Evaluation of extended-life pheromone formulations used with and without dichlorvos for boll weevil (Coleoptera: Curculionidae) trapping

Boll weevil traps baited with a ComboLure (25 of mg grandlure + 30 mg of eugenol + 90 of mg dichlorvos [DDVP]), an extended-release lure (25 mg of grandlure + 30 mg of eugenol + 60 of mg DDVP kill-strip), and extended-release lure with no DDVP were evaluated for boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), captures in South Texas cotton, Gossypium hirsutum L., fields during February-March 2005 and March-April 2006. The traps were serviced once a week for five consecutive weeks by using the same methodology as active boll weevil eradication programs. Mean captured boll weevils from extended-release lures with no DDVP were significantly higher in five of 10 trapping weeks compared with captures of the ComboLure and extended lure. Weekly mortality of boll weevils captured was similar for the ComboLure (72.6 +/- 4.7%) and extended lure + DDVP (73.5 +/- 4.0%), and both were significantly higher than the extended lure (32.8 +/- 5.0%) with no DDVP. The presence or absence of DDVP did not significantly affect the sex ratio of field-captured boll weevils. We found no functional reasoning for using DDVP in large scale trapping of boll weevils regardless of the formulation or presentation in the trap. We conducted two additional trapping evaluations after the 2005 and 2006 studies, but the numbers of boll weevils captured were too low for statistical comparisons, indicating that boll weevil eradication is reducing populations in the Rio Grande Valley of Texas.     

Boll weevil (Coleoptera: Curculionidae) bait sticks: toxicity and malathion content

Assays of malathion content and toxicity to boll weevil, Anthonomus grandis grandis Bohemian, were conducted on boll weevil bait sticks, now marketed as Boll Weevil Attract and Control Tubes (BWACTs; Plato Industries, Houston, TX). In general, the longer BWACTs were in the field, the lower the mortality of weevils that were exposed to them. Bioassays of weevil mortality correlated with hexane washes of BWACT surfaces showed highly variable mortality when surface malathion fell below approximately 20 ng per 1 microl of hexane, but consistently high mortality (> or = 90%) when surface malathion was above 30 ng per 1 microl of hexane. A linear equation was calculated to predict mortality as a function of malathion on a BWACT surface. Although mortality was related to surface amounts of malathion, it was unrelated to the total amount of malathion present in BWACTs. Similarly, surface malathion was unrelated to the total amount present in BWACTs. As with mortality, amount of surface malathion declined with time, but total malathion did not decline with time. Boll weevils placed on fresh BWACTs tended to accumulate more malathion and died in greater numbers as time spent on fresh tubes increased, but not as time spent on tubes aged in the field (for 5 mo total) increased. Weevils that landed on tubes after a short flight died in approximately the same numbers as those that were placed on tubes using proper methodology. The amount of malathion expected to cause 90% mortality of boll weevils subjected to proper methodology was 47% higher than for a less stringent methodology (34.3 versus 23.4 ng), which demonstrates the importance of strictly adhering to proper methodology; nevertheless, chemical assay of malathion on the BWACT surface proved to be a more consistent measure of BWACT toxicity than bioassay, and it should replace the bioassay.     

Grandlure dosage and attraction of boll weevils (Coleoptera: Curculionidae)

The effects of grandlure dosage on of boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), attraction were assessed. Traps collected more boll weevils under field and laboratory conditions as the amount of grandlure in laminated plastic strips was increased from 0 to 10, 30, and 60 mg. Spreading the point source of the lure by cutting the strip into quarters and positioning each quarter on separate corners of the large capacity trap to create an expanded source for the pheromone plume, however, resulted in fewer trap captures than traps with quartered lures all positioned on a single corner. The large capacity trap with the quartered lure on one corner also caught more weevils than the traps with an intact lure fastened to one corner. Although aging lure strips for three weeks reduced emissions of the four pheromone components and their attractiveness to boll weevils, cutting the aged lure into quarters resulted in greater emissions and attraction than lures that were aged intact or as quarters. Some pheromone components volatilized faster than others, resulting in time-related changes in blend ratios, but the underlying factor in boll weevil attraction to grandlure strips was dosage, the amount of volatilized pheromone available for interacting with an adult boll weevil.     

Effects of routine late-season field operations on numbers of boll weevils (Coleoptera: Curculionidae) captured in large-capacity pheromone traps

Flat and cylindrical adhesive boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), pheromone traps captured significantly more (P < or = 0.05) boll weevils than the Hercon (Hercon Environmental, Emigsville, PA) trap during the late cotton-growing season, and larger adhesive areas were associated with higher captures; a flat plywood board collected the most boll weevils because it had the largest surface area. The flat board trap, chosen for measuring large late-season adult boll weevil populations common to the Lower Rio Grande Valley of Texas in 2000 and 2001, collected more (P < or = 0.05) weevils when deployed in proximity to natural and cultivated perennial vegetation, and mean numbers of captured boll weevils were higher (P < or = 0.0001) on the leeward sides of the board traps than on the windward sides. The board trap had an estimated potential capacity of approximately 27,800 boll weevils, and the large capacity of the board trap allowed for more accurate measurements of large adult boll weevil populations than the more limited Hercon trap. Measurement of adult boll weevil numbers after the routine field operations of defoliation, harvest, shredding, and stalk-pulling, demonstrated that large populations of boll weevils persist in cotton fields even after the cotton crop has been destroyed. Increases (P < or = 0.05) in the percentage variation of trapped boll weevils relative to the numbers collected just before each field operation were observed after defoliation, harvest, shredding, and stalk-pulling, but the percentage variations followed a quadratic pattern with significant correlation (P < 0.0001; 0.59 < adjusted r2 < 0.73). Numbers of adult boll weevils caught on board traps deployed at 15.24-m intervals on windward and leeward edges of cotton fields suggested that boll weevil populations in flight after field disturbances might be affected by large-capacity trapping.     

Boll weevil (Coleoptera: Curculionidae) survival through cotton gin trash fans

There is concern that cotton gins may serve as loci for reintroduction of boll weevils, Anthonomus grandis grandis Boheman, to eradicated or suppressed zones when processing weevil-infested cotton from neighboring zones. Previous work has shown that virtually all weevils entering the gin in the seed cotton will be removed before they reach the gin stand. Those not killed by the seed cotton cleaning machinery will be shunted alive into the trash fraction, which passes through a centrifugal trash fan before exiting the gin. The objective of this study was to determine survival potential of boll weevils passed through a trash fan. Marked adult weevils were distributed in gin trash and fed through a 82.6-cm (32.5-in.) diameter centrifugal fan operated across a range of fan-tip speeds. A small number of boll weevils were recovered alive immediately after passage through the fan, but all were severely injured and did not survive 24 h. In another experiment, green bolls infested with both adult- and larval-stage weevils were fed through the fan. Several teneral adults survived 24 h, and there was no evidence that fan-tip speed affected either initial survival of weevils, or the number of unbroken boll locks that could harbor an infesting weevil. Thus, designating a minimum fan-tip speed for ensuring complete kill is not possible for the boll weevil. Experiments suggest that a device installed in a gin that partially crushes or cracks bolls open before entering a trash fan will increase mortality, possibly enough that further precautions would be unnecessary.     

Efficacy of diatomaceous earth to control internal infestations of rice weevil and maize weevil (Coleoptera: Curculionidae)

Densities of 10, 20, and 30 hard red winter wheat kernels, Triticum aestivum L., were infested with different life stages of the rice weevil, Sitophilus oryzae (L.), mixed with 35 g of wheat treated with 300 ppm of the Protect-It (Mississauga, Ontario, Canada) formulation of diatomaceous earth (DE), and held at 22, 27, and 32 degrees C. A similar test was conducted by exposing densities of 6, 12, and 18 corn kernels infested with different life stages of the maize weevil, Sitophilus zeamais Motschulsky, mixed with 30 g of corn, Zea mays L., treated with 300 ppm of DE. Mortality of adults emerging from kernels in wheat treated with DE was always greater than controls, and ranged from 56 to 90% at 22 degrees C and was >90% at 27 and 32 degrees C. In most treatment combinations, exposure to DE suppressed F1 progeny by 60-90% relative to untreated controls. Mortality of adult maize weevils on treated corn held at 22 and 27 degrees C was lower than mortality of rice weevils on wheat, and ranged from 4 to 84%. F1 production was low in corn held at 22 degrees C, and no F1s were produced in either the controls or the treatments at 32 degrees C. In treated corn held at 27 degrees C, exposure to the DE suppressed F1 progeny by approximately 70-80% relative to the untreated controls. Results of this study show that rice weevils and maize weevils emerging from infested kernels as adults are susceptible to DE, and these results are comparable to other studies in which adult weevils were exposed directly on wheat or corn treated with DE. Although adult weevils will be killed by exposure to DE, some oviposition could still occur and progeny suppression may not be complete; however, application of DE to commodities already infested with internal feeders, such as the rice weevil and the maize weevil, could help eliminate or suppress the infestation.     

Naturally-occurring biological control of the boll weevil [Col.: Curculionidae]

Red imported fire ants,Solenopsis invicta Buren, are effective predators of the boll weevil,Anthonomus grandis Boheman, in east Texas cotton fields. Boll weevils caused no economic loss in 11 years due to mortality attributed primarily to ants. Removal of the ants resulted in an increase in crop damage by the boll weevil. Insecticides used for cotton pests greatly reduce the abundance of the ants. To capitalize on this effective predation of boll weevils by ants, unnecessary applications of insecticides should be eliminated.     

Susceptibility of the boll weevil to Steinernema riobrave and other entomopathogenic nematodes

The susceptibility of the boll weevil (BW), Anthonomus grandis Boheman, to Steinernema riobrave and other nematode species in petri dishes, soil (Hidalgo sandy clay loam), and cotton bolls and squares was investigated. Third instar weevils were susceptible to entomopathogenic nematode (EN) species and strains in petri dish bioassays at 30 degrees C. Lower LC(50)'s occurred with S. riobrave TX- 355 (2 nematodes per weevil), S. glaseri NC (3), Heterorhabditis indicus HOM-1 (5), and H. bacteriophora HbL (7) than H. bacteriophora IN (13), S. riobrave TX (14), and H. bacteriophora HP88 (21). When infective juveniles (IJs) of S. riobrave were applied to weevils on filter paper at 25 degrees C, the LC(50) of S. riobrave TX for first, second, and third instars, pupae, and 1-day-old and 10-days-old adult weevils were 4, 5, 4, 12, 13, and 11IJs per weevil, respectively. The mean time to death, from lowest to highest concentration, for the first instar (2.07 and 1.27days) and second instar (2.55 and 1.39days) weevils were faster than older weevil stages. But, at concentrations of 50 and 100IJs/weevil, the mean time to death for the third instar, pupa and adult weevils were similar (1.84 and 2.67days). One hundred percent weevil mortality (all weevil stages) occurred 3days after exposure to 100IJs per weevil. Invasion efficiency rankings for nematode concentration were inconsistent and changed with weevil stage from 15 to 100% when weevils were exposed to 100 and 1IJs/weevil, respectively. However, there was a consistent relationship between male:female nematode sex ratio (1:1.6) and nematode concentration in all infected weevil stages. Nematode production per weevil cadaver increased with increased nematode concentrations. The overall mean yield of nematodes per weevil was 7680IJs. In potted soil experiments (30 degrees C), nematode concentration and soil moisture greatly influenced the nematode efficacy. At the most effective concentrations of 200,000 and 400,000IJs/m(2) in buried bolls or squares, higher insect mortalities resulted in pots with 20% soil moisture either in bolls (94 and 97% parasitism) or squares (92 and 100% parasitism) than those of 10% soil moisture in bolls (44 and 58% parasitism) or squares (0 and 13% parasitism). Similar results were obtained when nematodes were sprayed on the bolls and squares on the soil surface. This paper presents the first data on the efficacy of S. riobrave against the boll weevil, establishes the potential of EN to control the BW inside abscised squares and bolls that lay on the ground or buried in the soil.     

Killing power of the red imported fire ant [Hym.: Formicidae]: a key predator of the boll weevil [Col.: Curculionidae]

The red imported fire ant,Solenopsis invicta Buren, was identified as a key predator of the boll weevil,Anthonomus grandis Boheman. Although key factor analysis does not guarantee that the key factor is the causative agent, the evidence of boll weevil mortality was so clear that the fire ant could be identified as causing the mortality. Ant predation on immature boll weevils during the summer of 1981 averaged 84%. When this predation was combined with other natural mortality factors, the weevil population density throughout the season never exceeded levels that required control measures.     

Temperature-dependent development and reproduction of the boll weevil (Coleoptera: Curculionidae)

Abstract Effects of temperature on development, survival, and fecundity of boll weevil, Anthonomus grandis grandis Boheman, were assessed at 10, 11, 12, 15,20,25,30,35,45, and 46 °C; 65% relative humidity; and a photoperiod of 13:11 (L: D) h. The mortality of boll weevil immature stages was 100% at 12°C and decreased to 36.4% as the temperature increased to 25°C. When the temperature increased from 30 °C to 45 °C, the mortality of weevils also increased from 50.1% to 100%. From 15°C to 35°C, the bollweevilpreimaginal development rate was linearly related to temperature. The average development time of total boll weevil immature lifestages decreased 3.6-fold and the preovipositional period decreased 3.3-fold when the temperature was increased from 15°C to 30°C. The lower threshold for development was estimated at 10.9, 6.6, 7.0, and 9.0 °C for eggs, larval, pupal, and total immature stages, respectively, with total thermal time requirement to complete immature stages of 281.8 DD (degree day) (15°C) and 247.8 DD (35 °C). At 1LC and 46°C, weevil females did not oviposit. Longevity of adult females decreased 4.6-fold with increasing temperatures from 15°C to 35°C. Fecundity increased with increasing temperatures up to 30°C and significantly decreased thereafter. These findings will be useful in creating a temperature-based degree-day model for predicting the occurrence of key life stages in the field. An accurate predictor of a pest's development can be very important in determining sampling protocols, timing insecticide applications, or implementing an integrated pest management control strategy targeting susceptible life stages.     

Ecology and phenology of the boll weevil (Coleoptera: Curculionidae) on an unusual wild host, Hibiscus pernambucensis, in southeastern Mexico.

The phenology and ecology of Hibiscus pernambucensis Arruda and its interaction and importance in maintaining populations of the boll weevil, Anthonomus grandis Boheman, were studied over a period of 3 yr in the Soconusco Region of the state of Chiapas, Mexico. H. pernambucensis is a small tree of Neotropical distribution, restricted to lowland areas, and generally associated with halophytic vegetation. This species is found exclusively along the shores of brackish estuaries, in or near mangrove swamps in southeastern Mexico. In this region, H. pernambucensis has a highly seasonal flowering pattern in which the greatest bud production occurs shortly after the start of the rainy season in May and the highest fruit production occurs in July and August. Boll weevil larvae were found in buds of H. pernambucensis during all months but February and densities of buds and weevils were highest from May through September. The percentage of buds infested with boll weevil larvae rarely exceeded 30%. Because plant densities and reproductive output of H. pernambucensis is relatively low and, consequently, the number of oviposition and larval development sites for boll weevils is limited, the importance of this plant as a source of boll weevils with potential of attacking commercial cotton is minimal in comparison with the quantity produced in cultivated cotton. However, the plant could be important as a reservoir of boll weevils in areas of boll weevil quarantine and eradication programs. The factors and circumstances that may have led to this apparent recent host shift of the boll weevil in this region are discussed.     

Sublethal effects of malathion on boll weevil (Coleoptera: Curculionidae) fecundity when maintained on cotton squares or artificial diet

Mated 3‐day‐old female boll weevils, Anthonomus grandis grandis Boheman, reared from field‐infested cotton (Gossypium hirsutum L.) squares were topically treated with an estimated LD₅₀ of malathion (2 μg) to assess its effects on fecundity, oviposition, and body fat condition. Two different food sources, cotton squares and artificial diet, were assessed in malathion‐treated and nontreated (control) weevils. The LD₅₀ caused ～50% mortality in the square‐fed malathion treatment, but the artificial diet‐fed malathion‐treated weevils were less susceptible. LD₅₀ survivors fed on the squares produced ≥ 9 times more chorionated eggs in the ovaries and oviposited ≥ 19‐fold more than survivors fed artificial diet, regardless of the malathion treatment. Boll weevils that survived a 2 μg LD₅₀ malathion and also fed squares were ～4.5‐fold leaner than diet‐fed weevils. Our findings demonstrate that non‐resistant boll weevils surviving a sublethal dose of malathion will reproduce without any delay or significant loss in fecundity, and the food source for which boll weevils are maintained when conducting these assays will directly affect the results. The significance of these findings and how they are related to the final stages of eradicating the boll weevil from the US are discussed.     

Common subtropical and tropical nonpollen food sources of the boll weevil (Coleoptera: Curculionidae)

It is known that substantial boll weevil, Anthonomus grandis grandis Boheman, individuals can survive mild subtropical winters in some habitats, such as citrus orchards. Our study shows that endocarp of the fruit from prickly pear cactus, Opuntia engelmannii Salm-Dyck ex. Engel.; orange, Citrus sinensis L. Osbeck.; and grapefruit, Citrus paradisi Macfad., can sustain newly emerged adult boll weevils for >5 mo, which is the duration of the cotton-free season in the subtropical Lower Rio Grande Valley of Texas and other cotton-growing areas in the Western Hemisphere. Cotton, Gossypium hirsutum L., and the boll weevil occur in the same areas with one or all three plant species (or other citrus and Opuntia species that might also nourish boll weevils) from south Texas to Argentina. Although adult boll weevils did not produce eggs when fed exclusively on the endocarps of prickly pear, orange, or grapefruit, these plants make it possible for boll weevils to survive from one cotton growing season to the next, which could pose challenges to eradication efforts.     

Survival of boll weevil （Coleoptera： Curculionidae） adults after feeding on pollens from various sources

The survival of overwintering boll weevil, Anthonomus grandis grandis （Boheman）, adults on non-cotton hosts in the Lower Rio Grande Valley （LRGV） of Texas was examined from 2001 to 2006. The success of the Boll Weevil Eradication Program, which was reintroduced into the LRGV in 2005, depends on controlling overwintering boll weevil populations. Laboratory studies were conducted using boll weevil adults that were captured in pheromone traps from September through March. The number of adults captured per trap declined significantly in the field from fall to the beginning of spring （3.5-7.0-fold）. The proportion of trapped males and females did not differ significantly. The mean weight of boll weevil adults captured in September was 13.3 mg, while those of captured adults from November to February were significantly lower and ranged from 6.7 to 7.8 mg. Our results show that boll weevil adults can feed on different plant pollens. The highest longevity occurred when adults were fed almond pollen or mixed pollens （72.6 days and 69.2 days, respectively） and the lowest when they fed on citrus pollen or a non-food source （9.7 days or 7.4 days, respectively）. The highest adult survival occurred on almond and mixed pollens [88.0%-97. 6% after 1st feeding period （10 days）, 78.0%-90.8% after 3rd feeding period （10 days）, 55. 0%-83.6% after 5th feeding period （10 days）, and 15.2%-32.4% after lOth feeding period （10 days）]. The lowest adult survival occurred on citrus pollen [52.0%-56.0% after 1st feeding period （10 days）, 13.3% after 3rd and 5th feeding periods （10 days）, and 0 after 6th feeding period （10 days）]. Pollen feeding is not a behavior restricted to adult boll weevils of a specific sex or physiological state. Understanding how boll weevil adults survive in the absence of cotton is important to ensure ultimate success of eradicating this pest in the subtropics.     

A model for long-distance dispersal of boll weevils (Coleoptera: Curculionidae)

The boll weevil, Anthonomus grandis (Boheman), has been a major insect pest of cotton production in the US, accounting for yield losses and control costs on the order of several billion US dollars since the introduction of the pest in 1892. Boll weevil eradication programs have eliminated reproducing populations in nearly 94%, and progressed toward eradication within the remaining 6%, of cotton production areas. However, the ability of weevils to disperse and reinfest eradicated zones threatens to undermine the previous investment toward eradication of this pest. In this study, the HYSPLIT atmospheric dispersion model was used to simulate daily wind-aided dispersal of weevils from the Lower Rio Grande Valley (LRGV) of southern Texas and northeastern Mexico. Simulated weevil dispersal was compared with weekly capture of weevils in pheromone traps along highway trap lines between the LRGV and the South Texas / Winter Garden zone of the Texas Boll Weevil Eradication Program. A logistic regression model was fit to the probability of capturing at least one weevil in individual pheromone traps relative to specific values of simulated weevil dispersal, which resulted in 60.4% concordance, 21.3% discordance, and 18.3% ties in estimating captures and non-captures. During the first full year of active eradication with widespread insecticide applications in 2006, the dispersal model accurately estimated 71.8%, erroneously estimated 12.5%, and tied 15.7% of capture and non-capture events. Model simulations provide a temporal risk assessment over large areas of weevil reinfestation resulting from dispersal by prevailing winds. Eradication program managers can use the model risk assessment information to effectively schedule and target enhanced trapping, crop scouting, and insecticide applications.     

Short-range dispersal and overwintering habitats of boll weevils (Coleoptera: Curculionidae) during and after harvest in the subtropics

Field experiments in the subtropical Lower Rio Grande Valley of Texas were conducted to determine the extent of adult boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), dispersal from cotton, Gossypium hirsutum L., fields during harvest operations and the noncotton-growing ("overwinter") period between 1 September and 1 February. Using unbaited large capacity boll weevil traps placed at intervals extending outward from commercial field edges, boll weevils did not move in substantial numbers during harvest much beyond 30 m, primarily in the direction of prevailing winds. From traps placed in fallow cotton; citrus; lake edge; pasture; treeline; sorghum, Sorghum bicolor (L.) Moench, and sugarcane, Saccharum spp., habitats during the overwinter period, the most boll weevils were collected in the fallow cotton fields and adjacent treelines during the fall. However, the greatest abundances of boll weevils were found in citrus orchards in the spring, before newly planted cotton fields began to square. One of the three lake edges also harbored substantial populations in the spring. Egg development in females was not detected between November and April, but in cotton fields most females were gravid between May and August when cotton fruiting bodies were available. Mated females, as determined by discoloration of the spermatheca, made up 80-100% of the female population during November and December but declined to approximately 50% in February. The lower incidence of mating indicates a reduction in physical activity, regardless of overwinter habitat, until percentages increased in March and April after cotton fields had been planted and squares were forming.     

Reducing boll weevil populations by clipping terminal buds and removing abscised fruiting bodies

Cotton pests damaging fruiting bodies (squares and young bolls) are difficult to control and their damage results in direct yield loss. Small growers, with low technological inputs, represent a large portion of cotton growers worldwide comprising more than 76 countries; they rely mainly on cultural practices to counteract pest attack in their crops. Boll weevil, Anthonomus grandis Boheman (Coleoptera: Curculionidae), oviposition involves puncturing cotton squares and young bolls, causing abscission. We examined the impact on boll weevil population of collecting abscised cotton fruiting bodies and clipping plant terminals at 50% boll maturation in the field during two cotton‐growing seasons and under field cage conditions. Greatest numbers of damaged squares occurred ca. 117 days after planting and clipped plants resulted in reduction of abscised structures and adult boll weevils compared with non‐clipped plants, irrespective of cotton variety. Damaged young bolls were found ca. 128 days after planting in 2009 and 2011, but clipping had no effect. Numbers of boll weevils found in plants of the varieties BRS 201 and BRS Rubi (both in 2009) and BRS Rubi (in 2011) were, respectively, 13‐, 17‐, and 20‐fold greater when clipping plus collecting abscised fruiting bodies were not practiced. Furthermore, the average percentage of the boll weevil parasitoid Bracon vulgaris Ashmead (Hymenoptera: Braconidae) emerging from abscised and collected structures was similar between clipped and non‐clipped plant terminals in both seasons. Clipping plant terminals did not result in yield reduction and reduced adult boll weevil production. Collecting abscised reproductive structures, clipping plant terminals, and using both practices together reduced boll weevil populations by as much as 63, 57, and 79%, respectively, in cage trials. Thus, these practices cause significant impact on boll weevil populations and are feasible of adoption, especially for smallholder cotton growers.     

Suppression of Boll Weevil (Coleoptera: Curculionidae) Infestations on South Texas Cotton by Augmentative Releases of the Parasite Catolaccus grandis (Hymenoptera: Pteromalidae)

Augmentative releases of Catolaccus grandis (Burks) were conducted in a series of south Texas cotton fields during 1992 (April 30-June 29) in an attempt to suppress infestations of boll weevil, Anthonomus grandis Boheman. Within each of three release sites, the average incidence of mortality occurring among susceptible host stages (94.4-96.4% and 86.1-96.6% apparent mortality among third-stage larvae and pupae, respectively) was substantially greater than that occurring among these same stages in controls devoid of parasites (2.2-9.6% and 1.8-7.9% apparent mortality, respectively). Such differential mortality produced two important effects: (1) a significant reduction in densities of adult boll weevils produced in release sites relative to controls (0.0-0.1 and 0.3-1.6 unemerged adults/m², respectively), and (2) a concomitant reduction in the incidence of damaged bells during the postbloom period (0.2-0.4% and 48.3-91.7% in release and control sites, respectively). These results conclusively demonstrated the ability of C. grandis to suppress and maintain boll weevil infestations at subeconomic levels when augmented in sufficient quantities during the period in which the first and second host generations normally develop on cultivated cotton. The potential for augmentative biological control of boll weevil in the south Texas cotton environment is discussed.     

Early-season colonization patterns of the boll weevil (Coleoptera: Curculionidae) in Central Texas cotton

It is commonly believed that colonization of early-season cotton, Gossypium hirsutum L., by overwintered boll weevils, Anthonomus grandis grandis Boheman, is concentrated on field margins. However, supporting experimental evidence is not available. In 1999 and 2000, we examined colonization patterns of overwintered boll weevils in Central Texas cotton on the bases of adult collections by a pneumatic sampler and hand collections of abscised infested squares. Samples were taken from sites arranged in a grid that extended inward >70 m from the field margin. Adults were collected from shortly after seedling emergence until the flowering stage, and infested squares were collected during the one-third grown square stage. Despite numerical trends, the numbers of adult weevils collected were not significantly different between years or sexes, or among plant phenological stages. Field-to-field variation among collections was considerable and likely prevented detection of differences among these factors. Spatial patterns represented by adult weevil and infested square collections were examined by logistic regressions fitted to the respective probabilities of weevil detection at each designated sample site. Although we observed trends for slightly decreased probability of weevil detection with increased distance from the field margin, these trends were too weak to be demonstrated statistically. Our results indicate the boll weevil does not consistently exhibit a strong edge-oriented colonization pattern, and that management tactics that are predicated on these patterns, such as border sprays, should be used with caution.     

Forensic pollen geolocation techniques used to identify the origin of boll weevil re-infestation

The boll weevil, Anthonomus grandis, entered the United States of America in the early twentieth century and became a major pest in cotton, Gossypium spp. Shortly after the passage of Tropical Storm Erin on 16 August 2007 through the South Texas/Winter Garden boll weevil eradication zone, over 150 boll weevils were captured in the Southern Rolling Plains (SRP) eradication zone that was essentially weevil-free since 2003. Pollen analyses were made of the SRP weevils and weevils collected in two suspected source zones, Cameron (Southern Blacklands eradication zone) and Uvalde (Winter Garden eradication zone). An additional examination of the palynological evidence and examination of additional pollen residue shed new light on this event and strengthens the conclusion that the Uvalde area was the source of the SRP weevils. A total of 192 pollen grains from 39 taxa were found in the SRP weevils: 1904 pollen grains from ten taxa from the Cameron weevils and 148 grains from 28 taxa in the Uvalde weevils. The SRP weevils shared 16 taxa, including Phermeranthus sp. (flameflower) with the Uvalde weevils and only five taxa with the Cameron weevils. Common taxa between SRP and Uvalde weevils and the lack of the dominant ‘low spine’ Asteraceae that occurred in all Cameron samples confirm that the SRP weevils originated from the South Texas/Winter Garden zone. Problems associated with this type of research are similar to those in forensic palynology. These problems include the unknown origin of the weevils, pollen contamination and care and storage of the samples.