scholarly journals Take-all Patch Suppression in Creeping Bentgrass with Manganese and Copper

HortScience ◽  
1999 ◽  
Vol 34 (5) ◽  
pp. 891-892 ◽  
Author(s):  
W.J. Hill ◽  
J.R. Heckman ◽  
B.B. Clarke ◽  
J.A. Murphy

Take-all patch, caused by Gaeumannomyces graminis (Sacc.) Arx. & D. Olivier var. avenae (E.M. Turner) Dennis (Gga), is a disease of creeping bentgrass (Agrostis stolonifera Huds.), which most often is associated with golf courses. Synthesis of ligneous and phenolic compounds by plants requires adequate Mn+2 and Cu+2 nutrition and may be a factor in disease resistance. An experiment was conducted on a creeping bentgrass fairway naturally infested with Gga to determine if foliar applications of Mn+2 (1.02 and 2.04 kg·ha–1 per application) and Cu+2 (0.68 kg·ha–1 per application) would reduce take-all severity. Prior to initiating treatments, soil pH was 6.4 and Mehlich-3 extractable Mn+2 and Cu+2 were 5 mg·kg–1 and 1.7 mg·kg–1, respectively. Manganese and copper sulfate treatments were initiated in July 1995 and foliarly applied every 4 weeks through 1997 with the exception of December, January, and February. Disease incidence was decreased from 20% on untreated turf to 5% with the high rate of MnSO4. For both years, turf treated with the high rate of Mn+2 had less disease than turf receiving the low rate of Mn+2. The application of CuSO4, however, did not influence disease development.

Plant Disease ◽  
2006 ◽  
Vol 90 (1) ◽  
pp. 33-38 ◽  
Author(s):  
S. L. Thomas ◽  
P. Bonello ◽  
P. E. Lipps ◽  
M. J. Boehm

Avenacinase activity has been shown to be a key factor determining the host range of Gaeumannomyces graminis on oats (Avena sativa). G. graminis var. avenae produces avenacinase, which detoxifies the oat root saponin avenacin, enabling it to infect oats. G. graminis var. tritici does not produce avenacinase and is unable to infect oats. G. graminis var. avenae is also reported to incite take-all patch on creeping bentgrass (Agrostis stolonifera). It is unknown whether creeping bentgrass produces avenacin and if the avenacin-avenacinase interaction influences G. graminis pathogenicity on creeping bentgrass. The root extracts of six creeping bentgrass cultivars were analyzed by fluorimetry, thin-layer chromatography, and high performance liquid chromatography for avenacin content. Avenacin was not detected in any creeping bentgrass cultivars, and pathogenicity assays confirmed that both G. graminis var. avenae and G. graminis var. tritici can infect creeping bentgrass and wheat (Triticum aestivum), but only G. graminis var. avenae incited disease on oats. These results are consistent with the root analyses and confirm that avenacinase activity is not required for creeping bentgrass infection by G. graminis.


2008 ◽  
Vol 22 (3) ◽  
pp. 481-485 ◽  
Author(s):  
Patrick E. McCullough ◽  
Stephen E. Hart

Sulfosulfuron was recently registered for grassy weed control in creeping bentgrass, but turf sensitivity is a concern for intensively managed golf courses. Field and growth chamber experiments in New Jersey investigated creeping bentgrass growth responses and tolerance to sulfosulfuron. Creeping bentgrass chlorosis increased with sulfosulfuron rate but turf had less chlorosis from sequential sulfosulfuron applications compared to bispyribac–sodium. Herbicide-treated turf had similar root weight compared to untreated turf on six sampling dates. In growth-chamber experiments, creeping bentgrass treated with sulfosulfuron had chlorosis and clipping weight reductions exacerbated by reductions in temperature from 25 to 15 C. Overall, creeping bentgrass appears to tolerate sequential sulfosulfuron applications better than or comparable to bispyribac-sodium in early summer, whereas creeping bentgrass sensitivity to sulfosulfuron increases at cooler temperatures.


1999 ◽  
Vol 13 (2) ◽  
pp. 216-220 ◽  
Author(s):  
Darin S. Bevard ◽  
Thomas L. Watschke

Dithiopyr was applied to ‘Penneagle’ creeping bentgrass seedlings 2, 4, and 8 wk after emergence (WAE) in separate studies in the summers of 1992 and 1993 to determine seedling tolerance. Dithiopyr emulsifiable concentrate (IEC) was applied at 0.14, 0.28, 0.42, and 0.56 kg ai/ha, and granular (G) dithiopyr (0.1G) was applied at 0.14, 0.21, 0.28, and 0.42 kg/ha. Dithiopyr applied 2 WAE caused unacceptable injury regardless of rate or formulation. Injury was characterized by stunting of plants, leaf tip die-back, yellowing of older leaves, and a visible decline in quality. Injury increased with increasing rate. In 1992, the EC and G formulation of dithiopyr caused similar responses, whereas in the summer of 1993, the EC caused greater turf injury. Dithiopyr applied 4 WAE caused less injury than when applied 2 WAE, and injury was acceptable. Dithiopyr applied 8 WAE only slightly injured creeping bentgrass at the high rate for both formulations in both years.


1989 ◽  
Vol 29 (1) ◽  
pp. 85 ◽  
Author(s):  
DR Coventry ◽  
HD Brooke ◽  
JF Kollmorgen ◽  
DJ Ballinger

The severity of take-all, caused by Gaeumannomyces graminis var. tritici, was measured with lime, rotation and flutriafol treatments in a long-term field experiment. The incidence of eyespot lesions caused by Pseudocercosporella herpotrichoides was also measured. Flutriafol reduced the number of plants with deadheads or no heads and resulted in 12-60% more grain yield. However flutriafol had no effect on the number of plants with eyespot lesions. The number of plants with deadheads or no heads was highest (50-53%) on the wheat which was a third consecutive crop and on soil which had been amended with 2.5 and 5.0 t/ha lime. Sowing wheat after a subterranean clover based pasture considerably reduced the number of deadheads. Control of annual grasses in the pasture by spray-topping further reduced deadheads and with this treatment and at nil and low lime there were 2-7% deadheads. The percentage of plants with eyespot lesions was higher with the continuous cropped wheat. Lime increased grain yield only where the disease incidence was low but had no effect on the percentage of eyespot lesions. This work demonstrates the importance of crop rotation for disease control, particularly where soils are limed to amend severe soil acidity; the value of controlling annual grasses in pasture in the year preceding wheat cropping; and the potential of fungicide treatment as a practical means for controlling take-all in field grown wheat.


1973 ◽  
Vol 26 (6) ◽  
pp. 1277 ◽  
Author(s):  
GC Mac Nish

A bioassay was employed to compare the effect of various treatments on the level of G. graminis var. tritici inoculum in soil cores taken from a take-all patch. In a comparison of undisturbed soil and mixed soil, mixing caused a small reduction in incidence, possibly due to a dilution of the inoculum in the surface soil. Graded degrees of sieving from 5 to O� 5 mm mesh size caused a significant reduction in inoculum levels, with the latter reducing incidence to 3 % in seedlings at 4 weeks. However, it was also shown that increasingly finer sieving caused an increase in disease incidence if the seedlings were allowed to grow to maturity. It was not established whether the sieving affected the soil in such a way as to favour the pathogen, lower the resistance of the plant, or both.


1973 ◽  
Vol 26 (6) ◽  
pp. 1319 ◽  
Author(s):  
GC Mac Nish

A bioassay was used to study the effect of various storage treatments on the survival of G. graminis var. tritici in soil cores removed from a take-all patch. There was no significant change in the incidence of the fungus when the soil was maintained either dry (-250 to -980 bars) and cool (15�C), or moist (-4'0 to -7,0 bars) and cool (15�C). When maintained very dry (-980 bars or less) and hot (35�C) or wet (-0'1 to -0,2 bar) and cool (15�C) there was a significant reduction in disease incidence, but considerable levels of viable fungus were still present after 45 weeks storage. Only in wet hot soil (-0'1 to -0,2 bar and 35�C) was the fungus eliminated rapidly.


1998 ◽  
Vol 49 (8) ◽  
pp. 1225 ◽  
Author(s):  
P. A. Gardner ◽  
J. F. Angus ◽  
P. T. W. Wong ◽  
G. D. Pitson

Take-all is a root disease of wheat caused by the fungus Gaeumannomyces graminis var. tritici (Ggt). The most common method of control, growing wheat after a break crop, is not always feasible. This study compared the use of a break crop with 5 alternative control methods in a series of field experiments in south-eastern Australia. The methods of control tested were: (1) fungicide added to fertiliser; (2) soil fumigation with methyl bromide; (3) applied chloride; (4) seed treatment with microbial antagonists; (5) a prior brassica break crop; and (6) a 12-month-long fallow. Eight experiments were conducted over 2 years but not all treatments were included in each experiment. The most successful control methods were growing wheat after a brassica break crop or a long fallow. Both methods gave 72% yield increases over wheat growing after wheat. None of the other methods gave consistent, significant, or profitable yield increases or disease control. The mean yield increases in the year of application were 8% for the fungicide, 6% for microbial antagonists, 4% for chloride, and 7% for fumigation. The probable reason that fungicide and microbial antagonists were ineffective was that they were localised in the furrow where they were applied, whereas roots became infected in the inter-row space. Probable reasons that chloride was ineffective were that the background soil chloride levels were generally above the responsive range, and that roots became infected with take-all after the chloride was leached from the topsoil. The limitation of fumigation was that it suppressed natural antagonists of the Ggt, apparently leading to reinfection at higher levels than before. There was also evidence of Ggt re-infection in the second year after break crops, leading to an apparent ‘boomerang’ effect. Take-all inocula at the sites were measured in pre-sowing soil bioassays, whereas disease incidence was determined in seedlings and as ‘whiteheads’ as crops approached maturity. The only consistent pattern among the measurements was low disease incidence after break crops and the long fallow. Otherwise, there were low correlations between the 3 sets of measurements, suggesting that environmental changes after the soil bioassay and seedling assessment played critical roles in the progress of the disease.


2000 ◽  
Vol 51 (4) ◽  
pp. 445 ◽  
Author(s):  
J. A. Kirkegaard ◽  
M. Sarwar ◽  
P. T. W. Wong ◽  
A. Mead ◽  
G. Howe ◽  
...  

Biofumigation refers to the suppression of soil-borne pathogens and pests by biocidal compounds released by Brassica crops when glucosinolates (GSL) in their residues decay in soil. We conducted field studies at 2 sites to investigate the hypothesis that biofumigation by Brassica break crops would reduce inoculum of the take-all fungus Gaeumannomyces graminis var. tritici (Ggt) to lower levels than non-Brassica break crops, and thereby reduce Ggt infection and associated yield loss in subsequent wheat crops. High and uniform levels of Ggt were established at the sites in the first year of the experiments by sowing wheat with sterilised ryegrass seed infested with Ggt. Ggt inoculum declined more rapidly under Brassica crops than under linola and this reduction coincided with the period of root decay and reduced root glucosinolate concentrations around crop maturity. There was no consistent difference in inoculum reduction between canola (Brassica napus) and Indian mustard (Brassica juncea), nor between cultivars with high and low root GSL within each species. Despite significant inoculum reduction attributable to biofumigation, there were no differences in the expression of disease and associated impacts on the yield of subsequent wheat crops across the sites. Seasonal conditions, in particular the distribution of rainfall in both the summer–autumn fallow following the break crops and during the subsequent wheat crop, influenced inoculum survival and subsequent disease development. In wet summers, inoculum declined to low levels following all break crops and no extra benefit from biofumigation was evident. In dry summers the lower inoculum levels following brassicas persisted until the following wheat crops were sown but subsequent development of the disease was influenced more by seasonal conditions than by initial inoculum levels. Significant extra benefits of biofumigation were observed in one experiment where wheat was sown within the break crops to simulate grass weed hosts of Ggt. Under these circumstances there was greater reduction in Ggt inoculum under canola than linseed and an associated decrease in disease development. For host-dependent pathogens such as Ggt, we hypothesise that the benefits of biofumigation to subsequent wheat crops will therefore be restricted to specific circumstances in which inoculum is preserved during and after the break crops (i.e. dry conditions, grass hosts present) and where conditions in the following wheat crop lead to significant disease development (early sowing, wet autumn and spring, dry periods during grain filling).


Plant Disease ◽  
2005 ◽  
Vol 89 (2) ◽  
pp. 204-204 ◽  
Author(s):  
L. P. Tredway

An unknown disease was observed in June 2002 and 2003 on creeping bentgrass (CRB [Agrostis stolonifera L.]) putting greens at The Country Club of Landfall in Wilmington, NC that were established in 2001 with a 1:1 blend of cvs. A-1 and A-4. Soil pH ranged from 7 to 8 at this location because of poor quality irrigation water. Symptoms appeared in circular patches of 0.3 to 1 m in diameter that exhibited signs of wilt followed by chlorosis and orange foliar dieback. The disease was initially diagnosed as take-all patch caused by Gaeumannomyces graminis (Sacc.) Arx & D. Olivier var. avenae (E.M. Turner) Dennis, based on the observation of necrotic roots and crowns that were colonized with dark, ectotrophic hyphae. However, the historical lack of take-all patch occurrence in this region led to the suspicion that G. graminis var. avenae was not involved. Sections of root and crown tissue were surface disinfested in 0.6% NaOCl for 5 min or 1% AgNO3 for 1 min and 5% NaCl for 30 s. Tissue was plated on SMGGT3 (2) or on potato dextrose agar containing 50 mg L-1 of tetracycline, streptomycin, and chloramphenicol. A fungus resembling Magnaporthe poae Landschoot & Jackson was consistently obtained regardless of isolation method. Teleomorph production was conducted on Sachs agar (4) overlaid with autoclaved wheat (Triticum aestivum L.) stem sections. Seven isolates were plated alone or paired with M. poae tester isolates 73-1 or 73-15 (3) and incubated at room temperature under continuous fluorescent illumination. Six isolates produced perithecia and ascospores typical of M. poae (3) when paired with 73-15 but not when plated alone or paired with 73-1; these isolates are, therefore, M. poae mating type ‘a’. Isolate TAP42 did not produce perithecia and remains unidentified. Cone-Tainers (3.8 × 20 cm) containing calcined clay were seeded with ‘A-4’ CRB (9.7 g cm-2) and inoculated 8 weeks later by placing four M. poae-infested rye (Secale cereale L.) grains below the soil surface. Inoculated Cone-Tainers were placed in growth chambers with 12-h day/night cycles at 30/25°C, 35/25°C, or 40/25°C. Field plots (1 m2) of ‘A-4’ CRB in Jackson Springs, NC were inoculated on 19 June 2003 by removing a soil core (1.9 × 10.3 cm) from the center of each plot, adding 25 cm3 of M. poae-infested rye grains, and then capping the hole with sand. Growth chamber and field inoculations were arranged in a randomized complete block with four replications. Eight weeks after inoculation in the growth chamber, isolates TAP35, TAP41, and SCR4 caused significant foliar chlorosis and dieback at 12-h day/night cycles of 30/25°C and 35/25°C, but only TAP41 induced symptoms at 40/25°C. Isolate TAP42 did not induce symptoms at any temperature regimen. Orange patches (10 to 15 cm in diameter) were observed in field plots inoculated with TAP41 on 27 August 2003. No other isolates induced aboveground symptoms. Roots and crowns of plants exhibiting foliar symptoms in the greenhouse and field were necrotic and colonized with ectotrophic hyphae, and M. poae was consistently isolated from this tissue. Although M. poae has been associated with CRB in Florida (1), to our knowledge, this is the first report of summer patch of CRB within the normal zone of adaptation for this turfgrass species. Observation of this disease highlights the need for accurate methods for diagnosis of diseases caused by ectotrophic root-infecting fungi. References: (1) M. L. Elliott. Plant Dis. 77:429, 1993. (2) M. E. Juhnke et al. Plant Dis. 68:233, 1984. (3) P. J. Landschoot and N. Jackson. Mycol. Res. 93:59, 1989. (4) E. S. Lutrell. Phytopathology 48:281, 1958.


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