Greenhouse studies were conducted to determine the influence of phosphorus (P) concentrations on the growth of lettuce, smooth pigweed, and common purslane in monocultures and in mixtures and to determine the P-absorption rate of each species over time. For the P-competition studies, lettuce–smooth pigweed and lettuce–common purslane mixtures were established in P-less hydroponic solutions. Each lettuce–weed mixture was established separately. Concentrations of P were 10, 20, 40, 80, and 160 mg L−1. Lettuce to weed planting proportions were 2:0, 0:2, and 1:1. In the mixtures, biomass of common purslane increased sharply between 10 and 20 mg P L−1, depressing lettuce growth. No biomass changes were observed in smooth pigweed as P concentration increased. However, both weeds increased their P content within this range, depriving lettuce of this nutrient. Common purslane competed for P for its own growth, whereas smooth pigweed absorbed P luxuriously. For the P-absorption studies, roots of lettuce, smooth pigweed, and common purslane plants were submersed in a 20 mg P L−1 solution for 1, 2.5, 5, 10, 20, 40, 60, 90, 180, 360, 720, and 1,440 min. Common purslane was shown to be the most aggressive species for the nutrient, absorbing 50% of the content in 295 min, whereas lettuce and smooth pigweed needed 766 and 825 min to absorb 10 mg P L−1.

Studies were conducted to determine the relative fitness and competitive ability of an acetolactate synthase (ALS) inhibitor–resistant (R) downy brome biotype compared with a susceptible (S) biotype. In previous research, the mechanism of resistance was determined to be an altered ALS enzyme. Seed germination of the R biotype was compared with that of the S biotype at 5, 15, and 25 C. There were no different germination characteristics between R and S biotypes at 15 and 25 C. However, the R biotype germinated 27 h earlier than the S biotype and had reached over 60% germination when the S biotype initially germinated at 5 C. Under noncompetitive greenhouse conditions, growth of the R biotype was similar to that of the S biotype on the basis of shoot dry weight, leaf area, and plant height. Seed production of the R biotype was 83%, when compared with the S biotype, but seeds of the R biotype were larger than those of the S biotype. Replacement series experiments were conducted in the greenhouse to determine the relative competitive ability of R and S biotypes. No difference in competitive ability was observed between R and S biotypes on the basis of shoot dry weight, leaf area, or plant height. Thus, it appears that ALS-resistance trait is not associated with growth penalty in either noncompetitive or competitive conditions. In the absence of ALS inhibitors, these results suggest that the R biotype would remain at a similar frequency in a population of R and S biotypes.

Greenhouse studies were conducted to assess the intensity of smooth pigweed and common purslane aboveground interference (AI) and belowground interference (BI) with lettuce and to determine primary mechanisms of interference of each species as affected by P fertility rates. Lettuce was transplanted in mixtures with either smooth pigweed or common purslane according to four partitioning regimes: no interference, full interference, BI, and AI. Soil used was low in P for optimum lettuce yields, therefore P was added at rates of 0, 0.4, and 0.8 grams of P per liter of soil. Shoot and root biomass and plant height were measured for each species, as well as P tissue content. The data obtained indicated that smooth pigweed interfered with lettuce primarily through light interception by its taller canopy. A secondary mechanism of interference was the absorption of P from the soil through luxury consumption, increasing the P tissue content without enhancing smooth pigweed biomass accumulation. In contrast, common purslane competed aggressively with lettuce for P. Because the weed grew taller than lettuce, light interception was a secondary interference factor.

The phylogenetic relationships within two major locoweed genera, Astragalus and Oxytropis, and among varieties of woolly loco found in New Mexico were analyzed by comparing their chloroplast rpoC1 and rpoC2 gene sequences. Nucleic acids from locoweed species and varieties collected from different geographical locations in New Mexico were amplified using specific primer sets and subjected to restriction fragment analyses. Identity of the amplicons was confirmed by determining the 5′-end sequences from pea and woolly loco var. matthewsii. The amplified sequences from all samples were digested with 16 different restriction enzymes. Presence or absence of individual restriction fragments was scored as binary characters and used to develop a similarity coefficient matrix for cladistic analyses to determine the phylogenetic relationships. The target sequence was conserved, yielding 7% polymorphic data. Oxytropis species were monophyletic and, as expected, formed a clade distinct from Astragalus. The average similarity coefficient among woolly loco varieties was very high (0.9733), but the varieties still separated into three different clades. The phylogenetic relationship among woolly loco varieties coincided with their geographic distribution but was unrelated to insect feeding preference.

Biennial wormwood has become an important weed problem in the northern Great Plains, but little is known about its biology. Biennial wormwood seeds were collected from Fargo, ND, and Fergus Falls, MN, for field experiments in 1999 and 2000 to determine the influence of transplanting date on growth, biomass, and seed production. Seeds were seeded in a greenhouse every 2 wk, and seedling rosettes were transplanted to the field 2 wk after emergence from April 30 until September 15 to simulate season-long emergence. Weekly destructive subsampling started 2 wk after transplanting and ended on September 29 in both years. All seedlings that grew for at least 5 wk after transplanting produced flowers by mid- to late August of the same year. Late-transplanted seedlings with less than 5 wk of growth did not flower or survive the winter. Biennial wormwood biomass allocation patterns resemble those of an annual species, with about 15% of the total dry weight allocated to roots, 20% to stems, 25% to leaves, and 40% to flowers. Transplant date had a substantial influence on biomass partitioning. Seedlings transplanted early in the growing season produced more biomass and seed than late-season transplants. Biennial wormwood seedlings transplanted on April 30 produced over 435,000 seeds per plant, whereas seedlings transplanted on August 15 produced 500 to 3,000 seeds. Biennial wormwood was photoperiod sensitive and flowered when the day length was about 14 h or less, between August 18 and 25, in both years.

Three Italian Lolium weed populations, one susceptible and two resistant to diclofop, were characterized by the technique of inter simple sequence repeats (ISSR). The goal of this study was to taxonomically identify these Lolium populations as well as to evaluate evidence for introgression of ISSR fragments from Festuca and the potential role of this introgression in the diclofop response. ISSR analysis confirmed the genomic background of the weed populations to be consistent with that of Lolium. However, the great range of variation in ISSR banding patterns highlighted that the three ryegrass accessions are mixed populations made up of individuals resulting presumably from intrageneric and intergeneric hybridization in the Lolium–Festuca complex. Two Festuca genus-discriminating and 20 Festuca species-discriminating ISSR markers were screened among all the three ryegrass populations. The resistant Tuscania population carried the highest percentage of Festuca genome (16.8%) followed by the resistant Roma (13.6%) and susceptible Vetralla (7.6%) populations. On the basis of these data some influence of Festuca genome in diclofop resistance levels of studied ryegrass populations could be hypothesized.

An induced mutation of the common wheat (2n = 6x = 42, AABBDD genomes) cultivar ‘Fidel’ has been shown to provide resistance to the imidazolinone class of herbicides. This class of herbicide gives broad-spectrum weed control including the weedy relative of wheat, jointed goatgrass (2n = 4x = 28, CCDD genomes). Because wheat and jointed goatgrass share a common genome, genes present on the D genome may transfer between the two species as a result of natural hybridization and selective pressures. Our objectives were to determine which genome of common wheat contained the herbicide resistance gene in the mutated Fidel and to genetically map its position. We investigated the chromosomal location of this gene using both durum (2n = 4x = 28, AABB genomes) and common wheat (6x) backgrounds. From crosses of durum wheat genotypes as the recurrent parent with mutated Fidel (cv. 9804, resistant), only BC1 plants containing chromosome 6D (inherited from cv. 9804) were resistant to applications of labeled rates of imazamox, an imidazolinone herbicide. No other D-genome chromosome was absolutely associated with herbicide resistance. To confirm this chromosomal location and genetically map the position of this gene, two populations of F3 families from the cross of cv. 9804 to the common wheat cultivars ‘Cashup’ and ‘Madsen’ were screened for reaction to imazamox, followed by genetic mapping with microsatellite markers. Two linked microsatellite markers were associated with the resistance trait, and one of them, Xgdm127, was located to chromosome 6D using aneuploid stocks, confirming the location of this gene on 6D. These results indicate that this resistance gene is in the genome that common wheat shares with jointed goatgrass. Therefore, imidazolinone-resistant wheat will need to be carefully managed to minimize the occurrence and spread of resistant jointed goatgrass, whether such plants arise because of hybridization with resistant common wheat or by independent mutation, a frequent occurrence with this herbicide class.

A plant's ability to detect and adjust morphologically to changes in light quality (red–far-red [R:FR] ratio) is one mechanism by which a crop plant responds to weeds. To test this hypothesis, two experiments were conducted where corn was grown in growth cabinets under different light environments. First, to determine the effect of R:FR ratio on corn growth and development, treatments of high R:FR (1.37) and low R:FR (0.67) ratio were compared. These were established by planting corn in pots and then placing trays of either turface (a baked clay medium with high R:FR) or commercial grass sod (low R:FR) on each side of a row of corn pots. Grass sod was used to simulate low-growing weeds. The low R:FR sod treatment resulted in corn plants which were taller, had larger leaves, and greater shoot–root ratio than plants growing in the high R:FR turface treatment. In the second experiment, the effect of R:FR ratio on corn leaf azimuth position was examined. This was accomplished by adding a third treatment where each corn row had sod placed on one side and turface on the other. The proportion of leaves in four azimuthal classes was recorded. In the presence of sod, the proportion of leaves perpendicular to the corn row decreased, and this altered the proportion of leaves in other classes. Therefore, corn seedlings detected changes in light quality caused by the presence of sod (which simulated low-growing weeds) and responded by adjusting carbon allocation and leaf orientation to optimize the interception of light quantity and quality. These results support our hypothesis that low-lying vegetation can alter the growth of corn seedlings before competition for resources occurs. This change in growth may help explain the importance of early-season weed control in corn.

Giant reed is one of the most widespread invasive species in riparian habitats in California and other coastal states of the United States. This species is thought to spread primarily asexually by flood dispersal of stem and rhizome pieces; viable seeds have not been found in the United States. Research was conducted to quantify genetic variation in giant reed along the Santa Ana River in California and to investigate the pattern of distribution of variation along this watershed. Populations at least 3.2 km apart were collected along the length of the Santa Ana River from the headwaters to the Pacific Ocean. One additional population from a different watershed was collected to serve as an out-group. Genetic analyses were conducted using both starch gel electrophoresis for isozyme analysis and random amplified polymorphic DNA (RAPD) analysis. Both isozyme and RAPD analyses revealed levels of genetic diversity comparable with those in the literature for clonal species, suggesting that asexual reproduction is the primary means of spread of giant reed. Most phenotypes were spread along the Santa Ana River, which is expected if water is the primary means of spread of vegetative propagules. Among the unique phenotypes found, two isozyme phenotypes and one RAPD phenotype were dominant and were found spread along the river, which may indicate greater fitness or competitive superiority to the other phenotypes that were less common. The dominant phenotypes were also found in the out-group population, possibly because of spread by humans. Because spread occurs mainly asexually, management efforts should focus on preventing establishment and spread of vegetative propagules. A moderate level of genetic diversity also suggests that biological control of this weed could be successful.

Field, laboratory, and greenhouse experiments were conducted to determine the seed production potential and effect of environmental factors on germination, emergence, and survival of texasweed. Texasweed produced an average of 893 seed per plant, and 90% were viable. Seed exhibited dormancy, and prechilling did not release dormancy. Percent germination ranged from 56% for seed subjected to no prechilling to 1% for seed prechilled at 5 C for 140 d. Seed remained viable during extended prechilling conditions, with 80% of seed viable after 140 d of prechilling. Texasweed seed germinated over a range of 20 to 40 C, with optimum germination (54%) occurring with a fluctuating 40/30 C temperature regime. Seed germinated with fluctuating 12-h light/dark and constant dark conditions. Texasweed seed germinated over a broad range of pH, osmotic potential, and salt concentrations. Seed germination was 31 to 62% over a pH range from 4 to 10. Germination of texasweed ranged from 9 to 56% as osmotic potential decreased from − 0.8 MPa to 0 (distilled water). Germination was greater than 52% at less than 40 mM NaCl concentrations and lowest (27%) at 160 mM NaCl. Texasweed seedlings emerged from soil depths as deep as 7.5 cm (7% emergence), but emergence was > 67% for seed placed on the soil surface or at a 1-cm depth. Texasweed seed did not germinate under saturated or flooded conditions, but seed survived flooding and germinated (23 to 25%) after flood removal. Texasweed seedlings 2.5 to 15 cm tall were not affected by emersion in 10-cm-deep flood for up to 14 d. These results suggest that texasweed seed is capable of germinating and surviving in a variety of climatic and edaphic conditions, and that flooding is not a viable management option for emerged plants of texasweed.

Four experiments were conducted in central Iowa during 2001 and 2002 to determine the effects of weed emergence time and corn row spacing on common waterhemp growth and fecundity. Four common waterhemp emergence cohorts were established in each experiment and corresponded to the VE, V3, V5, and V8 stages of corn grown in rows spaced 38 and 76 cm apart. Common waterhemp mortality averaged 20, 56, 97, and 99% for the first, second, third, and fourth cohorts, respectively. Mean mature common waterhemp height for the first cohort was 140 cm, whereas plants emerging at the V8 corn stage were only 5 cm tall. Biomass of the first cohort was 20% less in 38-cm rows than in 76-cm rows, but later cohorts were not affected by row spacing. Biomass and seed production of waterhemp emerging at the V3, V5, and V8 corn stages decreased 80, 97, and 99%, respectively in comparison with the first cohort. Overall results indicate that common waterhemp biomass, survival, and fecundity decline sharply with delayed emergence relative to corn, but weeds emerging at or before the V5 corn stage may still contribute significantly to the seed bank.

The inheritance of glyphosate-resistant goosegrass was studied by making reciprocal crosses between resistant (R) and susceptible (S) biotypes. Eighty-four F1 hybrids were confirmed using isozyme analyses. Reciprocal F1 hybrids displayed uniform levels of resistance intermediate (I) to that of the parental types, with no indication of maternal inheritance. The F1 hybrids were selfed to produce F2 populations. F3 populations were produced by selfing resistant and intermediate F2 phenotypes. A segregation ratio of 1:2:1 (S:I:R) was observed in the F2 and subsequently in the F3 generations derived from selfing intermediate F2 phenotypes. Individuals in F3 families derived from selfing resistant F2 phenotypes were resistant. Results from the present study show that glyphosate resistance in goosegrass is inherited as a single, nuclear, and incompletely dominant gene.

Jointed goatgrass is a troublesome weed in winter wheat with selective control only possible with a herbicide-resistant crop. Even with herbicide-resistant wheat, cultural control is still an important part of jointed goatgrass management. A study was conducted in 1998 and 2000 to determine whether using larger sized seed of a tall wheat variety at an increased seeding rate would reduce the effect of jointed goatgrass on winter wheat. Wheat seed size, seeding rate, and variety height had no effect on jointed goatgrass plant density. Tall (∼130 cm) wheat reduced mature jointed goatgrass biomass 46 and 16% compared with short (∼100 cm) wheat in years 1 and 2 of the experiment, respectively. Spikelet biomass was also reduced approximately 70 and 30% in the same respective years. One thousand–spikelet weight of jointed goatgrass was reduced 37 and 7% in years 1 and 2, respectively, when grown in competition with taller compared with shorter wheat. Moreover, dockage was 80 and 30% less in years 1 and 2, respectively, when grown in competition with taller than shorter wheat. Mature jointed goatgrass height was similar regardless of the competitive wheat height. However, jointed goatgrass was as much as 18% taller than the short wheat and 15% shorter than the tall wheat. Seeding rate had the most consistent effect on wheat yield. Wheat seed yield was about 10% greater with 60 than 40 seed m−1 of row when competing with jointed goatgrass. Results of this study indicate that growers could use a tall winter wheat variety to improve crop competition against jointed goatgrass. Results also indicate that plant breeders should consider plant height because herbicide-resistant varieties are developed for the integrated management of jointed goatgrass.

The emergence of annual species depends on the number of seeds present and the biotic and abiotic conditions directly surrounding those seeds (the microsite). A field experiment was conducted to study the relative importance of seed presence vs. microsite conditions in determining the emergence of four annual species. Green foxtail, wild mustard, wild oat, and canola were seeded at 200, 400, and 1,200 seeds m−2 in separate plots in a coarse, loamy, mixed Typic Haplocryoll and a fine, mixed Typic Haplocryoll soil. Five microsite modification treatments (control, irrigation, soil compaction, soil compaction plus irrigation, and no crop) were applied to all weed seed density treatments for each weed species. All plots were seeded to spring wheat. Irrigation or soil compaction increased percent emergence of wild oat. Green foxtail emergence tended to increase with soil compaction in 2001 but not in 2002. Wild mustard and canola emergence were largely unaffected by microsite modification treatments. Weed emergence increased with increasing seed density for all species, but the proportion of the total number of seeds emerging decreased with increasing seed density for all species. We suggest that the emergence of the four weed species in this experiment was both seed and microsite limited. Increasing the number of seeds in the soil increased the probability of seeds landing within an appropriate microsite. For these four species, therefore, weed spread and weed patch formation may be determined both by seed production and dispersal and by variability in soil microsite conditions. Results suggest that weed management practices should limit seed dispersal of all species and discourage weed emergence of hard-to-control species during critical establishment periods.

The fungus Pleospora papaveracea is a potential biocontrol agent for opium poppy. The objective of this study was to characterize the growth and production of propagules of P. papaveracea on various substrates and determine their infectivity on opium poppy. Pleospora papaveracea was grown on agar media containing wheat bran, corn cobs, soy fiber, cottonseed meal, rice flour, cornstarch, pectin, dextrin, or molasses, all with the addition of brewer's yeast (BY). Maximum radial growth of P. papaveracea occurred on molasses, soy fiber, and wheat bran media. Pleospora papaveracea produced chlamydospores on dextrin–BY and cornstarch–BY only. Pleospora papaveracea growth in liquid media with 1% (wt/v) dextrin, cornstarch, soy fiber, or wheat bran resulted in the production of greater than 106 colony-forming units (cfu) ml−1 within 3 to 5 d of incubation. Pleospora papaveracea produced less than 105 chlamydospores ml−1 after 10 d of incubation in wheat bran–BY and soy fiber–BY liquid media compared with the production of greater than 105 chlamydospores ml−1 after 5 d of incubation in dextrin–BY or cornstarch–BY liquid media. Fewer cfu were produced by P. papaveracea in 0.25% dextrin or 0.25 and 0.50% soy fiber liquid media than with 1 or 2% substrate. Greater than 107 chlamydospores g−1 dry weight and 108 cfu g−1 dry weight of P. papaveracea were produced in dextrin–BY liquid media in a commercial bench-top fermentor. After air drying biomass for 6 d, propagules of P. papaveracea remained infective on opium poppy. Mycelia and chlamydospores of P. papaveracea grew and formed appressoria during the infection process. Air-dried biomass, when rehydrated in 0.001% Tween 20, caused necrosis within 48 h after application to detached opium poppy leaves. At least 94% of the propagules from air-dried biomass that germinated and infected detached opium poppy leaves were of mycelial origin.

Because soil characteristics and weed densities vary within agricultural landscapes, determining which subfield areas are most favorable to weed species may aid in their management. Field and greenhouse studies were conducted to determine whether subfield environments characterized by higher soil organic carbon (SOC), or ridge vs. furrow microsites, affect common sunflower seed germination after winter burial, seedling emergence, or the control afforded by a preemergence herbicide in a ridge-tillage corn production system. Among seeds buried in situ during winter months and germinated in the laboratory, no differences in common sunflower seed germination or mortality were detected between high-SOC (1.8% mean) and low-SOC (1.1% mean) locations. However, seeds buried at 5-cm depth had about 40% laboratory germination compared with about 10% for seeds stratified on the soil surface or under crop residues. In field emergence and survival experiments, the SOC main-plot effect indicated 25% greater seedling survival in high- than in low-SOC locations. In the absence of herbicide, both emergence and survival were ≥ 35% greater in the ridge than in the furrow microsite, and seedling survival was 48% greater in high- vs. low-SOC furrow environments. However, common sunflower seedling survival was similar between herbicide-treated high- and low-SOC ridges. Greenhouse studies indicated a 13 to 24% increase in common sunflower seedling biomass per 1% increase in SOC under three atrazine doses. Altered or additional weed management tactics should be considered for common sunflower in high-SOC environments to offset the greater potential for seedling survival and growth.

Information on weed responses to soil fertility levels is needed to aid development of fertilizer management strategies as components of integrated weed management programs. A controlled environment study was conducted to determine shoot and root growth response of 22 agricultural weeds to fertilizer phosphorus (P) applied at 5, 10, 20, 40, or 60 mg kg−1 soil. An unfertilized control was included. Wheat and canola were included as control species. Shoot and root growth of all weeds increased with added P, but the magnitude of the response varied greatly among species. Many weeds exhibited similar or greater responses in shoot and root biomass to increasing amounts of soil P compared with wheat or canola. With increasing amounts of P, 17 weed species increased shoot biomass more than wheat, and 19 weed species increased shoot biomass more than canola. However, only 10 weed species exhibited greater increases in root biomass than canola, and no weed species increased root biomass more than wheat with added P. Canola was among species taking up the greatest percentage of available P at all P doses. However, percentage P uptake by wheat relative to other species varied with P dose. Only four weed species extracted more P than wheat at low P levels, but 17 weed species extracted more P at high soil P levels. These findings have significant implications as to how soil fertility may influence crop–weed competition.

Small broomrape, a holoparasitic weed, was recently introduced to the Pacific Northwest and contaminates a limited number of red clover fields in Oregon. Greenhouse and field studies were conducted to evaluate small broomrape response to common crop and weed species in the Pacific Northwest, and to evaluate a quick-screening method for plant species response to the parasite. In greenhouse studies, plants were grown in a hydroponic polyethylene bag system to allow for continuous visibility of their roots and monitoring of small broomrape seed germination and tubercle development. Results of the greenhouse study were validated in a field contaminated with small broomrape. In the greenhouse polyethylene bag study, small broomrape germinated and tubercles developed on alfalfa, arrowleaf clover, carrot, celery, crimson clover, lettuce, prickly lettuce, red clover, spotted catsear, subterranean clover, white clover, and wild carrot. Small broomrape germinated but did not develop tubercles when grown with barley, birdsfoot trefoil, common vetch, creeping bentgrass, cucumber, field corn, red fescue, flax, Italian ryegrass, nasturtium, oats, orchardgrass, perennial ryegrass, snap bean, sugar pea, sunflower, sweet corn, tall fescue, tomato, and wheat. In the field study, tubercles developed on alfalfa, arrowleaf clover, common vetch, crimson clover, red clover, subterranean clover, and white clover, but small broomrape flower stalks did not emerge in arrowleaf clover or crimson clover. Common vetch was a host for small broomrape in the field study but not in the hydroponic polyethylene bag system, thus, caution is warranted in using the quick screening method to elucidate potential small broomrape host species.

The effects of the fungal protein Nep1 and Pseudomonas syringae pv. tagetis (Pst) applied separately or in combination on Canada thistle, common ragweed, and common dandelion were examined in growth chamber experiments. Experiments examined five treatments: (1) untreated control, (2) Silwet L-77 (0.3%, v/v) control, (3) Nep1 (5 μg ml−1) plus Silwet L-77 (0.3%, v/v), (4) Pst (109 colony-forming units [cfu] ml−1) plus Silwet L-77 (0.3%, v/v), and (5) Pst (109 cfu ml−1) and Nep1 (5 μg ml−1) plus Silwet L-77 (0.3%, v/v). Foliar treatments were applied at 28, 26, and 21 d after planting for Canada thistle, common dandelion, and common ragweed, respectively. For all three species, foliar application of Nep1 alone or in combination with Pst caused rapid desiccation and necrosis of leaves, with the greatest effect on recent, fully expanded (RFE) leaves. Within 4 to 8 h after treatment (HAT), 60 to 80% of RFE leaves of all three species were necrotic. Measured 72 HAT, Pst populations in Canada thistle leaves treated with Nep1 plus Pst were approximately 105 cfu cm−2 compared with 107 cfu cm−2 for leaves treated with Pst alone. Measured 2 wk after treatment, foliar application of Nep1 reduced shoot dry weight of the three weeds by 30 to 41%. Treatment with Pst reduced shoot growth of common ragweed, Canada thistle, and common dandelion by 82, 31, and 41%, respectively. The large suppression of common ragweed shoot growth caused by Pst treatment was associated with a high percentage (60%) of leaf area exhibiting chlorosis. Treatment with Pst plus Nep1 did not result in significant decreases in shoot dry weight for Canada thistle and common dandelion compared with either treatment alone. For common ragweed, shoot growth reduction caused by applying Pst and Nep1 together was not greater than that caused by Pst alone.

Lanceleaved waterplantain is an exotic weed of rice that was introduced into Australia in the 1930s. Since its introduction, it has spread throughout much of the rice-growing region in southeastern Australia. The variability of lanceleaved waterplantain in these regions was studied using polymerase chain reaction-based, inter simple sequence repeat (ISSR) analysis. Deoxyribonucleic acid fingerprints from samples of the weed from southeastern Australia were compared between locations and with two samples of common waterplantain, a closely related species. The analysis indicated that there were two distinct groups of lanceleaved waterplantain that correlated with location. From the results of multidimensional scaling analysis, it is hypothesized that the Griffith group did not arise from hybridization between lanceleaved waterplantain and common waterplantain, and that it is more likely that the group arose from a separate introduction into the area. It is also suggested that there is seed movement between areas in the Murray Valley and Colleambally Irrigation areas. The implications of this variation for biological control of the weed are discussed.