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1

Watkins, Lee, and Donald A. Levin. "Outcrossing rates as related to plant density in Phlox drummondii." Heredity 65, no. 1 (August 1990): 81–89. http://dx.doi.org/10.1038/hdy.1990.73.

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2

Kelly, Martin G., and Donald A. Levin. "Directional selection on initial flowering date in Phlox drummondii (Polemoniaceae)." American Journal of Botany 87, no. 3 (March 2000): 382–91. http://dx.doi.org/10.2307/2656634.

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3

Levin, Donald A. "S-gene polymorphism in Phlox drummondii." Heredity 71, no. 2 (August 1993): 193–98. http://dx.doi.org/10.1038/hdy.1993.124.

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4

Tiku, A., M. K. Razdan, and S. N. Raina. "Production of triploid plants from endosperm cultures of Phlox drummondii." Biologia plantarum 58, no. 1 (March 1, 2014): 153–58. http://dx.doi.org/10.1007/s10535-013-0372-7.

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5

Schlichting, Carl D., and B. Devlin. "Male and Female Reproductive Success in the Hermaphroditic Plant Phlox drummondii." American Naturalist 133, no. 2 (February 1989): 212–27. http://dx.doi.org/10.1086/284911.

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6

Schwaegerle, K. E., and D. A. Levin. "Environmental Effects on Growth and Fruit Production in Phlox Drummondii." Journal of Ecology 78, no. 1 (March 1990): 15. http://dx.doi.org/10.2307/2261033.

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7

Kelly, Martin G., and Donald A. Levin. "Fitness Consequences and Heritability Aspects of Emergence Date in Phlox Drummondii." Journal of Ecology 85, no. 6 (December 1997): 755. http://dx.doi.org/10.2307/2960599.

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8

KOUL, K. K., and S. N. RAINA. "Male and female meiosis in diploid and colchitetraploid Phlox drummondii Hook. (Polemoniaceae)." Botanical Journal of the Linnean Society 122, no. 3 (November 1996): 243–51. http://dx.doi.org/10.1111/j.1095-8339.1996.tb02074.x.

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9

Raina, S. N., A. Parida, K. K. Koul, S. S. Salimath, M. S. Bisht, V. Raja, and T. N. Khoshoo. "Associated chromosomal DNA changes in polyploids." Genome 37, no. 4 (August 1, 1994): 560–64. http://dx.doi.org/10.1139/g94-080.

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The 2C and 4C nuclear DNA amounts were estimated in eight diploid species, belonging to three diverse genera (Vicia, Tephrosia, and Phlox) and their corresponding colchitetraploids. In P. drummondii, T. purpurea, and T. oxygona tetraploids the deviation from the expectation was highly significant. The DNA in P. drummondii was further discarded in subsequent (C1, C2) generations, thus attaining an overall reduction of about 25%. The DNA content in the subsequent generations was the same as that of C2. It is concluded that rapid DNA loss in the first and subsequent generations was not only associated with the substantial increase (30–66%) in the seed set, but it also helped in the establishment and stabilization of the tetraploid. The possible relationship between such a nucleotypic change and success of polyploids is discussed. The DNA change from the expected value in the P. drummondii tetraploid was achieved by equal decrement to each chromosome independent of size, i.e., small chromosomes loose the same amount of DNA as the large chromosomes.Key words: colchitetraploid, genome size, DNA loss, seed fertility, stability, DNA distribution.
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10

Liu, Dawei, Qiyue Liu, Peng Zhang, Kefei Tan, and Jingsheng Chen. "First Report of Powdery Mildew Caused by Golovinomyces magnicellulatus on Phlox drummondii in China." Plant Disease 104, no. 5 (May 2020): 1547. http://dx.doi.org/10.1094/pdis-06-19-1319-pdn.

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11

Majetic, Cassie J., Antonio R. Castilla, and Donald A. Levin. "Losing a Scent of One’s Self: Is There a Reduction in Floral Scent Emission in Self-Pollinating Phlox cuspidata versus Outcrossing Phlox drummondii?" International Journal of Plant Sciences 180, no. 1 (January 2019): 86–92. http://dx.doi.org/10.1086/701102.

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12

Heywood, J. S., and D. A. Levin. "Interactions between seed source, planting arrangement, and soil treatment in determining plant size and root allocation in Phlox drummondii." Oecologia 68, no. 2 (January 1986): 285–90. http://dx.doi.org/10.1007/bf00384801.

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13

Zale, Peter J., and Pablo Jourdan. "Genome Size and Ploidy of Phlox paniculata and Related Germplasm in Subsections Paniculatae and Phlox." Journal of the American Society for Horticultural Science 140, no. 5 (September 2015): 436–48. http://dx.doi.org/10.21273/jashs.140.5.436.

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Phlox is an important genus of herbaceous ornamental plants previously targeted for germplasm development, characterization, and enhancement by the U.S. Department of Agriculture, National Plant Germplasm System. Among Phlox in cultivation, Phlox paniculata is the most widely grown and intensively bred species, but little is known about variation in genome size and ploidy of this species or of related taxa that may be used for germplasm enhancement. The objective of this study was to assess cytotype variation in a diverse collection of cultivars and wild germplasm of P. paniculata (subsection Paniculatae) and of related taxa in subsections Paniculatae and Phlox. The collection included 138 accessions from seven species and two interspecific hybrids. Flow cytometry was used to estimate holoploid (2C) genome sizes and to infer ploidy levels. Chromosome counts were made to calibrate ploidy with genome size for a subset of taxa. Most cultivars were diploid (2n = 2x = 14) and had mean genome sizes that did not vary between subsections Paniculatae (14.33 pg) and Phlox (14.23 pg) although size variation was greater among cultivars within subsection Phlox. Triploid cultivars of P. paniculata, with a mean genome size of 21.36 pg and mitotic chromosome counts of 2n = 3x = 21, were identified. Such triploids suggests previous interploid hybridization within this taxon. Five tetraploid (2n = 4x = 28) cultivars were found in subsection Phlox; all were selections of P. glaberrima ssp. triflora, and had a mean genome size of 25.44 pg; chromosome counts in one of these confirmed they were tetraploid. The putative hybrid Phlox Suffruticosa Group ‘Miss Lingard’ showed an intermediate genome size of 21.21 pg supporting a triploid, hybrid origin of this taxon. Mean 2C genome sizes among wild-collected accessions were similar to values reported for cultivars (Paniculatae = 14.59 pg, Phlox = 14.23 pg), but taxa in subsection Phlox exhibited greater variation that included two tetraploids identified among wild-collected accessions; one, of P. pulchra, had a mean genome size of 26.17 pg, representing the first report of polyploidy in the taxon. This is the first report on genome size for the majority of species in the study. Although genome size could not be used to differentiate taxa in subsections Paniculatae and Phlox, the data provide further insights into cytotype variation of Phlox germplasm useful for plant breeders and systematists.
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14

Thomas Ruley, A., Nilesh C. Sharma, and Shivendra V. Sahi. "Antioxidant defense in a lead accumulating plant, Sesbania drummondii." Plant Physiology and Biochemistry 42, no. 11 (December 2004): 899–906. http://dx.doi.org/10.1016/j.plaphy.2004.12.001.

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15

Henson, M. S., S. R. Sharpe, and I. M. Meadows. "Annuals and Herbaceous Perennials Tolerant or Resistant to Phytophthora Species in the Landscape1." Journal of Environmental Horticulture 38, no. 3 (September 1, 2020): 107–13. http://dx.doi.org/10.24266/0738-2898-38.3.107.

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Abstract Plants of one or two cultivars of 16 annuals and 14 herbaceous perennials were evaluated based on desirability and anecdotal evidence of resistance to Phytophthora root or crown rot. Six plant cultivars served as susceptible controls. Three landscape beds were established in North Carolina and each was infested with three species of Phytophthora: P. nicotianae, P. drechsleri, and P. tropicalis. Plants were regularly rated for disease incidence and symptomatic plants were assayed to determine the presence of Phytophthora species. Ten cultivars of annuals and seven cultivars of herbaceous perennials did not exhibit symptoms of Phytophthora root or crown rot or other disease throughout the season (June 4 to October 15, 2018). Phytophthora spp. were recovered from seven and six cultivars of the evaluated annuals and herbaceous perennials, respectively. Phytophthora nicotianae, P. drechsleri, or P. cryptogea were recovered from a susceptible host in each landscape bed. P. tropicalis was recovered from one plant cultivar evaluated. Phytophthora cryptogea was recovered from three plant cultivars, although this species was not intentionally introduced in the landscape beds. We identified 22 plant cultivars within 13 herbaceous plant species that grew vigorously in landscape beds infested with species of Phytophthora. Index words: bedding plants, disease resistance, herbaceous perennials, landscape plants, Phytophthora nicotianae, Phytophthora drechsleri, Phytophthora tropicalis. Species used in this study: yarrow (Achillea millefolium L. ‘Desert Eve Red'), fernleaf yarrow (Achillea filipendulina Lam. ‘Moonshine Yellow'), angelonia (Angelonia angustifolia Benth. ‘ArchAngel Pink', ‘Serenita White'), annual vinca (Catharanthus roseus (L.) G. Don ‘Cora Apricot', ‘Cora Strawberry', ‘Pacifica Raspberry'), celosia (Celosia argentea L. ‘New Look'), tickseed (Coreopsis auriculata L. ‘Nana', ‘Yellow Jethro Tull'), purple coneflower (Echinacea purpurea (L.) Moench ‘Cheyenne Spirit', ‘PowWow Wild Berry'), blanket flower (Gaillardia x grandiflora Hort. ‘Goblin', ‘Mesa Bi-color'), Barberton daisy (Gerbera jamesonii Bolus ex Hooker f. ‘Crazy Daisy'), verbena (Glandularia canadensis ‘Homestead Purple'), >dusty miller (Jacobaea maritima (L.) Pelser & Meijden ‘Silver Dust'), New Guinea impatiens (Impatienshawkeri W.Bull ‘Hamony', ‘Sunpatiens Compact Orchid', ‘Sunpatiens Lilac'), sweet potato vine (Ipomoea batatas (L.) Lam. ‘Ace of Spades', ‘Bright Idea Tri-color'), West Indian lantana (Lantana camara L. ‘Miss Huff'), lantana (Lantana x hybrida ‘New Gold'), shasta daisy (Leucanthemum x superbum (Bergmans ex J.W. Ingram) Bergmans ex Kent. ‘Becky', ‘Snow Lady'), bee balm (Monarda didyma L. ‘Petite Delight', ‘Jacob Cline'), ornamental grass (Panicum virgatum L. ‘Rotstrahlbusch', ‘Shenandoah'), geranium (Pelargonium x hortorum L.H. Bailey (pro. sp.) ‘Bullseye Cherry', Calliope Dark Red'), calibrachoa (Petunia x calibrachoa ‘Super Cal'), petunia (Petunia x hybrida (Hooker) Vilmorin ‘Easy Wave Red', ‘Easy Wave White', ‘Wave Purple', ‘Yellow Madness', Violet Picotee'), annual phlox (Phlox drummondii Hook. ‘Intensia Red Hot', ‘Phlox Star'), garden phlox (Phlox paniculata L. ‘Amethyst True Gal'), black-eyed susan (Rudbeckia hirta L. ‘Indian Summer', ‘Prairie Sun'), mealy blue sage (Salvia farinacea Benth. ‘Victoria Blue'), African marigold (Tagetes erecta L. ‘Inca Yellow', ‘Proud Yellow'), French marigold (Tagetes patula L. ‘Disco Mix', ‘Disco Yellow'), narrowleaf zinnia (Zinnia angustifolia Kunth. ‘Star Orange', ‘Star White'), Phytophthora nicotianae Breda de Haan, Phytophthora cryptogea Pethybr. and Laff, Phytophthora drechsleri Tucker, Phytophthora tropicalis Aragaki and J.Y. Uchida, zinnia (Zinnia elegans Jacq. ‘Magellan Orange').
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16

Schmidt, Kurt P., and Donald A. Levin. "The Comparative Demography of Reciprocally Sown Populations of Phlox drummondii Hook. I. Survivorships, Fecundities, and Finite Rates of Increase." Evolution 39, no. 2 (March 1985): 396. http://dx.doi.org/10.2307/2408372.

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17

Israr, Mohd, and Shivendra V. Sahi. "Antioxidative responses to mercury in the cell cultures of Sesbania drummondii." Plant Physiology and Biochemistry 44, no. 10 (October 2006): 590–95. http://dx.doi.org/10.1016/j.plaphy.2006.09.021.

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18

Waitt, D. E., and D. A. Levin. "Phenotypic integration and plastic correlations inPhlox drummondii(Polemoniaceae)." American Journal of Botany 80, no. 10 (October 1993): 1224–33. http://dx.doi.org/10.1002/j.1537-2197.1993.tb15356.x.

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19

Díaz-Barradas, M. C., J. B. Gallego-Fernández, and M. Zunzunegui. "Plant response to water stress of native and non-native Oenothera drummondii populations." Plant Physiology and Biochemistry 154 (September 2020): 219–28. http://dx.doi.org/10.1016/j.plaphy.2020.06.001.

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20

D. A., Davydov. "NEW FINDINGS OF ALIEN PLANT ERGAZIOPHYTES IN THE LEFT BANK FOREST-STEPPE OF UKRAINE." Scientific Bulletin of Natural Sciences (Biological Sciences), no. 29 (January 11, 2021): 14–23. http://dx.doi.org/10.32999/ksu2524-0838/2020-29-2.

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The article summarizes the data on the distribution of 25 alien vascular plants in the territory of the Left Bank Forest-Steppe of Ukraine. All of them are ergaziophytes (mostly ornamental plants) escaped from their areas of cultivation. Ten species (Callistephus chinensis (L.) Nees, Iberis umbellata L., Lobularia maritima (L.) Desv., Ricinus communis L., Hemerocallis fulva (L.) L., Iris germanica L., Salvia sclarea L., Mirabilis jalapa L., Sorghum drummondii (Nees ex Steud.) Millsp. & Chase and Viola sororia Willd.) have been firstly found as wild plants in this region. Four species (Rudbeckia triloba L., Euphorbia marginata Pursh, Portulaca grandiflora Hook. and Solanum lycopersicum L.) are new for Poltava region, one(Solidago gigantea W.T. Aiton) – for Sumy region, two (Allium tuberosum Rottler ex Spreng. and Salvia sclarea L.) – for Kharkiv city and Kharkiv region. The data of distribution of Amaranthus caudatus L. in the Left Bank Forest-Steppe of Ukraine were confirmed by herbarium specimen. Other eight species (Allium schoenoprasum L., Calendula officinalis L., Heliopsis helianthoides (L.) Sweet, Symphyotrichum novae-angliae (L.) G.L. Nesom, Dianthus barbatus L., Phedimus spurius (M. Bieb.) 't Hart, Phlox paniculata L., Solanum tuberosum L.) belong to locally distributed alien plants. Based on analysis of the chorology of these species, it is found that eight alien plants have North-American origin, other main regional chorological groups are represented by species from Eastern Asia (4), South America (3) and Europe (3). Major part of the found alien plants includes ephemerophytes in the Left Bank Forest-Steppe of Ukraine (22 species), only three representatives (Heliopsis helianthoides, Phedimus spurius and Solidago gigantea) are naturalized on this territory and belong to the stable floristic component. Two species (Hemerocallis fulva and Iris germanica) are sporadically distributed in different locations, but represented by vegetative clones only and have not been considered as elements of the spontaneous flora. Key words: adventive plants, new localities, Forest-Steppe zone.
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21

D. A., Davydov. "NEW FINDINGS OF ALIEN PLANT ERGAZIOPHYTES IN THE LEFT BANK FOREST-STEPPE OF UKRAINE." Scientific Bulletin of Natural Sciences (Biological Sciences), no. 29 (January 11, 2021): 14–23. http://dx.doi.org/10.32999/ksu2524-0838/2020-29-2.

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The article summarizes the data on the distribution of 25 alien vascular plants in the territory of the Left Bank Forest-Steppe of Ukraine. All of them are ergaziophytes (mostly ornamental plants) escaped from their areas of cultivation. Ten species (Callistephus chinensis (L.) Nees, Iberis umbellata L., Lobularia maritima (L.) Desv., Ricinus communis L., Hemerocallis fulva (L.) L., Iris germanica L., Salvia sclarea L., Mirabilis jalapa L., Sorghum drummondii (Nees ex Steud.) Millsp. & Chase and Viola sororia Willd.) have been firstly found as wild plants in this region. Four species (Rudbeckia triloba L., Euphorbia marginata Pursh, Portulaca grandiflora Hook. and Solanum lycopersicum L.) are new for Poltava region, one(Solidago gigantea W.T. Aiton) – for Sumy region, two (Allium tuberosum Rottler ex Spreng. and Salvia sclarea L.) – for Kharkiv city and Kharkiv region. The data of distribution of Amaranthus caudatus L. in the Left Bank Forest-Steppe of Ukraine were confirmed by herbarium specimen. Other eight species (Allium schoenoprasum L., Calendula officinalis L., Heliopsis helianthoides (L.) Sweet, Symphyotrichum novae-angliae (L.) G.L. Nesom, Dianthus barbatus L., Phedimus spurius (M. Bieb.) 't Hart, Phlox paniculata L., Solanum tuberosum L.) belong to locally distributed alien plants. Based on analysis of the chorology of these species, it is found that eight alien plants have North-American origin, other main regional chorological groups are represented by species from Eastern Asia (4), South America (3) and Europe (3). Major part of the found alien plants includes ephemerophytes in the Left Bank Forest-Steppe of Ukraine (22 species), only three representatives (Heliopsis helianthoides, Phedimus spurius and Solidago gigantea) are naturalized on this territory and belong to the stable floristic component. Two species (Hemerocallis fulva and Iris germanica) are sporadically distributed in different locations, but represented by vegetative clones only and have not been considered as elements of the spontaneous flora. Key words: adventive plants, new localities, Forest-Steppe zone.
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22

Pilate, Gilles, Lucienne Sossountzov, and Emile Miginiac. "Hormone Levels and Apical Dominance in the Aquatic Fern Marsilea drummondii A. Br." Plant Physiology 90, no. 3 (July 1, 1989): 907–12. http://dx.doi.org/10.1104/pp.90.3.907.

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23

Adkins, Scott, John Hammond, Abed Gera, Clarissa J. Maroon-Lango, Irena Sobolev, Andrea Harness, Mohammad Zeidan, and Sara Spiegel. "Biological and Molecular Characterization of a Novel Carmovirus Isolated from Angelonia." Phytopathology® 96, no. 5 (May 2006): 460–67. http://dx.doi.org/10.1094/phyto-96-0460.

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A new carmovirus was isolated from Angelonia plants (Angelonia angustifolia), with flower break and mild foliar symptoms, grown in the United States and Israel. The virus, for which the name Angelonia flower break virus (AnFBV) is proposed, has isometric particles, ≈30 nm in diameter. The experimental host range was limited to Nicotiana species, Schizanthus pinnatus, Myosotis sylvatica, Phlox drummondii, and Digitalis purpurea. Virions were isolated from systemically infected N. benthamiana leaves, and directly from naturally infected Angelonia leaves, using typical carmovirus protocols. Koch's postulates were completed by mechanical inoculation of uninfected Angelonia seedlings with purified virions. Isometric particles were observed in leaf dips and virion preparations from both Angelonia and N. benthamiana, and in thin sections of Angelonia flower tissue by electron microscopy. In sodium dodecyl sulfate-polyacrylamide gel electrophoresis of dissociated purified virus preparations, a major protein component with a molecular mass of 38 kDa was observed. Virion preparations were used to produce virus-specific polyclonal antisera in both Israel and the United States. The antisera did not react with Pelargonium flower break virus (PFBV), Carnation mottle virus (CarMV), or Saguaro cactus virus (SgCV) by either enzyme-linked immunosorbent assay or immunoblotting. In reciprocal tests, antisera against PFBV, CarMV, and SgCV reacted only with the homologous viruses. The complete nucleotide sequence of a Florida isolate of AnFBV and the coat protein (CP) gene sequences of Israeli and Maryland isolates were determined. The genomic RNA is 3,964 nucleotides and contains four open reading frames arranged in a manner typical of carmoviruses. The AnFBV CP is most closely related to PFBV, whereas the AnFBV replicase is most closely related to PFBV, CarMV, and SgCV. Particle morphology, serological properties, genome organization, and phylogenetic analysis are all consistent with assignment of AnFBV to the genus Carmovirus.
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24

GERA, A., and J. COHEN. "Occurrence of cucumber mosaic virus in phlox in Israel." Plant Pathology 39, no. 3 (September 1990): 558–60. http://dx.doi.org/10.1111/j.1365-3059.1990.tb02533.x.

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25

FEHLBERG, SHANNON D., KRISTEN A. FORD, MARK C. UNGERER, and CAROLYN J. FERGUSON. "Development, characterization and transferability of microsatellite markers for the plant genus Phlox (Polemoniaceae)." Molecular Ecology Resources 8, no. 1 (January 2008): 116–18. http://dx.doi.org/10.1111/j.1471-8286.2007.01891.x.

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26

Zunzunegui, María, José Ángel Morales Sánchez, Mari Cruz Díaz Barradas, and Juan B. Gallego-Fernández. "Different tolerance to salinity of two populations of Oenothera drummondii with contrasted biogeographical origin." Plant Physiology and Biochemistry 162 (May 2021): 336–48. http://dx.doi.org/10.1016/j.plaphy.2021.03.001.

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27

Srivastava, A. K., P. Venkatachalam, K. G. Raghothama, and S. V. Sahi. "Identification of lead-regulated genes by suppression subtractive hybridization in the heavy metal accumulator Sesbania drummondii." Planta 225, no. 6 (December 2, 2006): 1353–65. http://dx.doi.org/10.1007/s00425-006-0445-3.

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28

Bjon, Gunvor S., Wolfram Braune, and Lars Olof Bjorn. "Light-induced, dark-reversible colour shifts in petals of Phlox." Physiologia Plantarum 64, no. 4 (August 1985): 445–48. http://dx.doi.org/10.1111/j.1399-3054.1985.tb08520.x.

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29

Ferguson, Carolyn J., Franziska Kramer, and Robert K. Jansen. "Relationships of Eastern North American Phlox (Polemoniaceae) Based on ITS Sequence Data." Systematic Botany 24, no. 4 (October 1999): 616. http://dx.doi.org/10.2307/2419646.

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30

BŁaszkowski, Janusz, Carsten Renker, and François Buscot. "Glomus drummondii and G. walkeri, two new species of arbuscular mycorrhizal fungi (Glomeromycota)." Mycological Research 110, no. 5 (May 2006): 555–66. http://dx.doi.org/10.1016/j.mycres.2006.02.006.

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31

Ruane, Lauren G., and Kathleen Donohue. "Environmental effects on pollen-pistil compatibility betweenPhlox cuspidataandP. drummondii(Polemoniaceae): implications for hybridization dynamics." American Journal of Botany 94, no. 2 (February 2007): 219–27. http://dx.doi.org/10.3732/ajb.94.2.219.

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32

Zunzunegui, María, José Ángel Morales Sánchez, Mari Cruz Díaz Barradas, and Juan B. Gallego-Fernández. "Corrigendum to “Different tolerance to salinity of two populations of Oenothera drummondii with contrasted biogeographical origin” [Plant Physiol. Biochem. 162(2021) 336–348]." Plant Physiology and Biochemistry 166 (September 2021): 999–1000. http://dx.doi.org/10.1016/j.plaphy.2021.07.008.

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33

Lubna, Sajjad Asaf, Rahmatullah Jan, Abdul Latif Khan, and In-Jung Lee. "Complete Chloroplast Genome Characterization of Oxalis Corniculata and Its Comparison with Related Species from Family Oxalidaceae." Plants 9, no. 8 (July 23, 2020): 928. http://dx.doi.org/10.3390/plants9080928.

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Oxalis corniculata L. (family Oxalidaceae) is a small creeper wood sorrel plant that grows well in moist climates. Despite being medicinally important, little is known about the genomics of this species. Here, we determined the complete chloroplast genome sequence of O. corniculata for the first time and compared it with other members of family Oxalidaceae. The genome was 152,189 bp in size and comprised of a pair of 25,387 bp inverted repeats (IR) that separated a large 83,427 bp single copy region (LSC) and a small 16,990 bp single copy region (SSC). The chloroplast genome of O. corniculata contains 131 genes with 83 protein coding genes, 40 tRNA genes, and 8 rRNA genes. The analysis revealed 46 microsatellites, of which 6 were present in coding sequences (CDS) regions, 34 in the LSC, 8 in the SSC, and 2 in the single IR region. Twelve palindromic repeats, 30 forward repeats, and 32 tandem repeats were also detected. Chloroplast genome comparisons revealed an overall high degree of sequence similarity between O. corniculata and O. drummondii and some divergence in the intergenic spacers of related species in Oxalidaceae. Furthermore, the seven most divergent genes (ccsA, clpP, rps8, rps15, rpl22, matK, and ycf1) among genomes were observed. Phylogenomic characterization on the basis of 60 shared genes revealed that O. corniculata is closely related to O. drummondii. The complete O. corniculata genome sequenced in the present study is a valuable resource for investigating the population and evolutionary genetics of family Oxalidaceae and can be used to identify related species.
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34

Pietsch, Grace M., and Neil O. Anderson. "Use of morphological, molecular markers and cytology to differentiate between closely related Gaura coccinea, G. drummondii for breeding purposes." Euphytica 183, no. 1 (August 14, 2011): 95–109. http://dx.doi.org/10.1007/s10681-011-0504-0.

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35

Hoot, Sara B., W. Carl Taylor, and Nancy S. Napier. "Phylogeny and Biogeography of Isoëtes (Isoëtaceae) Based on Nuclear and Chloroplast DNA Sequence Data." Systematic Botany 31, no. 3 (July 1, 2006): 449–60. http://dx.doi.org/10.1600/036364406778388511.

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Despite its ancient origins, worldwide distribution, and adaptation to diverse habitats, Isoëtes species have a highly conserved morphology, making it difficult to resolve phylogenetic relationships using morphological characters. In this paper, we report the results from various analyses (maximum parsimony, maximum likelihood, and Bayesian inference) for Isoëtes species from around the world based on nucleotide sequences from the nuclear internal transcribed spacer (ITS) and chloroplast atpB/rbcL intergenic spacer regions. The trees resulting from our analyses of the combined data contain six major well-supported clades (bootstrap ≥ 90%, posterior probabilities 1.00): A clade with possible Gondwanan affinities (I. australis, I. coromandelina, I. panamensis, I. cubana, I. jamaicensis); a South African clade (I. capensis, I. toximontana, I. stellenbossiensis, I. stephansenii); a largely Northern Hemisphere clade (I. nuttallii, I. orcuttii, I. minima, I. dixitei, I. abyssinica, I. olympica, I. longissima, I. velata); an Asian/Australasian clade (I. drummondii, I. gunnii, I. pusilla, I. kirkii, I. muelleri, I. taiwanensis, I. japonica, I. yunguiensis, I. habbemensis); a Mediterranean clade (I. histrix and I. setacea); and a poorly resolved clade consisting of 12 new world species (American species complex). Our results are compared to past classifications and various biogeographical scenarios are explored.
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36

Dobeš, Christoph, Thomas Mitchell-Olds, and Marcus A. Koch. "Intraspecific diversification in North AmericanBoechera stricta(=Arabis drummondii),Boechera×divaricarpa, andBoechera holboellii(Brassicaceae) inferred from nuclear and chloroplast molecular markers-an integrative approach." American Journal of Botany 91, no. 12 (December 2004): 2087–101. http://dx.doi.org/10.3732/ajb.91.12.2087.

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37

Raja, VarshaG, K. K. Koul, S. N. Raina, and Ajay Parida. "Ploidy-dependent genomic stability in the tissue cultures of ornamental Phlox drummondii Hook." Plant Cell Reports 12, no. 1 (December 1992). http://dx.doi.org/10.1007/bf00232414.

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38

"Ribosomal DNA Variation in the Native Plant Phlox divaricata." Molecular Biology and Evolution, November 1, 1987. http://dx.doi.org/10.1093/oxfordjournals.molbev.a040472.

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39

Vejsadová, Hana, Pavel Matiska, Bohuš Obert, Eva Ürgeová, and Anna PreŤová. "Somatic embryogenesis in Phlox paniculata – histological analysis." Biologia 71, no. 7 (January 1, 2016). http://dx.doi.org/10.1515/biolog-2016-0100.

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