WO2012143676A2 - Coating compositions for pathogen control in ornamentals - Google Patents

Abstract

Coating composition for applying to a plant structure of a dicotyledonous ornamental plant from which roots and shoots are capable of growing, wherein the said coating composition comprises an organic carrier material and one or more biological agents that possess an activity against at least one or more pathogens of a dicotyledonous ornamental plant

Description

COATING COMPOSITIONS FOR PATHOGEN CONTROL IN ORNAMENTALS

The present invention relates to coating compositions including an organic component and a biological agent for applying to plant structures of ornamental plants from which roots and shoots are capable of growing, uses of coating compositions on such structures, methods of producing such coating compositions and plant structures coated with such coating compositions. In particular, the invention relates to coating compositions that comprise an organic carrying material and biological agents selected from chemicals and biological agents active against one or more plant pathogens selected from bacterial, fungal and arthropod pathogens that infest plant structures of ornamental plants.

Losses in yield in ornamental crops are recorded annually and come about as a result of plant infestations due to pathogens such as bacteria, fungi and arthropods which can infest the plant at various stages of development, such as at the seed, tuber and/or bulb stage. Agronomic losses due to pathogen infestations remain high despite many defensive measures that have been devised by man to combat such infestations. Such defensive measures include the use of synthetic chemicals; the employment of genetic engineering; and the use of live biological agents that are applied in the form of coatings, sprays and washes and the like.

Pesticides in the form of chemical agents such as fungicides, bactericides and arthropodicides, typically in the form of insecticides and/or acaricides may be applied to the crop the form of liquid soil drenches, liquid seed treatments and the like. Such kinds of chemical treatments tend to be indiscriminate and may adversely affect beneficial bacteria, fungi and arthropods as well as the plant pathogens at which such treatments are targeted.

When conventional pesticides are used as seed treatments the seeds are coated with pesticide directly or the pesticide is applied to the seed in the presence of an inorganic carrier. Such seed treatments are typically applied in liquid form or as wet slurry and subsequently the seeds are dried. Such treatments are mostly aimed at providing direct protection against pathogens such as arthropods and/or seed borne microorganisms and/or soil borne microorganisms that attack the seed or other plant structure from which roots and shoots are able to emerge. The high level of chemicals that are typically used introduces a chemical load to the environment that may give rise to ecological concerns.

One problem in applying a biological agent that is a chemical agent in conventional plant structure coating procedures is that the chemical agent is typically applied as slurry and this may give rise to an uneven application of the coating whereby the seeds are not fully coated or a percentage of the seeds, up to 20% depending on seed type and coating procedure do not get coated. Furthermore, the seed coatings may not be uniform and this gives rise to physical weaknesses in the seed coat and the coating may flake off.

A further problem arises when using biological agents that are selected from beneficial live bacterial and fungal species that may be applied conventionally to plant structures, for example as spores in conjunction with an inorganic carrier in the form of particulate compositions or in the form of liquid compositions which may then be dried back, is that the applied biological agents rapidly lose viability. Without the intention of being bound by theory it is thought that as the seeds or storage organs are dried back, the micro-environment alters and the viability of applied live biological agents may be seen to decrease sharply and almost as soon as the applied composition is dried. The loss of viability of the biological agent is typically associated with the splitting of the fungal or bacterial spores which renders them non-viable.

It has now been found that by using an organic carrier material in conjunction with a biological agent, the viability of the biological agent is improved on the plant structure, such as a seed or a tuber and the like, relative to the viability of biological agents applied to such structures conventionally. Furthermore, the coating of the plant structure is less susceptible to flaking.

It is an object of the present invention to supply improved seed coatings comprising biological agents for use on plant structures, such as seeds, as herein defined. Furthermore, it is an object of the invention to supply seed coatings that utilise fewer chemical additives and/or lesser amounts of thereof for protecting seed and/or young plantlets from pathogens than conventional seed coatings. These and other objects of the invention will become apparent from the following description and examples.

According to the present invention there is provided a dicotyledonous ornamental plant structure coating composition, wherein the said coating composition comprises at least one organic carrier material in the form of particles wherein the carrier material is selected from waxes having a melting point of ≥50° Centigrade and one or more biological agents that possess an activity against one or more pathogens of a dicotyledonous ornamental plant.

For the purposes of the present invention "plant structures" are viable ornamental plant structures to which compositions of the invention may be applied and include seeds, seed tubers, tuberous roots (sometimes referred to as 'tubers', e.g. dahlia 'tubers'), bulbs, corms and rhizomes. Viable plant structures as provided herein means that the plant structures are capable of germinating to conventional levels of germination typical of ornamental plant seeds or in the case of seed tubers, tuberous roots, bulbs, corms and rhizomes of growing roots and shoots. Thus, viable plant structures as herein defined may be used for the planting of ornamentals such as varieties of tulip, amaryllis, hyacinth, daffodil, narcissus, cyclamen, lily, lily of the valley, iris, gladiolus, crocus, crocosmia, dahlia, snowdrop, bluebell, dahlia, freesia, gloxinia, anemone, fritillaria, alstromeria ligtu and hybrids thereof, camassia esculenta, arum italicum, muscari, agapanthus, begonia, acidanthera, ranunculus, ornamental allium and the like. Examples of ornamentals seeds that may be coated with compositions of the invention include seeds of viola (pansy), primula, petunia, polyanthus, tagetes, pelargoniums including P. Peitatum, begonia, cyclamen, achillea, ageratum, agrostemma, alyssum, amaranthus, antirrhinum, aquilegia, aster, calendula, campanula, carnation, chrysanthemum, helleborus, cineraria, clematis, convolvulus, Centaurea cyanus, cosrnea, dahlia, delphinium, dianthus, digitalis, myosotis, freesia, geranium, godetia, impatiens, cheiranthus cheiri, dianthus barbatus, lathyrus odoratus, salvia, salpiglossis, verbena, zinnia and the like. The online Sutton Seeds catalogue 2010 herein incorporated by reference provides examples of many varieties of ornamental plant which may be treated with the coating compositions of the present invention. Woody ornamental plant structures may also be treated with compositions of the invention. Woody ornamental plant structures include seeds of ornamental plants such as members of the arborvitae, acer, azalea, Chamaecyparis, dogwood, euonymus, rose, forsythia, Fraser fir, hemlock, Japanese holly, juniper, Pieris, rhododendron, Taxus, white pine, maple, elm, aspen, ash, beech, and oak.

The organic carrier material is selected from organic materials that can be applied to plant structures as defined herein such as seeds preferably as a dry powder wherein the powder particles are of a pre-determined volume mean diameter or as populations of particles presented in a liquid form, such as an oleaginous formulation or as an aqueous formulation.

Generally, the organic carrier material of use in the invention is present in the form of particles in a composition of the invention and possesses a volume mean diameter of a certain size as defined herein. To obtain particles of organic materials of a volume mean diameter applicable for use in the invention, organic materials in the form of, for example, 1 to 5 kilogram blocks or tablets may be broken up or kibbled into small millimetre-sized pieces (such as from 2mm - 8mm approximate diameter in size, for example from 4mm to 6mm) in a kibbling machine. The millimetre-sized pieces can then be passed through a comminuting means such as a standard mill, e.g. an Apex Comminuting mill, and milled or comminuted into particles having an approximate diameter in the range from 100pm - 500pm, for example from 250μητ> - 300pm. The micron-sized comminuted particles can then be passed through a micronising apparatus, such as an AFG micronising air mill to obtain particles of a desired VMD range, such as from 15 m - 20 m, that is of use in the present invention. The skilled addressee will appreciate that such procedures for obtaining small particles are well known in the art. Preferably, dry powder compositions of the invention comprise composite particles having a volume mean diameter of≥5pm, for example of 8μηι, 9μιη, 10pm, 11 m, 12pm, 13μηι, 14pm, 15pm up to 40pm or any value thereinbetween. As stated herein, the volume mean diameter of the composite particles is typically≥10pm or > 2pm and may lie in the range from 10pm to 200pm and may have a value that lies anywhere there inbetween. for example from≥10pm to 100pm; or from >10pm to 40pm; or from >10pm to 30pm or any desired volume mean diameter value in between. Preferably, dry powder compositions of the invention comprise particles having a volume mean diameter of≥8pm, for example of 8pm, 9pm, 9.7pm, 10pm, 11pm, 12pm, 13pm, 14pm, 15pm and the like up to any volume mean diameter of choice, such as up to 200pm or any volume mean diameter in between for example 40pm or 30pm. Particles of the invention that possess a volume mean diameter >10pm are considered to be less of a thoracic hazard to humans and are not thought to be allergenic.

The particles of the organic carrier material in liquid form may be applied as an oleaginous formulation or as an aqueous formulation in which particles of a pre-determined volume mean diameter are suspended, which once applied to a plant structure, is then permitted to dry on the plant structure using conventional drying procedures. Where the organic carrier material is applied to plant structures as herein defined, such as to seeds in a dry powder form, the particles of the organic powder material may have a volume mean diameter of any conventional size as herein described. To such organic carrier material of use in the invention such as in the form of dry powders, chemicals may be added that are of use against pathogens that are arthropods such as insects, arachnids or if appropriate, their larvae eggs, or pupae; chemicals of use against bacterial pathogens; and chemicals of use against fungal pathogens may be added prior to the coating of the ornamental plant structure, such as an ornamental plant seed. Additionally, beneficial live biological agents may be added to such dry powders of use in the present invention, the live biological agents being able to target bacterial pathogens of the ornamental plant andfor to target fungal pathogens of the ornamental plant. Spores of choice of beneficial live biological agents such as fungal conidia or hyphae or mycelia of fungi that do not form spores or conidia-like structures may also be added to dry powders of use in the present invention. Suitable organic carrier materials of use in the invention are typically made up of waxes having a melting point of≥50°C, more preferably of >60°C, and most preferably are made up of hard waxes having a melting point of >70°C.

Natural waxes of use in the present invention include camauba wax, beeswax, Chinese wax, shellac wax, spermaceti wax, myricyl palmitate, cetyl palmitate, candelilla wax, castor wax, ouricury wax, wool wax, sugar cane wax, retamo wax, rice bran wax and the like.

Synthetic waxes of use in the present invention include suitable waxes selected from paraffin wax, microcrystailine wax, Polyethylene waxes, Fischer-Tropsch waxes, substituted amide waxes, polymerized a-olefins and the like. Mineral waxes of use in the invention include montan wax (e.g. Lumax® Bayer) ceresin wax, ozocerite, peat wax and the like.

Suitable organic carrier particles may be selected from waxes such as carnauba wax, beeswax, montan wax, Chinese wax, shellac wax, spermaceti wax, myricy) palmitate, cetyl palmitate, candelilla wax, castor wax, ouricury wax, wool wax, sugar cane wax, retamo wax, and rice bran wax or a mixture of two or more thereof.. Such waxes typically display a high enthalpy of lattice energy during melt. Preferably the organic carrier material is carnauba wax which may be applied in liquid form, typically in the form of a suspension, or more preferably in powder form as discrete particles.

Additionally, the organic carrier particles of use in compositions of the invention may contain other components such as additives selected from UV blockers such as beta-carotene or p- amino benzoic acid, colouring agents such as optical brighteners and commercially available colouring agents such as food colouring agents, plasticisers such as glycerine or soy oil, antimicrobials such as potassium sorbate, nitrates, nitrites, propylene oxide and the like, antioxidants such as vitamin E, butylated hydroxyl anisole (BHA), butylated hydroxytoluene (BHT), and other antioxidants that may be present, or mixtures thereof. The skilled artisan will appreciate that the selection of such commonly included additives will be made depending on end purpose, and perceived need.

Liquid formulations of the invention may be formulated as an aqueous formulation or as an oleaginous formulation, depending on design. Aqueous formulations may include surfactants selected from commercially available surfactants such as Libsorb, Silwet L77, Tween 80, Torpedo II, Newmans T80, Fortune, Guard, Rhino, Biopower, and the like. Of these surfactants, Libsorb is the most preferred.

Oleaginous formulations, that is to say oil-based formulations, may contain any oil suitable for use in the present invention which may be selected from petroleum oils, such as paraffin oil, and vegetable oils such as rapeseed oil, soybean oil, sunflower oil, palm oil and the like. Oil formulations of use in the invention contain organic carrier particles as described herein and these in turn may be admixed with flow agents such as hydrophilic precipitated silicas, for example Sipernat 383 DS, Sipernat 320, EXP 4350, and Sipernat D-17 and the like. Such free-flowing agents may be dispersed in oils, for example, for anti-foaming purposes.

The skilled addressee will appreciate that where an aqueous or an oil formulation may be used to apply biological agents of use in the invention, the liquid element should be removed from the coated plant structure after coating is achieved for example by drying off using conventional drying processes, leaving a plant structure coating composition in dry particulate form in close association therewith or in contact therewith, wherein the coating composition is made up of the organic carrier as herein described and the at least one biological agent, also as herein described.

A biological agent for the purposes of the present invention is one that can be used to control the population of a plant pathogen of an ornamental plant, and may be selected from chemical fungicides, arthropodicides such as insecticides and acaricides, bactericides and from live biological agents that are able to control the population of one or more seed or soil borne pathogens of an ornamental plant structure as herein defined. Preferably, the population of the soil borne pathogen on or in the immediate proximity of the ornamental plant structure as herein defined is reduced either by the biological agent rendering it unable to reproduce or by killing it. Examples of biological agents of use the present invention that are chemicals of use on seeds of ornamentals include those chemical agents most commonly used on arthropods such as rice weevil, Sitophilus oryza; granary weevil, Sitophilus granaries; lesser grain borer, Rhyzopertha dominica; Angoumois grain moth, Sitotroga cerealella; cadelle, Tenebroides mauritanicus; saw-toothed grain beetle, Oryzaephilus surinamensis; flat grain beetle, Cryptolestes pusillus; flour beetles, Tribolium species; dermestids, Trogoderma species; bruchids, several bean and cowpea weevils; Indian-meal moth, Plodia interpunctella; and almond moth, Ephestia cautella. Examples of suitable chemicals of use in the invention may be selected from the pyrethroids, such as a- cypermethrin, λ-cyhalothrin, [cyano-(3-phenoxyphenyl)-methyl] 3-(2,2-dibromoethenyl)-2,2- dimethyl-cyclopropane-1 -carboxylate (deltamethrin), and τ-fluvalinate, the organophosphates such as chlorpyriphos (diethoxy-sulfanylidene-(3,5,6-trichloropyridin-2- y oxy-I^J-phosphane), malathion (diethyl 2 dimethoxyphosphino -thioyl- sulfanylbutanedioate), coumaphos (3-chloro-7-diethoxyphosphinothioyloxy-4- methylcoumarin), and stirifos ([(E)-2-chloro-1-(2,4,5-trichlorophenyl)ethenyl] dimethyl phosphate) the carbamates such as amitraz (N-(2,4-dimethylphenyl)-N-[(2,4- dimethylphenyl)iminomethyl]-N-methylmethanimidamide), the spinosans such as spinosad (Dow Agrichemical, France), the gamma amino butyric acid (GABA) inhibitors such as fipronil (5-amino-1 -[2,6-dichloro-4-(trifluoromethyl)phenyl]-4 (trifluoromethylsulfinyl) pyrazole- 3-carbonitrile), the neonicotinoids such as imidacloprid ( V-[1-[(6-Chloro-3-pyridyl)methyl]- 4,5-dihydroimidazol-2-yl)nitramide), the anthranilamides, the formononetins such as 7- Hydroxy-3-(4-methoxyphenyl)chromone, the essential oils such as tea tree oil, thyme oil (also known as thymol), citronella oil, and menthol, and the insect growth regulators such as methoxyfenozide (f\ -iert-butyl-A/-(3-methoxy-o-toluoyl)-3,5-xylohydrazide) and the like.

Examples of live biological agents (also known as biocontrol organisms or biocontrol agents) that are commonly referred to in the art as "biological antagonists" that may be used in coating compositions of the present invention include Pseudomonas spp., Trichoderma spp., Streptomyces spp., such as Streptomyces lydicus (available from Natural Industries Inc., Houston, Texas, USA), Ampelomyces quisqualis isolate -10 (available from Ecogen Inc. Langhorne, USA), Bacillus spp., such as Bacillus subtilis GB03, 8. lichenformis, and 8. megaterium (all available from Growth Products, White Plains, USA), Coniothyrium minitans (available from Prophyta Biologischer Pflanzenschutz GmbH, Germany), Agrobacterium radiobacter Strain 84 (available from AgbioChem Inc, Florida, USA), Erwinia amylovora HrpN harpin protein (available from Eden Bioscience Corp., Bothell WA, USA), Streptomyces griseoviridis strain 61 (available from Kemira Agro Oy, Helsinki, Finland), Agrobacterium radiobacter K1026 (available from Bio-care Technology, Australia), Gliocladium catenulatum (available from Kemira Agro Oy, Helsinki, Finland), Trichoderma harzianium Rifai strain RL-AG2 (T-22)(available from Bioworks Inc, Geneva, USA), and Gliocladium v/rens (aka Trichoderma virens) GL-21 (available from Certis Inc., Columbia, USA).

The skilled addressee will appreciate that compositions of the invention may also be added direct to the soil or growing medium into which plant structures as herein defined are to be planted. Such compositions may be added as powders and mixed with the soil or applied as liquid suspensions using conventional procedures.

Soil borne pathogens for the purposes of the present invention are ones that are able to colonise the ornamental plant structure as defined herein, such as the seed cuticle and/or ones that populate the soil and which are capable of acting on ornamental plant structures as defined herein. Such soil borne pathogens are typically bacteria and/or fungi. Examples of soil bome bacterial and fungal pathogens that attack ornamental plants include species of Rhizoctonia solani (e.g. active against verbena; anemone; dahlia; impatiens; primula; poinsettia), Botrytis spp. such as Botrytis cinerea (e.g. active against viola), Chalara elegans (e.g. active against verbena; cyclamen), Cylindrocarpon destructans (e.g. active against cyclamen), Cylindrocladiella peruvania (e.g. active against cyclamen), Erwinia chrysanthemi (e.g. active against Euphorbia pulcherrima (poinsettia)), Pythium spp (e.g. active against impatiens; primula), Agrobacterium tumefaciens (e.g active against anemone; carnation; dahlia; geraniums (pelargonium); primula; poinsetUa), Phytophthora spp. (e.g. active against impatiens; geraniums (pelargonium)); species such as phytophthora tentaculata (e.g. active against Chrysanthemum, Verbena, and Delphinium species, Sclerotinia sclerotiorum, Fusarium spp., and Verticillium spp., such as Verticillium albo-atrum (e.g. active against woody ornamentals such as maple, elm, aspen, ash, beech, and oak; chrysanthemum).

According to a further aspect of the invention there is provided use of organic carrier particles of wax in the manufacture of a coating composition as defined herein that includes a biological agent as defined herein above. In a preferment of this aspect of the invention, the coating composition is a seed coating composition. In a further preferment of this aspect of the invention the coating composition is a storage organ coating composition wherein the storage organ is selected from tubers, tuberous roots, corms, bulbs and rhizomes. The organic carrier particles are selected from natural waxes, synthetic waxes, and mineral waxes having a melting point of ≥50°C, more preferably of ≥60°C, and most preferably are made up of hard waxes having a melting point of≥70°C. Suitable waxes of use in this aspect of the invention may be selected from waxes such as carnauba wax, beeswax, montan wax, Chinese wax, shellac wax, spermaceti wax, myricyl palmitate, cetyl palmitate, candelilla wax, castor wax, ouricury wax, wool wax, sugar cane wax, retamo wax, and rice bran wax or a mixture of two or more thereof. Preferably, the seed coating that is employed in this aspect of the invention includes carnauba wax as the organic carrier. Preferably, in this aspect of the invention, the organic carrier particles have a mean volume diameter from >5pm, such as in the range >8pm to 200pm, as herein described.

In a third aspect of the invention there is provided use of wax as an organic carrier in particulate form in an ornamental structure coating composition as described herein. The organic carrier particles in this aspect of the invention are selected from natural waxes, synthetic waxes, and mineral waxes having a melting point of ≥50°C, more preferably of ≥60°C, and most preferably are made up of hard waxes having a melting point of 70°C. Suitable organic carrier particles of use in this aspect of the invention may be selected from carnauba wax, beeswax, montan wax, Chinese wax, shellac wax, spermaceti wax, myricyl palmitate, cetyl palmitate, candelilla wax, castor wax, ouricury wax, wool wax, sugar cane wax, retamo wax, and rice bran wax or a mixture of two or more thereof. Preferably, the wax carrier particles of use in this aspect of the invention comprise organic carrier particles of carnauba wax. Preferably still, the organic carrier particles of use in this aspect of the invention have a mean volume diameter >8pm, such as in the range of >10pm to 200pm.

In a fourth aspect of the invention there is provided a method of manufacturing a plant structure coating composition as herein described that comprises

1) selecting an organic carrier material wherein the carrier materia) is selected from waxes having a melting point of≥50° Centigrade;

2) comminuting said organic carrier material into particles of a desired mean volume diameter in the range from≥5pm, such as in the range≥8pm to 200pm; and

3) adding biological agent to the product particles of step 2).

The biological agent of use in this aspect of the invention is selected from a chemical agent which is an arthropodicide such as an insecticide or an acaricide or a mixture thereof, a fungus species and/or a bacterium species or a mixture of one or more thereof. Suitable fungus species and bacterium species may be selected from Pseudomonas spp., Trichoderma spp., Streptomyces spp., such as Streptomyces lydicus, Ampelomyces quisqua!is isolate M-10, Bacillus spp., such as Bacillus subtilis GB03, B. lichenfonnis, and B. megaterium, Coniothyrium minitans, Agrobacterium radiobacter Strain 84, Erwinia amylovora HrpN harpin protein, Streptomyces griseoviridis strain K61 , Agrobacterium radiobacter K1026, Gliociadium catenulatum, Trichoderma harzianium Rifai strain KRL-AG2 (T-22), and Gliociadium virens (aka Trichoderma virens) GL-21 and the like.

The organic carrier material in this aspect of the invention may be selected from waxes such as from those waxes as hereinbefore described. Suitable waxes may be selected from waxes such as carnauba wax, beeswax, montan wax, Chinese wax, shellac wax, spermaceti wax, myricyl palmitate, cetyl palmitate, candelilla wax, castor wax, ouricury wax, wool wax, sugar cane wax, retamo wax, and rice bran wax or a mixture of two or more thereof. Preferably, the wax carrier particles of use in this aspect of the invention comprise dry particles of carnauba wax.

In a further aspect of the invention, there is provided a plant structure coating composition produced by the method as described herein.

In a further aspect of the invention there is provided a coating composition as described herein for use on a plant structure as defined herein. The coating composition may be applied to any ornamental plant structure such as those selected from those of varieties of tulip, amaryllis, hyacinth, daffodil, narcissus, cyclamen, lily, lily of the valley, iris, gladiolus, crocus, crocosmia, dahlia, snowdrop, bluebell, dahlia, freesia, gloxinia, anemone, fritillaria, alstromeria ligtu and hybrids thereof, camassia esculenta, arum italicum, muscari, agapanthus, begonia, acidanthera, ranunculus, ornamental allium; seeds of viola (pansy), primula, petunia, polyanthus, tagetes, pelargoniums including P. Peltatum_: begonia, cyclamen, achillea, ageratum, agrostemma, alyssum, amaranthus, antirrhinum, aquilegia, aster, calendula, campanula, carnation, chrysanthemum, helleborus, cineraria, clematis, convolvulus, Centaurea cyanus, cosmea, dahlia, delphinium, dianthus, digitalis, myosotis, freesia, geranium, godetia, impatiens, cheiranthus cheiri, dianthus barbatus, lathyrus odoratus, salvia, salpiglossis, verbena, zinnia; and seeds of ornamental plants of the arborvitae, acer, azalea, Chamaecyparis, dogwood, euonymus, rose, forsythia, Fraser fir, hemlock, Japanese holly, juniper, Pieris, rhododendron, Taxus, white pine, maple, elm, aspen, ash, beech, and oak.

In a further aspect of the invention there is provided a method of coating an ornamental plant structure with a coating composition that comprises an organic carrier material and a biological antagonist to one or more fungal or bacterial pathogens so as to limit damage by the said pathogens to the said plant structure, the method comprising adding a biological antagonist to an organic carrier material wherein the organic carrier material is in dry particulate form, mixing the two components together and applying the resulting composition in dry particulate form to the ornamental plant structure. Thus, the ornamental plant structure coating composition is applied in dry particulate form. Naturally, the skilled addressee will appreciate that the organic carrier material may also contain added pigments, plasticisers and other minor components as herein described. In an alternative, the seed coating may be applied in liquid form as herein described and then the seeds dried, leaving a coating composition that is in dry particulate form when on the seed. However, it is preferred that the coating composition is applied in dry, particulate form for ease of application and production costs are kept low. The plant structure in this aspect of the invention is selected from seeds, tubers, tuberous roots, corms, bulbs and rhizomes. The treatment composition is applied to the plant structure in dry particulate form or liquid form as hereinbefore described, and preferably in dry particulate form. The organic carrier material in this aspect of the invention may be selected from camauba wax, beeswax, montan wax, Chinese wax, shellac wax, spermaceti wax, myricyl palmitate, cetyl palmitate, candelilla wax, castor wax, ouricury wax, wool wax, sugar cane wax, retamo wax, and rice bran wax or a mixture of two or more thereof. Preferably, the organic carrier material is camauba wax in dry particulate form..

The treatment composition in this aspect of the invention includes one or more biological agents selected from chemical arthropodicides such as insecticides and acaricides, fungicides, bactericides and live biological agents. Preferably, the biological agents are selected from Pseudomonas spp., Thchoderma spp., Streptomyces spp., such as Streptomyces lydicus, Ampelomyces quisquatis isolate M-10, Bacillus spp., such as Bacillus subtilis GB03, β. lichenformis, and B. megaterium, Coniothyrium minitans, Agrobacterium radiobacter Strain 84, Erwinia amylovora HrpN harpin protein, Streptomyces griseoviridis strain K61 , Agrobacterium radiobacter K1026, Gliocladium catenulatum, Trichoderma tiarzianium Rifai strain KRL-AG2 (T-22), and Gliocladium virens (aka Trichoderma virens) GL-21.

There now follow examples that illustrate the invention. It is to be understood that the examples are not to be construed as limiting the invention in any way.

Examples Section

Control of Botrytis cinerea [United Kingdom National Culture Collection (UKNCC)] on pansy (Viola sp.) by means of seed treatments

Using the antagonists Trichoderma harzianum [Pseudomonas fluorescens and Bacillus subtilis [United Kingdom National Culture Collection (UKNCC)]

Grey Mould

Symptoms

Flowers turn a papery brown and become covered with grey, fuzzy masses. Senescing flowers are particularly susceptible. Tan to brown spots with a target-like appearance can also develop on the leaves. These patches are often associated with flowers which have dropped onto the leaf surface. This disease is particularly troublesome during periods of extended cloudy, humid, wet weather.

Disadvantages of Conventional Seed Treatment i) Limited dose capacity - The amount of pesticide that can be applied is limited by how much will actually stick to the

ii) Limited duration of protection - The duration is often short due to the relatively small amount of biological agent (e.g. chemical) applied to the seed, dilution of the biological agent as the plant grows, and breakdown of the biological agent. iii) Limited shelf life of treated seed - Producing excess treated seed is undesirable because the shelf life of treated seed may be limited.

All three of these limitations may be overcome or significantly reduced through the inclusion of carnauba wax particles as a carrier for a biological agent, in this case dormant microorganisms that are applied to seeds. Under favourable conditions, the microorganisms grow and colonize the exterior of the developing seed or seedling. Biological agents may help in reducing seed decay, seedling diseases, or root rot.

The following tests are performed to examine the potential effect of the inclusion of carnauba wax particles.

Phase One - isolate Cultures 1. Culture Maintenance

Records are kept with each isolate sub-culture being assigned an accession number. All plates and slides relating to that sub-culture are labelled with an accession number.

In addition, permanent lactophenol (LP) mount slide are made from each of the original cultures and file for reference purposes No more than three generations of sub-culture occur before passaging through a living host and re-isolating in order to maintain the fitness of the organism.

Sub-cultures are stored for future use on Potato Dextrose Agar (POA) at 4°c.

Each isolate is assigned an accession number and sub-cultures are labelled with that number.

DNA is extracted for identity verifications and stored at -20^'C. A reference sample of the pure culture is stored on glycerol at -20^"C. Upon completion of the experiment DNA identification of the culture is repeated to confirm that the organism has not mutated during the course of the work.

2. Culturing of the causal agent

Isolation of a pathogenic fungus from diseased tissue into pure culture is one of the standard techniques in identifying and describing a disease. It is an essential step in proving the pathogenicity of previously un-encountered organisms.

Techniques commonly involve: a. Surface-sterilisation treatment

b. Plating (possibly on selective medium) of samples of diseased tissue, with appropriate precautions.

c. Sub-culturing to get pure cultures.

3. Purification of Cultures

Small disinfected root pieces of an artificially inoculated plant are cultured on water agar. The fungal colonies that appear most frequently are likely the target pathogen. Several saprophytes may also be present in infected plant tissues and they may grow into the medium with the principal pathogen. Routine surface-sterilisation consists of wiping the tissue with (or immersing in) 0.1% solution of sodium hypochlorite (NaOCI - sometimes referred to as "NaCIO") followed by rinsing with sterile distilled water. To obtain a pure culture of the pathogen, a small sample is taken from the growing edge of a colony with a flamed loop or scalpel and streaked over the surface of a pre-poured plate of PDA. The inclusion of chloramphenicol (a bacteriostatic anti-microbial) at 30mg/l reduces the risk of bacterial contamination. As the streak progresses over the agar, fungal spores are separated until single spores are obtained from which separate colonies will grow. Repeat this procedure until pure cultures are obtained.

4. Single Spore Isolation

Single spore isolations are important to investigate pathogenic variability. An inoculum of spores is placed in a tube containing 10 ml of sterile water. This spore suspension is streaked along a marked line on the surface of a thin tap water agar medium, and incubated at 22°C. After 24hr incubation, select germinated spores using a stereoscopic microscope and transferred one spore at a time to another agar plate.

5. Slide Preparation for Microscopic examination and reference

Identification of the pathogen, rather than the disease, requires microscopic examination of infected tissue. The tissue may be sectioned or surface scraped and then mounted in water/lactophenol. Fungal structures seen macroscopically may be separated from the host tissue to be examined and identified. Identification depends on spore formation and therefore infected material is incubated in a moist environment overnight prior to examination in order to encourage sporulation. Cotton blue stain is added to the lactophenol in order to highlight fungal structure. The specimen is placed in a drop of stain on a glass slide and gently warmed by passing through a low flame for a few seconds before mounting in lactophenol.

Whole mount sections can be cleared and stained for ease of identification using the following method:

Leaf disks are rendered clear by heating in tube in lactophenol until clear (up to 20 minutes), without boiling. Stain by heating in 0.5%cotton blue in lactophenol on a slide for 5-10 minutes. Rinse thoroughly in lactophenol and mount in the same.

6. Growth and Media

Sub-cultures are assessed for growth and germination at a range of temperatures, 13.5°C, 18°C and 22.5°C. A range of media is examined for suitability. Whilst PDA is generally suitable for most fungal species it has been found that use of a low nutrient agar, such as tap-water agar, reduce prolific growth and can encourage sporulation. Therefore PDA, tap- water agar, and a selective media from literature, Czapek's Dox agar (Dawson (1962) Saboutaudia 1. 214-219), are included within the assessment trials

A 5mm diameter disk is cut from the margin of an actively growing culture using a flamed cork borer. This is placed upside down in the centre of the pre-poured media plates. Five replicates are made for each media type and temperature (45 plates in total). Complete randomisation is applied to plates in each incubator. Plates are observed until one culture succeeds in completely covering the plate in any one media. At this point the following measurements are taken: fungus colony diameter, colour and margin. In addition, the level of sporulation is recorded.

Five 5mm disks are cut from each plate using a flamed cork borer and suspended in 20ml of distilled water (+0.05% Tween 20®). The sample is then sonicated for 2 minutes to release the spores and then vortexed to aid the formation of a uniform spore suspension. Samples are assessed for spore concentration using an Improved Neubauer haemocytometer using standard counting methodology.

The mean for each media type is calculated and ANOVA is applied to examine the results for significant differences.

Phase Two - In vitro studies:

1. Screen microorganisms and carnauba wax to determine interactions

In order to explain effects observed the microorganisms, pathogens and antagonists, are screened against carnauba wax to identify any carrier only effect. This enables the determination of treatment effect as well as any synergy occurring as a result of the use of using an antagonist with carnauba wax particles. a. Plates of appropriate media are used based on the findings of the experiment above.

Air-milled carnauba wax is sterilised using the autoclave and then ground using a twin blade mill, producing particles with an approximate VMD of 130pm. The sterilised media is then cooled to 50°C (molten stage). The carnauba wax is then incorporated into the media. Two concentrations of carnauba wax are tested; 1g/l and 10gfl. A 5mm diameter disk is cut from the margin of an actively growing culture using a flamed cork borer. This is placed upside down in the centre of the pre-poured media/carnauba wax plates. Five replicates are made for each concentration and incubated at the optimum temperature for growth/sporulation (as determined in previous experiment). Growth rates and characteristics are compared to the controls using data from the Growth and Media experiment above.

Differences are analysed using ANOVA. b. Disks of the pathogen and antagonists are dusted with different carnauba wax treatments and put on appropriate media. The carnauba wax particles need to be free of microorganisms to be able to carry out this experiment. Growth of treated and untreated organisms is compared. 2. investigate antagonist action against pathogens i. Effect of antagonists on viability of B.cinerea mycelium (in vitro assay I)

All antagonistic isolates are tested in a dual culture assay against pathogenic fungi on PDA or alternative pre-defined media. Agar plugs of 8. cinerea and the antagonist isolate to be tested are arranged 7 cm apart on 9cm agar plates. Inhibition zones and zones of overlapping are assessed after 7 days incubation at 13.5°C, 8°C and 22.58°C. Where an antagonist overgrows the mycelium of B.cinerea, the zone of hyphal interaction between both is investigated microscopically (100x). Fungal strains without a microscopically visible effect on mycelium of B.cinerea are excluded from further experiments. Furthermore, the viability of B.cinerea in the region of interaction is tested by transfer of mycelial discs onto water agar plates 5 days after first contact. The B.cinerea mycelium is assessed as viable when the growth of typical hyphae is observed microscopically (100x). Each experiment is repeated three times with three samples per replicate. ii. Effect of antagonists on germination of B.cinerea sclerotia produced in vitro (in vitro assay H)

Sclerotia of B.cinerea of uniform size are placed on a 6 day old culture (PDA, 20°C) of the fungal antagonist. After incubation for 14, 28 and 35 days at 20°C, eight sclerotia per replicate (three replicates per antagonist) are transferred from the agar plate onto water agar. Mycelial growth from these sclerotia is assessed under a light microscope ( 00x).

3. Confirmation of pathogenicity

Steps to perform Koch's postulates (Koch 1890, criteria designed to establish a causal relationship between a causative microbe and a disease)

a) Describe the symptoms expressed by the diseased crop plants.

b) Isolate the suspected pathogen— the same cultures should be isolated from plants with similar symptoms

c) Obtain a pure culture and use it to inoculate healthy plant material.

d) Observe the symptoms expressed by the inoculated plants— symptoms should be the same as those observed originally in the crop plants.

e) Re-isolate the pathogen from the newly diseased material. The culture should be the same as the original purified culture. i. Indirect Application - Plant Using healthy plants - soil can be inoculated directly using a spore suspension made from a pure agar culture or from a culture grown in flasks. A fungal spore or bacterial suspension can be added post-emergence so that the root system is drenched by the suspension. Plants are then observed over 7 days and symptoms recorded. Koch's Postulates are applied in order to confirm that the symptoms relate to the inoculated pathogen. Direct Application - Seed

Inoculum for preparing spore suspensions is grown on water agar containing sterile seeds. Fungal spores and hyphae or bacterial spore and vegetative growth are scraped from the colony and transfer to sterile water. This spore suspension is then applied to seeds and mixed to ensure a uniform distribution. Seeds are then:

• Placed on moist filter paper and incubated at optimum growth temperature for 5 days.

• sown in heat sterilised potting compost and incubated in a propagator at optimum growth temperature for 7 days

Symptom expression and germination is recorded for both sets of experiments and Koch's postulates applied

4. Carnauba Wax/Antagonist co-location analysis

A dry powder formulation of spores is produced using a spore separator. Moisture content of the formulation is reduced to below 5% using a dehumidifier and silica beads. Spore concentration is determined using a Neubauer haemocytometer and standardised counting methodology.

Steps in Air Milling in Boyes Micronisation Process (for carnauba wax particles with a VMD o approx. 15pm and 75pm, respectively)

1. 2kg carnauba wax blocks are first kibbled into approximately 4 to 6mm pieces in a KT Handling Ltd Model 04 kibbler (serial no. 729/C) following the manufacturer's instructions.

2. The kibbled pieces are then passed through an Apex Construction Ltd Model 314.2 Comminuting Mill (serial no. A21306) and reduced further in size to a range of 250 to 300um.

3. The comminuted particles are then passed through a Hosokawa Micron Ltd Alpine 100AFG jet mill (serial no. 168092) following the manufacturer's instructions, setting the mill at a suitable speed (a speed of 8000rpm for particles having a VMD of 15pm or at a speed of 2500rpm for particles having a V D of 75pm), with a positive system pressure of 0.03bar.

4. The grinding air is to be kept to 6 bar, the system rinsing air flow and Classifying Wheel gap rinsing air are both to be set at a minimum of 0.5 bar and no more than 0.75bar, the cleaning air filter is to register a delta of no more than 5bar to achieve a final particle size with a VMD of 5um or 75pm as required.

Entostat was combined with viola (pansy) seed at three loadings (see below).

Two sizes of camauba wax particle having V Ds of 15pm and 75pm, respectively, are examined in combination with the spore formulation at two different ratios (1:3, 2:2). Samples of the camauba wax/spore mixture are analysed using electron photomicroscopy to determine the co-location effect. Any variation observed is recorded.

In addition, both sizes of camauba wax referred to, are mixed with a homogenised sample of mycelium and examined as described above.

5. Camauba Wax Particle loading

Camauba wax particle adhesion to seeds is approximated through the use of photomicroscopy (qualitative) and fluorometric analysis (quantitative). Two sizes of camauba wax particles (with 1 % glo-brite) are used having a VMD of 15pm and 75pm, respectively. Four combinations: Two ratios of camauba wax/spore formulation, together with one mycelial and a vehicle control (camauba wax only), makes a total of eight treatments. Treatments will be applied to 10g of seed and replicated three times. Three subsamples are taken from each replicate and the mean used in analysis.

For fluorometric analysis three 1g samples are each be added to 5ml of ethanol and sonicated to aid the release of the carnauba wax particles from the seeds. Samples are analysed using a Perkin Elmer L55 Fluorometer (Perkin Elmer, Ma, USA). Statistical analysis of variation between treatments is performed using ANOVA.

Seed size and architecture varies greatly between crop species and this influences application rates and method. A homogeneous mix is attained through tumbling seed and carnauba wax formulation in a cylinder, adapted to produce lateral mixing/tumbling through the inclusion of angled interior vanes, placed on a Wheaton roller for 5 minutes.

Phase Three - In vivo:

B.cinerea, together with the most successful antagonist model is used in a series of in vivo experiments. The basic design is a split-plot experiment with temperature being the main plot factor (13.5X, 18°C and 22.5°C) and camauba wax antagonist ratio (3 treatments: 2x spore, 1 x mycelial) being the sub-plot. Four homogeneous mixes of each treatment are prepared using the method described above and these represent the replicates. Treatments:

1 ) Application rate 1 - 7.5 x 10⁶ conidia kg^"1

2) Application rate 2 ~ 7.5 x 10^s conidia kg^"1

3) Application 3 - Mycelia

4) Control 1 - Vehicle control (Carnauba wax only)

5) Control 2 - no treatment Mixes (true replicates): A, B, C, D Subsamples of each mix: α, β, y

Mixes and treatments are arranged according to a Randomised Block design. Pot studies

Each temperature (growth chamber) contains 60 plant pots.

Treated seed is sown in accordance with supplier's recommendation. Soil/compost (1 :1 John Innes No.2 and peat compost) is heat sterilised prior to inoculation with 10ml of B.cinerea spore suspension and thoroughly mixed before sowing.

Plants are placed in the growth chambers for a period of 21 days with observations of symptom expression made every 48 hours post emergence. Water is applied through capillary matting twice daily.

After 21 days plants are removed from their pots and the following assessment measurements taken:

• % germination

• % pre-emergence damping off

• % post-emergence damping off

• Root weight

• Shoot weight

In addition, symptom expression is assessed based on a damage scale.

Means of the measurements taken from the subsamples α, β, y are compared for each treatment using ANOVA. Samples are taken from 5 plants exhibiting symptoms and Koch's Postulates applied to confirm the causal organism (by comparison to the reference slide of the master culture).

The experiment is repeated.

Second Example

Control of Pythium spp. [United Kingdom National Culture Collection (UKNCC)] on pansy (Viola sp.) by means of seed treatments using fludioxonil.

Experimental Design - as Pot Study above

Carnauba wax is melted using copper pans. During cooling fludinoxonil is added at 1% of the mass of the carnauba. This mixture is allowed to solidify before chipping and processing through a mill to produce particles with a VMD of 25μιη via the process described in example 1.

Treatments for the Pot Study- Control 1 - Vehicle control (Carnauba wax only) Control 2 - no treatment

Treatment 1 - 1 % fludinoxonil carnauba wax at 10g per kg of seed Treatment 2 - 1 % fludinoxonil carnauba wax at 3.2g per kg of seed Assessment and analysis as with previous Pot Study Third Example

Control of Peridroma saucia, the cutworm on pansy (V7o/a sp.) by means of seed treatments using thiamethoxam.

Early-season wireworm damage consists of hollowed-out seeds where larvae have entered during germination. Seedling plants also can be injured or killed by larvae tunnelling into the plant below the soil line. Occasionally, wireworms bore into the stalks of larger plants and tunnel in a few inches, but the damage is not significant.

Experimental Design - as Pot Study above

Carnauba wax is melted using copper pans. During cooling thiamethoxam is added at 1% of the mass of the carnauba. This mixture is allowed to solidify before chipping and processing through a mill to produce particles having a VMD of 25pm via the process described in example 1.

Treatments for the Pot Study- Control 1 - Vehicle control (Camauba wax only) Control 2 - no treatment

Treatment 1 - 1 % thiamethoxam carnauba wax at 4.2g per kg of seed

Treatment 2 - 1 % thiamethoxam camauba wax at 1.3g per kg of seed

Empty pots are lined with a nylon mesh screening material before filling with potting soil. A wire frame is constructed and the nylon meshed tied off over the frame to provide a caged experimental arena designed so that the insect cannot escape the treated area.

Seeds are allowed to germinate for three days before adding five 3^rd instar larvae to the soil surface of each pot before resealing the mesh cage.

Observations are made over 21 days.

Plants are assessed for:

• % germination

• Damage

• Root weight

• Shoot weight

The procedures detailed within Example One are followed to examine the antagonistic effect of Trichoderma harzianum [United Kingdom National Culture Collection (UKNCC)], Pseudomonas fluorescens [UKNCC] and Bacillus subtilis [UKNCC] on Alternaria sp., a fungal pathogen of Petunia (Petunia sp.).

The procedures detailed within Example One are followed to examine the antagonistic effect of Trichoderma harzianum [United Kingdom National Culture Collection (UKNCC)], Pseudomonas fluorescens [UKNCC] and Bacillus subtilis [UKNCC] on Botrytis cinerea, a fungal pathogen of Verbena (Verbena sp.). The procedures detailed within Example Two are followed to examine the effect of metalaxyl on Botrytis cinerea, a fungal pathogen of Petunia (Petunia sp.).

The procedures detailed within Example Two are followed to examine the effect of feranimol [(RS)-2,4'-dichloro-a-(pyrirnidin-5-yl) benzhydryl alcohol] on Thielaviopsis basicola, a fungal pathogen of verbena.

The procedures detailed within Example Three are followed to examine the effect of thiamethoxam on the verbena bud moth (Endothenia hebesanaan) insect pest of Verbena (Verbena sp.).

The procedures detailed within Example Three are followed to examine the effect of imidacloprid on variegated cutworm

{Peridroma saucia), an insect pest of Petunia (Petunia sp.).

Suppression of causal agents of fungal disease in Cyclamen (Cyclamen L.) using a seed coating comprised of Trichoderma sp. and carnauba wax particles

The potential for Trichoderma sp. (Ascomycota) as a biocontrol agent in the defence against plant pathogens is known.

Trichoderma hyphae are capable of penetrating the hyphae of other fungi and extracting nutrients from within, resulting in the suppression and eventual death of the host. Trichoderma exhibits rapid mycelial growth and is capable of out-competing other fungi for nutrients.

There are several commercially available formulations of Trichoderma marketed as crop protection products. These are commonly supplied as a wettable powder formulation and applied to the area of cultivation as a drench. The disadvantage of this form of application is that it is necessary to treat the entire cultivation area, whereas it is the region immediately surrounding the seed or plant that requires the treatment. The larger the number of conidia delivered to this area the greater the level of control they are able to impart. Therefore a targeted application system able to deliver sufficient conidia to the required area offers a distinct advantage in the use of Trichoderma over conventional applications.

Experimental Aim: To assess the potential use of Entostat as a seed-coating technology for the delivery of beneficial microbes

Methods

Steps in Air Milling in Boyes Micronisation Process (for carnauba wax particles with a VMD of approx. 10pm)

1. 2kg carnauba wax blocks are first kibbled into approximately 4 to 6mm pieces in a KT Handling Ltd Model 04 kibbler (serial no. 729/C) following the manufacturer's instructions. 2. The kibbled pieces are then passed through an Apex Construction Ltd Model 314.2 Comminuting Mill (serial no. A21306) and reduced further in size to a range of 250 to 300um.

3. The comminuted particles are then passed through a Hosokawa Micron Ltd Alpine 100AFG jet mill (serial no. 168092) following the manufacturer's instructions, setting the mill at a speed of 12,500rpm for particles having a VMD of 9.7pm), with a positive system pressure of 0.03bar.

4. The grinding air is to be kept to 6 bar, the system rinsing air flow and Classifying Wheel gap rinsing air are both to be set at a minimum of 0.5 bar and no more than 0.75bar, the cleaning air filter is to register a delta of no more than 5bar to achieve a final particle size with a VMD of 9.7μΓη.

Entostat was combined with cyclamen seed at three loadings (see below). 1. Baseline data: seed coating techniques

1.1. Seed Coating. Trichoderma harzianum (containing 7.75x10⁹ colony forming units g^"1 Sylvan Bio, Loches, France) with a germination percentage of 95% was applied to cyclamen seed (Hhp. Coum)) supplied by Nicky's Nursery, (Kent, UK) using carnauba wax particles with a VMD of 9.7pm. A target loading was set at 10⁵ conidia per seed based on information obtained from literature.

Carnauba particles were mixed with the dry conidia powder at different ratios and applied 0.01 g (0.2% by mass) directly to dry seed, 5g of seeds per concentration. For each concentration, four batches of 10 seeds were used for evaluation of conidia loading.

Conidia to carnauba ratios used were:

100% Conidia, 50% Conidia, 25% Conidia and 9% Conidia with the remainder in each case being made up of carnauba wax particles.

1.2. Enumeration. Direct enumeration to determine conidia loading of seeds was done through the use of a haemocyto meter (Improved Neubauer, Hawksley, Lancing, UK). Inoculum: Preparation of suspension.

Propagules are usually formulated in a water carrier, although those with hydrophobic cell walls (such as Trichoderma) are not readily suspended in water. To uniformly suspend hydrophobic propagules in water it is necessary to sonicate and/or use mechanical suspension methods. Mechanical suspension of propagules using micropestles provides good suspension of conidia in water without causing damage to cells. A surfactant may also facilitate suspension of propagules (Tween20 at 0.05%). To suspend hydrophobic conidia, harvested conidia are placed in a 1.5ml microcentrifuge tube, =0.5ml of sterile water is added to the tube, the micropestle is inserted into the tube, and the conidial mass is gently agitated with the micropestle by hand. The micropestle is the attached to the motor (e.g. Kontes, Argos pellet pestle motor) and the suspension is vigorously agitated while moving the pestle in and up and down, and side to side motion, circa. 30 seconds. Since the haemocytometer method does not distinguish between viable and non-viable propagules, it is necessary to determine spore viability so that doses can be prepared on the basis of viable propagules.

Seed washes and enumeration of Trichoderma loadings were done on 4 batches of seeds per treatment. Inoculum was washed from seeds by placing into 1 ml sterile 0.05% Tween20 (or substitute - similar non-ionic surfactant/dispersal agent) in a Eppendorf tube and vortexing for 30 seconds to remove conidia from the seed surface. Samples were then sonicated for two minutes to break up any conidial clumping. Counts obtained were used to calculate the mean conidia loading of seed coated with the various treatments. Results obtained using 100% conidia powder were used as a benchmark and the conidia/carnauba combination powders compared against it as a determination of efficiency of loading.

Confirmation of conidial viability was achieved by dilution plating on Trichoderma Specific Media (TSM) (see below). A dilution series was set up and duplicate plates inoculated from the series. Colony Forming Units (CFU) counts were made after 7 days, allowing inoculum levels on seeds to be quantified. In addition, fresh, unused conidia were plated to provide a comparison of before and after seed application.

Germination percentage was also measured. A satisfactory density of conidia was obtained by spreading approximately 10⁶ conidia in 100μΙ on the media in a 9cm petri dish. Conidia were incubated in the dark at 25°C for five days, and the area to be observed was then fixed using lactophenol. Phase contrast microscopy using an inverted compound microscope enabled sufficient examination of the conidia.

Conidia were considered viable if germtube lengths were two times the diameter of the propagule in question. Numbers of germinated and non-germinated conidia in arbitrarily- selected fields of view or in parallel transects, defined with an ocular micrometer, were counted. A minimum of 300 conidia were counted to provide an accurate estimate. It is desirable to determine the viability of propagules on replicate cultures and at various positions on the same plate.

This allowed calibration of the seed-coating techniques to obtain similar levels of Trichoderma loadings on the seeds for each coating method. 7.3. Seed Germination. One batch (5 seeds) of seeds from each treatment was placed on seed test paper (Whatman 181) in a 9cm Petri dish. Dishes were sealed with Parafilm and held at 20°C for 7-10 days and germination rate determined. This was repeated with untreated seed.

Trichoderma Selective Media (adapted from Williams, Clarkson et al 2003) was prepared as follows:

For 1000ml

Basal Medium Ingredients:

0.2g MgS0₄ 3.0g glucose

0.9g K₂HP0₄ 0.15g rose bengal

0.15g KCI 20g agar

1.0g NH₄N0₃ 950ml distilled water

Basal Medium Process

Mix liquid ingredients with all solid ingredients, except the agar in a 1L Erlenmeyer flask. Add the 20g agar and stir or shake. Plug with cyclamen wool and cover with foil. Autoclave.

Biocidal Medium (per litre)

0.25g crystallized chloramphenicol

0.2g quintozene

0.2g captan

1.2ml propamocarb (Previcur)

50ml sterile distilled water Summary

Cyclamen seed can be coated with Trichoderma spores in excess of the target 10⁵ spores seed^*1 for all treatments.

Use of Entostat increases the efficiency of spore delivery as a result of a reduction in wasted or lost spores.

The germination viability of the spores was unaffected by their use as a seed coating.

Enumeration through direct counting of spores using a haemocytometer or through the use of CFU counting gives statistically similar results and therefore either method may be used once germination viability has been proved unaffected by the treatment.

The described method for cyclamen L as provided above is used to assess the delivery efficiency of spores by Entostat to seeds of viola, pelargonium, and poinsettia. Similar results are obtained.

Effects of seed coating on disease suppression

Seeds are coated with Trichoderma using water or Entostat to achieve loadings of ca. 1Q⁴ and 10⁵ CFUs seed^"1. Water treatments are suspensions of spores in sterile water in which the seed samples are soaked for one hour. Seeds are then dried back, a likely commercial scenario, or sown wet coated. Entostat is applied at ratios of 3.1 , and 9: , Entostat to spores respectively. Seed treatment methods are then compared for their ability to protect germinating cyclamen seedlings from Phytophthora sp., one of the causal agent of root rot disease in cyclamen.

Inoculation of seeds with Trichoderma. Cyclamen Hhp. Coum is inoculated as follows (target concentration per seed):

) Trichoderma at 10⁴/seed using a water suspension (wet coating)

2) Trichoderma at 0⁵/seed using a water suspension (wet coating)

3) Trichoderma at 10⁴/seed using a water suspension (dry coating)

4) Trichoderma at 10⁵/seed using a water suspension (dry coating)

5) Trichoderma at 10 /seed using Entostat at 3:1

6) Trichoderma at 10⁵/seed using Entostat at 3:1

7) Trichoderma at 10⁴/seed using Entostat at 9:1

8) Trichoderma at 10⁵/seed using Entostat at 9:1 9) No Trichoderma, water only

10) No Trichoderma, Entostat only

11 ) Seed only

Enumeration. Trichoderma is quantified using standard dilution plating methods on Trichoderma specific media. This confirms CFU loadings per seed for treatments 1-8. Dilution platings are carried out in duplicate.

Phytophthora bioassay

inoculum preparation - Phytophthora sp., known to be pathogenic on many ornamentals, such as cyclamen, poinsettia, viola and pelargonium, are grown on PDA plates from stock cultures, and incubated at 20°C to produce actively growing colonies. Agar plugs are removed from the plates and used to inoculate sterilised (autoclaved at 21 °C for 20 mins) John Innes No.2 potting mix (60% moisture content; 60g) mixed with potato cubes (2 mm², 25g) in 500ml Erlenmeyer flasks. Flasks are incubated at 20°C for 14 days. Inoculum levels in the medium are quantified using a dilution plating method.

Effectiveness of seed treatment on Phytophthora. Seeds are sown into individual cells of seed trays containing Phytophthora -inoculated medium (approx. 15ml/cell). Four replicate batches of ten seeds per treatment are planted into the cells. Once sown, the trays are placed in a plant growth chamber (Weiss Gallenkamp Fitotron SG120) at 20°C with ca. 16h lighting. Cells are bottom watered. The number of seedlings surviving is recorded every 3 days for 21 days.

Time to emergence, percentage successful emergence and percentage plants expressing symptoms (including lesions and cankers) are recorded and the results analysed. Differences in Entostat treated seed and untreated seed are observed.

The described method for cylamen L. seed as provided above is used to assess time to emergence, percentage successful emergence and percentage plants expressing symptoms are recorded for seeds of viola, pelargonium, and poinsettia. Similar results as obtained for Entostat treated and untreated cyclamen seed are obtained. Differences in Entostat treated seed and untreated seed are observed.

Claims

1. A dicotyledonous ornamental plant structure coating composition, wherein the said coating composition comprises at least one organic carrier material in the form of particles wherein the carrier material is selected from waxes having a melting point of ≥50° Centigrade and one or more biological agents that possess an activity against at least one or more pathogens of a dicotyledonous ornamental plant.

2. A coating composition according to claim 1 wherein the plant structure is selected from seeds and storage organs such as tubers, tuberous roots, corms, bulbs and rhizomes.

3. A coating composition according to claim 1 or claim 2, wherein the plant structure is that of a seed of an ornamental plant.

4. A coating composition according to any one of claims 1 to 3, wherein the particles of wax have a volume mean diameter of >5pm.

5. A coating composition according to any one of claims 1 to 4, wherein the particles have a volume mean diameter in the range of from 8 to 200pm.

6. A coating composition according to any one of claims 1 to 5 wherein the biological agent is selected from a chemical agent, a fungus species and/or a bacterium species, or a mixture of two or more thereof.

7. A coating composition according to any one of claims 1 to 6 wherein the biological agent is selected from an insecticide and an acaricide.

8. A coating composition according to any one of claims 1 to 6 wherein the biological agent is selected from Pseudomonas spp., Trichoderma spp., Streptomyces spp., such as Streptomyces lydicus, Ampelomyces quisqualis isolate -10, Bacillus spp., such as Bacillus subtilis GB03, S. lichenformis, and B. megaterium, Coniothy um minitans, Agrobacterium radiobacter Strain 84, Erwinia amylovora HrpN harpin protein, Streptomyces griseoviridis strain K61 , Agrobacterium radiobacter K1026, Gliocladium catenulatum, Trichoderma harzianium Rifai strain KRL-AG2 (T-22), and Gliocladium virens (aka Trichoderma virens) GL-21 .

9. A coating composition according to any one of claims 1 to 8 wherein the organic carrier material is selected from waxes having a melting temperature of ≥50°C such as carnauba wax, beeswax, montan wax, Chinese wax, shellac wax, spermaceti wax, candelilla wax, castor wax, ouricury wax, and rice bran wax or a mixture of two or more thereof.

10. A coating composition according to any one of the preceding claims wherein the particles are carnauba wax particles.

11. A coating composition according to any preceding claim wherein the pathogen is a bacterial species, a fungal species or an arthropod species.

12. A coating composition according to any one of claims 1 to 6, 8 or 9 wherein the live biological agent is at least one biological antagonist is present in the form of bacterial spores and/or fungal spores located on the surface of the said particles and/or on the surface of the said ornamental plant structure.

13. Use of an organic carrier wherein the organic carrier is made up of particles of wax in the manufacture of a coating composition according to any one of claims 1 to 12 that includes a biological agent as defined in any one of claims 3 to 5.

14. Use according to claim 3 wherein the coating composition is an ornamental plant seed coating composition.

15. Use according to claim 13 wherein the coating composition is an ornamental plant storage organ coating composition wherein the storage organ is selected from tubers, tuberous roots, corms, bulbs and rhizomes.

16. Use according to any one of claims 13 to 15 wherein the organic carrier particles are selected from waxes having a melting temperature of ≥50°C such as carnauba wax, beeswax, montan wax, Chinese wax, shellac wax, spermaceti wax, candelilla wax, castor wax, ouricury wax, and rice bran wax; or a mixture of one or more thereof.

17. Use according to any one of claims 13 to 16 wherein the seed coating composition includes carnauba wax.

18. Use according to any one of claims 13 to 17 wherein the organic carrier particles have a mean volume diameter≥5pm, such as in the range≥8 m to 200pm.

19. A method of manufacturing a plant structure coating composition according to any one of claims 1 to 10 that comprises

1 ) selecting an organic carrier material;

2) comminuting said organic carrier material into particles of a desired volume mean diameter≥5pm, such as in the range 8pm to 200pm; and

3) adding a biological agent to the product particles of step 2).

20. A method according to claim 19 wherein the organic carrier material is selected from waxes having a melting temperature of ≥50^eC, such as carnauba wax, beeswax, montan wax, Chinese wax, shellac wax, spermaceti wax, candelilla wax, castor wax, ouricury wax, and rice bran wax or a mixture of two or more thereof.

21. A method according to claim 20 wherein the material is carnauba wax.

22. A coating composition according to any one of claims 1 to 12 and claim 20 when used on an ornamental plant structure as defined in claim 1.

23. A coating composition according to claim 22 wherein the ornamental plant structure is selected from those of varieties of tulip, amaryllis, hyacinth, daffodil, narcissus, cyclamen, lily, lily of the valley, iris, gladiolus, crocus, crocosmia, dahlia, snowdrop, bluebell, dahlia, freesia, gloxinia, anemone, fritillaria, atstromeria ligtu and hybrids thereof, camassia esculenta, arum italicum, muscari, agapanthus, begonia, acidanthera, ranunculus, ornamental allium; seeds of viola (pansy), primula, petunia, polyanthus, tagetes, pelargoniums including P. Peltatum, begonia, cyclamen, achillea, ageratum, agrostemma, alyssum, amaranthus, antirrhinum, aquilegia, aster, calendula, campanula, carnation, chrysanthemum, helleborus, cineraria, clematis, convolvulus, Centaurea cyanus, cosmea, dahlia, delphinium, dianthus, digitalis, myosotis, freesia, geranium, godetia, impatiens, cheiranthus cheiri, dianthus barbatus, lathyrus odoratus, salvia, salpiglossis, verbena, zinnia; and seeds of ornamental plants of the arborvitae, azalea, Chamaecyparis, dogwood, euonymus, rose, forsythia, Fraser fir, hemlock, Japanese holly, juniper, Pieris, rhododendron, Taxus, white pine, maple, elm, aspen, ash, beech, and oak.

24. A method of coating a plant structure with a coating composition wherein the coating composition comprises an organic carrier material that is a wax having a melting point of >50°C and at least one biological antagonist to one or more fungal or bacterial pathogens, the method comprising adding the said biological antagonist to the said organic carrier material, mixing the two components together and applying the resulting composition to the plant structure.

25. A method according to claim 24, wherein the plant structure is a non-germinated structure that is selected from seeds, tubers, tuberous roots, corms, bulbs and rhizomes.

26. A method according to claim 24 or claim 25 wherein the coating composition comprises a particulate composition that when applied to the plant structure is in a dry particulate form.

27. A method according to any one of claims 24 to 26, wherein the coating composition comprises an organic carrier material wherein the organic carrier material is awax having a melting point of≥50"C such as carnauba wax, beeswax, montan wax, Chinese wax, shellac wax, spermaceti wax, candelilla wax, castor wax, ouricury wax, and rice bran wax or mixtures of two or more thereof.

28. A method according to claim 27, wherein the coating composition includes one or more biological agents selected from insecticides and acaricides, fungicides, bactericides and live biological agents.

29. A method according to any one of claims 24 to 28 wherein the carrier material is camauba wax.

30. A method according to claim 28 or claim 29, wherein the biological agent is selected from Pseudomonas spp., Trichoderma spp., Streptomyces spp., such as Streptomyces lydicus, Ampeiomyces quisqualis isolate M-10, Bacillus spp., such as Bacillus subtilis GB03, B. lichenformis, and B. megatenum, Coniothyrium minitans, Agrobacterium radiobacter Strain 84„ Streptomyces griseoviridis strain K61 , Agrobacterium radiobacter K1026, Gl/ocladium catenulatum, Trichoderma harzianium ifai strain KRL-AG2 (T-22), and Gliocladium virens (aka Trichoderma virens) GL-21.

31. A dicotyledonous ornamental plant structure comprising a coating composition according to any one of claims 1 to 12, and claims 22 and 23.

32. A plant structure according to claim 31 that is a coated ornamental plant seed or a coated ornamental plant bulb or a coated ornamental plant tuber.

33. A plant structure according to claim 31 or claim 32 that is a coated ornamental plant seed.