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NZ614667B2 - Plant growth regulation composition - Google Patents
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NZ614667B2 - Plant growth regulation composition - Google Patents

Plant growth regulation composition Download PDF

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Publication number
NZ614667B2
NZ614667B2 NZ614667A NZ61466712A NZ614667B2 NZ 614667 B2 NZ614667 B2 NZ 614667B2 NZ 614667 A NZ614667 A NZ 614667A NZ 61466712 A NZ61466712 A NZ 61466712A NZ 614667 B2 NZ614667 B2 NZ 614667B2
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NZ
New Zealand
Prior art keywords
plant
surfactant
composition
plant growth
ethyl
Prior art date
Application number
NZ614667A
Other versions
NZ614667A (en
Inventor
Ulrich Johannes Haas
Richard Brian Perry Deceased
Philip Taylor
Original Assignee
Syngenta Limited
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
Priority claimed from GBGB1105526.6A external-priority patent/GB201105526D0/en
Priority claimed from GBGB1112815.4A external-priority patent/GB201112815D0/en
Application filed by Syngenta Limited filed Critical Syngenta Limited
Priority claimed from PCT/EP2012/055605 external-priority patent/WO2012130924A1/en
Publication of NZ614667A publication Critical patent/NZ614667A/en
Publication of NZ614667B2 publication Critical patent/NZ614667B2/en

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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
    • A01N2300/00Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
    • 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
    • A01N25/30Biocides, 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 characterised by the surfactants
    • 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
    • A01N33/00Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
    • A01N33/02Amines; Quaternary ammonium compounds
    • A01N33/12Quaternary ammonium compounds
    • 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
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/42Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing within the same carbon skeleton a carboxylic group or a thio analogue, or a derivative thereof, and a carbon atom having only two bonds to hetero atoms with at the most one bond to halogen, e.g. keto-carboxylic acids
    • 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/541,3-Diazines; Hydrogenated 1,3-diazines
    • 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647Triazoles; Hydrogenated triazoles
    • A01N43/6531,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • 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
    • A01N47/02Biocides, 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

Provided are plant growth regulation compositions comprising a plant growth regulator, a surfactant and optionally an agriculturally acceptable carrier. The surfactant is a branched non-ionic alcohol ethoxylate having an alkyl chain length of 8 carbon atoms, an average of from 1 to 7 propylene oxide units, and an average of from 4 to 9 ethylene oxide units. A preferred surfactant is 2-ethyl hexanol 6PO-8EO. Preferred plant growth regulators include trinexapac-ethyl, prohexadione-calcium and chlormequat-chloride.Further provided are methods for enhancing or regulating the growth of plants comprising applying said composition. units, and an average of from 4 to 9 ethylene oxide units. A preferred surfactant is 2-ethyl hexanol 6PO-8EO. Preferred plant growth regulators include trinexapac-ethyl, prohexadione-calcium and chlormequat-chloride.Further provided are methods for enhancing or regulating the growth of plants comprising applying said composition.

Description

PLANT GROWTH REGULATION COMPOSITION The present invention relates to an improved plant growth regulation composition sing a plant growth regulator and a surfactant. It also s to a method for enhancing or regulating the growth of plants comprising applying said composition.
Plant growth regulators are often used to regulate the growth and development of crop plants. For e, plant growth regulators are used to slow the pment of a crop (such as oil seed rape) so that it flowers at a desired time, reduce the height of a crop (such as in cereals) so that it is less susceptible to lodging, increase en efficiency, regulate flowering and fruit set of a crop (such as fruit trees), and slow turfgrass growth rate to reduce mowing frequency.
There are several different classes of plant growth regulator. Known classes include azoles (such as uniconazole, and paclobutrazol), cyclohexane carboxylates (such as trinexapac-ethyl, and prohexadione-calcium), pyrimidinyl carbinols (such as flurprimidol, and ancymidol), quarternary ammoniums (such as chlormequat-chlon'de, and mepiquat- chloride), and nyl-amino phenyl-acetamides (such as mefluidide).
Plant growth regulators operate by various modes of . For example, onium-type plant growth retardants such as chlormequat-chloride and mepiquat-chlon'de, that possess a positively charged ammonium, phosphonium or sulphonium group, functi on by blocking the synthesis of gibberellin early in the biosynthetic pathway. Growth retardants comprising a en-containing heterocycle, such as flurprimidol, paclobutrazol and uniconazole—P, act as inhibitors of monooxygenases that catalyse ive steps in gibberellin biosynthesis.
Structural mimics of 2-oxoglutaric acid, such as the clohexanediones trinexapac-ethyl and prohexadione—calcium, interfere with the late steps of gibberellin biosynthesis. Other plant growth regulators, such as mefluidide, inhibit cell division and differentiation.
Plant growth regulators such as trinexapac-ethyl are commonly used on crops to reduce the risk of lodging through stem ning and shortening, and improved rooting. It is well known in the art that treatment of crops with trinexapac—ethyl can increase yield both through reduction in lodging, and through improved rooting which makes the crop less susceptible to drought stress.
There is a need for ed plant growth regulating compositions that provide better growth regulating effects, both in terms of control of lodging and crop enhancement benefits.
W0 2012/130924 It is known that adjuvants such as surfactants are often built into formulations, or added to tank mixtures before application, to improve uptake of the active ingredient into the plant, Surprisingly, it has been found that applying trinexapac-ethyl in combination with a specific surfactant results in better plant growth regulating effects than when applied alone, or with other surfactants. In particular, this allows ent plant growth regulation and crop enhancement effects to be obtained at lower rates of plant growth regulator active ingredient. ing to the present invention, there is provided a composition comprising a plant growth regulator, a surfactant, and optionally an agriculturally acceptable carrier, wherein the surfactant is a branched non-ionic alcohol ethoxylate having an alkyl chain length of 8 carbon atoms, from 1 to 7 propylene oxide units, and from 4 to 9 ne oxide units.
In a further embodiment, there is provided a composition ting ially of a plant growth regulator, a surfactant, and optionally an agriculturally able carrier, wherein the surfactant is a branched non-ionic alcohol ethoxylate having an alkyl chain length of 8 carbon atoms, from 1 to 7 propylene oxide units, and from 4 to 9 ethylene oxide units.
In a further embodiment, there is provided a ition consisting of a plant grth regulator, a surfactant, and ally an agriculturally acceptable carrier, wherein the surfactant is a branched non-ionic alcohol ethoxylate having an alkyl chain length of 8 carbon atoms, from 1 to 7 propylene oxide units, and from 4 to 9 ethylene oxide units.
Suitably, the alkyl chain is ethyl—hexyl. The ing may be located at any position on the alkyl chain. Preferably, the alkyl chain is branched at the 2-position. More preferably the alkyl chain is 2-ethyl hexyl.
As is well known to those skilled in the art, the degree of lation represents a mean average, because the manufacturing process for such adj uvants is imprecise and results in products containing a distribution of molecules with ent levels of lation.
In one embodiment, the surfactant comprises from 5 to 9 ethylene oxide units. In a further embodiment, the surfactant comprises from 7 to 8 ethylene oxide units. Preferably, the surfactant comprises an average of 8 ethylene oxide units.
In a further ment, the surfactant comprises from 4 to 7 propylene oxide units. In another embodiment, the surfactant comprises from 5 to 6 propylene oxide units. Preferably, the surfactant ses an average of 6 propylene oxide units.
W0 2012/130924 Suitably, the ratio of ethylene oxide to propylene oxide units is from 8:1 to 1:1. More suitably, the ratio of ne oxide to propylene oxide units is 3:1. More suitably still, the ratio of ethylene oxide to propylene oxide units is 4:3. Preferably, the ratio of ethylene oxide to propylene oxide units is from 1.1:1 to 1.6:1. In one embodiment, it is about 1.4:1.
Preferably the surfactant comprises (on average) 8 ethylene oxide and 6 propylene oxide units.
In one aspect of the present invention, the surfactant consists of 2-ethyl hexanol having an average of 6 PO units and an average of 8 EO units. In a further aspect, the surfactant consists of Z-ethyl hexanol having 2 PO units and 8 E0 units.
In one embodiment, the surfactant is 2-ethyl hexanol PO-EO, which is available from Dow under the tradename Ecosurf® EH~6 (CAS 643667).
The composition of the present invention surprisingly provides better l of g at lower rates of active ient. r, the ability to apply the composition at a lower AI rate without loss of plant growth regulation efficacy enables ation at earlier plant growth stages — at a time when application of higher AI rates is typically phytotoxic to the plants. For example, on cereal crops the composition of the present invention may be applied at about growth stage 29-30, instead of growth stage 31-33. The ability to apply the composition at early growth stages maximises the crop enhancement benefits of the plant growth regulator compound itself, for example resulting in better root development, drought tolerance, and ultimately higher yield. The composition of the present invention may also give rise to a longer residual effect of the plant growth regulator, for example in terms of lodging control, crop enhancement benefits, or both.
Any plant growth regulator may be used in accordance with the present ion. A complete list of all commercially available plant growth regulators may be obtained from the Pesticide Manual (15‘11 edition, published by the British Crop Protection Council). In one embodiment, the plant growth regulator is selected from the group consisting of trinexapac- ethyl, prohexadione-calcium, paclobutrazol, uniconazole, flurprimidol, ide, mepiquatchloride , chlormequat—chloride, and a mixture thereof.
Suitably, the plant growth regulator is a gibberellin thesis inhibitor. ly, the plant growth regulator is a class A gibberellin biosynthesis inhibitor. Suitably, the plant growth tor is a class B gibberellin biosynthesis inhibitor. In a preferred embodiment the plant growth regulator is trinexapac—ethyl, prohexadione—calcium or chlormequat— W0 2012/130924 chloride. In one embodiment, the plant growth regulator is apac-ethyl. In one embodiment, the plant growth regulator is prohexadione-calcium. In one embodiment, the plant growth regulator is chlorrnequat-chloride. In one embodiment, the plant growth regulator is paclobutrazol. In one embodiment, the plant growth tor is midol.
In one embodiment, the composition of the t invention comprises at least 20% w/v tant. Suitably the composition of the present invention comprises at least 25% w/v surfactant. ly the composition ofthe present invention comprises at least 30% w/v surfactant. More suitably the composition of the t invention comprises at least 35% w/v surfactant. In a further embodiment, the composition of the present invention comprises at least 40% w/v surfactant. Preferably the composition of the present invention comprises about 40% w/v tant. Preferably the composition of the present invention comprises about 41% w/v surfactant. ably the composition of the present invention compri ses about 42% w/v surfactant. Preferably the composition of the present invention comprises about 43% W/V surfactant. Preferably the composition of the present invention comprises about 44% w/v surfactant. Preferably the composition of the present invention ses about 45% w/v surfactant. Preferably the composition of the present invention comprises about 46% w/v surfactant. Preferably the composition of the present invention comprises about 47% w/v surfactant. Preferably the composition of the present invention comprises about 48% w/v surfactant. Preferably the composition of the present invention comprises about 49% w/v surfactant. Preferably the composition of the present invention ses about 50% w/v surfactant.
The plant growth regulator is present in the composition in an amount sufficient to regulate plant growth. In one embodiment, the composition of the present invention comprises between 5% and 95% active ingredient, preferably between 5% and 50%. In one embodiment, the ition comprises about 25% w/v active ingredient.
In the present ion, the mixture ratio of plant growth regulator to surfactant lies within the range from about 1:10 to about 10:1 by weight. Suitably, the mixture ratio of plant growth regulator to surfactant is from about 1:5 to about 5:1 by weight. More suitably, the e ratio of plant growth regulator to surfactant is from about 2:1 to about 1:2 by weight.
The composition of the present invention is lly diluted prior to use. In one embodiment of the present invention, there is provided a plant growth regulation spray solution comprising a composition as defined above, wherein the surfactant is present at W0 2012/130924 between 0.1 and 0.5% w/v. Preferably, the surfactant is present in the spray solution at about 0.2% W/v.
The rate of application of the composition may vary within wide limits and depends upon the crop, the nature of the soil, the method of application, the prevailing climatic conditions, and other factors governed by the method of application and the time of ation. The composition of the present invention is generally d at a rate of 0.001 to 1 kg ai/ha, ally from 0.001 to 0.5 kg ai/ha. Suitably the composition is applied at a rate from about 50 to about 150 g ai/ha/ More suitably, the composition is applied at a rate of about 75g ai/ha.
According to the present invention there is provided a method for enhancing the growth of plants comprising applying to a plant, plant part, plant propagation material, or plant g locus a composition or plant growth regulation spray solution as defined above. In particular, the method results in improvements in plant yield, plant vigour, plant quality, and/or plant tolerance to stress factors. In one embodiment, the plants have improved tolerance to drought conditions.
The term ‘crop enhancement’ as used herein means an improvement in plant vigour, an improvement in plant y, improved tolerance to stress factors, and/or ed input use efficiency.
According to the t invention, an ‘improvement in plant vigour’ means that certain traits are improved qualitatively or quantitatively when compared with the same trait in a control plant which has been grown under the same conditions in the absence of the method of the invention. Such traits include, but are not d to, early and/or improved germination, improved emergence, the ability to use less seeds, increased root growth, a more developed root system, increased root nodulation, sed shoot , increased tillering, stronger tillers, more productive s, increased or improved plant stand, less plant verse (lodging), an increase and/or improvement in plant height, an increase in plant weight (fresh or dry), bigger leaf blades, greener leaf colour, increased pigment content, increased photosynthetic activity, earlier flowering, longer panicles, early grain maturity, increased seed, fruit or pod size, increased pod or ear number, sed seed number per pod or car, increased seed mass, enhanced seed filling, less dead basal leaves, delay of senescence, improved vitality of the plant and/or less inputs needed (e.g. less fertiliser, water and/or labour needed). A plant with improved vigour may have an increase in any of the aforementioned traits or any combination or two or more of the aforementioned traits.
According to the present invention, an ‘improvement in plant quality’ means that certain traits are improved qualitatively or quantitatively when compared with the same trait in a control plant which has been grown under the same conditions in the absence of the method of the invention. Such traits include, but are not limited to, ed visual appearance of the plant, reduced ethylene (reduced production and/or inhibition of reception), improved quality of harvested material, e.g. seeds, fruits, leaves, vegetables (such improved quality may manifest as improved visual appearance of the harvested material, improved carbohydrate content (e.g. increased quantities of sugar and/or starch, improved sugar acid ratio, ion of reducing sugars, increased rate of pment of sugar), improved protein content, improved oil content and composition, ed ional value, reduction in anti- nutritional compounds, ed organoleptic properties (e.g. improved taste) and/or improved er health benefits (e.g. sed levels of vitamins and anti-oxidants)), improved post-harvest characteristics (e. g. ed shelf-life and/or storage stability, easier processability, easier extraction of compounds) and/or ed seed quality (e.g. for use in following seasons). A plant with improved quality may have an increase in any of the aforementioned traits or any ation or two or more of the aforementioned traits. ing to the present invention, an ‘improved tolerance to stress factors’ means that certain traits are improved qualitatively or quantitatively when compared with the same trait in a control plant which has been grown under the same ions in the absence of the method of the invention. Such traits include, but are not limited to, an increased tolerance and/or resistance to c stress factors which cause timal growing conditions such as drought (e.g. any stress which leads to a lack of water content in plants, a lack of water uptake potential or a reduction in the water supply to plants), cold exposure, heat exposure, osmotic stress, UV stress, flooding, increased salinity (e. g. in the soil), increased mineral exposure, ozone exposure, high light exposure and/or d availability of nutrients (eg. nitrogen and/or phosphorus nutrients). A plant with improved tolerance to stress factors may have an increase in any of the aforementioned traits or any combination or two or more of the aforementioned traits. 1n the case of drought and nutrient stress, such improved tolerances may be due to, for example, more efficient uptake, use or retention of water and nutrients.
According to the t invention, an ‘improved input use efficiency’ means that the plants are able to grow more effectively using given levels of inputs compared to the grown W0 2012/130924 of control plants which are grown under the same conditions in the absence of the method of the invention. In particular, the inputs include, but are not limited to iser (such as nitrogen, phosphorous, potassium, micronutrients), light and water. A plant with improved input use efficiency may have an improved use of any of the aforementioned inputs or any combination of two or more of the aforementioned .
Other crop enhancements of the present invention include a decrease in plant height, or reduction in tillering, which are beneficial features in crops or conditions where it is ble to have less biomass and fewer s.
Any or all of the above crop enhancements may lead to an improved yield by improving e.g. plant physiology, plant growth and development and/or plant architecture. In the context of the present invention ‘yield’ includes, but is not limited to, (i) an se in biomass production, grain yield, starch content, oil content and/or protein content, which may result from (a) an increase in the amount produced by the plant per se or (b) an ed y to harvest plant matter, (ii) an improvement in the composition of the harvested material (e.g. improved sugar acid ratios, improved oil composition, increased nutritional value, reduction of anti—nutritional compounds, increased er health benefits) and/or (iii) an increased/facilitated ability to harvest the crop, improved processability of the crop and/or better storage stability/shelf life. Increased yield of an agricultural plant means that, where it is possible to take a quantitative measurement, the yield of a product of the respective plant is increased by a measurable amount over the yield of the same product of the plant produced under the same conditions, but without application of the present invention. According to the present invention, it is preferred that the yield be sed by at least 0.5%, more preferred at least 1%, even more red at least 2%, still more preferred at least 4% or even more. , preferably 5% Any or all of the above crop enhancements may also lead to an improved utilisation of land, i.e. land which was previously lable or sub-optimal for cultivation may become available. For e, plants which show an increased y to survive in drought conditions, may be able to be cultivated in areas of sub-optimal rainfall, e. g. perhaps on the fringe of a desert or even the desert itself.
According to the present invention there is also provided a method for regulating the growth of plants comprising applying to a plant, plant part, plant propagation material, or plant growing locus a composition or plant growth tion spray solution as defined above.
The composition of the present invention may be applied to any crop plants.
Examples of dicotyledon crops include beet (such as sugar beet or fodder beet); fruits (such as pomes, stone fruits or soft fruits, for example apples, pears, plums, peaches, almonds, cherries, strawberries, raspberries or blackberries); leguminous plants (such as beans, lentils, peas or soybeans); oil plants (such as rape, mustard, poppy, olives, sunflowers, coconut, castor oil plants, cocoa beans or groundnuts); cucumber plants (such as marrows, cucumbers or melons); fibre plants (such as cotton, flax, hemp or jute); citrus fruit (such as oranges, lemons, grapefruit or mandarins); bles (such as h, lettuce, cabbages, carrots, tomatoes, potatoes, cucurbits or paprika); lauraceae (such as avocados, cinnamon or camphor); tobacco; nuts; coffee; tea; vines; hops; durian; bananas; natural rubber plants; and ornamentals (such as flowers, shrubs, broad—leaved trees or evergreens, for example conifers). This list does not represent any limitation. In one embodiment, the crop plants are oil plants. In particular, the crop plants are oil seed rape plants.
Examples of monocotyledon crops include cereals (wheat, millet, sorghum, rye, triticale, oats, barley, teff, spelt, buckwheat, fonio and quinoa), rice, maize (corn), turfgrass and sugar cane. Suitably the crop plants are monocotyledonous plants. More ly, the crop plants are cereals, in particular wheat or . In one embodiment, the cereal crop is wheat. In a further embodiment, the cereal crop is barley. In a r embodiment, the crop plants are rice . In a further embodiment, the crop plants are sugar cane plants. In further embodiment, the crop plants are com plants.
Suitably the crop plant is turfgrass. Cool season turfgrasses include, for e: Bluegrasses (Poa L.), such as Kentucky Bluegrass (Poa sis L.), Rough Bluegrass (Poa trivialis L.), Canada ass (Poa compressor L.) and Annual ass (Poa annua L.); Bentgrasses (Agrostis L.), such as ng Bentgrass (Agv‘ostz’s palustris Huds.), Colonial Bentgrass (Agrosfis tem'us Sibth.), Velvet Bentgrass (Agrostz's canina L.) and Redtop (Agrostis alba L.); Fescues (Festuca L.), such as Creeping Red Fescue (Festuca rubra L.), Chewings Fescue (Festuca rubra var. commutata , Sheep Fescue (Festuca ovz‘na L.), Hard Fescue (Festuca olia), Tall Fescue (Festuca arundinacea Schreb.), Meadow Fescue (Festuca elatior L.); Ryegrasses (Lolium L.), such as Perennial ss (Lolium perenne L.), Annual an) Ryegrass (Lolium multzflorum Lam); Wheatgrasses (Agropyron Gaertn.), such as Fairway Wheatgrass (Agropyron cristaz‘um (L.) Gaertn.), W0 2012/130924 Western rass (Agropyron smithii Rydb.); Smooth Brome (Bromus s Leyss.); and Timothy (Phleum L.). Warm season turfgrasses include, for example Bermudagrasses (Cynodon L. C. Rich), Zoysiagrasses (Zoysia Willd.), St. Augustinegrass (Stenotaphrum secundazum (Walt) Kuntze), Centipedegrass (Eremochloa ophiuroz'des (Munro) Hack), Carpetgrass pus Beauv.), Bahiagrass (Paspalum notatum F1ugge.), Kikuyugrass (Pennisetum clandestinum Hochst. ex Chiov), Buffalograss (Buchloe dactyloides (Nutt.) .), Centipedegrass (Eremochloa spp) and Seashore paspalum (Paspalum vaginatum swartz).
Crops include those that have been ed tolerant to herbicides like bromoxynil or classes of herbicides (such as HPPD inhibitors, ALS inhibitors (for example primisulfuron, prosulfuron and trifloxysulfuron), EPSPS l-pyrovyl-shikimate—3—phosphate-synthase) inhibitors, GS (glutamine synthetase) inhibitors or PPO (protoporphyrinogen-oxidase) inhibitors) as a result of tional s of breeding or genetic engineering. An example of a crop that has been rendered nt to imidazolinones, e.g. imazamox, by conventional methods of breeding enesis) is Clearfield® summer rape (Canola).
Examples of crops that have been rendered tolerant to herbicides or s of herbicides by genetic engineering methods include glyphosate— and glufosinate—resistant maize varieties cially ble under the trade names RoundupReady® Herculex IO and LibertyLink®. Crops also includes plants that have been transformed by the use of recombinant DNA techniques so that they are capable of synthesising one or more selectively acting toxins, such as are known, for example, from toxin-producing bacteria, especially those of the genus Bacillus. Crops also es plants which have been transformed by the use of recombinant DNA techniques so that they are capable of synthesi sing antipathogenic substances having a selective , such as, for example, the so-called "pathogenesis-related proteins". Examples of such antipathogenic substances and transgenic plants capable of synthesi sing such antipathogenic substances are known, for example, from EP—A—0 392 225, WO 95/33818, and EP-A-0 353 191. The methods of producing such transgenic plants are generally known to the person skilled in the art and are described, for example, in the publications mentioned above.
The composition of the present invention is typically formulated for use on plants, and further comprises formulation adj uvants, such as carriers, solvents and surface-active substances. The ations can be in various physical forms, for example dusting powders, gels, wettable powders, water-dispersible granules, water-dispersible tablets, effervescent compressed tablets, emulsifiable trates, microemulsifiable trates, oil-in-water emulsions, oil flowables, aqueous dispersions, oil dispersions, suspoemulsions, e suspensions, emulsifiable granules, soluble liquids, water-soluble concentrates (with water or a water-miscible organic solvent as carrier), or impregnated polymer films. Such ations can either be used directly or are diluted prior to use. Diluted formulations can be prepared, for example, with water, liquid izers, micronutrients, biological organisms, oil or solvents. These formulations may contain as little as about 0.5% to as much as about 95% or more by weight of active ient. The optimum amount for any given compound will depend on formulation, application equipment and nature of the plants to be controlled. le powders are in the form of finely divided particles which disperse readily in water or other liquid carriers. The particles n the active ingredient retained in a solid matrix. Typical solid matrices include fuller’s earth, kaolin clays, silicas and other readily wet organic or inorganic solids. Wettable powders normally contain about 5% to about 95% of the active ingredient plus a small amount of wetting, dispersing or emulsifying agent.
Emulsifiable trates are homogeneous liquid compositions dispersible in water or other liquid and may consist entirely of the active compound with a liquid or solid emulsifying agent, or may also contain a liquid carrier, such as xylene, heavy aromatic naphthas, isophorone and other non-volatile organic solvents. In use, these concentrates are sed in water or other liquid and normally applied as a spray to the area to be treated.
The amount of active ient may range from about 0.5% to about 95% of the concentrate.
Granular formulations include both extrudates and relatively coarse particles and are usually applied without dilution to the area in which suppression of vegetation is desired.
Typical carriers for granular formulations include fertiliser, sand, fuller’s earth, attapulgite clay, bentonite clays, montmorillonite clay, vermiculite, perlite, calcium carbonate, brick, pumice, pyrophyllite, , dolomite, plaster, wood flour, ground corn cobs, ground peanut hulls, sugars, sodium chloride, sodium sulphate, sodium silicate, sodium borate, magnesia, mica, iron oxide, zinc oxide, titanium oxide, antimony oxide, cryolite, gypsum, diatomaceous earth, m sulphate and other organic or inorganic materials which absorb or which can be coated with the active compound. Particularly suitable is a fertiliser granule carrier.
Granular ations normally contain about 5% to about 25% active ingredients which may include surface—active agents such as heavy aromatic naphthas, kerosene and other petroleum fractions, or ble oils; and/or stickers such as dextrins, glue or synthetic resins. The granular substrate material can be one of the l carriers mentioned above and/or can be a W0 2012/130924 fertiliser material e.g. urea/formaldehyde fertilisers, ammonium, liquid nitrogen, urea, potassium chloride, ammonium compounds, phosphorus compounds, sulphur, similar plant nutrients and micronutrients and es or ations f. The plant growth regulator and surfactant may be neously distributed throughout the granule or may be spray impregnated or absorbed onto the granule substrate after the granules are formed.
Encapsulated granules are lly porous granules with porous membranes sealing the granule pore openings, retaining the active species in liquid form inside the granule pores.
Granules typically range from 1 millimetre to 1 centimetre, preferably 1 to 2 millimetres in diameter. Granules are formed by extrusion, agglomeration or prilling, or are lly occurring. Examples of such materials are vermiculite, sintered clay, kaolin, attapulgite clay, sawdust and granular carbon. Shell or membrane materials include natural and synthetic rubbers, cellulosic materials, styrene-butadiene copolymers, polyacrylonitriles, polyacrylates, polyesters, polyamides, polyureas, polyurethanes and starch xanthates.
Dusts are free-flowing admixtures ofthe active ingredient with finely divided solids such as talc, clays, flours and other organic and inorganic solids which act as dispersants and carriers.
Microcapsules are typically droplets or granules of the active material enclosed in an inert porous shell which allows escape of the enclosed al to the surroundings at controlled rates. Encapsulated ts are typically about 1 to 50 microns in diameter. The ed liquid lly tutes about 50 to 95% of the weight of the capsule and may include solvent in addition to the active compound.
Other useful formulations for plant growth regulation applications include simple ons of the active ingredients in a solvent in which it is completely soluble at the desired concentration, such as acetone, alkylated naphthalenes, xylene and other organic solvents.
Pressurised Sprayers, wherein the active ingredient is dispersed in finely-divided form as a result of vaporisation of a low boiling dispersant solvent carrier, may also be used.
Many of the ations described above include wetting, dispersing or fying agents. Examples are alkyl and alkylaryl sulphonates and sulphates and their salts, polyhydric alcohols; polyethoxylated ls, esters and fatty amines. These agents, when used, ly comprise from 0.1% to 15% by weight of the formulation.
Suitable agricultural adjuvants and carriers, either ated together and/or added separately, that are useful in formulating the compositions of the invention in the formulation W0 2012/130924 2012/055605 types described above are well known to those skilled in the at Suitable es of the ent classes are found in the non-limiting list below.
Liquid carriers that can be employed include water, toluene, xylene, petroleum naphtha, crop oils, AMS; acetone, methyl ethyl ketone, cyclohexanone, acetic anhydride, acetonitrile, acetophenone, amyl acetate, 2-butanone, chlorobenzene, cyclohexane, cyclohexanol, alkyl acetates, diacetonalcohol, 1,2-dichloropropane, diethanolamine, p- diethylbenzene, diethylene glycol, diethylene glycol abietate, diethylene glycol butyl ether, diethylene glycol ethyl ether, diethylene glycol methyl ether, N,N-dimethyl formamide, dimethyl sulfoxide, l,4-dioxane, ylene glycol, dipropylene glycol methyl ether, dipropylene glycol dibenzoate, itol, alkyl pyrrolidinone, ethyl acetate, 2-ethyl hexanol, ne carbonate, 1,1,1-t1ichloroethane, 2-heptanone, alpha , d—limonene, ethylene glycol, ethylene glycol butyl ether, ethylene glycol methyl ether, gamma-butyrolactone, glycerol, glycerol diacetate, glycerol monoacetate, glycerol triacetate, hexadecane, ne glycol, isoamyl acetate, isobomyl e, isooctane, rone, isopropyl benzene, isopropyl myristate, lactic acid, laurylamine, mesityl oxide, methoxy-propanol, methyl isoamyl ketone, methyl yl ketone, methyl laurate, methyl octanoate, methyl oleate, methylene chloride, m—xylene, n—hexane, n-octylamine, octadecanoic acid, octyl amine acetate, oleic acid, oleylamine, o-xylene, , polyethylene glycol (PEG400), propionic acid, ene glycol, propylene glycol monomethyl ether, p-xylene, toluene, triethyl phosphate, triethylene glycol, xylene sulfonic acid, paraffin, mineral oil, trichloroethylene, perchloroethylene, ethyl acetate, amyl acetate, butyl acetate, methanol, ethanol, isopropanol, and higher molecular weight alcohols such as amyl alcohol, tetrahydrofurfuryl alcohol, hexanol, octanol, etc. ethylene , propylene glycol, glycerine, N—methyl-Z-pyrrolidinone, and the like. Water is generally the carrier of choice for the dilution of concentrates. le solid carriers include talc, titanium dioxide, pyrophyllite clay, silica, attapulgite clay, guhr, chalk, diatomaxeous earth, lime, m ate, bentonite clay, fuller’s earth, fertiliser, cotton seed hulls, wheat flour, soybean flour, pumice, wood flour, walnut shell flour, lignin and the like.
In addition to the surfactant of the present invention, further surface-active agents may be advantageously employed in both said liquid and solid compositions, especially those designed to be diluted with carrier before application. The surface-active agents can be anionic, cationic, non-ionic or polymeric in character and can be employed as emulsifying , wetting agents, suspending agents or for other purposes. Typical surface active W0 2012/130924 agents include salts of alkyl sulfates, such as diethanolammonium lauryl sulphate; rylsulfonate salts, such as calcium lbenzenesulfonate; alkylphenol-alkylene oxide addition products, such as nonylphenol—C.sub. 18 ethoxylate; alcohol-alkylene oxide addition products, such as tridecyl alcohol-C.sub. 16 ethoxylate; soaps, such as sodium stearate; alkylnaphthalenesulfonate salts, such as sodium dibutylnaphthalenesulfonate; dialkyl esters of sulfosuccinate salts, such as sodium di(2-ethylhexyl) sulfosuccinate; sorbitol esters, such as sorbitol ; quaternary amines, such as lauryl trimethylammonium chloride; polyethylene glycol esters of fatty acids, such as polyethylene glycol stearate; block copolymers of ethylene oxide and propylene oxide; and salts of mono and dialkyl ate .
Other nts commonly utilized in agricultural compositions include - crystallisation inhibitors, viscosity modifiers, suspending agents, spray t modifiers, pigments, antioxidants, foaming agents, light-blocking agents, compatibilizing agents, antifoam agents, sequestering agents, neutralising agents and buffers, corrosion inhibitors, dyes, odorants, spreading agents, penetration aids, micronutrients, emollients, lubricants, sticking agents, and the like. The compositions can also be formulated with liquid fertilizers or solid, particulate fertiliser carriers such as ammonium nitrate, urea and the like.
These formulations can be applied to plants pre- or post-emergence, by conventional methods, for example sprinkling, spreading or spraying (by hand, tractor, airplane and the like), drench or in—furrow ation to soil, seed treatment, h addition to irrigation water and the like. Preferably the composition of the present invention is applied in the form of a spray application to the foliage plants after nce.
The present invention may optionally include one or more additional pesticides such as insecticides, nematicides, fungicides or herbicides or additional plant growth regulators. A list of pesticides that may be used with the t invention is available in Pesticide Manual (15th edition, hed by the British Crop Protection Council). For example, the composition of the present invention may comprise apac-ethyl and paclobutrazol, trinexapac-ethyl and prohexadione-calcium, or trinexapac-ethyl and acibenzolar—S-methyl.
Co-application of pesticides with the present ion has the added benefit of minimising farmer time spent ng products to crops, since only a single ation may be required to both provide growth regilation and control pests.
The apac-ethyl and further active ingredient may be applied either simultaneously or sequentially in any order. If administered sequentially, the components may be administered in any order in a suitable ale, for e, with no longer than 1 month, no longer than 1 week, or no longer than 24 hours between the time of administering the first component and the time of administering the last component. Suitably, the components are administered within a timescale of a few hours, such as one hour. If the tn'nexapac—ethyl and further active ingredient are administered simultaneously, they may be administered separately or as a tank mix or as a pre—formulated mixture. In one embodiment the mixture or composition of the t invention may be applied to the crop plants as a seed treatment prior to planting.
EXAMPLES Example 1 Summer barley, winter barley, summer wheat and winter wheat plants were grown in a glasshouse. Summer-barley was d at beginning of stem elongation (G83 2); winter barley, summer wheat and winter wheat plants were treated at the 3 leaf growth stage (G813).
Treatments were made as indicated in Table 1. Treatments were made by spraying with a boom sprayer and a spray volume of 200 l/ha.. Treatments were made by tank mixing Moddus® with the relevant nt. The adjuvants in treatments 2 and 3 were selected for their close structural similarity to that of treatment 1. The rate is expressed amount of trinexapac-ethyl (g ai/ha) and percentage of adjuvant in the spray solution.
Table 1: Treatment list Treatment Trinexapac nt Rate (trinexapac g ai/ha + adj uvant %) CHKa Moddus® (EC250) None 200 + 0 CHKb 100 + 0 CHKc 50 + 0 h—I S) Moddus® (EC250) EcosurfEH6 100 + 0.2 l—i O" (SL005) 100 + 0.1 p—A O 50 + 0.2 NSD Moddus® (EC250) Dowfax 20A64 100 + 0.2 [00" (SL005) 100 + 0.1 [\JO 50 + O. w m Moddus® (EC250) Genapol X090 100 + 0.2 Mb.) 00" (SL005) 100 + 0.1 50 + 0.2 Plant stand, including plant height and plant volume was assessed visually at 14, 21, 30 and 46 days after treatment, ing treated plants against the ted check. The results are shown in Table 2, expressed as a tage of plant stand reduction compared to W0 2012/130924 the nt untreated control. Note that the l4daa data is not presented because the plants were too young to demonstrate differences in plant height. Also, the 46daa data is not presented because at this late growth stage the plants were ing to ripen, and so the results did not give an accurate representation of the differences between treatments.
Table 2: Results - percentage plant stand reduction compared to control Treatment IIé SW 22.5 17.5 N K11 SB = Summer barley (v. Passadena); WB = Winter barley (v. ; W = Winter wheat (v. Anna); SW = summer wheat (v. Lona); daa = days after application = Better PGR effect than check at equivalent Moddus rates = Worse PGR effect than treatment 1 (less reduced plant stand) The data shows that treatment 1 (Moddus + Ecosurf EH6) gave a much better plant growth regulation effect than the check (Moddus alone) treatments at equivalent rates of trinexapac-ethyl.
Further, the data shows that treatment 1 (Moddus + Ecosurf EH6) surprisingly ed in a better plant growth regulation effect than treatments containing other adjuvants, W0 2012/130924 (namely treatment 2 Moddus + Dowfax 20A64, and treatment 3 Moddus + l X090), despite the close structural similarity and wetting properties of the adjuvants used in these treatments. Whilst there are a handful of data points for which treatment 1 gave a ly worse plant growth regulation effect than treatments 2 or 3, the person skilled in the art will appreciate that this is ly due to natural variation that is able in PGR biological trials — and that the overall data trend overwhelmingly supports the present ion.
Example 2 A field trial was setup in New Zealand. Treatments were applied to wheat, in the absence of lodging. The results in table 3 show that Wheat treated with compositions of the present invention performed better than Moddus® applied at equivalent rates of trinexapac-ethyl, resulting in better reduction in height, and higher yield.
Table 3: Results - Height and yield of wheat Height at Height at Treatment lSDAA (cm) cm) (dt/ha) Composition of invention* Composition of invention* * Contains 50% w/v Ecosurf EH6, and 25% w/v trinexapac-ethyl Example 3 W0 2012/130924 A field trial was setup in Brazil. Treatments were applied to various varieties of ane days before harvest, and the resulting amount of total recoverable sugars (‘ATR’) measured. The results (averages of replicates) in table 4 show that the sugarcane treated with a ition of the present invention results in higher a level of ATR than ® at lower rates to apac-ethyl.
Table 4: Results — Total recoverable sugars in sugarcane Treatment ATR (kg / ton of sugarcane) ai/ha) Varieties RB855453; Variety SP816250 SP791011;SP813250 Untreated Moddus® 250EC 134.57 _| Moddus® 250EC 135.56 Composition of invention* 133.49 Composition of invention* Composition of invention* * Contains 50% w/v EcosurfEH6, and 25% w/v trinexapac-ethyl

Claims (16)

WHAT IS CLAIMED IS:
1.
. A composition comprising a plant growth regulator, a surfactant, and optionally an agriculturally acceptable carrier, wherein the surfactant is a branched non-ionic alcohol ethoxylate having an alkyl chain length of 8 carbon atoms, an e of from 1 to 7 propylene oxide units, and an average of from 4 to 9 ethylene oxide units, and wherein the plant growth regulator is trinexapac-ethyl.
. A composition according to claim 1, n the alkyl chain is ethyl-hexyl.
. A composition according to claim 1 or 2, comprising an average of from 7 to 8 ethylene oxide units.
. A composition according to any one of claims 1 to 3, comprising an average of from 5 to 15 6 propylene oxide units.
. A composition according to any one of the ing claims, wherein the surfactant is 2- ethyl hexanol 6PO-8EO. 20 . A composition according to any one of the preceding claims comprising at least 20% w/v surfactant.
. A plant growth regulation spray on comprising a composition as defined in any one of claims 1 to 6, wherein the surfactant is present at between 0.1 and 0.5% w/v.
. A plant growth tion spray solution ing to claim 7, wherein the surfactant is present at about 0.2% w/v.
. A method for enhancing the growth ofplants comprising applying to a plant, plant part, 30 plant propagation material, or plant growing locus a composition as defined in any one of claims 1 to 6, or a plant growth tion spray solution as defined in claim 7 or 8.
10. A method according to claim 9 for improving plant yield, plant vigour, plant quality, plant tolerance to stress factors, and/or input use ncy, comprising applying to a plant, plant part, plant propagation material, or plant growing locus a composition as defined in any one of claims 1 to 6, or a plant growth regulation spray solution as defined in claim 7 or 8.
11. A method according to claim 10, wherein the plant has improved tolerance to drought conditions. 10
12. A method for regulating the growth of plants comprising applying to a plant, plant part, plant ation material, or plant growing locus a ition as defined in any one of claims 1 to 6, or a plant growth regulation spray solution as defined in claim 7 or 8.
13. A composition according to claim 1, substantially as herein described with reference to 15 any one of the es thereof.
14. A composition according to any one of claims 1 to 6, substantially as herein described.
15. A plant growth regulation spray according to claim 7 or 8, substantially as herein 20 described.
16. A method according to any one of claims 9 to 12, substantially as herein described.
NZ614667A 2011-03-31 2012-03-29 Plant growth regulation composition NZ614667B2 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
GBGB1105526.6A GB201105526D0 (en) 2011-03-31 2011-03-31 Pesticidal composition
GB1105526.6 2011-03-31
GBGB1112815.4A GB201112815D0 (en) 2011-07-25 2011-07-25 Pesticidal composition
GB1112815.4 2011-07-25
PCT/EP2012/055605 WO2012130924A1 (en) 2011-03-31 2012-03-29 Plant growth regulation composition

Publications (2)

Publication Number Publication Date
NZ614667A NZ614667A (en) 2014-11-28
NZ614667B2 true NZ614667B2 (en) 2015-03-03

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