ライフサイエンスコーパス: beetle

1 wings), Diptera (flies), and now Coleoptera (beetles).

2 thropod availability (i.e. large spiders and beetles).

3 bundles in the brain of the day-active dung beetle.

4 n, the pheromone attracted both sexes of the beetle.

5 nd incipient speciation in the mountain pine beetle.

6 enced emerald ash borer and bull-headed dung beetle.

7 constructed anatomical structure of a hister beetle.

8 t-parasitic nematode, but also by its vector beetle.

9 ng JH regulation of patency in the red flour beetle.

10 ve-dominated but only in the presence of the beetle.

11 ormation of lightweight rigid cuticle of the beetle.

12 llion years ago, before the origin of modern beetles.

13 assemblage composition of adult spiders and beetles.

14 ad on the carcass surface in the presence of beetles.

15 sceptible (S) and imidacloprid resistant (R) beetles.

16 nomic basis and evolution of wood-feeding in beetles.

17 evelopmental environment of Onthophagus dung beetles.

18 anism of sex ratio bias in midges, wasps and beetles.

19 ar phylogeny for Melanesian Exocelina diving beetles.

20 s the dominant orientation cue for nocturnal beetles.

21 , wasps, spiders, mites, bugs, and predatory beetles.

22 ssayed colonization by 35 species of aquatic beetles.

23 ls to the integrated pest management of bark beetles.

24 ting, is found both in animals (for example, beetles [2]) and in plants (on the petals of some animal

25 Beetles able to colonize live tree tissues are most like

26 the more recently disturbed ("focal") unit's beetle abundance was positively related to source unit a

27 We measured beetle abundances at three distances from the shared edg

28 Soon after fire, beetle abundances within management units were highest n

29 However, at the lifecycle level, dung beetles accounted for only a 0.05-0.13% reduction of ove

30 The rapid spread of the Colorado potato beetle across Eurasia illustrates the importance of evol

31 tropical insect herbivores, the rolled-leaf beetles, across both broad and narrow elevational gradie

32 has not increased in direct response to bark beetle activity.

33 biomass killed by bark beetle attacks across beetle-affected areas in western US forests from 2000 to

34 core is also a feature of the similar-sized beetle AFP that is a beta-helix with seven 12-residue co

35 The midge and beetle AFPs are not homologous and their ice-binding sit

36 rees N, we tested the role of the biocontrol beetle Agasicles hygrophila in mediating warming effects

37 ack, and in North America by the herbivorous beetle Agrilus planipennis.

38 Asian Longhorned Beetle (ALB) Anoplophora glabripennis is a serious invas

39 edators (Pardosa spider species and the rove beetle Aleochara bilineata).

40 distinctive termitophilous aleocharine rove beetles, all of which possess specialized swollen or hor

41 With beetles alone accounting for about 40% of all described

42 Burying beetles also carry phoretic mites (Poecilochirus carabi

43 entation behavior has made ball-rolling dung beetles an attractive model organism for the study of th

44 due to high susceptibility to mountain pine beetle and the non-native white pine blister rust (WPBR)

45 ation by inducing ecdysone production in the beetle and up-regulating ecdysone-dependent gene express

46 nt termite societies were quickly invaded by beetles and by multiple independent lineages of social p

47 associated with two guilds of insects - bark beetles and defoliators - which are responsible for subs

48 of key functional groups of termites, ants, beetles and earthworms, and an increase in the abundance

49 by a factor of 5.3 from the plants to adult beetles and further to bugs.

50 ved during development of Onthophagus horned beetles and have retained the ability to regulate A/P po

51 the occurrence of drought, presence of bark beetles and increased mortality of larger trees.

52 support a cleaning mutualism between burying beetles and P. carabi mites, but more work is needed to

53 ulating plant defenses have been observed in beetles and piercing-sucking insects, but the role of ca

54 Using Leptinotarsa decemlineata beetles and stinkbug (Podisus maculiventris) predators,

55 e literature on trapping bark and woodboring beetles and their associates and conducted meta-analyses

56 Using a wider suite of species (birds, dung beetles and trees) and a wider range of livestock-produc

57 Cucumber beetles and wolf spiders were equally heat tolerant (CTM

58 superior to multiple-funnel traps, (b) bark beetles and woodborers were captured in higher numbers i

59 y of profound impacts by phloem-feeding bark beetles, and species such as the mountain pine beetle (D

60 onghorned beetle, certain other phytophagous beetles, and to a lesser degree, other phytophagous inse

61 The Asian longhorned beetle (Anoplophora glabripennis) is a wood-feeding inse

62 comparative studies of the Asian longhorned beetle, Anoplophora glabripennis, a globally significant

63 n mimics (spider wasps) and Batesian mimics (beetles, antlions, and spiders; see references in).

64 Burying beetles are a suitable species to study how animals mana

65 We found evidence that only larger beetles are able to construct rounder carcass nests, and

66 abundance and richness of colonizing aquatic beetles are determined by patch quality and context-depe

67 Here, we demonstrate that myrmecoid rove beetles are strongly polyphyletic, with this adaptive mo

68 Beetles are the most diverse group of macroscopic organi

69 ss neurons in the central complex of diurnal beetles are tuned only to the sun, whereas the same neur

70 The longhorned beetle Aromia bungii (Coleoptera: Cerambycidae) is a maj

71 tra using Tribolium castaneum (the red flour beetle) as a model.

72 results demonstrated that exposure of adult beetles, as well as larvae to dvvgr or dvbol dsRNA in ar

73 Greater survival to mountain pine beetle attack in slow-growing families reflected, in par

74 th generalized hydraulic failure and/or bark-beetle attack, while long-term decrease in growth may be

75 ion is thought to be required for successful beetle attack.

76 We find that biomass killed by bark beetle attacks across beetle-affected areas in western U

77 control options dwindling, research on click beetle biology and ecology is of increasing importance i

78 l-Oriental disjunct distribution in the rove beetle Bolitogyrus, a suspected Eocene relict.

79 ically convergent with Early Cretaceous bark-beetle borings 120 million-years later.Numerous gaps rem

80 Bombardier beetles (Brachinini) use a rapid series of discrete expl

81 Mapping the neuropils of the dung beetle brain is thus a prerequisite to understand the ne

82 how celestial cues are processed in the dung beetle brain, little is known about its general neural l

83 s (Cerambycidae) and 38 metallic wood boring beetles (Buprestidae) intercepted in SWPM associated wit

84 colour and fluorescence are induced in this beetle by various liquids, although the mechanism has ne

85 ased on principles derived from Namib desert beetles, cacti, and pitcher plants--that synergistically

86 sorting in replicated invasions of the bean beetle Callosobruchus maculatus across homogeneous exper

87 on for food, South African ball-rolling dung beetles carve a piece of dung off a dung-pile, shape it

88 The pinewood nematode and its vector beetle cause pine wilt disease, which threatens forest e

89 Among BD agents, bark beetles caused most C fluxes (61%), and total insect-ind

90 o 2015, we obtained larvae of 338 longhorned beetles (Cerambycidae) and 38 metallic wood boring beetl

91 metabolic repertoire of the Asian longhorned beetle, certain other phytophagous beetles, and to a les

92 relationships of four species of net-winged beetles characterised by female neoteny.

93 litermes flavipes (Kollar), and spotted lady beetles, Coleomegilla maculate De Geer.

94 Wireworms, the larvae of click beetles (Coleoptera: Elateridae), have had a centuries-l

95 he bioluminescence, attract staphilinid rove beetles (coleopterans), as well as hemipterans (true bug

96 A new study shows that female burying beetles communicate their hormonal status to their male

97 to more than 200 species, of which flies and beetles constitute the majority.

98 ng and after breeding, to understand whether beetles could be "seeding" the carcass with particular m

99 gap, we used specialist pest Colorado potato beetle (CPB) and its host plant, potato, as a model syst

100 Colorado Potato Beetle (CPB) is a devastating invasive pest of potato bo

101 Colorado potato beetles (CPB; Leptinotarsa decemlineata) use several Sol

102 and colleagues [1] described an extinct rove beetle, Cretotrichopsenius burmiticus, from two specimen

103 The diving beetle Cybister japonicus Sharp shows a remarkable sexua

104 tle (Dendroctonus ponderosae) and the spruce beetle (D. rufipennis) have recently undergone epic outb

105 covering their full distributions, we found beetle damage on A. sessilis increased with rising tempe

106 evidence for one cohort, exemplified by the beetle Darwinylus marcosi, family Oedemeridae (false bli

107 e mortality and defoliation) and agent (bark beetles, defoliator insects, other insects, pathogens, a

108 beetle outbreaks, focusing on mountain pine beetle (Dendroctonus ponderosae) and Douglas-fir beetle

109 etles, and species such as the mountain pine beetle (Dendroctonus ponderosae) and the spruce beetle (

110 r strong herbivory caused by a mountain pine beetle (Dendroctonus ponderosae) outbreak.

111 ed by forest die-off caused by mountain pine beetle (Dendroctonus ponderosae), with implications for

112 le (Dendroctonus ponderosae) and Douglas-fir beetle (Dendroctonus pseudotsugae) in forests regenerati

113 +/- 0.6 mg/mL) in the larval hemolymph of a beetle, Dendroides canadensis, and demonstrate that the

114 Away from contiguously impacted patches (low beetle densities), infestations are characterized by app

115 The hide beetle Dermestes maculatus represents an intermediate be

116 and that this is a fundamental component of beetle development and fitness.

117 Once the beetle develops into the adult stage, it secretes ascaro

118 erpillars for the root-feeding larvae of the beetle Diabrotica virgifera virgifera, a major pest of m

119 mal maxima parameter (CTM50) of the cucumber beetle (Diabrotica undecimpunctata), wolf spider (Tigros

120 We show that burying beetles do not "preserve" the carcass by reducing bacter

121 gies are driven by fungal metabolism whereas beetle ecology is evolutionarily more flexible.

122 /kg bulk-CeO2 were presented to Mexican bean beetles (Epilachna varivestis), which were then consumed

123 ariance in CTmax values for most rolled-leaf beetles, especially high-elevation species, suggests tha

124 gly little is known about opsin evolution in beetles, even though they are the most species rich anim

125 B. bassiana lines evolving resistance to the beetles' external immune defences, not due to increased

126 1-diene and other sesquiterpenes observed in beetle extracts.

127 ion, a model of spot formation by dispersing beetles facing a local Allee effect is derived.

128 Inside mesocosms, beetle feeding increased with temperature, wolf spiders

129 ar to the phenotypes observed after starving beetles for 5 days PAE.

130 advances in applied chemical ecology of bark beetles for scientists and land managers.

131 tative evidence supporting the importance of beetle forewings in tolerating a variety of environmenta

132 ial tool in ongoing efforts to eradicate the beetle from regions of the world that it has already inv

133 sal area had been killed or impaired by bark beetles (from 7.1 +/- 0.22 mumol m(-2) s(-1) in 2005 to

134 The ambrosia beetle-fungus farming symbiosis is more heterogeneous th

135 Beetle-fungus specificity is clade dependent and ranges

136 phidae) when attacking three closely related beetles: Galerucella pusilla, Galerucella calmariensis a

137 s on the exoskeletal growth of the dock leaf beetle Gastrophysa viridula, capturing all aspects of it

138 The Asian longhorned beetle genome encodes a uniquely diverse arsenal of enzy

139 uingly, the largest insect Order Coleoptera (beetles) has evolved a unique approach, in which only a

140 se traits, in the developmental evolution of beetle horns, an evolutionary novelty, and horn polyphen

141 Diurnal beetles, however, persist in using a celestial body for

142 s showed that a single species of predacious beetle (i) reduced the density of the non-burrowing spec

143 t in the presence of above-ground predacious beetles: (i) non-burrowing detritivores will suffer mort

144 lated yearly maps of travel time to previous beetle impact.

145 ts of ecosystem engineering by a wood-boring beetle in a neotropical mangrove forest system.

146 iously published, likely-termitophilous rove beetle in Burmese amber [2].

147 uarantine surveillance efforts to detect the beetle in incoming shipments.

148 on carcasses and measured the effect on the beetle in the presence and absence of mites.

149 They employ Callosobruchus seed beetles in a clever array of linked habitat patches to c

150 erence differs between nocturnal and diurnal beetles in a manner that reflects their contrasting visu

151 two OBPs in the male foreleg tarsi of diving beetles in chemical communication.

152 pothesis that P. carabi mites assist burying beetles in clearing the carcass of bacteria as a side-ef

153 neuroethology of insects in general and dung beetles in particular.

154 tter levels resulted in greater abundance of beetles in such localities, which then compressed into t

155 level fire behavior models suggest that bark beetle-induced tree mortality increases flammability of

156 d and the overall composition was altered by beetle-induced tree mortality.

157 llion, 5.5 million, and 7 million species of beetles, insects, and terrestrial arthropods, respective

158 and phenolics in response to fungal and bark beetle invasion.

159 abies) is periodically attacked by the bark beetle Ips typographus and its fungal associate, Endocon

160 he structural colour of male Hoplia coerulea beetles is notable for changing from blue to green upon

161 Detailed information about bark beetles is seldom reported and their role is poorly unde

162 Coleoptera (beetles) is a massively successful order of insects, dis

163 ocity (u*) = 0.7 m s(-1)], during which bark beetles killed or infested 85% of the aboveground respir

164 emissions from heterotrophic respiration of beetle-killed biomass are balanced by forest regrowth an

165 i gen. have specialised setae from dermestid beetle larvae (hastisetae) attached to their bodies, lik

166 The beetle larvae feeding on nano-CeO2 exposed leaves accumu

167 in the hemolymph (or blood) of overwintering beetle larvae.

168 l and behavioral convergence, with replicate beetle lineages following a predictable phenotypic traje

169 ving trees, vectors of pathogenic fungi, and beetles living in rotten trees with a wood-decay symbion

170 erated traits, such as the mandibles of stag beetles (Lucanidae), the claspers of praying mantids (Ma

171 Here we tested green, yellow, and red beetle luciferases and optimized substrate conditions fo

172 erase produces light by converting substrate beetle luciferin into the corresponding adenylate that i

173 Several recent papers suggest that dung beetles may affect fluxes of GHGs from cattle farming.

174 Beetles may also "weed" the bacterial community by elimi

175 ontrast, we suggest that the effects of dung beetles may be accentuated in tropical countries, where

176 s describe a late Permian fossil wood-boring beetle microcosm, with the oldest known example of compl

177 on pastures, offering limited scope for dung beetle mitigation of GHG fluxes.

178 ead, with spatial distribution determined by beetle motility and the need to overcome the Allee effec

179 Although nocturnal beetles move in the same manner through the same environ

180 Mountain pine beetle (MPB, Dendroctonus ponderosae) is a significant m

181 Mountain pine beetles (MPB, Dendroctonus ponderosae Hopkins) are aggre

182 In the western United States, mountain pine beetles (MPBs) have killed pine trees across 71,000 km(2

183 Parenting in the burying beetle Nicrophorus vespilloides is complex and, unusuall

184 ring and parental performance in the burying beetle Nicrophorus vespilloides We found that offspring

185 e fitness costs of inbreeding in the burying beetle Nicrophorus vespilloides, an insect with facultat

186 Burying beetles (Nicrophorus vespilloides) breed on small verteb

187 problem, we combined experiments on burying beetles (Nicrophorus vespilloides) with theoretical mode

188 ng a model host-parasite system, the burying beetle, Nicrophorus vespilloides and the entomopathogeni

189 ere we test our hypothesis in female burying beetles, Nicrophorus vespilloides, an insect where carin

190 f these mechanisms best explains how burying beetles, Nicrophorus vespilloides, manipulate the bacter

191 ignificance and fitness consequences for the beetle of mite-associated changes to the bacterial commu

192 Inspired by the white beetle of the genus Cyphochilus, we fabricate ultra-thin

193 t, we were able to artificially induce adult beetles of Micromalthus debilis in order to describe its

194 Beetles of the genus Nicrophorus are well known for thei

195 Flour beetles of the genus Tribolium Macleay (Coleoptera: Tene

196 acts of a multivoltine introduced biocontrol beetle on the non-target native plant Alternanthera sess

197 enomic basis for the evolutionary success of beetles on plants.

198 the elevational distributions of rolled-leaf beetles on two mountains in Costa Rica.

199 We find that beetle oocytes and embryos of all stages are abundant in

200 the infrared sensors on the abdomens of some beetles or photoreceptors on the genitalia of some butte

201 arcasses that were either fresh, prepared by beetles or unprepared but buried underground for the sam

202 ng effects of precipitation on plants, ants, beetles, orthopterans, kangaroo rats, ground squirrels a

203 Here, we used a recent bark beetle outbreak in lodgepole pine (Pinus contorta) fores

204 case study featuring fire, harvest, and bark beetle outbreak, we illustrate how resultant fitted valu

205 e begun to examine the local impacts of bark beetle outbreaks in individual stands, but the full regi

206 have contributed to rapid expansion of bark beetle outbreaks killing millions of trees over a large

207 ation model to assess susceptibility to bark beetle outbreaks over 130 y of stand development.

208 tify the regional carbon impacts of the bark beetle outbreaks taking place in western US forests.

209 opment affects future susceptibility to bark beetle outbreaks, focusing on mountain pine beetle (Dend

210 rest disturbances such as wildfires and bark beetle outbreaks, thereby increasing the potential for s

211 perms and in case of intense drought or bark-beetle outbreaks.

212 provide important documentation of potential beetle pests that may cross country borders through the

213 S)-himachala-9,11-diene in the crucifer flea beetle Phyllotreta striolata, a compound previously iden

214 We tested four categories of stress on the beetles: physical damage to hindwings, predation, desicc

215 Burying beetles prepare an edible nest for their young from a sm

216 simply a by-product of the way in which the beetles prepare the carcass for reproduction, remains to

217 etabolic repertoire, the bacteria in Cassida beetles produce pectinases predicted to mediate degradat

218 nisms (e.g., cyanobacteria, dinoflagellates, beetles) produce structurally distinct toxins that are c

219 pene synthase activity was detected in crude beetle protein extracts, but only when (Z,E)-farnesyl di

220 sal third-stage nematode LIII larvae promote beetle pupation by inducing ecdysone production in the b

221 a have facilitated the remarkable success of beetle radiation.

222 and increase non-target effect occurrence by beetle range expansion to additional areas where A. sess

223 relationships, ratios with other taxa, plant:beetle ratios, and a completely novel body-size approach

224 At the first two levels, dung beetles reduced GHG emissions by up to 7% and 12% respec

225 fe habits and early evolution of wood-boring beetles remain shrouded in mystery from a limited fossil

226 re more manure is left on pastures, and dung beetles remove and aerate dung faster, and that this is

227 CTmax was determined for 1,252 individual beetles representing all populations across the gradient

228 the capacity to synthesize terpenes for bark beetle resistance, chemical feedstocks, and biofuels.

229 A study of dung beetles rolling dung balls to safety reveals unexpected

230 In characterizing the source of a leaf beetle's (Cassida rubiginosa) pectin-degrading phenotype

231 s to safety reveals unexpected facets of the beetle's acquisition and use of celestial information fo

232 nventional interpretation of the role of the beetle's bumpy surface geometry in promoting condensatio

233 nalysed bacterial communities in the burying beetle's gut, during and after breeding, to understand w

234 he bacterial community are adaptive from the beetle's perspective, or are simply a by-product of the

235 Moreover, the beetle's photonic structure is enclosed by a thin scale

236 lt head of both basal and derived scarabaeid beetle species (Onthophagini and Oniticellini).

237 al the patterns of opsin evolution across 62 beetle species and relatives.

238 ains of a day-active and a night-active dung beetle species based on immunostainings against synapsin

239 ediates sex-specific development in a horned beetle species by combining systemic dsx knockdown, high

240 es, the truly pertinent question is how many beetle species exist.

241 ochemical-based management of the major bark beetle species in western North America.

242 of neuropil structures between the two dung beetle species revealed differences that reflect adaptat

243 resent four new and independent estimates of beetle species richness, which produce a mean estimate o

244 lysis with fossils, we show that a whirligig beetle species, Heterogyrus milloti, inhabiting forest s

245 we show that the offspring of three burying beetle species, N. orbicollis, N. pustulatus, and N. ves

246 which produce a mean estimate of 1.5 million beetle species.

247 Much of beetle speciosity is attributable to myriad life habits,

248 Isolated beetle spots were sorted by travel time and compared wit

249 Using a laboratory model system (beetles spreading through artificial landscapes), we qua

250 arkable among these are many species of rove beetle (Staphylinidae) that exhibit ant-mimicking "myrme

251 mushrooms (Agaricales) and mycophagous rove beetles (Staphylinidae) from mid-Cretaceous Burmese ambe

252 ominant among these are the aleocharine rove beetles (Staphylinidae), a vast and ecologically diverse

253 lutionary history of the cosmopolitan diving beetle subfamily Colymbetinae, the majority of which are

254 ts, geometrid and arciinid moths and carabid beetles, subsequently investigating their respective und

255 e identified a Cactin gene from the mealworm beetle, Tenebrio molitor (TmCactin) and characterized it

256 axmoth, Galleria mellonella or adults of the beetle, Tenebrio molitor.

257 e to resurrect sexual adults in a species of beetle that reproduces by parthenogenetic paedogenesis,

258 Furthermore, western corn rootworm beetles that emerged from larval feeding on transgenic m

259 s marcosi, family Oedemeridae (false blister beetles), that had an earlier gymnosperm (most likely cy

260 Parker introduces the staphylinids or 'rove beetles', the most species-rich groups of insect on Eart

261 eviously observed that Phyllotreta striolata beetles themselves produce volatile glucosinolate hydrol

262 multi-scale colonization dynamics of aquatic beetles through the processes of contagion and compressi

263 ttackers, creating an Allee effect requiring beetles to attack en masse to successfully reproduce.

264 account of motion detection in animals from beetles to humans.

265 osed crowns(4,15), and the tendency for bark beetles to preferentially attack larger trees(16).

266 We show that mites: 1) cause beetles to reduce the antibacterial activity of their ex

267 ntially facilitating their movement into the beetle trachea for transport to the next pine tree.

268 onging to the obligately termitophilous rove beetle tribe Trichopseniini, display the protective hors

269 evolving replicate populations of the flour beetle Tribolium castaneum for 6 to 7 years under condit

270 g in both the blastoderm and germband of the beetle Tribolium castaneum is based on the same flexible

271 The red flour beetle Tribolium castaneum is widely used as a model ins

272 use new fluorescent transgenic lines in the beetle Tribolium castaneum to show that the EE tissues d

273 e set out to describe cellularization in the beetle Tribolium castaneum, the embryos of which exhibit

274 atterning genes in embryos and larvae of the beetle Tribolium castaneum, we provide the first molecul

275 s are required for cell intercalation in the beetle Tribolium castaneum.

276 portant model and pest insect, the red flour beetle Tribolium castaneum.

277 as is found in the pair-rule circuit of the beetle Tribolium Taken together, our results suggest tha

278 Using the flour beetle (Tribolium castaneum) in a microcosm experiment,

279 Here we use flour beetles (Tribolium castaneum) to show experimentally tha

280 Using a model system, red flour beetles (Tribolium castaneum), we either allowed or cons

281 The red flour beetle, Tribolium castaneum, is an emerging model organi

282 ungus, Beauveria bassiana, and the red flour beetle, Tribolium castaneum, which has a well-documented

283 NAi) screen targeting GPCRs in the red flour beetle, Tribolium castaneum.

284 male accessory gland (MAG) in the red flour beetle, Tribolium castaneum.

285 died due to biotic attacks (especially bark-beetles) typically showed relatively small and short-ter

286 hree separate channels for colour vision) in beetles up to 12 times and more specifically, duplicatio

287 om the busy dung pile, at night and day, the beetles use a wide repertoire of celestial compass cues.

288 Diurnal and nocturnal African dung beetles use celestial cues, such as the sun, the moon, a

289 rect observation of explosions inside living beetles using synchrotron x-ray imaging.

290 infection, growth, and survival of this bark beetle-vectored fungus and may play a major role in the

291 ated emergence of stands susceptible to bark beetles was not temporally synchronized but was protract

292 Beetles were maintained on one of five diets that varied

293 Beetles were present throughout the gradient.

294 mmunity-wide mortality was high or when bark beetles were present.

295 microbials imposes a fitness cost on burying beetles, which rises with the potency of the antimicrobi

296 set of the network morphology within a white beetle wing scale.

297 essful radiation of this taxon, by providing beetles with protection against a variety of harsh envir

298 ed a significant advantage compared to those beetles with their elytra experimentally removed.

299 (TSF) on abundances of a specialist palmetto beetle within and between fire management units in Apala

300 Introduction of dung beetles would minimize sources connected to waterways by