Greenhouse cage studies were conducted to determine the influence of shoot morphology and genetic variation on establishment of Spurgia esulae gall midge on seven leafy spurge genotypes. The genotypes were collected from South Dakota, North Dakota, Nebraska, Montana, Wyoming, Manitoba, and Austria. Genotypes from South Dakota and Nebraska were most susceptible to gall formation and had the highest larvae survival, while the genotypes from Montana and Manitoba were most resistant. Morphological characteristics of the leafy spurge stem tips, such as stem diameter, leaf length, width, and area did not correlate with gall formation or larvae survival. Chloroplast DNA restriction fragment length polymorphism analysis of the genotypes identified six chloroplast types among the seven leafy spurge genotypes. The two genotypes most resistant to galling by S. esulae, Manitoba and Montana, had the same chloroplast genotype, but also were closely related to the two most susceptible genotypes. Because eggs were laid on all genotypes, it appears that adult females were not preferentially selecting appropriate host genotypes, but that egg and larvae survival was strongly influenced by genotype.

Laboratory experiments were conducted to identify adjuvants that improve absorption of imazethapyr, 2,4-D amine, and picloram by leafy spurge. Adjuvants (0.25% v/v) included crop oil concentrate (COC), methylated seed oil (MSO), nonionic surfactant (NIS), organosilicones (Silwet L-77®, Sylgard® 309, Silwet® 408), 3:1 mixtures of acetylinic diol ethoxylates (ADE40, ADE65, ADE85) with Silwet L-77, ammonium sulfate (2.5 kg ha−1), and 28% urea ammonium nitrate (UAN, 2.5% v/v). Adjuvants were combined with 14C-herbicide and commercially formulated herbicide product. Leaves were harvested 2 DAT, rinsed with 10% aqueous methanol to remove surface deposits of herbicide, and dipped in 9:1 hexane:acetone to solubilize cuticular waxes. Imazethapyr absorption increased by 38 to 68% when UAN was combined with COC, NIS, or MSO. Total absorption of imazethapyr plus COC, MSO, or NIS exceeded 86% 2 DAT when UAN was added. Urea ammonium nitrate reduced the amount of imazethapyr associated with the cuticular wax by 2.0%. Imazethapyr absorption was similar on both the abaxial and adaxial leaf surface when UAN was not added; however, 12% more imazethapyr was absorbed from the abaxial leaf surface than from the adaxial leaf surface when UAN was combined with Sylgard 309. Uptake of 2,4-D ranged from 54 to 78% and was greatest with Silwet 408 and 3:1 mixture of ADE40: Silwet L-77. Picloram absorption ranged from 3 to 19%. Buffering picloram treatment solutions to pH 7 and including 2.5 kg ha-1 ammonium sulfate increased picloram absorption to 37%.

The effect of glyphosate applied alone and with 2,4-D as a commercial mixture on 30 native or introduced grass species was evaluated. Grass yield averaged 98 and 87% of the untreated controls when glyphosate was applied in the fall at 0.2 or 0.4 kg ae ha-1, respectively, alone or with 2,4-D at 0.35 or 0.7 kg ae ha-1. Western wheatgrass production decreased more than any other species present in a native rangeland site following either a spring or fall glyphosate application. In seeded plots, intermediate wheatgrass was the most and ‘Fairway’ crested wheatgrass the least susceptible to glyphosate plus 2,4-D with average yields of 57 and 97% compared with untreated controls of each species, respectively. Glyphosate reduced the yield of ‘Nordan’ standard crested wheatgrass more than that of Fairway crested wheatgrass or other diploid cultivars. The greater the spring precipitation following a fall application of glyphosate, the less effect of glyphosate on forage yield. Glyphosate plus 2,4-D can be used for weed control in pasture and rangeland provided some yield reduction is acceptable.

Rhizobacteria have been shown to be phytotoxic to leafy spurge in laboratory assays. This field study investigated the influence of two strains of Pseudomonas fluorescens [Trevisan, (Migula)], deleterious rhizobacteria (DRB), on root weight, root bud number, and root carbohydrate content of leafy spurge at three sites located in northeast and north-central South Dakota. Soils were inoculated with 2 g of starch-based granules containing no bacteria or starch granules containing 108colony-forming units (cfu)/g of either bacterial strain LS102 (Montana origin) or LS174 (South Dakota origin). Bacterial strains were detected on root samples from treated areas. Root weight and root carbohydrate content were reduced about 20% compared to roots from control plots.

Germinability and viability of leafy spurge seeds following ingestion by sheep and goats were evaluated. Four sheep and four goats were separated into eight pens and fed individually a known number of leafy spurge seeds. Following ingestion, goats and sheep passed leafy spurge seeds for 4 and 9 d, respectively. Eighteen percent of the seeds fed were recovered in the fecal material of both species of livestock. Number of seeds recovered, expressed as percent of total seeds fed, decreased with time (P < 0.01). Germinability and viability of the recovered seeds were less than the control (P < 0.01). Sheep were more effective than goats in reducing germinability and viability of leafy spurge seeds (P < 0.01). Results indicate that sheep and goats are effective biological tools for reducing spread of leafy spurge seeds. However, animals grazing mature leafy spurge should be confined for 5 d, until all viable seeds have passed through the digestive system, before they are rotated onto pastures that are devoid of leafy spurge.