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Publication #IG479

Stink Bugs in Florida Rice1

Ron Cherry2

Introduction

Although many different insects can be found in rice fields in Florida, stink bugs are currently considered the most important pest. Jones and Cherry (1986) reported that the rice stink bug, Oebalus pugnax, was the dominant species, comprising more than 95% of the total stink bug population. Cherry et al. (1998) reported that the stink bug Oebalus ypsilongriseus was widespread in Florida rice fields. This was the first report of this species being found in commercial rice fields in the United States. Cherry and Nuessly (2010) reported that the stink bug Oebalus insularis is now widespread in Florida rice fields. This was the first report of this species being found in commercial rice fields in the United States. The stink bug complex attacking Florida rice is the most diversified and unique stink bug complex in US rice production (Table 1).

Figure 1. 

Rice stink bugs are usually sampled with sweep nets.


[Click thumbnail to enlarge.]

Damage

Rice stink bugs cause economic losses in two major ways. Both the adult and nymphal stages feed on individual grains of rice as the panicle develops. With their sucking mouthparts, they can completely remove a grain's content in the milk stage of grain development, thereby reducing yields. More seriously, grains attacked in the dough stage become shriveled kernels with spots varying from light yellow to black. This condition, called "pecky rice," has the greatest impact on rice quality and marketability. Research has shown that much of the pecky rice is due to kernel wounding by the feeding behavior of the rice stink bug. This wounding introduces fungi and other microorganisms that cause the undesirable discoloration (peck) in the grain.

Biology

A large complex of these shield-shaped bugs occurs on rice. They are particularly fond of the developing grain of rice, other small grains, and various developing grass seeds. While a few species are almost specific to graminaceous plants, some species are equally fond of legumes and other crops. All of these bugs are similar in their life histories and habits. They have a gradual metamorphosis from egg through nymphal instars to adult. Nymphs of most species tend to be more colorful than adults. Nymphs become progressively larger with each molt, and the wing pads become progressively more prominent. All species share the protective ability to emit an ill-smelling substance from ventrally located osteolar canals (Genung et al. 1979).

Figure 2. 

The most abundant rice stink bug in Florida rice is Oebalus pugnax. The adult is shown.


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Natural Control

Stink bugs have many general and specific natural enemies. Rice stink bug eggs are often attacked by egg parasites, particularly Telonomus sp. (Scelionidae). Stink bugs are also attacked by a variable group of insect predators. A benbicid wasp (Bicyrtes quadrifasciata) provisions its subterranean nests with green stink bugs and other pentatomids. The assassin bug (Zelus bilobus) feeds on nymphs as well as adults. Among several species of spiders that prey on stink bugs, a common jumping spider (Phidippus audax) is especially prominent.

Many species of birds feed to some extent on stink bugs. Data based on stomach contents analysis showed that 14% of meadowlark (Sturnella magna), 10% of red-winged blackbird (Agelaius phoeniceus), 16% of boat-tailed grackle (Cassidix mexicanus), and 14% of cattle egret (Bubulcus ibis) stomachs contained these insects (Genung et al. 1979). These data may look impressive, but they do not show evidence that bird predation is reducing stink bug populations significantly. More recently, Borkhataria et al. (2012) used bird exclosures to evaluate the effects of blackbirds on stink bug populations in Florida rice. There was no difference in abundance of rice stink bugs (Oebalus spp.) in environments where blackbirds had been excluded versus control environments, indicating that predation by birds did not reduce stink bug populations. Pecky rice damage rates in exclosure environments and control environments were similar as well. These data suggest that despite their conspicuous presence, blackbirds had little effect on stink bug populations in Florida rice fields.

Figure 3. 

The stink bug Oebalus ypsilongriseus was first reported in Florida rice in 1988. The adult is shown.


[Click thumbnail to enlarge.]

Cultural Control

Timing of planting date has shown positive results in keeping stink bugs away from crops at their most vulnerable time. Litsinger (1994) gives examples of planting dates being used to reduce insect damage of numerous rice pests including stink bugs. Data in Table 2 suggest that planting date could be used to move rice heading from the period of greatest flight activity, thus reducing stink bug populations in the rice. However, moving rice planting dates may pose other problems for rice growers. Planting rice too early may result in frost damage, and rice in Florida may alternate with other crops such as corn and sugarcane grown at different times on the same land. Hence, rice planting and harvesting are frequently timed in conjunction with these other crops. Our data suggest that changing the planting date can avoid stink bug damage in rice, but the planting date is frequently contingent upon other grower considerations, which often makes changing it difficult or impossible

The effect of weeds on rice stink bug, Oebalus pugnax (F.), populations was studied in Florida rice fields (Cherry and Bennett 2005). Fall panicum, Panicum dichotomiflorum, was the most common grassy weed found in weedy areas of rice fields, and significantly more rice stink bugs were found in these weedy areas than were found in non-weedy areas in the fields. Large numbers of rice stink bugs also were found in unmowed roadsides containing heading weeds, especially coast cockspur, Echinochloa walteri. In contrast, few rice stink bugs were found in mowed roadsides, presumably because mowing prevented weed heading around rice fields. The Cherry and Bennett study showed that weed control helps reduce rice stink bug populations in Florida rice.

Chemical Control

Insect sweep-nets should be used for sampling. Treat when there are 30 stink bugs per 100 sweeps during the first two weeks of heading and when there are 100 stink bugs per 100 sweeps until two weeks before harvest (LSU 2013).

Cherry and Deren (2000) studied the effect of time of day and weather conditions on sweep-net catches of stink bugs in Florida rice fields. Their data showed that except in rainy, stormy, or very windy conditions, time of day is not a significant factor in sweep-net catches of stink bugs in Florida rice fields. Also, air temperature and wind speed, except when very windy, generally had little effect on stink bug catches in sweep nets.

Rice fields in Florida were sampled for the rice stink bug O. pugnax to determine its spatial distribution in Florida rice (Foster et al.1989). This most important stink bug pest of Florida rice had an aggregated distribution. However, the grower practice of sampling ends of fields rather than the entire field is satisfactory because stink bug catches from the ends of the fields accurately predict the overall field populations of the stink bugs.

Insecticide applications currently used by Florida rice growers are effective. However, population reduction of stink bugs may be only temporary (Jones and Cherry 1986). Insecticide recommendations do change over time. Hence, growers should contact their county extension agent for currently labeled insecticides for stink bug control.

Figure 4. 

The stink bug Oebalus insularis was first reported in Florida rice in 2010. The adult is shown.


[Click thumbnail to enlarge.]

References Cited

Borkhataria, R., G. Nuessly, E. Pearlstine, and R. Cherry. 2012. “Effects of blackbirds (Agelaius phoenicius) on stink bug (Hemiptera: Pentatomidae) populations, damage, and yield in Florida rice.” Florida Entomol. 95: 143-149

Cherry, R. and A. Bennett. 2005. “Effect of weeds on rice stink bug (Hemiptera: Pentatomidae) populations in Florida rice fields.” J. Entomol. Science. 40: 378-384.

Cherry, R., D. Jones, and C. Deren. 1998. “Establishment of a new stink bug pest, Oebalus ypsilongriseus (Hemiptera: Pentatomidae) in Florida rice.” Florida Entomologist. 81: 216-220.

Cherry, R., and G. Nuessly. 2010. “Establishment of a new stink bug pest, Oebalus insularis (Hemiptera: Pentatomidae) in Florida rice.” Florida Entomologist. 93: 291- 293.

Cherry, R., and C. Deren. 2000. “Sweep net catches of stink bugs (Hemiptera: Pentatomidae) in Florida rice fields at different times of day.” J. Entomol. Science. 35: 490-493.

Cherry, R. and A. Wilson. 2011. “Flight activity of stink bug (Hemiptera: Pentatomidae) pests of Florida rice.” Florida Entomologist. 94: 359-360.

Foster, R., R. Cherry, and D. Jones. 1989. “Spatial distribution of the rice stink bug (Heteroptera: Pentatomidae) in Florida rice.” J. Econ. Entomol. 82: 507-509.

Genung, W. G., G. H. Snyder, and V. E. Green, Jr. 1979. “Rice field insects in the Everglades.” Belle Glade Res. Rep. EV-1979-7. Univ. of Florida, Gainesville.

Jones, D. B., and R. H. Cherry. 1986. “Species composition and seasonal abundance of stink bugs (Heteroptera: Pentatomidae) in southern Florida rice.” J.Econ. Entomol. 79: 1226-1229.

Litsinger, J. 1994. “Cultural, mechanical, and physical control of rice insects,” pp. 549-583. In E. Heinricks (ed), Biology and Management of Rice Insects. John Wiley and Sons. New York.

LSU Ag. Center. 2013. Louisiana Insect Pest Management Guide: Rice-2013 Guide.

Tables

Table 1. 

Relative Abundance of Stink Bugs Found in Southern Florida Rice Fields in 2008 and 2009 (Cherry and Nuessly 2010).

     

Total

Species1

Adults

Nymphs

Number

%

E. ictericus

2

0

2

<1

M. pictiventris

49

0

49

4

N. viridula

10

4

14

1

O. insularis

200

27

227

20

O. pugnax

550

68

618

54

O. ypsilongriseus

181

30

211

18

Unknown

22

10

32

3

         

Total

1014

139

1153

100

1 Euschistus ictericus, Mormidea pictiventris, Nezara viridula, Oebalus insularis, pugnax, and ypsilongriseus.

Table 2. 

Rice Stink Bugs Caught1 in a Blacklight Trap Twice Weekly from 1 January 2008 through 1 January 2010 (Cherry and Wilson 2011).

     

Oebalus

Month

E. ictericus

N. viridula

insularis

pugnax

ypsilongriseus

January

0 b

0 c

0 c

0 b

0 b

February

0 b

0.2 c

0 c

0.7 b

0 b

March

0 b

0 c

0 c

0 b

0 b

April

0 b

0 c

0 c

0 b

0 b

May

0 b

0.8 c

0 c

1.9 b

0 b

June

0.6 b

4.9 c

0.2 c

4.2 b

0 b

July

16.7 a

22.3 a

8.6 a

233.0 a

2.3 a

August

3.4 b

12.5 b

3.8 b

15.9 b

1.9 a

September

0.6 b

2.3 c

0.7 c

3.4 b

0 b

October

0.1 b

1.9 c

0 c

0.1 b

0.3 b

November

0 b

0.7 c

0 c

0 b

0 b

December

0 b

0.6 c

0 c

0.1 b

0 b

1 Means in a column followed by the same letter are not significantly different (alpha = 0.05) using the Least Significant Difference Test.

Footnotes

1.

This document is IG479, one of a series of the Entomology and Nematology Department, UF/IFAS Extension. Original publication date October 2013. Visit the EDIS website at http://edis.ifas.ufl.edu.

2.

Ron Cherry, professor, Department of Entomology and Nematology, Everglades Research and Education Center, Belle Glade, FL; UF/IFAS Extension, Gainesville, FL 32611.


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