ライフサイエンスコーパス: oviposition

1 and locate appropriate sites for egg laying (oviposition).

2 in turn, caused embryos to dry out following oviposition.

3 center for decision-making during Drosophila oviposition.

4 ole of these compounds in affecting P. rapae oviposition.

5 osition site, clutch size, and supernumerary oviposition.

6 ntibody production ensued following parasite oviposition.

7 r orientation of a female to host plants for oviposition.

8 subsequent oogenic processes, as well as in oviposition.

9 is, reaching a maximum on day 7, just before oviposition.

10 mate in swarms and females die shortly after oviposition.

11 oice oviposition assay significantly reduces oviposition.

12 havioral response to an odorant that affects oviposition.

13 onstrated predator avoidance behavior during oviposition.

14 d previously undescribed degrees of flexible oviposition.

15 water more quickly than those with flexible oviposition.

16 what may be the earliest evidence of insect oviposition.

17 vector behavior of predator avoidance during oviposition.

18 chs selected plots with fewer arthropods for oviposition.

19 d female adults and females after mating and oviposition.

20 ts' behavioral decisions during foraging and oviposition.

21 to dispersal, territoriality, courtship and oviposition.

22 maternal factors injected into hosts during oviposition.

23 parasitoid wasps leads to a sharp decline in oviposition.

24 g acceptance of those plants for feeding and oviposition.

25 re Manduca sexta with respect to feeding and oviposition.

26 nds on bare ground for mating, foraging, and oviposition.

27 ng of AaCAT1 reduces egg yield of subsequent ovipositions.

28 attraction to acetic acid to ensure optimal oviposition.(2) How such mechanosensory feedback modulat

29 nth segments are specialized differently for oviposition: 20 ovipositor motor neurons were found in t

30 und that ASM female flight was reduced after oviposition, a comparison of gene expression before and

31 f 0.1 to 1 larvae-equivalent per milliliter, oviposition activity increased in a dose-dependent manne

32 ed during the dark phase to choose sites for oviposition adds a new dimension to our understanding of

33 ons show that: (i) the refractory time after oviposition affects the value of superparasitism, with s

34 l to stimulate vitellogenesis and subsequent oviposition (anautogeny), but some autogenous individual

35 ffspring before washing and 25% reduction in oviposition and 50% reduction in offspring after 20 wash

36 ponent; Royal Guard induced 83% reduction in oviposition and 95% reduction in offspring before washin

37 ree-component sugar-wax blend replicated the oviposition and caterpillar response observed with the p

38 mRNA levels then declined after oviposition and during pregnancy.

39 only natural differential attractiveness for oviposition and feeding, but also other attributes that

40 of the Xenopus laevis egg that occur during oviposition and fertilization have been thoroughly studi

41 gic/tyraminergic signalling is essential for oviposition and hatching rate.

42 e presence of glucosinolates as a signal for oviposition and larval feeding.

43 t into the fly pupa by N. vitripennis during oviposition and N. vitripennis larvae developing infecti

44 have evolved in ways that maintain effective oviposition and pollination.

45 1 and ALAT2 in the female mosquitoes delayed oviposition and reduced egg production.

46 and inhibition of its biosynthesis in males, oviposition and refractoriness to further mating in the

47 they are acquired by parasitic wasps during oviposition and subsequently transmitted to new hosts.

48 rial infection of Drosophila females reduces oviposition and that peptidoglycan, the component that a

49 the relationship between the time spent for oviposition and the availability of aquatic habitats, we

50 Towards this goal, we examined WFT oviposition and TSWV inoculation behavior on tomato line

51 iles interacted to mediate resistance to WFT oviposition and TSWV inoculation on tomato leaves.

52 ve fitness by negatively impacting egg load, oviposition, and eclosion, and promoting an increase in

53 strain, PVY , affected the host preference, oviposition, and egg hatch rate of Lso-free or Lso-carry

54 h resistant lines (B75 and B96) with reduced oviposition, and increased resting and web-building time

55 pment and apoptosis, postmating behavior and oviposition, and nutrient sensing.

56 15, 20, 25, 30 and 35 C) on adult longevity, oviposition, and nymph development of the brown planthop

57 ior, impacting sperm storage/use, ovulation, oviposition, and remating receptivity.

58 a disruption in blood digestion, excretion, oviposition, and reproduction.

59 eir host finding, dietary range, mating, and oviposition are discussed.

60 humidity-inhibiting odorants in a two-choice oviposition assay significantly reduces oviposition.

61 In cage oviposition assays, FAW moths preferred to oviposit on m

62 In oviposition assays, we found that non-host odors varied

63 show that C. elegans persistently suppresses oviposition at high CO2.

64 clization is illustrated by the synthesis of oviposition attractant pheromone of the mosquito Culex p

65 ors, CquiOR10 and CquiOR2, narrowly tuned to oviposition attractants and well conserved among mosquit

66 mines may also serve as feeding attractants, oviposition attractants, or social cues.

67 ned volumetric space to accommodate specific oviposition attractants.

68 where strains generally showed preferential oviposition away from the acaricides.

69 s with respect to timing of adult emergence, oviposition behavior and larval habitat.

70 n between the reaction mass and remating and oviposition behavior argues that divergence has been pro

71 ome fertile as sperm become motile, and that oviposition behavior increases sharply after females rea

72 lant tissue concealment.(2)(,)(3) Endophytic oviposition behavior is currently common in many lineage

73 ion in Encarsia pergandiella but changed the oviposition behavior of females.

74 the roles of CO(2) cues in the foraging and oviposition behavior of phytophagous insects and in beha

75 occurs through a different component of the oviposition behavior than in the yucca moths.

76 This change in oviposition behavior, mediated by neuropeptide F, is ret

77 Endophytic oviposition behavior, the insertion of eggs into plant t

78 nctions in female reproduction by modulating oviposition behavior.

79 n exists on how conspecific signals modulate oviposition behavior.

80 gs and tended to more frequently divert from oviposition behavior.

81 pollination behaviors, but plant-seeking and oviposition behaviors are sustained through additional O

82 oincided with the shift from host-seeking to oviposition behaviors in blood-fed female mosquitoes.

83 ent plant species influence host-seeking and oviposition behaviors of swede midge?

84 ble roles during mate-finding, foraging, and oviposition behaviors.

85 oderate deviations in reproductive rate when oviposition behaviour is allowed to co-evolve in the sim

86 ductive rates among female size classes, and oviposition behaviour is predicted to co-evolve with rep

87 hen tested the effects of weaver ants on the oviposition behaviour of pollinating and non-pollinating

88 r of host plant quality during mixed feeding-oviposition bouts on Datura and Nicotiana plants.

89 mpact on C. sonorensis survival/longevity or oviposition but has a significant negative effect on mid

90 r, RHBP knockdown did not cause reduction in oviposition but led to the production of heme-depleted e

91 on the distal oviduct may be specialized for oviposition but there is no vagina.

92 In females, the pattern was phase-coupled to oviposition, but persisted after the connections with th

93 tested, pollinators and both traits increase oviposition by a hawkmoth herbivore, with nectar being m

94 in larval regurgitant contributes to reduced oviposition by adult females on larvae-infested plants.

95 h greenhouse and field settings, landing and oviposition by cabbage root fly females were positively

96 od genets to nutrient or shade stress and to oviposition by E. solidaginis.

97 surrounding scree habitat experience reduced oviposition by female butterflies and herbivory by cater

98 be a counter-adaptive mechanism for reducing oviposition by P. rapae and perhaps other crucifer-speci

99 d that pre-existing PVY infection can reduce oviposition by the Lso-carrying vector, the preference o

100 After oviposition, CD4(+), CD8(+), and CD19(+) splenocytes and

101 ed exposure to the net were kept in separate oviposition chambers and observed for the reproductive e

102 Furthermore, in oviposition choice tests in a wind tunnel, maize with or

103 ive response of Viburnum spp. against insect oviposition contrasts with little difference in the qual

104 that indole glucosinolates are an important oviposition cue.

105 etic analysis identified two unique, unitary oviposition cues for An. gambiae, 2-propylphenol and 4-m

106 yet imperfectly understood, role in sensing oviposition cues.

107 ers of egg batches produced during the first oviposition cycle on both the susceptible and resistant

108 and draw down spermatozoa reserves with each oviposition cycle.

109 of aquatic habitats, we show that prolonged oviposition cycles induced by source reduction account f

110 and 30 C, adult females achieved up to three oviposition cycles on the susceptible variety, but only

111 d larger batches during the second and third oviposition cycles on the susceptible variety; however,

112 ous from those that had undergone one or two oviposition cycles with an accuracy of 87%.

113 s the most important factor affecting female oviposition decisions.

114 ylsucrose amounts increased, WFT egg-laying (oviposition) decreased and TSWV inoculation was suppress

115 However, long-term persistence of oviposition depression after predator removal requires n

116 y regulation using a parasitoid wasp-induced oviposition depression paradigm in Drosophila melanogast

117 o predator elicits both an acute and learned oviposition depression, mediated through the visual syst

118 Activation of female-specific oviposition descending neurons (oviDNs) is necessary and

119 the discovery of microbial-derived repellent/oviposition-deterrent compounds that could be used in be

120 o-choice studies to determine the repellent, oviposition-deterrent, and insecticidal effects of C. fi

121 vity of the oviposition stimulants overcomes oviposition deterrents contained in Juglans leaves.

122 However, the early increase in oviposition did not result in more offspring in the 8 ho

123 gene expression before and after mating and oviposition did not reveal any genes which were consiste

124 gration polyphenism, spatial distribution of oviposition, egg size, and other miscellaneous traits.

125 Recent studies concerning mating and oviposition, especially as they impact the likelihood of

126 ng the idea that the behavioral component of oviposition evolves before other adaptations associated

127 oviDNs and their major excitatory input, the oviposition excitatory neurons (oviENs).

128 Nonlethal effects of predators on mosquito oviposition, foraging, and life history are common, and

129 hydroxyphenylacetic acid elicit increases in oviposition frequency in zebrafish mating pairs.

130 as a potent aggregation pheromone and as an oviposition guidance cue for females.

131 capes as a natural model system to study how oviposition habitat selection of Diptera responds to the

132 consequence of source reduction on mosquito oviposition has largely been neglected in evaluations of

133 t the evolution of parasitoidism and aquatic oviposition help to explain the diversification in the s

134 is the innately preferred nectar source and oviposition host for M. sexta Hence, the hawkmoth is an

135 In addition, significant differences in oviposition, host-choice and longevity were observed amo

136 e (maggots) for the estimation of time since oviposition (i.e., egg laying) for post mortem interval

137 one (20E) is a key regulator of monandry and oviposition in An. gambiae.

138 exes-courtship pursuit in males and communal oviposition in females.

139 mical analyses, which elicits attraction and oviposition in laboratory assays, as well as attraction

140 lopment, survival, host tree association and oviposition in large enclosures with trees planted two y

141 depletion of JNK pathway components inhibits oviposition in mated females, whereas JNK activation by

142 r sexual refractoriness but instead licenses oviposition in mated individuals once a 20E-inhibiting k

143 esigned to measure attraction for feeding or oviposition in relation to their host plants or specific

144 earning using a specific biological example: oviposition in the Lepidoptera.

145 dimorphism, protogyny, parthenogenesis, and oviposition in the pupal case.

146 Here we show that 20E-triggered oviposition in these mosquitoes is regulated by the stre

147 lool, reported to oppositely affect M. sexta oviposition, in the Arizona and Utah accessions.

148 dropsophus, which demonstrates that flexible oviposition (individuals laying eggs both in and out of

149 ality far more efficiently by remotely using oviposition-induced plant volatiles (OIPVs).

150 increases tomato defense against TPW through oviposition-induced responses, which promotes recruitmen

151 Moreover, oviposition inhibition rate in adult female of An. steph

152 gulator ( Pyriproxyfen) resulted in complete oviposition inhibition.

153 ABAergic (gamma-aminobutyric-acid-releasing) oviposition inhibitory neurons (oviINs) mediate feed-for

154 Another trait, oviposition into flowers, has evolved repeatedly within

155 e show that exposure to ethanol reduces wasp oviposition into fruit fly larvae.

156 ses are transmitted with the wasp egg during oviposition into lepidopteran insects, enabling the surv

157 When oviposition is imminent, female South African clawed fro

158 Drosophila melanogaster oviposition is one such important behavior, in which fem

159 Oviposition is stimulated by cues from water containers,

160 Oviposition is typically rare in virgin females but is i

161 A uniquely female behavior in grasshoppers, oviposition, is driven by neural circuitry in the termin

162 A specialized behavior, oviposition, is produced by the eighth and ninth abdomin

163 gravid females (adulticidal) or larvae post-oviposition (larvicidal).

164 , taste impacts processes including feeding, oviposition, locomotion, mating, and memory formation.

165 factors such as saliva and oral secretions, oviposition materials, and even feces.

166 Although oviposition normally occurs only after sexual maturity,

167 c) were divided among seven treatments after oviposition; normoxia (control; 21% O(2)), or hypoxia (1

168 e pre-oviposition period and period of first oviposition of migrants treated with JHA were significan

169 cals, for instance NeemAzal and NSE deterred oviposition of S. litura.

170 egulating the establishment, maturation, and oviposition of schistosomes and the progression of schis

171 Behavioral response also affected the oviposition of T. urticae, where strains generally showe

172 Oviposition of the Lso-carrying psyllids was lower on PV

173 In Drosophila melanogaster, oviposition on a substrate containing ethanol enhances f

174 , individuals can be selected to concentrate oviposition on an abundant low-quality host, whilst igno

175 the impact of larval host age at the time of oviposition on development time, mother longevity and of

176 match, quantifying the impact of error-prone oviposition on larval performance in a specialized speci

177 Pea weevil (Bruchus pisorum L.) oviposition on pods of specific genetic lines of pea (Pi

178 Adult marking appeared to deter oviposition only in the presence of an unmarked substrat

179 , disrupted nitrogen waste disposal, delayed oviposition onset, and decreased fecundity in vitellogen

180 ntaining highly toxic Se levels and shows no oviposition or feeding deterrence, in contrast to relate

181 rn by experimental methods that activate the oviposition pattern in females.

182 cies have led to sweeping generalizations of oviposition patterns across entire mosquito genera.

183 el oviposition performance; individual-level oviposition performance; and key developmental factors.

184 traction to host volatiles; population-level oviposition performance; individual-level oviposition pe

185 The pre-oviposition period and period of first oviposition of mi

186 Immature developmental duration, adult pre-oviposition period and total pre-oviposition periods, ad

187 antly enhanced key fitness traits, including oviposition period, adult longevity, net reproductive ra

188 on led to a male-biased sex ratio, shortened oviposition period, and decreased life-time reproductive

189 ed the pre-oviposition period, shortened the oviposition period, decreased the number of eggs deposit

190 formance metrics such as mating success, pre-oviposition period, number of eggs laid, duration of egg

191 It significantly prolonged the pre-oviposition period, shortened the oviposition period, de

192 These changes in males led to prolonged pre-oviposition periods and decreased fecundity in females.

193 males, resulting in significant reduction of oviposition periods and fecundity in females, and signif

194 sperm competitions (each running over 30-day oviposition periods) shows that males producing both rel

195 , adult pre-oviposition period and total pre-oviposition periods, adult longevity, fecundity, and sex

196 e recorded no difference in the body weight, oviposition periods, and longevity compared to controls.

197 ulex quinquefasciatus (CquiOBP1) bound to an oviposition pheromone (5R,6S)-6-acetoxy-5-hexadecanolide

198 nd variable mortality risks in each may make oviposition plasticity adaptive.

199 is the development of a lure that stimulates oviposition plus a toxin with no deterrent effect.

200 Mismatches between female oviposition preference and larval performance can lead t

201 Oviposition preference changed over time.

202 Female flies showed no oviposition preference for treated or untreated diets.

203 6b are essential in sour GRNs of females for oviposition preference on acid-containing food.

204 Oviposition preference resulted from reduced levels of r

205 here competing dopaminergic systems modulate oviposition preference to adjust to changes in natural o

206 The enantiomers had opposite effects on oviposition preference, but the magnitude of the effect

207 c correlation between larval performance and oviposition preference, indicating that female moths do

208 ereas there was no significant difference in oviposition preference.

209 Although studies have demonstrated that oviposition preferences of successive insects were affec

210 Females show strong oviposition preferences that correspond with larval perf

211 t volatile emissions, herbivore settling and oviposition preferences, and herbivore population growth

212 transduction in adult females with different oviposition preferences.

213 osine methylation machinery to platyhelminth oviposition processes.

214 hensi exposed to pyriproxyfen was 100% while oviposition rate in adult female of An.stephensi in the

215 reproductive performance was evidenced by an oviposition rate of 35%.

216 Oviposition rates among ovitraps placed in three Treatme

217 Reexposed baboons with low worm recovery and oviposition rates and small (modulated) hepatic granulom

218 aps within 20-25 m of each other and compare oviposition rates at these sites with background oviposi

219 osition rates at these sites with background oviposition rates in Control and Vector Areas.

220 h primary infections, when worm recovery and oviposition rates were high and hepatic schistosome egg

221 Adult survival/longevity, oviposition rates, number of eggs deposited, egg hatch r

222 Survival/longevity of the blood-fed adults, oviposition rates, number of eggs deposited, larval stag

223 , the specialist BGM showed no difference in oviposition, resting and web-building time across all ma

224 Currently, traps baited with oviposition semiochemicals play an important role in det

225 supplemented with MSN, prior exposure to TPW oviposition shifted subsequent egg-laying from a prefere

226 rons fine tune the physical assessment of an oviposition site and determine where the female fly lays

227 Habitat selection, including oviposition site choice, is an important driver of commu

228 Finding a suitable oviposition site is a challenging task for a gravid fema

229 t hygrosensory pathways in blood feeding and oviposition site seeking and suggest Ir40a-dependent Dry

230 Moist Cells to promote blood feeding, while oviposition site seeking is driven specifically by Ir68a

231 iative learning can affect processes such as oviposition site selection and host preference, it is ti

232 ur understanding of the risk and benefits of oviposition site selection by gravid An. gambiae females

233 that female insects perceive and use during oviposition site selection is complex and varies by spec

234 Mosquito oviposition site selection is essential for vector popul

235 ing mate and food localization, mate choice, oviposition site selection, kin recognition, and predato

236 trategies, voltinism, diapause, aestivation, oviposition site, clutch size, and supernumerary oviposi

237 receptor abolishes aggregation behavior and oviposition site-selection towards 9-tricosene and E2-he

238 ent studies have shown that behaviour during oviposition site-selection, host location and even host

239 Understanding choice of oviposition sites and dispersal behavior is important fo

240 ain chemical information on mating partners, oviposition sites and food.

241 The antenna is involved in finding food, oviposition sites and mates.

242 m of host marking and re-assessment of prior oviposition sites during the decision-making process.

243 climate-induced reductions in water depth at oviposition sites have caused high mortality of embryos

244 Selection of appropriate oviposition sites is essential for progeny survival and

245 o promote blood feeding and locate potential oviposition sites is shared between the malaria vector A

246 tion of resources to eggs, and the choice of oviposition sites may all be influenced by plant quality

247 opheles gambiae mosquitoes identify suitable oviposition sites through a repertoire of cues, but the

248 Females prefer oviposition sites with pheromone concentrations correspo

249 ensitivity to identify appropriate habitats, oviposition sites, and food sources, to date no nonnavig

250 e hormone analogue (JHA) between resting and oviposition sites.

251 mount of time required for vectors to locate oviposition sites.

252 ghly sensitive detectors of food, mates, and oviposition sites.

253 f colony con-specifics, and determination of oviposition sites.

254 o coincide with the availability of food and oviposition sites.

255 directly and indirectly with conspecifics at oviposition sites.

256 ent tuning of their olfactory system towards oviposition sites.

257 al for nocturnal moths to locate feeding and oviposition sites.

258 edes aegypti, seeking blood-meals as well as oviposition sites.

259 such as locating food, sexual partners, and oviposition sites.

260 l sources, most notably blood meal hosts and oviposition sites.

261 Blowflies use odors to locate food and oviposition sites; therefore, olfaction might have playe

262 e percentages of OFM in the egg maturation & oviposition stage, which could be used as an indicator i

263 s because the leaves do not contain specific oviposition stimulant(s).

264 Larval extracts contained both oviposition stimulant(s)/attractant(s) and deterrent(s),

265 e leaves were treated with a Lyonia-specific oviposition stimulant, although they do not lay eggs on

266 ylic acids and methyl esters serve as potent oviposition stimulants for gravid Ae. aegypti.

267 Otherwise, the activity of the oviposition stimulants overcomes oviposition deterrents

268 riterpenoid glycosides were characterized as oviposition stimulants.

269 and ODS column chromatography to isolate the oviposition stimulants.

270 at microorganisms in leaf infusions produced oviposition-stimulating kairomones, and using a combinat

271 rsity of tachinids, examine the evolution of oviposition strategies and host associations, review kno

272 dominant effects of resource allocation and oviposition strategies, and of mechanical constraints.

273 (number and duration of probing events) and oviposition studies with non-viruliferous and virulifero

274 roposed that ovariole number correlated with oviposition substrate [2-4] but sampled largely one clad

275 Furthermore, we show that oviposition substrate evolution is linked to changes in

276 ed to food containing acetic acid (AA) as an oviposition substrate.

277 n preference to adjust to changes in natural oviposition substrates.

278 , gentamicin-fed ticks showed a reduction in oviposition success compared to ticks artificially fed o

279 bacterial VOCs did not induce A. biguttatus oviposition, suggesting their role in beetle behavior is

280 ash was less preferred for adult feeding and oviposition than susceptible hosts, more resistant to la

281 females do not easily conform to artificial oviposition, the genetic refreshment of this GSS is a ch

282 After oviposition, the species of parent was molecularly deter

283 due to the unanticipated impact of wAnga on oviposition timing.

284 By contrast, the reduced TPP oviposition trait in LA3952 is independent of Lso.

285 Prolonged oviposition triggered pigmentation in the basal cells of

286 vation method are: embryos at 15-30 min post oviposition, two incubation steps in 100% deuterated met

287 rial peptidoglycan reduces Drosophila female oviposition via NF-kappaB pathway activation in some neu

288 After oviposition, viral quantification revealed that seven of

289 Mite oviposition was also recorded after 72 h.

290 ducts to cyp79B2 cyp79B3 mutants showed that oviposition was increased by indole-3-carbinol and decre

291 ffect of pyriproxyfen on mosquito fecundity (oviposition) was also assessed over four days after 72 h

292 Upon oviposition, wasps inject these viruses into their hosts

293 hatched without cold within 19-32 days post oviposition, we were able to develop a non-diapausing co

294 Bacteria known to stimulate oviposition were found in both wild and mass-reared flie

295 Experimental methods that activate oviposition were found to also activate a rhythmical mot

296 Consumption and oviposition were positively correlated; however, the rel

297 her foraging-related traits, consumption and oviposition, were also detected among inbred lines.

298 The maternal control of the sex ratio during oviposition, which is well known in other hymenopterans,

299 have either obligate aquatic or terrestrial oviposition, with eggs that are specialized for developi

300 ence of wAnga in female mosquitoes following oviposition, with the caveat that we could not rule out