Effect of patch size on seed removal by harvester ants

The harvester ant Messor barbarus can be responsible for high weed seed losses in dry land cereals in Spain. Because weeds occur in patches, harvester ants have to be able to find and exploit patches. However, seed patches can differ in size and may, therefore, differ in the probability of being discovered and exploited. Here, 90 patches varying in size from 0.25 to 9 m² were created in three 50 × 50 m subareas in a cereal field. Oat seeds were sown as weed seed surrogates in the patches at 2000 seeds m^?2. After 24 h, those remaining were collected and the exploitation rate (the percentage of seeds removed per patch discovered by ants) was estimated. Harvester ant nests and the location of the seed patches were georeferenced and used to estimate distances between them. The patch encounter rate (the proportion of patches discovered by the ants) decreased slightly, but significantly, with decreasing patch size, though not the exploitation rate, which was lowest in the smallest patches (78–94%) and highest in the largest (99–100%). Seed patches that were not found or partially exploited were mostly located in subareas with a lower ant nest density or a longer distance away from the nearest nest than seed patches that were fully exploited. The results of this study indicate that the interaction between the spatial distribution of ant nests and the patchy distribution of seeds can create opportunities for seeds to be subjected to lower levels of predation.     

Ecophysiological study on weed seed banks and weeds in Cambodian paddy fields with contrasting water availability

Weed infestations are a major cause of yield reduction in rice (Oryza sativa) cultivation, particularly with direct‐seeding methods, but the relationship between weed dynamics and water availability in Cambodian paddy fields has not been documented previously. We surveyed the weed abundance and weed seed banks in the soil of paddy fields with inferred differences in their water regime in 22 farm fields in three provinces of Cambodia in the 2005 and 2006 rainy seasons. We studied rain‐fed lowland fields in upslope and downslope topographic positions and fields at different distances from the irrigation water source inside an irrigation rehabilitation area. The weed seed banks were estimated by seedling emergence in small containers and weed abundance and vigor were estimated by a simple scoring system. The estimated weed seed bank in the top 5 cm of soil ranged from 52.1 to 167 × 10³ seeds m^?2 (overall mean of 8.5 × 10³ seeds m^?2) and contained a high proportion (86%) of sedge species, such as Fimbristylis miliacea L. and Cyperus difformis. Several fields had particularly large seed banks, including one near the reservoir. No clear difference was found in the weed seed banks between the irrigated fields that were located close to (upstream) and distant from (downstream) the water source or between the irrigated and rain‐fed lowland fields, but the weed scores were larger in the rain‐fed fields and the downstream fields within the irrigated area. A water shortage during the late growing season in 2005 led to a proliferation of weeds in some fields and an associated increase in weed seedbank size in 2006. However, the weed scores in 2006 were more strongly associated with that year's water conditions than with the weed seedbank size.     

The effect of crop,cultivation and seed addition for birds on surface weed seed densities in arable crops during winter

Weed seeds present an agronomic threat, but are also an important food resource for wildlife in winter. Weed seed densities on the soil surface in winter were examined from 1999 to 2002 in 105 fields on three different farms in UK. The effect of the preceding crop, cultivation, position within the field and the application of seed for birds (bird seed) on surface seed abundance and species composition was tested. Six or fewer species comprised c. 80% of the weed seeds. By January of each study year, the densities of seeds important for farmland birds (key seeds) were 73% or 87% lower compared with early winter on two of the farms, but were stable on the third where seeds were incorporated through cultivation. At the edge and mid‐field, seed densities only exceeded 400 m^?2 in 17%, 10% and 12% of fields for total, key and dicotyledonous seeds respectively. The preceding crop only affected seed densities at one site; stubbles of winter barley had fewer seeds compared with winter wheat or spring barley. Seed densities varied between the edge and mid‐field, but trends were inconsistent between sites. The density of the larger seeds (Atriplex patula, Viola arvensis, Polygonum aviculare and Chenopodium album) were reduced in fields receiving bird seed. The objectives of weed control and conservation may not be mutually exclusive because seed return was most reduced where the ground remained uncultivated through the winter, yet this also provided the best foraging opportunities for surface feeding seed predators.     

Weed seed rain interception by grass cover depends on seed traits

Weed management requires a better understanding of the dynamics of the weed seedbank, which is a primary source of weeds in a field. Seeds reaching the ground after seed rain replenish the seedbank and therefore contribute to future weed infestations. Our investigation is based on the hypothesis that a permanent vegetation cover, such as a grassland, can prevent weed seeds from reaching the ground. Therefore, we developed an innovative experimental device to simulate in controlled conditions the seed rain of 12 weed species (Capsella bursa‐pastoris, Conyza canadensis, Myosotis arvensis, Papaver rhoeas, Poa annua, Polygonum aviculare, Ranunculus sp., Rumex obtusifolius, Sonchus asper, Stellaria media, Taraxacum officinale and Veronica persicaria). We quantified the interception of weed seeds by a grass cover. Grass cover height, seed size and seed appendage (e.g. pappus, wing or awn) increased seed interception, in contrast to seed weight and shape index. From these results, we established a linear model to predict weed seed interception by a grass cover as a function of their seed trait values. The relationship between the predicted interception and weed community dynamics observed in grasslands was negative for some species, indicating that other processes may be involved depending on weed species. The weed seed interception model will be incorporated into an existing model of weed population dynamics to simulate the impact of grassland insertion into arable crop rotations.     

Seed survival and predation of Anoda cristata in soyabean crops

Anoda cristata is a troublesome annual broad-leaved weed in summer crops in the rolling Pampa in Argentina; seeds are the only source of regeneration of this species. Seed persistence or depletion is the result of survival and loss processes, including predation. The objective of this study was to determine survival at two burial depths in undisturbed soil and predation rates of A. cristata seeds in soyabean crops in different rotations and tillage systems. Survival was discontinuous and decreased to 25% after 35 months, after which no further reduction in survival was observed to the end of the experiment at 96 months. No differences in seed survival between seeds placed on the soil surface and buried 5 cm below the soil surface were found at 80 months, but at later times survival was lower for seeds placed on the soil surface. Predation rates ranged between 0.3% day⁻¹ and 6.7% day⁻¹. Of the models tested, a polynomial regression of the rate of predation with time gave the best representation of seed predation. From January to July, predation was higher in non-tillage plots in the wheat/soyabean rotation. There was no significant difference in predation rates between tillage systems in the soyabean monoculture and no difference between planting densities. Higher crop residue levels in non-tillage plots in the wheat/soyabean rotation was the dominant factor influencing seed predation, probably because such habitat favours the presence of seed predators.     

Diversity in weed seed production and the soil seed bank: Contrasting responses between two agroecosystems

This study was carried out to compare the diversity in seed production and the soil seed bank in a dryland and an irrigated agroecosystem in the dry tropics. Both agroecosystems showed a comparable number of species, but only 25% and 38% similarity during the winter and rainy cropping seasons, respectively. In the irrigated agroecosystem, the amount of seed production diversity was almost double in the winter season, compared to the rainy season. The weed seedbank diversity was low but was sensitive to cropping practices and seasons in both agroecosystems. A considerably smaller soil seedbank size in the irrigated agroecosystem (cf. dryland) was related to lowered weed seed production. The dryland agroecosystem showed a greater accumulation of the seeds of broad‐leaved weeds, whereas the irrigated agroecosystem accumulated more seeds of the grasses or sedges. About three‐fourths of the seeds during the winter season were accounted for by Anagallis arvensis and Chenopodium album in the dryland agroecosystem and by C. album and Melilotus indica in the irrigated agroecosystem. However, during the rainy season, Ammannia baccifera, Echinochloa colona and Cyperus rotundus dominated in both agroecosystems. The changes in the weed seed bank and its diversity are mainly attributed to differences in water management, which tends to reduce species diversity, especially at a lower depth, but leads to the dominance of some potentially noxious weeds (e.g. Phalaris minor and M. indica). Approximately double the soil seedbank size and a greater diversity at a lower depth might indicate an adaptive mechanism in the storage of weed seeds in the dryland agroecosystem.     

Postdispersal seed predation by Teleogryllus emma (Orthoptera: Gryllidae) reduces the seedling emergence of a non‐native grass weed,Italian ryegrass (Lolium multiflorum)

The potential impact of postdispersal seed predation by the field cricket, Teleogryllus emma (Ohmachi et Matsuura), on the seedling emergence of Italian ryegrass (Lolium multiflorum Lam.), a non‐native grass weed in Japan, was determined. The relationship between cricket density and the proportion of seedling emergence was investigated by conducting manipulative experiments in duplicate, using enclosures. One‐thousand seeds of Italian ryegrass were exposed to adult crickets at different densities (zero, one, two, four and eight individuals per 2.25 m² enclosure) for 2 weeks. The proportion of seedling emergence decreased with increasing cricket density. The proportion of seedling emergence in the enclosures without the crickets was 90.9–97.2%, whereas the seedling emergence in the enclosures with eight crickets greatly decreased, to 0.5–2.5%. These results suggest that postdispersal seed predation by T. emma can substantially decrease the abundance of Italian ryegrass at an early life stage and reduce its population in environments with a high density of crickets.     

Temperature influences postdispersal predation of weed seeds

Temperature is a key factor for the living organisms on earth. It influences weed management practices, either directly or indirectly. Field experiments were conducted to determine the effect of temperature on the postdispersal seed predation of four important weed species (Cuscuta compestris, Stellaria media, Taraxacum officinale and Veronica persica) in two lucerne fields in Mashhad and Chenaran, north‐eastern Iran. These two cities have the same climate: temperate and cold alpine but the temperature varies between them. Wire mesh cages were used to determine the relative importance of birds in predation and pitfall traps were used to detect the species and the activity density of invertebrate predators. The results showed that the predation preference of different weed species was significantly different between and within fields. Seed predation fluctuated widely throughout the sampling periods, matching the periodic forage harvest and regrowth cycle of lucerne. Despite the level of seed predation fluctuating, it declined toward the last sampling periods. Using wire mesh exclusion cages showed no significant effect of birds on weed seed predation in both fields. Ants, crickets and carabid beetles were the invertebrate seed predators that were caught in the pitfall traps. There were significant correlations between the mean temperature and predator activity densities and also between the predated seeds and the mean air temperature in both locations. The results of this study indicate the significant effect of temperature on postdispersal weed seed predation. Therefore, with respect to climate change and increasing global warming, it would be possible to focus on postdispersal seed predation in weed management in the future.     

Post-dispersal seed predation of non-target weeds in arable crops

Field experiments were conducted to quantify the natural levels of post-dispersal seed predation of arable weed species in spring barley and to identify the main groups of seed predators. Four arable weed species were investigated that were of high biodiversity value, yet of low to moderate competitive ability with the crop. These were Chenopodium album, Sinapis arvensis, Stellaria media and Polygonum aviculare. Exclusion treatments were used to allow selective access to dishes of seeds by different predator groups. Seed predation was highest early in the season, followed by a gradual decline in predation over the summer for all species. All species were taken by invertebrates. The activity of two phytophagous carabid genera showed significant correlations with seed predation levels. However, in general carabid activity was not related to seed predation and this is discussed in terms of the mainly polyphagous nature of many Carabid species that utilized the seed resource early in the season, but then switched to carnivory as prey populations increased. The potential relevance of post-dispersal seed predation to the development of weed management systems that maximize biological control through conservation and optimize herbicide use, is discussed.     

Impact of cropping systems on the weed seed banks in the northern Great Plains, USA

Very little research has been done on weed seedbank communities in the northern Great Plains region of the USA. The objectives of this study were to evaluate the effects of management systems on the weed seed banks and to assess the relationship between the weed seed banks and the above-ground weed communities. The seed banks were sampled along a range of areas of above-ground weed diversity in organic and conventional spring wheat production fields near Big Sandy, Montana, over 2 years. Eight 1 m × 0.33 m areas were selected in each field to encompass a wide range of above-ground weed diversity and soil cores were taken in each area to a depth of 20 cm and split in half at 10 cm. The number of seeds recovered from the top 10 cm of soil and the 10–20 cm depth were significantly affected by the sampling year and an interaction between the cropping system and the sampling year. The year was the only significant predictor affecting the weed seedbank diversity at both depths. A significant interaction between the management system and the year observed at the 10–20 cm sampling depth reflected the higher rate of decrease in diversity occurring between 2005 and 2006 in the conventionally managed fields compared with the organic fields. A multivariate ordination indicated that, although the year played a significant role in determining the weed seedbank communities, the management system had a role only during 2006. We failed to detect strong correlations between the above-ground and underground weed communities. The results of this study suggest that, in the studied region, yearly fluctuations in environmental factors have significant impacts on the weed seed banks.     

You cannot fight fire with fire: a demographic model suggests alternative approaches to manage multiple herbicide‐resistant Avena fatua

Multiple herbicide‐resistant (MHR ) weed populations pose significant agronomic and economic threats and demand the development and implementation of ecologically based tactics for sustainable management. We investigated the influence of nitrogen fertiliser rate (56, 112, 168, or 224 kg N ha^?1) and spring wheat seeding density (67.3 kg ha^?1 or 101 kg ha^?1) on the demography of one herbicide susceptible and two MHR Avena fatua populations under two cropping systems (continuous cropping and crop‐fallow rotation). To represent a wide range of environmental conditions, data were obtained in field conditions over 3 years (2013–2015). A stochastic density‐dependent population dynamics model was constructed using the demographic data to project A. fatua populations. Elasticity analysis was used to identify demographic processes with negative impacts on population growth. In both cropping systems, MHR seedbank densities were negatively impacted by increasing nitrogen fertilisation rate and wheat density. Overall, MHR seedbank densities were larger in the wheat‐ fallow compared with the continuous wheat cropping system and seedbank densities stabilised near zero in the high nitrogen and high spring wheat seeding rate treatment. In both cropping systems, density‐dependent seed production was the most influential parameter impacting population growth rate. This study demonstrated that while the short‐term impact of weed management tactics can be investigated by field experiments, evaluation of long‐term consequences requires the use of population dynamics models. Demographic models, such as the one constructed here, will aid in selecting ecologically based weed management tactics, such as appropriate resource availability and modification to crop competitive ability to reduce the impact of MHR .     

Weed seedbank size and composition in a long‐term tillage and crop sequence experiment

Knowledge of the effects of agricultural practices on weed seedbank dynamics is essential for predicting future problems in weed management. This article reports data relative to weed seedbank structure after 18 years of continuous application of conventional tillage (CT, based on mouldboard ploughing) or no tillage (NT) within three crop sequences (continuous wheat, W_W; wheat–faba bean, W_F; and wheat–berseem clover, W_B). Tillage system did not affect the size of the total weed seedbank, but altered both its composition and the distribution of seeds within the soil profile. In particular, the adoption of CT favoured some species (mainly Polygonum aviculare), whereas the continuous use of NT favoured other species (Papaver rhoeas, Phalaris spp. and Lactuca serriola). The effects of tillage system on weed seedbank size and composition were less pronounced in the W_B cropping system than in either the W_W or W_F. Compared with W_F and W_B, W_W resulted in an increase in total weed seedbank density (about 16 000 seedlings m^?2 in W_W, compared with 10 000 and 6000 seedlings m^?2 in W_F and W_B, respectively) and a reduction in weed diversity, with a strong increase in some species (e.g. Polygonum aviculare). Our results for the effect of NT application on weed seedbank size and composition suggest that farmers should only apply such a conservative technique within an appropriate crop sequence.     

Weed seed decay in conventional and diversified cropping systems

Diversified cropping systems can have high soil microbial biomass and thus strong potential to reduce the weed seedbank through seed decay. This study, conducted in Iowa, USA, evaluated the hypothesis that weed seed decay is higher in a diversified 4‐year maize–soyabean–oat/lucerne–lucerne cropping system than in a conventional 2‐year maize–soyabean rotation. Mesh bags filled with either Setaria faberi or Abutilon theophrasti seeds and soil were buried at two depths in the maize phase of the two cropping systems and sampled over a 3‐year period. Setaria faberi seed decay was consistently greater at 2 cm than at 20 cm burial depth and was higher in the more diverse rotation than in the conventional rotation in 1 year. Abutilon theophrasti seeds decayed very little in comparison with seeds of S. faberi. Separate laboratory and field experiments confirmed differences in germination and seed decay among the seed lots evaluated each year. Fusarium, Pythium, Alternaria, Cladosporium and Trichoderma were the most abundant genera colonising seeds of both species. A glasshouse experiment determined a relationship between Pythium ultimum and S. faberi seed decay. Possible differences in seed susceptibility to decay indicate the need to evaluate weed seedbank dynamics in different cropping systems when evaluating overall population dynamics and formulating weed management strategies.     

Enhanced weed‐crop competition effects on growth and seed production of herbicide‐resistant and herbicide‐susceptible annual sowthistle (Sonchus oleraceus)

Enhanced crop competition could aid in the management of annual sowthistle (Sonchus oleraceus L.), a dominant weed of Australian cropping systems. A two‐year pot study was conducted to evaluate the effect of wheat (Triticum aestivum L.) planting densities (0, 82, and 164 wheat plants/m²) on growth and seed production of glyphosate‐resistant (GR) and glyphosate‐susceptible (GS) biotypes of annual sowthistle. Without competition, both biotypes produced a similar number of leaves and biomass, but the GS biotype produced 80% more seeds (46,050 per plant) than the GR biotype. In competition with 164 wheat plants/m², the number of leaves in the GR and GS biotypes was reduced by 62 and 61%, respectively, in comparison with the no‐competition treatment, and similarly, weed biomass was reduced by 78 and 77%, respectively. Compared to no‐competition treatment, the seed production of GR and GS biotypes was reduced by 33 and 69%, respectively, when grown with 82 wheat plants/m², but increasing wheat density from 82 to 164 plants/m² reduced the number of seeds only in the GS biotype (81%). Both biotypes produced greater than 6,000 seeds per plant when grown in competition with 164 plants/m², suggesting that increased crop density should be integrated with other weed management strategies for efficient control of annual sowthistle.     

Seed dormancy and soil seedbank of the invasive weed Chenopodium hybridum in north‐western China

Seed dormancy and persistence in the soil seedbank play a key role in timing of germination and seedling emergence of weeds; thus, knowledge of these traits is required for effective weed management. We investigated seed dormancy and seed persistence on/in soil of Chenopodium hybridum, an annual invasive weed in north‐western China. Fresh seeds are physiologically dormant. Sulphuric acid scarification, mechanical scarification and cold stratification significantly increased germination percentages, whereas dry storage and treatments with plant growth regulators or nitrate had no effect. Dormancy was alleviated by piercing the seed coat but not the pericarp. Pre‐treatment of seeds collected in 2012 and 2013 with sulphuric acid for 30 min increased germination from 0% to 66% and 62% respectively. Effect of cold stratification on seed germination varied with soil moisture content (MC) and duration of treatment; seeds stratified in soil with 12% MC for 2 months germinated to 39%. Burial duration, burial depth and their interaction had significant effects on seed dormancy and seed viability. Dormancy in fresh seeds was released from October to February, and seeds re‐entered dormancy in April. Seed viability decreased with time for seeds on the soil surface and for those buried at a depth of 5 cm, and 39% and 10%, respectively, were viable after 22 months. Thus, C. hybridum can form at least a short‐lived persistent soil seedbank.     

Soil seedbanks in slash‐and‐burn rice fields of northern Laos

Crops in shifting cultivation fields often suffer from severe weed infestation when long fallow periods are replaced by short fallow periods. The soil seedbank as a source of weed infestation was studied in four fields that differed in their last fallow duration. The effect of burning was analysed by comparing adjacent pre‐burn and post‐burn samples (two sites). Surface vegetation was monitored from burning to harvest in the plots from which soil samples were taken to determine the fraction of the seedbank germinating (three sites). Seedbank size (1700–4000 seedlings m^?2) varied depending on a single species, Mimosa diplotricha. Burning reduced emergence of most species, but stimulated emergence in others. Densities in the seedbank were not correlated with above‐ground abundances in the field, except for some species. Most species emerging after 50 days from the soil samples (40% of seedlings) were absent from the field after 190 days. Whilst the data from this study are derived from only four fields, the weed problems after short‐term fallowing appeared to be due to a larger fraction of the seedbank emerging, possibly due to shallow burial, and to a floristic shift towards adaption to burning, rather than the size of the seedbank per se.     

Seed dynamics in populations of A vena sterilis ssp. ludoviciana

Seed populations of Avena sterilis ssp. ludoviciana (Durieu) Nyman were monitored in a naturally occurring infestation throughout its life cycle. Considering the large weed population present (298panicles m^?2), total seed production was relatively low: 3838 seeds m^?2. Only 68% of these seeds were recovered from the soil surface and a further 3% were removed with wheat grain and straw during harvest operations. The numbers of seeds from the stubble between mid-July and mid-September were relatively low (10%). Ploughing the stubble in October buried most of the recently produced seed rain and resulted in a relatively uniform vertical distribution of the seedbank. Maximum seed persistence in the soil ranged from 27 to 43 months (depending on the experimental technique used to do the study). Seed decline followed an exponential pattern on a yearly basis, with the greatest decline taking place between October and April (57–90% in year 1 and 10–40% in year 2), Between May and September the buried seed populations remained practically constant. Seedbank depletion was primarily due to seedling production (25%) and ‘lethal’ germination (24%). Although the depth of burial had very little effect on seed survival, the mode of seed disappearance was closely related to their depth in the soil. Seed depletion through ‘lethal’ germination increased with increasing depth in the soil, whereas depletion through seedling emergence decreased with increasing depth.     

Contribution of the seed microbiome to weed management

Seed‐attacking microorganisms have an undefined potential for management of the weed seedbank, either directly through inundative inoculation of soils with effective pathogenic strains, or indirectly by managing soils in a manner that promotes native seed‐decaying microorganisms. However, research in this area is still limited and not consistently successful because of technological limitations in identifying the pathogens involved and their efficacy. We suggest that these limitations can now be overcome through application of new molecular techniques to identify the microorganisms interacting with weed seeds and to decipher their functionality. However, an interdisciplinary weed management approach that includes weed scientists, microbiologists, soil ecologists and molecular biologists is required to provide new insights into physical and chemical interactions between different seed species and microorganisms. Such insight is a prerequisite to identify the best candidate organisms to consider for seedbank management and to find ways to increase weed seed suppressive soil communities.     

Spatial stability of Avena sterilis ssp. ludoviciana populations under annual applications of low rates of imazamethabenz

Long‐term experiments were conducted in two winter barley fields in central Spain to determine the spatial stability of Avena sterilis ssp. ludoviciana populations under annual applications of low rates of imazamethabenz herbicide. Weed density was sampled every year (over 5 years in the first field and over 3 years in the second) on the same grid locations prior to herbicide application. Although weed patches were stable in their location, weed density decreased in most of the years. In the first field, the populations decreased exponentially over the 5‐year period. The rates of population decline were dependent on the initial density of the population, being higher for the central core of the patches and lower for the low‐density areas. Under the conditions present in this experiment, it was possible to reduce heavy weed patches (up to 1200 seedlings m^?2) down to relatively safe levels (18 seedlings m^?2) in a period of 3 years using a density‐specific control programme, applying low rates of herbicides when weed densities were below a given level (1000 seedlings m^?2). However, under adverse environmental conditions, half rates of the herbicide failed to control the weed populations adequately. The stability of the location of patches of A. sterilis ssp. ludoviciana suggest that weed seedling distributions mapped in one year are good predictors of future seedling distributions. However, the actual densities established each year will depend on the control level achieved the previous year and the climatic conditions present during the establishment period.     

Potential of weed seedbanks for managing weeds: a review of recent New Zealand research

Weed seedbanks are the primary source of weeds in cultivated soils. Some knowledge of the weed seedbank may therefore be appropriate for integrated weed management programs. It would also be very useful in planning herbicide programs and reducing the total herbicide use. However, a number of problems are inherent in the estimation of the seedbank size for arable weeds that usually have annual life cycles. In a long-term research project we have investigated the dynamics of weed seedbanks in corn fields for the past 8 years. Specific studies have included (i) developing cheap and efficient methods for estimating the weed seedbank; (ii) developing guidelines for efficient soil sampling (including the number and size of samples); (iii) influence of cultivation methods on weed seed distribution; (iv) mapping the spatial variability of the seedbank; (v) estimating the rate of seedbank decline for certain weed species; and (vi) assessing the potential of using the weed seed content in the soil to predict future weed problems. This paper reviews and summarizes the results of our research on the above aspects. The strong correlation between seedlings emerged in the greenhouse and seeds extracted in the laboratory for the most abundant weed species has demonstrated the potential for using the weed seed content of the soil to predict future weed infestations. The next step is to establish correlations with field emergence under commercial conditions using the sampling guidelines developed in our studies. Subsequently, we aim to offer the weed seedbank estimation as a commercial service to farmers for planning the most appropriate weed management options.