GB2116160A - Plant growth regulation method and composition - Google Patents
Plant growth regulation method and composition Download PDFInfo
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- GB2116160A GB2116160A GB08306333A GB8306333A GB2116160A GB 2116160 A GB2116160 A GB 2116160A GB 08306333 A GB08306333 A GB 08306333A GB 8306333 A GB8306333 A GB 8306333A GB 2116160 A GB2116160 A GB 2116160A
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- Prior art keywords
- ccc
- pyrimidinemethanol
- crop
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Classifications
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- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05G—MIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
- C05G3/00—Mixtures of one or more fertilisers with additives not having a specially fertilising activity
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- 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
- A01N47/02—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 no bond to a nitrogen atom
Abstract
A method of regulating plant growth, particularly of a cereal crop, comprises applying to the crop or crop locus where the regulation is desired from 0.025 to 3.5 kg/ha of a pyrimidinemethanol of formual I <CHEM> wherein R is CF3, [CF2]2H or C2F5, or an acid addition salt thereof and from 0.1 to 3.5 kg/ha of CCC.
Description
1
GB211616QA 1
SPECIFICATION
Plant growth regulation method and composition
5 This invention relates to methods of regulating plant growth, and to compositions for use in that method. The ingredients are known growth regulating agents, but the compositions of the present invention have surprising and improved properties over the respective ingredients, synergism being observed.
The plant growth regulation art has now advanced to a stage in which compounds are 10 available which can cause very specific and selective effects upon the growth and development of certain plants. It is now apparent that synthetic growth-regulating chemicals are becoming extremely important and valuable in the commercial control of crop growth, in both agriculture and horticulture. For example, several agents are now in commercial use which can alter the growth habit of crops such as sugar cane, cotton, potatoes and many others, for example, so as 15 to increase the ease of mechanical harvesting and final yield.
Chlormequat chloride, hereinafter referred to as CCC, is a well known plant growth regulator which shortens stem growth in, for example, wheat and poinsettias. It is fully described in the 6th edition of The Pesticide Manuel, published in 1979 by The British Crop Protection Council. The compounds of formula (I) as described hereunder, are known compounds and were 20 disclosed in GB Patent No. 1,468,840, together with their growth regulating properties in crop plants, ornamental plants, woody plants and turf. The compound in which R is CF3 is hereinafter referred to as EL 500.
This invention relates to a method of regulating the growth of a crop which comprises applying to the crop or crop locus from 0.025 to 3.5 kg/ha of a pyrimidinemethanol of formula 25 1
CH3 CH3
35
wherein R is CF3, (CF2)2H or C2F5, and from 0.1 to 3.5 kg/ha of CCC. Preferably, the pyrimidinemethanol is applied at from 0.025 to 2.0 kg/ha. the CCC is preferably applied at from 0.1 to 3.0 kg/ha. More preferably, the pyrimidinemethanol is applied at from 0.025 to 0.75 kg/ha whilst that of CCC is from 0.1 to 0.7 kg/ha.
40 Thus the ratio in which the pyrimidinemethanol and CCC are applied lies in the range 1 :140 to 35:1. The preferred ratio lies in the range 1:120 to 20:1, and more preferably is in the range 1 :28 to 7.5:1.
The preferred pyrimidinemethanol of formula I is that in which R is CF3.
The active compounds may be applied sequentially or, preferably, simultaneously. Particularly 45 useful results are obtained when the method is applied to cereal crops, such as barley and wheat, and also oilseed rape. As examples of other crops may be given rice, rye and herbage grasses as well as amenity grass and lawns.
The invention also provides a composition for regulating the growth of a crop which comprises from 1 to 35 parts by weight of a pyrimidinemethanol, preferably EL 500, and from 50 1 to 1 35 parts by weight of CCC, the preferred composition having from 1 to 20 parts of pyrimidinemethanol and from 1 to 120 parts of CCC. Thus the weight ratio of pyrimidinemethanol : CCC is in the range 1 :140 to 35:1. Preferably the composition comprises a weight ratio of pyrimidinemethanol to CCC of 1 :120 to 20:1, most preferably from 1 :28 to 7.5:1. A third active component, which may for example be a fungicide such as nuarimol, or a selective 55 herbicide may advantageously be incorporated in the composition.
It is preferred that the composition should also comprise an inert carrier. Other excipients may be incorporated.
The carrier utilized in preparing compositions of the invention may be any inert dry or liquid carrier. In the case of dry carriers, various types may be employed. Typical solid carriers and 60 diluents include clay, diatomaceous earth, sand, talc, synthetic carriers and the like. Dry compositions may be blended and formulated as wettable powders and applied as sprays using water as a vehicle. Alternatively, the dry compositions may be formulated without a wetting agent and applied as a dust or in the form of granules or pellets.
The active ingredients of the composition can also be formulated as ready to dilute aqueous 65 suspensions or oils or emulsifiable concentrates. They can additionally take the form of non-
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GB2116160A
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aqueous solutions or suspensions utilizing adjuvants and diluents such as xylene, toluene, acetone and the like.
The formulations will generally contain from 1 to 90% of active ingredient, the so-called concentrates, whether solid or liquid, intended for dilution prior to application, containing from 5 20 to 95% of active ingredients, the balance being carriers, excipients etc.
The active ingredients may be present as the free compounds or in the form of salts of other suitable derivatives, for example, the acid addition salts formed with non-phytotoxic acids such as hydrochloric, hydrobromic, sulphuric, phosphoric, nitric, oxalic, p-toluenesulphonic, benzene-sulphonic, methanesulphonic or maleic. It will be understood by those skilled in the art that 10 suitable salts include those which are not substantially more phytotoxic than the free bases from which they are derived.
The invention may usefully be applied to the crops at any time, but the best results on cereals are obtained when applications are made before tillering, before stem elongation and/or at mid stem elongation. In the case of cereal crops application is preferably made once, during mid 15 stem elongation.
The effect of a single application to cereal crops during mid stem elongation has the effect not only of reducing the height of the crop, thus reducing the incidence of lodging and facilitating the harvesting of the crop, but also of concentrating the plant energy into the formation of seeds, thus increasing the crop yield per plant.
20 The method and compositions of the invention provide a degree of growth regulation which would not be predicted from the teaching of the art. By virtue of the use of the invention, lower amounts of the active ingredients are used to obtain a given degree of growth control than would otherwise have been required.
Although the invention is particularly effective when applied to cereal crops, in particular 25 spring wheat, spring barley and winter barley, other crops may also benefit from the invention. Such other crops include, for example, oilseed rape, rice, ryegrass and other grasses, including amenity grass and lawns. The invention can also be applied with advantage to ornamental crops, such as tulips, chrysanthemum spp, lilies, poinsettias and carnations.
As previously mentioned, sequential or simultaneous application of the active ingredients may 30 be employed. Simultaneous application is preferred and for such purpose it is preferred to employ a combined composition according to the invention after suitable dilution, if appropriate. However, tank mixes may be employed involving separate addition of the active ingredients to a diluent, such as water, to form an appropriate application medium such as a spray liquor, immediately prior to use. For such latter method and also for enabling sequential application to 35 be made, the present invention also provides a two component pack, the pack comprising a first container containing the pyrimidinemethanol, preferably EL 500, and a second container containing CCC, the amounts in each container preferably corresponding to the desired and preferred ratio of the components when used according to the method of the invention.
When the active ingredients are applied sequentially, the applications should be within 4 40 weeks of each other, but preferably within 5 days and most preferably within 24 hours.
The following Examples illustrate the invention, whilst not limiting it.
EXAMPLE 1
Winter oilseed rape (Elvera) was grown in a medium loam with a 2% organic content in 16 45 cm X 16 cm plastic pots in the open, 10 seeds being hand sown per pot. After 34 days, post-emergence of the crop, the plants were sprayed using a microsprayer with an Allman Number Zero nozzle operating at 2 kg/cm2 with a volume rate of 40 ml/m2 (400 l/ha).
EL 500 was used in the form of a 50% wettable powder and CCC as a 62% aqueous suspension. The rate of application of EL 500 was 0.50 kg/ha while that of CCC was 0.70 50 kg/ha.
Plants which were treated with a combination of EL 500 and CCC were compared in height with other plants which had not been treated. Simultaneous tests were carried out on plants treated singly with EL 500 or CCC. Height measurements were taken at different periods after treatment, to determine the percentage reduction in crop height of the treated plants as 55 compared with untreated plants. Those plants treated with CCC alono, after 15 days, showed no plant height reduction compared with untreated plants, while those treated with EL 500 alone showed an 87.8% height reduction in the same period. When treated with EL 500 plus CCC, plants showed an 89.6% reduction. At 45 days after treatment the respective figures were 17.2, 82.4 and 93.3 while at 76 days the figures were 1.9, 77.4 and 88.1.
60 The Colby equation, which provides a measure of synergism, is as follows:
Y(100 — X)
Expected effect = X 4
100 ,
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60
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GB2116160A
3
where X and Y are the individual effects of two treatments. If the effect of the combination of the two treatments is greater than that calculated from the above equation, synergism is observed.
When the Colby equation is applied to the above figures, the expected and observed values 5 are:
% Reduction in Crop Height
Days after
Expected
Observed treatment
(Colby)
15
87.8
89.6
45
85.4
93.3
76
77.8
88.1
Thus a marked degree of synergism was observed in this experiment.
20 EXPERIMENT 2
Following the procedure of Example 1, winter oilseed rape was treated 34 days after planting with either (i) 0.70 kg/ha of CCC, (ii) 0.75 kg/ha of EL 500 or (iii) a combination of 0.70 kg/ha of CCC and 0.75 kg/ha of EL 500. Observations made 1 5, 45 and 76 days after treatment gave the following results.
25
% Reduction in Crop Height
CCC 4- EL 500
30
Days after treatment
CCC alone
EL 500 alone
Expected (Colby)
Observed
15
0
87.8
87.8
91.3
45
17.2
92.6
93.8
95.8
35
76
1.9
90.6
90.7
91.5
As in Example 1, synergism was observed throughout the growth period.
40 EXAMPLES
Following the procedure of Example 1, plants of spring wheat were treated 34 days after planting with either (i) 0.25 kg/ha of EL 500 or (ii) 0.7 kg/ha of CCC or (iii) 0.25 kg/ha of EL 500 plus 0.7 kg/ha of CCC. Measurements taken 31 days after treatment and compared with the height of untreated plants gave the following results.
% Reduction in Crop Height
Crop
CCC alone
EL 500 alone
CCC + EL 500 Expected (Colby) Observed
Spring Wheat
24.8
18.7
38.8 47.5
A marked degree of synergism was observed.
EXAMPLE 4
Example 3 was repeated with spring wheat and spring barley, but using an application rate of 60 0.5 kg/ha of EL 500 with the following results.
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GB211616QA
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% Reduction in Crop Height
Crop
CCC alone
EL 500 alone
CCC + EL 500 Expected (Colby) Observed
Spring Wheat Spring Barley
24.8 37.6
34.7 31.5
50.8 56.9 57.2 58.6
10
15
A small degree of synergism was observed in spring barley, while spring wheat showed it to a marked degree.
EXAMPLE 5
Example 4 was repeated, but using an application rate of 0.75 kg/ha of EL 500, with the following results.
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25
30
% Reduction in Crop Height
CCC + EL 500
Crop
CCC
EL 500
alone alone
Expected (Colby) Observed
Spring Wheat Spring Barley
24.8 37.6
38.0 41.7
53.3 74.0 63.6 69.8
A marked degree of synergism was observed in both spring wheat and barley.
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EXAMPLE 6
Using the procedure of Example 1, plants of spring wheat and spring barley were treated 34 35 days after planting with either (i) 0.75 kg/ha of EL 500 or (ii) 0.7 kg/ha of CCC or (iii) 0.75 kg/ha of EL 500 plus 0.7 kg/ha of CCC and their heights compared 59 days after treatment with untreated plants. The results were as follows:
35
40 % Reduction in Crop Height 40
CCC + EL 500
Crop CCC EL 500
alone alone Expected (Colby) Observed
45 45
Spring Wheat 34.5 26.1 51.5 63.0
Spring Barley 19.3 26 40.2 46.2
50 A marked degree of synergism was observed. 50
EXAMPLE 7
Following the procedure of Example 1, plants of oilseed rape were treated after 34 days with (i) 0.25 kg/ha of EL 500 or (ii) 0.7 kg/ha of CCC or (iii) a combination of the two, and their 55 heights compared 15 days after treatment with untreated plants. The reduction in crop heights 55 are shown in the following table for the different growth periods
5
GB2116160A
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10
% Reduction in Crop Height
Crop
Period after
Treatment
CCC alone
EL 500 alone
CCC 4- EL 500 Expected (Colby) Observed
Oilseed Rape
15 days
0
81.7
81.7 87.7
10
15
EXAMPLE 8
Following the procedure of Example 1, plants of spring wheat were treated after 34 days with (i) 0.25 kg/ha of EL 500 or (ii) 0.7 kg/ha of CCC or (iii) a combination of the two, and their heights compared 15 and 45 days after treatment with untreated plants. The reduction in crop heights are shown in the following table for the different growth periods
% Reduction in Crop Height
Crop
Period
CCC
EL 500
CCC + EL 500
after alone alone
Treatment
Expected (Colby) Observed
Spring Wheat
15 days
29.1
0.9
29.7 31.8
45 days
27.2
25.2
45.5 46.9
EXAMPLE 9
30 The procedure of Example 8 was repeated using oilseed rape and spring wheat, but using 0.7 30 kg/ha of EL 500, with the following results.
35
% Reduction in Crop Height
50
45
Crop
Period after
Treatment
CCC alone
EL 500 alone
CCC + EL 500 Expected (Colby) Observed
Oilseed Rape
15 days
0
87.8
87.8
97.3
45 days
17.7
92.6
93.8
95.8
Spring Wheat
15 days
29.1
19.1
42.6
42.7
45 days
27.2
46
60.6
64.6
EXAMPLE 10
Following the procedure of Example 1, plants of winter wheat were treated 83 or 131 days after planting with (i) EL 500, (ii) CCC or (iii) a combination of the two. The dosage level of EL 500 was varied from 37.5 to 250 gms/ha. Measurements of the plant heights were taken 105 or 57 days after treatment. The reduction in crop height when compared with untreated plants is tabulated below for the combinations tested.
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GB211610OA
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% Reduction in Crop Height
Days after planting (treatment)
83
131
Days after treatment (observation)
105
57
Compound
Dose
Expected
Observed
Expected
Observed
gm/ha
EL 500
37.5
0
0
75
0
1.9
125
5.3
4.4
250
20.3
7.9
CCC
700
0.2
5.3
EL 500 + CCC
37.5 + 700
0.2
3.6
5.3
8.7
75.0 + 700
0.2
15.5
7.0
5.3
125.0 + 700
5.4
28.3
9.4
24.1
250.0 + 700
20.4
31.7
12.7
28.8
Marked synergism was observed at 7 of the 8 data points where the combination was used.
Overall plant height is a function of the distance between internodes. Assessment was made of the distance between nodes 2 and 3. These nodes were produced after the applications were 25 made. 25
% Reduction in Distance between Nodes 2 and 3
30 Days after planting (treatment) 83 131 30
35 35
Days after planting (treatment)
83
131
Days after treatment (observation)
105
57
Compound
Dose
Expected
Observed
Expected
Observed
gm/ha
EL 500
37.5
7.2
0
75
0
0
125
7.2
7.2
250
28.6
14.3
CCC
700
14.3
28.2
EL 500 + CCC
37.5 + 700
20.5
14.3
28.2
21.4
75.0 + 700
14.3
25.0
28.2
32.8
125.0 + 700
20.5
46.2
33.3
50.0
250.0 + 700
38.8
64.3
38.4
55.6
40 CCC 700 14.3 28.2 40
45 45
Marked synergism was observed at 6 of the 8 data points where the combination was used.
EXAMPLE 11
50 Example 10 was repeated using winter barley. The results are set out in the following tables.
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GB2116160A 7
% Reduction in Crop Height
5 Days after planting (treatment) 83 131 5
Days after treatment (observation) 105 57
Compound
Dose gm/ha
Expected
Observed
Expected
Observed
EL 500
37.5
0
0
75
0
0
125
0
0
250
3.2
0
CCC
700
0
0
EL 500 + CCC
37.5 + 700
0
0
0
0
75.0 + 700
0
0
0
0
125.0 + 700
0
4.5
0
17.2
250.0 + 700
3.2
20.6
0
12.6
% Reduction in Distance Between Nodes 2 and 3
25
30
35
40
Days after planting (treatment)
83
131
Days after treatment (observation)
105
57
Compound
Dose
Expected
Observed
Expected
Observed
gm/ha
EL 500
37.5
0
0
75
0
0
125
0
0
250
0
0
CCC
700
0
0
EL 500 + CCC
37.5 + 700
0
0
0
0
75.0 + 700
0
0
0
4.2
125.0 + 700
0
4.2
■o
25.0
250.0 + 700
0
33.3
0
16.7
25
30
35
40
Marked synergism was observed at 5 of the 8 data points where the combination was used. For winter wheat the lowest application rate of the combination tested (EL 500 37.5 + chlor-45 mequat 700 gm/ha) generally displayed synergism as did higher application rates (13 of 16 45 data points). The growth stage at which the application was made appeared to be immaterial. For winter barley a generally higher application rate than that which was required for wheat was necessary to reduce crop height. Thus EL 500 at rates equal to or greater than 75 gm/ha in combination with 700 gm/ha chlormequat was synergistic at 9 of 1 2 occasions. As with wheat, 50 the growth stage of the crop at the time of application appeared to be immaterial. 50
EXAMPLE 12
Four seeds of spring barley (variety "Golden Promise") were planted in 4" (10 cm) square pots filled with steam sterilized soil. The seeds and soil were covered with 30 ml of medium-55 sized vermiculite. The pots were lightly sprayed with water and kept in the growth room under a 55 combination of fluorescent and incandescent lights at 235 microeinsteins m~2 sec-1 at 33°C. The pots were watered daily by sub-irrigation for 10 days, by which time they were at a 2-leaf stage. The plants were thinned to two plants per pot before treatment.
60 Compound formulation 60
Stock solutions containing 1 mg/ml of CCC and compounds to be tested in combination with CCC were prepared, using 1% Toximul R/Toximul S (1 :1) in 1:1 acetone :ethanol as a solvent, and .05% Toximul R/Toximul S (1.5:1) in deionised water was used as a diluent in preparing the test solutions, according to the following table.
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GB21161SQA
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Treatment
Vol. of
Stock Soln. (ml)
Vol. of
Bate
Test Compound
CCC
Diluent (ml)
5
(lb/acre)
(ml)
.1
.29
8.7
.2
.57
8.4
.4
1.14
7.9
10
.5
1.43
7.6
1
2.86
6.1
.1 + .5
.29
1.43
7.3
.2 + .5
.57
1.43
7.0
.4+ .5
1.14
1.43
6.4
15
.1 + 1
.29
2.86
6.4
.2 + 1
.57
2.86
5.9
.4 + 1
1.14
2.86
5.6
10
15
20 Treatment procedure 20
Plants were sprayed with a DeVilbiss compressed air sprayer at the rate of 3 ml/pot. All experiments were set up in a randomized block design and replicated three times.
Data Collection Procedure
25 Treated plants were moved to a greenhous and kept under meta halide lights at 190 25
microeimsteins m~2 sec-1 and 29°C. Data were collected on the plants fourteen days after treatment.
Plant height was determined by measuring the plants from the pot edge to the tip of the tallest leaf. Both plants in the pot were measured and the results recorded as an average of the
30 two in centimeters. The data were converted from centimeters to a percent of the average height 30 of the control plants and the percentage reduction in height of the treated plants determined.
The following compounds were tested by this procedure, EL 500 (A), a-isopropyl-o:-(p-1,1,2,2-tetrafluoroethoxyphenyl)-5-pyrimidinemethanol (B), and a-isopropyl-a-(p-pentafluoroethoxyphe-nyl)-5-pyrimidinemethanol (C).
35 The results of this treatment are set out in the following tables. 35
% Reduction
40
Compound
Dose lb/acre
Expected
Observed
CCC
.5
9.4
1.0
14.2
45
EL 500
.1
12.3
.2
12.3
.4
9.4
CCC + EL 500
.5
1
20.5
21.7
2
20.5
25.0
50
4
17.9
32.5
1.0
1
24.8
21.7
2
24.8
33.Q
4
22.3
31.6
GB 2116160A
% Reduction
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Compound
Dose
Expected
Observed
CCC
5
9.4
1
0
14.2
'B'
1
5.2
2
1.4
4
11.3
CCC + 'B'
.5
1
14.1
12.7
2
10.7
17.0
4
19.6
16.0
1.0
1
18.7
19.3
2
15.4
20.8
4
23.9
27.4
10
20
25
30
35
% Reduction
Compound
Dose
Expected
Observed
CCC
.5
9.4
1
.0
14.2
'C
.1
10.8
.2
9.9
.4
12.3
CCC + 'C
.5
.1
19.2
19.3
.2
18.4
28.3
.4
20.5
30.2
1.0
.1
23.5
33.5
2
22.7
25.9
.4
24.8
38.7
20
25
30
35
EXAMPLE 13
Plants of barley (Golden Promise) were cultivated in 4" pots as in Example 12 and the effect of a soil drench on their growth rate was determined. The treatment solutions were prepared by 40 dissolving the active ingredients in a 1:1 acetone: ethanol mixture and diluting with deiortized water to prepare a stock solution, which could be diluted as required. The solution volume of the drench was 20 ml in each treatment, which was applied 8 days after planting, and measurements were made 17 days later.
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45
% Reduction
Compound
Dose
Expected
Observed
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CCC
.5
13.4
1.0
12.5
EL 500
.1
42.7
.2
50.7
.4
54.4
55
CCC + EL 500
.5 .1
50.4
46.5
.2
57.3
48.8
.4
60.5
51.1
1 .1
49.8
49.2
.2
56.9
52.5
60
.4
60.1
53.9
45
50
55
60
EXAMPLE 14
Plants of Spring Barley (Larker) were grown in the open in rows 6" apart in clay soil with 65 small clods. The plants were sprayed after 27 days, using a C02 Backpack sprayer operating at 65
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GB2116160A 10
25 psi using an 8002E Tee Jet nozzle. The plant heights were subsequently measured at various intervals, the results being summarized in the following table, which shows the reduction in plant height of treated plants relative to untreated plants at different periods of time following the treatment.
5 5
10
% Reduction
No. of Days
CCC
EL 500
CCC + EL 500
1.5 lb/acre
3 lb/acre
1.5 lb/acre
1.5 + 1.5
3+ 1.5
33
1.8
0
10.2
0.6
6.6
39
0
0
10.7
0
7.1
45
1.5
0
7.7
4.6
7.7
55
1.5
0
7.7
4.6
7.7
10
15
EXAMPLE 15
20 Example 15 was repeated with Spring Barley (Larker) planted on clay soil with no clods. The backpack sprayer was operated at 30 psi. The results are shown in the following table.
20
25
% Reduction
CCC
EL 500
CCC + EL 500
No. of Days
1.5 lb/acre
3 lb/acre
1.5 lb/acre
1.5 + 1.5
3 + 1.5
45
7.9
0
4.8
1.6
0
55
7.9
0
4.8
1.6
0
25
30
EXAMPLE 16
35 Winter Barley (Pike) was planted in the open in rows 6" apart in the autumn. One application 35 of a growth regulator formulation was made, in spring, using a C02 backpack sprayer operating at 20 psi, and using an 8002E Tee Jet nozzle. The plant heights were measured and compared with untreated plants after 13 and 30 days. The formulation compositions and calculated growth reduction, as a percentage of the central plants, are shown in the following table.
40 40
45 (lb/acre) (lb/acre) (lb/acre) 45
% Reduction
No. of Days
CCC
EL 500
CCC + EL 500
(lb/acre)
(lb/acre)
(lb/acre)
1 2 3
1.5
1.5+ 1.5
3 + 1.5
13
4.6 4.7 1.8
3.0
1.3
6.4
30
2.6 7.1 4.3
1.5
1.5
5.4
50 50
Formulations containing the active ingredients were prepared as in the following Examples. EXAMPLE 17
55 The following ingredients were carefully blended in conventional mixing equipment, to 55
provide a wettable powder.
11
GB 2116160A 11
% by wt.
5 EL 500 1 5
CCC 28
Sodium dioctyl sulphosuccinate 5
Naphthalene/formaldehyde condensate 3
Precipitated silicon dioxide 25
10 Kaolin to 100 10
EXAMPLE 18
Example 17 was repeated, using the following make-up of ingredients: 15 15
% by wt.
EL 500 45
20 CCC 6 20
Sodium dioctyl sulphosuccinate 5
Naphthalene/formaldehyde condensate 3
Precipitated silicon dioxide 1 5
Kaolin to 100
25 25
In the following Examples, suspension concentrates were prepared having the constituents indicated.
30 EXAMPLE 19 30
% w/v
35 EL 500 2 35
CCC 56 Ethylene oxide/propylene oxide block copolymer 3
Lignin sulphonate 5
40 Ethylene glycol 10 40
Silicone antifoam emulsion 0.5
Xanthan gum 1.0
Water to 100
45 45
EXAMPLE 20
% w/v
50 50
EL 500 45 CCC 6 Ethylene oxide/propylene oxide block copolymer 3 55 Lignin sulphonate 5 55 Ethylene glycol 10 Silicone antifoam emulsion 0.5 Xanthan gum 0.5 Water to 100 60 60
Claims (22)
1. A method of regulating the growth of a crop which comprises applying to the crop or crop locus where the regulation is desired from 0.025 to 3.5 kg/ha of a pyrimidinemethanol of 65 formula I 65
12
GB2110160A
12
<>k>-
/\
CH3 CH3
10 10
wherein R is CF3, (CF2)2H or C2F5, or an acid addition salt thereof and from 0.1 to 3.5 kg/ha of CCC.
2. A method according to claim 1 wherein the pyrimidinemethanol is applied at from 0.025 to 2.0 kg/ha and CCC from 0.1 to
3.0 kg/ha.
15 3. A method according to claim 1 or claim 2 wherein R is CF3. 15
4. A method according to any one of claims 1 to 3 wherein the ratio of the pyrimidinemethanol to CCC is in the range of 1 :28 to 7.5:1.
5. A method according to any one of claims 1 to 4 wherein the pyrimidinemethanol and the CCC are applied simultaneously.
20
6. A method according to any one of claims 1 to 4 wherein the pyrimidinemethanol and the 20 CCC are applied sequentially.
7. A method according to any one of claims 1 to 6 wherein the crop is spring wheat, spring barley or winter barley.
8. A method according to any one of claims 1 to 7 wherein the crop is treated during mid-
25 stem elongation. 25
9. A method according to any one of claims 1 to 8 wherein the crop is treated by foliar application.
10. A plant growth regulator composition which comprises from 1 to 35 parts by weight of a pyrimidinemethanol as defined in claim 1 and from 1 to 135 parts by weight of CCC.
30
11. A composition according to claim 10 which comprises from 1 to 20 parts by weight of 30 a pyrimidinemethanol and from 1 to 120 parts by weight of CCC.
12. A composition according to claim 10 or claim 11 wherein the pyrimidinemethanol is ct-isopropyl-ffi-(p-trifluoromethoxyphenyl)-5-pyrimidinemethanol.
13. A composition according to any one of claims 10 to 12 in which the ratio of
35 pyrimidinemethanol to CCC in in the range of 1 :28 to 7.5:1. 35
14. A composition according to any one of claims 10 to 13 also comprising a third component.
15. A composition according to claim 14 in which the third component is a fungicide.
16. A composition according to claim 1 5 in which the fungicide is nuarimol.
40
17. A composition according to any one of claims 10 to 16 which also comprises an inert 40 carrier.
18. A method of producing a plant growth regulating composition which comprises bringing into admixture from 1 to 35 parts by weight of a pyrimidinemethanol of formula (I) as defined in claim 1 and from 1 to 135 parts by weight of CCC, together with an inert carrier therefor.
45
19. A method according to any one of claims 1 to 9 which comprises applying a 45
composition according to any one of claims 10 to 17.
20. A composition of claim 10 as herein described with especial reference to the Examples.
21. A method of claim 1 as herein described with especial reference to the Examples.
22. A method of claim 18 as herein described with especial reference to the Examples.
Printed for Her Majesty's Stationery Office by Burgess & Son (Abingdon) Ltd.—1983.
Published at The Patent Office, 25 Southampton Buildings, London, WC2A 1AY, from which copies may be obtained.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8206999 | 1982-03-10 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| GB8306333D0 GB8306333D0 (en) | 1983-04-13 |
| GB2116160A true GB2116160A (en) | 1983-09-21 |
| GB2116160B GB2116160B (en) | 1985-08-29 |
Family
ID=10528908
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB08306333A Expired GB2116160B (en) | 1982-03-10 | 1983-03-08 | Plant growth regulation method and composition |
Country Status (16)
| Country | Link |
|---|---|
| EP (1) | EP0088631B1 (en) |
| JP (1) | JPS58185501A (en) |
| KR (1) | KR840004051A (en) |
| AT (1) | ATE18333T1 (en) |
| AU (1) | AU554132B2 (en) |
| BR (1) | BR8301146A (en) |
| CA (1) | CA1196511A (en) |
| DD (1) | DD210191A5 (en) |
| DE (1) | DE3362372D1 (en) |
| ES (1) | ES8404149A1 (en) |
| GB (1) | GB2116160B (en) |
| GR (1) | GR77958B (en) |
| IL (1) | IL68037A (en) |
| NZ (1) | NZ203480A (en) |
| PL (1) | PL136459B1 (en) |
| SU (1) | SU1409118A3 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106135213A (en) * | 2016-07-01 | 2016-11-23 | 北京天辰云农场科技股份有限公司 | A kind of Semen Tritici aestivi hot-dry wind tolerance spraying resistant to lodging liquor and preparation and application thereof |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1468840A (en) * | 1974-05-21 | 1977-03-30 | Lilly Co Eli | Substituted nitrogen hetero-cycles |
| AU545889B2 (en) * | 1980-05-09 | 1985-08-08 | Eli Lilly And Company | Plant growth regulatory combination |
-
1983
- 1983-03-03 AU AU12012/83A patent/AU554132B2/en not_active Ceased
- 1983-03-03 IL IL68037A patent/IL68037A/en unknown
- 1983-03-04 NZ NZ203480A patent/NZ203480A/en unknown
- 1983-03-04 GR GR70681A patent/GR77958B/el unknown
- 1983-03-07 PL PL1983240920A patent/PL136459B1/en unknown
- 1983-03-08 JP JP58038106A patent/JPS58185501A/en active Pending
- 1983-03-08 BR BR8301146A patent/BR8301146A/en unknown
- 1983-03-08 GB GB08306333A patent/GB2116160B/en not_active Expired
- 1983-03-08 DE DE8383301266T patent/DE3362372D1/en not_active Expired
- 1983-03-08 EP EP83301266A patent/EP0088631B1/en not_active Expired
- 1983-03-08 AT AT83301266T patent/ATE18333T1/en not_active IP Right Cessation
- 1983-03-09 ES ES520426A patent/ES8404149A1/en not_active Expired
- 1983-03-09 CA CA000423188A patent/CA1196511A/en not_active Expired
- 1983-03-09 KR KR1019830000950A patent/KR840004051A/en not_active Application Discontinuation
- 1983-03-09 SU SU833560847A patent/SU1409118A3/en active
- 1983-03-10 DD DD83248698A patent/DD210191A5/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU1201283A (en) | 1983-09-15 |
| BR8301146A (en) | 1983-11-22 |
| DD210191A5 (en) | 1984-06-06 |
| ES520426A0 (en) | 1984-04-16 |
| GR77958B (en) | 1984-09-25 |
| PL136459B1 (en) | 1986-02-28 |
| NZ203480A (en) | 1985-10-11 |
| CA1196511A (en) | 1985-11-12 |
| AU554132B2 (en) | 1986-08-07 |
| JPS58185501A (en) | 1983-10-29 |
| KR840004051A (en) | 1984-10-06 |
| EP0088631B1 (en) | 1986-03-05 |
| DE3362372D1 (en) | 1986-04-10 |
| SU1409118A3 (en) | 1988-07-07 |
| IL68037A0 (en) | 1983-06-15 |
| EP0088631A1 (en) | 1983-09-14 |
| PL240920A1 (en) | 1983-10-24 |
| ES8404149A1 (en) | 1984-04-16 |
| GB8306333D0 (en) | 1983-04-13 |
| ATE18333T1 (en) | 1986-03-15 |
| IL68037A (en) | 1986-07-31 |
| GB2116160B (en) | 1985-08-29 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PCNP | Patent ceased through non-payment of renewal fee |