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.

Hairy nightshade is the most widespread nightshade species in North America. Increased knowledge of hairy nightshade germination biology would facilitate development of an optimum control program. Germination of hairy nightshade seeds as affected by environmental and chemical factors was studied under greenhouse and controlled-environment growth chamber conditions. Hairy nightshade seeds were in an innate dormant state when initially separated from the berries. Moist compared with dry storage was more effective for breaking dormancy at 4 C, but dry storage was more effective at 17 C. Hairy nightshade seeds germinated equally well under both a 14-h photoperiod and continuous darkness. These germinated at constant temperatures ranging from 19 to 39 C, with optimum germination attained between 27 and 33 C. Germination markedly declined as osmotic potential of the germination medium decreased. The optimum pH range for germination of hairy nightshade seeds was between 6 and 8, although some seeds germinated at pH 4 and 9. Maximum hairy nightshade emergence occurred with seeding depths of 2 cm or less. No emergence occurred when seeding depth reached 8 cm.

Field trials were conducted from 2006 through 2008 to determine the influence of ethofumesate applied at planting followed by dimethenamid-p or s-metolachlor applied to emerged sugarbeet for late-season weed control in glyphosate-resistant sugarbeet. The entire plot area was kept weed-free until mid-June by applying glyphosate at the four- and eight-true-leaf sugarbeet growth stages. Glyphosate was not applied from mid-June until late-July to allow weed growth as a measure of the residual benefit from ethofumesate, dimethenamid-p, and s-metolachlor applied earlier in the growing season. Dimethenamid-p was not as effective as s-metolachlor in reducing weed density in mid-July. Late-season weed suppression from both s-metolachlor and dimethenamid-p benefitted from ethofumesate applied at planting. Dimethenamid-p applied when sugarbeet reached the six-true-leaf growth stage reduced weed density and sugarbeet injury more than earlier applications. The lowest weed density in mid-July was achieved when s-metolachlor was applied at the six- to eight-true-leaf sugarbeet growth stage compared to earlier growth stages. A planting time application of ethofumesate followed by two glyphosate applications plus s-metolachlor at the eight-true-leaf sugarbeet growth stage provided 89% more weed control in mid-July than glyphosate alone. Suppressing late-season weed development increased sugarbeet root yield 15% compared with areas not receiving ethofumesate and s-metolachlor.

The effects of spring tillage sequence on summer annual weed populations were evaluated over two cycles of a 3-yr crop rotation of snap beans, sweet corn, and winter wheat. Continuous no-till (N) planting of vegetable crops each spring (NNNN) reduced summer annual weed density 63 to 86% compared to that of continuous conventional tillage (CCCC), depending upon site and herbicide level. Hairy nightshade populations were reduced by 88 to 96% when spring tillage was eliminated from the crop rotation. The effects of the NNNN spring tillage sequence on weed density were similar at two sites even though the crop rotations at the two sites began with different crops. The rotational tillage sequence of NCNC at the East site, in a crop rotation that began with corn, reduced summer annual weed density by 46 to 51% compared to that of continuous conventional tillage and planting (CCCC) at low and medium herbicide rates, respectively. In contrast, the tillage sequence of CNCN in the same crop rotation and at the same site increased weed density by 80% compared to that of CCCC at a low herbicide rate. The effects of the NCNC and CNCN rotational tillage sequences on weed density were reversed at the West site, and was probably caused by pairing sweet corn with conventional tillage rather than no tillage. The reduction in summer annual weed density caused by reduced spring tillage frequency did not significantly increase crop yields.

Hairy nightshade is a common weed in potato rotations in the western United States. As a close relative of potato, hairy nightshade can host numerous potato nematodes, diseases, and insect pests. Hairy nightshade hosts three common parasitic nematodes of potato, Columbia and northern root-knot nematodes, and stubby root nematode. Tubers of a potato breeding line with roots that are resistant to Columbia root-knot nematode—race 1, were damaged when grown in the presence of hairy nightshade. The weed provided an alternate host for the nematode, which then allowed the nematode to infect susceptible tubers. Stubby root nematodes transmit tobacco rattle virus (TRV), the causal agent for corky ringspot disease (CRS) of potato. CRS disease was maintained in soil when hairy nightshade was present in rotation crops of alfalfa or Scotch spearmint that otherwise eliminated the disease. Hairy nightshade also is a host of potato leaf roll virus (PLRV), which is transmitted by green peach aphids (GPA). GPA preferentially land and readily reproduce on hairy nightshade. Aphid transmission of PLRV from hairy nightshade to potato was four times greater than the virus transmission rate from potato to potato. Integrated management of these potato nematodes, diseases, and insect pests also should include strategies to control hairy nightshade in potato and rotation crops.

Understanding the factors regulating recruitment in diverse tillage systems will improve the efficacy of weed-management strategies. Experiments measured the effect of hairy nightshade winter seed position (burial depth) on seedling recruitment and seed germination, dormancy, and mortality. Hairy nightshade seeds were placed in soil tubes at 1 cm below the soil line and buried in the fall so that seeds were positioned in the soil at 1, 6, 13, and 25 cm below the soil surface. Tubes with undisturbed soil and seeds were removed from the field in March, April, and May of 2004 and 2005 and placed in wells in a heated, aluminum block with a linear temperature gradient from 22.7 to 36.0 C at 2.7 C intervals, and recruitment was measured. Seeds were also recovered from the soil tubes to determine effects of seed position on germination rate, mortality, and seed dormancy. Hairy nightshade seedling recruitment was greater for seeds positioned at 6, 13, and 25 cm during the winter than at 1 cm. Seed dormancy and mortality were greatest for seeds positioned at 1 cm, but that did not adequately account for the significant decrease in recruitment at 1 cm compared to seeds buried at 6, 13, or 25 cm. Protecting the seeds buried at 1 cm from rainfall during the winter increased seedling recruitment from 0 to 20% of buried seeds but had a negligible effect on seed mortality and dormancy. Soil density was negatively correlated with recruitment.