A screening method was used to characterize seed thermal responses of prostrate knotweed and common purslane, two important weeds invading wheat in the humid Pampa. Through this method, it was possible to detect thermal conditions that induce or break dormancy in both species. In addition, we were able to quantify changes in dormancy level in seed populations as a function of time of burial after dispersal, through changes in width of the thermal range within which germination can occur. Plotting the overlap of this thermal range and observed soil temperature throughout the year allowed the prediction of the seedling emergence period. This prediction was in agreement with observed seedling emergence in the field for both species, during 2 consecutive yr. From the analysis carried out under laboratory conditions, it was also possible to estimate required thermal time for germination of the nondormant fraction of the population and the base temperature above which thermal time is accumulated. The results obtained from this study are the basis for the formulation of seed germination models that predict not only the occurrence of seedling emergence in the field, but also the dynamics of germination within those periods.

In a semiarid Mediterranean site in central Spain, field experiments were conducted on a Calcic Haploxeralf (noncalcic brown soil), which had been managed with three crop rotations and two tillage systems (no-tillage and conventional tillage) since 1987. The crop rotations consisted of barley→vetch, barley→sunflower, and a barley monoculture. The study took place in two growing seasons (1992–1994) to assess the effects of management practices on the weed seedbank. During this period, spring weed control was not carried out in winter crops. In the no-tillage system, there was a significant increase in the number of seeds of different weed species: anacyclus, common purslane, corn poppy, knotted hedge-parsley, mouse-ear cress, spring whitlowgrass, tumble pigweed, venus-comb, and Veronica triphyllos. Conversely, the presence of prostrate knotweed and wild radish was highest in plots under conventional tillage. These results suggest large differences in the weed seedbank as a consequence of different soil conditions among tillage systems, but also the necessity of spring weed control when a no-tillage system is used. With regard to crop rotations, the number of seeds of knotted hedge-parsley, mouse-ear cress, and spring whitlowgrass was greater in the plots under the barley→vetch rotation. Common lambsquarters dominated in the plots under the barley→sunflower rotation, whereas venus-comb was the most frequent weed in the barley monoculture. Larger and more diverse weed populations developed in the barley→vetch rotation rather than in the barley→sunflower rotation or the barley monoculture.

Field experiments, conducted from 1991 to 1994, generated information on weed seedbank emergence for 22 site-years from Ohio to Colorado and Minnesota to Missouri. Early spring seedbank densities were estimated through direct extraction of viable seeds from soil cores. Emerged seedlings were recorded periodically, as were daily values for air and soil temperature, and precipitation. Percentages of weed seedbanks that emerged as seedlings were calculated from seedbank and seedling data for each species, and relationships between seedbank emergence and microclimatic variables were sought. Fifteen species were found in 3 or more site-years. Average emergence percentages (and coefficients of variation) of these species were as follows: giant foxtail, 31.2 (84%); velvetleaf, 28.2 (66); kochia, 25.7 (79); Pennsylvania smartweed, 25.1 (65); common purslane, 15.4 (135); common ragweed, 15.0 (110); green foxtail, 8.5 (72); wild proso millet, 6.6 (104); hairy nightshade, 5.2 (62); common sunflower, 5.0 (26); yellow foxtail, 3.4 (67); pigweed species, 3.3 (103); common lambsquarters, 2.7 (111); wild buckwheat, 2.5 (63), and prostrate knotweed, 0.6 (79). Variation among site-years, for some species, could be attributed to microclimate variables thought to induce secondary dormancy in spring. For example, total seasonal emergence percentage of giant foxtail was related positively to the 1st date at which average daily soil temperature at 5 to 10 cm soil depth reached 16 C. Thus, if soil warmed before mid April, secondary dormancy was induced and few seedlings emerged, whereas many seedlings emerged if soil remained cool until June.

Yield loss was related to weed species composition and density in permanent plots, recorded several weeks after sowing of spring cereals in southern Sweden. A range of agronomic situations was included by experimentally varying fertilizer application and sowing density in 33 field trials in different locations during 3 yr. Direct gradient analysis, using yield loss as the sole predictor, arranged weed community composition in the spring along a gradient of small to large yield losses. Yield loss could be explained, to some extent, by the species composition in the spring. Species associated with situations with large losses were hempnettle and wild radish, whereas several benign species were identified based on their association with lack of yield loss. The results suggest that possible predictive tools using spring species composition would be improved if they also considered soil type and seed rate. Some agronomically important weed species were not identified as associated with yield loss when assessed in terms of their abundance in the spring, which may limit the possibilities of basing management decisions on weed plant density in the spring.

Intercropping is an eco-friendly approach for reducing weed problems through nonchemical methods. Intercrop effects on weed community structure have rarely been studied. A 6-yr study was initiated in 1999 and the response of aboveground weed flora (1999–2002 and 2005) and seed bank (2005) to the intercropping of saffron and black zira, two perennial crops was investigated. Mixtures consisted of 0/100, 25/75, 50/50, 75/25, and 100/0 saffron/black zira ratios, each planted at three densities: 30, 50, and 70 plant m−2. The effect of planting density on weed populations was variable and in most cases not significant. However, mixture ratios caused drastic species compositional changes in the weed community for which univariate and multivariate analyses explored four major associations: (1) weeds that favored a higher ratio of saffron in mixtures (e.g., grasses, field bindweed, pigweeds), (2) weeds that preferred a higher ratio of black zira in mixtures (e.g., Persian speedwell, Brassicaceae complex, Polygoaceae complex, and earthsmoke), (3) weeds that were more abundant in 50/50 mixtures (e.g., Caryophyllaceae complex), and (4) weeds that showed no specific pattern (e.g., common lambsquarterss). Pigweeds, prostrate knotweed, and common lambsquarters dominated the viable seed bank with relative densities of 48, 28, and 8%, respectively. The seed bank of most weed species responded to mixture ratios in a similar manner to those of their corresponding aboveground flora. Seed density decreased as soil depth increased, leading to the accumulation of 66, 22, and 12% of viable seeds in soil layers of 0–5, 5–15 and 15–25 cm, respectively. Greater weed and seed densities were found in more pure stands of black zira. These findings contribute to improving current understanding of crop–weed community structures and may help in developing weed management practices.

A study at Fairbanks, AK, was started in 1984 to determine soil seed longevity of 17 weed species. Seeds were buried in mesh bags 2 and 15 cm deep and were recovered 0.7, 1.7, 2.7, 3.7, 4.7, 6.7, 9.7, and 19.7 yr later. Viability was determined by germination and tetrazolium tests. Seed viability data were fit to an exponential model, separately for each depth, and the likelihood-ratio test was used to determine whether seed-viability decline was affected by burial depth. Depth of burial had a significant effect on viability decline of prostrate knotweed, marsh yellowcress, bluejoint reedgrass, and wild oat. By 19.7 years after burial (YAB), all seeds of common hempnettle, quackgrass, wild oat, foxtail barley, and bluejoint reedgrass were dead. Seeds of 12 other species were still viable: corn spurry (0.1%), prostrate knotweed (0.3% at 2 cm, 0.8% at 15 cm), flixweed (0.5%), pineapple-weed (0.6%), shepherd's-purse (1.3%), wild buckwheat (1.5%), common chickweed (1.6%), rough cinquefoil (1.8%), common lambsquarters (3.0%), Pennsylvania smartweed (3.3%), marsh yellowcress (8.5% at 2 cm, 0.3% at 15 cm), and American dragonhead (62.2%). Seed dormancy at 19.7 YAB was very low for all species (< 4%) except for American dragonhead, common lambsquarters, Pennsylvania smartweed, and shepherd's-purse, which had seed dormancies of 100, 27, 25, and 38%, respectively. Seed longevity was not increased by cold, subarctic temperatures.

A 50-yr study at Fairbanks, AK, was started in 1984 to determine soil seed longevity of 17 weed species. Seeds were buried in mesh bags 2- and 15-cm deep and were recovered 0.7, 1.7, 2.7, 3.7, 4.7, 6.7, 9.7, 19.7, and 24.7 yr later. Viability was determined using germination and tetrazolium tests. By 24.7 yr after burial (YAB), no viable seeds were found for common hempnettle, flixweed, foxtail barley, quackgrass, and wild oat. Bluejoint reedgrass, which had no live seed 19.7 YAB, again had viability (1% at 15 cm) 24.7 YAB. Seeds of 11 other species were still viable: American dragonhead (52%), marsh yellowcress (11 and 3.0% at 2 and 15 cm respectively), common lambsquarters (2.8%), prostrate knotweed (2.8% at 15 cm), shepherd's-purse (2.8%), pineapple-weed (2.6%), rough cinquefoil (2.3%), Pennsylvania smartweed (1.1%), common chickweed (0.4%), wild buckwheat (0.3%), and corn spurry (0.1%). Seed dormancy 24.7 YAB was very low (< 10%) for all species except American dragonhead (99%), shepherd's-purse (40%), marsh yellowcress (23% at 2 cm), Pennsylvania smartweed (18%), and rough cinquefoil (14%). At the beginning of the study, declines in seed longevity were uniform between replicates, but variability between replicates increased over time for all species except American dragonhead, suggesting that some soil microsites are more favorable for seed survival and may be seedbank “safe sites.” Results of this study demonstrate that nonrandom seed mortality contributes to the spatial heterogeneity of seed populations in the soil seedbank.

The utility of solaria (1 by 1-m plastic sheets) to predict densities of a few weed species in summer crops has been demonstrated previously, but needed further research to be adopted by farmers and advisors. We tested the method to detect important weeds in Argentina and Minnesota, and determined the minimum number of solaria required to predict the presence of emerged weed seedlings in the forthcoming growing season. Three experiments were performed in Buenos Aires Province, Argentina, and one in Minnesota. Solaria were placed in fields with different previous crops and soil management: no tillage (two fields) and conventional tillage (two fields). Preceding crops were corn (one field), wheat (one field), and double-cropped wheat/soybean (two fields). After weeds were enumerated, solaria were removed, sunflower (one field) and soybean (three fields) were planted, and weeds later assessed in each crop. Results indicate that one solarium per 1.9 ha can detect common lambsquarters with 95% confidence within the next summer crop. For other species, one solarium per 4.2, 1.2, 1.0, and 1.8 to 2.7 ha (depending upon field site) for large crabgrass, prostrate knotweed, wild buckwheat, and green foxtail, respectively, was required. The low cost and simplicity of assessment make this technique more suitable than that of soil seed-bank samples to predict weed emergence. The number of solaria required to forecast weed infestation levels confidently is sufficiently low that their use may be justified, especially in small fields of high-value crops.

Progress in bioherbicide development has been hindered by the strict moisture and temperature requirements of the living active ingredient. Application of a jute fabric to areas treated with a Sclerotinia minor granular bioherbicide improved broadleaf weed control and broadened the effective application period to include the warm summer season. When turfgrass plots treated with the bioherbicide were covered with burlap fabric for 3 d, broadleaf weed (dandelion, white clover, broadleaf plantain, buckhorn plantain, ground ivy, and prostrate knotweed) control was greatly enhanced. The cover was made of natural jute fibers that retained water but had sufficient transparency to allow 33% light penetration for continued growth of the grass. Virulence of the bioherbicide was maintained under elevated temperatures that would otherwise reduce efficacy. The bioherbicide was ineffective in the summer unless covered, but dandelion density, broadleaf weed ground cover, and dandelion survival were all reduced by the bioherbicide when plots were covered, even if applications were made in July. The efficacy of the bioherbicide was also enhanced under favorable conditions, and covering permitted reduced application rates without loss of efficacy. When applied at a rate of 20 g/m2 and covered, S. minor granules exerted significantly greater biocontrol of dandelion than 40 g/m2 without covering. Covering for up to 5 d did not cause any adverse effects on the turfgrass. This approach may overcome one obstacle to the commercialization of the Sclerotinia minor bioherbicide, permitting its deployment under challenging environmental conditions.