Translator Disclaimer
1 September 2016 Effect of plant Growth Regulators on Blissus insularis (Hemiptera: Blissidae)
Author Affiliations +
Abstract

Plant growth regulators are known to influence a plant's characteristics and therefore can be used as an alternative strategy in making Blissus insularis Barber (Hemiptera: Blissidae) habitat unfavorable for this insect's survival. The reduction of B. insularis population densities following the application of mefluidide and trinexapac-ethyl in field plots indicated the indirect effect of plant growth regulator application on B. insularis for its management in St. Augustinegrass.

Use of plant growth regulators is a common practice by turfgrass managers to regulate grass canopy heights and reduce mowing frequency (Watschke et al. 1992). Plant susceptibility to insect herbivory can be manipulated by using plant growth regulators to change a plant's physical or biochemical properties (Singer & Smith 1976; Coffelt & Schultz 1988; Campbell 1998; Turgeon 1999). In this study, we sought to investigate the indirect effect of 2 plant growth regulators on turf physiology and Blissus insularis Barber (Hemiptera: Blissidae) abundance in St. Augustinegrass, Stenotapharum secundatum Kuntze (Poaceae).

A field experiment was established in summer 2013 using ‘Floratam’ St. Augustinegrass plots (2 × 2 m) with buffer zones (1 × 1 m) in randomized complete block design with 5 replicates consisting of 2 plant growth regulator treatments and untreated water control at the University of Florida (UF) Plant Science Unit in Citra, Florida. We hypothesized that plant growth regulators would influence B. insularis abundance by altering habitat suitability by changing the chemical and morphological characteristics of the St. Augustinegrass. To ensure a baseline number of insects in each plot, 30 B. insularis individuals (a mixture of 4th and 5th nymphal instars, and unsexed adults from an established laboratory colony maintained according to Vázquez' [2010] protocol on St. Augustinegrass plugs and yellow corn, respectively) were released in the center of each plot on 6 May 2013. Trinexapacethyl (Primo Maxx®, Syngenta Crop Science, Raleigh, North Carolina) and mefluidide (Embark®, Gordon Corporation, Kansas City, Missouri) were applied on 5 Jun, 3 Jul, and 5 Aug 2013 at the rate of 0.45 and 0.17 L active ingredient (a.i.) per ha, respectively, by using a 4 nozzle, 1.8 m boom connected to a 35 psi CO2 pressurized backpack sprayer.

To evaluate treatment effects, the center of each plot (700 cm2 area) was vacuum sampled for 30 s by using a TroyBilt TB320BV blower vacuum (TroyBilt, Cleveland, Ohio) (Crocker 1993; Nagata & Cherry 1999) on 12 Jun, 12 Jul, and 12 Aug 2013 between 1000 and 1400 h. Insects were collected in a white bucket and counted (in the field if ≤20 or in the laboratory if >20) and returned to their respective plots within 24 h. Turf management practices like irrigation and fertilization can play a significant role in altering the habitat's properties like moisture, nutrition, and thatch thickness to influence insect abundance. We measured turf parameter readings on each sampling date to account for the influence of plant growth regulator applications on habitat suitability characteristics of turf. Thatch thickness was determined by inserting a 2 cm diameter soil probe into the plot, and the layer between the soil and living plant tissue of the core was measured with a ruler (cm). Turf color and chlorophyll index were determined using a Field-Scout TCM 500 NDVI Turf Color Meter (Spectrum Technologies, Inc., Plainfield, Illinois) and FieldScout CM-1000 Normalized Difference Vegetative Index (NDVI) (Spectrum Technologies, Inc., Plainfield, Illinois), respectively. Soil moisture was measured with a TDR 300 Soil Moisture Probe (Spectrum Technologies, Inc., Plainfield, Illinois). Total Kjeldahl nitrogen concentration (TKN) was estimated by clipping 10 turf sprigs (about 5 g), which were oven dried at 70 to 80 °C for ≥⃒48 h, weighed, ground, and analyzed by the UF Institute of Food and Agricultural Sciences Analytical Research Laboratory. Sampling data were analyzed using mixed model analyses (PROC MIXED, SAS Version 9.3, SAS Institute, Inc., Cary, North Carolina). Effects with P ≤ 0.05 were considered significant. When appropriate, means were separated using Tukey's HSD test. Thatch thickness, turf color, turf chlorophyll content, soil moisture, and TKN concentration were included in the linear mixed model to identify the most significant factor associated with B. insularis density.

Although no significant differences existed between treatment and control plots during 2 sampling dates (Fig. 1), when data were pooled for all 3 dates evaluated, significantly fewer B. insularis individuals (F = 15.54; df = 2,8; P = 0.0018) were recovered in plots treated with a plant growth regulator (mefluidide = 7.0 ± 1.7; trinexapac-ethyl = 5.9 ± 1.3) compared with the control plots (12.6 ± 1.3) (Fig. 1). Turf TKN concentration was significantly and positively associated with B. insularis densities (Table 1) (F = 9.09; df =1,16; P = 0.008). Turf TKN represents a total nitrogen concentration and in plant growth regulator treated plots, reduced nitrogen availability may have impacted insect abundance. The plant growth regulator application did not affect thatch thickness or turf quality among treatments, possibly due to short test duration.

Fig. 1.

Mean Blissus insularis densities (± SE) in St. Augustinegrass, Stenotaphrum secundatum, treated with mefluidide, trinexapac-ethyl, or untreated control. Means with the same letter within a sampling date did not differ statistically (ANOVA, P > 0.05); there were 5 replicates per treatment.

f01_557.jpg

Table 1.

Turf health parameters influencing Blissus insularis densities in ‘Floratam’ St. Augustinegrass, Stenotaphrum secundatum, from 12 Jun to 12 Aug 2013.

t01_557.gif

Honeyborne (1969) and Coffelt & Schultz (1988) indicated that mefluidide slowed the development of azalea lace bug, Stephanitis pyrioides (Scott) (Hemiptera: Tingidae) on Rhododendron sp. (Ericaceae) because of reduced nutrient availability. Tsagkarakis et al. (2012) found that Diaphorina citri Kuwayama (Hemiptera: Liviidae) adults reared on Citrus volkameriana (Rutaceae) trees treated with prohexadione calcium and mefluidide showed significant reductions in both fecundity and survivorship. However, no effect of plant growth regulator use on the suitability of creeping bentgrass against black cutworms, Agrotis ipsilon Hufnagel (Lepidoptera: Noctuidae), and sod webworms (Lepidoptera: Pyralidae) was evident (Rogers et al. 2001). We suggest further testing with plant growth regulators to provide more robust recommendations for B. insularis management.

We are grateful to P. Ruppert for his technical assistance. Funding was provided by the State of Florida and the USDA-NIFA Pest Management Alternatives Program (2010-02650).

References Cited

1.

Campbell BC. 1998. The effects of plant growth regulators and herbicides on host plant quality to insects, pp. 205–247 In Heinrichs EA [ed.], Plant Stress- Insect Interactions. Wiley, New York, New York. Google Scholar

2.

Coffelt MA, Schultz PB. 1988. Influence of plant growth regulators on the development of the azalea lace bug (Hemiptera: Tingidae). Journal of Economic Entomology 81: 290–292. Google Scholar

3.

Crocker RL. 1993. Chemical control of southern chinch bug in St. Augustinegrass. International Turfgrass Society Research Journal 7: 358–365. Google Scholar

4.

Honeyborne CHB. 1969. Performance of Aphis fabae and Brevicoryne brassicae on plants treated with growth regulators. Journal of the Science of Food and Agriculture 20: 388–390. Google Scholar

5.

Nagata RT, Cherry RH. 1999. Survival of different life stages of the southern chinch bug (Hemiptera: Lygaeidae) following insecticidal applications. Journal of Entomological Science 34: 126–131. Google Scholar

6.

Rogers ME, Held DW, Williams DW, Potter DA. 2001. Effects of two plant growth regulators on suitability of creeping bentgrass for black cutworms and sod webworms. International Turfgrass Society Research Journal 9: 806–809. Google Scholar

7.

SAS Software. 2010. Version 9.3. SAS Institute, Cary, North Carolina. Google Scholar

8.

Singer MC, Smith BD. 1976. Use of the plant growth regulator chlormequat chloride to control the aphid Hyperomyzus lactucae on black currants. Annals of Applied Biology 82: 407–414. Google Scholar

9.

Tsagkarakis AE, Rogers ME, Spann TE. 2012. Applications of plant growth regulators to container-grown citrus trees affect the biology and behavior of the Asian citrus psyllid. Journal of the American Society for Horticultural Science 137: 3–10. Google Scholar

10.

Turgeon AJ. 1999. Turfgrass Management, 5th ed. Prentice Hall, Upper Saddle River, New Jersey. Google Scholar

11.

Vázquez JC, Hoy MA, Royalty RN, Buss EA. 2010. A synchronous rearing method for Blissus insularis (Hemiptera: Blissidae). Journal of Economic Entomology 103: 726–734. Google Scholar

12.

Watschke TL, Prinster MG, Breuninger JM. 1992. Plant growth regulators and turfgrass management, pp. 557–588 In Waddington DV, Carrow RN, Shearman RC [eds.], Turfgrass, 1st ed. American Society of Agronomy. Madison, Wisconsin. Google Scholar
Navneet Kaur, Jennifer L. Gillett-Kaufman, and Eileen A. Buss "Effect of plant Growth Regulators on Blissus insularis (Hemiptera: Blissidae)," Florida Entomologist 99(3), 557-558, (1 September 2016). https://doi.org/10.1653/024.099.0336
Published: 1 September 2016
JOURNAL ARTICLE
2 PAGES


SHARE
ARTICLE IMPACT
Back to Top