다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
NTIS 바로가기
Plants, v.9 no.8, 2020년, pp.927 -
Martínez-Harms, Jaime (Institut fü) , Hadar, Ravit (r Biologie-Neurobiologie, Freie Universitä) , Márquez, Natalia (t Berlin, Kö) , Menzel, Randolf (nigin-Luise Str. 1–) , Shmida, Avi (3, 14195 Berlin, Germany) , Stavenga, Doekele G. (ravit.hadar@charite.de (R.H.)) , Vorobyev, Misha (nmarquez@zedat.fu-berlin.de (N.M.))
AI-Helper
Evolutionary change is considered a major factor influencing the invasion of new habitats by plants. Yet, evidence on how such modifications promote range expansion remains rather limited. Here we investigated flower color modifications in the red poppy, Papaver rhoeas (Papaveraceae), as a result of...
1. Parker I.M. Pollinator limitation of Cytisus scoparius (Scotch broom), an invasive exotic shrub Ecology 1997 78 1457 1470 10.1890/0012-9658(1997)078[1457:PLOCSS]2.0.CO;2
2. Larson K.C. Fowler S.P. Walker J.C. Lack of pollinators limits fruit set in the exotic Lonicera japonica Am. Midl. Nat. 2002 148 54 60 10.1674/0003-0031(2002)148[0054:LOPLFS]2.0.CO;2
3. Baker H.G. The evolution of weeds Annu. Rev. Ecol. Syst. 1974 5 1 24 10.1146/annurev.es.05.110174.000245
4. Lloyd D.G. Self- and cross-fertilization in plants. II. The selection of self- fertilization Int. J. Plant. Sci. 1992 153 370 380 10.1086/297041
5. Morgan M.T. Wilson W.G. Self-fertilization and the escape from pollen limitation in variable pollination environments Evolution 2005 59 1143 1148 10.1111/j.0014-3820.2005.tb01050.x 16136811
6. Eckert C.G. Kalisz S. Geber M.A. Sargent R. Elle E. Cheptou P.O. Goodwillie C. Johnston M.O. Kelly J.K. Moeller D.A. Plant mating systems in a changing world Trends Ecol. Evol. 2010 25 35 43 10.1016/j.tree.2009.06.013 19683360
7. Gabra S. Papaver species and opium through the ages Bull. Inst. Egypte 1954 37 39 56
8. Kadereit J.W. Some suggestions on the geographical origin of the central, west and north European synanthropic species of Papaver L. Bot. J. Linn. Soc. 1990 103 221 231 10.1111/j.1095-8339.1990.tb00185.x
9. Colledge S. Conolly J. Shennan S. Archaeobotanical Evidence for the Spread of Farming in the Eastern Mediterranean Curr. Anthropol. 2004 45 S35 S58 10.1086/422086
10. Willerding U. Zur Geschichte der Unkrauter Mitteleuropas Wachholtz Neumunster, Germany 1986
11. Zohary D. Hopf M. Domestication of Plants in the Old World: The Origin and Spread of Cultivated Plants in West Asia, Europe, and the Nile Valley 2nd ed. Clarendon Press Oxford, UK 1993
12. Godwin H. The History of the British Flora: A Factual Basis for Phytogeography 2nd ed. Cambridge University Press Cambridge, UK 1975
13. McNaughton I.H. Harper J.L. The comparative biology of closely related species living in the same area I. External breeding barriers between Papaver species New Phytol. 1960 59 15 26 10.1111/j.1469-8137.1960.tb06197.x
14. Dafni A. Bernhardt P. Shmida A. Ivri Y. Greenbaum S. Red bowl-shaped flowers: Convergence for beetle pollination in the Mediterranean region Isr. J. Bot. 1990 39 81 92
15. Dobson H.E.M. Groth I. Bergstrom G. Pollen advertisement: Chemical contrasts between whole-flower and pollen odors Am. J. Bot. 1996 83 877 885 10.1002/j.1537-2197.1996.tb12779.x
16. Proctor M. Yeo P. The Pollination of Flowers Collins London, UK 1973
17. Lawrence M.J. Genetics of self-incompatibility in Papaver rhoeas Proc. R. Soc. B 1975 188 275 285 10.1098/rspb.1975.0019
18. Foote H.C. Ride J.P. Franklin-Tong V.E. Walker E.A. Lawrence M.J. Franklin F.C. Cloning and expression of a distinctive class of self-incompatibility (S) gene from Papaver rhoeas L. Proc. Natl. Acad. Sci. USA 1994 91 2265 10.1073/pnas.91.6.2265 8134385
19. Wheeler M.J. de Graaf B.H.J. Hadjiosif N. Perry R.M. Poulter N.S. Osman K. Vatovec S. Harper A. Franklin F.C.H. Franklin-Tong V.E. Identification of the pollen self-incompatibility determinant in Papaver rhoeas Nature 2009 459 992 10.1038/nature08027 19483678
20. Martinez-Harms J. Vorobyev M. Schorn J. Shmida A. Keasar T. Homberg U. Schmeling F. Menzel R. Evidence of red sensitive photoreceptors in Pygopleurus israelitus (Glaphyridae: Coleoptera) and its implications for beetle pollination in the southeast Mediterranean J. Comp. Physiol. A 2012 198 451 463 10.1007/s00359-012-0722-5
21. Peitsch D. Fietz A. Hertel H. Desouza J. Ventura D.F. Menzel R. The spectral input systems of hymenopteran insects and their receptor-based color vision J. Comp. Physiol. A 1992 170 23 40 10.1007/BF00190398 1573568
22. Martinez-Harms J. Palacios A.G. Marquez N. Estay P. Arroyo M.T.K. Mpodozis J. Can red flowers be conspicuous to bees? Bombus dahlbomii and South American temperate forest flowers as a case in point J. Exp. Biol. 2010 213 564 10.1242/jeb.037622 20118307
23. Streinzer M. Roth N. Paulus H.F. Spaethe J. Color preference and spatial distribution of glaphyrid beetles suggest a key role in the maintenance of the color polymorphism in the peacock anemone ( Anemone pavonina , Ranunculaceae) in Northern Greece J. Comp. Physiol. A 2019 205 735 743 10.1007/s00359-019-01360-2
24. Lotmar R. Neue Untersuchungen uber den Farbensinn der Bienen, mit besonderer Berucksichtigung des Ultravioletts Z. Vergl. Physiol. 1933 19 673 723 10.1007/BF00395648
25. Kugler H. Hummeln und die UV-Reflexion an Kronblattern Naturwissenschaften 1947 34 315 316 10.1007/BF00623640
26. Daumer K. Blumenfarben, wie sie die Bienen sehen Z. Vergl. Physiol. 1958 41 49 110 10.1007/bf00340242
27. Lunau K. Interspecific diversity and uniformity of flower colour patterns as cues for learned discrimination and innate detection of flowers Experientia 1993 49 1002 1010 10.1007/BF02125649
28. Van der Kooi C.J. Stavenga D.G. Vividly coloured poppy flowers due to dense pigmentation and strong scattering in thin petals J. Comp. Physiol. A 2019 205 363 372 10.1007/s00359-018-01313-1
29. Chittka L. Waser N.M. Why red flowers are not invisible to bees Isr. J. Plant. Sci. 1997 45 169 183 10.1080/07929978.1997.10676682
30. Sakai A.K. Allendorf F.W. Holt J.S. Lodge D.M. Molofsky J. With K.A. Baughman S. Cabin R.J. Cohen J.E. Ellstrand N.C. The population biology of invasive species Annu. Rev. Ecol. Syst. 2001 32 305 332 10.1146/annurev.ecolsys.32.081501.114037
31. Stockwell C.A. Hendry A.P. Kinnison M.T. Contemporary evolution meets conservation biology Trends Ecol. Evol. 2003 18 94 101 10.1016/S0169-5347(02)00044-7
32. Lambrinos J.G. How interactions between ecology and evolution influence contemporary invasion dynamics Ecology 2004 85 2061 2070 10.1890/03-8013
33. Barrett S.C.H. Colautti R.I. Eckert C.G. Plant reproductive systems and evolution during biological invasion Mol. Ecol. 2008 17 373 383 10.1111/j.1365-294X.2007.03503.x 17868309
34. Richardson D.M. Allsopp N. D’Antonio C.M. Milton S.J. Rejmanek M. Plant invasions―The role of mutualisms Biol. Rev. 2000 75 65 93 10.1017/S0006323199005435 10740893
35. Dudek B. Schneider B. Hartmut H.H. Stavenga D.G. Martinez-Harms J. Highly different flavonol content explains geographic variations in the UV reflecting properties of flowers of the corn poppy, Papaver rhoeas ( Papaveraceae ) Phytochemistry 2020 10.1016/j.phytochem.2020.112457
36. Haribal M.M. Feeny P.P. Combined roles of contact stimulant and deterrents in assessment of host-plant quality by ovipositing zebra swallowtail butterflies J. Chem. Ecol. 2003 29 653 670 10.1023/A:1022820719946 12757326
37. Mallikarjuna N. Kranthi K.R. Jadhav D.R. Kranthi S. Chandra S. Influence of foliar chemical compounds on the development of Spodoptera litura (Fab.) in interspecific derivatives of groundnut J. Appl. Entomol. 2004 128 321 328 10.1111/j.1439-0418.2004.00834.x
38. Sosa T. Chaves N. Alias J.C. Escudero J.C. Henao F. Gutierrez-Merino C. Inhibition of mouth skeletal muscle relaxation by flavonoids of Cistus ladanifer L.: A plant defense mechanism against herbivores J. Chem. Ecol. 2004 30 1087 1101 10.1023/B:JOEC.0000030265.45127.08 15303316
39. Hollosy F. Effects of ultraviolet radiation on plant cells Micron 2002 33 179 197 10.1016/S0968-4328(01)00011-7 11567887
40. Rozema J. van de Staaij J. Bjorn L.O. Caldwell M. UV-B as an environmental factor in plant life: Stress and regulation Trends Ecol. Evol. 1997 12 22 28 10.1016/S0169-5347(96)10062-8 21237957
41. Shirley B.W. Flavonoid biosynthesis: ‘new’ functions for an ‘old’ pathway Trends Plant. Sci. 1996 1 377 382 10.1016/S1360-1385(96)80312-8
42. Havaux M. Kloppstech K. The protective functions of carotenoid and flavonoid pigments against excess visible radiation at chilling temperature investigated in Arabidopsis npq and tt mutants Planta 2001 213 953 966 10.1007/s004250100572 11722132
43. Albert A. Sareedenchai V. Heller W. Seidlitz H.K. Zidorn C. Temperature is the key to altitudinal variation of phenolics in Arnica montana L. cv. ARBO Oecologia 2009 160 1 8 10.1007/s00442-009-1277-1 19194724
44. Jansen M.A.K. Gaba V. Greenberg B.M. Higher plants and UV-B radiation: Balancing damage, repair and acclimation Trends Plant. Sci. 1998 3 131 135 10.1016/S1360-1385(98)01215-1
45. Del Valle J.C. Buide M.L. Casimiro-Soriguer I. Whittall J.B. Narbona E. On flavonoid accumulation in different plant parts: Variation patterns among individuals and populations in the shore campion ( Silene littorea ) Front. Plant. Sci. 2015 6 939 10.3389/fpls.2015.00939 26579180
46. Koski M.H. Ashman T.-L. An altitudinal cline in UV floral pattern corresponds with a behavioral change of a generalist pollinator assemblage Ecology 2015 96 3343 3353 10.1890/15-0242.1 26909439
47. Koski M.H. Ashman T.-L. Floral pigmentation patterns provide an example of Gloger’s rule in plants Nat. Plants 2015 1 14007 10.1038/nplants.2014.7 27246054
48. Jaakola L. Hohtola A. Effect of latitude on flavonoid biosynthesis in plants Plant. Cell Env. 2010 33 1239 1247 10.1111/j.1365-3040.2010.02154.x 20374534
49. Seckmeyer G. Pissulla D. Glandorf M. Henriques D. Johnsen B. Webb A. Siani A.-M. Bais A. Kjeldstad B. Brogniez C. Variability of UV irradiance in Europe Photochem. Photobiol. 2008 84 172 179 10.1111/j.1751-1097.2007.00216.x 18173717
50. Darwin C. The Effects of Cross and Self Fertilization in the Vegetable Kingdom John Murray London, UK 1876
51. Grant V. Pollination systems as isolating mechanisms in angiosperms Evolution 1949 3 82 97 10.1111/j.1558-5646.1949.tb00007.x 18115119
52. Levin D.A. The origin of reproductive isolating mechanisms in flowering plants Taxon 1971 20 91 113 10.2307/1218538
53. Grant V. Modes and origins of mechanical and ethological isolation in angiosperms Proc. Natl. Acad. Sci. USA 1994 91 3 10 10.1073/pnas.91.1.3 11607448
54. Grant V. Isolation and hybridization between Aquilegia formosa and A. pubescens El Aliso 1952 2 341 360
55. Chen Z. Liu C.-Q. Sun H. Niu Y. The ultraviolet colour component enhances the attractiveness of red flowers of a bee-pollinated plant J. Plant. Ecol. 2020 13 354 360 10.1093/jpe/rtaa023
56. Lunau K. Papiorek S. Eltz T. Sazima M. Avoidance of achromatic colours by bees provides a private niche for hummingbirds J. Exp. Biol. 2011 214 1607 10.1242/jeb.052688 21490268
57. Koski M.H. Ashman T.-L. Dissecting pollinator responses to a ubiquitous ultraviolet floral pattern in the wild Funct. Ecol. 2014 28 868 877 10.1111/1365-2435.12242
58. Mitich L.W. Corn Poppy ( Papaver rhoeas L.) Weed Technol. 2000 14 826 829 10.1614/0890-037X(2000)014[0826:CPPRL]2.0.CO;2
59. Keasar T. Harari A.R. Sabatinelli G. Keith D. Dafni A. Shavit O. Zylbertal A. Shmida A. Red anemone guild flowers as focal places for mating and feeding by Levant glaphyrid beetles Bot. J. Linn. Soc. 2010 99 808 817 10.1111/j.1095-8312.2010.01384.x
60. Sabatinelli G. Eberle J. Fabrizi S. Ahrens D. A molecular phylogeny of Glaphyridae (Coleoptera: Scarabaeoidea): Evolution of pollination and association with ‘Poppy guild’ flowers Syst. Entomol. 2020 10.1111/syen.12429
61. Meyer R.S. Purugganan M.D. Evolution of crop species: Genetics of domestication and diversification Nat. Rev. Genet. 2013 14 840 852 10.1038/nrg3605 24240513
62. Darwin C. The Variation of Animals and Plants under Domestication John Murray London, UK 1868 Volume 2
63. Dewet J.M.J. Harlan J.R. Weeds and domesticates: Evolution in man-made habitat Econ. Bot. 1975 29 99 107 10.1007/BF02863309
64. Barrett S.H. Crop mimicry in weeds Econ. Bot. 1983 37 255 282 10.1007/BF02858881
65. Vorobyev M. Osorio D. Receptor noise as a determinant of colour thresholds Proc. R. Soc. B 1998 265 351 358 10.1098/rspb.1998.0302
66. Vorobyev M. Brandt R. Peitsch D. Laughlin S.B. Menzel R. Colour thresholds and receptor noise: Behaviour and physiology compared Vis. Res. 2001 41 639 653 10.1016/S0042-6989(00)00288-1 11226508
67. Koshitaka H. Kinoshita M. Vorobyev M. Arikawa K. Tetrachromacy in a butterfly that has eight varieties of spectral receptors Proc. R. Soc. B 2008 275 947 954 10.1098/rspb.2007.1614
68. Goldsmith T.H. Butler B.K. The roles of receptor noise and cone oil droplets in the photopic spectral sensitivity of the budgerigar, Melopsittacus undulatus J. Comp. Physiol. A 2003 189 135 142 10.1007/s00359-002-0385-8 12607042
69. Lind O. Chavez J. Kelber A. The contribution of single and double cones to spectral sensitivity in budgerigars during changing light conditions J. Comp. Physiol. A 2013 200 197 207 10.1007/s00359-013-0878-7 24366429
70. Wyszecki G. Stiles W.S. Color Science: Concepts and Methods, Quantitative Data and Formulae 2nd ed. John Wiley & Sons New York, NY, USA 1982
*원문 PDF 파일 및 링크정보가 존재하지 않을 경우 KISTI DDS 시스템에서 제공하는 원문복사서비스를 사용할 수 있습니다.
오픈액세스 학술지에 출판된 논문
Copyright KISTI. All Rights Reserved.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.