Asynchronous flowering was noted in a recently discovered infestation of siam weed in north Queensland. This may indicate some genetic diversity in the infestation, increasing concerns about the origin of the infestation. Internal transcribed spacer 1 (ITS1) sequence data were obtained for siam weed individuals from north Queensland, Indonesia, Thailand, South Africa, Ivory Coast, Brazil, Colombia, and the U.S. The ITS1 region is 258 base pairs long, and the populations that flower at different times in north Queensland differ by four base substitutions. The genotype common in north Queensland is also reported throughout the native and introduced ranges. The other genotype is reported only in north Queensland and southern Brazil. These data, in conjunction with prior investigations into possible origins, indicate that Brazil is the most likely source of the infestation in Australia.

Two previously identified triazine-resistant annual bluegrass (Poa annua) biotypes in Mississippi were evaluated to determine the level as well as the mode of resistance compared to a triazine-susceptible biotype. Annual bluegrass seeds were collected at two sites (Meridian and Tupelo, MS) from field plots previously treated with 11.2 kg ai/ha simazine. Seeds were planted on agar containing simazine (0, 0.001, 0.01, 0.1, 1, 10, or 100 mM) or diuron (0, 0.01, 0.1, 1, 10, 100, or 1,000 μM), placed in the growth chamber with an 8 h daylength and alternating temperatures of 15 and 20 C, and allowed to grow for 3 wk, after which fresh weight was determined. Data were subjected to regression analyses and the amount of simazine or diuron required to reduce fresh weight to 50% of the untreated plants was determined. These data indicated a greater than 1,000-fold level of resistance to simazine with either biotype. Diuron concentrations of 5.0, 3.0, and 3.2 μM were required to reduce fresh weight to 50% of the untreated for the triazine-susceptible, Meridian, and Tupelo biotypes, respectively. Sequencing a portion of the chloroplast psbA gene revealed a serine 264 to glycine mutation, which reduced the affinity of the triazine herbicides for the QB-binding niche on the D1 protein in photosystem II.

Red rice is a major weed of rice in the southern U.S. and can intercross with rice. Knowledge of the plant phenotypes from such crosses would be valuable for identification and management of these plants. Male-sterile long-grain tropical japonicas ‘Kaybonnet-1789’ and ‘Cypress-1819’ were crossed with two awned and two awnless U.S. red rice types. F1 plants produced pubescent leaves, red pericarp, and medium-grain seeds. Crosses involving awned LA3 and TX4 red rice produced F1 plants with reddish-purple basal leaf sheaths and usually flowered within the same time periods as the parents, whereas those involving awnless StgS red rice had green basal leaf sheaths, flowered much later than either parent, and produced awnless F1 and F2 offspring. Crosses involving awned red rice produced F1 plants with long awns and F2 plants with awns ranging in length from zero to that of red rice parents. F1 plants were taller than either parent and produced intermediate culm angles similar to red rice, whereas F2 plants had culms ranging from erect (like rice) to more open than red rice. Thus, true F1 hybrids from crosses between pure breeding (homozygous) rice and red rice can be positively identified by a combination of traits including pubescent leaves, medium-grain seeds with red pericarps, open plant types, and heights greater than the red rice parent. F1 hybrids may be awned or awnless, have purple or green stems, or have normal or delayed heading. F2 plants have a broad combination of phenotypic traits found in both parents and F1 hybrids.

In the state of Illinois, waterhemp and smooth pigweed are among the worst agricultural weeds. Previous research shows high potential for hybridization between these two species. However, the actual occurrence of hybrids in natural settings is still uncertain. Morphological similarity between hybrids and waterhemp makes field surveys of hybrids difficult to conduct. The main purpose of this study was to characterize the morphology of waterhemp × smooth pigweed F1 hybrids, emphasizing evaluation of characters that may allow for hybrid discrimination in field Amaranthus communities. Concurrently, the study characterized hybrid reproductive fitness, chromosome number, and DNA content. To accomplish this, hybrids were obtained from field crosses. A species-specific polymorphism in the ALS gene was used to verify hybrid identity. Significant differences (α = 0.05) between hybrids and individuals of the parental species were observed for five staminate and five carpellate characters. Of these, five characters differentiated hybrids from waterhemp. However, clustering analyses using these characters indicated that morphological differences were not reliable enough, by themselves, for unambiguous hybrid identification. Also, hybrid homoploidy (2n = 32) with respect to parental species excluded chromosome counts in hybridity determinations. However, DNA content analysis may be used for such purpose. Hybrids had an average of 1.21 pg of DNA per 2C nucleus, a value intermediate to that of parental species. Hybrids produced 3.3 or 0.7% the seed output of parental and sibling waterhemp individuals, respectively. Percent micropollen in hybrids was 95-times greater than in parental species. Hybrid sterility appears to be the most reliable feature for hybrid discrimination when conducting field surveys. However, molecular and cytogenetic analyses as employed in this study may be desired for ultimate identity corroboration.

Red rice has long been a troublesome, conspecific weed of cultivated rice. Rice varieties carrying certain herbicide-resistant traits acquired through genetic modification (herbicide-resistant varieties) now offer new options for red rice control. In concert with this innovation is the risk of gene flow, which can result in the transfer of that specific herbicide resistance to red rice and thus render this weed control measure ineffective. Gene flow in concept is simple, however, the parameters that determine the establishment of a new trait in a weed population are complex. Cross-pollination to make hybrid seed and the subsequent fate of those hybrid families in the general weed population are some of the biological factors that influence gene flow between red rice and cultivated rice. Natural outcrossing among rice plants is generally low. Most of the pollen dispersal studies published to date indicated that rice × rice outcrossing rates were less than 1.0%. Numerous reports summarized in this study suggest that outcrossing rates between rice and red rice can be highly variable but usually are similar to or lower than this level. However, once hybrids form, they may introgress into a red rice population within only a few generations. If hybrid seed families are to persist and establish herbicide-resistant red rice populations, they must successfully compete in the crop–weed complex. The ability to survive a herbicide applied to a herbicide-resistant rice variety would be a strong selective advantage for these hybrid families. Thus, the well-established principles of weed resistance management appear to be relevant for herbicide-resistant crop systems and should be used in combination with practices to minimize coincident flowering to mitigate the potential impact of gene flow from herbicide-resistant rice into red rice. For the rice–red rice crop–weed complex, there are both biological factors and agricultural practices that can work together to preserve these new weed control options.

Crop allelopathy has seldom been used effectively by farmers in weed management. Traditional breeding methods have not been successful in producing highly allelopathic crops with good yields. Genetic engineering may have the potential for overcoming this impasse. Crops have been made resistant to insects, pathogens, and herbicides with transgenes, but biotechnology has not produced crops that control weeds with allelochemicals. The strategies for producing allelopathic crops by biotechnology are relatively complex, usually involving multiple genes. One can choose to enhance production of allelochemicals already present in a crop or to impart the production of new compounds. The first strategy involves identification of the allelochemical(s), determination of the enzymes and genes encoding them, and the use of genetic engineering to enhance their production. The latter strategy employs altering existing biochemical pathways by insertions of transgenes to produce new allelochemicals. With either strategy, there are potential problems with tissue-specific promoters, autotoxicity, metabolic imbalances, and proper movement of the allelopathic compound to the rhizosphere.

Tropical soda apple samples were collected from 31 populations across the southeastern United States and from four populations in a portion of its native range in Brazil. The genetic relationships among these populations were examined by single primer amplification reactions (SPAR) and by sequencing a portion of the chloroplast genome. SPAR revealed no variation among the 132 individuals and only two chloroplast haplotypes were detected in the 50 individuals sequenced. The most common haplotype was present in all samples from the United States and most of the Brazilian samples, whereas the second haplotype was only found in one of the Brazilian populations. Within the limitations of these data, we conclude that Brazil is the best location to seek a potential biological control agent for tropical soda apple, and that, if identified, this agent should prove useful for populations throughout the United States.