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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

26 eggs into figs and fewer pollinators entered figs.

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

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

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

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

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

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

33 ars associated with 21 sympatric New Guinean figs.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

49 l defined (frequently hybridizing) groups of figs.

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

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

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

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

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

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

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

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

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

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

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

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

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