WO1999049728A1 - Tuberous root/tuber thickening promoters and crop yield increasing agents - Google Patents

Tuberous root/tuber thickening promoters and crop yield increasing agents Download PDF

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Publication number
WO1999049728A1
WO1999049728A1 PCT/JP1999/001591 JP9901591W WO9949728A1 WO 1999049728 A1 WO1999049728 A1 WO 1999049728A1 JP 9901591 W JP9901591 W JP 9901591W WO 9949728 A1 WO9949728 A1 WO 9949728A1
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Prior art keywords
group
tuber
crop
treatment
indole
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Application number
PCT/JP1999/001591
Other languages
French (fr)
Japanese (ja)
Inventor
Katsutoshi Hirose
Masayuki Hirose
Kouhei Ikeda
Naonori Hirata
Original Assignee
Kobe Natural Products & Chemicals Co., Ltd.
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Publication of WO1999049728A1 publication Critical patent/WO1999049728A1/en

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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N39/00Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
    • A01N39/02Aryloxy-carboxylic acids; Derivatives thereof
    • A01N39/04Aryloxy-acetic acids; Derivatives thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N37/00Biocides, 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
    • A01N37/10Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N37/00Biocides, 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
    • A01N37/18Biocides, 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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/36Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
    • A01N43/38Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings condensed with carbocyclic rings

Definitions

  • the present invention relates to a tuber (bulb, sukumei) of a plant such as vegetables (crops) and flowers.
  • Tuber and tuber hypertrophy promoters which are preferably used to promote root and tuber (underground) enlargement, as well as increasing the number of flowers and ears of various crop fields (plants), tillering, or fruit (fruit,
  • the present invention relates to a crop enhancer that is suitably used to promote the enlargement of seeds and increase the yield.
  • a tuberous root and tuber hypertrophy promoter that is safe and can be mass-produced, which can increase the yield by increasing the tubers and tubers of vegetables.
  • an agent for promoting tuber and tuber hypertrophy which is capable of enlarging bulbs of flowers and has excellent safety and can be mass-produced.
  • the present invention has been made in view of the above-mentioned conventional problems, and has an object to be used for promoting the enlargement of tuberous roots and tubers of plants such as vegetables and flowers, which can be used safely.
  • the inventors of the present application have intensively studied a tuber / tuber hypertrophy promoter and a crop increasing agent.
  • plants such as vegetables (crops) and flowers, etc.
  • a compound having a specific molecular structure that is, a compound having an indole skeleton, a compound having a benzene skeleton, and a compound having a naphthalene skeleton having a specific molecular structure.
  • the compound has a physiological activity that promotes the enlargement of the tuberous root (bulb / capital root) and tuber (underground stem), and that the compound is excellent in safety and can be mass-produced.
  • an indole skeleton-containing compound having a specific molecular structure has a physiological activity to promote the hypertrophy of fruits (fruits and seeds) of various crops (plants).
  • the inventors have also found that they have a physiological activity that promotes tillering, and have completed the present invention.
  • known indole skeleton-containing compounds have completely different physiological activities to plants depending on, for example, the substitution position and the number of chlorine atoms. Therefore, even if the molecular structures are similar, it is impossible at all to predict the biological activity of an unknown compound from a known similar compound.
  • tuber and tuber hypertrophy promoter of the present invention has the general formula (1)
  • X represents a hydrogen atom, a chlorine atom or a methoxy group
  • R 1 represents — — CHO group, one CH 2 CHO group, one CH 2 CN group, — COOR 2 group, — CH 2 COOR 2 group , — CH 2 CH 2 COOR 2 groups, — CH (CH 3 ) COOR 2 groups, — CH 2 CH 2 CH 2 COOR 2 groups, — CH (CH 3 ) CH 2 COOR 2 groups, — CH (CH 3 ) CH 2 CH 2 COOR 2 group or —CH 2 C 0 C 00 R 2 group
  • R 2 is a hydrogen atom, an alkali metal atom, an alkaline earth metal atom, Represents an alkyl group, a monosaccharide glycoside or an oligosaccharide glycoside
  • R 3 represents a hydrogen atom, an alkali metal atom, an alkaline earth metal atom, an alkyl group having 1 to 4 carbon atoms, a monosaccharide glycoside or an oligosaccharide glycoside.
  • R 4 represents a hydrogen atom, a chlorine atom, a methyl group or a hydroxymethyl group
  • R 5 represents a hydroxyl group or an amino group
  • the agent for promoting tuber root and tuber hypertrophy according to the present invention is characterized in that, in addition to the above constitution, the above compound is an indole skeleton-containing compound.
  • Indole skeleton-containing compounds, benzene skeleton-containing compounds, and naphthalene skeleton-containing compounds having the above-mentioned specific molecular structure have a physiological activity to promote the enlargement of tuberous roots and tubers of plants such as vegetables and flowers. are doing. These compounds are safe and can be mass-produced.
  • the reaction for synthesizing the above-mentioned indole skeleton-containing compound having a substituent at the 4-position of the indole ring is relatively simple. Therefore, according to the above configuration, tuber and tuber hypertrophy which is excellent in safety and can be mass-produced can be suitably used to promote the enlargement of tubers and tubers of plants such as vegetables and flowers.
  • An accelerator can be provided.
  • the tuber / tuber hypertrophy promoter of the present invention may be such that the indole skeleton-containing compound is a natural compound, or that the indole skeleton-containing compound is 4-hydroxyl.
  • ND-3—It is characterized by acetic acid and its esters. According to the above configuration, since the compound is a natural compound, it is possible to provide a tuber and tuber hypertrophy-promoting agent that is more excellent in safety even when it remains in a plant, for example.
  • the crop increasing agent according to the present invention is characterized by containing an indole skeleton-containing compound represented by the general formula (1) in order to achieve the above object.
  • the indole skeleton-containing compound having the above specific molecular structure has a physiological activity that promotes the increase in the number of flowers and ears of various crops (plants), tillering, or hypertrophy of fruits (fruits and seeds). I have. Therefore, according to the above configuration, it can be suitably used to increase the number of flowers and ears of various crops, increase tillering, or increase the yield by promoting actual hypertrophy. It is possible to provide a crop increasing agent capable of mass production.
  • the crop increasing agent according to the present invention may be arranged such that the indole skeleton-containing compound is a natural compound, or the indole skeleton-containing compound is indole-3-.
  • the compound is a natural compound, it is possible to provide a crop yield enhancer that is more excellent in safety even when it remains in a crop, for example.
  • the crop increasing agent according to the present invention is characterized in that it further contains a reducing agent in addition to the above-mentioned constitution.
  • Crops are usually used when diluted with tap water. Often. According to the above arrangement, since the crop increasing agent contains a reducing agent, the reducing agent reacts with chlorine remaining in tap water used for dilution. Therefore, the chlorine-based compound does not decompose the indole skeleton-containing compound, so that the crop-producing agent exerts its effect sufficiently even at a lower concentration even when diluted with tap water. can do.
  • tuber and tuber hypertrophy agent will be described.
  • the agent for promoting tuber root and tuber hypertrophy comprises: an indole skeleton-containing compound represented by the general formula (D); a benzene skeleton-containing compound represented by the general formula (2); )) Contains at least one compound selected from the group consisting of naphthalene skeleton-containing compounds, that is, the tuber / tuber hypertrophy promoter of the present invention contains the above compound as an active ingredient.
  • these compounds have a bioactivity that promotes tuberous root tuber hypertrophy.
  • indole skeleton-containing compound represented by the general formula (1) include, for example, indole-3-carboxylic acid, 4-chloroindole-13-caprolubonic acid, 4—Methoxyindole 3—Capillonic acid, indole—3-Acetic acid (3_indolylacetic acid), 4—Clotindole-3-monoacetic acid, 4—Methoxyindole—3—acetic acid, Indole—3—propionic acid, 4—cloindole—3—propionic acid, 4-methoxyindole—3—propionic acid, indole—3—butyric acid, 4 Rhu 3-butyric acid, 4-methoxyindole 3-butyric acid, and alkali metal or alkaline earth metal salts, esters or these compounds of these compounds Glycosides formed by combining these compounds with monosaccharides or oligosaccharides are exemplified.
  • a compound having an ester bond in the substituent represented by R 1 (and R 2 ), that is, an indole skeleton-containing compound having an ester bond is more easily absorbed by plants.
  • the indole skeleton-containing compound having an ester bond exhibits physiological activity by being hydrolyzed and converted into a carboxyl group (carboxylic acid) after being absorbed by a plant.
  • a compound in which the substituent represented by R 2 is an alkali metal or an alkaline earth metal, that is, an indole skeleton-containing compound that forms a salt Is more stable, and is excellent in storage and preservation.
  • the alkali metal include sodium and steel.
  • specific examples of the alkaline earth metal include calcium and the like.
  • the substituent represented by X in the indole skeleton-containing compound represented by the general formula (1) is a hydrogen atom
  • the substituent represented by R 1 (and R 2 ) is —CHO Group, — CH 2 CHO group, _ CH 2 CN group, one C ⁇ OH group, — CH 2 COOH group, _ CH 2 COOCH 3 group, — CH 2 CH 2 COOH group, — CH 2 CH 2 CH 2 COOH group
  • R 2 is a monosaccharide glycoside or an oligosaccharide glycoside _ CH 2 C 00
  • a compound in which R 2 is a natural compound
  • a substituent represented by X When is a chlorine atom, a compound in which the substituent represented by R 1 (and R 2 ) is one CH 2 COOH group and —CH 2 C 00 CH a group is a natural compound, and
  • the substituent represented by X is a methoxy group
  • the compound in which the substituent represented by R 1 is a CH 2
  • the substituent represented by X is a hydrogen atom, one substituent represented by R 1 CH 2 C 00 H Group indole-3 —acetic acid, the substituent represented by X is a chlorine atom, and the substituent represented by R 1 is —CH 2 COOH group 4 1-closed indole-3 —acetic acid
  • the substituent represented by X is a chlorine atom
  • the substituent represented by R 1 is a CH 2 C 00 CH 3 group, methyl—4 chloroindol—3—acetate
  • the substituent represented by R 1 is a hydrogen atom
  • the substituent represented by R 1 is a CH 2 CH 2 COOH group
  • the substituent represented by X is a hydrogen atom.
  • indole-3-butyric acid in which the substituent represented by R 1 is a —CH 2 CH 2 CH 2 C 00 H group.
  • 4-monoindole-3-acetic acid and its methyl ester are contained in, for example, immature seeds of edible endow and can be extracted from the immature seeds.
  • it is relatively easy to mass-produce 4-Lokundole-13-acetic acid and its methyl ester by synthesis.
  • Examples of the benzene skeleton-containing compound represented by the general formula (2) include, for example, p-chlorophenoxyacetic acid, 2,4-dichlorophenoxyacetic acid, 4-chloro-2-hydroxymethyl-2-acetic acid, In addition, alkali metal salts and alkaline earth metal salts of these compounds, esters, and glycosides obtained by combining these compounds with monosaccharides or oligosaccharides are also included.
  • Specific examples of the naphthalene skeleton-containing compound represented by the general formula (3) include 1-naphthylacetic acid (naphthalene_1-acetic acid) and 1-naphthyl Acetate amide.
  • indole skeleton-containing compounds benzene skeleton-containing compounds and naphthalene skeleton-containing compounds may be used alone or in combination of two or more.
  • an indole skeleton-containing compound is more preferable. It is more preferable that the indole skeleton-containing compound is a natural compound, and it is particularly preferable that the indole skeleton-containing compound is 4-chloroindol-13-acetic acid and / or an ester thereof.
  • the method for producing the above compound is not particularly limited, and a method of extracting from a plant using a general method, a method of producing by synthesis, or the like can be adopted.
  • the reaction for synthesizing the indole skeleton-containing compound having a substituent at the 4-position of the indole ring, the reaction for synthesizing the benzene skeleton-containing compound, and the reaction for synthesizing the naphthalene skeleton-containing compound are relatively simple. Yes, a known method can be adopted.
  • the agent for promoting tuberous root and tuber hypertrophy according to the present invention contains the above compound as an active ingredient.
  • the above compounds can be used as they are, but if necessary, in order to promote or stabilize the effect, for example, by mixing with various adjuvants such as adjuvants used in agricultural chemicals, It can also be used in various formulations such as powders, granules, condyles, wettable powders, flowables, emulsions, pastes and the like.
  • the tuberous root and tuber hypertrophy-promoting agent according to the present invention may contain the above-mentioned adjuvant if necessary. Can be.
  • auxiliary agents examples include solvents (diluents), emulsifiers, dispersants, Examples include various carriers, various substrates, spreading agents, wetting agents, fixing agents, disintegrating agents, and the like.
  • solvents diiluents
  • emulsifiers emulsifiers
  • dispersants examples include various carriers, various substrates, spreading agents, wetting agents, fixing agents, disintegrating agents, and the like.
  • the above-mentioned various preparations which are tuber and tuber hypertrophy promoters, can be used as they are. Accordingly, it can be used after being diluted to a predetermined concentration with water.
  • the tuber / tuber hypertrophy promoter can be diluted to a predetermined concentration with water without using the above solvent.
  • suitable solvents for preparing solutions, flowables, and emulsions include, for example, aromatic hydrocarbons such as toluene and xylene; methyl alcohol, ethyl alcohol, and a). Alcohols such as isopropyl alcohol, butyl alcohol, and ethylene glycol; ketones such as acetone and methylethyl ketone; amides such as N, N-dimethylformamide; dimethyl Sulfoxides such as sulfoxide; cyclohexane, tetrahydronaphthalene, methylnaphthalene; animal and vegetable oils, fatty acid-fatty acid esters; and the like, but are not particularly limited thereto.
  • aromatic hydrocarbons such as toluene and xylene
  • Alcohols such as isopropyl alcohol, butyl alcohol, and ethylene glycol
  • ketones such as acetone and methylethyl ketone
  • the surfactant is an anionic surfactant such as a higher alcohol sulfate ester salt, or a ionic surfactant such as a quaternary ammonium salt).
  • Surfactants, amphoteric surfactants such as betains, etc., and nonionic surfactants (nonionic surfactants) such as ethers, etc. By using a surfactant, the above compounds can be more effectively used in plants. It becomes easier to be absorbed.
  • the carrier suitable for supporting the compound include, but are not limited to, clay, kaolin, talc, diatomaceous earth, silica, alumina, calcium carbonate, and the like. , Bentonite (montmorillonite), feldspar, quartz, sawdust, etc., but are not particularly limited. These carriers may be used alone or in a combination of two or more.
  • Suitable base materials for converting the above compound into a paste include, for example, petrolatum, lanolin, synthetic resin, and rubber. Not something. One of these base materials may be used alone, or two or more may be used in combination.
  • Plants to which the agent for promoting tuber and tuber hypertrophy according to the present invention can be applied are plants having tubers (bulbs and lodgings) and tubers (rhizome).
  • Specific examples of the plant include potatoes (potatoes), sweet potatoes (sweet potatoes), sweet potatoes, sweet potatoes such as make-up, baron, and dejima, potatoes, potatoes, evening loimo, sassava, carrots, Korean carrots, radish, Vegetables (crops) such as radish, turnip, sugar beet, burdock, rust, edible lily, evening onion, garlic, lotus root, laccasei; lily, tulip, friesia, gladiolus, hyacinth, etc.
  • Examples of the method of using the tuber / tube enlarger ie, the method of treating plants using the tuber / tube enlarger, include, for example, foliage treatment, soil treatment, immersion treatment, and powder (powder) treatment. Injection treatment or the like can be employed, but is not particularly limited.
  • planting of tuber root and tuber hypertrophy examples include foliage (including rhizomes), roots (including bulbs and vines), seeds, flowers, fruits, and the like, but are not particularly limited.
  • the use form of the tuber root / tuber hypertrophy promoter may be any means capable of exerting a physiological activity on the plant by being absorbed by the plant. Specifically, for example, spraying Immersion, contact, injection, and the like. In short, the form of use that is most easily absorbed by the plant may be selected according to the type of the target plant, the time of use (purpose of use), and the like.
  • the use time of the tuber and tuber thickening promoter is not particularly limited, but when the plant is a vegetable (crop), the time at which the tuber or tuber begins to enlarge is more preferable. When the plant is a flower, it is more preferable that the bulb and the like start to enlarge after the flower blooms. In addition, for example, if a tuber / tuber hypertrophy promoter is used before the bulbs of flowers and plants are separated, the enlargement of the main bulb can be promoted.
  • the use of an agent can promote spheroid hypertrophy.
  • the amount of the compound used as an active ingredient may be determined according to the composition of the compound, the form of the tuber / tuber hypertrophy promoter, the type of plant to be treated, the treatment method, the time of use (purpose of use), and the like. , but it is not particularly limited - 1 per ares, in the range of 1 0- 7 g to 5 g is more preferable. More specifically, when the tuber and tuber hypertrophy accelerator is used as an aqueous solution for the foliage treatment. The accelerator is diluted so that the concentration of the above compound is about 0.001 ppm to 500 ppm. It is more preferable to spray the prepared aqueous solution within a range of 0.1 L to 20 L per are.
  • tuber and tuber hypertrophy promoter when used as an aqueous solution for the immersion treatment, it is more preferable to immerse the plant in the aqueous solution having the above concentration for a certain period of time.
  • the tuber and tuber hypertrophy-promoting agent according to the present invention the function of accumulating starch in tubers (bulbs and lodgings) and tubers (rhizome) in plants is improved, so that these tubers and tubers are not used. It can be enlarged to 1.5 times or more, more preferably 2 times or more by weight. That is, the tuber and tuber hypertrophy promoter according to the present invention has a function as a crop yield enhancer.
  • the tuber and tuber hypertrophy promoter according to the present invention includes an indole skeleton-containing compound represented by the general formula (1), a benzene skeleton-containing compound represented by the general formula (2), and
  • the structure includes at least one compound selected from the group consisting of naphthalene skeleton-containing compounds represented by the general formula (3).
  • the compound has a physiological activity of promoting the enlargement of tuberous roots and tubers of plants such as vegetables and flowers, and is excellent in safety and can be mass-produced. Therefore, according to the above configuration, it is possible to provide a tuber / tuber hypertrophy promoter which is suitably used for accelerating tuber and tuber hypertrophy, and which is excellent in safety and can be mass-produced.
  • tuber / tuber hypertrophy promoter of the present invention has a configuration in which the indole skeleton-containing compound is a natural compound.
  • the tuber / tuber hypertrophy promoter according to the present invention has a configuration in which the indole skeleton-containing compound is 4-chloroindole-13-acetic acid and Z or an ester thereof. According to the above configuration, since the compound is a natural compound, it is possible to provide a tuber / tuber hypertrophy promoting agent which is more excellent in safety even when it is left in a plant, for example. Next, the crop increasing agent will be described.
  • the crop increasing agent according to the present invention contains an indole skeleton-containing compound represented by the general formula (1). That is, the crop increasing agent according to the present invention contains the above compound as an active ingredient.
  • the compound in particular, the natural compound has a physiological activity that promotes the increase of the number of flowers and ears of various crops (plants), the tillering, or the hypertrophy of fruits (fruits, seeds). It is completely unexpected from known analogs.
  • the indole skeleton-containing compound only one kind may be used, or two or more kinds may be used in combination. More preferably, the indole skeleton-containing compound is a natural compound.
  • the group consisting of indole-3—acetic acid, 4-cycloindole-3—acetic acid, indole-3-butyric acid, and esters of these compounds It is particularly preferred that it be at least one compound selected, most preferred are 4-chloroindole-13-acetic acid and indole-3-butyric acid.
  • the crop increasing agent according to the present invention contains the above compound as an active ingredient.
  • the above compounds can be used as they are, but if necessary, in order to promote or stabilize the effect, for example, by mixing with various adjuvants such as adjuvants used in pesticides, As illustrated, it can also be used in various formulation forms. That is, the crop increasing agent according to the present invention may contain the above-mentioned auxiliary agent as needed, and therefore, the crop increasing agent can take the above-mentioned various formulation forms.
  • the above-mentioned various preparations which are crop-harvesting agents, can be used as they are, but if necessary, they can be used after being diluted to a predetermined concentration with water. When the compound is water-soluble, for example, by forming a salt, the solvent must be used. Also, the crop enhancer can be diluted to a predetermined concentration with water.
  • indole plant hormone can be stably present in a plant, but is decomposed in, for example, tap water by reacting with chlorine remaining in the tap water.
  • spraying common indole-based plant hormones on plants has had little effect because chlorine acts as an oxidizing agent and degrades indole-based plant hormones. Because it was causing it.
  • the crop increasing agent according to the present invention when used in a state diluted with tap water, for example, the crop increasing agent preferably contains a reducing agent.
  • the reducing agent include sodium bisulfite and the like.
  • any compound that reacts with an oxidizing agent such as chlorine and has no adverse effect on plants can be used.
  • the amount of the reducing agent used may be set according to the amount of chlorine remaining in the tap water.
  • the compound containing the indole skeleton is not decomposed by chlorine, so that even when diluted with tap water, the effect of the crop enhancer can be sufficiently improved at a lower concentration. Can be demonstrated. It is not practical to dilute the crop-producing agent with water that does not contain chlorine, such as distilled water, because of the high cost. Further, instead of using the reducing agent, the decomposition of the indole skeleton-containing compound can be avoided by diluting the crop yield using the solvent.
  • the crops to which the crop yield enhancer according to the present invention can be applied include the number of flowers and ears Any plant that can increase the number, increase tillering, or increase the yield of fruits (fruits, seeds) by increasing the yield can be used.
  • Specific examples of the plant include beans such as soybeans, black soybeans, endu beans (sayaendu), red beans, soybeans, and peanuts; wheats such as wheat, barley, and barley; corn and rice. , Ivy, castor, sesame, buckwheat; sugar beet; fruits, such as strawberries, watermelons, apples; so-called vegetables, such as pumpkin and tomato; It is not limited.
  • the method of using the crop enhancer is, for example, at the time of sowing, mixing treatment (soil treatment) for soil, For immersion and dust (powder) treatments; in the period after germination, injection treatment (irrigation treatment) for soil and foliage treatment for plants can be used.
  • the sites where the crop-producing agent is used for plants include foliage (including rhizomes), roots (including bulbs and puddles), seeds (including immature seeds), flowers, fruits, and the like.
  • the selection may be made according to the type and purpose of use, and is not particularly limited.
  • the form of use of the crop-harvesting agent may be any means capable of exerting a physiological activity on the plant by being absorbed by the plant. Specifically, for example, spraying, dipping, contacting , Injection and the like.
  • the form of use that is most easily absorbed by the plant may be selected according to the type of the target plant and the time of use (purpose of use).
  • the use time of the crop-harvesting agent may be set according to the type of plant and the purpose of use, and is not particularly limited. For example, at the time of sowing, when several true leaves are prepared, before flowering, and at the time of flowering , When immature seeds are produced (after flowering) I can do it.
  • the amount of the active compound to be used may be determined according to the composition of the compound, the form of the crop enhancer, the type of the target plant, the treatment method, the time of use (purpose of use), and the like, and is particularly limited. It is not limited to, a per one are, 1 0- 7 g ⁇ 5 g range, more preferable arbitrariness of. More specifically, when the crop enhancer is used as an aqueous solution and used for foliage treatment, the crop enhancer is diluted so that the concentration of the compound is about 0.001 ppm to 500 ppm. More preferably, the diluted aqueous solution is sprayed in a range of 0.1 L to 100 L per are.
  • the crop-enhancing agent when used as an aqueous solution for immersion treatment, it is more preferable to immerse the seed or plant (after germination) in the aqueous solution having the above concentration for a certain period of time.
  • the crop enhancer instead of using the above aqueous solution, that is, instead of using the crop enhancer dissolved in water (diluted with water), the crop enhancer may be added to a mixture of water and the solvent as necessary. It can be used in a state of being dissolved (diluted with a mixed solution), or in a state in which the crop enhancer is dissolved in the above-mentioned solvent (diluted with the solvent).
  • the use of the crop-increasing agent according to the present invention can increase the number of flowers and ears of a plant, promote tillering, or promote the actual hypertrophy, so that the yield of various crops can be compared with the case where no crop is used. And can be increased.
  • the crop increasing agent according to the present invention is configured to include the indole skeleton-containing compound represented by the general formula (1).
  • the compounds have a physiological activity that promotes the increase in the number of flowers and ears, tillering, or actual hypertrophy of various crops. Further, the compound is excellent in safety and can be mass-produced. Therefore, according to the above-mentioned configuration, it is suitable for increasing the number of flowers and ears of various crops, tillering, or promoting the hypertrophy of fruits to increase the yield. It is possible to provide safe and mass-producible crop enhancers that can be used.
  • the crop increasing agent according to the present invention has a configuration in which the indole skeleton-containing compound is a natural compound.
  • the crop-increasing agent according to the present invention is characterized in that the indole skeleton-containing compound comprises indole-3-acetic acid, 4-monoindole-3-acetic acid, indole-3-butyric acid, and
  • the composition is at least one compound selected from the group consisting of esters of these compounds. According to the above configuration, since the compound is a natural compound, even if it remains in the crop, for example, it is possible to provide a crop-enhancing agent which is more excellent in safety.
  • crop sales agent of the present invention according to the configuration of the c the a configuration including the to et the reducing agent, also crop sales agent odor when diluted with tap water, than at lower concentrations Therefore, the effect can be fully exhibited.
  • tuber root and tuber hypertrophy promoter and the crop-promoting agent according to the present invention may be various plant growth regulators, fertilizers (sugars, amino acids, organic acids-various minerals, etc.), herbicides, if necessary. , Fungicides, insecticides, acaricides, nematicides, fungicides for agriculture and horticulture, soil fungicides, soil improvers, etc.o Still other objects of the present invention The features, characteristics, and strengths will be more fully understood from the description below. Also, the benefits of the present invention will become apparent in the following description.
  • Examples 1 to 14 are examples relating to the tuberous root and tuber hypertrophy promoter
  • Examples 15 to 22 are examples relating to the crop increasing agent.
  • the sweet potato was treated using the tuber and tuber hypertrophy promoter of the present invention.
  • Commercially available sweet potato vines severe vines
  • these tips were planted in a field so that the stems of the three leaves at the base were buried in the soil.
  • the planting interval between the tip portions was about 60 cm.
  • IAA indole—3—acetic acid
  • a foliage treatment was performed by spraying a predetermined amount of an aqueous solution of p-chlorofunooxyacetic acid, or four of each aqueous solution.
  • the plants were treated using the tuber and tuber hypertrophy promoter of the present invention (first, potted plants were planted (a plurality of pots). Then, toxo plants whose growth states were substantially the same as each other were selected. in a concentration of 3 X 1 0 - by the 1 AA solution, a predetermined amount sprayed by one pot for each solution, - 5 mol ZL and 1 X 1 0- 5 mol ZL in which two 4 one C 1 In addition, instead of the above-mentioned aqueous solution, a control was made of Toxos which was sprayed with a predetermined amount of water.
  • the bulbs (toxoids) of Toxos are dug out, their weights (shown as weight in Table 2) are measured, and the weight ratio to the control (the same as the weight ratio) ) was calculated.
  • the same foliar treatment and measurement were performed using Yunnan Tokiso, Kiboushi and Lily instead of Tokiso.
  • Et al is, for lilies, 4 - instead of C 1 one IAA solution, tuberous • tubers hypertrophy accelerator, concentrations 3 X 1 0 - 5 the mole / L Lee emissions
  • IBA indole-3 butyric acid
  • concentration of 3 X 1 0 5 mol / L, 1 X 1 0 5 mol / L and 1 X 1 0 6 mol ZL is three kinds of 4 C 1 - to IAA solution, not a three strains each solution Soil treatment was performed by spraying a predetermined amount each.
  • Acapulco (3 strains) in which a predetermined amount of water was sprayed was used as a control.
  • Acapulco bulbs (tubes) were dug out, and their weight (indicated as weight in Table 3) and the perimeter of the bulb (indicated as perimeter) were measured.
  • the average weight of the bulb (same as the average weight) and the weight ratio to the control (same as the weight ratio), the average circumference of the bulb (same as the same as the average circumference) and the control
  • the length ratio to the length was calculated. Table 3 summarizes these results.
  • Tuberose treatment was carried out using the tuber and tuber hypertrophy promoter of the present invention.
  • tuberose bulbs were planted in the field.
  • a foliage treatment was performed by spraying a predetermined amount of an aqueous solution of 41 C 1 -IAA having a concentration of 3 ⁇ 10 5 mol / L on the three tube roses.
  • three tuberoses in which a predetermined amount of water was sprayed instead of the above-mentioned aqueous solution were used as a control opening.
  • Satoimo was treated using the tuber and tuber hypertrophy promoter of the present invention.
  • these seed potatoes were planted in the field. The planting interval between them was about 60 cm.
  • the radish was treated for 20 days using the tuber and tuber hypertrophy promoter of the present invention.
  • radish seeds manufactured (many) were sparsely sown in two 34 cm x 68 cm planters and grown at room temperature. After two months, thinning was performed so that the number of radishes per planter would be about 40.
  • thinning was performed so that the number of radishes per planter would be about 40.
  • the control of the radish on the 20th was used as the control.
  • the cut portion was adjusted to a concentration of 5 ⁇ 1.
  • the immersion treatment was performed by immersion in an aqueous solution of 4-C1-IAA at 0 to 15 mol / L for 2 hours.
  • the radish for 20 days can be obtained. It was found that root enlargement was promoted. It was also found that the combined use of the foliage treatment and the injection treatment or the immersion treatment further promoted the root enlargement of Japanese radish.
  • Nonio emissions based surfactant US, V Alent trade name: X- 7 7
  • a plurality of potatoes having substantially the same size as each other were prepared, and half of the potatoes were immersed in the aqueous solution for 2 hours to perform an immersion treatment. The remaining potatoes were not subjected to the above treatment.
  • 10 plants (pieces) were treated, 15 were not treated and 15 pieces (pieces). Planted in the field. Ridge width was 1 m, and the planting interval was 40 cm.
  • the potatoes of the first group were cut into two pieces (halved) and then immersed in an aqueous solution having the same composition as in Example 7 for 2 hours.
  • the second group of potatoes are nonionic surfactants
  • the (X 7 7) in a proportion of 2 0 ppm, by immersing 2 hours IBA solution the concentration is 5 x 1 0 6 mol ZL, after the immersion treatment, cut into two (2 etc. Minute).
  • Potato fourth group includes a surfactant (S orpo 1 7 1 5 7 ) at a rate of 1 0 ppm, by concentration immersed for 2 hours in IBA solution is 3 x 1 0 5 mol / L After the immersion treatment, it was cut into two (halved). The fifth and sixth groups of potatoes were cut in two (halved). These six groups of potatoes were then planted on the field on August 28. The ridge width was 1 m and the planting interval was 40 cm.
  • S orpo 1 7 1 5 7 a surfactant at a rate of 1 0 ppm, by concentration immersed for 2 hours in IBA solution is 3 x 1 0 5 mol / L After the immersion treatment, it was cut into two (halved). The fifth and sixth groups of potatoes were cut in two (halved). These six groups of potatoes were then planted on the field on August 28. The ridge width was 1 m and the planting interval was 40 cm.
  • the nonionic surfactant (X-77) was added to 20 ppm at the stage when the aerial part grew to about 10 leaves (September 29).
  • the foliage treatment was performed by spraying an IBA aqueous solution having a concentration of 5 ⁇ 10 5 mol / L in a ratio of 120 m 1 / m 2 .
  • the sixth potato was not subjected to the immersion treatment and the foliage treatment.
  • the potato (baron) immersion treatment and foliage treatment using the tuber and tuber hypertrophy-promoting agent according to the present invention promoted the potato tuber hypertrophy, In other words, the yield increased.
  • Japanese radish was treated using the tuber and tuber hypertrophy promoter of the present invention.
  • seeds (many) of radish variety: Oshin) were sown at 30 cm intervals and grown.
  • half of the radish was replaced with a nonionic surfactant (manufactured by Wako Pure Chemical Industries, Ltd., trade name: Tween 8 0) at a concentration of 500 ppm, and a concentration of 5 x 10 — 5 mol ZL is sprayed with an aqueous solution of 4 1 C 1 and 1 IAA at a spray rate of 85 m 1 / m 2.
  • a nonionic surfactant manufactured by Wako Pure Chemical Industries, Ltd., trade name: Tween 8 0
  • a concentration of 5 x 10 — 5 mol ZL is sprayed with an aqueous solution of 4 1 C 1 and 1 IAA at a spray rate of 85 m 1 / m 2.
  • foliage treatment was performed.
  • Ligustrum lily was treated.
  • bulbs bulb circumference 6 cm to 7 cm
  • two ridges 1.1 m wide and 5 m long.
  • a nonionic surfactant ( X — 7 7) at a concentration of 20 ppm and a concentration of 5 x 10 — 5 mol / L 4 — CI — IAA solution is sprayed at a spray rate of 0.9 L / m 2
  • foliage treatment was performed.
  • the remaining grape lily (the other ridge) on which a predetermined amount of water was sprayed was used as a control.
  • Tulip treatment was performed using the tuber / tuber hypertrophy promoter of the present invention.
  • approximately 800 bulbs variety: Oxford (red flower), bulb circumference 10 cm
  • 500 ppm of nonionic surfactant Tween 80
  • concentration 4 is 5 x 1 0 one 5 mol / L - CI -.
  • Example 7 Satomo treatment was performed in the same manner as in Example 7. First, an IAA aqueous solution containing a nonionic surfactant (X — 77) at a ratio of 20 ppm and having a concentration of 5 ⁇ 10 — 5 mol / L was prepared. Next, a plurality of taros having substantially the same size were prepared, and half of the taros were immersed in the aqueous solution for 2 hours to perform immersion treatment. The above process was not applied to the remaining satimo. Then, 12 treated taros and 11 untreated taros were planted in the field in early April. The ridge width was 1 m and the planting interval was 30 cm.
  • a nonionic surfactant X — 77
  • the evening foliage treatment was performed using the crop increasing agent according to the present invention. First, on May 22nd, ⁇ evening seeds (many) were directly sown in the field and raised. After that, on July 14th, three plants, each of which grew to a height of about 90 cm and had not yet flowered, were selected as two groups (six in total).
  • Endow foliage treatment was carried out using the crop yield enhancer according to the present invention.
  • the seeds of endou variety: Azumino 30 day silk pod PMR
  • concentration of 5 X 1 0 - by spraying Te than in spraying amount of 5 mol / L is 4 one C 1 one IAA water solution 4 0 L / a
  • Gyotsu the foliage treatment was.
  • the other group's endowment (16 strains) was Instead, water was sprayed at a spraying rate of 40 L / a to control.
  • Wheat was treated using the crop increasing agent according to the present invention.
  • First, wheat seeds were divided into seven groups of 250 g each. 1 February 1 5 days, wheat first group, concentration by immersing 5 hours 4 _ C 1 one IAA solution is 1 X 1 0- 5 mol ZL, has been dipped.
  • a second group of wheat was immersed in an aqueous solution of IBA (crop-growth enhancer) at a concentration of 1 ⁇ 10 mol / L for 5 hours.
  • IBA crop-growth enhancer
  • a non-ionic surfactant manufactured by Toho Chemical Industry Co., Ltd., trade name: Sorbon T—80 was added to each of the above two aqueous solutions at a level of 20 pp. m.
  • -Foliage treatment was performed by spraying the IAA aqueous solution at a spraying rate of 20 LZa (effective dose 0.21 g / a).
  • an aqueous solution of IBA at a concentration of 5 X 10 — 5 mol / L was sprayed at 20 LZ a to the wheat of the fourth group that grew in the same manner. g / a) for foliage treatment.
  • a nonionic surfactant (same as above) was added at a ratio of 500 pprn.
  • Et al is, on April 1 7, grown on the ground portion 4 0 cm as high as, and for the fifth group of wheat not yet heading, concentration 5 X 1 0 one 5
  • the foliage treatment was performed by spraying an aqueous solution of 41-CI-IAA, which is mol / L, at a spraying rate of 40 LZa (effective dose: 0.42 g / a).
  • spraying amount of concentration 5 X 1 0 _ 5 mol / L in which IBA aqueous solution 4 0 LZ a (effective agent amount 0.4 Foliage treatment was performed by spraying at 1 g / a).
  • a nonionic surfactant (same as above) was added to the two aqueous solutions at a ratio of 500 ppm.
  • the wheat in the seventh group was controlled by spraying a predetermined amount of water without performing any of the above treatments.
  • the corn seeds (many) were grouped into 10 groups.
  • the concentration of 4 is 5 X 1 0 _ 6 mol / L - C 1 - by immersing 2 hours IAA solution, has been dipped.
  • the corn second group concentration 5 X 1 0- 6 mole 7 L a is 4 - performed by immersing for 3 0 seconds IAA Echiruaruko Lumpur solution, the immersion treatment - C 1 was.
  • the third Group - corn flop, concentration 5 X 1 0 - a 6 mol ZL IBA solution The immersion treatment was performed by immersing the sample for 2 hours.
  • a fourth group of corn was harvested at a concentration of 5 ⁇ 10 6 mol ZL by IAA
  • concentration of 1 X 1 0- 4 mol ZL 4 - CI - spraying amount of the IAA solution 4 0 L / a (effective drug amount
  • the foliage treatment was performed by spraying with 0.84 g / a).
  • concentration of 5 X 1 0 - spraying amount of 5 mol / L in a IAA aqueous solution 4 0 LZ a (effective agent amount 0.3 Foliage treatment was performed by spraying at 5 g / a).
  • a nonionic surfactant (same as above) was added to each of the three kinds of aqueous solutions at a ratio of 500 ppm.
  • the corn of the 10th group was controlled by spraying a predetermined amount of water without performing any of the above treatments.
  • foliage treatment was performed on rice (American ivy). First, on May 8, ⁇ evening seeds (many) were directly sowed at 50 cm intervals and cultivated. After that, I divided the data into three groups. Three weeks after sowing, the first group of ivy (6 strains), which grew to about 6 leaves, was treated with a nonionic surfactant (Wako Pure Chemical Industries, Ltd.). : the T ween 8 0) in a proportion of 1 0 0 ppm, by spraying concentration of IAA solution is 5 X 1 0 5 mol / L Te than in spraying amounts of 2 0 L / a, foliage treatment ( Initial).
  • aqueous solution (same composition) was sprayed onto the second group of ivy (7 strains) at a spraying rate of 20 L / a to obtain foliage. Processing (middle term) was performed. The control was applied to the third group of potatoes (14 strains) by spraying a predetermined amount of water without any of the above treatments.
  • the early harvest can be increased by performing the foliage treatment in the evening using the crop-harvesting agent according to the present invention, and the total yield can be reduced to the first.
  • the increase was 12% in the group and 32% in the second group.
  • Rice was treated using the crop yield enhancer according to the present invention.
  • rice seeds fir
  • 20 ppm of nonionic surfactant manufactured by Va1ent, USA; trade name: X-77
  • Concentration is 1 x 10 — 7 mol ZL
  • the immersion treatment was performed by immersing in an IA A aqueous solution for 2 hours.
  • the grown rice seedlings were transplanted to the paddy field.
  • the planting interval (between plants) was 25 cm, and rice was planted so that one group had 18 mx 3 rows.
  • Wheat was treated using the crop increasing agent according to the present invention. First, one mid-February to seeds 2 5 0 g of wheat, were grouped into three, it was seeded in a field of the area 7. 5 m 2, respectively. At this time, for the wheat of the first group, before sowing, it contains a nonionic surfactant (Tween 80) at a ratio of 20 ppm, and the concentration is 1 ⁇ 10 mol / L.
  • Tween 80 nonionic surfactant
  • the immersion treatment was performed by immersion for 2 hours.
  • nonionic surfactant Teween 80
  • the foliage treatment was performed by spraying an aqueous IAA solution having a concentration of 5 ⁇ 10 5 mol / L at a spray rate of 200 m 1 / m 2 .
  • the third group of wheat was controlled by spraying a predetermined amount of water without any of the above treatments.
  • the foliage treatment of tomato was performed using the crop increasing agent according to the present invention. First, tomato seedlings whose growth conditions were almost the same were selected and planted on May 20 at 40 cm intervals in a field.
  • a nonionic surfactant (X-77) was contained at a ratio of 20 ppm to the first group of tomatoes whose aerial parts grew to a height of about 20 cm. concentration by spraying Te than 1 0 0 spraying amount of m 1 / m 2 the IAA solution is 1 X 1 0- 5 mol ZL, were foliar treatment.
  • the second group of tomatoes contained 20 ppm of nonionic surfactant (as above) at a concentration of 1 X 10 — 5 mol / L 4 C 1 -IAA aqueous solution was sprayed at a spraying rate of 100 m 1 / m 2 to perform foliage treatment.
  • the third group of tomatoes was controlled by spraying a predetermined amount of water without any of the above treatments.
  • Three months after planting (mid-August), the yield, that is, the number of tomatoes (fruits) was calculated, and the control ratio was calculated. The results are summarized in Table 22.
  • the tuber / tuber hypertrophy promoter comprises an indole skeleton-containing compound represented by the general formula (1), a benzene skeleton-containing compound represented by the general formula (2), and 3) Including the naphthalene skeleton
  • the composition includes at least one compound selected from the group consisting of organic compounds.
  • the tuber and tuber hypertrophy promoter can be suitably used to promote tuber and tuber hypertrophy of plants such as vegetables and flowers, and is excellent in safety and can be mass-produced. .
  • the crop increasing agent according to the present invention is configured to contain the indole skeleton-containing compound represented by the general formula (1).
  • the crop-harvesting agent can be suitably used for increasing the number of flowers and ears of various crops (plants), increasing the number of tillers, or promoting the hypertrophy of fruits (fruits and seeds) to increase the yield. It is excellent in safety and can be mass-produced.

Abstract

Tuberous root/tuber thickening promoters and crop yield increasing agents containing, for example, compounds with an indole skeleton represented by general formula (1): wherein X represents H, Cl or -OCH3; R1 represents -CHO, -CH¿2?CHO, -CH2CN, -COOR?2, -CH¿2COOR2, -CH2CH2COOR2, -CH(CH¿3?)COOR?2, -CH¿2CH2CH2COOR2, -CH(CH¿3?)CH2COOR?2¿, -CH(CH¿3?)CH2CH2COOR?2¿ or -CH¿2?COCOOR?2¿, (wherein R2 represents H, an alkali metal, an alkaline earth metal, C¿1-4? alkyl, a monosaccharide glycoside or an oligosaccharide glycoside. Thus, it is possible to provide tuberous root/tuber thickening promoters and crop yield increasing agents which are highly safe and can be produced on a mass scale.

Description

塊根 ·塊茎肥大促進剤、 並びに、 作物増収剤 Tuber and tuber hypertrophy, and crop-producing agent
技術分野 本発明は、 野菜類 (作物) や花卉類等の植物が有する塊根 (球根 ·宿 明 TECHNICAL FIELD The present invention relates to a tuber (bulb, sukumei) of a plant such as vegetables (crops) and flowers.
根) や塊茎 (地下茎) の肥大を促進させるのに好適に用いられる塊根 · 塊茎肥大促進剤、 並びに、 各種作物田(植物) の花数や穂数の増加、 分蘖、 或いは、 実 (果実、 種子) の肥大を促進させて収量を増加させるのに好 適に用いられる作物増収剤に関するものである。 Tuber and tuber hypertrophy promoters, which are preferably used to promote root and tuber (underground) enlargement, as well as increasing the number of flowers and ears of various crop fields (plants), tillering, or fruit (fruit, The present invention relates to a crop enhancer that is suitably used to promote the enlargement of seeds and increase the yield.
背景技術 Background art
従来より、 野菜類 (作物) が有する塊根 (球根 ,宿根) や塊茎 (地下 茎) を肥大させて収量を増加させるベく (即ち、 食料を増産すべく) 、 種々提案がなされている。 例えば、 イ ン ドール骨格含有化合物の一種で ある 5, 6 —ジクロロイ ン ドール— 3 —酢酸に、 ジャガイモの塊茎 (地 下茎) の肥大を促進させる生理活性 (作用) があることは知られている (特公平 6 — 6 2 5 6 3号公報、 1 9 9 4年 8月 1 7 日公告 (日本国)  Conventionally, various proposals have been made to increase the yield by enlarging the tubers (bulbs and roots) and tubers (underground stems) of vegetables (crops) (that is, to increase food production). For example, it is known that 5,6-dichloroindole-3-acetic acid, one of the indole skeleton-containing compounds, has a physiological activity (action) that promotes the enlargement of potato tubers (underground stems). (Japanese Patent Publication No. 6-625653, published on August 17, 1994, Japan)
) o ) o
また一方、 従来より、 各種作物 (植物) を増収させる方法と して、 例 えば、 雄性不稔剤を利用して、 優れた 種子を創製する方法や、 矮化 剤を利用して、 植物の倒伏防止を行う方法等が行われている。 そして、 上記 5, 6 —ジクロロイ ン ド一ルー 3 —酢酸には、 小麦の一粒当たりの 重さを増加させる (実の肥大を促進させる) 生理活性 (作用) があるこ とが知られている (特公平 6 — 6 2 5 6 3号公報) 。 そこで、 上記 5 , 6 —ジクロ口イ ン ドールー 3 —酢酸を作物増収剤と して用い、 各種作物 の収量を增加させることが提案されている。 On the other hand, conventionally, as a method of increasing the yield of various crops (plants), for example, a method of creating excellent seeds by using a male sterile agent, or a method of producing a plant by using a dwarfizing agent, Methods for preventing lodging, etc., have been implemented. And, the above-mentioned 5, 6-dichloroindole 3-acetic acid has a physiological activity (action) that increases the weight per grain of wheat (promotes the growth of fruit). (Japanese Patent Publication No. 6-625663). Therefore, it has been proposed to increase the yield of various crops by using the above-mentioned 5, 6-dichroic indole-3-acetic acid as a crop increasing agent.
しかしながら、 イ ン ドール環の 5, 6位に置換基を有する上記 5, 6 ージクロ口イ ン ド一ルー 3 —酢酸を合成する反応は複雑であり、 このた め、 該化合物を大量生産することは困難である。 また、 該化合物は合成 化合物であつて天然には存在しないので、 例えばジャガイモ等の野菜類 (作物) や各種作物 (植物) に残留した場合には、 安全性に優れている とは言い難い。  However, the reaction for synthesizing the above-mentioned 5,6-dichloroindole-3- (acetic acid) having a substituent at the 5- or 6-position of the indole ring is complicated, and therefore, it is necessary to mass-produce the compound. It is difficult. Further, since the compound is a synthetic compound and does not exist in nature, it is hard to say that it is excellent in safety when it remains in vegetables (crops) such as potatoes and various crops (plants).
それゆえ、 野菜類が有する塊根や塊茎を肥大させて収量を増加させる ことができる、 安全性に優れかつ大量生産可能な塊根 ·塊茎肥大促進剤 が求められている。 また、 花卉類が有する例えば球根を肥大させること ができる、 安全性に優れかつ大量生産可能な塊根 ·塊茎肥大促進剤も求 められている。  Therefore, there is a need for a tuberous root and tuber hypertrophy promoter that is safe and can be mass-produced, which can increase the yield by increasing the tubers and tubers of vegetables. There is also a need for an agent for promoting tuber and tuber hypertrophy, which is capable of enlarging bulbs of flowers and has excellent safety and can be mass-produced.
さ らに、 各種作物 (植物) の実 (果実、 種子) の肥大を促進させて収 量を増加させることができる、 安全性に優れかつ大量生産可能な作物増 収剤が求められている。 また、 各種作物の花数や穂数の増加、 分蘖を促 進させて収量を増加させることができる、 安全性に優れかつ大量生産可 能な作物増収剤も求められている。  In addition, there is a need for a safe and mass-producing crop enhancer that can increase the yield by promoting the growth of fruits (fruits, seeds) of various crops (plants). There is also a need for a crop enhancer that is safe and can be mass-produced, which can increase the number of flowers and ears of various crops and increase the yield by promoting tillering.
本発明は、 上記従来の問題点に鑑みなされたものであり、 その目的は- 野菜類や花卉類等の植物が有する塊根や塊茎の肥大を促進させるのに好 適に用いることができる、 安全性に優れかつ大量生産可能な塊根 · 塊茎 肥大促進剤を提供すること、 並びに、 各種作物の花数や穂数の増加、 分 蘖、 或いは、 実の肥大を促進させて収量を増加させるのに好適に用いる ことができる、 安全性に優れかつ大量生産可能な作物増収剤を提供する ことにある。 発明の開示 The present invention has been made in view of the above-mentioned conventional problems, and has an object to be used for promoting the enlargement of tuberous roots and tubers of plants such as vegetables and flowers, which can be used safely. To provide tuber and tuber hypertrophy promoters that are excellent in quality and can be mass-produced, and to increase the number of flowers and ears of various crops, tillers, or to increase the yield by promoting fruit hypertrophy. Preferably used It is an object of the present invention to provide a crop enhancer that is safe and can be mass-produced. Disclosure of the invention
本願発明者等は、 上記の目的を達成すべく、 塊根 ·塊茎肥大促進剤、 並びに、 作物増収剤について鋭意検討した。 その結果、 特定の分子構造 を有する化合物、 つまり、 特定の分子構造を有するィ ン ドール骨格含有 化合物やベンゼン骨格含有化合物、 ナフタ レン骨格含有化合物に、 野菜 類 (作物) や花卉類等の植物が有する塊根 (球根 · 宿根) や塊茎 (地下 茎) の肥大を促進させる生理活性があること、 並びに、 該化合物が安全 性に優れかつ大量生産することができることを見い出した。 また、 特定 の分子構造を有するイ ン ドール骨格含有化合物に、 各種作物 (植物) の 実 (果実、 種子) の肥大を促進させる生理活性があることを見い出した さ らに、 該化合物に、 各種作物の一穂当たりの粒数や穂数を増加させる 効果や、 花が咲く前においては花数を増加させる効果、 或いは分蘖を促 進させる効果、 つまり、 各種作物の花数や穂数の増加、 分蘖を促進させ る生理活性があることも見い出して、 本発明を完成させるに至った。 尚、 既知のイ ン ドール骨格含有化合物は、 例えば塩素原子の置換位置 並びに個数によって、 植物に対する生理活性が全く異なる。 従って、 分 子構造が類似していても、 既知の類似化合物から未知の化合物の生理活 性を予測することは、 全く不可能である。  In order to achieve the above object, the inventors of the present application have intensively studied a tuber / tuber hypertrophy promoter and a crop increasing agent. As a result, plants such as vegetables (crops) and flowers, etc., have a compound having a specific molecular structure, that is, a compound having an indole skeleton, a compound having a benzene skeleton, and a compound having a naphthalene skeleton having a specific molecular structure. It has been found that the compound has a physiological activity that promotes the enlargement of the tuberous root (bulb / capital root) and tuber (underground stem), and that the compound is excellent in safety and can be mass-produced. In addition, they have found that an indole skeleton-containing compound having a specific molecular structure has a physiological activity to promote the hypertrophy of fruits (fruits and seeds) of various crops (plants). The effect of increasing the number of grains and ears per ear of a crop, the effect of increasing the number of flowers before blooming, or the effect of promoting tillering, that is, increasing the number of flowers and ears of various crops, The inventors have also found that they have a physiological activity that promotes tillering, and have completed the present invention. Note that known indole skeleton-containing compounds have completely different physiological activities to plants depending on, for example, the substitution position and the number of chlorine atoms. Therefore, even if the molecular structures are similar, it is impossible at all to predict the biological activity of an unknown compound from a known similar compound.
即ち、 本発明にかかる塊根 ·塊茎肥大促進剤は、 上記の目的を達成す るために、 一般式 ( 1 )
Figure imgf000006_0001
That is, the tuber and tuber hypertrophy promoter of the present invention has the general formula (1)
Figure imgf000006_0001
(式中、 Xは、 水素原子、 塩素原子またはメ トキシ基を表し、 R 1 は- — C H O基、 一 C H 2 C H O基、 一 C H 2 C N基、 — C O O R 2 基、 ― C H 2 C O O R 2 基、 — C H 2 C H 2 C O O R 2 基、 — C H (C H 3) C O O R 2 基、 — C H 2 C H 2 C H 2 C O O R 2 基、 — C H (C H 3) C H 2 C O O R 2 基、 — C H (C H 3) C H 2 C H 2 C O O R 2 基、 または— C H 2 C 0 C 00 R 2 基を表し、 かつ、 上記 R 2 は、 水素原子、 アル力 リ金属原子、 アルカ リ土類金属原子、 炭素数 1〜 4のアルキル基、 単糖 の配糖体またはォリ ゴ糖の配糖体を表す) (In the formula, X represents a hydrogen atom, a chlorine atom or a methoxy group, and R 1 represents — — CHO group, one CH 2 CHO group, one CH 2 CN group, — COOR 2 group, — CH 2 COOR 2 group , — CH 2 CH 2 COOR 2 groups, — CH (CH 3 ) COOR 2 groups, — CH 2 CH 2 CH 2 COOR 2 groups, — CH (CH 3 ) CH 2 COOR 2 groups, — CH (CH 3 ) CH 2 CH 2 COOR 2 group or —CH 2 C 0 C 00 R 2 group, and R 2 is a hydrogen atom, an alkali metal atom, an alkaline earth metal atom, Represents an alkyl group, a monosaccharide glycoside or an oligosaccharide glycoside)
で示されるィ ン ドール骨格含有化合物、 一般式 ( 2 ) An indole skeleton-containing compound represented by the general formula (2)
Figure imgf000006_0002
Figure imgf000006_0002
(式中、 R 3 は、 水素原子、 アルカ リ金属原子、 アルカ リ土類金属原 子、 炭素数 1〜 4のアルキル基、 単糖の配糖体またはォリ ゴ糖の配糖体 を表し、 R 4 は、 水素原子、 塩素原子、 メチル基またはヒ ドロキシメチ ル基を表す) (Wherein, R 3 represents a hydrogen atom, an alkali metal atom, an alkaline earth metal atom, an alkyl group having 1 to 4 carbon atoms, a monosaccharide glycoside or an oligosaccharide glycoside. And R 4 represents a hydrogen atom, a chlorine atom, a methyl group or a hydroxymethyl group)
で示されるベンゼン骨格含有化合物、 および、 一般式 ( 3 )
Figure imgf000007_0001
A benzene skeleton-containing compound represented by the general formula (3)
Figure imgf000007_0001
(式中、 R 5 は、 ヒ ドロキシル基またはア ミ ノ基を表す) (Wherein, R 5 represents a hydroxyl group or an amino group)
で示されるナフタ レン骨格含有化合物からなる群より選ばれる少なく と も一種の化合物を含むことを特徴としている。 また、 本発明にかかる塊 根 ·塊茎肥大促進剤は、 上記構成に加えて、 上記化合物がィ ン ドール骨 格含有化合物であることを特徵としている。 And at least one compound selected from the group consisting of naphthalene skeleton-containing compounds represented by Further, the agent for promoting tuber root and tuber hypertrophy according to the present invention is characterized in that, in addition to the above constitution, the above compound is an indole skeleton-containing compound.
上記特定の分子構造を有するィ ン ドール骨格含有化合物やベンゼン骨 格含有化合物、 ナフタ レ ン骨格含有化合物は、 野菜類や花卉類等の植物 が有する塊根や塊茎の肥大を促進させる生理活性を有している。 これら 化合物は、 安全性に優れかつ大量生産することができる。 例えばイ ン ド ール環の 4位に置換基を有する上記ィン ドール骨格含有化合物を合成す る反応は、 比較的簡単である。 従って、 上記の構成によれば、 野菜類や 花卉類等の植物が有する塊根や塊茎の肥大を促進させるのに好適に用い ることができる、 安全性に優れかつ大量生産可能な塊根 ·塊茎肥大促進 剤を提供することができる。  Indole skeleton-containing compounds, benzene skeleton-containing compounds, and naphthalene skeleton-containing compounds having the above-mentioned specific molecular structure have a physiological activity to promote the enlargement of tuberous roots and tubers of plants such as vegetables and flowers. are doing. These compounds are safe and can be mass-produced. For example, the reaction for synthesizing the above-mentioned indole skeleton-containing compound having a substituent at the 4-position of the indole ring is relatively simple. Therefore, according to the above configuration, tuber and tuber hypertrophy which is excellent in safety and can be mass-produced can be suitably used to promote the enlargement of tubers and tubers of plants such as vegetables and flowers. An accelerator can be provided.
さ らに、 本発明にかかる塊根 ·塊茎肥大促進剤は、 上記構成に加えて 上記イ ン ドール骨格含有化合物が天然化合物であること、 或いは、 上記 ィ ン ドール骨格含有化合物が 4 —クロ口イ ン ド一ルー 3 —酢酸およ またはそのエステルであることを特徴としている。 上記の構成によれば、 該化合物が天然化合物であるので、 例えば植物 に残留した場合においても、 安全性により一層優れた塊根 ·塊茎肥大促 進剤を提供することができる。 Furthermore, in addition to the above constitution, the tuber / tuber hypertrophy promoter of the present invention may be such that the indole skeleton-containing compound is a natural compound, or that the indole skeleton-containing compound is 4-hydroxyl. ND-3—It is characterized by acetic acid and its esters. According to the above configuration, since the compound is a natural compound, it is possible to provide a tuber and tuber hypertrophy-promoting agent that is more excellent in safety even when it remains in a plant, for example.
また一方、 本発明にかかる作物増収剤は、 上記の目的を達成するため に、 前記一般式 ( 1 ) で示されるイ ン ドール骨格含有化合物を含むこと を特徴と している。  On the other hand, the crop increasing agent according to the present invention is characterized by containing an indole skeleton-containing compound represented by the general formula (1) in order to achieve the above object.
上記特定の分子構造を有するィ ン ドール骨格含有化合物は、 各種作物 (植物) の花数や穂数の増加、 分蘖、 或いは、 実 (果実、 種子) の肥大 を促進させる生理活性を有している。 従って、 上記の構成によれば、 各 種作物の花数や穂数の増加、 分蘖、 或いは、 実の肥大を促進させて収量 を增加させるのに好適に用いることができる、 安全性に優れかつ大量生 産可能な作物増収剤を提供することができる。  The indole skeleton-containing compound having the above specific molecular structure has a physiological activity that promotes the increase in the number of flowers and ears of various crops (plants), tillering, or hypertrophy of fruits (fruits and seeds). I have. Therefore, according to the above configuration, it can be suitably used to increase the number of flowers and ears of various crops, increase tillering, or increase the yield by promoting actual hypertrophy. It is possible to provide a crop increasing agent capable of mass production.
また、 本発明にかかる作物増収剤は、 上記構成に加えて、 上記イ ン ド ール骨格含有化合物が天然化合物であること、 或いは、 上記ィン ドール 骨格含有化合物が、 イ ン ドール— 3 -酢酸、 4 一クロ口イ ン ドールー 3 —酢酸、 イ ン ドールー 3 —酪酸、 および、 これら化合物のエステルから なる群より選ばれる少なく とも一種の化合物であることを特徴としてい る o  Further, in addition to the above constitution, the crop increasing agent according to the present invention may be arranged such that the indole skeleton-containing compound is a natural compound, or the indole skeleton-containing compound is indole-3-. Acetic acid, 4-monoindole-3—acetic acid, indole-3-butyric acid, and at least one compound selected from the group consisting of esters of these compounds o
上記の構成によれば、 該化合物が天然化合物であるので、 例えば作物 に残留した場合においても、 安全性により一層優れた作物増収剤を提供 することができる。  According to the above configuration, since the compound is a natural compound, it is possible to provide a crop yield enhancer that is more excellent in safety even when it remains in a crop, for example.
さ らに、 本発明にかかる作物増収剤は、 上記構成に加えて、 還元剤を さ らに含むことを特徴としている。  Further, the crop increasing agent according to the present invention is characterized in that it further contains a reducing agent in addition to the above-mentioned constitution.
作物増収剤は、 通常、 水道水を用いて希釈された状態で使用される場 合が多い。 上記の構成によれば、 作物増収剤に還元剤が含まれているの で、 該還元剤は、 希釈に用いた水道水に残留している塩素と反応する。 従って、 該塩素によってィ ン ドール骨格含有化合物が分解されることが 無く なるので、 作物増収剤は、 水道水を用いて希釈した場合においても、 より低濃度で以て、 その効果を充分に発揮することができる。 Crops are usually used when diluted with tap water. Often. According to the above arrangement, since the crop increasing agent contains a reducing agent, the reducing agent reacts with chlorine remaining in tap water used for dilution. Therefore, the chlorine-based compound does not decompose the indole skeleton-containing compound, so that the crop-producing agent exerts its effect sufficiently even at a lower concentration even when diluted with tap water. can do.
以下、 本発明について詳しく説明する。 始めに、 塊根 ·塊茎肥大促進 剤について説明する。 Hereinafter, the present invention will be described in detail. First, the tuber and tuber hypertrophy agent will be described.
本発明にかかる塊根 ·塊茎肥大促進剤は、 前記一般式 ( D で示され るイ ン ドール骨格含有化合物、 前記一般式 ( 2 ) で示されるベンゼン骨 格含有化合物、 および、 前記一般式 ( 3 ) で示されるナフタ レン骨格含 有化合物からなる群より選ばれる少なく とも一種の化合物を含んでいる つまり、 本発明にかかる塊根 ·塊茎肥大促進剤は、 有効成分として上記 化合物を含んでいる。 尚、 これら化合物が塊根 '塊茎の肥大を促進させ る生理活性を備えていることは、 全く予期できないことである。  The agent for promoting tuber root and tuber hypertrophy according to the present invention comprises: an indole skeleton-containing compound represented by the general formula (D); a benzene skeleton-containing compound represented by the general formula (2); )) Contains at least one compound selected from the group consisting of naphthalene skeleton-containing compounds, that is, the tuber / tuber hypertrophy promoter of the present invention contains the above compound as an active ingredient. However, it is completely unexpected that these compounds have a bioactivity that promotes tuberous root tuber hypertrophy.
前記一般式 ( 1 ) で示されるイ ン ドール骨格含有化合物としては、 具 体的には、 例えば、 イン ドール— 3 —カルボン酸、 4 一クロ口イ ン ド一 ル一 3 —力ルボン酸、 4 —メ トキシイ ン ドールー 3 —力ルボン酸、 イ ン ドール— 3 ―酢酸 ( 3 _イ ン ドリル酢酸) 、 4 —クロ口イ ン ドールー 3 一酢酸、 4 —メ トキシイ ン ドール— 3 —酢酸、 イ ン ドール— 3 —プロピ オン酸、 4 —クロ口イン ドール一 3 —プロピオン酸、 4 ーメ トキシイ ン ドール一 3 —プロピオン酸、 イ ン ドール— 3 —酪酸、 4 一クロ口イ ン ド —ルー 3 —酪酸、 4 —メ トキシイン ドールー 3 —酪酸、 並びに、 これら 化合物のアルカリ金属塩やアルカリ土類金属塩、 エステル、 或いは、 こ れら化合物が単糖またはォリ ゴ糖と結合してなる配糖体等が挙げられる。 そして、 R 1 (および R 2 ) で表される置換基にエステル結合を有し ている化合物、 つまり、 エステル結合を有しているイ ン ドール骨格含有 化合物は、 植物により一層吸収され易い。 尚、 エステル結合を有してい るィ ン ドール骨格含有化合物は、 植物に吸収された後、 該エステルが加 水分解されてカルボキシル基 (カルボン酸) に変化することにより、 生 理活性を示す。 Specific examples of the indole skeleton-containing compound represented by the general formula (1) include, for example, indole-3-carboxylic acid, 4-chloroindole-13-caprolubonic acid, 4—Methoxyindole 3—Capillonic acid, indole—3-Acetic acid (3_indolylacetic acid), 4—Clotindole-3-monoacetic acid, 4—Methoxyindole—3—acetic acid, Indole—3—propionic acid, 4—cloindole—3—propionic acid, 4-methoxyindole—3—propionic acid, indole—3—butyric acid, 4 Rhu 3-butyric acid, 4-methoxyindole 3-butyric acid, and alkali metal or alkaline earth metal salts, esters or these compounds of these compounds Glycosides formed by combining these compounds with monosaccharides or oligosaccharides are exemplified. A compound having an ester bond in the substituent represented by R 1 (and R 2 ), that is, an indole skeleton-containing compound having an ester bond is more easily absorbed by plants. The indole skeleton-containing compound having an ester bond exhibits physiological activity by being hydrolyzed and converted into a carboxyl group (carboxylic acid) after being absorbed by a plant.
また、 前記一般式 ( 1 ) 中、 R 2 で表される置換基がアルカリ金属ま たはアル力 リ土類金属である化合物、 つまり、 塩を形成しているィ ン ド ール骨格含有化合物は、 より一層安定であるので、 貯蔵 · 保存等に優れ ている。 該ァルカ リ金属と しては、 具体的には、 例えば、 ナ ト リ ウム、 力リ ゥム等が挙げられる。 また、 アル力 リ土類金属としては、 具体的に は、 例えば、 カルシウム等が挙げられる。 Further, in the general formula (1), a compound in which the substituent represented by R 2 is an alkali metal or an alkaline earth metal, that is, an indole skeleton-containing compound that forms a salt Is more stable, and is excellent in storage and preservation. Specific examples of the alkali metal include sodium and steel. Further, specific examples of the alkaline earth metal include calcium and the like.
前記一般式 ( 1 ) で示されるイ ン ドール骨格含有化合物のうち、 Xで 表される置換基が水素原子である場合には、 R 1 (および R 2 ) で表さ れる置換基が— C H O基、 — C H 2 C H O基、 _ C H 2 C N基、 一 C〇 O H基、 — C H 2 C O O H基、 _ C H 2 C O O C H 3 基、 — C H 2 C H 2 C O O H基、 — C H 2 C H 2 C H 2 C O O H基、 および、 R 2 が単糖 の配糖体またはオリ ゴ糖の配糖体である _ C H 2 C 00 R 2 基である化 合物が天然化合物であり、 また、 Xで表される置換基が塩素原子である 場合には、 R 1 (および R 2 ) で表される置換基が一 C H 2 C O O H基、 および、 — C H 2 C 00 C H a 基である化合物が天然化合物であり、 さ らに、 Xで表される置換基がメ トキシ基である場合には、 R 1 で表され る置換基が一 C H 2 C N基である化合物が天然化合物である。 尚、 これ ら天然化合物が塊根 · 塊茎の肥大を促進させる生理活性を備えているこ とは、 全く予期できないこ とである。 When the substituent represented by X in the indole skeleton-containing compound represented by the general formula (1) is a hydrogen atom, the substituent represented by R 1 (and R 2 ) is —CHO Group, — CH 2 CHO group, _ CH 2 CN group, one C〇OH group, — CH 2 COOH group, _ CH 2 COOCH 3 group, — CH 2 CH 2 COOH group, — CH 2 CH 2 CH 2 COOH group And R 2 is a monosaccharide glycoside or an oligosaccharide glycoside _ CH 2 C 00 A compound in which R 2 is a natural compound, and a substituent represented by X When is a chlorine atom, a compound in which the substituent represented by R 1 (and R 2 ) is one CH 2 COOH group and —CH 2 C 00 CH a group is a natural compound, and When the substituent represented by X is a methoxy group, the compound in which the substituent represented by R 1 is a CH 2 CN group is a natural compound. In addition, this It is completely unexpected that natural compounds have the physiological activity of promoting tuber and tuber hypertrophy.
そ して、 天然化合物であるィ ン ドール骨格含有化合物と しては、 例え ば、 Xで表される置換基が水素原子であり、 R 1 で表される置換基が一 C H 2 C 00 H基であるイ ン ドールー 3 —酢酸、 Xで表される置換基が 塩素原子であり、 R 1 で表される置換基が— C H 2 C O O H基である 4 一ク ロ口イ ン ドールー 3 —酢酸、 Xで表される置換基が塩素原子であり、 R 1 で表される置換基が一 C H 2 C 00 C H 3 基であるメチル— 4 ーク ロロイ ン ドールー 3 —アセテー ト、 Xで表される置換基が水素原子であ り、 R 1 で表される置換基が一 C H 2 C H 2 C O O H基であるイ ン ド一 ルー 3 —プロピオン酸、 Xで表される置換基が水素原子であり、 R 1 で 表される置換基が _ C H 2 C H 2 C H 2 C 00 H基であるイ ン ドール— 3 —酪酸等が挙げられる。 例えば、 4 一クロ口イ ン ドールー 3 —酢酸や そのメ チルエステルは、 例えば食用に供されるェン ドウの未熟種子等に 含まれており、 該未熟種子等から取り出すことができる。 また、 4 ーク 口ロイ ン ドール一 3 —酢酸やそのメチルエステルは、 合成によって大量 生産することが比較的容易である。 Their to, is a fin d'skeleton-containing compound is a naturally occurring compound, For example, the substituent represented by X is a hydrogen atom, one substituent represented by R 1 CH 2 C 00 H Group indole-3 —acetic acid, the substituent represented by X is a chlorine atom, and the substituent represented by R 1 is —CH 2 COOH group 4 1-closed indole-3 —acetic acid Wherein the substituent represented by X is a chlorine atom, and the substituent represented by R 1 is a CH 2 C 00 CH 3 group, methyl—4 chloroindol—3—acetate, represented by X In which the substituent represented by R 1 is a hydrogen atom, and the substituent represented by R 1 is a CH 2 CH 2 COOH group, and the substituent represented by X is a hydrogen atom. And indole-3-butyric acid in which the substituent represented by R 1 is a —CH 2 CH 2 CH 2 C 00 H group. For example, 4-monoindole-3-acetic acid and its methyl ester are contained in, for example, immature seeds of edible endow and can be extracted from the immature seeds. In addition, it is relatively easy to mass-produce 4-Lokundole-13-acetic acid and its methyl ester by synthesis.
前記一般式 ( 2 ) で示されるベンゼン骨格含有化合物と しては、 具体 的には、 例えば、 p—クロロフエノキシ酢酸、 2, 4 ージクロロフエノ キシ酢酸、 4 —クロ口 — 2 —メ チルフヱノキシ酢酸、 並びに、 これら化 合物のアルカ リ金属塩やアルカ リ土類金属塩、 エステル、 或いは、 これ ら化合物が単糖またはォリ ゴ糖と結合してなる配糖体等が挙げられる。 前記一般式 ( 3 ) で示されるナフタ レン骨格含有化合物と しては、 具 体的には、 1 —ナフチル酢酸 (ナフタ レン _ 1 —酢酸) 、 1 —ナフチル ァセ トアミ ドが挙げられる。 Examples of the benzene skeleton-containing compound represented by the general formula (2) include, for example, p-chlorophenoxyacetic acid, 2,4-dichlorophenoxyacetic acid, 4-chloro-2-hydroxymethyl-2-acetic acid, In addition, alkali metal salts and alkaline earth metal salts of these compounds, esters, and glycosides obtained by combining these compounds with monosaccharides or oligosaccharides are also included. Specific examples of the naphthalene skeleton-containing compound represented by the general formula (3) include 1-naphthylacetic acid (naphthalene_1-acetic acid) and 1-naphthyl Acetate amide.
これらイ ン ドール骨格含有化合物、 ベンゼン骨格含有化合物、 および、 ナフタ レ ン骨格含有化合物は、 一種類のみを用いてもよく、 また、 二種 類以上を併用してもよい。 上記例示の化合物のうち、 ィ ン ドール骨格含 有化合物がより好ま しい。 また、 イ ン ドール骨格含有化合物が天然化合 物であることがさ らに好ま しく、 イ ン ドール骨格含有化合物が 4 一クロ ロイ ン ドール一 3 —酢酸および/またはそのエステルであることが特に 好ま しい。  These indole skeleton-containing compounds, benzene skeleton-containing compounds and naphthalene skeleton-containing compounds may be used alone or in combination of two or more. Among the compounds exemplified above, an indole skeleton-containing compound is more preferable. It is more preferable that the indole skeleton-containing compound is a natural compound, and it is particularly preferable that the indole skeleton-containing compound is 4-chloroindol-13-acetic acid and / or an ester thereof. New
上記化合物の製造方法は、 特に限定されるものではなく、 植物から一 般的手法を用いて取り出す方法、 或いは、 合成によって製造する方法等 を採用することができ、 比較的容易に大量生産することができる。 イ ン ドール環の 4位に置換基を有する上記ィ ン ドール骨格含有化合物を合成 する反応や、 ベンゼン骨格含有化合物を合成する反応、 ナフタ レ ン骨格 含有化合物を合成する反応は、 比較的簡単であり、 公知の手法を採用す ることができる。  The method for producing the above compound is not particularly limited, and a method of extracting from a plant using a general method, a method of producing by synthesis, or the like can be adopted. Can be. The reaction for synthesizing the indole skeleton-containing compound having a substituent at the 4-position of the indole ring, the reaction for synthesizing the benzene skeleton-containing compound, and the reaction for synthesizing the naphthalene skeleton-containing compound are relatively simple. Yes, a known method can be adopted.
本発明にかかる塊根 ·塊茎肥大促進剤は、 有効成分と して上記化合物 を含んでいる。 上記化合物は、 そのまま使用することができるが、 必要 に応じて、 その効果を助長若しく は安定化させるために、 例えば、 農薬 に用いられる補助剤等の各種補助剤と混合して、 液剤、 粉剤、 粒剤、 顆 粒剤、 水和剤、 フロアブル剤、 乳剤、 ペース ト剤等の種々の製剤形態で 以て使用することもできる。 つまり、 本発明にかかる塊根 ·塊茎肥大促 進剤は、 必要に応じて上記の補助剤を含んでいてもよく、 従って、 該塊 根 · 塊茎肥大促進剤は、 上記種々の製剤形態を採ることができる。  The agent for promoting tuberous root and tuber hypertrophy according to the present invention contains the above compound as an active ingredient. The above compounds can be used as they are, but if necessary, in order to promote or stabilize the effect, for example, by mixing with various adjuvants such as adjuvants used in agricultural chemicals, It can also be used in various formulations such as powders, granules, condyles, wettable powders, flowables, emulsions, pastes and the like. In other words, the tuberous root and tuber hypertrophy-promoting agent according to the present invention may contain the above-mentioned adjuvant if necessary. Can be.
上記の補助剤としては、 例えば、 溶剤 (希釈剤) 、 乳化剤、 分散剤、 各種担体、 各種基材、 展着剤、 湿展剤、 固着剤、 崩壊剤等が挙げられる そして、 塊根 ·塊茎肥大促進剤である上記各種製剤は、 そのまま使用す ることができるが、 必要に応じて、 水で所定の濃度に希釈して使用する こともできる。 尚、 上記化合物が塩を形成する等して水溶性を備えてい る場合には、 上記溶剤を用いなく とも、 塊根 ·塊茎肥大促進剤を水で所 定の濃度に希釈することができる。 Examples of the above auxiliary agents include solvents (diluents), emulsifiers, dispersants, Examples include various carriers, various substrates, spreading agents, wetting agents, fixing agents, disintegrating agents, and the like.The above-mentioned various preparations, which are tuber and tuber hypertrophy promoters, can be used as they are. Accordingly, it can be used after being diluted to a predetermined concentration with water. When the above compound has water solubility by forming a salt or the like, the tuber / tuber hypertrophy promoter can be diluted to a predetermined concentration with water without using the above solvent.
液剤やフロアブル剤、 乳剤 (エマルシヨ ン) を調製するのに好適な溶 剤と しては、 具体的には、 例えば、 トルエン、 キシレン等の芳香族炭化 水素類 ; メ チルアルコール、 エチルアルコール、 イ ソプロピルアルコー ル、 ブチルアルコール、 エチレングリ コール等のァルコ一ル類 ; ァセ ト ン、 メ チルェチルケ ト ン等のケ ト ン類 ; N , N —ジメチルホルムア ミ ド 等のア ミ ド類 ; ジメチルスルホキシ ド等のスルホキシ ド類 ; シク ロへキ サン、 テ トラ ヒ ドロナフタ レン、 メチルナフタ レン ; 動植物油、 脂肪酸- 脂肪酸エステル ; 等が挙げられるが、 特に限定されるものではない。 こ れら溶剤は、 一種類のみを用いてもよく、 また、 二種類以上を併用して もよい。  Examples of suitable solvents for preparing solutions, flowables, and emulsions (emulsions) include, for example, aromatic hydrocarbons such as toluene and xylene; methyl alcohol, ethyl alcohol, and a). Alcohols such as isopropyl alcohol, butyl alcohol, and ethylene glycol; ketones such as acetone and methylethyl ketone; amides such as N, N-dimethylformamide; dimethyl Sulfoxides such as sulfoxide; cyclohexane, tetrahydronaphthalene, methylnaphthalene; animal and vegetable oils, fatty acid-fatty acid esters; and the like, but are not particularly limited thereto. One of these solvents may be used alone, or two or more thereof may be used in combination.
乳化剤または分散剤としては、 各種界面活性剤を用いることができる ( 該界面活性剤としては、 例えば、 高級アルコール硫酸エステル塩等の陰 ィォン系界面活性剤、 四級ァンモニゥム塩等の陽ィォン系界面活性剤、 ベタイ ン型等の両性界面活性剤、 エーテル型等の非イオン系界面活性剤 (ノニオン系界面活性剤) 等が挙げられる。 界面活性剤を用いることに より、 上記化合物が植物により一層吸収され易く なる。 As the emulsifier or dispersant, various surfactants can be used ( for example, the surfactant is an anionic surfactant such as a higher alcohol sulfate ester salt, or a ionic surfactant such as a quaternary ammonium salt). Surfactants, amphoteric surfactants such as betains, etc., and nonionic surfactants (nonionic surfactants) such as ethers, etc. By using a surfactant, the above compounds can be more effectively used in plants. It becomes easier to be absorbed.
上記化合物を担持するのに好適な担体としては、 具体的には、 例えば ク レー、 カオリ ン、 タルク、 珪藻土、 シリカ、 アルミナ、 炭酸カルシゥ ム、 ベン トナイ ト (モンモリ ロナイ ト) 、 長石、 石英、 おが屑等が挙げ られるが、 特に限定されるものではない。 これら担体は、 一種類のみを 用いてもよく、 また、 二種類以上を併用してもよい。 Specific examples of the carrier suitable for supporting the compound include, but are not limited to, clay, kaolin, talc, diatomaceous earth, silica, alumina, calcium carbonate, and the like. , Bentonite (montmorillonite), feldspar, quartz, sawdust, etc., but are not particularly limited. These carriers may be used alone or in a combination of two or more.
上記化合物をペース ト状 (剤) にするのに好適な基材と しては、 具体 的には、 例えば、 ワセリ ン、 ラノ リ ン、 合成樹脂、 ゴム等が挙げられる 力く、 特に限定されるものではない。 これら基材は、 一種類のみを用いて もよ く、 また、 二種類以上を併用してもよい。  Suitable base materials for converting the above compound into a paste (agent) include, for example, petrolatum, lanolin, synthetic resin, and rubber. Not something. One of these base materials may be used alone, or two or more may be used in combination.
本発明にかかる塊根 ·塊茎肥大促進剤を適用することができる植物は、 塊根 (球根 ·宿根) や塊茎 (地下茎) を有する植物である。 該植物と し ては、 具体的には、 例えば、 メークイ ンや男爵、 出島等のジャガイモ ( 馬鈴薯) 、 サツマィモ (甘藷) 、 サ トィモ、 ャマイモ、 夕ロイモ、 キヤ ッサバ、 ニンジン、 朝鮮ニンジン、 ダイコン、 二十日ダイ コン、 カブ、 テンサイ、 ゴボウ、 ヮサビ、 食用ユリ、 夕マネギ、 ニンニク、 レンコン、 ラッカセィ等の野菜類 (作物) ; テツボウユリ等のユリ、 チューリ ップ、 フ リ ージア、 グラジオラス、 ヒヤシンス、 球根べゴニァ、 チグリ シァ、 ダリ ア、 カラー、 ァネモネ、 ムスカ リ、 ラナンキュラス、 クロ ッカス、 コルチカム、 スィセン、 アイ リ ス、 ァリ ュウム、 カタク リ、 ォ一二ソガ ラム、 ハブランサス、 グロ ッパ、 リ コ リ ス、 ネリ ネ、 チオノ ドクサ、 ト キソゥ、 雲南 トキソゥ、 ギボウシ、 アカプルコ、 チューべローズ等の花 卉類 ; 等が挙げられるが、 特に限定されるものではない。  Plants to which the agent for promoting tuber and tuber hypertrophy according to the present invention can be applied are plants having tubers (bulbs and lodgings) and tubers (rhizome). Specific examples of the plant include potatoes (potatoes), sweet potatoes (sweet potatoes), sweet potatoes, sweet potatoes such as make-up, baron, and dejima, potatoes, potatoes, evening loimo, sassava, carrots, Korean carrots, radish, Vegetables (crops) such as radish, turnip, sugar beet, burdock, rust, edible lily, evening onion, garlic, lotus root, laccasei; lily, tulip, friesia, gladiolus, hyacinth, etc. Bulb Begonias, Tigrisia, Darias, Colors, Anemones, Musculi, Ranunculus, Crocus, Colchicum, Sissen, Iris, Aryum, Catakuri, Ossigaram, Habransas, Groppa, Li Coli, Nerine, Chiono doxa, Tok ゥ, Yunnan Tok ゥ, Hosta, Acapulco, Tuberose, etc .; and other plants, but are not particularly limited.
塊根 ·塊茎肥大促進剤の使用方法、 即ち、 塊根 ·塊茎肥大促進剤を用 いた植物の処理方法としては、 具体的には、 例えば、 茎葉処理、 土壌処 理、 浸漬処理、 粉剤 (粉末) 処理、 注入処理等を採用することができる が、 特に限定されるものではない。 つま り、 塊根 ·塊茎肥大促進剤の植 物に対する使用部位としては、 茎葉 (地下茎を含む) 、 根 (球根 ·宿根 を含む) 、 種子、 花、 果実等が挙げられるが、 特に限定されるものでは ない。 塊根 ·塊茎肥大促進剤の使用形態としては、 植物に吸収されるこ とによつて該植物に対して生理活性を発揮させることができる手段であ ればよく、 具体的には、 例えば、 撒布、 浸漬、 接触、 注入等が挙げられ る。 要するに、 対象とする植物の種類や使用時期 (使用目的) 等に応じ て、 該植物に最も吸収され易い使用形態を選択すればよい。 Examples of the method of using the tuber / tube enlarger, ie, the method of treating plants using the tuber / tube enlarger, include, for example, foliage treatment, soil treatment, immersion treatment, and powder (powder) treatment. Injection treatment or the like can be employed, but is not particularly limited. In other words, planting of tuber root and tuber hypertrophy Examples of the parts used for objects include foliage (including rhizomes), roots (including bulbs and vines), seeds, flowers, fruits, and the like, but are not particularly limited. The use form of the tuber root / tuber hypertrophy promoter may be any means capable of exerting a physiological activity on the plant by being absorbed by the plant. Specifically, for example, spraying Immersion, contact, injection, and the like. In short, the form of use that is most easily absorbed by the plant may be selected according to the type of the target plant, the time of use (purpose of use), and the like.
塊根 ·塊茎肥大促進剤の使用時期は、 特に限定されるものではないが、 植物が野菜類 (作物) である場合には、 塊根または塊茎が肥大し始める 時期がより好ま しい。 植物が花卉類である場合には、 花が咲いた後、 球 根等が肥大し始める時期がより好ま しい。 また、 例えば花卉類の球根が 分球する前に塊根 ·塊茎肥大促進剤を使用すると、 本球の肥大を促進す ることができる一方、 花卉類の球根が分球した後に塊根 ·塊茎肥大促進 剤を使用すると、 分球の肥大を促進することができる。  The use time of the tuber and tuber thickening promoter is not particularly limited, but when the plant is a vegetable (crop), the time at which the tuber or tuber begins to enlarge is more preferable. When the plant is a flower, it is more preferable that the bulb and the like start to enlarge after the flower blooms. In addition, for example, if a tuber / tuber hypertrophy promoter is used before the bulbs of flowers and plants are separated, the enlargement of the main bulb can be promoted. The use of an agent can promote spheroid hypertrophy.
有効成分である上記化合物の使用量は、 該化合物の組成、 塊根 ·塊茎 肥大促進剤の製剤形態、 対象とする植物の種類、 処理方法、 使用時期 ( 使用目的) 等に応じて設定すればよく、 特に限定されるものではないが- 1 アール当たり、 1 0— 7 g〜 5 gの範囲内がより好ましい。 より具体的 には、 塊根 ·塊茎肥大促進剤を水溶液にして茎葉処理に用いる場合には. 該促進剤を上記化合物の濃度が 0 . 0 0 1 p p m〜 5 0 0 p p m程度と なるように希釈した水溶液を、 1アール当たり、 0 . 1 L〜 2 0 Lの範 囲内で撒布することがより好ましい。 また、 塊根 ·塊茎肥大促進剤を水 溶液にして浸漬処理に用いる場合には、 上記濃度の水溶液に植物を一定 時間浸漬することがより好ま しい。 本発明にかかる塊根 ·塊茎肥大促進剤を使用することによって、 植物 における塊根 (球根 ·宿根) や塊茎 (地下茎) にデンプンを蓄える機能 が向上されるので、 これら塊根や塊茎を、 使用しない場合と比較して重 量比で 1 . 5倍以上、 より好ま しく は 2倍以上に肥大させることができ る。 即ち、 本発明にかかる塊根 ·塊茎肥大促進剤は、 作物増収剤として の機能を備えている。 The amount of the compound used as an active ingredient may be determined according to the composition of the compound, the form of the tuber / tuber hypertrophy promoter, the type of plant to be treated, the treatment method, the time of use (purpose of use), and the like. , but it is not particularly limited - 1 per ares, in the range of 1 0- 7 g to 5 g is more preferable. More specifically, when the tuber and tuber hypertrophy accelerator is used as an aqueous solution for the foliage treatment. The accelerator is diluted so that the concentration of the above compound is about 0.001 ppm to 500 ppm. It is more preferable to spray the prepared aqueous solution within a range of 0.1 L to 20 L per are. In addition, when the tuber and tuber hypertrophy promoter is used as an aqueous solution for the immersion treatment, it is more preferable to immerse the plant in the aqueous solution having the above concentration for a certain period of time. By using the tuber and tuber hypertrophy-promoting agent according to the present invention, the function of accumulating starch in tubers (bulbs and lodgings) and tubers (rhizome) in plants is improved, so that these tubers and tubers are not used. It can be enlarged to 1.5 times or more, more preferably 2 times or more by weight. That is, the tuber and tuber hypertrophy promoter according to the present invention has a function as a crop yield enhancer.
以上のように、 本発明にかかる塊根 ·塊茎肥大促進剤は、 前記一般式 ( 1 ) で示されるイ ン ドール骨格含有化合物、 前記一般式 ( 2 ) で示さ れるベンゼン骨格含有化合物、 および、 前記一般式 ( 3 ) で示されるナ フタ レン骨格含有化合物からなる群より選ばれる少なく とも一種の化合 物を含む構成である。 上記化合物は、 野菜類や花卉類等の植物が有する 塊根や塊茎の肥大を促進させる生理活性を有しており、 しかも、 安全性 に優れかつ大量生産することができる。 従って、 上記の構成によれば、 塊根や塊茎の肥大を促進させるのに好適に用いることができる、 安全性 に優れかつ大量生産可能な塊根 ·塊茎肥大促進剤を提供することができ る。  As described above, the tuber and tuber hypertrophy promoter according to the present invention includes an indole skeleton-containing compound represented by the general formula (1), a benzene skeleton-containing compound represented by the general formula (2), and The structure includes at least one compound selected from the group consisting of naphthalene skeleton-containing compounds represented by the general formula (3). The compound has a physiological activity of promoting the enlargement of tuberous roots and tubers of plants such as vegetables and flowers, and is excellent in safety and can be mass-produced. Therefore, according to the above configuration, it is possible to provide a tuber / tuber hypertrophy promoter which is suitably used for accelerating tuber and tuber hypertrophy, and which is excellent in safety and can be mass-produced.
また、 本発明にかかる塊根 ·塊茎肥大促進剤は、 上記イ ン ドール骨格 含有化合物が天然化合物である構成である。 さ らに、 本発明にかかる塊 根 ·塊茎肥大促進剤は、 上記ィ ン ドール骨格含有化合物が 4 -クロロイ ン ドール一 3 —酢酸および Zまたはそのエステルである構成である。 上 記の構成によれば、 該化合物が天然化合物であるので、 例えば植物に残 留した場合においても、 安全性により一層優れた塊根 ·塊茎肥大促進剤 を提供することができる。 次に、 作物増収剤について説明する。 In addition, the tuber / tuber hypertrophy promoter of the present invention has a configuration in which the indole skeleton-containing compound is a natural compound. Further, the tuber / tuber hypertrophy promoter according to the present invention has a configuration in which the indole skeleton-containing compound is 4-chloroindole-13-acetic acid and Z or an ester thereof. According to the above configuration, since the compound is a natural compound, it is possible to provide a tuber / tuber hypertrophy promoting agent which is more excellent in safety even when it is left in a plant, for example. Next, the crop increasing agent will be described.
本発明にかかる作物増収剤は、 前記一般式 ( 1 ) で示されるイ ン ドー ル骨格含有化合物を含んでいる。 つまり、 本発明にかかる作物増収剤は、 有効成分と して上記化合物を含んでいる。 尚、 該化合物、 特に、 天然化 合物が各種作物 (植物) の花数や穂数の増加、 分蘖、 或いは、 実 (果実、 種子) の肥大を促進させる生理活性を備えていることは、 既知の類似化 合物からは全く予期できないことである。  The crop increasing agent according to the present invention contains an indole skeleton-containing compound represented by the general formula (1). That is, the crop increasing agent according to the present invention contains the above compound as an active ingredient. It should be noted that the compound, in particular, the natural compound has a physiological activity that promotes the increase of the number of flowers and ears of various crops (plants), the tillering, or the hypertrophy of fruits (fruits, seeds). It is completely unexpected from known analogs.
ィ ン ドール骨格含有化合物は、 一種類のみを用いてもよく、 また、 二 種類以上を併用してもよい。 イ ン ドール骨格含有化合物は、 天然化合物 であることがより好ま しい。 そして、 上記例示の化合物のうち、 イ ン ド ール— 3 —酢酸、 4 一 ク ロ 口イ ン ドール— 3 —酢酸、 イ ン ドール— 3 — 酪酸、 および、 これら化合物のエステルからなる群より選ばれる少なく とも一種の化合物であることが特に好ま しく、 4 一クロ口イ ン ドール一 3 一酢酸、 および、 ィ ン ドール— 3 —酪酸が最も好ま しい。  As the indole skeleton-containing compound, only one kind may be used, or two or more kinds may be used in combination. More preferably, the indole skeleton-containing compound is a natural compound. Among the compounds exemplified above, the group consisting of indole-3—acetic acid, 4-cycloindole-3—acetic acid, indole-3-butyric acid, and esters of these compounds It is particularly preferred that it be at least one compound selected, most preferred are 4-chloroindole-13-acetic acid and indole-3-butyric acid.
本発明にかかる作物増収剤は、 有効成分として上記化合物を含んでい る。 上記化合物は、 そのまま使用することができるが、 必要に応じて、 その効果を助長若しく は安定化させるために、 例えば、 農薬に用いられ る補助剤等の各種補助剤と混合して、 前記例示の通り、 種々の製剤形態 で以て使用することもできる。 つまり、 本発明にかかる作物増収剤は、 必要に応じて前記の補助剤を含んでいてもよく、 従って、 該作物増収剤 は、 前記種々の製剤形態を採ることができる。 そして、 作物増収剤であ る上記各種製剤は、 そのまま使用することができるが、 必要に応じて、 水で所定の濃度に希釈して使用することもできる。 尚、 上記化合物が塩 を形成する等して水溶性を備えている場合には、 上記溶剤を用いなく と も、 作物増収剤を水で所定の濃度に希釈することができる。 The crop increasing agent according to the present invention contains the above compound as an active ingredient. The above compounds can be used as they are, but if necessary, in order to promote or stabilize the effect, for example, by mixing with various adjuvants such as adjuvants used in pesticides, As illustrated, it can also be used in various formulation forms. That is, the crop increasing agent according to the present invention may contain the above-mentioned auxiliary agent as needed, and therefore, the crop increasing agent can take the above-mentioned various formulation forms. The above-mentioned various preparations, which are crop-harvesting agents, can be used as they are, but if necessary, they can be used after being diluted to a predetermined concentration with water. When the compound is water-soluble, for example, by forming a salt, the solvent must be used. Also, the crop enhancer can be diluted to a predetermined concentration with water.
ところで、 自然界のイ ン ドール系植物ホルモンは、 1 X 1 0 — 8モル/ L ( 1 0 - 8 M ) 程度の極めて低濃度で存在しているにも関わらず、 種々 の効果を発揮している。 しかしながら、 該イ ン ドール系植物ホルモンは、 植物内では安定して存在することができるものの、 例えば水道水中では、 該水道水に残留している塩素と反応することによつて分解されてしまう つま り、 従来、 一般的なィ ン ドール系植物ホルモンを植物に撒布しても、 殆ど効果が得られなかった原因は、 塩素が酸化剤として作用し、 イ ン ド —ル系植物ホルモンの分解を引き起こしていたためである。 Meanwhile, Lee emissions doll system phytohormones nature, 1 X 1 0 - 8 mol / L (1 0 - 8 M ) of about despite being present at very low concentrations, it exerts various effects I have. However, the indole plant hormone can be stably present in a plant, but is decomposed in, for example, tap water by reacting with chlorine remaining in the tap water. Conventionally, spraying common indole-based plant hormones on plants has had little effect because chlorine acts as an oxidizing agent and degrades indole-based plant hormones. Because it was causing it.
そこで、 本発明にかかる作物増収剤を、 例えば水道水を用いて希釈し た状態で使用する場合には、 該作物増収剤は、 還元剤を含んでいること が好ま しい。 該還元剤と しては、 具体的には、 例えば、 重亜硫酸ナ ト リ ゥム等が挙げられるが、 塩素等の酸化剤と反応し、 かつ、 植物に対して 悪影響を及ぼさない化合物であればよく 、 特に限定されるものではない また、 還元剤の使用量は、 水道水に残留している塩素の量等に応じて設 定すればよい。  Therefore, when the crop increasing agent according to the present invention is used in a state diluted with tap water, for example, the crop increasing agent preferably contains a reducing agent. Specific examples of the reducing agent include sodium bisulfite and the like. However, any compound that reacts with an oxidizing agent such as chlorine and has no adverse effect on plants can be used. There is no particular limitation, and the amount of the reducing agent used may be set according to the amount of chlorine remaining in the tap water.
これにより、 塩素によってィ ン ドール骨格含有化合物が分解されるこ とが無く なるので、 作物増収剤は、 水道水を用いて希釈した場合におい ても、 より低濃度で以て、 その効果を充分に発揮することができる。 尚、 作物増収剤を、 蒸留水等の、 塩素を含まない水を用いて希釈することは、 費用等が嵩むため、 実用的ではない。 また、 還元剤を用いる代わりに、 前記溶剤を用いて作物増収剤を希釈することにより、 イ ン ドール骨格含 有化合物の分解を回避することもできる。  As a result, the compound containing the indole skeleton is not decomposed by chlorine, so that even when diluted with tap water, the effect of the crop enhancer can be sufficiently improved at a lower concentration. Can be demonstrated. It is not practical to dilute the crop-producing agent with water that does not contain chlorine, such as distilled water, because of the high cost. Further, instead of using the reducing agent, the decomposition of the indole skeleton-containing compound can be avoided by diluting the crop yield using the solvent.
本発明にかかる作物増収剤を適用することができる作物は、 花数や穂 数の増加、 分蘖、 或いは、 実 (果実、 種子) の肥大を促進させて収量を 増加させることができる植物であればよい。 該植物と しては、 具体的に は、 例えば、 大豆、 黒大豆、 エン ドゥ豆 (サャエン ドゥ) 、 小豆、 空豆、 ピーナツッ等の豆類 ; 小麦、 大麦、 力ラスムギ等の麦類 ; トウモロコシ、 イネ、 ヮタ、 ヒマヮ リ、 ゴマ、 ソバ ; 甜菜 (ビー ト) ; イチゴ、 西瓜、 メ 口ン等の果物類 ; カボチヤ、 トマ ト等の、 いわゆる実の成る野菜類 ; 等が挙げられるが、 特に限定されるものではない。 The crops to which the crop yield enhancer according to the present invention can be applied include the number of flowers and ears Any plant that can increase the number, increase tillering, or increase the yield of fruits (fruits, seeds) by increasing the yield can be used. Specific examples of the plant include beans such as soybeans, black soybeans, endu beans (sayaendu), red beans, soybeans, and peanuts; wheats such as wheat, barley, and barley; corn and rice. , Ivy, castor, sesame, buckwheat; sugar beet; fruits, such as strawberries, watermelons, apples; so-called vegetables, such as pumpkin and tomato; It is not limited.
作物増収剤の使用方法、 即ち、 作物増収剤を用いた植物の処理方法と しては、 具体的には、 例えば、 播種時においては、 土壌に対しては混和 処理 (土壌処理) 、 種子に対しては浸漬処理や粉剤 (粉末) 処理 ; 発芽 した後の時期においては、 土壌に対しては注入処理 (灌注処理) 、 植物 に対しては茎葉処理 ; 等を採用することができるが、 特に限定されるも のではない。 つまり、 作物増収剤の植物に対する使用部位としては、 茎 葉 (地下茎を含む) 、 根 (球根 ·宿根を含む) 、 種子 (未熟種子を含む ) 、 花、 果実等が挙げられるが、 該植物の種類や使用目的に応じて選択 すればよく、 特に限定されるものではない。  The method of using the crop enhancer, that is, the method of treating the plant with the crop enhancer, is, for example, at the time of sowing, mixing treatment (soil treatment) for soil, For immersion and dust (powder) treatments; in the period after germination, injection treatment (irrigation treatment) for soil and foliage treatment for plants can be used. It is not limited. In other words, the sites where the crop-producing agent is used for plants include foliage (including rhizomes), roots (including bulbs and puddles), seeds (including immature seeds), flowers, fruits, and the like. The selection may be made according to the type and purpose of use, and is not particularly limited.
作物増収剤の使用形態と しては、 植物に吸収されることによって該植 物に対して生理活性を発揮させることができる手段であればよく、 具体 的には、 例えば、 撒布、 浸漬、 接触、 注入等が挙げられる。 要するに、 対象とする植物の種類や使用時期 (使用目的) 等に応じて、 該植物に最 も吸収され易い使用形態を選択すればよい。  The form of use of the crop-harvesting agent may be any means capable of exerting a physiological activity on the plant by being absorbed by the plant. Specifically, for example, spraying, dipping, contacting , Injection and the like. In short, the form of use that is most easily absorbed by the plant may be selected according to the type of the target plant and the time of use (purpose of use).
作物増収剤の使用時期は、 植物の種類や使用目的に応じて設定すれば よく 、 特に限定されるものではないが、 例えば、 播種時、 本葉が数枚揃 う時期、 開花前、 開花時、 未熟種子が生成される時期 (開花後) 等が挙 げられる。 The use time of the crop-harvesting agent may be set according to the type of plant and the purpose of use, and is not particularly limited. For example, at the time of sowing, when several true leaves are prepared, before flowering, and at the time of flowering , When immature seeds are produced (after flowering) I can do it.
有効成分である上記化合物の使用量は、 該化合物の組成、 作物増収剤 の製剤形態、 対象とする植物の種類、 処理方法、 使用時期 (使用目的) 等に応じて設定すればよく、 特に限定されるものではないが、 1 アール 当たり、 1 0— 7 g〜 5 gの範囲内がより好ま しい。 より具体的には、 作 物増収剤を水溶液にして茎葉処理に用いる場合には、 該作物増収剤を上 記化合物の濃度が 0 . 0 0 1 p p m〜 5 0 0 p p m程度となるように希 釈した水溶液を、 1 アール当たり、 0 . 1 L〜 1 0 0 Lの範囲内で撒布 することがより好ま しい。 また、 作物増収剤を水溶液にして浸漬処理に 用いる場合には、 上記濃度の水溶液に種子または植物 (発芽後) を一定 時間浸漬することがより好ま しい。 尚、 上記水溶液を用いる代わりに、 つまり、 作物増収剤を水に溶解させた (水で希釈した) 状態で用いる代 わりに、 必要に応じて、 作物増収剤を水と前記溶剤との混合液に溶解さ せた (混合液で希釈した) 状態で用いること、 或いは、 作物増収剤を前 記溶剤に溶解させた (溶剤で希釈した) 状態で用いることもできる。 本発明にかかる作物増収剤を使用することによって、 植物の花数や穂 数の増加、 分蘖、 或いは、 実の肥大を促進させることができるので、 各 種作物の収量を、 使用しない場合と比較して増加させることができる。 The amount of the active compound to be used may be determined according to the composition of the compound, the form of the crop enhancer, the type of the target plant, the treatment method, the time of use (purpose of use), and the like, and is particularly limited. It is not limited to, a per one are, 1 0- 7 g~ 5 g range, more preferable arbitrariness of. More specifically, when the crop enhancer is used as an aqueous solution and used for foliage treatment, the crop enhancer is diluted so that the concentration of the compound is about 0.001 ppm to 500 ppm. More preferably, the diluted aqueous solution is sprayed in a range of 0.1 L to 100 L per are. In addition, when the crop-enhancing agent is used as an aqueous solution for immersion treatment, it is more preferable to immerse the seed or plant (after germination) in the aqueous solution having the above concentration for a certain period of time. Instead of using the above aqueous solution, that is, instead of using the crop enhancer dissolved in water (diluted with water), the crop enhancer may be added to a mixture of water and the solvent as necessary. It can be used in a state of being dissolved (diluted with a mixed solution), or in a state in which the crop enhancer is dissolved in the above-mentioned solvent (diluted with the solvent). The use of the crop-increasing agent according to the present invention can increase the number of flowers and ears of a plant, promote tillering, or promote the actual hypertrophy, so that the yield of various crops can be compared with the case where no crop is used. And can be increased.
以上のように、 本発明にかかる作物増収剤は、 前記一般式 ( 1 ) で示 されるイ ン ドール骨格含有化合物を含む構成である。 上記化合物は、 各 種作物の花数や穂数の増加、 分蘖、 或いは、 実の肥大を促進させる生理 活性を有している。 また、 化合物は、 安全性に優れかつ大量生産するこ とができる。 従って、 上記の構成によれば、 各種作物の花数や穂数の増 加、 分蘖、 或いは、 実の肥大を促進させて収量を増加させるのに好適に 用いることができる、 安全性に優れかつ大量生産可能な作物増収剤を提 供することがでぎる。 As described above, the crop increasing agent according to the present invention is configured to include the indole skeleton-containing compound represented by the general formula (1). The compounds have a physiological activity that promotes the increase in the number of flowers and ears, tillering, or actual hypertrophy of various crops. Further, the compound is excellent in safety and can be mass-produced. Therefore, according to the above-mentioned configuration, it is suitable for increasing the number of flowers and ears of various crops, tillering, or promoting the hypertrophy of fruits to increase the yield. It is possible to provide safe and mass-producible crop enhancers that can be used.
また、 本発明にかかる作物増収剤は、 上記イ ン ドール骨格含有化合物 が天然化合物である構成である。 さ らに、 本発明にかかる作物増収剤は、 上記イ ン ドール骨格含有化合物が、 イ ン ドールー 3 —酢酸、 4 一クロ口 イ ン ドールー 3 —酢酸、 イ ン ドール— 3 —酪酸、 および、 これら化合物 のエステルからなる群より選ばれる少なく とも一種の化合物である構成 である。 上記の構成によれば、 該化合物が天然化合物であるので、 例え ば作物に残留した場合においても、 安全性により一層優れた作物増収剤 を提供することができる。  Further, the crop increasing agent according to the present invention has a configuration in which the indole skeleton-containing compound is a natural compound. Further, the crop-increasing agent according to the present invention is characterized in that the indole skeleton-containing compound comprises indole-3-acetic acid, 4-monoindole-3-acetic acid, indole-3-butyric acid, and The composition is at least one compound selected from the group consisting of esters of these compounds. According to the above configuration, since the compound is a natural compound, even if it remains in the crop, for example, it is possible to provide a crop-enhancing agent which is more excellent in safety.
また、 本発明にかかる作物増収剤は、 還元剤をさ らに含む構成である c 上記の構成によれば、 作物増収剤を水道水を用いて希釈した場合におい ても、 より低濃度で以て、 その効果を充分に発揮することができる。 Moreover, crop sales agent of the present invention, according to the configuration of the c the a configuration including the to et the reducing agent, also crop sales agent odor when diluted with tap water, than at lower concentrations Therefore, the effect can be fully exhibited.
尚、 本発明にかかる塊根,塊茎肥大促進剤、 並びに、 作物増収剤は、 必要に応じて、 各種の植物生長調節剤、 肥料 (糖類、 アミ ノ酸、 有機酸- 各種ミネラル等) 、 除草剤、 殺黴剤、 殺虫剤、 殺ダニ剤、 殺線虫剤、 農 園芸用殺菌剤、 土壌殺菌剤、 土壌改良剤等の薬剤と併用することもでき る o 本発明のさ らに他の目的、 特徴、 および優れた点は、 以下に示す記載 によって充分判るであろう。 また、 本発明の利益は、 次の説明で明白に なるであろう。 発明を実施するための最良の形態 以下、 実施例により、 本発明をさ らに具体的に説明するが、 本発明は これらにより何ら限定されるものではない。 尚、 実施例 1〜 1 4 は、 塊 根 · 塊茎肥大促進剤にかかる実施例であり、 実施例 1 5〜 2 2 は、 作物 増収剤にかかる実施例である。 In addition, the tuber root and tuber hypertrophy promoter and the crop-promoting agent according to the present invention may be various plant growth regulators, fertilizers (sugars, amino acids, organic acids-various minerals, etc.), herbicides, if necessary. , Fungicides, insecticides, acaricides, nematicides, fungicides for agriculture and horticulture, soil fungicides, soil improvers, etc.o Still other objects of the present invention The features, characteristics, and strengths will be more fully understood from the description below. Also, the benefits of the present invention will become apparent in the following description. BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described more specifically with reference to Examples, but the present invention is not limited thereto. It should be noted that Examples 1 to 14 are examples relating to the tuberous root and tuber hypertrophy promoter, and Examples 15 to 22 are examples relating to the crop increasing agent.
〔実施例 1〕  (Example 1)
本発明にかかる塊根 ·塊茎肥大促進剤を用いてサツマィモの処理を行 つた。 先ず、 互いに生長状態がほぼ揃っている市販のサツマィモのつる (複数本) を選択し、 先端部から 5枚の葉が茎に残るようにして水切り した。 次いで、 これら先端部分を、 根元側の 3葉分の茎が土壌に埋まる ようにして畑に植え付けた。 上記先端部分同士の植え付け間隔は、 約 6 0 c mと した。  The sweet potato was treated using the tuber and tuber hypertrophy promoter of the present invention. First, commercially available sweet potato vines (several vines) whose growth conditions were almost the same were selected and drained so that five leaves remained on the stem from the tip. Next, these tips were planted in a field so that the stems of the three leaves at the base were buried in the soil. The planting interval between the tip portions was about 60 cm.
そして、 2か月間経過後、 畑に植え付けた上記サッマイモ (複数株) に、 塊根 ·塊茎肥大促進剤である 4 一クロ口イ ン ド一ルー 3 -酢酸 (以 下、 4 — C 1 一 I A Aと略す) の水溶液、 メチル— 4 —ク ロ口イ ン ドー ル— 3 —アセテー トの水溶液、 イ ン ドール— 3 —酢酸 (以下、 I A Aと 略す) の水溶液、 1 一ナフチルァセ トア ミ ドの水溶液、 または、 p —ク ロロフ ノキシ酢酸の水溶液を、 各水溶液ごとに 4株ずつ所定量撒布す ることにより、 茎葉処理を行った。 4 一 C 1 一 I A A水溶液の濃度は、 1 X 1 0— 4モル Z L、 3 X 1 0— 5モル/し、 1 X 1 0— 5モル Z L、 およ び、 1 X 1 0 — 6モル Z Lの 4種類とした。 また、 メチルー 4 —クロロイ ン ドール— 3 —アセテー ト水溶液、 I A A水溶液、 1 —ナフチルァセ ト アミ ド水溶液、 および、 p—クロロフヱノキシ酢酸水溶液の濃度は、 1 X 1 0 — 5モル Z Lとした。 また、 上記水溶液の代わりに水を所定量撒布 したサツマィモ ( 4株) を、 比較の対象と した (以下、 処理を行わない 植物をコ ン トロールと記す) 。 After a lapse of two months, the above sweet potatoes (several strains) planted in the field were added to the tuberous root and tuber hypertrophy-promoting agent, 4-l-in-l-l-3-acetic acid (hereinafter, 4-C1 IAA). Aqueous solution of methyl-4—cloindole—3—acetate aqueous solution, indole—3—acetic acid (hereinafter abbreviated as IAA) aqueous solution, and aqueous solution of 1-naphthylacetamide A foliage treatment was performed by spraying a predetermined amount of an aqueous solution of p-chlorofunooxyacetic acid, or four of each aqueous solution. 4 one C 1 concentration one IAA aqueous solution, 1 X 1 0- 4 mol ZL, 3 X 1 0- 5 mol / to, 1 X 1 0- 5 mol ZL, and, 1 X 1 0 - 6 mol There are four types of ZL. Furthermore, methyl-4 - Kuroroi emissions Doll - 3 - Asete DOO aqueous IAA solution, 1 - Nafuchiruase DOO ami de solution, and the p- Kurorofuwenokishi aqueous acetic acid concentration, 1 X 1 0 - was 5 mol ZL. In addition, Satsumaimo (4 strains) in which a predetermined amount of water was sprayed instead of the above aqueous solution was used for comparison (hereinafter, no treatment is performed). Plants are referred to as controls).
茎葉処理を行ってから 3か月間経過後、 全てのサツマィモを掘り出し て、 収穫量、 即ち、 芋 (塊根) の重量を測定し、 1個当たりのサッマイ モの平均重量 (表 1で 1個重量と記す) 、 1株当たりのサッマイモの平 均重量 (同、 1株重量と記す) 、 および、 1株当たりのサッマイモのコ ン トロールに対する重量比 (同、 重量比と記す) を算出した。 結果を表 Three months after the foliage treatment, all the sweet potatoes were dug out and the yield, that is, the weight of potatoes (tubes) was measured, and the average weight of sweet potatoes per one (Table 1 shows the weight of one sweet potato) ), The average weight of sweet potato per share (the same shall be referred to as one share weight), and the weight ratio of the sweet potato to the control per share (the same shall be referred to as weight ratio) were calculated. Table of results
1 にまとめた。 Summarized in 1.
表 1  table 1
Figure imgf000023_0001
表 1 の結果から明らかなように、 本発明にかかる塊根 ·塊茎肥大促進 剤を用いてサッマイモの茎葉処理を行う ことにより、 該サッマイモの芋 の肥大が促進されること、 つまり、 収穫量が増加することが判った。 〔実施例 2 〕
Figure imgf000023_0001
As is evident from the results in Table 1, the foliage treatment of sweet potato using the tuber and tuber hypertrophy promoter according to the present invention promotes the enlargement of the sweet potato potato, that is, increases the yield. I found out. (Example 2)
本発明にかかる塊根 ·塊茎肥大促進剤を用いて花卉類の処理を行つた ( 先ず、 トキソゥを鉢植え (複数鉢) した。 次いで、 互いに生長状態がほ ぼ揃っている トキソゥを選択し、 該トキソゥに、 濃度が 3 X 1 0 — 5モル Z Lおよび 1 X 1 0— 5モル Z Lである 2種類の 4 一 C 1 ― 1 A A水溶液 を、 各水溶液ごとに 1鉢ずつ所定量撒布することにより、 茎葉処理を行 つた。 また、 上記水溶液の代わりに水を所定量撒布した トキソゥをコン トロールと した。 The plants were treated using the tuber and tuber hypertrophy promoter of the present invention (first, potted plants were planted (a plurality of pots). Then, toxo plants whose growth states were substantially the same as each other were selected. in a concentration of 3 X 1 0 - by the 1 AA solution, a predetermined amount sprayed by one pot for each solution, - 5 mol ZL and 1 X 1 0- 5 mol ZL in which two 4 one C 1 In addition, instead of the above-mentioned aqueous solution, a control was made of Toxos which was sprayed with a predetermined amount of water.
茎葉処理を行ってから 2か月間経過後、 トキソゥの球根 (塊根) を掘 り出してその重量 (表 2で重量と記す) を測定すると共に、 コン トロー ルに対する重量比 (同、 重量比と記す) を算出した。 また、 トキソゥの 代わりに、 雲南トキソゥ、 キボウシ、 およびユリを用いて、 同様の茎葉 処理並びに測定等を行った。  Two months after the foliage treatment, the bulbs (toxoids) of Toxos are dug out, their weights (shown as weight in Table 2) are measured, and the weight ratio to the control (the same as the weight ratio) ) Was calculated. In addition, the same foliar treatment and measurement were performed using Yunnan Tokiso, Kiboushi and Lily instead of Tokiso.
さ らに、 ユリについては、 4 — C 1 一 I A A水溶液の代わりに、 塊根 •塊茎肥大促進剤である、 濃度が 3 X 1 0 — 5モル/ Lであるイ ン ドール 一 3 —プロピオン酸およびイ ン ドールー 3 —酪酸 (以下、 I B Aと略す ) を用いて、 同様の茎葉処理並びに測定等を行った。 これら結果を表 2 にまとめた。 Et al is, for lilies, 4 - instead of C 1 one IAA solution, tuberous • tubers hypertrophy accelerator, concentrations 3 X 1 0 - 5 the mole / L Lee emissions Doll one 3 - propionic acid and The same foliage treatment and measurement were performed using indole-3 butyric acid (hereinafter abbreviated as IBA). Table 2 summarizes these results.
表 2 植 物 塊根 水溶液濃度 重量比 肥大促進剤 (モル/ L) ( g ) Table 2 Plants Tuberous roots Aqueous solution concentration Weight ratio Hypertrophy (mol / L) (g)
3 X 1 0 2 0. 5 1. 6 9 3 X 1 0 2 0.5 0.5 1.69
4 - C 1 I A A 4-C 1 I A A
トキソゥ 1 X 1 0 1 6. 8 1. 3 9 コ ン ト ローノレ 1 2. 1  Toxo 1 × 10 1 6.8 1.39 Control
4 C 1 I A A 3 X 1 0 1. 7 8 9 トキソゥ 4 C 1 I A A 3 X 1 0 1.7 8 9
コ ン ト ロール 0. 9  Control 0.9
4 - C 1 I A A 3 x 1 0 1 6. 4 1. 3 6 キボウシ 4-C 1 I A A 3 x 10 1 6.4 1. 3 6
コ ン ト ローノレ 1 4. 8  Contour Nore 14.8
4 - C 1 - I A A 3 X 1 0 4 2. 2 1. 3 8 インド-ル- 3-ブ αピオン酸 3 x 1 0 4 1. 1 1. 3 5 ュ 4-C 1-I A A 3 X 10 4 2.2 1. 3 8 Indole-3-Bu α-Pionic acid 3 x 10 4 1.11.35
I B A 3 X 1 0 4 1 1. 3 7 コ ン ト ロ一ノレ 3 0. 5 表 2の結果から明らかなように、 本発明にかかる塊根 · 塊茎肥大促進 剤を用いて トキソゥゃ雲南 トキソゥ、 キボウシ、 ユリの茎葉処理を行う ことにより、 これら花卉類の球根や宿根の肥大が促進されることが判つ た。 〔実施例 3〕 本発明にかかる塊根 · 塊茎肥大促進剤を用いてアカプルコ (ユリ科) の処理を行った。 先ず、 5月に落花した後、 互いに生長状態がほぼ揃つ ているアカプルコを選択し、 9月上旬に、 該アカプルコ (複数株) に、 濃度が 3 X 1 0 5モル/ L、 1 X 1 0 5モル/ Lおよび 1 X 1 0 6モル Z Lである 3種類の 4 C 1 — I A A水溶液を、 各水溶液ごとに 3株ず つ所定量撒布することにより、 土壌処理を行った。 また、 上記水溶液の 代わりに水を所定量撒布したアカプルコ ( 3株) をコン トロールと した,IBA 3 X 104 1 1.37 7 Control 30.5 As is clear from the results in Table 2, the tuberous root / tuber hypertrophy promoter of the present invention was used to promote Toxo (Yunnan Toxo) and Kiboushi. It was also found that the application of foliage treatment to lilies promotes the enlargement of bulbs and lodgings of these flowers. [Example 3] Acapulco (Liliaceae) was treated using the tuber and tuber hypertrophy promoter of the present invention. First, after abscission in May, select Acapulco are substantially Soroitsu is growing with each other, in early September, to the Acapulco (multiple strains), concentration of 3 X 1 0 5 mol / L, 1 X 1 0 5 mol / L and 1 X 1 0 6 mol ZL is three kinds of 4 C 1 - to IAA solution, not a three strains each solution Soil treatment was performed by spraying a predetermined amount each. In addition, instead of the above aqueous solution, Acapulco (3 strains) in which a predetermined amount of water was sprayed was used as a control.
1 0月下旬にアカプルコの球根 (塊根) を掘り出して、 その重量 (表 3で重量と記す) 並びに球根周囲の長さ (同、 周囲長と記す) を測定し た。 そして、 球根の平均重量 (同、 平均重量と記す) およびコン トロ一 ルに対する重量比 (同、 重量比と記す) 、 並びに、 球根の平均周囲長 ( 同、 平均周囲長と記す) およびコン トロールに対する長さ比 (同、 長さ 比と記す) を算出した。 これら結果を表 3にまとめた。 In late October, Acapulco bulbs (tubes) were dug out, and their weight (indicated as weight in Table 3) and the perimeter of the bulb (indicated as perimeter) were measured. The average weight of the bulb (same as the average weight) and the weight ratio to the control (same as the weight ratio), the average circumference of the bulb (same as the same as the average circumference) and the control The length ratio to the length was calculated. Table 3 summarizes these results.
表 3 Table 3
Figure imgf000027_0001
Figure imgf000027_0001
表 3の結果から明らかなように、 本発明にかかる塊根 ·塊茎肥大促進 剤を用いてアカプルコの土壌処理を行う ことにより、 該アカプルコの球 根の肥大が促進されることが判った。  As is evident from the results in Table 3, it was found that the soil enlargement of Acapulco using the agent for promoting tuber and tuber enlargement according to the present invention promoted the enlargement of the bulbs of Acapulco.
〔実施例 4〕  (Example 4)
本発明にかかる塊根 ·塊茎肥大促進剤を用いてチューべローズの処理 を行った。 先ず、 チューべローズの球根を圃場に植え付けた。 次いで、 互いに生長状態がほぼ揃っているチユーべローズを選択して摘花を行つ た後、 該チュ一べローズ 3本に、 濃度が 3 X 1 0 — 5モル/ Lである 4 一 C 1 - I A A水溶液を所定量撒布することにより、 茎葉処理を行った。 また、 上記水溶液の代わりに水を所定量撒布したチューべローズ 3本を コン ト口一ノレとした。 Tuberose treatment was carried out using the tuber and tuber hypertrophy promoter of the present invention. First, tuberose bulbs were planted in the field. Next, select the bellows whose growth status is almost the same, and perform flower removal. After that, a foliage treatment was performed by spraying a predetermined amount of an aqueous solution of 41 C 1 -IAA having a concentration of 3 × 10 5 mol / L on the three tube roses. In addition, three tuberoses in which a predetermined amount of water was sprayed instead of the above-mentioned aqueous solution were used as a control opening.
茎葉処理を行ってから 2か月間経過後、 チューべローズの球根 (塊根 ) を掘り出してその重量を測定し、 平均重量 (同、 平均重量と記す) お よびコン トロールに対する重量比 (同、 重量比と記す) を算出した。 結 果を表 4にまとめた。  Two months after the foliage treatment, the bulbs (tubes) of tuberose were dug out and weighed, and the average weight (the same as the average weight) and the weight ratio to the control (the same as the weight) Ratio). Table 4 summarizes the results.
表 4  Table 4
Figure imgf000028_0001
Figure imgf000028_0001
表 4の結果から明らかなように、 本発明にかかる塊根 ·塊茎肥大促進 剤を用いてチューべローズの茎葉処理を行う ことにより、 該チューべ口 ーズの球根の肥大が促進されることが判った。  As is evident from the results in Table 4, it can be seen that by performing the foliage treatment of tuberose with the tuberous root / tuber hypertrophy promoter of the present invention, the bulb enlargement of the tuberous mouth is promoted. understood.
〔実施例 5〕  (Example 5)
本発明にかかる塊根 ·塊茎肥大促進剤を用いてサ トィモの処理を行つ た。 先ず、 互いにほぼ等しい重量を有するサ トイモの種芋 (塊茎) を 2 個用意し、 一方の種芋を濃度が 3 x 1 0— 5モル/ Lである 4 — C 1 ― I A A水溶液に 3時間浸漬することにより、 浸漬処理を行った。 他方の種 芋には上記処理を行わなかった。 次いで、 これら種芋を圃場に植え付け た。 両者の植え付け間隔は、 約 6 0 c mとした。 そして、 2か月間経過後、 圃場に植え付けた種芋のうち、 浸漬処理を 行つた種芋に、 濃度が 3 x 1 0 5モル Z Lである 4 C 1 I A A水溶 液を所定量撒布することにより、 茎葉処理を行った。 浸漬処理を行わな かった種芋には、 茎葉処理を行わなかった。 Satoimo was treated using the tuber and tuber hypertrophy promoter of the present invention. First, seed potatoes of Sa Toimo the (tubers) and two ready to have approximately equal weight to each other, one of the seed tuber concentration is 3 x 1 0- 5 mol / L 4 - C 1 - immersed 3 hours in IAA solution Thereby, the immersion treatment was performed. The other potato was not subjected to the above treatment. Next, these seed potatoes were planted in the field. The planting interval between them was about 60 cm. Then, after 2 months, of seed potatoes which planted in the field, dipped in KoTsuta seed tuber, by concentration is sprayed predetermined amount 4 C 1 IAA aqueous solution is 3 x 1 0 5 mol ZL, foliage Processing was performed. Seed potatoes without immersion treatment were not subjected to foliage treatment.
茎葉処理を行ってから 3か月間経過後、 全てのサ トイモを掘り出して. 収穫量、 即ち、 芋 (塊茎) の重量を測定し、 サ トィモの全重量 (表 5で. 全重量と記す) 、 および、 コン トロールに対する重量比 (同、 重量比と 記す) を算出した。 結果を表 5 にまとめた。  Three months after the foliage treatment, all the taros are dug out. The yield, that is, the weight of potatoes (tubes) is measured, and the total weight of satimo (shown as total weight in Table 5) , And the weight ratio with respect to the control (hereinafter, referred to as weight ratio) were calculated. Table 5 summarizes the results.
表 5  Table 5
Figure imgf000029_0001
Figure imgf000029_0001
表 5の結果から明らかなように、 本発明にかかる塊根 ·塊茎肥大促進 剤を用いてサ トィモの浸漬処理および茎葉処理を行う ことにより、 該サ トイモの芋の肥大が促進されること、 つまり、 収穫量が増加することが 判った。  As is clear from the results in Table 5, the taro immersion treatment and the foliage treatment using the tuber and tuber hypertrophy promoter according to the present invention promote the taro sweet potato hypertrophy, that is, However, it was found that the yield increased.
〔実施例 6〕  (Example 6)
本発明にかかる塊根 ·塊茎肥大促進剤を用いて二十日ダイコンの処理 を行った。 先ず、 1 1月 2 8 日に二十日ダイ コンの種 (多数) を 3 4 c m X 6 8 c mの大きさのプランター 2つにまばらに播き、 室温で育成し た。 2か月間経過後、 プランタ一 1つ当たりの二十日ダイコンの本数が 約 4 0本となるように、 間引きを行った。 そして、 2月 1 2 日に、 二十 日ダイコンの根茎が、 発達する直前の状態となったので、 一方のプラン ターに植えられている二十日ダイ コ ンに対して、 以下の処理を行う と共 に、 他方のプランターに植えられている二十日ダイコンをコン トロール と した。 The radish was treated for 20 days using the tuber and tuber hypertrophy promoter of the present invention. First, on January 28, 20 days, radish seeds (many) were sparsely sown in two 34 cm x 68 cm planters and grown at room temperature. After two months, thinning was performed so that the number of radishes per planter would be about 40. And on February 12th, twenty Since the rhizomes of Japanese radish were in a state just before development, the following treatment was applied to the twenty-day radish planted in one planter, and it was planted in the other planter. The control of the radish on the 20th was used as the control.
即ち、 一方のブラン夕一の二十日ダイコンに、 濃度が 3 X 1 0 — 5モル Z Lである 4 — C 1 一 I A A水溶液を 8 0 0 m l ( 1本当たり 2 0 m l ) 撒布することにより、 茎葉処理を行った。 その翌日、 茎葉処理を行つ た二十日ダイコンのうちの 5本に対して、 該二十日ダイコンの茎に、 濃 度が 2 X 1 0 —2モル/ Lである 4 — C 1 一 I A A水溶液を、 シリ ンジを 用いて 1 0 μ 1 ずつ注入することにより、 注入処理を行つた。 また、 茎 葉処理を行った二十日ダイコンのうちの他の 5本に対して、 該二十日ダ ィコンの葉の先端を約 1 c m切断した後、 該切断部を濃度が 5 X 1 0 一5 モル/ Lである 4 一 C 1 一 I A A水溶液に 2時間浸漬することにより、 浸漬処理を行った。 That is, one of Bran evening one radish, concentration 3 X 1 0 - by C 1 one IAA aqueous 8 0 0 ml (2 0 ml per one) to sample - 5 mol is ZL 4 The foliage treatment was performed. The next day, the foliage treatment against five of Gyotsu was radish, the stems of the radish, concentration is 2 X 1 0 - a 2 mol / L 4 - C 1 one The injection treatment was performed by injecting an aqueous solution of IAA at a rate of 10 μl using a syringe. Further, after cutting the tip of the leaves of the radish of about 20 cm from the other five radishes treated with the foliage treatment, the cut portion was adjusted to a concentration of 5 × 1. The immersion treatment was performed by immersion in an aqueous solution of 4-C1-IAA at 0 to 15 mol / L for 2 hours.
3月 6 日に全ての二十日ダイコンを掘り出して、 プランターごとの二 十日ダイ コ ンの全重量 (表 6で全体重量と記す) 、 並びに、 根 (塊根) の全重量 (同、 全大根重量と記す) を測定した。 そして、 二十日ダイコ ン 1本当たりの根の重量 (同、 平均重量と記す) 、 およびコン トロール に対する重量比 (同、 重量比と記す) を算出した。 これら結果を表 6 に まとめた。 表 6 On March 6, all the twenty-day radish was dug out, and the total weight of the twenty-day radish per planter (shown as the total weight in Table 6), and the total weight of the roots (tubes) Radish weight) was measured. Then, the weight of the root per 20-day radish (the same as the average weight) and the weight ratio to the control (the same as the weight ratio) were calculated. Table 6 summarizes these results. Table 6
Figure imgf000031_0001
Figure imgf000031_0001
表 6の結果から明らかなように、 本発明にかかる塊根 · 塊茎肥大促進 剤を用いて二十日ダイ コ ンの茎葉処理や注入処理、 浸漬処理を行う こと により、 該二十日ダイ コ ンの根の肥大が促進されることが判った。 また、 茎葉処理と、 注入処理または浸漬処理とを併用することにより、 二十日 ダイコンの根の肥大がより一層促進されることが判った。  As is evident from the results in Table 6, by applying the foliage treatment, injection treatment, and immersion treatment of the radish for 20 days using the tuber and tuber hypertrophy promoter according to the present invention, the radish for 20 days can be obtained. It was found that root enlargement was promoted. It was also found that the combined use of the foliage treatment and the injection treatment or the immersion treatment further promoted the root enlargement of Japanese radish.
〔実施例 7〕  (Example 7)
本発明にかかる塊根 ·塊茎肥大促進剤を用いて春作のジャガイモ (メ —ク イ ン) の処理を行った。 先ず、 ノニオ ン系界面活性剤 (米国, V a l e n t社製、 商品名 : X— 7 7 ) を 2 0 p p mの割合で含む、 濃度が 3 X 1 0 _ 5モル/ Lである I B A水溶液を調製した。 次に、 互いにほぼ 等しい大きさのジャガイモを複数個用意し、 該ジャガイモのうちの半分 を上記水溶液に 2時間浸漬することにより、 浸漬処理を行った。 残りの ジャガイモには上記処理を行わなかった。 次いで、 これらジャガイモを 2つに切った ( 2等分した) 後、 処理を行った方を 1 0株 (個) 、 処理 を行わなかった方を 1 5株 (個) 、 3月 8 日に圃場に植え付けた。 畝幅 は 1 m、 植え付け間隔は 4 0 c mと した。 Spring potatoes (me-quin) were treated using the tuber and tuber hypertrophy promoter of the present invention. First, Nonio emissions based surfactant (US, V Alent trade name: X- 7 7) a in a proportion of 2 0 ppm, the IBA solution the concentration is 3 X 1 0 _ 5 mol / L Preparation did. Next, a plurality of potatoes having substantially the same size as each other were prepared, and half of the potatoes were immersed in the aqueous solution for 2 hours to perform an immersion treatment. The remaining potatoes were not subjected to the above treatment. Next, after cutting these potatoes into two pieces (halved), 10 plants (pieces) were treated, 15 were not treated and 15 pieces (pieces). Planted in the field. Ridge width Was 1 m, and the planting interval was 40 cm.
そして、 凡そ 3か月間経過後 ( 6月上旬) 、 全てのジャガイモを掘り 出して、 収穫量、 即ち、 ジャガイモ (塊茎) の重量を測定し、 1株当た りのジャガイモの平均個数 (表 7で 1株個数と記す) 、 1株当たりのジ ャガイモの平均重量 (同、 1株重量と記す) 、 および、 1株当たりのジ ャガイモのコ ン ト ロールに対する重量比 (同、 重量比と記す) を算出し た。 結果を表 7 にまとめた。  After about three months (early June), all potatoes were dug out, the yield, that is, the weight of potatoes (tubes) was measured, and the average number of potatoes per share (Table 7) , The average weight of potatoes per share (also referred to as the weight of one share), and the weight ratio of potatoes per control to the control (also referred to as the weight ratio) ) Was calculated. Table 7 summarizes the results.
表 7  Table 7
Figure imgf000032_0001
Figure imgf000032_0001
表 7 の結果から明らかなように、 本発明にかかる塊根 ·塊茎肥大促進 剤を用いてジャガイモ (メークイ ン) の浸漬処理を行う ことにより、 該 ジャガイモの塊茎の肥大が促進されること、 つまり、 収穫量が 3 8 %増 加することが判つた。  As is clear from the results in Table 7, the potato (make-in) immersion treatment using the agent for promoting tuber root and tuber hypertrophy according to the present invention promotes the tuber tuber hypertrophy. It was found that the yield increased by 38%.
〔実施例 8〕  (Example 8)
本発明にかかる塊根 ·塊茎肥大促進剤を用いて秋作のジャガイモ (出 島) の処理を行った。 先ず、 互いにほぼ等しい大きさのジャガイモを複 数個用意し、 該ジャガイモのうちの半分を実施例 7 と同一組成の水溶液 に 2時間浸漬することにより、 浸漬処理を行った。 残りのジャガイモに は上記処理を行わなかった。 次いで、 これらジャガイモを切らずに 1 5 株 (個) ずつ、 8月 2 8 日に圃場に植え付けた。 畝幅は 1 m、 植え付け 間隔は 4 0 c mとした。 Autumn potatoes (Dejima) were treated using the tuber and tuber hypertrophy promoters of the present invention. First, a plurality of potatoes having substantially the same size as each other were prepared, and half of the potatoes were immersed in an aqueous solution having the same composition as in Example 7 for 2 hours to perform an immersion treatment. The remaining potatoes were not subjected to the above treatment. The potatoes were then planted on the field on August 28 without cutting 15 potatoes (pieces). Ridge width 1 m, planting The interval was 40 cm.
そして、 凡そ 3か月間経過後 ( 1 2月上旬) 、 全てのジャガイモを掘 り出して、 収穫量、 即ち、 ジャガイモ (塊茎) の重量を測定し、 1株当 たりのジャガイモの平均個数 (表 8で 1株個数と記す) 、 1株当たりの ジャガイモの平均重量 (同、 1株重量と記す) 、 および、 1株当たりの ジャガイモのコ ン トロールに対する重量比 (同、 重量比と記す) を算出 した。 結果を表 8にまとめた。  After about three months (early February), all potatoes were dug out, the yield, that is, the weight of potatoes (tubes) was measured, and the average number of potatoes per share (table) 8, the average weight of potatoes per share (also referred to as one share weight), and the weight ratio of potato to control per share (same as weight ratio). It was calculated. Table 8 summarizes the results.
表 8  Table 8
Figure imgf000033_0001
Figure imgf000033_0001
表 8 の結果から明らかなように、 本発明にかかる塊根 ·塊茎肥大促進 剤を用いてジャガイモ (出島) の浸漬処理を行う ことにより、 該ジャガ ィモの塊茎の肥大が促進されること、 つまり、 収穫量が 4 9 %増加する ことが判つた。  As is clear from the results in Table 8, the potato (Dejima) immersion treatment using the agent for promoting tuber root and tuber hypertrophy according to the present invention promotes the enlargement of the tuber of the potato. However, it was found that the yield increased by 49%.
〔実施例 9〕  (Example 9)
本発明にかかる塊根 ·塊茎肥大促進剤を用いて秋作のジャガイモ (男 爵) の処理を行った。 先ず、 互いにほぼ等しい大きさのジャガイモを複 数個用意し、 6つのグループに分けた。  Autumn potatoes (baron) were treated using the tuber and tuber hypertrophy promoter according to the present invention. First, several potatoes of almost the same size were prepared and divided into six groups.
そして、 第 1のグループのジャガイモは、 2つに切った ( 2等分した ) 後、 実施例 7 と同一組成の水溶液に 2時間浸漬することにより、 浸漬 処理を行った。 第 2のグループのジャガイモは、 ノニオン系界面活性剤 (X 7 7 ) を 2 0 p p mの割合で含む、 濃度が 5 x 1 0 6モル Z Lで ある I B A水溶液に 2時間浸漬することにより、 浸漬処理を行った後、 2つに切った ( 2等分した) 。 第 3のグループのジャガイモは、 界面活 性剤 (東邦化学工業株式会社製、 商品名 : S o r p o l 7 1 5 7 ) を 1 p p mの割合で含む、 濃度が 3 X 1 0 5モル Z Lである I B A水溶液 に 2時間浸漬することにより、 浸漬処理を行った後、 2つに切った ( 2 等分した) 。 第 4のグループのジャガイモは、 界面活性剤 ( S o r p o 1 7 1 5 7 ) を 1 0 p p mの割合で含む、 濃度が 3 x 1 0 5モル/ L である I B A水溶液に 2時間浸漬することにより、 浸漬処理を行つた後 2つに切った ( 2等分した) 。 第 5および第 6のグループのジャガイモ は、 2つに切った ( 2等分した) 。 次いで、 これら 6つのグループのジ ャガイモを、 8月 2 8 日に圃場に植え付けた。 畝幅は 1 m、 植え付け間 隔は 4 0 c mとした。 The potatoes of the first group were cut into two pieces (halved) and then immersed in an aqueous solution having the same composition as in Example 7 for 2 hours. The second group of potatoes are nonionic surfactants The (X 7 7) in a proportion of 2 0 ppm, by immersing 2 hours IBA solution the concentration is 5 x 1 0 6 mol ZL, after the immersion treatment, cut into two (2 etc. Minute). Potato third group, surface active agent (TOHO Chemical Industry Co., Ltd., trade name: S orpol 7 1 5 7) the a proportion of 1 ppm, the concentration is 3 X 1 0 5 mole ZL IBA After immersion treatment by immersion in an aqueous solution for 2 hours, it was cut into two (halved). Potato fourth group includes a surfactant (S orpo 1 7 1 5 7 ) at a rate of 1 0 ppm, by concentration immersed for 2 hours in IBA solution is 3 x 1 0 5 mol / L After the immersion treatment, it was cut into two (halved). The fifth and sixth groups of potatoes were cut in two (halved). These six groups of potatoes were then planted on the field on August 28. The ridge width was 1 m and the planting interval was 40 cm.
そして、 上記第 5のグループのジャガイモに対しては、 地上部が 1 0 葉程度に生長した段階 ( 9月 2 9 日) で、 ノニオン系界面活性剤 (X— 7 7 ) を 2 0 p p mの割合で含む、 濃度が 5 x 1 0 5モル/ Lである I B A水溶液を 1 2 0 m 1 /m 2 の撒布量で以て撒布することにより、 茎 葉処理を行った。 尚、 第 6のジャガイモには上記浸漬処理および茎葉処 理を行わなかった。 For the potatoes of the fifth group, the nonionic surfactant (X-77) was added to 20 ppm at the stage when the aerial part grew to about 10 leaves (September 29). The foliage treatment was performed by spraying an IBA aqueous solution having a concentration of 5 × 10 5 mol / L in a ratio of 120 m 1 / m 2 . The sixth potato was not subjected to the immersion treatment and the foliage treatment.
そして、 植え付けてから凡そ 3か月間経過後 ( 1 2月上旬) 、 全ての ジャガイモを掘り出して、 収穫量、 即ち、 ジャガイモ (塊茎) の重量を 測定し、 1株当たりのジャガイモの平均個数 (表 9で 1株個数と記す) 1株当たりのジャガイモの平均重量 (同、 1株重量と記す) 、 および、 1株当たりのジャガイモのコン トロールに対する重量比 (同、 重量比と 記す) を算出した。 結果を表 9 にまとめた。 About three months after planting (early December), all potatoes are dug out, and the yield, that is, the weight of potatoes (tubes) is measured, and the average number of potatoes per plant (table) The average weight of potatoes per share (also referred to as the weight of one share) and the weight ratio of potato to control per share (same as the weight ratio) ) Was calculated. Table 9 summarizes the results.
表 9 ジャガイモ (男爵) Table 9 Potatoes (baron)
·. ·.
7、、 7,
ノ itレ ¾¾¾ ' 企 小 /仪/展 /又 怀 ftX. 1丄 *怀Φ^ΚΙ¾τ  ノ it レ ¾¾¾ '工 小 / 仪 / 展 / も ft ftX. 1 丄 * 怀 Φ ^ ΚΙ¾τ
ープ 肥大促進剤 (モル/ L) (株) (個) (g)  Soup enlarger (mol / L) (stock) (pieces) (g)
1 3 X 1 0 " X- 7 7 2 0 浸漬 8 5. 0 4 0 8 1. 0 1 3 X 10 "X- 7 7 2 0 Immersion 8 5.0 4 0 8 1. 0
2 5 X 1 0 "6 X- 7 7 2 0 浸漬 6 4. 7 4 4 8 1. 5 3 2 5 X 10 " 6 X- 7 7 2 0 Immersion 6 4. 7 4 4 8 1. 5 3
3 I B A 3 X 1 0 -5 Sorpol 7157 1 浸漬 9 3. 8 4 7 7 1. 6 3 3 IBA 3 X 1 0 - 5 Sorpol 7157 1 dip 9 3.8 4 7 7 1.6 3
4 3 X 1 0 -5 Sorpol 7157 1 0 浸漬 4 4. 3 5 8 6 2. 0 1 4 3 X 1 0 - 5 Sorpol 7157 1 0 dip 4 4.3 5 8 6 2.0 1
5 3 X 1 0-5 X- 7 7 2 0 茎葉 5 3. 4 3 5 8 1. 2 3 5 3 X 1 0- 5 X- 7 7 2 0 foliage 5 3.4 3 5 8 1.2 3
6 コントロール 7 3. 1 2 9 2 6 Control 7 3. 1 2 9 2
表 9の結果から明らかなように、 本発明にかかる塊根 · 塊茎肥大促進 剤を用いてジャガイモ (男爵) の浸漬処理や茎葉処理を行うことにより、 該ジャガイモの塊茎の肥大が促進されること、 つまり、 収穫量が増加す ることが判った。 As is clear from the results in Table 9, the potato (baron) immersion treatment and foliage treatment using the tuber and tuber hypertrophy-promoting agent according to the present invention promoted the potato tuber hypertrophy, In other words, the yield increased.
〔実施例 1 0〕  (Example 10)
本発明にかかる塊根 ·塊茎肥大促進剤を用いてダイコンの処理を行つ た。 先ず、 4月 1 0 日にダイコン (品種 : おしん) の種子 (多数) を、 3 0 c m間隔で播種して育成した。 そして、 地上部が 1 0 c m程度の高 さに生長した段階 ( 1 8 日後) で、 該ダイコ ンのうちの半分に、 ノニォ ン系界面活性剤 (和光純薬工業株式会社製、 商品名 : T w e e n 8 0 ) を 5 0 0 p p mの割合で含む、 濃度が 5 x 1 0 — 5モル Z Lである 4 一 C 1 一 I A A水溶液を 8 5 m 1 / m 2 の撒布量で以て撒布することによ り、 茎葉処理を行った。 また、 上記水溶液の代わりに水を所定量撒布し た残りのダイコンをコン トロールと した。 Japanese radish was treated using the tuber and tuber hypertrophy promoter of the present invention. First, on April 10, seeds (many) of radish (variety: Oshin) were sown at 30 cm intervals and grown. Then, at the stage when the above-ground portion grew to a height of about 10 cm (after 18 days), half of the radish was replaced with a nonionic surfactant (manufactured by Wako Pure Chemical Industries, Ltd., trade name: Tween 8 0) at a concentration of 500 ppm, and a concentration of 5 x 10 — 5 mol ZL is sprayed with an aqueous solution of 4 1 C 1 and 1 IAA at a spray rate of 85 m 1 / m 2. As a result, foliage treatment was performed. The remaining radish, in which a predetermined amount of water was sprayed instead of the above aqueous solution, was used as a control.
そして、 播種してから凡そ 2か月間経過後、 全てのダイコンを引き抜 いて、 収穫量、 即ち、 ダイ コンの地上部 (茎葉) および地下部 (塊根) の重量を測定し、 1本当たりのダイ コ ンの地上部平均重量 (表 1 0で地 上部重量と記す) 、 1本当たりのダイコ ンの地下部平均重量 (同、 地下 部重量と記す) 、 並びに、 1本当たりのダイコンのコン トロールに対す る地上部および地下部の重量比 (同、 重量比と記す) を算出した。 結果 を表 1 0にまとめた。 表 1 0 About two months after sowing, all radish was extracted, and the yield, that is, the weight of the above-ground part (foliage) and underground part (tube) of the radish was measured. Above-ground average weight of radish (referred to as ground weight in Table 10), average underground weight of radish per unit (also referred to as underground weight), and radish per unit The weight ratio of the aboveground part and the underground part with respect to the troll was calculated. The results are summarized in Table 10. Table 10
Figure imgf000038_0001
Figure imgf000038_0001
表 1 0 の結果から明らかなように、 本発明にかかる塊根 ·塊茎肥大促 進剤を用いてダイコンの茎葉処理を行う ことにより、 該ダイコンの塊根 の肥大が促進されること、 つまり、 収穫量が地下部で 6 2 %増加するこ とが判った。  As is evident from the results in Table 10, by performing the foliage treatment of radish using the tuber and tuber hypertrophy-promoting agent according to the present invention, the enlargement of the tuberous root of the radish is promoted. Increased by 62% in the underground.
〔実施例 1 1〕  (Example 11)
本発明にかかる塊根 ·塊茎肥大促進剤を用いてテッボウユリの処理を 行つた。 先ず、 9月中旬に、 凡そ 3 0 0個の球根 (球根周囲長 6 c m 〜 7 c m ) を、 幅 1 . 1 m、 長さ 5 mの畝 ( 2本) に植え付けた。 そして、 地上部が 8 c m程度の高さで 1 5 〜 2 5葉程度に生長した段階 ( 1月 9 日) で、 該テツボウユリのうちの半分 (一方の畝) に、 ノニオン系界面 活性剤 (X — 7 7 ) を 2 0 p p mの割合で含む、 濃度が 5 x 1 0 — 5モル / Lである 4 — C I — I A A水溶液を 0 . 9 L / m 2 の撒布量で以て撒 布することにより、 茎葉処理を行った。 また、 上記水溶液の代わりに水 を所定量撒布した残りのテツボウユリ (他方の畝) をコン トロールとし た。 Using the tuber and tuber hypertrophy promoter according to the present invention, Ligustrum lily was treated. First, in mid-September, about 300 bulbs (bulb circumference 6 cm to 7 cm) were planted in two ridges 1.1 m wide and 5 m long. At the stage when the aerial part grew to about 15 to 25 leaves at a height of about 8 cm (January 9), half of the lily of the valley (one ridge) was coated with a nonionic surfactant ( X — 7 7) at a concentration of 20 ppm and a concentration of 5 x 10 — 5 mol / L 4 — CI — IAA solution is sprayed at a spray rate of 0.9 L / m 2 Thus, foliage treatment was performed. In addition, instead of the above aqueous solution, the remaining grape lily (the other ridge) on which a predetermined amount of water was sprayed was used as a control.
そして、 7月 3 日に、 全ての球根を掘り出して、 収穫量、 即ち、 テツ ボウユリの球根 (塊根) の総重量を測定し、 1 0 0個当たりの球根の重 量 (表 1 1で 1 0 0個重量と記す) 、 および、 該球根のコン トロールに 対する重量比 (同、 重量比と記す) を算出した。 結果を表 1 1 にまとめ た。 Then, on July 3, all the bulbs were dug out, and the harvest amount, that is, the total weight of the bulbs of tube lilies was measured, and the weight of bulbs per 100 bulbs was measured. The amount (expressed as 100 weights in Table 11) and the weight ratio of the bulb to the control (also expressed as weight ratio) were calculated. The results are summarized in Table 11.
表 1 1  Table 11
Figure imgf000039_0001
Figure imgf000039_0001
表 1 1 の結果から明らかなように、 本発明にかかる塊根 ·塊茎肥大促 進剤を用いてテッボウユリの茎葉処理を行う ことにより、 該テッポゥュ リの球根 (塊根) の肥大が促進されること、 つまり、 収穫量が 2 3 %増 加することが判つた。  As is evident from the results in Table 11, by performing the foliar treatment of tebo lily using the tuber and tuber hypertrophy-promoting agent according to the present invention, it is possible to promote the enlargement of the bulb (tube) of the teppori. In other words, the yield increased by 23%.
〔実施例 1 2 〕  (Example 12)
本発明にかかる塊根 ·塊茎肥大促進剤を用いてチューリ ッ プの処理を 行つた。 先ず、 1 0月 1 8 日に、 凡そ 8 0 0個の球根 (品種 : オックス フ ォー ド (赤花) 、 球根周囲長 1 0 c m ) を、 5 c m間隔で植え付けた ( そして、 地上部が 1 0 c m程度の高さで 2 3葉程度に生長した段階 ( 4月上旬) で、 該チューリ ップのうちの半分に、 ノニオン系界面活性剤 ( T w e e n 8 0 ) を 5 0 0 p p mの割合で含む、 濃度が 5 x 1 0 一 5 モル/ Lである 4 — C I — I A A水溶液を 4 0 0 m 1 / m 2 の撒布量で 以て撒布することにより、 茎葉処理を行った。 また、 上記水溶液の代わ りに水を所定量撒布した残りのチューリ ップをコ ン ト ロールとした。 そして、 8月上旬に、 全ての球根 (塊根) を掘り出して、 該チュ リ ップの球根の周囲長を測定し、 大きさ毎に集計した。 結果を表 1 2 ま とめた。 Tulip treatment was performed using the tuber / tuber hypertrophy promoter of the present invention. First, on October 18th, approximately 800 bulbs (variety: Oxford (red flower), bulb circumference 10 cm) were planted at 5 cm intervals (and the aerial part was planted). At the stage of growing to about 23 leaves at a height of about 10 cm (early April), 500 ppm of nonionic surfactant (Tween 80) was added to half of the tulips. a proportion, concentration 4 is 5 x 1 0 one 5 mol / L - CI -. by sprayed Te than in the IAA solution 4 0 0 spraying amount of m 1 / m 2, were subjected to foliage treatment also The remaining tulips, to which a predetermined amount of water had been sprayed instead of the above aqueous solution, were used as controls. In early August, all bulbs (lumps) were dug out, the perimeters of the bulbs of the tulips were measured, and totaled for each size. The results are summarized in Table 12.
表 1 2  Table 1 2
Figure imgf000040_0001
Figure imgf000040_0001
表 1 2の結果から明らかなように、 本発明にかかる塊根 ·塊茎肥大促 進剤を用いてチューリ ップの茎葉処理を行う ことにより、 該チューリ ッ プの球根 (塊根) の肥大が促進されること、 つまり、 周囲長が 1 3 c m 以上の球根の個数が増加することが判った。  As is evident from the results in Table 12, by performing the foliage treatment of the tulip using the tuber and tuber hypertrophy-promoting agent according to the present invention, the enlargement of the bulb (tube) of the tulip is promoted. In other words, it was found that the number of bulbs with a perimeter of 13 cm or more increased.
〔実施例 1 3〕  (Example 13)
実施例 7 と同様にして春作のジャガイモ (メ一クイ ン) の処理を行つ た。 先ず、 ノニォン系界面活性剤 (X— 7 7 ) を 2 0 p p mの割合で含 む、 濃度が 3 X 1 0 _ 5モル Z Lである I A A水溶液を調製した。 次に、 互いにほぼ等しい大きさのジャガイモを複数個用意し、 該ジャガイモの うちの半分を上記水溶液に 2時間浸漬することにより、 浸漬処理を行つ た。 残りのジャガイモには上記処理を行わなかった。 次いで、 これらジ ャガイモを 2つに切った ( 2等分した) 後、 処理を行った方を 1 0株 ( 個) 、 処理を行わなかった方を 1 2株 (個) 、 3月上旬に圃場に植え付 けた。 畝幅は 1 m、 植え付け間隔は 4 0 c mとした。 そして、 凡そ 3か月間経過後 ( 6月上旬) 、 全てのジャガイモを掘り 出して、 収穫量、 即ち、 ジャガイモ (塊茎) の重量を測定し、 1株当た りのジャガイモの平均個数 (表 1 3で 1株個数と記す) 、 1株当たりの ジャガイモの平均重量 (同、 1株重量と記す) 、 および、 1株当たりの ジャガイモのコン トロールに対する重量比 (同、 重量比と記す) を算出 した。 結果を表 1 3にまとめた。 ジャガイモ (メークイ ン) の収穫量は 2 9 %増加した。 In the same manner as in Example 7, spring potatoes (maquins) were processed. First, including Nonion-based surfactant (X- 7 7) in a proportion of 2 0 ppm, the concentration of IAA solution was prepared a 3 X 1 0 _ 5 mol ZL. Next, a plurality of potatoes having substantially the same size as each other were prepared, and half of the potatoes were immersed in the above aqueous solution for 2 hours to perform an immersion treatment. The above potato was not subjected to the above treatment. Then, after cutting these potatoes into two (halved), the treated group had 10 shares (units) and the untreated group had 12 shares (units). Planted in the field. The ridge width was 1 m and the planting interval was 40 cm. After approximately three months (early June), all potatoes were dug out, the yield, that is, the weight of potatoes (tubes) was measured, and the average number of potatoes per share (Table 1) Calculate the potato weight per share (same as the weight of one share), and the weight ratio of potato to control per share (same as the weight ratio). did. The results are summarized in Table 13. Potato (make-in) yield increased by 29%.
表 1 3  Table 13
Figure imgf000041_0001
Figure imgf000041_0001
〔実施例 1 4〕  (Example 14)
実施例 7 と同様にしてサ トィモの処理を行った。 先ず、 ノニォン系界 面活性剤 (X — 7 7 ) を 2 0 p p mの割合で含む、 濃度が 5 x 1 0 — 5モ ル/ Lである I A A水溶液を調製した。 次に、 互いにほぼ等しい大きさ のサ トィモを複数個用意し、 該サ トイモのうちの半分を上記水溶液に 2 時間浸漬することにより、 浸漬処理を行った。 残りのサ トィモには上記 処理を行わなかった。 次いで、 処理を行ったサ トイモを 1 2株 (個) 、 処理を行わなかったサ トイモを 1 1株 (個) 、 4月上旬に圃場に植え付 けた。 畝幅は 1 m、 植え付け間隔は 3 0 c mとした。 Satomo treatment was performed in the same manner as in Example 7. First, an IAA aqueous solution containing a nonionic surfactant (X — 77) at a ratio of 20 ppm and having a concentration of 5 × 10 — 5 mol / L was prepared. Next, a plurality of taros having substantially the same size were prepared, and half of the taros were immersed in the aqueous solution for 2 hours to perform immersion treatment. The above process was not applied to the remaining satimo. Then, 12 treated taros and 11 untreated taros were planted in the field in early April. The ridge width was 1 m and the planting interval was 30 cm.
そして、 凡そ 7か月間経過後 ( 1 1月上旬) 、 全てのサ トイモを掘り 出して、 収穫量、 即ち、 芋 (塊茎) の重量を測定し、 1株当たりのサ ト ィモの平均個数 (表 1 4で 1株個数と記す) 、 1株当たりのサ トイモの 平均重量 (同、 1株重量と記す) 、 および、 1株当たりのサ トイモのコ ン ト ロールに対する重量比 (同、 重量比と記す) を算出した。 結果を表 1 4 にまとめた。 サ トイモの収穫量は、 2 2 %増加した。 After about seven months (early January), all the taros were dug out, and the yield, that is, the weight of potatoes (tubes) was measured, and the weight per plant was determined. The average number of potatoes (denoted as one share in Table 14), the average weight of taro per share (also denoted as one share weight), and the control of the taro per share The weight ratio (same as the above) is calculated. The results are summarized in Table 14. Taro yields increased by 22%.
表 1 4  Table 14
Figure imgf000042_0001
Figure imgf000042_0001
〔実施例 1 5〕  (Example 15)
本発明にかかる作物増収剤を用いてヮ夕の茎葉処理を行った。 先ず、 5月 2 2 日にヮ夕の種子 (多数) を畑に直播きして育成した。 その後、 7月 1 4 日に、 9 0 c m程度の高さに生長し、 かつ、 未だ開花していな いヮ夕を 3株ずつ、 2つのグループ (計 6株) と して選択した。  The evening foliage treatment was performed using the crop increasing agent according to the present invention. First, on May 22nd, ヮ evening seeds (many) were directly sown in the field and raised. After that, on July 14th, three plants, each of which grew to a height of about 90 cm and had not yet flowered, were selected as two groups (six in total).
そして、 一方のグループのヮタに対して、 濃度が 1 X 1 0 5モル/ L である 4 C 1 I A A (作物増収剤) 水溶液を 4 0 L Z a の撒布量で 以て撒布することにより、 茎葉処理を行った。 また、 他方のグループの ヮ夕に対して、 上記水溶液の代わりに水を 4 0 L Z aの撒布量で以て撒 布することにより、 コン トロールと した。 Then, the Wa data of one group, by concentration to sprayed Te than in spraying amount of 1 X 1 0 5 mol / L in a 4 C 1 IAA (crop sales agent) aqueous solution 4 0 LZ a, Foliage treatment was performed. In addition, for the other group, water was sprayed at a spraying rate of 40 LZa instead of the above aqueous solution to control.
1 0月 1 5 日に上記のヮタを収穫し、 収穫量、 即ち、 実 (種子) の個 数を数えた。 結果を表 1 5 にまとめた。 表 1 5 On October 15th, the above-mentioned potatoes were harvested, and the harvest amount, that is, the number of seeds (seed) was counted. The results are summarized in Table 15. Table 15
Figure imgf000043_0001
表 1 5の結果から明らかなように、 本発明にかかる作物増収剤を用い てヮ夕の茎葉処理を行うことにより、 ヮ夕の花数の増加が促進されるこ とが判った。
Figure imgf000043_0001
As is evident from the results in Table 15, it was found that performing the foliage treatment of the evening using the crop-producing agent according to the present invention promoted the increase in the number of evening flowers.
〔実施例 1 6〕  (Example 16)
本発明にかかる作物増収剤を用いてェン ドウの茎葉処理を行った。 先 ず、 1 1月中旬にェン ドゥ (品種 : あずみ野 3 0 日絹莢 P M R ) の種子 Endow foliage treatment was carried out using the crop yield enhancer according to the present invention. First of all, in mid-January, the seeds of endou (variety: Azumino 30 day silk pod PMR)
(多数) を、 畝幅 9 0 c mの畑に、 株間 2 0 c mとなるように播種して 育成した。 3 0 日間経過後、 生長したェン ドウに施肥すべく、 畑に化成 肥料 (新東化学工業株式会社製) を 5 0 g / 5 0本の割合で投与した。 (Many) were sown and grown in a field with a ridge width of 90 cm so that the inter-strain was 20 cm. After a lapse of 30 days, a fertilizer (manufactured by Shinto Kagaku Kogyo Co., Ltd.) was administered to the field at a ratio of 50 g / 50 to fertilize the grown endow.
そして、 播種してから 5 ヶ月間経過し、 花が付き始めた頃に、 エン ド ゥを 2つにグループ分けした。 次いで、 一方のグループのエン ドゥ ( 2 Five months after sowing, when the flowers began to grow, Endo was divided into two groups. Then, the ending of one group (2
4株) に対して、 濃度が 5 X 1 0 — 5モル/ Lである 4 一 C 1 一 I A A水 溶液を 4 0 L / aの撒布量で以て撒布することにより、 茎葉処理を行つ た。 また、 他方のグループのェン ドウ ( 1 6株) に対して、 上記水溶液 の代わりに水を 4 0 L / aの撒布量で以て撒布することにより、 コン ト ロールと した。 Against four strains), concentration of 5 X 1 0 - by spraying Te than in spraying amount of 5 mol / L is 4 one C 1 one IAA water solution 4 0 L / a, Gyotsu the foliage treatment Was. In addition, the other group's endowment (16 strains) was Instead, water was sprayed at a spraying rate of 40 L / a to control.
5月初旬に上記のェン ドウを収穫し、 実であるサヤエン ドウの収穫量 即ち、 1株当たりのサヤエン ドウの重量 ( g) 、 および、 コン トロール に対する重量比 (以下、 対コ ン トロール比と記す) を測定した。 結果を 表 1 6 にまとめた。  Harvesting the above-mentioned window in early May, the harvested amount of the snowy dough, that is, the weight (g) of the snowy dough per plant and the weight ratio to the control (hereinafter referred to as the control ratio) ) Was measured. The results are summarized in Table 16.
表 1 6  Table 16
Figure imgf000044_0001
表 1 6の結果から明らかなように、 本発明にかかる作物増収剤を用い てェン ドゥの茎葉処理を行うことにより、 サャエン ドゥの肥大が促進さ れ、 収量が増加することが判った。
Figure imgf000044_0001
As is evident from the results in Table 16, it was found that by performing the foliage treatment on the endou using the crop-producing agent according to the present invention, the thickening of Sayaendu was promoted and the yield was increased.
〔実施例 1 7〕  (Example 17)
本発明にかかる作物増収剤を用いて小麦の処理を行った。 先ず、 小麦 の種子を 2 5 0 gずつ、 7つにグループ分けした。 1 2月 1 5 日に、 第 1のグループの小麦を、 濃度が 1 X 1 0— 5モル Z Lである 4 _ C 1 一 I A A水溶液に 5時間浸漬することにより、 浸漬処理を行った。 また、 同 日に、 第 2のグループの小麦を、 濃度が 1 X 1 0 モル/ Lである I B A (作物増収剤) 水溶液に 5時間浸漬することにより、 浸漬処理を行つ た。 尚、 上記二種類の水溶液には、 非イオ ン界面活性剤 (東邦化学工業 株式会社製、 商品名 : S o r b o n T— 8 0 ) を、 それぞれ 2 0 p p mの割合で添加した。 Wheat was treated using the crop increasing agent according to the present invention. First, wheat seeds were divided into seven groups of 250 g each. 1 February 1 5 days, wheat first group, concentration by immersing 5 hours 4 _ C 1 one IAA solution is 1 X 1 0- 5 mol ZL, has been dipped. On the same day, a second group of wheat was immersed in an aqueous solution of IBA (crop-growth enhancer) at a concentration of 1 × 10 mol / L for 5 hours. A non-ionic surfactant (manufactured by Toho Chemical Industry Co., Ltd., trade name: Sorbon T—80) was added to each of the above two aqueous solutions at a level of 20 pp. m.
次に、 同日に、 上記 7つのグループの小麦を、 それぞれ一区画 ( 7. 4 m 2 ) の畑に播種して、 圃場試験を行った。 Next, on the same day, wheat from the above seven groups was sown in a field of one plot (7.4 m 2 ), and a field test was performed.
そして、 2月 1 9 日に、 地上部が 1 0 c m程度の高さに生長した第 3 のグループの小麦に対して、 濃度が 5 X 1 0 — 5モル 7 Lである 4 — C 1Then, on February 19th, the concentration of 5 X 10 — 5 mol 7 L for a third group of wheat whose aerial part grew to a height of about 10 cm 4 — C 1
- I A A水溶液を 2 0 L Z aの撒布量 (有効薬量 0. 2 1 g / a ) で以 て撒布することにより、 茎葉処理を行った。 また、 同日に、 同様に生長 した第 4のグループの小麦に対して、 濃度が 5 X 1 0 — 5モル/ Lである I B A水溶液を 2 0 L Z aの撒布量 (有効薬量 0. 2 0 g / a ) で以て 撒布することにより、 茎葉処理を行った。 尚、 上記二種類の水溶液には、 非ィォン界面活性剤 (同上) を、 それぞれ 5 0 0 p p rnの割合で添加し た。 -Foliage treatment was performed by spraying the IAA aqueous solution at a spraying rate of 20 LZa (effective dose 0.21 g / a). On the same day, an aqueous solution of IBA at a concentration of 5 X 10 — 5 mol / L was sprayed at 20 LZ a to the wheat of the fourth group that grew in the same manner. g / a) for foliage treatment. To the two aqueous solutions, a nonionic surfactant (same as above) was added at a ratio of 500 pprn.
さ らに、 4月 1 7 日に、 地上部が 4 0 c m程度の高さに生長し、 かつ、 未だ出穂していない第 5のグループの小麦に対して、 濃度が 5 X 1 0一 5 モル/ Lである 4 一 C I — I A A水溶液を 4 0 L Z aの撒布量 (有効薬 量 0. 4 2 g/ a ) で以て撒布することにより、 茎葉処理を行った。 ま た、 同日に、 同様に生長した第 6のグループの小麦に対して、 濃度が 5 X 1 0 _5モル/ Lである I B A水溶液を 4 0 L Z aの撒布量 (有効薬量 0. 4 1 g/ a ) で以て撒布することにより、 茎葉処理を行った。 尚、 上記二種類の水溶液には、 非イオン界面活性剤 (同上) を、 それぞれ 5 0 0 p p mの割合で添加した。 Et al is, on April 1 7, grown on the ground portion 4 0 cm as high as, and for the fifth group of wheat not yet heading, concentration 5 X 1 0 one 5 The foliage treatment was performed by spraying an aqueous solution of 41-CI-IAA, which is mol / L, at a spraying rate of 40 LZa (effective dose: 0.42 g / a). Also, on the same day, with respect to wheat sixth group of grew similarly, spraying amount of concentration 5 X 1 0 _ 5 mol / L in which IBA aqueous solution 4 0 LZ a (effective agent amount 0.4 Foliage treatment was performed by spraying at 1 g / a). A nonionic surfactant (same as above) was added to the two aqueous solutions at a ratio of 500 ppm.
また、 第 7のグループの小麦に対しては、 上記処理を全く行わないで 水を所定量撒布することにより、 コン トロールと した。  In addition, the wheat in the seventh group was controlled by spraying a predetermined amount of water without performing any of the above treatments.
6月 1 6 日に上記 7つのグループの小麦をそれぞれ収穫し、 収穫量 ( k g Z区画) 、 および、 1穂当たりの平均粒数 (個、 2 0本平均) を測 定した。 結果を表 1 7にまとめた。 On June 16 each of the above seven groups of wheat was harvested and the yield ( kg Z section), and the average number of grains per ear (20 pieces / average) were measured. The results are summarized in Table 17.
表 1 7  Table 17
Figure imgf000046_0001
Figure imgf000046_0001
表 1 7 の結果から明らかなように、 本発明にかかる作物増収剤を用い て小麦の処理を行う ことにより、 1穂当たりの粒数が増加が促進され、 これにより、 小麦の収量が増加することが判った。  As is clear from the results in Table 17, by treating the wheat with the crop-harvesting agent according to the present invention, the number of grains per ear is promoted, thereby increasing the yield of wheat. It turns out.
〔実施例 1 8〕  (Example 18)
本発明にかかる作物増収剤を用いてトウモロコシの処理を行った。 先 ず、 トウモロコシの種子 (多数) を 1 0 にグループ分けした。 4月 1 7 日に、 第 1 のグループの トウモロコシを、 濃度が 5 X 1 0 _ 6モル/ Lで ある 4 — C 1 — I A A水溶液に 2時間浸漬することにより、 浸漬処理を 行った。 また、 同日に、 第 2のグループの トウモロコシを、 濃度が 5 X 1 0— 6モル 7 Lである 4 — C 1 - I A Aェチルアルコ ール溶液に 3 0秒 間浸漬することにより、 浸漬処理を行った。 また、 同日に、 第 3のグル —プの トウモロコシを、 濃度が 5 X 1 0 — 6モル Z Lである I B A水溶液 に 2時間浸漬することにより、 浸漬処理を行った。 また、 同日に、 第 4 のグループの トウモロコシを、 濃度が 5 X 1 0 6モル Z Lである I A AMaize was treated using the crop increasing agent according to the present invention. First, the corn seeds (many) were grouped into 10 groups. On April 1 7, the corn a first group, the concentration of 4 is 5 X 1 0 _ 6 mol / L - C 1 - by immersing 2 hours IAA solution, has been dipped. Further, on the same day, the corn second group concentration 5 X 1 0- 6 mole 7 L a is 4 - performed by immersing for 3 0 seconds IAA Echiruaruko Lumpur solution, the immersion treatment - C 1 Was. Further, on the same day, the third Group - corn flop, concentration 5 X 1 0 - a 6 mol ZL IBA solution The immersion treatment was performed by immersing the sample for 2 hours. On the same day, a fourth group of corn was harvested at a concentration of 5 × 10 6 mol ZL by IAA
(作物増収剤) 水溶液に 2時間浸漬することにより、 浸漬処理を行った c 尚、 上記四種類の溶液には、 非イオン界面活性剤 (東邦化学工業株式会 社製、 商品名 : S o r b o n T— 8 0 ) を、 それぞれ 5 0 0 p p mの 割合で添加した。 (Crop increasing agent) Immersion treatment was carried out by immersion in an aqueous solution for 2 hours. C The above four types of solutions include nonionic surfactants (manufactured by Toho Chemical Industry Co., Ltd., trade name: S orbon T —80) was added at a rate of 500 ppm each.
次に、 4月 1 9 日に、 上記 1 0のグループの トウモロコシを、 それぞ れ苗箱に播種した。 次いで、 4月 3 0 日に、 生長した苗を畑に移植した c そして、 5月 1 日 (播種してから 1 2 日後) に、 地上部が 1 0 c m程 度の高さに生長した第 5のグループの トウモロコシに対して、 濃度が 5 X 1 0 5モル/ Lである 4 — C I — I A A水溶液を 4 0 L / aの撒布量 (有効薬量 0. 4 2 g / a ) で以て撒布することにより、 茎葉処理を行 つた。 また、 同日に、 同様に生長した第 6のグループの トウモロコシに 対して、 濃度が 1 X 1 0— 4モル Z Lである 4 — C I — I A A水溶液を 4 0 L / aの撒布量 (有効薬量 0. 8 4 g / a ) で以て撒布することによ り、 茎葉処理を行った。 また、 同日に、 同様に生長した第 7のグループ の トウモロコシに対して、 濃度が 5 X 1 0 - 5モル/ Lである I A A水溶 液を 4 0 L Z aの撒布量 (有効薬量 0. 3 5 g / a ) で以て撒布するこ とにより、 茎葉処理を行った。 尚、 上記三種類の水溶液には、 非イオン 界面活性剤 (同上) を、 それぞれ 5 0 0 p p mの割合で添加した。 Next, on April 19, the corns of the above 10 groups were sown in seedling boxes, respectively. Then, on April 30, the grown seedlings were transplanted to the field.c . On May 1 (12 days after sowing), the aerial part grew to a height of about 10 cm. for the 5 groups of maize, concentration is 5 X 1 0 5 mol / L 4 - CI - than in spraying amount of 4 0 L / a the IAA solution (effective agent quantity 0. 4 2 g / a) By foliar spraying, foliage treatment was performed. Further, on the same day, for the corn sixth group of grew similarly, concentration of 1 X 1 0- 4 mol ZL 4 - CI - spraying amount of the IAA solution 4 0 L / a (effective drug amount The foliage treatment was performed by spraying with 0.84 g / a). Further, on the same day, with respect to the seventh group of corn was grown in the same manner, concentration of 5 X 1 0 - spraying amount of 5 mol / L in a IAA aqueous solution 4 0 LZ a (effective agent amount 0.3 Foliage treatment was performed by spraying at 5 g / a). Incidentally, a nonionic surfactant (same as above) was added to each of the three kinds of aqueous solutions at a ratio of 500 ppm.
さ らに、 6月 3 0 日 (播種してから 7 2 日後) に、 実が付き始めた第 8のグループの トウモロコシに対して、 濃度が 5 X 1 0 5モル/ Lであ る 4 C 1 I A A水溶液を 4 0 L / aの撒布量 (有効薬量 0. 4 2 g / a ) で以て撒布することにより、 茎葉処理を行った。 また、 同日に、 同様に生長した第 9のグループの トウモロコシに対して、 濃度が 5 X 1 0 5モル Z Lである I A A水溶液を 4 0 L Z aの撒布量 (有効薬量 0 . 3 5 g / a ) で以て撒布することにより、 茎葉処理を行った。 尚、 上記 二種類の水溶液には、 非イオン界面活性剤 (同上) を、 それぞれ 5 0 0 p p mの割合で添加した。 In addition, on June 30 (72 days after seeding), the 8th group of corn that began to bear fruit had a concentration of 5 X 10 5 mol / L with 4 C Foliage treatment was performed by spraying 1 IAA aqueous solution at a spraying rate of 40 L / a (effective dose of 0.42 g / a). Also, on the same day, Against corn ninth group of grew similarly, concentration is sprayed amount of 4 0 LZ a the IAA solution is 5 X 1 0 5 mole ZL (effective drug amount 0. 3 5 g / a) Te following Foliage treatment was performed by spraying. A nonionic surfactant (same as above) was added to the two aqueous solutions at a ratio of 500 ppm.
また、 第 1 0のグループの トウモロコシに対しては、 上記処理を全く 行わないで水を所定量撒布することにより、 コン トロールとした。  Further, the corn of the 10th group was controlled by spraying a predetermined amount of water without performing any of the above treatments.
8月 6 日に上記 1 0のグループの トウモロコシをそれぞれ収穫し、 収 穫量、 即ち、 トウモロコシの全重量 ( k g ) を測定すると共に、 1株当 たりの重量 (k g ) 、 および、 対コン トロール比を算出した。 結果を表 1 8 にまとめた。 Above 1 0 group of corn were harvested respectively on August 6, yield Karyou, i.e., with measuring the total weight of maize (k g), the per share Weight (kg), and, to-Con The trawl ratio was calculated. The results are summarized in Table 18.
表 1 8 グル 作物増収剤 水溶液濃度 有効薬量 処理 株 数 Table 1 8 Guru Crop increase agent Aqueous solution concentration Effective dose Amount treated
ープ ( / a) 方法 (株) (k g)  (/ A) Method Co., Ltd. (kg)
1 4一 C 1一 I AA 5 X 1 0 4 7 1 9. 9 1 1 4 1 C 1 1 I AA 5 X 1 0 4 7 1 9.9 1
4 - C 1 - I A A 5 x 1 0一6 1 2 4. 2 1 4-C 1-IAA 5 x 10 0 1 6 1 2 4.2 1
ェチルアル] -ル溶液  Etilal]-solution
I B A 5 1 0 2 5 9. 9 2 I B A 5 1 0 2 5 9. 9 2
I A A 5 X 1 0 2 3 8. 5 5 I A A 5 X 1 0 2 3 8.5 5 5
4一 C 1一 I AA 5 x 1 0 0. 42 2 6 1 0. 8 1 6 4 1 C 1 1 I AA 5 x 1 0 0.42 2 6 1 0.8 1 6
4一 C 1一 I AA 1 x 1 0 0. 84 2 5 1 0. 3 0 4 1 C 1 1 I AA 1 x 1 0 0.84 2 5 1 0.3 0
I A A 5 x 1 0一5 0. 3 5 2 2 7. 8 3 IAA 5 x 10 0 1 5 0 .3 5 2 2 7. 8 3
4 - C 1 - I A A 5 X 1 0 0. 4 2 2 3 8. 7 7 4-C 1-I A A 5 X 1 0 0. 4 2 2 3 8. 7 7
I AA 5 x 1 0 0. 3 5 2 0 7. 3 0 I AA 5 x 1 0 0. 3 5 2 0 7.30
1 0 コン トローノレ 7 2 2 2. 7 1 1 0 Contronore 7 2 2 2. 7 1
表 1 8 の結果から明らかなように、 本発明にかかる作物増収剤を用い て トウモロコシの処理を行う ことにより、 実の肥大が促進されて収量が 増加することが判った。 As is evident from the results in Table 18, it was found that the corn treatment using the crop-producing agent according to the present invention promoted actual hypertrophy and increased the yield.
〔実施例 1 9〕  (Example 19)
本発明にかかる作物増収剤を用いてヮ夕 (アメ リカヮタ) の茎葉処理 を行つた。 先ず、 5月 8 日にヮ夕の種子 (多数) を 5 0 c m間隔で圃場 に直播き して育成した。 その後、 ヮタを 3つにグループ分けした。 そし て、 播種してから 3週間経過後に、 6葉程度に生長した第 1のグループ のヮタ ( 6株) に対して、 ノニオン系界面活性剤 (和光純薬工業株式会 社製、 商品名 : T w e e n 8 0 ) を 1 0 0 p p mの割合で含む、 濃度 が 5 X 1 0 5モル/ Lである I A A水溶液を 2 0 L / aの撒布量で以て 撒布することにより、 茎葉処理 (初期) を行った。 Using the crop-producing agent of the present invention, foliage treatment was performed on rice (American ivy). First, on May 8, ヮ evening seeds (many) were directly sowed at 50 cm intervals and cultivated. After that, I divided the data into three groups. Three weeks after sowing, the first group of ivy (6 strains), which grew to about 6 leaves, was treated with a nonionic surfactant (Wako Pure Chemical Industries, Ltd.). : the T ween 8 0) in a proportion of 1 0 0 ppm, by spraying concentration of IAA solution is 5 X 1 0 5 mol / L Te than in spraying amounts of 2 0 L / a, foliage treatment ( Initial).
次いで、 播種してから 7週間経過後に、 第 2のグループのヮタ ( 7株 ) に対して、 上記水溶液 (同一組成) を 2 0 L / aの撒布量で以て撒布 することにより、 茎葉処理 (中期) を行った。 第 3のグループのヮタ ( 1 4株) に対しては、 上記処理を全く行わないで水を所定量撒布するこ とにより、 コン トロールと した。  After 7 weeks from the sowing, the above aqueous solution (same composition) was sprayed onto the second group of ivy (7 strains) at a spraying rate of 20 L / a to obtain foliage. Processing (middle term) was performed. The control was applied to the third group of potatoes (14 strains) by spraying a predetermined amount of water without any of the above treatments.
そして、 これら 3つのグループに対し、 綿摘みを 1 0月 1 2 日、 1 1 月 9 日および 1 2月 3 日の 3回行って、 それぞれヮタを収穫し、 収穫量 即ち、 種子を含むヮタの 1株当たりの重量を測定すると共に、 対コン ト ロール比を算出した。 結果を表 1 9 にまとめた。 Then, cotton picking was performed on these three groups three times on October 12, October 9, and January 3, and harvested potatoes, respectively. We measured the weight of each peta stock and calculated the ratio to control. The results are summarized in Table 19.
表 1 9 グル 作物 水溶液濃度 処理方法 株 数 10月収穫量 (g) 11月収穫量 (g) 12月収穫量 (g) 総収穫量 (g) ープ 増収剤 Table 1 9 Gour Crops Aqueous solution concentration Treatment method Number of plants Number of October harvest (g) November harvest (g) December harvest (g) Gross harvest (g)
(モル/ (株) 対コン -ル比 対コント π-ル比 対コント ル比 対コント α-ル比 茎葉 7 6. 7 1 2 0. 0 5 6. 7 2 5 3. 4 (Mol / Co., Ltd. to control ratio to control π-control ratio to control ratio to control α-control ratio Foliage 7 6. 7 1 2 0 .0 5 6. 7 2 5 3. 4
1 6 1 6
(初期) 1. 5 1. 3 8 0. 6 6 1. 1 2 (Initial) 1. 5 1. 3 8 0.6. 6 1. 1. 2
I AA 5 X 1 0 -5 I AA 5 X 1 0 - 5
茎葉 8 7. 3 1 0 3. 6 1 0 7. 1 2 9 8. 0 Foliage 8 7. 3 1 0 3.6 1 0 7. 1 2 9 8.0
2 7 2 7
(中期) 1. 6 5 1. 1 9 1. 2 5 1. 3 2  (Medium term) 1. 6 5 1. 1 9 1. 2 5 1.
3 コントロール 1 4 5 2. 9 8 7. 1 8 5. 7 2 2 5. 7 3 Control 1 4 5 2. 9 8 7. 1 8 5. 7 2 2 5. 7
表 1 9 の結果から明らかなように、 本発明にかかる作物増収剤を用い てヮ夕の茎葉処理を行うことにより、 早期の収穫量を増加させることが できると共に、 総収穫量が第 1のグループでは 1 2 %、 第 2のグループ では 3 2 %、 それぞれ増加することが判った。 As is evident from the results in Table 19, the early harvest can be increased by performing the foliage treatment in the evening using the crop-harvesting agent according to the present invention, and the total yield can be reduced to the first. The increase was 12% in the group and 32% in the second group.
〔実施例 2 0〕  (Example 20)
本発明にかかる作物増収剤を用いてイネ (コシヒカ リ) の処理を行つ た。 先ず、 5月上旬にイネの種子 (モミ) を 3つにグループ分けして苗 箱に播種した。 このとき、 第 1のグループのイネの種子に対しては、 播 種前に、 ノ二オン系界面活性剤 (米国, V a 1 e n t社製、 商品名 : X - 7 7 ) を 2 0 p p mの割合で含む、 濃度が 1 x 1 0 — 7モル Z LであるRice (Koshihikari) was treated using the crop yield enhancer according to the present invention. First, rice seeds (fir) were divided into three groups and sown in seedling boxes in early May. At this time, 20 ppm of nonionic surfactant (manufactured by Va1ent, USA; trade name: X-77) was added to the seeds of the first group of rice before sowing. Concentration is 1 x 10 — 7 mol ZL
I A A水溶液に 2時間浸漬することにより、 浸漬処理を行った。 The immersion treatment was performed by immersing in an IA A aqueous solution for 2 hours.
一方、 5月 2 6 日に、 地上部が 1 0 c m程度の高さに生長した第 2の グループのイネに対して、 ノニオン系界面活性剤 (T w e e n 8 0 ) を 1 0 0 p p mの割合で含む、 濃度が 5 X 1 0 — 5モル/ Lである I A A 水溶液を、 苗箱 1箱当たり 5 0 0 m 1 の撒布量で以て撒布することによ り、 茎葉処理を行った。 第 3のグループのイネに対しては、 上記処理を 全く行わないで水を所定量撒布することにより、 コン トロールと した。 On the other hand, on May 26, 100 ppm of nonionic surfactant (Tween 80) was added to the rice of the second group, whose height above the ground was about 10 cm. The foliage treatment was carried out by spraying an aqueous solution of IAA having a concentration of 5 × 10 — 5 mol / L containing 5,000 m 1 per seedling box. A third group of rice was controlled by spraying a predetermined amount of water without any of the above treatments.
そして、 苗箱に播種してから 1 力月間育成した後、 生長したイネの苗 を水田に移植した。 植え付け間隔 (株間) は 2 5 c mとし、 1つのグル 一プが 1 8 m X 3列となるように田植えした。  After sowing the seedlings in the seedling box and growing for one month, the grown rice seedlings were transplanted to the paddy field. The planting interval (between plants) was 25 cm, and rice was planted so that one group had 18 mx 3 rows.
9月 2 3 日にイネを刈り取り、 乾燥して脱穀することにより、 イネ ( コメ) を収穫し、 収穫量、 即ち、 1株当たりのコメの重量を測定すると 共に、 対コン トロール比を算出した。 結果を表 2 0にまとめた。 表 2 0 On September 23, rice was harvested, dried and threshed to harvest the rice (rice), and the yield, that is, the weight of rice per plant, was measured, and the ratio to control was calculated. . The results are summarized in Table 20. Table 20
Figure imgf000053_0001
表 2 0の結果から明らかなように、 本発明にかかる作物増収剤を用い てイネの処理を行う ことにより、 コメの収量が増加することが判つた。 〔実施例 2 1〕
Figure imgf000053_0001
As is clear from the results in Table 20, it was found that the rice yield was increased by treating the rice with the crop increasing agent according to the present invention. (Example 21)
本発明にかかる作物増収剤を用いて小麦の処理を行った。 先ず、 1 2 月中旬に小麦の種子を 2 5 0 gずつ、 3つにグループ分けし、 それぞれ 面積 7. 5 m 2 の畑に播種した。 このとき、 第 1のグループの小麦に対 しては、 播種前に、 ノニォン系界面活性剤 (Tw e e n 8 0 ) を 2 0 p p mの割合で含む、 濃度が 1 X 1 0 モル/ Lである I A A水溶液にWheat was treated using the crop increasing agent according to the present invention. First, one mid-February to seeds 2 5 0 g of wheat, were grouped into three, it was seeded in a field of the area 7. 5 m 2, respectively. At this time, for the wheat of the first group, before sowing, it contains a nonionic surfactant (Tween 80) at a ratio of 20 ppm, and the concentration is 1 × 10 mol / L. IAA solution
2時間浸漬することにより、 浸漬処理を行った。 The immersion treatment was performed by immersion for 2 hours.
一方、 2月下旬に、 地上部が 1 0 c m程度の高さに生長した第 2のグ ループの小麦に対して、 ノニォン系界面活性剤 (Tw e e n 8 0 ) を 1 0 0 p mの割合で含む、 濃度が 5 X 1 0 5モル/ Lである I A A水 溶液を 2 0 0 m 1 /m 2 の撒布量で以て撒布することにより、 茎葉処理 を行った。 第 3のグループの小麦に対しては、 上記処理を全く行わない で水を所定量撒布することにより、 コン トロールとした。 On the other hand, in late February, nonionic surfactant (Tween 80) was added at a rate of 100 pm to a second group of wheat, whose tops grew to a height of about 10 cm. The foliage treatment was performed by spraying an aqueous IAA solution having a concentration of 5 × 10 5 mol / L at a spray rate of 200 m 1 / m 2 . The third group of wheat was controlled by spraying a predetermined amount of water without any of the above treatments.
そして、 6月中旬に上記 3つのグループの小麦をそれぞれ収穫し、 収 穫量 ( k g/区画) と共に、 対コン トロール比を算出した。 結果を表 2 1 にまとめた。 In mid-June, the three groups of wheat were harvested, and the yield (kg / plot) and the ratio to control were calculated. Table 2 shows the results Summarized in 1.
表 2 1  Table 2 1
Figure imgf000054_0001
Figure imgf000054_0001
表 2 1の結果から明らかなように、 本発明にかかる作物増収剤を用い て小麦の処理を行う ことにより、 収穫量が第 1のグループでは 2 4 %、 第 2のグループでは 2 0 %、 それぞれ増加することが判った。  As is evident from the results in Table 21, by processing the wheat using the crop enhancer according to the present invention, the yield was 24% in the first group, 20% in the second group, and It was found that each increased.
〔実施例 2 2〕  (Example 22)
本発明にかかる作物増収剤を用いて トマ 卜の茎葉処理を行った。 先ず、 互いに生長状態がほぼ揃っている トマ トの苗 (複数) を選択し、 5月 2 0 日に、 4 0 c m間隔で圃場に植え付けて育成した。  The foliage treatment of tomato was performed using the crop increasing agent according to the present invention. First, tomato seedlings whose growth conditions were almost the same were selected and planted on May 20 at 40 cm intervals in a field.
6月 3 日に、 地上部が 2 0 c m程度の高さに生長した第 1のグループ の トマ トに対して、 ノニォン系界面活性剤 (X— 7 7 ) を 2 0 p p mの 割合で含む、 濃度が 1 X 1 0— 5モル ZLである I A A水溶液を 1 0 0 m 1 /m2 の撒布量で以て撒布することにより、 茎葉処理を行った。 一方- 同日に、 第 2のグループの トマ トに対して、 ノニォン系界面活性剤 (同 上) を 2 0 p p mの割合で含む、 濃度が 1 X 1 0 —5モル/ Lである 4 C 1 - I A A水溶液を 1 0 0 m 1 /m 2 の撒布量で以て撒布することに より、 茎葉処理を行った。 第 3のグループの トマ トに対しては、 上記処 理を全く行わないで水を所定量撒布するこ とによ り、 コ ン ト ロールと し た。 そして、 植え付けてから 3か月間経過後 ( 8月中旬) 、 収穫量、 即ち トマ 卜の実の数 (結実数) を求めると共に、 対コン トロ -ル比を算出し た。 結果を表 2 2 にまとめた。 On June 3, a nonionic surfactant (X-77) was contained at a ratio of 20 ppm to the first group of tomatoes whose aerial parts grew to a height of about 20 cm. concentration by spraying Te than 1 0 0 spraying amount of m 1 / m 2 the IAA solution is 1 X 1 0- 5 mol ZL, were foliar treatment. On the other hand, on the same day, the second group of tomatoes contained 20 ppm of nonionic surfactant (as above) at a concentration of 1 X 10 — 5 mol / L 4 C 1 -IAA aqueous solution was sprayed at a spraying rate of 100 m 1 / m 2 to perform foliage treatment. The third group of tomatoes was controlled by spraying a predetermined amount of water without any of the above treatments. Three months after planting (mid-August), the yield, that is, the number of tomatoes (fruits) was calculated, and the control ratio was calculated. The results are summarized in Table 22.
表 2 2  Table 2 2
Figure imgf000055_0001
表 2 2 の結果から明らかなように、 本発明にかかる作物増収剤を用い て トマ 卜の茎葉処理を行う ことにより、 実の総数が第 1のグループでは 2 3 %、 第 2のグループでは 2 7 %、 それぞれ増加することが判つた。 尚、 発明を実施するための最良の形態の項においてなした具体的な実 施態様または実施例は、 あく までも、 本発明の技術内容を明らかにする ものであって、 そのような具体例にのみ限定して狭義に解釈されるべき ものではなく、 本発明の精神と次に記載する特許請求の範囲内で、 いろ いろと変更して実施することができるものである。 産業上の利用可能性
Figure imgf000055_0001
As is evident from the results in Table 22, the foliage treatment of tomato using the crop-producing agent according to the present invention resulted in a total number of fruits of 23% in the first group and 2% in the second group. 7%, respectively. It should be noted that the specific embodiments or examples made in the section of the best mode for carrying out the invention merely clarify the technical contents of the present invention, and such specific examples The present invention should not be construed as being limited to only the above, but can be implemented with various modifications within the spirit of the present invention and the scope of the claims described below. Industrial applicability
本発明にかかる塊根 ·塊茎肥大促進剤は、 前記一般式 ( 1 ) で示され るイ ン ドール骨格含有化合物、 前記一般式 ( 2 ) で示されるベンゼン骨 格含有化合物、 および、 前記一般式 ( 3 ) で示されるナフタ レン骨格含 有化合物からなる群より選ばれる少なく とも一種の化合物を含む構成で ある。 該塊根 ·塊茎肥大促進剤は、 野菜類や花卉類等の植物が有する塊 根や塊茎の肥大を促進させるのに好適に用いることができ、 しかも、 安 全性に優れかつ大量生産可能である。 The tuber / tuber hypertrophy promoter according to the present invention comprises an indole skeleton-containing compound represented by the general formula (1), a benzene skeleton-containing compound represented by the general formula (2), and 3) Including the naphthalene skeleton The composition includes at least one compound selected from the group consisting of organic compounds. The tuber and tuber hypertrophy promoter can be suitably used to promote tuber and tuber hypertrophy of plants such as vegetables and flowers, and is excellent in safety and can be mass-produced. .
また、 本発明にかかる作物増収剤は、 前記一般式 ( 1 ) で示されるィ ン ドール骨格含有化合物を含む構成である。 該作物増収剤は、 各種作物 (植物) の花数や穂数の増加、 分蘖、 或いは、 実 (果実、 種子) の肥大 を促進させて収量を増加させるのに好適に用いることができ、 しかも、 安全性に優れかつ大量生産可能である。  Further, the crop increasing agent according to the present invention is configured to contain the indole skeleton-containing compound represented by the general formula (1). The crop-harvesting agent can be suitably used for increasing the number of flowers and ears of various crops (plants), increasing the number of tillers, or promoting the hypertrophy of fruits (fruits and seeds) to increase the yield. It is excellent in safety and can be mass-produced.

Claims

求 の 般式 ( 1 The general formula (1
一 ( 1 ) One (1)
Figure imgf000057_0001
Blue
Figure imgf000057_0001
(式中、 Xは、 水素原子、 塩素原子またはメ トキシ基を表し、 R 1 は、 — C H O基、 — C H 2 C H O基、 — C H 2 C N基、 — C O O R 2 基、 ― C H 2 C 00 R 2 基、 _ C H 2 C H 2 C O O R 2 基、 — C H (C H 3) C 00 R 2 基、 — C H 2 C H 2 C H 2 C O O R 2 基、 — C H (C H 3) C H 2 C O O R 2 基、 — C H (C H 3) C H 2 C H 2 C O O R 2 基、 または— C H 2 C 0 C 00 R 2 基を表し、 かつ、 上記 R 2 は、 水素原子、 アル力 リ金属原子、 アルカ リ土類金属原子、 炭素数 1〜 4のアルキル基、 単糖 の配糖体またはォリ ゴ糖の配糖体を表す) (Wherein, X represents a hydrogen atom, a chlorine atom or a methoxy group, and R 1 is — CHO group, — CH 2 CHO group, — CH 2 CN group, — COOR 2 group, — CH 2 C 00 R 2 group, _ CH 2 CH 2 COOR 2 group, - CH (CH 3) C 00 R 2 group, - CH 2 CH 2 CH 2 COOR 2 group, - CH (CH 3) CH 2 COOR 2 group, - CH ( CH 3 ) CH 2 CH 2 COOR 2 group or —CH 2 C 0 C 00 R 2 group, and R 2 is a hydrogen atom, an alkali metal atom, an alkaline earth metal atom, the number of carbon atoms Represents an alkyl group of 1-4, a monosaccharide glycoside or an oligosaccharide glycoside)
で示されるイ ン ドール骨格含有化合物、 一般式 ( 2 ) An indole skeleton-containing compound represented by the general formula (2)
Figure imgf000057_0002
Figure imgf000057_0002
(式中、 R 3 は、 水素原子、 アルカリ金属原子、 アルカリ土類金属原 子、 炭素数 1〜 4のアルキル基、 単糖の配糖体またはォリ ゴ糖の配糖体 を表し、 R 4 は、 水素原子、 塩素原子、 メチル基またはヒ ドロキシメチ ル基を表す) (Wherein, R 3 is a hydrogen atom, an alkali metal atom, an alkaline earth metal atom, an alkyl group having 1 to 4 carbon atoms, a monosaccharide glycoside or an oligosaccharide glycoside) And R 4 represents a hydrogen atom, a chlorine atom, a methyl group or a hydroxymethyl group)
で示されるベンゼン骨格含有化合物、 および、 一般式 ( 3 ) A benzene skeleton-containing compound represented by the general formula (3)
Figure imgf000058_0001
(式中、 R 5 は、 ヒ ドロキシル基またはアミ ノ基を表す)
Figure imgf000058_0001
(Wherein, R 5 represents a hydroxyl group or an amino group)
で示されるナフタ レン骨格含有化合物からなる群より選ばれる少なく と も一種の化合物を含むことを特徴とする塊根 ·塊茎肥大促進剤。 A tuberous root / tuber hypertrophy accelerator comprising at least one compound selected from the group consisting of naphthalene skeleton-containing compounds represented by the formula:
2 . 上記化合物がィ ン ドール骨格含有化合物であることを特徴とする請 求項 1記載の塊根 ·塊茎肥大促進剤。  2. The tuber / tuber hypertrophy promoter according to claim 1, wherein the compound is an indole skeleton-containing compound.
3 . 上記イ ン ドール骨格含有化合物が天然化合物であることを特徴とす る請求項 2記載の塊根 ·塊茎肥大促進剤。  3. The tuber / tuber hypertrophy promoter according to claim 2, wherein the indole skeleton-containing compound is a natural compound.
4 . 上記ィ ン ドール骨格含有化合物が 4 —クロ口イ ン ドール— 3 —酢酸 および/またはそのエステルであることを特徴とする請求項 2または 3 記載の塊根 ·塊茎肥大促進剤。  4. The tuber / tuber hypertrophy promoter according to claim 2 or 3, wherein the indole skeleton-containing compound is 4-cloindindole-3-acetic acid and / or an ester thereof.
5 . 界面活性剤をさ らに含むことを特徴とする請求項 1、 2、 3 または 5. The method according to claim 1, 2, 3 or 3, further comprising a surfactant.
4記載の塊根 ·塊茎肥大促進剤。 Tuberous root according to 4 · Tuber hypertrophy promoter.
6 . 植物生長調節剤、 肥料、 除草剤、 殺黴剤、 殺虫剤、 殺ダニ剤、 殺線 虫剤、 農園芸用殺菌剤、 土壌殺菌剤、 および土壌改良剤からなる群より 選ばれる少なく とも一種の薬剤と併用することを特徴とする請求項 1 な いし 5の何れか 1項に記載の塊根 ·塊茎肥大促進剤。 6. At least one selected from the group consisting of plant growth regulators, fertilizers, herbicides, fungicides, insecticides, acaricides, nematicides, agricultural and horticultural fungicides, soil fungicides, and soil conditioners. Claim 1 which is used in combination with a kind of drug 6. The agent for promoting tuberous root and tuber hypertrophy according to any one of item 5 above.
7. 1 アール当たりの使用量が 1 0— 7 g〜 5 gの範囲内であることを特 徵とする請求項 1ないし 6の何れか 1項に記載の塊根 ·塊茎肥大促進剤 c7. The tuber and tuber hypertrophy promoter c according to any one of claims 1 to 6, wherein the amount used per are is in the range of 10 to 7 g to 5 g.
8. 水で希釈されていることを特徴とする請求項 1ないし 7の何れか 1 項に記載の塊根 ·塊茎肥大促進剤。 8. The tuber / tuber hypertrophy promoter according to any one of claims 1 to 7, wherein the agent is diluted with water.
9. 液剤、 粉剤、 粒剤、 顆粒剤、 水和剤、 フロアブル剤、 乳剤、 および ペース ト剤からなる群より選ばれる少なく とも一種の製剤形態を採って いることを特徴とする請求項 1ないし 7の何れか 1項に記載の塊根 · 塊 茎肥大促進剤。  9. The pharmaceutical composition according to claim 1, wherein the composition is in at least one type of formulation selected from the group consisting of liquids, powders, granules, granules, wettable powders, flowables, emulsions, and pastes. 7. The tuberous root / tubule enlargement promoter according to any one of 7 above.
1 0. 茎葉処理、 土壌処理、 浸漬処理、 粉剤処理、 および注入処理から なる群より選ばれる少なく とも一種の処理方法に適用されることを特徴 とする請求項 1ないし 9の何れか 1項に記載の塊根 ·塊茎肥大促進剤。 10. The method according to any one of claims 1 to 9, wherein the method is applied to at least one kind of treatment method selected from the group consisting of foliage treatment, soil treatment, immersion treatment, dust treatment, and injection treatment. Tuberous root described. Tuber hypertrophy promoter.
1 1. 茎葉、 根、 種子、 花、 および果実からなる群より選ばれる少なく とも一種の植物部位に適用されることを特徴とする請求項 1ないし 9の 何れか 1項に記載の塊根 ·塊茎肥大促進剤。 1 1. The tuber and tuber according to any one of claims 1 to 9, wherein the tuber is applied to at least one plant part selected from the group consisting of foliage, roots, seeds, flowers, and fruits. Hypertrophy.
1 2. 一般式 ( 1 )  1 2. General formula (1)
Figure imgf000059_0001
Figure imgf000059_0001
(式中、 Xは、 水素原子、 塩素原子またはメ トキシ基を表し、 R 1 は 一 C H O基、 — C H 2 C H O基、 — C H 2 C N基、 — C O O R 2 基、 ― C H 2 C 00 R 2 基、 — C H 2 C H 2 C 00 R 2 基、 — C H (C H 3) C 00 R 2 基、 — C H 2 C H 2 C H 2 C 00 R 2 基、 — C H (C H 3) C H 2 C 00 R 2 基、 一 C H (C H 3) C H 2 C H 2 C 00 R 2 基、 または一 C H 2 C O C O O R 2 基を表し、 かつ、 上記 R 2 は、 水素原子、 アル力 リ金属原子、 アルカ リ土類金属原子、 炭素数 1〜 4のアルキル基、 単糖 の配糖体またはォリ ゴ糖の配糖体を表す) (Wherein, X represents a hydrogen atom, a chlorine atom or a methoxy group, and R 1 represents one CHO group, —CH 2 CHO group, —CH 2 CN group, —COOR 2 group, —CH 2 C 00 R 2 Groups, — CH 2 CH 2 C 00 R 2 groups, — CH (CH 3 ) C 00 R 2 groups, — CH 2 CH 2 CH 2 C 00 R 2 groups, — CH (CH 3 ) CH 2 C 00 R 2 groups, 1 CH (CH 3 ) CH 2 CH 2 C 00 R 2 groups, or 1 Represents a CH 2 COCOOR 2 group, and R 2 is a hydrogen atom, an alkali metal atom, an alkaline earth metal atom, an alkyl group having 1 to 4 carbon atoms, a monosaccharide glycoside or an oligosaccharide. Represents sugar glycoside)
で示されるイ ン ドール骨格含有化合物を含むことを特徴とする作物増収 剤。 A crop increasing agent comprising an indole skeleton-containing compound represented by the formula:
1 3. 上記ィ ン ドール骨格含有化合物が天然化合物であることを特徴と する請求項 1 2記載の作物増収剤。  13. The crop increasing agent according to claim 12, wherein the indole skeleton-containing compound is a natural compound.
1 4. 上記イ ン ドール骨格含有化合物が、 イ ン ドールー 3 -酢酸、 4 一 クロ口イ ン ドール— 3 —酢酸、 イ ン ドールー 3 —酪酸、 および、 これら 化合物のエステルからなる群より選ばれる少なく とも一種の化合物であ ることを特徴とする請求項 1 2 または 1 3記載の作物増収剤。  1 4. The compound containing the indole skeleton is selected from the group consisting of indole-3-acetic acid, 4-methylindole-3-acetate, indole-3-butyric acid, and esters of these compounds. 14. The crop enhancer according to claim 12, wherein the crop enhancer is at least one compound.
1 5. 上記ィ ン ドール骨格含有化合物が、 4 一クロ口イ ン ドールー 3 — 酢酸、 および/または、 イ ン ドールー 3 —酪酸であることを特徴とする 請求項 1 2 または 1 3記載の作物増収剤。  1 5. The crop according to claim 12 or 13, wherein the indole skeleton-containing compound is 4 mono-indole 3-acetic acid and / or indole 3-butyric acid. Increasing agent.
1 6. 還元剤をさ らに含むことを特徴とする請求項 1 2、 1 3、 1 4 ま たは 1 5記載の作物増収剤。  16. The crop enhancer according to claim 12, 13, 14, or 15, further comprising a reducing agent.
1 7. 還元剤が重亜硫酸ナ ト リ ゥムであることを特徴とする請求項 1 6 記載の作物増収剤。  17. The crop increasing agent according to claim 16, wherein the reducing agent is sodium bisulfite.
1 8. 植物生長調節剤、 肥料、 除草剤、 殺黴剤、 殺虫剤、 殺ダニ剤、 殺 線虫剤、 農園芸用殺菌剤、 土壌殺菌剤、 および土壌改良剤からなる群よ り選ばれる少なく とも一種の薬剤と併用することを特徴とする請求項 1 2ないし 1 7の何れか 1項に記載の作物増収剤。 1 8. Selected from the group consisting of plant growth regulators, fertilizers, herbicides, fungicides, insecticides, acaricides, nematicides, agricultural and horticultural fungicides, soil fungicides, and soil conditioners The crop increasing agent according to any one of claims 12 to 17, which is used in combination with at least one kind of drug.
1 9 . 1 アール当たりの使用量が 1 0 — 7 g〜 5 gの範囲内であることを 特徴とする請求項 1 2ないし 1 8の何れか 1項に記載の作物増収剤。 The crop increasing agent according to any one of claims 12 to 18, wherein the amount used per 19.1 is in the range of 10 to 7 g to 5 g.
2 0 . 水で希釈されていることを特徴とする請求項 1 2ないし 1 9の何 れか 1項に記載の作物増収剤。 20. The crop enhancer according to any one of claims 12 to 19, which is diluted with water.
2 1 . 液剤、 粉剤、 粒剤、 顆粒剤、 水和剤、 フロアブル剤、 乳剤、 およ びペース ト剤からなる群より選ばれる少なく とも一種の製剤形態を採つ ていることを特徴とする請求項 1 2ないし 1 9の何れか 1項に記載の作 物増収剤。  2 1. It is characterized in that it takes at least one type of formulation selected from the group consisting of liquids, powders, granules, granules, wettable powders, flowables, emulsions, and pastes 10. The crop enhancer according to any one of claims 12 to 19.
2 2 . 茎葉処理、 土壌処理、 浸漬処理、 粉剤処理、 および注入処理から なる群より選ばれる少なく とも一種の処理方法に適用されることを特徴 とする請求項 1 2ないし 2 0の何れか 1項に記載の作物増収剤。  22. The method according to any one of claims 12 to 20, wherein the method is applied to at least one kind of treatment method selected from the group consisting of foliage treatment, soil treatment, immersion treatment, dust treatment, and injection treatment. Item 8. A crop-promoting agent according to Item.
2 3 . 茎葉、 根、 種子、 花、 および果実からなる群より選ばれる少なく とも一種の植物部位に適用されることを特徴とする請求項 1 2ないし 2 0の何れか 1項に記載の作物増収剤。  23. The crop according to any one of claims 12 to 20, wherein the crop is applied to at least one plant part selected from the group consisting of foliage, roots, seeds, flowers, and fruits. Increasing agent.
PCT/JP1999/001591 1998-03-30 1999-03-26 Tuberous root/tuber thickening promoters and crop yield increasing agents WO1999049728A1 (en)

Applications Claiming Priority (4)

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JP10/84397 1998-03-30
JP8439798 1998-03-30
JP26676398 1998-09-21
JP10/266763 1998-09-21

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1667520A4 (en) * 2003-08-22 2010-05-19 Stoller Ets Methods for improving growth and crop productivity of plants by adjusting plant hormone levels, ratios and/or co-factors
US8207091B2 (en) 2004-03-02 2012-06-26 Stoller Enterprises, Inc. Methods for improving growth and crop productivity of plants by adjusting plant hormone levels, ratios and/or co-factors
US8252722B2 (en) 2003-08-22 2012-08-28 Stoller Enterprises, Inc. Controlling plant pathogens and pests with applied or induced auxins

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS272219B1 (en) * 1950-04-25 1952-06-17
JPS3812529B1 (en) * 1961-02-13 1963-07-18
JPS4999807A (en) * 1973-01-26 1974-09-20
JPS5265077A (en) * 1975-11-18 1977-05-30 Philagro Sa Composotion for increasing sugar component of sugar cane and usage of same
JPS5921601A (en) * 1982-07-29 1984-02-03 Kanesho Kk Coloring promotor
JPS61500689A (en) * 1983-09-15 1986-04-10 ユニバ−シティ・オブ・バス Contact lens disinfection composition, disinfection solution and disinfection method
JPH0662563B1 (en) * 1986-01-08 1994-08-17 Nippon Kayaku Kk
JPH08245308A (en) * 1995-03-08 1996-09-24 M T I:Kk Antibacterial liquid
JPH09241239A (en) * 1996-03-06 1997-09-16 Agency Of Ind Science & Technol Esters of 4-chloroindole-3-acetic acid

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS272219B1 (en) * 1950-04-25 1952-06-17
JPS3812529B1 (en) * 1961-02-13 1963-07-18
JPS4999807A (en) * 1973-01-26 1974-09-20
JPS5265077A (en) * 1975-11-18 1977-05-30 Philagro Sa Composotion for increasing sugar component of sugar cane and usage of same
JPS5921601A (en) * 1982-07-29 1984-02-03 Kanesho Kk Coloring promotor
JPS61500689A (en) * 1983-09-15 1986-04-10 ユニバ−シティ・オブ・バス Contact lens disinfection composition, disinfection solution and disinfection method
JPH0662563B1 (en) * 1986-01-08 1994-08-17 Nippon Kayaku Kk
JPH08245308A (en) * 1995-03-08 1996-09-24 M T I:Kk Antibacterial liquid
JPH09241239A (en) * 1996-03-06 1997-09-16 Agency Of Ind Science & Technol Esters of 4-chloroindole-3-acetic acid

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Chemical Abstracts Service (C A S); 1 January 1970 (1970-01-01), ALAGAPPAN R M: "GROWTH RESPONSES IN SWEET POTATO IN INDOLE-3-ACETIC ACID AND ALPHA-NAPHTHALENE ACETIC ACID", XP002919118 *
Chemical Abstracts Service (C A S); 1 January 1980 (1980-01-01), KUMAR P, BAIJAL B D: "ROLE OF VARIOUS GROWTH REGULATORS ON GROWTH AND DEVELOPMENT OF POTATO (SOLANUM TUBEROSUM L.) II. STOLON DEVELOPMENT, TUBER INDUCTION AND YIELD", XP002919117 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1667520A4 (en) * 2003-08-22 2010-05-19 Stoller Ets Methods for improving growth and crop productivity of plants by adjusting plant hormone levels, ratios and/or co-factors
US8252722B2 (en) 2003-08-22 2012-08-28 Stoller Enterprises, Inc. Controlling plant pathogens and pests with applied or induced auxins
US8207091B2 (en) 2004-03-02 2012-06-26 Stoller Enterprises, Inc. Methods for improving growth and crop productivity of plants by adjusting plant hormone levels, ratios and/or co-factors

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