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Artículos de revistas sobre el tema "Floral variation"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 19 de febrero de 2022

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1

Soltis, Pamela S., Samuel F. Brockington, Mi-Jeong Yoo, et al. "Floral variation and floral genetics in basal angiosperms." American Journal of Botany 96, no. 1 (2009): 110–28. http://dx.doi.org/10.3732/ajb.0800182.

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2

Majetic, Cassie J., Robert A. Raguso, and Tia-Lynn Ashman. "Sources of floral scent variation." Plant Signaling & Behavior 4, no. 2 (2009): 129–31. http://dx.doi.org/10.4161/psb.4.2.7628.

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3

Shibusawa, Naoe, Isao Nohara, and Ryo Ohsawa. "Interspecific variation of scent characteristics in the Cyclamen genus and the utility of the variation." Horticultural Science 45, No. 4 (2018): 193–204. http://dx.doi.org/10.17221/111/2017-hortsci.

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All the currently available interspecific scented cyclamen were bred by crossing Cyclamen persicum with only a wild species, C.purpurascens. To develop cyclamen with a wider variety of fragrances, we clarified the diversity of volatile compounds emitted from the flowers of 17 wild cyclamen species. We found that 14 of the wild species emitted fragrant compounds. In particular, C. pseudibericum, C. cyprium, C. libanoticum, C. purpurascens, C. cilicium and C. alpinum emitted floral compounds, and C. mirabile emitted fruity compounds. We produced interspecific hybrids between two C. persicum cult
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4

Huang, Daihong, Fuchen Shi, Minwei Chai, Ruili Li, and Houhun Li. "Interspecific and Intersexual Differences in the Chemical Composition of Floral Scent inGlochidionSpecies (Phyllanthaceae) in South China." Journal of Chemistry 2015 (2015): 1–14. http://dx.doi.org/10.1155/2015/865694.

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Plants of theGlochidion(Phyllanthaceae) genus are pollinated exclusively by host-specificEpicephala(Gracillariidae) moths. Floral scent has been thought to play key role in the obligate pollination mutualism betweenGlochidionplants andEpicephalamoths, but few studies have been reported about chemical variation in floral volatiles ofGlochidionspecies in China. Floral volatiles of male and female flowers of fiveGlochidionspecies in south China were collected by dynamic headspace absorption technique and then were chemically analyzed by using gas chromatography-mass spectrometry. A total of 69 co
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5

Cash-Arcia, Norman, William Cetzal-Ix, Edgar Mó, Hermes Vega, and Saikat Kumar Basu. "First record of Lepanthes appendiculata Ames (Orchidaceae: Pleurothallidinae) from Nicaragua, with comments on the morphological variation, geographical distribution, and conservation status." Check List 12, no. 4 (2016): 1941. http://dx.doi.org/10.15560/12.4.1941.

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Lepanthes appendiculata Ames, a new record for the orchid flora of Nicaragua is presented, with comments on its geographical distribution, floral variations, and analysis of conservation status following IUCN criteria. Additionally, we include iconography of its floral variations, habitats, and a detailed distribution map. Based on the herbarium records and iconography, we also accept and corroborate 10 species of Lepanthes Sw. in Nicaragua.
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6

Chen, Gao, Wei-Chang Gong, Jia Ge, Johann Schinnerl, Bin Wang, and Wei-Bang Sun. "Variation in floral characters, particularly floral scent, in sapromyophilous Stemona species." Journal of Integrative Plant Biology 59, no. 11 (2017): 825–39. http://dx.doi.org/10.1111/jipb.12580.

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7

Weber, Urs K., Scott L. Nuismer, and Anahí Espíndola. "Patterns of floral morphology in relation to climate and floral visitors." Annals of Botany 125, no. 3 (2019): 433–45. http://dx.doi.org/10.1093/aob/mcz172.

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Abstract Background and Aims The diversity of floral morphology among plant species has long captured the interest of biologists and led to the development of a number of explanatory theories. Floral morphology varies substantially within species, and the mechanisms maintaining this diversity are diverse. One possibility is that spatial variation in the pollinator fauna drives the evolution of spatially divergent floral ecotypes adapted to the local suite of pollinators. Another possibility is that geographic variation in the abiotic environment and local climatic conditions favours different
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8

Kitazawa, Miho S. "Developmental stochasticity and variation in floral phyllotaxis." Journal of Plant Research 134, no. 3 (2021): 403–16. http://dx.doi.org/10.1007/s10265-021-01283-7.

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AbstractFloral phyllotaxis is a relatively robust phenotype; trimerous and pentamerous arrangements are widely observed in monocots and core eudicots. Conversely, it also shows variability in some angiosperm clades such as ‘ANA’ grade (Amborellales, Nymphaeales, and Austrobaileyales), magnoliids, and Ranunculales. Regardless of the phylogenetic relationship, however, phyllotactic pattern formation appears to be a common process. What are the causes of the variability in floral phyllotaxis and how has the variation of floral phyllotaxis contributed to floral diversity? In this review, I summari
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9

Roberts, D., A. McMinn, N. Johnston, D. B. Gore, M. Melles, and H. Cremer. "An analysis of the limnology and sedimentary diatom flora of fourteen lakes and ponds from the Windmill Islands, East Antarctica." Antarctic Science 13, no. 4 (2001): 410–19. http://dx.doi.org/10.1017/s0954102001000578.

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The limnology and sedimentary diatom flora of fourteen lakes and ponds from the Windmill Islands, East Antarctica, is presented. Saline lakes, saline ponds and freshwater ponds are represented in this dataset. The Windmill Island lake diatom flora represents an intermediate floral assemblage between that of the freshwater lakes of the Larsemann Hills and the saline lakes of Vestfold Hills, East Antarctica. Variations within this assemblage are related to water chemistry variables in the Windmill Island lakes. In particular, a lakewater salinity/phosphate gradient can explain the variation obse
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10

van de Kerke, Sara J., Tiemen van Engelenhoven, Anne L. van Es, et al. "Capturing variation in floral shape: a virtual3D based morphospace for Pelargonium." PeerJ 8 (April 2, 2020): e8823. http://dx.doi.org/10.7717/peerj.8823.

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Background Variation in floral shapes has long fascinated biologists and its modelling enables testing of evolutionary hypotheses. Recent comparative studies that explore floral shape have largely ignored 3D floral shape. We propose quantifying floral shape by using geometric morphometrics on a virtual3D model reconstructed from 2D photographical data and demonstrate its performance in capturing shape variation. Methods This approach offers unique benefits to complement established imaging techniques (i) by enabling adequate coverage of the potential morphospace of large and diverse flowering-
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11

Ros, P., B. C. Anderson, and A. Ellis. "Pollinator-driven floral variation in Tritoniopsis revoluta." South African Journal of Botany 74, no. 2 (2008): 377. http://dx.doi.org/10.1016/j.sajb.2008.01.103.

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12

Affre, L., and J. D. Thompson. "Floral trait variation in fourCyclamen (Primulaceae) species." Plant Systematics and Evolution 212, no. 3-4 (1998): 279–93. http://dx.doi.org/10.1007/bf01089743.

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13

Burdon, Rosalie C. F., Robert A. Raguso, André Kessler, and Amy L. Parachnowitsch. "Spatiotemporal Floral Scent Variation of Penstemon digitalis." Journal of Chemical Ecology 41, no. 7 (2015): 641–50. http://dx.doi.org/10.1007/s10886-015-0599-1.

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14

Orozco-Obando*, Warner, and Hazel Y. Wetzstein. "Genotypic Variation in Flower Bud Development in Hydrangea macrophylla." HortScience 39, no. 4 (2004): 757B—757. http://dx.doi.org/10.21273/hortsci.39.4.757b.

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The general doctrine of flowering in Hydrangea is that floral induction occurs during the previous season on last year's growth and usually at the stem's terminal bud. However, Hydrangea cultivars widely differ in their relative abundance and duration of flower production. The objective of this study was to determine how developmental flowering patterns compare among different genotypes. Flowering was characterized in 18 H. macrophylla cultivars by assessing the extent of flower initiation and development in terminal and lateral buds of dormant shoots (i.e., after they have received floral ind
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15

Azad, Rumana, K. L. Wasantha Kumara, Gamini Senanayake, R. A. A. K. Ranawaka, D. K. N. G. Pushpakumara, and Sudarshanee Geekiyanage. "Flower morphological diversity of cinnamon (Cinnamomum verum Presl) in Matara District, Sri Lanka." Open Agriculture 3, no. 1 (2018): 236–44. http://dx.doi.org/10.1515/opag-2018-0025.

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Abstract The cinnamon flowers exhibit protogynous dichogamy with 2 flower types “Type A” and “Type B” which first flowers during morning and evening respectively. This floral cycle causes a temporal barrier to the maintenance of elite breeding material and for hybridization with desired parents. Determination of variation in flower and inflorescence morphology can shed light on functional diversity in “Type A” and “Type B” flowers. In order to study these variations, a survey of cultivated cinnamon lands and wild habitats was conducted in fifteen locations in the Matara district. Peduncle leng
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16

Orozco-Obando, Warner, Gwen N. Hirsch, and Hazel Y. Wetzstein. "Genotypic Variation in Flower Induction and Development in Hydrangea macrophylla." HortScience 40, no. 6 (2005): 1695–98. http://dx.doi.org/10.21273/hortsci.40.6.1695.

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The general doctrine of flowering in Hydrangea macrophylla (Thunb.) Ser. is that floral induction occurs during the fall months with the flower appearing the following spring or summer. However, hydrangea cultivars differ widely in their relative abundance and duration of flower production. The objective of this study was to determine how developmental flowering patterns compared among different hydrangea genotypes. Flowering was characterized in 18 cultivars by assessing flower initiation in dormant buds of 1-year-old stems that received natural outdoor inductive conditions. Terminal and late
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17

Macnair, M. R., and Q. J. Cumbes. "The genetic architecture of interspecific variation in mimulus." Genetics 122, no. 1 (1989): 211–22. http://dx.doi.org/10.1093/genetics/122.1.211.

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Abstract The genetic architecture of various floral and morphological differences between Mimulus cupriphilus and Mimulus guttatus is investigated. M. cupriphilus is believed to have speciated from M. guttatus in the recent past. The two parent species, the F(1) and F(2), and two backcrosses were grown and scored for 23 different characters. The analysis of means revealed significant epistasis for a number of the floral characters, particularly those involving the length of parts. Dominance was generally toward M. guttatus, except for the characters related to flowering time. Analysis of the g
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18

Warner, Ryan M., and John E. Erwin. "Variation in Floral Induction Requirements of Hibiscus sp." Journal of the American Society for Horticultural Science 126, no. 3 (2001): 262–68. http://dx.doi.org/10.21273/jashs.126.3.262.

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Thirty-six Hibiscus L. species were grown for 20 weeks under three lighting treatments at 15, 20, or 25 ± 1.5 °C air temperature to identify flowering requirements for each species. In addition, species were subjectively evaluated to identify those species with potential ornamental significance based on flower characteristics and plant form. Lighting treatments were 9 hour ambient light (St. Paul, Minn., November to May, 45 °N), ambient light plus a night interruption using incandescent lamps (2 μmol·m-2·s-1; 2200 to 0200 hr), or ambient light plus 24-hour supplemental lighting from high-press
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19

Klinkhamer, Peter G. L., and Catharina A. M. van der Veen-van Wijk. "Genetic Variation in Floral Traits of Echium vulgare." Oikos 85, no. 3 (1999): 515. http://dx.doi.org/10.2307/3546700.

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20

Schemske, Douglas W., and Carol C. Horvitz. "Temporal Variation in Selection on a Floral Character." Evolution 43, no. 2 (1989): 461. http://dx.doi.org/10.2307/2409220.

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21

Schemske, Douglas W., and Carol C. Horvitz. "TEMPORAL VARIATION IN SELECTION ON A FLORAL CHARACTER." Evolution 43, no. 2 (1989): 461–65. http://dx.doi.org/10.1111/j.1558-5646.1989.tb04240.x.

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22

Battey, Nicholas H., and Fiona Tooke. "Molecular control and variation in the floral transition." Current Opinion in Plant Biology 5, no. 1 (2002): 62–68. http://dx.doi.org/10.1016/s1369-5266(01)00229-1.

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23

Richards, Jennifer H., and Suzanne Koptur. "FLORAL VARIATION AND DISTYLY IN GUETTARDA SCABRA (RUBIACEAE)." American Journal of Botany 80, no. 1 (1993): 31–40. http://dx.doi.org/10.1002/j.1537-2197.1993.tb13764.x.

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24

Brock, Marcus T., Jennifer M. Dechaine, Federico L. Iniguez-Luy, Julin N. Maloof, John R. Stinchcombe, and Cynthia Weinig. "Floral Genetic Architecture: An Examination of QTL Architecture Underlying Floral (Co)Variation Across Environments." Genetics 186, no. 4 (2010): 1451–65. http://dx.doi.org/10.1534/genetics.110.119982.

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25

Ellis, Allan G., Samuel F. Brockington, Marinus L. de Jager, Gregory Mellers, Rachel H. Walker, and Beverley J. Glover. "Floral trait variation and integration as a function of sexual deception in Gorteria diffusa." Philosophical Transactions of the Royal Society B: Biological Sciences 369, no. 1649 (2014): 20130563. http://dx.doi.org/10.1098/rstb.2013.0563.

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Phenotypic integration, the coordinated covariance of suites of morphological traits, is critical for proper functioning of organisms. Angiosperm flowers are complex structures comprising suites of traits that function together to achieve effective pollen transfer. Floral integration could reflect shared genetic and developmental control of these traits, or could arise through pollinator-imposed stabilizing correlational selection on traits. We sought to expose mechanisms underlying floral trait integration in the sexually deceptive daisy, Gorteria diffusa , by testing the hypothesis that stab
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26

Kong, Ying, Jinrong Bai, Lixin Lang, et al. "Variation in Floral Scent Compositions of Different Lily Hybrid Groups." Journal of the American Society for Horticultural Science 142, no. 3 (2017): 175–83. http://dx.doi.org/10.21273/jashs03934-16.

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Lilium cultivars have a wide range of variation in floral scent phenotypes. Using gas chromatography–mass spectrometry (GC/MS) analyses of volatile emissions during the night, the floral scent compositions of 35 lily cultivars from seven different hybrid groups were studied. The results showed that there was a positive correlation between volatile emission levels and scent intensities. Nonscented lily cultivars belonging to Asiatic hybrids hardly emitted volatiles, light-scented Longiflorum × Asiatic hybrids emitted low levels of volatiles, and scented lily cultivars (belonging to Oriental, Tr
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27

Sinjushin, Andrey, Ekaterina Bykova, and Vladimir Choob. "Interaction between Floral Merism and Symmetry: Evidence from Fasciated Mutant of Lupinus angustifolius L. (Leguminosae)." Symmetry 11, no. 3 (2019): 321. http://dx.doi.org/10.3390/sym11030321.

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A significant diversity of flower structure in angiosperms is defined by few parameters, among which one may list floral merism and symmetry as the most important. However, observation of normal variation in different taxa indicates that high floral merism (more than six organs) is very rarely associated with a monosymmetry. Precise mechanisms underlying this tendency, as well as the mode of interaction between regulatory pathways of floral symmetry and merism, remain unidentified. In this work, we observed the floral ontogeny in normal plants of Lupinus angustifolius L. (Leguminosae), describ
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28

Jacquemyn, Hans, and Rein Brys. "Lack of strong selection pressures maintains wide variation in floral traits in a food-deceptive orchid." Annals of Botany 126, no. 3 (2020): 445–53. http://dx.doi.org/10.1093/aob/mcaa080.

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Abstract Background and Aims Angiosperms vary remarkably in traits such as colour, size and shape of flowers, yet such variation generally tends to be low within species. In deceptive orchids, however, large variation in floral traits has been described, not only between but also within populations. Nonetheless, the factors driving variation in floral traits in deceptive orchids remain largely unclear. Methods To identify determinants of variation in floral traits, we investigated patterns of fruit set and selection gradients in the food-deceptive orchid Orchis purpurea, which typically presen
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29

Vannette, Rachel L. "The Floral Microbiome: Plant, Pollinator, and Microbial Perspectives." Annual Review of Ecology, Evolution, and Systematics 51, no. 1 (2020): 363–86. http://dx.doi.org/10.1146/annurev-ecolsys-011720-013401.

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Flowers at times host abundant and specialized communities of bacteria and fungi that influence floral phenotypes and interactions with pollinators. Ecological processes drive variation in microbial abundance and composition at multiple scales, including among plant species, among flower tissues, and among flowers on the same plant. Variation in microbial effects on floral phenotype suggests that microbial metabolites could cue the presence or quality of rewards for pollinators, but most plants are unlikely to rely on microbes for pollinator attraction or reproduction. From a microbial perspec
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30

Iwamoto, A., A. Shimizu, and H. Ohba. "Floral development and phyllotactic variation in Ceratophyllum demersum (Ceratophyllaceae)." American Journal of Botany 90, no. 8 (2003): 1124–30. http://dx.doi.org/10.3732/ajb.90.8.1124.

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31

van der Niet, Timotheüs, Christoph P. E. Zollikofer, Marcia S. Ponce de León, Steven D. Johnson, and H. Peter Linder. "Three-dimensional geometric morphometrics for studying floral shape variation." Trends in Plant Science 15, no. 8 (2010): 423–26. http://dx.doi.org/10.1016/j.tplants.2010.05.005.

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32

Ros, P., B. Anderson, and A. G. Ellis. "Pollinator mediated floral variation and hybridization in Tritoniopsis revoluta." South African Journal of Botany 75, no. 2 (2009): 418. http://dx.doi.org/10.1016/j.sajb.2009.02.099.

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33

Newman, Ethan, and Bruce Anderson. "Character displacement drives floral variation in Pelargonium (Geraniaceae) communities." Evolution 74, no. 2 (2020): 283–96. http://dx.doi.org/10.1111/evo.13908.

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34

Dormont, Laurent, Nina Joffard, and Bertrand Schatz. "Intraspecific Variation in Floral Color and Odor in Orchids." International Journal of Plant Sciences 180, no. 9 (2019): 1036–58. http://dx.doi.org/10.1086/705589.

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35

Moya, Samuel, and James D. Ackerman. "Variation in the floral fragrance of Epidendrum ciliare (Orchidaceae)." Nordic Journal of Botany 13, no. 1 (1993): 41–47. http://dx.doi.org/10.1111/j.1756-1051.1993.tb00009.x.

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36

GUITIAN, J. "Variation in Floral Sex Allocation in Polygonatum odoratum (Liliaceae)." Annals of Botany 94, no. 3 (2004): 433–40. http://dx.doi.org/10.1093/aob/mch163.

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37

Meagher, Thomas R. "Linking the Evolution of Gender Variation to Floral Development." Annals of Botany 100, no. 2 (2007): 165–76. http://dx.doi.org/10.1093/aob/mcm035.

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38

Obi Johnson, Bettie, Annette M. Golonka, Austin Blackwell, Iver Vazquez, and Nigel Wolfram. "Floral Scent Variation in the Heterostylous Species Gelsemium sempervirens." Molecules 24, no. 15 (2019): 2818. http://dx.doi.org/10.3390/molecules24152818.

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Gelsemium sempervirens (L.) W.T. Aiton, a distylous woody vine of the family Gelsemiaceae, produces sweetly fragrant flowers that are known for the toxic alkaloids they contain. The composition of this plant’s floral scent has not previously been determined. In this study, the scent profiles of 74 flowers obtained from six different wild and cultivated populations of G. sempervirens were measured by solid phase microextraction-gas chromatography-mass spectrometry (SPME-GC-MS). There were 81 volatile organic compounds identified and characterized as benzenoids, terpenoids, fatty acid derivative
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39

Burkle, Laura A., William R. Glenny, and Justin B. Runyon. "Intraspecific and interspecific variation in floral volatiles over time." Plant Ecology 221, no. 7 (2020): 529–44. http://dx.doi.org/10.1007/s11258-020-01032-1.

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40

Gaskett, Anne C., Elena Conti, and Florian P. Schiestl. "Floral Odor Variation in Two Heterostylous Species of Primula." Journal of Chemical Ecology 31, no. 5 (2005): 1223–28. http://dx.doi.org/10.1007/s10886-005-5351-9.

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41

Kitazawa, Miho S. "Correction to: Developmental stochasticity and variation in floral phyllotaxis." Journal of Plant Research 134, no. 3 (2021): 645. http://dx.doi.org/10.1007/s10265-021-01307-2.

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42

Le Maitre, N. C., M. D. Pirie, and D. U. Bellstedt. "An approach to determining anthocyanin synthesis enzyme gene expression in an evolutionary context: an example from Erica plukenetii." Annals of Botany 124, no. 1 (2019): 121–30. http://dx.doi.org/10.1093/aob/mcz046.

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Abstract Background and Aims Floral colour in angiosperms can be controlled by variations in the expression of the genes of the anthocyanin pathway. Floral colour shifts influence pollinator specificity. Multiple shifts in floral colour occurred in the diversification of the genus Erica (Ericaceae), from plesiomorphic pink to, for example, red or white flowers. Variation in anthocyanin gene expression and its effects on floral colour in the red-, pink- and white-flowered Erica plukenetii species complex was investigated. Methods Next generation sequencing, reverse transcriptase PCR and real-ti
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43

Kiełtyk, Piotr. "Patterns of floral allocation along an elevation gradient: variation in Senecio subalpinus growing in the Tatra Mountains." Alpine Botany 131, no. 1 (2021): 117–24. http://dx.doi.org/10.1007/s00035-021-00247-w.

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AbstractThis study examined the morphological variation in Senecio subalpinus W.D.J. Koch. (Asteraceae) along a 950-m elevation gradient in the Tatra Mountains, Central Europe, with emphasis on floral allocation patterns. Fifteen morphological traits were measured in 200 plants collected in the field from 20 sites then the findings were modelled by elevation using linear mixed-effects models. Plant aboveground biomass and height decreased steadily with increasing elevation; however, the most distinctive feature was the elevational shift in floral allocation patterns. Low-elevation plants had g
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44

Tucic, Branka, S. Manitasevic, A. Vuleta, and Gordana Matic. "Linking Hsp90 function to micro-environmental and stochastic variation in floralorgans of Iris pumila L." Archives of Biological Sciences 60, no. 3 (2008): 411–19. http://dx.doi.org/10.2298/abs0803411t.

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Hsp90 is an environmentally responsive molecular chaperone that was found to play a key role in buffering against genetic and non-genetic perturbations in the model organisms Arabidopsis and Drosophila. Here we analyzed the buffering capacity of Hsp90 against two kinds of non-genetic factors - stochastic noise and micro-environmental varia?tion of floral organ traits in naturally growing Iris pumila plants. We found no statistical association between the endog?enous level of Hsp90 and the floral organ radial symmetry produced by stochastic developmental noise. Conversely, floral organ plastici
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45

Petrén, Hampus, Per Toräng, Jon Ågren, and Magne Friberg. "Evolution of floral scent in relation to self-incompatibility and capacity for autonomous self-pollination in the perennial herb Arabis alpina." Annals of Botany 127, no. 6 (2021): 737–47. http://dx.doi.org/10.1093/aob/mcab007.

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Abstract Background and Aims The transition from outcrossing to selfing is a frequent evolutionary shift in flowering plants and is predicted to result in reduced allocation to pollinator attraction if plants can self-pollinate autonomously. The evolution of selfing is associated with reduced visual floral signalling in many systems, but effects on floral scent have received less attention. We compared multiple populations of the arctic–alpine herb Arabis alpina (Brassicaceae), and asked whether the transition from self-incompatibility to self-compatibility has been associated with reduced vis
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46

Juenger, Thomas, Michael Purugganan, and Trudy F. C. Mackay. "Quantitative Trait Loci for Floral Morphology in Arabidopsis thaliana." Genetics 156, no. 3 (2000): 1379–92. http://dx.doi.org/10.1093/genetics/156.3.1379.

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Abstract A central question in biology is how genes control the expression of quantitative variation. We used statistical methods to estimate genetic variation in eight Arabidopsis thaliana floral characters (fresh flower mass, petal length, petal width, sepal length, sepal width, long stamen length, short stamen length, and pistil length) in a cosmopolitan sample of 15 ecotypes. In addition, we used genome-wide quantitative trait locus (QTL) mapping to evaluate the genetic basis of variation in these same traits in the Landsberg erecta × Columbia recombinant inbred line population. There was
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Friberg, Magne, Christopher Schwind, Paulo R. Guimarães, Robert A. Raguso, and John N. Thompson. "Extreme diversification of floral volatiles within and among species ofLithophragma(Saxifragaceae)." Proceedings of the National Academy of Sciences 116, no. 10 (2019): 4406–15. http://dx.doi.org/10.1073/pnas.1809007116.

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A major challenge in evolutionary biology is to understand how complex traits of multiple functions have diversified and codiversified across interacting lineages and geographic ranges. We evaluate intra- and interspecific variation in floral scent, which is a complex trait of documented importance for mutualistic and antagonistic interactions between plants, pollinators, and herbivores. We performed a large-scale, phylogenetically structured study of an entire plant genus (Lithophragma, Saxifragaceae), of which several species are coevolving with specialized pollinating floral parasites of th
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Moré, Marcela, Florencia Soteras, Ana C. Ibañez, Stefan Dötterl, Andrea A. Cocucci, and Robert A. Raguso. "Floral Scent Evolution in the Genus Jaborosa (Solanaceae): Influence of Ecological and Environmental Factors." Plants 10, no. 8 (2021): 1512. http://dx.doi.org/10.3390/plants10081512.

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Floral scent is a key communication channel between plants and pollinators. However, the contributions of environment and phylogeny to floral scent composition remain poorly understood. In this study, we characterized interspecific variation of floral scent composition in the genus Jaborosa Juss. (Solanaceae) and, using an ecological niche modelling approach (ENM), we assessed the environmental variables that exerted the strongest influence on floral scent variation, taking into account pollination mode and phylogenetic relationships. Our results indicate that two major evolutionary themes hav
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Díaz Jiménez, Pedro, Heiko Hentrich, Pedro Adrián Aguilar-Rodríguez, et al. "A Review on the Pollination of Aroids with Bisexual Flowers." Annals of the Missouri Botanical Garden 104, no. 1 (2019): 83–104. http://dx.doi.org/10.3417/2018219.

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This paper presents an exhaustive review of the current knowledge on pollination of Araceae genera with bisexual flowers. All available studies on floral morphology, flowering sequence, floral scent, floral thermogenesis, floral visitors, and pollinators were carefully examined, with emphasis on the species-rich genera Anthurium Schott, Monstera Adans., and Spathiphyllum Schott. Genera with bisexual flowers are among the early-diverging lineages in Araceae, but present adaptations in their floral ecology to a great variety of pollination vectors, such as bees, beetles, flies, and, unusually, w
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Zhao, Tingting, Dawei Li, Lulu Li, et al. "The Differentiation of Chilling Requirements of Kiwifruit Cultivars Related to Ploidy Variation." HortScience 52, no. 12 (2017): 1676–79. http://dx.doi.org/10.21273/hortsci12410-17.

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Kiwifruit (Actinidia chinensis Planchon) is an economically important fruit, and its flowering and production are affected by the chill accumulation in winter. In this study, the chilling requirements of nine kiwifruit cultivars with three ploidy levels (diploid, tetraploid, and hexaploid) were analyzed by using the Dynamic Model, Utah Model, and chilling hours (CH) Model. The chilling requirements for vegetative budbreak of these kiwifruit cultivars were 24–55 chill portions (CP), 316–991 chill units (CU), and 222–853 CH, and the chilling requirements for floral emergence were 45–69 CP, 825–1
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