JPH02273104A - Husked seed for culture and production thereof - Google Patents
Husked seed for culture and production thereofInfo
- Publication number
- JPH02273104A JPH02273104A JP25936789A JP25936789A JPH02273104A JP H02273104 A JPH02273104 A JP H02273104A JP 25936789 A JP25936789 A JP 25936789A JP 25936789 A JP25936789 A JP 25936789A JP H02273104 A JPH02273104 A JP H02273104A
- Authority
- JP
- Japan
- Prior art keywords
- seed
- seeds
- germination
- peeled
- coating agent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 239000011248 coating agent Substances 0.000 claims abstract description 46
- 235000015097 nutrients Nutrition 0.000 claims abstract description 9
- 239000005871 repellent Substances 0.000 claims abstract description 5
- 239000005556 hormone Substances 0.000 claims abstract description 4
- 229940088597 hormone Drugs 0.000 claims abstract description 4
- 239000002917 insecticide Substances 0.000 claims abstract description 4
- 239000003086 colorant Substances 0.000 claims abstract description 3
- 230000002940 repellent Effects 0.000 claims description 4
- 230000000844 anti-bacterial effect Effects 0.000 claims description 2
- 239000003899 bactericide agent Substances 0.000 claims description 2
- 230000035784 germination Effects 0.000 abstract description 58
- 238000000034 method Methods 0.000 abstract description 24
- 238000000576 coating method Methods 0.000 abstract description 19
- 235000009337 Spinacia oleracea Nutrition 0.000 abstract description 13
- 239000007788 liquid Substances 0.000 abstract description 12
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract description 6
- 244000300264 Spinacia oleracea Species 0.000 abstract description 3
- 239000001569 carbon dioxide Substances 0.000 abstract description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract description 3
- 240000008620 Fagopyrum esculentum Species 0.000 abstract description 2
- 235000009419 Fagopyrum esculentum Nutrition 0.000 abstract description 2
- 239000003795 chemical substances by application Substances 0.000 abstract description 2
- 239000004927 clay Substances 0.000 abstract description 2
- 239000000843 powder Substances 0.000 abstract description 2
- 239000007921 spray Substances 0.000 abstract description 2
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- 239000010903 husk Substances 0.000 abstract 1
- 239000003507 refrigerant Substances 0.000 abstract 1
- 239000002689 soil Substances 0.000 description 21
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- 230000000694 effects Effects 0.000 description 12
- 239000011521 glass Substances 0.000 description 12
- 238000009331 sowing Methods 0.000 description 12
- 241000219315 Spinacia Species 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 230000001737 promoting effect Effects 0.000 description 6
- 239000007789 gas Substances 0.000 description 5
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 4
- 206010052428 Wound Diseases 0.000 description 4
- 208000027418 Wounds and injury Diseases 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 235000007516 Chrysanthemum Nutrition 0.000 description 3
- 244000189548 Chrysanthemum x morifolium Species 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000007710 freezing Methods 0.000 description 3
- 230000008014 freezing Effects 0.000 description 3
- 238000003306 harvesting Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 241000228212 Aspergillus Species 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 229930191978 Gibberellin Natural products 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- IXORZMNAPKEEDV-UHFFFAOYSA-N gibberellic acid GA3 Natural products OC(=O)C1C2(C3)CC(=C)C3(O)CCC2C2(C=CC3O)C1C3(C)C(=O)O2 IXORZMNAPKEEDV-UHFFFAOYSA-N 0.000 description 2
- 239000003448 gibberellin Substances 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 230000009931 harmful effect Effects 0.000 description 2
- 229940125697 hormonal agent Drugs 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 230000007226 seed germination Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 description 1
- 240000004507 Abelmoschus esculentus Species 0.000 description 1
- 244000291564 Allium cepa Species 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- 240000005528 Arctium lappa Species 0.000 description 1
- 235000003130 Arctium lappa Nutrition 0.000 description 1
- 235000008078 Arctium minus Nutrition 0.000 description 1
- 235000016068 Berberis vulgaris Nutrition 0.000 description 1
- 241000335053 Beta vulgaris Species 0.000 description 1
- 244000067456 Chrysanthemum coronarium Species 0.000 description 1
- 235000007871 Chrysanthemum coronarium Nutrition 0.000 description 1
- 244000146493 Cryptotaenia japonica Species 0.000 description 1
- 235000004035 Cryptotaenia japonica Nutrition 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000208818 Helianthus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- PWWVAXIEGOYWEE-UHFFFAOYSA-N Isophenergan Chemical compound C1=CC=C2N(CC(C)N(C)C)C3=CC=CC=C3SC2=C1 PWWVAXIEGOYWEE-UHFFFAOYSA-N 0.000 description 1
- FAIXYKHYOGVFKA-UHFFFAOYSA-N Kinetin Natural products N=1C=NC=2N=CNC=2C=1N(C)C1=CC=CO1 FAIXYKHYOGVFKA-UHFFFAOYSA-N 0.000 description 1
- 240000008415 Lactuca sativa Species 0.000 description 1
- 235000003228 Lactuca sativa Nutrition 0.000 description 1
- 208000002720 Malnutrition Diseases 0.000 description 1
- NWBJYWHLCVSVIJ-UHFFFAOYSA-N N-benzyladenine Chemical compound N=1C=NC=2NC=NC=2C=1NCC1=CC=CC=C1 NWBJYWHLCVSVIJ-UHFFFAOYSA-N 0.000 description 1
- 206010067482 No adverse event Diseases 0.000 description 1
- 240000009164 Petroselinum crispum Species 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- -1 Polycoat (trade name Chemical compound 0.000 description 1
- 244000184734 Pyrus japonica Species 0.000 description 1
- 239000005708 Sodium hypochlorite Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- AZFNGPAYDKGCRB-XCPIVNJJSA-M [(1s,2s)-2-amino-1,2-diphenylethyl]-(4-methylphenyl)sulfonylazanide;chlororuthenium(1+);1-methyl-4-propan-2-ylbenzene Chemical compound [Ru+]Cl.CC(C)C1=CC=C(C)C=C1.C1=CC(C)=CC=C1S(=O)(=O)[N-][C@@H](C=1C=CC=CC=1)[C@@H](N)C1=CC=CC=C1 AZFNGPAYDKGCRB-XCPIVNJJSA-M 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 210000002257 embryonic structure Anatomy 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 230000009610 hypersensitivity Effects 0.000 description 1
- 230000009545 invasion Effects 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- QANMHLXAZMSUEX-UHFFFAOYSA-N kinetin Chemical compound N=1C=NC=2N=CNC=2C=1NCC1=CC=CO1 QANMHLXAZMSUEX-UHFFFAOYSA-N 0.000 description 1
- 229960001669 kinetin Drugs 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 210000001161 mammalian embryo Anatomy 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007721 medicinal effect Effects 0.000 description 1
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 description 1
- 229910052754 neon Inorganic materials 0.000 description 1
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 235000018343 nutrient deficiency Nutrition 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 235000011197 perejil Nutrition 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000004304 potassium nitrite Substances 0.000 description 1
- 235000010289 potassium nitrite Nutrition 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001846 repelling effect Effects 0.000 description 1
- BCVNCJWDDOITBB-UHFFFAOYSA-N s-(dimethylcarbamoylsulfanyl) n,n-dimethylcarbamothioate;methyl n-[1-(butylcarbamoyl)benzimidazol-2-yl]carbamate Chemical compound CN(C)C(=O)SSC(=O)N(C)C.C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 BCVNCJWDDOITBB-UHFFFAOYSA-N 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 230000021217 seedling development Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
Landscapes
- Pretreatment Of Seeds And Plants (AREA)
Abstract
Description
【発明の詳細な説明】
【産業上の利用分野]
本発明は、播種した硬実種子の発芽時間を短縮し、発芽
の不揃いをなくする硬実種子の発芽促進法に関するもの
である。
[従来の技術]
播種した硬実種子を時間的に均一成長させ、しかも高い
発芽率で生育することは、例えば、特に成長の速いホウ
レンソウなどを収穫良く生産する上で大変重要である。
硬実種子の発芽には、まず吸水することが必要である。
硬実種子は、通常その外被部が硬い種皮で覆われていて
、この種皮が水を吸収して、次いで種皮内部の胚などが
吸水することになる。
そのため通常の栽培では、発芽をスムーズになさしめる
為に、播種する前に種子を20〜24時間水に浸漬して
種皮に十分吸水せしめてから播種することが多い。
種子は水分を吸収した後、種皮内部では貯蔵栄養分が分
解され、ホルモンが合成され、幼苗の発育と幼根の伸長
を開始させるのである。
この様な水による発芽促進の他にジベレリン、ベンジル
アデニン、カイネチン、チオ尿素、エスレル、過酸化水
素水、亜硝酸カリウム及び次亜塩素酸ソーダなどの化学
物質の存在下で処理することも知られている。
r発明が解決しようとする課題】
しかしながら、水に硬実種子を浸漬した場合この種子を
土中や水耕栽培用のスボンヂなどに播種すると均一に発
芽しないため、生育した苗は不揃いであり、苗を束ねる
ときに成長の遅いものを除去して選別しなくてはならず
効率及び作業性が悪かった。
また、一方化学物質によって種皮の処理、例えば、アル
カリ処理などを行うと種皮内部にまで薬剤が浸透して正
常な種子に却って悪影響を及ぼすことがあり、好ましい
ものではなかった。
そのため、剥皮種子の発芽成長に悪影響なく、均一に発
芽し、発芽時間が短く、収穫効率の向上する剥皮種子及
びその製造方法が強く要望されている。
[課題を解決するための手段〕
本発明者らは、上述の欠陥を解消するため鋭意研究を重
ねた結果、低温において種皮を剥離処理することが、剥
離の際に内部の種子の種皮を傷付けず、また、低温処理
が種子の発芽を促進するという一石二鳥の効果を与え、
極めて有効であることを見い出し、また、剥皮種子に人
工の種皮すなわちコーティング剤を被覆するとさらにこ
の効果が助長されることを見い出し、これらの知見に基
づいて、本発明に到達したものである。
すなわち、本発明は、次の6項目からなるものである。
1 種皮付き種子を一5℃以下の低温に維持して、種皮
を破壊して得た栽培用剥皮種子。
2 種皮付き種子を温度−5℃以下特に−30℃以下に
おいて、種皮を破壊して、種皮を除去し、所望によりコ
ーティング剤を塗布することを特徴とする栽培用剥皮種
子の製造方法。
3 温度が一30℃以下の超低温である項1記載の栽培
用剥皮種子。
4 剥皮種子をコーティング剤で被覆した項l又は3記
載の栽培用剥皮種子。
5 コーティング剤が殺菌剤、殺虫剤、ホルモン剤、栄
養剤又は鳥忌避剤を含有するものである環4記載の栽培
用剥皮種子。
6 コーティング剤に着色剤を添加した項4又は5記載
の栽培用剥皮種子。
〔作用〕
本発明の種子の発芽促進法が発芽揃いがよく、かつ発芽
率も高いという特性は以下の理由によるものと推測され
る。
まず種子を低温処理することにより、種子の内部まで刺
激をうけ胚が活性化れ、発芽の起爆の引金になることが
挙げられる。
次に、種皮が除去されているので水分の吸収が速いのが
発芽が速いことが挙げられる。
そしてまた低温処理した後に種皮を剥離途去するため、
−5°0以下の温度では種皮が凍結して弾力を失い、特
に−30℃、さらに、好ましくは、−70〜−130℃
の温度にすると、さらに種皮が脆くなりわずかな変形で
も種皮が破壊される。
常温では、種皮に弾力があり、これを破壊しようとする
と、内部の種子本体の種皮に傷が付きやすい。かかる傷
が付くと、この傷口から子葉が先に種子から突出するい
わゆるアティビカル発芽が多くなり、正規に発根するも
のと混在し、発芽の均一性が乱れる。
これに対して、本発明のように低温特に超低温に維持し
て種皮を破壊すると、種皮が凍結し脆くなっているので
、種皮が脆く内部の種子の種皮を損なわずに種皮だけが
除去できる。
これにより、発芽の均一性が良くなっているものと推定
される。
以下、本発明を更に詳細に説明する。
本発明の発芽促進法に使用される種子としては、例えば
ホウレンソウ、みつば、オクラ、シュンギク、ビート、
ソバ、ヒマワリ、ごぼう、うり類、レタス、ねぎ類、パ
セーリ、豆類などが挙げられる。
次に上記した種子を超低温処理する方法としては、液体
ヘリウム、液体ネオン、液体アルゴン、液体窒素、液体
酸素、液化炭酸ガス、液体空気、フロンなどを使用する
ことができるが、これらの中で、液体窒素若しくは液体
空気及び液化炭酸ガスなどが沸点及び経済性の点で適し
ている。これらの液化ガスはスプレー式に直接種子に噴
射され、系内で気化する方式で冷却するので効率的にか
つ確実に冷却することができる。
種子に直接噴射する冷却はどのような方法であってもよ
いが、例えば、種子を連続的に冷却筒の中に仕込み、こ
れを螺旋状のスクリューで送りだしながら冷却筒内に設
けた液化ガス管のノズルから液化ガスを噴出させて冷却
し、冷却筒の他端から冷凍された種子を送り出すことが
できる。
使用したスプレー式7リーザー冷気循環式フリーザーな
どの急速凍結装置により冷却庫内設定温度−10〜−1
96℃、好ましくは−70〜−130℃で30秒〜40
分旭理を行う。
超低温処理を行った種子は、更にその種皮を剥離するが
、種皮を剥離する方法としては、例えば、2本の回転ロ
ール、振動篩、高速回転翼による破砕、種子ジェット流
衝突方式などの装置が使用される。その他、皮取り器、
荒挽きロールボールミルなどの装置によっても種皮を剥
離することができる。
このような種皮の剥離は、冷凍状態及び乾燥状態のまま
行う必要があるが、液体窒素などの液化ガスの噴射によ
り冷凍すれば、冷凍系から粉砕系までを簡単に密閉する
だけで、噴射された液化ガスが蒸発して、常に系内から
外に冷気が流れ出すので、種皮の温度上昇及び外気の湿
度の侵入はなく、乾燥状態かつ凍結状態のままで粉砕す
ることができる。
この様な装置を使用することで種皮が脆くなっているの
で、弱い力で種皮を粉砕できる。
粉砕力が小さいため種子の内部が傷付かずに種皮のみを
容易に剥離分離することができる。
種皮を粉砕するに際して、従来種子を食用として採取す
る場合は、採取種子の表面に傷の有無は、食用としては
なにも悪影響はないが、本発明のように栽培用として剥
皮種子を製造する場合は、アティビカル発芽を起こさな
いため剥皮種子の表面に傷のない種子にする必要がある
。
本発明の冷凍種皮の粉砕除去では種皮の表面を傷つけな
いように種々注意して粉砕するのが望ましい。
また、本発明により得た剥皮種子は、種皮がないため運
送中、貯蔵中などの衝撃により傷が付きやすい。
冷凍剥皮工程によっても肉眼では見えない傷が剥皮種子
の表面に発生している可能性がある。
剥皮種子表面に傷がついていると、運送中又は店頭から
栽培農家に亙る流通過程において環境の変化を受けやす
く、発芽率の低下を生じゃすい。
なお、長期間の保存中又は播種後の土壌中でも、剥皮種
子の表面に傷がある場合は、種々の病原菌が傷口から侵
入して汚染されやすくなり、また、湿度、温度などの環
境の変化に対して過敏に影響を受け、発芽率が低下し、
成育速度も不均一となる。
本発明の剥皮種子を、コーティング剤、例えば、チバガ
イギー社製商品名ポリコートのような酸化アルミ、酸化
チタンなどの無機粉末からなるもの又は各種粘土などで
コーティングすれば、衝撃によって発生しt;傷を防ぎ
、微生物の侵入を防止し、環境の変化に対する抵抗性を
増大させることができる。
本発明者らは、このコーティング被覆によって、発芽口
を揃え、アティピカル発芽を押さえる本発明の効果をさ
らに向上させることを見い出した。
本発明剥皮種子には、特に、水分の侵入を妨げない限り
、また種子の発芽成長に有害な物質でない限り、剥皮種
子表面に固定できるコーテイング物質としては特に制限
なくどのようなものでも使用することができる。
また、場合に応じて、微生物による弊害を防止するため
、殺菌剤、例えばベンレートT(デュポン社製商品名)
、リドミル(チバガイギー社製商品名)などを含むコー
ティング剤で種子をコートするのが望ましい。
さらに、ホルモン剤、例えば、ジベレリンなどを含有す
るコーティング剤で種子をコーティングすることによっ
て、発芽及び生育を一層早めることもできる。
さらに、殺虫剤、例えば、プロメット(チバガイギー社
商品名)をコーティング剤として、使用することができ
る。
また、栄養剤をコーティング剤に含有させることができ
る。一般に、皮付き種子の種類によっては、種皮が単な
る種子の保護に止どまらず、土壌中の発芽に際して、種
皮中の成分が成長に必要な栄養剤としての役割を果たす
ものもある。
この場合の栄養不足を補うために、無機栄養剤又は有機
栄養剤をコーティング剤に含有させることができる。
無機栄養剤としては、窒素、リン系肥料などが使用でき
、有機栄養剤としては各種ビタミン又は本発明の剥皮工
程において除去された種皮を乾燥して粉末化したものを
コーティング剤に含有させることができる。
本発明のコーティング剤には、鳥忌避剤を少量混入する
ことができる。
一般に、鳥は発芽した種子を食べない習性があるが、撒
かれた発芽前の種子は鳥の好物となる。
これを防ぐために、鳥の嫌う匂い又は色などを着けた鳥
忌避剤を含有するコーティング剤を使用することができ
る。
コーティングする方法は、公知のコーティング方法、例
えば、種子粒流を上から落下させてこれにコーティング
剤溶液又は懸濁液を噴霧し、溶液を乾燥する方法などに
よりコーティングすることができる。
コーティングは、剥皮種子の表面を全面的に被覆でき、
しかもその厚さが均一であることが望ましい。コーティ
ング剤の使用量は、コーティング方法にも依存し、とく
に制限はないが、例えば、種子100重量部に対して、
1〜20重量部のコーティング剤を使用することができ
る。
なお、前記したコーティング剤には、染料や顔料などの
色素を含有せしめておくとコーティング種子の識別又は
コーティング剤の識別ができ、播種の際に品種及び播種
量、播種間隔の判別をするのに好都合である。
〔実施例〕
以下、実施例により本発明を更に具体的に説明する。
実施例1
ホウレンソウ種子として、ハイバック(アスグロウ社製
商品名)を用いて、液体窒素供給容器及び噴射ノズルを
備えたフリーザー装置(温度設定−150℃)内に入れ
15分間超低温魁理した後、種子を取り出し、これを家
庭用ミキサーを改造した高速回転翼装置に入れて1分間
の種皮破砕処理を行い、これをふるいにかけて、種皮を
剥離したホウレンソウ種子のみを分離した。
該種皮剥離種子と種皮付き無処理種子とについて、次の
処方により、ガラスシャーレ置床法と土壌直撤法の両方
により発芽試験を行った。
エ ガラスシャーレ置床法
低温剥皮処理種子と無処理の種皮付き種子をそれぞれ1
区に100粒の種子を4区のウレタンホームの床に同時
に種子を撒いた。
発芽状況を24時間毎に観察し、結果を第1表に示した
。
(以下余白)
低温剥皮処理したものは3日速く発芽する上に発芽の半
分以上が2日目に集中しており、均一に速い発芽の効果
が認められる。
現在、ウレタン床で水耕栽培されているホウレンソウは
29日周期で収穫するので、3日速く発芽することは収
穫サイクルを短縮して生産性を10%以上向上させ、し
かも、均一成育により、さらに2日速く収穫できること
になる。
従来は、速く収穫するために、成長の遅いものは間引い
て廃棄していた。この間引きの手間が省ける上、収量も
上がる。このような効果はホウレンソウ栽培において大
きな効果である。
■ 土壌直撒法
この場合は、種皮付き種子は撒く前に24時間水中に浸
けてから、低温剥離処理種子と同時に土壌に撒いた。
発芽の状況は第2表に示した。
(以下余白)
この結果から、低温剥離処理種子は発芽率もよく、第1
日めに50%以上が集中して2日以内で殆どが一斉に発
芽していることが分かる。
無処理の種皮付き種子は発芽率が悪い上、4日間に発芽
時期が広がり成育が不揃いである。
実施例2
実施例1と同様の低温処理して得たホウレンソウの種子
と超低温処理を行わないで、手作業によって種皮を剥離
したホウレンソウの種子とをガラスシャーレ置床法によ
り発芽時間の比較を行った。その結果を第3表に示す。
(以下余白)
(数値は1区100粒で4区の平均値である)(数値は
発芽率%)
第3表から明らかなように、超低温処理した後に種皮を
剥離したホウレンソウの種子は、置床後27時間で発芽
率は60%となるが、超低温処理を行わないで種皮を剥
離したのみのホウレンソウの種子は、発芽率が約60%
に達するのに約20時間遅れる。
実施例3
液体窒素供給容器、液体窒素噴射用ノズル、温度センサ
ーなどを備えたフリーザー装置にシュンギクの種子を入
れ、設定温度−85℃で15分間超低温処理した後、種
子を取り出し、これを振動篩装置に入れて、7時間振動
処理し、種皮を剥離したシュンギクに種子を得た。
次いで実施例2により得たシュンギクの種子と超低温処
理を行わないで荒挽きロールのみによって種皮を剥離し
たシュンギクの種子とを土壌直播法によって発芽時間を
比較した。その結果を第4表に示す。
(以下余白)
第4表
(1区100粒)
比較例は途中であるので数字を(
)とした。
第4表の結果から明らかなように超低温処理した後に種
皮を剥離したシュンギクの種子は、土壌播種倹約4日で
発芽率約75%となるが、超低温処理を行わないシュン
ギクの種子は、土壌播種後7日経過しても25〜40%
の発芽率であった。
実施例4
品種ワーグナー(出隅種苗製)を使用して、実施例1と
同様の低温処理後剥皮して得たホウレンソウの剥皮種子
をコーティングした。
コーティング剤は、チバガイギー社製商品名ポリコート
を使用し、この懸濁液を種子上に均等に噴霧させて、こ
れを乾燥して種子100重量部に対して、ポリコート8
重量部(固形分重量)をコーティングさせた。
これを次の処方で、土壌及びガラスシャーレの栽培試験
をしてコーティングする前の剥皮種子の栽培結果と比較
し、土壌試験結果を第5表に、ガラスシャーレ試験結果
を第6表に示した。
〔土壌試験処方〕
供試種子数400粒(1区)
播種口 平成1年8月12日
播種法 蒸気消毒した土壌に播種
温 度 常温
〔ガラスシャーレ試験処方〕
供試種子数 1区、100粒の4区
置床日 8月22日
播種法 9cmガラスシャーレに露紙2枚、水分量6c
cに100粒ずつ置床。
温度20’0
(以下余白)
第 5
表
第 6
表
土壌試験の第5表の結果からコーティング処理種子は未
処理種子に比べその発芽の63%が4日目に集中してい
る。他方未処理種子は4〜6日目に分散して発芽し74
%の発芽に達している。
種皮を剥離すると発芽が揃うが、これにコーティング処
理することでさらに発芽を促進することが解った。
第6表の結果より、土壌試験と同様にコーティング処理
種子の発芽はその72%が2日目に集中している。未処
理種子は2日間に渡って発芽しており、主な発芽は3日
目に集中している。
アティビカル発芽についてもコーティング処理種子は1
0%程度低く、コティングすることで、種皮の傷を覆う
効果が認められた。なお、各区1%程度の不発芽があっ
た。
実施例5
株張りシュンギクS型(山陽種苗株式会社製)を実施例
2と同様に低温処理して得たシュンギクの剥皮種子を粘
土でコーティング処理した。
これを栽培試験をしてコーティングする前の剥皮種子の
栽培結果と比較した。
コーティング剤は、ポリコートを使用し、種子100重
量部に対して、ポリコート剤8重量部を実施例4と同様
にコーティングさせI;。
これを次の処方で、土壌及びガラスシャーレの栽培試験
をしてコーティングする前の剥皮種子の栽培結果と比較
し、土壌試験結果を第7表に、ガラスシャーレ試験結果
を第8表に示した。
〔土壌試験処方〕
供試種子数400粒(1区)
播種日 平成1年8月8日
播種法 蒸気消毒した土壌に播種
温 度 常温
〔ガラスシャーレ試験処方〕
供試種子数 1区、100粒の4区
置床日 平成1年8月8日
播種法 9cyaガラスシヤーレに露紙2枚、水分量6
ccに100粒ずつ置床。
温度20℃
第 7
表
第 8
表
土壌試験の結果からコーティング剤処理種子は未処理種
子に比べその発芽の64%が4日目に集中している。他
方未処理種子は4〜6日目に分散して発芽し60%の発
芽に達している。果被を剥離すると発芽が揃う、これに
コーティング処理することでさらに発芽を促進すること
が解った。
ガラスシャーレ試験の結果から、発芽試験はコーティン
グ処理種子の発芽はその47%が1日目に発芽している
。未処理種子は2日目に63%が発芽しており、コーテ
ィング種子は発芽が早まっている。
アビティカル発芽についてもコーティング種子は7%程
度低く、コートすることで、種皮の傷を覆う効果が認め
られた。なお、各区8%程度の不発芽があった。
[発明の効果]
本発明の処理法によって低温処理して種皮を剥離除去し
た種子は、種皮付き種子と比較して、発芽率、成育の均
一性において非常にすぐれていて、さらに、低温処理を
行わずにただ単に種皮のみを剥離除去した種子と比べて
も、例えばホウレンソウなどでは60%発芽率達成時間
比で約20時間早くなり大変早く発芽し、しかも発芽揃
いも良好で苗の選別に時間を要しないで済むなどの効果
があり、土壌栽培、水耕栽培における種子の均−発芽促
進法として極めて有益である。
さらに、剥皮種子をコーティングして種子表面を保護す
ると、発芽の均−性及びアビティカル発芽の防止に効果
があり、コーティング剤として薬効又はのある物質を使
用するとそれぞれの薬効により、栄養剤又はホルモン剤
による成長促進、病原菌防護、殺虫及び鳥忌避の効果が
得られる。また、コーティング剤に着色して種子又はコ
ーティングの種類を識別することができる。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a method for promoting germination of hard seeds that shortens the germination time of sown hard seeds and eliminates uneven germination. [Prior Art] It is very important for sown hard seeds to grow uniformly over time and to grow at a high germination rate, for example, in order to produce particularly fast-growing spinach with a good yield. For hard seeds to germinate, they first need to absorb water. Hard seeds are usually covered with a hard seed coat, and this seed coat absorbs water, which in turn is absorbed by the embryo inside the seed coat. Therefore, in normal cultivation, in order to ensure smooth germination, seeds are often soaked in water for 20 to 24 hours to allow the seed coat to absorb sufficient water before sowing. After the seed absorbs water, stored nutrients are broken down within the seed coat, and hormones are synthesized to initiate seedling development and radicle elongation. In addition to promoting germination with water, it is also known to treat seeds in the presence of chemicals such as gibberellin, benzyladenine, kinetin, thiourea, ethrel, hydrogen peroxide, potassium nitrite, and sodium hypochlorite. There is. [Problem to be Solved by the Invention] However, when hard seeds are soaked in water and sown in soil or in a substrate for hydroponic cultivation, they do not germinate uniformly, and the seedlings that grow are irregular. When bundling seedlings, slow-growing ones had to be removed and sorted, resulting in poor efficiency and workability. On the other hand, if the seed coat is treated with a chemical substance, for example, an alkali treatment, the chemical may penetrate into the seed coat and have an adverse effect on normal seeds, which is not preferable. Therefore, there is a strong demand for a peeled seed and a method for producing the same, which have no adverse effects on the germination and growth of the peeled seed, germinate uniformly, have a short germination time, and improve harvest efficiency. [Means for Solving the Problems] As a result of extensive research in order to eliminate the above-mentioned defects, the present inventors have found that peeling the seed coat at low temperatures damages the seed coat of the inner seed during peeling. In addition, low-temperature treatment has the effect of promoting seed germination, killing two birds with one stone.
We have found that this is extremely effective, and that this effect is further enhanced when the peeled seeds are coated with an artificial seed coat, i.e., a coating agent.Based on these findings, we have arrived at the present invention. That is, the present invention consists of the following six items. 1. A peeled seed for cultivation obtained by destroying the seed coat by maintaining the seed coated seed at a low temperature of -5°C or lower. 2. A method for producing peeled seeds for cultivation, which comprises destroying the seed coat of the seed coated seed at a temperature of -5°C or lower, particularly -30°C or lower, removing the seed coat, and optionally applying a coating agent. 3. The peeled seeds for cultivation according to item 1, wherein the temperature is an ultra-low temperature of 130°C or less. 4. The peeled seed for cultivation according to item 1 or 3, wherein the peeled seed is coated with a coating agent. 5. The peeled seeds for cultivation according to ring 4, wherein the coating agent contains a bactericide, an insecticide, a hormone, a nutrient, or a bird repellent. 6. The peeled seeds for cultivation according to item 4 or 5, wherein a coloring agent is added to the coating agent. [Effect] The characteristics that the method for promoting seed germination of the present invention has good uniform germination and high germination rate are presumed to be due to the following reasons. First, by treating seeds at low temperatures, the inside of the seeds are stimulated and the embryos are activated, which triggers germination. Second, since the seed coat has been removed, moisture absorption is rapid, which leads to faster germination. And after the low temperature treatment, the seed coat is peeled off,
At temperatures below -5°C, the seed coat freezes and loses its elasticity, particularly -30°C, more preferably -70 to -130°C.
If the temperature is raised to , the seed coat becomes even more brittle and even the slightest deformation will destroy the seed coat. At room temperature, the seed coat is elastic, and if you try to break it, the inner seed coat of the seed body is likely to be damaged. When such a wound occurs, so-called ativistic germination, in which the cotyledons first protrude from the seed through the wound, increases and is mixed with those that normally germinate, disrupting the uniformity of germination. On the other hand, when the seed coat is destroyed by maintaining it at a low temperature, particularly an ultra-low temperature, as in the present invention, the seed coat is frozen and becomes brittle, so that only the seed coat can be removed without damaging the inner seed coat of the seed. It is presumed that this improves the uniformity of germination. The present invention will be explained in more detail below. Seeds used in the germination promotion method of the present invention include, for example, spinach, mitsuba, okra, shungiku, beet,
Examples include buckwheat, sunflowers, burdock, cucurbits, lettuce, green onions, parsley, and beans. Next, as a method for ultra-low temperature treatment of the seeds described above, liquid helium, liquid neon, liquid argon, liquid nitrogen, liquid oxygen, liquefied carbon dioxide, liquid air, chlorofluorocarbon, etc. can be used, but among these, Liquid nitrogen, liquid air, and liquefied carbon dioxide are suitable in terms of boiling point and economy. These liquefied gases are sprayed directly onto the seeds and cooled by vaporizing within the system, allowing for efficient and reliable cooling. Any method can be used to cool the seeds directly, but for example, a liquefied gas pipe installed in the cooling cylinder that continuously feeds the seeds into the cooling cylinder and sends them out with a spiral screw. The seeds can be cooled by blowing out liquefied gas from the nozzle, and the frozen seeds can be sent out from the other end of the cooling tube. The set temperature inside the refrigerator can be set at -10 to -1 using a quick freezing device such as the spray type 7 Reaser cold air circulation type freezer used.
96°C, preferably -70 to -130°C for 30 seconds to 40
Perform the separation. Seeds that have undergone ultra-low temperature treatment are further stripped of their seed coats. Methods for stripping the seed coats include, for example, devices such as two rotating rolls, a vibrating sieve, crushing with high-speed rotary blades, and a seed jet impingement method. used. Others, skin remover,
The seed coat can also be peeled off using equipment such as a rough roll ball mill. Peeling of seed coats like this needs to be done in a frozen and dry state, but if freezing is done by injection of liquefied gas such as liquid nitrogen, the injection can be done by simply sealing the area from the freezing system to the grinding system. The liquefied gas evaporates and cold air constantly flows out from the system, so there is no rise in temperature of the seed coat and no humidity from the outside air enters, and the seed coat can be ground in a dry and frozen state. By using such a device, the seed coat becomes brittle, so it can be crushed with a weak force. Since the crushing force is small, only the seed coat can be easily peeled off and separated without damaging the inside of the seed. Conventionally, when seed coats are crushed, when seeds are collected for food, the presence or absence of scratches on the surface of the collected seeds does not have any adverse effect on the food, but when peeled seeds are produced for cultivation as in the present invention. In this case, it is necessary to use peeled seeds with no scratches on their surfaces to prevent ativistic germination. When removing the frozen seed coat by crushing it in accordance with the present invention, it is desirable to take various precautions in crushing the seed coat so as not to damage the surface of the seed coat. Moreover, since the peeled seeds obtained according to the present invention do not have a seed coat, they are easily damaged by impacts during transportation, storage, etc. The freeze-peeling process may also cause scratches on the surface of the peeled seeds that are invisible to the naked eye. If the surface of the peeled seeds is damaged, they are susceptible to environmental changes during transportation or during the distribution process from the store to the grower, leading to a drop in germination rate. In addition, if there are scratches on the surface of peeled seeds during long-term storage or in the soil after sowing, various pathogenic bacteria can easily enter through the scratches and become contaminated, and they may also be susceptible to changes in the environment such as humidity and temperature. The germination rate decreases due to hypersensitivity to
The growth rate will also be uneven. If the peeled seeds of the present invention are coated with a coating agent, for example, one made of inorganic powder such as aluminum oxide or titanium oxide, such as Polycoat (trade name, manufactured by Ciba Geigy), or various clays, scratches will not occur due to impact. can prevent, prevent the invasion of microorganisms, and increase resistance to environmental changes. The present inventors have discovered that this coating further improves the effect of the present invention in aligning germination openings and suppressing atypical germination. For the peeled seeds of the present invention, any coating material that can be fixed on the surface of the peeled seeds may be used without particular restriction, as long as it does not prevent the intrusion of moisture or is harmful to the germination and growth of the seeds. I can do it. In addition, depending on the case, in order to prevent harmful effects caused by microorganisms, disinfectants such as Benlate T (trade name manufactured by DuPont) may be used.
It is desirable to coat the seeds with a coating agent containing, for example, Ridomil (trade name, manufactured by Ciba Geigy). Furthermore, germination and growth can be further accelerated by coating seeds with a coating agent containing a hormonal agent, such as gibberellin. Furthermore, an insecticide such as Promet (trade name of Ciba Geigy) can be used as a coating agent. Additionally, nutrients can be included in the coating agent. In general, depending on the type of coated seed, the seed coat does not stop at simply protecting the seed; in some cases, components in the seed coat serve as nutrients necessary for growth during germination in soil. In order to compensate for nutritional deficiencies in this case, inorganic or organic nutrients can be included in the coating agent. As inorganic nutrients, nitrogen and phosphorus-based fertilizers can be used, and as organic nutrients, various vitamins or the dried and powdered seed coat removed in the peeling process of the present invention can be included in the coating agent. can. A small amount of bird repellent can be mixed into the coating agent of the present invention. Birds generally do not have the habit of eating germinated seeds, but scattered ungerminated seeds become their favorite food. To prevent this, a coating containing a bird repellent with an odor or color that birds dislike can be used. Coating can be carried out by a known coating method, for example, by dropping a stream of seed grains from above, spraying a coating agent solution or suspension thereon, and drying the solution. The coating can cover the entire surface of the peeled seeds,
Moreover, it is desirable that the thickness be uniform. The amount of coating agent used depends on the coating method and is not particularly limited, but for example, for 100 parts by weight of seeds,
1 to 20 parts by weight of coating agent can be used. In addition, if the above-mentioned coating agent contains pigments such as dyes or pigments, it is possible to identify the coated seeds or the coating agent. It's convenient. [Example] Hereinafter, the present invention will be explained in more detail with reference to Examples. Example 1 Spinach seeds were placed in a freezer (temperature set at -150°C) equipped with a liquid nitrogen supply container and an injection nozzle using Hyback (trade name manufactured by Asgrow) for 15 minutes at an ultra-low temperature. The seeds were taken out, placed in a high-speed rotary blade device that was a modified household mixer, and subjected to seed coat crushing treatment for 1 minute, and then sieved to separate only the spinach seeds from which the seed coat had been peeled off. Germination tests were conducted on the seeds with peeled seed coats and untreated seeds with seed coats, using both the glass Petri dish bed method and the direct soil removal method, using the following formulation. D. Glass petri dish bed method: 1 low-temperature peeled seed and 1 untreated seed coated seed each.
100 seeds were scattered simultaneously on the floor of the urethane platform in 4 wards. The germination status was observed every 24 hours, and the results are shown in Table 1. (Margins below) Those treated with low-temperature peeling germinate three days faster, and more than half of the germination is concentrated on the second day, indicating a uniformly rapid germination effect. Spinach, which is currently grown hydroponically on urethane beds, is harvested every 29 days, so germinating three days faster will shorten the harvest cycle and increase productivity by more than 10%. This means that it can be harvested in two days faster. Previously, in order to harvest quickly, slow-growing plants were thinned out and discarded. This will save you the trouble of thinning, and will also increase your yield. Such an effect is a great effect in spinach cultivation. ■ Direct sowing method in the soil In this case, the seeds with seed coats were soaked in water for 24 hours before sowing, and then sown on the soil at the same time as the cold-exfoliated seeds. The germination status is shown in Table 2. (Margins below) From these results, the seeds treated with low-temperature peeling have a good germination rate and
It can be seen that more than 50% of the seeds were concentrated on the same day, and most of them germinated all at once within two days. Untreated seeds with seed coats have a poor germination rate, and the germination period is spread over 4 days, resulting in uneven growth. Example 2 The germination time of spinach seeds obtained by the same low-temperature treatment as in Example 1 and spinach seeds whose seed coats were manually peeled off without ultra-low-temperature treatment was compared using a glass Petri dish bed method. . The results are shown in Table 3. (The following margins) (The numbers are the average values for 4 plots with 100 grains in 1 plot) (The numbers are germination percentage%) As is clear from Table 3, spinach seeds whose seed coats have been peeled off after ultra-low temperature treatment are After 27 hours, the germination rate will be 60%, but spinach seeds whose seed coats have been peeled off without undergoing ultra-low temperature treatment have a germination rate of about 60%.
It takes about 20 hours to reach this point. Example 3 Seeds of Japanese chrysanthemum were placed in a freezer equipped with a liquid nitrogen supply container, a liquid nitrogen injection nozzle, a temperature sensor, etc., and subjected to ultra-low temperature treatment at a set temperature of -85°C for 15 minutes.The seeds were then taken out and passed through a vibrating sieve. The seeds were placed in an apparatus and subjected to vibration treatment for 7 hours, and the seed coat was peeled off to obtain seeds. Next, the germination time was compared using the direct soil seeding method between the seeds of Aspergillus annuus obtained in Example 2 and the seeds of Aspergillus annuus whose seed coats were peeled off only by rough grinding rolls without ultra-low-temperature treatment. The results are shown in Table 4. (Margins below) Table 4 (100 grains per section) The comparative example is in the middle, so the numbers are in parentheses. As is clear from the results in Table 4, the seeds of the Japanese chrysanthemum whose seed coats have been peeled off after ultra-low temperature treatment have a germination rate of about 75% within 4 days of soil sowing, but the seeds of the Chinese chrysanthemum that are not subjected to the ultra-low temperature treatment have a germination rate of approximately 75% when sown in the soil. 25-40% after 7 days
The germination rate was . Example 4 Peeled spinach seeds obtained by peeling after low temperature treatment in the same manner as in Example 1 were coated using Variety Wagner (manufactured by Isumi Seeds Co., Ltd.). As a coating agent, Polycoat (trade name) manufactured by Ciba Geigy is used. This suspension is evenly sprayed onto the seeds, dried, and Polycoat 8 is applied to 100 parts by weight of the seeds.
parts by weight (solids weight) were coated. Using the following formulation, we conducted a soil and glass petri dish cultivation test and compared it with the cultivation results of peeled seeds before coating, and the soil test results are shown in Table 5 and the glass petri dish test results are shown in Table 6. . [Soil test recipe] Number of test seeds: 400 seeds (1 section) Seed port: August 12, 1999 Sowing method: Sowing into steam-sterilized soil Temperature: Normal temperature [Glass petri dish test recipe] Number of test seeds: 1 section, 100 seeds Planting date in 4th section: August 22nd Sowing method: 2 sheets of open-air paper in a 9cm glass petri dish, moisture content: 6c
Place 100 grains each in c. Temperature 20'0 (blank below) Table 5 Table 6 From the soil test results in Table 5, 63% of the germination of coated seeds was concentrated on the 4th day compared to untreated seeds. On the other hand, untreated seeds dispersed and germinated on the 4th to 6th day.74
% germination has been reached. Peeling off the seed coat facilitates germination, but it has been found that coating the seed coat further promotes germination. From the results in Table 6, 72% of the germination of the coated seeds was concentrated on the second day, similar to the soil test. Untreated seeds germinated over two days, with main germination concentrated on the third day. Regarding ativical germination, coated seeds are also 1
Coating was found to be effective in covering wounds in the seed coat at a low level of about 0%. In addition, about 1% of the seeds failed to germinate in each section. Example 5 Dehulled seeds of Sternium japonica S type (manufactured by Sanyo Seedlings Co., Ltd.) were treated at low temperature in the same manner as in Example 2, and the peeled seeds were coated with clay. A cultivation test was conducted on this and compared with the cultivation results of peeled seeds before coating. Polycoat was used as the coating agent, and 100 parts by weight of seeds were coated with 8 parts by weight of the polycoat agent in the same manner as in Example 4. Using the following formulation, we conducted a soil and glass petri dish cultivation test and compared it with the cultivation results of peeled seeds before coating.The soil test results are shown in Table 7, and the glass petri dish test results are shown in Table 8. . [Soil test recipe] Number of test seeds: 400 seeds (1 section) Sowing date: August 8, 1999 Sowing method: Sowing in steam-sterilized soil Temperature: Room temperature [Glass petri dish test recipe] Number of test seeds: 1 section, 100 seeds Planting date in 4th section: August 8, 1999 Sowing method: 2 sheets of exposed paper in a 9cya glass shear, moisture content: 6
Place 100 grains in each cc. Temperature 20°C Table 7 Table 8 The soil test results show that 64% of the germination of seeds treated with the coating agent was concentrated on the fourth day compared to untreated seeds. On the other hand, untreated seeds dispersed and germinated on the 4th to 6th day, reaching 60% germination. It was found that peeling off the fruit cover facilitates germination, and that coating it with a coating treatment further promotes germination. From the results of the glass petri dish test, 47% of the coated seeds germinated on the first day. 63% of the untreated seeds germinated on the second day, and the coated seeds germinated faster. Avitical germination was also found to be about 7% lower for coated seeds, indicating that coating had the effect of covering wounds in the seed coat. In addition, about 8% of the seeds failed to germinate in each section. [Effects of the Invention] Seeds whose seed coats have been peeled off and removed by low temperature treatment using the treatment method of the present invention are extremely superior in germination rate and uniformity of growth compared to seeds with seed coats. Even compared to seeds whose seed coats are simply stripped and removed, spinach, for example, germinates very quickly, about 20 hours faster than the time it takes to achieve a 60% germination rate. This method is extremely useful as a method for promoting uniform germination of seeds in soil cultivation and hydroponic cultivation. Furthermore, coating peeled seeds to protect the seed surface is effective for uniform germination and prevention of abiotic germination, and when a substance with medicinal properties is used as a coating agent, nutritional or hormonal agents may be added. It has the effect of promoting growth, protecting against pathogens, killing insects, and repelling birds. Additionally, the type of seed or coating can be identified by coloring the coating agent.
Claims (1)
を破壊して得た栽培用剥皮種子。 2 種皮付き種子を温度−5℃以下において、種皮を破
壊して、種皮を除去し、所望によりコーティング剤を塗
布することを特徴とする栽培用剥皮種子の製造方法。 3 温度が−30℃以下の超低温である請求項1記載の
栽培用剥皮種子。 4 剥皮種子をコーティング剤で被覆した請求項1又は
3記載の栽培用剥皮種子。 5 コーティング剤が殺菌剤、殺虫剤、ホルモン剤、栄
養剤又は鳥忌避剤を含有するものである請求項4記載の
栽培用剥皮種子。 6 コーティング剤に着色剤を添加した請求項4又は5
記載の栽培用剥皮種子。[Claims] 1. A peeled seed for cultivation obtained by maintaining a seed coated seed at a low temperature of -5°C or lower to destroy the seed coat. 2. A method for producing peeled seeds for cultivation, which comprises destroying the seed coat of the seed coated seed at a temperature of -5°C or lower, removing the seed coat, and applying a coating agent if desired. 3. The peeled seed for cultivation according to claim 1, wherein the temperature is an ultra-low temperature of -30°C or lower. 4. The peeled seed for cultivation according to claim 1 or 3, wherein the peeled seed is coated with a coating agent. 5. The peeled seeds for cultivation according to claim 4, wherein the coating agent contains a bactericide, an insecticide, a hormone, a nutrient, or a bird repellent. 6. Claim 4 or 5, wherein a coloring agent is added to the coating agent.
Dehulled seeds for cultivation as described.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1259367A JP2579822B2 (en) | 1988-10-19 | 1989-10-04 | Method for producing peeled seeds for cultivation |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63-263321 | 1988-10-19 | ||
JP26332188 | 1988-10-19 | ||
JP1259367A JP2579822B2 (en) | 1988-10-19 | 1989-10-04 | Method for producing peeled seeds for cultivation |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02273104A true JPH02273104A (en) | 1990-11-07 |
JP2579822B2 JP2579822B2 (en) | 1997-02-12 |
Family
ID=26544096
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1259367A Expired - Lifetime JP2579822B2 (en) | 1988-10-19 | 1989-10-04 | Method for producing peeled seeds for cultivation |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2579822B2 (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002003308A (en) * | 2000-04-18 | 2002-01-09 | Inkotekku Japan Kk | Agrochemical-coated rice seed |
WO2001078507A3 (en) * | 2000-04-18 | 2002-06-27 | Incotec Japan Co Ltd | Rice seed coated with an agricultural chemical |
WO2003092410A1 (en) * | 2002-04-30 | 2003-11-13 | Aipop Co., Ltd. | Method of extracting rutin from buck wheat growed by hydroponics |
CN103039155A (en) * | 2013-01-18 | 2013-04-17 | 通化师范学院 | Integrated after-ripening method of taxus cuspidate seeds |
CN103650697A (en) * | 2012-09-21 | 2014-03-26 | 张勇 | Method for promoting cynomorium songaricum seeds to germinate |
CN106973577A (en) * | 2016-10-27 | 2017-07-25 | 重庆市农业科学院 | A kind of simple asparagus lettuce seed accelerating germination method |
CN108243656A (en) * | 2018-02-09 | 2018-07-06 | 芜湖欧标农业发展有限公司 | A kind of method for treating seeds before wealth and rank forsythia viridissima Lindl sowing |
CN109220058A (en) * | 2018-10-31 | 2019-01-18 | 海南大学 | A method of improving cymose buckwheat rhizome percentage of seedgermination |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5131751A (en) * | 1974-09-12 | 1976-03-18 | Mitsubishi Monsanto Chem | SHINKUSEIKEIYONANSHITSUHORIENKABINIRUENBOSUSHIITO NO SEIZOHO |
JPS58157619U (en) * | 1982-04-16 | 1983-10-21 | 株式会社イデヤ | Resin tablet heating device |
JPS6296005A (en) * | 1985-10-23 | 1987-05-02 | 日本甜菜製糖株式会社 | Treatment of seed |
-
1989
- 1989-10-04 JP JP1259367A patent/JP2579822B2/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5131751A (en) * | 1974-09-12 | 1976-03-18 | Mitsubishi Monsanto Chem | SHINKUSEIKEIYONANSHITSUHORIENKABINIRUENBOSUSHIITO NO SEIZOHO |
JPS58157619U (en) * | 1982-04-16 | 1983-10-21 | 株式会社イデヤ | Resin tablet heating device |
JPS6296005A (en) * | 1985-10-23 | 1987-05-02 | 日本甜菜製糖株式会社 | Treatment of seed |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002003308A (en) * | 2000-04-18 | 2002-01-09 | Inkotekku Japan Kk | Agrochemical-coated rice seed |
WO2001078507A3 (en) * | 2000-04-18 | 2002-06-27 | Incotec Japan Co Ltd | Rice seed coated with an agricultural chemical |
JP4724309B2 (en) * | 2000-04-18 | 2011-07-13 | インコテックジャパン株式会社 | Pesticide-coated rice seed |
WO2003092410A1 (en) * | 2002-04-30 | 2003-11-13 | Aipop Co., Ltd. | Method of extracting rutin from buck wheat growed by hydroponics |
CN103650697A (en) * | 2012-09-21 | 2014-03-26 | 张勇 | Method for promoting cynomorium songaricum seeds to germinate |
CN103039155A (en) * | 2013-01-18 | 2013-04-17 | 通化师范学院 | Integrated after-ripening method of taxus cuspidate seeds |
CN106973577A (en) * | 2016-10-27 | 2017-07-25 | 重庆市农业科学院 | A kind of simple asparagus lettuce seed accelerating germination method |
CN106973577B (en) * | 2016-10-27 | 2020-07-28 | 重庆市农业科学院 | Simple asparagus lettuce seed germination accelerating method |
CN108243656A (en) * | 2018-02-09 | 2018-07-06 | 芜湖欧标农业发展有限公司 | A kind of method for treating seeds before wealth and rank forsythia viridissima Lindl sowing |
CN109220058A (en) * | 2018-10-31 | 2019-01-18 | 海南大学 | A method of improving cymose buckwheat rhizome percentage of seedgermination |
CN109220058B (en) * | 2018-10-31 | 2021-01-29 | 海南大学 | Method for improving germination rate of wild buckwheat rhizome seeds |
Also Published As
Publication number | Publication date |
---|---|
JP2579822B2 (en) | 1997-02-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP3307066B1 (en) | Seed disinfection method | |
Nerson | Seed production and germinability of cucurbit crops | |
US4061488A (en) | Plant treating mixtures and methods utilizing spores of Bacillus uniflagellatus | |
EP2793570B1 (en) | Seed treatment composition | |
HU222817B1 (en) | Method for increasing the shelf life of seeds | |
Dorna et al. | Germination, vigour and health of primed Allium cepa L. seeds after storage | |
BRPI0715498A2 (en) | new antifungal composition | |
TW201733442A (en) | Vaporized administration of pesticides | |
JPH02273104A (en) | Husked seed for culture and production thereof | |
CN102948280A (en) | Treatment agent for hard seeds | |
Sweet et al. | The surface decontamination of seeds to produce axenic seedlings | |
Chala et al. | Review on seed process and storage condition in relation to seed moisture and ecological factor | |
CN104380875A (en) | Method for cold resistance treatment on corn seed to eliminate rogue | |
Thomas | Seed treatments and techniques to improve germination | |
Huang et al. | Cold water treatment promotes ethylene production and dwarfing in tomato seedlings | |
US11420806B2 (en) | Method for improving the storability of seeds | |
Siddiqui et al. | Influence of sprout inhibiting treatments and packaging methods on storage performance of Kufri Chipsona 4 potato | |
Sudhakar et al. | Technological Advances in Agronomic Practices of Seed Processing, Storage, and Pest Management: An Update | |
Begum et al. | Effect of Harvesting Stages on Seed Yield and Quality of Okra (Abelmoschus esculentus L. Moench). | |
JPH0614810B2 (en) | Seed with seed coat and method for producing the same | |
CN106068777A (en) | A kind of Radix Notoginseng seed bar processing method improving Radix Notoginseng survival rate | |
JP3833793B2 (en) | Vegetation seed and vegetation sheet using the seed | |
Elkashif et al. | Effect of cultivar, packaging treatments and temperature on post-harvest quality of okra | |
CN114980743A (en) | Compositions and methods for treating plants and plant parts with volatile spoilage biocontrol actives | |
CN113207580A (en) | Rapid seedling raising method for holboellia latifolia seeds |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20071107 Year of fee payment: 11 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20081107 Year of fee payment: 12 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20091107 Year of fee payment: 13 |
|
EXPY | Cancellation because of completion of term |