Boll weevil (Coleoptera: Curculionidae) survival through the seed cotton cleaning process in the cotton gin

There is concern that gins located in boll weevil, Anthonomus grandis grandis Boheman, eradication zones may become points of reintroduction when they process cotton grown in a neighboring infested area. We estimated boll weevil survival through two typical machine sequences used in commercial cotton gins to clean and dry the seed cotton in advance of the gin stand, as well as separately through two incline cylinder cleaners or one or two tower dryers operating at different temperatures. Large numbers of laboratory-reared adult boll weevils were marked with fluorescent powder, fed into the test system, and recovered with the assistance of blacklights. We found no evidence of survival through the seed cotton cleaning systems even when the dryers were not heated, or when passed separately through the two incline cleaners alone. Upper confidence limits (95%) were calculated for the observed zero recoveries based on sample size and the binomial distribution, and these represent the statistical worst-case (i.e., highest) survival potential. Survival through heated tower dryers declined rapidly to zero at higher temperatures, especially when two dryers were running. Although we conclude that the potential for survival of weevils in the seed cotton to the gin stand is zero or close to zero, a small percentage of live weevils was recovered in the green boll/rock trap, which may represent the greatest threat of reintroduction at the gin. Escape of live weevils with the gin trash is also possible, and studies addressing this issue will be presented elsewhere.     

Potential for transport of boll weevils (Coleoptera: Curculionidae) to the cotton gin within cotton modules

There is concern that cotton gins located in boll weevil, Anthonomus grandis grandis Boheman, eradication zones serving customers in adjacent infested zones may serve as a site for boll weevil reintroductions if weevils are transported alive inside cotton modules. We surveyed fields in three distinct areas of Texas and found that weevils can be present in large numbers in cotton fields that have been defoliated and desiccated in preparation for harvest, both as free adults and as immatures inside unopened bolls. Harvested cotton taken from module builders indicated that approximately = 100-3700 adult boll weevils were packed inside modules constructed at the sampled fields. Marked weevils were forced through a laboratory field cleaner (bur extractor) commonly mounted on stripper-harvesters, and 14% were recovered alive in the seed cotton fraction and lived at least to 24 h. Survival of weevils placed inside modules declined over time up to 7 d, but the magnitude of the decline varied with experimental conditions. In one experiment, 91% of the weevils survived to 7 d, whereas under harsher environmental conditions, only 11% survived that long. Together, our results indicate that when cotton is harvested in an infested area, boll weevils likely will be packed alive into cotton modules, and many will still be alive by the time the module is fed into the gin, at least up to 7 d after the module's construction.     

Potential for escape of live boll weevils (Coleoptera: Curculionidae) into cottonseed, motes, and cleaned lint at the cotton gin

Reintroductions of the boll weevil, Anthonomus grandis grandis Boheman, into areas of the United States where it has been eradicated or suppressed are very expensive to mitigate. There is concern that a cotton gin in an eradication zone may serve as a site of boll weevil reintroductions when processing cotton harvested in a neighboring infested zone. Similarly, there is a question whether weevil-free areas can safely import gin products, such as cottonseed and baled lint, from infested areas without risking an introduction. Many countries require fumigation of imported U.S. cotton bales to protect against boll weevil introductions, costing the U.S. cotton industry millions of dollars annually. In previously reported experiments, we quantified the potential for boll weevils to survive passage through precleaning machinery in the gin. In this study, we quantified survival potential of boll weevils passing through the gin stand and segregating into the cottonseed, mote, or lint fractions. We also examined boll weevil survival when passed with ginned lint through a lint cleaner. We present a flow chart of experimentally determined survival potentials of boll weevils passing through the various subprocesses of the gin, from which one can calculate the risk of a live boll weevil reaching any point in the process. Our data show that there is virtually no chance of a boll weevil being segregated alive into the cottonseed or of one surviving in the lint to approach the bale press. Therefore, quarantine or fumigation of cottonseed and cotton bales to guard against boll weevil introductions is unnecessary.     

Effects of burial and soil condition on postharvest mortality of boll Weevils (Coleoptera: Curculionidae) in fallen cotton fruit

Effects of soil condition and burial on boll weevil, Anthonomus grandis grandis Boheman, mortality in fallen cotton, Gossypium hirsutum L., fruit were assessed in this study. During hot weather immediately after summer harvest operations in the Lower Rio Grande Valley of Texas, burial of infested fruit in conventionally tilled field plots permitted significantly greater survival of weevils than in no-tillage plots. Burial of infested squares protected developing weevils from heat and desiccation that cause high mortality on the soil surface during and after harvest in midsummer and late summer. A laboratory assay showed that burial of infested squares resulted in significantly greater weevil mortality in wet than in dry sandy or clay soils. Significantly fewer weevils rose to the soil surface after burial of infested bolls during winter compared with bolls set on the soil surface, a likely result of wetting by winter rainfall. A combination of leaving infested fruit exposed to heat before the onset of cooler winter temperatures and burial by tillage when temperatures begin to cool might be an important tactic for reducing populations of boll weevils that overwinter in cotton fields.     

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.     

Dispersal of boll weevils (Coleoptera: Curculionidae) from cotton modules before ginning

We characterized the level of risk of boll weevil, Anthonomus grandis grandis Boheman, reintroduction to an eradication zone posed by dispersal from cotton modules during and after transport to the gin. Mark-release-recapture experiments in August and September in Texas indicated that most weevils disperse rapidly from the module surface, temperature permitting, unless confined under a module tarp, where most died. Nevertheless, 1-5% of released weevils were recovered alive after 24 h on the side and top surfaces of modules, representing potential dispersants. Mortality of boll weevils caged on the top surface of a module was 95-100% after 1-4 d when maximum air temperatures were > or = 33 degrees C and 72-100% when minimum temperatures were -7 degrees C or lower, but a few survived even after experiencing a minimum daily temperature of -12 degrees C. Under warm (daily maximum temperatures > or = 25 degrees C) and cold (daily minimum temperatures < or = 0 degrees C) weather conditions, survival was higher under the tarp than on the open surface of the module (20 versus 7% and 42 versus 26%, respectively), but mortality was 100% in both locations when temperatures reached 34 degrees C. Our results indicate that although the threat to an eradication zone posed by boll weevil dispersal from an infested module is very low under most environmental conditions, it is probably greatest when 1) a module is constructed and transported from an infested zone during weather too cool for flight, followed by warm weather favorable for flight at the gin yard; or 2) such a module is transported immediately after construction in moderate-to-warm weather.     

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.     

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.     

Influence of cotton fruit stages as food sources on boll weevil (Coleoptera: Curculionidae) fecundity and oviposition

Boll weevil, Anthonomus grandis grandis Boheman (Coloeoptera: Curculionidae), populations in the Lower Rio Grande Valley of Texas increase strongly during the squaring stage, and preemptive insecticide sprays at the pinhead square stage were designed to capitalize on that association. Laboratory assays showed that cotton plant volatiles, or leaves as a food source, do not elicit egg production in wild weevils. Boll weevils fed on large (5.5-8-mm diameter) squares for 7 d resulted in > or = 3.8-fold more gravid females that developed 4.8-fold more chorionated eggs per female than weevils fed on match-head-sized squares, or postbloom, young (5-10-d-old), or old (3-5-wk-old) bolls. When presented with a choice, nongravid females preferred to feed on young and old bolls 4.7- and 8.4-fold more, respectively, than on large squares. In the field, large squares had 7.8- and 25-fold more feeding punctures than match-head-sized squares and bolls, respectively. Oviposition increased > or = 2.7-fold when females fed on large squares compared with match-head-sized squares and bolls. Greater feeding on large squares during squaring and the associated greater fecundity explain rapid weevil population buildups shortly after large squares become well established.     

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.     

Relationships of abscised cotton fruit to boll weevil (Coleoptera: Curculionidae) feeding, oviposition, and development

Abscised cotton, Gossypium hirsutum L., fruit in field plots planted at different times were examined to assess adult boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), use of squares and bolls during 2002 and 2003 in the Lower Rio Grande Valley of Texas. Although boll abscission is not necessarily related to infestation, generally more bolls abscised than squares and abundances of fallen bolls were not related to the planting date treatments. During 2003, fallen squares were most abundant in the late-planted treatment. Although large squares (5.5-8-mm-diameter) on the plant are preferred for boll weevil oviposition, diameter of abscised squares is not a reliable measurement because of shrinkage resulting from desiccation and larval feeding. Fallen feeding-punctured squares and bolls were most abundant in late plantings but differences between fallen feeding-punctured squares versus fallen feeding-punctured bolls were found in only one treatment in 2003. During the same year, fallen oviposition-punctured squares were more numerous in the late-planted treatment than in the earlier treatments. Treatment effects were not found on numbers of oviposition-punctured bolls, but fallen oviposition-punctured squares were more common than bolls in the late-planted treatment compared with earlier treatments each year. Dead weevil eggs, larvae, and pupae inside fallen fruit were few and planting date treatment effects were not detected. Living third instars and pupae were more abundant in fallen squares of the late-planted treatment than in the earlier treatments and bolls of all three treatments. This study shows that fallen squares in late-planted cotton contribute more to adult boll weevil populations than bolls, or squares of earlier plantings.     

Reproductive potential of field-collected overwintering boll weevils (Coleoptera: Curculionidae) fed on pollen in the laboratory

Abstract  The reproductive potential of overwintering boll weevil, Anthonomus grandis grandis (Boheman), females collected from pheromone traps in September, November and January, fed for 1, 3, and 5 weeks on plant pollens, and then provided cotton squares, was determined in the laboratory at 27 ± 1°C, 65% RH, and a photoperiod 13 : 11 (L : D) h. Duration of pollen feeding by overwintering boll weevils did not significantly influence egg and feeding punctures, or puncture ratios (egg to total punctures) for any of the three months of parent weevil collections when provided cotton squares on a daily basis. However, punctures and puncture ratios are significantly different when comparing mean data between months of boll weevil collections. When boll weevils were provided with cotton squares daily, the pre-ovipositional periods of female parents captured in September, November and January were 5, 9 and 14 days, respectively. The rate of eggs by females was significantly lower during November and January than September. Female parents collected in September produced a significantly higher percentage of eggs yielding adult progeny than those collected in November and January. Life table parameters indicated that net reproductive rate ( R _o) of boll weevil females collected in September was 1.2-fold higher than those collected in November and 10.7-fold higher than those collected in January. Except for testes size, no differences in male reproductive parameters were observed during the cotton-free period compared with males captured during mid-cotton (June). The number of oocytes in the ovarioles and the number of oocytes containing yolk were significantly lower during September, November and January compared with June. The reproductive potential of overwintering boll weevil females collected in different months is an important consideration in determining the success of any control strategy.     

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.     

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.     

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.     

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.     

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.     

Effects of kaolin-based particle film application on boll weevil (Coleoptera: Curculionidae) injury to cotton

This study examined a non-insecticidal tactic for suppressing boll weevil, Anthonomus grandis grandis Boheman, damage to cotton, Gossypium hirsutum L. In cage assays, kaolin, a reflective white mineral, applied to excised cotton squares or to the cotton foliage, initially resulted in lower levels of boll weevil injury to squares than nontreated squares. Boll weevil oviposition and feeding on kaolin-treated squares and squares on kaolin-treated cotton plants increased when nontreated squares and cotton plants were in short supply. A laboratory assay and field trials suggested that boll weevils distinguished between cotton plots based on color differences caused by kaolin and this appeared to influence levels of damage to squares. Random sampling in small plots indicated that oviposition damage to squares in plots treated with kaolin was reduced (P < 0.05) compared with nontreated controls, except when rain washed the kaolin off the foliage. Lint yield differences were not detected between the small plots, but the kaolin-treated small plots yielded as much as 2.36 times more cotton lint than a large but unreplicated adjacent nontreated control plot, and up to 1.39 times more than another large but unreplicated adjacent plot sprayed twice with preemptive applications of azinphosmethyl when cotton squares were first developing (pinhead stage). Potentially important avenues for future research on boll weevil injury suppression using kaolin are discussed.     

Reproductive potential of overwintering, F1, and F2 female boll weevils (Coleoptera: Curculionidae) in the Lower Rio Grande Valley of Texas

The feeding and oviposition activity of overwintering boll weevils, Anthonomus grandis grandis (Boheman), and seasonal fluctuations in development, survival, and reproduction of progeny of overwintering and first- and second-generation boll weevil females were determined in the laboratory at 27 degrees C, 65% RH, and a photoperiod of 12:12 (L:D) h. During the cotton-free period in the Lower Rio Grande Valley, female boll weevils without access to cotton resorb their unlaid eggs and enter reproductive diapause. However, when they were provided daily with greenhouse-grown cotton squares, commencement of oviposition began after 7, 15, or 20 d, depending on when they were captured. Females captured later in the winter fed longer before laying eggs than those captured in the early fall, suggesting that it may take females longer to terminate diapause the longer they have been dormant. The rate of feeding by females was significantly less during the winter months, and this may have affected the rate of diet-mediated termination of dormancy. Females of the first and second generations after the overwintering generation produced a significantly higher percentage of progeny surviving to adulthood and a higher proportion of these progeny were females. Offspring development time from overwintering female parents was significantly longer than that from first and second generations under the same laboratory conditions. The total number of lifetime eggs produced by females of the second generation during the cotton-growing season were approximately 9.9-fold higher than for overwintering females and 1.5-fold higher than for first-generation females. Life table calculations indicated that the population of second-generation boll weevils increased an average of 1.5-fold higher each generation than for females of the first generation and 22.6-fold higher than for overwintering females. Our data showed variation in boll weevil survival, development, and reproductive potential among the overwintering and first- and second-generation females, suggesting inherent seasonal fluctuations in these parameters.     

Longevity and egg development of adult female boll weevils fed exclusively on different parts and stages of cotton fruiting bodies

The capacities of the rind (i.e., the developing calyx and petals of squares; and the outer casing, or husk, of bolls) and the internal reproductive portion of cotton, Gossypium hirsutum L. (Malvaceae), squares of three sizes, and bolls of three ages to influence adult female boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), longevity and egg production were evaluated in laboratory bioassays. While feeding on the reproductive portion of squares was expected to support adult boll weevils for considerable periods of time (e.g., medium square reproductive portion: ≈185 days), feeding on rinds also resulted in substantial longevity (e.g., medium square rind: ≈120 days). As anticipated, feeding on the reproductive portion of squares resulted in formation of chorionated eggs in mated females, but a diet comprised exclusively of rinds, particularly from large squares, was associated with gravidity and high fecundity relative to rinds of young and mature bolls. The reproductive portion and rind of post‐bloom and young bolls as sources of food resulted in limited gravidity while mature bolls were not associated with any egg formation. These findings further our understanding of how boll weevils feed on different parts of the cotton plant and how those parts as food sources are related to the biology and ecology of the boll weevil.