5th Sem Applied Zoology
5th Sem Applied Zoology
5th Sem Applied Zoology
Beneficial Interactions
The beneficial interactions such as symbiosis (mutualism), proto cooperation, and
commensalism are found to operate among the soil inhabitants.
Symbiosis (Mutualism)
Mutualism is an example of symbiotic relationship in which each organism benefits
from the association. One type of mutualistic association is that involving the
exchange of nutrients, between two species, a phenomenon called syntrophisms.
Many microorganism’s synthesis vitamins and amino acids in excess of their
nutritional requirements. Others have a requirement for one or more of these nutrients.
Symbiosis is an obligatory relationship between two populations that benefit both the
populations. Both populations are living together for mutual benefit. The relationship
between algae and fungi that result in the formation of lichens is a classical example of
mutualistic intermicrobial relationship. Lichens are composed of primary producer, the
phycosymbiont (algae) and a consumer the mycosymbiont (fungus).
Commensalism
In a commercial relationship between two microbial populations, one population is
benefited and other population remains unaffected. Commensalism is a unidirectional
relationship between two populations. The unaffected population does not benefit by
the action of second population. For receiving population, the benefit provided may be
essential.
In commensalism, the unaffected population modifies the habitat in such a
way that another population benefits. For example, a population of facultative
anaerobes utilizes oxygen and creates a habitat suitable for the growth of anaerobes.
In soil, vitamin and growth factors producing organisms benefit vitamin and growth
factors requiring organisms.
Q: -Define Zoonosis.
Ans: - The word “zoonoses” (singular zoonosis) originated from the Greek word
„zoon‟ meaning animal, „nosos‟ meaning disease and it was Rudolf Virchow who first
used this term in 1855 in his famous „Handbook of Communicable Disease‟ to
describe the animal diseases secondarily transmissible to man.
Zoonosis refers to diseases that can be passed from animals to humans.
They are sometimes called zoonotic diseases. Animals can carry harmful germs, such
as bacteria, fungi, parasites, and viruses. These are then shared with humans and cause
illness. Zoonotic diseases range from mild to severe, and some can even be fatal.
Classification of Zoonosis
As per classification adopted by the joint WHO/FAO Expert Group on zoonoses, the
zoonoses have been grouped into three categories:
[A] Based in terms of reservoir host:
1. Anthropozoonoses: The infections transmitted to man from lower vertebrates are
termed as Anthropozoonoses. e.g., Ascariosis.
2. Zooanthroponoses: The infections transmitted to lower vertebrate animals from
man referred as zooanthroponoses. The infections are primarily of human origin, e.g.
Schistosomosis, Hymenolepiosis.
3. Amphixenoses: The infection maintained between man and lower vertebrate
animals, which may be transmitted in either direction, e.g. Salmonellosis.
[B] Based upon the type of life cycle:
1. Direct zoonoses: The infection transmitted from the infected vertebrate host to a
susceptible vertebrate host (e.g. Man) either by direct contact, contact with a fomite or
by a mechanical vector. During transmission the agent undergoes no developmental
and little or no propagative changes e.g. Trichinellosis.
2. Cyclozoonoses: The infection requires more than one vertebrate host species in
order to complete the life cycle of the agent. No invertebrate hosts are required.
Type I - Obligatory Cyclozoonoses - Man must be one of the vertebrate hosts in these
cycles e.g. Taenia saginata and T. solium infections.
Type II - Non-obligatory Cyclozoonoses - Man is sometime involved, but the human
involvement is the exception rather than the rule e.g. hydatid disease.
3. Metazoonoses: The infection is transmitted biologically by the invertebrate vectors.
In the invertebrate, the agent multiplies (Propagative or cyclopropagative
transmission), in which case the invertebrate also serves as reservoir of infection or the
agent merely develops (developmental transmission). In the metazoonoses there is
always an extrinsic incubation period in the invertebrate hosts before transmission to
another vertebrate hosts is possible.
Depending upon the hosts required, at least four subtypes of metazoonoses
may be distinguished:
Subtype I - requiring one vertebrate host and one invertebrate host e.g. yellow fever.
Subtype II - requiring one vertebrate host and two invertebrate hosts e.g.
paragonimosis.
Subtype III - requiring two vertebrate hosts and one invertebrate host e.g.
clonorchiosis.
Subtype IV - representing transovarian trans mission e.g. tick-borne encephalitis.
4. Saprozoonoses:Saprozoonoses are those zoonoses which require a non-animal site
to serve either as a true reservoir of infection or as a site for an essential phase of
development. Considered as nonanimal are organic matter (including food), soil and
plants e.g. various forms of larva migrans.
[C] Based upon etiological agent:
1. Bacterial zoonoses: Zoonoses caused by bacterial agents e.g. brucellosis, plague,
salmonellosis, anthrax.
2. Viral zoonoses: Zoonoses caused by viruses e.g. rabies, influenza, yellow fever.
3. Rickettsial zoonoses: Zoonoses caused by rickettsia e.g. Qfever, tick typhus.
4. Protozoan zoonoses: Zoonoses caused by protozoans e.g. toxoplasmosis,
trypanosomosis, leishmaniosis.
5. Helminthic zoonoses: Zoonoses caused by helminthes e.g. hydatidosis, taeniosis,
schistosomosis, trichinellosis.
6. Fungal zoonoses: Zoonoses caused by fungal agents e.g. histoplasmosis,
cryptococcosis.
7. Ectoparasitic zoonoses: Zoonoses caused by ectoparasites e.g. scabies, myiasis.
Factors Responsible for Emergence /Reemergent Of Zoonotic Diseases
Population explosion
Exploitation of newer Geographical areas.
Construction of pipe lines, roads, rivers, dams, new colonies, mining and similar
ecology damaging activities
Change in foods and food technology etc.
Q: - What is tuberculosis?
Ans: - Tuberculosis is an infectious disease that usually affects the lungs. Compared
with other diseases caused by a single infectious agent, tuberculosis is the second
biggest killer, globally.
Doctors make a distinction between two kinds of tuberculosis infection: latent and
active.
Latent TB - the bacteria remain in the body in an inactive state. They cause no
symptoms and are not contagious, but they can become active.
Active TB - the bacteria do cause symptoms and can be transmitted to others.
Zoonotic tuberculosis (TB) is a form of tuberculosis in people caused by
Mycobacterium bovis, which belongs to the M. tuberculosis complex. Cattles are most
important animal reservoir for M. bovis in relation to zoonotic exposure of humans.
But the disease can affect many other species snd become established in wildlife
reservoirs. It often affects sites other than the lungs (extrapulmonary), but in many
cases is clinically indistinguishable from TB caused by M. tuberculosis.
Prevention And control:
Improve the Scientific Evidence Base
1. Systematically survey, collect, analyse and report better quality data on the
incidence of zoonotic TB in people, and improve surveillance and reporting of bovine
TB in livestock and wildlife.
2. Expand the availability of appropriate diagnostic tools and capacity for testing to
identify and characterize zoonotic TB in people.
3. Identify and address research gaps in zoonotic and bovine TB, including
epidemiology, diagnostic tools, vaccines, effective patient treatment regimens, health
systems and interventions coordinated with veterinary services.
Reduce Transmission at The Animal-Human Interface
4. Develop strategies to improve food safety.
5. Develop capacity of the animal health sector to reduce the prevalence of TB in
livestock.
6. Identify key populations and risk pathways for transmission of zoonotic TB.
Strengthen Intersectoral And Collaborative Approaches
7. Increase awareness of zoonotic TB, engage key public and private stakeholders and
establish effective intersectoral collaboration.
8. Develop and implement policies and guidelines for the prevention, surveillance,
diagnosis, and treatment of zoonotic TB, in line with intergovernmental standards
where relevant.
9. Identify opportunities for community-tailored interventions that jointly address
human and animal health.
10. Develop an investment case to advocate for political commitment and funding to
address zoonotic TB across sectors at the global, regional and national levels
Q: - What is typhoid?
Ans: -Typhoid is a bacterial infection that can lead to a high fever, diarrhea, and
vomiting. It can be fatal. It is caused by the bacteria Salmonella typhi.
The infection is often passed on through contaminated food and drinking water,
and it is more prevalent in places where handwashing is less frequent. It can also be
passed on by carriers who do not know they carry the bacteria.
Annually, there are around 5,700 cases in the United States, and 75 percent of
these start while traveling internationally. Globally, around 21.5 million people a year
contract typhoid.
If typhoid is caught early, it can be successfully treated with antibiotics; if it is
not treated, typhoid can be fatal.
SYMPTOMS:
SYMPTOMS: Headache & typhoid fever which rise to the Headache & typhoid fever
which rise to the maximum in the afternoon. Maximum in the afternoon. High fever in
the second weak & then gradually High fever in the second weak & then gradually
declines during third & fourth week. Declines during third & fourth week.
PREVENTION:
PREVENTION: Proper sanitation. Proper sanitation. TAB-vaccination provides
immunity. TAB-vaccination provides immunity. Typhoral oral vaccine also prevents
typhoid. Typhoral oral vaccine also prevents typhoid.
CONTROL:
CONTROL: There are standard drugs against There are standard drugs against
typhoid which cure the disease. Typhoid which cure the disease.
Q: -Explain the life cycle of Entamoeba histolytica?
Ans: - Entamoeba histolytica is a parasitic protozoan and lives as an endo-parasite in
the upper part of the large intestine, i.e., colon of man. It inhabits the mucous and sub-
mucous layers of the large intestine. It feeds mainly on the tissues of the intestinal wall
and often produces severe ulcers and abscesses. The parasite is worldwide in
distribution and more common in most countries of trop-ics and subtropics rather than
temperate zones. E. histolytica is scarcely pathogenic found in human beings of
temperate zones.
Life Cycle of Entamoeba histolytica:
The life cycle of E. histolytica is completed through a single host-man. Hence it is
called monogenetic. Trophozoite and cyst stages of the parasite are concerned with the
life cycle.
Encystment: Entamoeba histolytica multi-plies by binary fission in the trophozoite
stage. They have the capacity to encyst. Unfavourable conditions in the habitat such as
lack of nutrients, temperature deviations from the optimum range, decreased O2
tensions, lowered pH and accumulation of metabolic wastes may be the causes for
encystment.
Precystic form: Prior to encystment the trophozoite of each parasite loses its pseu-
dopodium, eliminates food vacuoles and becomes spherical, called a precystic form.
The diameter of this stage varies 10-20 µm and the structure of the nucleus is like the
trophozoite stage of the parasite.
Mature cyst form: The precystic form secrets a thin, tough and transparent mem-
brane around it, called the cyst wall. The animal having a cyst is called a cyst. The
process of enclosing in a cyst is called encystment or encystation. At the early stage
the cyst contains a single nucleus. The single nucleus is divided mitotically forming
two nuclei. This is called binucleate cystic stage. Then the two nuclei are divided by
mitosis and four nuclei occur. The nuclear divisions take place without cytoplasmic
division and this tetra-nucleate cyst is called mature cyst. The whole process of
encystment takes a few hours and the mature cyst lives in the lumen of the intestine of
host only two days.
Tolerance of the cyst: The cysts of E. histolytica can survive about one month in
water and about 12 days on dry land. They can tolerate the temperature up to 50°
Celsius and 4 hours in formaldehyde solution.
Infection: At the tetranucleate stage the cyst is infective to a new host. The infective
cysts pass out through the host’s faeces and are introduced into the gut lumen of a new
host through the contaminated drink, food and vegetables.
Excystment: Then the infective cysts pass into the lower portion of the small intestine
(colon) of the new host. Here the process of excystment occurs. The excystment is the
process by which the cysts are transformed into the trophozoites. The cyst wall in the
colon becomes permeable by the action of intestinal enzymes, the trypsin of the intes-
tine. The cyst wall ruptures and 4-nucleate amoeba emerges out from the cyst.
Factors for excystment: Temperature, pH, chemical composition of the medium and
the flora of the bacteria may be the reasons for excystment.
Metacystic form: After the emergence of quadrinucleate amoeba, the division of cyto-
plasm immediately ensues and produces four small metacystic trophozoites.
Trophozoites: Both the nucleus and cytoplasm of each metacystic trophozoite divide
and as a result 8 small amoebulae are produced. These are called young uninucleate
trophozoites. They are motile and penetrate the mucous membrane.
The young trophozoites feed on host tissues, blood, bacteria and yeast and
gradually in-crease in size to attain maturity. Inside the tissues the trophozoites
multiply and start the procystic form of the life cycle. Transformation of a
quadrinucleate metacystic stage of entamoeba histolytica to eight uninucleate
trophozoites
Transmission: Cysts of Entamoeba are transmitted from one individual to another in a
variety of ways:
1. The cysts are generally transmitted with food or drink.
2. House flies and cockroaches may trans-mit cysts mechanically.
3. Raw vegetable is also another source of infection.
4. In many countries human faeces are used as fertilizer and thus roots and leaves of
plants remain contaminated with viable cysts. Food handlers are also sometimes
responsible for the spread of infection owing to imperfect personal sanitary measures.
Q: - Explain the pathogenicity of Entamoeba histolytica?
Ans: Entamoeba histolytica causes amoebiasis or amoebic dysentery or intestinal
amoebiasis or tropical amoebiasis.
Trophozoites dissolve the mucosal lining by histolysin. It causes ulcers. These
ulcers contain cellular debris, lymphocytes, RBC and bacteria.
It leads into formation of abscesses in the wall of large intestine. It results in stool
with blood and mucous.
Some persons do not exhibit any symptoms in spite of having cysts. They are called
as carriers or asymptomatic cyst passers.
Trophozoites rupture the wall of capillaries enters the blood stream and reach the
liver where they cause abscesses (secondary amoebiasis). From there they go to lungs,
heart, brain, kidneys gonads and cause abscesses in them.
Following measures are essential in the prevention of the disease:
1. Sanitary disposal of faecal matter.
2. Perfect sanitation and protection of water and vegetables from pollution.
3. Washing of hands with antiseptic soap and water before touching the food.
4. Cleanliness in preparing the food.
5. Protection of foods and drinks from houseflies, cockroaches, etc.
6. Raw and improperly washed and cooked vegetables should be avoided.
Q: -Describe the life cycle of Plasmodium vivax in man?
Ans. Life cycle of Plasmodium vivax in man: -In man, Plasmodium reproduces by
asexual reproduction known as schizogony. It occurs in hepatocytes of liver as hepatic
schizogony and erythrocytes (RBC) as erythrocytic schizogony.
Hepatic Schizogony: it was explained by Shortt and Garnham. Sporozoites of
Plasmodium enter into the blood of man from female Anopheles and reach the
hepatocytes within half an hour and undergo pre-erythrocytic and exo-erythrocytic
cycles in the following manner.
1. Pre-erythrocyticcycle:
a) sporozoites transform into trophozoites and feed on the contents of hepatic cells
and attain maximum size and becomes Schizontstage.
b) Nucleus divides for many times mitotically which is followed by cytoplasmic
divisions and thus form 12,000 cryptozoites or 1st generationmerozoites.
c) cryptozoites enter the sinusoids of liver. It takes place in 8days.
d) Some of them enter RBCs and majority of them enter fresh livercells.
2. Exo-erythrocyticcycle:
a) cryptozoites after entering the liver cells undergo same changes of pre-erythrocytic
cycle and form into second generation merozoites orMetacryptozoites.
b) Metacryptozoites are of two types
a) Smaller micro-metacryptozoites
b) Larger Macro-metacryptozoites.
c) Macro-metacryptozoites attack fresh liver cells and continue another exo-
erythrocytic cycle.
d) Micro-metacryptozoites enter RBC to continue erythrocytic cycles and
produce merozoites.
3. Erythrocytic cycle:
i) life cycle of Plasmodium vivax in erythrocytes of man was described by Camillo
Golgi. So, it is called as Golgi cycle.
ii) Golgi cycle is started by either cryptozoites of pre-erythrocytic
cycle or the micrometacryptozites of exo-erythrocytic cycle.
iii) In fresh RBC, Plasmodium gets spherical shaped trophozoites. It develops a small
vacuole which enlarges in size and pushes the cytoplasm and nucleus to periphery.
iv) Plasmodium looks like a finger ring. So, this stage is known as signet ring stage.
v) It loses vacuole and develops pseudopodia and becomes amoeboid stage or late
trophozoite stage.
vi) It feeds on contents of RBC with pseudopodia and increases in size. It results the
doubling of the size of RBC. This condition is known as hypertrophy.
vii) Plasmodium digests the globin part of ingested haemoglobin and converts the
soluble haem into an insoluble hamozoin (malaria pigment).
viii) Small red coloured dots appear in the cytoplasm of the RBC known as
Schuffner’s dots. They are antigens formed by parasite.
ix) Plasmodium loses pseudopodia and increases in size, occupies the entire RBC and
becomes a Schizont.
x) It undergoes schizogony (a type of multiple fission) and produces 12-24
erythrocytic merozoites. They are arranged irregularly in RBC.
xi) Erythrocyte bursts and releases the merozoites along with haemozoin into the
blood. It is completed in 48 hours/2days.
Q: -Describe the life cycle of Plasmodium in mosquito or Ross cycle?
Ans. Gametocytes of Plasmodium enter into the crop of female Anopheles mosquito.
In mosquito the life cycle of Plasmodium continues in the following stages….
a) Gametogony
b) Fertilization
c) Formation of ookinete & oocysts
d) Sporogony
A) Gametogony: it is the formation of male and female gametes from the
gametocytes.
It occurs in the lumen of crop of mosquito.
1. Formation of male gametes: nucleus of microgametocyte divides into 8 daughter
nuclei known as pronuclei. They reach the periphery. Cytoplasm is pushed out in
the form of 8 flagella like processes. Each process receives one pronucleus and
forms a micro gamete or male gamete
male gametes show lashing movements like flagella and get separated from
cytoplasm of microgametocyte. This process is known as exflagellation.
2. Formation of female gametes: female gametocyte undergoes a few changes and
transform into a female gamete by maturation. Nucleus of female gamete moves
towards the periphery and Cytoplasm at that point forms a projection known as
fertilizationcone.
B) Fertilization: fusion of male and female gametes is known as fertilization. It
occurs in crop of mosquito. Actively moving microgamete comes in contact with
female gamete at fertilization cone. Later pronuclei and cytoplasm of both gametes
fuse and form a synkaryon. This type of fusion of dissimilar gametes is known as
anisogamy. Female gamete with synkayon is known as Zygote which is round and non
motile.
C) Formation of Ookinete and Oocysts:
Zygote remains inactive for some time and transform into a long, slender, motile,
vermiform within 18-24 hours. Ookinete pierces the wall of crop and settles beneath
the basement rane. It becomes round and secretes a cyst around the body and becomes
OOCYST. About 50-500 oocyts are formed on the wall of crop and appear as nodules.
D)Sporogony:
Formation of sporozoites in oocyts is known as sporogony. According to Bano, the
nucleus of oocyts first undergoes reduction division followed by Repeated mitotic
divisions which result in the formation of sporoblasts. Each nucleus is surrounded by a
little bit of cytoplasm and transforms into sickle shaped Sporozoites. Oocyts with
sporozoites is known as Sporocyst. By rupturing of sporocyst about 10,000 sporozoites
are released into the haemocoel of Mosquito. They enter into salivary glands of
mosquito and are ready for infection. Life cycle of Plasmodium in mosquito is
completed in about 10-24days.
Life cycle in tsetse fly: When this insect vector sucks the blood of an infected person,
it also takes short stumpy forms of trypomastigote along with the sucked blood. Now
these stumpy forms continue development in the midgut of insect vector.
Development in the Midgut of Insect Fly: Further change of trypomastigote occurs
in the insect vector’s midgut within peritrophic membrane and the short stumpy forms
of the parasites trans-form into long slender forms. Now these long slender forms
appear which pass to posterior end of the extraperitrophic space (a space between the
peritrophic membrane and epithelial cells), where they continue to multiply for some
days. By the 15th day they escape from the peritrophic space and enter the lumen of
the proventriculus (the periventricular form is the same as that of the midgut form).
Development within the Salivary Gland of Insect Fly: Later the long slender forms
make their way into salivary glands through the hypo- pharynx. Here they multiply
and change their morphology, first into epimastigote and then into the metacyclic stage
(short stumpy forms of trypo-mastigote) which are infective to man. It has been
reported that the time taken for the complete evolution of the infective forms
(metacyclic stage) inside the vector insect is about 20 days. These flies remain
infective for the rest of their lives, a period extending up to 185 days. When the vector
fly bites a healthy person, it transfers the metacyclic forms along with saliva into his
blood where they initiate another infection.
Pathogenicity and Symptoms of Trypanosoma gambiense:
The bite of an infected fly is usually followed by itching and irritation near the wound,
and frequently a local dark red lesion develops. In blood, the parasite multiplies and
absorbs nutrients from it. After a few days, fever and headache develop, recurring at
regular intervals accompanied by increasing weakness, loss of weight and anaemia.
Usually, the parasites succeed in penetrating the lymphatic glands. Because of
its infection, the lymphatic glands swell and after it the parasites enter the
cerebrospinal fluid and brain causing a sleeping sickness like condition. Development
of lethargic condition and recurrence of fever are the symptoms of its infection.
Trypanosoma gambiense causes trypanosomiasis; most commonly referred to as
sleeping sickness leading to coma stage and finally resulting into the death of the
patient. In fact, two types of diseases are caused by Trypanosome which are essentially
similar in symptoms. These are Gambian and Rhodesian sleeping sickness. The
Gambian sleeping sickness occurs in western part of Africa and its vector is Glossina
palpalis, while Rhodesian sleeping sickness occurs in rest of Africa and its vector is
Glossinamorsitans. The only difference between the two is that the latter is more rapid
causing the death of the patient within 3-4 months of infection.
Diagnosis, Treatment and Prevention of Disease Caused by Trypanosoma
gambiense: The diagnosis is confirmed by examining fresh or stained peripheral blood
or by examining the cerebrospinal fluid obtained by lumbar puncture or by examining
the extract of enlarged lymphatic glands.
Treatment (Therapy): Arsenic and antimony compounds were until recently the
drugs for treatment of trypanosomiasis, but now they are rarely used except for late
stages when the parasites have invaded the central nervous system.
Prevention (Prophylaxis): The following measures are suggested for preventing the
infection of this parasite:
1. By eradicating the vectors. The infection of this parasite can be checked by
completely eradicating the secondary host (Tsetse fly). For this, the endemic areas
should be kept clean and regular spray of insecticides like DDT is suggested which
help in eradicating the fly.
2. Care should be taken to keep the reservoir hosts free from its infection.
3. Preventive medicines should be taken frequently and periodically which help to a
great extent from its infection
Q: - Explain the life cycle of Ancylostoma duodenale?
Ans: -Ancylostoma duodenale is a species of the roundworm genus Ancylostoma. It is
a parasitic nematode worm and commonly known as the Old-World hookworm. It
lives in the small intestine of hosts such as humans, cats and dogs, where it is able to
mate and mature. It is also called the common hookworm.
Life History of Ancylostoma duodenale:
The life history of Ancylostoma duodenale is monogenetic as no intermediate host is
required; man is the only main host for Ancylostoma duodenale.
Copulation and Fertilization: Copulation occurs in the intestine of the host, during
the process the copulatory bursa of male is applied on the vulva of female and sperms
are transferred. In fact, during copulation the worms (a male and a female) assume a
Y-shaped figure owing to the position of the genital openings. The sperms, thus,
transferred come to lie in the seminal receptacles where fertilisation takes places. The
fertilised eggs are then pushed into the uteri for laying through vagina and gonopore.
Egg Laying: The female worm lays eggs in the intestine of the host which pass out
with faeces. On an average nearly 9,000 eggs are laid per day by a female. The eggs
are oval or elliptical in shape measuring 65 pm in length by 40 pm in breadth,
colourless and protected by a transparent hyaline shell-membrane. An egg that comes
out of the host body possesses an embryo up to 4-celled or 8- celled stage. The eggs,
which passed out with the faeces, are not infective to man.
Development in Soil: Under favourable conditions of environment like moisture,
oxygen and temperature (about 68-85°F), the embryo develops into a rhabditiform
larva or first stage juvenile; it is about 250 µm in length. This larva hatches out of the
egg in the soil in about 48 hours. This larva possesses the mouth, buccal capsule,
elongated pharynx, bulb-like oesophagus and intestine. It feeds on bacteria and other
debris of the soil and moults twice, on the third day and the fifth day. It then develops
into a filariform larva measuring about 500 to 600 pm in length. It is the infective stage
of the parasite. This larva does not feed but remains infective and alive for several
weeks under favourable conditions. The time taken for development from eggs to
filiform larvae, is on an average 8 to 10 days.
Infection to New Host: The filiform larvae are infective to man. The larvae cast off
their sheaths and penetrate the skin of a human host. The anterior end of the larva is
provided with oral spears by which it penetrates the soft skin of the feet and hands,
generally through hair follicles.
Migration and Later Development: On reaching the subcutaneous tissues, the larvae
enter into the lymphatic’s and small venules. They pass through the lymphatic-
vascular system into the venous circulation and are carried through the right heart into
the pulmonary capillaries, where they break through the capillary walls to enter into
the alveolar spaces. They then migrate on the bronchi → trachea → larynx, and crawl
over the epiglottis to the back of the pharynx and are finally swallowed. During its
migration, when it reaches to oesophagus, its third moulting occurs and a terminal
buccal capsule is formed. The time taken in this migration is about 10 days. Thus,
finally the growing larvae settle down in the small intestine and undergo fourth and
final moult to become the adults. In about 3 to 4 weeks’ time they become sexually
mature to repeat the life history again. The life span of the adult worm in human
intestine has been estimated differently by different workers; generally, it is believed
to be 3 to 4 years.
Diagnosis, Disease and Pathogenicity of Ancylostoma duodenale:
The infection of hookworm is easily diagnosed by the presence of its eggs in faecal
smear from the patient. The disease caused by its infection is generally referred to as
ancylostomiasis.
The hookworms are the most dangerous parasitic nematodes because they hold
on to the intestinal villi and suck blood and body fluids of the host by their muscular
pharynx, they also cut holes in the intestinal mucosa and leave bleeding wounds. It
causes severe anaemia. In children, where incidence of infection is very great, they
retard the physical and mental growth.
Some toxins secreted by the glands in the head region of worms cause
stomachache, food fermentation, diarrhoea, constipation, dyspnea, palpitation of heart,
eosinophilia, ill health and the patient may finally collapse.
During penetration of larvae in the skin, local irritation is caused resulting into
inflammation of the surrounding tissues; these may result into tiny sores. The
migratory larvae in lungs may cause haemorrhage and bronchial pneumonites.
Treatment and Prevention of Infection Caused by Ancylostoma duodenale
Drugs like carbon tetrachloride, thymol, oil of chenopodium, hexylresorcinol, etc., are
used effectively to control the infection of Ancylostoma. Some other anti-helminth
drugs like tetrachloroethylene and blephenium are found to be more effective and are
safe to be used.
Prevention of Infection by Ancylostoma duodenale: The infection of Ancylostoma
duodenale can be checked effectively by improving the sanitary conditions to avoid
the contamination of faeces with the soil and other edibles, by protecting feet and
hands from being touched with the soil. Children should be directed to keep their
hands and nails clean.
Q: - Explain the life cycle of Wuchereria bancrofti?
Ans: -Wuchereria bancrofti is a dreadful endoparasite of man; adults harbouring the
lymphatic vessels and lymph nodes. Its life history is digenetic, as it involves a
secondary host, the blood-sucking insects, i.e., the female mosquitoes of the genus
Culex, Aedes or Anopheles; the secondary host for W. bancrofti in India and China is
Culex pipiens, in Pacific Islands (except Fiji and New Caledonia) is Anopheles
punctatus and in Polynesian Islands is Aedes polynesiensis. Wuchereria bancrofti is a
human parasitic roundworm that is the major cause of lymphatic filariasis.
Life History of Wuchereria bancrofti:
We know that Wuchereria bancrofti is digenetic, i.e., its life history is completed in
two hosts; man is the main host, while female mosquito, usually Culex pipiens, is the
secondary host. Mature male and female worms copulate in the lymph glands of man
where they usually live. Since female worm is viviparous or ovoviviparous, it delivers
numerous larvae called microfilariae. The microfilariae are born in very immature
stage.
However, microfilariae find their way into the blood stream where they can live for a
considerable time without undergoing any developmental changes. As referred to, due
to their nocturnal periodicity they are sucked up by the secondary host when it comes
to take its blood-meal from the human body.
Pathogenic manifestations of heavy infection of Wuchereria
The microfilariae, after reaching in the body of the secondary host, undergo further
development to become infective to man. In fact, immediately after their entry in the
stomach of mosquito, the sheaths around their bodies are shed off and then they
penetrate the gut wall within an hour or two and migrate to the thoracic muscles.
Here they become short and thick like sausages within 2 days having short spiky
tails and measure 124 to 250 µm in length and 10 to 17 pm in diameter, they also
possess rudimentary digestive tract. These are first stage larvae. Within next 3 to 7
days they grow rapidly and moult once or twice to become the second stage larvae;
they measure 225 to 330 µm in length and 15 to 30 pm in diameter.
Finally, by 10th or 11th day they become fully grown and are referred to as third
stage larvae; they measure about 1500 to 2000 pm in length and 18 to 23 µm in
diameter. This stage is infective to man. These larvae are inactive and come to lie in
the labium of the mosquito.
When the mosquito bites the warm and moist skin of man, the larvae creep out
of the labium to the human skin, then they penetrate into the skin and finally come to
settle down in the lymphatic’s. Here, they grow and become fully adult and sexually
mature within a period of 5 to 18 months.
These sexually mature worms start reproduction to repeat the life history again.
The life span of adult worms is very long, probably ranging from 5 to 10 years.
UNIT-II
1. Insects of Economic Importance
Biology, control and damage caused by Helicoverpaarmigera, Pyrillaperpusilla and
papiliodemoleus, Callosobruchuschinesis, Sitophilus oryzaeTriboliumcastaneum
2. Insects of Medical Importance
Medical importance and control of Pediculus humans corporis, Anopheles, Culex, Aedes
Xenopsyllacheopis
3. Insect pests
Of crops, vegetables, oilseeds, coffee, tea
4. Insect pest management
Damage: Both adults and nymphs suck the cell sap of succulent leaves of sugarcane
by their rostrum. As a result the leaves turn pale yellow. They secrete a sweet sticky
transparent liquid known as honey dew which attracts the harmful fungi resulting into
a good growth of black shooty mould due to which the photosynthesis is affected and
hence productivity also. Because of the attack of this pest the quality and quantity of
sugar is affected.
Control: The egg masses should be collected and destroyed by burning, burying or
spraying phenyl water. The pest can be controlled by spraying 0.05% of parathion,
malathion, thiodon, fenitrothion or rogor. Dusting the plants with 10% Aldrin or
dieldrin also helps.
3. Papilio demoleus
Biology: This is a common pest of all citrus plants. Adult is a large butterfly and has
prominent black and yellow markings on the wings. They are active fliers and found
throughout the year in plains. Eggs are small, round, smooth, yellowish and laid singly
glued on to the tender leaves. They hatch in 3-6 days. First three instars of the larvae
resemble bird droppings as they are brownish-black in colour, with one or two white
patches. Last two instars are green in colour, sometimes with greyish markings.
Pupation takes place on the plant. Pupa, which is called chrysalis, greenish to brown in
colour, resembles a twisted leaf and remains attached to a branch with a fine silken
thread. Pupal period is 8-15 days.
Damage: Larvae are voracious feeders of tender leaves and defoliate the trees. They
eat leaves from margin inwards, leaving the larger veins intact. Younger plants cannot
withstand defoliation and die.
Control: Handpicking and destruction of the larvae which are so prominent on the
leaves helps to save the plants in nurseries. Dusting the trees with sodium fluosilicate
or BHC 5% or spraying malathion, endosulfan, parathion, fentrothion 0.02% or lead
arsenate 0.25% effectively controls the pests orchards.
Spraying spores of Bacillus thuringiensis gives high mortality of caterpillars.
4. Callosobruchus chinensis
Biology: It is commonly called pulse beetle. A pest of pulses, cowpea, soybean, gram,
pigeon pea, lablab etc. Cosmopolitan in the tropics and subtropics of the world. Adult
beetle is 3-4 mm long, female being larger, brownish in colour, broader at shoulders
and rounded posteriorly. Adults show sexual dimorphism. Males possess deeply
emarginated or indented eyes and prominently serrate antennae, while in female these
characters are not distinctly marked. Fecundity is about 100 eggs per female. Eggs are
whitish, elongated and stuck on the grains or on pods and sometimes on the surface of
the container. Grubs are scarabeiform or eruciform, plump and with short legs and
yellowish in colour. First instar larvae bear functional legs and a pair of thoracic plates
to facilitate boring into the seeds. They feed on the inner contents of the grain and may
damage several grains during development. Completion of life cycle takes 4-5 weeks
and there may be 6-7 overlapping generations in a year.
Damage: Both larvae and adults cause damage to the grains. They bite holes in the
grains to enter inside and feed on kernel, damaging several grains in the process. As
the beetles can actively fly, the infestation can start in the fields, where the beetles
deposit their eggs on the pods.
Control: Callosobruchus spp. may be controlled by fumigation treatment with
phosphine Intercropping maize with cowpeas, and not harvesting crops late
significantly reduced infestation by C. maculatus Good store hygiene plays an
important role in limiting infestation by these species. The removal of infested residues
from last season's harvest is essential, as is general hygiene. Solarization (or drying
and heating) can be used to control infestations of C. maculatus without affecting seed
germination.
5. Sitophilus oryzae
Biology: It is commonly called the rice weevil. This is primarily a pest of rice but
occasionally attacks wheat, corn, jowar, flour, beans, dry fruits and biscuits. Adults are
2-3 mm long dark brown weevils, with four faint yellow spots on the elytra. Body is
punctured with minute pits. Adults do not fly but try to crawl away when disturbed.
Their longevity can be up to 5 months. Eggs are whitish, oval, 0.7 mm long. Females
chew a small depression on the surface of rice grain, lay an egg in it and seal it with a
gelatinous fluid for protection. Grubs make their way into seed to feed on kernel. They
are plump,3-4 mm long, legless, dirty white in colour with a brownish head. Pupation
takes place inside the grain. Pupa is light yellowish but later turns dark brown. Adult
emerges by cutting a hole in the grain.
Damage: Larva as well as the adult cause damage to
grains. Larvae feed inside the seed and make in
hollow and exit by making a circular hole on the
surface. Adults can damage several seeds by cutting
an irregularly lined circular hole, through which they
feed on the kernel.
Control: Good store hygiene plays an important role in limiting infestation by S.
oryzae he removal of infested residues from last season's harvest is essential. Grain
may be protected by the admixture of insecticide. Sitophilus spp. have a low
susceptibility to synthetic pyrethroids but are readily killed by organophosphorous
compounds such as fenitrothion and pirimiphos-methyl.
6. Tribolium castaneum
Biology: It is commonly called red flour beetle. It is a worldwide pest of stored
products, particularly food grains. They are cosmopolitan in distribution. Larval and
adult both the stages are found infesting and causing damage. The adults are reddish
brown and are very active and survive in moderately cold winter in unheated buildings
and often live for 2 years in adult stage during which period the fertilized female
produces eggs. Eggs hatch into larva which are reddish yellow in colour which after 6
to 7 moultings change into pupae from which the adults arise.
Damage: These beetles cause serious damage in monsoon period. They heavily
damage flour in the mills but sometimes damage the grains in store. Both the adult and
larva are infective stages.
Damage: These beetles cause serious
damage in monsoon period. They heavily
damage flour in the mills but sometimes
damage the grains in store. Both the adult
and larva are infective stages.
Control: Flour mills should be kept clean
and dry. The infested portion of the flours
should be removed. The adults or its other
life stages should be removed from stores
or go downs
Insects of Medical Importance
1. Pediculus humanus corporis:
Commonly known as body louse, it is the
blood sucking ectoparasite of man and is cosmopolitan in distribution. It is found in
the hairs of the armpits, clothes and garments. The asults are wingless, flattened,
greyish white insects. It is comparatively larger then the head louse (Pediculus
humanus capitis).
Medical Importance: They suck the blood, cause
annoyance, itching and irritation and transmit
certain diseases.
Epidemic typhus: This disease is caused by a
PPLO, Ricketsia prowazeki, which multiplies in
the gut of lice. Spores are released through faeces
within 5 days of infection and can remain viable for 4 months in the dry conditions.
They get into the human system through contact with blood, through wounds,
conjunctive or by inhalation into lungs. The disease spreads in epidemic form and is
capable of causing 100% fatality. Reservoir hosts are sheep and goats.
Trench fever: This is caused by Ricketsia quintana. The disease was common among
soldiers during the world war II, when soldiers had to spend several days trapped in
trenches and lice transmitted the disease in epidemic form. The mode of transmission
is similar to the epidemic typhus.
Relapsing fever: This disease is transmitted by a spirochaet, Borrelia recurrentis
which breeds in the haemolymph of the louse and escapes when the louse is crushed or
dies due to the parasite. It gets into the human blood through wounds or scratches. This
disease spread in great epidemic form during the World War I and II.
Local urticaria and itching: This is also called the Vagabond disease. Itching, rashes
and discoloration of the skin takes place due to the allergic reaction to the bites and
blood sucking by lice.
Control: Cleanliness and hygiene eradicates lice. In case of severity of infestation,
clean shaving of head brings relief. Application of kerosene mixed with olive oil in
equal ratio on the head kills lice. Lindane ointment, malathion (Lycil) and Mediker
shampoo (also contains malathion) or any insecticide mixed with oil kills all lice on
head. The application has to be repeated every week to kill nymphs emerging from
eggs. Body lice can be controlled by steaming or boiling of clothes and bedding or
rinsing clothes in weak insecticide solution.
2. Mosquitoes: Anopheles, Culex, Aedes.
Mosquitoes are cosmopolitan in distribution. They are nocturnal in habit and are found
in abundance in damp, marshy lands near stagnant water. Only female mosquitoes are
adapted to suck the blood of human beings and function as carrier of viral, protozoan
and nematode diseases.
Culex mosquitoes serve as the vectors for filariasis or elephantiasis. This disease is
caused by the nematode parasite, Wuchereria bancrofti. It is commonly known as
filarial worm. It is found in the lymphatic vessels and lymph glands of man. The
female worms give birth to living embryos known as microfilariae. The microfilariae
normally circulate at night (10 to 2 am) in the peripheral blood. At that time they are
ingested by the mosquito along with blood, the mosquito is not just a mechanical
carrier of the parasite. Developmental changes take place in the body of the parasite.
When the infected mosquito next bites another person, the larvae penetrate the
superficial skin to find their way into the lymphatic vessels, and attain sexual maturity.
In severe infection the adults cause blocking of lymphatic system which results in the
enlargement of legs, arms, scrotum, and mammary glands. It is known as
elephantiasis.
Anopheles. Adults are dull whitish in colour having wings with blackish spots and
dark veins. They make no noise while flying. There may be scattered scales on the
abdomen. Thorax without any markings on the dorsal side and scutellum not lobed and
has uniformly distributed hairs on its posterior margin. Maxillary palps in both sexes
are equal to proboscis but in male they are clubbed at the tip. Adult in resting position
makes an angle of 45 degrees against the surface. Anopheles mosquitoes are best
known for spreading malaria, although they can transmit other diseases. They are
active between sunrise and sunset, and can be found both indoors and outdoors. The
females feed on both humans and animals, but some species have a preference for one
over the other; species that favour humans pose the greatest risk for transmitting
malaria.
Another type of mosquito, Aedes transmits yellow fever through a virus.
Aedes: This is called zebra mosquito as it has black and white bands on the abdomen
and legs. The Aedes mosquitoes are the carriers of many viral diseases including Zika,
dengue, chikungunya, yellow fever, and Rift Valley disease. The Aedes mosquitoes
can be identified by the distinctive black and white markings on their bodies and legs.
Unlike most other mosquitoes, Aedes mosquitoes are active and bite only during the
daytime, with peak activity during the early morning and in the evening before dusk.
There are two specific species of Aedes that are important transmitters of viruses –
Aedes aegypti and Aedes albopictus. Aedes aegypti, also known as the yellow fever
mosquito, is found in urban areas, is active both indoors and outdoors, and has a
preference for humans as the source of its blood meal. Aedes albopictus, commonly
referred to as the Asian tiger mosquito, is mostly associated with areas of vegetation
and is found primarily outdoors; the female will bite domestic and wild animals, as
well as humans. Because the Aedes aegypti mosquitoes live near and prefer to feed on
people, they are more likely to spread viral diseases than are the Aedes albopictus
mosquitoes.
Medical Importance: These groups of mosquitoes cause irritation during biting, lead
to allergy and suck blood. But their main role is in transmission of number of diseases.
Chikungunya virus causes a disease that, while rarely fatal, can cause debilitating joint
pain that can last for weeks. Typical symptoms include fever and rash, as well as pain.
The virus, which is classified as an alphavirus, is similar to dengue virus. The two
viruses produce many of the same symptoms and both are carried by the Aedes
mosquitoes, primarily Aedes aegypti.
Dengue virus causes dengue fever, a disease characterized by high fever,
headache, joint pain, and rash. A more severe form, dengue hemorrhagic fever, can
include bleeding and breathing difficulty and is fatal in some cases. There are four
types of dengue virus, and they belong to a class of viruses known as flavi viruses –
the family that also includes the West Nile, yellow fever, and Zika viruses. Dengue,
transmitted predominantly by Aedes aegypti mosquitoes, is found in more than 100
countries.
Yellow fever virus most commonly causes fever, headache, muscle pain, and
nausea in those individuals who develop symptoms (many do not); these symptoms
can initially be mistaken for malaria. The virus, classified as a flavi virus, is generally
transmitted by Aedes aegypti mosquitoes, the reason that these mosquitoes are also
known as yellow fever mosquitoes.
Zika virus, the most recent of these mosquito-borne viruses to emerge, causes no
symptoms or only a mild disease that may involve fever, rash, and joint pain in most
people who become infected. However, the disease can cause severe neurological
defects in the developing foetuses of pregnant women who are infected with Zika
virus. Zika virus is classified as a Flavi virus and is transmitted principally by the
Aedes aegypti mosquito.
West Nile virus can cause death in humans and different bird species. Most
people (80%) do not develop any symptoms. Most of the remaining individuals who
become infected develop West Nile fever, which is associated with fevers, aches, and
nausea. A small percentage (about 1 in 150 infected persons) develops West Nile
encephalitis, a more serious disease that produces high fever, neck stiffness,
convulsions, muscle weakness, paralysis, and possibly death. West Nile virus belongs
to the flavi virus family of viruses. It is transmitted principally by Culex mosquitoes.
Birds are the reservoir for the virus and mosquitoes acquire the virus when they feed
on infected birds.
Culex (female) is the vector of filarial worm Wuchereria bancrofti, which causes
filariasis in humans. Different species of anopheles mosquito transmit malaria causing
protozoan called plasmodium.
MOSQUITO CONTROL:
Mosquito control efforts have not been successful because of the ability of mosquitoes
to develop resistance against insecticides very quickly and their capacity to inhabit a
variety of environmental conditions. The following measures are generally adopted to
reduce mosquito populations.
Personal preventive measures: Use of mosquito nets is an effective method to
prevent adults from biting and transmitting malaria. Application of mosquito repellent
chemicals, such as citronella oil, dimethylphthalate, odomos cream or pyrethrum
cream also prevent mosquitoes from sucking blood. Mosquito repelling fumigants, e.g.
tortoise mosquito coil contains pyrethrum in it and Good night mats or All out liquids
contain synthetic pyrethroids such as deltamethrin, decamethrin and allethrin. They
effectively repel and confuse mosquitoes.
Anti-larval measures: Removal of breeding places effectively reduces mosquito
population. Broken pots, old tyres, tins and other containers should be removed from
the surroundings as they serve as breeding places for Aedes. Coolers and overhead
water tanks should be periodically cleaned or treated with potassium permagnate to
kill the larvae. Small water bodies, ditches and ponds that cannot be filled should be
sprayed with light diesel or petroleum oil that makes a thin film on the water surface
and clogs respiratory siphons of larvae. Use of Paris green (copper aceto-arsenite) also
kills larval and pupal stages. Biological control of larvae and pupae in ponds has been
achieved by releasing larvivorous fishes, such as the native Gambusia and
Nothobranchius guntheri introduced by CIBC from Africa. These fishes actively feed
on the larvae and can aestivate in mud when ponds dry up in the summer months.
Naiads of dragonflies and damselflies are also effective predators of mosquito larvae
and pupae.
Anti-adult measures: -Trapping of adults by hanging black cloths to serve as hiding
places during day time and then killing the adults by spraying insecticide should be
done daily. UV electrocuting traps should be used to attract and kill adults. Destruction
of tall grasses and bushes serve as resting places for mosquitoes in day time and hence
should be removed from the surrounding areas.
Use of malathion and endosulfan aerosols in the colonies periodically has been
effective in reducing their populations. Aerial sprays of pyrethrum, carbaryl,
carbofuran, arprocarb mixed with mineral oil are still effective in killing adults.
Synthetic pyrethroids are quite effective and new chemicals used against mosquitoes
but are prohibitively expensive.
3. Xenopsyllacheopis
Fleas are small wingless insects, 2-3 mm long, with highly sclerotised, laterally
compressed bodies and reddish-brown colour. Antennae short, stout, pectinate or
clubbed and concealed in a groove. Mouth parts are modified for piercing and sucking.
Legs adapted for clinging with curved claws. Hind leg longer, modified for jumping.
The Oriental rat flea (Xenopsyllacheopis), also known as the tropical rat flea, is a
parasite of rodents, primarily of the genus Rattus, and is a primary vector for bubonic
plague and murine typhus.
Medical importance: Fleas transmit plague that is caused by the safety pin bacillus
called Yersinia pestis or Pasturella pestis. The disease is caused in man as well as in
rats and produces three types of symptoms in man.
1. Bubonic plague. The bacillus infects lymphatic system, causing swelling and pain
in the lymph glands but no fever occurs. Rats also suffer from similar symptoms.
2. Septicemic plague. Infection spreads to the blood vascular system causing fever.
There is headache and pain in the back. Sudden chilliness, blood-shot eyes, rapid
pulse, thick speech and high fever are other symptoms. In the case of prolonged illness
spleen enlarges and becomes brick-red in colour and liver is also enlarged. Comma
and death can occur due to heart failure in about a week.
3. Pneumonic plague. In this case bacillus multiplies in the lungs and pleural cavity,
causing pneumonia-like symptoms. Yellowish fluid fills the lungs and pleural cavity,
causing excessive coughing and heavy breathing. Infection can spread directly from
man to man through droplets release during coughing. This is the most dangerous type
of plague as it spreads very fast by droplet infection, particularly in high population
density areas and brings about quick deaths.
Murine typhus: This is another disease transmitted by Xenopsylla cheopis. It is a mild
typhoid fever caused by the PPLO, Rickettsia mooseri. The causative organism
multiplies in the gut of flea and is excreted through faeces. Man gets infected either by
contamination of wounds by the flea faeces or by inhalation of dust containing faeces.
Some fleas act as intermediate hosts for the tape worms like, Dipylidium caninum and
Hymenolepis diminuta.
Control of fleas: Control of rats is an effective method of controlling fleas. Trapping,
baiting and fumigation can eradicate rats. Cyanogas fumigation kills not only rats but
also all stages of fleas in the rat burrows. Fumigation should be done every 2-3
months. Construction of rat proof godown having metalled doors and meshed windows
is also an effective method to keep the rats away from human dwellings. Dusting the
houses, floors, godowns and other places frequented by rats should be done frequently
using residual insecticides such as BHC, endosulfan, dieldrin, aldrin etc. This will kill
all stages of fleas as they breed in dust and abandoned corners.
Patients suffering from plague can be treated with streptomycin injections or oral
doses of antibiotics such as tetracycline, sulphadiazene, chloramphenicol, doxycycline,
azithromycin etc. given two or three times in a day.
2.2 Insect pests
Insect pests of crops
S. PEST DESCRIPTION
NO
Q: - What is Aquaculture?
Ans: - Aquaculture is a branch of science that deals with the farming of economically
important aquatic organisms and plants, under controlled and in a confined
environment.
Brief history:
Aquaculture is an ancient culture technique. It was first practiced in Asia. Chinese, in
3500 BC raised carps in ponds. They also developed breeding techniques for increased
production. Today China dominates in Aquaculture industry. Currently Aquaculture
practices all over the world are growing as fast as any other type of agriculture.
Aquaculture in India is one hundred years old. Till the end of 19th century the method
of pond management was mainly confined to West Bengal, Bihar and Orissa. Later, it
gradually spread to other states including Tamilnadu.
Prospects of Aquaculture:
1. There is an increasing global demand for food. It is predicted that in another fifteen
years animal proteins alone will provide 40% of the world’s need.
2. As the growing population needs more food, increased aquaculture production
would reduce the pressure on natural population.
3. Aquaculture helps to promote economic development in rural and under developed
areas.
4. Culture of selected varieties of fish will help in good yield of commercial forms
5. The desirable fish being cultured in pond makes the process of harvesting easy and
economical.
6. Fishes are healthy sources for animal proteins and are easy to digest and such an
animal protein can be harvested on demand.
4.1 Genetic improvements in aquaculture industry, Induced breeding
INTRODUCTION
The wild harvest of fish, invertebrates (mainly molluscs and crustaceans), and aquatic
plants (mainly seaweeds), has provided human populations across the globe with
important sources of nutrition from ancient times. Today aquaculture and capture
fisheries directly employ over 180 million people, supporting the livelihood of 8
percent of the world’s population, and each sector provides about 50 percent of the
world’s aquatic food supply.1 There are more than 31 000 species of finfish, 85 000
species of mollusk, 47 000 species of crustacean and 13 000 species of seaweed, with
more than 5000 species accessed in wild fisheries and about 400 species used in
aquaculture. Aquatic genetic resources underpin the productivity and sustainability of
world aquaculture and capture fisheries, and the essential services provided by aquatic
ecosystems in marine, brackish and freshwaters.
The application of genetic principles to aquatic species used in aquaculture is a
relatively recent phenomenon and the sector has not yet made full use of available
technologies to increase production as other food producing sectors have done. Indeed,
it is only over the past two decades that there has been widespread acceptance that
genetic improvement and the application of biotechnologies has an important role to
play in aquaculture development and that very significant genetic gains can be
achieved through the appropriate application of well-planned genetic breeding
programmes for aquatic species.
APPLICATION OF GENETIC TECHNOLOGIES IN AQUACULTURE
PRODUCTION
Genetic technologies can be utilized in aquaculture for a variety of reasons, although
the main use is to improve production. Improvements in marketability, disease
resistance, body shape, color, culturability, and the conservation of natural resources
can be facilitated by the appropriate genetic technology. Genetic improvement
programmes can be used to provide short-term or long-term gains. The short-term
gains are usually immediate, within two generations, and generally not cumulative
(unless combined with other long-term programmes), whereas the long-term
programmes such as selective breeding produce gains that accumulate each generation.
Long-term genetic improvement strategies
Domestication and the full potential for the utilization of aquatic genetic resources will
only be realized through long-term breeding programmes. The aquaculture sector lags
far behind the crop and livestock sectors with regard to the development of
domesticated and genetically improved strains.
Selective breeding
Growth rate is the characteristic most often improved in selective breeding
programmes and increases of up to 20% per generation have been reported. Other
traits have been shown to have additive genetic variance and therefore, amenable to
improvement. Traits such as disease and stress resistance, timing of maturity and flesh
quality are now being increasingly included in selective breeding programmes.
Breeding programmes have been expanded and their design optimized, and new ones
initiated. Examples of species used in recent breeding programmes include Atlantic
cod, Atlantic salmon, common carp, gilthead seabream, hybrid striped bass, Lake
Malawi tilapia, Mediterranean Sea bass, Nile tilapia, red sea bream and rohu carp.
On disease resistance, the adoption of domesticated and genetically improved
whiteleg shrimp Penaeus vannamei resulted in a drastic increase in shrimp aquaculture
output but also posed serious risks of persistent infections, e.g. with viral pathogens
that can be passed from broodstock to postlarvae. The use of specific pathogen free
(SPF) domesticated shrimp should be supported by robust biosecurity as a prime
consideration.
Another potential application of genetic selection techniques is in the area of
enhancing feed utilization, i.e. to determine whether carnivorous fish with natural
capacity for protein utilization asmain energy source can be genetically selected.
Classic selective breeding programmes will continue to be the main engine driving the
global finfish aquaculture industry forward.
Genetic engineering
Genetic engineering technology is now beginning to find application in the production
of aquaculture feed to assist in reducing the dependency on fishmeal and fish oil and to
improve the terrestrial animal- and plant-based feed ingredients. Examples include:
genetically engineered yeast for production of important feed ingredients such as fish
growth hormone and carotenoid pigments; preprocessing techniques of plant material
to reduce the effects of antinutritional factors, breeding of plants with a better amino
acid profile and less antinutritional factors, and converting low grade land animal by-
products into high-value protein.
Transgenic fish has been produced since the mid-1980s with most research
focused on the transfer of growth hormone genes. In several cases, significant
increases in growth have been reported. Currently, no transgenic fish have been
approved for commercial release as food for humans.
Short term genetic improvement strategies
Short-term genetic improvement techniques may not require the same level of record
keeping nor management as long-term projects and can impart significant gains with
simple technologies in a short period of time.
Hybridization and crossbreeding
Crossbreeding and hybridization can be utilized to combine favourable qualities from
two genetically different groups and to take advantage of hybrid vigour (heterosis).
Interspecific hybridization has resulted in fish with improved growth rates,
manipulated sex ratios, sterile animals, improved flesh quality, increased disease
resistance, improved tolerance to environmental extremes and other altered traits.
Chromosome set manipulation
Manipulation of chromosome-sets (polyploidization) has been accomplished for many
aquatic species through thermal and chemical shocks to developing embryos. Triploid
organisms are useful because they are sterile and therefore able to put more energy
into the growth process rather than into maturation and reproduction. Whilst
chromosome-set manipulations have not resulted in many commercial applications for
finfish, the use of triploids has become an important part of the oyster farming industry
and may have similar potential in other shellfish. For example, triploid Pacific oysters
have shown 14 - 159% growth improvement over diploid controls. At the same time,
sterility reduces the risk of breeding with native species which may be of importance
in stocking programmes such as the use of grass carp for vegetation control or to
address environmental impacts of fish escaping from farms.
Sex manipulation
Manipulation of sex can be of advantage in species with sexual dimorphism in
important traits or when reduced chance of reproduction is desired. Monosex male
stocks have considerable commercial benefit in a number of species, most notably in
tilapia due to problems of both precocious maturation and unwanted reproduction
within the production system exhibited by this species. Also, female trout and salmon
grow better and female sturgeon produce caviar. The sex of fish can be easily
manipulated using hormonal treatments, but there has been concern about the use of
hormones in animal production resulting in an increased use of other biotechnologies
in those developing countries whose production goes to export markets.
Emerging technologies
A number of new genetic technologies are now beginning to be applied in cultured
aquatic species. Genome technologies include DNA marker, novel sequencing, gene
discovery, genome mapping (showing the relative positions of genes along a
chromosome) and genome expression technologies that examine how genes actually
function in the organisms. These technologies will be useful to find important genes
affecting traits such as disease resistance, growth rate and sex determination, allowing
more precisely targeted selection to improve aquaculture performance.
Induced breeding
Induced breeding in fish culture
The practice involved in prompting the fish to breed in confined water is known as
induced breeding. Induced breeding technique enhances seed productions. It is
performed by a technique called hypophystation. The hypophystation is a process of
stimulating the breeding activity of fish through the injection of pituitary extract
resulting timely release of eggs and sperms from the ripe gonads. The extract should
come from the healthy pituitary gland of healthy fish of the same species or closely
related one.
Induced breeding technique
This technique involves (i) preparation of pituitary extract (ii) selection of breeder (iii)
injection to breeder (iv) spawning in breeding hapa.
(i) Preparation of pituitary extract: For the preparation of extract, the pituitary gland
is removed by dissecting the head from gravid donor fish. The removed pituitary
glands are kept in absolute alcohol for dehydration. Then the glands are preserved in
fresh alcohol contained in dark colouredpvals and stored in a refrigerator. The
preserved pituitary glands are then softened in an instrument called homogenizer with
distilled water. The extract prepared by centrifugation method is stored in vials
(ii) Selection of Breeder: The breeder to be selected must be healthy, fully ripe and of
medium size. The preferable age group may be ranging from two to four years and
weight may be ranging from 1 to 5 kg.
(iii) Injection to breeder: Intramuscular injection of pituitary extract is administered
with a hypodermic syringe. In usual practice, female alone is administered with a
stimulating dose of 2 to 3mg/kg weight. After 6 hours a second dose of extract with 5
to 8 mg/kg is also injected. Similarly, males are also injected with the first dose of 2-3
mg/kg of body weight of the recipient fish.
(iv) Spawning in breeding hapa : The injected male and female breeders are kept
together in a rectangular enclosure called ‘Hapa’. The hapa is made of mosquito net
cloth to prevent breeders from escaping. The release of matured eggs and sperms
called spawning, takes place after 3-6 hours.
What are the advantages of induced breeding?
i) Eggs and spawns of carps at the collected from the river bed, there are every
possibility of mixture of other fishes of eggs and spawns. Whereas, in the induced
breeding there is no possibility of mixture and as a result the pure form of fish seeds
are obtained.
ii) Desired species of carps can be cultured through the induced breeding.
iii) Large numbers of eggs are available from a fish through induced breeding.
iv) In the same season, a carp can be induced to breed more than once.
v) Transportation cost becomes very low as the carps can be breed in any desired
pond.
vi) Between the different species of fishes hybridization can be done and it is possible
to get hybrid variety of fishes.
4.2 Prawn fisheries-culture
The prawn production in India accounts for about 15% of the total world production of
prawn and shrimps. For marine prawns, the percentage of Indian production to the
world production is about 20%. The major commercial prawn species reared in India
are Macrobrachium. rosenbergii and M. malcolmsonii.
BIOLOGY
Macrobrachiumrosenbergii, also known as the giant river prawn or the giantfreshwater
prawn, is native to the Indo-Pacific and northern Australian Regions. The adult is
found in freshwater, while its larval stages live in brackish water after the juvenile
stage. During mating, the male attaches its spermatophore on the ventral side of the
abdomen of female’s body and the eggs coming out of female genital opening are
fertilised by the sperms derived from spermatophores.
The fertilised eggs are held in the brood chamber or egg basket, which is made by the
interlocking appendixinterna of the pleopods and are aerated by vigorous movements
of the swimmerets for 2-3 weeks. This is in contrast to shrimps, whose fertilized eggs
are released into the sea. Females can lay 80,000-100,000 eggs during one spawning
and eggs take an average of 20 days at 28°C to hatch into larvae.
After hatching, larvae are dispersed by the rapid movements of the abdominal
appendages of the female. Larvae are
planktonic and swim upside down actively with
tail first posture and feed on small planktons.
Larvae complete development in 15-20 days
and metamorphose into post larvae, which
resemble miniature adults and generally feed
near bottom and then begin to migrate upstream into freshwater rivers within one or
two weeks after metamorphosis and are soon able to swim against the rapidly flowing
currents (contranatant behaviour) and can also crawl over the stones in shallow waters.
HATCHERIES AND NURSERIES
Freshwater prawn hatcheries need supplies for both freshwater and sea water; the latter
can be drawn from areas where the salinity is 30 to 35 ppt. The brackish water derived
from the mixture of seawater, brine or artificial sea salts mixed with freshwater should
have salinity of 12-16 ppt, pH of 7.0 to 8.5 and dissolved oxygen level of 5 ppm.
The prawn farm site should also have the following facilities:
• A secure power supply to ensure that the components of hatchery, e.g. aeration, water
flow etc. can continue to function uninterrupted.
• An uninterrupted access for incoming and outgoing materials by road.
• Access to the uninterrupted seawater and freshwater supplies.
• Farm should not be close to cities, mines and industrial centres or to other activities
that may pollute the water supply.
• Farm should be situated in a climate where the temperature range of 28-31°C can be
easily maintained.
• Food supplies for larvae should be easily procured when required.
• Should have access to biological and veterinary assistance whenever required.
• Should be close to other nursery facilities feed sites.
• Should be close to the market for quick selling after harvesting.
OBTAINING BERRIED FEMALE PRAWNS
Berried females are those that carry fertilised eggs in their egg basket. They can be
obtained from rivers, canals, lakes and estuaries, where they are most abundant in the
beginning of rainy season. In the tropics, berried females can be obtained all the year
round from farm ponds containing adult animals. Selecting fast-growing, berried
females from ponds has a positive effect on the weight of prawns at harvest.
In the tropics, where berried females are readily available, special brood holding
facilities are not required but in temperate areas, indoor brood stocking facilities are
essential. Brood stock is disinfected by placing into freshwater containing 0.2-0.5 ppm
of copper sulphate or 15-20 ppm of formalin for about 30 minutes. Prawns should be
fed daily at the rate of 1-3% of total biomass.
Berried females can be collected from the holding system and placed in tanks
where the eggs will hatch into first instar larvae, which are collected by netting. The
hatching tanks should be covered to prevent bright sunlight to reach larvae for which
the inner side of the tanks should also be painted with black epoxy-resin paint.
LARVAL REARING TANKS
Different designs of containers can be used to grow freshwater prawn larvae, which
may be circular flat-bottom tanks, circular conical-bottomed plastic tanks, plastic-lined
wooden tanks, rectangular concrete tanks, concrete-faced brick tanks and earthen water
jars. Good drainage system is essential as water has to be removed from tanks at
harvesting time. Mixing tanks are also required for preparing the brackish water to be
used in the hatchery as well as storage tanks. Aeration of water is also essential which
can be done through PVC pipes, with holes cut at one-foot intervals.
Larvae should not be exposed to direct sunlight, for which 90% of the tan area should
be covered and shady. Some natural light is essential for good larval survival, which
can be provided through transparent roofs over the hatcheries. Physical filters that
include sand filters, drum screen filters, and medium filters should be easy to clean and
designed to minimize water loss.
Water needs to be chemically treated before it can be used in rearing tanks and
also should be physically filtered by passing through the sand bed before transferring it
to another tank for treatment. Mix the seawater or brine with freshwater to form 12 ppt
of brackish water. The optimum temperature range for M. rosenbergii is 28-31°C.
Below 24-26°C the larvae will not grow well and the time taken for them to reach
metamorphosis will be longer.
LARVAL FEEDING
A wide range of feeding material is used by different hatcheries, which includes
nauplius larvae of shrimps, freshwater cladocerans, fish eggs, squid flesh, frozen adult
Artemia, rotifers, fish flesh, egg custard, worms and commercial feeds available in the
market. The quantity of food to be given depends on the utilization of feed by larvae
that vary from place to place. The quantity of feed consumed will increase as the
larvae grow.
HARVESTING POST LARVAE
When post larvae are about 7-8 mm long, they can withstand transfer from 12 ppt
water into freshwater. However, they should not be harvested from the larval tanks and
transferred directly into holding tanks containing freshwater but should be
acclimatized to fresh water in the larval tanks itself. When majority of larvae have
metamorphosed, water level in tanks should be reduced to about 35 cm. Then
gradually the tank should be flushed with freshwater over a period of 12 hours. The
post larvae can then be collected and transferred or the larval tanks can be refilled to
70 cm with fresh water and the animals temporarily held in them. The best way to
harvest post larvae from the larval tanks is to reduce the water level and then remove
them by nets.
HOLDING POST LARVAE BEFORE SALE
Post larvae cannot be held in holding tanks for more than a week or two prior to
stocking in nurseries. When the post larvae are in the holding tanks, the rearing water
should be changed every 2-3 days) to provide aeration. Post larvae can be stocked at
densities of about 5,000/m2 for one week, although survival increases by reducing the
density.
REARING PONDS
Pond size should be such that can be managed easily. Generally, most farms have
ponds of around 0.2- 0.6 ha size. Large ponds are normally wider than 30 m and often
drained for harvesting. The average depth of water in freshwater prawn ponds in
tropical areas should be about one meter; with a minimum of 0.75 m and a maximum
of 1.2 m. Deeper ponds are used in colder areas to maintain more stable water
temperatures. The banks of the ponds or embankments or bunds must be high enough
for the highest water level expected in the pond, which generally should be 1-2 feet
higher than water level. The flow of water into each pond must be controlled by
valves, stop-logs or plugs. Paddle wheels are the most efficient method of increasing
dissolved oxygen levels in the pond water.
STOCKING
Stocking the ponds quickly reduces competitors and predators, which have less time to
become established. Often post larvae that are a week or two old after metamorphosis
are used to stock ponds, where they remain until harvesting. A stocking density of
about 40,000/ha is recommended for the monoculture of Macrobrachium rosenbergii.
Using larger juveniles for stocking increases the survival rate as well as the average
weight of the animals by as much as about 30%.
FEED TYPE
Natural productivity of the ponds generally gives small production from the ponds.
Therefore, intensive farming must involve supplementary feeding to increase
productivity. Some farms claim to rely on fertilizers, rather than feeding at the
beginning of the rearing period, which stimulates algal bloom and lot of micro flora
and fauna in the ponds. Others find that providing feed from the beginning of the
rearing period improves performance and is cost-effective. Commercial feeds are the
most productive and reliable to use but they are expensive and unaffordable to small
farmers.
HARVESTING MARKETABLE PRAWNS
Basically, there are two methods of harvesting: culling and draining. The time of
harvesting depends partly on the growth rate and partly on the size of animals for
market requirements. Culling is used to harvest market-sized animals from the ponds
to remove faster growing prawns which increase density quickly. In tropics culling
usually starts 5-7 months after post larvae have been stocked to take out the market-
sized animals for selling and keeping the smaller ones and soft-shelled animals in the
pond for further growth. After about 8-11 months ponds are drained and all animals
are sold. In cull harvesting, a seine net is pulled through the pond to remove market-
sized animals, while in drain harvesting, a harvesting sump is installed in front of the
gate or outside the pond, in which prawns will accumulate while water is being
drained.
DISEASE CONTROL
Several diseases affect freshwater prawn larvae as well as adults. Some hatcheries use
formalin at the rate of 200 ppm daily as an effective remedy for protozoan and
hydrozoan parasites and fungal diseases. Formalin can also be used at a lower level of
about 30 ppm for longer periods, followed by water change after 24 hours. Larvae can
also be transferred to disinfecting tanks every 5-10 days to get rid of diseases and
parasites. Daily dip of larvae in Malachite green (0.2 ppm) for 30 min has also been
used for treatment. Also, dipping in copper sulphate 0.4 ppm solution for 6 hours is
recommended. Antibiotics and sulfa drugs are sometimes used to control filamentous
bacteria and some hatcheries use lime (CaO) as a prophylactic measure.
4.3 Freshwater fish culture
Fish farming or pisciculture involves raising fish commercially in tanks or enclosures
such as fish ponds, usually for food. It is the principal form of aquaculture, while other
methods may fall under mari-culture. A facility that releases juvenile fish into the wild
for recreational fishing or to supplement a species' natural numbers is generally
referred to as a fish hatchery. Worldwide, the most important fish species produced in
fish farming are carp, tilapia, salmon, and catfish.
Indian aquaculture has been growing at a fast pace over the last two decades,
with freshwater aquaculture contributing over 95% of the production. The three Indian
major carps, namely catla (Catlacatla), rohu (Labeorohita) and mrigal
(Cirrhinusmrigala) contribute to the bulk of production amounting to about two million
tonnes annually (FAO, 2003). Silver carp, grass carp and common carp formthe
second important group for fish production. Average national production from
pondfisheries has increased from 0.6 tonnes/ha/year in 1974 to 2.2 tonnes/ha/year in
2002 (Tripathi, 2003).
COMPOSITE FISH CULTURE
The three major carps cultured in India, namely, catla (Catla catla), rohu (Labeo
rohita) and mrigal (Cirrhinus mrigala), contribute as much as 87 percent of the total
Indian aquaculture production. Three exotic carps were also introduced, namely, silver
carp (Hypophthalmichthys molitrix); grass carp (Ctenopharyngodon idella) and
common carp (Cyprinus carpio). There are also several other medium and minor carp
species, namely, Labeo calbasu, L. fimbriatus, L. gonius, L. bata, L. ariza, Cirrhinus
mrigala, Puntius sarana, Hypselobarbus pulchellus, H. kolus and Amblypharyngodon
mola, which are important in aquaculture. Among catfishes, magur (Clarias
batrachus) is the only species that is widely cultured, while the catfish, ‘Singhi’
(Heteropneustes fossilis) is cultured to some extent in the eastern states.
Attempts have also been made to culture the other catfishes like Pangasius
pangasius, Wallago attu, Sperata seenghala, S. aor and Ompok pabda. The finfish
species of importance include climbing perch (Anabas testudineus), murrels (Channa
striata and C. marulius) and tilapia (Oreochromis mossambicus and Oreochromis
niloticus).
PREPARATION OF PONDS
Pond preparation involves making the ponds weed and predator-free and generating
adequate natural food for the survival and growth of fishes. Control of aquatic weeds,
removal of undesirable flora and fauna and improvement of soil and water quality are
important aspects of fish management. Weeds have to be removed from the ponds
first, after which the tank is fertilized with both organic and inorganic fertilizers, such
as Oil Cake and raw Cow Dung @ 5,000 kg/acre.
The PH of pond water should be 7.5 – 8.00, for which lime is added in the tanks
@ 200 kg/acre per annum. The lime increases pH and also helps in eradicating fish
parasites. The organic fertilizer in the form of raw cow dung is added in the tank @
500 kg/acre per annum. This is followed by the application of inorganic fertilizers like
Super Phosphate @ 120 kg/acre and Ammonium Sulphate @ 200 kg/acre, in spaced
intervals.
SPAWNING
Because of constant temperature and favourable weather conditions, carps spawn all
the year round in India. Spawning takes place early in the morning when the water
surface cools down to about18 degrees. The female carp swims near the water surface
followed by the male carp in nuptial swimming and rubbing each other’s bodies.
Female lays egg and male releases its milt and eggs are fertilised.
Three days after fertilization, the eggs begin to hatch. The newly hatched larva
is about 5.5 mm long, delicate and transparent, with a yolk sac attached to the belly. It
rarely swims but settles on the bottom or on some floating object. On the second day,
the larva starts swimming and on the third day swims actively from surface to bottom.
During these stages, the larva or fry gets its nourishment from the yolk sac, which
disappears on the third day and the fry now must search for food and eat.
Supplementary fry-feed in the form of hard-boiled egg yolk or powdered milk
can be applied on the water surface at this time.
Carpscan feed on almost anything like insects, shells and worms and can also eat
aquatic plants, bread crumbs, rice bran and fish meal made from corn, copra and
soybean.
CHOOSING BROODERS
Both female and male brood fish should be carefully tended for 2-3 months before
induced spawning operations are carried out and males and females should be
segregated and kept in separate ponds.
To be good brooders the fish must be more
than one year old and 150 gm in weight. Sex
can be determined by the shape of the genital
papilla which is pointed in male and oval in
female. When the female is ready for induced
spawning operations, It should have a bulging
abdomen that is soft to touch. The cloaca is
reddish and prominent, and the contour of the
enlarged ovaries can be seen on both sides of the abdomen. The head should be small
and the snout pointed.
Nursery ponds are constructed to rear carp fry or larvae. A normal sized nursery pond
measures 5 x 10 m, with a depth of 0.5 m. Before filling up water the pond should be
cleaned thoroughly to get rid of predators and parasites that may be destructive the
larvae. About 1,500 to 3,000 fries can be stocked in the nursery pond andfed with
milk, wheat flour or boiled egg yolk by spreading it on the water surface. This feed can
be supplemented with rice bran, bread crumbs or fish meal, which can be given twice a
day, in the morning and in the afternoon.
Rearing ponds, where adult carps are cultured until they reach marketable size, are
needed, which have dimensions of 15 x 50 m and depth of 1.5 to 2 m. Rearing ponds
should also be thoroughly cleaned before filling them with water. This is done by
exposing the bottom and letting it dry thoroughly. Next step involves application of
fertilizers, which encourages growth of aquatic plants, moss and algae, which are
important natural food and also lead to growth of micro fauna. Manure in the form of
chicken dropping is the most commonly used being cheaper and more readily available
in large quantities. When carp fry reaches the length of about 5 to 7 cm, they are
transferred from the nursery pond to the rearing pond and allowed to grow to adult
stage.
STOCKING OF PONDS
Ponds are stocked with fish fries of appropriate size. Fingerlings of over 10 cm in size
are recommended for stocking in culture ponds. Stocking of smaller fishes may result
in higher mortalities and slow growth during the initial months. In fish polyculture a
fingerling size of 50-100 g is preferred for stocking to ensure higher survival and
better growth. Generally, a density of 5,000 fingerlings is kept as a standard stocking
rate per ha for carp polyculture, which will give a yield of 3-5 ton/ha/yr.
Prior to stocking, the fish fries should be dippedin 3-5% potassium
permanganate solution for 15 seconds to kill parasites. In composite fish farming, a
combination of six species are cultured, namely, Catla, Rohu, Mrigal and exotic Carps
like Silver Carps, bass and common Carp. Supplementary feeds like Groundnut Oil
cake and Rice Bran are fed to fishes during culture. At the end of the culture period of
say 12 months, the fish will reach marketable size and fetch attractive prices.
POST-STOCKING POND MANAGEMENT
While fertilizing the carp ponds, 20-25% of the total amount of organic manures is
applied a fortnight before stocking and the remaining amount is applied in equal
instalments on a bimonthly basis. Other commonly used organic manures include
poultry manure, pig dung, duck droppings, cow dung, domestic sewage, etc. Azolla, a
nitrogen-fixing fern is used as a bio-fertilizer for aquaculture at the rate of 40
tonnes/ha/yr, which supplements nutrients required for intensive carp culture. The
bioprocessed organic manure, biogas slurry has also been used as manure in carp
culture.
The supplementary feed in carp polyculture is usually restricted to a mixture of
groundnut/mustard oil-cake and rice bran. Grass carps are fed with aquatic vegetation
such as Hydrilla, Najas, Ceratophylum, duck weeds, etc. which can be kept in special
enclosures in corners of the pond. Feeding preferably twice-a-day is advocated @ 5%
of the initial biomass of stocking material for first month and then gradually reducing
it.
Aeration may be done mechanically to increase the concentration of dissolved oxygen
in ponds, by paddle wheel aerators, aspirator aerators and submersible pond aerators. It
is also necessary to replace certain amount of water at regular intervals.
HARVESTING
Harvesting of fishes is usually done after a culture period of 10 months to one year.
However, fishes attaining the marketable size can be harvested periodically depending
on several factors, which also reduces the pressure of density in the ponds and thereby
providing sufficient space for the growth of fishes.
4.4 Pearl and Lac culture
Q: -What do you mean by Pearl Culture?
Ans: -History of Pearl Industry: For the first time the idea of pearl industry was
evoked in Japan which was carried out in the Bay of Japan located at South coast of
Hansoo. But in Japan, pearl culturists feel difficulty due to unfavourable climatic
conditions. Kokichi Mikimoto (1858-1954) is referred to be the father of pearl
industry. Pearl is a concretion formed by molluscs. It consists of nacre or mother of
pearl. It is characterised by iridescence and translucence.
Pearls is produced by the marine molluscs such as pearl oyster and mussel.
Types of pearls: Pearls are of seven types. They are the following -
(1) Linghapearl: This is the best quality pearl obtained from marine oysters.
(2) Seed pearls: The small pearls are called seed pearls.
(3) Baroque pearls: These are spherical pearls formed inside the body.
(4) Blister pearls: These are pearls attached to the shell. They are half-spherical in
shape.
(5) Oriental pearls: These are true pearls with a great lustre, beauty and a smooth
surface.
(6) Natural pearls: These are the pearls obtained from pearl oysters of deep oceans.
(7) Cultured pearls: These are the pearls obtained from cultivated species of pearl
oysters.
Composition of pearl: Pearl comprises of water, organic matter, calcium carbonate
and the residue.
(1) Water 24
(2) Organic matter 3.55.9
(3) Calcium carbonate 90
(4) Residue 0.10.8
The pearl is formed of nacre. The nacre is formed of two substances namely a calcium
carbonate which is in the form of argonite or calcite and an albuminoid substance
called conchiolin/colchitin
Pearl-producing animals: Pearls are produced by bivalve molluscs. There are marine
as well as fresh water animals.