Interest in cover crops is increasing but information is limited on integrating them into crop rotations especially in the relatively short growing season on the northern Great Plains. A 3-yr research project, initiated in 2009 near Mandan, North Dakota, USA, evaluated (1) what impact cover crops may have on subsequent cash crops yields and (2) whether cover crop mixtures are more productive and provide additional benefits compared to cover crop monocultures. The study evaluated 18 different cover crop monocultures and mixtures that were seeded in August following dry pea (Pisum sativum L.). The following year, spring wheat (Triticum aestivum L.), corn (Zea mays L.), soybean (Glycine max L.) and field pea were seeded into the different cover crop treatments and a non-treated control. A lack of timely precipitation in 2009 resulted in a low cover crop yield of 17 g m2 compared to 100 and 77 g m2 in 2008 and 2010, respectively. Subsequent cash crop yield was not affected by late-seeded cover crops. Cool-season cover crop monocultures were more productive than warm-season monocultures and some mixtures in 2008 and 2010. Relative yield total did not differ from one in any cover crop mixture suggesting that overyielding did not occur. Species selection rather than species diversity was the most important contributor to cover crop yield. Cover crops can be grown following short-season cash crops in the northern Great Plains, but precipitation timing and species selection are critical.

Avena fatua seeds remaining on the plant at harvest and taken into the combine harvester may be dispersed over large areas. The objective of this study was to characterize the development of A. fatua in comparison to spring Triticum aestivum. As part of this objective, the rate of seed shed in A. fatua relative to development of T. aestivum was determined. Avena fatua and T. aestivum had similar phyllochron intervals within locations but differed between locations. Plant development as measured by the Zadoks plant development scale was consistent within plant species between locations. Seed shed in A. fatua was also consistent between locations. Most of the seed shed occurred within 2 wk, and the cumulative seed shed followed a sigmoidal pattern. The seed shed occurred as T. aestivum was ripening, and the percentage of seed shed appears to be related to the water content of the T. aestivum spike. Because of this relationship, the proportion of seed remaining on A. fatua at harvest could be managed by changing the timing of crop harvest.

The dynamics of the host–parasite relationship between tomato cv. Brigade and Egyptian broomrape is temperature-related. This relationship was utilized for the development of an equation on the basis of thermal time (as measured by growing degree days, GDD, C) to predict the parasitism dynamics of Egyptian broomrape in tomato. To obtain a reliable prediction from thermal time values, studies based on a wide range of temperatures are essential. Four temperature-regime treatments and five levels of infestation with Egyptian broomrape seeds were tested in a multiclimate greenhouse (phytotron) and a temperature-controlled greenhouse, respectively. The day/night temperature regimes were 20/12 C, 23/15 C, 26/18 C, and 29/21 C and the infestation levels were 0 (noninfested control), 1, 5, 10, and 25 mg of Egyptian broomrape seeds per liter of soil. As expected, increasing temperature or infestation levels resulted in faster appearance and higher rate of attachments, respectively. The relation between development of attachments and GDD was described as a three-parameter logistic curve. In both temperature-regime and infestation-level experiments, the development of attachments began 200 GDD after planting and the maximal number of attachments was recorded 800 GDD after planting. A significant reduction in the aboveground biomass of the tomato plants due to increased Egyptian broomrape biomass was recorded only for the 26/18 C and 29/21 C day/night treatments and the three highest infestation levels (5, 10, and 25 mg L−1 soil). The ability to predict the start of parasitism can be used to develop a climate-based system for Egyptian broomrape control with herbicides.