MXPA96003861A - Arbo protection - Google Patents
Arbo protectionInfo
- Publication number
- MXPA96003861A MXPA96003861A MXPA/A/1996/003861A MX9603861A MXPA96003861A MX PA96003861 A MXPA96003861 A MX PA96003861A MX 9603861 A MX9603861 A MX 9603861A MX PA96003861 A MXPA96003861 A MX PA96003861A
- Authority
- MX
- Mexico
- Prior art keywords
- pesticide
- alkyl
- tree
- haloalkyl
- cut
- Prior art date
Links
- 238000000034 method Methods 0.000 claims abstract description 30
- 241000607479 Yersinia pestis Species 0.000 claims abstract description 9
- 230000001066 destructive effect Effects 0.000 claims abstract description 7
- 239000000575 pesticide Substances 0.000 claims description 39
- 125000000217 alkyl group Chemical group 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 14
- 238000009472 formulation Methods 0.000 claims description 13
- 235000013399 edible fruits Nutrition 0.000 claims description 11
- 125000001188 haloalkyl group Chemical group 0.000 claims description 10
- 241000234295 Musa Species 0.000 claims description 9
- 125000005843 halogen group Chemical group 0.000 claims description 9
- 239000002917 insecticide Substances 0.000 claims description 9
- DIPLXSBTYRDLGV-UHFFFAOYSA-N 2-methyl-2-methylsulfanylpropanal Chemical compound CSC(C)(C)C=O DIPLXSBTYRDLGV-UHFFFAOYSA-N 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 239000005645 nematicide Substances 0.000 claims description 8
- 240000008790 Musa x paradisiaca Species 0.000 claims description 7
- 235000018290 Musa x paradisiaca Nutrition 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical group NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 230000008030 elimination Effects 0.000 claims description 3
- 238000003379 elimination reaction Methods 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
- KZAUOCCYDRDERY-UHFFFAOYSA-N oxamyl Chemical compound CNC(=O)ON=C(SC)C(=O)N(C)C KZAUOCCYDRDERY-UHFFFAOYSA-N 0.000 claims description 3
- WCXDHFDTOYPNIE-RIYZIHGNSA-N (E)-acetamiprid Chemical compound N#C/N=C(\C)N(C)CC1=CC=C(Cl)N=C1 WCXDHFDTOYPNIE-RIYZIHGNSA-N 0.000 claims description 2
- 239000005875 Acetamiprid Substances 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 240000000907 Musa textilis Species 0.000 claims description 2
- 239000005950 Oxamyl Substances 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- KXRPCFINVWWFHQ-UHFFFAOYSA-N cadusafos Chemical compound CCC(C)SP(=O)(OCC)SC(C)CC KXRPCFINVWWFHQ-UHFFFAOYSA-N 0.000 claims description 2
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 2
- 125000001072 heteroaryl group Chemical group 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 claims 2
- ZOPGSELPSVHSIY-UHFFFAOYSA-N CNC(O)=O.CC1(OC2=C(C1)C=CC=C2)C Chemical compound CNC(O)=O.CC1(OC2=C(C1)C=CC=C2)C ZOPGSELPSVHSIY-UHFFFAOYSA-N 0.000 claims 1
- 239000005906 Imidacloprid Substances 0.000 claims 1
- VSHURSPEQITHNX-UHFFFAOYSA-N [5-[4-(dimethylamino)piperidin-1-yl]-1h-imidazo[4,5-b]pyridin-2-yl]-(2-isoquinolin-4-ylpyridin-4-yl)methanone Chemical compound C1CC(N(C)C)CCN1C1=CC=C(N=C(N2)C(=O)C=3C=C(N=CC=3)C=3C4=CC=CC=C4C=NC=3)C2=N1 VSHURSPEQITHNX-UHFFFAOYSA-N 0.000 claims 1
- WCXDHFDTOYPNIE-UHFFFAOYSA-N acetamiprid Chemical compound N#CN=C(C)N(C)CC1=CC=C(Cl)N=C1 WCXDHFDTOYPNIE-UHFFFAOYSA-N 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- NAGJZTKCGNOGPW-UHFFFAOYSA-K dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [O-]P([O-])([S-])=S NAGJZTKCGNOGPW-UHFFFAOYSA-K 0.000 claims 1
- 229940056881 imidacloprid Drugs 0.000 claims 1
- 239000012669 liquid formulation Substances 0.000 claims 1
- 241000013557 Plantaginaceae Species 0.000 abstract description 4
- 241000234615 Musaceae Species 0.000 abstract description 3
- 241000196324 Embryophyta Species 0.000 description 20
- 238000003306 harvesting Methods 0.000 description 7
- 235000021015 bananas Nutrition 0.000 description 6
- 241000244206 Nematoda Species 0.000 description 4
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 235000003805 Musa ABB Group Nutrition 0.000 description 3
- 235000015266 Plantago major Nutrition 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 description 2
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 description 2
- 241000254171 Curculionidae Species 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 description 2
- UYVQYZKGUSYZOP-UHFFFAOYSA-N ethoxy-hydroxy-sulfanyl-sulfanylidene-$l^{5}-phosphane Chemical compound CCOP(O)(S)=S UYVQYZKGUSYZOP-UHFFFAOYSA-N 0.000 description 2
- 239000000417 fungicide Substances 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
- 238000003780 insertion Methods 0.000 description 2
- 230000037431 insertion Effects 0.000 description 2
- -1 nitromethylenes Chemical class 0.000 description 2
- 239000005648 plant growth regulator Substances 0.000 description 2
- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 1
- ZOCSXAVNDGMNBV-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound NC1=C(S(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZOCSXAVNDGMNBV-UHFFFAOYSA-N 0.000 description 1
- 244000099147 Ananas comosus Species 0.000 description 1
- 235000007119 Ananas comosus Nutrition 0.000 description 1
- 101100247611 Arabidopsis thaliana RCF3 gene Proteins 0.000 description 1
- 239000005741 Bromuconazole Substances 0.000 description 1
- 241001212534 Cosmopolites sordidus Species 0.000 description 1
- 239000005976 Ethephon Substances 0.000 description 1
- 239000005980 Gibberellic acid Substances 0.000 description 1
- 229930191978 Gibberellin Natural products 0.000 description 1
- 241001445511 Helicotylenchus multicinctus Species 0.000 description 1
- 241000243783 Heteroderidae Species 0.000 description 1
- 241000243786 Meloidogyne incognita Species 0.000 description 1
- 241000201375 Radopholus similis Species 0.000 description 1
- 241001132771 Rotylenchus buxophilus Species 0.000 description 1
- 241000189579 Thripidae Species 0.000 description 1
- 230000007059 acute toxicity Effects 0.000 description 1
- 231100000403 acute toxicity Toxicity 0.000 description 1
- 230000009418 agronomic effect Effects 0.000 description 1
- QGLZXHRNAYXIBU-UHFFFAOYSA-N aldicarb Chemical compound CNC(=O)ON=CC(C)(C)SC QGLZXHRNAYXIBU-UHFFFAOYSA-N 0.000 description 1
- QGLZXHRNAYXIBU-WEVVVXLNSA-N aldicarb Chemical compound CNC(=O)O\N=C\C(C)(C)SC QGLZXHRNAYXIBU-WEVVVXLNSA-N 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 description 1
- MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- HJJVPARKXDDIQD-UHFFFAOYSA-N bromuconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCC(Br)C1 HJJVPARKXDDIQD-UHFFFAOYSA-N 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000002894 chemical waste Substances 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 235000012055 fruits and vegetables Nutrition 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000003448 gibberellin Substances 0.000 description 1
- IXORZMNAPKEEDV-OBDJNFEBSA-N gibberellin A3 Chemical compound C([C@@]1(O)C(=C)C[C@@]2(C1)[C@H]1C(O)=O)C[C@H]2[C@]2(C=C[C@@H]3O)[C@H]1[C@]3(C)C(=O)O2 IXORZMNAPKEEDV-OBDJNFEBSA-N 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000001069 nematicidal effect Effects 0.000 description 1
- 239000003090 pesticide formulation Substances 0.000 description 1
- 239000000447 pesticide residue Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 230000002792 vascular Effects 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Abstract
A method to protect trees of the Musaceae or Plantaginaceae families from destructive pests, in which the trees to be protected share a common system of
Description
TREE PROTECTION DESCRIPTION OF THE INVENTION
This invention relates to a new method to protect trees of the Musaceae (banana) and Plan-tagináceas families (llantenes) from harmful or destructive pests. Global regulatory requirements on the use of pesticides are increasingly demanded, particularly in relation to unmanageable or unnecessary pesticide residues. Thus, there are mutually contradictory requirements on the part of farmers that, on the one hand, the need to totally suppress destructive pests demands that more pesticides be used, and, on the other hand, the increasing pressures of regulatory bodies demand that they be used. less pesticides. These regulatory demands aim to protect the safety and health of agricultural workers and the general public. It is also known that the general public would like less chemical waste in fruits and vegetables. A particular consequence of this situation is that there is a growing need to have more effective methods of protecting bananas and plantains. It is known that said fruit trees attract a large number of pests, particularly insects and destructive nematodes. A common technique for growing bananas or plantains is to let them grow in large blocks or plantations. The trees are arranged as mother plants that have a series (for example 1 to 5, generally 1 to 3) of shoots or shoots, that is to say daughters plants, that leave the bulb (it is de-cir, of the base of the pseudo-trunk ) of the mother plant. Therefore, mothers and daughters share a common root system. At an appropriate time before harvesting the fruit of the mother plants or trees, all the daughter plants are cut except one for the mother plant, with the agri-farmer deciding which one has the best chance of survival. This practice allows the REF to be easily produced: 23096 next generation of banana or plantain plants. The elimination of the daughter plants after the harvest of the mother plants is possible, but it is preferable to do it before for agronomic reasons. The fruits of the bananas are harvested by cutting the bunches of fruits. Next, the mother trees are cut to eliminate the cups. The remaining pseudo-logs generally have a height range of 0.5 meters to 2.5 meters. This practice facilitates the growth of daughter plants. The pseudo-stem stock is then left until it withers or is cut in stages until only one pseudo-stem child remains. Accordingly, there is a need to provide an improved method for protecting pineapple bananas and plantains, which is effective against destructive pests, especially insects and nematodes and in which the interval from treatment of said trees by a pesticide to the harvest is as long as possible and in which the worker's exposure is at a minimum level. It has now been found that these needs can be met in whole or in part by means of the present invention. According to the invention, a pesticide is found which is more advantageously applied to the pseudo-stem of the cut mother tree to protect the son tree. In another embodiment, after the initial removal of the crown from the parent tree, the daughter plants can be allowed to develop and the size of the pseudo-parent stem gradually reduced by subsequent cuts. During this time a pesticide can be applied to the pseudo-stem stock at any point, including when the pseudo-stem stock has been effectively removed. However, it is more advantageous to apply the pesticide in the first part of the development of the daughter plant to maximize the treatment-harvest time interval. The present invention relates to a method for protecting two or more trees of the Musaceae or Plan-taigaceae families from destructive pests, in which the trees to be protected share a common system of roots, said method comprising: (a) cutting one of the trees that share said root system to collect its fruit, and (b) subsequently introducing a pesticide into said cut tree. The pesticide can be introduced into any portion of said cut tree. According to one aspect of the invention, the pesticide is introduced into the cut of the tree. According to another aspect of the invention, the tree is cut to eliminate its crown after the separation of the fruit and before the introduction of the pesticide. The pesticide, in a preferred aspect of the invention, is then introduced into the cut of the tree formed by the elimination of the cup. The pesticide is generally an insecticide, nematocide, fungicide or plant growth regulator, preferably an insecticide or nematicide. The pesticide is preferably transportable and more preferably soluble in water at room temperature, the solubility in water being generally greater than 0.5 g / 1, preferably greater than 2 g / 1 at room temperature. The pesticide may be provided in a formulation that is generally transportable and more preferably soluble in water at room temperature. Banana or plantain species that are preferably protected according to the present invention are Musa textilis, Musa sapientum or Musa paradisica. The pesticide is generally introduced into the tree from zero to about thirty days after one of the trees is cut, preferably from about one to about seven days and even more preferably from about two to about three days. A preferred group of insecticides or nematicides according to the invention are carbamates. Carbamates are a well-known group of pesticides: those skilled in the art will recognize them in The Pesticide Manual 10th Edition, edited by C. Tomlin, British Crop Protection Council, United Kingdom, 1994. A preferred group of carbamates are N-methyl. -carbamates, which are the substances that possess the substituent -OC (0) NHMe. A particularly preferred carbamate that can be used according to the present invention is 2-methyl-2- (methylthio) -propionaldehyde (aldicarb) O-methylcarba-moyloxime. Other carbamates which can be used according to the invention are 2,3-dihydro-2,2-dimethylbenzo-furan-7-yl methylcarbamate (carbofuran) and N, N-dimethyl-2-methylcarbamoyloxy-mino-2- (methylthio) acetamide (oxamyl). A carbamate can be used alone or in combination with other pesticides. Other insecticides or nematicides that can be used according to the present invention alone or in combination with other pesticides include: nitromethylenes or nitroimines, including l- (6-chloro-3-pyridylmethyl) -N-nitroimidazolidin-2-ylidenamine (imino) dacloprid); cyanoimines, including (E) -N1 - [(6-chloro-3-pyridyl) methyl] -N2-cyano-N; L-methylacetamidine (acetamiprid); and organophosphates, including O-ethyl phosphorodithioate and S, S-di-sec-butyl (cadusafos); (RS) -2-oxo-l, 3-thiazolidin-3-ylphosphonothioate of O-ethyl and S-sec-butyl (fostiazate); and S, S-dipropyl and O-ethyl phosphorodithioate (ethopro-fos). Other insecticides or nematicides that can be used according to the present invention alone or in combination with other pesticides include the compounds of formula (I):
(I) wherein: Rx is -CN or methyl; R2 is -S (0) nR3; R3 is alkyl or haloalkyl; R4 represents a hydrogen or halogen atom or a member of a group consisting of -NR5R6, -S (0) mR7, -C (0) 0-R7, alkyl, haloalkyl, -0Rβ and -N = C (R « ,) (R10) > Rs and R "independently represent the hydrogen atom or an alkyl, haloalkyl, -C (0) alkyl, alkoxycarbonyl or -S (0)? RCF3 radical; or Rs and R6 may together form a divalent alkylene radical which may be interrupted by one or two divalent heteroatoms, such as oxygen or sulfur; R- represents an alkyl or haloalkyl radical; Ra represents an alkyl or haloalkyl radical or a hydrogen atom; R9 represents an alkyl radical or a hydrogen atom; R10 represents a phenyl or heteroaryl group which is unsubstituted or substituted by one or more halogen atoms or a member of the group consisting of -OH, -O-alkyl, -S-alkyl, cyano and alkyl; X represents a trivalent nitrogen atom or a radical -C-R12, the other three valences of the carbon atom forming part of the aromatic ring; R? And Ri2 represent, independently of each other, a hydrogen or halogen atom; R., 3 represents a halogen atom or a haloalkyl, haloalkoxy, -SÍO ^ CFa or SFS group; m, n, q and r represent, independently of one another, an integer equal to 0, 1 or 2; with the proviso that, when Rx is methyl, R3 is haloalkyl, R4 is -NH2, RX1 is -Cl, R13 is CF3 and X is N. The term "alkyl" is understood to mean carbon chains of one to six atoms. of carbon that have linear or branched chains. By the term "alkylene divalen-te" is meant a carbon chain which is attached at two points to the nitrogen atom of the radical R4. A preferred group of compound of formula (I) is that wherein: Rx is CN; R3 is a haloalkyl radical; R? It's NH2:
RX1 and R12 represent, independently of one another, a halogen atom; and R13 is a haloalkyl radical. A more preferred compound of formula (I) is 5-amino-1- (2,6-dichloro-4-trifluoromethyl-phenyl) -4-trifluoromethylsulfinyl-3-cyanopyrazole. The compounds of formula (I) can be prepared according to known procedures, for example as described in International Patent Publication Nos. WO 87/3781, 93/6089 and 94/21606 as well as in European Patent Applications 295117, 403300 , 385809 or 679650, German Patent Publication 19511269 and United States Patents 5232940 and 5236938 or other process according to the knowledge of those skilled in the art of chemical synthesis. Pests that can be repressed according to the present invention include Cosmopolites sordidus (banana weevil), Radopholus similis (excavator nematode), Heli-cotylenchus multicinctus (spiral nematode), Meloidogyne incognita (nematode root knot) and pests of the families Heteroderidae and Thripidae. Fungicides that can be used according to the present invention include: methyl l- (butylcarbamoyl) benzimidazol-2-ylcarbamate (benomyl); triazoles, which include (±) -l- [2- (2, 4-dichlorophenyl) -4-propyl-l, 3-dioxolan-2-ylmethyl] -lH-l, 2,4-triazole (propicone-zol); and 1- [(2RS, 4RS; 2RS, 4SR) -4-bromo-2- (2,4-dichlorophenyl) tetrahydrofurfuryl] -1H-1,2,4-triazole (bromuconazole). Plant growth regulators that may be employed in accordance with the present invention include: a gibberellin, such as gibberellic acid or 2-chloroethylphosphonic acid (ethephon). The amount of pesticide used is an agronomically acceptable and effective amount per tree. In the case of 2-methyl-2- (methylthio) propional-dehyde O-methylcarbamoyloxime, amounts of 0.01 to 5 g per tree, preferably 0.3 to 0.9 g per tree may be appropriate. The introduction of the pesticide into the pseudo-trunk of the tree is carried out by inserting a composition, which can be of liquid or solid formulation, preferably solid, in order to reduce worker exposure, especially with compound that have relatively very acute toxicity. A solid formulation for 2-methyl-2- (methylthio) propionaldehyde O-methylcarbamoyloxime is preferred. The formulations are chosen to accelerate the transmission of the active ingredient in an aqueous phase, such as vascular tissue normally present in plants or trees. Formulations are also chosen to minimize the exposure of agricultural workers to the pesticide. Even more preferred are substantially pulverulent formulations, for example those whose particle size is greater than 0.1 mm, preferably 0.4 to 0.8 mm. Acceptable formulations can be prepared by mixing the active ingredient with a polymer, especially a water soluble polymer. Gels can also be used. The introduction of the pesticide into the pseudo-stem of the parent tree can be carried out by suitable means. One possibility is the injection of the pesticide into the pseudo-trunk. Another possibility is to make or drill holes in the tree and put in them the formulation and then plug or seal the holes. The holes can be made in the lateral part of the pseudo-trunk, but it is preferred to perform the insertion where the pseudo-trunk was cut to eliminate the cup. Another method of introducing the pesticide is to separate a wedge from the pseudo-stem, add the pesticide formulation and replace the wedge in the space where it was. An especially preferred embodiment of this insert is to separate the wedge from the cut surface made to remove the cup. Another embodiment is the insertion into the pseudo-stem of a water soluble capsule containing a dose of the desired pesticide. The following non-limiting example is given to illustrate the invention.
EXAMPLE Bananas grow in plantation. The trees are arranged as mother plants that have a series (1 to 5) of daughter plants growing from the bulb. Just before harvesting the mother plants, the daughter plants are cut except one daughter plant per mother plant. The fruit of the bananas is collected by cutting the bunches of fruits. After a week of this harvest, the pseudo-trunks of these plants are cut to eliminate the cups. After two days a wedge is cut from the surface resulting in the removal of the cup from each pseudo-stem of each parent tree. A dose of 0.5 g per tree of O-methylcarbamoyloxime of 2-methyl-2- (methylthio) -propionaldehyde is placed in the form of a granular formulation at 15% w / w in the empty concave space from which it is separated. wedge and the wedges are replaced. The daughters plants are protected against nema-all as well as weevils until the time of the harvest of the daughter trees that occurs 35 weeks later, thus providing an economically acceptable fruit. The risk of worker exposure is greatly reduced.
It is noted that in relation to this date, the best method known to the applicant to carry out the aforementioned invention, is that which is clear from the present description of the invention. Having described the invention as above, property is claimed as contained in the following:
Claims (15)
1. - A method to protect two or more trees of the Musaceous or Plantaginaceous families of destructive pests, in which the trees to be protected share a common system of roots, characterized because it involves: (a) cutting one of the trees that they share said root system to collect their fruit, and (b) then introduce a pesticide into said cut tree.
2. A method according to claim 1, characterized in that the cut tree is cut to remove its crown after the removal of the fruit and before the introduction of the pesticide.
3. A method according to claim 1 or claim 2, characterized in that the pesticide is introduced in the cut of the tree.
4. - A method according to any one of the preceding claims, characterized in that the pesticide is introduced in the cut of the tree formed by the elimination of the cup.
5. - A method according to claim 1 or claim 2, characterized in that the pesticide is introduced in the lateral portion of the tree.
6. A method according to any one of the preceding claims, characterized in that the pesticide is transferred from zero to approximately thirty days after the tree has been cut.
7. - A method according to any one of the preceding claims, characterized by the pesticide is an insecticide or ne aicide.
8. A method according to any one of the preceding claims / characterized in that the pesticide is transportable at room temperature.
9. A method according to any one of the preceding claims, characterized in that the pesticide is provided as a formulation that is soluble in water at room temperature.
10. A method according to any one of the preceding claims, characterized in that the trees are Musa textilis, Musa sapientum or Musa paradisica.
11. A method according to any one of the preceding claims, characterized in that the insecticide or nema ticide is carbamate, preferably an N-methyl carbamate.
12. - A method according to claim 10, characterized in that the insecticide or nematicide is O-methylcarbamoyloxy-2-methyl-2- (methylthio) propionaldehyde or methylcarbamate 2,3-dihydro-2,2-dimethylbenzofuran -7-ilo.
13. - A method according to claim 12, characterized in that the amount of O-methylcarbamoyloxime of 2-methyl-2- (methylthio) propionaldehyde used per tree is 0.01 g and 5 g per tree, preferably from 0.3 g to 0.9 g per tree.
14. A method according to any one of claims 1 to 10, characterized in that the insecticide or nematicide is: 1- (6-chloro-3-pyridylmethyl) -N-nitroimidazolidin-2-ylidenamine (imidacloprid); (E) -N1 - [(6-chloro-3-pyridyl) methyl] -N2-cyano-N1-methylacetamidine (acetamiprid); N, N-dimethyl-2-methylcarbamoyloxyimino-2- (methylthio) -acetamide (oxamyl) phosphorodithioate 0-ethyl and S, S-di-sec-butyl (cadusafos); (RS) -2-oxo-l, 3-thiazolidin-3-ylphosphonothioate 0-ethyl and S-sec-butyl (fostiazate); and S, S-dipropyl and 0-ethyl phosphorodithioate (etoprofos).
15. A method according to any one of claims 1 to 10, characterized in that the pesticide is a ccm-post of formula: (D wherein: R-L is -CN or methyl? R2 is -S (0) "R3; R3 is alkyl or haloalkyl; R4 represents a hydrogen or halogen atom or a member of a group consisting of NRSR6, S (0) mR7, C (0) 0-R7, alkyl, haloalkyl, 0RS and -N = C (R9) (R10); R5 and R6 independently represent the hydrogen atom or an alkyl, haloalkyl, C (0) alkyl, alkoxycarbonyl or S (0) 3_CF3 radical; or Rs and R6 may together form a divalent alkylene radical which may be interrupted by one or two divalent heteroatoms, such as oxygen or sulfur; R-7 represents an alkyl or haloalkyl radical; Rβ represents an alkyl or haloalkyl radical or a hydrogen atom; R9 represents an alkyl radical or a hydrogen atom; Rxo represents a phenyl or heteroaryl group which is unsubstituted or substituted by one or more halogen atoms or a member of the group consisting of OH, -O-alkyl, -S-alkyl, cyano and alkyl; X represents a trivalent nitrogen atom or a C-R12 radical / the other three valences of the carbon atom forming part of the aromatic ring; R and Ri2 represent, independently of one another, a hydrogen or halogen atom; R13 represents a halogen atom or a haloalkyl, haloalkoxy, S (0) qCF3 or SFS group; m, n, q and r represent, independently of one another, an integer equal to 0, 1 or 2; with the proviso that, when Rx is methyl, R3 is haloalkyl, R? is NH2, R12_ is Cl, R13 is CF3 and? is N. 16.- A method according to any one of claims 1 to 10, and 15, characterized in that the compound of formula (I) is 5-amino-3-cyano-1- (2,6-dichloro- 4-trif luorome-tilphenyl) -4-trif luoromethylsulfonylpyrazole. 17. A method according to any one of the preceding claims, characterized in that the pesticide used is presented as a solid or liquid formulation, preferably a solid formulation. 18. A method according to claim 17, characterized in that the formulation is substantially pulverulent. 19. A method according to claim 17 or claim 18, characterized in that the formulation has a particle size greater than 0.1 mm, preferably 0.4 to 0.8 mm.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9510575A FR2738112B1 (en) | 1995-09-05 | 1995-09-05 | METHOD FOR IMPROVING BANANA FRUIT YIELDS |
| FR9510575 | 1995-09-05 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MX9603861A MX9603861A (en) | 1997-07-31 |
| MXPA96003861A true MXPA96003861A (en) | 1997-12-01 |
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