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At least 1,117 records · Page 62Linked to original sources
PubMed2001

Optimum timing of miticide applications for control of Varroa destructor (Acari: Varroidae) in Apis mellifera (Hymenoptera: Apidae) in Washington State, USA.

Seven treatments for the control of Varroa destructor (Anderson & Trueman) were tested to determine the optimum timing of miticide application. Threshold mite levels indicating miticide application were determined for three possible treatment dates: April, August, and October. The treatments were as follows: (1) fluvalinate in April, (2) fluvalinate in August, (3) fluvalinate in October, (4) fluvalinate in April and October, (5) fluvalinate applied continuously (except during honey flow) with replacement every 42 d, (6) control (no treatment), and (7) coumaphos in April. The number of miticide applications in a season had no effect on brood area or colony bee population a year after initiating the experiment. However, the absence of any treatment significantly reduced brood area and colony bee population and significantly increased colony mite population. Date of treatment had significant effects on colony mortality rates, mite levels, and brood area the following spring. When coupled with sampling and threshold recommendations, a single, late-season application of fluvalinate is as effective for the control of V. destructor as semiannual or continuous miticide applications. Treatment thresholds were recommended for ether roll and 48-h sticky board sampling methods in April (three and 24 mites, respectively) and August (14 and 46 mites, respectively) and for ether rolls in October (three mites) in cold climates.

Animals↗
PubMed2003

Field trials using the fungal pathogen, Metarhizium anisopliae (Deuteromycetes: Hyphomycetes) to control the ectoparasitic mite, Varroa destructor (Acari: Varroidae) in honey bee, Apis mellifera (Hymenoptera: Apidae) colonies.

The potential for Metarhizium anisopliae (Metschinkoff) to control the parasitic mite, Varroa destructor (Anderson and Trueman) in honey bee colonies was evaluated in field trials against the miticide, tau-fluvalinate (Apistan). Peak mortality of V. destructor occurred 3-4 d after the conidia were applied; however, the mites were still infected 42 d posttreatments. Two application methods were tested: dusts and strips coated with the fungal conidia, and both methods resulted in successful control of mite populations. The fungal treatments were as effective as the Apistan, at the end of the 42-d period of the experiment. The data suggested that optimum mite control could be achieved when no brood is being produced, or when brood production is low, such as in the early spring or late fall. M. anisopliae was harmless to the honey bees (adult bees, or brood) and colony development was not affected. Mite mortality was highly correlated with mycosis in dead mites collected from sticky traps, indicating that the fungus was infecting and killing the mites. Because workers and drones drift between hives, the adult bees were able to spread the fungus between honey bee colonies in the apiary, a situation that could be beneficial to beekeepers.

Animals↗
PubMed2004

Formic acid treatment for control of Varroa destructor (Mesostigmata: Varroidae) and safety to Apis mellifera (Hymenoptera: Apidae) under southern United States conditions.

The efficacy of a formic acid pad formulation was field tested for control of the honey bee parasitic mite Varroa destructor Anderson & Trueman in Florida and Texas. This pad formulation gave 39.8 +/- 11.1% control at the end of a 6-wk treatment period, which did not significantly differ from the initial sample date. Coumaphos treatment provided poor control (38.4 +/- 11.1%) over the 6-wk period, confirming reports of coumaphos resistance in the region. Under relatively warm winter conditions in southern Texas, formic acid caused mortality of developing eggs and brood. If resistance by V. destructor to the two acaricides registered for its control in the United States continues, the formic acid pad could provide an alternative compound to use as part of an integrated pest management approach. Given the low control seen in this trial, however, modifications of application technology would seem necessary.

Animals↗
PubMed2005

Evaluation of drone brood removal for management of Varroa destructor (Acari: Varroidae) in colonies of Apis mellifera (Hymenoptera: Apidae) in the northeastern United States.

The efficacy of drone brood removal for the management of Varroa destructor Anderson & Trueman in colonies of the honey bee, A. mellifera L., was evaluated. Colonies were treated with CheckMite+ in the fall of 2002. The following spring, quantities of bees and brood were equalized, but colonies were not retreated. The brood nest of each colony consisted of 18 full-depth worker combs and two full-depth drone combs. Each worker comb had <12.9 cm2 of drone cells. Standard management practices were used throughout the season. Colonies were randomly assigned to one of two groups. In the control group, drone combs remained in place throughout the season. In the treatment group, drone combs were removed on 16 June, 16 July, 16 August, and 16 September and replaced with empty drone combs (16 June) or with drone combs removed on the previous replacement date. In the early fall, the average mite-to-bee ratio in the control group was significantly greater than the corresponding ratio in the treatment group. Drone brood removal did not adversely affect colony health as measured by the size of the worker population or by honey production. Fall worker populations were similar in the two groups. Honey production in treatment colonies was greater than or similar to production in control colonies. These data demonstrate that drone brood removal can serve as a valuable component in an integrated pest management program for V. destructor and may reduce the need for other treatments on a colony-by-colony basis.

Acari↗
PubMed1997

Some preliminary studies on the ability of Africanized honey bees (Apis mellifera L.) to tolerate cold temperatures when placed inside a refrigerator.

Cold is often suggested as an ecological mechanism to prevent the migration of Africanized honey bees. The ability of Africanized honey bees to tolerate cold temperatures was investigated. In one study an observation hive was placed inside a refrigerator at 25 degrees C. The study was conceptualized as a choice experiment in which the colony could remain in a cold environment or leave for a warm environment. Analysis indicated that the bees remained at 9 +/- 1 degrees C for 14 days before leaving. In a second series of studies, testing the tolerance to 0 degree C, 280 bees were placed individually in small metal tubes. The data gathered included survival rate, time to regain consciousness, and ability to feed. Analysis indicated that Africanized bees can survive for up to 3 hr. at 0 degree C with few ill effects. At 4 hr., however, the survival rate is low. Limitations of the study, the use of cold as a possible deterrent to honey bee mites, and suggestions for additional research are discussed.

Animals↗
PubMed2003

Development of an ethanol model using social insects: II. Effect of Antabuse on consumatory responses and learned behavior of the honey bee (Apis mellifera L.).

The ability of Antabuse (disulfiram) to influence ethanol consumption and learning in harnessed honey bees was investigated. In the first series of experiments a factorial design was used with 5 levels of ethanol concentration (0%, 1%, 5%, 10%, 20%), 4 doses of Antabuse (0, 37 microg/g, 3.7 microg/g, .37 microg/g), and 2 testing intervals (1 min., 10 min.). Animals were fed a single 1 microl dose of Antabuse and contact time with an ethanol solution measured. A second series of experiments investigated the influence of Antabuse on the formation of Pavlovian conditioning of the proboscis extension reflex. A factorial design was used with two levels of training (paired, unpaired), three levels of ethanol (0%, 1%, 5%), and 2 levels of pretreatment (distilled water, 3.7 microg/g). Analysis of the consumption experiments indicate that pretreatment with Antabuse reduces ethanol intake, although there was substantial variability. The findings of the Pavlovian experiments suggest that pretreatment with Antabuse significantly reduced responding to a CS signaling the availability of ethanol.

Alcohol Deterrents↗
PubMed2004

Development of an ethanol model using social insects: IV. Influence of ethanol on the aggression of Africanized honey bees (Apis mellifera L.).

Experiments were designed to determine whether ethanol influenced aggression in honey bees. Two experiments are reported. In Exp. 1, harnessed honey bees were fed a 1%, 5%, 10%, or 20% ethanol solution. Two control groups received either a sucrose solution only or no pretreatment, respectively. The dependent variable was the number of sting extensions over 10 min. Analysis showed that aggression in harnessed bees was not influenced by prior ethanol consumption. Because there was some suspicion that the extension of the sting apparatus may be hindered by harnessing, and the authors wanted to use a design that increased ecological validity, Exp. 2 was conducted with free-flying bees. Sucrose or 20% ethanol solutions were placed in front of beehives, and the number of stings on a leather patch dangled in front of the hive served as the dependent variable. The experiment was terminated after 5 hr. because bees exposed to ethanol became dangerously aggressive. A unique aspect of the study was that Africanized honey bees were used.

Aggression↗
PubMed2000

Senescence and learning in honeybee (Apis mellifera) workers.

Foraging by honeybee workers was investigated from the moment of the first foraging flight until death. To minimise the influence of factors other than senescence the foragers were trained to collect food from an artificial flower close to their hive. During each foraging trip the workers repeatedly visited an artificial flower, collecting one microlitre of 50% sugar solution per visit. During the first 50 flights the mean time taken to collect one portion of food decreased significantly and the number of visits to the artificial flower per flight increased significantly. During flights following the 50th flight, the mean time taken to collect one portion of food increased significantly and the number of visits to the artificial flower per flight decreased significantly. The results confirm earlier observations that the foraging behaviour of honeybee workers is not only influenced by learning, but also by the effects of senescence.

Aging↗
PubMedDate not supplied

Early development of mushroom bodies in the brain of the honeybee Apis mellifera as revealed by BrdU incorporation and ablation experiments.

In the honeybee the mushroom bodies are prominent neuropil structures arranged as pairs in the dorsal protocerebrum of the brain. Each mushroom body is composed of a medial and a lateral subunit. To understand their development, the proliferation pattern of mushroom body intrinsic cells, the Kenyon cells, were examined during larval and pupal stages using the bromodeoxyuridine (BrdU) technique and chemical ablation with hydroxyurea. By larval stage 1, approximately 40 neuroblasts are located in the periphery of the protocerebrum. Many of these stem cells divide asymmetrically to produce a chain of ganglion mother cells. Kenyon cell precursors underly a different proliferation pattern. With the beginning of larval stage 3, they are arranged in two large distinct cell clusters in each side of the brain. BrdU incorporation into newly synthesized DNA and its immunohistochemical detection show high mitotic activity in these cell clusters that lasts until mid-pupal stages. The uniform diameter of cells, the homogeneous distribution of BrdU-labeled nuclei, and the presence of equally dividing cells in these clusters indicate symmetrical cell divisions of Kenyon cell precursors. Hydroxyurea applied to stage 1 larvae caused the selective ablation of mushroom bodies. Within these animals a variety of defects were observed. In the majority of brains exhibiting mushroom body defects, either one mushroom body subunit on one or on both sides, or three or four subunits (e.g., complete mushroom body ablation) were missing. In contrast, partial ablation of mushroom body subunits resulting in small Kenyon cell clusters and peduncles was observed very rarely. These findings indicate that hydroxyurea applied during larval stage 1 selectively deletes Kenyon stem cells. The results also show that each mushroom body subunit originates from a very small number of stem cells and develops independently of its neighboring subunit.

Animals↗
PubMed2000

Detection of nerve growth factor (NGF) in venoms from diverse source: isolation and characterization of NGF from the venom of honey bee (Apis melifera).

Pearce (1973) reported the absence of NGF in the venoms of bees, scorpions, spiders, and toads. Contrary to the negative findings in the past, results of this research prove the presence of NGF in bee and scorpion venoms. Venoms from various species of snake, bee, scorpion, and toad were screened by two methods: immunological test ELISA using antibodies versus mouse NGF and venom NGF and the biological test of neurite outgrowth, the characteristic of NGF on PC cells. The presence of NGF was detected in snake, bee, and scorpion venoms, but not in toad venom by these tests. NGF was isolated from bee venom by HPLC fractionation using ion exchange chromatography. The molecular weight of bee NGF was found to be 14.0 kDa resolving into a single band by PAGE. The biological activity of bee NGF on PC12 cells was found to be 1/10 of the venom NGF.

Animals↗
PubMed2000

The development of an ethanol model using social insects I: behavior studies of the honey bee (Apis mellifera L.).

BACKGROUND: The purpose of this experiment was to test the feasibility of creating an animal model of ethanol consumption using social insects. Honey bees were selected as the model social insect because much is known about their natural history, physiology, genetics, and behavior. They are also inexpensive to procure and maintain. Of special interest is their use of communication and social organization. METHODS: Using both between- and within-experiment designs, studies were conducted with harnessed foragers to determine whether honey bees would consume ethanol mixed with sucrose (and, in some cases, water). Shuttle-box and running-wheel studies were conducted to examine the effect of ethanol on locomotion. The effect of ethanol on stinging behavior in harnessed foragers was investigated. The effect of ethanol on Pavlovian conditioning of proboscis extension was also investigated. Finally, in a self-administration study, foraging honey bees were trained to fly to an artificial flower containing ethanol. RESULTS: (1) Harnessed honey bees readily consume 1%, 5%, 10%, and 20% ethanol solutions; (2) 95% ethanol will also be consumed as long as the antennae do not make contact with the solution; (3) with the exception of 95% ethanol, consumption as measured by contact time or amount consumed does not differ in animals that consume 1%, 5%, 10%, and 20% ethanol solutions; (4) exposure to a lesser (or greater) concentration of ethanol does not influence consumption of a greater (or lesser) concentration; (5) consumption of 10% and 20% ethanol solutions decreases locomotion when tested in both a shuttle-box and running-wheel situation; (6) consumption of 1%, 5%, 10%, and 20% ethanol does not influence stinging behavior in harnessed foragers; (7) ethanol solutions greater than 5% significantly impair Pavlovian conditioning of proboscis extension; and (8) free-flying honey bee foragers will readily drink from an artificial flower containing 5% ethanol. CONCLUSIONS: The experiments on consumption, locomotion, and learning suggest that exposure to ethanol influences behavior of honey bees similar to that observed in experiments with analogous vertebrates. The honey bee model presents unique research opportunities regarding the influence of ethanol in the areas of language, social interaction, development, and learning. Although the behavioral results are interesting, similarity between the physiologic effects of ethanol on honey bees and vertebrates has not yet been determined.

Aggression↗
PubMed1975

[Electron microscopic studies on the retina of the honey bee (Apis mellifica): II. Investigations on reactions of the fine structure of the rhabdomeric tubuli after exposure to various experimental influences, especially to light of different wavelength (author's transl)].

Electron microscopic studies were made on the fine structure of the rhabdomeric tubuli of the honey bee-eye after exposure to white and monochromatic light. Several preparation and fixation techniques were tested. A method to irradiate the eyes in vitro by high intensity of white or monochromatic light was developped.

Animals↗