{"id":1158,"date":"2026-07-27T19:23:19","date_gmt":"2026-07-27T23:23:19","guid":{"rendered":"https:\/\/site.caes.uga.edu\/entomologyresearch\/?p=1158"},"modified":"2026-07-28T08:36:18","modified_gmt":"2026-07-28T12:36:18","slug":"pasture-mealybug-the-grass-specialist-threatening-your-turfgrass","status":"publish","type":"post","link":"https:\/\/site.caes.uga.edu\/entomologyresearch\/2026\/07\/pasture-mealybug-the-grass-specialist-threatening-your-turfgrass\/","title":{"rendered":"Pasture Mealybug: The Grass Specialist Threatening Your Turfgrass"},"content":{"rendered":"\n<p><strong><u>Pasture mealybug (<em>Heliococcus summervillei<\/em>) has not yet been confirmed in Georgia.<\/u><\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"563\" src=\"https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-1-1024x563.jpg\" alt=\"\" class=\"wp-image-1160\" srcset=\"https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-1-1024x563.jpg 1024w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-1-300x165.jpg 300w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-1-768x422.jpg 768w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-1-1536x845.jpg 1536w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-1-2048x1126.jpg 2048w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><figcaption class=\"wp-element-caption\">Fig. 1. Pasture mealybug on (A) sugarcane and (B) pasture grass (<mark class=\"has-inline-color has-primary-color\">red <\/mark>arrows). Photo credits: A, De-fen Mou, University of Florida; B, Nicole F. Quinn, University of Florida.<\/figcaption><\/figure>\n\n\n\n<p>The pasture mealybug (<em>Heliococcus summervillei<\/em>) (Fig. 1) is a destructive, invasive sap-sucking insect native to South and Southeast Asia that has recently emerged as a threat to agriculture in the United States. After first becoming a serious pasture pest in Queensland, Australia, in 1928, it spread to the Caribbean islands around 2019 and was officially confirmed in the continental U.S. (specifically southeastern Texas) in October 2025, likely introduced via wind currents from tropical storms. This pest is a severe concern because it reproduces explosively (Fig. 2), injects toxins that cause rapid plant dieback, overwinters underground, and currently lacks labeled chemical controls. As a strict grass specialist, it poses an immediate economic threat to livestock and forage systems by decimating major grazing grasses, such as bermudagrass and bahiagrass, while also causing heavy yield losses in row-crop agriculture (such as rice and sugarcane, etc) and threatening commercial turfgrass and sod industries.<\/p>\n\n\n\n<figure class=\"wp-block-image aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"505\" src=\"https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-2-1-1024x505.jpg\" alt=\"\" class=\"wp-image-1162\" srcset=\"https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-2-1-1024x505.jpg 1024w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-2-1-300x148.jpg 300w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-2-1-768x379.jpg 768w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-2-1-1536x757.jpg 1536w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-2-1-2048x1010.jpg 2048w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><figcaption class=\"wp-element-caption\">Fig. 2. Pasture mealybug infestation on (A) sugarcane and (B) pasture grass. Photo credits: A, De-fen Mou, University of Florida; B, Nicole F. Quinn, University of Florida.<\/figcaption><\/figure>\n\n\n\n<h2 class=\"wp-block-heading\">Biology and life cycle<\/h2>\n\n\n\n<p>The pasture mealybug is named for its unique preference for grazing and forage grasses, and it reproduces exclusively through sexual reproduction, producing up to three generations per year with population peaks during warm, wet late-summer months. The species exhibits extreme sexual dimorphism: damaging, sap-sucking nymphs progress through four oval, creamy-white instars ranging from 0.2 mm crawlers to 2.0 mm fuzzy, wax-covered nymphs, while the non-feeding adults look entirely different. Adult males are tiny, winged, gnat-like insects measuring under 1.0 mm that live only a few days to mate, whereas adult females are wingless, retain a juvenile appearance (Fig. 1), measure 2.0 mm to 5.0 mm long, and turn a distinctive pink color after mating (Fig. 3), rapidly producing up to 100 offspring in a single 24-hour period. These various life stages shift dynamically throughout the environment, with feeding nymphs clustering on grass leaves and stems, mating adults hiding in the thick thatch and plant crowns, and egg-laying females crawling into the soil, roots, or beneath cow patties where they can safely overwinter.<\/p>\n\n\n\n<figure class=\"wp-block-image aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"337\" src=\"https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-3-1024x337.jpg\" alt=\"\" class=\"wp-image-1163\" srcset=\"https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-3-1024x337.jpg 1024w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-3-300x99.jpg 300w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-3-768x253.jpg 768w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-3-1536x506.jpg 1536w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-3-2048x674.jpg 2048w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><figcaption class=\"wp-element-caption\">Fig. 3. Mated female of pasture mealybug on grass (arrows). Photo credit: Nicole F. Quinn, University of Florida.<\/figcaption><\/figure>\n\n\n\n<h2 class=\"wp-block-heading\">Hosts<\/h2>\n\n\n\n<p>The pasture mealybug is a grass specialist that reproduces exclusively on monocotyledonous plants within the Poaceae (true grasses) and Cyperaceae (sedges) families. Its primary reproductive hosts include vital forage and pasture options, including buffelgrass, bermudagrass, bahiagrass, and limpograss, alongside major row crops, such as sugarcane and rice. While adult females may occasionally crawl onto broadleaf weeds or neighboring non-grass plants, they cannot successfully mate, lay eggs, or sustain subsequent generations on them. Instead, the pest relies on dense turfgrasses like St. Augustinegrass and aggressive wild weeds, such as Johnsongrass, to act as permanent breeding grounds and reservoirs that fuel its spread.<\/p>\n\n\n\n<figure class=\"wp-block-image aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"681\" src=\"https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-4-1024x681.jpg\" alt=\"\" class=\"wp-image-1164\" srcset=\"https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-4-1024x681.jpg 1024w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-4-300x200.jpg 300w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-4-768x511.jpg 768w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-4-1536x1022.jpg 1536w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-4-2048x1362.jpg 2048w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><figcaption class=\"wp-element-caption\">Fig. 4. Pasture mealybug damage on grass. (Photo credits: Nicole F. Quinn and Issac Esquivel, University of Florida.<\/figcaption><\/figure>\n\n\n\n<figure class=\"wp-block-image aligncenter size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"609\" height=\"342\" src=\"https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-5.jpg\" alt=\"\" class=\"wp-image-1165\" srcset=\"https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-5.jpg 609w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-5-300x168.jpg 300w\" sizes=\"auto, (max-width: 609px) 100vw, 609px\" \/><figcaption class=\"wp-element-caption\">Fig. 5. Pasture mealybug damage on sugarcane. Photo credit: De-fen Mou, University of Florida.<\/figcaption><\/figure>\n\n\n\n<h2 class=\"wp-block-heading\">Damage<\/h2>\n\n\n\n<p>Damage from the immature nymph stage of the pasture mealybug manifests as a destructive combination of sap extraction, toxic saliva injection, and secondary infections by pathogens such as Fusarium. Early signs of an infestation appear within roughly one week, mimicking drought or nutrient stress as leaves begin yellowing at the tips, stunting overall growth, and producing a sticky honeydew that promotes black sooty mold.<\/p>\n\n\n\n<p>Symptoms vary distinctly by host: forage and pasture grasses, especially limpograss, bermudagrass, and bahiagrass, experience profound stunting accompanied by severe red or purple leaf discoloration that rapidly gives way to dead patches and catastrophic &#8220;pasture dieback&#8221; (Fig. 4); conversely, sugarcane primarily responds with widespread leaf yellowing and extensive regressive death of tillers without turning red (Fig. 5). Meanwhile, across all hosts, the insects actively target hidden areas including the undersides of leaves, plant crowns, and root systems.<\/p>\n\n\n\n<figure class=\"wp-block-image aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"768\" src=\"https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-6-1024x768.jpg\" alt=\"\" class=\"wp-image-1166\" srcset=\"https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-6-1024x768.jpg 1024w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-6-300x225.jpg 300w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-6-768x576.jpg 768w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-6-1536x1152.jpg 1536w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-6-2048x1536.jpg 2048w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><figcaption class=\"wp-element-caption\">Fig. 6. Mated female of pasture mealybug on grass. Photo credits: Nicole F. Quinn and Issac Esquivel, University of Florida.<\/figcaption><\/figure>\n\n\n\n<p><em><strong>Based on their feeding and the damage they cause to pasture grasses, the following symptoms or scenarios are suspected in turfgrass: <\/strong><\/em>When the pasture mealybug colonizes managed turfgrasses such as St. Augustinegrass or bermudagrass, its subterranean, dense-thatch feeding habits trigger severe secondary cosmetic and structural problems. The immature nymphs continuously excrete sugary, sticky honeydew onto the lower shoots and thick thatch layer, creating an ideal breeding environment for black sooty mold fungus to coat the blades, block photosynthesis, and leave a dark, &#8220;toasted&#8221; or burnt look across the lawn. Simultaneously, the combination of physical sap depletion and toxic saliva injection severely stunts root systems, leaving turfgrass vulnerable to secondary soil-borne pathogens such as Fusarium root rot, which rapidly decompose weakened crowns. As these compounding issues thin out the yard and cause patchy dieback, opportunistic broadleaf weeds face zero pressure from the grass-specialist pest, allowing them to aggressively overgrow the vacant, dying patches of turfgrass.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Monitoring<\/h2>\n\n\n\n<p>Monitoring the pasture mealybug requires physical field scouting because no commercially available pheromone traps, lures, or effective color-attraction sticky cards are available for this species. Because the destructive nymphs and adult females are wingless crawlers that live subterraneanly or deep within the dense turfgrass thatch, they are likely to be unresponsive to traditional yellow or blue overhead sticky traps. To confirm an infestation, you must first look for the stark visual contrast of yellowing, purpling, or dying grass patches sitting immediately adjacent to perfectly healthy, green, immune legumes like clover. Instead of inspecting completely dead grass, which the pests actively abandon, you should target the stressed grass at the margins of a dying patch by pulling back the canopy to perform leaf-flip inspections for tiny, white, waxy insects on the lower leaf undersides. Because these pests heavily colonize hidden structures, checking for secondary signs like heavy ant trails and black sooty mold fungus on the lower stems, or using a trowel to execute a root and thatch excavation, remains the only definitive way to expose the white, powdery residue and clusters of bugs actively feeding on the root zone.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">Management<\/h2>\n\n\n\n<p>Proper identification is the most important first step. If you suspect pasture mealybug, send the samples to your local county agents, who can help with identification. <strong><em><u>To date, there is no confirmed record of pasture mealybug in Georgia.<\/u><\/em><\/strong><\/p>\n\n\n\n<p>Because the early stages of pasture mealybug occur in the soil, reducing the thatch layer with verti-cutting may help reduce population size. Avoiding over-fertilizing can reduce the new flush of succulent grass tissue that would otherwise accelerate mealybug reproduction. Thus, precise nitrogen may be necessary. Additionally, maintaining a strict mowing height at the upper end of the turf species&#8217; recommended range encourages deep, robust root architecture that can withstand subterranean sap feeding, while practicing deep, infrequent irrigation would allow the soil surface to dry out and become inhospitable to moisture-loving nymphs. Establishing rigorous equipment sanitation protocols, such as power-washing mowers and aerators between locations, helps prevent the accidental transfer of waxy crawlers and egg masses from infested lawns to clean properties. They could hitchhike via our clothing material (Fig. 7) and spread to new areas.<\/p>\n\n\n\n<figure class=\"wp-block-image aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"682\" src=\"https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-7-1024x682.jpg\" alt=\"\" class=\"wp-image-1167\" srcset=\"https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-7-1024x682.jpg 1024w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-7-300x200.jpg 300w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-7-768x511.jpg 768w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-7-1536x1022.jpg 1536w, https:\/\/site.caes.uga.edu\/entomologyresearch\/files\/2026\/07\/Fig.-7-2048x1363.jpg 2048w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><figcaption class=\"wp-element-caption\">Fig. 7. Pasture mealybug hitchhiking on clothing. Photo credit: Nicole F. Quinn and Issac Esquivel, University of Florida.<\/figcaption><\/figure>\n\n\n\n<p>There is no insecticide registered specifically for pasture mealybug on turfgrass. Based on research activities in TX and FL pastures, imidacloprid and thiamethoxam were effective in reducing all stages of pasture mealybug. More research is warranted before recommending other insecticides at this time. If you suspect mealybug in turfgrass as pasture mealybug, please report it to your local UGA Extension Agent. <\/p>\n\n\n\n<h2 class=\"wp-block-heading\">References<\/h2>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Brookes, H. M. (1978). A new species of <em>Heliococcus<\/em> \u0160ulc from Australia and Pakistan and a redescription of <em>Heliococcus<\/em> glacialis (Newstead) Comb. N. (Homoptera: Pseudococcidae). <em>Australian Journal of Entomology<\/em>, <em>17<\/em>(3), 241\u2013245. <a href=\"https:\/\/doi.org\/10.1111\/j.1440-6055.1978.tb00151.x\">https:\/\/doi.org\/10.1111\/j.1440-6055.1978.tb00151.x<\/a><\/li>\n\n\n\n<li>Garc\u00eda Morales, M., Denno, B. D., Miller, D. R., Miller, G. L., Ben-Dov, Y., &amp; Hardy, N. B. (2016). ScaleNet: A literature-based model of scale insect biology and systematics. <em>Database<\/em>, <em>2016<\/em>, Article baw118. <\/li>\n\n\n\n<li>Aca-Mart\u00ednez, E. A., Hern\u00e1ndez-Ju\u00e1rez, A., &amp; Arredondo-Bernal, H. C. (2025). <em>Heliococcus summervillei<\/em> Brookes (Hemiptera: Pseudococcidae), a new potential pest of sugarcane in North America. <em>Southwestern Entomologist<\/em>, <em>50<\/em>(4), 1011\u20131014. <\/li>\n\n\n\n<li>Powell, E. C., &amp; Hauxwell, C. (2026). <em>Pasture mealybug, Heliococcus summervillei Brookes (Hemiptera: Coccomorpha: Pseudococcidae), a serious invasive pest of pasture grass, turf grass, and sugarcane, has been detected in Florida, USA<\/em> (Pest Alert). Florida Department of Agriculture and Consumer Services, Division of Plant Industry. <a href=\"https:\/\/www.fdacs.gov\/Agriculture-Industry\/Pests-and-Diseases\/Plant-Pests-and-Diseases\/Pasture-Mealybug\">https:\/\/www.fdacs.gov\/Agriculture-Industry\/Pests-and-Diseases\/Plant-Pests-and-Diseases\/Pasture-Mealybug<\/a><\/li>\n\n\n\n<li>Hauxwell, C. (2018, January). <em>Mealybugs and pasture dieback: Technical note<\/em>. Queensland University of Technology. https:\/\/doi.org\/10.13140\/RG.2.2.24502.87369<\/li>\n\n\n\n<li>Xu, H., Humpal, J. A., Wilson, B. A. L., Ash, G. J., &amp; Powell, K. S. (2024). Mealybug Population Dynamics: A Comparative Analysis of Sampling Methods for&nbsp;<em>Saccharicoccus sacchari<\/em>&nbsp;and&nbsp;<em>Heliococcus summervillei<\/em>&nbsp;in Sugarcane (<em>Saccharum<\/em>&nbsp;sp. Hybrids).&nbsp;<em>Insects<\/em>,&nbsp;<em>15<\/em>(7), 492. https:\/\/doi.org\/10.3390\/insects15070492<\/li>\n<\/ul>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Pasture mealybug (Heliococcus summervillei) has not yet been confirmed in Georgia. The pasture mealybug (Heliococcus summervillei) (Fig. 1) is a destructive, invasive sap-sucking insect native to South and Southeast Asia that has recently emerged as a threat to agriculture in the United States. After first becoming a serious pasture pest in Queensland, Australia, in 1928, [&hellip;]<\/p>\n","protected":false},"author":499,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-1158","post","type-post","status-publish","format-standard","hentry","category-fall-armyworm"],"_links":{"self":[{"href":"https:\/\/site.caes.uga.edu\/entomologyresearch\/wp-json\/wp\/v2\/posts\/1158","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/site.caes.uga.edu\/entomologyresearch\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/site.caes.uga.edu\/entomologyresearch\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/site.caes.uga.edu\/entomologyresearch\/wp-json\/wp\/v2\/users\/499"}],"replies":[{"embeddable":true,"href":"https:\/\/site.caes.uga.edu\/entomologyresearch\/wp-json\/wp\/v2\/comments?post=1158"}],"version-history":[{"count":6,"href":"https:\/\/site.caes.uga.edu\/entomologyresearch\/wp-json\/wp\/v2\/posts\/1158\/revisions"}],"predecessor-version":[{"id":1183,"href":"https:\/\/site.caes.uga.edu\/entomologyresearch\/wp-json\/wp\/v2\/posts\/1158\/revisions\/1183"}],"wp:attachment":[{"href":"https:\/\/site.caes.uga.edu\/entomologyresearch\/wp-json\/wp\/v2\/media?parent=1158"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/site.caes.uga.edu\/entomologyresearch\/wp-json\/wp\/v2\/categories?post=1158"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/site.caes.uga.edu\/entomologyresearch\/wp-json\/wp\/v2\/tags?post=1158"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}