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1 December 2002 OLD TRAPS FOR NEW WEEVILS: NEW RECORDS FOR CURCULIONIDS (COLEOPTERA: CURCULIONIDAE), BRENTIDS (COLEOPTERA: BRENTIDAE) AND ANTHRIBIDS (COLEOPTERA: ANTHRIBIDAE) FROM JEFFERSON CO., FLORIDA
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Abstract

Trapping studies using three different types of traps placed in several wild and cultivated habitats in North Florida (Jefferson Co.) produced 97 different species of adult weevils in the family Curculionidae and the closely related primitive families Anthribidae, Brentidae and Ithyceridae. Sixty-one of 97 species trapped have not been reported previously from Jefferson Co. Furthermore, seven species of Curculionidae are first records for the state, with four of these being important agricultural pests (Hypera meles, H. nigrirostris, H. punctata and Sitona lineatus). In addition, some weevils taken in our traps represent undescribed species of Apteromechus, Cercopeus and Conotrachelus. Herein we include: (1) an alphabetical listing of species collected in these traps, (2) a description and illustration of the traps used, and (3) months of the year and generalized habitats where traps were placed and specimens were collected. Information on host associations is provided for many species.

Weevils (Coleoptera: Curculionidae) are extremely important insects as plant pests and as beneficial biological control agents for noxious weeds. More than 863 genera and 7,000 species currently are recognized in North America (O’Brien & Wibmer 1982). Native species such as the plum curculio, Conotrachelus nenuphar (Herbst), and the cosmopolitan maize weevil, Sitophilus zeamais (Motschulsky), feed on everything from agronomic and fruit crops to stored products. Thousands of foreign species, particularly from the Caribbean and southeast Asia, are potential invaders of the United States, following the pattern of such destructive exotic pests as the boll weevil, Anthonomus grandis grandis Boheman, and the recently detected Myllocerus undatus Marshall in Florida (C. W. O., unpublished data).

The Florida beetle fauna is one of the most diverse in North America, given the many tropical species entering south Florida from the West Indies (Peck & Thomas 1998). In the most recent distributional checklist for the Coleoptera of Florida (Peck & Thomas 1998) the authors indicate that close to 18% (or ≈ 825 species) belong to the superfamily Curculionoidea (as defined in Alonso-Zarazaga & Lyal 1999). Some of the species can be very abundant at particular sites and times of the year and, as such, can be collected with relative ease. An example of this is the Fuller rose beetle, Naupactus cervinus (Boheman) (R. F. M., unpublished data). However, many Curculionoidea are cryptic and nocturnally active, and collecting them can prove difficult. As a result, exotic pest weevils entering the state may remain undetected for many years until their population builds-up to economically important levels.

We conducted a series of trapping studies over a period of nine years (1993-2001) in several wild and cultivated habitats in North Florida near the town of Monticello. Three different types of traps previously reported as effective for capturing a variety of economically important weevils (Tedders & Wood 1994, Mizell & Tedders 1999) were tested for their ability to capture other species. Ninety-seven different species of adult weevils, Curculionidae, and the closely related primitive families Anthribidae, Brentidae and Ithyceridae (as treated in Alonso-Zarazaga & Lyal 1999) were collected. In this paper we include: (1) a table with information on all of the species collected, (2) months of the year when specimens were collected, (3) descriptions and photographs of the traps used, and (4) information on host associations for most species. Our results are discussed in the context of the importance of visual cues for weevils and the use of traps in early detection of pest weevil introductions.

Materials and Methods

Sites

Traps were placed in various wild and cultivated habitats on the grounds of the University of Florida, North Florida Research and Education Center in Monticello, FL, which is located in Jefferson County about 16 km S of the Florida-Georgia state line. Different traps or trap combinations were placed in pecan (PCN) (Carya illinoiensis) and peach (PCH) (Prunus persica) orchards and in small plantings of Japanese persimmon (PSN) (Diospyros kaki) (Table 1). These cultivated areas are interspersed with several wet woodland sites (WD) containing tree species that are typical for North Florida, including slash pine (Pinus elliottii), loblolly pine (P. taeda), longleaf pine (P. palustris), tupelo or black gum (Nyssa sylvatica), sweet gum (Liquidambar styraciflua), water oak (Quercus nigra), red oak (Quercus rubra) and shagbark hickory (Carya ovata) (USDA 1989). In addition, other weedy, forage and ornamental plant species were present in the surrounding habitats. Among these were mixed bahia-grass (Paspalum notatum), vetch (Vicia sativa), red clover (Trifolium pratense), rabbit-eye blueberries (Vaccinium ashei), Lantana camara, and Sesbania spp.

Traps. Three types of traps were tested for their ability to capture weevils. We used two active pyramidal-shaped traps (Fig. 1a and Fig. 1b) similar (equal dimensions) to those described in Tedders and Wood (1994) and Mizell and Tedders (1999). Trap bodies were manufactured from 1.3 cm thick masonite and painted black (Ace® acrylic flat latex house paint #103A105) or safety yellow (Glidden® alkyd industrial formula #4540). The screen cone and collecting cylinder components of the boll weevil trap (Anonymous 1990) were used to capture the adult weevils in the black traps, while the window screen top collection device described by Mizell and Tedders (1995) was used to capture the weevils in the yellow pyramidal trap. In this manuscript we refer to the black pyramidal trap as a Tedders trap (T in Table 1) and the yellow pyramidal trap as a Stinkbug trap (SB) (after Mizell & Tedders 1995). The third trap used was a passive Circle trap (C) (Fig. 1c), made of aluminum insect screening, similar to the one described by Mulder et al. (2000) to capture the pecan weevil and the plum curculio in Oklahoma. As above for the Tedders trap, a boll weevil trap top was modified to fit the top of the circle trap to capture adult weevils.

The total number of traps of each type varied from year to year, but at no time were fewer than 20 traps of each type present in the field. Tedders, Stinkbug and Circle traps were placed in all habitats except for peach orchards, which did not receive Circle traps. All traps were unbaited and were serviced 1-3 times per week throughout the course of the study. Trap tops were emptied, cleaned of debris and replaced. Captured insects were preserved in 95% ethyl alcohol and brought back to the laboratory, where a representative series of all weevils from each trap were mounted and labeled. Taxonomic determinations to species were made by C.W.O. Trap(s), habitat(s) and month(s) of the year when each species of weevil was collected were summarized, and the information is presented in Table 1. Species for which host associations are provided in the text are indicated in Table 1, as are the species that have been introduced into North America.

Results and Discussion

Ninety-seven species of adult Curculionidae and the closely related primitive families Anthribidae, Brentidae and Ithyceridae were collected in our traps from 1993-2001 (Table 1). The preponderance of species collected was advanced weevils (89 species), with only six species of Anthibidae, one species of Brentidae and the one species of Ithyceridae being captured. Table 1 indicates the species for which host associations are provided in the text (see below under First records from Florida and Host Associations). Host information was not available for 21 species of Curculionidae. Sixty-one (or almost 63%) of the species captured have not been reported previously from Jefferson Co., FL (* in Table 1) and seven species are first records for the state (** in Table 1) (see earlier list in Peck & Thomas 1998). More importantly, four of the first time records for Florida are for species that are important agricultural pests in other parts of the United States (Hypera meles, H. nigrirostris, H. punctata and Sitona lineatus). Some weevils collected in our traps represent undescribed species belonging to Apteromechus, Cercopeus and Conotrachelus. The taxonomic descriptions of the new species will be published elsewhere.

Several economically important species captured in our traps have had a number of taxonomic name changes over the past five decades, which can cause confusion when searching the literature for pest information. We believe it is useful to list some of these names here in order to aid researchers in their studies of these weevils. The anthribid weevil, Araecerus coffeae (Fabricius), was known as A. fasciculatus DeGeer until 1994, when Zimmerman published notes on the long ignored synonymy of this widespread stored product pest (Zimmerman 1994). However, there is controversy over this synonymy and, as such, the name changes may continue for this important pest species. The vegetable weevil, Listroderes difficilis Germain, has been called L. costirostris Schoenherr, which is actually a distinct Argentine species known in the United States only from California and Arizona (O’Brien & Wibmer 1982). The Fuller rose beetle, Naupactus cervinus (Boheman), has been introduced into many countries from its home in Argentina, including into the United States (Lanteri et al. 2002). It has been placed in and referred to as belonging to the genera Aramigus, Asynonychus, Pantomorus and Naupactus, the latter in which it is currently placed (Alonso-Zarazaga & Lyal 1999). In addition, its specific name has several junior synonyms that have been used in older literature, including Aramigus fulleri (Horn), Asynonychus godmanni (Crotch), Pantomorus olindae (Perkins) and Naupactus simplex Pascoe. Finally, Naupactus peregrinus (Buchanan) is another species still referred to under several different genera including Graphognathus and Pantomorus. It is important that researchers be aware of all names used for the species they investigate if they wish to make use of earlier research studies regarding life history, distribution, control options or information on natural enemies. Sources of such names are found most often in catalogs or checklists, as well as in revisions and monographs of many groups of economically important insects.

First records for Florida

1) A single adult of Acanthoscelidius curtus (Say) was found on 19 May 1995 in a Stinkbug trap placed in a peach orchard. We continued to have Stinkbug traps at this location, however, no other specimens of this species were collected. Blatchley and Leng (1916) report it as occurring on Polygonum sp. in swamps in New York. Polygonum spp. (Polygonaceae) are commonly known as knotweeds and grow in marshes, swamps, wet forests and ditches. Acanthoscelidius curtus is found in South Carolina, Kentucky, Virginia and North Carolina, as well as in the north eastern and north central United States (O’Brien & Wibmer 1982). Two other species of Acanthoscelidius, A. acephalus (Say) and A. mendicus (Dietz), are listed as occurring in north Florida (Peck & Thomas 1998) but were not collected in our study. Most Acanthoscelidius species breed in evening primrose (Oenothera spp.) (C. W. O., unpublished data).

2) We collected specimens of Brachystylus acutus (Say) in Tedders and Circle traps placed in pecan and Japanese persimmon orchards. Very few specimens were obtained (8 total) and these collections occurred from April to June in 2000 and in June 2001. Blatchley and Leng (1916) call this species the gray persimmon weevil (although this is not an approved ESA common name, ESA 1997) and report that it has been collected from hickory and persimmon and swept from low herbage. They suggest that it probably is found wherever persimmon is grown. Brachystylus acutus is found in Georgia, Alabama, Kentucky, Mississippi, North Carolina, South Carolina, the northeastern states, and Missouri. No other species of Brachystylus are reported to occur in the United States (O’Brien & Wibmer 1982).

3) We collected 40 adults of Cryptorhynchus woodruffi Sleeper mostly from woodland habitats in Tedders and Circle traps. Two adults were captured in traps placed in pecan orchards and one in a peach orchard. The first specimen was found in May 1999 and additional collections were made in 2000 and 2001. Sleeper (1955) described the male and female of C. woodruffi collected at Cranberry Bog, Buckeye Lake, Ohio in June 1953, however, no information on host associations were provided for the species.

4-6) Three of the new Florida records that are important agricultural pests belong to the genus Hypera, and include Hypera meles (Fabricius) (the clover head weevil), H. nigrirostris (F.) (the lesser clover weevil) and H. punctata (F.) (the clover leaf weevil). These species are native to the Old World but have been reported from the southeastern United States (O’Brien & Wibmer 1982). Hypera meles has been reported to feed on alfalfa (= lucerne), red, zigzag and crimson clovers and black medik. Hypera nigrirostris feeds on alsike, white, red, crimson and zigzag clovers, alfalfa and black medik, while H. punctata feeds on red, crimson and white clovers, alfalfa and Jerusalem artichoke (Helianthus tuberosus) in Europe (Titus 1911). We collected ten H. meles from Tedders traps placed in a pecan orchard in September 1993. Specimens of H. nigrirostris were found in both Tedders and Stinkbug traps placed in pecan and peach orchards, respectively. A few specimens also were collected in Tedders traps located in forested habitats adjacent to the orchards. These weevils were collected in July 1993 and May 1995. Adults of H. punctata were taken from the same traps and habitats as H. nigrirostris, but were collected during September and November 1993, August and November of 1994 and in June 2001. The genus Hypera is primarily Palearctic in distribution (Puttler et al. 1973), although seventeen species are listed as occurring in North America, six of which are introduced from Europe (O’Brien & Wibmer 1982). Until now, only two species of Hypera, H. postica (Gyllenhal) and H. compta (Say), were listed as occurring in Florida (Peck & Thomas 1998). Hypera postica, the alfalfa weevil, is an immigrant from Europe and a major pest of alfalfa and other legumes (Puttler et al. 1973), and H. compta is semiaquatic and breeds externally on leaves of Polygonum in Florida (C.W.O., unpublished data).

7) Nineteen Sitona lineatus (Linneaus), the pea leaf weevil, adults were collected in Tedders (11 specimens), Stinkbug (4) and in Circle traps (4) placed in pecan, peach and Japanese persimmon orchards. Specimens were collected from February-June and in September and December from 1996-2001. This is the first record for S. lineatus in the southeastern United States. C. W. O. has since collected additional specimens in Tallahassee, FL. It previously had been reported to occur in Idaho, Oregon, Washington and in British Columbia, Canada, where it is a serious pest of edible legumes, especially peas, Pisum sativum (Schotzko & Quisenberry 1999). Hoebeke and Wheeler (1985) also collected it in coastal areas of Virginia. Bright (1994) reports it as occurring on peas, beans, sweet peas, alfalfa, various varieties of clover, bird’s foot trefoil, wild and cultivated vetch, chickpea (Cicer arietinum) and thrashed oats. Of the twenty species of Sitona present in North America, four are reported to occur in the southeastern United States. With this new state record for S. lineatus, all four species are now reported as occurring in Florida (O’Brien & Wibmer 1982, Peck & Thomas 1998).

First records for Jefferson County

Fifty-four species trapped during this study are first records for Jefferson County (designated with * in Table 1). When the seven new weevil records for the state are included, the number of species new to Jefferson County increases to 61. The list includes seven species of Conotrachelus, six Curculio, three each of Cryptorhynchus and Cophes, two each of Chalcodermus, Eudiagogus, Myrmex, Sitona, Sphenophorus, and Tyloderma, and one species each of Acalles, Anthonomus, Aphrastus, Atrichonotus, Cyrtepistomus, Geraeus, Hypera, Listroderes, Madarellus, Ochyromera, Odontocorynus, Odontopus, Pandeleteius, Pheloconus, Phyrdenus, Pissodes, Pseudomus, and Tanymecus. Three species of Anthribidae and one each of Brentidae and Ithyceridae are also new records for Jefferson Co.

Host associations for weevils collected during this study (see above for 1st state records)

Anthribidae. Araecerus coffeae (F.), the coffee bean weevil, is a well-known pest of coffee beans, but larvae can develop in seeds of many kinds of plants (Zimmerman 1994). Brachycorynus rectus (LeConte) has been reared from Celtis laevigatus, black locust and dead wood of sugar maple (Valentine 1998). Euparius marmoreus (Olivier) feeds on several species of polypore fungi (Trametes hirsutus, T. versicolor, Megasporoporia setulosa, Trichaptum biforme, T. abietinus, T. sector, Phlebia hydnoides, Panis rudis and Pereniporia medulla-panis) (Valentine 1998). Goniocloeus bimaculatus (Olivier) has been collected on Biscogniauxia sp. fungus on winter-killed sugar maple, on Xylaria sp. and Diatrype sp. fungi and has been also been found under bark of dead oaks (Valentine 1998). Adults and larvae of Piesocorynus mixtus LeConte eat pyrenomycete fungi of the order Sphaeriales, families Zylariaceae and Diatrypaceae (Valentine 1998). Toxonotus cornutus (Say) has been found boring in persimmon (Diospyrus sp.), and has been collected from Prosopis and oak seedlings (Valentine 1998).

Brentidae. Arrenodes minutus (Drury) occurs beneath the bark of recently felled or dying oak, poplar and beech trees (Blatchley & Leng 1916).

Ithyceridae. Ithycerus noveboracensis (Forster) is associated with trees from the families Betulaceae (Carpinus caroliniana, Betula populifolia), Juglandaceae (Juglans cinerea, Carya cordiformis, C. ovata) and Fagaceae (Fagus grandifolia, Castanea dentata, Quercus alba, Q. macrocarpa, Q. bicolor, Q. coccinea, Q. prinus, Q. ellipsoids & Q. borealis). Large numbers of adults occasionally are taken from fruit trees in the family Rosaceae, such as apple (Malus sylvestris), plum (Prunus americana) and peach (Sanborne 1981).

Curculionidae. The larvae of Anthonomus quadrigibbus Say feed around the core of apple, pear and haw (Crataegus sp.) but are rarely very injurious. They have also been collected from flowers of red haw, Crataegus, and hazel, shadebush (Amelanchier), and various fruit trees (Blatchley & Leng 1916). Apteromechus ferratus (Say), as well as other species of Apteromechus, breed in twigs and branches of many hardwood trees and shrubs (C. W. O., unpublished data). Atrichonotus taeniatulus (Berg) feeds on a variety of plants, with a preference for Leguminosae. Host plants for this species include lucern, subterranean clover, bean, hibiscus, dahlia, rose, eucalyptus, sunflower and roots of grasses (Lanteri & O’Brien 1990). Bagous magister LeConte is commonly collected feeding on water lily (Nymphaea odorata) (C. W. O., unpublished data). Chalcodermus aeneus Boheman, the cowpea curculio, infests field peas, string beans, soybean, lima bean, cotton and strawberry. Several leguminous weeds, including vetch, also are hosts (Blatchley & Leng 1916).

Schoof (1942) and references cited therein, report that larvae of Conotrachelus affinis Boheman attack nuts of Juglandaceae (pignut, shagbark, mockernut and bitternut hickory). Conotrachelus anaglypticus (Say) is considered an economic pest of peach and larvae have been reported to attack cotton bolls (Gossypium hirsutum), and the cambium and inner bark of several fruit and shade trees (apple, pear, pignut hickory, American hornbeam, sweet birch, American beech, American chestnut, white, chestnut, and red oak, tulip tree, service berry, red maple, tupelo, flowering dogwood and sourwood), as well as columbine (Aquilegia), cowpea, Japanese plum, mulberry elm and Crataegus. Conotrachelus aratus (Germar) attack several species of Juglandaceae (pecan, bitternut, shagbark and pignut hickory), while C. carolinensis Schoof attacks peaches and has been collected in cotton fields. Pheloconus cribicollis (Say), formerly in the genus Conotrachelus, have been collected on Pinus palustris, cotton, Ambrosia and peach while C. elegans (Say) has been reported on Pinus rigida, and feeding on leaves and nuts of various species of Juglandaceae (pecan, mockernut and pignut hickory) as well as on plum and cotton. They have been found breeding in galls caused by Phylloxera on leaves of hickory and pecan. Conotrachelus geminatus LeConte have been bred from flowerheads of beggar-tick (Bidens) and giant ragweed (Ambrosia trifida). Conotrachelus hicoriae Schoof attack the nuts of pecan and peach. Conotrachleus naso LeConte breed in the fruit of hawthorn (Crataegus sp.), and in acorns of post, live, white and chestnut oaks and other species of Fagaceae, and on cotton and on dogwood. Conotrachelus nenuphar (Herbst), the plum curculio, has been reported from plum, cherry, peach, nectarine, apple, wild crabapple, pear and quince. In addition, huckleberry, grape, strawberry, currant, gooseberry and persimmon are listed as occasional hosts. Conotrachelus posticatus Boheman breeds in acorns of various species of Quercus (Schoof 1942). Conotrachelus similis Boheman breeds in the berries of wooly buckthorn (Bumelia lanuginosa) (Blatchley & Leng 1916).

Cophes fallax (LeConte) can be found when sifting the soil under beech logs, and it breeds in dead limbs of hickory and dead stems of Cassia (Blatchley & Leng 1916). Cossonus corticola Say occurs under the bark of pine and is reported to feed on pine, while C. impressifrons Boheman occurs under bark of butternut, sycamore, oak, chestnut and other hardwood trees (Blatchley & Leng 1916). Cryptorhynchus fuscatus LeConte breeds in dead branches of hardwood trees, while C. minutissimus LeConte has been extracted from dead branches of pecan (C. W. O., unpublished data).

Seven species of Curculio were captured in our traps. Gibson (1969) reports that the pecan weevil, Curculio caryae (Horn) breeds in most species of the genus Carya (pecan, hickory). Curculio fulvus Chittenden has been found breeding exclusively in live oak (Q. virginiana). Curculio sulcatulus (Casey) has been found breeding in 29 species of oaks (Quercus), preferring the acorns of the red oak group of species, and is the only Curculio reported infesting Q. mohriana. Curculio proboscideus (Fabricius) attacks 21 species of oaks, while C. pardalis (Chittenden) has been reported from 18, C. longidens Chittenden from 11 and C. humeralis (Casey) from 13 Quercus species. In addition, C. pardalis is the only Curculio found attacking Quercus robur and Q. chapmani, while C. humeralis is the only Curculio listed as attacking Quercus margaretta (Gibson 1969).

Cyrtepistomus castaneus (Roelofs), the Asiatic oak weevil, attacks many species of woody plants but seems to prefer oak and chestnut. The larval stage is a root feeder, while the adults attack the leaves. Eubulus bisignatus (Say) breeds in twigs and branches of many hardwood trees and shrubs (C. W. O., unpublished data). Eubulus parochus Herbst was reportedly beaten from elm and found under the bark of butternut. Larvae mine the inner bark and wood of weakened and decayed walnut (Blatchley & Leng 1916). Eudiagogus maryae Warner has been found feeding on and defoliating species of Sesbania, Cassia and Daubentonia, while E. rosenschoeldi Fahraeus are associated almost exclusively with three species of Sesbania, S. vesicaria (bagpod sesbania), S. drummondii (Drummond rattlebox) and S. exaltata (hemp sesbania) (Warner 1979). Hylobius pales (Herbst), the pales weevil, is an important pest of new pine and Christmas tree plantations throughout eastern North America (Fettig & Salom 1998). Listroderes apicalis Waterhouse is a pest of beets (Beta vulgaris), sunflower (Helianthus annus) and wheat (Triticum aestivum) (Lanteri et al. 2002). The host list for Listroderes difficilis Germain, the vegetable weevil, includes bean, beet, burdock, cabbage, carrot, cauliflower, celery, chard, Chinese cabbage, garlic, head cabbage, kale, lettuce, mustard, mustard cabbage, onion, pepper, peanut, potato, radish, rape, spinach, tomato, turnip and sweet potato. Cultivated flowers attacked include pansy, petunia, poppy, phlox and verbena. The principal weed hosts include dandelion, mallow, milk thistle, mustard, wild aster, wild radish and wild parsnip (High 1939). Madarellus undulatus (Say) occurs on wild grape, poison ivy and Virginia creeper and bores in the latter (Blatchley & Leng 1916). Myrmex dichrous (LeConte) breeds in dead fronds of palmetto and Sabal palms (C. W. O., unpublished data), while M. floridanus (Casey) has been collected from oak and Bumelia (Peck & Thomas 1998). Naupactus cervinus (Boheman), the Fuller rose beetle, is injurious to citrus trees and ornamentals such as rose and geranium (Lanteri et al. 2002). The larvae of Naupactus peregrinus (Buchanan) are serious pests of many crops and ornamental plants in the southeastern United States. Ochyromera ligustri Warner breeds in fruits of Ligustrum (C. W. O., unpublished data). Odontocorynus salebrosus (Casey) has been swept from huckleberry and collected from Asclepias and Achillea lanulosa (Blatchley & Leng 1916). The larvae of Odontopus calceatus (Say) mine the leaves of sassafras and Liriodendron (Blatchley & Leng 1916). Pachnaeus opalus (Olivier) has been collected from crabapple and on Irish juniper (C. W. O., unpublished data). Like the pales weevil, Pachylobius picivorus (Germar), the pitch-eating weevil, is an important pest of new pine and Christmas tree plantations throughout eastern North America (Fettig & Salom 1998). Pandeleteius hilaris (Herbst) has been reported from the leaves of oak, hickory and chestnut as well as from beech, smart-weed and Ceanothus (Howden 1959). Phyrdenus divergens (Germar) occurs on black night-shade (Solanum nigrum) (Blatchley & Leng 1916). Pissodes nemorensis Germar, the Eastern pine weevil, attacks the trunks of young trees of Virginia pine, Pinus virginiana.

Sitona californius Fahraeus has been recorded from native lupine (Lupinus polyphyllus), Ceanothus divaricata and from a variety of plants including plum, peach, crabapple, alfalfa, apple, wild sunflower, Lotus scoparius and Eleocharis macrostachya (Bright 1994). Sitona hispidulus (F.) occurs on various forage legumes, alfalfa and varieties of clover (Bright 1994). Sitona lineellus (Bonsdorff) occurs mainly on alfalfa but also can be found on vetch, several varieties of clover, peas, alsike and many garden plants (Bright 1994). The rice weevil, Sitophilus oryzae (L.), and the maize weevil, S. zeamais Motschulsky are cosmopolitan pests of wheat, maize, oats, barley, sorghum, buckwheat, rye, rice, stored cotton, table beans and cashew nuts. Adults are reported to burrow into grapes, apples, and pears (Lanteri et al. 2002). The rice weevil is so called only because rice is the food on which it was first described. Sphenophorus cariosus (Olivier) generally feeds on rushes and sedges but has proven destructive to corn. The horned or beaked rush (Rhynchospora corniculata) is the preferred host, although it occurs in several species of Cyperus and Scirpus (Vaurie 1951). Sphenophorus coesifrons Gyllenhal has been collected from centipede grass (C.W.O., unpublished data), and adults can damage corn and are injurious to rice (Vaurie 1951). Sphenophorus inaequalis (Say) is reported from Bermuda grass (Cynodon dactylon) (Vaurie 1951). Tanymecus lacaena (Herbst) feeds on ragweed (Ambrosia artemisiifolia) (C.W.O., unpublished data). Tyloderma foveolatum (Say) breeds in the stems of evening primrose (Oenothera biennis) and the cut-leaved primrose (O. laciniata); it has also been reported as feeding on corn stalks and ripe strawberries (Wibmer 1981). Several life stages of T. variegatum (Horn) were collected from lizard’s tail (Saururus cernuus) by Wibmer (1981).

Trap Mode of Action

Active Tedders and Stinkbug traps and passive Circle traps have been used previously to capture many economically important weevils (Sherman & Mizell 1995, Tedders & Wood 1995, Tedders et al. 1996, Stansly et al. 1997, Prokopy & Wright 1998), as well as other selected Coleoptera (Braman et al. 2002). However, we know of no earlier study where these traps have captured as many species of weevils as we report herein. Furthermore, Mizell and Tedders (1999) and Mizell et al. (2002) used baited Tedders traps to study the behavioral response to visual and olfactory cues in H. pales and Pachylobius picivorus, two pests of Christmas trees in Florida. Unlike the Tedders and Stinkbug traps, which function as silhouette mimicking structures when placed on the ground, the Circle trap is normally attached to the tree bole where it acts as a passive funnel that captures insects walking up the bole of the tree.

Raney and Eikenbary (1968) reported that 60-80% of pecan weevil adults emerging from their pupal cells (in the soil under pecan trees) reach the tree bole by walking rather than flying. Similar behavior has been observed in many weevils that attack fruit trees or that feed on the tender new growth of their host trees (e. g., Diaprepes abbreviatus (L.) on citrus). Availability of all of these food resources (young nuts, fruits and tender foliage) is highly variable in time and space (Hunter & Lechowicz 1992). Yields in fruit and nut trees and the timing of citrus growth flushes are genetically programmed but are highly plastic, allowing for modification in their expression through interaction with the environment. For example, pecan is an alternate bearing nut tree with cycles of high and low nut production, which vary for individual trees (Wood & McMeans 1981, Sparks 1991).

Presumably in response to the unpredictability in the nut resource, the pecan weevil has evolved a two and partial three-year life cycle, and adults tend to aggregate year after year on those trees with the highest yield of nuts. We hypothesize that the walking behavior exhibited by the pecan weevil is an adaptation that enhances the probability that emerging adults will return to the tree of their larval development, which over evolutionary time would be those trees with the highest yield of nuts. As such, we would expect the pecan weevil, as well as other weevils that use the bole as a visual cue to locate host trees after emergence, to be captured in either the silhouette mimicking traps or in traps attached to the tree trunk. Our examination of the host associations for the weevils captured during our study suggests that the preponderance of species captured are associated with tree species found in the study area. However, this hypothesis does not explain the capture of species that breed in weedy hosts or that pupate in their host plant. Nevertheless, we have demonstrated that active pyramidal (Tedders & Stinkbug) and passive Circle traps are valuable tools for capturing rare weevils and to monitor for economically important weevil immigrants.

Acknowledgments

We thank Cheryl Manasa, Ryan Mizell and Charlie Riddle for their help in servicing and maintaining traps and Dr. Lois O’Brien for labeling most of the weevils. We thank M. Oraze, M. Thomas, S. Reitz, and K. Bloem, for their helpful suggestions on earlier versions of this manuscript. We thank the USDA-APHIS Science Fellows Program for funding to support Dr. Stephanie Bloem. The research of Dr. Charles W. O’Brien was supported in part by a grant, FLAX 97007, CSREES, USDA (Cooperative State Research Education and Extension Service, U.S. Department of Agriculture). Contribution of the Florida Agricultural Experiment Station Journal Series number R-08903.

References Cited

  1. M. A. Alonso-Zarazaga and C. H C. Lyal . 1999. A world catalogue of families and genera of Curculionoidea (Insecta: Coleoptera) (excepting Scolytidae and Platypodidae). Entomopraxis, S.C.P., Barcelona, Spain. 315 pp.  Google Scholar

  2. Anonymous 1990. The boll weevil trap: an eradication tool. Fact Sheet. USDA-APHIS. 1 pp.  Google Scholar

  3. W. S. Blatchley and C. W. Leng . 1916. Rhynchophora or weevils of North Eastern America. The Nature Publishing Company, Indianapolis, IN. 682 pp.  Google Scholar

  4. K. Braman, B. L. Sparks, W. L. Tedders, R. F. Mizell III, and W. G. Hudson . 2002. Effects of trap color and bait type on collections of Coleoptera in pyramid traps in commercial nurseries. J. Entomol. Sci. Submitted. Google Scholar

  5. D. E. Bright 1994. Revision of the genus Sitona (Coleoptera: Curculionidae) of North America. Ann. Entomol. Soc. America 87::277–306. Google Scholar

  6. Entomological Society of America 1997. Common names of insects and related organisms. Entomol. Soc. America, Lanham, MD. 232 pp.  Google Scholar

  7. C. J. Fettig and S. M. Salom . 1998. Comparisons of two trapping methods for Hylobius pales (Coleoptera: Curculionidae) in Virginia. Environ. Entomol. 27::572–577. Google Scholar

  8. L. P. Gibson 1969. Monograph of the genus Curculio in the New World (Coleoptera: Curculionidae). Part I. United States and Canada. Misc. Pub. Entomol. Soc. America. 6::240–285. Google Scholar

  9. M. M. High 1939. The Vegetable Weevil. U.S. Department of Ag. Circ. # 530. 26 pp.  Google Scholar

  10. E. R. Hoebeke and A. G. Wheeler Jr. . 1985. Sitona lineatus (L.), The pea leaf weevil: first records in eastern North America (Coleoptera: Curculionidae). Proc. Entomol. Soc. Washington 87::216–220. Google Scholar

  11. A. T. Howden 1959. A revision of the species of Pandeleteius Schonherr and Pandeleteinus Champion of America North of Mexico (Coleoptera: Curculionidae). Proc. California Acad. Sci. 29::361–421. Google Scholar

  12. A. F. Hunter and M. J. Lechowicz . 1992. Predicting the timing of budburst in temperate trees. J. Appl. Ecol. 29::597–604. Google Scholar

  13. A. A. Lanteri and C. W. O’Brien . 1990. Taxonomic revision and cladistic analysis of Atrichonotus Buchanan (Coleoptera:Curculionidae). Trans. American Entomol. Soc. 116::697–725. Google Scholar

  14. A. A. Lanteri, A. E. Marvaldi, and S. M. Suarez . 2002. Gorgojos de la Argentina y sus plantas huespedes. Tomo I: Apionidae y Curculionidae. Soc. Entomol. Argentina. Special Publication 1. San Miguel de Tucuman. 98 pp.  Google Scholar

  15. R. F. Mizell III and W. L. Tedders . 1995. A new monitoring method for detection of the stinkbug complex in pecan orchards. Proc. Southeastern Pecan Growers Assoc. 88::36–40. Google Scholar

  16. R. F. Mizell III and W. L. Tedders . 1999. Evaluation of trap type and color for monitoring Hylobius pales and Pachylobius picivorus in Florida. Florida Entomol. 82::615–624. Google Scholar

  17. R. F. Mizell III, F. W. Martin, and W. L. Tedders . 2002. Visual and odor cues affect trap efficiency for Hylobius pales (Herbst), Pachylobius picivorus (Germar) (Coleoptera: Curculionidae) and Xylotrechus sagitattus (Germar) (Coleoptera: Cerambycidae). Canadian Entomol. Submitted. Google Scholar

  18. P. J. Mulder, B. D. McGraw, W. Reid, and R. A. Grantham . 2000. Monitoring adult weevil populations in pecan and fruit trees in Oklahoma. Oklahoma State University Extension Facts. F-7190: 1-8.  Google Scholar

  19. C. W. O’Brien and G. J. Wibmer . 1982. Annotated checklist of the weevils (Curculionidae sensu lato) of North America, Central America, and the West Indies (Coleoptera: Curculionoidea). Mem. American Entomol. Inst. #34. Ann Arbor, MI. 382 pp.  Google Scholar

  20. S. B. Peck and M. C. Thomas . 1998. A distributional checklist of the beetles (Coleoptera) of Florida. Volume 16. Arthropods of Florida and neighboring land areas. Florida Dept. of Agriculture and Consumer Services, DPI, Gainesville, FL. 180 pp.  Google Scholar

  21. R. J. Prokopy and S. E. Wright . 1998. Plum curculio (Coleoptera: Curculionidae) response to unbaited pyramid and cone traps. J. Econ. Entomol. 91::226–234. Google Scholar

  22. B. Puttler, S. E. Thewke, and R. E. Warner . 1973. Bionomics of three Nearctic species, one new, of Hypera (Coleoptera:Curculionidae), and their parasites. Ann. Entomol. Soc. America 66::1299–1306. Google Scholar

  23. H. G. Raney and R. D. Eikenbary . 1968. Investigations on flight habits of the pecan weevil, Curculio caryae (Coleoptera: Curculionidae). Canadian Entomol. 100::1091–1095. Google Scholar

  24. M. Sanborne 1981. Biology of Ithycerus noveboracensis (Forster) (Coleoptera) and weevil phylogeny. Evol. Mon. 4::1–209. Google Scholar

  25. H. F. Schoof 1942. The genus Conotrachelus DeJean (Coleoptera, Curculionidae) in the North Central United States. Contr. Entomol. Lab. University of Illinois. 223::1–170. Google Scholar

  26. D. J. Schotzko and S. S. Quisenberry . 1999. Pea leaf weevil (Coleoptera: Curculionidae) special distribution in peas. Environ. Entomol. 28::477–484. Google Scholar

  27. W. Sherman and R. F. Mizell III . 1995. Pachneaus spp. root weevils in Florida peach. Proc. Florida St. Hort. Soc. 108::348–349. Google Scholar

  28. E. L. Sleeper 1955. New Ohio Rhynchophora (Coleoptera: Curculionidae). I. The Ohio J. Sci. 55::54–60. Google Scholar

  29. D. Sparks 1991. Geographical origin of pecan cultivars influences the time required for fruit development and nut size. J. American Hort. Soc. 116::627–631. Google Scholar

  30. P. Stansly, R. F. Mizell III, and C. McCoy . 1997. Monitoring Diaprepes abbreviatus with Tedders traps in southwest Florida citrus. Proc. Florida St. Hort. Soc. 110::22–26. Google Scholar

  31. W. L. Tedders and B. W. Wood . 1994. A new technique for monitoring pecan weevil emergence (Colepotera: Curculionidae). J. Entomol. Sci. 29::18–30. Google Scholar

  32. W. L. Tedders and B. W. Wood . 1995. Pyramidal traps for monitoring the presence of pecan weevil (Coleoptera: Curculionidae). J. Entomol. Sci. 30::534–544. Google Scholar

  33. W. L. Tedders, R. F. Mizell III, and B. W. Wood . 1996. Influence of trap color on pecan weevil monitoring. J. Entomol. Sci. 31::414–419. Google Scholar

  34. E. G. Titus 1911. The genus Hypera and Phytonomus (Coleoptera: Family Curculionidae) in America north of Mexico. Ann. Entomol. Soc. America 4::383–494. Google Scholar

  35. USDA-Soil Conservation Service 1989. Soil survey of Jefferson County, Florida. United States Department of Agriculture. Soil Conservation Service. 193 pp.  Google Scholar

  36. B. D. Valentine 1998. A review of Nearctic and some related Anthribidae (Coleoptera). Insecta Mundi 12::251–312. Google Scholar

  37. P. Vaurie 1951. Revision of the genus Calendra (formerly Sphenophorus) in the United States and Mexico (Coleoptera, Curculionidae). Bull. American Mus. Nat. Hist. 98::33–186. Google Scholar

  38. R. E. Warner 1979. The genus Eudiagogus (Coleoptera: Curculionidae: Leptopiinae), with two new species on the weed Sesbania (Leguminosae). Proc. Entomol. Soc. Washington 81::304–320. Google Scholar

  39. G. J. Wibmer 1981. Revision of the new world weevil genus Tyloderma in America north of Mexico (Coleoptera: Curculionidae: Cryptorhynchinae). Southwestern Entomol. Supplement 3. 95 pp.  Google Scholar

  40. B. W. Wood and J. L. McMeans . 1981. Carbohydrate changes in various organs of bearing and nonbearing pecan trees. J. American Hort. Soc. 106::758–761. Google Scholar

  41. E. C. Zimmerman 1994. Australian weevils (Coleoptera: Curculionoidea). Volume 1. Anthribidae to Attelabidae. CSIRO, Australia 741 pp.  Google Scholar

Appendices

Fig. 1a. Black (Tedders) pyramidal-shaped trap with modified insect collecting top

i0015-4040-85-4-632-f01.gif

Fig. 1b. Yellow (Stinkbug) pyramidal-shaped trap with modified insect collecting top

i0015-4040-85-4-632-f02.gif

Fig. 1c. Circle trap

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Table 1.

Summary of trapping results in Jefferson County, Florida where three different types of traps were evaluated for their ability to capture weevils in several wild and cultivated habitats from 1993-2001. The traps used were black Tedders traps (T), yellow Stinkbug traps (SB) and Circle traps (C). The first column indicates the family (F) to which each species belongs (Anthribidae (A), Brentidae (B), Ithyceridae (I) or Curculioniade (C)) and whether the capture represents a new record for Jefferson County (*) or for the state of Florida (**). Intro ? indicates whether or not the species is exotic to North America. An “x” in the column for Host info ? indicates whether additional host association information is provided in the text

i0015-4040-85-4-632-t01.gif
Stephanie Bloem, Russell F. Mizell, and Charles W. O’Brien "OLD TRAPS FOR NEW WEEVILS: NEW RECORDS FOR CURCULIONIDS (COLEOPTERA: CURCULIONIDAE), BRENTIDS (COLEOPTERA: BRENTIDAE) AND ANTHRIBIDS (COLEOPTERA: ANTHRIBIDAE) FROM JEFFERSON CO., FLORIDA," Florida Entomologist 85(4), 632-644, (1 December 2002). https://doi.org/10.1653/0015-4040(2002)085[0632:OTFNWN]2.0.CO;2
Published: 1 December 2002
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