scholarly journals Population Dynamics of the Lance Nematode (Hoplolaimus galeatus) in Creeping Bentgrass

Plant Disease ◽  
2006 ◽  
Vol 90 (1) ◽  
pp. 44-50 ◽  
Author(s):  
D. M. Settle ◽  
J. D. Fry ◽  
T. C. Todd ◽  
N. A. Tisserat

The effects of management practices and nematode population density on the seasonal fluctuationsin lance nematode (Hoplolaimus galeatus) populations in creeping bentgrass were studiedin a naturally infested experimental putting green and in artificially infested microplots. In general, H. galeatus populations increased from late spring through midsummer, declined in August, and increased again in the fall. Population increase in microplots was strongly density dependent, with final population densities inversely proportional to inoculum levels. Ectoparasitic populationsof H. galeatus in both studies were composed of adults and juveniles, whereas endoparasiticpopulations were almost exclusively juveniles. H. galeatus populations in the naturallyinfested site were aggregated spatially, but the aggregation was not temporally stable. Nematodepopulations were not affected by bentgrass cultivar selection or irrigation frequency.

Plant Disease ◽  
2007 ◽  
Vol 91 (9) ◽  
pp. 1170-1179 ◽  
Author(s):  
D. M. Settle ◽  
J. D. Fry ◽  
G. A. Milliken ◽  
N. A. Tisserat ◽  
T. C. Todd

We compared photosynthesis and multispectral radiometry (MSR) measurements with visual quality ratings for assessment of feeding injury to creeping bentgrass caused by the lance nematode (Hoplolaimus galeatus) using artificially infested microplots and a naturally infested putting green. Nematode feeding resulted in negative visual and MSR effects on creeping bentgrass in microplots. Visual quality ratings were correlated more consistently with nematode densities than either individual MSR variables or factor models of MSR variables. Threshold estimates for H. galeatus population densities associated with unacceptable bentgrass quality in microplots varied widely by month and year. Similarly, the relationship between H. galeatus population density and turf health indicators (including MSR measurements, visual ratings, and net photosynthetic rate) varied with cultivar and management practice (irrigation frequency and mowing height) in the naturally infested putting green. Notably, negative effects of nematode feeding were not consistently associated with more stressful management practices, suggesting that stress avoidance is not a reliable deterrent to H. galeatus damage in creeping bentgrass. Damage thresholds for this nematode–host association are dynamic and should be used with caution.


2002 ◽  
Vol 127 (2) ◽  
pp. 224-229 ◽  
Author(s):  
Maxim J. Schlossberg ◽  
Keith J. Karnok ◽  
Gil Landry

Subjection of intensively managed creeping bentgrass [Agrostis stolonifera L. var. palustris (Huds.). Farw., (syn. Agrostis palustris Huds.)] to supraoptimal soil temperatures is deleterious to root viability and longevity. The ability to estimate viable root length would enable creeping bentgrass managers to more accurately schedule certain management practices. The purpose of this rhizotron study was to develop a model, based on an accumulated degree-day (ADD) method, capable of estimating viable root length density of established `Crenshaw' and `L93' creeping bentgrass maintained under putting green conditions. Viable root length density observations were made biweekly and soil temperature data collected April through September 1997, and January through August 1998 and 1999. Relative viable root length density (RVRLD) is defined as the measured viable root length density divided by the maximum density attained that spring. In both years, maximum annual viable root length density for all plots was reached, on average, by 138 days from the beginning of the year (18 May). Cultivar and year effects were nonsignificant (P = 0.67 and 0.20, respectively). Degree-day heat units were calculated using an array of base temperatures by integral and arithmetical methods. Although the two accumulative methods proved suitable, the model regressing arithmetical degree-day accumulations against the bentgrass RVRLD provided a better fit to the data set. Use of the 10 °C base temperature in the arithmetical ADD calculations provided the following model; RVRLD = 0.98 - [1.30 × 10-4 (ADD)], accounting for 83.8% of the experimental variability (P < 0.0001). As several abiotic/edaphic factors have been shown to significantly influence root growth and viability, development of a widely usable model would include additional factors.


Plant Disease ◽  
2009 ◽  
Vol 93 (8) ◽  
pp. 846-846 ◽  
Author(s):  
L. Simard ◽  
G. Bélair ◽  
S. Miller

Creeping bentgrass, Agrostis stolonifera L., is the most important turfgrass species cultivated on golf greens in Canada. The needle nematode, Longidorus breviannulatus Norton & Hoffman, has several plant hosts including Gramineae such as corn, Zea mays L. (3), and creeping bentgrass (1). This large, plant-parasitic nematode is found most frequently in sandy soils and is encouraged by irrigation (2). In 2006, irregular, yellowish/chlorotic, and dead turfgrass patches were observed for the first time on several sand-based creeping bentgrass cv. Penncross greens on a golf course in Bromont, Québec (45°19′N, 72°39′W). Furthermore, a noticeable decline of the turfgrass root system was observed. Creeping bentgrass was grown with the following management practices: mowing height 3.18 mm, fertilization 2.27 kg N/0.45 kg P2O5/3.18 kg K2O/92.9 m2/year, aeration two times per year with 9.53-mm-diameter hollow core. On 5 July 2006, soil (0.5 kg) was sampled from two damaged areas of green no. 11. Three plugs (5-cm diameter × 15 cm deep) were taken from each area with a soil probe and pooled to form two separate samples. Another set of soil samples was collected on 12 July from three golf greens (nos. 10, 11, and 16). One sample was taken from each of three damaged areas and two healthy areas of each green. Plant-parasitic nematodes were extracted from 100-ml volumes of each soil sample by the Baermann pan and funnel extraction methods. Numbers of L. breviannulatus from the soil sampled on 5 July were counted with a stereo-microscope after 4 days of extraction, while numbers of L. breviannulatus in the rest of the samples were counted after 7 days of extraction. Identification was determined by morphological examination of a small number of adult female nematodes (n = 7). Characteristics distinguishing these specimens as L. breviannulatus include: amphidial pouches (bilobed and extending to the guiding ring), length 5,115 μm (4,780 to 6,230 μm), distance of the guiding ring from the oral aperture 26 μm (24 to 30 μm), odontostyle length 83 μm (78 to 90 μm), and tail length 42 μm (37 to 50 μm). In the two soil samples collected on 5 July, 0 and 183 juveniles per kilogram of dry soil were recovered with the Baermann pan method. In samples collected on 12 July from damaged areas of three greens, averages of 16 (min 0 and max 60) and 22 (min 0 and max 80) juveniles per kilogram of dry soil were obtained with the Baermann pan and funnel methods, respectively. No L. breviannulatus was found in any sample from healthy areas. Although no damage threshold has been established for L. breviannulatus in creeping bentgrass, low numbers of needle nematodes can be damaging in other crops such as corn. In our study, the occurrence of the damage was related to populations of the needle nematode, and therefore, the nematode was the likely cause of the damage. In Canada, L. breviannulatus is reported from Ontario (4). To our knowledge, this is the first report of the occurrence of L. breviannulatus in Québec. References: (1) L. B. Forer. Plant Dis. Rep. 61:712, 1977. (2) R. B. Malek et al. Plant Dis. 64:1110, 1980. (3) D. C. Norton and J. K. Hoffmann. J. Nematol. 7:168, 1975. (4) W. Ye and R. T. Robbins. J. Nematol. 36:220, 2004.


1980 ◽  
Vol 60 (4) ◽  
pp. 1209-1213 ◽  
Author(s):  
J.L. EGGENS

The effectiveness of thatch control practices commonly employed in Ontario on Penncross creeping bentgrass turf maintained as a putting green was evaluated from July 1976 to October 1979. The most effective treatments were coring and vertical mowing followed by topdressing, and topdressing alone. The least amount of winter injury occurred in plots where coring was followed by topdressing. Coring reduced thatch accumulation more than did vertical mowing. Vertical mowing increased winter injury and annual bluegrass content in the plots more than did coring. Thatch accumulation was less at the 5-mm than at the 8-mm mowing height. Nitrogen treatments of 2 and 4 kg N∙100 m−2 did not influence thatch accumulation.


Plant Disease ◽  
1999 ◽  
Vol 83 (6) ◽  
pp. 516-520 ◽  
Author(s):  
Yan Feng ◽  
Peter H. Dernoeden

Putting green samples (n = 109) were inspected for the presence of Pythium oospores in roots of plants from golf courses (n = 39) in Maryland and adjacent states. Twenty-eight Pythium isolates were recovered from creeping bentgrass (Agrostis palustris) (n = 25) and annual bluegrass (Poa annua) (n = 3) plants. Most isolates associated with Pythium-induced root dysfunction were from greens less than 3 years of age and were obtained primarily between March and June, 1995 to 1997. Eight Pythium species (P. aristosporum, P. aphanidermatum, P. catenulatum, P. graminicola, P. torulosum, P. vanterpoolii, P. volutum, and P. ultimum var. ultimum) were isolated from creeping bentgrass and two species (P. graminicola and P. torulosum) were from annual bluegrass. All species, except P. catenulatum, were pathogenic to ‘Crenshaw’ creeping bentgrass seedlings in postemergence pathogenicity tests. P. aristosporum (n = 3) and P. aphanidermatum (n = 1) were highly aggressive at a low (18°C) and a high temperature (28°C). P. graminicola (n = 1) was low to moderately aggressive. P. torulosum (n = 12) was the most frequently isolated species, but most isolates were either nonpathogenic or caused very little disease. P. aristosporum (n = 3) and P. aphanidermatum (n = 1) were highly aggressive and were associated with rapid growth at 18 and 28°C on cornmeal agar. P. volutum (n = 1) was highly aggressive at 18°C, but was one of slowest growing isolates. Infected roots were generally symptomless, and the number of oospores observed in roots was not always a good indicator of disease or of the aggressiveness of an isolate. Large numbers of oospores of low or even nonpathogenic species may cause dysfunction of creeping bentgrass roots.


1986 ◽  
Vol 76 (2) ◽  
pp. 265-274 ◽  
Author(s):  
M. J. Samways

AbstractParasitoids of Aonidiella aurantii (Maskell) on citrus in South Africa were monitored using two types of yellow sticky trap. One of these traps was highly efficient, being fluorescent with peak reflectance at about 530 nm. Aphytis spp. populations were low before February and high thereafter. Citrus surrounded by natural bush was an isolated reservoir of high host and parasitoid population levels. Aphytis spatial distribution within the orchard was extremely patchy, with over 100-fold differences in population levels over a distance of a few metres. This patchiness mirrored that of its host. This contagious spatial pattern was maintained despite 1000-fold seasonal changes in population levels. These temporal changes were characteristic and general throughout an orchard, and independent of patchiness. Initial Aphytis population levels did not dictate the final population level at the end of the season. Comperiella bifasciata Howard and its hyperparasitoid Marietta javensis (Howard) also showed clear seasonal population trends, but not of the same magnitude as those of Aphytis. There was no statistically significant correlation between the spatial distribution of one parasitoid with that of another, even between C. bifasciata and M. javensis. The patchiness of these two species was not correlated with overall host density. Aphytis and C. bifasciata were partially mutually exclusive. Aphytis was by far the most economically important of the parasitoids. Pest management practices, therefore, should aim at conserving the pool of Aphytis within the orchard as far as practicable.


2009 ◽  
Vol 23 (3) ◽  
pp. 425-430 ◽  
Author(s):  
Patrick E. McCullough ◽  
Stephen E. Hart

Bispyribac-sodium is an efficacious herbicide for annual bluegrass control in creeping bentgrass fairways, but turf tolerance and growth inhibition may be exacerbated by low mowing heights on putting greens. We conducted field and greenhouse experiments to investigate creeping bentgrass putting green tolerance to bispyribac-sodium. In greenhouse experiments, creeping bentgrass discoloration from bispyribac-sodium was exacerbated by reductions in mowing height from 24 to 3 mm, but mowing height did not influence clipping yields or root weight. In field experiments, discoloration of creeping bentgrass putting greens was greatest from applications of 37 g/ha every 10 d, compared to 74, 111, or 222 g/ha applied less frequently. Chelated iron effectively reduced discoloration of creeping bentgrass putting greens from bispyribac-sodium while trinexapac-ethyl inconsistently reduced these effects. Overall, creeping bentgrass putting greens appear more sensitive to bispyribac-sodium than higher mowed turf, but chelated iron and trinexapac-ethyl could reduce discoloration.


1991 ◽  
Vol 71 (2) ◽  
pp. 595-599 ◽  
Author(s):  
D. J. Cattani ◽  
M. H. Entz ◽  
K. C. Bamford

Tiller production and dry matter accumulation were monitored in six creeping bentgrass (Agrostis palustris Hud.) genotypes maintained as a putting green. Core samples for tiller density and aboveground biomass determinations were collected at intervals between October 1987 and October 1989. Two experimental lines, UM84-01 and UM86-01, produced more (P < 0.05) tillers and higher (P < 0.05) aboveground biomass than the commercial cultivars Penneagle, National, Emerald and Seaside. Both tiller density and aboveground biomass rankings among genotypes were consistent over the study period. Although lower tillering genotypes had a significantly higher aboveground biomass per tiller, total aboveground biomass was influenced more by tiller density than by biomass per tiller. The relationship between tiller density and tiller dry weight was expressed mathematically to determine potential wear stress resistance among genotypes. Key words: Creeping bentgrass, tillering, biomass accumulation


HortScience ◽  
1994 ◽  
Vol 29 (8) ◽  
pp. 880-883 ◽  
Author(s):  
B. Jack Johnson

Three field experiments were conducted to determine if several preemergence and postemergence herbicides were safe to apply to creeping bentgrass (Agrostis stolonifera L. `Penncross') maintained at putting green height. When dithiopyr was applied at preemergence in late February or early March, the emulsifiable concentrate formulation (≤1.7 kg·ha-1) and granular formulation (≤1.1 kg·ha-1) did not reduce the quality or cover of creeping bentgrass. Applied at preemergence, bensulide plus oxadiazon at 6.7 + 1.7 kg·ha-1 and 13.4 + 3.4 kg·ha-1 reduced turfgrass quality for 2 to 3 weeks and 8 weeks after treatment, respectively. When MON 12051 and monosodium salt of methylarsonic acid (MSMA) (≤0.14 and ≤2.2 kg·ha-1, respectively) were applied at postemergence to creeping bentgrass in early June, the reduction in turfgrass quality varied from slight to moderate for 1 to 2 weeks, but turfgrass fully recovered with no effect on turfgrass cover. Quinclorac applied at postemergence in early June at ≥0.6 kg·ha-1 severely reduced creeping bentgrass quality and cover for ≥8 weeks. Diclofop at 0.6 kg·ha-1 applied to creeping bentgrass in June, July, or August maintained consistently higher quality and cover ratings than when applied at ≥1.1 kg·ha-1. Diclofop applied at 0.6 kg·ha-1 in June and repeated at the same rate in July reduced quality of creeping bentgrass less than when applied at 1.1 kg·ha-1 at any date. Chemical names used: O,O-bis (1-methylethyl) S-{2-[(phenylsulfonyl)amino]ethyl} phosphorodithioate (bensulide); (±)-2-[4-(2,4-dichlorophenoxy)phenoxy]propanoic acid (diclofop); S,S-dimethyl-2-(difluoromethyl)-4-(2-methylpropyl)-6-(trifluoromethyl)-3,5-pyridinedicarbothioate (dithiopyr); methyl-5-{[(4,6-dimethoxy-2-pyrimidinyl)amino] carbonylaminosulfonyl}-3-chloro-1-methyl-1-H-pyrazol-4-carboxylate (MON 12051); 3-[2,4-dicloro-5-(1-methylethoxy)phenyl]-5-(1,1-dimethylethyl)-1,3,4-oxadiazol-2-(3H)-one (oxadiazon); 3,7-dicloro-8-quinolinecarboxylic acid (quinclorac).


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