ライフサイエンスコーパス: fig

1 fig codes for a predicted PP2C phosphatase.

2 fig has two different promoters which produce two differ

3 o decades since Janzen described how to be a fig, more than 200 papers have appeared on fig wasps (Ag

4 modified across multiple trophic levels in a fig wasp community according to climate.

5 g a model interaction network comprised of a fig and fig wasp mutualist, eight non-pollinating fig wa

6 Herein, we characterize the efficacy of a fig fruit extract of ABA in promoting glycemic control.

7 Here we assemble high-quality genomes of a fig species, Ficus pumila var. pumila, and its specific

8 Additionally, figs presented greater sources of amino acids (725.07 mg

9 iniscent of green, herbaceous notes but also figs and cooked fruit.

10 urposes (monotropic and oligotropic bees and fig wasps).

11 l interaction network comprised of a fig and fig wasp mutualist, eight non-pollinating fig wasp (NPFW

12 lation genetic data from neotropical fig and fig wasp species that suggest that a more accurate model

13 lized pollinator mutualisms such as figs and fig wasps and yuccas and yucca moths.

14 n losses), the nested arrangement of kay and fig is conserved in all species.

15 ggest that the nested arrangement of kay and fig may be due to a functional relationship between them

16 ated by serine/threonine phosphorylation and fig is a predicted PP2C phosphatase specific for serine/

17 ver ants on fig wasp community structure and fig seed production were then compared between trees wit

18 gest that these pollinator host-switches and fig hybridization events are a dominant feature of fig/w

19 ing and nutritional components of leaves and figs from several Spanish varieties of Ficus carica L.

20 ly specialized pollinator mutualisms such as figs and fig wasps and yuccas and yucca moths.

21 ity, with no significant differences between fig and blackthorn extracts.

22 In the mutualism between fig trees and their pollinating wasps both partners depe

23 n of host sanctions in the mutualism between fig trees and their pollinating wasps.

24 y examine the idea that codivergence between figs and their pollinators has been dominated by strict-

25 sity-dependent facultative mutualism between figs, pollinator wasps and the nematode.

26 Both fig transcripts are also detected in all stages tested.

27 les, provides an important resource for both fig breeding and for fundamental research into the relat

28 a high-energy lifestyle fueled primarily by fig juice.

29 beta-d-glucopyranoside, Ficus capensis (Cape fig) the most 3-CQA and 5-CQA, and Parinari curatellifol

30 Since early in the man history, common fig was appreciated as food and for its medicinal proper

31 PC) and antioxidant activity from fresh dark fig (Ficus carica L.) have been investigated using respo

32 tion, with pollinators' offspring dominating figs produced by trees inhabited by weaver ants, and off

33 total of 300 samples of hazelnuts and dried fig were analysed for the incidence of any aflatoxins (A

34 Three hazelnuts and six dried fig samples exceeded the European maximum limits (MLs) o

35 Sixteen dried fig samples (12.3%) contained AFs ranging from 0.1 to 28

36 dorant zone reminiscent of coconut and dried figs as 5,6-dihydro-6-pentyl-2H-pyran-2-one (C10 massoia

37 tomatoes, spinach, brined olives, and dried figs using shotgun metagenomics.

38 to AFs exposure is higher than that of dried figs.

39 eggs into figs and fewer pollinators entered figs.

40 cus nymphaeifolia act at the level of entire figs (syconia), not at the level of the individual flowe

41 Multitrophic communities of wasps exploiting fig fruits, which first evolved about 75MYA, do not show

42 Ficus (figs) and their agaonid wasp pollinators present an ecol

43 + CFS was employed as packaging material for fig fruit to prolong the shelf life.

44 transcripts, both in the same reading frame, fig-alpha and beta.

45 ity were successfully synthesized from fresh fig fruit using a one-step pyrolysis method.

46 analysis of kayak (kay) and fos intron gene (fig), a divergently transcribed gene located in a kay in

47 region is a nested gene, fos-intronic gene (fig) which is transcribed in the opposite direction.

48 One gene, fig-1, encodes a labile protein with conserved thrombosp

49 ars associated with 21 sympatric New Guinean figs.

50 rgely conserved across the range of the host fig, despite limited correspondence between the ranges o

51 Furthermore, the antioxidant capacity in fig achenes' oil was assessed by employing two different

52 yield, stability and bioactive compounds in fig, black cumin and rosehip oils.

53 independently confirmed that differences in fig traits predict differences in dispersers.

54 eroxide value (PV) increased dramatically in fig (182.7 %) and rosehip (221.1 %) oils, while PV of Me

55 MeTHF extracted oils was not significant in fig and rosehip oils.

56 MeTHF increased oil yield in fig (11.7 %), black cumin (28.3 %) and rosehip (13.2 %).

57 the non-pollinator P. mayri most abundant in figs on trees inhabited by other ants.

58 with unbiased estimates of odor and color in figs, we demonstrate that fruit traits evolve in concert

59 h do not bring pollen, to avoid sanctions in figs to which other wasps bring pollen.

60 xcluded, more non-pollinators laid eggs into figs and fewer pollinators entered figs.

61 two non-pollinator tribes developing in its figs each contained only four species.

62 phemeral and highly sought-after fruit, like figs, than sites with less ephemeral fruit that can be m

63 of common fruit plants such as olive, mango, fig and medicinal herbs that have been used to treat ski

64 and population genetic data from neotropical fig and fig wasp species that suggest that a more accura

65 plores the in vitro biological activities of fig latex and elucidates its possible mechanisms of acti

66 t time, we have immobilized scFv antibody of fig mosaic virus (FMV) on the magnetic nanoparticles (MN

67 characterized the multitrophic community of fig wasps associated with Ficus racemosa and then applie

68 The present work describes the evaluation of fig peels and blackthorn fruit extracts as natural purpl

69 A phylogenetic examination of fig revealed that there are three subfamilies of PP2C ph

70 bridization events are a dominant feature of fig/wasp coevolutionary history, and by generating novel

71 adaptation and cospeciation between pairs of fig and wasp species that are associated in highly speci

72 h a non-commercially available proteinase of fig-leaf gourd fruit (Cucurbita ficifolia) increased the

73 Three newly discovered species of fig-living nematodes display remarkable diversity in hea

74 This new synthesis of fig wasp research attempts to integrate recent contribut

75 resident lineages and local colonisations of figs by other insect lineages.

76 l defined (frequently hybridizing) groups of figs.

77 The effects of weaver ants on fig wasp community structure and fig seed production wer

78 a fig, more than 200 papers have appeared on fig wasps (Agaonidae) and their host plants (Ficus spp.,

79 Overall, PVA + FM + GG + CFS-based packed fig fruits has prolonged shelf life of till 12 days.

80 Pantropical fig-wasp communities represent a remarkably well-replica

81 Gall wasps pollinate fig trees.

82 on of resource conflicts between pollinating fig wasps, their hosts, and their parasites.

83 nd fig wasp mutualist, eight non-pollinating fig wasp (NPFW) antagonists/commensals and a nematode pr

84 ls of host specificity among non-pollinating fig wasps and quantify geographical variation in communi

85 behaviour of pollinating and non-pollinating fig wasps in an ant-exclusion experiment.

86 ct high dispersal ability in non-pollinating fig wasps to result in lower geographical turnover in co

87 specificity in two genera of non-pollinating fig wasps.

88 phical turnover in comparison to pollinating fig wasps.

89 nd natural sweeteners (dried apples, prunes, figs, raisins, apricots, carrot and sweet potato, stevia

90 ne of the oldest known domesticated species, fig (Ficus carica L.), using Pacific Biosciences single-

91 Such fig-level sanctions allow uncooperative wasps, which do

92 These data indicate that fig achenes oil of F. carica could be potentially useful

93 Our data shows that fig latex inhibits properties that are associated with H

94 The fig genome is ~333 Mbp in size, of which 80% has been an

95 the prevalence of uncooperative wasps in the fig tree-fig wasp mutualism.

96 erred how this influences the fitness of the fig-pollinator mutualists.

97 knowledge of the evolutionary history of the fig/fig-wasp mutualism.

98 Our results indicated that the fig achenes' oil is a rich source of bioactive molecules

99 t Oecophylla smaragdina, associated with the fig tree Ficus racemosa in southwest China.

100 generating novel genomic combinations in the figs have likely contributed to the remarkable diversity

101 oncentration of 4MMB in VOO samples and the 'fig tree leaf' sensory attribute.

102 ost-switching by the pollinators, leading to fig hybridization, even between distantly related clades

103 The application of coatings (CFA-PAHF) to figs significantly reduced (p <= 0.05) weight loss and m

104 lence of uncooperative wasps in the fig tree-fig wasp mutualism.

105 ween epigenetic changes and phenotype, using fig as a model species.

106 nclosed communities of wasps associated with figs as study system.