USPP6247P - Geranium plant "Helen" - Google Patents
Geranium plant "Helen" Download PDFInfo
- Publication number
- USPP6247P USPP6247P US06/882,129 US88212986V US6247P US PP6247 P USPP6247 P US PP6247P US 88212986 V US88212986 V US 88212986V US 6247 P US6247 P US 6247P
- Authority
- US
- United States
- Prior art keywords
- cultivar
- geranium
- sup
- kaempferol
- diglucoside
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 241000208152 Geranium Species 0.000 title claims abstract description 12
- 229930002877 anthocyanin Natural products 0.000 claims abstract description 9
- 235000010208 anthocyanin Nutrition 0.000 claims abstract description 9
- 239000004410 anthocyanin Substances 0.000 claims abstract description 9
- 150000004636 anthocyanins Chemical class 0.000 claims abstract description 9
- HVQAJTFOCKOKIN-UHFFFAOYSA-N flavonol Natural products O1C2=CC=CC=C2C(=O)C(O)=C1C1=CC=CC=C1 HVQAJTFOCKOKIN-UHFFFAOYSA-N 0.000 claims abstract description 9
- 235000011957 flavonols Nutrition 0.000 claims abstract description 9
- 150000007946 flavonol Chemical class 0.000 claims abstract description 5
- 238000004519 manufacturing process Methods 0.000 claims abstract description 3
- IYRMWMYZSQPJKC-UHFFFAOYSA-N kaempferol Chemical compound C1=CC(O)=CC=C1C1=C(O)C(=O)C2=C(O)C=C(O)C=C2O1 IYRMWMYZSQPJKC-UHFFFAOYSA-N 0.000 description 14
- MWDZOUNAPSSOEL-UHFFFAOYSA-N kaempferol Natural products OC1=C(C(=O)c2cc(O)cc(O)c2O1)c3ccc(O)cc3 MWDZOUNAPSSOEL-UHFFFAOYSA-N 0.000 description 13
- REFJWTPEDVJJIY-UHFFFAOYSA-N Quercetin Chemical compound C=1C(O)=CC(O)=C(C(C=2O)=O)C=1OC=2C1=CC=C(O)C(O)=C1 REFJWTPEDVJJIY-UHFFFAOYSA-N 0.000 description 12
- UBSCDKPKWHYZNX-UHFFFAOYSA-N Demethoxycapillarisin Natural products C1=CC(O)=CC=C1OC1=CC(=O)C2=C(O)C=C(O)C=C2O1 UBSCDKPKWHYZNX-UHFFFAOYSA-N 0.000 description 7
- 238000004458 analytical method Methods 0.000 description 7
- 235000008777 kaempferol Nutrition 0.000 description 7
- UXOUKMQIEVGVLY-UHFFFAOYSA-N morin Natural products OC1=CC(O)=CC(C2=C(C(=O)C3=C(O)C=C(O)C=C3O2)O)=C1 UXOUKMQIEVGVLY-UHFFFAOYSA-N 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- ZVOLCUVKHLEPEV-UHFFFAOYSA-N Quercetagetin Natural products C1=C(O)C(O)=CC=C1C1=C(O)C(=O)C2=C(O)C(O)=C(O)C=C2O1 ZVOLCUVKHLEPEV-UHFFFAOYSA-N 0.000 description 6
- HWTZYBCRDDUBJY-UHFFFAOYSA-N Rhynchosin Natural products C1=C(O)C(O)=CC=C1C1=C(O)C(=O)C2=CC(O)=C(O)C=C2O1 HWTZYBCRDDUBJY-UHFFFAOYSA-N 0.000 description 6
- 235000005875 quercetin Nutrition 0.000 description 6
- 229960001285 quercetin Drugs 0.000 description 6
- 239000003643 water by type Substances 0.000 description 6
- DIRROHKULXIUCB-DHJOXOLYSA-N 3,5-Bis(glucosyloxy)-4',7-dihydroxyflavylium chloride Chemical compound [Cl-].O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC(C(=[O+]C1=CC(O)=C2)C=3C=CC(O)=CC=3)=CC1=C2O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 DIRROHKULXIUCB-DHJOXOLYSA-N 0.000 description 5
- 229930003935 flavonoid Natural products 0.000 description 5
- 150000002215 flavonoids Chemical class 0.000 description 5
- 235000017173 flavonoids Nutrition 0.000 description 5
- 241000196324 Embryophyta Species 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- YPWHZCPMOQGCDQ-HMGRVEAOSA-N kaempferol 7-O-beta-D-glucopyranoside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=CC(O)=C2C(=O)C(O)=C(C=3C=CC(O)=CC=3)OC2=C1 YPWHZCPMOQGCDQ-HMGRVEAOSA-N 0.000 description 4
- 229910003944 H3 PO4 Inorganic materials 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 150000002216 flavonol derivatives Chemical class 0.000 description 3
- FUKUFMFMCZIRNT-UHFFFAOYSA-N hydron;methanol;chloride Chemical compound Cl.OC FUKUFMFMCZIRNT-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229930015717 petunidin Natural products 0.000 description 3
- 235000006384 petunidin Nutrition 0.000 description 3
- AFOLOMGWVXKIQL-UHFFFAOYSA-O petunidin Chemical compound OC1=C(O)C(OC)=CC(C=2C(=CC=3C(O)=CC(O)=CC=3[O+]=2)O)=C1 AFOLOMGWVXKIQL-UHFFFAOYSA-O 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- MQVRGDZCYDEQML-UHFFFAOYSA-N Astragalin Natural products C1=CC(OC)=CC=C1C1=C(OC2C(C(O)C(O)C(CO)O2)O)C(=O)C2=C(O)C=C(O)C=C2O1 MQVRGDZCYDEQML-UHFFFAOYSA-N 0.000 description 2
- ZQMDJECDLYTUCE-LCENJUANSA-N Delphinidin-3,5-diglucoside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C(C=2C=C(O)C(O)=C(O)C=2)OC2=CC(=O)C=C(O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O3)O)C2=C1 ZQMDJECDLYTUCE-LCENJUANSA-N 0.000 description 2
- YPWHZCPMOQGCDQ-UHFFFAOYSA-N Populnin Natural products OC1C(O)C(O)C(CO)OC1OC1=CC(O)=C2C(=O)C(O)=C(C=3C=CC(O)=CC=3)OC2=C1 YPWHZCPMOQGCDQ-UHFFFAOYSA-N 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- JPUKWEQWGBDDQB-QSOFNFLRSA-N kaempferol 3-O-beta-D-glucoside Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C(C=2C=CC(O)=CC=2)OC2=CC(O)=CC(O)=C2C1=O JPUKWEQWGBDDQB-QSOFNFLRSA-N 0.000 description 2
- KZMACGJDUUWFCH-UHFFFAOYSA-O malvidin Chemical compound COC1=C(O)C(OC)=CC(C=2C(=CC=3C(O)=CC(O)=CC=3[O+]=2)O)=C1 KZMACGJDUUWFCH-UHFFFAOYSA-O 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 210000003462 vein Anatomy 0.000 description 2
- YRSDVHGZBOKELJ-DHXGRXBNSA-N (2s,3r,4s,5s,6r)-2-[2-(3,4-dihydroxy-5-methoxyphenyl)-7-hydroxy-3-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-5-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol;chloride Chemical compound [Cl-].OC1=C(O)C(OC)=CC(C=2C(=CC=3C(O[C@H]4[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O4)O)=CC(O)=CC=3[O+]=2)O[C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)=C1 YRSDVHGZBOKELJ-DHXGRXBNSA-N 0.000 description 1
- RHKJIVJBQJXLBY-FTIBDFQESA-N (2s,3r,4s,5s,6r)-2-[7-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-5-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol;chloride Chemical compound [Cl-].COC1=C(O)C(OC)=CC(C=2C(=CC=3C(O[C@H]4[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O4)O)=CC(O)=CC=3[O+]=2)O[C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)=C1 RHKJIVJBQJXLBY-FTIBDFQESA-N 0.000 description 1
- BDCDNTVZSILEOY-WNJKXWAASA-N 3-[(2s,3r,4r,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one Chemical compound O[C@@H]1[C@@H](O)[C@@H](CO)O[C@H]1OC1=C(C=2C=C(O)C(O)=CC=2)OC2=CC(O)=CC(O)=C2C1=O BDCDNTVZSILEOY-WNJKXWAASA-N 0.000 description 1
- YLNDNABNWASMFD-UHFFFAOYSA-N 4-[(1,3-dimethylimidazol-1-ium-2-yl)diazenyl]-n,n-dimethylaniline Chemical compound C1=CC(N(C)C)=CC=C1N=NC1=[N+](C)C=CN1C YLNDNABNWASMFD-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
- RDFLLVCQYHQOBU-GPGGJFNDSA-O Cyanin Natural products O([C@H]1[C@H](O)[C@H](O)[C@H](O)[C@H](CO)O1)c1c(-c2cc(O)c(O)cc2)[o+]c2c(c(O[C@H]3[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O3)cc(O)c2)c1 RDFLLVCQYHQOBU-GPGGJFNDSA-O 0.000 description 1
- SHZGCJCMOBCMKK-UHFFFAOYSA-N D-mannomethylose Natural products CC1OC(O)C(O)C(O)C1O SHZGCJCMOBCMKK-UHFFFAOYSA-N 0.000 description 1
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 1
- XCTGXGVGJYACEI-BYNFETKLSA-O Delphin Natural products O([C@H]1[C@@H](O)[C@H](O)[C@H](O)[C@H](CO)O1)c1c(-c2cc(O)c(O)c(O)c2)[o+]c2c(c(O[C@H]3[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O3)cc(O)c2)c1 XCTGXGVGJYACEI-BYNFETKLSA-O 0.000 description 1
- 208000035240 Disease Resistance Diseases 0.000 description 1
- 229910004373 HOAc Inorganic materials 0.000 description 1
- YYVIFBVXJYYHCW-UHFFFAOYSA-N Malvin Natural products COc1cc(cc(OC)c1O)C2=C(Cc3c(OC4OC(CO)C(O)C(O)C4O)cc(O)cc3O2)OC5OC(CO)C(O)C(O)C5O YYVIFBVXJYYHCW-UHFFFAOYSA-N 0.000 description 1
- 241000208181 Pelargonium Species 0.000 description 1
- IPVSUYLZIAYTOK-VWVAXHKFSA-O Peonin Natural products O(C)c1c(O)ccc(-c2c(O[C@H]3[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O3)cc3c(O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O4)cc(O)cc3[o+]2)c1 IPVSUYLZIAYTOK-VWVAXHKFSA-O 0.000 description 1
- NSZQOXBBEWYGQH-UHFFFAOYSA-N Quercetin-3-rhamnosid Natural products CC1OC(O)C(O)C(OC2=C(Oc3cc(O)cc(O)c3C2=O)c4ccc(O)c(O)c4)C1O NSZQOXBBEWYGQH-UHFFFAOYSA-N 0.000 description 1
- 206010037867 Rash macular Diseases 0.000 description 1
- SOSLMHZOJATCCP-AEIZVZFYSA-N afzelin Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1OC1=C(C=2C=CC(O)=CC=2)OC2=CC(O)=CC(O)=C2C1=O SOSLMHZOJATCCP-AEIZVZFYSA-N 0.000 description 1
- SOSLMHZOJATCCP-PADPQNGGSA-N afzelin Natural products O([C@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](C)O1)C1=C(c2ccc(O)cc2)Oc2c(c(O)cc(O)c2)C1=O SOSLMHZOJATCCP-PADPQNGGSA-N 0.000 description 1
- OVVGHDNPYGTYIT-ROUHPGRKSA-N alpha-L-Rhap-(1->6)-D-Glcp Chemical group O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)C(O)O1 OVVGHDNPYGTYIT-ROUHPGRKSA-N 0.000 description 1
- 229930014669 anthocyanidin Natural products 0.000 description 1
- 150000001452 anthocyanidin derivatives Chemical class 0.000 description 1
- 235000008758 anthocyanidins Nutrition 0.000 description 1
- 150000008209 arabinosides Chemical group 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000012742 biochemical analysis Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- RDFLLVCQYHQOBU-ZOTFFYTFSA-O cyanin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC(C(=[O+]C1=CC(O)=C2)C=3C=C(O)C(O)=CC=3)=CC1=C2O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 RDFLLVCQYHQOBU-ZOTFFYTFSA-O 0.000 description 1
- AYVZVUMKUBCNQZ-UHFFFAOYSA-N delphinidin 3,5-diglucoside Natural products OCC(O)C(O)C(O)C(O)COC1=C(Oc2cc(O)cc(OCC(O)C(O)C(O)C(O)CO)c2C1)c3cc(O)c(O)c(O)c3 AYVZVUMKUBCNQZ-UHFFFAOYSA-N 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- -1 flavonol compounds Chemical class 0.000 description 1
- 150000008195 galaktosides Chemical class 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229930182478 glucoside Natural products 0.000 description 1
- 150000008131 glucosides Chemical group 0.000 description 1
- ALRFYJWUVHBXLV-UHFFFAOYSA-N guaijaverin Natural products OC1COC(COC2=C(Oc3cc(O)cc(O)c3C2=O)c4ccc(O)c(O)c4)C(O)C1O ALRFYJWUVHBXLV-UHFFFAOYSA-N 0.000 description 1
- 238000003898 horticulture Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 235000009584 malvidin Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 229940023569 palmate Drugs 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- HKUHOPQRJKPJCJ-UHFFFAOYSA-N pelargonidin Natural products OC1=Cc2c(O)cc(O)cc2OC1c1ccc(O)cc1 HKUHOPQRJKPJCJ-UHFFFAOYSA-N 0.000 description 1
- 235000006251 pelargonidin Nutrition 0.000 description 1
- XVFMGWDSJLBXDZ-UHFFFAOYSA-O pelargonidin Chemical compound C1=CC(O)=CC=C1C(C(=C1)O)=[O+]C2=C1C(O)=CC(O)=C2 XVFMGWDSJLBXDZ-UHFFFAOYSA-O 0.000 description 1
- 229930015721 peonidin Natural products 0.000 description 1
- 235000006404 peonidin Nutrition 0.000 description 1
- XFDQJKDGGOEYPI-UHFFFAOYSA-O peonidin Chemical compound C1=C(O)C(OC)=CC(C=2C(=CC=3C(O)=CC(O)=CC=3[O+]=2)O)=C1 XFDQJKDGGOEYPI-UHFFFAOYSA-O 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 230000000644 propagated effect Effects 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- QDAMORAIRIHJCS-UHFFFAOYSA-N quercetin 3-rhamnoside Natural products CC1OC(OC2=C(Oc3ccc(O)c(O)c3C2=O)c4ccc(O)c(O)c4)C(O)C(O)C1O QDAMORAIRIHJCS-UHFFFAOYSA-N 0.000 description 1
- OXGUCUVFOIWWQJ-HQBVPOQASA-N quercitrin Chemical compound O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1OC1=C(C=2C=C(O)C(O)=CC=2)OC2=CC(O)=CC(O)=C2C1=O OXGUCUVFOIWWQJ-HQBVPOQASA-N 0.000 description 1
- 230000033458 reproduction Effects 0.000 description 1
- 230000001850 reproductive effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000008265 rhamnosides Chemical class 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Images
Definitions
- the present invention relates to a new and distinct cultivar of geranium Pelargonium ⁇ hortorum called "Helen”.
- the cultivar is particularly well adapted to both commercial greenhouse production and garden performance.
- the cultivar's novel characteristics include more fully double flowers, better garden performance and better heat tolerance when compared with "Ivalo”.
- the cultivar is further characterized by unique biochemical fingerprint profiles.
- the cultivar was developed from an organized, scientifically designed breeding program carried out at the Department of Horticulture, The Pennsylvania State University, University Park, Pa. 16802 and specifically resulted from selection in the progeny of a cross between geranium cultivars "Bruni" ⁇ "Ivalo". The selection was asexually propagated by cuttings and the reproductions ran true.
- test plant was grown in full sun under glass, 62° F. night and 68° F. cloudy days, 75° F. sunny days. Soilless medium was fertilized once per week with 15-15-15 at 275 ppm N. Color readings were taken under cool white fluorescent lamps at 150 footcandles and color identification was by reference to the Royal Horticultural Society Colour Charts except where common terms of color definition are employed.
- FIG. 1 illustrates in color the cultivar including foliage and flowers.
- FIG. 2 illustrates the anthocyanin profile obtained from HPLC. Quantitative values are found in the tables. Analyses included a single peak that represented both pelargonidin and petunidin 3,5-diglucosides. Corrections were made in accompanying tables.
- FIG. 3 illustrates the flavonol profile obtained from HPLC. Quantitative values are found in the tables._______________________________________________Peak No._____________________________________________.1. Quercetin 3-rhamnosylgalactoside2. Quercetin 3-rutinoside3. Quercetin 3-galactoside4. Quercetin 3-glucoside5. Kaempferol 3-rhamnosylgalactoside6. Kaempferol 3-galactoside7. Kaempferol 3-rutinoside8. Kaempferol 3-glucoside; Kaempferol 7-glucoside; Quercetin 3-rhamnoside9. Kaempferol 3-xyloside10. Kaempferol 3-arabinoside11. Kaempferol 3-rhamnoside_______________________________
- Ribs and veins are--Palmate veins. Ribs suppressed and distinct. Fan 3, yellow-green group 144-D (RHSCC).
- Petioles Stalked 5.0-7.0 cm long, medium caliper.
- Shape Initially ovate.
- Blooming habit Smaller bloom but more floriferous than typical geranium; flat top; flowers borne close to foliage.
- Pedicel 2.5-3.0 cm in length.
- Peduncle 11.0-16.0 cm long; strong.
- Lasting quality Excellent, 3 weeks or longer.
- Style.--Green 0.5 cm.
- Ovaries Green; globe-shaped; 5- or 6-lobed; pubescent.
- Flavonoid extraction The sample size for flavonoid identification consisted of the petals from six florets just after anthesis. Three different samples were collected from each cultivar and handled separately for analysis. The petals were weighed, ground in 20 ml of 1% HCl-MeOH with a mortar and pestle, filtered through one layer of Whatman #1 filter paper, and washed with 1% HCl-MeOH. The volume was adjusted to 90 ml and 2-15 ml aliquots were removed for the analysis and handled separately. Each aliquot was taken to dryness at 40° C. in vacuo. All traces of HCl were removed by azeotropic distillation with MeOH.
- One of the dried extracts was reconstituted in 2 ml of 1% HCl-MeOH and was used for anthocyanin analysis.
- the other was reconstituted in 2 ml of MeOH and was used for flavonol analysis.
- Each sample was stored at -34° C. until analyzed.
- the flavonoids were quantified by injecting standards and comparing their peak areas with those from the plant samples. The results are expressed as ug of flavonoid/g fresh weight of plant material.
- Kaempferol 3-rhamnoside could not be quantitated for several cultivars and is designated as ND (not determined).
- the chromatograms showed a small, wide peak in the region of elution for this compound. If a substantial amount of this compound were present, a distinct peak appeared but minute quantities, if present, were masked.
Landscapes
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
Abstract
This invention relates to a new distinct cultivar of geranium, substantially as illustrated and described, characterized as being particularly well adapted to both commercial greenhouse production and garden performance, possessing unique flavonol and anthocyanin profiles and having more fully double flowers, better garden performance, and better heat tolerance when compared with geranium cultivar "Ivalo".
Description
The present invention relates to a new and distinct cultivar of geranium Pelargonium×hortorum called "Helen". The cultivar is particularly well adapted to both commercial greenhouse production and garden performance. The cultivar's novel characteristics include more fully double flowers, better garden performance and better heat tolerance when compared with "Ivalo". The cultivar is further characterized by unique biochemical fingerprint profiles.
The cultivar was developed from an organized, scientifically designed breeding program carried out at the Department of Horticulture, The Pennsylvania State University, University Park, Pa. 16802 and specifically resulted from selection in the progeny of a cross between geranium cultivars "Bruni"×"Ivalo". The selection was asexually propagated by cuttings and the reproductions ran true.
With reference to the detailed description of the cultivar which follows, the test plant was grown in full sun under glass, 62° F. night and 68° F. cloudy days, 75° F. sunny days. Soilless medium was fertilized once per week with 15-15-15 at 275 ppm N. Color readings were taken under cool white fluorescent lamps at 150 footcandles and color identification was by reference to the Royal Horticultural Society Colour Charts except where common terms of color definition are employed.
FIG. 1 illustrates in color the cultivar including foliage and flowers.
FIG. 2 illustrates the anthocyanin profile obtained from HPLC. Quantitative values are found in the tables. Analyses included a single peak that represented both pelargonidin and petunidin 3,5-diglucosides. Corrections were made in accompanying tables.
______________________________________
Peak No.
______________________________________
1. Delphinidin 3,5-diglucoside
2. Cyanidin 3,5-diglucoside
3. Pelargonidin 3,5-diglucoside
4. Peonidin 3,5-diglucoside
5. Malvidin 3,5-diglucoside
______________________________________
FIG. 3 illustrates the flavonol profile obtained from HPLC. Quantitative values are found in the tables.______________________________________Peak No.______________________________________1. Quercetin 3-rhamnosylgalactoside2. Quercetin 3-rutinoside3. Quercetin 3-galactoside4. Quercetin 3-glucoside5. Kaempferol 3-rhamnosylgalactoside6. Kaempferol 3-galactoside7. Kaempferol 3-rutinoside8. Kaempferol 3-glucoside; Kaempferol 7-glucoside; Quercetin 3-rhamnoside9. Kaempferol 3-xyloside10. Kaempferol 3-arabinoside11. Kaempferol 3-rhamnoside______________________________________
Classification:
Botanical.--Pelargonium×hortorum.
Tradename.--#714 (80-220-1)="Helen".
Form: Compact, globe.
Height: 21.0-25.0 cm.
Growth: Short internodes, self branching; medium-size stem (diameter); flowers borne close to foliage.
Leaves:
Size.--6.0-9.0 cm across.
Shape.--Reniform, variously lobed.
Margin.--Crenate.
Texture.--Pubescent.
Color.--Fan 3, green group, 137-C (RHSCC) Top; 138-B (RHSCC) Bottom.
Ribs and veins.--Palmate veins. Ribs suppressed and distinct. Fan 3, yellow-green group 144-D (RHSCC).
Petioles: Stalked 5.0-7.0 cm long, medium caliper.
Stem: Medium caliper.
Color.--Fan 3, green group 143-C (RHSCC).
Internodes: 1.5-2.0 cm.
Shape: Initially ovate.
Size: 1.5 cm diameter.
Blooming habit: Smaller bloom but more floriferous than typical geranium; flat top; flowers borne close to foliage.
Size: 8.0-12.0 cm across.
Borne: Heavy, strong peduncle; modified umbel.
Florets:
Form.--Round, irregular; cupped; 3.5-4.5 cm; semi-double; overall clear pink with ruby-red blotch on petals.
Petals.--11-14.
Size.--2.0-2.5 cm long and 1.0-2.0 cm wide.
Texture and appearance.--Smooth; dull color. Base: Pure white to red-purple, Fan 2, red-purple group 62-B (RHSCC). Mid-veins and blotch: Fan 2, red-purple group 57-A (RHSCC). Top: Fan 2, red-purple group 61-D (RHSCC). Reverse: Fan 2, red-purple group 62-B (RHSCC).
Petaloids:
Quantity.--4-6.
Shape.--1.5-2.5 cm long; narrow and twisted.
Color.--Same as petals.
Pedicel: 2.5-3.0 cm in length.
Peduncle: 11.0-16.0 cm long; strong.
Persistence: Non-shattering; will hold 3-4 weeks.
Disease resistance: Not evaluated.
Lasting quality: Excellent, 3 weeks or longer.
Stamens: 3-4.
Anthers.--Small, brown 2.0-3.0 mm.
Filaments.--Flat white, 1.0 cm long; tips tinted rose-purple; small twisted petaloids attached.
Pollen.--Straw-colored (mature).
Pistils:
Number.--1.
Length.--0.75-1.0 cm.
Stigma.--5- or 6-lobed; rose-colored.
Style.--Green; 0.5 cm.
Ovaries: Green; globe-shaped; 5- or 6-lobed; pubescent.
Fruit: None.
In recent years, biochemical analysis has played an increasing role in plant systematics and taxonomy. In order to further characterize the cultivar, flavonols and anthocyanins were extracted from florets of the cultivar and its parents and subjected to analysis by high pressure liquid chomatography (HPLC). Background information supporting the validity of the HPLC technique can be found in an article by Asen & Griesbach ("High Pressure Liquid Chromatographic Analysis of Flavonoids in Geranium Florets as an Adjunct for Cultivar Identification", S. Asen and R. Griesbach, J. Amer. Soc. Hort. Sci. 108(5):845-850 (1983)), the contents of which are incorporated herein by reference. Briefly, the method for performing the analysis was carried out as follows:
Flavonoid extraction. The sample size for flavonoid identification consisted of the petals from six florets just after anthesis. Three different samples were collected from each cultivar and handled separately for analysis. The petals were weighed, ground in 20 ml of 1% HCl-MeOH with a mortar and pestle, filtered through one layer of Whatman #1 filter paper, and washed with 1% HCl-MeOH. The volume was adjusted to 90 ml and 2-15 ml aliquots were removed for the analysis and handled separately. Each aliquot was taken to dryness at 40° C. in vacuo. All traces of HCl were removed by azeotropic distillation with MeOH. One of the dried extracts was reconstituted in 2 ml of 1% HCl-MeOH and was used for anthocyanin analysis. The other was reconstituted in 2 ml of MeOH and was used for flavonol analysis. Each sample was stored at -34° C. until analyzed.
HPLC. Samples were analyzed on a Waters High Performance Liquid Chromatograph equipped with an automatic injection system (Waters Assoc. Wisp 71OA), dual pumps (Waters Assoc. Model 6000A), solvent programmer (Waters Assoc. Model 600), data module (Waters Assoc.), variable wavelength detector (Waters Assoc. Model 480), and a C18 column (25 cm×0.46 cm and 5 μm particle size, Supelco).
Most of the flavonol compounds were separated by a linear gradient of 8% to 23% pump B over 55 min (pump A=1% triethylamine buffered to pH 3.0 with H3 PO4 (TEAP); pump B=CH3 CN) at a flow rate of 1.2 ml/min and a chart speed of 0.5 cm/min. Detection was at 340 nm.
The anthocyanins were resolved by a linear gradient of 30% to 50% pump B over 40 min (pump A=1.5% H3 PO4 ; pump B=20% HOAc+25% CH3 CN+55% of 1.5% H3 PO4) at a flow rate of 1.0 ml/min and a chart speed of 0.5 cm/min. Detection was at 546 nm utilizing a fixed wavelength detector.
The flavonoids were quantified by injecting standards and comparing their peak areas with those from the plant samples. The results are expressed as ug of flavonoid/g fresh weight of plant material.
Chromatographic profiles for anthocyanins and flavonols are presented in FIGS. 2 and 3, respectively; quantification of these profiles by comparison to standards is presented in Tables 1 and 2, respectively.
The anthocyanins petunidin and pelargonidin 3,5-diglucoside were not resolved by the solvent system used. Past research has shown only negligible amounts of petunidin 3,5-diglucoside to be present in geranium florets compared to pelargonidin 3,5-diglucoside. In light of this, the peak corresponding to petunidin and pelargonidin 3,5-diglucoside was quantified as pelargonidin 3,5-diglucoside.
Kaempferol 3-rhamnoside could not be quantitated for several cultivars and is designated as ND (not determined). The chromatograms showed a small, wide peak in the region of elution for this compound. If a substantial amount of this compound were present, a distinct peak appeared but minute quantities, if present, were masked.
Barriers to quantitation of several flavonols existed. Kaempferol 3-glucoside, kaempferol 7-glucoside, and quercetin 3-rhamnoside all had the same retention time under these conditions. If these compounds are needed to distinguish between cultivars, they would have to be separated by other solvents or column types. Quercetin 3-xyloside appeared in several of the comparisons, but standards were not available to quantify this compound.
TABLE 1
______________________________________
Anthocyanin concentration in petals of geranium florets
μg anthocyanidin 3,5-diglucoside/g fresh wt.
Delph- Cyan- Pelar-
Cultivar
inidin idin gonidin
Peonidin
Malvidin
Total
______________________________________
714 --.sup.z
23 t.sup.y
422 t 455
Bruni --.sup. 78 5251 2418 -- 7747
Ivalo t 42 t.sup.
351 t 408
______________________________________
.sup.z -- = not detected
.sup.y t = trace < 10 μg
TABLE 2
______________________________________
Flavonol concentration in petals of geranium florets
______________________________________
μg/g fresh wt.
Qu3-.sup.z
Qu3- Qu3- Qu3- Km3- Km3-
Cultivar
rhagal rut gal glu rhagal
gal
______________________________________
714 22 51 t.sup.y
t 189 11
Bruni 11 34 --.sup.w
t 307 47
Ivalo 11 32 t.sup.
t 132 t
______________________________________
μg/g fresh wt.
Km3- Km3- Km3- Km3-
Cultivar
rut xyl arab rha Total
______________________________________
714 617 21 22 126 1069
Bruni 1257 13 49 185 1908
Ivalo 470 t 10 114 789
______________________________________
.sup.z Abbreviations: Km = Kaempferol; Qu = Quercetin; arab = arabinoside
gal = galactoside; glu = glucoside; rha = rhamnoside; rhagal =
rhamnosylgalactoside; rut = rutinoside; xyl = xyloside.
.sup.y t = trace < 10 μg.
.sup.w -- = not detected.
Claims (1)
1. A new distinct cultivar of geranium, substantially as illustrated and described, characterized as being particularly well adapted to both commercial greenhouse production and garden performance, possessing unique flavonol and anthocyanin profiles and having more fully double flowers, better garden performance, and better heat tolerance when compared with geranium cultivar "Ivalo".
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/882,129 USPP6247P (en) | 1986-07-03 | 1986-07-03 | Geranium plant "Helen" |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/882,129 USPP6247P (en) | 1986-07-03 | 1986-07-03 | Geranium plant "Helen" |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USPP6247P true USPP6247P (en) | 1988-08-16 |
Family
ID=25379948
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/882,129 Expired - Lifetime USPP6247P (en) | 1986-07-03 | 1986-07-03 | Geranium plant "Helen" |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USPP6247P (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USPP9488P (en) * | 1995-02-06 | 1996-03-26 | Gerd Endisch | Geranium plant named Lorca |
-
1986
- 1986-07-03 US US06/882,129 patent/USPP6247P/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USPP9488P (en) * | 1995-02-06 | 1996-03-26 | Gerd Endisch | Geranium plant named Lorca |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| USPP6247P (en) | Geranium plant "Helen" | |
| USPP6379P (en) | Geranium plant "Siren" | |
| USPP6219P (en) | Geranium plant "Paris" | |
| USPP6220P (en) | Geranium plant "Cassandra" | |
| USPP6218P (en) | Geranium plant "Ben Franklin" | |
| USPP6378P (en) | Geranium plant "Calypso" | |
| USPP12242P2 (en) | Echinacea plant named ‘Kim's Knee High’ | |
| USPP6064P (en) | Variety of geranium named Victoria | |
| USPP7627P (en) | Geranium plant `208(81-344-3)` | |
| USPP6063P (en) | Variety of geranium named Claret | |
| USPP6066P (en) | Variety of geranium named Diplomat | |
| USPP6065P (en) | Variety of geranium named Valerie | |
| US8084674B2 (en) | Flower pigmentation in Pelargonium hortorum | |
| USPP9970P (en) | Variety of geranium named `Penve` | |
| USPP7467P (en) | Regal Pelargonium `Allure` | |
| USPP7343P (en) | Regal Pelargonium `Crystal` | |
| USPP7083P (en) | Distinct variety of geranium plant named Fox | |
| USPP5311P (en) | Variety of geranium named `Alex` | |
| USPP5312P (en) | Variety of geranium named `Perlenkette` | |
| USPP5315P (en) | Variety of geranium named `Palais` | |
| USPP5314P (en) | Variety of geranium named `Jubilaeum` | |
| USPP7656P (en) | Regal pelargonium `315-(83-48-1)` | |
| USPP5313P (en) | Variety of geranium named `Lachsball` | |
| USPP13187P3 (en) | Geranium plant named ‘Fisdidin’ | |
| USPP12917P2 (en) | Geranium plant named ‘Fisrored’ |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: RESEARCH CORPORATION, 25 BROADWAY, NEW YORK, NEW Y Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:CRAIG, RICHARD;REEL/FRAME:004575/0624 Effective date: 19860625 |