Studies were conducted to determine lethal temperatures for Cyperus esculentus and Cyperus rotundus tubers using diurnal oscillations in soil temperature with maxima of 40, 45, 50, and 55 C and a minimum of 26 C. Growth of Cyperus spp. plants was faster at 40 C than at a constant temperature of 26 C. The 45 C treatment delayed Cyperus spp. emergence but was not lethal to tubers. Tuber mortality was 100% for both Cyperus spp. with the 50 and 55 C temperature regimes. Soil solarization with thermal-infrared-retentive (TIR) films resulted in higher soil temperatures than with a 30-μm low-density polyethylene (LDPE) clear film. With TIR films, greater proportions of emerged C. rotundus plants were killed by foliar scorching, and 6 wk of soil solarization was more effective at reducing C. rotundus density than with the LDPE film. Four weeks after film removal, the lowest level of control was obtained with the LDPE film. For C. rotundus tubers planted 5 and 10 cm deep, 62% control was obtained with the LDPE film, and it decreased to 32% with a 15-cm planting depth. The best residual control was 95 and 92% with the 75-and 100-μm TIR films, respectively. With the TIR films, there was no significant change in C. rotundus control with planting depth.

Greenhouse experiments were conducted to evaluate the effect of the fungus Dactylaria higginsii on the interference of Cyperus rotundus (purple nutsedge) with Lycopersicon esculentum (tomato ‘Agroset'). Cyperus rotundus plants established from tubers were planted at initial densities equivalent to 40, 80, 160, and 320 tubers m−2 with L. esculentum in 35-cm-diam pots. Cyperus rotundus plants were inoculated by spraying with a spore suspension of D. higginsii containing 0.5% Metamucil as a carrier. The treatments were Metamucil only, 104 conidia ml−1 + Metamucil, or 106 conidia ml−1 + Metamucil. In the absence of D. higginsii, C. rotundus at densities of 80, 160, and 320 tubers m−2 reduced L. esculentum yield by 14, 68, and 70%, respectively. In contrast, yield of L. esculentum treated with D. higginsii at 106 conidia ml−1 was equal to that in the weed-free control. The rate of disease increase (r G) was higher in treatments with 106 conidia ml−1 (r G = 0.126 to 0.136) compared to 104 conidia ml−1 (r G = 0.046 to 0.050). At 106 conidia ml−1D. higginsii reduced the interference from C. rotundus, controlled C. rotundus better, and increased L. esculentum yield compared to the weedy checks.

The objective of this study was to identify some epidemiological conditions that affect the pathogenicity and weed control efficacy of the fungal pathogen Dactylaria higginsii on Cyperus rotundus. In controlled environments, the fungus required a minimum dew period of 12 h and a temperature of 25 C during the dew period to produce severe disease on four- and six-leaf-stage plants inoculated with 106 conidia ml−1. Under these conditions, 75% disease (percent leaf area damaged) and excellent weed control (nearly 100% plant mortality) were achieved. In experiments to test the interaction among dew period temperature, dew period duration, and plant growth stages, younger plants (four- to six-leaf) were more susceptible to D. higginsii than older (eight-leaf-stage) plants. At the dew period duration of 24 h and dew period temperature of 30 C, the number of days to obtain 50% disease severity on four- to six-leaf-stage plants was significantly less (10 d) compared with older plants (16 d). To achieve effective control, D. higginsii should be applied early in the growing season when C. rotundus plants are young and the temperature and dew period requirements are not limiting. The need for a long dew period (>12 h) for infection and disease development may be a limiting factor in this pathosystem. This limitation may be overcome by using inoculum amended with moisture-retaining gels.

Field studies were conducted in 1996 and 1997 to determine the response of Cyperus rotundus and Cyperus esculentus, Kyllinga brevifolia, and Kyllinga gracillima to mowing regimens common to recreational turfgrass. Treatments were selected to simulate Cynodon dactylon golf course management and included mowing at 1.3 and 3.8 cm with mowing frequencies of three times per week and once a week, respectively. A nonmowed check was included for comparison. Reductions in C. rotundus shoot number were observed beginning 6 wk after initial treatment (WAIT) in 1996 and 9 WAIT in 1997 for the 1.3-cm mowing regime. The 3.8-cm mowing regime did not reduce C. rotundus shoot number until the final evaluation of each year. Reductions in C. rotundus rhizome length, tuber number, and tuber size were observed for both mowing regimes in both years. Cyperus esculentus shoot number was reduced by the 1.3-cm treatment at each evaluation date in 1996 and 1997. Cyperus esculentus shoot number reductions in the 3.8-cm regime were first observed 4 and 6 WAIT in the 2 yr and continued until termination. The 1.3-cm regime reduced C. esculentus spread beginning 6 WAIT in 1996 and 3 WAIT in 1997. Cyperus esculentus spread was also reduced by the 3.8-cm treatment, but reduction began at later evaluations (8 and 9 WAIT). Tuber production by C. esculentus was completely inhibited by the two mowing regimes in both years. The only treatment effect observed in K. brevifolia and K. gracillima in 1996 was a reduction in internode length of K. gracillima by the 1.3-cm mowing regime. In 1997, the 1.3-cm regime reduced K. brevifolia shoot number at 15 and 18 WAIT and plant spread beginning 6 WAIT and continuing until termination. The 3.8-cm treatment did not affect K. brevifolia shoot number and reductions in spread were only observed at the final evaluation. Kyllinga gracillima shoot number and plant spread were reduced by the 1.3-cm mowing regime at each 1997 evaluation. Reductions in K. gracillima shoot number occurred at the final evaluation, and reductions in spread began 12 WAIT when subjected to the 3.8-cm treatment. Both mowing regimes reduced K. brevifolia and K. gracillima internode length. Kyllinga brevifolia total rhizome length and total node number were reduced by the 1.3-cm regime only. Kyllinga gracillima rhizome length, internode length, and node number were reduced by both regimes in 1997.