JP2008189593A - Defloration agent and defloration method - Google Patents

Defloration agent and defloration method Download PDF

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JP2008189593A
JP2008189593A JP2007025762A JP2007025762A JP2008189593A JP 2008189593 A JP2008189593 A JP 2008189593A JP 2007025762 A JP2007025762 A JP 2007025762A JP 2007025762 A JP2007025762 A JP 2007025762A JP 2008189593 A JP2008189593 A JP 2008189593A
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flowering
polysaccharide
chitosan
agent
weight
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Akio Morita
明雄 森田
Kanako Shibata
歌菜子 柴田
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Shizuoka University NUC
Yaizu Suisan Kagaku Kogyo Co Ltd
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Shizuoka University NUC
Yaizu Suisan Kagaku Kogyo Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a defloration agent and a defloration method, hardly affecting a human body, a plant and the environment, and having excellent defloration effects. <P>SOLUTION: The defloration method includes spraying the defloration agent containing at least one kind selected from polysaccharides, decomposition products of the polysaccharides, and chemical derivatives thereof as an active ingredient on flowers of the plant. The polysaccharide is preferably at least one kind selected from chitin, chitosan and cellulose. The decomposition product of the polysaccharides is preferably at least one kind selected from the decomposition products of the chitin, chitosan and the cellulose. The chemical derivative is preferably the one obtained by chemically binding the sugar chain of the polysaccharide and/or the decomposition product of the polysaccharide with another saccharide. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

本発明は、人体や植物や環境への影響が少なく、摘花効果に優れた摘花剤及び摘花方法に関する。   The present invention relates to a flowering agent and a flowering method that have little effect on human bodies, plants, and the environment, and that have an excellent flowering effect.

果樹には同一品種の花粉の受粉(自家受粉)で種子ができる(結実する)自家和合性のものと、自家受粉では結実しない自家不和合性のものがある。自家和合性の場合、放っておけば多数の結実が生じることから、養分の過剰消耗を防ぎ果実の発育を促す目的で、摘花による果実数の制限が行われている。   There are two types of fruit trees: self-compatibility, which can be seeded (fruited) by pollination of pollen of the same variety (self-pollination), and self-incompatibility, which does not bear fruit by self-pollination. In the case of self-compatibility, if it is left untreated, a number of fruits are produced. Therefore, in order to prevent excessive consumption of nutrients and promote fruit development, the number of fruits is restricted by flowering.

摘花以外にも着果数を制限し、果実の肥大化を促す作業として摘雷、摘果がある。敵雷、摘花、摘果は果実品質を大きく作用する重要な作業であるが、その作業を決められた短期間に終える必要性があるため、果樹農家にとってこれらの作業は非常に大きな負担となっている。例えば、リンゴではこれらの作業が全作業に占める割合は約半分を占めているといわれ、特に日本では、農業人口の高齢化問題もあり、作業の省力化は大きな課題である。この敵雷、摘花、摘果はリンゴのみならず、ナシ、モモ、ブドウ、カキ、柑橘類等においても必要な作業とされている。   In addition to picking flowers, there are lightning and fruit removal operations that limit the number of fruits and promote fruit enlargement. Enemy thunder, flowering, and fruit extraction are important tasks that greatly affect fruit quality. However, these operations are extremely burdensome for fruit farmers because they need to be completed in a short period of time. Yes. For example, apples are said to account for about half of all these tasks, especially in Japan, with the problem of aging of the agricultural population, and labor saving is a major issue. This enemy thunder, flowering and fruit picking are considered to be necessary not only for apples but also for pears, peaches, grapes, oysters, citrus fruits and the like.

このうちの摘花の方法のひとつとして、花を手作業で摘み取る方法があるが、この方法は早期摘花や省力化が困難でありあまり行われていない。また、摘花は手作業で行う方法以外に、摘花剤を散布する方法があり、摘花剤を散布する方法は省力化という点で優れている。   One of the methods for picking flowers is a method of picking flowers by hand, but this method is not often performed because early flowering and labor saving are difficult. In addition to the manual method of flowering, there is a method of spraying a flowering agent, and the method of spraying a flowering agent is excellent in terms of labor saving.

この摘花剤は、主に開花時に適用して必要な花のみを結実させるものであり、石灰硫黄合剤を有効成分とする摘花剤が、汎用的に使用されている。   This flowering agent is applied mainly at the time of flowering to produce only necessary flowers, and a flowering agent containing a lime sulfur mixture as an active ingredient is widely used.

また、下記特許文献1には、有機の水溶性酸のクエン酸,グルコン酸,コハク酸,乳酸,フマル酸,リンゴ酸,酢酸,酒石酸,プロピオン酸等の有機酸及び有機酸塩を有効成分とする摘花剤が開示されている。   Patent Document 1 listed below includes organic water-soluble acids such as citric acid, gluconic acid, succinic acid, lactic acid, fumaric acid, malic acid, acetic acid, tartaric acid, and propionic acid as active ingredients. A flowering agent is disclosed.

また、下記特許文献2には、特定の表面積及び粒径を有するケイ酸塩鉱物、炭酸カルシウム、ゼオライト、リン酸マグネシウム、炭酸マグネシウム等の水難溶性無機化合物に、縮合リン酸及びその塩、レシチン、ステロール、アミノ酸、ショ糖脂肪酸エステル等の添加物を、含浸・吸着させた摘花剤が開示されている。
特開2001−206805号公報 国際公開2004−12507号パンフレット 特開昭63−216804号公報
Further, in Patent Document 2 below, silicate minerals having a specific surface area and particle size, calcium carbonate, zeolite, magnesium phosphate, magnesium carbonate, and other poorly water-soluble inorganic compounds include condensed phosphoric acid and salts thereof, lecithin, Flowering agents in which additives such as sterols, amino acids, sucrose fatty acid esters and the like are impregnated and adsorbed are disclosed.
JP 2001-206805 A International Publication No. 2004-12507 Pamphlet JP 63-216804 A

石灰硫黄合剤は、一定の効果があるものの、強い塩基性であると共に強い異臭を有し人体に悪影響をおよぼす恐れがあるため、マスクや保護眼鏡、防御服等で防護措置をとる必要がある等、作業性が悪く取り扱い面に問題があった。なお、石灰硫黄合剤に配合されている生石灰の配合量を減らせばpHを中性近くにすることができるが、元々石灰は硫黄の薬害(葉が茶褐色にやける)を防止するための成分であり、石灰の配合量を減らした場合には、硫黄の薬害が顕著になる問題があった。   Although lime-sulfur mixture has certain effects, it must be protected with a mask, protective glasses, protective clothing, etc. because it is strongly basic and has a strong off-flavor and may adversely affect the human body. The workability was poor and there were problems with handling. In addition, if the amount of quicklime blended in the lime sulfur mixture is reduced, the pH can be made close to neutral, but lime is originally a component to prevent sulfur phytotoxicity (leaves turn brown) There is a problem that the phytotoxicity of sulfur becomes remarkable when the amount of lime is reduced.

また、上記特許文献1の摘花剤は、有効成分としての有機酸による酸の影響を受けて、樹皮や葉等に薬害症状が発生する場合があり、安定した摘花効果を得るため、摘花剤の濃度調整が難しい問題があった。   In addition, the flowering agent of Patent Document 1 may be affected by an acid caused by an organic acid as an active ingredient, and may cause phytotoxic symptoms on the bark, leaves, etc. In order to obtain a stable flowering effect, There was a problem that density adjustment was difficult.

また、上記特許文献2に開示された摘花剤は、特定の粒径及び表面積を有する水難溶性無機化合物を用いているため、原料コストがかかる問題があり、更には、添加剤による薬害のおそれもあった。   In addition, the flowering agent disclosed in Patent Document 2 uses a poorly water-soluble inorganic compound having a specific particle size and surface area, and thus has a problem of starting material costs, and further, there is a risk of phytotoxicity due to the additive. there were.

一方、上記特許文献3には、キトサンオリゴ糖には、植物の根の生育を抑制する作用を有することが報告されているものの、キトサンオリゴ糖による摘花効果については何ら開示されていない。   On the other hand, Patent Document 3 reports that chitosan oligosaccharide has an action of suppressing the growth of plant roots, but does not disclose any flowering effect of chitosan oligosaccharide.

よって、本発明の目的は、人体や果樹や環境への影響が少なく、摘花効果に優れた摘花剤及び摘花方法を提供することである。   Accordingly, an object of the present invention is to provide a flowering agent and a flowering method that have little effect on the human body, fruit tree, and environment, and that have an excellent flowering effect.

本発明者らは、多糖類の機能を研究する中で、意外にも多糖類が、花粉管の成長を阻害する効果を有することを見出し、本発明を完成するに至った。   The inventors of the present invention have unexpectedly found that the polysaccharide has an effect of inhibiting the growth of the pollen tube while studying the function of the polysaccharide, and completed the present invention.

すなわち、本発明の摘花剤は、多糖類、多糖類分解物、及びこれらの化学的誘導体から選ばれる少なくとも一種を有効成分とする。   That is, the flowering agent of the present invention contains at least one selected from polysaccharides, polysaccharide degradation products, and chemical derivatives thereof as an active ingredient.

本発明の摘花剤の有効成分である多糖類、多糖類分解物、及びこれらの化学的誘導体は、花粉管の成長を効果的に阻害できるので、受精が妨げられて、優れた摘花効果が発揮される。さらには、安全性が高く、人体や環境や果樹に対する薬害が極めて生じにくい。   The polysaccharides, polysaccharide degradation products, and chemical derivatives thereof, which are active ingredients of the flowering agent of the present invention, can effectively inhibit pollen tube growth, so that fertilization is hindered and an excellent flowering effect is exhibited. Is done. Furthermore, it is highly safe and hardly causes phytotoxicity to the human body, environment and fruit trees.

本発明の摘花剤は、前記多糖類が、キチン、キトサン、セルロースから選ばれる少なくとも一種であることが好ましい。   In the flowering agent of the present invention, the polysaccharide is preferably at least one selected from chitin, chitosan, and cellulose.

また、本発明の摘花剤は、前記多糖類の重量平均分子量が、4,000〜200,000であることが好ましい。   In the flowering agent of the present invention, the polysaccharide preferably has a weight average molecular weight of 4,000 to 200,000.

また、本発明の摘花剤は、前記多糖類分解物が、キチン分解物、キトサン分解物、セルロース分解物から選ばれる少なくとも一種であることが好ましい。   In the flowering agent of the present invention, the polysaccharide degradation product is preferably at least one selected from a chitin degradation product, a chitosan degradation product, and a cellulose degradation product.

また、本発明の摘花剤は、前記多糖類分解物が、2〜20量体のオリゴ糖類であることが好ましい。   Moreover, as for the flowering agent of this invention, it is preferable that the said polysaccharide degradation product is a 2-20 mer oligosaccharide.

また、本発明の摘花剤は、前記化学的誘導体が、前記多糖類及び/又は前記多糖類分解物の糖鎖に、他の糖類が化学結合してなるものであることが好ましい。   In the flowering agent of the present invention, the chemical derivative is preferably formed by chemically bonding another saccharide to the sugar chain of the polysaccharide and / or the polysaccharide degradation product.

上記各態様によれば、特に優れた摘花効果が得られるので、摘花剤の使用量を大幅に削減することができる。   According to each aspect described above, a particularly excellent flowering effect can be obtained, so that the amount of flowering agent used can be greatly reduced.

一方、本発明の摘花方法は、上記摘花剤を植物の花に散布することを特徴とする。   On the other hand, the flowering method of the present invention is characterized in that the flowering agent is sprayed on a plant flower.

本発明の摘花方法によれば、上述したように、摘花剤の有効成分である多糖類及び/又はその分解物が、花粉管の成長を効果的に阻害するので、受精が妨げられて摘花効果が発揮される。そして、多糖類及びその分解物は安全性が高いので、摘花剤を散布した際、人体や環境に対して悪影響を及ぼしにくく、更には植物に対する薬害が極めて生じにくい。   According to the flowering method of the present invention, as described above, the polysaccharide and / or its degradation product, which is an active ingredient of a flowering agent, effectively inhibits the growth of pollen tubes. Is demonstrated. And since a polysaccharide and its decomposition product are high safety, when spraying a flowering agent, it is hard to have a bad influence with respect to a human body or an environment, and also it is hard to produce the phytotoxicity to a plant very much.

また、本発明の摘花方法は、前記摘花剤を植物の花の開花期及び/又は満開期以降に散布することが好ましい。例えば、果樹の花は一斉に開花するわけではなく、数日〜1週間程度にわたって順次開花するのが普通である。また、一般に先に開花した花による果実ほど良果になる傾向がある。したがって、良果を得るには、先に開花した花を結実させ、後から開花した花を摘花することが好ましい。よって、この実施形態によれば、花の開花期及び/又は満開期以降に散布することで、先に開花した花を結実させ、後から開花した花の受精を妨げて摘花でき、良果を得ることができる。   In the flowering method of the present invention, the flowering agent is preferably sprayed after the flowering period and / or the full blooming period of the plant. For example, the flowers of fruit trees do not bloom all at once, but usually bloom sequentially over several days to a week. Moreover, generally the fruit by the flower which blossomed previously tends to become good fruit. Therefore, in order to obtain a good fruit, it is preferable to produce a flower that has flowered earlier and to pick a flower that has flowered later. Therefore, according to this embodiment, by spraying after the flowering period and / or the full blooming period of the flower, it is possible to produce a flower that has flowered earlier, to prevent fertilization of the flower that has been flowered later, and to flower, Obtainable.

本発明によれば、人体や環境に対し悪影響を及ぼすことなく、更には薬害により樹勢を弱めることなく、効果的に植物の摘花を行うことができ、高品質の果実を得ることができる。   According to the present invention, a plant can be effectively flowered without adversely affecting the human body and the environment, and further without weakening the tree by phytotoxicity, and a high-quality fruit can be obtained.

本発明の摘花剤は、多糖類、多糖類分解物、及びこれらの化学的誘導体から選ばれる少なくとも一種を有効成分として含むものである。   The flowering agent of the present invention contains at least one selected from polysaccharides, polysaccharide degradation products, and chemical derivatives thereof as an active ingredient.

本発明の摘花剤において上記多糖類としては、キチン、キトサン、セルロースが好ましく挙げられる。   In the flowering agent of the present invention, preferred examples of the polysaccharide include chitin, chitosan, and cellulose.

キチンは、カニ殻を酸およびアルカリ処理することで得られるものであり、天然由来の多糖類である。そして、本発明においては、キチンの重量平均分子量は、4,000〜200,000が好ましく、4,000〜50,000がより好ましい。   Chitin is obtained by treating the crab shell with acid and alkali, and is a naturally occurring polysaccharide. In the present invention, the weight average molecular weight of chitin is preferably 4,000 to 200,000, and more preferably 4,000 to 50,000.

キトサンは、キチンを脱アセチル化処理して得られるものであり、天然由来の多糖類である。そして、本発明においては、キトサンは、脱アセチル化度が20〜100%であることが好ましく、40〜100%がより好ましい。また、キトサンの重量平均分子量は、4,000〜200,000が好ましく、4,000〜50,000がより好ましい。   Chitosan is obtained by deacetylating chitin and is a naturally derived polysaccharide. In the present invention, chitosan preferably has a degree of deacetylation of 20 to 100%, more preferably 40 to 100%. Moreover, the weight average molecular weight of chitosan is preferably 4,000 to 200,000, and more preferably 4,000 to 50,000.

セルロースは、植物細胞の細胞壁または繊維から得られるものであり、天然由来の多糖類である。そして、本発明においては、セルロースの重量平均分子量は、4,000〜200,000が好ましく、4,000〜50,000がより好ましい。   Cellulose is obtained from plant cell walls or fibers, and is a naturally occurring polysaccharide. In the present invention, the weight average molecular weight of cellulose is preferably 4,000 to 200,000, more preferably 4,000 to 50,000.

なお、重量平均分子量は、例えば、蒸気圧浸透法、光散乱法、電気泳動法、GPC−HPLC法等の方法により測定することができる。   In addition, a weight average molecular weight can be measured by methods, such as a vapor pressure osmosis method, a light-scattering method, an electrophoresis method, and GPC-HPLC method, for example.

また、本発明の摘花剤において上記多糖類分解物としては、キチン分解物、キトサン分解物、セルロース分解物が好ましく挙げられる。   In the flowering agent of the present invention, preferred examples of the polysaccharide degradation product include chitin degradation products, chitosan degradation products, and cellulose degradation products.

キチン分解物は、キチンを酸又は酵素で加水分解して得られる低分子キチンや、キチンオリゴ糖である。そして、本発明においては、キチン分解物は2〜20量体のオリゴ糖であることが好ましく、2〜10量体のオリゴ糖であることがより好ましい。   Chitin degradation products are low molecular chitin obtained by hydrolyzing chitin with an acid or an enzyme, and chitin oligosaccharide. In the present invention, the chitin degradation product is preferably a 2-20 mer oligosaccharide, and more preferably a 2-10 mer oligosaccharide.

キトサン分解物は、キトサンを、酸又は酵素で加水分解して得られる低分子キトサンや、キトサンオリゴ糖である。そして、本発明においては、キトサン分解物は2〜20量体のオリゴ糖であることが好ましく、2〜10量体のオリゴ糖であることがより好ましい。   The chitosan degradation product is a low-molecular chitosan obtained by hydrolyzing chitosan with an acid or an enzyme, or chitosan oligosaccharide. In the present invention, the chitosan degradation product is preferably a 2 to 20-mer oligosaccharide, and more preferably a 2 to 10-mer oligosaccharide.

セルロース分解物は、セルロースを、例えば酸又は酵素で加水分解して得られるものである。そして、本発明においては、2〜20量体のオリゴ糖であることが好ましく、2〜10量体のオリゴ糖であることがより好ましい。   The cellulose degradation product is obtained by hydrolyzing cellulose with an acid or an enzyme, for example. And in this invention, it is preferable that it is a 2-20 mer oligosaccharide, and it is more preferable that it is a 2-10 mer oligosaccharide.

また、本発明の摘花剤において上記化学的誘導体は、上記多糖類及び/又は上記多糖類分解物の糖鎖に、他の糖類が化学結合してなるものである。主骨格となる糖鎖に誘導される上記他の糖類としては、ラクトース、メリビオース、カルボキシル化ラクトース、グルコース、マルトース、ラミナリビオース、セロビオース、マンノビオース、ジガラクトサミン、ジグルコサミンが挙げられ、特に安価に製造できるという理由からラクトース、グルコースが好ましい。また、主骨格となる糖鎖に対する、上記他の糖類の誘導率は、1〜80%が好ましく、5〜50%がより好ましい。具体的にはキトサンラクトース等が挙げられる。   In the flowering agent of the present invention, the chemical derivative is formed by chemically bonding another saccharide to the sugar chain of the polysaccharide and / or the polysaccharide degradation product. Examples of other saccharides derived from the sugar chain as the main skeleton include lactose, melibiose, carboxylated lactose, glucose, maltose, laminaribiose, cellobiose, mannobiose, digalactosamine, and diglucosamine. Lactose and glucose are preferable because they can be used. Moreover, 1-80% is preferable and the induction | guidance | derivation rate of the said other saccharides with respect to the sugar_chain | carbohydrate used as a main skeleton is more preferable 5-50%. Specific examples include chitosan lactose.

また、本発明の摘花剤は、上記多糖類、多糖類分解物、及びこれらの化学的誘導体の他に、人体、環境、果樹に対して薬害を与えない範囲で添加剤を使用してもよい。添加剤としては、展着効果としてポリオキシエチレンアルキルフェニルエーテル、固着効果としてパラフィン樹脂肪酸エステル、飛散防止としてポリオキシエチレンジノニルフェニルエーテルなどの展着剤や微生物による分解を防止するための抗菌剤等が挙げられ、これらを1種又は2種以上を組み合わせて用いることができる。そして、添加剤の含有量は、0.01〜99質量%が好ましく、0.1〜50質量%がより好ましい。   In addition to the polysaccharides, polysaccharide degradation products, and chemical derivatives thereof, the flowering agent of the present invention may use additives within a range that does not cause phytotoxicity to the human body, environment, and fruit trees. . Additives such as polyoxyethylene alkyl phenyl ether as spreading effect, paraffin tree fatty acid ester as sticking effect, polyoxyethylene dinonyl phenyl ether as anti-scattering agent and antibacterial agent to prevent decomposition by microorganisms These can be used, and these can be used alone or in combination of two or more. And 0.01-99 mass% is preferable and, as for content of an additive, 0.1-50 mass% is more preferable.

そして、本発明の摘化剤は、多糖類、多糖類分解物、及びこれらの化学的誘導体から選ばれる少なくとも一種と、必要に応じて添加剤とを、水に溶解又は分散し、水溶液又は懸濁液とすることが好ましい。   The plucking agent of the present invention comprises at least one selected from polysaccharides, polysaccharide degradation products, and chemical derivatives thereof, and additives as necessary, dissolved or dispersed in water to form an aqueous solution or suspension. It is preferable to use a turbid liquid.

また、本発明の摘化剤は、多糖類、多糖類分解物、及びこれらの化学的誘導体を、合計量で0.1〜10,000ppm含むことが好ましく、10〜10,000ppm含むことがより好ましく、100〜10,000ppm含むことが特に好ましい。これらの合計含有量が0.1ppm未満であると、摘花効果が乏しくなる。また、10,000ppmを超えると、摘花効果はさほど向上しないので、原料コストが増加して経済的に好ましくない。   Further, the plucking agent of the present invention preferably contains 0.1 to 10,000 ppm, more preferably 10 to 10,000 ppm of the total amount of polysaccharides, polysaccharide degradation products, and chemical derivatives thereof. The content is preferably 100 to 10,000 ppm. If the total content thereof is less than 0.1 ppm, the flowering effect becomes poor. On the other hand, if it exceeds 10,000 ppm, the flowering effect is not improved so much, which increases the raw material cost and is not economically preferable.

次に、本発明の摘花方法について説明する。   Next, the flowering method of the present invention will be described.

本発明の摘花方法は、上記摘花剤を、果樹等の植物の花に散布することである。   The flowering method of the present invention is to spray the flowering agent on flowers of plants such as fruit trees.

本発明の摘花方法において、適用可能な植物としては、特に限定はなく、リンゴ、ナシ、モモ、ブドウ、カキ、柑橘類等の果樹が好ましく挙げられる。   In the flowering method of the present invention, the applicable plant is not particularly limited, and fruit trees such as apples, pears, peaches, grapes, oysters, citrus fruits are preferably mentioned.

本発明の摘花方法において、摘花剤の散布は、植物の花の開花期及び/又は満開期以降に散布することが好ましく、植物の花の満開期に一回目の散布を行い、満開期から2〜3日後に更に散布を行うことが好ましい。   In the flowering method of the present invention, the flowering agent is preferably sprayed after the flowering period and / or after the full blooming period of the plant, and the first spraying is performed during the full blooming period of the plant. It is preferable to further spray after 3 days.

果樹等の植物の花は一斉に開花するわけではなく、植物によって異なるが、一般的に数日〜1週間程度にわたって順次開花する。例えば、リンゴ等の落葉果実の開花は、頂芽の中心花がまず満開になる。その後、頂芽の側花がやや遅れて満開となり、更に数日から1週間後、腋花が満開となる。また、一般に、先に開花した花による果実ほど良果になる傾向がある。よって、植物の花の開花期及び/又は満開期以降に散布することで、先に開花した花を結実させ、後から開花した花の受精を妨げて摘花でき、良果を得ることができる。   The flowers of plants such as fruit trees do not bloom at the same time, and generally vary sequentially over several days to one week, although they vary depending on the plant. For example, in the flowering of deciduous fruits such as apples, the central flower of the top bud is first in full bloom. Thereafter, the side flowers of the top buds are in full bloom with a slight delay, and after a few days to a week, the spikes are in full bloom. Moreover, generally the fruit by the flower which blossomed previously tends to become good fruit. Therefore, by spraying after the flowering period and / or the full blooming period of the plant, the flower that has been flowered earlier can be ripened, the fertilization of the flower that has been flowered later can be prevented, and flowering can be obtained.

具体的には、植物の種類により、結実に適さない花の花序内の位置が異なるため、摘花対象となる花の開花にあわせた散布が好ましく、例えば、リンゴ等の落葉果実の場合、頂芽の中心花が満開になった際に摘花剤を散布することが好ましい。   Specifically, since the position in the inflorescence of the flower that is not suitable for fruiting varies depending on the type of plant, it is preferably sprayed according to the flowering of the flower to be flowered. For example, in the case of deciduous fruits such as apples, It is preferable to spray a flower-picking agent when the central flower is fully bloomed.

なお、本発明において植物の花の満開期とは、全花芽(つぼみ)に対して開花した花の数の割合が50%となった時期を意味する。   In the present invention, the full bloom period of a plant means a period when the ratio of the number of flowers bloomed to the total flower buds (buds) is 50%.

そして、本発明の摘花剤の散布量は、50〜1,000L/10aが好ましく、100〜500L/10aがより好ましい。散布量が50L/10a未満であると、摘花効果が乏しくなる。一方、散布量が1,000L/10aを超えても、摘花効果がさほど向上しないので、原料コストが増加して経済的に好ましくない。   And the application quantity of the flowering agent of this invention has preferable 50-1,000L / 10a, and 100-500L / 10a is more preferable. If the application amount is less than 50 L / 10a, the flowering effect becomes poor. On the other hand, even if the application amount exceeds 1,000 L / 10a, the flowering effect is not improved so much, which increases the raw material cost and is not economically preferable.

以下実施例を挙げて本発明を具体的に説明するが、これらの実施例は本発明の範囲を限定するものではない。   EXAMPLES Hereinafter, the present invention will be specifically described with reference to examples, but these examples do not limit the scope of the present invention.

(試験例1)
茶花粉5mgを、液体培地(キトサンオリゴ糖(5糖):0ppm〜10ppm,スクロース:8%、Ca(NO:0.5mM、HBO:1.0mM)20mlに静置し、暗所、25℃、20時間培養した。その後、液体培地をろ過処理した後、茶花粉の重量を測定し、重量変化により花粉管の成長度を観測した。結果を図1に記す。図中の横軸は、キトサンオリゴ糖(5糖)の濃度(ppm)であり、縦軸は、キトサンオリゴ糖(5糖)が無添加時のときの重量を100とした時の相対量(%)である。
(Test Example 1)
Leave 5 mg of tea pollen in 20 ml of liquid medium (chitosan oligosaccharide (pentose): 0 ppm to 10 ppm, sucrose: 8%, Ca (NO 3 ) 2 : 0.5 mM, H 3 BO 3 : 1.0 mM). Incubated in the dark at 25 ° C. for 20 hours. Thereafter, after filtering the liquid medium, the weight of tea pollen was measured, and the degree of growth of the pollen tube was observed by the change in weight. The results are shown in FIG. The horizontal axis in the figure is the concentration (ppm) of chitosan oligosaccharide (pentose), and the vertical axis is the relative amount when the weight when no chitosan oligosaccharide (pentose) is added is 100 ( %).

(試験例2)
茶花粉5mgを、液体培地(キトサンオリゴ糖(7糖):0ppm〜10ppm,スクロース:8%、Ca(NO:0.5mM、HBO:1.0mM)20mlに静置し、暗所、25℃、20時間培養した。その後、液体培地をろ過処理した後、茶花粉の重量を測定し、重量変化により花粉管の成長度を観測した。結果を図2に記す。図中の横軸は、キトサンオリゴ糖(7糖)の濃度(ppm)であり、縦軸は、キトサンオリゴ糖(7糖)が無添加時のときの重量を100とした時の相対量(%)である。
(Test Example 2)
Leave 5 mg of tea pollen in 20 ml of liquid medium (chitosan oligosaccharide (7 sugar): 0 ppm to 10 ppm, sucrose: 8%, Ca (NO 3 ) 2 : 0.5 mM, H 3 BO 3 : 1.0 mM). Incubated in the dark at 25 ° C. for 20 hours. Then, after filtering the liquid medium, the weight of tea pollen was measured, and the degree of growth of the pollen tube was observed by the change in weight. The results are shown in FIG. The horizontal axis in the figure is the concentration (ppm) of chitosan oligosaccharide (7 sugar), and the vertical axis is the relative amount when the weight when no chitosan oligosaccharide (7 sugar) is added is 100 ( %).

(試験例3)
茶花粉5mgを、液体培地(キトサンオリゴ糖(8糖):0ppm〜10ppm,スクロース:8%、Ca(NO:0.5mM、HBO:1.0mM)20mlに静置し、暗所、25℃、20時間培養した。その後、液体培地をろ過処理した後、茶花粉の重量を測定し、重量変化により花粉管の成長度を観測した。結果を図3に記す。図中の横軸は、キトサンオリゴ糖(8糖)の濃度(ppm)であり、縦軸は、キトサンオリゴ糖(8糖)が無添加時のときの重量を100とした時の相対量(%)である。
(Test Example 3)
Leave 5 mg of tea pollen in 20 ml of liquid medium (chitosan oligosaccharide (8 sugar): 0 ppm to 10 ppm, sucrose: 8%, Ca (NO 3 ) 2 : 0.5 mM, H 3 BO 3 : 1.0 mM). Incubated in the dark at 25 ° C. for 20 hours. Then, after filtering the liquid medium, the weight of tea pollen was measured, and the degree of growth of the pollen tube was observed by the change in weight. The results are shown in FIG. The horizontal axis in the figure is the concentration (ppm) of chitosan oligosaccharide (octasaccharide), and the vertical axis is the relative amount when the weight when no chitosan oligosaccharide (octasaccharide) is added is 100 ( %).

(試験例4)
茶花粉5mgを、液体培地(キトサンオリゴ糖(9糖):0ppm〜10ppm,スクロース:8%、Ca(NO:0.5mM、HBO:1.0mM)20mlに静置し、暗所、25℃、20時間培養した。その後、液体培地をろ過処理した後、茶花粉の重量を測定し、重量変化により花粉管の成長度を観測した。結果を図4に記す。図中の横軸は、キトサンオリゴ糖(9糖)の濃度(ppm)であり、縦軸は、キトサンオリゴ糖(9糖)が無添加時のときの重量を100とした時の相対量(%)である。
(Test Example 4)
Leave 5 mg of tea pollen in 20 ml of liquid medium (chitosan oligosaccharide (9 sugar): 0 ppm to 10 ppm, sucrose: 8%, Ca (NO 3 ) 2 : 0.5 mM, H 3 BO 3 : 1.0 mM). Incubated in the dark at 25 ° C. for 20 hours. Then, after filtering the liquid medium, the weight of tea pollen was measured, and the degree of growth of the pollen tube was observed by the change in weight. The results are shown in FIG. The horizontal axis in the figure is the concentration (ppm) of chitosan oligosaccharide (9 sugars), and the vertical axis is the relative amount when the weight when no chitosan oligosaccharide (9 sugars) is added is 100 ( %).

(試験例5)
茶花粉5mgを、液体培地(キトサンオリゴ糖(2〜20糖ミクスチャー):0ppm〜100ppm,スクロース:8%、Ca(NO:0.5mM、HBO:1.0mM)20mlに静置し、暗所、25℃、20時間培養した。その後、液体培地をろ過処理した後、茶花粉の重量を測定し、重量変化により花粉管の成長度を観測した。結果を図5に記す。図中の横軸は、キトサンオリゴ糖(2〜20糖ミクスチャー)の濃度(ppm)であり、縦軸は、キトサンオリゴ糖(2〜20糖ミクスチャー)が無添加時のときの重量を100とした時の相対量(%)である。
(Test Example 5)
5 mg of tea pollen in 20 ml of liquid medium (chitosan oligosaccharide (2 to 20 sugar mixture): 0 ppm to 100 ppm, sucrose: 8%, Ca (NO 3 ) 2 : 0.5 mM, H 3 BO 3 : 1.0 mM) The mixture was allowed to stand and cultured in the dark at 25 ° C. for 20 hours. Then, after filtering the liquid medium, the weight of tea pollen was measured, and the degree of growth of the pollen tube was observed by the change in weight. The results are shown in FIG. The horizontal axis in the figure is the concentration (ppm) of chitosan oligosaccharide (2 to 20 sugar mixture), and the vertical axis is 100 when the chitosan oligosaccharide (2 to 20 sugar mixture) is not added. The relative amount (%).

(試験例6)
茶花粉5mgを、液体培地(低分子キトサン(重量平均分子量4,000):0ppm〜100ppm,スクロース:8%、Ca(NO:0.5mM、HBO:1.0mM)20mlに静置し、暗所、25℃、20時間培養した。その後、液体培地をろ過処理した後、茶花粉の重量を測定し、重量変化により花粉管の成長度を観測した。結果を図6に記す。図中の横軸は、低分子キトサン(重量平均分子量4000)の濃度(ppm)であり、縦軸は、低分子キトサン(重量平均分子量4000)が無添加時のときの重量を100とした時の相対量(%)である。
(Test Example 6)
5 mg of tea pollen was added to a liquid medium (low molecular chitosan (weight average molecular weight: 4,000): 0 ppm to 100 ppm, sucrose: 8%, Ca (NO 3 ) 2 : 0.5 mM, H 3 BO 3 : 1.0 mM) And cultured at 25 ° C. for 20 hours in the dark. Thereafter, after filtering the liquid medium, the weight of tea pollen was measured, and the degree of growth of the pollen tube was observed by the change in weight. The results are shown in FIG. The horizontal axis in the figure is the concentration (ppm) of low molecular chitosan (weight average molecular weight 4000), and the vertical axis is when the weight when no low molecular chitosan (weight average molecular weight 4000) is added is 100. Relative amount (%).

(試験例7)
茶花粉5mgを、液体培地(低分子キトサン(重量平均分子量20,000):0ppm〜100ppm,スクロース:8%、Ca(NO:0.5mM、HBO:1.0mM)20mlに静置し、暗所、25℃、20時間培養した。その後、液体培地をろ過処理した後、茶花粉の重量を測定し、重量変化により花粉管の成長度を観測した。結果を図7に記す。図中の横軸は、低分子キトサン(重量平均分子量20000)の濃度(ppm)であり、縦軸は、低分子キトサン(重量平均分子量20000)が無添加時のときの重量を100とした時の相対量(%)である。
(Test Example 7)
5 mg of tea pollen in 20 ml of liquid medium (low molecular chitosan (weight average molecular weight 20,000): 0 ppm to 100 ppm, sucrose: 8%, Ca (NO 3 ) 2 : 0.5 mM, H 3 BO 3 : 1.0 mM) And cultured at 25 ° C. for 20 hours in the dark. Then, after filtering the liquid medium, the weight of tea pollen was measured, and the degree of growth of the pollen tube was observed by the change in weight. The results are shown in FIG. The horizontal axis in the figure is the concentration (ppm) of low molecular chitosan (weight average molecular weight 20000), and the vertical axis is when the weight when no low molecular chitosan (weight average molecular weight 20000) is added is 100. Relative amount (%).

(試験例8)
茶花粉5mgを、液体培地(キトサンラクトース:0ppm〜100ppm,スクロース:8%、Ca(NO:0.5mM、HBO:1.0mM)20mlに静置し、暗所、25℃、20時間培養した。その後、液体培地をろ過処理した後、茶花粉の重量を測定し、重量変化により花粉管の成長度を観測した。結果を図8に記す。図中の横軸は、キトサンラクトースの濃度(ppm)であり、縦軸は、キトサンラクトースが無添加時のときの重量を100とした時の相対量(%)である。
(Test Example 8)
5 mg of tea pollen is left in a liquid medium (chitosan lactose: 0 ppm to 100 ppm, sucrose: 8%, Ca (NO 3 ) 2 : 0.5 mM, H 3 BO 3 : 1.0 mM) in the dark, 25 The culture was performed at 20 ° C. for 20 hours. Then, after filtering the liquid medium, the weight of tea pollen was measured, and the degree of growth of the pollen tube was observed by the change in weight. The results are shown in FIG. The horizontal axis in the figure is the concentration (ppm) of chitosan lactose, and the vertical axis is the relative amount (%) when the weight when no chitosan lactose is added is 100.

(試験例9)
茶花粉5mgを、液体培地(キチンオリゴ糖(2〜10糖ミクスチャー):0ppm〜100ppm,スクロース:8%、Ca(NO:0.5mM、HBO:1.0mM)20mlに静置し、暗所、25℃、20時間培養した。その後、液体培地をろ過処理した後、茶花粉の重量を測定し、重量変化により花粉管の成長度を観測した。結果を図9に記す。図中の横軸は、キチンオリゴ糖(2〜10糖ミクスチャー)の濃度(ppm)であり、縦軸は、キチンオリゴ糖(2〜10糖ミクスチャー)が無添加時のときの重量を100とした時の相対量(%)である。
(Test Example 9)
5 mg of tea pollen in 20 ml of liquid medium (chitin oligosaccharide (2 to 10 sugar mixture): 0 ppm to 100 ppm, sucrose: 8%, Ca (NO 3 ) 2 : 0.5 mM, H 3 BO 3 : 1.0 mM) The mixture was allowed to stand and cultured in the dark at 25 ° C. for 20 hours. Then, after filtering the liquid medium, the weight of tea pollen was measured, and the degree of growth of the pollen tube was observed by the change in weight. The results are shown in FIG. The horizontal axis in the figure is the concentration (ppm) of chitin oligosaccharide (2 to 10 sugar mixture), and the vertical axis is 100 when the chitin oligosaccharide (2 to 10 sugar mixture) is not added. The relative amount (%).

(試験例10)
茶花粉5mgを、液体培地(セロオリゴ糖(2糖):0ppm〜100ppm,スクロース:8%、Ca(NO:0.5mM、HBO:1.0mM)20mlに静置し、暗所、25℃、20時間培養した。その後、液体培地をろ過処理した後、茶花粉の重量を測定し、重量変化により花粉管の成長度を観測した。結果を図10に記す。図中の横軸は、セロオリゴ糖(2糖)の濃度(ppm)であり、縦軸は、セロオリゴ糖(2糖)が無添加時のときの重量を100とした時の相対量(%)である。
(Test Example 10)
5 mg of tea pollen was allowed to stand in 20 ml of a liquid medium (cellooligosaccharide (disaccharide): 0 ppm to 100 ppm, sucrose: 8%, Ca (NO 3 ) 2 : 0.5 mM, H 3 BO 3 : 1.0 mM), The cells were cultured in the dark at 25 ° C. for 20 hours. Then, after filtering the liquid medium, the weight of tea pollen was measured, and the degree of growth of the pollen tube was observed by the change in weight. The results are shown in FIG. The horizontal axis in the figure is the concentration (ppm) of cellooligosaccharide (disaccharide), and the vertical axis is the relative amount (%) when the weight when no cellooligosaccharide (disaccharide) is added is 100. It is.

(試験例11)
茶花粉5mgを、液体培地(セロオリゴ糖(5糖):0ppm〜100ppm,スクロース:8%、Ca(NO:0.5mM、HBO:1.0mM)20mlに静置し、暗所、25℃、20時間培養した。その後、液体培地をろ過処理した後、茶花粉の重量を測定し、重量変化により花粉管の成長度を観測した。結果を図11に記す。図中の横軸は、セロオリゴ糖(5糖)の濃度(ppm)であり、縦軸は、セロオリゴ糖(5糖)が無添加時のときの重量を100とした時の相対量(%)である。
(Test Example 11)
5 mg of tea pollen was left in a liquid medium (cello-oligosaccharide (pentose): 0 ppm to 100 ppm, sucrose: 8%, Ca (NO 3 ) 2 : 0.5 mM, H 3 BO 3 : 1.0 mM), The cells were cultured in the dark at 25 ° C for 20 hours. Then, after filtering the liquid medium, the weight of tea pollen was measured, and the degree of growth of the pollen tube was observed by the change in weight. The results are shown in FIG. The horizontal axis in the figure is the concentration (ppm) of cellooligosaccharide (pentose), and the vertical axis is the relative amount (%) when the weight when no cellooligosaccharide (pentose) is added is 100. It is.

上記結果より、多糖類、多糖類分解物、及びこれらの化学的誘導体は、花粉管の成長を効果的に抑制する働きがあることが分かる。特にキトサンオリゴ糖、低分子キトサン、キトサンラクトースは花粉管の成長抑制作用に優れていた。   From the above results, it can be seen that polysaccharides, polysaccharide degradation products, and chemical derivatives thereof have a function of effectively suppressing the growth of pollen tubes. In particular, chitosan oligosaccharide, low-molecular chitosan, and chitosan lactose were excellent in pollen tube growth inhibitory action.

キトサンオリゴ糖(5糖)による花粉管の成長に対する影響を示す図表である。It is a graph which shows the influence with respect to the growth of the pollen tube by chitosan oligosaccharide (pentasaccharide). キトサンオリゴ糖(7糖)による花粉管の成長に対する影響を示す図表である。It is a graph which shows the influence with respect to the growth of the pollen tube by chitosan oligosaccharide (7 sugar). キトサンオリゴ糖(8糖)による花粉管の成長に対する影響を示す図表である。It is a graph which shows the influence with respect to the growth of the pollen tube by chitosan oligosaccharide (octasaccharide). キトサンオリゴ糖(9糖)による花粉管の成長に対する影響を示す図表である。It is a graph which shows the influence with respect to the growth of the pollen tube by chitosan oligosaccharide (9 sugars). キトサンオリゴ糖(2〜20糖ミクスチャー)による花粉管の成長に対する影響を示す図表である。It is a graph which shows the influence with respect to the growth of a pollen tube by chitosan oligosaccharide (2-20 sugar mixture). 低分子キトサン(重量平均分子量4,000)による花粉管の成長に対する影響を示す図表である。It is a graph which shows the influence with respect to the growth of a pollen tube by low molecular chitosan (weight average molecular weight 4,000). 低分子キトサン(重量平均分子量20,000)による花粉管の成長に対する影響を示す図表である。It is a graph which shows the influence with respect to the growth of a pollen tube by a low molecular chitosan (weight average molecular weight 20,000). キトサンラクトースによる花粉管の成長に対する影響を示す図表である。It is a graph which shows the influence with respect to the growth of the pollen tube by chitosan lactose. キチンオリゴ糖(2〜10糖ミクスチャー)糖による花粉管の成長に対する影響を示す図表である。It is a graph which shows the influence with respect to the growth of a pollen tube by chitin oligosaccharide (2-10 sugar mixture) sugar. セロオリゴ糖(2糖)による花粉管の成長に対する影響を示す図表である。It is a graph which shows the influence with respect to the growth of the pollen tube by cellooligosaccharide (disaccharide). セロオリゴ糖(5糖)による花粉管の成長に対する影響を示す図表である。It is a graph which shows the influence with respect to the growth of pollen tube by cellooligosaccharide (pentasaccharide).

Claims (8)

多糖類、多糖類分解物、及びこれらの化学的誘導体から選ばれる少なくとも一種を有効成分とする摘花剤。   A flowering agent comprising at least one selected from polysaccharides, polysaccharide degradation products, and chemical derivatives thereof as an active ingredient. 前記多糖類が、キチン、キトサン、セルロースから選ばれる少なくとも一種である請求項1に記載の摘花剤。   The flower picking agent according to claim 1, wherein the polysaccharide is at least one selected from chitin, chitosan, and cellulose. 前記多糖類の重量平均分子量が、4,000〜200,000である請求項1又は2に記載の摘花剤。   The flowering agent according to claim 1 or 2, wherein the polysaccharide has a weight average molecular weight of 4,000 to 200,000. 前記多糖類分解物が、キチン分解物、キトサン分解物、セルロース分解物から選ばれる少なくとも一種である請求項1に記載の摘花剤。   The flowering agent according to claim 1, wherein the polysaccharide degradation product is at least one selected from a chitin degradation product, a chitosan degradation product, and a cellulose degradation product. 前記多糖類分解物が、2〜20量体のオリゴ糖類である請求項4に記載の摘花剤。   The flowering agent according to claim 4, wherein the polysaccharide degradation product is a 2 to 20-mer oligosaccharide. 前記化学的誘導体が、前記多糖類及び/又は前記多糖類分解物の糖鎖に、他の糖類が化学結合してなるものである請求項1〜5のいずれか一つに記載の摘花剤。   The flowering agent according to any one of claims 1 to 5, wherein the chemical derivative is obtained by chemically bonding another saccharide to a sugar chain of the polysaccharide and / or the polysaccharide degradation product. 請求項1〜6のいずれか一つに記載の摘花剤を、植物の花に散布することを特徴とする摘花方法。   A flowering method characterized by spraying the flowering agent according to any one of claims 1 to 6 on a flower of a plant. 前記摘花剤を、植物の花の開花期及び/又は満開期以降に散布する請求項7に記載の摘花方法。   The flowering method according to claim 7, wherein the flowering agent is sprayed after a flowering period and / or a full blooming period of a plant.
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JP7279088B2 (en) 2018-03-14 2023-05-22 クック チャン,イン Flower picking composition and flower picking method using the same

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