KR100271887B1 - 식물에서의 개화를 가속화 및 연장시키는 방법 - Google Patents
식물에서의 개화를 가속화 및 연장시키는 방법 Download PDFInfo
- Publication number
- KR100271887B1 KR100271887B1 KR1019940701268A KR19940701268A KR100271887B1 KR 100271887 B1 KR100271887 B1 KR 100271887B1 KR 1019940701268 A KR1019940701268 A KR 1019940701268A KR 19940701268 A KR19940701268 A KR 19940701268A KR 100271887 B1 KR100271887 B1 KR 100271887B1
- Authority
- KR
- South Korea
- Prior art keywords
- plants
- flowering
- plant
- ppm
- avg
- Prior art date
Links
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 title claims abstract description 32
- 241000196324 Embryophyta Species 0.000 claims abstract description 58
- 239000000203 mixture Substances 0.000 claims abstract description 37
- 240000002024 Gossypium herbaceum Species 0.000 claims abstract description 20
- 235000004341 Gossypium herbaceum Nutrition 0.000 claims abstract description 20
- 238000009472 formulation Methods 0.000 claims abstract description 18
- 239000003112 inhibitor Substances 0.000 claims abstract description 11
- 150000003839 salts Chemical class 0.000 claims abstract description 5
- PAJPWUMXBYXFCZ-UHFFFAOYSA-N 1-aminocyclopropanecarboxylic acid Chemical compound OC(=O)C1(N)CC1 PAJPWUMXBYXFCZ-UHFFFAOYSA-N 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 41
- 230000000694 effects Effects 0.000 claims description 9
- USGUVNUTPWXWBA-JRIXXDKMSA-N (e,2s)-2-amino-4-(2-aminoethoxy)but-3-enoic acid Chemical compound NCCO\C=C\[C@H](N)C(O)=O USGUVNUTPWXWBA-JRIXXDKMSA-N 0.000 claims description 8
- 239000002736 nonionic surfactant Substances 0.000 claims description 7
- 210000003128 head Anatomy 0.000 claims description 6
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- 239000003945 anionic surfactant Substances 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 125000000129 anionic group Chemical group 0.000 claims description 3
- 240000003421 Dianthus chinensis Species 0.000 claims 1
- 230000004373 eye development Effects 0.000 claims 1
- 238000011282 treatment Methods 0.000 abstract description 13
- 241000218922 Magnoliophyta Species 0.000 abstract description 12
- 229920000742 Cotton Polymers 0.000 description 11
- 241000219146 Gossypium Species 0.000 description 11
- 230000001133 acceleration Effects 0.000 description 11
- 239000004094 surface-active agent Substances 0.000 description 11
- 238000011156 evaluation Methods 0.000 description 8
- NQRKYASMKDDGHT-UHFFFAOYSA-N (aminooxy)acetic acid Chemical compound NOCC(O)=O NQRKYASMKDDGHT-UHFFFAOYSA-N 0.000 description 7
- 238000005507 spraying Methods 0.000 description 7
- 240000005020 Acaciella glauca Species 0.000 description 6
- 235000018782 Dacrydium cupressinum Nutrition 0.000 description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 6
- 239000005977 Ethylene Substances 0.000 description 6
- 235000013697 Pinus resinosa Nutrition 0.000 description 6
- 239000007921 spray Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 230000003442 weekly effect Effects 0.000 description 6
- 101710194665 1-aminocyclopropane-1-carboxylate synthase Proteins 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 4
- 238000004806 packaging method and process Methods 0.000 description 4
- 230000035882 stress Effects 0.000 description 4
- 240000006497 Dianthus caryophyllus Species 0.000 description 3
- 235000009355 Dianthus caryophyllus Nutrition 0.000 description 3
- 102000003960 Ligases Human genes 0.000 description 3
- 108090000364 Ligases Proteins 0.000 description 3
- 206010063493 Premature ageing Diseases 0.000 description 3
- 208000032038 Premature aging Diseases 0.000 description 3
- -1 hexitol anhydrides Chemical class 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229920000136 polysorbate Polymers 0.000 description 3
- 238000002791 soaking Methods 0.000 description 3
- SOWBFZRMHSNYGE-UHFFFAOYSA-N Monoamide-Oxalic acid Natural products NC(=O)C(O)=O SOWBFZRMHSNYGE-UHFFFAOYSA-N 0.000 description 2
- ZSILVJLXKHGNPL-UHFFFAOYSA-L S(=S)(=O)([O-])[O-].[Ag+2] Chemical compound S(=S)(=O)([O-])[O-].[Ag+2] ZSILVJLXKHGNPL-UHFFFAOYSA-L 0.000 description 2
- 230000001186 cumulative effect Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000003306 harvesting Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- 241000219322 Dianthus Species 0.000 description 1
- 241000974966 Dianthus sp. Species 0.000 description 1
- 241000208152 Geranium Species 0.000 description 1
- 241000241602 Gossypianthus Species 0.000 description 1
- HLOPMQJRUIOMJO-ZPYNKGFJSA-N L-2-amino-4-methoxy-trans-but-3-enoic acid Chemical compound CO\C=C\[C@H](N)C(O)=O HLOPMQJRUIOMJO-ZPYNKGFJSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 229920004896 Triton X-405 Polymers 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- UGJQDKYTAYNNBH-UHFFFAOYSA-N amino cyclopropanecarboxylate Chemical compound NOC(=O)C1CC1 UGJQDKYTAYNNBH-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 230000034303 cell budding Effects 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 238000003967 crop rotation Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 210000004907 gland Anatomy 0.000 description 1
- 230000030400 head development Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 238000011369 optimal treatment Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000008121 plant development Effects 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 230000003938 response to stress Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 108700012359 toxins Proteins 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000009966 trimming Methods 0.000 description 1
- 238000009424 underpinning Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cultivation Of Plants (AREA)
- Fertilizers (AREA)
- Enzymes And Modification Thereof (AREA)
Abstract
Description
Claims (9)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US77920491A | 1991-10-18 | 1991-10-18 | |
US7/779204 | 1991-10-18 | ||
PCT/US1992/008915 WO1993007746A1 (en) | 1991-10-18 | 1992-10-16 | Method of accelerating and prolonging flowering in plants |
Publications (1)
Publication Number | Publication Date |
---|---|
KR100271887B1 true KR100271887B1 (ko) | 2000-11-15 |
Family
ID=25115658
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019940701268A KR100271887B1 (ko) | 1991-10-18 | 1992-10-16 | 식물에서의 개화를 가속화 및 연장시키는 방법 |
Country Status (14)
Country | Link |
---|---|
US (1) | US5523281A (ko) |
EP (1) | EP0609364B1 (ko) |
JP (1) | JPH07500250A (ko) |
KR (1) | KR100271887B1 (ko) |
AT (1) | ATE199208T1 (ko) |
AU (1) | AU661350B2 (ko) |
CA (1) | CA2116325C (ko) |
DE (1) | DE69231697T2 (ko) |
DK (1) | DK0609364T3 (ko) |
ES (1) | ES2156115T3 (ko) |
GR (1) | GR3035799T3 (ko) |
IL (1) | IL103465A (ko) |
MX (1) | MX9205972A (ko) |
WO (1) | WO1993007746A1 (ko) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE217755T1 (de) * | 1995-12-21 | 2002-06-15 | Basf Corp | Aminoethoxyvinylglycine in kombination mit mepiquatchlorid |
AU1348297A (en) * | 1995-12-21 | 1997-07-14 | Basf Corporation | Enhancing the rate of seed germination with application of ethylene biosynthesis inhibitors |
WO1997023133A1 (en) * | 1995-12-21 | 1997-07-03 | Basf Corporation | Low rate application of inhibitors of ethylene biosynthesis or action |
US5801119A (en) * | 1996-12-31 | 1998-09-01 | Abbott Laboratories | Process for inhibiting stem elongation in bulbous plants and cut flowers therefrom |
BRPI0718215A2 (pt) * | 2006-11-03 | 2013-11-12 | Valent Biosciences Corp | Formulação, e, método para a inibição de etileno em uma planta de colheita. |
EP2052612A1 (de) | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
DE102008037629A1 (de) | 2008-08-14 | 2010-02-18 | Bayer Cropscience Ag | Herbizid-Kombination mit Dimethoxytriazinyl-substituierten Difluormethansulfonylaniliden |
CN114982758B (zh) * | 2022-05-30 | 2023-04-18 | 山东省农业科学院 | 一种促进棉花水分吸收助剂、制备方法及使用方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4441918A (en) * | 1982-07-01 | 1984-04-10 | Estech, Inc. | Ethylene inhibition in plants |
US4744811A (en) * | 1986-04-23 | 1988-05-17 | Basf Aktiengesellschaft | Substituted oxime-ethers and their use as bioregulators to lower the endogenous ethylene level in plants |
WO1991009112A1 (en) * | 1989-12-12 | 1991-06-27 | Agritope, Inc. | Genetic control of ethylene biosynthesis in plants |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3928406A (en) * | 1973-04-04 | 1975-12-23 | Amchem Prod | Plant growth regulant compositions and methods |
GB1509068A (en) * | 1974-05-27 | 1978-04-26 | Mitsubishi Petrochemical Co | Phosphonic and thiophosphonic acid derivatives and their use as plant growth regulants |
US4554017A (en) * | 1978-06-03 | 1985-11-19 | Bayer Aktiengesellschaft | Method and compositions for regulating plant growth using cycloalkane-carboxylic acid compounds |
-
1992
- 1992-10-16 US US08/196,081 patent/US5523281A/en not_active Expired - Lifetime
- 1992-10-16 CA CA002116325A patent/CA2116325C/en not_active Expired - Fee Related
- 1992-10-16 DE DE69231697T patent/DE69231697T2/de not_active Expired - Fee Related
- 1992-10-16 MX MX9205972A patent/MX9205972A/es unknown
- 1992-10-16 AT AT92922741T patent/ATE199208T1/de not_active IP Right Cessation
- 1992-10-16 EP EP92922741A patent/EP0609364B1/en not_active Expired - Lifetime
- 1992-10-16 JP JP5507861A patent/JPH07500250A/ja active Pending
- 1992-10-16 DK DK92922741T patent/DK0609364T3/da active
- 1992-10-16 ES ES92922741T patent/ES2156115T3/es not_active Expired - Lifetime
- 1992-10-16 WO PCT/US1992/008915 patent/WO1993007746A1/en active IP Right Grant
- 1992-10-16 AU AU28930/92A patent/AU661350B2/en not_active Ceased
- 1992-10-16 KR KR1019940701268A patent/KR100271887B1/ko not_active IP Right Cessation
- 1992-10-18 IL IL10346592A patent/IL103465A/en not_active IP Right Cessation
-
2001
- 2001-04-27 GR GR20010400647T patent/GR3035799T3/el not_active IP Right Cessation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4441918A (en) * | 1982-07-01 | 1984-04-10 | Estech, Inc. | Ethylene inhibition in plants |
US4744811A (en) * | 1986-04-23 | 1988-05-17 | Basf Aktiengesellschaft | Substituted oxime-ethers and their use as bioregulators to lower the endogenous ethylene level in plants |
WO1991009112A1 (en) * | 1989-12-12 | 1991-06-27 | Agritope, Inc. | Genetic control of ethylene biosynthesis in plants |
Also Published As
Publication number | Publication date |
---|---|
AU2893092A (en) | 1993-05-21 |
IL103465A0 (en) | 1993-03-15 |
GR3035799T3 (en) | 2001-07-31 |
DK0609364T3 (da) | 2001-05-07 |
CA2116325A1 (en) | 1993-04-29 |
MX9205972A (es) | 1995-01-31 |
DE69231697D1 (de) | 2001-03-29 |
EP0609364A4 (en) | 1994-11-17 |
WO1993007746A1 (en) | 1993-04-29 |
AU661350B2 (en) | 1995-07-20 |
US5523281A (en) | 1996-06-04 |
EP0609364A1 (en) | 1994-08-10 |
DE69231697T2 (de) | 2001-09-20 |
IL103465A (en) | 1999-08-17 |
JPH07500250A (ja) | 1995-01-12 |
EP0609364B1 (en) | 2001-02-21 |
ES2156115T3 (es) | 2001-06-16 |
ATE199208T1 (de) | 2001-03-15 |
CA2116325C (en) | 1999-05-04 |
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Patent event date: 19940418 Patent event code: PA01051R01D Comment text: International Patent Application |
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Comment text: Notification of reason for refusal Patent event date: 19990828 Patent event code: PE09021S01D |
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Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20000603 |
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Comment text: Registration of Establishment Patent event date: 20000821 Patent event code: PR07011E01D |
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