moisture to support its establishment. In addition to the weed moving south in Pakistan due to irrigation, it will also move north due to temperature increases. The CLIMEX model indicated that there are many more areas within South Asia that are suitable for parthenium weed growth, both under the present and a future climate scenario. Most of the south-western and north-eastern parts of Afghanistan are suitable under the current climate, but more areas are likely to become suitable under climate change scenarios. Under climate change, the suitability of southern parts of Pakistan is likely to decrease.
ABSTRACT
The development of a cell suspension culture system for the scaling up of coconut embryogenic callus (EC) production would drastically improve efforts to achieve the large-scale production of high-quality clonal plantlets. To date, the hard nature of coconut EC appeared to be the main constraint for developing cell suspension cultures. Hence, this study attempted to acquire friable EC through the following approaches: The manipulation of (1) medium type and subculture frequency, (2) a reduced 2,4-dichlorophenoxy acetic acid concentration during subculture, (3) the nitrate level and the ammonium-to-nitrate ratio, and the addition of amino acid mixture, (4) the addition of L-proline, and (5) the reduction of medium nutrients. Unfortunately, none of these culture conditions produced friable coconut EC. Even though friable EC was not achieved via these approaches, some of the conditions were found to influence the formation of compact EC, therefore these results are important for further studies focused on somatic embryogenesis in coconut and other species.
ABSTRACT
Coconut (Cocos nucifera L.) is an important perennial crop adapted to a wide range of habitats. Although global coconut demand has increased sharply over the past few years, its production has been decreasing due to palm senility, as well as abiotic and biotic stresses. In fact, replanting efforts are impeded due to the lack of good quality seedlings. In vitro technologies have a great potential; however, their applications may take time to reach a commercial level. Therefore, traditional seed propagation is still critical to help meet the rising demand and its practice needs to be improved. To achieve an improved propagation via seeds, it is important to understand coconut fruit biology and its related issues. This review aims to provide a comprehensive summary of the existing knowledge on coconut fruit morpho-anatomy, germination biology, seed dispersal, distribution, fruit longevity and storage. This will help to identify gaps where future research efforts should be directed to improve traditional seed propagation.
ABSTRACT
Coconut [Cocos nucifera L.] is often called "the tree of life" because of its many uses in the food, beverage, medicinal, and cosmetic industries. Currently, more than 50% of the palms grown throughout the world are senile and need to be replanted immediately to ensure production levels meet the present and increasing demand for coconut products. Mass replanting will not be possible using traditional propagation methods from seed. Recent studies have indicated that in vitro cloning via somatic embryogenesis is the most promising alternative for the large-scale production of new coconut palms. This paper provides a review on the status and prospects for the application of somatic embryogenesis to mass clonal propagation of coconut.
ABSTRACT
Parthenium weed (Parthenium hysterophorus L.) is an invasive plant species in around 50 countries and a 'Weed of National Significance' in Australia. This study investigated the relative toxicity of the leaf, shoot and root extracts of two geographically separate and morphologically distinct biotypes of parthenium weed in Queensland, Australia. Parthenium weed exhibited higher phytotoxic, cytotoxic and photocytotoxic activity in leaf tissue extracts in contrast to shoot and root. The germination and seedling growth of a dicot species (garden cress) were inhibited more than those of a monocot species (annual ryegrass) using a phytotoxicity bioassay. The cytotoxicity of leaf extracts was assessed in a mouse fibroblast cell suspension assay and increased under high ultraviolet A(UV-A) radiation. A major secondary metabolite, parthenin, was found in abundance in leaf extracts and was positively correlated with cytotoxicity but not with photocytotoxicity or phytotoxicity. Ambrosin and chlorogenic acid were also detected and were positively correlated with germination inhibition and the inhibition of radicle elongation, respectively. In addition, other currently unidentified compounds in the leaf extracts were positively correlated with phytotoxicity, cytotoxicity and photocytotoxicity with two to three molecules strongly correlated in each case. Both parthenium weed biotypes investigated did not differ with respect to their relative toxicity, despite their reported differences in invasive potential in the field. This suggests that secondary chemistry plays a limited role in their invasion success.
Subject(s)
Asteraceae/toxicity , Metabolome , Metabolomics , Plant Extracts/toxicity , Plant Weeds/toxicity , Animals , Asteraceae/growth & development , Asteraceae/metabolism , Cell Survival/drug effects , Dose-Response Relationship, Drug , Fibroblasts/drug effects , Fibroblasts/pathology , Germination/drug effects , Mice , NIH 3T3 Cells , Parthenogenesis , Plant Extracts/metabolism , Plant Leaves/metabolism , Plant Leaves/toxicity , Plant Roots/metabolism , Plant Roots/toxicity , Plant Shoots/metabolism , Plant Shoots/toxicity , Plant Weeds/growth & development , Plant Weeds/metabolism , Queensland , Secondary MetabolismABSTRACT
We studied the effects of a biological control agent, Epiblema strenuana Walker (Lepidoptera: Tortricidae) alone and together with a sown native grass, Astrebla squarrosa C.E. Hubb. and an introduced pasture plant, Clitoria ternatea L. on growth and seed production of Parthenium hysterophorus L. Astrebla squarrosa and C. ternatea individually reduced shoot dry biomass of P. hysterophorus by 30 and 42%, respectively; and by 48 and 70%, respectively in the presence of biological control agent, E. strenuana. Similarly, A. squarrosa and C. ternatea individually reduced weed seed production up to 48 and 64%, respectively; and by 73 and 81%, respectively in the presence of E. strenuana. In the presence of E. strenuana, the biomass of A. squarrosa and C. ternatea was increased by 13 and 10%, respectively. The biological control agent induced more galls per P. hysterophorus plant when either of the competing plants were present than when grown alone. The abundance of galls increased with pasture competition, but only for C. ternatea, and not for A. squarrosa. The biological control agent worked synergistically with the two competitive plants to reduce the growth and production of viable seed, which should lead to a decrease in the P. hysterophorus soil seed banks in the field, and eventually seedling recruitment in future generations of P. hysterophorus.
Subject(s)
Asteraceae , Plant Weeds , Seedlings , SoilABSTRACT
BACKGROUND: The rise in atmospheric CO2 has huge impacts on the biology and management of invasive weed species such as Parthenium hysterophorus. This study evaluated the effect of ambient (400 ppm) and elevated (700 ppm) CO2 concentrations on P. hysterophorus growth, reproductive output and response to glyphosate applied at several doses including the recommended dose (800 g a.e. ha-1 ). RESULTS: The plants in control treatment (no herbicide) grew taller (41%), produced a larger number of leaves (13%) and flowers (39%), and higher dry biomass (34%) at elevated CO2 as compared to the ambient CO2 . Glyphosate caused significant reduction in chlorophyll content of P. hysterophorus plants grown at both CO2 concentrations in a dose-dependent manner. The percentage herbicide injury was relatively less at elevated CO2 as compared to the ambient CO2 at 7 and 14 days after glyphosate application but it was almost similar at 21 days after application. This shows that elevated CO2 might have slowed the translocation of glyphosate initially, but most plants were killed eventually close to 21 days after application. The survival rate was higher under elevated as compared to the ambient CO2 at recommended and lower doses of glyphosate. There was a negligible difference between the two CO2 concentrations for the plant dry biomass reduction over the control treatment. CONCLUSIONS: P. hysterophorus growth and reproductive potential (indicated by number of flowers) improved significantly by CO2 enrichment but there was little effect on the overall efficacy of glyphosate applied to control this species. © 2019 Society of Chemical Industry.
Subject(s)
Asteraceae/drug effects , Asteraceae/physiology , Carbon Dioxide/metabolism , Glycine/analogs & derivatives , Herbicides/pharmacology , Weed Control , Asteraceae/growth & development , Dose-Response Relationship, Drug , Glycine/pharmacology , GlyphosateABSTRACT
Coconut farming is not only a vital agricultural industry for all tropical countries possessing humid coasts and lowlands, but is also a robust income provider for millions of smallholder farmers worldwide. However, due to its longevity, the security of production of this crop suffers significantly from episodes of natural disasters, including cyclone and tsunami, devastating pest and disease outbreaks, while also affected by price competition for the principal products, especially the oil. In order to reduce these pressures, high-value coconut varieties (makapuno and aromatics) have been introduced in some regions, on a limited scale, but with positive outcomes. Even though these two varieties produce fruit with delicious solid or flavoursome liquid endosperm, their distinct biochemical and cellular features unfortunately prevent their in situ germination. In fact, embryo rescue and culture have been developed historically to nurture the embryo under in vitro conditions, enabling effective propagation. In an attempt to provide a comprehensive review featuring these elite coconut varieties, this paper firstly introduces their food values and nutritional qualities, and then discusses the present knowledge of their biology and genetics. Further possibilities for coconut in general are also highlighted, through the use of advanced tissue culture techniques and efficient seedling management for sustainable production of these highly distinct and commercially attractive varieties of coconut.
Subject(s)
Cocos/growth & development , Plant Breeding/methods , Cocos/genetics , Cocos/metabolism , Crops, Agricultural/genetics , Crops, Agricultural/growth & development , Crops, Agricultural/metabolism , Endosperm/genetics , Endosperm/metabolism , Genes, Plant , Genetic Variation , Germination , Nutritive ValueABSTRACT
MAIN CONCLUSION: The present review discusses not only advances in coconut tissue culture and associated biotechnological interventions but also future research directions toward the resilience of this important palm crop. Coconut (Cocos nucifera L.) is commonly known as the 'tree of life'. Every component of the palm can be used to produce items of value and many can be converted into industrial products. Coconut cultivation faces a number of acute problems that reduce its productivity and competitiveness. These problems include various biotic and abiotic challenges as well as an unstable market for its traditional oil-based products. Around 10 million small-holder farmers cultivate coconut palms worldwide on c. 12 million hectares of land, and many more people own a few coconut palms that contribute to their livelihoods. Inefficiency in the production of seedlings for replanting remains an issue; however, tissue culture and other biotechnological interventions are expected to provide pragmatic solutions. Over the past 60 years, much research has been directed towards developing and improving protocols for (i) embryo culture; (ii) clonal propagation via somatic embryogenesis; (iii) homozygote production via anther culture; (iv) germplasm conservation via cryopreservation; and (v) genetic transformation. Recently other advances have revealed possible new ways to improve these protocols. Although effective embryo culture and cryopreservation are now possible, the limited frequency of conversion of somatic embryos to ex vitro seedlings still prevents the large-scale clonal propagation of coconut. This review illustrates how our knowledge of tissue culture and associated biotechnological interventions in coconut has so far developed. Further improvement of protocols and their application to a wider range of germplasm will continue to open up new horizons for the collection, conservation, breeding and productivity of coconut.
Subject(s)
Biotechnology/methods , Cocos/embryology , Seeds/cytology , Cryopreservation , Seeds/growth & developmentABSTRACT
Protocols are proposed for the low (-20 degree C) and ultra-low (-80 degree C) temperature storage of coconut (Cocos nucifera L.) embryos. A tissue dehydration step prior to storage, and a rapid warming step upon recovery optimized the protocol. The thermal properties of water located within embryos were monitored using differential scanning calorimetry (DSC). In the most efficient version of the protocol, embryos were dehydrated under a sterile air flow in a dehydration solution containing glucose (3.33 M) and glycerol (15 percent) for 16 hours. This protocol decreased the embryo water content from 77 to 29 percent FW and at the same time reduced the amount of freezable water down to 0.03 percent. The dehydrated embryos could be stored for up to 3 weeks at -20 degree C (12 percent producing normal plants upon recovery) or 26 weeks at -80 degree C (28 percent producing normal plants upon recovery). These results indicate that it is possible to store coconut germplasm on a medium term basis using an ultra-deep freezer unit. However for more efficient, long term storage, cryopreservation remains the preferred option.
Subject(s)
Cocos/embryology , Cryopreservation/methods , Seeds/growth & development , Calorimetry, Differential Scanning , Cocos/chemistry , Cocos/growth & development , Seeds/chemistry , Water/chemistryABSTRACT
⢠Seed longevity, which is essential for germplasm conservation and survival of many land plant species, can vary considerably within species and cultivars. Here, we explore the relationship between parental and offspring phenotypes to elucidate how pre-zygotic environment affects seed longevity. ⢠Plants of the wild species Plantago cunninghamii were exposed to wet or dry soil within a warm or cool glasshouse until flowering and then moved to a common environment. Seeds subsequently produced were collected at maturity, and longevity was assessed by controlled ageing at 45°C, 60% relative humidity. Multivariate analysis was used to examine relationships between the parental and offspring phenotypes. ⢠The pre-zygotic environment resulted in a highly plastic parental response which was passed on to offspring seeds and changed their longevity (p(50)) by more than a factor of 2. Seed longevity is a function of the seed population's distribution of deaths in time (σ) and quality (K(i)); σ was associated with plant size, and K(i) with reproductive plant traits. ⢠The pre-zygotic growth environment modulated seed longevity via a parental effect. Reproductive performance and seed quality (K(i)) were highly correlated with each other and unrelated to the maternal plant phenotype. Hence seed quality may be associated with the paternal plant response to the environment.
Subject(s)
Environment , Plantago/physiology , Seeds/physiology , Multivariate Analysis , Phenotype , Plantago/embryology , Reproduction , SoilABSTRACT
Cryopreservation of coconut can be used as a strategy to back up the establishment of living collections which are expensive to maintain and are under constant threat from biotic and abiotic factors. Unfortunately, cryopreservation protocols still need to be developed that are capable of producing a sizeable number of field-grown plants. Therefore, we report on the development of an improved cryopreservation protocol which can be used on a wide range of coconut cultivars. The cryopreservation of zygotic embryos and their recovery to soil-growing plants was achieved through the application of four optimised steps viz.: (i) rapid dehydration; (ii) rapid cooling; (iii) rapid warming and recovery in vitro and (iv) acclimatization and soil-supported growth. The thermal properties of water within the embryos were monitored using differential scanning calorimetry (DSC) in order to ensure that the freezable component was kept to a minimum. The feasibility of the protocol was assessed using the Malayan Yellow Dwarf (MYD) cultivar in Australia and then tested on a range of cultivars which were freshly harvested and studied in Indonesia. The most efficient protocol was one based on an 8-h rapid dehydration step followed by rapid cooling step. Best recovery percentages were obtained when a rapid warming step and an optimised in vitro culture step were used. Following this protocol, 20% (when cryopreserved 12 days after harvesting) and 40% (when cryopreserved at the time of harvest) of all MYD embryos cryopreserved could be returned to normal seedlings growing in soil. DSC showed that this protocol induced a drop in embryo fresh weight to 19% and significantly reduced the amount of water remaining that could produce ice crystals (0.1%). Of the 20 cultivars tested, 16 were found to produce between 10% and 40% normal seedlings while four cultivars generated between 0% and 10% normal seedlings after cryopreservation. This new protocol is applicable to a wide range of coconut cultivars and is useful for the routine cryopreservation of coconut genetic resources.
Subject(s)
Cocos/growth & development , Cryopreservation/methods , Dehydration , Seedlings/growth & development , Acclimatization , Biodiversity , Cocos/genetics , Desiccation/methods , Seeds/growth & developmentABSTRACT
The present study aimed at exploring the fidelity of coconut (Cocos nucifera L.) plants recovered from cryopreservation. Zygotic embryos from various different cultivars were cryopreserved following four successive steps, namely: rapid dehydration, rapid freezing, rapid thawing and in vitro recovery followed by acclimatization. At the end of the acclimatization period, the seedlings were compared to counterparts of the same age, which were produced from non-cryopreserved embryos. Both series were submitted to morphological, cytological and molecular comparisons. No significant differences in terms of growth rates could be measured. In addition, no morphological variation could be detected through the measurement of shoot elongation rates, production of opened leaves, and the number and total length of primary roots. Karyotype analysis revealed the same chromosome number (2n = 32) in all studied cultivars independently of cryopreservation. No significant differences could be observed between control and cryopreserved material concerning the type of chromosomes, the length of the long and short arms, the arm length ratio and the centromeric index. However, idiogram analysis did show a greater number of black banding on chromosomes isolated from cryopreserved material. Genetic and epigenetic fidelity was assessed through microsatellite (SSR) analysis and global DNA methylation rates; no significant differences would be observed between genomic DNAs isolated from seedlings originating from cryopreserved embryos and respective controls. In conclusion, our results suggest that the method of cryopreservation under study did not induce gross morphological, genetic or epigenetic changes, thus suggesting that it is an appropriate method to efficiently preserve coconut germplasm.
Subject(s)
Cocos/embryology , Cocos/growth & development , Cryopreservation/methods , Seedlings/embryology , Seedlings/growth & development , Seeds/embryology , Seeds/growth & development , Cocos/cytology , Cocos/genetics , DNA Methylation , Microsatellite Repeats/genetics , Seedlings/cytology , Seedlings/genetics , Seeds/cytology , Seeds/genetics , ZygoteABSTRACT
BACKGROUND AND AIMS: The period during which seeds develop on the parent plant has been found to affect many seed characteristics, including dormancy, through interactions with the environment. Goodenia fascicularis (Goodeniaceae) seeds were used to investigate whether seeds of an Australian native forb, harvested from different environments and produced at different stages of the reproductive period, differ in dormancy status. METHODS: During the reproductive phase, plants were grown ex situ in warm (39/21 degrees C) or cool (26/13 degrees C) conditions, with adequate or limited water availability. The physiological dormancy of resulting seeds was measured in terms of the germination response to warm stratification (34/20 degrees C, 100 % RH, darkness). KEY RESULTS: Plants in the cool environment were tall and had high above-ground biomass, yet yielded fewer seeds over a shorter, later harvest period when compared with plants in the warm environment. Seeds from the cool environment also had higher viability and greater mass, despite a significant proportion (7 % from the cool-wet environment) containing no obvious embryo. In the warm environment, the reproductive phase was accelerated and plants produced more seeds despite being shorter and having lower above-ground biomass than those in the cool environment. Ten weeks of warm stratification alleviated physiological dormancy in seeds from all treatments resulting in 80-100 % germination. Seeds that developed at warm temperatures were less dormant (i.e. germination percentages were higher) than seeds from the cool environment. Water availability had less effect on plant and seed traits than air temperature, although plants with reduced soil moisture were shorter, had lower biomass and produced fewer, less dormant seeds than plants watered regularly. CONCLUSIONS: Goodenia fascicularis seeds are likely to exhibit physiological dormancy regardless of the maternal environment. However, seeds collected from warm, dry environments are likely to be more responsive to warm stratification than seeds from cooler, wetter environments.
Subject(s)
Germination/physiology , Magnoliopsida/physiology , Seeds/physiology , Australia , Climate , Temperature , Time FactorsABSTRACT
Grass weed populations resistant to aryloxyphenoxypropionate (APP) and cyclohexanedione herbicides that inhibit acetyl-CoA carboxylase (ACCase; EC 6.4.1.2) represent a major problem for sustainable agriculture. We investigated the molecular basis of resistance to ACCase-inhibiting herbicides for nine wild oat (Avena sterilis ssp. ludoviciana Durieu) populations from the northern grain-growing region of Australia. Five amino acid substitutions in plastid ACCase were correlated with herbicide resistance: Ile-1,781-Leu, Trp-1,999-Cys, Trp-2,027-Cys, Ile-2,041-Asn, and Asp-2,078-Gly (numbered according to the Alopecurus myosuroides plastid ACCase). An allele-specific PCR test was designed to determine the prevalence of these five mutations in wild oat populations suspected of harboring ACCase-related resistance with the result that, in most but not all cases, plant resistance was correlated with one (and only one) of the five mutations. We then showed, using a yeast gene-replacement system, that these single-site mutations also confer herbicide resistance to wheat plastid ACCase: Ile-1,781-Leu and Asp-2,078-Gly confer resistance to APPs and cyclohexanediones, Trp-2,027-Cys and Ile-2,041-Asn confer resistance to APPs, and Trp-1,999-Cys confers resistance only to fenoxaprop. These mutations are very likely to confer resistance to any grass weed species under selection imposed by the extensive agricultural use of the herbicides.