ライフサイエンスコーパス: corolla

1 he M. lewisii flower, thus prepatterning the corolla.

2 ntral genes in an intermediary region of the corolla.

3 al to the lateral and abaxial regions of the corolla.

4 es examined and could extend into sepals and corolla.

5 identity and are highly expressed in petunia corollas.

6 st-pollination ethylene synthesis in petunia corollas.

7 ight hours, paralleling PhCCD1 expression in corollas.

8 sensitivity and ABA accumulation in petunia corollas.

9 a role in specifying dorsal identity in the corolla and androecium of monosymmetric (bilateral) flow

10 revealed that PhCCD1 is highly expressed in corollas and leaves, where it constitutes approximately

11 af petiole, flower and fruit pedicel, flower corolla, and fruit calyx.

12 as induced by pollination in both WT and IPT corollas, but this increase was delayed in IPT flowers.

13 senescence, was significantly greater in WT corollas, confirming that floral senescence was delayed

14 sociation between mouthparts' length and the corolla depth of the visited flowers, thus favouring tra

15 ber of cell divisions that took place during corolla development.

16 Such pleiotropic effects may underlie the corolla dimorphism frequently observed in gynodioecious

17 espite seasonal pulses of flowers with short-corollas, hummingbirds consistently foraged on well-matc

18 gth and nectar consumption (fly benefit) and corolla length and pollen deposition (plant benefit).

19 Selection between corolla length and proboscis length was reciprocal at th

20 the major driving force for the evolution of corolla length of R. purpurea and proboscis length of P.

21 loral display area, inflorescence height and corolla length of R. purpurea by comparing selection gra

22 Visitation also peaked at an intermediate corolla length, while its relationship to corolla width

23 hat (1) JA-Ile/COR-based signaling regulates corolla limb opening and a JA-negative feedback loop; (2

24 le-sterile flowers had significantly smaller corollas, longer styles and greater stigmatic exsertion

25 We studied hummingbird bill and plant corolla matching during seasonal variation in flower ava

26 lling anthocyanin pigmentation in the entire corolla of M. lewisii and two R2R3-MYB genes, PELAN and

27 ate pathway to the synthesis of FVBPs in the corolla of Petunia x hybrida cv. 'Mitchell Diploid'.

28 76% decrease in beta-ionone synthesis in the corollas of selected petunia lines, indicating a signifi

29 t flower), which differs from Antirrhinum in corolla (petal) symmetry and pollination mode.

30 ned, such as floral phenology, display size, corolla pigment, and inflorescence height.

31 es to induce endogenous ethylene production, corolla senescence, and up-regulation of the senescence-

32 While most floral trait values, including corolla size and nectar, increased linearly with increas

33 at male sterility is associated with reduced corolla size.

34 ve but may not correlate with transitions in corolla symmetry.

35 ike genes are thought to affect evolution of corolla symmetry.

36 duet for the main function of a sympetalous corolla, that of advertising for and rewarding pollinato

37 white region (i.e., light areas) around the corolla throat of M. lewisii flowers by diverting dihydr

38 70%, and total chorismate mutase activity in corolla tissue is reduced by 80-85% compared to control

39 lls within the ventral petal which adapt the corolla to specialised functions in pollination.

40 The various elaborations of corolla tube attributes, such as length, width and curva

41 e genetic and developmental control of these corolla tube attributes.

42 Different axes of corolla tube complexity can be disentangled at the devel

43 g linear selection imposed by pollinators on corolla tube length at all sites, but there was no consi

44 Local corolla tube length was correlated with local fly probos

45 idy on floral morphology in Nicotiana, using corolla tube measurements and geometric morphometrics to

46 loral traits (e.g., carotenoid pigmentation, corolla tube structure, nectar volume, pistil and stamen

47 ulus lewisii, with a substantial decrease in corolla tube width but no change in tube length.

48 s also located in the inner epidermis of the corolla tube with little BAMT protein detected in the ou

49 three functions: trichome production in the corolla tube, conical cell development in the petal hing

50 and between lower and upper portions of the corolla tube, defined by the stamen insertion boundary.

51 ies produce flowers with petals fused into a corolla tube.

52 small pollen from anthers located within the corolla tube.

53 Pollination of flowers with long corolla tubes by long-tongued hawkmoths has been invoked

54 s and is the sole pollinator of a plant with corolla tubes of matching length.

55 polyploids tend to evolve shorter and wider corolla tubes, suggesting that allopolyploidy could prov

56 pollinators specialize on flowers with deep corolla tubes, whereas shorter-tongued pollinators gener

57 te corolla length, while its relationship to corolla width varied across sites.

58 rect effects and vice versa for the trait of corolla width, which may be due, at least in part, to th

59 ls are only known as flowers, more precisely corollas with stamens and styles.

60 henylethyl benzoate, both present in petunia corollas, with similar catalytic efficiencies.

61 CYC2-like genes correlate with the origin of corolla zygomorphy are poorly understood.

62 YC2-like genes correlates with the origin of corolla zygomorphy.

63 es are probably crucial for the evolution of corolla zygomorphy.