GB2304575A - Protection of trees sharing a common root system - Google Patents
Protection of trees sharing a common root system Download PDFInfo
- 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
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Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N25/00—Biocides, 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
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N47/00—Biocides, 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
- A01N47/08—Biocides, 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, 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.
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)
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)
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)
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 |
-
1995
- 1995-09-05 FR FR9510575A patent/FR2738112B1/en not_active Expired - Fee Related
-
1996
- 1996-09-03 AU AU64419/96A patent/AU725638B2/en not_active Ceased
- 1996-09-03 AU AU64420/96A patent/AU728772B2/en not_active Ceased
- 1996-09-04 CO CO96047089A patent/CO4480714A1/en unknown
- 1996-09-04 ZA ZA967479A patent/ZA967479B/en unknown
- 1996-09-04 ZA ZA967477A patent/ZA967477B/en unknown
- 1996-09-05 GB GB9618525A patent/GB2304708B/en not_active Expired - Lifetime
- 1996-09-05 OA OA60885A patent/OA10589A/en unknown
- 1996-09-05 OA OA60884A patent/OA10328A/en unknown
- 1996-09-05 GB GB9618548A patent/GB2304575B/en not_active Expired - Lifetime
Cited By (7)
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 |
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