Leafy spurge, a noxious perennial weed, is a major threat to the prairie ecosystem in North America. Strategic planning to control leafy spurge requires monitoring its spatial distribution and spread. The ability to detect flowering leafy spurge at two biological control sites in southern Saskatchewan, Canada, was investigated using an unmanned aerial vehicle (UAV) system. Three flight missions were conducted on June 30, 2016, during the leafy spurge flowering period. Imagery was acquired at four flight heights and one or two acquisition times, depending on the site. The sites were reflown on June 28, 2017, to evaluate the change in flowering leafy spurge over time. Mixture tuned matched filtering (MTMF) and hue, intensity, and saturation (HIS) threshold analyses were used to determine flowering leafy spurge cover. Flight height of 30 m was optimal; the strongest relationships between UAV and ground estimates of leafy spurge cover (r2 = 0.76 to 0.90; normalized root mean square error [NRMSE] = 0.10 to 0.13) and stem density (r2 = 0.72 to 0.75) were observed. Detection was not significantly affected by the image analysis method (P > 0.05). Flowering leafy spurge cover estimates were similar using HIS (1.9% to 14.8%) and MTMF (2.1% to 10.3%) and agreed with the ground estimates (using HIS: r2 = 0.64 to 0.93, NRMSE = 0.08 to 0.25; using MTMF: r2 = 0.64 to 0.90, NRMSE = 0.10 to 0.27). The reduction in flowering leafy spurge cover between 2016 and 2017 detected using UAV images and HIS (8.1% at site 1 and 2.7% at site 2) was consistent with that based on ground digital photographs (10% at site 1 and 1.8% at site 2). UAV imagery is a useful tool for accurately detecting flowering leafy spurge and could be used for routine monitoring purposes in a biological control program.

Aphthona spp. flea beetles were released in two ecological sites of the Little Missouri National Grasslands in southwestern North Dakota in 1999 to control leafy spurge. The change in leafy spurge density and soil seedbank composition was monitored to evaluate the effectiveness of the biological weed control agent and the associated change in plant communities 5, 10, and 15 yr after release in loamy overflow (valleys) and loamy sites (ridges). In 2014, 15 yr after release, leafy spurge stem density had decreased 94% from 110 to 7 stems m−2 in the loamy overflow sites and 88% from 78 to 9 stems m−2 in the loamy sites. Leafy spurge represented only 2% and 6% of the loamy overflow and loamy seedbanks in 2004, respectively, compared with nearly 67% and 70%, respectively, in 1999. There was a slow shift to reintroduction of native species into the seedbank over the last 15 yr. The number of desirable species increased to 21 by 2014 (more than three times the number of species in 1999) in the loamy overflow sites, and doubled to 14 species in the loamy sites, while less desirable forb species doubled in both sites. Desirable grass species doubled in the loamy overflow sites by 2014 but remained unchanged in loamy sites. Aphthona spp. successfully controlled leafy spurge for more than 15 yr without any additional control methods or costs to land managers and resulted in the slow return of a subset of native species.

Levels of inter- and intrapopulation genetic variation were determined in five North American populations of leafy spurge using chloroplast DNA (cpDNA) RFLPs and RAPD markers. Thirteen plastome types were identified among 123 individuals collected from five geographically separated populations. Number of plastomes within a population ranged from one to seven, with four of the populations having a predominate type plus one or more rarer types. Some plastome types were shared by populations, but plastome distribution among populations was nonrandom. RAPD markers indicated greatest relatedness among individuals within a population. Relatedness among populations as established through RAPDs was greater for geographically closer populations; this relationship was not observed for cpDNA markers. Differences in the range of movement for pollen and seed may account for differences between results of the cpDNA and RAPD analyses. The high degree of genetic variability among North American leafy spurge suggests possible multiple introductions or a high degree of variability within leafy spurge populations in its native range.

The productivity and native species diversity of Great Plains grasslands have been substantially reduced by past management that facilitated the establishment of invasive exotic weeds and displacement of native species. Management strategies are needed to rapidly restore the productive capacity and biological diversity of these degraded grasslands. Critically important phases of the grassland restoration process are the reintroduction and establishment of native species. Weed interference is the primary constraint to successful establishment of native plants. The goal of our research is to develop strategies that use multiple technologies, including herbicides, to expedite grassland revegetation with native grasses and forbs. Imidazolinone herbicides (AC 263,333, imazapyr, and imazethapyr) were used successfully to improve establishment of native perennial grasses (big bluestem, switchgrass, little bluestem) and selected forbs (blackeyed-susan, purple prairieclover, Illinois bundleflower, trailing crownvetch, and upright prairie coneflower) on cropland and as components of a strategy to revegetate leafy spurge-infested rangeland with native tallgrasses. Imazethapyr at 70 or 110 g ai/ha applied at planting resulted in stands of big bluestem and little bluestem that were similar or superior to stands established where atrazine was applied. Seedling grasses were susceptible to imazapyr at two of three study sites. Imazapyr at 560 g ai/ha plus sulfometuron at 100 g ai/ha applied in fall was the optimum treatment for suppression of leafy spurge and exotic cool-season grasses and establishment of big bluestem and switchgrass on degraded rangeland sites. Establishment of selected forbs was improved by PRE treatment with AC 263,222 or imazethapyr at 70 g ai/ha. This research provides evidence that the imidazolinone herbicides can be important components of integrated weed management strategies designed to reverse deterioration of grasslands by reestablishing native species, improving grassland productivity, and decreasing the prevalence of exotic weeds.

Euphorbia esula is an exotic perennial weed that is estimated to infest 650,000 ha in North and South Dakota, Montana, and Wyoming. The estimated annual economic effect of E. esula infestations in the four-state area is about $130 million. We present the results of a survey of ranchers, local decision makers, and public land managers of grazing and nongrazing property from a five-county area in North and South Dakota, Montana, and Wyoming. A total of 565 ranchers, local decision makers, and public land managers were surveyed, which resulted in 267 completed questionnaires. The main objective of the survey was to evaluate respondent's perspectives of managerial, institutional, and social factors that may affect the rate and extent of implementation of various E. esula control strategies. The reasons for not using the various E. esula controls generally fell into environmental, financial, and educational categories. In many cases, little can be done to remove environmental constraints; however, financial constraints may be addressed through cost-share programs either offered locally or through state agencies. The other main reason for not using some controls was a lack of knowledge to work with various controls (e.g., grazing and biological controls). These obstacles could be addressed with workshops, demonstrations, or educational bulletins. These educational tools could be provided by universities or governmental agencies, as respondents indicated this was their choice for information dissemination. Disagreements among the survey groups were not substantial, and many share similar concerns in controlling the weed.

Microarray analysis was used to follow changes in gene expression coinciding with seasonal changes in the dormancy status of crown buds of field-grown leafy spurge. Known cold-regulated genes were induced, and numerous gibberellic acid–responsive genes were down-regulated during the transition from paradormancy to endodormancy. Genes involved in photomorphogenesis were induced during endodormancy. Also, ethylene signaling responses were observed during ecodormancy rather than endodormancy. These results provide additional insights into the signals regulating expression of several genes previously associated with transition from paradormancy to growth in root buds.

Real-time polymerase chain reaction (real-time PCR), also known as quantitative PCR, is used to determine relative gene expression or to quantify exact levels of mRNA in cells or tissues. Before the advent of real-time PCR, the major difficulty associated with traditional quantitative or semiquantitative PCR was to ensure that PCR reactions were quantified within the exponential phase of amplification. Real-time PCR alleviates that problem by detecting and quantifying fluorescent signals after each amplification cycle. Additionally, it does not require running gels and thus is able to produce data in 2 to 3 h. Four different types of chemistries, DNA-binding agents (SYBR Green), hydrolysis probes (TaqMan), hairpin probes (molecular beacons, scorpions), and fluorescent-labeled hybridization probes (Light Cycler), have been commonly used for real-time PCR. Among those chemistries, SYBR Green is the most economical choice. We have used real-time PCR and SYBR Green to examine the expression of a number of leafy spurge genes after growth induction and during normal seasonal growth. Because no reliable endogenous reference genes have been identified in leafy spurge, we performed PCR without an endogenous reference gene and analyzed messenger RNA (mRNA) expression based on the threshold cycle (CT) value of amplification. Excluding an endogenous reference gene from that data analysis was rather straightforward and reliable if RNA was properly prepared and quantified. Given that genomic tools, such as expressed sequence tags (ESTs), and their expression profiles are lacking for most weedy species, avoiding the use of endogenous reference genes in real-time PCR simplifies the optimization process and reduces the cost tremendously. However, we found that using a passive reference dye (ROX) to normalize non-PCR–related fluctuations in fluorescent signal is desirable.

We evaluated the efficacy of the biological control agent, red-headed leafy spurge stem borer, against the nonnative invasive plant leafy spurge. Our three treatments were release of the biological control agent into uncaged plots, release of the biological control agent into plots caged to prevent agent escape, and control plots caged to prevent agent entry. These treatments were replicated three times at six sites in the western United States. We measured leafy spurge biomass for 1 or 2 yr following release. We also measured the percentage of leafy spurge stems showing evidence of red-headed leafy spurge stem borer oviposition for either 1 or 2 yr following agent release, depending on the site. Red-headed leafy spurge stem borer did not demonstrably reduce leafy spurge biomass in our study. Moreover, compared to the release year, evidence of red-headed leafy spurge stem borer oviposition declined with time, suggesting the agent population was diminishing. This suggests the agent is incapable of building large populations capable of controlling leafy spurge at the sites we studied. However, after being released, populations of biological control agents sometimes go through long lag phases and then begin rapid population increases, so we cannot completely dismiss the possibility that red-headed leafy spurge stem borer might become effective given more time.

Diversified grasslands that contain native plant species can produce biofuels, support sustainable grazing systems, and produce other ecosystem services. However, ecosystem service production can be disrupted by invasion of exotic perennial plants, and these plants can have soil-microbial “legacies” that may interfere with establishment and maintenance of diversified grasslands even after effective management of the invasive species. The nature of such legacies is not well understood, but may involve suppression of mutualisms between native species and soil microbes. In this study, we tested the hypotheses that legacy effects of invasive species change colonization rates, diversity, and composition of arbuscular-mycorrhizal fungi (AMF) associated with seedlings of co-occurring invasive and native grassland species. In a glasshouse, experimental soils were conditioned by cultivating three invasive grassland perennials, three native grassland perennials, and a native perennial mixture. Each was grown separately through three cycles of growth, after which we used T-RFLP analysis to characterize AMF associations of seedlings of six native perennial and six invasive perennial species grown in these soils. Legacy effects of soil conditioning by invasive species did not affect AMF richness in seedling roots, but did affect AMF colonization rates and the taxonomic composition of mycorrhizal associations in seedling roots. Moreover, native species were more heavily colonized by AMF and roots of native species had greater AMF richness (number of AMF operational taxonomic units per seedling) than did invasive species. The invasive species used to condition soil in this experiment have been shown to have legacy effects on biomass of native seedlings, reducing their growth in this and a previous similar experiment. Therefore, our results suggest that successful plant invaders can have legacies that affect soil-microbial associations of native plants and that these effects can inhibit growth of native plant species in invaded communities.

In this review, we examine current techniques and recent advances directed toward understanding cellular mechanisms involved in controlling dormancy in vegetative propagules. Vegetative propagules (including stems, rhizomes, tubers, bulbs, stolons, creeping roots, etc.) contain axillary and adventitious buds capable of producing new stems/branches under permissive environments. Axillary and adventitious buds are distinct in that axillary buds are formed in the axil of leaves and are responsible for production of lateral shoots (branches). Adventitious buds refer to buds that arise on the plant at places (stems, roots, or leaves) other than leaf axils. Both axillary and adventitious buds generally undergo periods of dormancy. Dormancy has been described as a temporary suspension of visible growth of any plant structure containing a meristem (Lang et al. 1987). Dormancy can be subdivided into three categories: (1) ecodormancy-arrest is under the control of external environmental factors; (2) paradormancy-arrest is under the control of external physiological factors within the plant; and (3) endodormancy-arrest is under the control of internal physiological factors. One common feature in all of these processes is prevention of growth under conditions where growth should otherwise continue. There is growing evidence that lack of growth is due to blockage of cell division resulting from interactions between the signaling pathways controlling dormancy and those controlling the cell cycle.

Genomics programs in the weed science community have not developed as rapidly as that of other crop, horticultural, forestry, and model plant systems. Development of genomic resources for selected model weeds are expected to enhance our understanding of weed biology, just as they have in other plant systems. In this report, we describe the development, characteristics, and information gained from an expressed sequence tag (EST) database for the perennial weed leafy spurge. ESTs were obtained using a normalized cDNA library prepared from a comprehensive collection of tissues. During the EST characterization process, redundancy was minimized by periodic subtractions of the normalized cDNA library. A sequencing success rate of 88% yielded 45,314 ESTs with an average read length of 671 nucleotides. Using bioinformatic analysis, the leafy spurge EST database was assembled into 23,472 unique sequences representing 19,015 unigenes (10,293 clusters and 8,722 singletons). Blast similarity searches to the GenBank nonredundant protein database identified 18,186 total matches, of which 14,205 were nonredundant. These data indicate that 77.4% of the 23,472 unique sequences and 74.7% of the 19,015 unigenes are similar to other known proteins. Further bioinformatics analysis indicated that 2,950, or 15.5%, of the unigenes have previously not been identified suggesting that some may be novel to leafy spurge. Functional classifications assigned to leafy spurge unique sequences using Munich Information Center for Protein or Gene Ontology were proportional to functional classifications for genes of arabidopsis, with the exception of unclassified or unknowns and transposable elements which were significantly reduced in leafy spurge. Although these EST resources have been developed for the purpose of constructing high-density leafy spurge microarrays, they are already providing valuable information related to sugar metabolism, cell cycle regulation, dormancy, terpenoid secondary metabolism, and flowering.