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ACTUAL WORK EXPERIENCE
ENTOMOLOGY DEPARTMENT
(MASS PRODUCTION OF BIO-AGENTS AND BIO-PESTICIDES
Course no -SRP-EL-ENTO 406
Student’s name-Jyothsna.A
Reg.Number-K/17/095
Semester-VII
2021-2022
Introduction
India is a country rich in biological diversity. So, biological control of insects, weeds, and diseases
by using their natural enemies has been practiced in India from many years ago .Due to high success
rate, biological control has been used as a promising alternative to chemical control In our country.
entomology module was a great opportunity to know more about different bio-control agents and
its production. We learnt a lot things, which include the preparation Metarhizium bio-pesticide
preparation of the media for the growth of M.anisopliae ,rearing of laboratory hosts, quality control
testing methods etc.
TThe manager of this module is Dr. A S Bagade sir .This module was allotted to student’s batch of
40 which is subdivided into 2 batches of 20 students each. And each batch Is again divided into 4 group
containing 5 students in each group. the weekly schedule is assigned to each group.
For the proper allotment works for ESRP EL ENTO 406 mass production of bio agents and bio
pesticides the module in charge alloted the batches of each batch and and alote them working
schedule for each day. My group members were,
G.R Ghanvant S.S Gurgude P.C Jdav
Y. V Jangamwar Jyothsna A
Weekly schedule
Monday Mixing and packing
Tuesday Inoculation
Wednesday Media preparation
Thursday Lab cleaning
Friday Mixing and packing
Saturday Inoculation
Sunday Media preparation
Work performed
Preparation of metarhizium Rearing of mealy bud
Quality control testes
Rearing of Helicoverpa armigera
Other extension activities
Media preparation
Cleaning of lab and lab utensils
Rearing of Corcyra cephalonica
Lab cleaning
• Maintenance and cleaning of labs are very important to prevent contamination in culture at
laborataries. In the module we have to clean EPN lab, inoculation room,store room,and the
room where powder mixing take place.
• We also want to wash the lab utensils,used for Metarhizium culture preparation&media
preparation
Washing lab utensils Cleaning lab
Media preparation
Take 5L of water
and add 500 ml
of molasses into
it
Mix the solution
well with grinder
Add 100 ml of
the solution into
each conical
flasks
Cover it with
cotton plug.and
tie it with paper
and rubber
After that keep
the conical
flasks in the
autoclave
@121°c for 15
psi
Take the fully matured
culture and grind it
well
Mix the culture ell
with talcum powder
seive it twice with
mesh
Weighing of the
packets
Powder preparation and packing
Packed phule
metarhizium
Packing the
metarhizium packets
Keeping the packets
in the rack
Cook the potato pieces in 500
ml of water for 30 mints.
collect extract of cooked potato by
filtering through muslin cloth
add 20 g of dextrose to the extract Add agar –agar
Take 250 g potato peel off the
skin and cut it into small pieces
P. D. A Preparation
After cooling Pour into
petri-dish
Pour PDA into the
conical flasks
Covering the flask’s
mouth with paper
Autoclave the media for 15
psi pressure
Rearing of Corcyra cephalonica
• Take the wooden box of 45×30×15 cm and clean it properly.
• Sterilise the sorghum or wheat grains by oven for 30 minutes.and spray it with 0.1% of
formalin.
• Mill the grain to make 3-5 pieces of grains .
• Then fill the wooden box with,
1. 2.5kg of Crushed jowar or wheat grains
2. 25 g of crushed groundnut
3. 2g of protein
4. 1-1.5g of sulphur powder
5. 0.5 g of streptocyclin
6. 0.5 cc Corcyra cephalonica egg.
• Mix the materials properly after filling it in the box .and cover it with lid
• Keep it in the iron rack for 40-45 days
• After 45-50 days the moths of Corcyra cephalonica will emerge out
• Then collect the moths in the ovipositor cage.
Pupa formed
Filling container Mixing the ingredients
Adding eggs of rice moth
Rearing of Helicoverpa armigera
• Collected the larvae of H.armigera from chick pea field at pod formation stage.Collected
• Procedure for preparation of artificial diet
Then one cube is provided to each larvae for feeding
Then cut it into Cube size of 1×1×1 cm approximate
It allowed to cool
The grinded material mixed in agar-agar solution.this semi solid diet poured in a
aluminium tray
Then grinded the rest meterial in 300 ml water
We warmed agar-agar in 300ml water in a big container
First we waited Gram flour 105 gm.,distilled water 600ml,agar-agar 12.5gm,ascorbic acid-2gm
,sorbic acid-1gm,B-complex 1tablespoon.
Mass culturing of mealy Bug on red pumpkin
Pumpkin after mealy bug infestation
• Take a well developed red pumpkin with more no. of
furrows
• Dip it in the bavistin solution(0.1%) to prevent
contamination
• After drying fill the injuries or holes with paraffin wax
• Then tie the threads along with ridges which helps the
crawlers to crawl
• Then transfer the ovisacs of mealy bug to the
pumpkin with help of a camel hair brush
• Allow the mealy bugs for growth. And they develop
after 30-40 days
PDA media is
used for the
preparation of
mother culture.
Media is
sterilized at 121
degree celsius
for 30 min in
autoclave
Test tubes kept in
slanting position
Then it is
inoculated with
stock culture
Incubated at
room
temperature
PREPARATION OF
MOTHER
CULTURE
Inoculation
On the laminar airflow & on the UV light
for 20 minutes
On the daylight & sterilize surface & hand
with 0.1% Hgcl2
Lit spirit lamp and heat the needle
Insert hot needle on mother culture
Inoculate the media bottle with fungi
Seal the flask with cotton plug and keep in
the rack
Serial
dilution
Procedure
• Prepare 10 test tubes with 1oml of distilled water in one and 9 ml of distilled water in remaining test tubes(it
will be 10^-1 concentration )
• After that add 1g of Metarhizium powder in the first test tube.
• Shake it well to make a homogenous solution.
• Then puppet out 1ml of the dilutent from the first test tube and transfer it into the second test tube.
• Shake the test tube well.and again transfer 1ml of dilutent to the next test tube
• Repeat the process upto 10th test tube.
• The last test will be of 10^-10 concentration
Adding 1g of metarhizium powder into
10 ml water and shaking it
Pippeting out 1 ml of the solution Adding it into test tube containing 9ml of
distilled water
COLONY COUNTING
Transfer 1 ml of
dilutebt from
each test tube
of
concentration
10^-1 to 10^-
10 into petri
plates
Add small
quantity of PDA
into petri plates
Allow it to
solidify and tie it
with rubber
Keep it in B O
D Incubator for
5 days in
inverted
position
After 5 days
take colony
count on colony
counter
EXTENSION
ACTIVITIES
Giving information about metarhizium to
the farmers
Preparation of neem seed kernel extract
Method of preparation
 neem seed kernels are collected ,washed
,cleaned in pure water and shade dried for a few
days
The outer rind of seed is broken and kernels are
gathered and ground well as paste form
20 litre of water and 15 ml of soap solution are
added and kept undisturbed for overnight
Filter it and spray in the morning
Home activities
Method of preparation
 take a 200 litre vessel ( either plastic drum or similar ones)
Pour the water first
Submerge all 10 different leaves in the water
Pour cow urine and cow dung on top of the submerged leaves
Mix them well and leave it for 5 days
On the sixth day ,add 5-7 litre of water and again mix all the content in the vessel
Leave the same as it is for a month
The Dashparni ark is ready to use after filtering it
Preparation of Dashparni ark
Submerging the leaves Adding cow urine Adding cow dung Mixing it well
Business area coverage
Area covered by RCSM kolhapur entomology unit is all over kolhapur district and its 12 talukas and also nearby
districts. Of kolhapur. Also farmers from satara, sangli districts and from nipani districts of karnataka are coming
to buy the product
Distribution strategy
kolhapur is a district with majority population engaged in agriculture and large number of farmers were aware about
the mass production unit and bio-pesticides at AC kolhapur
Business networking is through contact with the farnmers,nursary growers,gardners,krishi seva kendra etc
Marketing channels
Department Farmers
Entomology module gave us opportunity to develop business networking skills being genuine,
, authentic and by building trust.
Focus
Empathy
Communication and
listening
Mutual support
Positive perspective
Diverse thinking
Business network skills acquired
Social skills
Communication and listening skills
Creative thinking
Teamwork and leadership skills
Ambition
Willingness to learn
Time management and organizational
skills
Customer service skills
courage and risk bearing
Entrepreneurship skills
MARKETING STRATEGY
• Marketing of the bio pesticide was done with the help of
folders,leaflets
1
• The rural agricultural work experience (Rawe) program is conducted
by universities for student where they spent 6 months in village and
guides farmers about the modern techniques in agriculture
2
• Organizes group discussion and lectures on the Agriculture topics by
professors of college, for awareness and guidance
3
• Visit to the field,mass discussion by agriculture professors and
scientist
4
SWOT Analysis
SWOT Analysis is a simple but useful framework for analyzing the organization's strengths,
weaknesses, opportunities, and threats. It helps us to build on what we do well, to address we you're
lacking, to minimize risks, and to take the greatest possible advantage of chances for success.
STRENGHTHS
Proper guidance
Better utilization of resources
Availability of adequate manpower
Customer reliability
Infrastructure availability
Better team work
WEAKNESS
Tedious legal procedure for registration
Regular application required
Lack of awareness of bio pesticides among
farmers
It’s efficiency depend upon the climate
Opportunities
Wide market of kolhapur
Chances of extending the business
coverage
High demand for bio agents
Threats
Risk of new entrant in market
Total cost Rs 9,39,376
Production of 3 months 5523 kg
Rate per kg Rs 200
Per kg cost of production 170.08 Rs /kg
Receipts for 3 Month Rs 1106400
Net profit Rs 167042
B.C ratio 1.17:1
Economic analysis
Thank you …

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1623312726776_work experience ppt ento jo.pptx

  • 1. ACTUAL WORK EXPERIENCE ENTOMOLOGY DEPARTMENT (MASS PRODUCTION OF BIO-AGENTS AND BIO-PESTICIDES Course no -SRP-EL-ENTO 406 Student’s name-Jyothsna.A Reg.Number-K/17/095 Semester-VII 2021-2022
  • 2. Introduction India is a country rich in biological diversity. So, biological control of insects, weeds, and diseases by using their natural enemies has been practiced in India from many years ago .Due to high success rate, biological control has been used as a promising alternative to chemical control In our country. entomology module was a great opportunity to know more about different bio-control agents and its production. We learnt a lot things, which include the preparation Metarhizium bio-pesticide preparation of the media for the growth of M.anisopliae ,rearing of laboratory hosts, quality control testing methods etc. TThe manager of this module is Dr. A S Bagade sir .This module was allotted to student’s batch of 40 which is subdivided into 2 batches of 20 students each. And each batch Is again divided into 4 group containing 5 students in each group. the weekly schedule is assigned to each group.
  • 3. For the proper allotment works for ESRP EL ENTO 406 mass production of bio agents and bio pesticides the module in charge alloted the batches of each batch and and alote them working schedule for each day. My group members were, G.R Ghanvant S.S Gurgude P.C Jdav Y. V Jangamwar Jyothsna A Weekly schedule Monday Mixing and packing Tuesday Inoculation Wednesday Media preparation Thursday Lab cleaning Friday Mixing and packing Saturday Inoculation Sunday Media preparation
  • 4. Work performed Preparation of metarhizium Rearing of mealy bud Quality control testes Rearing of Helicoverpa armigera Other extension activities Media preparation Cleaning of lab and lab utensils Rearing of Corcyra cephalonica
  • 5. Lab cleaning • Maintenance and cleaning of labs are very important to prevent contamination in culture at laborataries. In the module we have to clean EPN lab, inoculation room,store room,and the room where powder mixing take place. • We also want to wash the lab utensils,used for Metarhizium culture preparation&media preparation Washing lab utensils Cleaning lab
  • 6. Media preparation Take 5L of water and add 500 ml of molasses into it Mix the solution well with grinder Add 100 ml of the solution into each conical flasks Cover it with cotton plug.and tie it with paper and rubber After that keep the conical flasks in the autoclave @121°c for 15 psi
  • 7. Take the fully matured culture and grind it well Mix the culture ell with talcum powder seive it twice with mesh Weighing of the packets Powder preparation and packing
  • 8. Packed phule metarhizium Packing the metarhizium packets Keeping the packets in the rack
  • 9. Cook the potato pieces in 500 ml of water for 30 mints. collect extract of cooked potato by filtering through muslin cloth add 20 g of dextrose to the extract Add agar –agar Take 250 g potato peel off the skin and cut it into small pieces P. D. A Preparation
  • 10. After cooling Pour into petri-dish Pour PDA into the conical flasks Covering the flask’s mouth with paper Autoclave the media for 15 psi pressure
  • 11. Rearing of Corcyra cephalonica • Take the wooden box of 45×30×15 cm and clean it properly. • Sterilise the sorghum or wheat grains by oven for 30 minutes.and spray it with 0.1% of formalin. • Mill the grain to make 3-5 pieces of grains . • Then fill the wooden box with, 1. 2.5kg of Crushed jowar or wheat grains 2. 25 g of crushed groundnut 3. 2g of protein 4. 1-1.5g of sulphur powder 5. 0.5 g of streptocyclin 6. 0.5 cc Corcyra cephalonica egg. • Mix the materials properly after filling it in the box .and cover it with lid • Keep it in the iron rack for 40-45 days • After 45-50 days the moths of Corcyra cephalonica will emerge out • Then collect the moths in the ovipositor cage.
  • 12. Pupa formed Filling container Mixing the ingredients Adding eggs of rice moth
  • 13. Rearing of Helicoverpa armigera • Collected the larvae of H.armigera from chick pea field at pod formation stage.Collected • Procedure for preparation of artificial diet Then one cube is provided to each larvae for feeding Then cut it into Cube size of 1×1×1 cm approximate It allowed to cool The grinded material mixed in agar-agar solution.this semi solid diet poured in a aluminium tray Then grinded the rest meterial in 300 ml water We warmed agar-agar in 300ml water in a big container First we waited Gram flour 105 gm.,distilled water 600ml,agar-agar 12.5gm,ascorbic acid-2gm ,sorbic acid-1gm,B-complex 1tablespoon.
  • 14.
  • 15. Mass culturing of mealy Bug on red pumpkin Pumpkin after mealy bug infestation • Take a well developed red pumpkin with more no. of furrows • Dip it in the bavistin solution(0.1%) to prevent contamination • After drying fill the injuries or holes with paraffin wax • Then tie the threads along with ridges which helps the crawlers to crawl • Then transfer the ovisacs of mealy bug to the pumpkin with help of a camel hair brush • Allow the mealy bugs for growth. And they develop after 30-40 days
  • 16. PDA media is used for the preparation of mother culture. Media is sterilized at 121 degree celsius for 30 min in autoclave Test tubes kept in slanting position Then it is inoculated with stock culture Incubated at room temperature PREPARATION OF MOTHER CULTURE
  • 17. Inoculation On the laminar airflow & on the UV light for 20 minutes On the daylight & sterilize surface & hand with 0.1% Hgcl2 Lit spirit lamp and heat the needle Insert hot needle on mother culture Inoculate the media bottle with fungi Seal the flask with cotton plug and keep in the rack
  • 18. Serial dilution Procedure • Prepare 10 test tubes with 1oml of distilled water in one and 9 ml of distilled water in remaining test tubes(it will be 10^-1 concentration ) • After that add 1g of Metarhizium powder in the first test tube. • Shake it well to make a homogenous solution. • Then puppet out 1ml of the dilutent from the first test tube and transfer it into the second test tube. • Shake the test tube well.and again transfer 1ml of dilutent to the next test tube • Repeat the process upto 10th test tube. • The last test will be of 10^-10 concentration Adding 1g of metarhizium powder into 10 ml water and shaking it Pippeting out 1 ml of the solution Adding it into test tube containing 9ml of distilled water
  • 19. COLONY COUNTING Transfer 1 ml of dilutebt from each test tube of concentration 10^-1 to 10^- 10 into petri plates Add small quantity of PDA into petri plates Allow it to solidify and tie it with rubber Keep it in B O D Incubator for 5 days in inverted position After 5 days take colony count on colony counter
  • 20. EXTENSION ACTIVITIES Giving information about metarhizium to the farmers
  • 21. Preparation of neem seed kernel extract Method of preparation  neem seed kernels are collected ,washed ,cleaned in pure water and shade dried for a few days The outer rind of seed is broken and kernels are gathered and ground well as paste form 20 litre of water and 15 ml of soap solution are added and kept undisturbed for overnight Filter it and spray in the morning Home activities
  • 22. Method of preparation  take a 200 litre vessel ( either plastic drum or similar ones) Pour the water first Submerge all 10 different leaves in the water Pour cow urine and cow dung on top of the submerged leaves Mix them well and leave it for 5 days On the sixth day ,add 5-7 litre of water and again mix all the content in the vessel Leave the same as it is for a month The Dashparni ark is ready to use after filtering it Preparation of Dashparni ark
  • 23. Submerging the leaves Adding cow urine Adding cow dung Mixing it well
  • 24. Business area coverage Area covered by RCSM kolhapur entomology unit is all over kolhapur district and its 12 talukas and also nearby districts. Of kolhapur. Also farmers from satara, sangli districts and from nipani districts of karnataka are coming to buy the product Distribution strategy kolhapur is a district with majority population engaged in agriculture and large number of farmers were aware about the mass production unit and bio-pesticides at AC kolhapur Business networking is through contact with the farnmers,nursary growers,gardners,krishi seva kendra etc Marketing channels Department Farmers
  • 25. Entomology module gave us opportunity to develop business networking skills being genuine, , authentic and by building trust. Focus Empathy Communication and listening Mutual support Positive perspective Diverse thinking Business network skills acquired Social skills
  • 26. Communication and listening skills Creative thinking Teamwork and leadership skills Ambition Willingness to learn Time management and organizational skills Customer service skills courage and risk bearing Entrepreneurship skills
  • 27. MARKETING STRATEGY • Marketing of the bio pesticide was done with the help of folders,leaflets 1 • The rural agricultural work experience (Rawe) program is conducted by universities for student where they spent 6 months in village and guides farmers about the modern techniques in agriculture 2 • Organizes group discussion and lectures on the Agriculture topics by professors of college, for awareness and guidance 3 • Visit to the field,mass discussion by agriculture professors and scientist 4
  • 28. SWOT Analysis SWOT Analysis is a simple but useful framework for analyzing the organization's strengths, weaknesses, opportunities, and threats. It helps us to build on what we do well, to address we you're lacking, to minimize risks, and to take the greatest possible advantage of chances for success. STRENGHTHS Proper guidance Better utilization of resources Availability of adequate manpower Customer reliability Infrastructure availability Better team work WEAKNESS Tedious legal procedure for registration Regular application required Lack of awareness of bio pesticides among farmers It’s efficiency depend upon the climate Opportunities Wide market of kolhapur Chances of extending the business coverage High demand for bio agents Threats Risk of new entrant in market
  • 29. Total cost Rs 9,39,376 Production of 3 months 5523 kg Rate per kg Rs 200 Per kg cost of production 170.08 Rs /kg Receipts for 3 Month Rs 1106400 Net profit Rs 167042 B.C ratio 1.17:1 Economic analysis