ライフサイエンスコーパス: honeybee

1 an Peninsula countries (honey from A-lineage honeybees).

2 arily conserved and can also be found in the honeybee.

3 ression of piggyBac-derived cassettes in the honeybee.

4 a uniform model of olfactory learning in the honeybee.

5 thways mediate learned food aversions in the honeybee.

6 (Varroa destructor), an ecto-parasite of the honeybee.

7 ortive meiotic division, which occurs in the honeybee.

8 icing changes upon pesticide exposure in the honeybee.

9 in recombination rate between subspecies of honeybee.

10 ch varies depending on the flora used by the honeybees.

11 d limiting the utilisation of visual cues in honeybees.

12 source, i.e., attacked and/or freshly killed honeybees.

13 estructor, are a major threat to the world's honeybees.

14 plant with pitfall flowers, mimics attacked honeybees.

15 environmental pollutant toxicities for adult honeybees.

16 ly, dependent on the pollination activity of honeybees.

17 d colony-level effects in free-flying worker honeybees.

18 nding of processes underlying the biology of honeybees.

19 oyal jelly, induces queen differentiation in honeybees.

20 that impair olfactory learning and memory in honeybees.

21 aching in ants and behavioural traditions in honeybees.

22 contributes to higher recombination rates in honeybees.

23 cantly reduced survival of long-lived winter honeybees.

24 developed to differentiate C- and M-lineages honeybees.

25 role in learning and memory is not clear in honeybees.

26 Honeybees(1) and bumblebees(2) perform learning flights

27 rees C) than sweat bees (50.3 degrees C) and honeybees (49.1 degrees C).

28 Honeybees [6] and ants [7, 8] foraging from their nest c

29 (51.7%), followed by bumblebees (63.7%) and honeybees (74.2%).

30 Comparing the ant genomes with those of the honeybee, a lineage that evolved eusociality independent

31 important commercial pollinator, the Western honeybee, a major concern in the Northern Hemisphere.

32 t themselves and their provisions, paralyzed honeybees, against mold fungi.

33 Highly aggressive Africanized honeybees (AHB) invaded Puerto Rico (PR) in 1994, displa

34 cium imaging of odor induced activity in the honeybee AL to evaluate the relevance of this temporal d

35 IP-Seq datasets derived from Apis mellifera (honeybee), an invertebrate species that contains more as

36 In honeybees, an elaborate language could evolve because re

37 lomerular numbers are higher in the eusocial honeybee and a sexual dimorphism of the relative investm

38 , but haploid-only and male-haploid (such as honeybee and ant) species have been described.

39 question, we use calcium imaging of isolated honeybee and Drosophila Kenyon cells (KCs), which are ta

40 Comparing island honeybee and wild bumblebee populations with and without

41 V) and the exotic parasite Nosema ceranae in honeybees and bumblebees is linked; as honeybees have hi

42 es on commercially bred species (principally honeybees and bumblebees) have identified sub-lethal eff

43 lysis virus (SBPV), cause lethal diseases in honeybees and bumblebees, resulting in agricultural loss

44 l projection patterns resemble situations in honeybees and Drosophila.

45 Nevertheless, in insects as diverse as honeybees and houseflies, Sxl seems not to determine sex

46 sities of bumblebees, solitary bees, managed honeybees and hoverflies were negatively related to the

47 for further work on compound conditioning in honeybees and other animals are considered.

48 Despite this risk, honeybees and other sequenced social insects have far fe

49 Bumblebees, honeybees and stingless bees can distinguish flowers bas

50 s, whereas it is clearly present in eusocial honeybees and stingless bees.

51 estructor drives DWV prevalence and titre in honeybees and sympatric bumblebees.

52 in areas where international trade has moved honeybees and their disease.

53 centrations that are encountered by foraging honeybees and within the hive, and are additive with com

54 systems of these bumblebees, two species of honeybee, and a solitary leafcutting bee, are strikingly

55 We compared the genomes of seven ants, the honeybee, and various solitary insects to examine whethe

56 as t(1.7) for ants, from t(1.6) to t(5) for honeybees, and from t(1.46) to t(2.9) for termites.

57 del of the nest-choice dynamics in swarms of honeybees, and have concluded that both interdependence

58 are similarly depauperate in bumblebees and honeybees, and multiple categories of genes linked to so

59 lia scalaris, mosquitoes, butterfly, beetle, honeybee, ant, and aphid.

60 o link changes in structural organization of honeybees' antennal lobes with their behavioural perform

61 We used the honeybee Apis mellifera and conducted a series of experi

62 new genomes to those of the highly eusocial honeybee Apis mellifera and other Hymenoptera, we identi

63 ly spread from a common source, the European honeybee Apis mellifera.

64 dentify neuronal cell types of the CX in the honeybee Apis mellifera.

65 cing in the sex determination cascade of the honeybee Apis mellifera.

66 g important pollinators such as the European honeybee Apis mellifera.

67 Honeybees Apis mellifera are important pollinators of wi

68 simulate effects of pesticides on different honeybee (Apis mellifera L.) life stages, we used the BE

69 Concern over reported honeybee (Apis mellifera spp.) losses has highlighted ch

70 the flour beetle (Tribolium castaneum), the honeybee (Apis mellifera) and the fruit fly (Drosophila

71 multiple RNA viruses in co-occurring managed honeybee (Apis mellifera) and wild bumblebee (Bombus spp

72 perception and the circadian clock using the honeybee (Apis mellifera) as a model.

73 If a honeybee (Apis mellifera) colony loses its queen, worker

74 The honeybee (Apis mellifera) dance communication system is

75 Social evolution in the honeybee (Apis mellifera) has resulted in queens with 20

76 The honeybee (Apis mellifera) is a eusocial insect displayin

77 The pressures on honeybee (Apis mellifera) populations, resulting from th

78 ere, we further explored these models in the honeybee (Apis mellifera) using worker nutrition rearing

79 Honeybee (Apis mellifera) venom (HBV) has been a subject

80 inum hydroxide (Al[OH](3))-adsorbed purified honeybee (Apis mellifera) venom (HBV) preparations can r

81 most damaging bacterial brood disease of the honeybee (Apis mellifera), causing colony deaths on all

82 ts of the csd gene among 76 genotypes of the honeybee (Apis mellifera).

83 Free-flying honeybees (Apis mellifera carnica) are known to learn th

84 During olfactory learning in honeybees (Apis mellifera) and Drosophila melanogaster t

85 Honeybees (Apis mellifera) can use stimulus onset asynch

86 ood is the most destructive brood disease of honeybees (Apis mellifera) globally.

87 In a recent experiment on short-term memory, honeybees (Apis mellifera) learned to choose between 2 c

88 d sweat bees (Agapostemon sericeus), western honeybees (Apis mellifera), and common eastern bumblebee

89 Honeybees (Apis mellifera), important pollinators for cr

90 but demonstrated only recently in work with honeybees (Apis mellifera), that the different treatment

91 Honeybees (Apis mellifera), the prevailing managed insec

92 Honeybees (Apis mellifera), which are important pollinat

93 l correlates of visual attention in behaving honeybees (Apis mellifera).

94 s and gene conversions in 22 colonies of the honeybee, Apis mellifera, and 9 colonies of the bumblebe

95 We here show that antennal movements of the honeybee, Apis mellifera, are governed by combined visua

96 The Western honeybee, Apis mellifera, is the most important managed

97 In the advanced eusocial honeybee, Apis mellifera, studies suggest that microRNAs

98 a specific task by using allogrooming in the honeybee, Apis mellifera, where worker behaviour might l

99 Honeybees, Apis mellifera, are able to distinguish mixtu

100 s, while the "socio-genomes" of ants and the honeybee are broadly characterized by a pervasive patter

101 Honeybees are an excellent model system for examining ho

102 Tasks performed by worker honeybees are distributed in time and space.

103 and honey and determinates in what extension honeybees are exposed to them.

104 Honeybees are exposed to two widely used classes of chol

105 DWV prevalence, and sympatric bumblebees and honeybees are infected by the same DWV strains, Apis is

106 ausing colony deaths on all continents where honeybees are managed.

107 Honeybees are models for studying how animals with relat

108 The results suggest that at colony level, honeybees are relatively robust to the effects of clothi

109 Honeybees are typically used as a model organism to inve

110 Multiple RNA viruses associated with honeybees are widespread in sympatric wild bumblebee pop

111 r systems, for example, hydra, squid and the honeybee, are valuable alternative models to address spe

112 of honeybees with the aim of developing the honeybee as a model for understanding how an individual'

113 orientation has been extensively studied in honeybees at the behavioral level, most electrophysiolog

114 These tools are difficult to apply in honeybees because the unit of reproduction is the colony

115 ances in dissecting the complex processes of honeybee behavior have been limited in the recent past d

116 e can bind to two characterized receptors in honeybees, both of which are coupled to intracellular cA

117 plore this hypothesis by asking where in the honeybee brain AmCREB-dependent processes might take pla

118 an be induced into the antennal lobes of the honeybee brain by injecting ferrous ammonium citrate (FA

119 shroom body Kenyon cells in acutely isolated honeybee brain, we show that the neonicotinoids imidaclo

120 In honeybee brains, CREB-dependent genes are regulated in a

121 In honeybee brains, it labels different structures which pr

122 ion can significantly improve the success of honeybee breeding programs.

123 ethylation can affect learning and memory of honeybees by regulating other epigenetic modification pr

124 New research shows that honeybees can classify arrangements of two visual patter

125 Recent studies reported that honeybees can perform elemental learning by associating

126 Ants, like honeybees, can set their travel direction along foraging

127 European honeybees collect this honeydew and make it into a type

128 tainably high losses of managed A. mellifera honeybee colonies in many regions of the world.

129 overwinter decline (workforce mortality) of honeybee colonies in the field.

130 Honeybee colonies reproduce two ways: producing swarms c

131 d spread of chemosensory preferences through honeybee colonies via classical conditioning procedures.

132 A three-day treatment of honeybee colonies with 25 mM LiCl in 1L/day sucrose solu

133 lterated honey samples obtained from feeding honeybee colonies with different levels (5, 20 and 100 L

134 nd predicting of the swarming process within honeybee colonies, using vibro-acoustic information.

135 portant and increasing threat to the managed honeybee colonies, which are vital in crop pollination.

136 ulations and driven by trade and movement of honeybee colonies.

137 ned larvae exhibiting rebel traits emerge in honeybee colonies.

138 rlying polyethism and social organization in honeybee colonies.

139 help explain, in part, the global decline of honeybee colonies.

140 bees with an additional year and new data on honeybee colony development, swarming, mortality, pathog

141 Recently, the causes of honeybee colony losses have been intensely studied, show

142 For more than a decade, high percentages of honeybee colony losses have been reported worldwide.

143 The large numbers of honeybee colony losses reported in recent years have bee

144 e stressors have been implicated in elevated honeybee colony losses.

145 sophisticated and hierarchical structure of honeybee combs and measure the elastic properties of fre

146 over interference are significantly lower in honeybees compared to bumblebees, which may be one mecha

147 onal states across species and suggests that honeybees could be regarded as exhibiting emotions.

148 ting that there might be a role for neuronal honeybee CREB (Apis mellifera CREB, or AmCREB) in the be

149 ngredient mass basis) to kill over a billion honeybees daily.

150 information using a symbolic 'language' (the honeybee dance) and the rapid spread of chemosensory pre

151 worldwide on corn crops have been blamed for honeybee decline.

152 Recombinants of the honeybee deformed wing virus and the Varroa destructor v

153 The first morphological worker mutants in honeybees demonstrate that the response to nutrition rel

154 ived arabinogalactan proteins (AGPs) and the honeybee-derived protein apisimin are present in varieti

155 Here, we ask whether honeybees display a pessimistic cognitive bias when they

156 Honeybees display a unique biolocomotion strategy at the

157 We report that honeybee dsx is sex-specifically spliced and that it pro

158 We suggest that parallel processing via the honeybee dual olfactory pathway provides enhanced odor p

159 ica, providing the palaeoecological range of honeybees during prehistory.

160 ory regions of the more ancient mosquito and honeybee E(spl) bHLH genes.

161 ico (PR) in 1994, displacing gentle European honeybees (EHB) in many locations.

162 and landscape-scale field data to show that honeybee EIDs are indeed widespread infectious agents wi

163 Free-flying honeybees exhibit remarkable cognitive capacities but th

164 We analyzed landscape-level honeybee foraging ecology patterns over two years by dec

165 t alone, suggesting unexpected complexity in honeybee foraging networks.

166 Honeybees form complex societies with a division of labo

167 Honeybees form societies in which thousands of members i

168 wers protects both the plant and pollinating honeybees from pathogens (phytopathogenic fungus Botryti

169 xperiments with odors and colors free-flying honeybees gave no evidence of blocking; separate reinfor

170 Some honeybee genome features thought to underpin advanced eu

171 Artificial selection for disease-resistant honeybee genotypes has previously only been carried out

172 ry conditions that electrostatically charged honeybees, green bottle flies, fruit flies, aphids, and

173 otic exposure on the size and composition of honeybee gut communities.

174 ects on both the size and composition of the honeybee gut microbiome.

175 mosome pairs, some hymenopterans such as the honeybee have been shown to produce haploid sperm throug

176 These findings reveal that honeybees have evolved a secreted dietary RNA-binding fa

177 ae in honeybees and bumblebees is linked; as honeybees have higher DWV prevalence, and sympatric bumb

178 This is remarkable because worker honeybees have reduced reproductive organs and are norma

179 Honeybees have remarkable visual cognitive abilities, al

180 is shows that DWV is globally distributed in honeybees, having recently spread from a common source,

181 e if dysbiosis of the gut microbiome impacts honeybee health, and we performed experiments to determi

182 ight the importance of the gut microbiome in honeybee health, but they also provide insights into how

183 using accelerometers placed in the heart of honeybee hives.

184 g and understanding the impact of DWV in non-honeybee hosts are major new goals.

185 ht the predominance of honeys from C-lineage honeybees in Europe, except in Iberian Peninsula countri

186 l sweet substance produced by Apis mellifera honeybees in Europe.

187 ometry and corridor-centering in free-flying honeybees, including previously unaccounted for manipula

188 th increasing cover of MFCs but densities of honeybees increased.

189 unknown function secreted from the glands of honeybees into Royal Jelly, forming a complex with apalb

190 demonstrated horizontal RNA transfer between honeybees involving secretion and ingestion of worker an

191 The honeybee is a model organism for studying learning and m

192 Pollen hoarding (pln) in honeybees is a complex trait associated with a well-char

193 Virus prevalence in honeybees is a significant predictor of virus prevalence

194 In honeybees, it is assumed to have functions in modulating

195 In the whole population of honeybee KCs we find that pairing of acetylcholine (ACh)

196 nsecticides may constitute a major hazard to honeybees, leading to colony collapse disorder.

197 evels of neonicotinoids are known to disrupt honeybee learning and behaviour, the neurophysiological

198 In honeybees, learning flights become longer when the rewar

199 , despite clear evidence of strong effect on honeybee longevity of widely-employed neonicotinoid inse

200 may be a major cause of elevated overwinter honeybee loss.

201 o efficient and effective foraging by aiding honeybee memory of a learned olfactory association [4],

202 This specialist honeybee mite vectors deformed wing virus (DWV), an impo

203 ogy of neurons that constitute the CX in the honeybee mostly enigmatic.

204 rom simple neural circuits, in this case the honeybee mushroom body.

205 hours and that it can be transferred between honeybee nestmates during trophallaxis.

206 Here we show that honeybees not only detect toxins but can also learn to a

207 extensive involvement of DNA methylation in honeybee olfactory learning and memory process.

208 The honeybee olfactory system is a well-established model fo

209 s to the observed behavioural performance of honeybees on these cues.

210 resistance in mice to the lethal effects of honeybee or Russell's viper venom.

211 ogen spillover from managed pollinators like honeybees or commercial colonies of bumblebees.

212 t differ in selection between bumblebees and honeybees, or between the social and solitary clades.

213 The content of GOx of honeybee origin was believed to be the main predictor of

214 potential to interact with its pollinators (honeybees, other bees, butterflies and flies) through ir

215 e event durations experienced by a colony of honeybees over their entire lifetimes.

216 d wing virus (DWV), an important re-emerging honeybee pathogen that also infects wild bumblebees.

217 Varroa destructor, the primary honeybee pathogen, is kept in check by various chemical

218 New research on ants and honeybees points to DNA methylation as a crucial factor

219 ntly mediated by European and North American honeybee populations and driven by trade and movement of

220 Although DWV was previously present in honeybee populations, the arrival and global spread of a

221 is higher in wild bumblebees than in managed honeybee populations.

222 rrent and next generation pesticides pose to honeybee populations.

223 ecting for distance, dances demonstrate that honeybees possess a significant preference for rural lan

224 Honeybees possess an elaborate olfactory system with uni

225 ounds which may enter the human diet through honeybee products.

226 by a lower level of sociality than ants and honeybees provide new insights into the origin and evolu

227 or, an ectoparasitic viral vector in Western honeybees, provides a unique opportunity to examine how

228 However, honeybee queens mate with many males and so each colony

229 Honeybees quickly learn to associate floral cues with fo

230 Using honeybees radar-tracked during their orientation flights

231 nforming to patterns readily learned even by honeybees, rats, and sleeping human neonates.

232 hive-based olfactory information transfer to honeybee recruitment events.

233 A new behavioural study shows that honeybees remember visual panoramas in a compass-based c

234 RNA viruses associated with honeybees represent a potential threat to other insect p

235 Honeybees rewarded with caffeine, which occurs naturally

236 y to remember a learned floral scent as were honeybees rewarded with sucrose alone.

237 Maeterlinck did not mean to suggest that honeybees rival humans in intelligence - rather he saw i

238 e during conditioning and testing improved a honeybee's ability to learn, recognize, and differentiat

239 esting whether odor concentration affected a honeybee's ability to learn, recognize, and discriminate

240 We further report that the honeybee's channel is also sensitive to permethrin and f

241 Radar studies of a honeybee's flights when it first leaves its nest suggest

242 uch changes in recognition may impact upon a honeybee's foraging efficiency and therefore the pollina

243 rmacological characterization of the western honeybee's sodium channel (Apis Mellifera NaV1).

244 ater surface may increase the water-foraging honeybee's survival chances when they fall on the water.

245 lso the basis of a neural 'front end' of the honeybee's visual odometer.

246 Honeybees show a fairly abrupt increase in response afte

247 New findings on foraging honeybees show that co-existing strategies, where some i

248 Myoglobin was embedded in transparent honeybee silk protein films.

249 eveals previously unrecognized plasticity in honeybee social organization.

250 In honeybee societies, distinct caste phenotypes are create

251 ce amounts and is nearly absent in sympatric honeybee species (respectively only 0.07% and 0.44% as m

252 f rapid-onset systemic allergic reactions to honeybee stings and positive specific IgE levels to eval

253 In European honeybee stocks bidirectionally selected for pln, worker

254 Honeybee swarms and complex brains show many parallels i

255 higher rates measured in the highly eusocial honeybee than the primitively social bumblebee.

256 These flies are well known to feed on honeybees that are eaten by spiders, which we thus predi

257 Compared with the Western honeybee, the degree of sexual dimorphism in Eucera is m

258 In the honeybee, their main sensory input regions are large, do

259 Honeybees therefore appear to have a unique, evolutionar

260 stimated--route of environmental exposure of honeybees to and intoxication with neonicotinoid insecti

261 To test this, we trained foraging-age honeybees to learn to associate floral scent with a rewa

262 ificantly reduced the ability of the trained honeybees to recognize the altered odour.

263 ith field-realistic doses of caffeine caused honeybees to significantly increase their foraging frequ

264 Extrapolating the toxicity scaling for honeybees to the lifespan of winter bees suggests that i

265 Many insecticides are bird, fish, and honeybee toxicants, whereas herbicides and fungicides po

266 Honeybees transmit food-related information to nestmates

267 reaching a speed up to 3 body lengths.s(-1) Honeybees use their wetted wings as hydrofoils for their

268 Honeybees utilise floral odours when foraging for flower

269 sitization to the only available recombinant honeybee venom (HBV) allergen, rApi m 1, in patients wit

270 reactivity to recombinant yellow jacket and honeybee venom allergens by Immulite3 g.

271 r mastocytosis, a panel of yellow jacket and honeybee venom allergens was applied on a widely used Ig

272 obubbles (PLA2denat -MB) in a mouse model of honeybee venom allergy.

273 evels to evaluate the safety and efficacy of honeybee venom immunotherapy (HBVIT) combined with Advax

274 ed different effects on resistance to RVV or honeybee venom in BALB/c versus C57BL/6 mice that had re

275 We found that mice injected with amounts of honeybee venom similar to that which could be delivered

276 ne and specific immunoglobulin G4 (sIgG4) to honeybee venom, but not with total IgE or sIgE.

277 te that IgE also can enhance defense against honeybee venom.

278 re essential for such acquired resistance to honeybee venom.

279 fe-threatening allergic reaction following a honeybee, vespid, or ant sting.

280 WV recombinants constitute the most virulent honeybee viruses in the UK.

281 The impressive repertoire of honeybee visually guided behaviors, and their ability to

282 The state of individual honeybees was manipulated by either starving donor bees

283 The individual variability of worker honeybees was nonzero but less than that of humans, poss

284 calcium imaging of projection neurons in the honeybee, we studied neuronal mechanisms of odor-backgro

285 r CT(max) in more urbanized locations, while honeybees were closer to their CWC.

286 Clothianidin residues in pollen, nectar and honeybees were consistently higher at clothianidin-treat

287 Honeybees were most sensitive to insecticides (clothiani

288 Honeybees were trained to recognise the full synthetic o

289 tion after Hymenoptera sting (11 wasp and 12 honeybee) were treated with VIT.

290 nii is comparable to volatiles released from honeybees when under simulated attack.

291 It now seems that this has also happened in honeybees, where the sex-determining gene has now been s

292 V is now an important reemerging pathogen of honeybees, which are undergoing a worldwide manmade epid

293 PCR assay was proposed to identify A-lineage honeybees, while a second method based on real-time PCR

294 -choice decisions on a single day, except in honeybees whose queens can conduct mating flights for se

295 hianidin seed-treated oilseed rape fields on honeybees with an additional year and new data on honeyb

296 correlation among the artificial feeding of honeybees with carbohydrate supplements and the chemical

297 l interactions and food sharing behaviour of honeybees with the aim of developing the honeybee as a m

298 DWV is now the most prevalent virus in honeybees, with a minimum average of 55% of colonies/api

299 Our study demonstrates that honeybees, with their great foraging range and sensitive

300 genetic maps of human, mouse, rat, chicken, honeybee, worm, and yeast are discussed.