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Pesticidal Composition And A Process For Its Preparation

Abstract: The present disclosure relates to a pesticidal composition comprising a synergistic combination of cartap hydrochloride, at least one anilide, and tricyclazole. The pesticidal composition of the present disclosure provides a stable, and ready to use pesticidal composition exhibiting synergistic activity and enhanced efficacy. The present disclosure also provides a process for preparing the pesticidal composition. The pesticidal composition can be used for the protection of crops from pests to obtain improved yield of crops.

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Patent Information

Application #
Filing Date
07 August 2017
Publication Number
11/2019
Publication Type
INA
Invention Field
AGROCHEMICALS
Status
Email
dewan@rkdewanmail.com
Parent Application
Patent Number
Legal Status
Grant Date
2020-10-15
Renewal Date

Applicants

INDOFIL INDUSTRIES LIMITED
Kalpataru Square 4th Floor, Andheri (E) Kondivita Road, Off Andheri- Kurla Rd. Mumbai Maharashtra INDIA 400 059

Inventors

1. RAO, Jayprakash Gopalkrishnan
Gokulnagari Nx- K-5/502 Khadakpada, Kalyan(W) Mumbai Maharashtra INDIA 42130
2. BORSE, Mayur
Ram Niwas appt , Near Apna Bazar Market Kalher Tal Bhiwandi, Dist Thane. Maharashtra INDIA
3. PATIL,Vilas Kashinath
Flat no 201 , A-wing Om Sai Appt Swapna nagari, Shantnu Society, Badlapur (west) Mumbai Maharashtra INDIA

Specification

DESC:FIELD
The present disclosure relates to a pesticidal composition and a process for its preparation.
DEFINITIONS
As used in the present disclosure, the following terms are generally intended to have the meaning as set forth below, except to the extent that the context in which they are used indicate otherwise.
Pesticide: Pesticides are substances that are meant to control pests or weeds. The term pesticide includes all of the following: herbicide, insecticide, insect growth regulator, nematicide, termiticide, molluscicide, piscicide, avicide, rodenticide, bactericide, insect repellent, animal repellent, antimicrobial, fungicide, disinfectant (antimicrobial), and sanitizer.
Nereistoxin: The term “nereistoxin” refers to a naturally occurring toxin capable of blocking both muscle and neuronal nicotinic acetylcholine receptors.
BACKGROUND
The background information herein below relates to the present disclosure but is not necessarily prior art.
In order to satisfy the food requirements of the growing population, it is important to maximize food production. One way of increasing the food production is to protect crops from harmful pests that reduce food production. Conventionally, chemicals such as organochlorines, organophosphates, organosulfurs, carbamates, formamidines, dinitrophenols, organotins, pyrethroid, pyrazoles, phenylpyrazoles, and pyrroles are used to control/manage pests.
Cartap hydrochloride is an insecticide belonging to the thiocarbamate class of insecticides. Cartap hydrochloride is a systemic insecticide having stomach and contact action, and is used for controlling chewing and sucking pests, which results in insect paralysis, and hence insects are not able to feed, and die of starvation. Cartap hydrochloride is typically used, at a concentration in the range of 0.4-1.0 kg/ha, for control of chewing and sucking insects (particularly Lepidoptera and Coleoptera), at almost all stages of development, on many crops, including rice (Chilo suppressalis, Cnaphalocrocis medinalis, Lissorhoptrus oryzophilus and rice-leaf beetle), potatoes, cabbage and other vegetables (Agromyzidae, Leptinotarsa decemlineata and Plutella xylostella); also on soya beans, peanuts, sunflowers, maize, sugar beet, wheat, pearl barley, pome fruit, stone fruit, citrus fruit, vines, chestnuts, ginger, tea, cotton, and sugar cane.
The structure of cartap hydrochloride is given herein below as Formula-1.


Formula-1
Tricyclazole is a fungicide belonging to the triazole class of fungicides. Tricyclazole is a systemic fungicide for protecting paddy crops. Tricyclazole is applied in the form of a flat drench, transplant root soak, and foliar application. Conventionally, one or two applications by the aforestated methods provide a season long control of the disease. The IUPAC name of tricyclazole is 5-Methyl-1,2,4-triazolo [3,4-b] [1,3] benzothiazole. The structure of tricyclazole is given herein below as Formula-2.


Formula-2
Anilides are a diverse group of fungicides. Anilides are aromatic molecules with the chemical formula C6H5NH2. Anilides are the broader class of anilines, which are often classified as amines due to the –NH2 group. Different molecular groups may be attached to the phenol group (which makes the molecule an aromatic) and determined the product and their biological activity. Unquestionably the greatest group of anilides is the phenylamide fungicides. The anilide fungicides have exceptional protectant activity on the genera Botrytis, Monilinia, and Sclerotinia. The mode of action of anilides is inhibition of succinate dehydrogenase, an enzyme in both the electron transport system and citric acid cycle that converts glucose into Adenosine triphosphate (ATP). Combating resistance becomes an issue with the wide scale use of these fungicides.
The mode of action for cartap, anilide and tricyclazole are totally different, as they are unique in their targeted pest(s). However, these pesticides are applied individually at different times, during the growth of the plant crop, and are therefore labour intensive and time consuming.
Therefore, there is felt a need for a synergistic pesticidal composition having enhanced efficacy and ready to use form in a single application. There also exists the need for pesticidal composition that combine knock-down activity with prolonged control, i.e., with long lasting action and help prevent/overcome resistance.
OBJECTS
Some of the objects of the present disclosure, which at least one embodiment herein satisfies, are as follows:
It is an object of the present disclosure is to ameliorate one or more problems of the prior art or to at least provide a useful alternative.
Another object of the present disclosure is to provide a synergistic pesticidal composition which solves the problems of reducing the dosage rate.
Still another object of the present disclosure is to provide a stable and ready to use pesticidal composition.
Yet another object of the present disclosure is to provide a pesticidal composition having enhanced efficacy or enhancing the spectrum of activity.
It is therefore an object of the present disclosure to provide a pesticidal composition which show enhanced action against pests compared to the control rates that are possible with the individual compounds and/or is suitable for improving the health of plants when applied to plants, parts of plants, plant propagation materials, or at their locus of growth.
Other objects and advantages of the present disclosure will be more apparent from the following description, which is not intended to limit the scope of the present disclosure.

SUMMARY
The present disclosure provides a pesticidal composition and a process for its preparation. The present disclosure provides a pesticidal composition comprising cartap hydrochloride, at least one anilide and a tricyclazole.
The pesticidal composition comprises a synergistic combination of cartap hydrochloride in an amount in the range of 0.1 wt% to 50 wt% of the composition, at least one anilide in an amount in the range of 0.1 wt% to 40 wt % of the composition, and tricyclazole in an amount in the range of 0.1 wt% to 40 wt% of the composition. The pesticidal composition further comprises agrochemically acceptable additives selected from the group consisting of the group consisting of at least one surfactant, at least one stabilizer, at least one filler, at least one coloring agent, at least one acidifying agent, and at least one carrier.
The synergistic action of cartap hydrochloride, anilide, and tricyclazole, along with the specific combination of the ingredients used in the present disclosure provides improved bio-efficacy. The pesticidal composition of the present disclosure may be used to prevent/treat multiple pests through a single application.
DETAILED DESCRIPTION
Embodiments are provided so as to thoroughly and fully convey the scope of the present disclosure to the person skilled in the art. Numerous details, are set forth, relating to specific components, and methods, to provide a complete understanding of embodiments of the present disclosure. It will be apparent to the person skilled in the art that the details provided in the embodiments should not be construed to limit the scope of the present disclosure. In some embodiments, well-known processes, and well-known techniques are not described in detail.
The terminology used, in the present disclosure, is only for the purpose of explaining a particular embodiment and such terminology shall not be considered to limit the scope of the present disclosure. As used in the present disclosure, the forms "a,” "an," and "the" may be intended to include the plural forms as well, unless the context clearly suggests otherwise. The terms "comprises," "comprising," “including,” and “having,” are open ended transitional phrases and therefore specify the presence of stated features, integers, steps, operations, elements, modules, units and/or components, but do not forbid the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof. The particular order of steps disclosed in the method and process of the present disclosure is not to be construed as necessarily requiring their performance as described or illustrated. It is also to be understood that additional or alternative steps may be employed.
It is desirable to provide farmers with a ready to use formulation of two or more active ingredients which can simply be put into a tank and then sprayed or broadcasted directly. However, all the combinations may not be compatible or stable over long periods and therefore it is necessary in many cases to mix the active ingredients prior to application. The present disclosure envisages a stable and ready to use synergistic pesticidal composition having enhanced efficacy.
In an aspect of the present disclosure, there is provided a synergistic pesticidal composition comprising cartap hydrochloride, at least one anilide, and tricyclazole.
Cartap-HCl is an insecticide of Nereistoxin analogue group, which provides effective control of insect pests through its contact, systemic and stomach poison action and has a remarkable capacity to control caterpillars. It is safe for environment, is suitable for Integrated Pest Management (IPM) system, and is a persistent insecticide that controls the pests for a longer period. Farmers generally apply the granules of cartap hydrochloride, 15-25 days after the plantation, to prevent stem borer infestations, and leaf roller at later stages.
In accordance with the embodiments of the present disclosure, the amount of cartap hydrochloride can be in the range of 0.1 wt% to 50 wt% of the composition.
Typically, the anilide can be selected from the group consisting of benalaxy, benalaxyl-M, bixafen, boscalid, carboxin, fenhexamid, fluxapyroxad, isotianil, metalaxyl, metalaxyl-M, metsulfovax, ofurace, oxadixyl, oxycarboxin, penflufen, pyracarbolid, pyraziflumid, sedaxane, thifluzamide, tiadinil, and vangard.
In accordance with the embodiments of the present disclosure, the anilide can be selected from the group consisting of anilide is selected from the group consisting of bixafen, boscalid, carboxin, fenhexamid, fluxapyroxad, ofurace, oxycarboxin, penflufen, pyracarbolid, pyraziflumid, sedaxane, thifluzamide and tiadinil.
In an embodiment of the present disclosure, the anilide can be selected from thifluzamide, boscalid, fulxapyroxad and fenhexamid.
In accordance with the embodiments of the present disclosure, the amount of anilide can be in the range of 0.1 wt% to 40 wt% of the composition.
The pesticidal composition of the present disclosure also comprises tricyclazole. Tricyclazole belongs to the group of melanin biosynthesis inhibitors. It inhibits the melanin formation in fungi. Tricyclazole inhibits sporulation and secondary infection. It is a systemic fungicide that gets rapidly absorbed and translocated all over the plants. Tricyclazole is a systemic fungicide that effectively controls paddy blast disease; Tricyclazole is generally applied by farmers around 25 days after planting to 25 days before harvest to control blast (Pyricularia oryzae), as this disease can appear during any stage of the paddy.
In accordance with the embodiments of the present disclosure, the amount of tricyclazole can be in the range of 0.1 wt% to 40 wt% of the composition.
Farmers usually apply different insecticide/ fungicide such as cartap, anilide, and tricyclazole to the plants based on the time of applications. The targets are totally different for each chemical as they are unique in their targeted pest(s). However, these pesticides are applied individually at different times, during the growth of the plant crop, and are therefore labour intensive and time consuming. The synergistic pesticidal composition of the present disclosure has enhanced efficacy, is available in a ready to use form in a single application. The labour consumption for the application of the synergistic pesticidal composition of the present disclosure is comparatively lower and hence, is cost effective. Further, the synergistic and the compatible pesticidal composition of the present disclosure is more effective than the tank mix/sand mix and avoids repeated spraying of different pesticides and further reduces cost, which will help the farming community. So the mixture of cartap, tricyclazole and anilide chemicals adds great value to the farmer for improved yields by preventing the pest/s in time and adds further value by reducing the cost of labour, which is a herculean task, to repeat the sprays with a target to control different pest/s at different times of crop stage.
The composition of the present disclosure is economical and feasible to apply in the situation where co-existing of pest takes place. The pesticidal composition of the present disclosure is more suitable for application to address multiple pest and diseases at a time and available ready to use form.
The pesticidal composition of the present disclosure further comprises one or more agrochemically acceptable additives. Typically, the additives can be selected from the group consisting of at least one surfactant, at least one stabilizer, at least one filler, at least one coloring agent, at least one carrier, at least one acidifying agent, and combinations thereof.
In accordance with the embodiments of the present disclosure, the typical amounts of the additives are:
- surfactant in the range of 0.5 wt% to 10 wt% of the composition,
- stabilizer in the range of 0.1 wt% to 10 wt% of the composition,
- filler in the range of 0.1 wt% to 10 wt% of the composition,
- coloring agent in the range of 0.1 wt% to 5 wt% of the composition,
- acidifying agent in the range of 0.1 wt% to 5 wt% of the composition,
- carrier in the range of 1 wt% to 90 wt% of the composition.
The surfactant can be selected from the group consisting of non-ionic surfactants, wetting agent, dispersing agent such as ethoxylated aliphatic alcohol, polyglycerol alkyl ethers, glycol ethers, crownethers, ester-linked surfactants, polyoxyethylene alkyl ethers, Brij, Spans (sorbitan esters) Tweens (Polysorbates), Sodium lignosulphonte, sodium lauryl sulphate, ammonium lauryl sulfate alkyl naphthalene sulphonate, dioctyl sodium sulfosuccinate and alkyl naphthalene sulphonate condensate.
The stabilizer can be selected from acids and phosphates.
The filler can be selected from clay, sand, silica, sodium sulphates.
The coloring agent is selected from anthraquinone class.
The acidifying agent can be selected from weak acids such as phosphoric acid, oxalic acid and acetic acid.
In an embodiment of the present disclosure, the pesticidal composition comprises cartap hydrochloride in an amount in the range of 0.1 wt% to 40 wt% of the composition, at least one anilide in an amount in the range of 0.1 wt% to 30 wt% of the composition, tricyclazole in an amount in the range of 0.1 wt% to 30 wt% of the composition, and one or more agrochemically acceptable additives.
In another embodiment of the present disclosure, the pesticidal composition comprises cartap hydrochloride in an amount in the range of 0.1 wt% to 30 wt% of the composition, at least one anilide in an amount in the range of 0.1 wt% to 15 wt% of the composition, tricyclazole in an amount in the range of 0.1 wt% to 15 wt% of the composition, and agrochemically acceptable additives selected from the group consisting of at least one surfactant, at least one stabilizer, at least one filler, at least one coloring agent, at least one acidifying agent, carrier and combinations thereof.
The present disclosure in another aspect provides a process for preparing a synergistic pesticidal composition.
The pesticidal composition of the present disclosure can be in a dosage form selected from the group consisting of encapsulated granules, water dispersible granules, and wettable powder.
In an embodiment of the present disclosure, the pesticidal composition is in the form of encapsulated granules.
The process for preparing the pesticidal composition in the form of encapsulated granules is described hereinafter in detail.
Pre-determined quantities of at least one surfactant, at least one stabilizer, at least one acidifying agent, and at least one coloring agent are blended in a drum fitted with a heating coil to obtain a blended mixture (Mixture A). In accordance with the embodiments of the present disclosure, the heating coil can be maintained at a temperature in the range of 60°C to 65°C
Pre-determined quantity of a carrier is charged into a rotating blender. The so obtained blended mixture (Mixture A) obtained is heated to a temperature in the range of 55 °C to 65 °C and then sprayed over the carrier in the rotating blender to obtain an admixture (Mixture B). In accordance with the embodiments of the present disclosure, the heating can be carried out at a temperature in the range of 55 °C to 65 °C.
The so obtained admixture (Mixture B) is then cooled to room temperature, typically at a temperature in the range of 10 °C to 40°C, and further pre-determined quantity of carrier is charged into the rotating blender to obtain a blended admixture (Mixture C). The blended admixture is typically blended for a time period in the range of 20 minutes to 60 minutes.
Pre-determined quantities of cartap, at least one anilide and tricyclazole are charged into a ribbon blender, mixed and ground in a mill to obtain wettable powder (Mixture D). Typically, the particle size of the wettable powder can be in the range of 2 micron to 8 micron.
The wettable powder (Mixture D) is then blended/mixed with the blended admixture (Mixture C) for a time period in the range of 40 minutes to 120 minutes to obtain coated granules.
The coated granules are then blended with a pre-determined quantity of a filler for a time period in the range of 20 minutes to 60 minutes to obtain the pesticidal composition of the present disclosure in the form of encapsulated granules.
In another embodiment of the present disclosure, the pesticidal composition is in the form of wettable powder.
The process for preparing the pesticidal composition in the form of wettable powder is described hereinafter in detail.
Pre-determined amounts of a filler and a surfactant are blended to obtain a mixture (Mixture A). Typically, the blending is carried out in a ribbon blender for a time period in the range of 90 minutes to 150 minutes.
Pre-determined amounts of cartap hydrochloride, at least one anilide and tricyclazole are mixed with the mixture to obtain a resultant mixture (Mixture B). The mixing is typically carried out for a time period in the range of 2 hours to 5 hours.
Pre-determined amounts of a acidifying agent (phosphoric acid), a surfactant and a stabilizer are blended to the resultant mixture to obtain a blended mixture. The blending is typically carried out for a time period in the range of 40 minutes to 120 minutes.
The blended mixture is then milled for a time period in the range of 40 minutes to 120 minutes to obtain a milled mixture. Typically, the milling is carried out in a jet mill. Milling is carried out to reduce the particle size to be in the range of 2 micron to 10 micron.
A pre-determined amount of a dispersing agent is blended to the milled mixture to obtain the pesticidal composition of the present disclosure in the form of wettable powder.
The present disclosure further provides a kit configurable as a pesticidal composition. The kit comprises cartap hydrochloride, at least one anilide, tricyclazole and agrochemically acceptable additives, and is adapted to be stored, transported, and discharged for treatment of plants, its habitat, soil, a crop or a crop field.
The pesticidal composition of the present disclosure comprising cartap hydrochloride, at least one anilide and tricyclazole can be used for treatment of plants, its habitat, soil, a crop or a crop field.
The present disclosure also provided a method for controlling pests. The method comprises contacting an infested site with a pesticidal composition comprising cartap hydrochloride, at least one anilide and tricyclazole by applying an effective amount of the composition thereon.
The pesticidal composition of the present disclosure exerts a synergistic action due to the combined effect of cartap hydrochloride, at least one anilide and tricyclazole, and thereby results in enhanced bio-efficacy. Further, as the different pesticides having different modes of action are present as a ready-to-use single kit, it is easy to apply and an enhanced bio-efficacy can be achieved by reduced number of applications.
The foregoing description of the embodiments has been provided for purposes of illustration and not intended to limit the scope of the present disclosure. Individual components of a particular embodiment are generally not limited to that particular embodiment, but, are interchangeable. Such variations are not to be regarded as a departure from the present disclosure, and all such modifications are considered to be within the scope of the present disclosure.
The present disclosure is further described in light of the following experiments which are set forth for illustration purpose only and not to be construed for limiting the scope of the disclosure. The following experiments can be scaled up to industrial/commercial scale and the results obtained can be extrapolated to industrial scale.
Experimental Detail
Experiment-1: Cartap hydrochloride 4% + Thifluzamide 0.4% + Tricyclazole 1.2% GR
4 g of phosphoric acid, 10.00 g of propol PAP, 5.00 g of Propal PAD and 6.2 g of Acid green 25 were charged in a metal drum fitted with heating coil, and was blended for 30 minutes at a temperature of 60 °C to obtain Mixture A. 670 g of river sand was charged into a rotating blender. Mixture A was further heated to 65 °C and then sprayed over the river sand in the rotating blender to obtain Mixture B. Mixture B was then cooled to 30 °C and then 204.95 g of river sand was charged into the rotating blender and mixed for 30 minutes to obtain Mixture C. 42.30 g of Cartap hydrochloride, 4.40 g of Thifluzamide technical, and 13.15 g of Tricyclazole technical was charged into a ribbon blender and was ground in a mill to obtain Mixture D, i.e., wettable powder having particle size in the range of 2 to 8 micron. Mixture D was then charged in Mixture C in a rotating blender for 60 minutes to obtain coated granules. 40 g of Clay was blended with the coated granules for 30 minutes to obtain the pesticidal composition of the present disclosure in the form of encapsulated granules.
Experiment-2: Cartap hydrochloride 4% + Thifluzamide 1.5% + Tricyclazole 2.5% GR
4 g of phosphoric acid, 10.00 g of propol PAP, 5.00 g of Propol PAD, and 6 g of Acid green 25 were charged in the metal drum fitted with heating coil, and was blended for 30 minutes at a temperature of 60 °C to obtain Mixture A. 650 g of river sand was charged into a rotating blender. Mixture A was further heated to 65 °C and then sprayed over the river sand in the rotating blender to obtain Mixture B. Mixture B was then cooled to 30 °C and then 218.04 g of river sand was charged into the rotating blender and mixed for 30 minutes to obtain Mixture C. 42.30 g of Cartap hydrochloride, 16.31 g of Thifluzamide technical, and 26.35 g of Tricyclazole technical was charged into a ribbon blender and was ground in a mill to obtain Mixture D in the form of wettable powder having particle size in the range of 2 to 8 micron. Mixture D was then mixed with Mixture C in a rotating blender for 60 minutes to obtain coated granules. 22.0 g of Clay was blended with the coated granules for 30 minutes to obtain the pesticidal composition of the present disclosure in the form of encapsulated granules.
The GR compositions obtained in experiments 1 and 2 were subjected to accelerated storage study (temperature of 54 °C for 14 days), and the result obtained is summarized in Table-1.
Table-1
Actives Experiment-1 Experiment-2
Initial After ageing Initial After ageing
Cartap hydrochloride content 4.05 4.04 4.06 4.02
Thifluzamide content 0.44 0.42 1.55 1.56
Tricyclazole content 1.21 1.20 2.55 2.53

It is seen from Table-1 that there was no significant decrease in the amount of the actives after the storage period, thus indicating that the pesticidal composition prepared of the present disclosure was stable. Further, the bio-efficacy of the pesticidal composition was also retained after the storage period.
Experiment-3: Cartap hydrochloride 25% + thifluzamide 4.5% + Tricyclazole 10% WP
471 g of clay, 20 g of sodium lauryl sulphate, and 20 g of silica were charged in to a ribbon blender and was blended for 2 hours to obtain Mixture A. 270 g of cartap hydrochloride, 47 g of Thifluzamide technical, and 112 g of Tricyclazole technical was added to Mixture A and blended for 3 hours to obtain Mixture B. 10 g of phosphoric acid, 10 g of propol PAP, 5 g of Propol PAD were charged to Mixture B and was blended for one hour. The obtained mixture was then ground in jet mill to reduce the particle size in the range of 2 micron to 10 micron. The milled mixture was further blended with 35 g of Tamol 8906 to obtain the pesticidal composition of the present disclosure in the form of in wettable powder form.
Experiment-4: Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP
235 g of clay, 236 g of sodium sulphate, 20 g of sodium lauryl sulphate, 20 g of silica were charged in to a ribbon blender and was blended for 2 hours to obtain Mixture A. 270 g of cartap hydrochloride, 47 g of Thifluzamide technical, and 112 g of Tricyclazole technical was added to obtain Mixture B. 10 g of phosphoric acid 10 g of propol PAP, and 5 g of Propol PAD were charged to Mixture B and blended for one hour. The obtained mixture was then ground in jet mill to reduce the particle size in the range of 2 to 10 micron. The milled mixture was further blended with 35 g of Morwet D425 to obtain the pesticidal composition of the present disclosure in the form of in wettable powder form.
Experiment-5: Cartap hydrochloride 4% + Boscalid 0.4% + Tricyclazole 1.2% GR
6 g of phosphoric acid, 10.00 g of propol PAP, 5.00 g of Propal PAD and 6.5 g of Acid green 50 were charged in a metal drum fitted with heating coil, and was blended for 30 minutes at a temperature of 60 °C to obtain Mixture A. 650 g of river sand was charged into a rotating blender. Mixture A was further heated to 65 °C and then sprayed over the river sand in the rotating blender to obtain Mixture B. Mixture B was then cooled to 30 °C and then 222.55 g of river sand was charged into the rotating blender and mixed for 30 minutes to obtain Mixture C. 42.30 g of Cartap hydrochloride, 4.50 g of Boscalid technical, and 13.15 g of Tricyclazole technical was charged into a ribbon blender and was ground in a mill to obtain Mixture D, i.e., wettable powder having particle size in the range of 2 to 8 micron. Mixture D was then charged in Mixture C in a rotating blender for 60 minutes and 40 g of Clay was mixed and the mixture was blended for 30 minutes to obtain the pesticidal composition of the present disclosure in the form of encapsulated granules.
Experiment-6: Cartap hydrochloride 4% + Fluxapyroxad 0.5% + Tricyclazole 1.2% GR
6 g of phosphoric acid, 10.00 g of propol PAP, 5.00 g of Propal PAD and 6.5 g of Acid green 25 were charged in a metal drum fitted with heating coil, and was blended for 30 minutes at a temperature of 60 °C to obtain Mixture A. 650 g of river sand was charged into a rotating blender. Mixture A was further heated to 65 °C and then sprayed over the river sand in the rotating blender to obtain Mixture B. Mixture B was then cooled to 30 °C and then 220 g of river sand was charged into the rotating blender and mixed for 30 minutes to obtain Mixture C. 42.30 g of Cartap hydrochloride, 5.2 g of Fluxapyroxad technical, and 13.15 g of Tricyclazole technical was charged into a ribbon blender and was ground in a mill to obtain Mixture D, i.e., wettable powder having particle size in the range of 2 to 8 micron. Mixture D was then charged in Mixture C in a rotating blender for 60 minutes and 41.85 g of Clay was mixed and the mixture was blended for 30 minutes to obtain the pesticidal composition of the present disclosure in the form of encapsulated granules.
Experiment-7: Cartap hydrochloride 4% + Fenhexamid 0.5% + Tricyclazole 1.2% GR
6.5 g of phosphoric acid, 10.00 g of propol PAP, 5.00 g of Propal PAD and 6.0 g of Acid green 25 were charged in a metal drum fitted with heating coil, and was blended for 30 minutes at a temperature of 60 °C to obtain Mixture A. 650 g of river sand was charged into a rotating blender. Mixture A was further heated to 65 °C and then sprayed over the river sand in the rotating blender to obtain Mixture B. Mixture B was then cooled to 30 °C and then 220 g of river sand was charged into the rotating blender and mixed for 30 minutes to obtain Mixture C. 42.30 g of Cartap hydrochloride, 5.3 g of Fluxapyroxad technical, and 13.15 g of Tricyclazole technical was charged into a ribbon blender and was ground in a mill to obtain Mixture D, i.e., wettable powder having particle size in the range of 2 to 8 micron. Mixture D was then charged in Mixture C in a rotating blender for 60 minutes and 41.75 g of Clay was mixed and the mixture was blended for 30 minutes to obtain the pesticidal composition of the present disclosure in the form of encapsulated granules.
Experiment-8: Study of bioefficacy and phytotoxicity of the pesticidal composition of the present disclosure in the form of encapsulated granules (experiment-1 and experiment-2)
The details of the crop used, the target pests, the application duration, and the treatment details of the pesticidal composition used are summarized in Tables 2-4.
The pesticidal composition of experiment-1 (Cartap hydrochloride 4% + Thifluzamide 0.4% + Tricyclazole 1.2% GR) and experiment-2 (Cartap hydrochloride 4% + Thifluzamide 1.5% + Tricyclazole 2.5% GR) were used in this study.
Table-2
a) Crop : Paddy (Oryza sativa)
b)
c) Variety/Cultivar
Date of Transplanting :
: Ganga Kaveri, Paddy.
01/12/2016
d) Target pest
: Stem borer (Scirpophaga incertulas),
Leaf folder (Cnaphalocrocis medinalis),
Sheath Blight (Rhizoctonia solani)
Blast (Pyricularia oryzae)
e) Plot Size : 5 m X 6 m (30 sq. m.)
f) Spacing : 10 cm X 15 cm
g) Design of Experiment : Randomized Block Design (RBD)
h) No. of Treatments : 7 (Bioefficacy), 5 (Phytotoxicity)
i) No. of Replications : 3
j) Cropping Season : Rabi 2016-17

k) Number of Applications : 2 applications at an interval of 30 days
l) Date of Applications : 1st - 20/01/2017 (Maximum tillering stage)
2nd - 14/02/2017 (Panicle initiation stage)
m) Method of Application : Soil Application by Broad casting GR formulations and WP/SC mixed with sand and broadcasted in soil
n) Water volume for spray : NA
o)

p)

q) Time of observation

Package of Practices

Date of Harvesting :

:

: Bio-efficacy- Before 1st Application and 10, 15 & 20 days after 1st application and 0, 5, 10 & 15 days after 2nd Application
Phyto-toxicity- 1, 3, 5, 7, 10 & 15 days after application
All university recommended package of practices were followed to grow the crop
31/04/2017

Table-3: Bio-efficacy Treatment Details
Tr. No Treatment Details Dose
(g a.i./ha) Dose
(ml or g/ha)

T1 Cartap hydrochloride 4% + Thifluzamide 0.4% + Tricyclazole 1.2% GR (Experiment-1) 1000+ 100 + 300 25000
T2 Cartap hydrochloride 4% + Thifluzamide 1.5% + Tricyclazole 2.5% GR (Experiment-2) 1000 + 375 + 625 25000
T3 Cartap hydrochloride 4% GR + Thifluzamide 24% SC+ Tricyclazole 75% WP (TM) 1000+ 375+ 625 1000+1562.5+833
T4 Cartap hydrochloride 4% GR 1000 25000
T5 Thifluzamide 24% SC 375 1562.5
T6 Tricyclazole 75% WP 625 833.3
T7 Untreated Control - -

Table-4: Phytotoxicity Treatment Details
Tr. No Treatment Details Dose
(g a.i./ha) Dose
(ml or g/ha)

T1 Cartap hydrochloride 4% + Thifluzamide 0.4% + Tricyclazole 1.2% GR (Experiment-1) 1000+ 100 + 300 25000
T2 Cartap hydrochloride 4% + Thifluzamide 1.5% + Tricyclazole 2.5% GR(Experiment-2) 1000 + 375 + 625 25000
T3 Cartap hydrochloride 4% + Thifluzamide 0.4% + Tricyclazole 1.2% GR (Experiment-1) 2000+ 200+ 600 50000
T4 Cartap hydrochloride 4% + Thifluzamide 1.5% + Tricyclazole 2.5% GR (Experiment-2) 2000 + 750 + 1250 50000
T5 Untreated Control - -
A ready granular formulation test insecticide (1) + Fungicide (2), the three way combinations of Cartap hydrochloride (I) + Thifluzamide (F) + Tricyclazole (F) were tested at given concentrations with Ready mix combination of Cartap hydrochloride 4% + Thifluzamide 0.4% + Tricyclazole 1.2% GR (Experiment-1), Cartap hydrochloride 4% + Thifluzamide 1.5% + Tricyclazole 2.5% GR (Experiment-2) along with solo insecticide i e. Cartap hydrochloride 4% GR, & Fungicides i.e., Thifluzamide 24% SC & Tricyclazole 75% WP and Untreated Control against Lepidopteran pests- Stem Borer, Leaf Folder, Sheath Blight & Leaf Blast on Paddy. All the test products & insecticides were applied as broadcasting in Soil as preventive in the field. Two applications were given at an interval of 30 days.
One day prior of the initiation of the experiment, pest incidences was recorded, and subsequent observations were recorded after 10, 15 and 20 days after first application and 0, 5, 10 & 15 days after 2nd Application. For Stem Borer (Dead hearts & White ears per hill was recorded), Leaf Folder (Number of newly infected leaves) were counted on 10 pre-tagged hills per plot. For Sheath Blight & Leaf Blast, the disease rating (Scale 0-9) was used and calculated PDI as formula given below (Table- (a) & (b). Mean PDI values were derived for the treatments and used for Statistical analysis of the data.
The standard Disease Rating Scale for Paddy Blast is given below:
Disease Rating Leaf blast
0 No lesions observed
1 Small brown specks of pin-point size or larger brown specks without sporulating center
2 Small roundish to slightly elongated, necrotic gray spots, about 1-2 mm in diameter, with a distinct brown margin
3 Lesion type is the same as in scale 2,but a significant number of lesions are on the upper leaves
4 Typical susceptible blast lesions 3mm or longer, infecting less than 4% of the leaf area
5 Typical blast lesions infecting 4-10% of the leaf area
6 Typical blast lesions infecting 11-25% of the leaf area
7 Typical blast lesions infecting 26-50% of the leaf area
8 Typical blast lesions infecting 51-75% of the leaf area and many leaves are dead
9 >75% leaf area affected

The standard for Disease Rating Scale for Paddy Sheath Blight is given below:
SCALE (relative lesion height: disease progress relative to plant height
0 No infection observed
1 Lesions limited to lower 20% of plant height
3 20-30%
5 31-45%
7 46-65%
9 More than 65%
Percent disease index (PDI) was calculated using the following formula:
Sum of all numerical ratings
PDI = --------------------------------------------------------------------- X 100
Total plants observed X Maximum rating scale

Paddy yield from each net plot was recorded at harvesting and weighed separately. Total yield from each net plot was calculated and computed on hectare basis (Kg/ha) and statistical analyzed the data.
Observations were taken on damage caused to plants, if any, by the application of different treatments by taking into the account phytotoxic symptoms viz. leaf injury on tips and leaf surface, wilting, vein clearing, necrosis, Epinasty and hyponasty on ten plants per plot. The observations were recorded before spray and 1, 3, 5, 7 & 10th day after applications. For Phytotoxicity study on leaf injury on tips and leaf surface the Scale (0-10) used is given below.
The standard Phytotoxicity Rating Scale (PRS) is given below:
Crop response/ Crop injury Rating
0-00 0
1-10% 1
11-20% 2
21-30% 3
31-40% 4
41-50% 5
51-60% 6
61-70% 7
71-80% 8
81-90% 9
91-100% 10

The statistical analysis of variance was calculated by using MS- Excel Computer Program and the results are summarized in Tables 5 to 10.
Observation:
a) Bio-efficacy of the pesticidal composition of the present disclosure against Stem borer
After first application the observations were recorded as no of Dead hearts due to Stem Borer incidence. The results obtained are summarized in Table-5.
Table-5: Bio-efficacy of different treatments against Stem Borer (Scirpophaga incertulas) of Paddy
Tr. No. Treatments DOSE/ ha 1st application 2nd application
No. dead hearts/Hill
(Avg. Mean) No. White hearts/Hill
(Avg. Mean)
g a.i. Formulation (g/ml) 0
DAA 10
DAA 15
DAA 20
DAA 0
DSA 5
DSA 10
DSA 15
DSA
T1 Cartap hydrochloride 4% + Thifluzamide 0.4% + Tricyclazole 1.2% GR (Experiment-1) 1000+ 100 + 300 25000 0.00
(0.0) 0.14
(0.79) 0.34
(0.92) 0.87
(1.17) 0.00
(0.0) 0.00
(0.0) 0.00
(0.0) 0.87
(1.17)
T2 Cartap hydrochloride 4% + Thifluzamide 1.5% + Tricyclazole 2.5% GR (Experiment-2) 1000 + 375 + 625 25000 0.00
(0.0) 0.10
(0.77) 0.40
(0.95) 0.94
(1.19) 0.00
(0.0) 0.00
(0.0) 0.00
(0.0) 0.80
(1.14)
T3 Cartap hydrochloride 4% GR + Thifluzamide 24% SC+ Tricyclazole 75% WP (TM) 1000+ 375+ 625 1000+1562.5+ 833 0.00
(0.0) 0.47
(0.98) 0.74
(1.11) 1.17
(1.3) 0.00
(0.0) 0.00
(0.0) 0.00
(0.0) 1.20
(1.3)
T4 Cartap hydrochloride 4% GR 1000 25000 0.00
(0.0) 0.27
(0.86) 0.44
(0.97) 0.94
(1.2) 0.00
(0.0) 0.00
(0.0) 0.00
(0.0) 1.34
(1.36)
T5 Thifluzamide 24% SC 375 1562.5 0.00
(0.0) 1.64
(1.46) 1.97
(1.57) 2.80
(1.82) 0.00
(0.0) 0.00
(0.0) 0.00
(0.0) 7.00
(2.73)
T6 Tricyclazole 75% WP 625 833 0.00
(0.0) 1.34
(1.36) 1.74
(1.5) 2.40
(1.71) 0.00
(0.0) 0.00
(0.0) 0.00
(0.0) 5.57
(2.46)
T7 Untreated Control - - 0.00
(0.0) 1.77
(1.51) 2.14
(1.62) 2.87
(1.84) 0.00
(0.0) 0.00
(0.0) 0.00
(0.0) 9.57
(3.16)
CD @ 5 % NS 0.26 0.23 0.2 NS NS NS 0.39
Figures in parenthesis are Square root transformed values. DAA- Days After 1st Application, DSA- days After 2nd Application, NS- Non significant
It is seen from Table-5 that at the time of initiation of trial there was no pest infestation in any of the treatments. At 10 days after first application, the highest Dead hearts infestation was recorded in Control (1.51/hill). All the insecticide treatments significantly reduced the Stem borer infestation than Untreated Control and Fungicide applications but the significant lowest number of Dead hearts was observed in T2 (0.77/Hill), T1 (0.79/ Hill), T3 (0.98) & T4 (0.86/Hill) which was superior over rest of all treatments and after 15 & 20 Days after first application (DAA) similar trend was observed in controlling dead hearts of Stem borer after first application.
After second application observations were taken as no of White ears due to Stem Borer incidence. After 2nd application at 0, 5, 10 days after second application (DSA) there was i.e., highest White ears were observed in Untreated Control (3.16/Hill) at 15 Days after second application (DSA) and T2 (1.14/Hill), T1 (1.17/Hill), T3 (1.30/Hill) & T4 (1.36/Hill) recorded lowest white ear infestation than rest of the treatments.
b) Bio-efficacy of the pesticidal composition of the present disclosure against Leaf Folder
It is seen from Table-6 that at the time of initiation of trial there was no pest observed. At 10 days after first application, the highest number of Leaf infestation was recorded in Control (1.97/Hill). The significant lowest Leaf infestation was observed in T1 (0.71/Hill), T2 (0.71/Hill), T3 (0.71/ Hill) & T4 (0.76/Hill). The treatments T1, T2 & T3 were significantly superior over rest of all the treatments and they are on par with each other on 15 & 20 days after first application (DAA) and Untreated Control recorded 2.50/hill.


Table-6: Bio-efficacy of different treatments against Leaf Folder (Cnaphalocrocis medinalis) of Paddy
Tr. No. Treatment DOSE/ ha 1st application 2nd application
No. of Infected Leaves/Hill
(Avg. Mean) No. of Infected Leaves/Hill
(Avg. Mean)
g a.i. Formulation (g/ml) 0
DAA 10
DAA 15
DAA 20
DAA 0
DSA 5
DSA 10
DSA 15
DSA
T1 Cartap hydrochloride 4% + Thifluzamide 0.4% + Tricyclazole 1.2% GR (Experiment-1) 1000+ 100 + 300 25000 0.00
(0.0) 0.00
(0.71) 0.07
(0.76) 0.34
(0.92) 2.00
(1.59) 0.47
(0.99) 0.67
(1.07) 1.67
(1.47)
T2 Cartap hydrochloride 4% + Thifluzamide 1.5% + Tricyclazole 2.5% GR (Experiment-2) 1000 + 375 + 625 25000 0.00
(0.0) 0.00
(0.71) 0.07
(0.76) 0.27
(0.88) 0.74
(1.11) 0.40
(0.95) 0.54
(1.01) 1.60
(1.45)
T3 Cartap hydrochloride 4% GR + Thifluzamide 24% SC+ Tricyclazole 75% WP (TM) 1000+ 375+ 625 1000+ 1562.5+ 833 0.00
(0.0) 0.00
(0.71) 0.14
(0.8) 0.44
(0.97) 0.87
(1.17) 0.54
(1.01) 0.54
(1.01) 1.60
(1.45)
T4 Cartap hydrochloride 4% GR 1000 25000 0.00
(0.0) 0.07
(0.76) 0.54
(1.02) 0.94
(1.2) 1.14
(1.27) 0.47
(0.99) 0.67
(1.08) 1.74
(1.5)
T5 Thifluzamide 24% SC 375 1562.5 0.00
(0.0) 1.84
(1.53) 2.47
(1.73) 3.34
(1.96) 3.47
(2.00) 4.40
(2.22) 7.07
(2.75) 8.87
(3.06)
T6 Tricyclazole 75% WP 625 833 0.00
(0.0) 2.34
(1.68) 3.00
(1.88) 3.60
(2.03) 4.67
(2.28) 5.00
(2.35) 6.67
(2.67) 9.07
(3.10)
T7 Untreated Control - - 0.00
(0.0) 3.37
(1.97) 3.60
(2.02) 5.74
(2.5) 6.87
(2.72) 7.14
(2.77) 8.67
(3.03) 12.14
(3.56)
CD @ 5 % NS 0.16 0.17 0.14 0.23 0.4 0.36 0.21
Figures in parenthesis are Square root transformed values. DAA- Days After 1st Application, DSA- days After 2nd Application, NS- Non significant
At 0 days after second application, least infestation was observed in T2 (1.11/Hill) and which is on par with T3 (1.17/Hill) & T4 (1.27/Hill) and at 5 days after second application, there was significant suppression of Leaf Folder infestation in the treatments. Less Leaf infestation was observed in T2 (0.95/Hill) and on par with T1 (0.99/Hill), T4 (0.99/Hill) & T3 (1.01/Hill) which were significantly lowest superior over rest of the treatments and the highest infestation was observed in Untreated Control that is T7 (2.77/Hill). At 10 days after second application also similar trend observed with highest infestation in untreated control (3.03/Hill).
At 15 days after second application also similar trend observed. The significant lowest Leaf Folder was observed in all T1, T2, T3 & T4 treatments (1.47, 1.45, 1.45 & 1.50/Hill respectively) and which was superior over rest of all treatments. The highest infestation of Leaf Folder was observed in Untreated Control (3.56/Hill).
c) Bio-efficacy of the pesticidal composition of the present disclosure against Sheath Blight
It is seen from Table-7 that at 10 days after first application, the highest percent disease incidence (PDI) of Sheath Blight was recorded in Untreated Control (P31.08%). The significant lowest Sheath Blight was observed in T2 (PDI 0.0%). The treatment T2 was on par with T3 (2.86%) and significantly superior over rest of all treatments. Similarly at 15 & 20 days after first application T2 (5.72% & 6.92% respectively) recorded least disease incidence over all the treatments and Untreated recorded (41.38% & 62.23% respectively).
At 0 days after second application, T2 (15.54%) was on par with T3 (20.12%) and superior over rest of the treatments. At 5 days after second application, there was good suppression of Sheath Blight incidence in all the combination treatments & Thifluzamide 24% SC. The treatment T2 was recorded (2.86%) from Sheath Blight infestation, which is significantly lowest among all the treatments and the highest incidence of Sheath Blight was noticed in Untreated Control T7 (59.45%). Same kind
of trend was recorded on 10 days after second application with Untreated Control T7 (59.0%).
Table-7: Bio-efficacy of different treatments against Sheath Blight (Rhizoctonia solani) of Paddy
Tr.
No. Treatment DOSE/ ha 1st application 2nd application
Avg. Mean (PDI) Avg. Mean (PDI)
g a.i. Formulation (g/ml) 0
DAA 10 DAA 15 DAA 20 DAA 0
DSA 5
DSA 10 DSA 15
DSA
T1 Cartap hydrochloride 4% + Thifluzamide 0.4% + Tricyclazole 1.2% GR (Experiment-1) 1000+ 100 + 300 25000 0.00
(0.0) 2.97
(9.78) 5.19
(14.04) 9.63
(23.2) 11.12
(28.53) 5.93
(28.13) 6.67
(34.82) 16.30
(40.06)
T2 Cartap hydrochloride 4% + Thifluzamide 1.5% + Tricyclazole 2.5% GR (Experiment-2) 1000 + 375 + 625 25000 0.00
(0.0) 2.23
(0.0) 3.71
(5.72) 8.89
(6.92) 12.6
(15.54) 5.19
(2.86) 7.41
(6.92) 15.56
(18.62)
T3 Cartap hydrochloride 4% GR + Thifluzamide 24% SC+ Tricyclazole 75% WP (TM) 1000+ 375+ 625 1000+1562.5+ 833 0.00
(0.0) 2.23
(2.86) 4.45
(10.98) 8.89
(13.11) 14.08
(20.12) 5.93
(10.98) 6.67
(16.47) 16.30
(27.86)
T4 Cartap hydrochloride 4% GR 1000 25000 0.00
(0.0) 22.97
(29.62) 40.75
(40.95) 50.38
(48.62) 60.0
(50.84) 65.19
(60.42) 70.15
(61.9) 84.45
(64.57)
T5 Thifluzamide 24% SC 375 1562.5 0.00
(0.0) 6.67
(14.83) 10.38
(14.83) 11.86
(17.97) 14.82
(22.63) 5.19
(13.11) 11.12
(19.42) 16.30
(33.43)
T6 Tricyclazole 75% WP 625 833 0.00
(0.0) 17.04
(24.35) 46.67
(43.09) 60.0
(46.93) 51.86
(55.11) 48.15
(59.45) 56.3
(61.95) 63.71
(67.46)
T7 Untreated Control - - 0.00
(0.0) 26.67
(31.08) 43.71
(41.38) 62.23
(49.96) 72.60
(58.58) 75.56
(59.45) 80.0
(59.0) 89.63
(63.45)
CD @ 5 % 0.00 4.01 4.55 7.17 7.63 4.35 5.5 8.62
Figures in parenthesis are arcsine transformed values. DAA- Days After 1st Application, DSA- days After 2nd Application, NS- Non significant
At 15 days after second application also similar trend was observed. The significant lowest Sheath Blight was recorded in treatment T2 (18.62%), which was superior over rest of all the treatments. The highest Sheath Blight was observed in Untreated Control (63.45%).
d) Bio-efficacy of the pesticidal composition of the present disclosure against Leaf Blast
It is seen from Table-8 that, at the time of initiation of trial, the incidence of pest was uniformly prevalent across the plot and was building up. At 10 days after first application, the highest percent of Leaf Blast was recorded in Untreated Control (29.10%). The significant lowest Leaf blast was observed in T1 (0.00%) & T2 (0.00%). The treatment T2 (0.00%) was on par with T1 (0.00%) & T3 (2.86%) and significantly superior over rest of all treatments.
At 15 & 20 days after first application, the incidences of Leaf Blast in Untreated Control (34.38% & 36.30% respectively) & T2 recorded significantly superior over all the treatments at 15 & 20 DAA.
Table-8: Bio-efficacy of different treatments against Leaf Blast (Pyricularia oryzae) of Paddy
Tr.
No. Treatment DOSE/ ha 1st application 2nd application
Avg. Mean (PDI) Avg. Mean (PDI)
g a.i. Formulation (g/ml) 0
DAA 10
DAA 15
DAA 20
DAA 0
DSA 5
DSA 10
DSA 15
DSA
T1 Cartap hydrochloride 4% + Thifluzamide 0.4% + Tricyclazole 1.2% GR (Experiment-1) 1000+ 100 + 300 25000 0.00
(0.0) 0.00
(0.0) 2.97
(21.65) 7.41
(23.2) 19.26
(34.35) 4.45
(35.72) 8.15
(38.79) 13.34
(41.38)
T2 Cartap hydrochloride 4% + Thifluzamide 1.5% + Tricyclazole 2.5% GR (Experiment-2) 1000 + 375 + 625 25000 0.00
(0.0) 0.00
(0.0) 2.23
(2.86) 6.67
(4.06) 19.26
(17.97) 4.82
(10.98) 8.89
(14.04) 14.08
(20.59)
T3 Cartap hydrochloride 4% GR + Thifluzamide 24% SC+ Tricyclazole 75% WP (TM) 1000+ 375+ 625 1000+1562.5+ 833 0.00
(0.0) 0.75
(2.86) 6.67
(14.43) 11.12
(19.23) 14.08
(21.98) 7.41
(13.41) 11.12
(19.42) 14.82
(24.73)
T4 Cartap hydrochloride 4% GR 1000 25000 0.00
(0.0) 13.34
(21.38) 21.49
(34.28) 25.93
(31.97) 37.78
(39.6) 48.89
(45.22) 55.56
(48.23) 61.49
(51.7)
T5 Thifluzamide 24% SC 375 1562.5 0.00
(0.0) 21.86
(27.34) 31.12
(30.96) 34.82
(36.16) 49.63
(38.34) 47.41
(43.35) 54.08
(47.37) 61.49
(51.82)
T6 Tricyclazole 75% WP 625 833 0.00
(0.0) 5.93
(13.04) 8.15
(16.33) 14.82
(22.55) 20.75
(24.12) 4.82
(14.99) 11.86
(19.42) 14.45
(25.44)
T7 Untreated Control - - 0.00
(0.0) 23.71
(29.10) 30.38
(34.36) 36.3
(37.93) 39.26
(38.74) 51.86
(46.07) 60.75
(52.1) 67.41
(57.57)
CD @ 5 % NS 5.99 8.09 6.76 7.39 8.46 7.44 8.26
Figures in parenthesis are arcsine transformed values. DAA- Days After 1st Application, DSA- days After 2nd Application, NS- Non significant

At 0 days after second application, there was significantly less percent of Leaf Blast disease observed in treatment T2 (17.97%) was on par with tank mix combination. The highest Leaf blast disease was recorded in Control (PDI 38.74%). The significant lowest disease incidence was recorded in T2, which was superior over rest of all the treatments.
5 days after second application, the disease incidence was suppressed in all the treatments except Untreated Control (46.07%). The treatment T2 was recorded least PDI of Leaf Blast (10.98%), which is significantly lowest among all the treatments. Same trend continued at 10 days after second application.
At 15 days after second application also similar trend observed. The significant lowest disease incidence was observed in treatment T2 (20.59%), which was superior over rest of the treatments. The highest PDI was observed in Untreated Control (57.57%).
c) Effect of the pesticidal composition on Yield
Table-9: Bio-efficacy of different treatments against yield of Paddy
Sl No. Treatment DOSE/ ha Mean Yield
(Kg/ha)
g a.i. Formulation (g/ml)
1 Cartap hydrochloride 4% + Thifluzamide 0.4% + Tricyclazole 1.2% GR (Experiment-1) 1000+ 100 + 300 25000 4766
2 Cartap hydrochloride 4% + Thifluzamide 1.5% + Tricyclazole 2.5% GR (Experiment-2) 1000 + 375 + 625 25000 5433
3 Cartap hydrochloride 4% GR + Thifluzamide 24% SC+ Tricyclazole 75% WP (TM) 1000+ 375+ 625 1000+1562.5+ 833.3 4666
4 Cartap hydrochloride 4% GR 1000 25000 4433
5 Thifluzamide 24% SC 375 1562.5 4500
6 Tricyclazole 75% WP 625 833.3 4563
7 Untreated Control - - 3566
CD @ 5 % 589
Figures in parenthesis are arcsine transformed values.
It is seen from Table-9 the treatments significantly increase the yield than Untreated Control (3566 Kg/ha). The highest yield was observed in treatment T2 (5433 Kg/ha), which was significantly superior over rest of the treatments followed by T1 (4766 Kg/ha).

d) Effect of the pesticidal composition on Phytotoxicity
The pesticidal compositions of the present disclosure were applied to check the phytotoxic effects like Leaf injury on tips/surface, Vein clearing, Necrosis, Hyponasty and Epinasty on the Paddy crop at X and 2X dosages. The observations on these Phytotoxicity parameters were observed on before application and at 3, 5, 7 and 10 days after application.
Table-10: Phyto-toxicity effect of different treatments on Paddy
Tr. No. Treatment Details
Dose *Phytotoxicity
(Based on 0-10 Phytotoxicity Rating Scale)
g a.i./ha g/ha Before Spray Days after application (DAA)
1 3 5 7 10
T1 Cartap hydrochloride 4% + Thifluzamide 0.4% + Tricyclazole 1.2% GR (Experiment-1) 1000+ 100 + 300 25000 0 0 0 0 0 0
T2 Cartap hydrochloride 4% + Thifluzamide 1.5% + Tricyclazole 2.5% GR (Experiment-2) 1000 + 375 + 625 25000 0 0 0 0 0 0
T3 Cartap hydrochloride 4% + Thifluzamide 0.4% + Tricyclazole 1.2% GR (Experiment-1) 2000+ 200+ 600 50000 0 0 0 0 0 0
T4 Cartap hydrochloride 4% + Thifluzamide 1.5% + Tricyclazole 2.5% GR (Experiment-2) 2000 + 750 + 1250 50000 0 0 0 0 0 0
T5 Untreated Control - - 0 0 0 0 0 0
*For phototoxic symptoms- Leaf injury on tips and Leaf surface, Wilting, Vein Clearing, Necrosis, Epinasty and Hyponasty
It is seen from Table-10 that there was no phytotoxicity observed on the crop after application of any of the treatments. There was no adverse effect noticed on the Paddy crop in the field applied with these test combinations.
It is clearly seen from the above studies that the pesticidal composition of the present disclosure is effective against insect pests and diseases of Paddy. It is observed that Cartap hydrochloride 4% + Thifluzamide 1.5% + Tricyclazole 2.5% GR (Experiment-2) provides the most effective control insect pests and diseases.
The efficacy of the pesticidal composition of the present disclosure (Cartap hydrochloride + Thifluzamide + Tricyclazole) is far better than the commercially available pesticides, such as Cartap hydrochloride 4% GR, Thifluzamide
24% SC, Tricyclazole 75% WP and their tank mix combination for controlling pest complex of Paddy. It is also observed that as the pesticidal composition of the present disclosure provided significantly improved bio-efficacy and hence is capable of producing higher Paddy yield. Further, there is no phytotoxicity effect of the insecticidal composition on Paddy. The pesticidal composition of the present disclosure exhibits synergistic effect in controlling the pests of paddy crop, and can be used effectively and safely used for the management of pests as compared to individual use of Cartap HCl, Thifluzamide and tricyclazole alone.
Experiment-9: Study of bioefficacy and phytotoxicity of the pesticidal composition of the present disclosure in the form of wettable powder (experiments 3-4)
The details of the crop used, the target pests, the application duration, and the treatment details of the pesticidal composition used are summarized in Tables 11-13.
The pesticidal composition of experiment-3 (Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP) and experiment-4 (Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP) were used in this study.
Table-11:
a) Crop : Paddy (Oryza sativa)
b)
c) Variety/Cultivar
Date of Transplanting :
: Ganga Kaveri, Paddy
14/12/2016
d) Target pest
: Stem borer (Scirpophaga incertulas),
Leaf folder (Cnaphalocrocis medinalis ),
Sheath Blight (Rhizoctonia solani)
Blast (Pyricularia oryzae)
e) Plot Size : 5 m X 6 m (30 sq. m.)
f) Spacing : 10 cm X 15 cm
g) Design of Experiment : Randomized Block Design (RBD)
h) No. of Treatments : 7 (Bioefficacy), 5 (Phytotoxicity)
i) No. of Replications : 3
j) Cropping Season : Rabi 2016-17
k) Number of Applications : 2 applications at an interval of 20 days
l) Date of Applications : 1st - 01/02/2017
2nd - 21/02/2017
m) Method of Application : By Knapsack Sprayer fitted with hallow cone nozzle
n) Water volume for spray : 500 L/ha
o)

p)

q) Time of observation

Package of Practices

Date of Harvesting :

:

: Bio-efficacy- Before 1st Spray and 5, 10 & 15 days after each sprays
Phyto-toxicity- 1, 3, 5, 7, 10 & 15 days after application
All university recommended package of practices were followed to grow the crop
08/04/2017

Table-12: Bio-efficacy Treatment Details
Tr. No Treatment Details Dose
(g a.i./ha) Dose
(ml or g/ha)

T1 Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-3) 500+90+200 2000
T2 Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-4) 500+90+200 2000
T3 Cartap hydrochloride 50% WP + Thifluzamide 24% SC + Tricyclazole 75% WP (Tank Mix) 500+90+200 1000+375+267
T4 Cartap hydrochloride 50% SP 500 1000
T5 Thifluzamide 5% SC 90 375
T6 Tricyclazole 75% WP 225 300
T7 Untreated control - -

Table-13: Phytotoxicity Treatment Details
Tr. No Treatment Details Dose
(g a.i./ha) Dose
(ml or g/ha)

T1 Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-3) 500+90+200 2000
T2 Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-4) 500+90+200 2000
T3 Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-3) 1000+180+400 4000
T4 Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-4) 1000+180+400 4000
T5 Untreated control - -
A ready formulations of test Insecticide (1) + Fungicides (2), the three way combinations of Cartap hydrochloride (I) + Thifluzamide (F) + Tricyclazole (F) were tested at given concentrations i e. Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-3), Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-4) & tank mixture of Cartap hydrochloride 50% WP + Thifluzamide 24% SC + Tricyclazole 75% WP (Tank Mix) along with solo individual Insecticide, Cartap hydrochloride 50% WP & Fungicides Thifluzamide 5% SC & Tricyclazole 75% WP and Untreated Control against Lepidopteran pests (Stem Borer & Leaf Folder) and diseases (Sheath Blight & Blast) of Paddy. The test products were applied as foliar spray with Knapsack Sprayer fitted with hollow cone nozzle. The application was initiated with the incidence of pests in the field. Two applications were given at an interval of 20 days.
One day prior of the initiation of the experiment, pest incidences were recorded, and subsequent observations was recorded after 5, 10 and 15 days of each spray. The Stem Borer & Leaf folder incidence was recorded as Dead hearts, White ears and newly infected leaves respectively on 10 pre-tagged hills per plot. And for Blast & Sheath Blight the observations were recorded on 10 pre-tagged hills per plot based on the disease rating scale as given below. The PDI was calculated as per given formula. Mean values were derived for the treatment and used for Statistical Analysis of the data.
The standard Disease Rating Scale for Paddy Blast is given below:
Disease Rating Leaf blast
0 No lesions observed
1 Small brown specks of pin-point size or larger brown specks without sporulating center
2 Small roundish to slightly elongated, necrotic gray spots, about 1-2 mm in diameter, with a distinct brown margin
3 Lesion type is the same as in scale 2,but a significant number of lesions are on the upper leaves
4 Typical susceptible blast lesions 3mm or longer, infecting less than 4% of the leaf area
5 Typical blast lesions infecting 4-10% of the leaf area
6 Typical blast lesions infecting 11-25% of the leaf area
7 Typical blast lesions infecting 26-50% of the leaf area
8 Typical blast lesions infecting 51-75% of the leaf area and many leaves are dead
9 >75% leaf area affected
The standard for Disease Rating Scale for Paddy Sheath Blight is given below:
SCALE (relative lesion height: disease progress relative to plant height
0 No infection observed
1 Lesions limited to lower 20% of plant height
3 20-30%
5 31-45%
7 46-65%
9 More than 65%
Percent disease index (PDI) was calculated using the following formula:
Sum of all numerical ratings
PDI = --------------------------------------------------------------------- X 100
Total plants observed X Maximum rating scale
Individual plot wise yield was recorded and calculated treatment wise mean yield and converted into yield per hectare (Kg/ha) and statistically analyzed the mean data.
Observations were taken on damage caused to Paddy crop, if any, by the application of different treatments by taking into the account phytotoxic symptoms viz. leaf injury on tips and leaf surface, wilting, vein clearing, necrosis, epinasty and hyponasty on ten plants per plot. The observations were recorded before spray and 1, 3, 5, 7, 10 & 15th day after applications. For Phytotoxicity study on leaf injury on tips and leaf surface the Scale (0-10) used is given below.
The standard Phytotoxicity Rating Scale (PRS) is given below:
Crop response/ Crop injury Rating
0-00 0
1-10% 1
11-20% 2
21-30% 3
31-40% 4
41-50% 5
51-60% 6
61-70% 7
71-80% 8
81-90% 9
91-100% 10
The statistical analysis of variance was calculated by using MS- Excel Computer Program and the results are summarized in Tables 14-19.
Observation:
a) Bio-efficacy of the pesticidal composition of the present disclosure against Stem borer
It is seen from Table-14 that at the time of initiation of trial there was non- significant pest population in all the treatments. After first application the observations wer recorded for Dead hearts. At 5 days after first application, the lowest Dead hearts were recorded in T2 (0.92/ Hill) which was at par with T1 (0.98/ Hill) and superior over rest of the treatments, Similar observation trend was observed in 10 & 15 days after first application. The treatment T7 Untreated Control recorded the highest Dead hearts (2.25/ Hill) at 15 days after first application.

Table-14: Bio-efficacy of different treatments of tests products against Stem Borer of Paddy

Treatment DOSE/ ha 1st application 2nd application
No. of Dead hearts/Hill (Avg. Mean) No. of White ears/Hill (Avg. Mean)
g a.i. Formulation (g/ml) 0 DAFA 5
DAFA 10
DAFA 15
DAFA 0 DASA 5 DASA 10
DASA 15
DASA
T1: Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-3) 500+90+200 2000 1.04
(1.24) 0.47
(0.98) 0.67
(1.08) 1.14
(1.28) 0.00
(0.00) 0.00
(0.00) 0.00
(0.00) 2.94
(1.84)
T2: Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-4) 500+90+200 2000 1.74
(1.49) 0.34
(0.92) 0.57
(1.03) 1.20
(1.31) 0.00
(0.00) 0.00
(0.00) 0.00
(0.00) 2.87
(1.93)
T3: Cartap hydrochloride 50% WP + Thifluzamide 24% SC + Tricyclazole 75% WP (Tank Mix) 500+90+200 1000+375+267 1.14
(1.28) 0.70
(1.09) 1.20
(1.31) 2.00
(1.59) 0.00
(0.00) 0.00
(0.00) 0.00
(0.00) 3.2
(1.92)
T4: Cartap hydrochloride 50% SP 500 1000 1.34
(1.36) 0.74
(1.11) 1.37
(1.35) 1.94
(1.56) 0.00
(0.00) 0.00
(0.00) 0.00
(0.00) 3.2
(2.34)
T5: Thifluzamide 5% SC 90 375 1.20
(1.31) 1.40
(1.38) 1.80
(1.52) 4.00
(2.12) 0.00
(0.00) 0.00
(0.00) 0.00
(0.00) 4.94
(2.26)
T6: Tricyclazole 75% WP 225 300 1.27
(1.33) 1.47
(1.41) 1.80
(1.52) 4.34
(2.2) 0.00
(0.00) 0.00
(0.00) 0.00
(0.00) 4.6
(2.40)
T7: Untreated control - - 1.27
(1.33) 1.54
(1.43) 2.07
(1.61) 4.54
(2.25) 0.00
(0.00) 0.00
(0.00) 0.00
(0.00) 5.27
(2.25)
CD @ 5 % NS 0.20 0.22 0.21 NS NS NS 0.25
Figures in parenthesis are square root transformed values DAFA- Days After First Application, DASA- Days After Second Application, NS- Non significant
After second application the observations were recorded for White ears. At 0, 5 & 10 days after second application there was no White ears observed in any of the treatment. Only 15 days after second application the White ears were observed. Where, the lowest White ears were recorded in T1 (1.84/ Hill) which was at par with T2 ((1.93/ Hill) and significantly superior over rest of the treatments. The treatment T7 Untreated Control found the highest no of White ears (2.25/ Hills)
b) Bio-efficacy of the pesticidal composition of the present disclosure against Leaf Folder
It is seen from Table-15 that at the time of initiation of the trial incidence of Leaf Folder were started but there was no significant difference between the treatments which indicates the uniform prevalence of the pest. At 5 days after first application, the highest no of infested leaves were observed in T7 Untreated Control (2.36/ Hill). The lowest infected leaves were recorded in T1, T2, T3 & T4 (0.71, 0.71, 071 & 0.76 /Hill respectively), which were at par with each other and significantly superior over rest of the treatments. The similar trends of observations were observed on 10 & 15 days after first application.
Table-15: Bio-efficacy of different treatments of tests products against Leaf Folder of Paddy
Treatment DOSE/ ha 1st Application 2nd Application
No. of Infected leaf/Hill (Avg. Mean) No. of Infected leaf/Hill (Avg. Mean)
g a.i. Formulation (g/ml) 0
DAFA 5
DAFA 10
DAFA 15
DAFA 0
DASA 5
DASA 10
DASA 15
DASA
T1: Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-3) 500+90+200 2000 3.7
(2.05) 0.00
(0.71) 0.00
(0.71) 0.27
(0.87) 1.60
(1.45) 0.20
(0.84) 0.54
(1.02) 0.80
(1.13)
T2: Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-4) 500+90+200 2000 3.2
(1.93) 0.00
(0.71) 0.00
(0.71) 0.27
(0.88) 2.14
(1.61) 0.27
(0.88) 0.60
(1.05) 0.80
(1.14)
T3: Cartap hydrochloride 50% WP + Thifluzamide 24% SC + Tricyclazole 75% WP (Tank Mix) 500+90+200 1000+375+267 3.27
(1.95) 0.00
(0.71) 0.00
(0.71) 0.40
(0.94) 2.54
(1.74) 0.40
(0.95) 0.94
(1.20) 1.00
(1.22)
T4: Cartap hydrochloride 50% SP 500 1000 3.87
(2.09) 0.07
(0.76) 0.27
(0.88) 0.80
(1.14) 2.54
(1.74) 0.40
(0.95) 1.00
(1.23) 1.07
(1.25)
T5: Thifluzamide 5% SC 90 375 4.00
(2.13) 4.74
(2.29) 5.2
(2.39) 6.37
(2.62) 9.40
(3.14) 11.10
(3.4) 11.47
(3.46) 14.0
(3.81)
T6: Tricyclazole 75% WP 225 300 3.94
(2.11) 4.54
(2.25) 4.8
(2.31) 5.44
(2.44) 9.00
(3.08) 10.57
(3.33) 11.47
(3.46) 13.87
(3.79)
T7: Untreated control - - 3.47
(2.00) 5.07
(2.36) 5.4
(2.43) 6.97
(2.74) 11.00
(3.37) 11.67
(3.47) 12.20
(3.55) 13.87
(3.79)
CD @ 5 % NS 0.11 0.10 0.27 0.50 0.45 0.40 0.26
Figures in parenthesis are square root transformed values DAFA- Days After First Application, DASA- Days After Second Application, NS- Non significant
After second application also at 0, 5, 10 & 15 days after similar trend was observed where insecticide (Cartap hydrochloride) included treatments showed at par best results and which were significantly superior over Untreated Control (T7) and only Fungicide treatments (T5 & T6).
c) Bio-efficacy of the pesticidal composition of the present disclosure against Sheath Blight
It is seen from Table-16 that at the time of initiation of trial, the disease was not observed and were uniform across the treatments. At 5 days after first application, the highest PDI was recorded in T7 Untreated Control (3.51%). The significant lowest PDI was observed in T2 (1.03%) which was at par with T1 & T3 (1.22 & 1.34% respectively) and significantly superior over rest of the treatments. Similar kinds of observations were recorded on 10 & 15 days after first application.
Table-16: Bio-efficacy of different treatments of tests products against Sheath Blight of Paddy
Treatment DOSE/ ha 1st Application 2nd Application
Mean PDI Mean PDI
g a.i. Formulation (g/ml) 0
DAFA 5
DAFA 10
DAFA 15
DAFA 0
DASA 5
DASA 10
DASA 15
DASA
T1: Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-3) 500+90+200 2000 0.00
(0.00) 1.49
(1.22) 1.86
(1.53) 5.93
(2.47) 11.12
(3.4) 5.19
(2.34) 9.63
(3.16) 13.34
(3.72)
T2: Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-4) 500+90+200 2000 0.00
(0.00) 0.75
(1.03) 1.49
(1.34) 5.19
(2.38) 9.63
(3.16) 4.45
(2.23) 8.89
(3.01) 12.60
(3.6)
T3: Cartap hydrochloride 50% WP + Thifluzamide 24% SC + Tricyclazole 75% WP (Tank Mix) 500+90+200 1000+375+267 0.00
(0.00) 1.49
(1.34) 2.23
(1.53) 5.93
(2.53) 15.56
(4.01) 15.93
(3.47) 19.63
(4.12) 14.08
(3.82)
T4: Cartap hydrochloride 50% SP 500 1000 0.00
(0.00) 11.86
(3.52) 19.26
(4.45) 42.23
(6.53) 42.23
(6.54) 46.67
(6.87) 51.12
(7.18) 65.19
(8.11)
T5: Thifluzamide 5% SC 90 375 0.00
(0.00) 2.97
(2.85) 5.93
(2.53) 12.6
(3.6) 18.52
(4.35) 17.41
(3.77) 18.86
(4.50) 17.04
(4.19)
T6: Tricyclazole 75% WP 225 300 0.00
(0.00) 11.12
(3.4) 16.30
(4.10) 33.71
(5.78) 49.63
(7.06) 57.04
(7.57) 62.23
(7.91) 71.12
(8.46)
T7: Untreated control - - 0.00
(0.00) 11.86
(3.51) 17.04
(4.18) 42.97
(6.59) 49.63
(7.08) 56.3
(7.54) 59.26
(7.73) 68.15
(8.29)
CD @ 5 % NS 0.9 0.74 1.08 0.75 0.95 1.01 0.54
Figures in parenthesis are arcsine transformed values, DAFA- Days After First Application, DASA- Days After Second Application, NS- Non significant

But at 0 days after second application, the significant lowest PDI was also observed in T2 (3.16%) which was at par with only T1 (3.4%) and significantly superior over rest of the treatments. On 5, 10 & 15 days after second application also, same trend of observations were observed. The T7 Untreated Control recorded highest PDI (8.29%) at 15 days after second application. So overall, T2 and T1 were found superior for controlling the Sheath Blight disease.
d) Bio-efficacy of the pesticidal composition of the present disclosure against Leaf Blast
It is seen from Table-17 that, at the time of initiation of trial, there was just initiated the Leaf Blast disease and it was uniformly distributed in all trial plots. At 5 days after first application, the highest PDI was recorded in T7 Untreated Control (4.04%). The significant lowest PDI was observed in T2 (0.71%) which was at par with T1 & T3 (1.34% both) and significantly superior over rest of the treatments. At 10 days after first application lowest disease was found in T2 (0.71%) which was significantly superior over rest of all the treatments followed by T1 (2.43%). On 15 days after first application again same trend of observations as of 5 days was observed.
Table-17: Bio-efficacy of different treatments of tests products against Leaf Blast of Paddy
Treatment (Leaf blast) DOSE/ ha 1st Application 2nd Application
Mean PDI Mean PDI
g a.i. Formulation (g/ml) 0
DAFA 5
DAFA 10
DAFA 15
DAFA 0
DASA 5
DASA 10
DASA 15
DASA
T1: Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-3) 500+90+200 2000 0.84
(1.16) 1.49
(1.34) 5.93
(2.43) 9.63
(3.16) 17.04
(4.19) 5.19
(2.32) 8.89
(3.05) 16.3
(4.1)
T2: Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-4) 500+90+200 2000 0.70
(1.09) 0.00
(0.71) 0.00
(0.71) 9.26
(3.09) 16.67
(4.14) 4.45
(2.19) 8.15
(2.88) 13.71
(3.74)
T3: Cartap hydrochloride 50% WP + Thifluzamide 24% SC + Tricyclazole 75% WP (Tank Mix) 500+90+200 1000+375+267 1.20
(1.3) 1.49
(1.34) 6.67
(2.58) 9.63
(3.16) 17.04
(4.19) 5.19
(2.38) 8.89
(3.03) 15.56
(3.99)
T4: Cartap hydrochloride 50% SP 500 1000 0.90
(1.18) 11.86
(3.51) 18.52
(4.36) 31.86
(5.69) 45.19
(6.75) 51.86
(7.24) 57.78
(7.64) 64.45
(8.06)
T5: Thifluzamide 5% SC 90 375 1.57
(1.44) 9.63
(3.16) 15.93
(4.05) 34.82
(5.94) 45.19
(6.73) 51.86
(7.22) 56.30
(7.54) 62.97
(7.96)
T6: Tricyclazole 75% WP 225 300 0.70
(1.1) 2.23
(1.65) 8.15
(2.93) 18.49
(4.43) 18.52
(4.35) 18.15
(4.94) 17.04
(4.15) 21.49
(4.64)
T7: Untreated control - - 1.84
(1.53) 15.93
(4.04) 15.93
(4.04) 45.93
(6.79) 56.30
(7.54) 60.75
(7.83) 65.19
(8.11) 75.56
(8.72)
CD @ 5 % NS 0.70 0.94 0.95 0.79 0.84 0.89 0.9
Figures in parenthesis are arcsine transformed values, DAFA- Days After First Application, DASA- Days After Second Application, NS- Non significant

At the time of second application (0 days) similar trend as of first application was observed. Where T2, T1 & T3 showed least PDI (4.14, 4.19, 4.19% respectively) which were at par with each other and significantly superior over rest of the treatments. At 5, 10 & 15 days after second application similar results were found. So for Leaf Blast also overall, T2, T1 & T3 were found superior for controlling the disease.
c) Effect of the pesticidal composition on Phytotoxicity
The test Insecticide + Fungicides three way combinations of the present disclosure were sprayed to check the phytotoxic effects like leaf injury on tips/surface, vein clearing, necrosis, hyponasty and epinasty on the Paddy crop at X and 2X dosages along with Untreated Control. The observations on these phytotoxicity parameters were observed on before spray and at 3, 5, 7, 10 & 15 days after application and the results are summarized in Table-18.
Table-18: Phyto-toxicity effect of different treatments on Paddy
Tr. No. Treatment Details
Dose *Phytotoxicity
(Based on 0-10 Phytotoxicity Rating Scale)
g a.i./ha ml or g/ha Before Spray Days after application (DAA)
1 3 5 7 10 15
T1 Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-3) 500+90+200 2000 0 0 0 0 0 0 0
T2 Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-4) 500+90+200 2000 0 0 0 0 0 0 0
T3 Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-3) 1000+180+400 4000 0 0 0 0 0 0 0
T4 Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-4) 1000+180+400 4000 0 0 0 0 0 0 0
T5 Untreated control - - 0 0 0 0 0 0 0
*For phototoxic symptoms- Leaf injury on tips and Leaf surface, Wilting, Vein Clearing, Necrosis, Epinasty and Hyponasty

It is seen from Table-18 that there was no any phytotoxicity observed on the crop after application of any of the treatment. There was no any adverse effect noticed on the crop in the field applied with these test products.
d) Effect of the pesticidal composition on Yield
Table-19: Effect of different treatments on Paddy Yield
Tr. No Treatment Details Dose (g a.i./ha) Dose (ml or g/ha) Yield (kg/ha)

T1 T1: Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-3) 500+90+200 2000 5250
T2 T2: Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-4) 500+90+200 2000 5369
T3 T3: Cartap hydrochloride 50% WP + Thifluzamide 24% SC + Tricyclazole 75% WP (Tank Mix) 500+90+200 1000+375+267 5081
T4 T4: Cartap hydrochloride 50% SP 500 1000 5076
T5 T5: Thifluzamide 5% SC 90 375 4615
T6 T6: Tricyclazole 75% WP 225 300 4864
T7 T7: Untreated control - - 3312
CD (P = 0.05) 204

It is seen from Table-19 that all the treatments significantly increase the yield than T7 Untreated Control (3312 Kg/ha). The highest yield was observed in treatment T2 (5369 Kg/ha), which was at par with T1 (5250 Kg/ha) and significantly superior over rest of the treatments.
It is clearly seen from the above studies that the pesticidal composition of the present disclosure is effective against insect pests and diseases of Paddy. It is observed that the three way combinations of the present disclosure, namely, Insecticide (1) & Fungicides (2), Cartap Hydrochloride + Thifluzamide + Tricyclazole gives effective control of lepidopteran insect pests (Leaf Folder & Stem Borer) and diseases (Sheath Blight & Blast) of Paddy. Both, the test products of this combination, Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-3) & Cartap hydrochloride 25% + Thifluzamide 4.5% + Tricyclazole 10% WP (Experiment-4) perform better. The efficacy of the pesticidal composition of the present disclosure (Cartap Hydrochloride + Thifluzamide + Tricyclazole) is far better than commercially available pesticides, such as Cartap Hydrochloride 50% WP and Thifluzamide 5% SC & Tricyclazole 75% WP for controlling lepidopteran insect pests and disease complex of Paddy. Further, there is no phytotoxicity effect of the insecticidal composition on Paddy. It is also observed that as the pesticidal composition of the present disclosure provided significantly improved bio-efficacy and hence is capable of producing higher Paddy yield. The pesticidal composition of the present disclosure exhibits synergistic effect in controlling the pests of paddy crop, and can be used effectively and safely used for the management of pests as compared to individual use of Cartap HCl, Thifluzamide and tricyclazole alone.
TECHNICAL ADVANCEMENTS
The present disclosure described herein above has several technical advantages including, but not limited to, the realization of a stable, and ready to use pesticidal composition having enhanced efficacy.
The embodiments herein and the various features and advantageous details thereof are explained with reference to the non-limiting embodiments in the following description. Descriptions of well-known components and processing techniques are omitted so as to not unnecessarily obscure the embodiments herein. The examples used herein are intended merely to facilitate an understanding of ways in which the embodiments herein may be practiced and to further enable those of skill in the art to practice the embodiments herein. Accordingly, the examples should not be construed as limiting the scope of the embodiments herein.
The foregoing description of the specific embodiments so fully reveal the general nature of the embodiments herein that others can, by applying current knowledge, readily modify and/or adapt for various applications such specific embodiments without departing from the generic concept, and, therefore, such adaptations and modifications should and are intended to be comprehended within the meaning and range of equivalents of the disclosed embodiments. It is to be understood that the phraseology or terminology employed herein is for the purpose of description and not of limitation. Therefore, while the embodiments herein have been described in terms of preferred embodiments, those skilled in the art will recognize that the embodiments herein can be practiced with modification within the spirit and scope of the embodiments as described herein.
The use of the expression “at least” or “at least one” suggests the use of one or more elements or ingredients or quantities, as the use may be in the embodiment of the disclosure to achieve one or more of the desired objects or results.
Any discussion of documents, acts, materials, devices, articles or the like that has been included in this specification is solely for the purpose of providing a context for the disclosure. It is not to be taken as an admission that any or all of these matters form a part of the prior art base or were common general knowledge in the field relevant to the disclosure as it existed anywhere before the priority date of this application.
The numerical values mentioned for the various physical parameters, dimensions or quantities are only approximations and it is envisaged that the values higher/lower than the numerical values assigned to the parameters, dimensions or quantities fall within the scope of the disclosure, unless there is a statement in the specification specific to the contrary.
While considerable emphasis has been placed herein on the components and component parts of the preferred embodiments, it will be appreciated that many embodiments can be made and that many changes can be made in the preferred embodiments without departing from the principles of the disclosure. These and other changes in the preferred embodiment as well as other embodiments of the disclosure will be apparent to those skilled in the art from the disclosure herein, whereby it is to be distinctly understood that the foregoing descriptive matter is to be interpreted merely as illustrative of the disclosure and not as a limitation.
,CLAIMS:WE CLAIM:
1. A pesticidal composition comprising cartap hydrochloride, at least one anilide and tricyclazole.
2. The pesticidal composition as claimed in claim 1 comprising cartap hydrochloride in an amount of 0.1 wt% to 50 wt% of the composition.
3. The pesticidal composition as claimed in claim 1 comprising anilide in an amount of 0.1 wt% to 40 wt% of the composition.
4. The pesticidal composition as claimed in claim 1 comprising tricyclazole in an amount of 0.1 wt% to 40 wt% of the composition.
5. The pesticidal composition as claimed in claim 1, wherein said anilide is selected from the group consisting of benalaxy, benalaxyl-M, bixafen, boscalid, carboxin, fenhexamid, fluxapyroxad, isotianil, metalaxyl, metalaxyl-M, metsulfovax, ofurace, oxadixyl, oxycarboxin, penflufen, pyracarbolid, pyraziflumid, sedaxane, thifluzamide, tiadinil, and vangard.
6. The pesticidal composition as claimed in claim 5, wherein said anilide is selected from the group consisting of bixafen, boscalid, carboxin, fenhexamid, fluxapyroxad, ofurace, oxycarboxin, penflufen, pyracarbolid, pyraziflumid, sedaxane, thifluzamide and tiadinil.
7. The pesticidal composition as claimed in claim 1 comprising one or more agrochemically acceptable additives.
8. The composition as claimed in claim 7, wherein said additive is selected from the group consisting of at least one surfactant, at least one stabilizer, at least one filler, at least one coloring agent, at least one carrier, at least one acidifying agent, and combinations thereof.
9. The pesticidal composition as claimed in claim 1 comprising:
- cartap hydrochloride in an amount in the range of 0.1 wt% to 40 wt% of the composition;
- at least one anilide in an amount in the range of 0.1 wt% to 30 wt% of the composition;
- tricyclazole in an amount in the range of 0.1 % to 30 % weight of the composition; and
- one or more agrochemically acceptable additives.
10. The pesticidal composition as claimed in claim 1 comprising:
- cartap hydrochloride in an amount in the range of 0.1 wt% to 30 wt% of the total composition;
- at least one anilide in an amount in the range of 0.1 wt% to 15 wt% weight of the total composition;
- tricyclazole in an amount in the range of 0.1 wt% to 15 wt% weight of the total composition; and
- agrochemically acceptable additives selected from the group consisting of at least one surfactant, at least one stabilizer, at least one filler, at least one coloring agent, at least one acidifying agent, carrier and combinations thereof.
11. The pesticidal composition as claimed in claim 1, wherein said pesticidal composition is in at least one dosage form selected from the group consisting of encapsulated granules, water dispersible granules and wettable powder.
12. A process for preparing a pesticidal composition as claimed in claim 1 in the form of encapsulated granules, the process comprising the following steps:
- blending pre-determined quantities of at least one surfactant, at least one stabilizer, at least one acidifying agent, and at least one coloring agent to obtain a blended mixture;
- heating said blended mixture at a temperature in the range of 55 °C to 65 °C and admixing with pre-determined quantity of a carrier to obtain an admixture;
- cooling said admixture to a temperature in the range of 10 °C to 40 °C, followed by addition of pre-determined quantity of a carrier and blending to obtain a blended admixture;
- milling pre-determined quantities of cartap, at least one anilide and tricyclazole to obtain wettable powder;
- blending said wettable powder with said blended admixture for a time period in the range of 40 minutes to 120 minutes to obtain coated granules; and
- blending said coated granules with a pre-determined amount of filler for a time period in the range of 20 minutes to 60 minutes to obtain said pesticidal composition in the form of encapsulated granules.
13. A process for preparing a pesticidal composition as claimed in claim 1 in the form of wettable powder, the process comprising the following steps:
- blending pre-determined amounts of a filler, and a surfactantto obtain a mixture;
- mixing pre-determined amounts of cartap hydrochloride, at least one anilide and tricyclazole to said blended mixture to obtain a resultant mixture;
- blending pre-determined amounts of a acidifying agent, a surfactant, and a stabilizer to said resultant mixture to obtain a blended mixture;
- milling said blended mixture for a time period in the range of 40 minutes to 120 minutes to obtain a milled mixture; and
- blending a pre-determined amount of a dispersing agent to said milled mixture to obtain said pesticidal composition in the form of wettable powder.
14. A method for controlling pests comprising contacting an infested site with a pesticidal composition comprising cartap hydrochloride, at least one anilide and tricyclazole by applying an effective amount of the composition thereon.
15. A kit configurable as a pesticidal composition adapted to be stored, transported, and discharged for treatment of plants, its habitat, soil, a crop or a crop field, comprising cartap hydrochloride, at least one anilide, tricyclazole and agrochemically acceptable additives.
16. Use of a pesticidal composition as claimed in claim 1, comprising cartap hydrochloride, at least one anilide and tricyclazole for treatment of plants, its habitat, soil, a crop or a crop field.

Documents

Application Documents

# Name Date
1 201721028021-STATEMENT OF UNDERTAKING (FORM 3) [07-08-2017(online)].pdf 2017-08-07
2 201721028021-PROVISIONAL SPECIFICATION [07-08-2017(online)].pdf 2017-08-07
3 201721028021-PROOF OF RIGHT [07-08-2017(online)].pdf 2017-08-07
4 201721028021-POWER OF AUTHORITY [07-08-2017(online)].pdf 2017-08-07
5 201721028021-DECLARATION OF INVENTORSHIP (FORM 5) [07-08-2017(online)].pdf 2017-08-07
6 201721028021-Proof of Right (MANDATORY) [12-03-2018(online)].pdf 2018-03-12
7 201721028021-ENDORSEMENT BY INVENTORS [06-08-2018(online)].pdf 2018-08-06
8 201721028021-CORRESPONDENCE-OTHERS [06-08-2018(online)].pdf 2018-08-06
9 201721028021-COMPLETE SPECIFICATION [06-08-2018(online)].pdf 2018-08-06
10 201721028021-ORIGINAL UNDER RULE 6 (1A)-FORM 1-140318.pdf 2018-08-11
11 201721028021-REQUEST FOR CERTIFIED COPY [22-08-2018(online)].pdf 2018-08-22
12 201721028021-FORM 18 [24-08-2018(online)].pdf 2018-08-24
13 201721028021-CORRESPONDENCE(IPO)-(CERTIFIED COPY)-(23-8-2018).pdf 2018-08-28
14 201721028021-FORM 3 [06-09-2018(online)].pdf 2018-09-06
15 201721028021-FORM 3 [07-09-2018(online)].pdf 2018-09-07
16 201721028021-FORM 3 [20-03-2019(online)].pdf 2019-03-20
17 201721028021-FER.pdf 2019-09-26
18 201721028021-FORM 3 [14-12-2019(online)].pdf 2019-12-14
19 201721028021-Information under section 8(2) (MANDATORY) [19-12-2019(online)].pdf 2019-12-19
20 201721028021-FORM-26 [21-12-2019(online)].pdf 2019-12-21
21 201721028021-ORIGINAL UR 6(1A) FORM 26-271219.pdf 2019-12-30
22 201721028021-FER_SER_REPLY [20-03-2020(online)].pdf 2020-03-20
23 201721028021-CLAIMS [20-03-2020(online)].pdf 2020-03-20
24 201721028021-FORM 3 [04-04-2020(online)].pdf 2020-04-04
25 201721028021-US(14)-HearingNotice-(HearingDate-07-08-2020).pdf 2020-07-01
26 201721028021-FORM-26 [04-08-2020(online)].pdf 2020-08-04
27 201721028021-Correspondence to notify the Controller [04-08-2020(online)].pdf 2020-08-04
28 201721028021-Written submissions and relevant documents [20-08-2020(online)].pdf 2020-08-20
29 201721028021-PatentCertificate15-10-2020.pdf 2020-10-15
30 201721028021-IntimationOfGrant15-10-2020.pdf 2020-10-15
31 201721028021-RELEVANT DOCUMENTS [17-09-2021(online)].pdf 2021-09-17
32 201721028021-RELEVANT DOCUMENTS [23-07-2022(online)].pdf 2022-07-23
33 201721028021-RELEVANT DOCUMENTS [23-08-2023(online)].pdf 2023-08-23

Search Strategy

1 SEARCHstrategy_23-09-2019.pdf
2 SEARCHstrategyAE_23-03-2020.pdf

ERegister / Renewals

3rd: 05 Nov 2020

From 07/08/2019 - To 07/08/2020

4th: 05 Nov 2020

From 07/08/2020 - To 07/08/2021

5th: 16 Jul 2021

From 07/08/2021 - To 07/08/2022

6th: 27 Jun 2022

From 07/08/2022 - To 07/08/2023

7th: 25 Jul 2023

From 07/08/2023 - To 07/08/2024

8th: 02 Aug 2024

From 07/08/2024 - To 07/08/2025