Number Of Adult Bees Research Articles

Resource gaps pose the greatest threat for bumblebees during the colony establishment phase

Abstract A common management intervention to support declining wild pollinators is ‘pollinator planting’. However, despite years of inclusion in conservation initiatives, global pollinator declines continue. Using the agent‐based model BEE‐STEWARD with two example species, Bombus terrestris (L. 1758) and B. pascuorum (Scopoli, 1763) (Hymenoptera: Apidae), we explore when during the year bumblebee resource demand is the highest and how that relates to seasonal changes in colony composition (numbers of eggs, larvae, pupae and adults). We then examine the impact of two‐week periods of resource scarcity across the year. Finally, we explore how enhancement with early spring‐blooming herbaceous species or trees changes colony survival and queen production. In the United Kingdom, there is a previously under‐appreciated ‘hungry gap’ for bumblebees in March–April, before the peak flight period, driven by the demands of larvae for protein and thermoregulation in the colony, rather than the number of adult bees. A 2‐week gap in forage availability during this period drives a 50%–87% drop in the production of daughter queens. Adding early‐blooming species in the model had significant, positive, long‐term effects on colony survival probability and daughter queen production. Pollinator‐planting initiatives in both national and international conservation schemes need to include plants that flower up to 1 month before the adults of target social pollinator species are apparent in the field, during the period that larvae dominate the colony. This approach is likely to increase colony survival and queen production, contributing towards halting and reversing global pollinator decline.

Colony size of amazonian stingless bees and its assessment through intrinsic parameters

Stingless bees live in populous colonies that vary in size from a few hundred individuals to tens of thousands, although information on actual colony size is limited. The objectives of this study were to determine the colony size of five Amazonian stingless bee species (Melipona flavolineata, Melipona fasciculata, Scaptotrigona aff. postica, Frieseomelitta longipes, and Plebeia minima), and to identify biological parameters that covary with colony size. The number of brood cells, adult bees, and food stocks were counted under laboratory conditions, alongside field assessments of egg-laying rate and external activity of adult workers. To identify covariates of colony size, the number of adult bees was regressed against the number of brood cells, egg-laying rate, external activity of adult workers, and food stocks, and the best candidate models were ranked using the Akaike Information Criterion. Mean (±s.d.) adult populations were: in M. flavolineata, 1046 ± 185; in M. fasciculata, 593 ± 300; in S. aff. postica, 7404 ± 1391; in F. longipes, 2425 ± 1000 and in P. minima, 405 ± 254. Thus, we showed that the external activity is the biological parameter, after the number of brood cells, that presents the best relationship with the number of adult bees, which can be easily evaluated in the field. Determining colony sizes using easily measurable biological parameters are important steps to understanding stingless bee’s life histories, ecology, and evolution, and to ease their keeping and utilization for pollination.

Integrated Pest Management Strategies to Control Varroa Mites and Their Effect on Viral Loads in Honey Bee Colonies.

Honey bee viruses in combination with varroa mite are very damaging for honey bee colonies worldwide. There are no effective methods to control the viral load in honey bee colonies except regular and effective control of mites. Integrated Pest Management strategies are required to effectively control mites with veterinary medicines based on organic compounds. We evaluated the effect of two brood interruption techniques, queen caging (QC) and trapping comb (TC), followed by an oxalic acid treatment, on the mite fall, colony strength, and viral load of Deformed Wing Virus (DWV) and Acute Bee Paralysis Virus (ABPV). In this paper, we report the data obtained in two experimental sites, in Slovenia and Italy, in terms of the varroacide efficacy, colony strength, and viral load. The number of adult bees after the adoption of the two techniques showed similar decreasing trends in both locations. The viral load of Acute Bee Paralysis Virus did not show any significant reduction after 25 days, reported as the number of Real-Time PCR cycles needed to detect the virus. The viral load of DWV also did not show a significant reduction after 25 days. The acaricidal efficacy of the applied protocols was high in both experimental groups and in both apiaries. Both the queen caging and trapping comb techniques, followed by an oxalic acid treatment, can be considered effective varroa treatment strategies, but further studies should be carried out to evaluate the long-term effects on viral loads to plan the Integrated Pest Management strategy with the right timing before wintering.

Oxalic acid application method and treatment intervals for reduction of Varroa destructor (Mesostigmata: Varroidae) populations in Apis mellifera (Hymenoptera: Apidae) colonies.

Oxalic acid (OA) is a popular miticide used to control Varroa destructor (Mesostigmata: Varroidae) in western honey bee (Apis mellifera L.) (Hymenoptera: Apidae) colonies. Our aim was to investigate which method of OA application (dribbling, fogging, or vaporizing) was the most effective at reducing V. destructor infestations (Experiment 1) and to improve upon this method by determining the treatment interval that resulted in the greatest V. destructor control (Experiment 2). We used the product Api-Bioxal (97% OA) and maintained 40 honey bee colonies (10/treatment) in both experiments. In Experiment 1, the treatments included (i) dribbling 50 ml of 3% OA solution, (ii) vaporizing 4 g of solid OA, (iii) using an insect fogger supplied with 2.5% OA dissolved in ethyl alcohol, and (iv) an untreated control. After 3 weeks, only the vaporization method reduced V. destructor infestations (from 9.24 mites/100 bees pretreatment to 3.25 mites/100 bees posttreatment) and resulted in significantly increased brood amounts and numbers of adult bees over those of the controls. In Experiment 2, all colonies were treated with 4 applications of OA via vaporization at a constant concentration of 4 g OA/colony. In this experiment, the groups were separated by treatment intervals at either 3-, 5-, or 7-day intervals. We observed that 5- and 7-day treatment intervals significantly reduced V. destructor populations from pretreatment levels over that of the controls and 3-day intervals. Our data demonstrate the efficacy of OA in reducing V. destructor infestation, particularly vaporizing 4 g every 5-7 days as the most effective method of application.

An approach to the modeling of honey bee colonies

Abstract. In this work, populations of adult and immature honeybees and their honey production are studied through mathematical and statistical modeling approaches. Those models are complementary and are presented in disjunct form. They were used to show different modeling methods for honey bee population dynamics. The statistical approach consisted of a generalized linear model using data from the Department of Agriculture of the United States of America (USDA), which showed that the relationship between the number of colonies and the rate of honey production is not constant in time but decrease over the years. These models showed that when a bee population is subjected to a stress factor (i.e., habitat destruction, Varroa mite, climate variability, season, neonicotinoids, among others), the abundance of individuals decreases over time as well as the honey produced by the colonies. Finally, the mathematical approach consisted of two models: (1) a smooth model, in which conditions of existence and stability of the equilibrium solutions are determined by an ecological threshold value, and (2) a non-smooth model where the mortality rate of bees is included as a function of the number of adult bees in the population.

Plant-based supplement containing B-complex vitamins can improve bee health and increase colony performance

It is common knowledge that nutritive stress resulting from decreased diversity and quality of food, pollution of food sources and beekeeping errors may lead to increased susceptibility of bees to pathogens and pesticides. The dearth of adequate food is frequently compensated with supplements. Thus, this research was aimed to study the effects of the plant-based supplement B + on colony strength (assessed according to open and sealed brood area, honey and pollen/bee bread reserves, and the number of adult bees). In addition, Nosema ceranae spores and viruses were quantified and the level of infestation with Varroa destructor assessed. The experiment was conducted in late summer and early spring. In colonies which were given B + in feed a significant increase (p < 0.05) in the parameters of colony strength were noticed in comparison to the control (colonies fed on sugar syrup). Moreover, it was proven that the bees from these colonies had significantly lower (p < 0.05) N. ceranae spore counts, and acute bee paralysis, deformed wing and sacbrood virus loads. Our results suggest that the addition of B + supplement to the colonies provide them with nutrients, contribute to their strengthening, might prevent nutritive stress and increase the success of bees in combating pathogens.

Comparison of long-term changes in size and longevity of bee colonies in mid-west Japan and Maui with and without exposure to pesticide, cold winters, and mites.

Four long-term field experiments in mid-west Japan (Shika) made it clear that extinction of colonies exposed to neonicotinoid was much higher than for colonies exposed to organophosphates. The incidence of hive death for of organophosphate-exposed and control (pesticide-free) colonies was similar. We conducted a field experiment in Maui for 271 days using the same pesticides (dinotefuran: 0.2 ppm, clothianidin: 0.08 ppm, fenitrothion: 1 ppm) as used in Shika with the honeybee, Apis mellifera, colonies without mites. Numbers of adult bees, capped brood, mites and other hive parameters were accurately counted on photographs of combs and on the inside of the hives. All six neonicotinoid (dinotefuran & clothianidin)-exposed colonies failed during the experiment. One of three organophosphate (fenitrothion)-exposed colonies and one of the three control colonies also failed. The findings from Maui, where colonies displayed no mites, provides evidence from Shika, with mites, that neonicotinoids are more hazardous to honeybee colonies than organophosphates. The apparent longevity of honeybee colonies on Maui was estimated by numbers of adult bees and capped brood using a mathematical model previously proposed. Seasonal changes in longevity on Maui differ greatly from changes at Shika, the latter showing distinct seasonal variation. Longevity on Maui remains nearly constant throughout the year with wide variations. At Shika, it increases drastically in winter, by six- to ten fold more than the other seasons. Differences seem to depend on the existence of cold winters and the length of flowering seasons. In a perpetually hospitable environment, small changes in conditions can be sensitively reflected in apparent longevity. Examining wide variations in apparent longevity that are seemingly incoherent, we recognized several differences in apparent longevity between neonicotinoid-exposed and organophosphate-exposed colonies: The colony that failed in after organophosphate-exposure colony group exhibited the longest apparent longevity and the fewest number of newly capped brood, as also was the case in control colonies. Extended longevity when few brood are newly produced is reasonable to maintain the colony from a physiological point of view. Extension of apparent longevity is not seen in neonicotinoid-exposed colonies when the number of newly capped brood is fewer. This finding suggests that neonicotinoid pesticides may inhibit normal apian physiology.

A three-year large scale study on the risk of honey bee colony exposure to blooming sunflowers grown from seeds treated with thiamethoxam and clothianidin neonicotinoids

Despite the restriction of the use of neonicotinoids in the EU, including thiamethoxam and clothianidin, the debate over their risk on honey bees has not been fully settled. This study presents results of a three-year study working with 180 honey bee colonies in ten replicates. Colonies were sorted into three treatments (60 colonies per treatment) exposed to sunflower blooms grown from seeds treated with thiamethoxam, clothianidin and a non-treated control. Each colony was assessed at six moments: one before to exposition to sunflower, two during the exposition (short-time risk), two after exposition (medium-time risk) and one after wintering (long-time risk). The health and development of the colonies were assessed by monitoring adult bee population, brood development, status of the queen, food reserves and survival. No significant difference among treatments when raw data was considered. However, when evolution from initial status of the colony was evaluated, a significant difference was observed from the first week of exposure to sunflower blooms. In this period, the number of adult bees and the amount of brood were slightly lower in the bee hives exposed to neonicotinoids, although such differences disappeared in subsequent evaluations. The concentration of residues in samples of beebread and adult bees was at the level of ng·g−1. Magnitude of the effect of the treatment factor on the variability of colony health and development related parameters was low. The most important factor was the hive, followed by the replicate and year, and to a lesser extent the initial strength of the colonies.

Organic farming positively affects honeybee colonies in a flower‐poor period in agricultural landscapes

Abstract Conventional farming has been implicated in global biodiversity and pollinator declines and organic farming is often regarded as a more ecological alternative. However, the effects of organic farming on honeybees remain elusive, despite honeybees’ importance as pollinators of crops and wild plants. Using 6 years of data from a large‐scale study with fortnightly measurements of honeybee colony performance traits (10 apiaries per year distributed across a 435 km2‐large research site in France), we related worker brood area, number of adult bees and honey reserves to the proportions of organic farmland in the surroundings of the hives at two spatial scales (300 m and 1,500 m). We found evidence that, at the local scale, organic farming increased both worker brood production and number of adult bees in the period of flower scarcity between the blooms of oilseed rape and sunflower (hereafter ‘dearth period’). At the landscape scale, organic farming increased honey reserves during the dearth period and at the beginning of the sunflower bloom. The results suggest that worker brood development benefitted from organic farming mostly through a more diverse diet due to an increase in the availability of diverse pollen sources in close proximity of their hives. Reduced pesticide drift may have additionally improved bee survival. Honey reserves were possibly mostly affected by increased availability of melliferous flowers in foraging distance. Synthesis and applications. Organic farming increases honeybee colony performance in a period of resource scarcity, likely through a continuous supply of floral resources including weeds, cover crops and semi‐natural elements. We demonstrate how worker brood area increases in the critical dearth period (between the blooms of oilseed rape and sunflower). This has previously been linked to winter colony survival, suggesting that organic farmland may mitigate repercussions of intensive farming on colony vitality. We conclude that organic farming benefits a crucial crop pollinator with potential positive implications for agriculture in the wider landscape.

Netted crop covers reduce honeybee foraging activity and colony strength in a mass flowering crop.

The widespread use of protective covers in horticulture represents a novel landscape‐level change, presenting the challenges for crop pollination. Honeybees (Apis mellifera L) are pollinators of many crops, but their behavior can be affected by conditions under covers. To determine how netting crop covers can affect honeybee foraging dynamics, colony health, and pollination services, we assessed the performance of 52 nucleus honeybee colonies in five covered and six uncovered kiwifruit orchards. Colony strength was estimated pre‐ and postintroduction, and the foraging of individual bees (including pollen, nectar, and naïve foragers) was monitored in a subset of the hives fitted with RFID readers. Simultaneously, we evaluated pollination effectiveness by measuring flower visitation rates and the number of seeds produced after single honeybee visits. Honeybee colonies under cover exhibited both an acute loss of foragers and changes in the behavior of successful foragers. Under cover, bees were roughly three times less likely to return after their first trip outside the hive. Consequently, the number of adult bees in hives declined at a faster rate in these orchards, with colonies losing on average 1,057 ± 274 of their bees in under two weeks. Bees that did forage under cover completed fewer trips provisioning their colony, failing to reenter after a few short‐duration trips. These effects are likely to have implications for colony health and productivity. We also found that bee density (bees/thousand flowers) and visitation rates to flowers were lower under cover; however, we did not detect a resultant change in pollination. Our findings highlight the need for environment‐specific management techniques for pollinators. Improving honeybee orientation under covers and increasing our understanding of the effects of covers on bee nutrition and brood rearing should be primary objectives for maintaining colonies and potentially improving pollination in these systems.

A mathematical model to estimate the seasonal change in apparent longevity of bee colony

The longevity of a honeybee colony is far more significant than the lifespan of an individual honeybee, a social insect. The longevity of a honeybee colony is integral to the fate of the colony. We have proposed a new mathematical model to estimate the apparent longevity defined in the upper limit of an integral equation. The apparent longevity can be determined only from the numbers of adult bees and capped brood. By applying the mathematical model to a honeybee colony in Japan, seasonal changes in apparent longevity were estimated in three long-term field experiments. Three apparent longevities showed very similar season-changes to one another, increasing from early autumn, reaching a maximum at the end of overwintering and falling approximately plumb down after overwintering. The influence of measurement errors in the numbers of adult bees and capped brood on the apparent longevity was investigated.

Effects of truck-mounted, ultra low volume mosquito adulticides on honey bees (Apis mellifera) in a suburban field setting.

Few studies have examined the impact of mosquito adulticides on honey bees under conditions that reflect actual field exposure. Whereas several studies have evaluated the toxicity of mosquito control products on honey bees, most have been laboratory based and have focused solely on acute mortality as a measure of impact. The goal of this study was to determine effects of routine applications of truck-based ultra-low volume (ULV) mosquito adulticides (i.e., Scourge, Duet, and Deltagard) on honey bees in a suburban setting. The mosquito adulticides used in this study were pyrethroids with active ingredients resmethrin (Scourge), prallethrin and sumithrin (Duet), and deltamethrin (Deltagard), in which resmethrin, prallethrin, and sumithrin were synergized with piperonyl butoxide. We measured and compared mortality and detoxification enzyme activities (esterase and glutathione S-transferase) from sentinel beehives within and outside of mosquito control areas. Concurrently, colony health (i.e., number of adult bees, brood quantity and brood quality) was compared throughout the study period. No significant differences were observed in honey bee mortality, colony health or detoxification enzyme activities between treated (five sprayed areas each received one to three insecticide treatment) and control sites (four unsprayed areas that did not receive insecticide treatment) over the seven week study period. However, our laboratory study showed that exposure to resmethrin, the active ingredient in Scourge, caused significant inhibition of esterase activity compared with the control group. Our findings suggest that proper application of truck based insecticides for mosquito control results in little or no exposure and therefore minimal effects on domestic honey bees.

An Evaluation of the Honey Bee (Hymenoptera: Apidae) Safety Profile of a New Systemic Insecticide, Flupyradifurone, Under Field Conditions in Florida.

Flupyradifurone (Sivanto) is a novel systemic insecticide from the butenolide class developed by Bayer. Based on available data (USEPA 2014), this insecticide appears to have a favorable safety profile for honey bee colonies. As a result, the label permits the product to be applied during prebloom and bloom in various crops, including citrus, except when mixed with azole fungicides during the blooming period. We placed 24 honey bee (Apis mellifera L.) colonies adjacent to eight flowering buckwheat (Fagopyrum esculentum Moench) fields that either had been sprayed with the maximum label rate of flupyradifurone or with water only (control fields), with three colonies placed adjacent to each field. We conducted colony strength assessments during which the number of adult bees, eggs, uncapped brood cells, capped brood cells, food storage cells, and weights of honey supers and brood chambers were determined prior to, during, and after the flowering period. We also analyzed bee-collected pollen and nectar for flupyradifurone residues. Overall, there were no differences in any colony strength parameter for colonies placed at control and flupyradifurone-treated buckwheat fields. Residue analyses showed that pollen (x = 565.8 ppb) and nectar (x = 259.4 ppb) gathered by bees on fields treated with flupyradifurone contained significantly higher flupyradifurone residues than did bee bread and unprocessed nectar collected by bees from control fields (75% of samples <LOD). Within the conditions set forth by our experimental design, our collective data suggest no adverse effects of flupyradifurone on honey bee colonies when following label directions.

Resource Effects on Solitary Bee Reproduction in a Managed Crop Pollination System.

Population density may affect solitary bee maternal resource allocation. The number of Megachile rotundata (F.), alfalfa leafcutting bee, females released for seed production of Medicago sativa L., alfalfa, may limit flower availability for nest provisioning. In turn, pollinator abundance also may affect crop yield. The M. sativa pollination system presents an opportunity to test for effects of density dependence and maternal manipulation on M. rotundata reproduction. A multiyear study was performed on M. sativa fields upon which M. rotundata densities were altered to induce low, medium, and high density situations. Numbers of adult bees and open flowers were recorded weekly; bee reproduction variables were collected once. Fields varied in plant performance for each site and year, and the intended bee densities were not realized. Therefore, the variable density index (DI) was derived to describe the number of female bees per area of flowers over the study period. As DI increased, percentages of pollinated flowers, established females, and healthy brood significantly increased, and the number of pollinated flowers per female and of dead or diseased brood significantly decreased. Sex ratio was significantly more female biased as DI increased. Overwintered offspring weights were similar regardless of DI, but significantly differed by year for both sexes, and for males also by field and year × field interaction. Overall, resource limitation was not found in this field study. Other density-dependent factors may have induced a bee dispersal response soon after bees were released in the fields that circumvented the need for, or impact of, maternal manipulation.

Evaluation of a novel bumble bee pollination station under summer greenhouse conditions

SummaryIn several world regions, greenhouse horticultural production is characterized by the use of simple low cost structures with limited climate control. Conditions in these are especially hard for bumble bee colonies during the summer months. Several factors can limit bumble bee activity and thus fruit set, including high temperatures, high radiation and poor quality and low volumes of pollen. In 2009 we carried out experiments to determine the influence of a commercial bumble bee “pollination station” on hive climate parameters and hive performance in tomato greenhouses under extreme summer environmental conditions. We found that air temperature and humidity fluctuation during the day was lower for the hives in the pollination station compared to control hives. Final numbers of adult bees and cocoons, and daily colony traffic were significantly higher (54%, 43% and 50.5% respectively) in the pollination stations than in control hives. This is the first report of a pollination station for bumble bees.

SuperBoost® synthetic brood pheromone enhances spring build-up of overwintered honey bee colonies

SummarySuperBoost® is a proprietary commercial product comprising the non-volatile 10-component honey bee brood pheromone, stabilized with an antioxidant, and delivered to a colony in a controlled release device. The pheromone (180 mg) is contained in a plastic pouch with a pheromone-permeable polyethylene release membrane and a pheromone-impermeable Mylar backing. The pouch is mounted in a solid plastic holder. A 12-replicate, 70-day, single-blind experiment was set up on 4 February 2009 at Abbotsford BC, Canada, to test the utility of SuperBoost for enhancing spring build-up of overwintered honey bee colonies. Colonies were randomly assigned as untreated controls or to be treated with freshly-loaded SuperBoost devices. Devices were replaced once (after 37 days). Supplementary pollen substitute (Bee Pro®) was fed to bees ad libitum. Measurements of BeePro consumption were made on nine occasions. On days 16 and 70 the area of brood comb and numbers of adult bees were determined. When colonies were divided (split), the numbers of daughter colonies were recorded. Two colonies treated with SuperBoost died during the experiment, as did one control colony. SuperBoost devices released 0.37 and 0.54 mg per day of pheromone over the two exposure periods, as determined gravimetrically. By Day 70, treated colonies had consumed 50% more BeePro than control colonies. Treated colonies had significantly more brood comb area (2.4 times) and adults (2.0 times) than control colonies. By day 96, six of the 10 surviving SuperBoost treated colonies had produced nine daughter colonies, a significantly higher proportion than the two of 11 control colonies, which produced four splits. We suggest that SuperBoost has substantial potential for enhancing the spring build-up of overwintered colonies.

The Effects of Four Insect Growth-Regulating (IGR) Insecticides on Honeybee (Apis mellifera L.) Colony Development, Queen Rearing and Drone Sperm Production

This study assessed the effects of exposure to IGRs on the long-term development of the honeybee colony, viability of queens and sperm production in drones and integrated the data into a honeybee population model. Colonies treated with diflubenzuron resulted in a short-term reduction in the numbers of adult bees and brood. Colonies treated with fenoxycarb declined during the season earlier and started the season slower. The number of queens that successfully mated and laid eggs was affected in the fenoxycarb treatment group but there were no significant differences in the drone sperm counts between the colonies. An existing honeybee population model was modified to include exposure to IGRs. In the model, fenoxycarb reduced the winter size of the colony, with the greatest effects following a June or an August application. Assuming a 'larvae per nurse bee' ratio of 1.5 for brood rearing capability, the reduction in winter size of a colony following a fenoxycarb application was at its worst about 8%. However, even if only those bees reared within 2 weeks of the IGR being applied are subject to premature ageing, this might significantly reduce the size of over-wintering colonies, and increase the chance of the bee population dwindling and dying in late winter or early spring.

Nest and colony characteristics of log-hived Melipona beecheii (Apidae: Meliponinae)

SUMMARYThe log hives of 19 colonies of the stingless bee Melipona beecheii were opened and adult and brood populations, stored nectar and pollen, and other nest characteristics were recorded. Adult populations were found to be between 500 and 2500. The presence of queen pupae in the brood and the size of the brood nest were found to be positively correlated. Adult gynes and males were seldom observed. Brood populations were generally found to be two to four times the number of adult bees. Honey stores were often smaller than pollen stores, and only few colonies contained more than 1litre. The volume of the cavity of the hives was between 5 litres and 16 litres. Blackened and useless pollen was found in several nests, usually in the bigger ones. New for Central American species of Melipona is the description of radiating entrance structures. The ultimate function of several nest structures is discussed in relation to the typical stingless bee biology and ecology. Recommendations for hive design are made.

TOXICITY EFFECTS AND CHALKBROOD INCIDENCE IN HONEY BEE1 COLONIES FED CONTROLLED DOSES OF FUNGICIDES2,3

Folpet and a combination with folpet, benomyl, citral, sodium propionate, and sorbic acid were fed or exposed to honey bee, Apis mellifera L., field colonies to: 1) determine their long-term toxic effects on the bees; and 2) to determine if chalkbrood (CB) disease, Ascosphaera apis (Maassen ex Claussen) Olive et Spiltor, is inhibited or controlled by the compounds. When folpet was fed to honey bee colonies in sucrose syrup, the group fed the highest rate (1000 ppm) never differed significantly (P &amp;gt; 0.05) from the control colonies. There was an equal number of adult bees, an equal amount of sealed brood, and mortality was identical. Analysis indicated significantly (P &amp;lt; 0.05) fewer CB mummies in treatment groups fed 10 or 1000 ppm folpet, but this apparent benefit may have been due to seasonal changes of reduced CB infection that occur in late summer. Folpet or a combination of folpet, benomyl, citral, sodium propionate, and sorbic acid (1000 ppm each, total 5000 ppm) incorporated into lipid/sucrose extender patties produced no significant (P &amp;gt; 0.05) effect of any kind on colonies to which they were applied, including CB infection. However, when the combination of five fungicides (5000 ppm) was impregnated into beeswax foundation and exposed to honey bee colonies, only a small amount of comb was drawn on the test foundation, indicating a repellent effect. Otherwise, the test foundation had no significant (P &amp;gt; 0.05) effect on the honey bees or the CB infection.