eChapters

Complete feed system is a system of ruminants feeding in which roughage and concentrate mixture are mixed homogenously in a predetermined ratio and processed in to pellet, briquette or block form to provide the animals a nutritionally balanced diet. Complete feed system is advantageous over conventional feed system as it reduces the cost of labour, transportation and storage of feed, besides ensuring uniform supply of nutrients and maintaining the optimum rumen environment due to the constant dietary roughage: concentrate ratio, which also avoids the selective feeding.

The Metric System

At present metric system is followed to calculate final results in analysis work. This system is quite simple in nature as well as in principle. The units of the metric system are: (1) the  metre (linear measure), (2) the litre (measure of capacity), and (3) the gram (measure of mass.)

One litre is the volume of pure water at 4ºC and 760 mm pressure which weigh 1 kilogram (kg). One litre equals 1000.027 cubic centimetres (Cm3) for most work, the units “millilitre”, “cubic centimetre” and used interchangeably.

At present there are three different temperature scales in common use. These are: the Fahrenheit (F), used chiefly in English-speaking countries. the centigrade (C), used universally in scientific work and the Absolute (T) or Kelvin (K) scale, differing from the centigrade only in the position of the zero point, its divisions being of the same size. its zero point is -273ºC. The kelvin scale is used especially in dealing with very high or very low temperature and in computations involving the laws of gases. The following formulae can be used for converting one scale to another:

Apparatus and Reagents

    1.    Soxhlet extraction asembly. This consists of 3 parts (a) condenser at the top, (b) the soxhlet or extractor in the middle, and (c) the receiver flask at the bottom. The 3 parts are assembled by means of their grounds glass interchangeable joints (Fig. 1).

    2.    Extraction thimble.

    3.    Petroleum ether (B.P. 40ºC to 60ºC)

    4.    Constant temperatue bath or six heater hot plate with temperature controlling device.

Isolation of RNA from Rat Liver
(Method of Schmidt and Thannhauser, 1945)
Principle

Most of the RNA (ribouncleic acid) of cells is found in the nucleoli and microsomes.These fractions of cells may be isolated by differential centrifugation of cellular homogenates and thus provide an enriched starting material for RNA extraction. Such methods require high speed  centrifugation. An alternate procedure used in the present method is to disrupt the whole cells by homogenization and isolate the nucleic acid of entire homogenate. This procedure consists of the following sequential steps.

I. Detection of Castor Husk in Oil Cakes and Oil Seed Meals (Method of ISI, (BIS), IS: 10165-1982)
Principle

The method is based on the fact that castor husk is not bleached under the conditions which cause the bleaching of almost all other materials of vegetable origin likely to be present in an oilcake. The method consists of the treatment of the material with dilute alkali and acid solutions followed by treatment with bleaching powder solution and the isolation of the unbleached castor husk.

  1.    Gender Sensitization: Change of Attitude of people towards gender equality, gender roles etc.

  2.    Public-Private Partnership: Involvement of private stakeholders with public entreprises

  3.    Information and Communication Technology (ICT): Use of computer. fax, video, telephones in information sharing & transfer of technology.

  4.    Cyber Extension: Use of computers in extension management.

  5.    Broad Based Extension: Farming system use for maximum use of all available resource to maximize profit

  6.    Bottom-up Approach: Planning from lowest level of society.

  7.    ITK (Indegenous Technological Knowledge): Use of farm community knowledge for development

  8.    Market Led Extension: Transfer of technology basing on assured & confirmed market of the product.

   Q.1.    How milk sample is collected for diagnosis of mastitis?
    Ans.    At first the end of teat is cleaned with a cotton swab dipped with 70% alcohol, then the dirt and wax are removed from the external sphincter by pressure. After this milk sample is collected in screw cap bottle.

    Q.2.    When milk sampling should be done in suspected cases of tubercular mastitis?
    Ans.    Last few streams of milking is crucial in cases of tubercular mastitis.

    Q.3.    What is the effect of freezing of milk sample on bacterial count?
    Ans.    On freezing of milk, Arcanobacter pyogenis and E. coli counts are decreased, coagulase negative bacteria counts increases whereas, Streptococcus and Staphylococcus spp. counts may be unaffected or increased.

    Q.4.    Which media is suitable for initial isolation of bacteria from milk samples?
    Ans.    Blood agar. However for isolation Streptococcus agalactiae selective media is required

Q1.    What is the etiology of Staphylococcus aureus mastitis?
    Ans.    Coagulase positive Staphylococcus aureus.

Q.2.    It causes contagious or environmental mastitis?
    Ans.    Contagious mastitis

Q3.    What are the important animal risk factors of S. aureus mastitis?
    Ans.
    (i)    Presence of coalgulase –ve Staphylococci and Corynebacterium bovis in the mammary gland act as protective factor for S. aureus mastitis.
    (ii)    Abrasion of teat orifice epithelium is a major risk factor of S. aureus mastitis.
    (iii)    Cows with increased parity are more prone to clinical and subclinical S. aureus mastitis.
    (iv)    Presence of different periparturient diseases like parturient peresis, retained placenta, dystocia, ketosis and ulcers in different organs are also risk    factors for S. aureus mastitis.
    (v)    Animals having very low SCC in milk are more prone to S. aureus mastitis.

Q.1.    Enumerate the etiological agents responsible for Coliform mastitis.
    Ans.    Different serotypes of E. coli, Klebsiella sp. and Enterobacter aerogens.

Q.2.    What is the primary reservoir of Coliform mastitis?
    Ans.    Primary reservoir of Coliform is the dairy cow’s environment as it is an environmental pathogen, however, infected mammary gland acts as reservoir of Coliform mastitis

Q.3.    What is the important factors of E. coli that affect the normal bactericidal activity of leukocytes?
    Ans.    Lipopolysaccharide-endotoxin, somatic and capsular factors. Similarly, fibronectin binding property of E. coli is also an important virulence factor which help to adhere to ductular epithelium.

    Q.1.    The mastitis-metritis-agalactia (MMA) is a disease syndrome of which animal species? 
    Ans.    Swine

    Q.2.    What is MMA syndrome?
    Ans.    MMA syndrome is post parturient disease of sows and manifested as fever, anorexia, lethargy, agalactia, mastitis, swollen udder and appearance of vulvar discharge due to development of metritis.
 
    Q.3.    What is the critical time of occurrence of MMA in sows?
    Ans.    The mastitis-metritis-agalactia (MMA) syndrome occurs between 12-48 hrs of farrowing in sows.

    Q.4.    What is the probable causes for the development of MMA syndrome?
    Ans.    The probable causes of MMA syndrome are infectious mastitis, metritis, more feeding at pregnant period, nutritional deficiency, endocrine disorders and constipation.

Pig Production on Scavenging

Pig farming has become a profitable enterprise since it possesses many economic traits e.g. high prolificacy, faster growth rate, shorter generation interval, low cost of rearing and high dressing percentage with better feed conversion efficiency. Pigs give quick return, convert inedible feed into valuable products, require less labor, adopt most types of farming systems, aid soil fertility, supplement other enterprises, etc. It is still considered as backward profession and unorganized rearing largely dominates the sector, and it is primarily in the hand of poor, landless and weaker section of society.

The genus was named after Morax who first isolated the organisms from human conjunctivitis in 1896.

Properties of genus

1.   Morphology :  Moraxella are gram negative, small rods occurring in pair (diplobacilli). The aged cultures exhibit pleomorphism, occurring in pairs or chains as short, plump rods with rounded ends. Some strains may appear as cocci. The capsule is present in fresh isolates of some species (except Moraxella catarrhalis). They are non-motile and non-sporing. Moraxella bovis contains numerous type IV fimbriae on its surface.

2.   Moraxella is aerobic, fastidious and non-fermenting in nature. However, some strains prefer anaerobic condition for their growth.    

3.   Classification : The genus Moraxella belongs to the Moraxellaceae family. Previously it was known as Branhamella. Most of the species are commensal except a few, which have disease producing capabilities. Important species are M. bovis, M. ovis, M. catarrhalis, M. boevrei, M. canis, M. caprae, M. caviae, M. cuniculi, M. phenylpyruvica.

4. Resistance : Resistance to physical and chemical agents is not remarkable. They are susceptible to desiccation and do not survive long outside the host. The beta- lactam antibiotic resistance is observed among M. catarrhalis isolates from clinical cases. This resistance is associated with the production of beta-lactamase enzyme.

Taylorella was first isolated by Taylor et al. (1978) as a causative agent of contagious equine metritis (CEM), a venereal disease of horses. The disease (CEM) was first reported in the mares of thoroughbred horses in UK in 1977 breeding season (Crowhurst, 1977). Initially the causative agent was assumed as Haemophilus equigenitalis. Later on the basis of numerical taxonomic characteristics, genomic G+C contents, DNA-DNA hybridisation studies, the new genus Taylorella was proposed in 1983 (Sugimoto et al., 1983). It was approved by the International Committee on Systematic Bacteriology.

Properties of genus

1.   Morphology :  Taylorella are gram negative, small rods or coccobacilli, measuring 5-6 µm by 0.8 µm. They are pleomorphic, piliated, encapsulated, non-sporing and non-motile.

2.   They are microaerophilic (require low O₂ tension for growth), non-fermentative, and non-proteolytic in nature.

3.         Classification : Taylorella belongs to β- subclass of class Proteobacteria (whereas, Haemophilus belongs to the γ- subclass of Proteobacteria). Major important species is Taylorella equigenitalis. The genus was considered as a ‘single species genus’ for a long time. Latter in   1997, National Veterinary Services Laboratories confirmed the identity of another Taylorella species, isolated from a donkey jack (Equus asinus) in California. It was named as T. asinigenitalis. The new species has minor difference in 16S rDNA sequence (97.6% similarity), DNA–DNA hybridization (23% similarity) and (G + C) composition with T. equigenitalis (Matsuda and Moore, 2003)
.

The genus Arcanobacterium was first described to include the bacteria originally isolated as Corynebacterium haemolyticum from American wounded soldiers (Collins et al., 1982). The bacteria had different cell wall and lipid composition in comparison to the other members of the genus Corynebacterium. So the new genus Arcanobacterium was created.

Properties of genus

1.         Morphology : Arcanobacterium pyogenes is a Gram positive, non-motile, non- spore forming, short, rod-shaped bacterium, measuring 0.5µm by 2 µm. They are non-capsulated and do not contain any metachromatic granule. Initially (during first 18 hour of growth) the bacterial cells may show characteristic ‘V’-arrangement like Corynebacterium, latter as the growth proceeds, the organisms become granular and segmented so that they resemble small and irregular cocci (whereas, A. hippocoleae and A. pluranimalium appear to be less coccoid). The cell wall is devoid of mycolic acid, arabinogalactan unlike ‘coryneform’ bacterial group (Mycobacterium, Corynebacterium, Rhodococcus, Nocardia). Cell wall peptidoglycan is composed of N-acetyl muramic acid, lysine. Being gram positive in nature, some strains exceptionally possess fimbriae.

Edmond Nocard (French Veterinarian) first isolated filamentous aerobic bacteria from clinical cases of ‘bovine farcy’ in 1888. In 1889, the genus Nocardia was formed by Trevisan, and the organism described by Nocard was named as Nocardia farcinica. In 1891 another similar organism (Nocardia asteroides) was isolated by Eppinger from a human brain abscess. Initially it was thought that they are the same organisms. Latter on the basis of the molecular studies their separate entity is established.

            However, 80 years later, re-examination of Nocard’s original isolate revealed two different filamentous organisms, one of which was Mycobacterium and the other was Nocardia. The cause of ‘bovine farcy’ has been subsequently attributed to Mycobacterium. Latter, it is proved that Mycobacterium farcinogenes is the actual causative agent of ‘bovine farcy’.

Dermatophilus congolensis was first described from clinical case of exudative dermatitis in cattle in Congo by Van Saceghem (Van Saceghem, 1915). It is primarily known as an animal pathogen causing acute, sub acute or chronic skin disease. The first cases of human infection with D. congolensis were reported in 1961 in four people who developed skin infection after handling an infected deer in a wildlife reserve in USA (Dean et al., 1961).

Properties of genus

1.   Morphology

Dermatophilus is a gram positive, non-acid fast, unusual bacterium having branched filaments. It follows a life cycle with different morphological features. It can be found in smears prepared from clinical samples in any form of its life cycle. Young filaments are 0.5 to 1.5 μm in diameter.  They enlarge within epidermis as they produce layers of transverse and longitudinal septations and reach 5 to 8 μm in diameter, surrounded by a mucoid capsule. The septations result in the formation of a sporangia (a kind of fungal fruiting body, sac like structure with spores) containing up to eight cocci cells. In the presence of liquid, the cocci are released and converted into flagellated motile zoospores, the infective form of the organism. It can infect the new site in the same animal or new host. These zoospores become visible in smear as parallel lines forming a ‘railway-track’ or ‘trum-track’ appearance (Fig.1). Under favourable conditions, the zoospores form germ tubes that develop into branching filaments. These filaments are the invasive form of the organism and the cycle is repeated.

Materials Required

Equipments and machinery used in Postharvest Technology laboratory for processing, packaging and quality analysis.

Procedure

    1.    Identify the equipments and machinery, note down the typical features about its shape, size, colour etc.

Materials Required

Fruits/vegetables, thermometer, refractometers, NaOH, Phenolphthalein, glassware, weighing balance, plastic crates for storage of commodity, water cooling facility.

Procedure

    1.    Harvest the fruit / vegetable
    2.    Count No. of unmarketable fruits in every 100 fruits harvested
    3.    Record the internal fruit temperature in about 5-10 randomly selected fruits with the help of a thermometer
    4.    Pre-cool the commodity in cold water (<5ºC), air or refrigerator till the temperature reaches near its optimum storage temperature
    5.    Record the internal fruit temperature
    6.    Record the time required to pre-cool the commodity
    7.    Keep the product for storage at ambient conditions alongwith control
    8.    Record the difference in the shelf life and quality during storage

Materials Required

Fruits juice, enzymes (pectinase, cellulase, pectinase CCM etc.), filter press, buchner filter apparatus, water bath, filter paper pulp, buchhi type rotary vacuum evaporator, freeze concentrator, membrane concentrator (whichever available), vacuum grease.

Procedure

    1.    Extract the juice as discussed in earlier exercises. Take a known quantity of juice in a conical flask.
    2.    Add enzymes i.e. pectinase @ 0.2% to the juice and keep in a water bath at temperature of 40-50ºC for 2 hrs.
    3.    Shake the flasks occasionally for uniform mixing of enzyme all throughout the flask during the enzymatic treatment.
    4.    Leave the flasks undisturbed for 10-12 hrs for allowing the insoluble solids to settle at the bottom of the flask.
    5.    Siphon the clear juice from the top of the flask.
    6.    Pass this siphoned juice through filter press or through a 0.4-0.5 cm thick bed of filter paper pulp in a Buchner filter apparatus or filter press.
    7.    Record the volume of the clarified juice obtained. Calculate the wastage.
    8.    Concentrate the juice in rotary vacuum evaporator at 50+2ºC temperature and at 28-30” Hg vacuum to a TSS of about 50 to 70º Brix. Record the exact TSS.
    9.    Record the volume of condensate obtained in the round bottom flask of the buchhi apparatus.
    10.    Calculate the folds of concentration

Materials Required

Fruit pulp, cane sugar, potable water, essence, citric acid, colours, preservatives, weighing balance, glass jars (500 ml capacity), jar closures, hand refractometer, steel pan, ladle etc.

Procedure

    1.    Select sound and fresh fruits, free from any blemishes. Generally a mixture of ripe and unripe fruits should be taken as the ripe fruits impart good flavour and the unripe fruits are rich in pectin, required for a good set.

    2.    Wash the fruits thoroughly. Cut into 4-8 pieces depending upon the fruit and size
    3.    Boil the fruit pieces for about 20-25 min in boiling water and pass through pulper to get a good pulp.
    4.    Weigh known quantity of fresh or preserved pulp and add about equal quantity of sugar (preferably in 45:55 ratio)
    5.    Cook the mixture on gas flame by occasional stirring. 
    6.    When the mixture becomes thick, perform sheet test.
    7.    Citric acid is added generally towards the end of cooking. Addition of all the acid in the beginning may result in stickiness and poor set. 
    8.    Remove from the flame when the mixture gives a clear sheet
    9.    Flavours, colours etc may also be added towards the end of boiling. 
    10.    Fill the jam in glass jars (preferably pre-warmed in hot air).
    11.    Close the jars with lug caps and allow to cool overnight.
    12.    Label and store in a cool place.

Materials Required

Fruit extract, cane sugar, potable water, essence, citric acid, colours, preservatives, weighing balance, glass jars (500 ml capacity), jar closures, hand refractometer, steel pan, ladle etc.

Procedure for Jelly

    1.    Select sound and fresh fruits, free from any blemishes. Generally a mixture of ripe and unripe fruits shouldbe taken as the ripe fruits impart good flavour and the unripe fruits are rich in pectin, required for a good set.
    2.    Wash the fruits thoroughly. Cut into 4-8 pieces depending upon the fruit and size
    3.    Boil the fruit pieces in water (about ½ to an equal weight of fruits for fruits like apple and 2-3 times the weight of sliced fruits in case of citrus fruits) for about 30 min. with occasional stirring. Strain the boiled mixture through coarse muslin cloth to get a clear pectin extract
    4.    A second extract may also be taken by boiling the same mass again and straining.
    5.    Add sugar (usually 3/4th to one part of the extract or in 45:55 ratio) to the pectin extract and boil in a stainless steel pan. Add required quantities of acid towards the end of boiling.
    6.    Remove the scum rising on the top of boiling mass occasionally.
    7.    To avoid charring, occasional stirring is also done.
    8.    To avoid destruction of pectin the cooking should be completed fast
    9.    Determine the end point of jelly as detailed ahead.
    10.    Fill in hot dry glass jars and cool rapidly
    11.    Pour a thin layer of hot molten paraffin wax seal to avoid moulding.   
    12.    Label and store in a cool place.

Materials Required

Lime fruits, green chillies, ginger salt (common), stainless steel pans, kinives, weighing balance, spices etc. 

Procedure

    1.    Select sound and mature fruits of lime, mature but green chillies having good size and ginger rhizomes.
    2.    Wash the lime fruits, ginger and chillies properly in running cold water.
    3.    Cut the lime fruits into pieces / halves. 
    4.    Remove the stalks of the chillies and cut into longitudinal slices. Peel ginger and cut into long thin slices.
    5.    Put the lime pieces, chilli and ginger slices in a wide mouthed pre-sterilized glass jar 
    6.    Add common salt @ 250g / Kg of material.
    7.    Squeeze some of the juice over the slices
    8.    Stir the mass well mixing thoroughly
    9.    In case the juice does not cover the material completely, add pre-boiled and cooled 5% solution of citric acid.
    10.    Keep the jar in Sun for about a week with occasional shaking of the material.
    11.    When the lime pieces start turning light brown, the pickle is ready for consumption.

Materials Required

Dehydrator, balance, thermometer, sulphur dioxide, blanching pan, fruits / vegetables, polythene or aluminium bags.

Procedure

    1.    Select sound fruits or vegetables 
    2.    Record their initial weight and wash them properly in plain water to remove any dirt or extraneous matter. 
    3.    Peel with stainless steel knife (as the case may be) and cut into thin uniform pieces or slices of  0.2-0.5 mm thickness
    4.    Blanch the slices in boiling water for 1-2 min. to inactivate the enzymes followed by immediate cooling.
    5.    Treat the slices with sulphur (sulphuring or sulphiting) in order to prevent darkening of the product during drying. 
    6.    Dry the slices in a mechanical air dehydrator at about 55 + 5oC temperature.
    7.    Record the weight of the product after every 2 hr till it becomes (almost) constant i.e. when there no more (significant) loss of moisture from the product.
    8.    Pack the product in ploythene or aluminium laminated pouches and seal them air tight. 
    9.    If it is to be converted into powder, the dried product can be ground in a grinder before packing.
    10.    Label the packages and store them in a cool dry place.
    11.    Plot the drying rate curve of the product on a graph paper and analyse it.
    12.    Record the initial and final moisture content of the product (as discussed in Exercise No. 19). 

Materials Required

Apple (or any local fruit), fruit mill, hydraulic press, weighing balance, Refractometer/sugar pectinol, diammonium hydrogen phosphate, Saccharomyces cerevisiae culture, Potassium metabisulphite (KMS) etc.

Procedure

    1.    Take a known quantity of apple (or any other fruit) say 20 Kg
    2.    Extract the juice as discussed in earlier exercises.
    3.    Add about 200 ppm of kms.
    4.    Add sugar syrup to increase the TSS to about 20 – 24ºBrix.
    5.    To about 10 Kg of juice diammonium hydrogen phosphate (10 g) and pectinol (20-25 g are added).
    6.    Take about 500 ml of this mixture in a conical flask and add pure Saccharomyces cerevisiae culture @ 1 % and plug the neck with cotton. Keep at 22-24ºC to complete the fermentation within one day and yeast culture is ready.
    7.    Add this culture to about 10 Kg of must for further fermentation (i.e. culture is added @ 5% therefore 500 g is added to 10 Kg must).
    8.    Record the TSS of the must before fermentation.
    9.    Keep must for fermentation in big jars (narrow mouth) filled to about 75 % of their volume. Close the mouth of jars or bottles with cotton plug.
    10.    Allow fermentation to take place at 22-24ºC for about 10–15 days.
    11.    When no more bubbles are coming out of the jars, fermentation is complete. At this stage the TSS reaches about 7º Brix.
    12.    Siphon the wine. Add filter aids if wine is not clear.
    13.    Blend the wine with sweetening agents if required.
    14.    Fill in beer bottles by keeping a head space of about 2.5 cm followed by crown corking them.
    15.    Pasteurize the bottles by keeping at 62.5ºC for 20 min.

Materials Required

Sample, 0.1 N NaOH solution, 1% phenolphthalein indicator solution, beakers, conical flasks, pestle and mortar, funnels, volumetric flasks, pipettes, pH meter, shaker.

Reagents

    1.    0.1 N NaOH: Dissolve 4 g NaOH (AR) crystals in sufficient water to make up the final vol. 1 litre.

    2.    1 % Phenolphthalein: Dissolve 1 g in 100 ml water. Readymade indicator solutions are more commonly used.  

Procedure

Preparation of sample: For fresh fruits and vegetables, prepare a well blended, uniform pulp in a pestle and mortar and for processed products, take out a representative sample and blend it well so that it becomes uniformly soluble when added to water. Filter through a fine muslin cloth or coarse filter paper if felt necessary. The liquid samples can be taken directly for estimation.
    1.    Take out a known weight / vol. (say 20 g) of sample in a beaker (in 3 replicates).
    2.    Make it to a known vol. (say 100 ml) with added distilled water.
    3.    Take 10 ml of this aliquot in a conical flask.
    4.    Add 1-2 drops of phenolphthalein indicator into the aliquot.
    5.    Titrate against 0.1 N solution of NaOH till light pink coloured end point is obtained.
    6.    For coloured products, i.e. tomato products where judgment of light pink colour is difficult, titration may be done over a shaker, and digital pH meter may be used for continuously measuring pH of aliquot which would show a steady increase with more and more addition of 0.1 N NaOH. Titre value may be recorded when pH of 8.3 is obtained.
    7.    Record the titre value and calculate the acidity of the sample as per the given formula.

Materials Required

Sample, reagents, beakers, conical flasks, pestle and mortar, funnels, volumetric flasks, pipettes, hot plate, weighing balance, spectrophotometer/colorimeter.

Reagents

    1.    0.1 N NaOH: Dissolve 4 g NaOH (AR) crystals in sufficient water to make up the final volume 1 Litre.
    2.    1 % Phenolphthalein: Dissolve 1 g in 100 ml water. Readymade indicator solutions are more commonly used.
    3.    Alkaline copper Tartarate
        a.    Dissolve 12.5 g anhydrous sodium carbonate, 10 g sodium bicarbonate, 12.5 g potassium sodium tartarate and 100 g anhydrous sodium sulphate in about 400 ml of distilled water and make up the final volume to 500 ml.
        b.    Dissolve 15 g copper sulphate in distilled water. Add one drop of sulphuric acid and make up to 100 ml in distilled water.
    4.    Always prepare fresh Alkaline Copper Tartarate reagent by mixing 96 ml of sol. a. and 4 ml of sol. b. and before use.
    5.     Arsenomolybdate Reagent: Dissolve 5.0 g ammonium molybdate (AR) in 90 ml of distilled water. Add about 5.0 ml of concentrated sulphuric acid and mix well. Add 600 mg of disodium hydrogen arsenate dissolved in 50 ml water. Mix well and incubate the prepared reagent at 37ºC for 24-48 hr or 55ºC for 30  min. with constant stirring.

SUMMARY

In the context of increasing population pressure, diminishing per capita land holding, and employment crisis, livelihood security of Indian rural population has become important concern today. The livelihood of the people is dynamic, diverse and complex in nature. The livelihood comprises the people themselves, the assets they posses, the activities they do and the output they gain from their activities. According to the need, availability of the resources and capacity, people used to select their livelihood strategies like agricultural intensification, livelihood diversification or they migrate to the other places to find alternative livelihoods.

A successfully developed new cultivar should have stable performance and broad adaptation over a range of environments, seasons and locations, in addition to high yield potential. Evaluating performance stability and range of adaptations is becoming increasingly important in breeding programs. Since stability and adaptability are important selection criteria in breeding programs, in depth research on stability is needed for a better estimate of crop performance and adaptability (Lin and Binns, 1988).

Having realized the importance of genotype × environment, several biometrical models have been developed to analyse the stability of genotypes. Such models have been discussed, critically reviewed comprehensively by Knight (1970), Freeman (1973), Hill (1975), Brain (1986) and Gautam et al. (1986).

However, the various methods proposed for the statistical analysis of genotype × environment are based on one of following approaches (Jain, 1982). In the first the variance interactions are estimated by equating the observed mean squares in the analysis of variance to their expectations on the random model. The second approach called phenotypic approach by Hill (1975) used the technique of partitioning the genotype _× environment component of variability into its linear and non-linear portions of assessing the stability of genotypes over a range of environments. This approach which is very widely adopted in plant breeding, came to be known as “Joint regression analysis”.

Many workers contributed for the development of this approach, notably Finlay and Wilkinson (1963), Eberhart and Russell (1966), Freeman and Perkins (1971) and Shukla (1972). The third approach called genotypic approach which also suggested by Hill (1975) is based on fitting of general models in which it specify, the contribution of genetic, environmental and genotype × environment to the generation means and variance. The contributions for he development of this approach were from Bucio (1966), Bucio and Hill (1966), Bucio et al. (1969), Perkins and Jinks (1968), Breese (1969), Hill and Perkins (1969) and Perkins (1970). Linear regression and joint regression models were more commonly used due to their simplicity and reliability in biological experiments. In general, these approaches fall conveniently into two parts.

Ramya (2012) studied stability of 12 hybrids in three environments. The researcher selected the 12 hybrids based on the standard heterosis. The hybrids are: P₂ × P₅, P₁ × P₅, P₃ × P₅, P₂ × P₇, P₂ × P₃ and P₁ × P₂. Among the twelve hybrids, the cross combinations viz., P₂ × P₅, P₂ × P₇ and P₂ × P₃ showed non-significant reciprocal effects for most of the traits including fruit yield per plant. The direct hybrid P₁ × P₂ showed less than 40 per cent standard heterosis for fruit yield per plant. It also exhibited low standard heterosis for number of fruits per plant. Eight hybrids viz., P₂ × P₅, P₅ × P₁, P₃ × P₅, P₂ × P₇, P₁ × P₅, P₂ × P₃, P₂ × P₁, P₅ × P₃, based on standard heterosis (>40 per cent) and their parents viz., P₁, P₂, P₃, P₅, P₇ were selected and grown in three different locations for finding their stable performance. Several authors have suggested different types of models to identify the stable genotypes. The model most commonly preferred by breeders is Eberhart and Russell (1966) model which was used in the present investigation. Various stability parameters were worked out on the available data and the results were discussed below.

Among the ten traits studied, days to first flowering, fruit weight and fruit girth showed non-significant genotype × environment interaction. Hence, the remaining seven traits were taken for further analysis. ANOVA across environment revealed highly significant mean sum of square for genotypes, indicating the presence of wide genotypic variability among the genotypes involved in the study for all the characters studied. High significant differences were observed for environments for the traits viz., number of branches per plant, fruit length and fruit yield per plant, indicating the divergence among the growing environments and differential response of genotypes to the various environments. The main factors contributing to the divergence of the environments might be temperature differences during crop season, intensity and duration of sun shine hours. Therefore, the genotypes must be tested over an extensive range of environments for proper assessment of stability of genotypes (Salesh Kumar Jindal et al.,2008).

Hendra, a disease of horse has been recognized in Australia since 1994-95 with zoonotic importance. It is caused by a virus under the genus Megamyxovirus and subfamily Paramyxovirinae and family Paramyxoviridae. This virus is also endemic in certain species of bat. Another zoonotic bat virus called Nipah virus has been placed under the same genus and family. It is transmitted between the horses through contact. Infected horses can develop a severe and fatal respiratory disease characterized by dyspnoea, vascular endothelial damage, pulmonary oedema and neurological signs. Experimental infection of cats and guinea pigs showed fatal respiratory disease. The transmission of virus from horse to horse and horse to man is through close contact. One person died of the disease due to respiratory failure and another one due to delayed onset of encephalitis. A number of diagnostic methods are available to provide prompt, sensitive and accurate diagnosis of the disease.

History: In 1994-95, a new viral zoonotic disease was identified in Queensland, Australia resulting in death of 2 human and 15 horses in two separate incidents. Again, in 1999 another horse died at the same place. The term 'Hendra' has been derived from the name of a place, suburb of Brisbane where first outbreak took place. In September 1994, a total of 15 horses died due to hyperacute respiratory disease. The trainer of the horse also died. In 1995, a farmer died of meningoencephalitis after having contact with a Hendra positive horse. In the 1999, a mare died of Hendra virus infections.

Etiology: The Hendra virus is under the new genus Megamyxovirus and family Paramyxoviridae. The Hendra virus was isolated in Vero cells from lung specimens and produced CPE within 3 days. The virus can grow in MDCK, BHK, RK13, LLC-MK2 and MRC5 cells. It also grows in cells derived from birds, reptiles, amphibians, fish and in embryonated chicken eggs. The virus does not have haemagglutinin or neuraminidase activity. The virus is pleomorphic in shape, 38-600 nm in diameter and enveloped with two glycosylated transmembrane proteins of different lengths (15 and 18 nm). It differs from respirovirus and rubulavirus in not using sialic acid containing receptors. The virions are labile and infectivity is destroyed by heat, lipid solvents, non-ionic detergents, formaldehyde and oxidizing agents. Virions contain one molecule of negative sense ssRNA about 15 Kb long which codes 8 proteins. The Hendra virus is the largest of all known viruses under Paramyxoviridae. The genetic studies showed that Hendra virus is more similar to Morbillivirus or intermediate between Morbillivirus and Respirovirus. The amino acid homology between Hendravirus and Morbillivirus varies from 17-21% (P protein) to 40-42% (M protein) compared to 6-10% and 8% respectively for other members of Paramyxoviridae. A new Hendra like virus has been identified as a cause of respiratory and neurological disease in pigs and humans in Malaysia, called Nipah virus, after a village where the first human case occurred. (The amino acid homology of N protein between Hendra and Nipah is 92%, whereas in case of P&V it is 80-85%). Like, Hendra virus, the Nipah virus is thought to have emerged from a fruit bat (Pteropus hypomelanus).

Organic C in agricultural soils contributes positively to soil fertility, soil tilth, crop production, and overall soil sustainability. Changes in agricultural management can potentially increase the accumulation rate of soil organic Cd (SOC), thereby sequesteringCO₂fromtheatmosphere.Optimizingagricultural management for accumulation of SOC can result in the sequestration of atmospheric CO₂, thereby partially mitigating the current increase in atmospheric Carbon dioxide. In addition to the environmental benefits of soil C sequestration, Carbon dioxide consideration has also been given to the implementation of a C credit trading system which may provide economic incentives for C sequestration initiatives.

Changes in agricultural practices for the purpose of increasing SOC must either increase organic matter inputs to the soil, decrease’decomposition of soil organic matter (SOM) and oxidation of SOC, or a combination thereof. These practices include, but are not limited to, reducing tillage intensity, decreasing or ceasing the fallow period, using a winter cover crop, changing from monoculture to rotation cropping, or altering soil inputs to increase primary production (e.g., fertilizers, pesticides, and irrigation). Implementing practices that sequester C can reverse the loss of SOC that may have occurred under intensive cultivation thereby increasing SOC to a new equilibrium

Objective: To identify drought tolerant genotypes by PEG method in laboratory.

Background information:

Among different abiotic stresses, drought is considered to be most detrimental for agricultural production. A drought is a period of below-average precipitation in a given climatic region that results in prolonged shortages in water availability, whether atmospheric, surface water or ground water. A drought can last for several months or years. Drought has substantial impact on ecosystem and agricultural productivity.

Some plant species are better able to tolerate drought stress than others. Genetic variability for drought tolerance also exists within many plant species (Blum, et al. 1980). The efficient exploitation of that variability for crop improvement would be facilitated by a fast and accurate screening method for identifying drought tolerant genotypes (Clark and Mc Craig, 1982). Several methods utilizing seedlings to screen for drought tolerance have been developed using an osmoticum such as polyethylene glycol (PEG) (Singh, et al. 1984). The other synonyms of PEG are Poly ethylene oxide (PEO) and Poly oxyethylene (POE); these other chemicals depend on the molecular weight. Chemical structure of PEG may be written as H”(O”CH₂”CH₂)_n”OH (Kahovec, et al. 2002). PEG is used in certain abiotic stress experiments to produce high degree of osmotic pressure, normally in the order of 'tens of atmosphere' PEG produces osmotic pressure due to its flexible nature and water soluble polymer. PEG also makes certain specific interactions with bio-molecules. Due to above properties PEG is used as a specific chemical to produce osmotic pressure in several biochemical and bio-membrane related experiments. For some genotypes, the seedling response apparently is a good indicator of the plant's reaction to drought stress later in its life cycle. However, early screening of seed plants via seedlings tests must still be considered as a method for identifying genotypes that will tolerate drought stress in the vegetative stage (Andersen, et al. 1987).

Objective: To identify salt tolerant genotypes by Glycine Betaine (GB) method in laboratory.

Background information:

Salt or salinity is a biggest danger that causes reduction in crop productivity worldwide. Salinity reduces the germination percentage, plant vigour and ultimately loss in final crop yield. There are different physiological parameters that are affected by high level of salinity viz., oxidative stress, physical alteration of bio-membrane, nutritional imbalance, loss of cell division & cell expansion, water stress, genotoxicity and ion toxicity. Together, these effects reduce plant growth, development and survival. During the onset and development of salt stress within a plant, all the major processes such as photosynthesis, protein synthesis and energy and lipid metabolism are affected. During initial exposure to salinity, plants experience water stress, which in turn reduces leaf expansion (Petronia, et al. 2011).

The water-soluble compounds which, are low in molecular weight, accumulate at certain concentration known as “compatible solutes” or “osmolytes” is the common strategy adopted by many organisms to combat the abiotic stresses. Some common compatible solutes are betaines, sugars (mannitol, sorbitol and trehalose), polyols, polyamines and amino acid (proline). Their accumulation is favored under water-deficit or salt stress as they provide stress tolerance to cell without interfering cellular machinery. The tolerant or sensitive species show difference in the stress tolerance level based on levels of accumulation of these compounds during abiotic stress condition. Accumulation of osmolytes like glycinebetaine (GB) in cells is known to protect organisms against abiotic stresses via osmoregulation or osmoprotection. Other roles of GB like cellular macromolecule protection and ROS detoxification have been suggested as mechanisms responsible for abiotic stress tolerance. In addition, GB also influences expression of several endogenous genes in plants.

Objective: To separate protein fragments by using SDS-PAGE method.

Background information

Electrophoresis is the motion of dispersed particles relative to a fluid under the effect of limited uniform field of electricity (Dukhin, and Derjaguin, 1974). Ferdin and Frederic Reuss (Reuss, 1809) first time observed such phenomena of electrokinetic nature in 1807. They found that the clay particles move in the water by giving constant supply of current. It happened due to interface of charged particles surface and the surrounding media. The technique is used widely in chemistry, biochemistry and molecular biology to separate different molecules based on difference in charge, binding affinity and size. Electrophoresis may be of two types viz., Anaphoresis and Cataphoresis. Anaphoresis is the electrophoresis of anions (-ve charged ions) while, Cataphoresis is electrophoresis of cations (+ve charged ions). Electrophoresis is a major analytical technique in biochemistry that is used for separation of macromolecules like protein, enzymes and nucleic acids. Electrophoresis is a technique used in laboratories in order to separate macromolecules based on size.

PAGE is abbreviated for Polyacrylamide gel electrophoresis that describes a technique widely used in biochemistry, forensics, genetics, molecular biology and biotechnology to separate biological macromolecules, usually proteins or nucleic acids, according to their electrophoretic mobility. Mobility is a function of the length, conformation and charge of the molecule.

Objective: To study peroxidase isozyme variation in rice seedlings by electrophoresis.

Background information

For electrophoresis and PAGE please see practical no. 4. For peroxidase please see practical no. 7.(Page 17-22)

Isozymes (isoenzymes or more generally as multiple forms of enzymes) are the enzymes that are differing in the sequence of amino acids but they work on same substrate or in other words catalyze same biochemical reaction. The isozymes have difference in K_M values and regulatory properties. Isozymes are very useful for proper tuning of metabolic activities and to meet the specific need of particular tissue or developmental stage, e.g. lactate dehydrogenase (LDH). Isozymes are coded by homologous genes that have diversity during evolutionary process. Although, strictly speaking, allozymes represent enzymes from different alleles of the same gene, and isozymes represent enzymes from different genes that process or catalyse the same reaction, the two words are usually used interchangeably.

Objective: To isolate DNA from plant sample by CTAB method and quantification by spectrophotometer.

Background information:

DNA isolation from different plant tissues viz., leaf, stem, root, flower and seed is a challenging task due to hindrance of variety of variety of biochemical compounds present and further problem increases with diverge plant species. In case of animal tissues the diversity in cellular bio-molecules in different species is much lower compared to plants. Two major phyto bio-molecules that have wide variation between species and pose serious problems in DNA isolation are: polyphenols and polysaccharides. These phyto bio-molecules if contaminated in DNA then may hinder further down applications like PCR, restriction digestion, sequencing, etc.

Several methods have been developed and reported that can remove polyphenols and polysaccharides efficiently during DNA isolation from plants. For this purpose two different chemicals are widely used,the first one is CTAB (cetyl trimethyl ammonium bromide) that is a cationic detergent and helps in removal of polysaccharides and the second one is polyvinylpyrrolidone that helps in removal of polyphenols. Due to above properties the CTAB based DNA extraction buffer is very common for plant DNA extraction.

Significance of different types of chemicals found in CTAB based plant DNA extraction method is explained as under:

Objective: To amplify DNA using RAPD primers and study on agarose gel.

Background information:

RAPD markers are decamer (10 nucleotide length) DNA fragments from PCR amplification of random segments of genomic DNA with single primer of arbitrary nucleotide sequence and which are able to differentiate between genetically distinct individuals. RAPD is applied to analyze the genetic diversity by random primers. Unlike traditional PCR analysis, RAPD does not require any prior DNA sequence information of the target organism: the identical 10-mer primers will or will not amplify a segment of DNA, depending on positions complementary with primers' sequence. For example, no fragment is produced if primers annealed too far apart or 3' ends of the primers are not facing each other. Therefore, if a mutation has occurred in the templ that was earlier complementary with primer, a PCR product will not be produced, resulting in a different pattern of amplified DNA segments on the gel. RAPD is a dominant marker means it cannot distinguish between heterozygous; single copy and homozygous; two copies. Rarely RAPD markers may be Co-dominant where different fragment length of DNA is amplified from the single locus. PCR is a molecular technique used for amplification of DNA, a complete enzyme based chemical reaction, therefore, the concentration and quality of template DNA, concentrations of PCR components, and the PCR cycling conditions may greatly influence the outcome. Thus, the RAPD technique is notoriously laboratory dependent and needs carefully developed laboratory protocols to be reproducible. Mismatches between the primer and the template may result in the total absence of PCR product or decreased amplified product. Thus, the RAPD results can be difficult to interpret.

Objective: To isolate RNA from plants using TRIzol reagent and its quantification by spectrophotometer.

Background information

RNA (Ribonucleic acid) is a polymeric substance present in living cells and many viruses, consisting of a long single-stranded chain of phosphate and ribose units with the nitrogen bases adenine, guanine, cytosine, and uracil, which are bonded to the ribose sugar. RNA is necessary in all the steps of protein synthesis in all living cells and carries the genetic information for many viruses.

The isolation of RNA with high quality is a crucial step required to perform various molecular biology experiment. TRIzol Reagent is a ready-to-use reagent used for RNA isolation from cells and tissues (Chomczynski, 1993).TRIzol works by maintaining RNA integrity during tissue homogenization, while at the same time disrupting and breaking down cells and cell components. Addition of chloroform, after the centrifugation, separates the solution into aqueous and organic phases. Aqueous phase contains RNA.

After transferring the aqueous phase, RNA can be recovered by precipitation with isopropyl alcohol. DNA and proteins can be recovered by sequential separation after the removal of aqueous phase. Ethanol precipitation needs DNA from the interphase, and an additional precipitation with isopropyl alcohol requires proteins from the organic phase. Total RNA extracted by TRIzol Reagent is free from the contamination of protein and DNA The isolated RNA can be further used in Northern blot analysis, in vitro translation, poly (A) selection, RNase protection assay and molecular cloning.

1. Introduction

Man (Homo sapiens) since his appearance on the sylvan Blue Planet started his search for healthcare and beautycare, besides food and shelter. Eventually, he also became conscious about his mind and attempted at ‘mindcare’. He employed leaves, flowers, fruits, etc. or some plant products altering his mind to remain aloof from his heavy worldly affairs, stress or even incurable diseases. He also endeavoured to use plants for his amusement. He exerted more pressure on local biodiversity, modified his study and observations on biodiversity which resulted into ‘cultural biodiversity’. He intensified his method of ‘trial and errors’ to search new sources or biodynamic chemicals. In recent times, he is emphasizing value-addition of the products in hand for his welfare. After food, medicine was his next priority to sustain life in primitive societies. Naturally, his study and research laid emphasis more on food and medicine in comparison to mind-altering bioresources. Even the modern man also paid more attention on the former rather that the latter. These trends have perforce led in partial negligence of research for psychoactive plants in his ambience. The present author, therefore, extended efforts to prepare an inventory of the mind-altering vis-à-vis psychoactive plants in the state of Maharashtra.

Phalsa (Grewia subinaequalis) is one of the hardiest, drought resistant and quick growing fruit crop. Different parts of the plant are used for curing variety of ailments. The ripe phalsa fruits are consumed fresh, in desserts or processed into refreshing fruit and soft drinks enjoyed during hot summers.

Climate and Soil

Phalsa prefers dry conditions and can therefore, withstand drought. It flourishes well under variable climatic conditions, and requires protection from the freezing cold temperature. Also, adequate sunlight and warm or hot temperatures are required for fruit ripening, development of appropriate fruit colour and good eating quality. Kandi areas are, therefore, quite suitable for its cultivation. It can also be grown under irrigated conditions. Phalsa plant grows vigorously under wide range of soils including fine sand, clay or even limestone. However, best results are obtained in well-drained, loamy soils.

Pecan (Carya illinoensis) is a highly nutritive and energy giving nut fruit. It has nutty flavor and superb tree characteristics. Area under pecannut in J&K is 414 hectares with annual production of 86 metric tonnes.

Climate and Soil

Pecan need warm temperate climate and extremes of both temperate and sub-tropical climates are undesirable. It needs adequate chilling hours ranging from 400-600 hours below 7.2^oC for different cultivars. Mean monthly temperature ranging from 24.0 to 29.5⁰C, with little diurnal variation during growing period is best for growth and fruiting. High humidity prevents pollination, increases the incidence of diseases and premature splitting of nuts.

Although pecan nuts are grown in varied soil conditions, but sandy loam soils (pH 5.0-8.0) which are deep, fertile and are rich in organic matter are best for its growth and fruiting. Symbiotic mycorrhiza and fibrous roots permeate the top 1 meter of soil.

Naïve panel: It refers to the sensory evaluation panel that has not been trained specifically regarding the product evaluation being undertaken in the study.

Nano technology: It is the art of manipulating materials on an atomic or molecular scale to build microscopic devices. The word “ nano’ meaning ‘dwarf” in Greek language refers to dimension / magnitude of the material / particle in the order of 10⁹. Nanotechnology is nothing but manipulating of particles into very small particles called nano-particles. These particles have dimensions in the scale of nano-meter and used to design / build materials and devices. Nanotechnology has been provisionally defined as relating to materials, systems and processes which operate at a scale of 100 nanometers (nm) or less. It will allow many things to be manufactured at low cost and with no pollution. The concept of nanotechnology was first given by Nobel Laureate physicist Richard P. Feynman in Southern California in 1959.

NaNO_2: Pink colour of cured meat is preserved by NaNO₂. It is effective against Cl. Botulinosm

Nanogram: It is one billionth of a gram.

Yak is among the most remarkable domestic animals. It is adapted to thrive in the harsh environment of high altitude and sustains livelihood of highlanders. Yak is handicapped because of lack of veterinary assistance and declining pastoral biomass. Marketing facilities for yak-based products are limited and the production potential of yak husbandry is on decline. Dearth of locally available trained manpower and prevailing illiteracy are other hindering factors for development of yak husbandry. Research and development with focus on upliftment of yak husbandry and yak products are therefore important.

Training is a major manpower management function. No organization can afford not to train its employees, regardless of his previous education, training, and experience. He has to be introduced into the work environment of his new employer inducted and taught to perform his assigned tasks in a new milieu. Moreover, changing technology, increasing automation in offices and factories and in almost all institutions is bringing about redesigned or altered jobs. People are constantly being “trained” and retrained by the way their superiors and other employees associate them with work. 
Training is a part of management development and also a form of organizational development. The most effective managers are those who can best develop the human resources of an organization for the purpose of achieving organizational goals and objectives. If the employees perceive training as a means to achieve their personal goals at work, they will welcome such opportunities. Some essentials about training may be borne in mind and they are:

Whatever may be the nature and strength of resistance to the performance appraisal, management cannot relinquish this practice. Without employee appraisal, salary increases, reassignments or promotions cannot be administered rationally. Each of these areas has its specific problems and one of the solutions of modern times has been offered by an unusually promising frame work offered by Peter Drucker concept of Management by Objectives (MBO).
MBO calls on the subordinate to set his short-term performance goals in consultation with his superior. Goals explicitly state the actions which the employee will follow. Instead of being appraised in a traditional way by his superior, the subordinate appraises his own performance by evaluating it vis-à-vis the goals. Before establishing a goal, the individual studies his job, assesses his potentialities, and formulates some specific plans to reach the goal. The supervisor is not the evaluator, but directs the goal-setting process to ensure that it matches the objectives of the organization.

TRANSFER

A transfer is a change in job assignment. It may involve a promotion or demotion or no change at all in responsibility and status. It is a change in assignment in which the employee moves to another job at approximately the same level of responsibility, the same skill, the level of pay. Transfer is to be distinguished from promotion and demotion which imply an ascending or descending change respectively, in the hierarchy of positions. A transfer may be either temporary or permanent, depending upon the need, and may occur within a department, between departments and divisions, or between plants or officers within a company/organization.

There are specific hazards associated with equipment, operation or a particular section. Such possible hazards and their preventive measures are discussed below.
I. Milk Reception Dock
    1.    Where the top of a vat, into which a 40 litre can of milk is to be dumped, is higher than the milk can, two men should lift and empty the can.
    2.    Where steam jet method of can washing is used, to avoid burning, employees would be furnished with protective equipment, including rubber boots and long aprons
    3.    Cans should be stacked in areas away from frequently used passage ways
    4.    Cans should not be stacked so high that they may fall and injure someone

Since time immemorial when man used primitive tools and machines to carry his loads, to draw his water, to till his land and to fabricate his building materials, he has been faced with the prospect of maintaining these assets until such time as he considered their useful life to be ended. Maintenance is very important to extend the useful life of an asset. Maintenance is usually viewed only as a repair function. It is, however, “a combination of any actions carried out to retain an item in, or restore it to, an acceptance condition”. In fact maintenance keeps or ensures that the entire production system is kept reliable, productive and efficient. All departments of a production system may have been designed beautifully without giving due consideration to maintenance management. The end result is obvious. Organizations like the National Productivity Council and others are playing a vital role in propagating the importance of Maintenance Management of all assets of the organization. In fact, all organizations must be having some assets, and hence the need for proper maintenance and ‘physical assets management’ which is synonymous with the word ‘Tero-technology’.

Concept of Inventory

‘Inventory’ may be defined as ‘usable but idle resource’. If resource is some physical and tangible object such as materials, then it is generally termed as stock. Thus stock or inventory are synonymous terms though inventory has wider implications. Broadly speaking, the problem of inventory management is one of maintaining, for a given financial investment, an adequate supply of something to meet an expected demand pattern. This could be raw materials work in progress finished products or the spares and other indirect materials. Inventory can be one of the indicators of the management effectiveness on the materials management front. Inventory turnover ratio (annual demand/average inventory) is an index of business performance. A soundly managed organization will have higher inventory turnover ratio and vice-versa. Inventory management deals with the determination of optimal policies and procedures for procurement of commodities. Since it is quite difficult to imagine a real work situation in which the required material will be made available at the point of use instantaneously, hence maintaining, inventories becomes almost necessary. Thus inventories could be visualized as ‘necessary evil’.

Air pollution is the introduction of chemicals, particulate matter, or biological materials into the atmosphere that cause harm or discomfort to humans or other living organisms, or cause damage to the natural environment. The concern to determine the importance of the airflow as a possible source of contamination in dairy and food industry is growing, because the airborne dust particles can introduce foreign matter including microbial contaminants into the dairy products. Maintenance of air quality in a dairy factory plays an important role and is very much monitored by controlling the temperature, humidity and particle concentration. Air quality control is required for the comfort and safety of employees. To reduce the possibility of contamination in products it is necessary to impose additional controls on air quality. Airborne contamination can be controlled by air filtration.