JPH0286717A - Method for proliferating algae - Google Patents
Method for proliferating algaeInfo
- Publication number
- JPH0286717A JPH0286717A JP63236892A JP23689288A JPH0286717A JP H0286717 A JPH0286717 A JP H0286717A JP 63236892 A JP63236892 A JP 63236892A JP 23689288 A JP23689288 A JP 23689288A JP H0286717 A JPH0286717 A JP H0286717A
- Authority
- JP
- Japan
- Prior art keywords
- algae
- precursor
- substrate
- coating film
- cured
- 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.)
- Pending
Links
- 241000195493 Cryptophyta Species 0.000 title claims abstract description 49
- 238000000034 method Methods 0.000 title claims description 33
- 230000002062 proliferating effect Effects 0.000 title 1
- 239000002243 precursor Substances 0.000 claims abstract description 80
- 238000000576 coating method Methods 0.000 claims abstract description 57
- 239000011248 coating agent Substances 0.000 claims abstract description 54
- 229920000642 polymer Polymers 0.000 claims abstract description 38
- 230000012010 growth Effects 0.000 claims abstract description 25
- 239000000758 substrate Substances 0.000 claims abstract description 19
- 239000000463 material Substances 0.000 claims description 21
- 239000007788 liquid Substances 0.000 claims description 10
- 235000012041 food component Nutrition 0.000 claims description 6
- 241001474374 Blennius Species 0.000 abstract description 29
- 239000000243 solution Substances 0.000 abstract description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 20
- 239000007864 aqueous solution Substances 0.000 abstract description 12
- 241001261506 Undaria pinnatifida Species 0.000 abstract description 11
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 abstract description 7
- 235000010413 sodium alginate Nutrition 0.000 abstract description 7
- 239000000661 sodium alginate Substances 0.000 abstract description 7
- 229940005550 sodium alginate Drugs 0.000 abstract description 7
- 241000251468 Actinopterygii Species 0.000 abstract description 6
- 238000001035 drying Methods 0.000 abstract description 4
- 230000035755 proliferation Effects 0.000 abstract description 3
- 238000007598 dipping method Methods 0.000 abstract description 2
- 239000007921 spray Substances 0.000 abstract 1
- 239000003973 paint Substances 0.000 description 17
- 239000002585 base Substances 0.000 description 15
- 230000000052 comparative effect Effects 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 229920005989 resin Polymers 0.000 description 10
- 239000007787 solid Substances 0.000 description 10
- 239000004567 concrete Substances 0.000 description 9
- 239000000835 fiber Substances 0.000 description 8
- 229920002472 Starch Polymers 0.000 description 7
- 235000010443 alginic acid Nutrition 0.000 description 7
- 229920000615 alginic acid Polymers 0.000 description 7
- 239000013535 sea water Substances 0.000 description 7
- 239000004372 Polyvinyl alcohol Substances 0.000 description 6
- -1 alginate alkylene glycol ester Chemical class 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 229920002451 polyvinyl alcohol Polymers 0.000 description 6
- 235000019698 starch Nutrition 0.000 description 6
- 239000008107 starch Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 229920006387 Vinylite Polymers 0.000 description 5
- 235000015097 nutrients Nutrition 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 229920001059 synthetic polymer Polymers 0.000 description 5
- 241000196324 Embryophyta Species 0.000 description 4
- 239000000783 alginic acid Substances 0.000 description 4
- 229960001126 alginic acid Drugs 0.000 description 4
- 150000004781 alginic acids Chemical class 0.000 description 4
- 230000001902 propagating effect Effects 0.000 description 4
- 230000003746 surface roughness Effects 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 229940072056 alginate Drugs 0.000 description 3
- 239000001110 calcium chloride Substances 0.000 description 3
- 229910001628 calcium chloride Inorganic materials 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
- 239000011976 maleic acid Substances 0.000 description 3
- 230000001737 promoting effect Effects 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 241000512259 Ascophyllum nodosum Species 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 229910021538 borax Inorganic materials 0.000 description 2
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
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- 229910052751 metal Inorganic materials 0.000 description 2
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- 235000015170 shellfish Nutrition 0.000 description 2
- 235000010339 sodium tetraborate Nutrition 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
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- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 2
- 239000003643 water by type Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 108010076119 Caseins Proteins 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 229920000896 Ethulose Polymers 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000001859 Ethyl hydroxyethyl cellulose Substances 0.000 description 1
- 102000020897 Formins Human genes 0.000 description 1
- 108091022623 Formins Proteins 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 240000003183 Manihot esculenta Species 0.000 description 1
- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 229920000602 Poly[(isobutylene-alt-maleic acid, ammonium salt)-co-(isobutylene-alt-maleic anhydride)] Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 230000005791 algae growth Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- VNSBYDPZHCQWNB-UHFFFAOYSA-N calcium;aluminum;dioxido(oxo)silane;sodium;hydrate Chemical compound O.[Na].[Al].[Ca+2].[O-][Si]([O-])=O VNSBYDPZHCQWNB-UHFFFAOYSA-N 0.000 description 1
- YYRMJZQKEFZXMX-UHFFFAOYSA-N calcium;phosphoric acid Chemical compound [Ca+2].OP(O)(O)=O.OP(O)(O)=O YYRMJZQKEFZXMX-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 235000019326 ethyl hydroxyethyl cellulose Nutrition 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- FWQHNLCNFPYBCA-UHFFFAOYSA-N fluoran Chemical compound C12=CC=CC=C2OC2=CC=CC=C2C11OC(=O)C2=CC=CC=C21 FWQHNLCNFPYBCA-UHFFFAOYSA-N 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
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- 229920005615 natural polymer Polymers 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 229910000273 nontronite Inorganic materials 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000012254 powdered material Substances 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000001850 reproductive effect Effects 0.000 description 1
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- 229910052708 sodium Inorganic materials 0.000 description 1
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- 239000002904 solvent Substances 0.000 description 1
- 229910001427 strontium ion Inorganic materials 0.000 description 1
- 239000002426 superphosphate Substances 0.000 description 1
- 229940100445 wheat starch Drugs 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A40/00—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
- Y02A40/80—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in fisheries management
- Y02A40/81—Aquaculture, e.g. of fish
Landscapes
- Artificial Fish Reefs (AREA)
- Cultivation Of Seaweed (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は人工魚礁体、あるいは滴定着用網、滴定着用ロ
ーブなどの藻増殖基材に、(海)水産植物、特にワカメ
、コンブ、ノリ等の海藻類の定着、増殖方法に関する。Detailed Description of the Invention (Field of Industrial Application) The present invention is applicable to artificial reef bodies, droplet fixing nets, droplet fixing lobes, and other algae growth substrates that contain (sea) aquatic plants, particularly wakame, kelp, and seaweed. Concerning methods for establishing and propagating seaweed.
(従来の技術及びその課題)
水産資源の消費量は年々増加の傾向にあり、もしも水産
資源の再生産を人工的に行なわないならば50年以内に
枯渇してしまうといわれている。(Prior art and its problems) The consumption of marine resources is increasing year by year, and it is said that if marine resources are not artificially reproduced, they will be exhausted within 50 years.
最近では資源ナショナリズムの世界的風潮から沿岸20
0海里の領海宣言が多くの国でなされていることを考え
ると、我が国沿岸漁業の振興の重要性は論議の余地がな
く、国家的見地から種々の施策が実施されている。その
1つが魚類、貝類、海藻類の養殖および増殖である。Recently, due to the global trend of resource nationalism, coastal
Considering that many countries have declared their territorial waters as zero nautical miles, there is no room for debate about the importance of promoting Japan's coastal fisheries, and various measures are being implemented from a national perspective. One of these is the cultivation and propagation of fish, shellfish, and seaweed.
魚類や貝類海藻類等の海産動植物の人工的生産の一方法
として人工魚礁および藻場が利用されており、かかる人
工魚礁および藻場としてはコンクリート、プラスチック
ゴムまたは網を基材とした人工魚礁体、さらには天然繊
維又は合成繊維製の海藻類定着用のロープや網を利用し
た藻場などがある。ところで、このような人工魚礁体や
藻場プラントがそのまま(海)水中に投入された場合、
その表面′に目的とする海藻類がより速くしかもできる
だけ多く繁殖することが望ましいのであるが、投入され
た海域によって生長速度や繁殖量に差があり、特に海水
中の栄養分が少い貧栄養海域では、海藻類の付着生育が
ほとんど期待できない。Artificial fish reefs and seaweed beds are used as a method for artificially producing marine animals and plants such as fish, shellfish, and seaweed. Such artificial reefs and seaweed beds include artificial reef bodies made of concrete, plastic rubber, or nets. In addition, there are seaweed beds using ropes and nets made of natural or synthetic fibers for fixing seaweed. By the way, if such an artificial fish reef body or seaweed bed plant is put into (sea) water as it is,
It is desirable for the target seaweed to reproduce as quickly and as much as possible on the surface of the seaweed, but the growth rate and amount of reproduction vary depending on the sea area where the seaweed is introduced. In this case, there is little expectation of attached growth of seaweed.
海藻類の生育を促進する目的で魚礁体、藻場プラントな
どの表面に栄養成分を含有する養藻用塗料を塗装して達
成しようとする方法については、特公昭35−1067
5号公報、特公昭47−8978号公報、特開昭49−
99889号公報、特公昭55−34186号公報、特
願昭55−141663において、藻類とくにワカメ、
コンブ、ノリ等の生長促進効果の大きい塗料組成物が提
案されている。For the purpose of promoting the growth of seaweed, a method of applying an algae-cultivating paint containing nutrients to the surfaces of fish reef bodies, seaweed bed plants, etc. is disclosed in Japanese Patent Publication No. 35-1067.
Publication No. 5, Japanese Patent Publication No. 1989-8978, Japanese Patent Application Publication No. 1977-
No. 99889, Japanese Patent Publication No. 55-34186, and Japanese Patent Application No. 55-141663, algae, especially seaweed,
Paint compositions that have a large growth promoting effect on kelp, seaweed, etc. have been proposed.
また、本出願人は、塗料中に配合する栄養成分の種類や
配合割合が増殖効果に大きく影響することのほか、塗膜
表面の凹凸、換言すれば表面粗さの程度が増殖性に極め
て大きな影響をもち、一般に平滑な塗面よりも適当な表
面粗さを持った塗面の方が海藻類に対する増殖効果の格
段と大きいことを見いだし、それにもとづいて、特定の
栄養成分を含み、かつ適当な表面粗さをもつ塗面を形成
する養藻用塗料についても特開昭57−177628号
公報ですでに提案した。In addition, the applicant has discovered that in addition to the fact that the types and proportions of nutritional components blended into the paint greatly affect the proliferation effect, the unevenness of the paint film surface, in other words, the degree of surface roughness, has an extremely large effect on the proliferation effect. In general, we found that a painted surface with appropriate surface roughness has a much greater growth effect on seaweed than a smooth painted surface. JP-A-57-177628 has already proposed an algae-cultivating paint that forms a coated surface with a certain surface roughness.
これらの栄養成分を含有する海藻類の養藻用塗料は、元
来、海藻の生長に必要な栄養成分の少ない、所謂、貧栄
養海域において特に効果ならしめることを主たる目的と
して用いるものであるが、一般にこの種の海域ではもと
もと海藻類が少ないこともあって、生殖生育によって藻
類の葉体となりうる前駆体(以下、「前駆体」と略称す
ることもある)の存在が少ないために、適性な栄養成分
を含有した塗料を塗布し、またその表面に適性な表面粗
度を与えて、前駆体の着生生長に好ましい環境を作って
も、海藻が着生、生育しないケースが多く認められるの
である。Paints for cultivating seaweed containing these nutritional components were originally intended to be particularly effective in so-called oligotrophic waters, where there are few nutrients necessary for the growth of seaweed. In general, seaweed is scarce in this type of sea area to begin with, and there are few precursors (hereinafter sometimes abbreviated as "precursors") that can become algae thallus through reproductive growth. Even if we create a favorable environment for the epiphytic growth of precursors by applying paint containing nutritional ingredients and giving the surface an appropriate surface roughness, there are many cases where seaweed does not adhere or grow. It is.
更に、栄養成分を含有する養藻用塗料から形成される塗
膜表面に、生殖、生育によって藻類の葉体となりうる前
駆体を付着させてお(方法(特開昭59−78633号
公報)及び養藻用塗料から形成される塗膜表面に、前駆
体を増養着生させた担体を結合した海藻増殖用被膜体(
特開昭58−193630号公報)が提案されている。Furthermore, precursors that can become algae fronds through reproduction and growth are attached to the surface of the coating film formed from the algae-cultivating paint containing nutritional components (method (Japanese Unexamined Patent Publication No. 78633/1983)). A coating material for seaweed growth, in which a carrier on which a precursor is grown and adhered is bonded to the surface of a coating formed from an algae cultivation paint.
JP-A-58-193630) has been proposed.
しかしながら、これらの方法は、塗膜表面に前駆体もし
くは前駆体を増養着生させた担体を付着、結合させたも
のを(海)水中に浸漬するまでの間に前駆体が乾燥して
枯死したり、また海(水)中で前駆体が塗膜もしくは支
持体から剥離したりする恐れがある。However, in these methods, the precursor or a carrier on which the precursor is grown and adhered is attached and bonded to the coating surface, and the precursor dries and dies before it is immersed in (sea) water. There is also a risk that the precursor may peel off from the coating or support in the sea (water).
また、栄養海域では種々の藻類が多量に存在するため食
用の藻類だけを生殖、生育させることは困難であること
から、通常、繊維、ロープ、網等の海藻類定着用基材に
直接前駆体を付着させておく方法が行なわれる。しかし
ながら、該方法においても、前記と同様に前駆体が枯死
したり、また前駆体が基材から剥離したりする恐れがあ
る。In addition, since it is difficult to reproduce and grow only edible algae in vegetative sea areas due to the abundance of various algae, it is common to use precursors directly on substrates for seaweed colonization, such as fibers, ropes, and nets. A method is used to keep it attached. However, in this method as well, there is a possibility that the precursor dies or dies, or the precursor peels off from the base material, as described above.
(課題を解決するための手段)
本発明者は、上記した欠点を克服する方法について種々
研究した結果、前記した従来の方法において、基材に付
着させ、た前駆体に水性高分子液を塗布することにより
、前駆体の乾燥による枯死及び(海)水中における前駆
体の剥離を防止できることを見い出し、本発明を完成す
るに至った。(Means for Solving the Problem) As a result of various studies on methods for overcoming the above-mentioned drawbacks, the present inventor found that in the conventional method described above, an aqueous polymer liquid is applied to a precursor that is attached to a base material. The inventors have discovered that by doing so, it is possible to prevent the precursor from dying due to drying and from peeling off in (sea) water, and have completed the present invention.
即ち、本発明は、基材に、生殖、生育によって藻類の葉
体となりうる前駆体を付着させたのち、水性高分子液を
塗装し、硬化もしくは未硬化の塗膜を形成させる藻類の
増殖方法並びに基材の表面に、前駆支持体を設けたのち
、水性高分子液を塗装し、硬化もしくは未硬化塗膜を形
成させる藻類の増殖方法、並びに基材に、藻類の栄養成
分を含有する養藻用塗膜を形成させたのち、生殖、生育
によって藻類の葉体となりうる前駆体を付着させ、次に
水性高分子液を塗装し硬化もしくは未硬化の塗膜を形成
させる藻類の増殖方法並びに基材に、藻類の栄養成分を
含有する養藻用塗膜を形成させたのち、該塗膜上に前駆
支持体を設け、次に水性高分子液を塗装し、硬化もしく
は未硬化塗膜を形成させることを特徴とする藻類の増殖
方法に係る。That is, the present invention provides a method for propagating algae, in which a precursor that can become an algal leaf through reproduction and growth is attached to a substrate, and then an aqueous polymer solution is applied to form a cured or uncured coating film. There is also a method for growing algae in which a precursor support is provided on the surface of a base material, and then an aqueous polymer solution is applied to form a cured or uncured coating film, and a method for growing algae in which a precursor support is provided on the surface of a base material, and a nutrient solution containing algae nutrients is applied to the base material. A method for propagating algae, in which a coating film for algae is formed, a precursor that can become an algae leaf body is attached through reproduction and growth, and then an aqueous polymer solution is applied to form a cured or uncured coating film; After forming an algae-cultivating coating film containing nutritional components of algae on a substrate, a precursor support is provided on the coating film, and then an aqueous polymer solution is applied to form a cured or uncured coating film. The present invention relates to a method for growing algae, characterized by forming algae.
本発明■〜■における基材、前駆体及び水性高分子液に
ついて述べる。The base material, precursor, and aqueous polymer liquid in the present invention (1) to (2) will be described.
基材としては、(海)水中に自然に存在する岩、石、又
は、人工的に設置した木、竹、石、コンクリート、プラ
スチック、ゴム、金属等の人工魚礁体、天然出維、合成
!Pi維等からなる網、ローブ等に構成される人工藻場
等が挙げられるが、これらに何ら限定されない。As a base material, rocks and stones that naturally exist in (sea) water, or artificial reefs such as artificially installed trees, bamboo, stones, concrete, plastic, rubber, metal, natural fibers, and synthetic! Examples include, but are not limited to, artificial seaweed beds constructed of nets, lobes, etc. made of Pi fibers, etc.
基材又は支持体に付着させる前駆体としては、生殖、生
育によって藻類の葉体となりうるものであって、例えば
藻類の遁走子、胞子(果胞子、殻胞子等)、幼芽、葉体
、葉体の粉状物(該粉状物は水に溶解もしくは分散させ
たものでもよい)等が使用できる。Precursors to be attached to the substrate or support include those that can become algal thallus through reproduction and growth, such as algal fumespores, spores (carospores, chlospores, etc.), buds, thallus, Powdered leaves (the powdered material may be dissolved or dispersed in water) can be used.
前駆体に塗装する水性高分子液としては、水を主な媒体
とする天然、;合成及び合成高分子類の水溶解液及び水
膨潤液等が使用できる。天然、半合成及び合成高分子類
は従来から公知の高分子類が使用できる6代表的な高分
子類を例示すると、天然高分子類としては、例えばかん
しょデンプン、ばれいしょデンプン、タピオカデンプン
、小麦デンプン、コーンスターチ等のデンプン質;フッ
ラン、寒天(ガラクタン)、アルギン酸、アルギン酸ナ
トリウム、カラゲナン等の海藻物質;にかわ、ゼラチン
、カゼイン、コラーゲン等のタンパク質;モンモリロナ
イト、バイデライト、ノントロナイト、サボナイト等の
モンモリロナイト系鉱物質等が挙げられる。半合成高分
子類としては、例えばビスコール、メチルセルロース、
エチルセルロース、ヒドロキシエチルセルロース、カル
ボキシメチルセルロース等のセルロース系:可溶性デン
プン、カルボキシメチルデンプン等のデンプン系;アル
ギン酸アルキレングリコールエステル等のアルギン酸誘
導体等が挙げられる6合成高分子類としては、例えばポ
リエチレングリコール、ポリプロピレングリコール等の
ポリアルキレングリコール類:ポリ(メタ)アクリル酸
、ポリ(メタ)アクリルアミド等のアクリル樹脂及びそ
の塩類;ポリビニルアルコール、ポリビニルピロリドン
等のビニル樹脂;ブチレン−(無水)マレイン酸、゛イ
ソブチレンー(無水)マレイン酸、ブタジェン−(無水
)マレイン酸等のマレイン化共重合体及びその塩類;ポ
リビニルアルコール−ポリ(メタ)アクリル酸等の共重
合体;ホウ酸ナトリウム等でポリビニルアルコールを架
橋した架橋ポリビニルアルコール及びアクリル繊維の加
水分解物等が挙げられる。上記塩としてはナトリウム、
カリウム、アンモニウムが挙げられる。上記水性高分子
は一種もしくは2種以上混合して使用できる。As the aqueous polymer liquid to be applied to the precursor, aqueous solutions and water-swollen liquids of natural, synthetic, and synthetic polymers that use water as a main medium can be used. As natural, semi-synthetic and synthetic polymers, conventionally known polymers can be used.6 Typical examples of the polymers include: natural polymers such as kansho starch, potato starch, tapioca starch, and wheat starch. , starch such as corn starch; seaweed substances such as fluoran, agar (galactan), alginic acid, sodium alginate, and carrageenan; proteins such as glue, gelatin, casein, and collagen; montmorillonite minerals such as montmorillonite, beidellite, nontronite, and savonite. Examples include quality. Examples of semi-synthetic polymers include biscol, methylcellulose,
Examples of synthetic polymers include cellulose types such as ethyl cellulose, hydroxyethyl cellulose, and carboxymethyl cellulose; starch types such as soluble starch and carboxymethyl starch; and alginic acid derivatives such as alginate alkylene glycol ester.6 Synthetic polymers include, for example, polyethylene glycol, polypropylene glycol, etc. Polyalkylene glycols: Acrylic resins and their salts such as poly(meth)acrylic acid and poly(meth)acrylamide; Vinyl resins such as polyvinyl alcohol and polyvinylpyrrolidone; Butylene-(anhydrous) maleic acid, ``isobutylene-(anhydrous) maleic acid'' Acid, maleated copolymers such as butadiene-(anhydrous)maleic acid and their salts; copolymers such as polyvinyl alcohol-poly(meth)acrylic acid; cross-linked polyvinyl alcohol and acrylic obtained by cross-linking polyvinyl alcohol with sodium borate, etc. Examples include fiber hydrolysates. The above salts include sodium,
Examples include potassium and ammonium. The above aqueous polymers can be used alone or in combination of two or more.
水性高分子類の中でも、アルギン酸、アルギン酸ナトリ
ウム等のアルギン酸高分子は、前駆体に対してからみや
すく、しかも繊維質等の基材または前駆体の支持体との
付着性に優れた糸状高分子であること、保水性に優れる
こと、前駆体の生育を阻害する性質がないこと、前駆体
が生殖、生育した藻類の葉体に対しても害を及ぼさない
こと、人体に対しても安全な物質であること等からこの
ものを使用することが好ましい。Among aqueous polymers, alginic acid polymers such as alginic acid and sodium alginate are filamentous polymers that are easy to entangle with precursors and have excellent adhesion to substrates such as fibers or supports for precursors. The substance has excellent water retention properties, does not have properties that inhibit the growth of the precursor, does not cause any harm to the leaflets of the algae in which the precursor reproduces and grows, and is safe for the human body. It is preferable to use this material because of the following reasons.
前駆体に塗布する水性高分子液は、水又は海水等の媒体
で希釈して、例えば浸漬スプレー、へケ等の塗装手段で
塗布できる。希釈した水性高分子液の固形分は塗装手段
によっても異なるが通常、約0.5〜60.0重量%、
好ましくは約3.0〜30.0重量%である。該固形分
が05重量%より低いと前駆体を被覆する水性高分子が
少なくなるので海(水)水の揮発が速くなり前駆体が枯
死したり、藻類の生殖生育が劣り好ましくない、他方、
固形分が60.0重量%より高いと塗装作業性が劣ると
ともに、前駆体に含まれた水分が水性高分子に吸着され
海(水)水に浸漬される前に前駆体が枯死する恐れがあ
るので好ましくない。The aqueous polymer liquid to be applied to the precursor can be diluted with a medium such as water or seawater, and applied by a coating method such as dip spraying or brushing. The solid content of the diluted aqueous polymer liquid varies depending on the coating method, but is usually about 0.5 to 60.0% by weight.
Preferably it is about 3.0-30.0% by weight. If the solid content is lower than 0.5% by weight, the amount of aqueous polymer that coats the precursor decreases, so the volatilization of sea water becomes faster and the precursor dies, and the reproduction and growth of algae becomes poor, which is undesirable.
If the solid content is higher than 60.0% by weight, painting workability will be poor, and there is a risk that the moisture contained in the precursor will be adsorbed by the aqueous polymer and the precursor will wither and die before it is immersed in seawater. I don't like it because it is.
また、水性高分子の硬化塗膜は、水性高分子液中に硬化
剤を含有させた高分子液を塗布するか、もしくは水性高
分子液を塗布した未硬化塗膜の上分子液に対してカルシ
ウムイオン、ストロンチウムイオン、アルミニウムイオ
ン等の多価イオン水溶性金属塩を硬化剤として使用する
系及びポリビニルアルコールの水性高分子液に対してホ
ウ酸ナトリウム等の塩を硬化剤として使用する系等が挙
げられる。Cured coatings of water-based polymers can be made by applying a polymer solution containing a curing agent in the water-based polymer solution, or by applying a polymer solution on top of an uncured coating coated with the water-based polymer solution. Systems that use polyvalent ion water-soluble metal salts such as calcium ions, strontium ions, and aluminum ions as hardening agents, and systems that use salts such as sodium borate as hardening agents for aqueous polymeric liquids of polyvinyl alcohol. Can be mentioned.
次に本発明方法について下記に述べる。Next, the method of the present invention will be described below.
まず本発明■の方法は基材に、前駆体を散布したのち、
水性高分子液を塗装し、硬化もしくは未硬化塗膜を形成
させ、次いでこのものを海(水)中に浸漬することによ
り実施できる。基材としては、好ましくは天然Ili維
、合成jJ!維からなる網、ローブ等の人工藻場が好ま
しい、水性高分子液の塗装は前駆体が被覆される程度に
塗布すれば充分と思われる。First, in the method of the present invention (2), after spraying a precursor on a base material,
This can be carried out by coating an aqueous polymer solution to form a cured or uncured coating, and then immersing this in the sea (water). The base material is preferably natural Ili fiber, synthetic jJ! Artificial seaweed beds such as nets and lobes made of fibers are preferable, and it is thought that it is sufficient to apply the aqueous polymer solution to the extent that the precursor is coated.
本発明■の方法は、基材に、前駆体と支持体で構成され
る前駆支持体を設けたのち、水性高分子液を塗装し硬化
もしくは未硬化の塗膜を形成させ、次いでこのものを海
(水)中に浸漬することにより実施できる。基材に前駆
支持体を設ける方法としては、例えば基材に例えばアク
リル樹脂、ビニル樹脂等の1B1脂を塗布したのち、該
tfiJ脂が乾燥する前′に支持体を結合させ、次に該
支持体に前駆体を付着させる方法もしくは予め前駆体を
支持体に付着させた前駆支持体を樹脂膜上に結合させる
ことにより実施できる。該方法において、前駆体が樹脂
膜中に入り込む恐れがないことから前者の方法が好まし
い。In the method of the present invention (2), a precursor support composed of a precursor and a support is provided on a base material, and then an aqueous polymer solution is applied to form a cured or uncured coating film. This can be done by immersing it in the sea (water). As a method for providing a precursor support on a base material, for example, after applying a 1B1 resin such as acrylic resin or vinyl resin to the base material, bonding the support before the TFIJ resin dries, and then applying the precursor support to the base material. This can be carried out by attaching a precursor to a body or by bonding a precursor support to which a precursor has been attached in advance onto a resin film. In this method, the former method is preferred since there is no fear that the precursor will enter the resin film.
支持体としては、前駆体が着生しやす(、かつ長期間(
海)水中に侵潰しても溶解、劣化しない材質であれば特
に制限なしに使用できる6代表例としては、例えば合成
繊維(ポリエチレン系、ポリエステル系、レーヨン、ア
セテート、ポリビニルアルコール系、ポリアクリル系、
ポリアクリロニトリル系等)、天然繊維(ヒツジ、ウマ
、ウサギ、キツネ、ラクダ、絹、綿花、マニラ麻、ザイ
ル麻、ラミー、パームトウイン(ジュロ)等)からなる
綿状、糸状、布状、ローブ状、網状等の形状のものが使
用できる。また、上記以外にも例えばポリウレタン、ポ
リスチレン、ポリ塩化ビニル、ポリエチレン等の発泡体
が使用できる。これらのものは、通常−辺の長さ又は直
径が1mm〜2.0cm程度のものを使用することが好
ましし)。As a support, precursors can easily adhere to it (and can be used for a long period of time).
6 Typical examples include synthetic fibers (polyethylene, polyester, rayon, acetate, polyvinyl alcohol, polyacrylic,
cotton-like, thread-like, cloth-like, robe-like, A net-like shape or the like can be used. In addition to the above, foams such as polyurethane, polystyrene, polyvinyl chloride, and polyethylene can be used. It is preferable to use these materials with a side length or diameter of about 1 mm to 2.0 cm).
前駆支持体に塗布する水性高分子液は前駆支持5kg/
m″程度で充分と思われる。The aqueous polymer solution applied to the precursor support is 5 kg/precursor support.
It seems that about m'' is sufficient.
本発明■において、支持体を用いると、簡単かつ強固に
基材に前駆体を固定化することができ・ること、前駆体
を着生させる面積が広くなるので基材の単位面積当りの
藻類の収穫量が多くなり生産能率が上昇する。更に前駆
支持体を水性高分子液で被覆させると前駆体が乾燥して
枯死したり、また前駆体が(海)水中で支持体から剥離
したりする恐れは全(ない。In the present invention (2), by using a support, the precursor can be easily and firmly immobilized on the base material, and since the area on which the precursor is attached is widened, the amount of algae per unit area of the base material can be increased. The yield will increase and production efficiency will increase. Furthermore, when the precursor support is coated with an aqueous polymer solution, there is no possibility that the precursor will dry out and die, or that the precursor will peel off from the support in (sea) water.
本発明■の方法は、基材に、養藻用塗膜を形成させたの
ち、前駆体を付着させ、次に水性高分子液を塗装し、硬
化もしくは未硬化の塗膜を形成することにより実施でき
る。養藻用塗膜を形成させる塗料としては、従来から公
知の養藻用塗料が使用できる。該養藻用塗料としては、
例えばチッ素含有物質、リン含有物質、アルカリ金属含
有物質、アルカリ土類金属含有物質を含有する塗料(特
開昭59−78633号公報、特開昭61−88829
号公報等)が使用できる。Method (2) of the present invention involves forming a coating film for algae cultivation on a substrate, adhering a precursor, and then coating an aqueous polymer solution to form a cured or uncured coating film. Can be implemented. As the paint for forming the algae cultivation coating, conventionally known algae cultivation paints can be used. As the algae-cultivating paint,
For example, paints containing nitrogen-containing substances, phosphorus-containing substances, alkali metal-containing substances, and alkaline earth metal-containing substances (JP-A-59-78633, JP-A-61-88829)
Publications, etc.) can be used.
養藻用塗膜に前駆体を付着させるには、養藻用塗料が粘
着性を有している間に前駆体を散布させるか、もしくは
前記特開昭59−78633号公報及び特開昭61−8
8829号公報等に2載される凹凸を有する塗膜に前駆
体を散布させることにより実施できる。In order to attach the precursor to the algae-cultivating coating, the precursor may be sprayed while the algae-cultivating coating is sticky, or the precursor may be applied as described in JP-A-59-78633 and JP-A-61. -8
This can be carried out by dispersing a precursor onto a coating film having irregularities as described in Japanese Patent No. 8829 and the like.
本発明■において、養藻用塗膜を用いると、栄養分の少
ない貧栄養海域で特に有効である。更に、養藻用塗膜上
に付着した前駆体を水性高分子液で被覆させると前駆体
が乾燥して枯死したり、また前駆体が(海)水中で養藻
用塗膜から剥離したりする恐れがない。In the present invention (2), the use of a coating film for algae cultivation is particularly effective in oligotrophic sea areas with few nutrients. Furthermore, if the precursor attached to the algae culture coating is coated with an aqueous polymer solution, the precursor may dry and die, or the precursor may peel off from the algae culture coating in (sea) water. There is no fear of it happening.
本発明■の方法は、基材に、養藻用塗膜を形成させ、次
いで該塗膜上に前駆体と支持体で構成される前駆支持体
を設けたのち、水性高分子液を塗装し硬化もしくは未硬
化の塗膜を形成させることにより実施できる。基材に養
藻用塗膜を形成させる方法としては、前記養藻用塗膜の
形成方法と同種の塗料及び方法で形成することができる
。該養藻用塗膜上に前駆支持体を設ける方法としては、
例えば基材にR’FA用塗料を塗布したのち、支持体を
散布し養藻用塗膜と結合させ、次に該支持体に前駆体を
付着させる方法もしくは予め前駆体を支持体に付着させ
た前駆支持体を養藻用塗膜上に結合させることにより実
施できる。支持体の種類及び大きさ並びに水性高分子液
の塗布量は、前記発明■に記載される同様のもの及び方
法が使用できる。In the method of the present invention (2), a coating film for algae cultivation is formed on a substrate, a precursor support composed of a precursor and a support is provided on the coating film, and then an aqueous polymer solution is applied. This can be carried out by forming a cured or uncured coating film. The algae-cultivating coating film can be formed on the substrate using the same type of paint and method as the method for forming the algae-cultivating coating described above. The method of providing a precursor support on the algae cultivation coating is as follows:
For example, after applying the R'FA paint to the base material, the support is sprayed and bonded to the algae cultivation coating, and then the precursor is attached to the support, or the precursor is attached to the support in advance. This can be carried out by bonding a precursor support on a coating film for algae cultivation. Regarding the type and size of the support and the amount of the aqueous polymer solution applied, the same ones and methods as described in the above-mentioned Invention (2) can be used.
本発明■において、本発明■記載の特徴以外に、本発明
■に養藻用塗膜を用いることにより貧栄養海域において
も前駆体を生殖、生育させることが可能となる。In the present invention (2), in addition to the features described in the present invention (2), by using the coating film for algae cultivation in the present invention (2), it becomes possible to reproduce and grow the precursor even in oligotrophic sea areas.
(作用及び発明の効果)
本発明方法は、特に前駆体に水性高分子液を塗布すると
、前駆体表面が湿潤保水されるため前駆体を(海)水中
に浸漬するまでの間に前駆体が乾燥して枯死する恐れは
全くないこと、水性高分子被膜が基材(支持体)及び前
駆体との付着性に優れることから長期間の(海)水浸漬
においても基材(支持体)から前駆体が剥離することが
全くないこと等の顕著な効果を奏するものである。(Function and Effects of the Invention) In the method of the present invention, in particular, when the aqueous polymer liquid is applied to the precursor, the surface of the precursor is kept moist and water-retained. There is no risk of it drying out and dying, and the water-based polymer film has excellent adhesion to the substrate (support) and precursors, so even when immersed in (sea) water for a long period of time, it will not stick to the substrate (support). This has remarkable effects such as no peeling of the precursor.
(実施例) 以下実施例を掲げて本発明方法を更に詳しく説明する。(Example) The method of the present invention will be explained in more detail below with reference to Examples.
実施例1
タレモナロープ(商品名、クラレ株式会社、ポリビニー
ルアルコール系繊維゛φ1cm長さ30cm” )にワ
カメ配偶体(前駆体)の水分tlIiifflを塗布し
た後、固形分5重量%アルギン酸ナトリウム水溶液を9
4g塗布した。Example 1 After applying water tlIiiffl of wakame gametophyte (precursor) to Taremona Rope (trade name, Kuraray Co., Ltd., polyvinyl alcohol fiber (φ1 cm, length 30 cm)), 9% of sodium alginate aqueous solution with a solid content of 5% by weight was applied.
4g was applied.
実施例2
前記実施例1で得た被塗物・・lを固形分2重量%塩化
カルシウム水溶液に浸漬塗装した。Example 2 The object to be coated obtained in Example 1 was coated by dipping in a calcium chloride aqueous solution having a solid content of 2% by weight.
実施例3
コンクリートブロック(幅2cmX縦10cmX横20
cm、以下、同様の意味を示す、)の上面にビニライト
VAGH(商品名、ユニオンカーバイト社製、ビニル系
樹脂)をキシレン溶剤に溶解した20重量%溶液を固形
分700g/ゴの塗布量で、ハケ塗りし、未乾燥の間に
クレモナローブ細片を250g/lrI″の量を表面に
散布し、乾燥させて、付着する。これに、ワカメの配偶
体(前駆体)の水分散液を塗布した後、固形分5重量%
アルギン酸ソーダー水溶液を2.5kg/ln”塗布し
た。Example 3 Concrete block (width 2cm x length 10cm x width 20cm)
cm (hereinafter the same meaning)) was coated with a 20% by weight solution of Vinylite VAGH (trade name, manufactured by Union Carbide Co., Ltd., vinyl resin) dissolved in xylene solvent at a coating amount of 700 g/kg solid content. , apply with a brush, and while it is still wet, sprinkle 250g/lrI'' of cremona lobe pieces on the surface, dry and adhere to it.Add an aqueous dispersion of wakame gametophyte (precursor) to the surface. After application, solids content 5% by weight
A sodium alginate aqueous solution was applied at 2.5 kg/ln.
実施例4
前記実施例3で得た塗装物表面を固形分2重1%塩化カ
ルシウム水溶液に浸漬塗装した。Example 4 The surface of the coated object obtained in Example 3 was dip-coated in a 1% solids calcium chloride aqueous solution.
実施例5
実施例3において、アルギン酸ソーダ水溶液に代えてア
ラソーブ100(商品名、荒用化学社製、高吸水性樹脂
)を海水に浸した固形分3重皿%吸水樹脂液を3kg/
m”塗布した以外は実施例3と同様にして行ない実施例
5のものを得た。Example 5 In Example 3, instead of the sodium alginate aqueous solution, 3 kg/3 kg of a water absorbing resin solution with a solid content of triple plate % of Arasorb 100 (trade name, manufactured by Arayo Kagaku Co., Ltd., super absorbent resin) soaked in seawater was used.
Example 5 was obtained in the same manner as in Example 3, except that the coating was applied with m''.
実施例6
実施例3において、アルギン酸ソータ水溶液を用いて塗
゛装する代わりにアラソープ100を海水に浸した固形
分4重量%吸水樹脂液及び5重量%アルギン酸ソーダ水
溶液を重量比1:1に混合した溶液を塗装し、更に2重
量%塩化カルシウム水溶液を3 kg/ m”塗装量で
塗装した以外は実施例3と同様にして行ない実施例6の
ものを得た。Example 6 In Example 3, instead of coating using the alginate sorter aqueous solution, Arasop 100 was soaked in seawater and a 4% solid content water-absorbing resin solution and a 5% by weight sodium alginate aqueous solution were mixed at a weight ratio of 1:1. Example 6 was obtained in the same manner as in Example 3, except that a 2% by weight calcium chloride aqueous solution was applied at a coating amount of 3 kg/m''.
実施例7
実施例3においてビニライトVAGHに代えて、養藻用
塗料用を300g/rri″塗布量を塗装した以外は、
実施例3と同様にして行ない実施例7のものを得た。Example 7 In Example 3, except that a coating for algae cultivation was applied at a coating amount of 300 g/rri'' instead of Vinylite VAGH.
Example 7 was obtained in the same manner as in Example 3.
(*)養藻用塗料
CR−20(商品名、加電化工業(株)、塩化ゴム系)
8.0g、ロジン8.0gをキシレン34.0gに溶解
し、更にこのものに骨粉10、Og、過リン酸石灰20
.0g、グリシン5、Ogを分#I混合した。(*) Algae cultivation paint CR-20 (product name, Kadenka Kogyo Co., Ltd., chlorinated rubber type)
Dissolve 8.0g of rosin and 8.0g of rosin in 34.0g of xylene, and add 10g of bone powder, Og, and 20g of superphosphate lime to this.
.. 0g, glycine 5, Og were mixed for min #I.
実施例8
実施例3においてビニライトVAGHに代えて、養藻°
用塗料国を同量塗装した以外は実施例3と同様にして行
ない実施例8のものを得た。Example 8 In Example 3, instead of vinylite VAGH, algae cultivation °
Example 8 was obtained in the same manner as in Example 3, except that the same amount of paint was applied.
比較例1
コンクリートブロックに20重量%ビニライトVAGH
溶液を700 g/ばでへケ塗りし常温で7日間乾燥さ
せ比較例1のものを得た。Comparative Example 1 20% by weight Vinylite VAGH on concrete block
The solution was applied at a rate of 700 g/bath and dried for 7 days at room temperature to obtain Comparative Example 1.
比較例2
コンクリートブロックに20重量%ビニライトVAGH
溶液を700g/m”でへケ塗りし、次いでクレモナー
ブ細片を250g/m″の量で散布し、乾燥を行ないワ
カメ配偶体の水分散液を塗布し比較例2のものを得た。Comparative example 2 20% by weight vinylite VAGH on concrete block
Comparative Example 2 was obtained by applying the solution at 700 g/m'', then scattering Cremonave strips at 250 g/m'', drying and coating with an aqueous dispersion of wakame gametophyte.
比較例3
実施例1と同様のクレモナローブにワカメ配偶体の水分
散液を塗布し、比較例3のものを得た。Comparative Example 3 An aqueous dispersion of wakame gametophyte was applied to the same Cremona lobe as in Example 1 to obtain Comparative Example 3.
比較例4
実施例3において、アルギン酸ソータ水溶液を用いない
以外は実施例3と同様にして比較例4のものを得た。Comparative Example 4 Comparative Example 4 was obtained in the same manner as in Example 3 except that the alginate sorter aqueous solution was not used.
結果をまとめて表−1に示す。The results are summarized in Table-1.
試験条件
室内浸漬試験
実施例及び比較例で得られたものを常温で一時間放置し
た後、海水槽に浸漬し、前駆体の生育を行なった。(海
水は静岡県賀茂郡東伊豆町沖で採水し、80°Cで一時
間滅菌したものを使用した。Test conditions Indoor immersion test The samples obtained in Examples and Comparative Examples were left at room temperature for one hour and then immersed in a seawater tank to grow the precursors. (The seawater used was collected off the coast of Higashiizu-cho, Kamo-gun, Shizuoka Prefecture, and sterilized at 80°C for one hour.
ワカメの生育状態を目視で観察した。評価は0:生育が
著しく良好、○:生育が良好、△:生育が若干認められ
る程度、×:生育が認められない、に基づいて行なった
。)
実海浸漬試験
実施例及び比較例で得られたものを常温で1時間放置し
た後、上記静岡県賀茂郡東伊豆町沖で昭和62年11月
から昭和63年3月まで浸漬した。(評価はO:コンク
リート表面90%以上ワカメ葉体が生育する、O:コン
クリート表面30〜89%ワカメ葉体が生育する、Δ:
コンクリート表面に5〜29%ワカメ葉体が生育する、
×:コンクリート表面に49%以下ワカメ葉体が生育も
しくは全く生育せず、に基づいて行なった。)平成
元年
月
/3
日
1、事件の表示
昭和63年
特許願
第236892号
2、発明の名称
藻類の増殖方法
3、補正をする者
事件との関係The growth status of wakame seaweed was visually observed. Evaluation was made on the basis of 0: growth is extremely good, ○: growth is good, Δ: growth is slightly observed, ×: no growth is observed. ) Actual sea immersion test The samples obtained in Examples and Comparative Examples were left at room temperature for 1 hour, and then immersed off the coast of Higashiizu-cho, Kamo-gun, Shizuoka Prefecture from November 1988 to March 1988. (Evaluation: O: Wakame leaves grow on more than 90% of the concrete surface, O: Wakame leaves grow on 30-89% of the concrete surface, Δ:
5-29% of wakame leaves grow on the concrete surface.
×: Wakame leaves grew on the concrete surface by 49% or less, or did not grow at all. ) Date 1989/3/1989 1. Indication of the case 1988 Patent Application No. 236892 2. Name of the invention Method for propagating algae 3. Person making the amendment Relationship with the case
Claims (4)
る前駆体を付着させたのち、水性高分子液を塗装し、硬
化もしくは未硬化塗膜を形成させることを特徴とする藻
類の増殖方法。(1) Propagation of algae characterized by attaching a precursor that can become an algal leaf through reproduction and growth to a substrate, and then coating with an aqueous polymer solution to form a cured or uncured coating film. Method.
る前駆体と支持体で構成される前駆支持体を設けたのち
、水性高分子液を塗装し、硬化もしくは未硬化塗膜を形
成させることを特徴とする藻類の増殖方法。(2) After providing a precursor support consisting of a support and a precursor that can become an algal leaf through reproduction and growth on the base material, an aqueous polymer liquid is applied to form a cured or uncured coating film. A method for growing algae, characterized by:
形成させたのち、該塗膜上に、生殖、生育によって藻類
の葉体となりうる前駆体を付着させ、次に水性高分子液
を塗装し、硬化もしくは未硬化塗膜を形成させることを
特徴とする藻類の増殖方法。(3) After forming an algae-cultivating coating film containing nutritional components of algae on the substrate, a precursor that can become an algae leaf through reproduction and growth is attached onto the coating film, and then an aqueous A method for growing algae, characterized by coating a polymer liquid and forming a cured or uncured coating film.
形成させたのち、該塗膜上に生殖、生育によって藻類の
葉体となりうる前駆体を支持体で構成される前駆支持体
を設け、次に水性高分子液を塗装し、硬化もしくは未硬
化塗膜を形成させることを特徴とする藻類の増殖方法。(4) After forming an algae-cultivating coating film containing nutritional components of algae on a substrate, a precursor composed of a support material is deposited on the coating film, which can become an algae leaf through reproduction and growth. A method for growing algae, which comprises providing a support and then coating an aqueous polymer solution to form a cured or uncured coating film.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63236892A JPH0286717A (en) | 1988-09-21 | 1988-09-21 | Method for proliferating algae |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63236892A JPH0286717A (en) | 1988-09-21 | 1988-09-21 | Method for proliferating algae |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0286717A true JPH0286717A (en) | 1990-03-27 |
Family
ID=17007315
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63236892A Pending JPH0286717A (en) | 1988-09-21 | 1988-09-21 | Method for proliferating algae |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0286717A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2014003930A (en) * | 2012-06-22 | 2014-01-16 | Hokkaido Univ | Structure for growing seaweed and method for producing the same |
-
1988
- 1988-09-21 JP JP63236892A patent/JPH0286717A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2014003930A (en) * | 2012-06-22 | 2014-01-16 | Hokkaido Univ | Structure for growing seaweed and method for producing the same |
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