Questions and Answers About Mycorrhiza
Questions and Answers About Mycorrhiza
Answer:
There are two main types of Mycorrhiza according to Ianson (2014):
ectomycorrhizae (ECM) and arbuscular mycorrhizae (AM).
a. Ectomycorrhizae (ECM) :
The ECM association is specific to roots of trees such as
birches, willows, pines, oaks and spruces. The fungi physically connect
with the roots of the host plant, improving the plants ability to take up
water and nutrients. They also form a sheath, or mantle, around the root,
which physically protects the root from some types of disease-causing
fungi. According to Muchovej (2001), Ectomycorrhizal inoculum is
easily produced for application in forest nurseries.
b. Arbuscular Mycorrhizae (AM):
The AM relationship affects both perennials and annuals. This
mycorrhizae is belonging to the Phylum Glomeromycota are symbionts
with terrestrial plant roots. It is now generally recognized that they
improve not only the phosphorus nutrition of the host plant but also its
growth, which may result in an increase in resistance to drought stress
and some diseases.
The main difference between the AM and ECM relationship is
that the AM relationship does not create a protective mantle around the
root the way the ECM relationship does. Instead, its hyphae enter the
plant cells, producing structures that facilitate water and nutrient uptake
by the plant. One way to spread AM fungi is to collect root tissue and
the soil immediately surrounding the root from a host plant that is
known to have the AM fungi and incorporate it into the soil of the new
plant. Management of arbuscular mycorrhizae focuses on maintaining
soil conditions favoring the fungi rather than constantly adding more
fungi-colonized tissue to the host plant. Establishing a successful
mycorrhizal relationship can be difficult because some of the species of
fungi may be site specific. But the necessity of AM inoculum
production via a host plant is still an obstacle to ample utilization of
AM fungi in agricultural crops as said by Muchovej (2001).
c. Orchid mycorrhizae
Orchid mycorrhizas are mutualistic interactions between fungi
and members of the Orchidaceae, the worlds largest plant family. The
majority of the worlds orchids are photosynthetic, a small number of
species are myco-heterotrophic throughout their lifetime, and recent
research indicates a third mode (mixotrophy) whereby green orchids
supplement their photosynthetically fixed carbon with carbon derived
from their mycorrhizal fungus. Molecular identification studies of
orchid-associated fungi indicate a wide range of fungi might be orchid
mycobionts, show common fungal taxa across the globe, and support
the view that some orchids have specific fungal interactions.
Confirmation of mycorrhizal status requires isolation of the fungi and
restoration of functional mycorrhizas. New methods may now be used
to store orchid-associated fungi, and store and germinate seed, leading
to more efficient culture of orchid species. However, many orchid
mycorrhizas must be synthesised before conservation of these
associations can be attempted in the field.
According to Dearnaley et al (2012) Orchid mycorrhizas are
predominantly represented by associations between photosynthetic
plants and rhizoctonia fungi. These associations, which likely
represent the plesiomorphic condition for orchids, gave rise through
repeated evolutionary shifts to interactions with other diverse fungal
lineages and diversification of orchid metabolism. How orchids recruit
and allow new fungi (even some nave fungi from non-mycorrhizal
clades) to enter the dual morphogenesis of mycorrhizas remains unclear.
However, orchid mycorrhizas are excellent models to reveal the general
properties of mycorrhizal systems as well as providing insights into the
fungal world via specificity aspects, ecological networks and evolution
of the mycorrhizal state.
d. Arbutoid mycorrhizae: Found in Californias chaparral plants.
e. Ericoid mycorrhizae:
According to Straker (1996), the ericoid mycorrhiza has been
regarded as the most specific of mycorrhizas because of its limitation to
b. Ectomychorriza
The hartig net is
formed by an ingrowth
of hyphae (often originating from the inner part of the surrounding
mantle) into the root of the plant host. The hyphae making up the Hartig
net penetrate and grow in a transverse direction to the axis of the
root, and thus form a network between the outer cells of the root axis.
This region of juxtaposition is where nutrient and carbon exchange
occurs.
Enveloping the root, and often containing more biomass than the
Hartig net interface, is a hyphal sheath known as the mantle. There
exists considerable variation in the structure of the mantle, ranging from
a loose network of hyphae to a structured and stratified arrangement of
tissue. Often, these layers resemble plant parenchyma tissue and are
referred to as pseudoparenchymatous
Extraradical hyphae extend outward from the mantle into
the soil, fulfilling the role of the suppressed root hairs by increasing the
surface area of the colonized root. These hyphae can spread out singly,
or in an aggregate arrangement known collectively as a rhizomorph.
Much as the Hartig net and mantle, composite hyphal organs can
display a wide range of structural difference. Some rhizomorphs are
simply parallel, linear collections of hyphae. Others yield more
complex organization such as aggregates where the central hyphae
possess enlarged diameters, or exhibiting apically extending hyphae
that superficially resemble meristematic activity.
Arranged by :
By:
E. A Lintang Wardyani ( H0713059)