ライフサイエンスコーパス: honeybee

1 ression of piggyBac-derived cassettes in the honeybee.

2 a uniform model of olfactory learning in the honeybee.

3 thways mediate learned food aversions in the honeybee.

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

5 tetraodon and frog and the insect genome of honeybee.

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

7 nding of processes underlying the biology of honeybees.

8 oyal jelly, induces queen differentiation in honeybees.

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

10 that impair olfactory learning and memory in honeybees.

11 aching in ants and behavioural traditions in honeybees.

12 L directly affecting the sucrose response of honeybees.

13 es would hybridize extensively with European honeybees.

14 d limiting the utilisation of visual cues in honeybees.

15 sing two selected, continually bred lines of honeybees.

16 tecture of the age of foraging initiation in honeybees.

17 ilarities in the learning of vertebrates and honeybees.

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

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

20 plant with pitfall flowers, mimics attacked honeybees.

21 environmental pollutant toxicities for adult honeybees.

22 ly, dependent on the pollination activity of honeybees.

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

24 Here, we report that desert ants, like honeybees [5] and hamsters [6], can also use PI to appro

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

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

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

28 s caused widespread death of managed African honeybee, A. m. scutellata, colonies.

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

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

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

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

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

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

35 host that develop much like the free-living honeybee and Drosophila.

36 l gene flow between European and Africanized honeybees and (2) the panmitic European population was r

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

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

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

40 ate- and glutamate-immunoreactive neurons in honeybees and cockroaches further suggests that neural a

41 In some insects, such as honeybees and fruit flies, octopamine has been shown to

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

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

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

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

46 Honeybees and some other insects, in learning the sun's

47 Bumblebees, honeybees and stingless bees can distinguish flowers bas

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

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

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

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

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

53 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.

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

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

56 sm for achieving thermal stability in flying honeybees, and this mechanism may occur commonly in endo

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

58 ctopamine release by one such pathway in the honeybee antennal lobe modulates olfactory processing in

59 Using a computational model of the honeybee antennal lobe, the authors show that changes in

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

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

62 questions, here we study the dsx gene of the honeybee Apis mellifera, a member of the most basal line

63 Flying endothermic insects, including the honeybee Apis mellifera, are believed to thermoregulate

64 to the calyces of the mushroom bodies of the honeybee Apis mellifera, the neurons' dendritic fields i

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

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

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

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

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

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

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

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

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

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

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

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

77 The honeybee (Apis mellifera) visual system contains three c

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

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

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

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

82 Honeybees (Apis mellifera) can use stimulus onset asynch

83 Previous experiments with honeybees (Apis mellifera) failed to show learned contro

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

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

86 Latent inhibition (LI) in honeybees (Apis mellifera) was studied by using a probos

87 Honeybees (Apis mellifera), important pollinators for cr

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

89 Honeybees (Apis mellifera), the prevailing managed insec

90 Honeybees (Apis mellifera), which are important pollinat

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

92 However, in the honeybee, Apis mellifera (A. mel.), the ventral midline

93 Relocation of the Cape honeybee, Apis mellifera capensis, by bee-keepers from s

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

95 In the honeybee, Apis mellifera, distinct gamma-tubulin foci ar

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

97 Honeybees, Apis mellifera, are able to distinguish mixtu

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

99 Honeybees are an excellent model system for examining ho

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

101 Honeybees are exposed to two widely used classes of chol

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

103 This pattern suggests that honeybees are innately informed of the general pattern o

104 Honeybees are known to fly a feeder-to-hive or hive-to-f

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

106 Honeybees are models for studying how animals with relat

107 s contrary to what these data might suggest: Honeybees are more, not less, able to discriminate among

108 Honeybees are typically used as a model organism to inve

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

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

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

112 Honeybees, beetles and roaches do not edit sytI.

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

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

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

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

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

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

119 In honeybee brains, it labels different structures which pr

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

121 communication of floral odour, as occurs in honeybees, bumble bees and some stingless bees, can be e

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

123 But I show here that naturalized, non-native honeybees can augment pollination and boost crop yields

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

128 Honeybee colonies reproduce two ways: producing swarms c

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

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

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

132 ned larvae exhibiting rebel traits emerge in honeybee colonies.

133 rlying polyethism and social organization in honeybee colonies.

134 behavior, division of labor among workers in honeybee colonies.

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

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

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

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

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

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

141 The honeybee dance language, in which foragers perform dance

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

143 Reported racial differences in honeybee dances could have arisen merely from difference

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

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

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

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

148 his trait in diploid worker and haploid male honeybees (drones) to learn more about the genetic archi

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

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

151 c heat production and wing-beat frequency in honeybees during hovering, agitated, or loaded flight.

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

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

154 ge provides new insight into its function in honeybee ecology.

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

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

157 In honeybees, employed foragers recruit unemployed hive mat

158 Snake or honeybee envenomation can cause substantial morbidity an

159 Free-flying honeybees exhibit remarkable cognitive capacities but th

160 In the honeybee, for example, the primary signal is the genotyp

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

162 Honeybees form complex societies with a division of labo

163 Honeybees form societies in which thousands of members i

164 The expansion of Africanized honeybees from South America to the southwestern United

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

166 Some honeybee genome features thought to underpin advanced eu

167 Furthermore, two maps of the honeybee genome were constructed from over 400 AFLP mark

168 ll currently predicted coding regions in the honeybee genome, a novel form of synonymous codon bias i

169 isms, including the recent sequencing of the honeybee genome, promises to advance our understanding o

170 he extraordinary recombinational size of the honeybee genome.

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

176 ecent studies of visual sequence learning in honeybees have investigated the bees' ability to perform

177 hown that during their expansion Africanized honeybees have low levels of introgressed alleles from r

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 (CAPE), an active component of propolis from honeybee hives, is known to have antimitogenic, anticarc

184 lic antioxidant derived from the propolis of honeybee hives.

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

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

187 y of neurons in the mushroom bodies of adult honeybees increases as a function of increasing age, but

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

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

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

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

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

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

194 In the present experiment, honeybees learned no less readily to choose between the

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

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

197 screening, we have cloned and sequenced the honeybee LW Rh gene.

198 in insects is a new understanding of how the honeybee measures the distance that it travels during it

199 virus that bore a construct that contained a honeybee melittin secretion (ms) signal attached to RT1.

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

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

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

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

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

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

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

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

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

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

210 ow for the first time a striking ontogeny to honeybee orientation flights.

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

212 A worker honeybee performs tasks within the hive for approximatel

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

214 Therefore, the resulting feral honeybee population of south Texas was best viewed as a

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

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

217 rrent and next generation pesticides pose to honeybee populations.

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

219 Honeybees possess an elaborate olfactory system with uni

220 Substitution of the SP from the honeybee protein mellitin resulted in threefold-higher c

221 ronizing neuronal firing in the brain of the honeybee provide new evidence that the oscillatory synch

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

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

224 Honeybees quickly learn to associate floral cues with fo

225 Using honeybees radar-tracked during their orientation flights

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

227 Honeybees rely primarily on the oxidation of hexose suga

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

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

230 Honeybees rewarded with caffeine, which occurs naturally

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

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

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

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

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

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

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

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

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

240 Honeybees show a fairly abrupt increase in response afte

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

242 Myoglobin was embedded in transparent honeybee silk protein films.

243 eveals previously unrecognized plasticity in honeybee social organization.

244 In honeybee societies, distinct caste phenotypes are create

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

246 In European honeybee stocks bidirectionally selected for pln, worker

247 tore egg diploidy), whereas workers of other honeybee subspecies are able to lay only haploid, male e

248 unctional imaging experiments in mammals and honeybees suggest a mechanism of odor coding that transl

249 Honeybee swarms and complex brains show many parallels i

250 For example, honeybees take repeated 'orientation' flights before bec

251 oser to Vmax in the flight muscles of flying honeybees than in other muscles previously studied.

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

253 syndrome is the pollen-hoarding syndrome in honeybees that ties together multiple behavioral phenoty

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

255 In the 'dance language' of honeybees, the dancer generates a specific, coded messag

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

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

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

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

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

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

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

263 Here we demonstrate that honeybees use an alternative strategy, hovering with rel

264 Honeybees utilise floral odours when foraging for flower

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

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

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

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

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

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

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

272 re essential for such acquired resistance to honeybee venom.

273 duced the morbidity and mortality induced by honeybee venom.

274 pecific blocker apamin, a peptide toxin from honeybee venom.

275 ide or the phospholipase A2 gene (PLA2) from honeybee venom.

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

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

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

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

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

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

282 Using honeybees, we now demonstrate that odour encoding involv

283 Honeybees were most sensitive to insecticides (clothiani

284 Honeybees were trained to recognise the full synthetic o

285 In this study, honeybees were trained with an improved technique to cho

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

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

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

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

290 dynamically scaled robot, the kinematics of honeybee wings generate prominent force peaks during the

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

292 Orientation flights provide honeybees with repeated opportunities to view the hive a

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

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

295 iation of foraging during the life course of honeybee workers is of central interest to understanding

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

297 speculated, but not shown, that Africanized honeybees would hybridize extensively with European hone