DDT (Dichloro-Diphenyl-Trichloroethane)[1]
DDT
was first prepared by O. Zeidler, a German Ph.D. student in 1874. Its insecticidal
properties were however discovered by a Swiss chemist Paul Muller in 1939. DDT
kills lice and mosquitoes which carries germs of typhus and malaria fever
respectively. DDT was the first chemical to have the property of killing
insects only by means of contact. DDT is still the backbone of many insects
control programs and is widely used as a household insecticide against leaf
hoppers and potatoes and in cotton insect control. DDT is a remarkable powerful
and persistent insecticide that is soluble in kerosene oil, petrol and ethyl
alcohol but insoluble in water. DDT is manufactured by exothermic condensation
of chlorobenzene with chloral at about 300C in the presence of oleum
or 99% sulphuric acid.
DDT (Dichloro Diphenyl
Tdrichloroethane) Fig II [1]
In
the 1940s, the properties of the new insecticide DDT seemed close to
miraculous. In tropic, DDT save millions of lives by killing the mosquitoes
that spread malaria, increase crop yields resulting from DDT’s destruction of
insects pests saved million or more from starvation
DDT
and other substances that undergo biological manifestation have two properties
that makes them dangerous;
§ They
do not readily break down into harmless substances
§ They
are fat soluble but not water soluble, therefore, they accumulate in the bodies
of animals particularly in the fat, rather than being broken down and excreted
in the watery urine. Because the transfer of energy from lower to higher tropic
level is extremely inefficient, herbivores must eat large quantities of plant
materials (which may have been spread with DDT), carnivores must eat many
herbivores and so on.
In1951,
the first DDT resistant strains of mosquitoes were reported from Greece, Panama
and U. S. A. In many parts of the world, spraying no longer prevents
transmission of malaria. In addition, the passage of persistent insecticides
such as DDT though the food chain become an increasing problem to birds and
mammals at the top of chain[4].
1.3.4 BIOLOGICAL INSECTICIDES
Recent
efforts to reduce bread spectrum toxins added to environment have brought
biological insecticides back to vogue. An example is the development and
increase in use of Bacillus thuringieness, a bacterial disease of Lepidopterans
and some other insects. It is used as a lavicide against a wide variety of caterpillars.
Because it has little effect on other organism. It is considered more
environmentally friendly than synthetic insecticides. The toxin forms.
Baccillus Thuringiensis. Baccillus Thuringiensis. Toxin has been incorporated
directly into plants through the use of genetic engineering[7].
1.3.5 TOXIC EFFECT OF REPELLENT
Some
insecticide kill or harm other creatures in addition to those they are intended
to kill. For example, birds may be poisoned when they eat food that was freshly
sprayed with insecticides or when they mistakes insecticides granules on the
ground for food and eat them.
Sprayed
insecticides may drift the area to which it is applied into wildlife areas,
especially when sprayed aerially[4].
DDT
can be a threat to health or the environment when used under wrong conditions.
It causes progressively higher concentration in the body of the animal farther
up the food chain.
Biological
parameters were used to evaluate the toxic effect of different brands of
mosquito coil smoke in experimental rats. The smoke from the coil produced
significant increase (P<0.05) in the level of total protein, total albumen,
bilirubin and blood/urea nitrogen when animals were exposed to smoke for 14
days[7].
Similarly,
the smoke from the coils also cause an elevation in the activities of aspirate
amino transference and alanine amino transference. Although the smoke from the
coil did not produce lesions in hearts, lungs and liver examined, the increase
in liver enzyme activities could be due to early liver damage[8].
Epidemiological
studies have shown that long-term exposure to mosquito coil smoke can induce
asthma and persistent wheeze in children. These studies also shows that one
burning mosquito coil produces the same amount of particulate mass (diameter up
to 2.5nm) as 75-137 burning cigarette would, and the coil can be as high as
that released from 51 burning cigarettes[8].
1.4 MOSQUITO COIL
Mosquito
coil is a mosquito repelling incense usually shaped into a spiral and typically
made from a dried paste of pyrethrum powder. Mosquito coils are widely used as
mosquito repellants. The major active ingredients of mosquito coilsare
purethrins accounting for about 0.3 – 0.4% of the coil mass. When a mosquito
coil is burnt, the insecticides evaporates (pyrethrin, PAH, aldehyde, etc) with
smoke, which prevent the mosquito from entering the room and harm those already
in the room. The remaining components of mosquito coils include filters,
binders, dyes and other additives capable of burning well without flame. He
components generates large amunt of submicrometer particles and gaseous
pollutants such as acenephthene, paranthrene, etc.
Mosquito
coils are often used overnight in sleeping quarters where continous exposures
may occur. Chronic exposure to coil smokes occur during rainy periods because
mosquitoes are found to be more active in the environment due to collection of
water and increase in green plants[9].
1.4.1 HOW
MOSQUITO COILS WORK
Mosquito
coils are burned on specially designed stands placed inside more attractive
looking mosquito coils holders which contain holes to let the smoke out. The
holders can usually be hung up or laid flat. Each mosquito coil slowly burns
for around 8 hours, during which time repelling active ingredients such as
pyrethoids or pyrethrum disperse with the smoke. The combination of ingredients
in the smoke coil either prevents mosquitoes from entering the surrounding
area, encourages them to leave the area if they have not already done so, or
knocks the insect down and kills the[10].
1.4.2 HOW
TO USE MOSQUITO COILS
Mosquito
coils are particularly useful for protection against mosquitoes when sitting
outside at night. They can be placed on a table so people can congregate around
them. It helps to stay in the vicinity of the smoke given off, but this may be
difficult if the smoke is carried away by the wind. A good tip is to place a
mosquito coil down on the ground by people’s ankle and feet, as this is an area
mosquitoes seem to bite frequently.
Again,
the less wind there is, the more likely the mosquito coil smoke will have a
chance to be effective. Mosquito coils are generally meant for use outdoors,
but if they have to be used indoors, it is wise to make sure rooms are well
ventilated. Packs of multiple mosquito coils are available with a coil stand
included[10].
1.4.3 ADVANTAGES
OF USING A MOSQUITO COIL
Mosquito
coils nowadays burn without flame for up to eight hours of continuous repelling
action. In quantitative tests, they provide about 80% protection. Mosquito
coils are also cheep and need no special equipment to use it in other than just
lighting it up. They are portable and fit into normal household practices of
lighting candles or incense[11].
1.4.4 DISADVANTAGES
OF USING MOSQUITO COILS
There
are several hazards that we know to be caused by mosquito coils. In 1999,
sparks from mosquito coils ignited a fire that swept through a three-story
dormitory building at a summer camp, 23 persons including 19 children died in
the blaze in South Korea[12].
The
long-term exposure calls for concerns on the potential toxicological effects of
smoke on humans[8].
1.4.5 ACTIVE INGREDIENTS IN MOSQUITO COIL
The
active ingredients found in mosquito coils can be some of the following;
·
PYRETHRUM
(Natural,
powdered material from a kind of chrysanthernum plant, performing moderated)
·
PYRETHRINS
(Extract
of insecticidal chemicals in pyrethrum)
·
ALLETHRIN Some
times d-trans-alletrin)
(The
first synthetic pyrethrin)
·
ESOBIOTHRIN (a
form of allethrin)
·
DIBUTYL
HYDROXYL TOLUENE (BHT) (an optional additive to prevent
pyrethroid from oxidizing during burning).
·
PIPERONYL
BUTOXIDE (PBO) (an optional additive to improve the
effectiveness of pyrethroid)
·
N-(2-ethylexyl)-bicyclo-(2,2,1)hept-5-ene-2,3-dicarboximide
(MGK 264) (an optional additive, to improve effectiveness of a pyrethroid)[13].
1.5
CITRUS
SINENSIS/ORANGE PLANT
The
orange plant is a hybrid of ancient cultivated origin, possibly between Pomelo
(citrus maxima) and tangerine (citrus reticulate). It is small
flavouring tree growing to about 10m tall with evergreen leaves, which are
arranged alternatively, of ovate shape with crenulate margins and 4-10cm long.
The orange fruit is a hesperidium, a type of berry[14].
Orange
originated in southeast Asia. The fruit of Citrus
sinensis is called sweet orange to distinguish it from citrus aurantium, the
bitter orange. The name is thought to ultimately derived from the sanskirt, for
the orange tree, with its final form developing languages. In a number of
languages.
In a
number of language,it is known as a “Chinese apple” (e.g Dutch Sinaasappel,
“China’s apple”.)[15].
Orange
can be found in almost all parts of Nigeria.
SPECIES OF CESTRUM
The
orange peels (cestrum) is gotten from sweet orange (ctrus sinensis)
1.5.1 IDENTIFICATION
Botanical name Citrus
Sinensis
English name Sweet Orange
Common name` Oroma (Igbo)
Family Rutaceae
Genus Citrus
Order Sapindales
1.5.2 USES OF CITRUS SINENSIS
1. 1. In the
home,oranges are commonly peeled segmented and utilized in fruit cups, salads,
gelatins and numerous other deserts and as garnishes on cake, meats and poultry
dishes.
2. They
are squeezed daily in the kitchen for juice.
3. In
South America, a dozen whole, peeled oranges are boiled in 3 pints (1.41
litres) of slightly sweetened water for 20min and then strained and the liquid
is poured over small squares of toast and slices of lemon and served as soup.
4. Whole
oranges are sliced, dried and pulverized and the powder is added to baked goods
as flavoring.
5. Dried
orange peels can be used as home made bath oils.
6. Limonene
carbon-base compounds that makes up around 95% of the oil found in orange peels
is often used to give household cleaners a citrus smell.
7. range
peels can be applied on the skin, in the night to repel mosquitoes.
8. Orange
peels can be used as scent.
1.5.3 FOOD VALUE.
The
Chemistry of the Orange is affected by many factors. On the average,
“Valencia”, Washington Navel”, and other commercial oranges have been found to
poses the value shown in the page.
FOOD VALUE PER 100G OF EDIBLE
PORTION
|
Fruit (fresh)
|
Juice (fresh)
|
Juice (canned unsweetened undiluted)
|
Frozen Concentrate (Unsaturated
undiluted)
|
Juice (dehydrated 380)
|
Orange peel (raw)
|
Calories
|
47-51
|
40-48
|
223
|
158
|
380
|
|
Moisture
|
86.0g
|
87.2-89.6g
|
42.0g
|
58.2g
|
1.0g
|
|
Protein
|
0.7-1.3g
|
0.5-1.0g
|
4.1g
|
2.3g
|
5.0g
|
1.5g
|
Fat
|
0.1-0.3g
|
0.1-0.3g
|
1.3g
|
0.2g
|
1.7g
|
0.2g
|
Carbohydrate
|
12.0-12.7g
|
9.3-11.3g
|
50.7g
|
38.0g
|
88.9g
|
25.0g
|
Fiber
|
0.5g
|
0.1g
|
0.5g
|
0.2g
|
0.8g
|
|
Ash
|
0.5-0.7g
|
0.4g
|
1.9g
|
1.3g
|
3.4g
|
0.8mg
|
Calcium
|
40-43mg
|
10-11mg
|
52mg
|
33mg
|
84mg
|
161mg
|
Phosphorus
|
17-22mg
|
25-19mg
|
86mg
|
55mg
|
134mg
|
21mg
|
Iron
|
0.2-0.8mg
|
0.2-0.3mg
|
1.3mg
|
0.4mg
|
1.7mg
|
0.8mg
|
Sodium
|
1.0mg
|
1.0mg
|
5mg
|
2mg
|
8.0mg
|
3.0mg
|
Potassium
|
190-200mg
|
190-208mg
|
942mg
|
657mg
|
1,728mg
|
212mg
|
Vitamin
A
|
200I.U
|
200I.U.
|
960I.u.
|
710I.U
|
1,680
I.U
|
420
I.U
|
Thiamine
|
0.10mg
|
0.09mg
|
0.39mg
|
0.30mg
|
0.67mg
|
0.12mg
|
Riboflavin
|
0.04mg
|
0.03mg
|
0.12mg
|
0.05mg
|
0.21mg
|
0.09mg
|
Niacin
|
0.4mg
|
0.4mg
|
1.7mg
|
1.2mg
|
2.9mg
|
0.9mg
|
Ascorbic
acid
|
45-61mg
|
37-61mg
|
229mg
|
158mg
|
359mg
|
136mg
|
1.5.4 ECONOMIC IMPORTANCE/USES
PULP: citrus
(3/4 being a by-product of orange juice extraction) is highly valued as
pelleted stocked feed with a protein content marketed as cat litter. It is a
source of edible yeast non-potable alcohol, ascorbic, and hesperidin.
PEEL: In
addition to its food uses, orange peel oil is a prized scent in perfume and
soaps because of its 90-95% limestone content, it has a lethal effect on
mosquitoes, houseflies, fleas and fireants. Its potential as an insecticide is
under investigation. Its being used in engine cleaners and in waterless
hand-cleaners in heavy mechanical repairs shops.
Terpenes
extract from the outer layer of the peels are important in resins and in
formulating paints for ships.
SEED: Oil
derived from orange and other citrus seeds is employed as a cooking oil and in
soap and plastics. The high- protein seed residue is suitable for human food
and an ingredient in cattle feed, and the hills enter into fertilizer mixtures.
FLOWER AND FOLIAGE: The essential oils distilled from orange
flowers and foliage are important in perfume manufacturing. Some petitgrain oil
is distilated from the leaves, flowers, twigs and small whole unripe fruits.
WOODS: The
wood is yellowish, it has been valued for furniture, cabinet work, turnery and
engraver’s blocks.
Branches
are fashioned into walking-sticks.
1.5.5 MEDICAL USES/IMPORTANCE
·
Orange are eaten to allay fever and catarrh
·
The roasted pulp is prepared as a poultice for
skin disease.
·
The fresh peel is rubbed on acne
·
In the mid-1950s, the health benefit of eating
peeled, whole oranges was much publicized because of its protopectin,
bioflavonoids and inositol (related to vitamin B).
·
Rutin and other bioflavonoids were for a while
much advocated for treating capillary fragility, hemorrhages and other
physiological problems.
·
An infusion of the immature fruit is taken to
relieve stomach and intestinal complaints.
·
The inner bark, macerated and infused in wine,
is taken as a tonic and carminative.
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