JPS5827769B2 - Plant growth regulator composition for cotton plants and method for applying the same - Google Patents
Plant growth regulator composition for cotton plants and method for applying the sameInfo
- Publication number
- JPS5827769B2 JPS5827769B2 JP53114018A JP11401878A JPS5827769B2 JP S5827769 B2 JPS5827769 B2 JP S5827769B2 JP 53114018 A JP53114018 A JP 53114018A JP 11401878 A JP11401878 A JP 11401878A JP S5827769 B2 JPS5827769 B2 JP S5827769B2
- Authority
- JP
- Japan
- Prior art keywords
- composition
- cotton
- growth regulator
- plant growth
- plants
- 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
Links
- 239000000203 mixture Substances 0.000 title claims description 99
- 239000005648 plant growth regulator Substances 0.000 title claims description 22
- 240000002024 Gossypium herbaceum Species 0.000 title claims description 19
- 235000004341 Gossypium herbaceum Nutrition 0.000 title claims description 19
- 238000000034 method Methods 0.000 title claims description 12
- 241000196324 Embryophyta Species 0.000 claims description 71
- 229920000742 Cotton Polymers 0.000 claims description 52
- 241000219146 Gossypium Species 0.000 claims description 44
- 238000003306 harvesting Methods 0.000 claims description 28
- UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 claims description 21
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 18
- 239000007864 aqueous solution Substances 0.000 claims description 15
- 230000023753 dehiscence Effects 0.000 claims description 15
- 239000002253 acid Substances 0.000 claims description 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 7
- 239000005977 Ethylene Substances 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 4
- 239000002689 soil Substances 0.000 claims description 4
- 244000204900 Talipariti tiliaceum Species 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000002699 waste material Substances 0.000 claims 17
- 238000001727 in vivo Methods 0.000 claims 1
- 230000000694 effects Effects 0.000 description 20
- 239000005976 Ethephon Substances 0.000 description 19
- 230000035613 defoliation Effects 0.000 description 19
- 238000012360 testing method Methods 0.000 description 16
- 239000000835 fiber Substances 0.000 description 13
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 12
- 230000012010 growth Effects 0.000 description 11
- 238000011282 treatment Methods 0.000 description 10
- 230000006378 damage Effects 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 7
- 238000005507 spraying Methods 0.000 description 7
- 235000013399 edible fruits Nutrition 0.000 description 6
- 230000001965 increasing effect Effects 0.000 description 6
- 230000035800 maturation Effects 0.000 description 6
- 230000004044 response Effects 0.000 description 6
- 244000070406 Malus silvestris Species 0.000 description 5
- 239000004480 active ingredient Substances 0.000 description 5
- 238000011161 development Methods 0.000 description 5
- 230000018109 developmental process Effects 0.000 description 5
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 4
- 235000011430 Malus pumila Nutrition 0.000 description 4
- 235000015103 Malus silvestris Nutrition 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- ZDXLFJGIPWQALB-UHFFFAOYSA-M disodium;oxido(oxo)borane;chlorate Chemical compound [Na+].[Na+].[O-]B=O.[O-]Cl(=O)=O ZDXLFJGIPWQALB-UHFFFAOYSA-M 0.000 description 4
- 210000004209 hair Anatomy 0.000 description 4
- 240000001624 Espostoa lanata Species 0.000 description 3
- 235000009161 Espostoa lanata Nutrition 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 235000021016 apples Nutrition 0.000 description 3
- 239000004067 bulking agent Substances 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- -1 fatty acid esters Chemical class 0.000 description 3
- 238000012794 pre-harvesting Methods 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 235000001543 Corylus americana Nutrition 0.000 description 2
- 240000007582 Corylus avellana Species 0.000 description 2
- 235000007466 Corylus avellana Nutrition 0.000 description 2
- 235000009438 Gossypium Nutrition 0.000 description 2
- 240000000047 Gossypium barbadense Species 0.000 description 2
- 240000007049 Juglans regia Species 0.000 description 2
- 244000141359 Malus pumila Species 0.000 description 2
- 230000006578 abscission Effects 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 229930188620 butyrolactone Natural products 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 239000002837 defoliant Substances 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 230000035784 germination Effects 0.000 description 2
- 239000005556 hormone Substances 0.000 description 2
- 229940088597 hormone Drugs 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 230000001939 inductive effect Effects 0.000 description 2
- 239000003701 inert diluent Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 238000000053 physical method Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000004904 shortening Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 235000006667 Aleurites moluccana Nutrition 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 240000008067 Cucumis sativus Species 0.000 description 1
- 235000009849 Cucumis sativus Nutrition 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 206010017533 Fungal infection Diseases 0.000 description 1
- 235000009429 Gossypium barbadense Nutrition 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 235000009496 Juglans regia Nutrition 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 208000031888 Mycoses Diseases 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 241000219094 Vitaceae Species 0.000 description 1
- 235000009754 Vitis X bourquina Nutrition 0.000 description 1
- 235000012333 Vitis X labruscana Nutrition 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 230000035601 cold sensitivity Effects 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000005059 dormancy Effects 0.000 description 1
- 239000006196 drop Substances 0.000 description 1
- 239000003221 ear drop Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 235000021021 grapes Nutrition 0.000 description 1
- 208000037824 growth disorder Diseases 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 230000014634 leaf senescence Effects 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000014571 nuts Nutrition 0.000 description 1
- 238000000424 optical density measurement Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- QPFYXYFORQJZEC-UHFFFAOYSA-N phenazopyridine Chemical compound NC1=NC(N)=CC=C1N=NC1=CC=CC=C1 QPFYXYFORQJZEC-UHFFFAOYSA-N 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000029553 photosynthesis Effects 0.000 description 1
- 238000010672 photosynthesis Methods 0.000 description 1
- 230000008654 plant damage Effects 0.000 description 1
- 230000008121 plant development Effects 0.000 description 1
- 230000037039 plant physiology Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000008771 sex reversal Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 230000005068 transpiration Effects 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/40—Introducing phosphorus atoms or phosphorus-containing groups
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/24—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing heterocyclic radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3808—Acyclic saturated acids which can have further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/572—Five-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/576—Six-membered rings
- C07F9/58—Pyridine rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/576—Six-membered rings
- C07F9/59—Hydrogenated pyridine rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6581—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms
- C07F9/6584—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and nitrogen atoms with or without oxygen or sulfur atoms, as ring hetero atoms having one phosphorus atom as ring hetero atom
- C07F9/65842—Cyclic amide derivatives of acids of phosphorus, in which one nitrogen atom belongs to the ring
- C07F9/65844—Cyclic amide derivatives of acids of phosphorus, in which one nitrogen atom belongs to the ring the phosphorus atom being part of a five-membered ring which may be condensed with another ring system
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
【発明の詳細な説明】
本発明は植物生長調整剤組成物に関するもので、特に普
通に生長する種々のゴシビウムアルボリウム(Goss
ypium arboreum )、多年生樹木変種(
perennial tree variety )
、ゴシビウムヒリシウム(Gossypium hir
supum ) 、多枝低木(multibranch
ed 5hrub 珈よびゴシビウムバルバデンス(G
ossypium barbadense )を包含す
る綿屑(ゴシビウム属)の植物に指向するもので、通常
の長い白い光沢性の繊維を有する低木の例としてはビマ
コツトン(pima cotton )である。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a plant growth regulator composition, in particular for various commonly growing Gossibium arborium (Gossibium arborium).
ypium arboreum ), perennial tree variety (
perennial tree variety)
, Gossypium hiricium
supum), multibranch shrub
ed 5hrub Coffee and Gosibium Barbadens (G
Directed to plants of the genus Gossybium, including Ossypium barbadense, an example of a shrub with the usual long white glossy fibers is pima cotton.
綿の木の生育は花芽の形成または綿ボール(cotto
n boil )に成熟するスクエア(5quare
)により開始する。Cotton tree growth begins with the formation of flower buds or cotton balls.
A square (5 square) that matures to n boil
).
成熱中、ボールは分裂し、長くて白い種子毛(リン)
(1int ) >よび3〜5本のさく片ボール蘇さく
(value boll capsule )に含ま
れている種子を覆っている短い毛(微毛(fuzz )
)の塊を露出する。During growth, the ball splits and produces long white seed hairs (phosphorus).
(1int) >Short hairs (fuzz) that cover the seeds contained in the 3-5 value boll capsules.
) to expose the mass.
ボールのこの破壊(breaking )または裂開(
dehiscence )は開いたボールから綿をむし
るスピンドル状ピッカー(5pindle−1ike
pickers )またはボール全体を収集するストリ
ッパー(5trippers )により収集することに
よって綿繊維を収穫する。This breaking or tearing of the ball
dehiscence) is a spindle-like picker (5pindle-1ike) that plucks cotton from an open ball.
The cotton fibers are harvested by collection by strippers (pickers) or strippers (5 strippers) that collect the whole ball.
一般に、ボール破壊を始めるスクエアからの期間経過は
比較的に長期間、例えば約40〜70日にわたり変化す
るが、しかも未開ボールの内側の綿繊維が成熟綿繊維の
生育するスクエアからの期間経過は約30〜35日であ
る。In general, the period from the square where ball destruction begins varies over a relatively long period of time, for example, about 40 to 70 days, but the period from the square where the cotton fibers inside the virgin ball grow into mature cotton fibers varies. Approximately 30-35 days.
裂開させる期間を延長させるために、1回以上の収穫作
業で綿を収集する必要があるとされているが、しかし気
候条件および著しい露出増加に基づき、通常低品質の綿
が第2収穫から回収される。In order to extend the splitting period, cotton may need to be collected in more than one harvest, but based on climatic conditions and significantly increased exposure, lower quality cotton is usually harvested from the second harvest. It will be collected.
多(の手段はボールを早く開かせることによって綿の生
長季節を短くすることに向けられている。Many measures are aimed at shortening the cotton growing season by opening the bolls earlier.
また、ボールを早く成熟させる強制処理の開発について
研究されている。Research is also being conducted on the development of forced processing that allows the ball to mature faster.
しかしながら、これらの処理は、一般に小さく軽いステ
ーブルド作物(5tapled crop )、すなわ
ち、増加した微毛を有する短くて、僅かな種子毛(5e
ed hairs )を生ずる。However, these treatments generally produce small, light stable crops (5tapled crops), i.e., short, scant seed hairs with increased microsets (5e).
ed hairs).
綿の収穫において考察される第2の重要なことは落葉(
defoliation )である。The second important thing to consider in cotton harvesting is defoliation (
defoliation).
収穫前における葉および葉柄の選択およびほとんど完全
な切除(abscissionγまピッカーに有利なボ
ールを作るのにおよび綿繊維を汚す望ましくないくず(
debris y)収集を避けるのに必要とされ、しか
も繊維の随伴破壊による分離問題を導びく。Selection and almost complete excision of leaves and petioles before harvest (abscission gamma to create balls favorable to the picker and undesirable debris contaminating the cotton fibers)
debris) is required to avoid collection, yet leads to separation problems due to concomitant destruction of the fibers.
多くの落葉剤が市販され、この目的のために使用されて
いるが、しかし望ましいことが証明されている落葉剤で
も落葉以外の任意の植物応答を促進しない。Many defoliants are commercially available and used for this purpose, but even those that have proven desirable do not promote any plant response other than defoliation.
また、成熟するボールが開く前または十分に発育する前
においては過度に速やかな落葉を避けるのが望ましい。It is also desirable to avoid excessively rapid defoliation before the mature ball opens or fully develops.
この理由としては著しい葉の落下(1ear drop
)は蒸散を遮断し、植物に不相応の圧力を生じさせ、
植物の発育を遮断する。The reason for this is significant leaf drop (1 ear drop).
) blocks transpiration and creates disproportionate pressure on plants,
Blocks plant development.
更に、発育するボールは葉の存在しないことにより養分
を失ない、植物システムは新しい葉の発育における生長
作用がその損失を補う傾向がある。Furthermore, the developing boll does not lose nutrients due to the absence of leaves, and the plant system tends to compensate for that loss through the growth process in the development of new leaves.
これらの作用は繊維安定の乏しい、かつ発育の低いボー
ルに貢献する。These effects contribute to a ball with poor fiber stability and poor growth.
綿の通常の価値は繊維の品質に基因する。The normal value of cotton is based on the quality of the fiber.
ステ−プルレングス(5taple length
)は主として重要であり、すなわち繊維が長くてより均
質であれば綿は一層価値が高まる。Staple length (5taple length)
) are of primary importance, i.e. the longer and more homogeneous the fibers, the more valuable the cotton.
また、色、強さおよび伸びを包含する他の考察される価
値は品質の判断に重要である。Other considered values including color, strength and elongation are also important in determining quality.
従って、綿を裂開後できるだけ早く収穫することが望ま
しく、このために降雨または葉くず(foliar d
ebris )に基づく汚染される原因を本質的に除去
する。Therefore, it is desirable to harvest the cotton as soon as possible after splitting, and for this purpose it is best
ebris)-based contamination is essentially eliminated.
ボール裂開は薬品により誘導され、かつ化学的に誘導さ
れた落葉は異なる割合で進行するから、および落葉が裂
開にほとんど影響を及ぼさないから、反対に収穫前に段
階間隔(staged 1ntervals )で現在
作物に数回態別に噴霧する必要がある。Ball dehiscence is induced by chemicals, and chemically induced defoliation proceeds at different rates, and defoliation has little effect on dehiscence, whereas defoliation is induced at staged intervals prior to harvest. Currently, crops need to be sprayed several times in different conditions.
明らかに、この手段は綿の製造コストを著しく増加させ
る。Obviously, this measure significantly increases the cost of cotton production.
最近、クロルエチルホスホン酸が綿の落葉剤として提案
されているが、しかしその使用において著しい落葉、す
なわち、35%以上の葉の落下に必要とされる薬量は2
0000−50000ppm酸の範囲にすることが報告
されている(米国特許第3879188号明細書)。Recently, chlorethylphosphonic acid has been proposed as a defoliant for cotton, but in its use, the dose required for significant defoliation, i.e., more than 35% leaf drop, is 2.
A range of 0,000-50,000 ppm acid has been reported (US Pat. No. 3,879,188).
これらの濃度レベルにおいて、裂開が非選択的であるこ
と、並びにボールおよび葉が処理によって落下すること
が確められている。At these concentration levels, it has been determined that dehiscence is non-selective and that balls and leaves fall off upon treatment.
ベルトワイドコットンリサーチコンフエレンス(Bel
twide Cotton Re5earchConf
erence )、1968年1月、ページ−W−モル
ガン(Page W、 Morgan )およびプラン
トフィジオロジー(P 1ant Physiolog
y ) )44 (3)1337−341.1969年
の研究報告書には、2000ppmのクロルエチルホス
ホン酸で処理したある種の綿はスクエア、花および成熟
ボールの落葉が比較的に速やかに生ずることが報告され
ている。Belt Wide Cotton Research Conference (Bel
wide Cotton Re5earchConf
erence), January 1968, Page W. Morgan and Plant Physiology.
y) ) 44 (3) 1337-341. A 1969 research report showed that certain types of cotton treated with 2000 ppm chloroethylphosphonic acid produced relatively rapid defoliation of squares, flowers, and mature balls. has been reported.
明らかに、落下したボールは回収しないで潜在収率(p
otentialyield )による損失として表わ
す。Obviously, the dropped ball should not be recovered and the potential yield (p
loss due to potential yield).
化学薬品の誘導成熟作用に関する限りにおいて、D、S
、キトツク氏(D、 S、 Kittock )その他
、r Journal Environ、 Qual、
Jl 973.2(3)、405〜8;およびC0L
、ハス氏(C,L、 Hsu )その他、rPhysi
ol、Plant J 1976.36(2J、150
〜3には二三の悪い副作用があるコツトン作物の強制成
熟により生ずることが報告されている。As far as the induced maturation effect of chemicals is concerned, D, S
, Mr. Kittock (D, S, Kittock) and others, r Journal Environ, Qual,
Jl 973.2(3), 405-8; and C0L
, Mr. Hsu (C, L, Hsu) and others, rPhysi
ol, Plant J 1976.36 (2J, 150
It has been reported that forced ripening of cotton crops has a few bad side effects.
特に、エセホン(ethephon ’)′IJ’正常
な繊維生長に抑制作用を有することが確められている。In particular, ethephon 'IJ' has been confirmed to have an inhibitory effect on normal fiber growth.
成熟を誘導する化学薬品の他の欠点としては、作物の生
長を幾分短くするけれども、成熟作用が無差別でありか
つすべての生育のステーブが同じ速度で進行するだけで
あるから、多収穫の必要性は無視することができない。Another disadvantage of maturation-inducing chemicals is that although they shorten crop growth somewhat, they do not produce high yields because the maturation effect is indiscriminate and all growing staves progress at the same rate. The need cannot be ignored.
従って、薬品または組成物の必要なことは通常得られる
より速い割合で未成熟ボールの成熟を進行させる後に葉
および葉柄を選択的に落下でき、未成熟ボールを選択的
に成熟すると共に成熟ボールの望ましくないボール破壊
させてボール破壊の時期を標準化し、このために多数回
収穫(multiple harvesting )
の必要性を省き、落葉に伴ないボール破壊を同時に起し
て異なる薬品の多数回被着の必要性を回避する。Therefore, the need for a chemical or composition that can selectively drop leaves and petioles after maturation of immature balls proceeds at a faster rate than is normally obtained, selectively maturing immature balls as well as mature balls. Multiple harvesting is used to standardize the timing of ball destruction by eliminating undesirable ball destruction.
To avoid the need for multiple applications of different chemicals by causing the balls to break simultaneously as the leaves fall.
本発明の目的は収穫前における綿の処理を有利に遠戚す
ることにある。The object of the invention is to advantageously improve the treatment of cotton before harvest.
本発明の他の目的は綿に対する単一の多目的組成物(s
ingle multi −purpose comp
osition)を提供することにある。Another object of the invention is to provide a single multi-purpose composition (s) for cotton.
ingle multi-purpose comp
The objective is to provide the following:
本発明の他の目的は綿の木においてボール裂開を誘導す
る組成物における成分の相剰組合せを提供することにあ
る。Another object of the invention is to provide a complementary combination of components in a composition that induces ball dehiscence in cotton plants.
本発明においては同時落葉−裂開作用の活性成分として
N−メチルピロリドンおよび2−ハD 、I。In the present invention, N-methylpyrrolidone and 2-HaD, I are used as active ingredients for simultaneous defoliation and dehiscence.
チルホスホン酸(この場合)・ロゲン原子は弗素、塩素
、臭素または沃素である)の如き第三アミンを含有する
綿の木の前収穫処理(preharvesttreat
ment )のための単コーテング組成物を得ることに
ある。Preharvest treatment of cotton plants containing tertiary amines such as tylphosphonic acid (in this case the rogene atom is fluorine, chlorine, bromine or iodine)
The objective is to obtain a single coating composition for ment).
ここに記載する「前収穫処理」とは綿ボールを植物から
採集する前に植物に被着処理することを意味する。As used herein, "pre-harvest treatment" means that the cotton balls are coated on the plants before they are collected from the plants.
N−メチルピロリドンおよび2−ハロエチルホスホン酸
は約o、o 5 : 1〜約4=1の範囲の重量比好ま
しくは約01:1〜約3:1の範囲の重量比で組合せる
。N-methylpyrrolidone and 2-haloethylphosphonic acid are combined in a weight ratio ranging from about o,o 5 :1 to about 4=1, preferably in a weight ratio ranging from about 01:1 to about 3:1.
この組成物は植物に直接に被着できるけれども、経済的
理由および良好な適用範囲のために組成物は通常不活性
稀釈剤または担体と混合する。Although the composition can be applied directly to plants, for economic reasons and good coverage the composition is usually mixed with an inert diluent or carrier.
かかる不活性稀釈剤または担体としては水、キシレン、
トルエン、シクロヘキザンまたは他のパラフィン類の如
き液体、鉱油留分、または他の不活性有機液体、または
不活性担体として通常使用されるこれらの混合物を用い
ることができる。Such inert diluents or carriers include water, xylene,
Liquids such as toluene, cyclohexane or other paraffins, mineral oil fractions, or other inert organic liquids, or mixtures thereof commonly used as inert carriers can be used.
噴霧溶液における上記組成物のN−メチルピロリドンの
濃度は約150ppm〜約12000ppm1好ましく
は約300ppm〜約110000ppの範囲にわたり
変えることができる。The concentration of N-methylpyrrolidone in the composition in the spray solution can vary over a range of about 150 ppm to about 12,000 ppm, preferably about 300 ppm to about 110,000 ppm.
液体担体または増量剤としてはポリオキシアルキレン脂
肪酸エステルまたはアルコールエーテル、リグニン、メ
チルセルロース等の如き表面活性剤を通常の割合で任意
に含有することができるけれども、本発明の上述する利
益を得るのに必要ではない。The liquid carrier or bulking agent may optionally contain surfactants such as polyoxyalkylene fatty acid esters or alcohol ethers, lignin, methyl cellulose, etc., in conventional proportions, but is not necessary to achieve the above-mentioned benefits of the invention. isn't it.
また、水稀釈剤は上記材料から選択する補助有機溶剤と
使用することができる。Water diluents can also be used with auxiliary organic solvents selected from the materials listed above.
しかしながら、また本発明の組成物はタルク、ベントナ
イト、クレー、珪藻土、カオリンおよび他の不活性の通
常の固体増量剤の如き増量剤を液体担体の場合と同じ濃
度範囲で使用することによりペースト、粉末または粒状
固体として植物に適用することができる。However, the compositions of the present invention can also be prepared by using bulking agents such as talc, bentonite, clay, diatomaceous earth, kaolin and other inert conventional solid bulking agents in the same concentration ranges as for liquid carriers. Or it can be applied to plants as a granular solid.
上記組成物は、収穫前およびボールが通常温度条件下で
固定(set ) した後に、綿の木に噴霧または撒布
することにより適用することができる。The composition can be applied by spraying or spreading to the cotton plants before harvest and after the bolls have set under normal temperature conditions.
上記組成物において植物に対してN−メチルピロリドン
を約0.0015〜約0.125?の範囲、好ましくは
約0.003〜約0.095?の範囲の植物適用量で使
用することによって望ましい効果を得ることができる。In the above composition, the amount of N-methylpyrrolidone is about 0.0015 to about 0.125? range, preferably from about 0.003 to about 0.095? Desired effects can be obtained by using plant dosages in the range of .
一般に、担体を包含する本発明の組成物は土壌面積のへ
クタール当り約0.1〜約100kg、好ましくは約1
〜約10kgの範囲の割合で作物に被着させる。Generally, the composition of the present invention, including the carrier, will be applied in an amount of about 0.1 to about 100 kg per hectare of soil area, preferably about 1 kg per hectare of soil area.
Cover the crop at a rate ranging from ~10 kg.
好ましい結果を得るためには、本発明の組成物をスクエ
アセラl−(5quare 5et)後少なくとも30
日にわたり適用する。In order to obtain favorable results, the compositions of the invention should be used for at least 30 minutes after square cellar l-(5 square 5et).
Apply over a period of days.
この適用は植物または植物繊維にいかなる損傷を与えな
い、初期ボール破壊を通じスクエア七ツト後の任意時期
に行うことができる。This application does not cause any damage to the plants or plant fibers and can be done at any time after the square seven through initial ball destruction.
本発明の組成物は植物に約183°C(65下)〜約3
5.0℃(95’T’)の範囲内の望ましい温度で適用
するが、しかし高温または低温における適用は植物損傷
に与えないけれども、低温においては適用期間を長くし
、高温においては短くするように植物応答期間が変化す
る。The compositions of the present invention can be applied to plants from about 183°C (below 65°C) to about 3°C.
Apply at the desired temperature within the range of 5.0°C (95'T'), but the application period should be longer at lower temperatures and shorter at higher temperatures, although application at higher or lower temperatures will not result in plant damage. The plant response period changes.
通常、適用の結果は活性成分の濃度および温度条件に依
存する処理後5〜4日内に得られる。Usually, the results of the application are obtained within 5 to 4 days after treatment, depending on the concentration of the active ingredient and the temperature conditions.
例えば、低レベル適用の場合には、8〜12日内で観察
され、高レベル適用の場合には5〜7日内で観察される
。For example, low level applications are observed within 8-12 days, and high level applications are observed within 5-7 days.
約35、OoC(95下)およびこれ以上のフィルド温
度(field temperature )はN−メ
チルビ0リドンの3000ppm以上の薬量レベルを必
要としないけれども、高い薬量レベルでも植物または綿
繊維に損傷を与えることなく使用することができる。Although field temperatures of about 35,00C (below 95) and above do not require dosage levels above 3000 ppm of N-methylbiolidone, even high dosage levels will damage plants or cotton fibers. It can be used without any problems.
また、本発明の組成物は担体または稀釈剤の外に表面活
性剤、普通殺虫剤および/または殺菌剤または望ましい
薬量レベルで綿の木の蔓延または感染の阻止、または予
防に適用する殺菌剤(biocides )を含有する
ことができる。In addition to the carrier or diluent, the compositions of the present invention may also include surfactants, commonly insecticides and/or fungicides or fungicides for use in inhibiting or preventing cotton plant infestation or infection at desired dosage levels. (biocides).
この場合、単一薬剤適用(single chemic
al application)は綿の木の成熟および
収穫に必要な多くの目的の役割をする。In this case, single chemical application
al applications) serve many purposes necessary for maturation and harvesting of cotton plants.
綿の前収穫処理のための本発明の組成物の適用により得
られる利点を次に列挙する=1゜ボール成熟、ボール裂
開および落葉に作用して多数回薬剤適用(rnulti
ple chemicalapplication )
の必要を回避する多目的組成物を得ることができる。The advantages obtained by the application of the composition of the invention for pre-harvest treatment of cotton are listed below:
ple chemical application)
A multipurpose composition can be obtained that avoids the need for.
2 ボール裂開の速度が高められ、第1収穫および同時
落葉に対してより均一に開いたボールを得ることができ
、このためにボールが十分に生育および開いた後に作用
する。2. The speed of ball dehiscence is increased and a more uniformly opened ball can be obtained for the first harvest and simultaneous defoliation, for which it acts after the ball has fully grown and opened.
3、組成物の成分相互間の相剰作用を達成し、個個の成
分により得られる効果の相より著しく高められた裂開に
おけるメタポリツク効果
(metabolic effects )を生ずる。3. Achieving synergy between the components of the composition, resulting in metabolic effects on cleavage that are significantly enhanced over the phase of effects obtained by the individual components.
4 成熟繊維を含有するボールの裂開を早く進行させる
と共に完全成熟破壊ボールにほとんど作用することがな
く、このために第1収穫において回収しうる綿の割合を
増加せしめ、かつ第2収穫の必要を最小限にするか、ま
たは省(ことができる。4. It speeds up the splitting of balls containing mature fibers and has little effect on fully mature broken balls, thereby increasing the proportion of cotton that can be recovered in the first harvest and reducing the need for a second harvest. can be minimized or eliminated.
5、固有の高品質の綿繊維を得ることができ、ある場合
には綿繊維の品質を改良することができる。5. Unique high quality cotton fibers can be obtained and in some cases the quality of cotton fibers can be improved.
6、植物温度感応性、および低温裂開に幻する抵抗性を
誘導することができる。6. Plant temperature sensitivity and resistance to cold dehiscence can be induced.
7、おそい植えつげおよび/または早期収穫を可能にす
ることができる。7. Can allow late planting and/or early harvesting.
8 綿の木の収穫を経済的にかつ作業を容易にすること
ができる。8. Cotton trees can be harvested economically and easily.
次に本発明を具体的に例を挙げて説明するけれども、本
発明の範囲はこれにより限定されるものではない。Next, the present invention will be explained with specific examples, but the scope of the present invention is not limited thereby.
次の例に示す量および割合は、特に記載しない限りはす
べて重量で示す。All amounts and proportions given in the following examples are by weight, unless otherwise stated.
例■
表■に示す試験は、(A)未処理植物、並びに種々の濃
度レベルで水溶液状態の(B)N−メチルピロリドンお
よびエセホン組成物、(qプロピレングリコールおよび
エセホン組成物、(D唯一の活性成分Nメチルピロリド
ンおよ店す唯一の活性成分エセホンで処理した植物によ
り得た半分開きボール(half −open bol
ls ) 、開いたボール(openboils )お
よび収穫できる状態の(harvestablebol
ls )ボールを包含する%ボールオプユング(% b
oll opening)を説明する比較例である。Examples ■ The tests shown in Table ■ tested (A) untreated plants and (B) N-methylpyrrolidone and ethephon compositions, (q propylene glycol and ethephon compositions, (D only) in aqueous solution at various concentration levels. Half-open bolls obtained from plants treated with the active ingredient N-methylpyrrolidone and the only active ingredient ethephon
ls ), open boils and harvestable bolls
ls) % ball opening (% b) containing the ball
This is a comparative example illustrating all openings.
均一条件下で30cm(1,2“)の土鈴(cla、y
pots )に入れた滅菌土壌で発育させた同じ種子源
(5eed 5ource )から生育した12週間た
った5本のゴシビウム パルバデンス植物(Gossy
piumbarbadense plants )の4
群(B〜E)のそれぞれを生育室(growth ch
amber )内で上述した4種の水溶液で処理してこ
れら植物の種々の生長☆☆調整状態の効果を比較した。A 30 cm (1,2") clay bell (cla, y) under uniform conditions
Only 5 Gossybium parvadens plants (Gossy
piumbarbadense plants) of 4
Each of the groups (B to E) was placed in a growth chamber.
amber) were treated with the four types of aqueous solutions mentioned above to compare the effects of various growth adjustment conditions on these plants.
植物の群Aは対照群として保留した。Group A of plants was retained as a control group.
特に、群Aは未処理植物を示し、群BはN−メチルピロ
リドンおよびエセホン組成物で処理した植物を示し、群
Cはプロピレングリコール/エセホン混合物で処理した
植物を示し、群りはN−メチルピロリドン単独で処理し
た植物を示しおよび群Eはエセホン単独で処理した植物
る示ず。In particular, group A represents untreated plants, group B represents plants treated with N-methylpyrrolidone and ethephon composition, group C represents plants treated with propylene glycol/ethephon mixture, and group N-methylpyrrolidone and ethephon mixture. Plants treated with pyrrolidone alone are shown and group E does not show plants treated with ethephon alone.
配合物の成分は水溶液の]lにおけるppmで示した。The components of the formulations are expressed in ppm in ]l of aqueous solution.
これらの試1験は同時に行ない、約21℃の日中の平均
温度および13℃の夜温度を成育室内において維持した
。These trials were conducted simultaneously and average daytime temperatures of approximately 21°C and night temperatures of 13°C were maintained in the growth chamber.
表■は噴霧後8.10および11日目子のポールオプニ
ングにおけるエセホン単独およびエセホン/プロピレン
グリコールと比較したN−メチルピロリドン/エセホン
組成物のポールオプニングの相対割合を示している。Table ■ shows the relative percentage of pole openings of the N-methylpyrrolidone/ethephon composition compared to ethephon alone and ethephon/propylene glycol in pole openings in pups 8.10 and 11 days after spraying.
例■
表■に示すデータは上述する組成物B〜Eおよび対照A
のそれぞれにより得られた収穫しうるボールの%に基つ
いた比較である。Example ■ The data shown in Table ■ are for compositions B to E and control A described above.
The comparison is based on the percentage of harvestable balls obtained by each.
収穫できる状態のボールは綿繊維が全露出し、ピッカー
に向げられるボールさく片により完全に開いたボールで
ある。A ball that is ready to be harvested is a ball that is fully open with all cotton fibers exposed and the ball flakes directed toward the picker.
表■に示すデータは組成物B、 CおよびE並び☆☆に
対照Aにより得た収穫できる状態のボールに発達する相
対割合に基づいた比較である。The data presented in Table ■ is a comparison based on the relative percentage of development into harvestable balls obtained with Compositions B, C, and E and ☆☆ and Control A.
組成物B−Eによる植物処理試験および対照Aに対する
試験において、噴霧後における観察を収穫できる状態の
ボールが優勢になる時期(すなわち、噴霧後10〜13
日目)に日収した以外は例■に記載すると同様にして行
なった。In plant treatment tests with Compositions B-E and against Control A, observations after spraying were made at the time when ready-to-harvest balls predominated (i.e., 10 to 13 days after spraying).
The procedure was carried out in the same manner as described in Example 2, except that the daily income was earned on day 1).
例■
表■に示すデータは上記組成物B〜Eおよび対照Aによ
り得た破壊(cracking )ボール、開放(op
ening )ボール、開℃)た( opened 、
) ボー、。EXAMPLE ■ The data shown in Table ■ are for cracking balls obtained with compositions B-E and control A above, open
ening ) ball, opened
) Beau,.
および収穫できる状態のボールを包含する全ボー☆☆ル
活性の%に基づく比較を示している。Comparisons are shown based on % of total ball activity encompassing balls and balls ready for harvest.
表■に示すデータは上記組成物B、 CおよびE並びに
対照Aにより得られた全ボール活性の相対割合に基づく
比較を示している。The data presented in Table 1 represents a comparison based on the relative percentage of total ball activity obtained with Compositions B, C and E above and Control A.
例IV
表■に示ずデータは上記組成物B〜Eおよび対照Aのそ
れぞれにより得た葉の落下(1eaf drop)の%
に基づく比較を示している。Example IV Data not shown in Table 1 is the % leaf drop obtained with each of the above compositions BE and Control A.
Comparisons are shown based on
表■1に示すデータは上記組成物B、 CおよびESl
pびに文・」照Aにより得た葉の落下の相対約合に基づ
く比較を示している。The data shown in Table 1 are for the above compositions B, C and ESL.
A comparison is shown based on the relative agreement of leaf fall obtained by P. and B. A.
例■
表■およびXに示す次の試1験のデータは綿の裂開応答
(dehiscence response )におけ
る高温度の効果を示している。EXAMPLE ■ The data from the following test shown in Tables ■ and X illustrate the effect of high temperature on the dehiscence response of cotton.
A、301(12つの上針に入れた滅菌土壌で同じ種子
源から発育させた12週間たった12本のゴシビウムバ
ルバデンス植物の3群をポールオプニングおよび葉の落
下のために生育室で試験した。A, 301 (3 groups of 12 Gossybium barbadens plants grown from the same seed source in sterile soil in 12 top needles for only 12 weeks in a growth chamber for pole opening and leaf drop) Tested.
群Aは薬剤を適用しない対照植物を示し、群Bは上記組
成物Bを噴霧した綿の木を示し、および群Cはエセホン
およびプロピレングリコールの組成物Cを噴霧した綿を
示している。Group A represents control plants with no drug applied, Group B represents cotton plants sprayed with composition B above, and Group C represents cotton sprayed with composition C of ethephon and propylene glycol.
表■に示す結果は同時に実施した各群に対して4回繰返
した試験の平均を示している。The results shown in Table ■ represent the average of four repeated tests for each group conducted simultaneously.
生育室内の気候条件は日中温度を27.2℃(81″F
)および夜温度を15.6°C(60下)にした。The climate conditions inside the growing room are such that the daytime temperature is 27.2°C (81″F).
) and the night temperature was 15.6°C (below 60°C).
鉢に生長した試験植物は高架グリッド ☆☆
(elevated grid )上に配置して温度お
よび温度条件を均一 にした。Test plants grown in pots were placed on an elevated grid to ensure uniform temperature and temperature conditions.
ppmで示す濃度の群BおよびCの組成物を含有する水
溶液を調整し、12週間たった綿の木に約21.1℃(
約70下の温度で均一に噴霧し、これら薬剤被着の結果
を噴霧後3日日および5日日で観察した。Aqueous solutions containing the compositions of groups B and C at concentrations in ppm were prepared and applied to cotton plants after 12 weeks at about 21.1°C (
They were uniformly sprayed at temperatures below about 70°C and the results of these drug depositions were observed 3 and 5 days after spraying.
応答の程度およびタイプを表■に示す。The degree and type of response is shown in Table ■.
温度の高いことは裂開応答を速めることを確めた。It was confirmed that higher temperature speeds up the cleaving response.
B8組組成物他の試験を35℃(95下)の日中温度お
よび夜温度18.3℃(65’F)で温室内★で実施し
た。B8 Compositions Other tests were conducted in a greenhouse at daytime temperatures of 35°C (below 95°C) and night temperatures of 18.3°C (65'F).
噴霧後5日日におけるこれらの試験結果を表Xに示す。The results of these tests 5 days after spraying are shown in Table X.
試験は各試験組成物に対し4回繰返して行なった。The test was repeated four times for each test composition.
一丘述するように、ポールオプニングは35.0℃(9
5下)で組成物Bにおいて著しく速(なることがわかる
。As mentioned above, the pole opening temperature is 35.0℃ (9
5 below) and significantly faster in composition B.
組成物Bは集熱繊維を含有する未熟ボールにおけるポー
ルオプニングを促進するが、しかし十分に成熟した破壊
ボールには影響を与えなかつた。Composition B promoted pole opening in immature balls containing heat collecting fibers, but had no effect on fully mature broken balls.
組成物Bで処理した十分に成熟したボールからの繊維の
劣化は認められず、および未成熟ボールにおいて誘発さ
れる裂開はボールの内側の潜伏(dormancy )
および菌類感染の潜伏期間(potential t
ime ) の減少により、および落葉前におけるポ
ールオプニングを誘導し、落葉が光合成を停止する前の
高い植物活力度におけるボール発育の速度を高めること
により繊維品質を改良ずろことを確めた。No degradation of fibers from fully mature balls treated with Composition B was observed, and the dehiscence induced in immature balls was due to dormancy inside the ball.
and the incubation period of fungal infection (potential t
ime) and improved fiber quality by inducing pole opening before defoliation and increasing the rate of ball development at high plant vigor before defoliation ceases photosynthesis.
例■
表Mに示す比較結果はフィールドにおける綿の木の裂開
応答における低温作用の結果を示してい★★る。Example ■ The comparative results shown in Table M show the consequences of cold effects on the dehiscence response of cotton plants in the field.
フィールド試験は、50CTL間隔で植えたゴシビウム
ヒリシュテウム変種(GossypiumHirsut
um variety )の12週間生育した綿の木に
ついて実施し、試験において未処理対照群A(2列に各
50本づつ植えた)、同じ本数の組成物Bで処理した植
物(群B)、同じ本数の組成物Cで処理した植物(群C
)および同じ本数のN−メチルピロリドンのみの組成物
りで処理した植物(群D)を使用した。Field trials were carried out using Gossypium Hirsut variety planted at 50 CTL spacing.
The test was carried out on cotton plants grown for 12 weeks of um variety), with untreated control group A (planted in two rows of 50 plants each), the same number of plants treated with composition B (group B), and the same number of plants treated with composition B (group B). Number of plants treated with composition C (group C
) and the same number of plants treated with a composition containing only N-methylpyrrolidone (group D) were used.
温度は44°c (,4−OT )日中温度から−3,
9℃(257’)夜温度に変化させた。The temperature is 44°C (,4-OT) -3,
The temperature was changed to 9°C (257') overnight.
結果を表Mに示す。表Mに示す上記試験において、組成
物Bはボール破壊に対する普通低温における植物抵抗性
が著しく少ないことがわかる。The results are shown in Table M. In the above tests shown in Table M, it can be seen that Composition B has significantly less plant resistance to ball breakage at normal low temperatures.
3125ppmエセホン濃度において、組成物Bは組成
物Cの場合におけるより著しく低い植物低温感受性を誘
導する。At a concentration of 3125 ppm ethephon, composition B induces significantly lower plant cold sensitivity than in the case of composition C.
落葉の効果は測定しなかった。The effect of defoliation was not measured.
この理由としては普通落葉を誘導する凍結温度以下のた
めに、この効果を測定することができないためである。The reason for this is that this effect cannot be measured because the temperature is below freezing, which normally induces defoliation.
上述するすべての試1験において、組成物Bを噴霧した
綿の木は繊維の脆弱または短縮を生じさせないことを確
めた。In all the tests mentioned above, it was determined that the cotton plants sprayed with Composition B did not suffer from weakening or shortening of the fibers.
収穫前および収穫後における汚染はほとんど除去するこ
とができ、裂開を本発明組成物により誘導した生育のお
くれたボールにおいても良好な繊維を得たことを確めた
。It was confirmed that most of the contamination before and after harvesting could be removed, and that good fibers were obtained even in slow-growing balls whose dehiscence was induced by the composition of the present invention.
上記試験結果から、N−メチルピロリドンおよびB−ハ
ロエチルホスホン酸の本発明組成物は態別の化学的落葉
適用の必要性を回避して綿の収穫を達成する多目的薬剤
組成物(multipurposetool )を得る
ことができること、およびこれらのメタポリツク作用の
割合が単収穫により良品質の綿を高収率で得るのに十分
利用されることが明らかにわかる。The above test results show that the composition of the present invention of N-methylpyrrolidone and B-haloethylphosphonic acid provides a multipurpose tool to achieve cotton yields, avoiding the need for separate chemical defoliation applications. It can clearly be seen that the rate of metapolising can be fully exploited to obtain high yields of good quality cotton in a single crop.
また、活性成分の相剰作用は試験結果から明らかであり
、潜在収率は第1収穫の場合に増加する。Also, a synergistic effect of the active ingredients is evident from the test results, with the potential yield increasing in the case of the first harvest.
上述する範囲の本発明において使用する成分の最適な組
合せは特別の綿の木の必要性に適合することができ、か
つ第2収穫の必要性を回避することができる。Optimal combinations of ingredients used in the present invention within the ranges described above can be tailored to the needs of a particular cotton plant and can avoid the need for a second harvest.
おそい植えつけを可能にしおよび/またに作物の自然回
転(natiral rotation )における収
穫を早めることにより綿の木に対する本発明の組成物お
よび適用方法の実際上の利益を得ろことができる。Practical benefits of the compositions and application methods of the present invention can be obtained for cotton plants by allowing for later planting and/or earlier harvest in the natural rotation of the crop.
また、上述する例において任意の他の2−・・ロエチル
ホスホン[!’lB−クロルエチルホスホン酸の代りに
用いて上述する本発明における利益を達成することがで
きる。Also, in the above example, any other 2-...loethylphosphone [! 'lB-chloroethylphosphonic acid can be used in place of it to achieve the benefits of the invention described above.
また、上述する例において3〜6個の炭素原子を有する
非環状第三アミン、例えばN−ジメチルホルムアミド、
N−N−ジメチルアセトアミド等をN−メチルピロリド
ンの代りに用いて収穫前の落葉の割合を高めることがで
きる。Also, in the examples mentioned above, acyclic tertiary amines having 3 to 6 carbon atoms, such as N-dimethylformamide,
N-N-dimethylacetamide or the like can be used in place of N-methylpyrrolidone to increase the rate of defoliation before harvest.
表■に示すこれらのアミド類および他の化合物は綿の木
に被着した場合に高い落葉特性を有する☆☆ことを見出
した。It has been found that these amides and other compounds shown in Table 1 have high defoliation properties when applied to cotton plants.
使用する組成物の代表的な成分について表■に示す量は
ppmで表わしている。The amounts shown in Table 1 for typical components of the compositions used are expressed in ppm.
次の化合物または組成物は単独またはN−メチルピロリ
ドン/エセホン組成物と組合せて用いて綿の木の落葉を
高めることができる。The following compounds or compositions can be used alone or in combination with the N-methylpyrrolidone/ethephon composition to enhance defoliation of cotton plants.
次のデータはブチロラクトン(BLO)−エセホン、ブ
チンジオール(B2O)へエセホンおよびジメチルホル
ムアミド(DMF)−エセホンのゴシビウムビリジウム
変種の15週間たった綿の木についての綿ボール活性に
おける効果を示している。The following data shows the effects of Gosibium viridium variants of butyrolactone (BLO)-ethephon, butynediol (BO)-ethephon and dimethylformamide (DMF)-ethephon on cotton boll activity on 15-week old cotton plants. .
生育室内の4本の植物の処理に一ヒ達する混合物の水溶
液を使用し、各植物に200’C(68下)つ噴★★霧
して湿らした。An aqueous solution of the mixture was used to treat four plants in the growth chamber and each plant was moistened by spraying at 200'C (68 below).
全ボール活性割合の%(ボール破壊、ポールオプニング
および収穫できる状態のボールを包含する)を表X■に
示す。The percentage of total ball activity (including ball breaks, pole openings and balls ready for harvest) is shown in Table X■.
表XIVは上記混合物の水溶液のそれぞれに対する収穫
できる状態のボールの%を示している。Table XIV shows the percentage of balls ready for harvest for each of the aqueous solutions of the above mixtures.
表X■およびXIVにおいて、使用成分の量は水液にお
けるppmで表わしている。In Tables X■ and XIV, the amounts of ingredients used are expressed in ppm of the aqueous solution.
生物学的活性
本発明の組成物は有効なエチレン遊離剤
(ethylene release agents
)でありおよび/または植物および植物組織によりエ
チレンの生体内生成を刺激する。Biologically active The compositions of the present invention are effective ethylene release agents.
) and/or stimulate the bioproduction of ethylene by plants and plant tissues.
従って、組成物は2−クロルエチルホスホン酸の標準生
理的作用特性を示す。Therefore, the composition exhibits the standard physiological action characteristics of 2-chloroethylphosphonic acid.
これらの作用の例はよく知られており、この作用には成
熟、成長抑制(stunting ) :頂芽優性損失
:発芽;花の促進、抑制および性転換:葉老衰、離脱、
花誘導等を包含する。Examples of these effects are well known and include maturation, stunting: loss of apical dominance: germination; promotion, suppression and sex reversal of flowers: leaf senescence, abscission,
Including flower induction etc.
本発明においてボール裂開の誘導が高められ、かつボー
ル収穫を著しく促進することは植物内におけるエチレン
ホルモンの特性によるものである。The enhanced induction of ball dehiscence and significant promotion of ball harvest in the present invention is due to the properties of ethylene hormone within the plant.
また、エチレンは綿の出芽を速めるのに使用することが
W、 C、Ha11氏ほかによるr Physiolo
giap lantarum j 10巻306頁(1
957)およびW、W、 Heck氏ほかによる「Te
xas、Experimental 5tation
、 Misc、PublicationJNP−613
(1962)に記載されており、綿におけるエチレンホ
ルモン作用において綿ボール裂開およびボール発育につ
いて多くの結果が得られている。Ethylene has also been shown to be used to speed up the germination of cotton, according to W. C. Ha11 et al.
giap lantarum j vol. 10 p. 306 (1
957) and “Te
xas, Experimental 5tation
, Misc, Publication JNP-613
(1962) and many results have been obtained on cotton ball dehiscence and ball development in ethylene hormone action in cotton.
例■
リンゴの赤変
リンゴの木のコルネル マクイントラシュ フルーツ(
Cornell McIntosh fruit )の
4つのグループに次の表X■に示す水溶液を噴霧した。Example ■ Red apple apple tree Cornel McIntrash fruit (
Four groups of Cornell McIntosh fruit (Cornell McIntosh fruit) were sprayed with the aqueous solution shown in Table X■ below.
他の対照グループには水溶液を噴霧しなかった。The other control group was not sprayed with the aqueous solution.
1週間後リンゴを収穫し、物理的測定を行なった。After one week, apples were harvested and physical measurements were taken.
これらの結果を平均して表に記録した。These results were averaged and recorded in a table.
エセホンの1.03ミリモル/リットルは類似処理(ホ
ルテイ力ルチュアル ザイエンスに関しザジャーナル
オブ アメリカン ソサエティ第99巻#3.239ペ
ージ、1974年5月に報告された論文の表■参照)に
おけるコルネルマクイントラシュ リンゴの72%赤変
率を得るのに必要とされることがわかる。1.03 mmol/liter of ethephon was treated in a similar manner (The Journal
of the American Society, Vol. 99, #3, page 239, Table ■ of the paper reported in May 1974).
例■
リンゴの赤変
4年たったミラスチュルデスプル リンゴの木(Mi
11ersturdeespur apple )の3
つのグループ(各グループは5本からなる)を表XVI
に示す水溶液を噴霧した。Example ■ Reddening of apples after 4 years Mirasturdespur apple tree (Mi
11ersturdeespur apple) no 3
Table XVI
The aqueous solution shown above was sprayed.
対照とする5本の他のグループには処理を行なわなかっ
た。The other group of five plants, which served as a control, were not treated.
2週間後、リンゴを収穫し、物理的測定を行なった。Two weeks later, the apples were harvested and physical measurements were taken.
この平均の結果例■
クルミの離れやすさく Walnut Looseni
ng )クルミの木のアシュレイ ナツツ(Ashle
ynut )の2つのグループ(各グループは5本から
なる)に表X■に示す水溶液を噴霧した。Example of the result of this average ■ Ease of separating walnuts Walnut Looseni
ng ) Walnut tree Ashley Natsutsu (Ashle)
ynut) were sprayed with the aqueous solution shown in Table X■.
5本の他の対照グループには処理を行なわなかった。The other control group of 5 bottles received no treatment.
10日後、試験結果を平均し、この結果を表に示す:
除去等級(abscissicn ratings )
において、3は過剰であり、1は僅かであり木をいため
ない。After 10 days, the test results are averaged and the results are shown in the table: Abscissicn ratings
In this case, 3 is excessive and 1 is slight and does not damage the tree.
上記表の収穫データは普通収穫中記録していた。The harvest data in the table above was normally recorded during harvest.
例X
ソワー チェリーの離れやすさ
ソワー チェリー(5our cherry )の木の
モントモレンシイ フルーツ(Montmorency
fruit )の2つのグループ(各グループは3本
の木からなる)に表X■に示す水溶液を噴霧した。Example
Two groups (each group consisting of 3 trees) of ``Fruit'' were sprayed with the aqueous solutions shown in Table X■.
対照とする3本の木のグループには処理を行なわなかっ
た。A control group of three trees received no treatment.
2週間後、結果を平均して表に示した。After two weeks, the results were averaged and shown in the table.
フルーツ除去力測定は各100個のフルーツについて7
日後に行なった。Fruit removal power measurement for each 100 fruits 7
I did it a day later.
上記フィールド試験において混合溶液に近い結果を得ろ
ためには約2倍のように多くのエセホンを必要とするこ
とがわかる。In the above field test, it was found that approximately twice as much ethephon was required to obtain results close to those of the mixed solution.
例M
ハシバミ(F 1lbert )の離れやすさハシバミ
(hazel )の木のバルセロナ ナツツ(Barc
ellona nut )の4つのグループ(各グルー
プは5本からなる)に表XIXに示す水溶液を噴霧した
。Example M Ease of separation of hazel (F 1lbert)Barcelona of hazel tree
ellona nut) were sprayed with the aqueous solution shown in Table XIX.
対照としての5本の他のグループには処理しなかった。Another group of 5 plants served as controls and were not treated.
2週間後、結果を平均して表に示す:ブドウの色増強(
Co1or enhancement )ブドウの木の
ジンファンデル フルーツ
(Zinfandel fruit )の4つのグルー
プ(各グループは5本からなる)に表XXに示す水溶液
を噴霧した。After two weeks, the results are averaged and shown in the table: Grape color enhancement (
Co1or enhancement) Four groups of vine Zinfandel fruit (each group consisting of five plants) were sprayed with the aqueous solution shown in Table XX.
対照としての5本の他のグループには処理しなかった。Another group of 5 plants served as controls and were not treated.
対照ブリックス(controlbrix ’)fr’
22%の時にブドウを収穫し、しかる後にブドウをジ
ュースにし、これから光学濃度測定を行なった。controlbrix(controlbrix')fr'
The grapes were harvested at 22%, after which they were juiced and optical density measurements were made.
結果を平均して表に示す:例xm
キ0ウリの性別(sex expressin )カラ
キシ キュウリ(Ga1axy cucumbers
)の2つのグループ(各グループは2本からなる)に表
XXIに示す水溶液を第1の真のリーフ ステージ(f
iret true 1eaf 5taze )後に噴
霧した。The results are averaged and shown in the table: Example xm Sex expressin Ga1axy cucumbers
) of the first true leaf stage (f
iret true 1eaf 5taze) and then sprayed.
対照として2本の植物には処理をしなかった。As a control, two plants were not treated.
結果を平均して表に示す:The results are averaged and shown in a table:
Claims (1)
酸の混合物からなる綿ボールの収穫前に適用することを
特徴とする綿屑植物の植物生長調整剤組成物。 2 N−メチルピロリドン対2−ハロエチルホスホン酸
の重量比を約0.05:1〜約4:1の範囲とする特許
請求の範囲第1項記載の綿屑植物の植物生長調整剤組成
物。 3N−メfルビロリトン対2−ハロエチルホスホン酸の
重量比を約0.1:1〜約3:1の範囲とする特許請求
の範囲第2項記載の綿屑植物の植物生長調整剤組成物。 42−ハロエチルホスホン酸を2−クロルエチルホスホ
ン酸とする特許請求の範囲第1項記載の綿屑植物の植物
生長調整剤組成物。 5 組成物を不活性担体に配合する特許請求の範囲第1
項記載の綿屑植物の植物生長調整剤組成物。 6 液体担体を水とする特許請求の範囲第5項記載の綿
屑植物の植物生長調整剤組成物。 7 組成物を不活性粒状担体に配合する特許請求の範囲
第1項記載の綿よ植物の植物生長調整剤組成物。 8 組成物を不活性担体に混合し、前記担体中のN−メ
チルピロリドンの濃度を約150ppm〜約12000
ppmの範囲にする特許請求の範囲第1項記載の綿屑植
物の植物生長調整剤組成物。 9 稀釈剤を水とし、組成物をこれに溶解する特許請求
の範囲第8項記載の綿屑植物の植物生長調整剤組成物。 10 稀釈剤をミイ・ラルスピリットとし、組成物を
これに分散させる特許請求の範囲第8項記載の綿、属植
物の植物生長調整剤組成物。 11 組成物はエチレンの生体内生成を刺激するエチ
レン発生能力を有する特許請求の範囲第1項記載の綿屑
植物の植物生長調整剤組成物。 12N−メfルビロリトンおよび2−ハロエチルホスホ
ン酸の混合物を収穫前に綿の水の裂開を誘導するのに十
分な量でかかる綿の木に被着処理することを特徴とする
綿屑植物の植物生長調整剤組成物の被着方法。 13 有効量は植物当り組成物中のN−メチルピロリド
ンを約0.0015〜約0.125@の範囲とする特i
i′t−請求の範囲第12項記載の綿屑植物の植物生長
調整剤組成物の接着方法。 14 有効量は植物当り組成物中のN−メチルピロリ
ドンを約0.003〜約0.095?の範囲とする特許
請求の範囲第13項記載の綿屑植物の植物生長調整剤組
成物の接着方法。 15 組成物の有効量をポールセット後植物に被着す
る特許請求の範囲第12項記載の綿屑植物の植物生長調
整剤組成物の被着方法。 16 組成物の有効量をポールセット後30〜40日
間植物に被着すη特許請求の範囲第15項記載の綿屑植
物の植物生長調整剤組成物の被着方法。 17組成物の有効量を植物に少なくとも15.6°C(
60下)の温度で被着する特許請求の範囲第12項記載
の綿屑植物の植物生長調整剤組成物の被着方法。 18組成物はN−メチルピロリドンおよび2−クロルエ
チルホスホン酸の共活性混合物を含有し、この共活性混
合物を液剤として植物に被着する特許請求の範囲第12
項記載の綿屑植物の植物生長調整剤組成物の被着方法。 19 組成物を水溶液の状態で植物に接触させる特許
請求の範囲第12項記載の綿屑植物の植物生長調整剤組
成物の被着方法。 20 組成物を綿の木のフィールドに土壌面積のへク
タール当り約0.1〜約100kgの割合で被着する特
許請求の範囲第18項記載の綿屑植物の植物生長調整剤
組成物の被着方法。[Scope of Claims] A plant growth regulator composition for cotton waste plants, characterized in that it is applied before harvesting cotton bolls, comprising a mixture of IN-methylvirolitone and 2-haloethylphosphonic acid. 2. The plant growth regulator composition for cotton waste plants according to claim 1, wherein the weight ratio of N-methylpyrrolidone to 2-haloethylphosphonic acid is in the range of about 0.05:1 to about 4:1. . The plant growth regulator composition for cotton waste plants according to claim 2, wherein the weight ratio of 3N-methylvirolitone to 2-haloethylphosphonic acid is in the range of about 0.1:1 to about 3:1. . The plant growth regulator composition for cotton waste plants according to claim 1, wherein the 42-haloethylphosphonic acid is 2-chloroethylphosphonic acid. 5 Claim 1 in which the composition is incorporated into an inert carrier
A plant growth regulator composition for cotton waste plants as described in 1. 6. The plant growth regulator composition for cotton waste plants according to claim 5, wherein the liquid carrier is water. 7. The plant growth regulator composition for cotton plants according to claim 1, wherein the composition is blended into an inert granular carrier. 8. Mixing the composition in an inert carrier and adjusting the concentration of N-methylpyrrolidone in the carrier from about 150 ppm to about 12,000 ppm.
The plant growth regulator composition for cotton waste plants according to claim 1, wherein the composition is in the ppm range. 9. The plant growth regulator composition for cotton waste plants according to claim 8, wherein the diluent is water and the composition is dissolved therein. 10. The plant growth regulator composition for plants of the genus Cotton according to claim 8, wherein the diluent is Mii Ral Spirit and the composition is dispersed therein. 11. The cotton waste plant growth regulator composition according to claim 1, wherein the composition has an ethylene generating ability that stimulates the in vivo production of ethylene. A cotton waste plant characterized in that the cotton plants are coated with a mixture of 12N-methylvirolitone and 2-haloethylphosphonic acid in an amount sufficient to induce water dehiscence in the cotton before harvesting. A method for applying a plant growth regulator composition. 13. The effective amount ranges from about 0.0015 to about 0.125 N-methylpyrrolidone in the composition per plant.
i't- A method for adhering a plant growth regulator composition for cotton waste plants according to claim 12. 14. The effective amount is about 0.003 to about 0.095 N-methylpyrrolidone in the composition per plant. A method for adhering a plant growth regulator composition for cotton waste plants according to claim 13. 15. A method for applying a plant growth regulator composition to cotton waste plants according to claim 12, wherein an effective amount of the composition is applied to the plants after pole setting. 16. A method for applying a plant growth regulator composition to cotton waste plants according to claim 15, wherein an effective amount of the composition is applied to the plant for 30 to 40 days after pole setting. 17. Apply an effective amount of the composition to plants at a temperature of at least 15.6°C (
13. A method for applying a plant growth regulator composition for cotton waste plants according to claim 12, wherein the composition is applied at a temperature of 60°C or lower. Claim 18: The composition contains a co-active mixture of N-methylpyrrolidone and 2-chloroethylphosphonic acid, and the co-active mixture is applied to plants as a liquid.
A method for applying a plant growth regulator composition to cotton waste plants as described in 2. 19. The method for applying a plant growth regulator composition to cotton waste plants according to claim 12, which comprises contacting the plant with the composition in the form of an aqueous solution. 20. Covering a field of cotton plants with the plant growth regulator composition of claim 18, wherein the composition is applied to a field of cotton trees at a rate of about 0.1 to about 100 kg per hectare of soil area. How to wear it.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US83375777A | 1977-09-16 | 1977-09-16 | |
AU75224/81A AU545673B2 (en) | 1977-09-16 | 1981-09-14 | Plant growth regulator containing an n-heterocyclic monoamide and a 2-halo-ethylphosphonic acid |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS54111468A JPS54111468A (en) | 1979-08-31 |
JPS5827769B2 true JPS5827769B2 (en) | 1983-06-11 |
Family
ID=25637870
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP53114018A Expired JPS5827769B2 (en) | 1977-09-16 | 1978-09-16 | Plant growth regulator composition for cotton plants and method for applying the same |
Country Status (7)
Country | Link |
---|---|
JP (1) | JPS5827769B2 (en) |
AR (1) | AR226815A1 (en) |
AU (1) | AU3990378A (en) |
DE (1) | DE2840063A1 (en) |
FR (1) | FR2408304A1 (en) |
IN (1) | IN149593B (en) |
ZA (1) | ZA785272B (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4328026A (en) | 1978-08-23 | 1982-05-04 | Gaf Corporation | Phosphoranyl derivatives containing nitrogen |
AU527254B2 (en) * | 1979-02-26 | 1983-02-24 | Stauffer Chemical Company | Synergistic herbicides |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4826936A (en) * | 1971-08-14 | 1973-04-09 | ||
JPS50132133A (en) * | 1974-04-15 | 1975-10-20 | ||
JPS50145531A (en) * | 1974-05-10 | 1975-11-21 | ||
JPS5295612A (en) * | 1976-02-05 | 1977-08-11 | Basf Ag | Phosphonic acid salts |
-
1978
- 1978-09-13 IN IN1005/CAL/78A patent/IN149593B/en unknown
- 1978-09-14 DE DE19782840063 patent/DE2840063A1/en active Granted
- 1978-09-15 AU AU39903/78A patent/AU3990378A/en not_active Abandoned
- 1978-09-15 FR FR7826524A patent/FR2408304A1/en active Granted
- 1978-09-15 AR AR273737A patent/AR226815A1/en active
- 1978-09-16 JP JP53114018A patent/JPS5827769B2/en not_active Expired
- 1978-09-18 ZA ZA785272A patent/ZA785272B/en unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4826936A (en) * | 1971-08-14 | 1973-04-09 | ||
JPS50132133A (en) * | 1974-04-15 | 1975-10-20 | ||
JPS50145531A (en) * | 1974-05-10 | 1975-11-21 | ||
JPS5295612A (en) * | 1976-02-05 | 1977-08-11 | Basf Ag | Phosphonic acid salts |
Also Published As
Publication number | Publication date |
---|---|
AU3990378A (en) | 1980-03-20 |
IN149593B (en) | 1982-02-06 |
AR226815A1 (en) | 1982-08-31 |
DE2840063C2 (en) | 1988-10-13 |
FR2408304B1 (en) | 1983-07-22 |
FR2408304A1 (en) | 1979-06-08 |
DE2840063A1 (en) | 1979-03-29 |
JPS54111468A (en) | 1979-08-31 |
ZA785272B (en) | 1980-06-25 |
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