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Biofertilizers and Mycorryza
Dr. Naveen Gaurav
Associate Professor and Head
Department of Biotechnology
Shri Guru Ram Rai University
Dehradun
Bio-fertilizers: It is estimated that more than 100 million tons of fixed nitrogen are
needed for global food production. The use of chemical/synthetic fertilizers is the
common practice to increase crop yields. Besides the cost factor, the use of fertilizers is
associated with environmental pollution.
Scientists are on a constant look for alternate, cheap and environmental-friendly sources
of nitrogen and other nutrients for plants. The term bio-fertilizers is used to refer to the
nutrient inputs of biological origin to support plant growth. This can be achieved by the
addition of microbial inoculants as a source of bio-fertilizers.
Bio-fertilizers broadly includes the following categories:
i. Symbiotic nitrogen fixers
ii. Asymbiotic nitrogen fixers
iii. Phosphate solubilizing bacteria/fungus
iv. Organic fertilizers.
The most important microorganisms used as bio-fertilizers along with the crops are listed
in Table 52.2.
Some of the important features of these bio-fertilizers are briefly described.
Symbiotic Nitrogen Fixers:
The diazotropbic microorganisms are the symbiotic nitrogen fixers that serve as bio-
fertilizers. e.g. Rhizobium sp and Brady rhizobium sp. The details on these bacteria with
special reference to nitrogen fixation must be referred now. Many attempts are being
made (although the success has been limited) to genetically modify the symbiotic
bacteria for improving nitrogen fixation.
Green manuring:
It is a farming practice wherein the leguminous plants which are benefited by the
symbiotic nitrogen fixing bacteria are ploughed into the soil and a non-leguminous crop
is grown to take benefits from the already fixed nitrogen. Green manuring has been in
practice in India for several centuries. It is a natural way of enriching the soil with
nitrogen, and minimizing the use of chemical fertilizers. Rhizobium sp can fix about 50-
150 kg nitrogen/hectare/annum.
Asymbiotic Nitrogen Fixers:
The asymbiotic nitrogen-fixing bacteria can directly convert the gaseous nitrogen to
nitrogen- rich compounds. When these asymbiotic nitrogen fixers die, they enrich the
soil with nitrogenous compounds, and thus serve as bio-fertilizers e.g. Azobacfer sp,
Azospirillum sp.
Blue-green algae (cynobacteria):
Blue-green algae multiply in water logging conditions. They can fix nitrogen in the form
of organic compounds (proteins, amino acids). The term algalization is used to the
process of cultivation of blue-green algae in the field as a source of bio-fertilizer.
Blue-green algae, besides fixing nitrogen, accumulate biomass, which improves the physical
properties of the soil. This is useful for reclamation of alkaline soils besides providing partial
tolerance to pesticides. Cynobacteria are particularly useful for paddy fields. The most
common blue-green algae are Azobacter sp and Azospirillum sp.
Azolla: Azolla is an aquatic fern, which contains an endophytic cynobacterium Anabaena
azollae in the leaf cavities providing a symbiotic relationship. Azolla with Anaebaena is
useful as biofertilizer.
But due to certain limitation (listed below), the use of Azolla has not become popular:
i. Azolla plant requires adequate supply of water.
ii. It can be easily damaged by pest diseases.
iii. Azolla cultivation is labour intensive.
Phosphate Solubilizing Bacteria: Certain bacteria (e.g. Thiobacillus, Bacillus) are capable of
converting non-available inorganic phosphorus present in the soil to utilizable (organic or
inorganic) form of phosphate. These bacteria can also produce siderophores, which chelates
with iron, and makes it unavailable to pathogenic bacteria. Thus, besides making phosphate
available, the plants are protected from disease – causing microorganisms.
Mycorrhizas: Mycorrhizas are the fungus roots (e.g. Glomus sp) with distinct morphological
structure. They are developed as a result of mutual symbiosis between certain root-
inhabiting fungi and plant roots. Mycorrhizas are formed in plants, which are limited with
nutrient supply. These plants may be herbs, shrubs and trees. For the development of
mycorrhizas, the fungus may be located on the root surface (ectomycorrhizas) or inside the
root (endomycorrhizas).
In recent years, an artificially produced inoculum of mycorrhizal fungi is used in crop fields. This
practice improves plant growth and yield, besides providing resistance against biotic (pathogens)
and abiotic (climatic changes) stress. Mycorrhizas also produce plant growth-promoting
substances.
Organic Fertilizers:
There are several organic wastes, which are useful as fertilizers. These include animal dung, urine,
urban garbage, sewage, crop residues and oil cakes. A majority of these wastes remain unutilized
as organic fertilizers. There exists a good potential for the development of organic manures from
these wastes.
Benefits of Bio-fertilizers:
i. Low cost and easy to produce. Small farmers are immensely benefited.
ii. Fertility of the soil is increased year after year.
iii. Free from environmental pollution.
iv. Besides nutrient supply, some other compounds, which promote plant growth, are also
produced e.g. plant growth hormones, antibiotics.
v. Bio-fertilizers increase physicochemical properties of the soil, soil texture, and water holding
capacity.
vi. Reclaimation of saline or alkaline soil is possible by using bio-fertilizers.
vii. Bio-fertilizers improve the tolerance of plants against toxic heavy metals.
viii. Plants can better withstand biotic and abiotic stresses and improve in product yield.
Limitations of Bio-fertilizers:
i. Bio-fertilizers cannot meet the total needs of the plants for nutrient supply.
ii. They cannot produce spectacular results, as is the case with synthetic fertilizers.
Considering the advantages and disadvantages of bio-fertilizers, a realistic and pragmatic
approach is to use combination of bio-fertilizers and synthetic fertilizers for optimum crop yield.
Note
Nitrogen Fixing Bacteria:
It is estimated that about 50% of the nitrogen needed by the plant comes from nitrogen
fixing bacteria. These are two types of nitrogen fixing microorganisms-asymbiotic and
symbiotic.
Asymbiotic nitrogen fixing microorganisms:
The gaseous nitrogen of the atmosphere is directly and independently utilized to produce
nitrogen-rich compounds. When these non- symbiotic organisms die, they enrich the soil
with nitrogenous compounds. Several species of bacteria and fungi can do this job e.g.
Clostridium pasturianum, Azatobacter chrooccum. The mechanism of nitrogen fixation by
asymbiotic bacteria is not clearly understood. It is believed that nitrogen is first converted
to hydroxylamine or ammonium nitrate, and then incorporated into biomolecules.
Symbiotic nitrogen fixing microorganisms:
These microorganisms live together with the plants in a mutually beneficial relationship,
phenomenon referred to as symbiosis. The most important microorganisms involved in
symbiosis belong to two related genera namely Rhizobium and Brady-rhizobium. These
symbiotic bacteria also referred to as nodule bacteria are Gram negative, flagellated and
rod-shaped. The host plants harbouring these bacteria are known as legumes e.g.
soybean, peas, beans, alfalfa, peanuts, and clover.
Mycorrhiza: Meaning, Types and Role
Meaning of Mycorrhiza:
Vitadini (1842) was the first to recognise the possible beneficial role of fungal mycelia which
mantle the root of higher plants, and this association is named as mycorrhiza (pl.
mycorrhizae) i.e., the fungal root, by Frank (1885).
Thus mycorrhizae are the symbiotic associations between plant root and fungi, with bidirec-
tional nutrient exchange between the partners.
The autotrophic host plant acts as the carbon source for the fungus, while the fungus
supplies mineral nutrients to the plant. About 90% of all land plants are associated with
mycorrhiza. The mycorrhizal association is not available in Cruciferae, Chenopodiaceae and
Resedaceae.
Features of Mycorrhiza:
Scannerini (1988) briefly pointed out the common features of mutualistic symbionts.
These include:
(i) Absence of any phytopathological symptoms in the partners during the active phase of
mutualism,
(ii) Presence of complex interfaces between cells of the partners with a predominant type of
perisymbiotic membrane, surrounding intracellular symbionts,
(iii) Presence of various types of phagocyte-like structures during establishment of symbionts
and during harvesting phase to control the symbiotic population by the host.
Types of Mycorrhiza:
Peterson and Farquhar (1994)
classified the mycorrhizae into
seven (7) distinct types.
These are :
(1) Ectomycorrhizae,
(2) Vesicular-arbuscular
mycorrhizae,
(3) Ectendomycorrhizae
(Arbutoid),
(4) Ericoid mycorrhizae,
(5) Centianoid mycorrhizae,
(6) Orchidoid mycorrhizae, and
(7) Monotropoid mycorrhizae.
(1) Ectomycorrhizae:
Ectomycorrhiza is commonly
called “sheathing mycorrhiza”.
They occur in 3% of all seed
plants in forests of temperate
regions, especially on pine,
beech, spruce, birch etc.
Generally they cause extensive branching and growth of roots and modification of branching
pattern, such as racemose type in dicots (Fagus) and dichotomous in gym- nosperms (Pinus). In
beech (Fagus) the ultimate lateral rootlets are differentiated into ‘long’ and ‘short’ roots.
The long roots show indefinite growth and their branches are the short roots that are thickened,
forked and mycorrhizal. They appear in various colours like white, brown, yellow, black etc.,
depending on the colour of the fungus. The fungus enters the cortex forming ‘Hartig net’, but
never goes inside the endodermis or stele. They form a mantle of varying thickness (Fig. 4.103A,
B).
Majority of the fungi belong to Agaricales of Hymenomycetes under Basidiomycotina. More than
100 species of toadstools are reported to form mycorrhiza. Most of the members are belonging to
the genera Amanita, Tricholoma, Boletus, Russula, Lactarius etc.
Members of Gastercmycetes under Basidiomycotina like Rhizopogon and Scleroderma are
involved in this process. Some members of Ascomycotina like Gyromitra esculenta, all species of
Tuber (T. melanospora) form mycorrhizae.
(2) Vesicular-arbuscular mycorrhizae (VAM):
It is a type of endomycorrhizal association, where both vesicles and arbuscles are developed
together. VAM is by far the commonest of all mycorrhizae and has been reported in more than
90% of land plants.
They are found in bryophytes, pteridophytes, gymnosperm (except Pinaceae) and most of
angiosperms, commonly in Leguminosae (Fabaceae), Rosaceae, Gramineae (Poaceae) and Palmae
(Arecaceae). VAM is not found in Ericaceae and Orchidaceae, where other type of association is
available. VAM has even been reported in Lower Devonian plant, Rhynia.
VAM is produced by aseptate mycelial fungi belong to Endogonaceae under Mucorales of
Zygomycotina and those members produced zygospores. The important genera involved in VAM
are Glomus, Gyrospora, Acaulospora etc. Most of the members are not culturable.
The VAM is so named because of the presence of two characteristic structures i.e., vesicles
and arbuscles:
(i) The vesicles are thin or thick walled vesicular structures produced intra-cellularly and
stored materials like polyphosphate and other minerals (Fig. 4.104).
(ii) The arbuscles are repeated dichotomously branched haustoria which grow intracellularly
(Fig. 4.104). The arbuscles live for four days and then get lysed releasing the stored food as
oil droplets, mostly polyphosphate.
There is no fungus mantle, but only a loose and very sparse network of septate hyphae
spread into the soil. These hyphae bear different types of spores, chlamydospores, or
aggregation of spores in sporocarp or zygospores. The superficial hyphae bear branches that
penetrate the epidermis and then grow intercellularly only in cortex.
Intercellular hyphae form arbuscles inside the parenchyma of cortex by repeated
dichotomous branching of the penetrating hyphae. The cell membrane of the penetrated
cell is invaginated and covers the arbuscles.
The hyphae also develop both inter- and intracellular thick-walled vesicles. The
chlamydospores may germinate on nutrient agar, but the hyphae stop growing when food
inside the spore is used up, thus they cannot be subcultured.
This type of association was present very early in the evolution land plants. Kidston and
Lang (1921) reported the VAM-like organism with Rhynia and Asteroxylon. Later, Pyrozinski
and Mallock (1975) proposed the mycorrhization/lichenisation association as a prelude to
land plant evolution.
(3) Ericoid mycorrhizae:
This is actually a type of endomycorrhiza. Ericoid
mycorrhizae are found in the different members
of Ericaceae like Erica, Calluna, Vaccinum,
Rhododendron etc. The fungi are slow-growing,
septate and mostly sterile. They are mostly
culturable. Both Pezizella ericae (Ascomycotina)
and Clavaria vermiculata (Basidiomycotina) have
been isolated from Rhododendrons.
During this association the rootlets of the plants
are covered by very sparse, loose, dark, septate
hyphae that penetrate the cortex forming
intercellular coils (Fig. 4.105). After 3-4 weeks the
coils degenerate like arbuscles of vesicular-
asbuscular mycorrhiza (VAM).
Most of the members of Ericaceae grow in acid
soil with less amount of P and N nutrition. The
fungus gets the photosynthate from the host and
improves the mineral uptake and nutrition of the
host, especially P and N. Many mycotrophs of
Ericaceae show high resistance to metals like Zn
and Cu. The mycorrhizal plants also show high
tolerance to these metals, which is totally absent
in non-infected plants.
(4) Ectendomycorrhizae (Arbutoid):
Some members of the family Ericaceae and members of other families of Ericales have
mycorrhizae intermediate in form between ecto- and endomycorrhizae types, called
ectendomycorrhizae. Arbustus and Arctostaphylos of Ericaceae show this type of mycorrhizal
association.
In Arbustus, the root system is differentiated into long and short roots. The short roots are
swollen and covered by hyphal mantle. Hartig net is absent in this association, but
intercellular coils develop in the outer cortical cells. Nothing is known about the fungi
involved in this association.
(5) Gentianoid mycorrhizae:
Seedlings of some members of Gentianaceae (Biackstonia perfoliata, Gentianella amarella,
etc.) get infected within 2 weeks of germination. In root, the cortical cells become full of
irregular coils of aseptate hyphae. With time the hyphae become lysed. Vesicles are
occasionally seen attached to these coils.
(6) Orchidoid mycorrhizae:
Orchids produce millions of tiny seeds per capsule, weighing about 0.3-14µg. The embryo of
seeds contains 10-100 cells and there is virtually no storage of food. The embryo is encircled
in a thin-walled net-like testa that helps in their dispersal.
Thus, majority of seeds are unable to germinate without exogenous supply of carbohydrates.
Therefore, mycorrhizal association is obligatory for the seeds to germinate. The fungus
provides C-nutrition to the seeds.
Initially the fungus enters the embryo and colonises, being restricted to the cortical cells and
provides the nutrition (Fig. 4.106). For non-green orchids, this is obligatory throughout their
lives. Apparently, it is a case of parasitism by orchids on the mycorrhizal fungi.
Fungi like Rhizoctonia (Basidiomycotina), are recognised by hyphal characteristics.
Corticium, Ceratobasidium etc., of Aphylloporales are associated in this type of mycorrhiza.
(7) Monotropoid mycorrhizae:
Monotropa hypopitys is a non-green saprophytic herb. It has short fleshy roots that are invested with
a hyphal sheath and often forming Hartig net in the cortical zone. Due to absence of chlorophyll, they
are unable to synthesise and supply carbohydrate to the fungus. Boletus is a mycorrhizal fungus asso-
ciated with roots of both pine and Monotropa.
When 14C glucose was injected into the phloem of Pinus trees, significant amount of radioactive
glucose (14C) was recorded in Monotropa (but not in other herbs) after 5 days. This indicates that the
fungus Boletus acts as a bridge between Monotropa and Pine plants.
Similarly, 32P injected into Monotropa was also detected in Pine roots within 2 hours. The above facts
indicate a bidirectional flow of nutrients between the plants through the fungus Boletus.
Role of Mycorrhizae in Agriculture and Foresty:
Role in Agriculture:
1. The mycorrhizal association helps in the formation of dichotomous branching and profuse root
growth, thus enhances plant growth.
2. Ectotrophic mycorrhiza helps in uptake of mineral ions and also acts as reservoir.
3. They also help in absorption of nutrients.
4. In nutrient deficient soil, the mycelial association helps in the absorption of N, Ca, P, Zn, Fe, Na and
others.
5. Mycorrhizal association is obligatory for the germination of orchid seeds.
Mycorrhizal growth in orchids (Rhizoctonia repens with Orchis militaris tuber tissues) causes the
synthesis of phytoalexins — orchinol and hirsinol. Both the compounds act as a barrier to protect
infection by other pathogens.
6. Inoculation of VAM as biofertiliser provides a distinct possibility for the uptake of P in phosphorus-
deficient soil.
Role in Foresty:
1. Mycorrhiza plays an important role to establish forest in unfavourable location, barren
land, waste lands etc.
2. Trees with facultative endomycorrhiza act as first invader in waste lands as pioneer in
plant succession.
3. The application of mycorrhizal fungi in forest bed enhances the formation of mycorrhizal
association that prevents the entry of fungal root pathogens. This method is very much
effective in the root of Pinus clausa against Phytophthora cinnamoni infection.
4. Mycorrhiza mixed nitrogenous compounds such as nitrate; ammonia etc. is available to
the plants. Thus it helps in plant growth, especially in acid soil.
Thank you
References: Online notes and Books by google search Engine

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  • 1. Biofertilizers and Mycorryza Dr. Naveen Gaurav Associate Professor and Head Department of Biotechnology Shri Guru Ram Rai University Dehradun
  • 2. Bio-fertilizers: It is estimated that more than 100 million tons of fixed nitrogen are needed for global food production. The use of chemical/synthetic fertilizers is the common practice to increase crop yields. Besides the cost factor, the use of fertilizers is associated with environmental pollution. Scientists are on a constant look for alternate, cheap and environmental-friendly sources of nitrogen and other nutrients for plants. The term bio-fertilizers is used to refer to the nutrient inputs of biological origin to support plant growth. This can be achieved by the addition of microbial inoculants as a source of bio-fertilizers. Bio-fertilizers broadly includes the following categories: i. Symbiotic nitrogen fixers ii. Asymbiotic nitrogen fixers iii. Phosphate solubilizing bacteria/fungus iv. Organic fertilizers. The most important microorganisms used as bio-fertilizers along with the crops are listed in Table 52.2.
  • 3. Some of the important features of these bio-fertilizers are briefly described. Symbiotic Nitrogen Fixers: The diazotropbic microorganisms are the symbiotic nitrogen fixers that serve as bio- fertilizers. e.g. Rhizobium sp and Brady rhizobium sp. The details on these bacteria with special reference to nitrogen fixation must be referred now. Many attempts are being made (although the success has been limited) to genetically modify the symbiotic bacteria for improving nitrogen fixation. Green manuring: It is a farming practice wherein the leguminous plants which are benefited by the symbiotic nitrogen fixing bacteria are ploughed into the soil and a non-leguminous crop is grown to take benefits from the already fixed nitrogen. Green manuring has been in practice in India for several centuries. It is a natural way of enriching the soil with nitrogen, and minimizing the use of chemical fertilizers. Rhizobium sp can fix about 50- 150 kg nitrogen/hectare/annum. Asymbiotic Nitrogen Fixers: The asymbiotic nitrogen-fixing bacteria can directly convert the gaseous nitrogen to nitrogen- rich compounds. When these asymbiotic nitrogen fixers die, they enrich the soil with nitrogenous compounds, and thus serve as bio-fertilizers e.g. Azobacfer sp, Azospirillum sp. Blue-green algae (cynobacteria): Blue-green algae multiply in water logging conditions. They can fix nitrogen in the form of organic compounds (proteins, amino acids). The term algalization is used to the process of cultivation of blue-green algae in the field as a source of bio-fertilizer.
  • 4. Blue-green algae, besides fixing nitrogen, accumulate biomass, which improves the physical properties of the soil. This is useful for reclamation of alkaline soils besides providing partial tolerance to pesticides. Cynobacteria are particularly useful for paddy fields. The most common blue-green algae are Azobacter sp and Azospirillum sp. Azolla: Azolla is an aquatic fern, which contains an endophytic cynobacterium Anabaena azollae in the leaf cavities providing a symbiotic relationship. Azolla with Anaebaena is useful as biofertilizer. But due to certain limitation (listed below), the use of Azolla has not become popular: i. Azolla plant requires adequate supply of water. ii. It can be easily damaged by pest diseases. iii. Azolla cultivation is labour intensive. Phosphate Solubilizing Bacteria: Certain bacteria (e.g. Thiobacillus, Bacillus) are capable of converting non-available inorganic phosphorus present in the soil to utilizable (organic or inorganic) form of phosphate. These bacteria can also produce siderophores, which chelates with iron, and makes it unavailable to pathogenic bacteria. Thus, besides making phosphate available, the plants are protected from disease – causing microorganisms. Mycorrhizas: Mycorrhizas are the fungus roots (e.g. Glomus sp) with distinct morphological structure. They are developed as a result of mutual symbiosis between certain root- inhabiting fungi and plant roots. Mycorrhizas are formed in plants, which are limited with nutrient supply. These plants may be herbs, shrubs and trees. For the development of mycorrhizas, the fungus may be located on the root surface (ectomycorrhizas) or inside the root (endomycorrhizas).
  • 5. In recent years, an artificially produced inoculum of mycorrhizal fungi is used in crop fields. This practice improves plant growth and yield, besides providing resistance against biotic (pathogens) and abiotic (climatic changes) stress. Mycorrhizas also produce plant growth-promoting substances. Organic Fertilizers: There are several organic wastes, which are useful as fertilizers. These include animal dung, urine, urban garbage, sewage, crop residues and oil cakes. A majority of these wastes remain unutilized as organic fertilizers. There exists a good potential for the development of organic manures from these wastes. Benefits of Bio-fertilizers: i. Low cost and easy to produce. Small farmers are immensely benefited. ii. Fertility of the soil is increased year after year. iii. Free from environmental pollution. iv. Besides nutrient supply, some other compounds, which promote plant growth, are also produced e.g. plant growth hormones, antibiotics. v. Bio-fertilizers increase physicochemical properties of the soil, soil texture, and water holding capacity. vi. Reclaimation of saline or alkaline soil is possible by using bio-fertilizers. vii. Bio-fertilizers improve the tolerance of plants against toxic heavy metals. viii. Plants can better withstand biotic and abiotic stresses and improve in product yield. Limitations of Bio-fertilizers: i. Bio-fertilizers cannot meet the total needs of the plants for nutrient supply. ii. They cannot produce spectacular results, as is the case with synthetic fertilizers. Considering the advantages and disadvantages of bio-fertilizers, a realistic and pragmatic approach is to use combination of bio-fertilizers and synthetic fertilizers for optimum crop yield.
  • 6. Note Nitrogen Fixing Bacteria: It is estimated that about 50% of the nitrogen needed by the plant comes from nitrogen fixing bacteria. These are two types of nitrogen fixing microorganisms-asymbiotic and symbiotic. Asymbiotic nitrogen fixing microorganisms: The gaseous nitrogen of the atmosphere is directly and independently utilized to produce nitrogen-rich compounds. When these non- symbiotic organisms die, they enrich the soil with nitrogenous compounds. Several species of bacteria and fungi can do this job e.g. Clostridium pasturianum, Azatobacter chrooccum. The mechanism of nitrogen fixation by asymbiotic bacteria is not clearly understood. It is believed that nitrogen is first converted to hydroxylamine or ammonium nitrate, and then incorporated into biomolecules. Symbiotic nitrogen fixing microorganisms: These microorganisms live together with the plants in a mutually beneficial relationship, phenomenon referred to as symbiosis. The most important microorganisms involved in symbiosis belong to two related genera namely Rhizobium and Brady-rhizobium. These symbiotic bacteria also referred to as nodule bacteria are Gram negative, flagellated and rod-shaped. The host plants harbouring these bacteria are known as legumes e.g. soybean, peas, beans, alfalfa, peanuts, and clover.
  • 7. Mycorrhiza: Meaning, Types and Role Meaning of Mycorrhiza: Vitadini (1842) was the first to recognise the possible beneficial role of fungal mycelia which mantle the root of higher plants, and this association is named as mycorrhiza (pl. mycorrhizae) i.e., the fungal root, by Frank (1885). Thus mycorrhizae are the symbiotic associations between plant root and fungi, with bidirec- tional nutrient exchange between the partners. The autotrophic host plant acts as the carbon source for the fungus, while the fungus supplies mineral nutrients to the plant. About 90% of all land plants are associated with mycorrhiza. The mycorrhizal association is not available in Cruciferae, Chenopodiaceae and Resedaceae. Features of Mycorrhiza: Scannerini (1988) briefly pointed out the common features of mutualistic symbionts. These include: (i) Absence of any phytopathological symptoms in the partners during the active phase of mutualism, (ii) Presence of complex interfaces between cells of the partners with a predominant type of perisymbiotic membrane, surrounding intracellular symbionts, (iii) Presence of various types of phagocyte-like structures during establishment of symbionts and during harvesting phase to control the symbiotic population by the host.
  • 8. Types of Mycorrhiza: Peterson and Farquhar (1994) classified the mycorrhizae into seven (7) distinct types. These are : (1) Ectomycorrhizae, (2) Vesicular-arbuscular mycorrhizae, (3) Ectendomycorrhizae (Arbutoid), (4) Ericoid mycorrhizae, (5) Centianoid mycorrhizae, (6) Orchidoid mycorrhizae, and (7) Monotropoid mycorrhizae. (1) Ectomycorrhizae: Ectomycorrhiza is commonly called “sheathing mycorrhiza”. They occur in 3% of all seed plants in forests of temperate regions, especially on pine, beech, spruce, birch etc.
  • 9. Generally they cause extensive branching and growth of roots and modification of branching pattern, such as racemose type in dicots (Fagus) and dichotomous in gym- nosperms (Pinus). In beech (Fagus) the ultimate lateral rootlets are differentiated into ‘long’ and ‘short’ roots. The long roots show indefinite growth and their branches are the short roots that are thickened, forked and mycorrhizal. They appear in various colours like white, brown, yellow, black etc., depending on the colour of the fungus. The fungus enters the cortex forming ‘Hartig net’, but never goes inside the endodermis or stele. They form a mantle of varying thickness (Fig. 4.103A, B). Majority of the fungi belong to Agaricales of Hymenomycetes under Basidiomycotina. More than 100 species of toadstools are reported to form mycorrhiza. Most of the members are belonging to the genera Amanita, Tricholoma, Boletus, Russula, Lactarius etc. Members of Gastercmycetes under Basidiomycotina like Rhizopogon and Scleroderma are involved in this process. Some members of Ascomycotina like Gyromitra esculenta, all species of Tuber (T. melanospora) form mycorrhizae. (2) Vesicular-arbuscular mycorrhizae (VAM): It is a type of endomycorrhizal association, where both vesicles and arbuscles are developed together. VAM is by far the commonest of all mycorrhizae and has been reported in more than 90% of land plants. They are found in bryophytes, pteridophytes, gymnosperm (except Pinaceae) and most of angiosperms, commonly in Leguminosae (Fabaceae), Rosaceae, Gramineae (Poaceae) and Palmae (Arecaceae). VAM is not found in Ericaceae and Orchidaceae, where other type of association is available. VAM has even been reported in Lower Devonian plant, Rhynia. VAM is produced by aseptate mycelial fungi belong to Endogonaceae under Mucorales of Zygomycotina and those members produced zygospores. The important genera involved in VAM are Glomus, Gyrospora, Acaulospora etc. Most of the members are not culturable.
  • 10. The VAM is so named because of the presence of two characteristic structures i.e., vesicles and arbuscles: (i) The vesicles are thin or thick walled vesicular structures produced intra-cellularly and stored materials like polyphosphate and other minerals (Fig. 4.104). (ii) The arbuscles are repeated dichotomously branched haustoria which grow intracellularly (Fig. 4.104). The arbuscles live for four days and then get lysed releasing the stored food as oil droplets, mostly polyphosphate. There is no fungus mantle, but only a loose and very sparse network of septate hyphae spread into the soil. These hyphae bear different types of spores, chlamydospores, or aggregation of spores in sporocarp or zygospores. The superficial hyphae bear branches that penetrate the epidermis and then grow intercellularly only in cortex. Intercellular hyphae form arbuscles inside the parenchyma of cortex by repeated dichotomous branching of the penetrating hyphae. The cell membrane of the penetrated cell is invaginated and covers the arbuscles. The hyphae also develop both inter- and intracellular thick-walled vesicles. The chlamydospores may germinate on nutrient agar, but the hyphae stop growing when food inside the spore is used up, thus they cannot be subcultured. This type of association was present very early in the evolution land plants. Kidston and Lang (1921) reported the VAM-like organism with Rhynia and Asteroxylon. Later, Pyrozinski and Mallock (1975) proposed the mycorrhization/lichenisation association as a prelude to land plant evolution.
  • 11.
  • 12. (3) Ericoid mycorrhizae: This is actually a type of endomycorrhiza. Ericoid mycorrhizae are found in the different members of Ericaceae like Erica, Calluna, Vaccinum, Rhododendron etc. The fungi are slow-growing, septate and mostly sterile. They are mostly culturable. Both Pezizella ericae (Ascomycotina) and Clavaria vermiculata (Basidiomycotina) have been isolated from Rhododendrons. During this association the rootlets of the plants are covered by very sparse, loose, dark, septate hyphae that penetrate the cortex forming intercellular coils (Fig. 4.105). After 3-4 weeks the coils degenerate like arbuscles of vesicular- asbuscular mycorrhiza (VAM). Most of the members of Ericaceae grow in acid soil with less amount of P and N nutrition. The fungus gets the photosynthate from the host and improves the mineral uptake and nutrition of the host, especially P and N. Many mycotrophs of Ericaceae show high resistance to metals like Zn and Cu. The mycorrhizal plants also show high tolerance to these metals, which is totally absent in non-infected plants.
  • 13. (4) Ectendomycorrhizae (Arbutoid): Some members of the family Ericaceae and members of other families of Ericales have mycorrhizae intermediate in form between ecto- and endomycorrhizae types, called ectendomycorrhizae. Arbustus and Arctostaphylos of Ericaceae show this type of mycorrhizal association. In Arbustus, the root system is differentiated into long and short roots. The short roots are swollen and covered by hyphal mantle. Hartig net is absent in this association, but intercellular coils develop in the outer cortical cells. Nothing is known about the fungi involved in this association. (5) Gentianoid mycorrhizae: Seedlings of some members of Gentianaceae (Biackstonia perfoliata, Gentianella amarella, etc.) get infected within 2 weeks of germination. In root, the cortical cells become full of irregular coils of aseptate hyphae. With time the hyphae become lysed. Vesicles are occasionally seen attached to these coils. (6) Orchidoid mycorrhizae: Orchids produce millions of tiny seeds per capsule, weighing about 0.3-14µg. The embryo of seeds contains 10-100 cells and there is virtually no storage of food. The embryo is encircled in a thin-walled net-like testa that helps in their dispersal. Thus, majority of seeds are unable to germinate without exogenous supply of carbohydrates. Therefore, mycorrhizal association is obligatory for the seeds to germinate. The fungus provides C-nutrition to the seeds.
  • 14. Initially the fungus enters the embryo and colonises, being restricted to the cortical cells and provides the nutrition (Fig. 4.106). For non-green orchids, this is obligatory throughout their lives. Apparently, it is a case of parasitism by orchids on the mycorrhizal fungi. Fungi like Rhizoctonia (Basidiomycotina), are recognised by hyphal characteristics. Corticium, Ceratobasidium etc., of Aphylloporales are associated in this type of mycorrhiza.
  • 15. (7) Monotropoid mycorrhizae: Monotropa hypopitys is a non-green saprophytic herb. It has short fleshy roots that are invested with a hyphal sheath and often forming Hartig net in the cortical zone. Due to absence of chlorophyll, they are unable to synthesise and supply carbohydrate to the fungus. Boletus is a mycorrhizal fungus asso- ciated with roots of both pine and Monotropa. When 14C glucose was injected into the phloem of Pinus trees, significant amount of radioactive glucose (14C) was recorded in Monotropa (but not in other herbs) after 5 days. This indicates that the fungus Boletus acts as a bridge between Monotropa and Pine plants. Similarly, 32P injected into Monotropa was also detected in Pine roots within 2 hours. The above facts indicate a bidirectional flow of nutrients between the plants through the fungus Boletus. Role of Mycorrhizae in Agriculture and Foresty: Role in Agriculture: 1. The mycorrhizal association helps in the formation of dichotomous branching and profuse root growth, thus enhances plant growth. 2. Ectotrophic mycorrhiza helps in uptake of mineral ions and also acts as reservoir. 3. They also help in absorption of nutrients. 4. In nutrient deficient soil, the mycelial association helps in the absorption of N, Ca, P, Zn, Fe, Na and others. 5. Mycorrhizal association is obligatory for the germination of orchid seeds. Mycorrhizal growth in orchids (Rhizoctonia repens with Orchis militaris tuber tissues) causes the synthesis of phytoalexins — orchinol and hirsinol. Both the compounds act as a barrier to protect infection by other pathogens. 6. Inoculation of VAM as biofertiliser provides a distinct possibility for the uptake of P in phosphorus- deficient soil.
  • 16. Role in Foresty: 1. Mycorrhiza plays an important role to establish forest in unfavourable location, barren land, waste lands etc. 2. Trees with facultative endomycorrhiza act as first invader in waste lands as pioneer in plant succession. 3. The application of mycorrhizal fungi in forest bed enhances the formation of mycorrhizal association that prevents the entry of fungal root pathogens. This method is very much effective in the root of Pinus clausa against Phytophthora cinnamoni infection. 4. Mycorrhiza mixed nitrogenous compounds such as nitrate; ammonia etc. is available to the plants. Thus it helps in plant growth, especially in acid soil. Thank you References: Online notes and Books by google search Engine