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Chromium is the 24th element in the periodic table and it is found in about 0.0122% of the
Earth's crust. It is named after the Greek word "chroma," meaning color. This element produces
many beautifully colored compounds, as well as a wide array of colored solutions. Chromium is
also a very useful industrial metal.
Introduction
Discovered in 1797 by Louis-Nicholas Vauquelin and isolated a year later, chromium is a very
hard steel-gray metal which takes its name from the Greek word chroma, for "color", suggesting
the wide variety of colors which characterize its compounds, many of which are used as oil paint
pigments. the pure metal is also a valuable alloying agent for spring steels and along with nickel,
in stainless steels. Chromium(III) oxide (a popular green pigment) is the ninth most abundant
chemical in the earth's crust.
3rdC BC - According to archaeologists, Qin Dynasty and the Terracotta Army weapons
were coated with Chromium.
1761 - Johann Gottlob Lehmann found an orange-red metal in the Ural Mountains which
was later found to be Lead chromate.
1770 - Peter Simon Pallas came to the site where Lehmann found the metal and Pallas
found the metal to be useful in paint.
1797 - Louis Nicolas Vauquelin discovered that he could isolate metallic chromium by
heating the oxide in a charcoal oven. This lead to the discovery of chromium metal.
1800s - Chromium was commonly used in paints and tanning salts.
Today - Chromium is now commonly used as metal alloys and in industrial factories.
Properties of Chromium
General Properties
Atomic Number 24
Physical Properties
Atomic Properties
Electronegativity 3.72 eV
Electron Affinity 64.3 kJ mol-1
Radius 124.9 pm
Metallic Properties
Chromium is a blue- gray metal that can be polished to achieve a high shine. It is extremely
lustrous and while it is relatively hard, it is also very brittle. Chromium is a fairly active metal.
While it does not react with water, it does react with most acids. It reacts with oxygen at room
temperature to form chromium (III) oxide. One of chromium's most important properties is its
self passivation. While it is stable in air, chromium will oxidize to form a thin layer that acts as a
protective coating to prevent further corrosion.
Magnetic Properties
Chromium is in elemental form, it displays paramagnetic properties. Recently, it has been
discovered that chromium can display different magnetic properties depending on its heating and
cooling, which affects the electrons' spinning alignments. Compounds of chromium, such as
chromium dioxide, are considered to be ferromagnetic. The ferromagnetic properties of these
compounds allow them to be used in data tape, a way to store information. Chromium can be
added to other compounds while maintaining its magnetic properties, and this depends on the
quantity of other elements in the compound. For example, some stainless steel compounds are
magnetic depending on the amount of chromium they contain.
Isotopes of Chromium
Chromium forms over 20 different isotopes. Three of them are considered stable while nineteen
are considered to be radioactive, and many have half lives shorter than 24 hours. The ones listed
below are the most stable and the most commonly found.
Isotopes Half-life
48 Cr 21.56 hours
49 Cr 42.3 mins
51 Cr 27.7025 days
52 Cr Stable
53 Cr Stable
54 Cr Stable
Occurrences of Chromium
Chromium is almost never found in its elemental state in nature, with the exception of a diamond
deposit in Russia. However, this diamond deposit has a reducing environment, which helps
produce small quantities of elemental chromium. Commonly it is found in numerous ores,
usually in the mineral chromite. Chromite is the complex of FeCr2O3FeCr2O3, or iron
chromium oxide. Chromium is also found in other minerals, including magnesiochromite
(MgCr2O4MgCr2O4). Chromite is found in earth's mantle and is mined most abundantly in
South Africa, India, Kazakhstan and Zimbabwe. Through the refining processes, chromite
produces both ferrochromium and metallic chromium.
Similar in characteristics and practical uses to vanadium and titanium, pure chromium has a
blue-white color. It is very brittle and corrosion resistant. It has three common oxidation states:
+2, +3, and +6. The metal ore (principally chromite, FeCr2O4FeCr2O4), is refined by heating in
the presence of Si or Al. The resulting ferrosilicon or ferroaluminum compound is separated
from the chromium by electrolysis.
Oxidation Compounds
State
-2 Na2[Cr(CO)5]Na2[Cr(CO)5]
-1 Na2[Cr(CO)10]Na2[Cr(CO)10]
0 Cr(CO)6Cr(CO)6
+1
+4 CrO2CrO2, CrF4CrF4
+5 CrF5CrF5
Chromium trioxide
Chromium trioxide or chromium (VI) oxide, CrO3 is acidic oxide, or acidic anhydride of chromic
acid. It will react with water to form chromic acid and will react with a base to form a chromium
salt. In solid form, it is a dark red-orange granular complex. It is used in chrome-plating as a
strong oxidizer, however, it is extremely toxic.
2CrO24(s)+2H+(aq)H2O(l)+Cr2O27(aq)Kc=3.210142CrO4(s)2+2H(aq)+H2O(l)+Cr2O7(a
q)2Kc=3.21014
In acidic solution, the forward reaction is favored. In basic solution, the reverse reaction is
favored.
Passivation of Chromium
Chromium is one of the few metals that has the property of passivation. Chromium will
spontaneously react to form a thin layer of oxide that protects the metal against further corrosion.
This surface is hard and nonreactive. This makes chromium ideal for electroplating other metals
to protect them from oxidizing, and because of it's hardness, it is used to harden the surface of
many objects, such as metal tools.
Quintuple Bond
First discovered in 2005, Chromium, Molybdenum, Tungsten, and Rhenium, all have a special
ability to form a quintuple bond; also known as a five fold bond. In Chromium cases, di-
chromium was discovered to have a quintuple bond, which means that 10 electrons are
participating in the bond with metal - metal. Chromium uses terphenyl ligand to perform this
action, thus making it relatively weak, but stable up to 200C. A quintuple bond is only possible
if chromium atom has only one other ligand in order to keep the bond stable. Although the
discovery is fairly recent, it has already provided great insight as to how transition metals are
able to bond with each other.
Production of Chromium
Chromium is produced from mined minerals such as chromite. The processes used to extract
chromium are similar to those of other metals. Chromium oxides can be heated with other
substances such as charcoal or aluminum. Through the process of heating, the carbon or
aluminum form oxides, leaving chromium in pure metal form. Pure chromium can also be
produced by running an electric current through some of its compounds. These are just two ways
of extracting chromium from its compounds. There are other processes to extract chromium such
the Thermite Process:
Fe2O3+2Al2Fe+Al2O3Fe2O3+2Al2Fe+Al2O3
Chromite and Ferrochromium can also be used directly to add chromium to other substances
such as steel.
Applications of Chromium
Chromium has many applications. It has been used in dyes to act as a mordant, which will
permanently fix dyes to different fabrics. Chromium has also been used in paints as pigments.
This is because chromium exhibits many different colors including; black, gray, green, blue,
violet, orange, yellow and red, depending on the compound. Chromium is used as an additive to
stainless steel, giving the steel its "stainless" property. Because chromium is self-passivating, it
will add a protective layer to the steel. It also acts to harden the steel. Stainless steel containing
chromium is a very useful alloy and is used in safes, ball bearings, and surgical tools.
Chrome plating is another application of chromium's self passivation. Metals and other
substances are chrome plated to add a protective and attractive outer coat. Chromium metal can
be polished to a high shine which will make the metal more attractive. The magnetic properties
of chromium make it perfect for magnetic tapes. Chromium dioxide is used in recording tapes.
Potassium dichromate has been used in the tanning of leather. Small trace quantities of
chromium have been found in semiprecious stones including: rubies, sapphires, emeralds,
serpentine and jade. Chromium is also used to line ovens and molds because of its high melting
point. This element is even found in the human body. Chromium is common in small quantities
in the body and has been connected to the body's use of sugar. It is commonly found in foods
such as romaine lettuce, onions and tomatoes. A deficiency of chromium leads to symptoms that
are commonly seen in diabetics. Although chromium is good in small quantities, larger quantities
of chromium can be extremely harmful to humans.
Problems
Answer the following:
Sumber :
https://chem.libretexts.org/Core/Inorganic_Chemistry/Descriptive_Chemistry/Elements_Organized_by_
Block/3_d-Block_Elements/Group_06%3A_Transition_Metals/Chemistry_of_Chromium
Chromium
Chromium is thought to influence how the hormone insulin behaves in the body. This means
meat
lentils
broccoli
potatoes
spices
You should be able to get all the chromium you need by eating a varied and balanced diet.
If you take chromium supplements, don't take too much as this might be harmful.
Having 10mg or less a day of chromium from food and supplements is unlikely to cause any
harm.
Sumber : https://www.nhs.uk/conditions/vitamins-and-minerals/others/#chromium
6. ESSENTIAL NUTRIENTS - MINERALS
Macroelements
Trace or microelements
Principal cations Principal anions
1
Underwood (1971); Reinhold (1975)
Minerals are essential constitutents of skeletal structures such as bones and teeth.
Minerals play a key role in the maintenance of osmotic pressure, and thus regulate the exchange
of water and solutes within the animal body.
Minerals serve as structural constituents of soft tissues.
Minerals are essential for the transmission of nerve impulses and muscle contraction.
Minerals play a vital role in the acid-base equilibrium of the body, and thus regulate the pH of the
blood and other body fluids.
Minerals serve as essential components of many enzymes, vitamins, hormones, and respiratory
pigments, or as cofactors in metabolism, catalysts and enzyme activators.
6.3 Macroelements
6.3.1 Calcium
Biological function: The principal biological functions of calcium may be summarised as follows;
Dietary sources and absorption: Rich dietary sources of calcium include limestone, oystershell grit, bone
meal, rock phosphate (4030%); crab meal, shrimp meal, meat and bone meal (2010%); white fish meal,
poultry manure, meat meal (105%); and brown fish meal, delactose whey powder, dried skim milk,
poultry by-product meal, kelp meal, alfalfa meal (51%).
Calcium is readily absorbed through the gastro-intestinal tract (through vitamin D3 action), gills, skin and
fins of fish and crustacea. In general, dietary calcium absorption is facilitated by dietary lactose (by
forming a soluble sugar-calcium complex) and by high gastric acidities (by aiding solubilization of the
calcium salt).
6.3.2 Phosphorus
Biological function: The principal biological functions of phosphorus may be summarized as follows;
Dietary sources and absorption: Rich dietary sources of phosphorus include rock phosphate, dicalcium
phosphate, bone meal (2010% P); meat and bone meal, meat meal, white fish meal, shrimp meal, poultry
by-product meal, dried poultry manure (52%); and rice bran, rice polishings, wheat bran, wheat mill run,
dried brewers yeast, sunflower seed meal, cottonseed meal, rapeseed meal, sesame seed meal, dried
delactose whey (21%).
Although soluble phosphorus salts can be absorbed through the skin, fins and gills of fish and shrimp, the
concentration of phosphorus in fresh and sea water is low, and consequently body phosphorus
requirements are usually met from dietary sources. Within plant foods, including cereals and oilseeds, 50
80% of the phosphorus occurs in the form of the calcium or magnesium salt of phytic acid; phytic acid
being the hexaphosphate ester of inositol. This organic form of phosphorus must first be hydrolyzed
within the gastro-intestinal tract by the enzyme phytase to inositol and phosphoric acid before it can be
utilized and absorbed by the animal. As with calcium, the absorption of inorganic phosphorus salts is
facilitated by high gastric acidity; the more soluble the salt the higher the availability and absorption of
phosphorus.
6.3.3 Magnesium
Biological function: The principal biological functions of magnesium may be summarised as follows;
Dietary sources and absorption: Rich dietary sources of magnesium include; meat and bone meal, rice
bran, kelp meal, sunflower seed meal (1.00.75% Mg); and wheat bran, wheat mill run, rice polishings,
rapeseed meal, shrimp meal, cottonseed meal, linseed meal, poultry manure and crab meal (0.750.5%).
Magnesium is readily absorbed through the gastro-intestinal tract, gills, skin and fins of fish and
crustacea. As with calcium and phosphorus, a proportion of the magnesium contained in plant foodstuffs
may be present in the form of phytin (Ca or Mg salt of phytic acid).
Biological function: Sodium, potassium, and chlorine occur almost entirely in the fluids and soft tissues
of the body, sodium and chlorine being found mainly in the body fluids, and potassium occuring mainly
in the cells. They serve a vital function in controlling osmotic pressures and acid-base equilibrium. They
also play important roles in water metabolism.
Sodium is the main monovalent ion of extracellular fluids; sodium ions constituting 93% of the ions
(bases) found in the blood stream. Although the principal role of sodium in the animal is connected with
the regulation of osmotic pressure and the maintenance of acid-base balance, sodium also has an effect on
muscle irritability, and plays a specific role in the absorption of carbohydrate.
Potassium is the major cation of intracellular fluid, and regulates intracellular osmotic pressue and acid-
base balance. Like sodium, potassium has a stimulating effect on muscle irritability. Potassium is also
required for glycogen and protein sysnthesis, and the metabolic breakdown of glucose.
Chlorine is the main monovalent anion of extracellular fluids; chlorine ions constituting about 65% of the
total anions of blood plasma and other extracellular fluids within the body (ie. gastric juice). Chlorine is
therefore essential for the regulation of osmotic pressue and acid-base balance. Chlorine also plays a
specific role in the transport of oxygen and carbon dioxide in the blood, and the maintenance of digestive
juice pH.
Dietary sources and absorption: Rich dietary sources of sodium, potassium and chlorine include: kelp
meal, condensed fish solubles, dried delactose whey, shrimp meal, white fish meal, meat meal, meat and
bone meal (41% Na in decreasing order); dehydrated cane molasses, condensed fish solubles, delactose
whey powder, alfalfa meal, dried torula yeast, soybean meal, rice bran (4-2% K in decreasing order);
dried brewers yeast, dried distillers solubles, wheat bran, cottonseed meal, meat and bone meal, wheat
mill run, copra meal, rapeseed meal, peanut meal, and sunflower seed meal (21% K in decreasing order);
salt (sodium chloride, 60% Cl) and potassium chloride (48% Cl).
Potassium, sodium and chloride are readily absorbed from the gastrointestinal tract, skin, fins and gills of
fish and crustacea.
6.3.5 Sulphur
Biological function: The principal biological functions of sulphur may be summarised as follows;
Sulphur is an essential component of several key amino acids (methionine and cystine), vitamins
(thiamine and biotin), the hormone insulin, and the crustacean exoskeleton.
As the sulphate, sulphur is an essential component of heparin, chondroitin, fibrinogen and taurine.
Several key enzyme systems such as coenzyme A and glutathione depend for their activity on
free sulphydryl (SH) groups.
Sulphur is believed to be involved in the detoxification of aromatic compounds within the animal
body.
Dietary sources and absorption: Rich dietary sources of the sulphur containing amino acids include fish
meal, chicken eggs, and hydrolysed feather meal (the latter containing primarily cystine, Table 5).
Sulphur containing amino acids and to a lesser extent inorganic sulphates are readily absorbed from the
gastrointestinal tract of fish and shrimp.
6.4 Microelements
6.4.1 Iron
Biological function: The principal biological functions of iron may be summarised as follows;
Dietary sources and absorption: Rich dietary sources of iron include; blood meal (0.30.2% Fe); kelp
meal, coconut meal, meat and bone meal, sunflower seed meal, dried distillers solubles (1000500
mg/kg); alfalfa meal, crab meal, condensed fish solubles, fish meal, meat meal, poultry by-product meal,
linseed meal, dried brewers yeast, dehydrated cane molasses, rice bran, delactose whey powder, and dried
poultry manure (500200 mg/kg).
Iron is readily absorbed through the gastro-intestinal tract, gills, fins and skin of fish and crustacea.
Dietary iron availability and absorption is usually depressed by high dietary intakes of phosphate,
calcium, phytates, copper and zinc. In general, inorganic sources of iron are more readily absorbed than
organic sources; the ferrous iron (Fe++) being more available for absorption than ferric iron (Fe+++).
Reducing substances such as vitamin C enhance the absorption of non-haem iron.
6.4.2 Zinc
Biological function: The principal biological functions of zinc may be summarised as follows;
Dietary sources and absorption: Rich dietary sources of zinc include chick hatchery meal (0.15% Zn),
dried Candida yeast, dehydrated fish solubles, dried distillers grains with solubles, dried poultry manure
(500200 mg/kg); fish meal, corn gluten meal, poultry by-product meal, wheat bran, rice mill run,
dehydrated cattle manure, wheat middlings, crab meal, sunflower seed meal, dried torula yeast (200100
mg/kg Zn).
Zinc is readily absorbed from the gastro-intestinal tract, gills, fins and skin of fish and crustacea. Dietary
zinc availability and absorption is reduced in the presence of phytates, and high dietary intakes of
calcium, phopshorus and copper.
6.4.3 Manganese
Biological function: The principal biological functions of managanese may be summarised as follows,
Manganese functions in the body as an enzyme activator for those enzymes that mediate
phosphate group transfer (ie. phosphate transferases and phosphate dehydrogenases), particularly
those concerned with the citric acid cycle including arginase, alkaline phosphatase and
hexokinase.
Manganese is an essential component of the enzyme pyruvate carboxylase
As a cofactor or component of several key enzyme systems, manganese is essential for bone
formation (re. mucopolysaccharide synthesis), the regeneration of red blood cells, carbohydrate
metabolism, and the reproductive cycle.
Dietary sources and absorption: Rich dietary sources of manganese include kelp meal (0.10% Mn), rice
bran, dehydrated poultry manure, palm kernel meal, crab meal, wheat bran, wheat germ meal, wheat mill
run, wheat middlings (300100 mg/kg); dehydrated cattle manure, corn distillers dried solubles, rye grain,
dehydrated cane molasses, dehydrated fish solubles, copra meal (10050 mg/kg); wheat, rapeseed meal,
sesame seed meal, linseed meal, brewers dried grains, safflower seed meal, shrimp meal and oats (5030
mg/kg).
Manganese is readily absorbed from the gastro-intestinal tract, gills, fins and skin of fish and crustacea.
Dietary manganese availability and absorption is reduced in the presence of phytates, and high dietary
intakes of calcium.
6.4.4 Copper
Biological function: The principal biological functions of copper may be summarised as follows;
Dietary sources and absorption: Rich dietary sources of copper include condensed fish solubles, corn
distillers dried solubles, dehydrated sugar cane molasses (100-75 mg/kg Cu); corn distillers grains with
solubles, dehydrated poultry manure (7550 mg/kg); dried brewers yeast, crab meal, corn gluten meal,
linseed meal, soybean meal, dried brewers grains, wheat mill run, millet, cottonseed meal, wheat
middlings, and copra meal (5020 mg/kg).
Copper is readily absorbed from the gastro-intestinal tract, gills, fins and skin of fish and crustacea.
Dietary copper availability and absorption is reduced in the presence of phytates, and high dietary intakes
of zinc, iron, molybdenum, cadmium, inorganic sulphates and calcium carbonate.
6.4.5 Cobalt
Biological function: The principal biological functions of cobalt may be summarised as follows;
Cobalt is an integral component of cyanocobalamin (vitamin B12), and as such is essential for red
blood cell formation and the maintenance of nerve tissue.
Although not confirmed, cobalt may also function as an activating agent for various enzyme
systems.
Dietary sources and absorption: Rich dietary sources of cobalt include copra meal (2 mg/kg Co), linseed
meal, dried brewers yeast, fish meal, meat meal, cottonseed meal, and soybean meal (0.50.1 mg/kg).
Cobalt is readily absorbed from the gastro-intestinal tract and the surrounding water by fish and crustacea.
Dietary cobalt availability and absorption is reduced in the presence of high dietary intakes of iodine.
6.4.6 Iodine
Biological function: Iodine is an integral component of the thyroid hormones, thyroxine and tri-iodo-
thyronine, and as such is essential for regulating the metabolic rate of all body processes.
Dietary sources and absorption: Rich dietary sources of iodine include all food stuffs of marine origin,
and in particular seaweed meals (which may contain up to 0.6% I) and marine fish and crustacean meals.
Iodine is readily absorbed from the gastro-intestinal tract and the surrounding water by fish and crustacea.
Dietary availability and absorption is reduced in the presence of high dietary intakes of cobalt.
6.4.7 Selenium
Biological function: Selenium is an essential component of the enzyme glutathione peroxidase, and as
such (together with the tocopherols - vitamin E) serves to protect cellular tissues and membranes against
oxidative damage. It has also been suggested that selenium participates in the biosynthesis of ubiquinone
(coenzyme Q; involved in cellular electron transport) and influences the absorption and retention of
vitamin E.
Dietary sources and absorption: Rich dietary sources of selenium include dehydrated fish solubles, fish
meal (52 mg/kg Se); dried brewers yeast, corn gluten meal, dried torula yeast, rapeseed meal, cottonseed
meal (21 mg/kg); and dried brewers grains, wheat bran, wheat middlings, linseed meal, hydrolyzed
feather meal, poultry by-product meal, meat meal and alfalfa (10.5 mg/kg). Selenium is readily absorbed
from the gastro-intestinal tract and the surrounding water by fish and crustacea.
6.4.8 Chromium
Biological function: Trivalent chromium is an integral component of the glucose tolerance factor (GTF; a
low molecular weight compound with trivalent chromium coordinated to two nicotinic acid molecules
with the remaining coordinates protected by amino acids) and acts as a cofactor for the hormone insulin.
Apart from its vital role in carbohydrate metabolism (ie. glucose tolerance and glycogen synthesis),
trivalent chromium is also believed to play an important role in cholesterol and amino acid metabolism.
Dietary sources and absorption: Rich dietary sources of trivalent chromium include chick shell meal (15
mg/kg), shrimp tail meat, Artemia salina, dried brewers yeast, shellfish, liver, poultry by-product meal
and fish meal (51 mg/kg dry weight). Trivalent chromium is readily absorbed from the gastrointestinal
tract and the surrounding water by fish and crustacea.
From the above it follows therefore that the dietary requirement of a fish or shrimp species for a particular
element will depend to a large extent upon the concentration of that element in the water body. At present
there is little information concerning the contribution of waterborne elements to the total mineral balance
of fish or shrimp (Tacon, Knox and Cowey, 1984).
Dietary mineral requirements are usually determined by feeding graded levels of each element within a
purified or semi-purified test diet; dietary requirement being taken at break-point on the basis of the
observed growth response, feed efficiency, or tissue enzyme indicator level (for review see Cowey and
Sargent, 1972; Cho, Cowey and Watanabe, 1985; Kanazawa, 1983; Lall, 1979; Nose and Arai, 1979;
NRC, 1983; and Robinson and Wilson, 1985). As with the vitamins, the majority of studies have been
conducted under controlled laboratory conditions and so little information exists on the dietary mineral
requirements of fish or shrimp under practical semi-intensive or intensive farming conditions using
practical diets.
Despite these limitations, the known dietary mineral requirements of the major aquaculture species are
summarised in Table 12.
CALCIUM
Channel catfish (I. punctatus) 1.50 % Andrews, Murai & Campbell (1973)
Red sea bream (C. major) 0.34 % Sakamoto & Yone (1973)
Red sea bream (C. major) >0.14 % Sakamoto & Yone (1976)
1
Dietary calcium requirement determined in calcium-free water
PHOSPHORUS
Red sea bream (C. major) 0.68 % Sakamoto & Yone (1973)
1
Basal diet contained 0.62% P derived mainly from plant sources and requireda minimum of 0.6% supplemental inorganic P as dibasic calcium
phosphate formaximum growth response
2
Available phosphorus requirement (as determined with fish)
3
Experiments conducted in floating cages suspended in an earthen pond, 100 fishof average size 120g/m3, and available P requirement based on
P availabilitiesof 70% for fish meal and Dicalcium phosphate and 33% for plant phosphorus
MAGNESIUM
Rainbow trout (S. gairdneri) 0.060.07 % Ogino, Takashima & Chiou (1978)
Rainbow trout (S. gairdneri) 0.05 % Knox, Cowey & Adron (1981, 1983)
Red sea bream (C. major) <0.012 % Sakamoto & Yone (1979)
1
No dietary requirement demonstrated
POTASSIUM 1
Red sea bream (C. major) 0.21 % Yone & Toshima (1979)
1
No dietary requirement or deficiency symptom demonstrated for sodium orchlorine in fish or shrimp to date
ZINC
Rainbow trout (S. gairdneri) 1530 mg/kg Ogino & Yang (1978)
Common carp (C. carpio) 1530 mg/kg Ogino & Yang (1979)
Channel catfish (I. punctatus) 150 mg/kg2 Gatlin & Wilson (1984)
1
Basal practical diet containing white fish meal as the major protein sourceand 60 mg/kg Zn; diet required supplemental Zn as ZnSO4.7H2O at
150 mg/kgdiet to prevent Zn deficiency and produce normal growth
2
Basal practical diet containing 1.1% phytic acid from soybean meal and rice,and requiring a dietary supplementation of 150 mg Zn/kg diet to
preventdeficiency symptoms
IRON
Channel catfish (I. punctatus) 30 mg/kg Gatlin & Wilson (1986)
Red sea bream (C. major) 150 mg/kg Sakamoto & Yone (1976a, 1978)
1
No dietary requirement demonstrated
COPPER
1
No dietary requirement demonstrated
MANGANESE
Rainbow trout (S. gairdneri) 1213 mg/kg Ogino & Yang (1980)
Common carp (C. carpio) 1213 mg/kg Ogino & Yang (1980)
Channel catfish (I. punctatus) 2.4 mg/kg 1 Robinson & Wilson (1985)
1
No dietary requirement demonstrated with fish fed purified diets for 13 weeks,and containing a basal manganese content of 2.4 mg/kg (studies
in press)
2
Recommended dietary Mn level for practical catfish feeds
IODINE
Chinook salmon (O. tshawytscha) 0.61.1 mg/kg Woodall & LaRoche (1964)
SELENIUM
Rainbow trout (S. gairdneri) 0.070.38 mg/kg Hilton, Hodson & Slinger (1980)
Channel catfish (I. punctatus) 0.10.25 mg/kg 1 Gatlin & Wilson (1984)
1
Dietary requirement of 0.25 mg/kg within purified diets, and a recommendeddietary requirement of 0.1 mg/kg Se within practical catfish feeds
CHROMIUM
Rainbow trout (S. gairdneri) 1.0 mg/kg Tacon & Beveridge (1982)
The following gross anatomical deficiency signs have been reported in juvenile fish or shrimp fed
experimental diets lacking in one or more essential mineral elements:
PHOSPHORUS
Common carp (C. carpio) Reduced growth, poor feed efficiency (1,2); bone demineralization,
skeletal deformity, abnormal calcification of ribs and soft rays of
pectoral fin (1); cranial deformity (1,3); increased visceral fat (4)
Channel catfish (I. punctatus) Reduced growth, poor feed efficiency (5); bone demineralization
(5,6)
Red sea bream (C. major) Reduced growth, poor feed efficiency, bone demineralization,
increased muscle, liver and vertebrae lipid content (7); curved and
enlarged spongy vertebrae (8); decreased liver glycogen (9)
Rainbow trout (S. gairdneri) Reduced growth, poor feed efficiency, bone demineralization (13,14)
Atlantic salmon (S. salar) Reduced growth, poor feed efficiency, bone demineralization (13,14)
CALCIUM
Channel catfish (I. punctatus) Reduced growth, low carcass ash, Ca and P content (fed vitamin D
deficienct diets, 6)
Rainbow trout (S. gairdneri) Anorexia, reduced growth and feed efficiency (15)
Eel (A. japonica) Anorexia, reduced growth and feed efficiency (16)
Red sea bream (C. major) Anorexia, reduced growth and feed efficiency (17)
MAGNESIUM
Common carp (C. carpio) Reduced growth (11, 18); sluggishness, anorexia, convulsions, high
mortality (11); cataracts (18)
Channel catfish (I. punctatus) Anorexia, reduced growth, sluggishness, muscle flacidity, high
mortality (19)
Rainbow trout (S. gairdneri) Reduced growth (2124); anorexia (22,23); cataracts (25);
sluggishness, calcinosis of kidney (21,22); increased mortality,
vertebral curvature, degener- ation of muscle fibres and epithelial
cells of pyloric caecae and gill filaments (23); reduced bone ash, Mg
and elevated Ca content (24)
Penaeids (P. japonicus) Reduced growth, poor survival and reduced feed efficiency (41)
ZINC
Channel catfish (I. punctatus) Reduced growth, anorexia, depressed bone Ca and Zn content (29)
Common carp (C. carpio) Reduced growth (18, 30); cataracts (18); anorexia, high mortality,
erosion of fins and skin, elevated tissue concentrations of Fe and Cu
in intestine and hepatopancreas (30)
Rainbow trout (S. gairdneri) Reduced growth (25,31,32); increased mortality (31, 32); cataracts
(25, 31); short body dwarfism (25); fin erosion (31)
MANGANESE
Tilapia (O. mossambicus) Reduced growth, anorexia, loss of equilibrium, mortality (33)
Common carp (C. carpio) Reduced growth (34, 18); short body dwarfism, cataracts (18)
Rainbow trout (S. gairdneri) Cataracts (25, 35); reduced growth, short body dwarfism (34, 35);
abnormal tail growth (34)
COPPER
Common carp (C. carpio) Reduced growth (34, 18); cataracts (18)
SELENIUM
Atlantic salmon (S. salar) Increased mortality, muscular dystrophy, depressed glutathione
peroxidase activity (36)
Common carp (C. carpio) Reduced growth (18, 37); cataracts (18); anaemia (37)
IODINE
1
1-Ogino & Takeda (1976); 2-Yone & Toshima (1979); 3-Ogino et al., (1979); 4-Takeuchi & Nakazoe (1981); 5-Andrews, Murai & Campbell
(1973); 6-Lovell & Li(1978); 7-Sakamoto & Yone (1980); 8-Sakamoto & Yone (1979); 9-Sakamoto & Yone(1978); 10-Arai, Nose & Kawatsu
(1974); 11-Ogino & Chiou (1976); 12-Ogino &Takeda (1978); 13-Ketola (1975); 14-Lall & Bishop (1977); 15-Arai et al. (1975);16-Arai, Nose
& Hashimoto (1975); 17-Sakamoto & Yone (1973); 18-Satoh et al.,(1983); 19-Gatlin et al., (1982); 20-Arai et al., (cited by Nose and Arai,
1979);21-Cowey et al., (1977); 22-Knox, Cowey & Adron (1981); 23-Ogino, Takashima &Chiou (1978); 24-Knox, Cowey & Adron (1983); 25-
Satoh et al., (1983a); 26-Sakamoto& Yone (1978a); 27-Sakamoto & Yone (1978); 28-Kawatsu (1972); 29-Gatlin& Wilson (1983); 30-Ogino &
Yang (1979); 31-Ogino & Yang (1978); 32-Wekell,Shearer & Houle (1983); 33-Ishak & Dollar (1968); 34-Ogino & Yang (1980);35-
Yamamoto et al., (1983); 36-Poston, Combs & Leibovitz (1976); 37-Lall (1979); 38-Gatlin & Wilson (1984a); 39-Woodall & LaRoche (1964);
40-NRC (1983);41-Kanazawa, Teshima & Sasaki (1984); 42-Gatlin & Wilson (1986).
Despite the adequate presence of macro and trace elements in virtually all raw ingredients commonly
used for fish feeding (Tacon and De Silva, 1983), and the ability of fish and shrimp to absorb certain trace
elements from the surrounding water, mineral deficiencies may arise under intensive culture conditions
through:
The absence of a specific macro or trace mineral premix within the diet (for details of specific
mineral premix formulations see NRC, 1983).
Reduced mineral bioavailability through dietary imbalances. The availability and utilization of
dietary trace elements in fish or shrimp is dependent upon the dietary source and form of the
element ingested, the adequacy of stores within the body, interactions with other mineral
elements present in the gastro-intestinal tract and within the body tissues (antagonisms), and
finally by element interactions with other dietary ingredients or their metabolites (ie. vitamins,
fibre and phytic acid). For example, Table 13 shows the relative availabilities or apparent
absorption efficiency of various forms or sources of dietary phosphorus for three fish species.
Phosphates
monobasic 94 94 94
dibasic 65 46 71
tribasic - 13 64
Fish meals
Protein sources
Egg albumin 71 - -
Casein 90 97 90
Brewers yeast - 93 91
Plant products
Rice bran - 25 19
Wheat germ - 57 58
Wheat middlings 28 - -
Corn, ground 25 - -
1
Source: NRC (1983)
For certain fish species the availability and absorption of phosphorus and other major elements (ie.
calcium) from fish meal and meat and bone meal is further complicated by the absence of an acid-
secreting stomach, which is essential for normal bone solubilization. For stomachless fish species soluble
monobasic inorganic salts or bioavailable organic salts must therefore be provided in the diet. Conversely,
within plant proteins a large proportion of phosphorus is present as organically bound phytates. Not only
is phytic acid phosphorus believed to be largely biologically unavailable, but phytic acid also has the
capacity to chelate other trace elements (iron, copper, zinc, cobalt, molybdenum) and by so doing may
render them biologically unavailable to the fish during digestion (Spinelli, 1980; Robinson and Wilson,
1985).
Under practical farming conditions mineral deficiency signs often arise from a dietary imbalance of
calcium; due to the antagonistic effect of excess dietary calcium on the absorption of phosphorus
(Nakamura, 1982) and the trace elements zinc, iron and manganese (Lall, 1979). For example, the
bioavailability of zinc, and to a lesser extent manganese within white fish meal has been found to be
much lower than that contained in brown fish meal (which has a much lower ash and calcium content;
Ketola, 1978; Watanabe, Takeuchi and Ogino, 1980). Thus in experimeental feeding trials with rainbow
trout, chum salmon and common carp fed on diets in which white fish meal was used without a trace
element supplement, overt trace element deficiency signs arise such as depressed growth, short body
dwarfism and cataracts (Watanabe, Takeuchi and Ogino, 1980; Satoh et al., 1983, 1983a; Yamamoto et
al, 1983).
A major hazard which may be associated with the use of dietary feed ingredients is the presence of
potentially toxic mineral elements such as the accumulative elements copper, lead, cadmium, mercury,
arsenic, fluorine, selenium, molybdenum and vanadium. For example, contamination with copper may
arise from products fermented within copper lined vessels (ie. brewery by-products), or within pig and
poultry excreta from the use of copper based growth stimulants or anti-fungal agents. Other feed
ingredients which may contain potentially toxic metal contaminants include: poultry manure (arsenic);
paper pulp waste (lead); fish meal (mercury, selenium, arsenic, cadmium, and lead); poultry by-product
meals (zinc); shellfish (zinc); seleniferous accumulating plants of the
genera Astragalus and Machaeranthera, or cereals grown in seleniferous soils (selenium); and Antartic
krill (fluorine).
Dietary toxicity signs which have been reported in fish and shrimp under controlled laboratory conditions
include:
Zinc Common carp (C. carpio) Reduced growth (dietary level above 300 mg/kg Zn; 1)
Selenium Reduced growth and feed efficiency, high mortality (dietary levels
Rainbow trout (S. gairdneri)
above 13 mg/kg; 3,4); nephrocalcinosis (4,5)
Channel catfish (I. punctatus) Reduced growth (dietary levels above 15 mg/kg; 6)
Chromium Rainbow trout (S. gairdneri) Reduced growth and feed efficiency (12)
0.014%; 13)
1
1-Jeng and Sun (1981); 2-Murai, Andrews & Smith (1981); 3-Hilton, Hodson &Slinger (1980); 4-Hicks, Hilton & Ferguson (1984); 5-Hilton &
Hodson (1983);6-Gatlin & Wilson (1984a); 7-Koyama & Itazawa (1977); 8-Koyama & Itazawa (1977a);9-Koyama & Itazawa (1979); 10-Roch
& Maly (1979); 11-Johansson-Sjbeck & Larsson(1979); 12-Tacon & Beveridge (1982); 13-Kanazawa, Teshima & Sasaki (1984)
2
Recent trials with channel catfish failed to demonstrate a deleterious effect of40 mg supplemental copper/kg diet on growth, feed efficiency or
blood chemistry(Gatlin and Wilson, 1986a). The absence of dietary copper toxicity has alsobeen reported for rainbow trout fed 150 mg
supplemental copper or 500 mg totaldietary copper (Knox, Cowey and Adron, 1982, 1984).
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