GB2304575A - Protection of trees sharing a common root system - Google Patents

Protection of trees sharing a common root system Download PDF

Info

Publication number
GB2304575A
GB2304575A GB9618548A GB9618548A GB2304575A GB 2304575 A GB2304575 A GB 2304575A GB 9618548 A GB9618548 A GB 9618548A GB 9618548 A GB9618548 A GB 9618548A GB 2304575 A GB2304575 A GB 2304575A
Authority
GB
United Kingdom
Prior art keywords
pesticide
alkyl
tree
foregoing
trees
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
Application number
GB9618548A
Other versions
GB2304575B (en
GB9618548D0 (en
Inventor
Jorge Cepeda
Juan Bocanegra
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer CropScience SA
Original Assignee
Rhone Poulenc Agrochimie SA
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Rhone Poulenc Agrochimie SA filed Critical Rhone Poulenc Agrochimie SA
Publication of GB9618548D0 publication Critical patent/GB9618548D0/en
Publication of GB2304575A publication Critical patent/GB2304575A/en
Application granted granted Critical
Publication of GB2304575B publication Critical patent/GB2304575B/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/24Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N57/00Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/12Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals

Abstract

Trees of the families Musaceae or Plantanginaceae which share a common root system are protected from destructive pests by cutting one of the trees to remove its fruit and then reintroducing a pesticide into the cut tree.

Description

Protection of trees This invention relates to a new method of protecting trees of the families Musaceae (banana) and Plantanginaceae (plantains) from harmful or destructive pests.
Global regulatory requirements are becoming more and more demanding with respect to the use of pesticides particularly with respect to unmanaged or unnecessary pesticide residues.
Thus there exist mutually contradictory requirements of farmers in that the need to control destructive pests very thoroughly demands that more pesticides be used, while increasing pressures from regulatory agencies demand that less pesticides be used These regulatory demands are aimed to protect the safety and health of agricultural workers and the general public.
It also well known that the general public would like less chemical residues on fruits and vegetables.
A particular consequence of this situation is that there is an increasing need to have more efficient methods of protection of banana trees and plantain trees. It is well known that such fruitproducing trees attract a large number of pests, particularly destructive insects and nematodes.
A common technique for cultivating banana trees or plantain trees is by growing them on large blocks or plantations. The trees are disposed as mother plants having a series (for example 1 to 5, generally 1 to 3) of followers or peeps, that is daughter plants, growing from the corm (that is, the base of the pseudotrunk) of the mother plant. In this respect the mother and daughter plants share a common root system. At an appropriate time before the harvest of the fruit of the mother plants or trees, all the daughter plants are removed except one per mother plant which are deemed by the grower to have the best chances of survival. Such a practice allows the next generation of banana or plantain plants to be readily produced. The removal of the daughter plants is possible after the harvest of the mother plants, but it is agronomically preferred to remove them beforehand.
The fruits of the banana trees are harvested by cutting off the bunches of fruit Afterwards, the mother trees are cut to remove the canopies. The pseudotrunks which are left are generally in a height range from 0.5 meters to 2.5 meters. Such a practice facilitates the growth of the daughter plants. The mother pseudotrunk is then left to decay or is cut down in stages until only a daughter pseudotrunk remains.
Therefore there exists a need to provide an improved method of protection for daughter banana trees and plantain trees from pests which is efficient against destructive pests, especially insects and nematodes and whereby the interval from the treatment of said trees by a pesticide to harvest is as long as possible and whereby the worker exposure is at a minimal level. It has now been found that these needs may be met in whole or in part by means of the instant invention The instant invention provides a method for the protection of two or more trees of the families Musaceae or Plantanginaceae from destructive pests wherein the trees to be protected share a common root system which method comprises: (a) cutting one of the trees sharing the said root system to remove its fruit and (b) then introducing a pesticide into the said cut tree.
The pesticide may be introduced into any portion of the said cut tree. According to a feature of the invention, the pesticide is introduced into the cut surface of the tree.
According to another feature of the invention, the tree is cut to remove its canopy after the removal of its fruit and before introducing pesticide. The pesticide is, in a preferred feature of the invention, then introduced into the cut surface of the tree formed by the removal of the canopy.
According to the invention, a pesticide is advantageously applied onto or into the pseudotrunk of the cut mother tree in order to protect the daughter tree. In another embodiment, after the initial removal of the canopy of the mother tree the daughter plants may be allowed to develop and the mother pseudotrunk gradually reduced in size by subsequent cuts. A pesticide may be applied onto or into the mother pseudotrunk during this time up to the time at which the mother pseudotrunk has been effectively removed.
However, it is most advantageous to apply the pesticide early in the development of the daughter plant in order to maximise the treatment-harvest time interval.
The pesticide is generally an insecticide, nematicide, fungicide or plant growth regulator, preferably an insecticide or nematicide. The pesticide is generally translocatable and more preferably water soluble at ambient temperature, the water solubility being generally higher than 0.5 gull, preferably higher than 2 gll at ambient temperature. The pesticide can be provided in a formulation that is generally translocatable and more preferably water soluble at ambient temperature.
Those species of banana or plantain trees to be 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 recognise these in The Pesticide Manual 10th ed., edited by C. Tomlin, British Crop Protection Council, United Kingdom, 1994. A preferred group of carbamates are N-methyl carbamates, that is those substances that possess the substituent -OC(O)NHMe. A particularly preferred carbamate that can be used according the instant invention is 2-methyl-2 (methylthio)propionaldehyde methylcarbamoylowne (aldicarb). Other cartamates that can be used according to the invention are 2,3-dibydro-2,2 dimethylbenzofuran-7-yl methylcarbamate (carbofuran) and NNaaadimethyl-2-methylcarbamoyloxyim (oxamyl).
A carbamate can be used alone or in combination with other pesticides.
Other insecticides or nematicides that can be used according to the instant invention either alone or in combination with other pesticides include: nitromethylenes or nitroimines including 1 -(6-chloro-3-pyridylmethyl)-N- nitroimidazolidin-2-ylideneamine (imidacloprid); cyanoimines including (E)-N-[(6-chloro-3-pyridyl)methyl]-N-cyano-N - methylacetamidine (acetamiprid);and organophosphates including S,S-di-sec-butyl O-ethyl phosphorodithioate (cadusafos); (RS)-S- sec-butyl O-ethyl 2-oxol,3-thiazolidin-3-yiphosphonothioate (fosthiazate); and O-ethyl S,S-dipropyl phosphorodithioate (ethoprophos).
Other insecticides or nematicides that can be used according to the instant invention either alone or in combination with other pesticides include compounds of formula a):
in which: R1 is -CN or methyl; R2 is -S(O)nR3; R3 is alkyl or haloalkyl; R4 represents a hydrogen or halogen atom or a member of a group consisting of -NR5R6, -S( )mR7. -C(O)0-R7, alkyl, haloalkyl, -OR8 and -N=C(R9)(RIO); Rs and R6 independently represent the hydrogen atom or an alkyl, haloalkyl, -C(O)alkyl, alkoxycarbonyl or -S(O)rCF3 radical; or Rg and R6 can together form a divalent alkylene radical which can be interrupted by one or two divalent heteroatoms, such as oxygen or sulfur; R7 represents an alkyl or haloalkyl radical; R8 represents an alkyl or haloalkyl radical or a hydrogen atom; Rg represents an alkyl radical or 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, 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; R1 1 and R12 represent, independently of one another, a hydrogen or halogen atom;; R13 represents a halogen atom or a haloalkyl, haloalkoxy, -S(O)qCF3 or SFg group; m, n, q, and r represent, independently of one another, an integer equal to 0, 1, or 2; provided that, when R1 is methyl, then R3 is haloalkyl, R4 is -NH2, Ri 1 is -C1, R13 is CF3 and X is N.
Alkyl groups and moieties in formula (I) are generally of 1 to 6 carbon atoms and are straight- or branched- chain. The ring formed by R5 and R6 with the nitrogen atom to which they are attached when they represent a divalent alkylene group is generally a 5-, 6- or 7- membered ring.
A preferred group of compounds of formula (')is one in which: R1 is CN; R3 is a haloalkyl radical; R4isNH2; X is C-R12; Ri 1 and R12 represent, independently of one another, a halogen atom;and R13 is a haloalkyl radical.
A preferred compound of formula (1) is 5-amino-1-(2,6dichloro s trifluoromethyl phenyl) 4-trinuoromethylsulfinyl-3cyanopyrazole.
Compounds of formula (1) may be prepared according to known processes, for example as described in International Patent Publications No. 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 a man skilled in the art of chemical synthesis.
Pests that may be controlled according to the instant invention include Cosmopolites sordidus (banana weevil), Radopholus similis (burrowing nematode), Helicotylenchus multicinctus (Spiral nematode), Meloidogyne incognita (Rootknot nematode) and pests of the families Heteroderidae and Thripidae.
Fungicides that may be used according to the instant invention include: methyl 1-(butylcarbamoyl)ben7imidazol-2-ylcarbamate (benomyl); triazoles including ( 1 -[2-(2,4-dichlorophenyi).4-propyl- 1 ,3dioxolan-2-ylmethyU - lH- 1,2,4-triazole (propiconazole);and I -[(2RS,4RS :2RSASR)bromo-2-(2,4dicMorophenyl)tetrrhydrnfrrfyU- lH- 1 ,2,4 triazole (bromuconazole).
Plant growth regulators that may be used according to the instant invention include: a gibbereilin such as gibberellic acid or 2chloroethylphosphonic acid (ethephon).
The amount of pesticide which is used is an effective and agronomically acceptable amount per tree. Appropriate amounts will be apparent to the normally skilled worker.
In the case of 2-methyl-2-(methylthio)propionaldehyde 0 methylcarbamoyloxime, quantities of from 0.01 to 5g per tree may be appropriate, preferably from 0.3 to 0.9g per tree.
The introduction of the pesticide in the pseudotrunk of the tree is made by insertion of a composition, which can be of liquid or solid formulation, preferably solid, in order to reduce worker exposure, especially with compounds having relatively high acute toxicity. A solid formulation is preferred for 2-methyl-2-(methylthio)propionaldehyde O-methylcarbamoyloxime.
Formulations are chosen so as to speed the transmission of the active ingredient into an aqueous phase such as the vascular tissue normally present in plants or trees. Formulations are also chosen in order to minimise the exposure of agricultural workers to the pesticide.
Still more preferable are those substantially dustless fonnulations, for example those whose particle size is greater than 0.1 mm, preferably from 0.4 to 0.8 mm. Acceptable formulations may be made by mixing the active ingredient with a polymer, especially a water soluble polymer. Gels may also be used.
The introduction of the pesticide into the pseudotrunk of the mother tree may be made by any suitable means. One possibility is the injection of the pesticide into the pseudotrunk. Another possibility is to make or drill holes in the tree and to put therein the formulation and then to plug or stop the holes. The holes may be made on the side of the pseudotrunk, but it is preferred to make the insertion where the pseudotrunk was cut to remove the canopy.
Another method of introduction of the pesticide is to cut a wedge out of the pseudotrunk, add the pesticidal formulation and replace the wedge back into the space from which it came. An especially preferred embodiment of this insertion is to cut the wedge out from the surface of the cut made by removing the canopy.
Another embodiment is the insertion into the pseudotrunk of a water-soluble capsule containing a dose of the desired pesticide.
The following non-limiting-example is given to illustrate the invention EXAMPLE Banana trees are grown in a plantation. The trees are disposed as mother plants having a series (1 to 5) of daughter plants growing from the corm. Just before harvesting the mother plants, the daughter plants are removed except one daughter plant per mother plant.
The fruit of the banana trees are harvested by cutting the sets of fruits. Within one week after this harvest, the pseudotrunks of these plants are cut to remove the canopies. After two days a wedge is cut from the surface resulting from the removal of the canopy of each pseudotrunk of each mother tree. A dose of 0.5 g per tree of 2-methyl-2 (methylthio)propionaldehyde O-methylcarbamoyloxime in the form of a 15 % w/w granular formulation is placed in the empty space from which each wedge was removed and the wedges are replaced.
The daughter plants are protected against both nematodes and weevils up to harvest time of the daughter trees which is 35 weeks later thus to provide economically acceptable fruit The risk of worker exposure is greatly reduced.

Claims (16)

1. A method for the protection of two or more trees of the families Musaceae or Plantanginaceae from destructive pests wherein the trees to be protected share a common root system which method comprises: (a) cutting one of the trees sharing the said root system to remove its fruit and (b) then introducing a pesticide into the said cut tree.
2. A method according to claim 1 wherein the cut tree is cut to remove its canopy after the removal of its fruit and before introducing the pesticide.
3. A method according to claim 1 or claim 2 wherein the pesticide is introduced into the cut surface of the tree.
4. A method according to anyone of the foregoing claims wherein the pesticide is introduced into the cut surface of the tree formed by the removal of the canopy.
5. A method according to claim 1 or claim 2 wherein the pesticide is introduced into the side of the tree
6. A method according to any one of the foregoing claims wherein the pesticide is introduced from zero to about thirty days after the tree is cut
7. A method according to any one of the foregoing claims wherein the pesticide is an insecticide or nematicide.
8. A method according to any one of the foregoing claims wherein the pesticide is translocatable at ambient temperature.
9. A method according to any one of the foregoing claims wherein the pesticide is provided in a formulation which is water soluble at ambient temperature.
10. A method according to any one of the foregoing claims wherein the trees are Musa textilis, Musa sapientum, or Musa paradisica
11. A method according to any one of the foregoing claims wherein the insecticide or nematicide is a carbamate.
12. A method according to claim 10 wherein the insecticide or nematicide is 2-methyl-2 (methylthio)propionaldehyde O-methylcarbamoyloxime or 2,3Zihydro-2,2dimethylbenzofuran-7- yl methylcarbamate.
13. A method according to claim 12 wherein the amount of 2-methyl-2 (methylthio)propionaldehyde O-methylcarbamoyloxime used per tree is from 0.01g and 5g per tree.
14. A method according to any one of claims 1 to 10 wherein the insecticide or nematicide is: 1 3-pyridylmethyl)-N-nitroimidazolidin-2-ylidwqmme; (E)-N-[(6-chloro-3-pyridyl)methyl]-N-cyano-N-methylacetamidine; N,N-dimethyl-2-methylcarbamoyloxyimino-2-(methylthio)acetamide; S,S-di-sec-butyl Methyl phosphorodithioate; (RSpS- sec-butyl methyl 2-oxo-13-thiazidin-3-ylphosphonothioat ;or O-ethyl S,S-dipropyl phosphorodithioate.
15. A method according to any one of claims 1 to 10 wherein the pesticide is a compound of formula:
in which: R1 is CN or methyl; R2 is S(O)nR3; R3 is alkyl or haloalkyl; R4 represents a hydrogen or halogen atom or a member of a group consisting of NRsR6, S(O)mR7, C(O)O-R7, alkyl, haloalkyl, OR8 and -N=C(R9)(RlO); Rg and R6 independently represent the hydrogen atom or an alkyl, haloalkyl, C(O)alkyl, alkoxycarbonyl or S(O)rCF3 radical; or Rg and R6 can together form a divalent alkylene radical which can be interrupted by one or two divalent heteroatoms, such as oxygen or sulfur; R7 represents an alkyl or haloalkyl radical; R8 represents an alkyl or haloalkyl radical or a hydrogen atom; Rg represents an alkyl radical or hydrogen atom; Rio 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 alryl; 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; R11 and R12 represent, independently of one another, a hydrogen or halogen atom;; R13 represents a halogen atom or a haloalkyl, haloalkoxy, S(O)qCF3 or SF5 group; m, n, q, and r represent, independently of one another, an integer equal to 0, 1, or 2; provided that, when R1 is methyl, then R3 is haloalkyl, R4 is NH2, R11 is Cl, R13 is CF3 and X is N.
16. A method according to any one of claims 1 to 10 and 15 wherein the pesticide is a compound of formula (I) which is 5-amino-3-cyano-1-(2,6-dichloro 4 trifluoromethylphenyl)-4-trifluoromethylsulfinylpyrazole .
17 A method according to any one of the foregoing claims wherein the pesticide used is in a solid or liquid formulation.
18 A method according to claim 17 wherein the formulation is substantially dustless.
19 A method according to claim 17 or claim 18 wherein the formulation has a particle size greater than 0.1 mm, preferably from 0.4 to 0.8 mm.
20 A method according to claim 1 substantially as hereinbefore described in the foregoing Example.
GB9618548A 1995-09-05 1996-09-05 Protection of trees Expired - Lifetime GB2304575B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR9510575A FR2738112B1 (en) 1995-09-05 1995-09-05 METHOD FOR IMPROVING BANANA FRUIT YIELDS

Publications (3)

Publication Number Publication Date
GB9618548D0 GB9618548D0 (en) 1996-10-16
GB2304575A true GB2304575A (en) 1997-03-26
GB2304575B GB2304575B (en) 1998-11-04

Family

ID=9482403

Family Applications (2)

Application Number Title Priority Date Filing Date
GB9618525A Expired - Lifetime GB2304708B (en) 1995-09-05 1996-09-05 Method for improving fruit yields from banana plants
GB9618548A Expired - Lifetime GB2304575B (en) 1995-09-05 1996-09-05 Protection of trees

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB9618525A Expired - Lifetime GB2304708B (en) 1995-09-05 1996-09-05 Method for improving fruit yields from banana plants

Country Status (6)

Country Link
AU (2) AU725638B2 (en)
CO (1) CO4480714A1 (en)
FR (1) FR2738112B1 (en)
GB (2) GB2304708B (en)
OA (2) OA10589A (en)
ZA (2) ZA967479B (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2334447A (en) * 1998-02-20 1999-08-25 Rhone-Poulenc Agro Sa Banana and plantain tree treatment
FR2775161A1 (en) * 1998-02-20 1999-08-27 Rhone Poulenc Agrochimie Induction of suckering in banana or plantain trees - by treatment with pesticide and a plant growth regulator
WO1999060840A1 (en) 1998-05-27 1999-12-02 Aventis Cropscience S.A. New method and device for delivering a phytoprotection product
WO2001013719A2 (en) * 1999-08-19 2001-03-01 Aventis Cropscience S.A. Container for pesticides

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU749429B2 (en) * 1996-06-19 2002-06-27 Bayer S.A.S. Method for improving the health of banana plants
WO1999004630A1 (en) * 1997-07-21 1999-02-04 Rhone-Poulenc Agro Agrochemical composition

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1453822A (en) * 1965-02-12 1966-07-22 Versatile composition intended in particular for the treatment of banana plantations and its preparation
IL29201A (en) * 1967-01-16 1972-07-26 Fmc Corp Plant growth regulant compositions and method using phosphonic acid derivatives
US3558302A (en) * 1968-12-20 1971-01-26 Exxon Research Engineering Co Stable oil-dithiocarbamate dispersions
FR2537395A1 (en) * 1982-12-10 1984-06-15 Rhone Poulenc Agrochimie FUNGICIDAL COMPOSITIONS BASED ON PHOSPHITE
FR2569530B1 (en) * 1984-08-29 1986-09-05 Rhone Poulenc Agrochimie FUNGICIDAL COMPOSITION BASED ON ALUMINUM TRIS ETHYL PHOSPHONATE
FR2543405B1 (en) * 1983-03-31 1986-01-03 Rhone Poulenc Agrochimie FUNGICIDAL COMPOSITION BASED ON ALUMINUM TRIS ETHYL PHOSPHONATE
IL82311A (en) * 1986-05-09 1992-06-21 Rhone Poulenc Agrochimie Bactericidal compositions based on phosphorous acid derivatives
US5514200B1 (en) * 1994-02-07 1997-07-08 Univ Formulation of phosphorus fertilizer for plants

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2334447A (en) * 1998-02-20 1999-08-25 Rhone-Poulenc Agro Sa Banana and plantain tree treatment
FR2775161A1 (en) * 1998-02-20 1999-08-27 Rhone Poulenc Agrochimie Induction of suckering in banana or plantain trees - by treatment with pesticide and a plant growth regulator
US6114285A (en) * 1998-02-20 2000-09-05 Rhone Poulenc Agro Compositions and methods for use in cropping bananas and plantain trees
ES2154580A1 (en) * 1998-02-20 2001-04-01 Rhone Poulenc Agrochimie Compositions and methods for use in cropping bananas and plantain trees
WO1999060840A1 (en) 1998-05-27 1999-12-02 Aventis Cropscience S.A. New method and device for delivering a phytoprotection product
WO2001013719A2 (en) * 1999-08-19 2001-03-01 Aventis Cropscience S.A. Container for pesticides
WO2001013719A3 (en) * 1999-08-19 2002-09-26 Aventis Cropscience Sa Container for pesticides

Also Published As

Publication number Publication date
GB2304708B (en) 1999-03-17
GB9618525D0 (en) 1996-10-16
OA10589A (en) 2002-07-10
AU725638B2 (en) 2000-10-19
ZA967477B (en) 1997-03-05
ZA967479B (en) 1997-03-05
GB2304575B (en) 1998-11-04
GB2304708A (en) 1997-03-26
AU6442096A (en) 1997-03-13
AU728772B2 (en) 2001-01-18
MX9603861A (en) 1997-07-31
FR2738112B1 (en) 1997-09-26
AU6441996A (en) 1997-03-13
FR2738112A1 (en) 1997-03-07
OA10328A (en) 1997-09-19
CO4480714A1 (en) 1997-07-09
GB9618548D0 (en) 1996-10-16

Similar Documents

Publication Publication Date Title
KR100458174B1 (en) Novel 5-amino-3-cyano-4-ethylsulfinyl-1-phenyl-pyrazole compounds and their use as pesticides
EA012465B1 (en) Selective insecticides for controlling insects and/or arachnides, use thereof and a method for controlling insects and/or arachnides
JP3880075B2 (en) Agricultural chemical treatment method of rice and seed rice treated with the treatment
FR2805971A1 (en) METHODS OF TREATING AND / OR PROTECTING CROPS AGAINST ARTHROPODS AND COMPOSITIONS USEFUL FOR SUCH METHODS
KR100428231B1 (en) Control of light moth grass by 1-arylpyrazole or 1-heteroarylpyrazole compound
US6071941A (en) Protection of trees
AU728772B2 (en) Protection of trees
EP1013170B1 (en) Method of insect control
CA2218511A1 (en) Use of a n-arylpyrazole or n-heteroarylpyrazole compound to regulate plant growth
SK160297A3 (en) Flea and tick control collar containing n-phenylpyrazole for use on cats and dogs
US6114285A (en) Compositions and methods for use in cropping bananas and plantain trees
KR19990028521A (en) Methods of Inhibiting Population of Insects by 1-arylpyrazole or 1-heteroarylpyrazole
MXPA96003861A (en) Arbo protection
AU724487B2 (en) Method of treatment of sugar plant to improve the sugar content
US6013661A (en) Protection of crops against birds using a compound of phenylpyrazole type
KR100478401B1 (en) Fungicidal and insecticidal compositions
IE45143B1 (en) Improvements in or relating to pesticides
MXPA99000681A (en) New compositions and methods for use in banana and silver cultivation
DE2135251A1 (en) Pesticides
US6051595A (en) Method for controlling flies infesting mushrooms by using a N-arylpyrazole or a n-heteroarylpyrazole compound
AU708045B2 (en) A method for controlling flies infesting mushrooms by using a N-arylpyrazole or a N-heteroarylpyrazole compound
FR2775161A1 (en) Induction of suckering in banana or plantain trees - by treatment with pesticide and a plant growth regulator
MXPA99008520A (en) Method of repression of insec
EP0962138A1 (en) Pesticidal method and composition
MXPA97008365A (en) Control of work rough roots by compounds 1-aril pirazol or 1-heteroaril pira