ライフサイエンスコーパス: oviposition

1 osition site, clutch size, and supernumerary oviposition.

2 ntibody production ensued following parasite oviposition.

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

4 subsequent oogenic processes, as well as in oviposition.

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

6 to dispersal, territoriality, courtship and oviposition.

7 maternal factors injected into hosts during oviposition.

8 parasitoid wasps leads to a sharp decline in oviposition.

9 g acceptance of those plants for feeding and oviposition.

10 re Manduca sexta with respect to feeding and oviposition.

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

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

13 center for decision-making during Drosophila oviposition.

14 ts' behavioral decisions during foraging and oviposition.

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

16 ng of AaCAT1 reduces egg yield of subsequent ovipositions.

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

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

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

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

21 mRNA levels then declined after oviposition and during pregnancy.

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

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

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

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

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

27 1 and ALAT2 in the female mosquitoes delayed oviposition and reduced egg production.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

44 nctions in female reproduction by modulating oviposition behavior.

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

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

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

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

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

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

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

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

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

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

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

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

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

58 that indole glucosinolates are an important oviposition cue.

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

60 yet imperfectly understood, role in sensing oviposition cues.

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

62 s the most important factor affecting female oviposition decisions.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

79 When oviposition is imminent, female South African clawed fro

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

81 Oviposition is stimulated by cues from water containers,

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

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

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

85 Although oviposition normally occurs only after sexual maturity,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

104 6b are essential in sour GRNs of females for oviposition preference on acid-containing food.

105 Oviposition preference resulted from reduced levels of r

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

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

108 Females show strong oviposition preferences that correspond with larval perf

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

110 osine methylation machinery to platyhelminth oviposition processes.

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

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

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

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

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

116 Mosquito oviposition site selection is essential for vector popul

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

141 After oviposition, viral quantification revealed that seven of

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

143 Upon oviposition, wasps inject these viruses into their hosts

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

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

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