Russian-olive is a nitrogen-fixing tree invading riparian corridors in western North America. The premise of revegetation after weed removal is that revegetation is required to return native species to a removal site and that revegetation improves site resistance to invasion or reinvasion via competitive exclusion. Therefore, we expected that revegetation would reduce invasive species cover and increase native species cover compared with non-revegetated controls. Native understory species diversity increased with time since removal. We recorded 18.2 native species in 2012, and 28.2 native species in 2016. Out of 22 planted species, 2 did not establish. Diversity in revegetated plots did not differ from unplanted controls, likely because species spread quickly across plot boundaries. Native perennial grass, seeded species, and annual bromes increased over time, while nonnative forbs and native forbs decreased over time. Only invasive perennial grass cover responded to the revegetation treatment with cover much higher in controls compared with revegetated plots (25.7% vs. 7.7%); this was likely a response to a preplanting herbicide treatment. All categories of species diversity except invasive species diversity increased over time. Only 4% of Russian-olive stumps resprouted in the first year of removal, less than 1% resprouted 2 yr after removal. There was no Russian-olive emergence from seed in the removal year, and seed emergence varied exponentially among following years. Seeded native species did not have trouble establishing once adequate spring moisture occurred in the second growing season after Russian-olive removal, indicating that removal did not present substantial obstacles to successful revegetation. Follow-up control of Russian-olive is critical after initial treatment.
Annual bromes (downy brome and Japanese brome) have been shown to decrease perennial grass forage production and alter ecosystem functions in northern Great Plains rangelands. Large-scale chemical control might be a method for increasing rangeland forage production. Although fall application has been shown to be the most effective and least likely to impact co-occurring native species, spring germination of downy brome may reduce the efficacy of fall-only herbicide application. We assessed the impact of a low glyphosate dose rate (210 g ha−1) applied to rangelands in fall or in fall and spring on nontarget species and on annual brome abundance at two sites in eastern Montana over 2 yr. We tested the following hypotheses: (1) nontarget effects are greater with spring herbicide application, (2) fall and spring herbicide application are necessary for effective downy brome control, and (3) fall herbicide application is sufficient to control Japanese brome. Few nontarget effects occurred; two dicotyledonous species exhibited small increases in response to herbicide. We found that that a single fall application reduced downy brome cover and seed bank density, but after the second fall application in the following year, downy brome did not continue to show a response to herbicide. After 2 yr of fall herbicide application, Japanese brome had denser seed banks in plots where herbicide had been applied. Blanket glyphosate application on rangelands is an unreliable method for controlling annual brome invasions in the northern Great Plains.
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On page 342 under the Experimental Design section in the original publication of this article, the spray concentrations were listed incorrectly. The following sentence has been corrected with the bolded text indicating the proper concentrations: "Resprouts and new Russian-olive seedlings were spot sprayed with a backpack using a mixture consisting of 1.25 g ae L − 1 Element® 4, 0.31 g ae L − 1 Milestone® (aminopyralid,
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