ライフサイエンスコーパス: weevil

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1 weevil (Callosobruchus maculatus F.) and pea weevil.

2 immediate and major diversification event in weevils.

3 tly evolved bacterial endosymbionts of maize weevils.

4 of hyperdiverse and flightless Trigonopterus weevils.

5 esistance of Sitka spruce against white pine weevil, a major North American forest insect pest of pin

6 nsis), but not against predation by the bean weevil (Acanthoscelides obtectus) or the Mexican bean we

7 so recorded the rate of acorn infestation by weevils and acorn germination rates of weekly collection

8 p and complex history of coevolution between weevils and angiosperms, including codiversification, re

9 with potent activity against the cotton boll weevil (Anthonomus grandis grandis Boheman).

10 Pea weevil (Bruchus pisorum L.) oviposition on pods of speci

11 est (Listronotus bonariensis; Argentine stem weevil) by an introduced parasitoid (Microctonus hyperod

12 Callosobruchus maculatus) and the azuki bean weevil (Callosobruchus chinensis), but not against preda

13 urthermore, scN substantially delayed cowpea weevil (Callosobruchus maculatus (F.)) growth and develo

14 cts that we have identified from both cowpea weevil (Callosobruchus maculatus F.) and pea weevil.

15 rtain species of bruchids such as the cowpea weevil (Callosobruchus maculatus) and the azuki bean wee

16 insecticidal activity when fed to the cowpea weevil, Callosobruchus maculatus (F.).

17 apoptosis in spruce budworm and cotton boll weevil cell cultures.

18 f host protein synthesis in budworm and boll weevil cells.

19 The African sweetpotato weevil Cylas brunneus is one of the most devastating pes

20 ollected life table data for the sweetpotato weevil, Cylas formicarius, grown on Ipomoea batatas and

21 Trypsin mRNA from the citrus weevil, Diaprepes abbreviatus, was reverse transcribed a

22 Comparative trends in weevil diversification and angiosperm dominance reveal t

23 Mechanical or Diaprepes root weevil (DRW) feeding damage to leaves caused a <10-fold

24 The 15 species in the weevil genus Galapaganus Lanteri 1992 (Entiminae: Curcul

25 resent a large-scale molecular phylogeny for weevils (herbivorous beetles in the superfamily Curculio

26 e analysis of fast-moving screw-and-nut-type weevil hip joints.

27 vely used in the French West Indies to fight weevils in banana plantations from 1973 to 1993.

28 ing and insecticidal activity against cowpea weevil, indicating that glycosylation and multimeric str

29 vergreen broad-leaved forests, and assess if weevil infestation contributes to low seedling recruitme

30 ersal strategies may mitigate the effects of weevil infestation of acorns in a population of Quercus

31 For most years: (i) the rate of weevil infestation was negatively density dependent (a g

32 nt use of EPNs in citrus for control of root weevils is also reported.

33 e exerted insecticidal activity against boll weevil larvae.

34 ent by translocating an abundant leaf-mining weevil Platynotocis sp., which largely escaped parasitis

35 In addition, weevil resistance to PA1b is correlated with bafilomycin

36 relatively higher levels of (+)-3-carene in weevil-resistant trees.

37 va) plants and its root herbivore rice water weevil (RWW; Lissorhoptrus oryzophilus), and how plant j

38 nearly 4-h video-recording of a female bean weevil's behavior.

39 Weevils, which represent one of the most diverse groups

40 canthoscelides obtectus) or the Mexican bean weevil (Zabrotes subfasciatus), insects that are common

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