ライフサイエンスコーパス: beetle

1 eleyi which can be locally eliminated by the beetle.

2 ecule produced by several species of blister beetle.

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

4 logical restoration in areas invaded by this beetle.

5 and its diverse variation in the ship-timber beetles.

6 ion of GSS activity in ermine moths and flea beetles.

7 e used as a guiding cue for the ball-rolling beetles.

8 , and flight modes as the extant ship-timber beetles.

9 tonic structures that evolved in cuticles of beetles.

10 ccompany the dietary shift towards plants in beetles.

11 versification and speciation in phytophagous beetles.

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

13 ssayed colonization by 35 species of aquatic beetles.

14 evelopmental environment of Onthophagus dung beetles.

15 interactions between conifer trees and bark beetles.

16 e caused by nematodes carried by pine sawyer beetles.

17 ls to the integrated pest management of bark beetles.

18 assemblage composition of adult spiders and beetles.

19 n both field-collected and laboratory-reared beetles.

20 may also aid in defense against herbivorous beetles.

21 els of sterols compared to laboratory-reared beetles (2,452-145,348 ng per beetle); cholesterol and s

22 sperm and egg function using Tribolium flour beetles, a warm-temperate-tropical insect model.

23 Beetles able to colonize live tree tissues are most like

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

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

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

27 istence in a community of 34 species of dung beetles across a gradient of environmental disturbance r

28 logical control agent the alligatorweed flea beetle (Agasicles hygrophila) do not completely overlap

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

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

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

32 Burying beetles also carry phoretic mites (Poecilochirus carabi

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

34 Both beetle and ant communities differed between treatments,

35 ce was significant overall as well for ant x beetle and beetle x beetle associations.

36 Unexpectedly, the beetle and grasshopper odors did not bias spiders away f

37 artmentalization by measuring pressures in a beetle and recording abdominal movements.

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

39 Both the beetle and the plant are well-documented to respond to d

40 The fire had little effect on the number of beetles and ants collected although beetle richness was

41 main component of tree defence against bark beetles and associated microbes; and (3) implementing co

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

43 date the modern saline (trona) pan show that beetles and other invertebrates inhabit this extreme env

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

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

46 y invertebrates with hard exoskeletons (e.g. beetles and snails), exhibit rougher microwear textures

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

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

49 ic interactions between herbivorous tortoise beetles and their obligate bacterial symbionts.

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

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

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

53 tural designs within the exoskeleton of this beetle, and examine the resulting mechanical response an

54 was strongly attractive to conspecific male beetles, and did not appear to attract other species.

55 ies, sterols were not detected in adult male beetles, and overall levels were generally low (total ng

56 known from fungi farmed by ants, termites or beetles, and plants farmed by humans or ants.

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

58 ffects of a low-intensity prescribed fire on beetles, ants and termites inhabiting log sections cut f

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

60 Ambrosia beetles are a threat to avocado where they have been fou

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

62 We not only found that beetles are more cooperative at carcasses when blowfly m

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

64 Beetles are the most diverse group of macroscopic organi

65 Tree-killing bark beetles are the most economically important insects in c

66 The longhorned beetle Arhopalus rusticus (Coleoptera: Cerambycidae, Spo

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

68 ertain plant tissues, the cuticles of crabs, beetles, arthropods, and beyond.

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

70 verall as well for ant x beetle and beetle x beetle associations.

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

72 ught-induced host-weakening was important to beetle attack success we used an iso-demographic approac

73 ny natural surfaces such as butterfly wings, beetles' backs, and rice leaves exhibit anisotropic liqu

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

75 ody size, and weaponry of male forked fungus beetles Bolitotherus cornutus as they influenced mating

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

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

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

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

80 ificantly altered the species composition of beetles captured in experiment plots.

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

82 ce of repellents was assessed by quantifying beetle catch on traps placed 'close' (~5-10 cm) and 'far

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

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

85 nian populations of the Neotropical tortoise beetle, Chelymorpha alternans, has been suspected but ne

86 oratory-reared beetles (2,452-145,348 ng per beetle); cholesterol and sitosterol were the dominant st

87 e obligate partnership between tortoise leaf beetles (Chrysomelidae: Cassidinae) and their pectinolyt

88 We used sevenspotted lady beetles (Coccinella septempunctata) to test how prey nut

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

90 The diversity and evolutionary success of beetles (Coleoptera) are proposed to be related to the d

91 Beetles (Coleoptera) comprise about one quarter of all d

92 Ambrosia beetles (Coleoptera: Curculionidae: Scolytinae and Platy

93 he smallest free-living insects, featherwing beetles (Coleoptera: Ptiliidae), and in larger represent

94 Ambrosia beetles collected on traps associated with all in-field

95 This raises the question of how the beetles combine multimodal orientation input to obtain a

96 own of PcGSS1 and PcGSS2 expression in adult beetles confirmed their function in vivo.

97 We show that beetles consuming an all-prey diet demonstrate normal gr

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

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

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

101 n-sequestering larvae of the banded cucumber beetle (D. balteata), while infectivity varied strongly

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

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

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

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

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

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

108 breaks over recent decades, including spruce beetle (Dendroctonus rufipennis).

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

110 The hide beetle Dermestes maculatus represents an intermediate be

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

112 The northern tamarisk beetle Diorhabda carinulata (Desbrochers) was approved f

113 and for plant feeding in general, in driving beetle diversification.

114 atments were identified to species to assess beetle diversity and community variation.

115 Beetle diversity was highest on traps deployed with low-

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

117 However, for projecting future bark beetle dynamics there is a critical lack of evidence to

118 exemplary species, the European spruce bark beetle (ESBB) (Ips typographus) and present a multivaria

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

120 inues in the posterior hindgut, and that the beetle excretes an energy- and nutrient-rich product on

121 South African ball-rolling dung beetles exhibit a unique orientation behavior to avoid c

122 n in three closely related species of horned beetles exhibiting strikingly diverse degrees of nutriti

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

124 Using an adult beetle feeding bioassay for oral ingestion of dsRNA, we

125 early in the season and after completion of beetle feeding revealed that variance in damage among br

126 ndings indicate that herbivory benefits lady beetle fitness across the Coccinellini, and that this wa

127 Here we explore how omnivory benefits lady beetle fitness.

128 ontrolled evolution experiments, we selected beetles for either specific or unspecific immune priming

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

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

131 derlying genetics we sampled a total of 3819 beetles from 28 sites across Panama, quantifying five di

132 tructures in two species of the stenine rove beetles from mid-Cretaceous Burmese amber.

133 We reared seven species of lady beetles-from five genera distributed across the tribe Co

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

135 Beetle-fungus specificity is clade dependent and ranges

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

137 However, evidence of changes in beetle gene repertoires driven by such interactions rema

138 ulates weapon size in the broad-horned flour beetle Gnatocerus cornutus.

139 ean eel Anguilla anguilla, and the whirligig beetle Gyrinus sp.) had been extirpated.

140 Field-collected beetles had higher levels of sterols compared to laborat

141 ormidea pama, Hemiptera), (3) Asian ladybird beetles (Harmonia axyridis, Coleoptera), and (4) eastern

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

143 stem, we tested how tree mortality from bark beetles impacts bee foraging habitats and populations.

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

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

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

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

148 We mated beetles in a 2 x 2 factorial design (males with or witho

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

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

151 and/or population establishment of ambrosia beetles in commercial avocado and function as an additio

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

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

154 Some lineages of ants, termites, and beetles independently evolved a symbiotic association wi

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

156 in soil or decaying wood, similar to extant beetle-infecting Ophiocordyceps species.

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

158 microbes; and (3) implementing conifer-bark beetle interactions in current models improves predictio

159 ol for detection of VLB in regions where the beetle is or may become established.

160 men extracted from scales of the Cyphochilus beetle, it will pose a limit to the achievable imaging r

161 We suggest that the jump from solitary beetle larva to ants within a colony exposed the fungus

162 Elaterid beetle larvae are among insect pests in soil that are in

163 We show that mites compete with beetle larvae for food in the absence of blowflies, and

164 likely arose from an ancestor that infected beetle larvae residing in soil or decaying wood, similar

165 Beetle larvae were more likely to move from damaged leav

166 by direct effects of warmer temperatures on beetle life cycles versus indirect effects of drought on

167 e primarily been driven by warming-amplified beetle life cycles whereas drought-weakened host defense

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

169 The two beetles' lineages probably diverged during the Pleniglac

170 in cells utilizing the split enhanced click beetle luciferase (Emerald Luc, ELuc) complementation te

171 Unlike other beetles, some ship-timber beetles (Lymexylidae) have extremely small elytra and la

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

173 The flightless beetle Merizodus soledadinus, native to the Falkland Isl

174 f symbiont metabolic range is shown to alter beetle metabolism of plant tissues and is implicated in

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

176 tectability of iridescent and non-iridescent beetle models and demonstrated that the iridescent treat

177 has affected its host-associated herbivorous beetle-Monochamus sartor.

178 response to some target dsRNAs causing 100% beetle mortality after ingestion.

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

180 We test this prediction in the Asian burying beetle Nicrophorus nepalensis, confirming that the diver

181 Using the Asian burying beetle Nicrophorus nepalensis, we demonstrate that mount

182 ratively breeding species, the Asian burying beetle Nicrophorus nepalensis.

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

184 ocus on the interactions between the burying beetle Nicrophorus vespilloides, an associated mite spec

185 Our experiments focus on the burying beetle Nicrophorus vespilloides, which naturally provide

186 Burying beetles (Nicrophorus vespilloides) breed on small verteb

187 We tested this prediction in the burying beetle, Nicrophorus vespilloides, a species where parent

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

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

190 uscumol was significantly more attractive to beetles of both sexes, than racemic fuscumol and a blend

191 Predatory lady beetles often consume non-prey foods like plant foliage

192 e origin of prothoracic horns in scarabaeine beetles, one of the most pronounced examples of secondar

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

194 l impact of the accidentally introduced leaf beetle Ophraella communa on the number of patients and h

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

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

197 June) and were not strongly affected by bark beetle outbreak; however, mean number of bee species and

198 g support for the view that irruptive spruce beetle outbreaks across North America have primarily bee

199 Landscape-scale bark beetle outbreaks alter forest structure with direct and

200 to previously proposed links between spruce beetle outbreaks and drought.

201 ienced widespread mortality caused by spruce beetle outbreaks in the 1990s, during a prolonged drough

202 clude that large-scale disturbance from bark beetle outbreaks may drive shifts in pollinator communit

203 Climate change has amplified eruptive bark beetle outbreaks over recent decades, including spruce b

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

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

206 e population dynamics of this and other bark beetle pests.

207 gatively influence larval growth of the leaf beetle Phaedon cochleariae (Coleoptera: Chrysomelidae) a

208 orewings (elytra) of the diabolical ironclad beetle, Phloeodes diabolicus.

209 y families of enzymes putatively involved in beetle-plant interactions that underwent adaptive expans

210 We explore the genomic consequences of beetle-plant trophic interactions by performing comparat

211 anol dispensers for manipulation of ambrosia beetle populations occurring in commercial avocado.

212 Furthermore, we show that lady beetles possess a state-dependent sterol-specific appeti

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

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

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

216 a) to test how prey nutrient content affects beetles' propensity to engage in herbivory.

217 Enzyme activity assays with crude beetle protein extracts revealed that glucosinolate sulf

218 herbivores, including the cabbage stem flea beetle (Psylliodes chrysocephala), prevent glucosinolate

219 c spider Nesticus barri and the troglobiotic beetle Ptomaphagus hatchi, each from four closely locate

220 come this limitation, the gene for the click beetle (Pyrophorus plagiophtalamus) red luciferase (luc)

221 evels were generally low (total ng of sterol/beetle range: 3-33 ng); the exception being Propylea qua

222 uordecimpunctata females (total ng of sterol/beetle range: 50-157 ng).

223 This revealed that the beetles register directional information provided by the

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

225 mites are especially effective at promoting beetle reproductive success at higher and lower natural

226 lies breed on the carrion too, mites enhance beetle reproductive success by eating blowfly eggs.

227 food in the absence of blowflies, and reduce beetle reproductive success.

228 umber of beetles and ants collected although beetle richness was significantly higher in burned logs

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

230 ombined in the spatial memory network in the beetle's brain.

231 es at ports of entry, and for monitoring the beetle's distribution and population trends in both ende

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

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

234 The burrows, probably produced by beetles, show that trace fossils can provide evidence fo

235 Unlike other beetles, some ship-timber beetles (Lymexylidae) have ext

236 ve tracts of pine forests, the southern pine beetle (SPB), Dendroctonus frontalis.

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

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

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

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

241 an introduced and a native Onthophagus dung beetle species in response to warming temperatures and h

242 We analysed the sterol profile of four beetle species reared on pea aphids-with or without foli

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

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

245 Using a community of beetle species, we show that when dispersal ability and

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

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

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

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

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

251 pondylis buprestoides (L.), and a rare click beetle, Stenagostus rufus (De Geer).

252 ed by multilayer cuticle reflectors in jewel beetle (Sternocera aequisignata) wing cases, provides ef

253 Laboratory-reared lady beetle sterol content was not significantly affected by

254 Indeed, the largest beetle suborder, Polyphaga, mostly includes plant eaters

255 representative of the two most species-rich beetle suborders.

256 egrates the many drivers governing this bark beetle system.

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

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

259 atus (Horn) (Coleoptera: Bostrichidae), is a beetle that is a member of a family that is primarily co

260 Odontotaenius disjunctus is a wood-feeding beetle that possesses a digestive tract with four main c

261 imilarly, there are other fossil families of beetles that are exclusively described from Cretaceous a

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

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

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

265 r the range margin of the alligatorweed flea beetle to test whether spatial variation in alligatorwee

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

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

268 show that intraspecific cooperation enables beetles to outcompete blowflies by recovering their opti

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

270 model system (Tribolium castaneum, red flour beetles) to test how the past environment of dispersing

271 Ambrosia beetle trap catches were reduced in the field more when

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

273 ex comprising MCU and EMRE subunits from the beetle Tribolium castaneum in complex with a human MICU1

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

275 ng specificity in an invertebrate model, the beetle Tribolium castaneum Using controlled evolution ex

276 On the contrary, here we show in the beetle Tribolium, whose development is broadly represent

277 two-species experimental system of the flour beetles Tribolium castaneum and Tribolium confusum, we s

278 rt of the blastoderm tissue of the red flour beetle (Tribolium castaneum) tightly adheres in a tempor

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 on of an MCU-EMRE complex from the red flour beetle, Tribolium castaneum, and a cryo-EM structure of

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

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

284 The velvet longhorned beetle, Trichoferus campestris (Faldermann) ("VLB"; Cole

285 predictions in the field using a specialist beetle Trirhabda pilosa that feeds on sagebrush Artemisi

286 re warming because maladaptation occurs when beetles try to breed at warmer temperatures.

287 miting resources, including food (rhinoceros beetles, Trypoxylus) and territories (fang blennies, Mei

288 We evolved replicate populations of burying beetles under two different regimes of parental care: So

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

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

291 es holds potential for manipulating ambrosia beetle vectors via push-pull management in avocado.

292 Beetles were maintained on one of five diets that varied

293 Previous laboratory results indicated that beetles were more likely to choose undamaged leaves comp

294 However, in preliminary field bioassays, beetles were not attracted by any known cerambycid phero

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

296 es are able to depolymerize RG-I relative to beetles whose symbionts lack the gene.

297 broader diversity of angiosperms than those beetles whose symbionts solely supplement polygalacturon

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

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

300 ificant overall as well for ant x beetle and beetle x beetle associations.