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COLLEGE OF AGRICULTURE,
ANAND AGRICULTURAL UNIVERSITY –
JABUGAM
CHHOTAUDEPUR – 391155
SEVENTH SEMESTER B.Sc. (Hons.) Agriculture
RAWE & AIA Programme
ON CAMPUS TRAINING PHASE
Phase P2 : On Campus Training
(During 17-08-2021 to 09-09-2021)
On Campus Training
Phase
SHRI AZADCHANDRA DAMOR
Co-ordinator of On Campus Training Phase
SHRI AZADCHANDRA DAMOR
Department of Genetics & Plant Breeding.
A presentation submitted in partial fulfilment of
the requirements for the degree of
BACHELOR OF SCIENCE IN AGRICULTURE
Prepared By
ASHISH SHIVJI BHUVA.
Registration number : 3010318006
SCHEDULE OF ORIENTATION PHASE WITH
RESPECTIVE COURSE TEACHERS
NO. DATE TEACHER SUBJECT
1. 17th Aug Dr. Manish Dabhi Ag. Entomology
2. 20th Aug Dr. Ranganathswamy. M
Shri Arjunsinh Rathava
Pathology &
Microbiology
3. 23rd Aug Dr. Vimal Patel
Dr. Rajkumar Shinde
Soil Science &
Ag. Chemistry
4. 26th Aug Dr. Rukshar Sheikh
Shri Azadchandra Damor
Plant Breeding & Genetics/
Seed Technology/ Biochem.
5. 31st Aug Dr. Sunil. R. Patel
Dr. Kiranben Chandravadia
Dr. Anil Macwan
Ag. Extension
6. 2nd Sept Dr. Pinakin Patel
Dr. Lokesh Yadav
Horticulture
7. 6th Sept Dr. Gajanan. L. Kadam
Dr. Vinod B. Mor
Agronomy
8. 7th Sept Dr. M. L. Gaur Ag. Engineering
9. 8th Sept Dr. Husen Mahammad Ag. Economics
Date : 17/08/2021 to 18/08/2021
Sub : Agricultural Entomology
Course Teacher : Dr. Manishkumar Dabhi
 General body organization of grasshopper
Classification of insects based on Orders
1. Pterygota
2. Apterygota
Recent Trends/ advances in Pest management.
I. INSECTS REPELLENTS.
 Types of repellents.
• Repellents are broadly classified as Physical and Chemical .
1. Physical Repellents
i) Contact stimuli repellents
ii ) Auditory repellents
iv) Excitatory repellents
v) Feeding repellents
2. Chemical repellents
i) Repellents of plant origin
ii) Synthetic repellents
MORPHOLOGYAND CLASSIFICATION OF INSECTS.
II. INSECT ANTIFEEDANT
 Groups of antifeedant
a) Triazines
b) Organotins
c) Carbamates
d) Botanical Extracts
i) Pyrethrum
ii) Margosa (Neem)
iii) Apple Factor
iv) Solanum alkaloids
III. INSECTS ATTRACTANTS
 Types of antifeedant
a) Pheromones
b) Natural food lures
c) Ovipostional lures
d) Poison baits
 Different Classification based on different modes.
 Classification based on mode of entry.
 Stomach
 Contact
 Fumigant
 Systemic
 Classification based on mode of action.
 Physical
 Respiratory
 Nerve
Based on toxicity.
 Extremely toxic
 Highly toxic
 Moderately toxic
 Less toxic
MASS PRODUCTION OF CORCYRA CEPHALONICA
(LAB HOST FOR TRICHOGRAMMA SPP.)
 Material required :
i. Sterilized Sorghum
ii. Corcyra rearing boxes
iii. Corcyra egg laying cage
iv. Racks for placing Corcyra eggs.
v. Streptomycin sulphate – 0.05 grams
 Procedure :
Grind the sorghum grains with grinding stone.
Place the flour in Corcyra rearing box.
Add protein X with eggs of Corcyra moth. Add 5 gm of wetable
Sulphur and streptomycin sulphate in each box.
Favorable temperature for rearing is 28+/-2 & Relative Humidity
75 %.
Moths start emerging after 30 to 35 days.
Collects eggs by passing different sieves of 10,15 and 20 mm
meshes.
Utilize Corcyra eggs for Trichogramma production or store them
in refrigerator at 10 degree Celsius for 7 days if required.
RESULT : After 3 weeks, moths emerged from eggs and
started to mating and produces eggs.
 Sprayer : is a device used in agriculture used to spray
liquids like water, insecticides, & Pesticides in agriculture.
 Types of Sprayer
o Knapsack sprayer
o Portable Sprayer
o Mist dust Sprayer
o HTP Sprayer
o Orchard Sprayer
o Knapsack Power Sprayer
 Types of Sprayers based on Volume (Area)
o High Volume Sprayer – 300 to 700 lit/ha
o Low Volume Sprayer – 50 to 100 lit/ha
o Ultra low Volume Sprayer – 1 to 5 lit/ha
 Duster : is a machine to apply chemical in dust form.
Dusters make use of air streams to carry pesticides in
finely divided dry form on plants.
 Types of Duster :
o Package Duster
o Plunger Duster
o Bellow Duster
o Rotary Duster
 Nozzle : The nozzle determines the amount of spray that is
generated over a given area, the uniformity of the spray
produced, the coverage obtained and the drift that occurs
 Types of nozzle :
o Flat fan nozzle
o Flood jet nozzle
o Adjustable nozzle
o Hollow cane nozzle
o Watched video recorded promotional film which showed
rearing of silk from silkworms, and how to produce honey
by beekeeping.
o Also watched CD- Video on how to prevent storage grain
pests and How to control it without tiresome.
o Watched video film on how to control Rats before damaging
crops.
o A CD- Video on Integrated Pest Management to control
Pest with effective measures and how to save crop before
infestation of destructive insects and pests via
AGRIMEDIA.
 Honey bee.
 Life cycle of honey bee.
 Types of Honey bees.
 Information about Honey bee.
 Management, growing methods.
 Honey rearing management.
 Honey rearing instruments and equipments.
 Silk worms.
 Types of silk worms.
 Life cycle of honey bee.
 Information about Silk.
 Eating's of worms, Growing management.
 Silk industry processing.
 Instruments and equipments and machines used for rearing silk.
HOW TO SPRAY
o Learned on different types of pesticides used for different
pests.
o Practically application of pesticides, how to handle pump,
how to prevent safety measures while spraying.
o Learned about different nozzles used in spraying pumps.
o How to handle pesticides and insecticides with safety
measures and what to do if unfortunately you get in touch
with danger and harmful pesticides.
o What type of sprayer, duster, and nozzles used for different
situations accordingly.
o What type of pesticide used for controlling different pests
and insects.
Date : 20/08/2021 to 21/08/2021
Sub : Plant Pathology & Microbiology
Course Teacher : Dr. Ranganathswamy. Math
 Seed Borne Disease & their Management.
 Important Terms related to Pathology.
 Introduction about Paul Neergaard : Father of Seed Pathology.
 Effects of Seed Infection.
 Significance of Seed Health.
 Seed Health Testing.
 Main objectives of Seed Health Test.
 About Fungi & Bacteria.
 Seed Health Testing Methods.
 Detail information on Blotting Method.
 Rolled Towel Method
 Deep Freeze Method
Procedure for slide preparation of spores of maydis leaf blight
(Cochliobolus heterostropus)
Slide preparation of spores of infected leaf (Maydis leaf
Blight)
Scraping of spores on slide
Dye : Bromophenol Cotton Blue & Safranin
View under microscope.
RESULT : Spores (Conidia viewed under microscope).
CONIDIA
Procedure for slide preparation of spores of bajra rust
(Puccinia pennisetti)
Slide preparation of spores of infected leaf (Bajra Rust)
Cutting of infected leaves on slide
Dye : Bromophenol Cotton Blue & Safranin
View under microscope.
RESULT : Uredospores occurs in group.
Uredospores of
Bajra Rust
ABOUT SEED HEALTH TESTING.
 TYPES OD SEED HEALTH TESTING METHODS
o Blotting method
o Rolled towel method/Seedling symptom test
o Deep Freeze Method
o Agar Plate Method.
 DIFFERENT SLIDE PREPARATION
o Anthracnose
o Maydis Leaf Blight
o Rust of Bajra
 ISOLATION OF RHIZOBIUM FROM ROOT NODULES.
 CULTURAL GROWTH OF ANTHRACNOSE (SOYBEAN)
PROCEDURE (Agar Plate Method)
Isolation of Internal Seed Borne Disease
 Clean the working area with alcohol to avoid other microbial
contaminations.
 Pour Sodium hypochlorite solution in first Petri plate.
 Pour autoclaved distilled water in another three Petri plates.
 Burn the spirit lamp behind the wooden slate for avoid contamination of
germs.
 Pour the seeds in
sodium hypochlorite
solution for about 3
minutes.
 After pouring the seeds in
solution wash it with
distilled water 3 times, in
each for 1 to 1.5 minutes.
 After transferring the seeds to 4th plate remove it after 2 minutes.
 Take out the wet seeds from plate with the help of pinchers.
 Transfer the seeds to tissue paper.
 Let them soak for 2 minutes.
 After soaking of
seeds transfer it to
the agar plate with
the help of pinchers,
one by one.
 Put seeds with
maximum space for
proper growth of
disease.
 After completing the
transfer of seeds to
media cover it with
paraffin wax and cover
it properly.
 Cover the plate
properly.
RESULT : Out of 9 seeds two (2) are infected by seed
borne disease. So, Sample taken if infested by fungi .
PROCEDURE (Blotting Method)
Isolation of Internal Seed Borne Disease
 Place the filter paper in the plate.Moisten the plate with water
 Place the soybean seeds in the plate and Count it.
 Cover the lid of plate and put it for 4 to 5 days .
RESULT : Out of 41 seeds 11 seeds are infected it
means sample is infected with seed borne disease
PROCEDURE (Rolled Towel Method)
Isolation of Internal Seed Borne Disease
 Take a germination paper and moist it with water place the
seeds on it.
 Count the seeds.
 Put another Germination paper on it, Cover it properly.
 Rolled it and place a rubber band around it
 Wait for 4 to 5 days.
RESULT : Out of
28 Seeds 9 are
infected with seed
borne disease,
taken sample if
infested with seed
borne diseases.
Date : 20/08/2021 to 21/08/2021
Sub : Plant Pathology & Microbiology
Course Teacher : Shri Arjunsinh Rathava
Isolation of rhizobium from the root nodules of leguminous plant
(Green gram & Soybean)
Isolation of Anthracnose (Colletrotrichum spp.) from Soybean and
grow its culture.
Method of Isolation of Pseudomonas spp. from soil by serial
dilution by streaking Method.
Slide preparation of Spores of Colletrotrichum spp.
Procedure for Pure culture of Anthracnose (Soybean)
(Colletotrichum truncatum)
Take the infected leaf and cut the portion infected with disease of
anthracnose.
Surface sterilize it with NaoCl (Sodium Hypochlorite).
Place it on PDA Media for growth of fungi by feeding nutients.
Incubate it for 4 days on 18 degree Celsius.
RESULT :
The cultural growth
of Pseudomonas.
Procedure for Isolation of Rhizobium from Black Gram and
Soybean
Properly wash the root nodules and Squash it in distilled water.
Make Serial Dilution up to 10-6 and take aliquot from last sample
and pour it in the PDA Media.
Pour the rhizobium in Plate by STREAKING method and with
help of inoculation loop.
Streak the rhizobium culture on PDA plates
Incubate it for 5 days at 22◦C.
RESULT :
Procedure for slide preparation of spores of Anthracnose
(Colletotrichum truncatum)
Slide preparation of spores of infected leaf (Maydis leaf Blight)
Scraping of spores on slide
Dye : Bromophenol Cotton Blue & Safranin
View under microscope.
RESULT : Acervuli containing conidiophores.
Acervuli
containing conidia
Date : 23/08/2021 to 25/08/2021
Sub : Plant Pathology & Microbiology
Course Teacher : Dr. Rajkumar Shinde
Dr. Vimal Patel
Soil sampling Collection from field by zig-zag method .
Collect sample from various different spots.
Collect sample Randomly.
Handle instruments carefully during processing.
Collect the soil sample with soil auger.
Mix the soil properly so the lesser variations in results.
Collect the sample in one bag and name it properly.
Mention the date and day and place from where the sample is
collected.
Transport it to the laboratory for analysis.
DETERMINATION OF ECe & PH FROM SOIL
The pH of a solution has been defined as the negative logarithm
of the hydrogen ion activity which in very dilute solutions can
be expressed as concentration, in gram mole per liter.
pH = -log10 [H+ ] or [H+ ]=10-pH
 Electric pH meter method :
 The instrument commonly used in this method is a glass
electrode pH meter with calomel reference electrode
introducing salt bridge.
 Most digital pH meter now days have single (combined)
electrode assembly.
 The instrument being a potentiometer requires to be
calibrated before use with buffer solutions of known pH
values.
EC is a measure of the ability of a salt solution to carry electric
current by the migration of ions under the influence of an
electric field. Like metallic conductor, solutions also obey
Ohm’s law. The unit of conductivity is dSm-1 which is the
reciprocal of resistance in Ohm’s cm1 .
Conductivity to ppm :
ppm = 0.64 x EC x 106 for irrigation water in the range 100 to
5000 micromhos/cm (EC in mhos x 103 = millimhos (dS/m)
and x 106 = micromhos).
DETERMINATION OF ECE & PH FROM SOIL
Sample pH ECe
soil 8.08 0.21 ds/m
DETERMINATION OF AVAILABLE PHOSPHORUS FROM SOIL
(Olsen’s method)
Principle of Spectrophotometer:
Lambert’s law: The intensity of emitted light decreased exponentially as
the thickness of absorbing medium increases arithmetically
Beer’s law: The intensity of beam of monochromatic light decreases
exponentially as the concentration of the absorbing substances increase
arithmetically.
Note: The absorbance is also known as optical density.
Reagents:
i. 0.5 M sodium bicarbonate
ii. 1.5 % Ammonium molybdate:
iii. Stannous chloride (SnCl2)
iv. Phosphorus free activated charcoal
v. Standard P solution (50 mg P/l
vi. Working standard (2 mg P/l)
 Weight 5 g soil in bottle. Add one teaspoon of activated charcoal and
100 ml 0.5 M NaHCO3 solution.
 Shake the bottle for 30 minute on mechanical shaker.
 Take 5 ml aliquot in a 25 ml volumetric flask & Add 5 ml
ammonium molybdate solution and add little quantity of distilled
water and shake well.
 Add 1 ml working SnCl2. Measure transmittance of the solution at
660 nm in Spectrophotometer:
 The 0.5M NaHCO3 pH 8.5 solution is most suitable for neutral to
alkaline soils and is design to control the ionic activity of calcium through
solubility product of CaCO3, thus extracting the most reactive forms of P
from Al-, Fe- and Ca-P.
 Phosphate in extract is measured by reaction of phosphate with
ammonium molybdate in an acid medium to form molybdo phosphoric
acid. Molybdophosphoric acid is then reduced to blue coloured complex
(reduced phosphomolybdenum blue).
P2O5 in soil (kg/ha) = Net OD x GF x 100 x 25 x 2.29 x 2.24
5
= 42 kg/ha
DETERMINATION OFAVAILABLE POTASSIUM FROM SOIL
(Flame photometric Method)
 Principle of instrument:
o Atomic emission is caused by the excitement of electron which jump
from lower energy level to higher energy level. These excited electrons
come back to their original energy level. While returning to their
original energy level, electrons give out the absorbed heat energy in the
form of characteristic radiation.
o By measuring the intensity of emitted radiation, we can measure the
amount of element present in the sample. The basic equation governing
the phenomena is:
ΔE = E1 - E0
 Reagents:
1. Neutral normal ammonium acetate solution
2. Standard K solution (1000 mg K/l
Take 5 g soil in 150 ml conical flask or plastic bottle. Add 25 ml of
neutral N ammonium acetate solution and shake for 30 min
Filter the content through a Whatman No. 1 filter paper
4. Set up flame photometer to 0 scale reading by atomizing distilled water,
and to 100 by atomizing 100 mg K/l solution
 Potassium in soil exists as water soluble, exchangeable, non
exchangeable (fixed) and lattice-K.
 The first two forms constitute only a small part, normally not more
than one per cent of the total content and are considered to be
easily available to the plant.
 Only when these two forms are depleted, part of non exchangeable
K moves to exchange sites and soil solution. Therefore, most of
the methods suggested are based on the determination of easily
available fraction i.e. water soluble and exchangeable K.
K2O in soil (kg/ha) = R x GF x 25 x 1.20 x 2.24
5
= 235 kg/ha
DETERMINATION OFAVAILABLE SULPHUR FROM SOIL
(Turbidity method)
 Principle:
o Besides some amount in soil solution, available S in mineral
soils occurs mainly as adsorbed SO4
2- ions. Both CaCl2 and
phosphate solutions are generally used for replacement of SO4
2-
ions. Uses of Ca salts have a distinct advantage over those of
Na and K, as Ca prevents deflocculating in heavy textured soils
and leads to easy filtration. SO4
2- in the extract can be estimated
turbid metrically using spectrophotometer.
 Reagents :
1. 0.15% CaCl2 2H2O
2. Morgan’s reagent.
3. Gum acacia solution
4. Barium chloride
5. Standard S solution (50 mg S/l):
Transfer 10 g soil into a 100 ml capacity plastic bottle & Add 50 ml 0.15%
CaCl2 to it
Shake it for 30 minute on mechanical shaker
Pipette 20 ml aliquot into 50 ml volumetric flasks & Add 20 ml
Morgan's reagent, 2 ml gum acacia and one spoon barium chloride.
After 20 minute, measure the turbidity in spectrophotometer at 410 nm
wavelength
S in soil (mg/kg) =
Net OD x GF x 50 x 50
10 x 20
=1.306 ppm
ESTIMATION OF AVAILABLE NITROGEN FROM SOIL
(By Alkaline KMnO4 Method)
 Principle:
o A known weight of sample is the mixed with excess alkaline
KMnO4 solution.
o Potassium permanganate is oxidized the part of organic
matter and alkaline media convert the organic N into
ammonia gas and it absorbed in boric acid.
o The content is then titrated with standard sulphuric acid
using a mixed indicator.
2KMnO4 + H2O 2KOH + 2MnO2 + 3(O)
R-CH NH2COOH + ½O2 R-CO-COOH + NH3
Reagents :
1. 0.1N H2SO4
2. 0.32% KMnO4 solution
3. 2.5% NaOH solution
4. Mixed indicator
5. Boric acid (4%)
6. Paraffin liquid
Transfer 20g soil in a 800ml distillation flask.
Add 100ml of 0.32% KMnO4 solution
Measure 25ml 4% boric acid containing mixed indicator in a 250ml
beaker and
place it under the receiver tube. Titrate the distillate with std. 0.1 N
H2SO4 up to pink colored end point.
Available N (kg/ha) =
(S-B) x 0.014 x N of H2SO4 x 100 x 10000 x 2.24
Weight of Soil
=125 kg/ha
Date : 12/08/2021
Sub : Seed Technology & Biochemistry.
Course Teacher : Dr. Rukshar Sheikh
 Steps of tissue culture.
 Problems in tissue culture.
 Introduction to Shoot Meristem
 Direct and Indirect Embryogenesis.
 About DNA Fingerprinting, DNA Extraction.
 Agarose gel electrophoresis is a basic and essential technique
in molecular biology. It is routinely used for analysis of PCR
products, plasmid DNA, and products of restriction enzyme
digestion. It is the first step for analysis of specific DNA and
RNA fragments by northern and Southern blots.
Instrument used Equipments used
DIAGRAMMATIC REPRESENTATION
Date : 13/08/2021
Sub : Plant Breeding and Genetics
Course Teacher : Shri Azadchandra Damor
Notification and Certification of Variety.
NSC- 1963
Showed how to perform emasculation and crossing in bajra.
Seed Certification standards in different crops.
Visited to field and discussed about Bagging, Emasculation &
Crossing.
Discussed about the germplasm of banana presented in campus.
Visited to Maize field & studied about genotypic differences &
variations.
Emasculation in greengram.
Studied about crossing in pearmillet.
Date : 31/08/2021 to 01/09/2021
Sub : Ag. Extension
Course Teacher : Dr. Sunil. R. Patel
 Important Extension teaching methods.
 Information on KVKs
 Mandates of KVKs.
 All over India has (722 KVK) & Gujarat has (30 KVK)
 Principles of Extension.
 Short information on method and Result demonstration.
 Steps in adoption process.
 Project evaluation Report.
 Different types of Group Contact Methods such as :
i. Panel Discussion
ii. Symposium
iii. Brain Storming.
iv. Syndicate Study
 Poster Making
 Individual Contact Methods
 Office call
 Personal Letter
 Group contact Methods
 Method Demonstration
 Result Demonstration
 Group Discussion
 Lecture method
 Seminar
 Panel Discussion
 Symposium
 Mass Contact Methods
 Leaflet
 Folder
 Bulletin
Date : 31/08/2021 to 01/09/2021
Sub : Ag. Extension
Course Teacher : Dr. Kiranben Chandravadia
Date : 02/09/2021 to 04/09/2021
Sub : Horticulture
Course Teacher : Dr. Lokesh Yadav.
Materials Req. Quantity
Lemon Juice 1 Lit.
Water 1 Lit.
Sugar 3 Kg
Potassium meta-
bisulphate
2 grams.
Preparation of Lemon Squash.
 About industry in food and Processing.
 Introduction to Jam, Jelly, Squash.
 Introduction to Post harvest technology.
 About Drying and Cooling in Horticulture.
 Different Machines used in Pre-Cooling.
 About General talks related to Horticulture.
 Shares in Market related to Marketing of Agriculture.
 TSS Content of different Fruits & Vegetables
Fruits TSS Content
Mango 5.0 to 6.0 Brix
Grapes 15 Brix
Aonla 19 Brix
Guava 8 to 10 Brix
Chickoo 4 Brix
Pomegranate 12 Brix
Fruits TSS Content
Barbadose
Cherry
1000-4000 mg/100gm
Aonla 600-100 mg/100gm
Guava 400 mg/100gm
Citrus 300 mg/100gm
Preparation of Tomato Ketchup
 Tomato Sauce is Thinner Consistency whereas Tomato ketchup
has Thicker Consistency.
 Tomato Ketchup is rich in nutrients like Vitamin C, B and
Potassium.
 It is excellent source of antioxidants, such as Lycopene, which
may reduce inflammation and reduces heart risk diseases and
also some cancers.
 It also regulates Blood Sugar.
 Promotes Growth skin, Stronger bones and Healthy Hair.
Materials Needed Quantity
Tomato 5 Kg
Sugar 600 gm
Ginger 100 gm
Cinnamon & Cardamom 5 gm
Black Pepper 10 gm
Onion 100 gm
Garlic 30 gm
Acetic Acid 20 ml
Chilli Powder 20 gm
Sodium Benzoate 3 gm
Salt 30 gm
Preparation of Mix Fruit Jam
The history of jam dates back to greeks, who used honey to
preserve quinces.In the 16th Century, cane sugar came to europe
from the new world, and it was used to preserve fruit, hence the
term introduce jam thereafter.
Fruit jam refers to a product made of whole fruit cut into pieces or
crushed, then heated with water and sugar until it reaches “jelling”
or setting point.
Materials Needed Quantity Required
Chickoo 250 gm
Pineapple 250 gm
Papaya 250 gm
Apple 250 gm
Sugar 700 gm
Lemon Powder 7 gm
Preparation of Apple Chutney
Material Needed Quantity
Apple 1 Kg
Sugar 1 Kg
Ginger 50 gm
Acetic Acid 15 ml
Salt 30 gm
Citric Acid 10 ml
Garam Masala 25 gm
 Advantages of Apple Chutney.
 Good for Weight loss
 Prebiotic Effects ang help to prevent cancer.
 Apples are linked to lower the risk of diabetes.
 Weeding of congress grass
near Research Station.
 Cleaned the College Campus
near Research Station.
 Parthenium spp. Are vey
difficult to control if once
entered in field.
 Cleaned the nursery area of
mango.
 Bio-control Agent :
Zygogramma
bicolorata
Grafting in Mango
 Usually mango seedlings are grafted using top/wedge grafting
Method.
 June is the best time for grafting in Mango.
 Branches with two or three buds are cutted from tree and is
joined with V-Shaped cutting in Scion & Root stock is simply
cutted in T- Shaped. Both are joined together.
 The cut is joined tightly and wrapped in plastic & keep it under
safe place.
Date : 06/08/2021
Sub : Agronomy.
Course Teacher : Dr. Gajanan. L. Kadam
 Discussed about general questions asked in exams.
 Full forms :
 Cell Division and expansion.
 Learnt about different terms used in agriculture.
 About Soil Fertility.
 Abstract about Bio-herbicide.
 Different families about weeds.
 Different Origin of Crops.
 About Soil Pores
 PWP
 UWP
 ASM
 BMP
 GAP
Frequently asked questions in exams :
 Types of rainfall i.,e Isohyet, Isopach, Isohel
 About Leeward and Windward
 Sesbania rostrata is a stem nodulating green manure crop
(West Africa).
 Urea is placed in reduced zone to minimize the losses.
 Biuret Content of Urea should not exceed 1.5
 Conversions from Celsius to Fahrenheit.
 Herbicide Required (Formula).
 NPK Content of Poultry Manure.
 Calculations on Gypsum Requirement and Fertilizer required
dose in Soil.
 Varieties of Cotton.
 RH of Saturated Air – 100 %
 About Active and Passive Remote Sensing.
Date : 06/08/2021
Sub : Agronomy.
Course Teacher : Dr. Vinod B. Mor
 Discussed about the herbicide widely used in Agriculture.
 Introduction to different crops present in field.
 Detail introduction to Field Capacity, Available Water.
 Brief introduction to irrigation system.
 Cropping intensity area in India.
 Visited campus area and discussed about common problems
Physical and Biological Classification of water.
Studied about crops present in area.
About different types of Farming system.
 Discuss about the Common problems present in agriculture.
 Rouging : Removal of Off types from field.
 Had done rouging in rice field.
ROUGING IN RICE FIELD
Date : 07/09/2021
Sub : Ag. Engineering
Course Teacher : Dr. M. L. Gaur
 General Status of soil conservation in India.
 Importance of soil conservation.
 History of soil erosion about five year plans.
 Principles of soil erosion.
 Different types of Water erosion.
 Different water harvesting techniques.
 About universal soil loss equation.
 Soil erodibility factor.
 Modified universal soil loss equation.
 Long term runoff harvesting Techniques.
 Principles of wind erosion and its control measures.
 Woodruff & Zing (1952) developed the following
relationship between the distance of full protection and the
height of wind break or shelter belt.
 Surveying & Field area Calculation.
 Types of Water Harvesting.
Date : 08/09/2021
Sub : Agricultural Economics
Course Teacher : Dr. M. T. Khorajiya
 Column and Line Charts on Agriculture Import (in crores) &
Agriculture export (in crores)
 Studied about : Mean Standard ,Error ,Median ,Mode ,Standard
Deviation Sample Variance ,Kurtosis, Skewness, Range,
Minimum, Maximum ,Sum Count.
 Average , SD, & CV on Market vise Data of different crops such
as Maize Pearl millet Sorghum Wheat.
 Regression Coefficient on Dependent and independent values
for Production function.
 Correlation between three different districts producing same
crop.
 Paired T – test.
THANK YOU

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ON CAMPUS TRAINING PHASE, JABUGAM

  • 1. COLLEGE OF AGRICULTURE, ANAND AGRICULTURAL UNIVERSITY – JABUGAM CHHOTAUDEPUR – 391155 SEVENTH SEMESTER B.Sc. (Hons.) Agriculture RAWE & AIA Programme ON CAMPUS TRAINING PHASE Phase P2 : On Campus Training (During 17-08-2021 to 09-09-2021)
  • 2. On Campus Training Phase SHRI AZADCHANDRA DAMOR
  • 3. Co-ordinator of On Campus Training Phase SHRI AZADCHANDRA DAMOR Department of Genetics & Plant Breeding. A presentation submitted in partial fulfilment of the requirements for the degree of BACHELOR OF SCIENCE IN AGRICULTURE Prepared By ASHISH SHIVJI BHUVA. Registration number : 3010318006
  • 4. SCHEDULE OF ORIENTATION PHASE WITH RESPECTIVE COURSE TEACHERS NO. DATE TEACHER SUBJECT 1. 17th Aug Dr. Manish Dabhi Ag. Entomology 2. 20th Aug Dr. Ranganathswamy. M Shri Arjunsinh Rathava Pathology & Microbiology 3. 23rd Aug Dr. Vimal Patel Dr. Rajkumar Shinde Soil Science & Ag. Chemistry 4. 26th Aug Dr. Rukshar Sheikh Shri Azadchandra Damor Plant Breeding & Genetics/ Seed Technology/ Biochem. 5. 31st Aug Dr. Sunil. R. Patel Dr. Kiranben Chandravadia Dr. Anil Macwan Ag. Extension 6. 2nd Sept Dr. Pinakin Patel Dr. Lokesh Yadav Horticulture 7. 6th Sept Dr. Gajanan. L. Kadam Dr. Vinod B. Mor Agronomy 8. 7th Sept Dr. M. L. Gaur Ag. Engineering 9. 8th Sept Dr. Husen Mahammad Ag. Economics
  • 5. Date : 17/08/2021 to 18/08/2021 Sub : Agricultural Entomology Course Teacher : Dr. Manishkumar Dabhi  General body organization of grasshopper
  • 6. Classification of insects based on Orders 1. Pterygota 2. Apterygota Recent Trends/ advances in Pest management. I. INSECTS REPELLENTS.  Types of repellents. • Repellents are broadly classified as Physical and Chemical . 1. Physical Repellents i) Contact stimuli repellents ii ) Auditory repellents iv) Excitatory repellents v) Feeding repellents 2. Chemical repellents i) Repellents of plant origin ii) Synthetic repellents MORPHOLOGYAND CLASSIFICATION OF INSECTS.
  • 7. II. INSECT ANTIFEEDANT  Groups of antifeedant a) Triazines b) Organotins c) Carbamates d) Botanical Extracts i) Pyrethrum ii) Margosa (Neem) iii) Apple Factor iv) Solanum alkaloids III. INSECTS ATTRACTANTS  Types of antifeedant a) Pheromones b) Natural food lures c) Ovipostional lures d) Poison baits
  • 8.  Different Classification based on different modes.  Classification based on mode of entry.  Stomach  Contact  Fumigant  Systemic  Classification based on mode of action.  Physical  Respiratory  Nerve Based on toxicity.  Extremely toxic  Highly toxic  Moderately toxic  Less toxic
  • 9. MASS PRODUCTION OF CORCYRA CEPHALONICA (LAB HOST FOR TRICHOGRAMMA SPP.)  Material required : i. Sterilized Sorghum ii. Corcyra rearing boxes iii. Corcyra egg laying cage iv. Racks for placing Corcyra eggs. v. Streptomycin sulphate – 0.05 grams  Procedure : Grind the sorghum grains with grinding stone. Place the flour in Corcyra rearing box. Add protein X with eggs of Corcyra moth. Add 5 gm of wetable Sulphur and streptomycin sulphate in each box.
  • 10. Favorable temperature for rearing is 28+/-2 & Relative Humidity 75 %. Moths start emerging after 30 to 35 days. Collects eggs by passing different sieves of 10,15 and 20 mm meshes. Utilize Corcyra eggs for Trichogramma production or store them in refrigerator at 10 degree Celsius for 7 days if required. RESULT : After 3 weeks, moths emerged from eggs and started to mating and produces eggs.
  • 11.  Sprayer : is a device used in agriculture used to spray liquids like water, insecticides, & Pesticides in agriculture.  Types of Sprayer o Knapsack sprayer o Portable Sprayer o Mist dust Sprayer o HTP Sprayer o Orchard Sprayer o Knapsack Power Sprayer  Types of Sprayers based on Volume (Area) o High Volume Sprayer – 300 to 700 lit/ha o Low Volume Sprayer – 50 to 100 lit/ha o Ultra low Volume Sprayer – 1 to 5 lit/ha
  • 12.  Duster : is a machine to apply chemical in dust form. Dusters make use of air streams to carry pesticides in finely divided dry form on plants.  Types of Duster : o Package Duster o Plunger Duster o Bellow Duster o Rotary Duster  Nozzle : The nozzle determines the amount of spray that is generated over a given area, the uniformity of the spray produced, the coverage obtained and the drift that occurs  Types of nozzle : o Flat fan nozzle o Flood jet nozzle o Adjustable nozzle o Hollow cane nozzle
  • 13. o Watched video recorded promotional film which showed rearing of silk from silkworms, and how to produce honey by beekeeping. o Also watched CD- Video on how to prevent storage grain pests and How to control it without tiresome. o Watched video film on how to control Rats before damaging crops. o A CD- Video on Integrated Pest Management to control Pest with effective measures and how to save crop before infestation of destructive insects and pests via AGRIMEDIA.
  • 14.  Honey bee.  Life cycle of honey bee.  Types of Honey bees.  Information about Honey bee.  Management, growing methods.  Honey rearing management.  Honey rearing instruments and equipments.  Silk worms.  Types of silk worms.  Life cycle of honey bee.  Information about Silk.  Eating's of worms, Growing management.  Silk industry processing.  Instruments and equipments and machines used for rearing silk.
  • 15. HOW TO SPRAY o Learned on different types of pesticides used for different pests. o Practically application of pesticides, how to handle pump, how to prevent safety measures while spraying. o Learned about different nozzles used in spraying pumps. o How to handle pesticides and insecticides with safety measures and what to do if unfortunately you get in touch with danger and harmful pesticides. o What type of sprayer, duster, and nozzles used for different situations accordingly. o What type of pesticide used for controlling different pests and insects.
  • 16. Date : 20/08/2021 to 21/08/2021 Sub : Plant Pathology & Microbiology Course Teacher : Dr. Ranganathswamy. Math  Seed Borne Disease & their Management.  Important Terms related to Pathology.  Introduction about Paul Neergaard : Father of Seed Pathology.  Effects of Seed Infection.  Significance of Seed Health.  Seed Health Testing.  Main objectives of Seed Health Test.  About Fungi & Bacteria.  Seed Health Testing Methods.  Detail information on Blotting Method.  Rolled Towel Method  Deep Freeze Method
  • 17. Procedure for slide preparation of spores of maydis leaf blight (Cochliobolus heterostropus) Slide preparation of spores of infected leaf (Maydis leaf Blight) Scraping of spores on slide Dye : Bromophenol Cotton Blue & Safranin View under microscope. RESULT : Spores (Conidia viewed under microscope). CONIDIA
  • 18. Procedure for slide preparation of spores of bajra rust (Puccinia pennisetti) Slide preparation of spores of infected leaf (Bajra Rust) Cutting of infected leaves on slide Dye : Bromophenol Cotton Blue & Safranin View under microscope. RESULT : Uredospores occurs in group. Uredospores of Bajra Rust
  • 19. ABOUT SEED HEALTH TESTING.  TYPES OD SEED HEALTH TESTING METHODS o Blotting method o Rolled towel method/Seedling symptom test o Deep Freeze Method o Agar Plate Method.  DIFFERENT SLIDE PREPARATION o Anthracnose o Maydis Leaf Blight o Rust of Bajra  ISOLATION OF RHIZOBIUM FROM ROOT NODULES.  CULTURAL GROWTH OF ANTHRACNOSE (SOYBEAN)
  • 20. PROCEDURE (Agar Plate Method) Isolation of Internal Seed Borne Disease  Clean the working area with alcohol to avoid other microbial contaminations.  Pour Sodium hypochlorite solution in first Petri plate.  Pour autoclaved distilled water in another three Petri plates.  Burn the spirit lamp behind the wooden slate for avoid contamination of germs.
  • 21.  Pour the seeds in sodium hypochlorite solution for about 3 minutes.  After pouring the seeds in solution wash it with distilled water 3 times, in each for 1 to 1.5 minutes.
  • 22.  After transferring the seeds to 4th plate remove it after 2 minutes.  Take out the wet seeds from plate with the help of pinchers.  Transfer the seeds to tissue paper.  Let them soak for 2 minutes.
  • 23.  After soaking of seeds transfer it to the agar plate with the help of pinchers, one by one.  Put seeds with maximum space for proper growth of disease.  After completing the transfer of seeds to media cover it with paraffin wax and cover it properly.  Cover the plate properly.
  • 24. RESULT : Out of 9 seeds two (2) are infected by seed borne disease. So, Sample taken if infested by fungi .
  • 25. PROCEDURE (Blotting Method) Isolation of Internal Seed Borne Disease  Place the filter paper in the plate.Moisten the plate with water  Place the soybean seeds in the plate and Count it.  Cover the lid of plate and put it for 4 to 5 days .
  • 26. RESULT : Out of 41 seeds 11 seeds are infected it means sample is infected with seed borne disease
  • 27. PROCEDURE (Rolled Towel Method) Isolation of Internal Seed Borne Disease  Take a germination paper and moist it with water place the seeds on it.  Count the seeds.  Put another Germination paper on it, Cover it properly.  Rolled it and place a rubber band around it  Wait for 4 to 5 days.
  • 28. RESULT : Out of 28 Seeds 9 are infected with seed borne disease, taken sample if infested with seed borne diseases.
  • 29. Date : 20/08/2021 to 21/08/2021 Sub : Plant Pathology & Microbiology Course Teacher : Shri Arjunsinh Rathava Isolation of rhizobium from the root nodules of leguminous plant (Green gram & Soybean) Isolation of Anthracnose (Colletrotrichum spp.) from Soybean and grow its culture. Method of Isolation of Pseudomonas spp. from soil by serial dilution by streaking Method. Slide preparation of Spores of Colletrotrichum spp.
  • 30. Procedure for Pure culture of Anthracnose (Soybean) (Colletotrichum truncatum) Take the infected leaf and cut the portion infected with disease of anthracnose. Surface sterilize it with NaoCl (Sodium Hypochlorite). Place it on PDA Media for growth of fungi by feeding nutients. Incubate it for 4 days on 18 degree Celsius. RESULT : The cultural growth of Pseudomonas.
  • 31. Procedure for Isolation of Rhizobium from Black Gram and Soybean Properly wash the root nodules and Squash it in distilled water. Make Serial Dilution up to 10-6 and take aliquot from last sample and pour it in the PDA Media. Pour the rhizobium in Plate by STREAKING method and with help of inoculation loop. Streak the rhizobium culture on PDA plates Incubate it for 5 days at 22◦C. RESULT :
  • 32.
  • 33. Procedure for slide preparation of spores of Anthracnose (Colletotrichum truncatum) Slide preparation of spores of infected leaf (Maydis leaf Blight) Scraping of spores on slide Dye : Bromophenol Cotton Blue & Safranin View under microscope. RESULT : Acervuli containing conidiophores. Acervuli containing conidia
  • 34. Date : 23/08/2021 to 25/08/2021 Sub : Plant Pathology & Microbiology Course Teacher : Dr. Rajkumar Shinde Dr. Vimal Patel Soil sampling Collection from field by zig-zag method . Collect sample from various different spots. Collect sample Randomly. Handle instruments carefully during processing. Collect the soil sample with soil auger. Mix the soil properly so the lesser variations in results. Collect the sample in one bag and name it properly. Mention the date and day and place from where the sample is collected. Transport it to the laboratory for analysis.
  • 35. DETERMINATION OF ECe & PH FROM SOIL The pH of a solution has been defined as the negative logarithm of the hydrogen ion activity which in very dilute solutions can be expressed as concentration, in gram mole per liter. pH = -log10 [H+ ] or [H+ ]=10-pH  Electric pH meter method :  The instrument commonly used in this method is a glass electrode pH meter with calomel reference electrode introducing salt bridge.  Most digital pH meter now days have single (combined) electrode assembly.  The instrument being a potentiometer requires to be calibrated before use with buffer solutions of known pH values.
  • 36. EC is a measure of the ability of a salt solution to carry electric current by the migration of ions under the influence of an electric field. Like metallic conductor, solutions also obey Ohm’s law. The unit of conductivity is dSm-1 which is the reciprocal of resistance in Ohm’s cm1 . Conductivity to ppm : ppm = 0.64 x EC x 106 for irrigation water in the range 100 to 5000 micromhos/cm (EC in mhos x 103 = millimhos (dS/m) and x 106 = micromhos). DETERMINATION OF ECE & PH FROM SOIL
  • 37. Sample pH ECe soil 8.08 0.21 ds/m
  • 38. DETERMINATION OF AVAILABLE PHOSPHORUS FROM SOIL (Olsen’s method) Principle of Spectrophotometer: Lambert’s law: The intensity of emitted light decreased exponentially as the thickness of absorbing medium increases arithmetically Beer’s law: The intensity of beam of monochromatic light decreases exponentially as the concentration of the absorbing substances increase arithmetically. Note: The absorbance is also known as optical density. Reagents: i. 0.5 M sodium bicarbonate ii. 1.5 % Ammonium molybdate: iii. Stannous chloride (SnCl2) iv. Phosphorus free activated charcoal v. Standard P solution (50 mg P/l vi. Working standard (2 mg P/l)
  • 39.  Weight 5 g soil in bottle. Add one teaspoon of activated charcoal and 100 ml 0.5 M NaHCO3 solution.  Shake the bottle for 30 minute on mechanical shaker.  Take 5 ml aliquot in a 25 ml volumetric flask & Add 5 ml ammonium molybdate solution and add little quantity of distilled water and shake well.  Add 1 ml working SnCl2. Measure transmittance of the solution at 660 nm in Spectrophotometer:
  • 40.  The 0.5M NaHCO3 pH 8.5 solution is most suitable for neutral to alkaline soils and is design to control the ionic activity of calcium through solubility product of CaCO3, thus extracting the most reactive forms of P from Al-, Fe- and Ca-P.  Phosphate in extract is measured by reaction of phosphate with ammonium molybdate in an acid medium to form molybdo phosphoric acid. Molybdophosphoric acid is then reduced to blue coloured complex (reduced phosphomolybdenum blue). P2O5 in soil (kg/ha) = Net OD x GF x 100 x 25 x 2.29 x 2.24 5 = 42 kg/ha
  • 41. DETERMINATION OFAVAILABLE POTASSIUM FROM SOIL (Flame photometric Method)  Principle of instrument: o Atomic emission is caused by the excitement of electron which jump from lower energy level to higher energy level. These excited electrons come back to their original energy level. While returning to their original energy level, electrons give out the absorbed heat energy in the form of characteristic radiation. o By measuring the intensity of emitted radiation, we can measure the amount of element present in the sample. The basic equation governing the phenomena is: ΔE = E1 - E0  Reagents: 1. Neutral normal ammonium acetate solution 2. Standard K solution (1000 mg K/l
  • 42. Take 5 g soil in 150 ml conical flask or plastic bottle. Add 25 ml of neutral N ammonium acetate solution and shake for 30 min Filter the content through a Whatman No. 1 filter paper 4. Set up flame photometer to 0 scale reading by atomizing distilled water, and to 100 by atomizing 100 mg K/l solution
  • 43.  Potassium in soil exists as water soluble, exchangeable, non exchangeable (fixed) and lattice-K.  The first two forms constitute only a small part, normally not more than one per cent of the total content and are considered to be easily available to the plant.  Only when these two forms are depleted, part of non exchangeable K moves to exchange sites and soil solution. Therefore, most of the methods suggested are based on the determination of easily available fraction i.e. water soluble and exchangeable K. K2O in soil (kg/ha) = R x GF x 25 x 1.20 x 2.24 5 = 235 kg/ha
  • 44. DETERMINATION OFAVAILABLE SULPHUR FROM SOIL (Turbidity method)  Principle: o Besides some amount in soil solution, available S in mineral soils occurs mainly as adsorbed SO4 2- ions. Both CaCl2 and phosphate solutions are generally used for replacement of SO4 2- ions. Uses of Ca salts have a distinct advantage over those of Na and K, as Ca prevents deflocculating in heavy textured soils and leads to easy filtration. SO4 2- in the extract can be estimated turbid metrically using spectrophotometer.  Reagents : 1. 0.15% CaCl2 2H2O 2. Morgan’s reagent. 3. Gum acacia solution 4. Barium chloride 5. Standard S solution (50 mg S/l):
  • 45. Transfer 10 g soil into a 100 ml capacity plastic bottle & Add 50 ml 0.15% CaCl2 to it Shake it for 30 minute on mechanical shaker Pipette 20 ml aliquot into 50 ml volumetric flasks & Add 20 ml Morgan's reagent, 2 ml gum acacia and one spoon barium chloride. After 20 minute, measure the turbidity in spectrophotometer at 410 nm wavelength
  • 46. S in soil (mg/kg) = Net OD x GF x 50 x 50 10 x 20 =1.306 ppm
  • 47. ESTIMATION OF AVAILABLE NITROGEN FROM SOIL (By Alkaline KMnO4 Method)  Principle: o A known weight of sample is the mixed with excess alkaline KMnO4 solution. o Potassium permanganate is oxidized the part of organic matter and alkaline media convert the organic N into ammonia gas and it absorbed in boric acid. o The content is then titrated with standard sulphuric acid using a mixed indicator. 2KMnO4 + H2O 2KOH + 2MnO2 + 3(O) R-CH NH2COOH + ½O2 R-CO-COOH + NH3
  • 48. Reagents : 1. 0.1N H2SO4 2. 0.32% KMnO4 solution 3. 2.5% NaOH solution 4. Mixed indicator 5. Boric acid (4%) 6. Paraffin liquid
  • 49. Transfer 20g soil in a 800ml distillation flask. Add 100ml of 0.32% KMnO4 solution Measure 25ml 4% boric acid containing mixed indicator in a 250ml beaker and place it under the receiver tube. Titrate the distillate with std. 0.1 N H2SO4 up to pink colored end point.
  • 50. Available N (kg/ha) = (S-B) x 0.014 x N of H2SO4 x 100 x 10000 x 2.24 Weight of Soil =125 kg/ha
  • 51. Date : 12/08/2021 Sub : Seed Technology & Biochemistry. Course Teacher : Dr. Rukshar Sheikh  Steps of tissue culture.  Problems in tissue culture.  Introduction to Shoot Meristem  Direct and Indirect Embryogenesis.  About DNA Fingerprinting, DNA Extraction.  Agarose gel electrophoresis is a basic and essential technique in molecular biology. It is routinely used for analysis of PCR products, plasmid DNA, and products of restriction enzyme digestion. It is the first step for analysis of specific DNA and RNA fragments by northern and Southern blots.
  • 54. Date : 13/08/2021 Sub : Plant Breeding and Genetics Course Teacher : Shri Azadchandra Damor Notification and Certification of Variety. NSC- 1963 Showed how to perform emasculation and crossing in bajra. Seed Certification standards in different crops. Visited to field and discussed about Bagging, Emasculation & Crossing. Discussed about the germplasm of banana presented in campus. Visited to Maize field & studied about genotypic differences & variations. Emasculation in greengram. Studied about crossing in pearmillet.
  • 55.
  • 56. Date : 31/08/2021 to 01/09/2021 Sub : Ag. Extension Course Teacher : Dr. Sunil. R. Patel  Important Extension teaching methods.  Information on KVKs  Mandates of KVKs.  All over India has (722 KVK) & Gujarat has (30 KVK)  Principles of Extension.  Short information on method and Result demonstration.  Steps in adoption process.  Project evaluation Report.  Different types of Group Contact Methods such as : i. Panel Discussion ii. Symposium iii. Brain Storming. iv. Syndicate Study
  • 57.  Poster Making  Individual Contact Methods  Office call  Personal Letter  Group contact Methods  Method Demonstration  Result Demonstration  Group Discussion  Lecture method  Seminar  Panel Discussion  Symposium  Mass Contact Methods  Leaflet  Folder  Bulletin Date : 31/08/2021 to 01/09/2021 Sub : Ag. Extension Course Teacher : Dr. Kiranben Chandravadia
  • 58.
  • 59. Date : 02/09/2021 to 04/09/2021 Sub : Horticulture Course Teacher : Dr. Lokesh Yadav. Materials Req. Quantity Lemon Juice 1 Lit. Water 1 Lit. Sugar 3 Kg Potassium meta- bisulphate 2 grams. Preparation of Lemon Squash.
  • 60.  About industry in food and Processing.  Introduction to Jam, Jelly, Squash.  Introduction to Post harvest technology.  About Drying and Cooling in Horticulture.  Different Machines used in Pre-Cooling.  About General talks related to Horticulture.  Shares in Market related to Marketing of Agriculture.  TSS Content of different Fruits & Vegetables Fruits TSS Content Mango 5.0 to 6.0 Brix Grapes 15 Brix Aonla 19 Brix Guava 8 to 10 Brix Chickoo 4 Brix Pomegranate 12 Brix Fruits TSS Content Barbadose Cherry 1000-4000 mg/100gm Aonla 600-100 mg/100gm Guava 400 mg/100gm Citrus 300 mg/100gm
  • 61. Preparation of Tomato Ketchup  Tomato Sauce is Thinner Consistency whereas Tomato ketchup has Thicker Consistency.  Tomato Ketchup is rich in nutrients like Vitamin C, B and Potassium.  It is excellent source of antioxidants, such as Lycopene, which may reduce inflammation and reduces heart risk diseases and also some cancers.  It also regulates Blood Sugar.  Promotes Growth skin, Stronger bones and Healthy Hair.
  • 62. Materials Needed Quantity Tomato 5 Kg Sugar 600 gm Ginger 100 gm Cinnamon & Cardamom 5 gm Black Pepper 10 gm Onion 100 gm Garlic 30 gm Acetic Acid 20 ml Chilli Powder 20 gm Sodium Benzoate 3 gm Salt 30 gm
  • 63.
  • 64. Preparation of Mix Fruit Jam The history of jam dates back to greeks, who used honey to preserve quinces.In the 16th Century, cane sugar came to europe from the new world, and it was used to preserve fruit, hence the term introduce jam thereafter. Fruit jam refers to a product made of whole fruit cut into pieces or crushed, then heated with water and sugar until it reaches “jelling” or setting point. Materials Needed Quantity Required Chickoo 250 gm Pineapple 250 gm Papaya 250 gm Apple 250 gm Sugar 700 gm Lemon Powder 7 gm
  • 65.
  • 66. Preparation of Apple Chutney Material Needed Quantity Apple 1 Kg Sugar 1 Kg Ginger 50 gm Acetic Acid 15 ml Salt 30 gm Citric Acid 10 ml Garam Masala 25 gm  Advantages of Apple Chutney.  Good for Weight loss  Prebiotic Effects ang help to prevent cancer.  Apples are linked to lower the risk of diabetes.
  • 67.
  • 68.  Weeding of congress grass near Research Station.  Cleaned the College Campus near Research Station.  Parthenium spp. Are vey difficult to control if once entered in field.  Cleaned the nursery area of mango.  Bio-control Agent : Zygogramma bicolorata
  • 69. Grafting in Mango  Usually mango seedlings are grafted using top/wedge grafting Method.  June is the best time for grafting in Mango.  Branches with two or three buds are cutted from tree and is joined with V-Shaped cutting in Scion & Root stock is simply cutted in T- Shaped. Both are joined together.  The cut is joined tightly and wrapped in plastic & keep it under safe place.
  • 70.
  • 71. Date : 06/08/2021 Sub : Agronomy. Course Teacher : Dr. Gajanan. L. Kadam  Discussed about general questions asked in exams.  Full forms :  Cell Division and expansion.  Learnt about different terms used in agriculture.  About Soil Fertility.  Abstract about Bio-herbicide.  Different families about weeds.  Different Origin of Crops.  About Soil Pores  PWP  UWP  ASM  BMP  GAP
  • 72. Frequently asked questions in exams :  Types of rainfall i.,e Isohyet, Isopach, Isohel  About Leeward and Windward  Sesbania rostrata is a stem nodulating green manure crop (West Africa).  Urea is placed in reduced zone to minimize the losses.  Biuret Content of Urea should not exceed 1.5  Conversions from Celsius to Fahrenheit.  Herbicide Required (Formula).  NPK Content of Poultry Manure.  Calculations on Gypsum Requirement and Fertilizer required dose in Soil.  Varieties of Cotton.  RH of Saturated Air – 100 %  About Active and Passive Remote Sensing.
  • 73. Date : 06/08/2021 Sub : Agronomy. Course Teacher : Dr. Vinod B. Mor  Discussed about the herbicide widely used in Agriculture.  Introduction to different crops present in field.  Detail introduction to Field Capacity, Available Water.  Brief introduction to irrigation system.  Cropping intensity area in India.  Visited campus area and discussed about common problems Physical and Biological Classification of water. Studied about crops present in area. About different types of Farming system.  Discuss about the Common problems present in agriculture.  Rouging : Removal of Off types from field.  Had done rouging in rice field.
  • 75. Date : 07/09/2021 Sub : Ag. Engineering Course Teacher : Dr. M. L. Gaur  General Status of soil conservation in India.  Importance of soil conservation.  History of soil erosion about five year plans.  Principles of soil erosion.  Different types of Water erosion.  Different water harvesting techniques.  About universal soil loss equation.  Soil erodibility factor.  Modified universal soil loss equation.  Long term runoff harvesting Techniques.  Principles of wind erosion and its control measures.
  • 76.  Woodruff & Zing (1952) developed the following relationship between the distance of full protection and the height of wind break or shelter belt.  Surveying & Field area Calculation.  Types of Water Harvesting.
  • 77. Date : 08/09/2021 Sub : Agricultural Economics Course Teacher : Dr. M. T. Khorajiya  Column and Line Charts on Agriculture Import (in crores) & Agriculture export (in crores)  Studied about : Mean Standard ,Error ,Median ,Mode ,Standard Deviation Sample Variance ,Kurtosis, Skewness, Range, Minimum, Maximum ,Sum Count.  Average , SD, & CV on Market vise Data of different crops such as Maize Pearl millet Sorghum Wheat.  Regression Coefficient on Dependent and independent values for Production function.  Correlation between three different districts producing same crop.  Paired T – test.