
Triungulin larvae of Nemognathinae found in flowers or attached to the hairs of bees are sometimes mistaken for those of Rhipiphoridae. In both groups, the body is navicular and heavily sclerotized and there is a definite pattern of setation. Nemognathine larvae are distinctive in having one to two (not four to five) stemmata on each side of the head, an ecdysial line on the thorax, and no pulvilli (bladderlike appendages).

Keys to genera for adult beetles and triungulin larvae are given in references (Arnett 1960) and (MacSwain 1956), respectively. Adults of most of the Florida species are described by Enns and Werner (Enns 1956, Werner 1945).

In the first instar or triungulin (T) phase the larva reaches its feeding site on its own (most Meloinae) or is carried there by an adult bee, to which the larva attaches from a flower (Meloini (not in Florida) and Nemognathinae). After feeding to repletion, the larva, with ecdysis, becomes scarabaeiform and enters a period of rapid growth (first grub phase, FG) that lasts until the end of instar five or six. In some species that prey on bees the FG larva uses only a single cell; in others it digs into nearby cells and devours their contents. In Meloinae the fully fed FG larva generally excavates a chamber apart from the feeding site. In instar six or seven, the larva typically becomes heavily sclerotized and immobile (coarctate phase, C). In this phase the musculature undergoes profound degeneration and respiration is reduced to an extremely low level, permitting survival for more than a year, if necessary. When development resumes the muscles regenerate and, with ecdysis, the larva once again becomes scarabaeiform (second grub phase, SG); at this point it may or may not excavate a pupal chamber. Nemognathinae are unusual in that the SG larva and following pupa and adult are encapsulated by the cast but intact skins of the last instar FG larva and the C larva.
Several alternative developmental pathways have been identified. In response to high temperature, many Epicauta larvae pupate directly from the FG phase or fail to diapause in the C phase; both patterns are conducive to multivoltinism. Rarely, a larva pupates directly from the C phase. Presumably in response to adverse environmental conditions, larvae of several genera of Meloinae can return to the C phase after reaching the SG phase. Most species pass the winter or dry season as coarctate larvae; a few do so as diapausing eggs, triungulin larvae, or adults.
Adults commonly live three months or more. Females typically mate and oviposit periodically throughout their adult lives.
The blistering agent is cantharidin, an odorless terpene (exo-1,2-cis-dimethyl-3,6-ep- oxyhexahydro-phthalic anhydride) occurring elsewhere only in beetles of the family Oedemeridae (Arnett 1984). Cantharidin or cantharides (dried, pulverized bodies of adult beetles) was once employed extensively in human and veterinary medicine, primarily as a vesicant and irritant and is still used in the U.S. as the active ingredient in a proprietary wart remover. Taken internally or absorbed through the skin, cantharidin is highly toxic to mammals. There is an extensive literature dealing with its reputed aphrodisiacal properties and numerous reports of human poisonings, both accidental and deliberate. Cantharides is sometimes specified as the Eurasian Spanishfly, Lytta vesicatoria (Linnaeus); however, other genera, particularly Mylabris and Epicauta, have been more commonly used, especially for extraction of cantharidin. Recorded cantharidin content of adult beetles (by dry weight) ranges from less than 1% to a high of 5.4%. Biological synthesis and function have been largely neglected. It is widely assumed that cantharidin confers chemical protection from predators, but there is little evidence for this. In at least some species, females receive large quantities of cantharidin from males during copulation. In any case, females incorporate the material in a coating applied to the eggs.
Cases of fatal poisonings of valuable horses in Florida, Oklahoma, Tennessee, and Texas by ingestion of blister beetles trapped in baled alfalfa hay (Mackay and Wollenman 1981, Schoeb and Panciera 1979) have revived interest in the pathology of cantharidin toxicosis and led to the development of a highly sensitive technique for detection of the compound (Ray et al. 1979). Poisonings have been traced to adults of Epicauta occidentalis Werner and, possibly, E. temexa Adams & Sel. Neither species occurs in Florida, but a close relative (the striped blister beetle, E. vittata (Fabricius)) and three other species of the genus (the clematis blister beetle, E. fabricii (LeConte); the black blister beetle, E. pennsylvanica (De Geer); and the margined blister beetle, E. pestifera Werner) occur in alfalfa fields here and pose a potential threat if horse owners turn to locally grown alfalfa as a source of hay. Research is available to indicate the amount of cantharidin levels present in common species, as well as the estimated number of beetles necessary to provide a lethal dose to horses (Sansome 2002).
Insect Management Guide: Vegetables
Insect Management Guide: Field Crops and Pastures
Pyrota limbalis LeConte. Washington, D.C., south to Highlands County, Florida. One record at light.
P. lineata (Olivier). Northern Florida, including the panhandle, south to Polk County. August-October. Several Compositae and Gerardia (Scrophulariaceae).
P. mutata (Gemm.). Northern Florida, including the panhandle, south to Polk County. Cicuta, Daucus, Eryngium, and several other Umbelliferae.
P. sinuata (Olivier). Coastal Plain from Mississippi to North Carolina; south in Florida to Highlands County. Gerardia (Scrophulariaceae).
Lytta polita Say. Georgia border south to Charlotte and Highlands counties. December-June. Has been taken in large numbers at lights.
Epicauta batesi Horn. Coastal Plain from New Jersey to Alabama; south in Florida to Polk County
E. excavatifrons Maydell. Coastal Mississippi and Alabama and south in Florida to Marion County. September-October. Recorded twice from grass.
E. fabricii (LeConte) - the ashgray blister beetle. Northern Florida, including the panhandle, south to Highlands County. April-May. Commonly on Leguminosae, including alfalfa, Baptisia, bean, pea, and sweetclover; sometimes attacks potato and glandless cotton. Often taken at lights.
E. floridensis Werner. Primarily coastal, from Texas and Oklahoma to New Jersey; probably statewide in Florida. Ipomoea (Convolvulaceae), Schrankia (Leguminosae), and (in captivity) Solanum (Solanaceae).
E. heterodera Horn. Coastal Mississippi to Georgia and south in Florida to Osceola County. September-November. Helenium and other Compositae.
E. pennsylvanica (De Geer) - the black blister beetle. Alachua, Leon, and Marion counties. Wide variety of plants, including many Compositae, Chenopodium (Chenopodiaceae), and such crops as alfalfa, beet, and potato.
E. pestifera Werner - the margined blister beetle. Northern Florida, including the panhandle, south to Indian River County Many Leguminosae and Solanaceae, including alfalfa, beet, egg plant, potato, soybean, and tomato.
E. sanguinicollis Horn. Alachua, Citrus, Sumter, and Brevard counties. Recorded in the literature only from Florida, but I have two specimens labeled "Savannah, Georgia." July and October. Compositae, Schrankia (Leguminosae), and cotton.
E. strigosa (Gyll.). Coastal Plain from Mississippi to New Jersey; probably statewide in Florida. Principally on Compositae, Opuntia (Cactaceae), Ipomoea (Convolvulaceae), and Vigna (Leguminosae). Common.
E. tenuis (LeConte). Described from an unspecified locality in Georgia and subsequently recorded in Florida from Baker and Volusia counties south to Highlands County. May-June.
E. torsa (LeConte). Oklahoma and east Texas, east on the Coastal Plain to Georgia and north to Massachusetts; probably statewide in Florida. April-June. Ilex (Aquifoliaceae), Sapindus (Sapindaceae), and Albizzia, Amorpha, and Robinia (Leguminosae).
E. vittata (Fabricius)- the striped blister beetle. Represented in Florida, where it occurs commonly throughout the state except for the Keys, by the "lemniscate" or southeastern coastal race (Adams and Selander 1979). March-May. Wide variety of plants, including Amaranthus (Amaranthaceae) and such crops as alfalfa, bean, beet, cotton, potato, and tomato. Attracted to lights.
Tetraonyx quadrimaculata (Fabricius). Trinidad, Lesser Antilles, Puerto Rico, Hispaņola, and the U.S. Coastal Plain from northern Florida (Alachua and Putnam counties) to Alabama and North Carolina. Convolvulaceae (Ipomoea) and Leguminosae (Bradburya, Coelosia) in the U.S. and these families and Bignoniaceae, Euphorbiaceae, and Verbenaceae in the West Indies. Reported damaging grapefruit flowers in Puerto Rico.
Nemognatha nemorensis Hentz. North Florida, south to Pinellas and Brevard counties. Several Compositae, including Bidens, Erigeron, Heterotheca, and, particularly, Rudbeckia.
N. piazata Fabricius. Represented in Florida by the nominate race (Mississippi to West Virginia south), which occurs statewide, including the Keys. Cirsium and Tetraognotheca (Compositae).
N. punctulata LeConte. Bahama and Cayman islands, Cuba, Jamaica, and the southeastern U.S. Recorded in Florida only from the Keys and Dade County. Bidens and "thistle" (Compositae). Not common.
Zonitis cribricollis (LeConte). Widely distributed in Florida, south to Dade County Achillea, Coreopsis, Helianthus, and Rudbeckia (Compositae). Rare.
Z. vittigera (LeConte). Represented in Florida, where it occurs south to Highlands County, by the nominate, eastern race. Numerous Compositae and Psoralea (Leguminosae).
Pseudozonitis longicornis (Horn). Kansas and east Texas east along the Coastal Plain to South Carolina; recorded in Florida from Highlands County south to the Keys. March-Jul. At lights. Rare.
P. pallida Dillon. Oklahoma and east Texas east to Florida, where it extends south through Dixie and Alachua counties to Hillsborough County. At lights. Not common.
P. schaefferi (Blatch.). A taxonomically isolated species known only from Florida (Pinellas, St. Johns, and Volusia counties) and Myrtle Beach, South Carolina (Kirk 1969). February-May.
Author: Richard B. Selander, Department of Genetics and Development, University of Illinois
at Urbana-Champaign; and Thomas R. Fasulo, University of Florida
Originally published as DPI Entomology Circular 268. Updated for this publication.
Photographs: Division of Plant Industry; John L. Capinera, University of Florida; and Samuel Grubb
Project Coordinator: Thomas R. Fasulo, University of Florida
Publication Number: EENY-166
Publication Date: October 2000. Latest revision: August 2003.
Copyright 2000-2003 University of Florida
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