Poa annua: An annual species?

As the Latin name annua implies, the species Poa annua L. is thought to have an annual life cycle. Yet, there are many reports in literature of P. annua persisting as a perennial. Considering that P. annua senescence patterns do not align with other true annual species, we hypothesized that P. annua is similar to other perennial, C3 turfgrass species that are subject to a confluence of environmental factors that can cause mortality. Four experiments were conducted in Knoxville, TN with the objective of determining environmental factors lethal to P. annua. A field monitoring study assessed 100 P. annua plants across ten grassland micro-environments from May to October 2020. Forty plants survived the summer and confirmed the existence of perennial P. annua ecotypes. Analysis of environmental factors at the time of plant death indicated soil moisture, soil temperature, and pathogenic infection were associated with mortality. A series of glasshouse or field experiments were conducted to investigate the effects of each factor on P. annua mortality. Soil moisture and soil temperature were not lethal to P. annua in the glasshouse, except under extreme conditions not typical in the field. A field study assessed mortality of plants from pathogenic infection and indicated that P. annua plants treated with fungicide throughout the summer survived year-round, whereas plants not receiving fungicide applications senesced. These findings support our hypothesis that P. annua is of a perennial life cycle, which can be influenced by environmental conditions. We suggest that the name P. annua is likely a misnomer based on its modern interpretation.

Modeling seasonal emergence of Poa annua in urban greenspace.

Turfgrasses are perennial components of urban greenspaces found in parks, recreational areas, golf courses, sports fields, and lawns that confer many ecosystem services. A copious seed producer, Poa annua is the most troublesome weed of turfgrass and continually threatens the ecosystem services provided by urban greenspaces. Field research was conducted in Knoxville, TN to better understand environmental conditions triggering P. annua seedling emergence patterns to assist managers with optimally timing interventions-both chemical and non-chemical-for control. Fluctuations in cooling degree day (CDD21C) accumulation accounted for 82% of the variance in yearly cumulative P. annua emergence data collected in a single irrigated sward of hybrid bermudagrass [C. dactylon (L.) Pers. x. C. transvaalensis Burtt-Davy]. However, non-linear models using CDD21C data developed ex post were not able to accurately predict P. annua emergence patterns ex ante. In both years, P. annua emergence changed most rapidly between the 40th and 43rd week of the year when seven-day mean soil temperature and rainfall were 18.9 °C and 12.7 mm, respectively. Future research should explore the efficacy of herbicide mixtures applied when P. annua emergence is most rapidly changing in lieu of developing models to predict when specific emergence thresholds occur.

Screening Tall Fescue for Resistance to Rhizoctonia solani and Rhizoctonia zeae Using Digital Image Analysis.

Brown patch, caused by Rhizoctonia solani, is a destructive disease on tall fescue. Compared with R. solani, Rhizoctonia zeae causes indistinguishable symptoms in the field but varies in geographic distribution. This may contribute to geographic variability observed in the resistance response of improved brown patch-resistant cultivars. This study examined R. solani and R. zeae susceptibility of four cultivars, selected based on brown patch performance in the National Turfgrass Evaluation Program (NTEP), and nine plant introductions (PIs). Twenty genotypes per PI/cultivar were evaluated by using four clonal replicates in a randomized complete block design. Plants were inoculated under controlled conditions with two repetitions per pathogen. Disease severity was assessed digitally in APS Assess, and analysis of variance and correlations were performed in SAS 9.3. Mean disease severity was higher for R. solani (65%) than for R. zeae (49%) (P = 0.0137). Interaction effects with pathogen were not significant for PI (P = 0.0562) but were for genotype (P < 0.001). Moderately to highly resistant NTEP cultivars compared with remaining PIs exhibited lower susceptibility to R. zeae (P < 0.0001) but did not differ in susceptibility to R. solani (P = 0.7458). Correlations between R. solani and R. zeae disease severity were not significant for either PI (R = 0.06, P = 0.8436) or genotype (R = 0.11, P = 0.09). Breeding for resistance to both pathogens could contribute to a more geographically stable resistance response. Genotypes were identified with improved resistance to R. solani (40), R. zeae (122), and both pathogens (26).

Development of SCAR markers and UP-PCR cross-hybridization method for specific detection of four major subgroups of Rhizoctonia from infected turfgrasses.

A rapid identification assay for Waitea circinata (anamorph: Rhizoctonia spp.) varieties zeae and circinata causing patch diseases on turfgrasses was developed based on the universally primed PCR (UP-PCR) products cross-blot hybridization. Tester isolates belonging to the two varieties of W. circinata were amplified with a single UP primer L21, which generated multiple DNA fragments for each variety. Probes were prepared with UP-PCR products of each tester isolate by labeling with digoxigenin. Fieldcollected W. circinata isolates and representative isolates of different R. solani anastomosis groups (AG) and AG subgroups were amplified with L21, immobilized on nylon membrane and cross hybridized with the two probes. Isolates within a W. circinata variety cross-hybridized strongly, while non-homologous isolates did not cross-hybridize or did so weakly. Closely related W. circinata varieties zeae and circinata were clearly distinguished with this assay. Sequence-characterized amplified region (SCAR) markers also were developed from UP-PCR products to identify isolates of Thanatephorus cucumeris (anamorph: R. solani) AG 1-IB and AG 2-2IIIB. These two AGs are commonly isolated from diseased, cool-season turfgrasses. The specific SCAR markers that were developed could differentiate isolates of AG 1-IB or AG 2-2IIIB groups. These SCAR markers did not amplify a product from genomic DNA of nontarget isolates of Rhizoctonia. The specificities and sensitivities of the SCAR primers were tested on total DNA extracted from several field-grown, cool-season turf species having severe brown-patch symptoms. First, the leaf samples from diseased turf species were tested for the anastomosis groups of the causal pathogen, and thereafter the total DNA was amplified with the specific primers. The specific primers were sensitive and unique enough to produce a band from total DNA of diseased turfgrasses infected with either AG 1-IB or AG 2-2IIIB.