Windmillgrass is a major weed in agricultural systems in northern Australia, and it has now become more common in southern Australia. Because little information is available on the biology of this weed species in southern Australia, studies were conducted to investigate plant development and seed biology. Under irrigated field conditions in South Australia, windmillgrass required 748 to 786 growing degree days from emergence to mature seed production. Freshly harvested seed had low dormancy with 16% to 40% germination. Seeds required light exposure for germination and less than 2% germination was observed in complete darkness. Seed could germinate over a wide temperature range (10 to 40 C) with maximum germination at 20 to 25 C. At 25 to 30 C, 50% germination occurred within 27.3 to 45.5 h, and the predicted base temperature for germination of the two populations investigated ranged from 9.2 to 11.2 C. The sodium chloride concentration and osmotic potential required to inhibit germination by 50% were 51 to 73 mM and −0.27 MPa, respectively. Seedling emergence was completely inhibited by burial of seed, which is consistent with its absolute requirement for light exposure to begin germination. Under field conditions, there was no clear effect of burial depth on seed viability in the first 2 yr with average rainfall, and seeds were completely nonviable after 12 mo. However, in the third year, with low spring–summer rainfall, buried seeds (37% viability after 14 mo) persisted longer than those left on the soil surface (6% viability after 14 mo). This study provides important information on plant development and seed biology of windmillgrass that will contribute to the development of a management program for this weed species in southern Australia.

Feather fingergrass is a major weed in agricultural systems in northern Australia and has now spread to southern Australia. To better understand the biology of this emerging weed species, its growth, development, and seed biology were examined. Under field conditions in South Australia, seedlings that emerged after summer rainfall events required 1,200 growing degree days from emergence to mature seed production and produced 700 g m−2 shoot biomass. Plants produced up to 1,000 seeds panicle−1 and more than 40,000 seeds plant−1, with seed weight ranging from 0.36 to 0.46 mg. Harvested seeds were dormant for a period of about 2 mo and required 5 mo of after-ripening to reach 50% germination. Freshly harvested seed could be released from dormancy by pretreatment with 564 mM sodium hypochlorite for 30 min. Light significantly increased germination. Seed could germinate over a wide temperature range (10 to 40 C), with maximum germination at 15 to 25 C. At 20 to 25 C, 50% germination was reached within 2.7 to 3.3 d, and the predicted base temperature to germinate was 2.1 to 3.0 C. The osmotic potential and NaCl concentration required to inhibit germination by 50% were −0.16 to −0.20 MPa and 90 to 124 mM, respectively. Seedling emergence was highest (76%) for seeds present on soil surface and was significantly reduced by burial at 1 (57%), 2 (49%), and 5 cm (9%). Under field conditions, seeds buried in the soil persisted longer than those left on the soil surface, and low spring–summer rainfall increased seed persistence. This study provides important information on growth, development, and seed biology of feather fingergrass that will contribute to the development of a more effective management program for this weed species in Australia.

Weed seedbanks have been studied intensively at local scales, but to date, there have been no regional-scale studies of weed seedbank persistence. Empirical and modeling studies indicate that reducing weed seedbank persistence can play an important role in integrated weed management. Annual seedbank persistence of 13 summer annual weed species was studied from 2001 through 2003 at eight locations in the north central United States and one location in the northwestern United States. Effects of seed depth placement, tillage, and abiotic environmental factors on seedbank persistence were examined through regression and multivariate ordinations. All species examined showed a negative relationship between hydrothermal time and seedbank persistence. Seedbank persistence was very similar between the two years of the study for common lambsquarters, giant foxtail, and velvetleaf when data were pooled over location, depth, and tillage. Seedbank persistence of common lambsquarters, giant foxtail, and velvetleaf from October 2001 through 2002 and October 2002 through 2003 was, respectively, 52.3% and 60.0%, 21.3% and 21.8%, and 57.5% and 57.2%. These results demonstrate that robust estimates of seedbank persistence are possible when many observations are averaged over numerous locations. Future studies are needed to develop methods of reducing seedbank persistence, especially for weed species with particularly long-lived seeds.

A study was conducted to quantify the magnitude and sources of variation in common waterhemp temporal patterns of emergence over 1 yr. In 2008 and 2010, emergence patterns in the absence of soil disturbance were determined for replicated samples of maternal families (progeny from one individual) separately harvested during the previous year from four plants within each of four agricultural fields (16 maternal families yr−1) at a university research farm near Urbana, IL. Combining data across years, variance partitioning indicated that seed sample within maternal family explained 48% of total variation in the percentage of viable, buried seeds that produced seedlings. Differences within, rather than among, maternal families also accounted for large fractions (60 to 99%) of total variation in cumulative percentage emergence at specific points during the growing season. Within years, seed samples characterized by delayed or accelerated emergence patterns did not originate from specific maternal plants. These results indicate that common waterhemp seed populations are without strong maternal plant effects that limit emergence to narrow intervals within the overall emergence period. Thus, results of this study support the use of contemporary approaches for modeling herbicide resistance evolution in common waterhemp, which assume seedling cohorts contain offspring from all individuals occurring within the maternal population.

Ripgut brome is a difficult weed to manage in cereal crops of southern Australia because only a few herbicides can provide effective control in cereals. Knowledge of seed-dormancy mechanisms, germination ecology, and emergence behavior in the field could facilitate development of effective weed control programs for this weed species. Ripgut brome populations from cropping fields were found to possess much longer seed dormancy than that reported previously in the literature. Furthermore, some ripgut brome populations from cropping fields showed longer seed dormancy than those collected from adjacent noncropped fence lines. For example, all seeds of one of the populations from the fence line (SA-1F) germinated at 3 mo after maturity, whereas seeds from the cropping field at the same site (SA-1C) showed little germination (< 3%) even at 8 mo after maturity. These highly dormant ripgut brome populations from cropping fields were responsive to cold stratification, with germination increasing significantly after 2 to 14 d of exposure. Germination of dormant ripgut brome populations increased with addition of gibberellic acid (0.001 M GA3), particularly when lemma and palea had been removed. Ripgut brome populations from cropping fields (VIC-2C and SA-1C) showed strong inhibition of seed germination when exposed to light. These differences in seed dormancy among ripgut brome populations were also expressed in seedling emergence pattern in the field. The nondormant populations collected from fence lines showed high seedling establishment (> 80%) during autumn, which coincided with the planting time of winter crops in southern Australia. In contrast, five populations from cropping fields showed much lower seedling establishment (3 to 17%) before the time of crop planting. Delayed seedling establishment in populations from cropping fields could lead to less effective preseeding weed control and higher weed infestations in field crops. Results of this study also showed that the seedbank of these highly dormant ripgut brome populations can readily persist from one year to the next. Effective management of ripgut brome populations with long seed dormancy and increased seedbank persistence would require a major change in cropping systems used by the growers in southern Australia.

Smooth barley has emerged as a problematic weed in cereal crops of South Australia. After the recent reports of herbicide resistance and increase in seed dormancy in smooth barley, it was considered important to determine the herbicide resistance status and seedbank behavior of field populations of this weed species. A field survey was undertaken in the Upper North and Eyre Peninsula regions of South Australia in October 2012. Of the 90 smooth barley populations screened for resistance to quizalofop, 15% exhibited some level of resistance and 85% were susceptible. Resistance to acetolactate synthase (ALS)-inhibiting herbicides was low, with only 3 and 12% of populations classified as developing resistance to imazamox + imazapyr and sulfosulfuron, respectively. No multiple resistance patterns were observed; however, two ALS-inhibiting herbicide-resistant populations had sulfonylurea-to-imidazolinone cross-resistance. At the start of the growing season, the majority of smooth barley populations emerged rapidly (median 50% time to emergence [T50] = 8 d). In contrast, some populations of smooth barley displayed an extremely slow emergence pattern, with T50 of > 20 d. No direct linkage between seed dormancy and herbicide resistance was observed. However, two acetyl coenzyme A carboxylase-inhibiting herbicide-resistant populations were highly dormant and exhibited delayed emergence. The majority of smooth barley populations showed low-level or no seedbank persistence, but a few populations persisted for 1 yr. However, some weed populations had up to 20% seedbank persistence from 1 yr to the next. Overall there was a strong negative relationship between smooth barley seedling emergence and the level of seed persistence (R2 = 0.84, P < 0.05). This association indicated that greater seed dormancy could be responsible for extended persistence of the seedbank of this weed species. The study provides valuable insights into the general pattern of herbicide resistance and the behavior of the seedbank of smooth barley populations on South Australian farms.

The predictability of the spring emergence period of kochia is a potentially exploitable attribute that may be applied to weed management. The emergence timing of kochia was monitored, during the spring and summer of 2005 and 2006, in 12 farmed fields in the northern region of the Northern Great Plains (NGP) of North America. Kochia emergence began at 50 cumulative growing-degree days (GDD Tbase 0 C, starting January 1) and continued into late summer. The onset of kochia emergence occurred well before the emergence onset of other weed species common to this region. Fall soil samples revealed few kochia seeds remained in the seedbank. In growth room studies, kochia seed placed at the soil surface had greater emergence compared with seed burial to a 10 mm or greater depth. Kochia did not emerge from seed planted 80 mm deep; however, radical emergence was evident indicating fatal germination. Kochia should be controlled early in the growing season, and burying seed will greatly reduce future kochia populations.

Seedbank persistence in canola seeds is related to their potential to develop secondary dormancy. This can result in volunteer weed problems many years after canola production. The potential to be induced into secondary dormancy is controlled by both the canola genetics and the environment of the mother plant. However, the effect of time of harvesting on secondary dormancy potential is not known. The objective of this study was to determine the effect of harvest timing on potential to develop seed dormancy in canola. Six harvest samples were collected weekly from two canola genotypes (5440 and 5020) starting from 10 to 20% seed color change on the main stem until they were fully ripened. Freshly harvested seeds of 5440 and 5020 showed 13 and 16% primary dormancy at 32 and 33 d after flowering (DAF), respectively, but dormancy decreased with harvest timings and no dormancy was observed when seeds were fully mature (78 DAF). After dormancy induction, 10% of 5440 seeds were dormant at 32 DAF, but 94% of seeds were dormant at 78 DAF. Similarly, 70% of 5020 seeds were dormant at 33 DAF, but 90% of seeds were dormant at 68 DAF. Thus, seeds had lower potential to secondary dormancy at early development but have a high potential to secondary dormancy induction at full maturity. This study suggests that windrowing these canola genotypes at the recommended time (60% seed color change on the main stem) may reduce ability of the seed to develop secondary dormancy and thus reduce the persistence of seeds in the soil seedbank.

With the recent interest in genetically engineered (GE) wheat and the commercialization of novel-trait imidazolinone herbicide-resistant wheat in North America, volunteer wheat as a weed has also been the subject of renewed interest, specifically, its recruitment and persistence in annual cropping systems. The recruitment of seed from a wheat seedbank established the previous autumn was monitored in a flax crop at two field sites in southern Manitoba, Canada, in 2003 and 2004. Seeds of eight Canadian Western Hard Red spring wheat cultivars, which exhibit a range of preharvest sprouting-resistance characteristics, were broadcast and incorporated into the soil in the autumn at 500 seeds m−2. Tillage treatments consisted of autumn tillage only, and autumn and spring tillage. Recruitment the following spring occurred very early in terms of accumulated growing–degree days (base temperature of 0 C) but expressed as a proportion of total seeds broadcast was low and variable. Total cumulative emergence of wheat over all 4 site yr ranged from 0.9 to 13.1%, with an overall average of 4.3%. There was no relationship between preharvest sprouting-resistance characteristics and recruitment proportion, and no significant influence of tillage treatment on wheat recruitment. Wheat seed that did not recruit was rapidly degraded in the soil and did not persist for more than 12 mo. However, some emerged volunteer wheat plants escaped all control measures normally used in establishing and growing a typical flax crop, and these escaped volunteer wheat plants set viable seed. Therefore, results of this study indicate that efforts and attention should be directed toward achieving very high levels of volunteer wheat control in subsequent rotational crops and that reseeding by escaped volunteer wheat plants may be a more important persistence mechanism for spring wheat than multiyear soil seedbank persistence.

Studies suggest that disturbance-induced reductions in soil seedbank density are diminished by periods of water scarcity after soil disturbance; however, this hypothesis has yet to be tested. The objectives of this study were (1) to determine the effects of increasing time between soil disturbance and flood irrigation on disturbance-induced reductions in soil seedbank density, and (2) to identify specific soil moisture levels that cause seedbank reductions under flood irrigation. Weed species in this study were junglerice, Palmer amaranth, and yellow foxtail. For Objective 1, artificial seedbanks with known numbers of seeds were disturbed 10, 3, or 0 d prior to flood irrigations under field conditions. For Objective 2, seeds were buried in soil mesocosms that were hydrated to specific soil water potentials (flooded, 0 kPa, −30 kPa, −60 kPa, and −180 kPa) and placed in laboratory conditions favorable for germination. For both objectives, seeds were recovered to determine the percentages of buried seeds that survived the disturbance or moisture treatments. Results for the field study indicated that soil disturbances reduced seedbank persistence of Palmer amaranth but did not affect seedbank persistence of junglerice and yellow foxtail. Disturbance-induced reductions in seedbank density were greatest when soil was disturbed 0 and 3 d prior to flood irrigations. For the laboratory study, results showed that waterlogged soil was not required for seedbank losses because rates of seedbank persistence were greater in saturated soils (0 kPa and flooded) compared to the lower moisture levels. These studies indicate that delays in irrigation can reduce the seedbank reduction potentials of soil disturbance events. Further, irrigation timing effects on disturbed soil seedbanks are likely to occur in all irrigation systems, including those that reduce the amount of water applied compared to flood irrigation.