Seedbank persistence of four summer grass weed species in the northeast cropping region of Australia

Summer grass weed species are a particular problem in the northeast cropping region of Australia because they are prolific seeders and favor no-till systems. Information on weed seed persistence levels can be used for the development of effective and sustainable integrated weed management programs. A field study was conducted over 42 months to evaluate the seedbank persistence of Chloris truncata, C. virgata, Dactyloctenium radulans, and Urochloa panicoides as affected by burial depth (0, 2, and 10 cm). Regardless of species, buried seeds persisted longer than surface seeds and there was no difference in seed persistence between 2 and 10 cm depths. Surface seeds of C. truncata depleted completely in 12 months and buried seeds in 24 months. Similarly, C. virgata seeds placed on the soil surface depleted in 12 months. Buried seeds of this species took 18 months to completely deplete, suggesting that C. truncata seeds persist longer than C. virgata seeds. Surface seeds of D. radulans took 36 months to completely deplete, whereas about 7% of buried seeds were still viable at 42 months. U. panicoides took 24 and 42 months to completely exhaust the surface and buried seeds, respectively. These results suggest that leaving seeds on the soil surface will result in a more rapid depletion of the seedbank. Information on seed persistence will help to manage these weeds using strategic tillage operations.

Seedbank persistence and emergence pattern of Argemone mexicana, Rapistrum rugosum and Sonchus oleraceus in the eastern grain region of Australia

A thorough understanding of the emergence pattern and persistence of weed seeds is a prerequisite in framing appropriate weed management options for noxious weeds. In a study conducted at the University of Queensland, Australia, the emergence and seed persistence behavior of three major weeds Sonchus oleraceous, Rapistrum rugosum, and Argemone mexicana were explored with seeds collected from Gatton and St George, Queensland, Australia, with an average annual rainfall of 760 and 470 mm, respectively. Seed persistence was evaluated by placing seeds at the surface layer (0 cm) or buried at 2 and 10 cm depths enclosed in nylon mesh bags and examined their viability for 42 months. In another study, the emergence pattern of four populations, each from these two locations, was evaluated under a rainfed environment in trays. In the mesh-bag study, rapid depletion of seed viability of S. oleraceous from the surface layer (within 18 months) and lack of seed persistence beyond two years from 2 and 10 cm depths were observed. In trays, S. oleraceous germinated 3 months after seeding in response to summer rains and there was progressive germination throughout the winter season reaching cumulative germination ranging from 22 to 29% for all the populations. In the mesh-bag study, it took about 30 months for the viability of seeds of R. rugosum to deplete at the surface layer and a proportion of seeds (5 to 13%) remained viable at 2 and 10 cm depths even at 42 months. Although fresh seeds of R. rugosum exhibit dormancy imposed due to the hard seed coat, a proportion of seeds germinated during the summer months in response to summer rains. Rapid loss of seed viability was observed for A. mexicana from the surface layer; however, more than 30% of the seeds were persistent at 2 and 10 cm depths at 42 months. Notably, poor emergence was observed for A. mexicana in trays and that was mostly confined to the winter season.

Seed bank dynamics of an invasive alien species, Helianthus annuus L.

Aims The ability to form persistent seed banks is one of the best predictors of species’ potential to establish in new ranges. Wild sunflower is native to North America where the formation of persistent seed banks is promoted by disturbance and it plays a key role on the establishment and persistence of native populations. However, the role of the seed banks on the establishment and persistence of invasive populations has not been studied. Here, we evaluated the role of seed bank and disturbance on the establishment and fitness, and seed persistence in the soil in several sunflower biotypes collected in ruderal (wild Helianthus annuus) and agrestal (natural crop–wild hybrid) habitats of Argentina as well as volunteer populations (progeny of commercial cultivars). Methods In a seed-bank experiment, we evaluated emergence, survival to reproduction, survival of emerged seedlings, inflorescences per plant and per plot under disturbed and undisturbed conditions over 2 years; in a seed-burial experiment, we evaluated seed persistence in the soil over four springs (6, 18, 30 and 42 months). Important Findings Overall, seedling emergence was early in the growing season (during winter), and it was promoted by disturbance, especially in the first year. Despite this, the number of inflorescences per plot was similar under both conditions, especially in ruderals. In the second year, emergence from the seed bank was much lower, but the survival rate was higher. In the seed-burial experiment, genetic differences were observed but seeds of ruderals and agrestals persisted up to 42 months while seeds of the volunteer did not persist longer than 6 months. The agrestal biotype showed an intermediate behavior between ruderals and volunteers in both experiments. Our findings showed that wild and crop–wild sunflower can form persistent seed banks outside its native range and that disturbance may facilitate its establishment in new areas.

Tillage and Cover Crop Effects on Weed Seed Persistence: Do Light Exposure and Fungal Pathogens Play a Role?

In a series of seed burial studies, we tested the hypothesis that reduced tillage and cereal rye (Secale cerealeL.) cover cropping influence seed persistence and that these effects are mediated by differences in fungal pathogens and exposure to light. Seeds of Powell amaranth (Amaranthus powelliiS. Watson) and large crabgrass [Digitaria sanguinalis(L). Scop.] were buried in mesh bags in a long-term experiment with two levels of tillage (full-width tillage [FWT] or strip tillage [ST]) and two levels of cover cropping (none or cereal rye). In Experiment 1, seeds were exhumed each spring for 3 yr and tested for viability. In Experiment 2, untreated and fungicide-treated seeds were buried, exhumed at shorter intervals, and tested for viability. In addition, a subset of seeds in FWT treatments were exhumed and stored in either light or darkness during tillage operations and evaluated for persistence at 8.5 mo after burial (MAB). In Experiment 1, the persistence ofD. sanguinalisseeds declined by 80% at 7 MAB regardless of cover crop or tillage treatment. The persistence ofA. powelliiseeds at 19 MAB declined by 95% in FWT compared with only 50% in ST. In Experiment 2, seed persistence of both species was greater in ST compared with FWT treatments, for seeds that had been exposed to light, but not for those that were maintained in darkness. Rye cover cropping resulted in a 2-fold increase in overwinter persistence of seeds ofD. sanguinalisregardless of fungicide treatment. These results demonstrate that increased persistence under ST was primarily due to reductions in light-induced fatal germination and that increased overwinter persistence ofD. sanguinalisin rye cover crop treatments could not be explained by differences in decay due to fungal pathogens controlled by the seed treatment.

Yellow bristle grass (Setaria pumila) germination biology

The presence of Setaria pumila in dairy pastures lowers feed quality and may cause grazing avoidance. More information is required about the germination biology of this weed to improve the effectiveness of control strategies. Base temperature and germination profile were determined on a thermo-gradient table. For emergence depth, seeds were buried at 0—50 mm and time to emerge recorded. Seed persistence was tracked at seven field sites over 5 years and in a laboratory-based controlled-ageing test. Base temperature for germination was 10.2˚C, germination was most rapid at 30—35˚C and most numerous from 20—30˚C. Emergence occurred from 2—50 mm depth but mostly from 2—15 mm. The controlled-ageing test indicated the seed was viable for <3 years. However, some Setaria pumila seed continued to germinate after 5 years of burial in all but the clay soil. Farmers should try to prevent this species from seeding for at least 5 years to reduce the seed bank. Soil inversion could promote dormancy and seed persistence. If followed by effective control, cultivation could stimulate germination and further reduce the seed bank.

Gamba grass (Andropogon gayanus Kunth.) seed persistence and germination temperature tolerance

Gamba grass (Andropogon gayanus Kunth.) is a highly invasive, naturalised Weed of National Significance in Australia due to its economic, environmental and social impacts. It outcompetes native pastures and fuels intense fires in northern Australian rangelands. To aid management of current infestations and to better understand its potential distribution, this study determined the germination response of gamba grass under a range of constant (13°C−48°C) and alternating (11/7°C–52/42°C) temperature regimes and quantified the potential longevity of soil seed banks. The effect of different soil types, levels of pasture cover and burial depths on seed longevity was investigated in the Dry Tropics of northern Queensland. Germination of gamba grass occurred under a wide range of both constant (17°C−39°C) and alternating day/night temperatures (16/12°C–47/39°C), although the level of germination declined at the lower and higher temperature ranges. At the cooler temperatures, seed viability was not affected, but seeds went into a state of dormancy. The highest level of seed viability was recorded at the lowest constant temperature regime (13°C) and at the two lowest alternating temperatures (11/7°C and 16/12°C). A gradual but variable decline in viability occurred thereafter with increasing temperatures. At the higher temperature range (e.g. constant temperatures of 39°C−43°C and alternating temperatures of 47/39°C) both dormancy and loss of seed viability were occurring, but once alternating and constant temperatures reached above 47/39°C and 43°C all seeds were rendered unviable after 9 and 6 weeks respectively. In the Dry Tropics of northern Queensland, viability of seeds was <1% after 12 months and nil after 24 months, irrespective of soil type or vegetation cover. However, burial depth had a significant effect, with surface located seeds exhibiting a faster rate of decline in germination and viability than seeds buried below ground (i.e. 2.5–10 cm). These findings have implications for the duration of control/eradication programs (i.e. seed persistence) and also suggest that gamba grass has the potential to greatly expand its current distribution into the relatively cooler southern latitude areas of Australia.

Aerobic environment ensures viability and anti-oxidant capacity when seeds are wet with negative effect when moist: implications for persistence in the soil

Interchangeable effects of temperature, moisture content and oxygen on seed longevity have been mostly examined to estimate seed viability during long-term dry storage, whereas few experiments have studied seed viability under near-natural conditions to evaluate seed persistence in the soil. To this end, we artificially aged seeds ofRanunculus baudotii, a hydrophyte widely distributed in temporary ponds constituting an abundant soil seed bank. Seeds were exposed to controlled ageing at three different relative humidities (RH) under both aerobic and anoxic conditions. Their viability, water content, membrane damage, oxidative stress and anti-oxidant enzymatic defence activity were evaluated. Seed survival was longer at higher relative humidity (97% RH), and lowest at a relative humidity (90% RH) simulating moist but not waterlogged soils. Anoxic conditions showed a protective role on viability at lower moisture contents (70% RH). Seed viability was negatively associated with hydrogen peroxide content and correlated with anti-oxidant enzyme activities, but not with membrane damage. Altogether, these results suggest negative roles for moist soils and anoxia in determining seed persistence in the field, but at higher moisture contents the negative effects of anaerobia diminished. The anti-oxidant system activation, even under unfavourable conditions, might recover seeds once all protective processes can operate, pointing out the plasticity of mechanisms involved in seed loss viability.