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*Corresponding author: Email: siddhant.ani@gmail.com;
Asian Journal of Advances in Agricultural Research
4(1): 1-5, 2017; Article no.AJAAR.38476
ISSN: 2456-8864
Spawned Casing vs Simple Casing
Siddhant1*
and O. P. Ukaogo2
1
Department of Botany, Durgesh Nandini Degree College, Faizabad (U.P.), India.
2
Envirnmental and Analytical Units, Department of Industrial Chemistry,
Abia State University, Nigeria.
Authors’ contributions
This work was carried out in collaboration between both authors. Author Siddhant designed the study,
performed the statistical analysis, wrote the protocol and wrote the first draft of the manuscript.
Authors Siddhant and OPU managed the analyses of the study. Author OPU managed the literature
searches. Both authors read and approved the final manuscript.
Article Information
DOI: 10.9734/AJAAR/2017/38476
Editor(s):
(1) Daniele De Wrachien, Professor, Department of Agricultural and Environmental Sciences,The State University of Milan,
Italy.
Reviewers:
(1) Hasan HĂĽseyin DoÄźan, Biology, Selcuk University,Turkey.
(2) Jayath P. Kirthisinghe, University of Peradeniya, Sri Lanka.
Complete Peer review History: http://www.sciencedomain.org/review-history/22292
Received 28th
November 2017
Accepted 7
th
December 2017
Published 14
th
December 2017
ABSTRACT
Effect of spawned and simple casing on the biological efficiency of pink oyster
mushroom Pleurotus eous was observed. The results exhibit that spawned casing not only takes
lesser time for case run but also produces early primordial development. A positive response on
mushroom biomass is also noticed in this technique.
Keywords: Simple casing; spawned casing; Pleurotus eous; yield; biological efficiency.
1. INTRODUCTION
The word 'casing' means covering of top of
mushroom beds with a layer of soil [1]. Though
the exact origin of this step in mushroom culture
is not known, yet its use seems to have been
more than two hundred year old. French were
first to find it essential to cover compost with a
casing layer, so as to stimulate vegetative
mycelium phase to encourage fruit [2]. It
regulates temperature and prevents quick drying
of spawned compost. It also gives mechanical
support to the mushroom sporophore. The
spawned casing technique was developed in
Original Research Article
Siddhant and Ukaogo; AJAAR, 4(1): 1-5, 2017; Article no.AJAAR.38476
2
Ireland during 1960’s and reported for the first
time by [3] in which small quantity of fully run
spawn/compost are added to casing medium
before spreading it over the mushroom beds.
This result in early pin head formation and
increase the yield [4]. This practice
is widely used for the cultivation of button
mushroom where pin is developed due to
nutritional stress provided by casing soil.
However, it is not necessary for oyster
mushroom cultivation where primordia develop
and economic optimum yield can be obtained
without using casing application. Present
investigation is an attempt to determine the effect
of spawned and simple casing on the biological
efficiency of pink oyster mushroom Pleurotus
eous.
2. MATERIALS AND METHODS
2.1 Mushroom Culture
The pure culture of Pleurotus eous was obtained
from the Mushroom Section of Plant Pathology
Department, Chandra Shekhar Azad University
of Agriculture and Technology, Kanpur (U.P.)
India. It was maintained on Potato Dextrose Agar
medium (peeled, sliced and boiled potato, 200 g;
dextrose, 20 g; agar, 20 g l
-1
) by using serial
subculture method [5].
2.2 Spawn Strategy
2.2.1 Spawn substrate
Wheat grain (Triticum aestivum) was used as a
spawn substrate which was purchased from the
seed market of Faizabad. The spawn was
prepared by the conventional method [5].
2.2.2 Spawn dose
Inoculation of substrate was made with spawn of
P. eous @ 15% w/w on dry weight basis under
aseptic conditions.
2.3 Substrate Preparation
The wheat straw substrate was collected
during threshing of harvested wheat crop by
avoiding pieces of leaf and leaf sheath
[6]. It was soaked in fresh water. When excess
water was drained off, it was then pasteurized in
the solution of Formaldehyde (500 ppm) and
Bavistin (75 ppm) for 18 hours as suggested by
[7].
2.4 Method of Cultivation
Plastic bag technology was employed in this
experiment. The beds were prepared from
pasteurized substrate by multilayered (3)
spawning following the procedure adopted by [8].
In this method, the wheat straw was placed at
the bottom of polythene bag. Later, a layer of
mushroom spawn was sprinkled. In the same
way, four layers of straw and three layer of
spawn were kept in the polythene bag. The
mouth of bags was then tightened with fibre
thread. The treatments were replicated thrice.
These bags were incubated in cultivation room at
22-30°C temperature for spawn run. Completely
colonized substrate was cased with casing
material. Watering was done at regular interval to
maintain moisture.
2.5 Casing Practise
2.5.1 Casing soil preparation
Farm yard manure and loam soil (1:1) were used
as casing materials, which were collected from
the village Madarahiya. These were properly
mixed to a uniform texture. The pH of mixture
was adjusted at 7.0-7.5 by addition of CaCO3. It
was then treated with 2% formaldehyde solution
and covered with the polythene sheet for next 72
hours. After this period, the mixture was
uncovered to remove the extra trace of
formaldehyde. It was then spread, collected and
store for use.
2.5.2 Casing application
Casing was applied on fully spawned run
substrate. It was achieved by following ways.
(1) Simple casing: In this method, the mouth
of bag was opened after completion of
spawn run which was then covered with 1-
1.25” thick layer of sterilized casing
material.
(2) Spawned casing: This was done by the
method suggested by [3]. In this method,
spawn was mixed to the casing soil @
0.1% (w/w) at the time of casing.
2.6 Concerning Data
2.6.1 Data regarding mushroom development
and yield parameters
It included time lapsed in spawn and case run,
fruit body initiation and maturation, number of
flushes, total yield, biological efficiency and
Siddhant and Ukaogo; AJAAR, 4(1): 1-5, 2017; Article no.AJAAR.38476
3
percent increase over control. The biological
efficiency of mushroom was worked out as
percentage yield of fresh mushroom in relation
to dry weight of the substrate as suggested by
[9].
2.6.2 Statistical analysis
Completely Randomized Design (CRD) was
followed for the experiment. The data were
statistically analysed by using the analysis of
veriance (ANOVA) at p= 5%. The critical
difference (CD) was worked out at five per cent
probability level.
3. RESULTS
3.1 Mushroom Development
All the sets took equal time (16 Days) for
substrate colonization from the date of spawning.
Once beds were fully covered with mushroom
mycelium, casing was applied. Spawned casing
seems to be significant in terms of early case
run. It took least time (20 Days) as compare to
simple casing (22 Days). Visual observations
regarding mycelia characters also indicated that
there was a compact mycelia growth with dense
strand in case of spawned casing. Results also
indicated that spawned casing produced early
sporophore production in comparison to simple
casing (Table 1).
3.2 Mushroom Yield
The crop of mushroom was harvested in three
flushes where yield and biological efficiency
ranged 344-354 gm, 68.8-70.8% in both the
casing techniques. Among them, spawned
casing gave higher yield and biological efficiency
(354 gm; 70.8%) over simple casing (344 gm;
68.8%), although, statistically both the casing
techniques were at par to each other, but if
choice is to be made between these, the
spawned casing was preferred over simple
casing due to early case run and primordial
development along with positive response on
mushroom biomass. The percent increase in
yield was also noticed in spawned cased beds
(Table 1).
Table 1. Effect of simple and spawned casing on various parameters of mushroom production
Casing Spawn
run
(days)
Case
run
(days)
Fruit
body
initiation
(days)
First
harvest
(days)
Total yield
from three
flushes
(gm/500 gm
dry substrate)
Biological
efficiency
(%)
%
increase
over
control
Spawned
casing
16 20 22 25 354 70.8 +2.90
Simple
casing
16 22 25 28 344 68.8 0.0
SE - 0.52 - - 4.86 0.97 -
CD
(P=0.05)
- 1.46 - - 13.51 2.70 -
Average of three replications
A) Spawned casing B) Simple casing
Plate 1. Effect of casing techniques on cropping of Pleurotus eous
Siddhant and Ukaogo; AJAAR, 4(1): 1-5, 2017; Article no.AJAAR.38476
4
4. DISCUSSION
In our investigation, spawned casing produced
early sporophore production in comparison to
simple casing. It was due to evenly distributed
inoculums in casing which equalized the mycelial
growth thorough out the casing [10] and ensured
all the mycelium on the bed surface at the same
stage of development and had equal access to
nutrients in the substrate [11] resulted early case
run and pin head formation in spawned casing
[4]. [12] suggested that specific bacterial
populations in the casing layer play an important
role in the formation of primordia and the
development of basidiome in P. ostreatus. It is
well established that casing in mushroom
cultivation has been principally associated with
aiding the change from the vegetative phase
(mycelium) to a reproductive one e.g. fruiting
[13]. In present investigation, spawned casing
produced higher mushroom biomass. Similar
observation has been made by [14,15,16] and
[17] who reported higher yield of oyster
mushroom from cased substrate.
5. CONCLUSION
Pleurotus eous is one of the edible mushrooms
that can be cultivated throughout the seasons in
different climatic zones of India except arid and
semi-arid regions. Simple cultivation technology,
low capital input, attractive fruit-bodies and long
shelf life are some of the qualities which
makes it a better choice for mushroom growers
and also consumers. The spawned casing
results early commencement of this mushroom
which simplifies the management of pre-fruiting
period. This technique has also a potential of
increasing the biological efficiency of mushroom
and to get early crop over simple casing.
COMPETING INTERESTS
Authors have declared that no competing
interests exist.
REFERENCES
1. Kaul TN. Casing. Indian Mushroom
Science. 1978;1:147-164.
2. Peerally A. Sporophore initiation in Agricus
bisphorus and Agricus bitorquis in relation
to bacteria and activated charcoal.
Mushroom Science. 1979;10:611–639.
3. MacCanna C, Flanagan JB. Casing type
and techniques. Mushroom Science. 1972;
8:727-731.
4. Shandilya TR, Seth PK, Munjal RL, Guleria
DS. Treating casing soil with steam +
benlate for better yield of mushrooms.
Indian Journal of Mycology and Plant
Pathology. 1976;6:5-7.
5. Naraian R, Sahu RK, Kumar S, Garg
SK, Singh CS, Kanaujia RS. Influence
of different nitrogen rich supplements
during cultivation of Pleurotus florida on
corn cob substrate. Environmentalist.
2009;29:1-7.
6. Siddhant, Yadav S, Ahmad A, Singh CS.
Effect of wheat straw component on
yield of Pleurotus eous. International
Journal of Current Microbiology and
Applied Sciences. 2013;2(8):221-225.
7. Vijay B, Sohi HS. Cultivation of Oyster
mushroom Pleurotus sajor-caju (Fr.)
Singer on chemically sterilized wheat
straw. Mushroom Journal for the Tropics.
1987;7:67-75.
8. Bano Z. Cultivation of Pleurotus flabellatus.
Second International Symposium on Plant
Pathology Held at IARI, New Delhi. 1971;
135.
9. Chang ST, Miles PG. Edible mushrooms
and their cultivation. Boca Raton: CRC
Press. 1989;256-274.
10. MacCanna C. Spawned casing. Mushroom
Journal. 1983;129:329-333.
11. Gupta Y, Vijay B, Sohi HS. Spawned
casing: Effect on yield of Agaricus bisporus
(Lang) Sing. Indian Journal of Mycology
and Plant Pathology. 1989;19(2):225-227.
12. Cho YS, Weon HY, Joh JO, Lim JH, Kim
KY, Son ES, et al. Effect of casing layer on
growth promotion of the edible mushroom
Pleurotus ostreatus. Mycobiology. 2008;
36(1):40-44.
13. Hayes WA, Nair HG. The cultivation of
Agaricus bisporus and other edible
mushroom. In: Smith JE, Berry OR,
editors. The Filamentous Fungi. London:
Edward Arnold; 1975.
14. Okhuoya JA, Okogbo FO. Cultivation of
Pleurotus tuber-regium (Fr.) Sing on
various farm wastes. Proc. Okla. Acad.
Sci. 1991;71:1-3.
15. Rodriguez Estrada AE, Del Mar Jimenez
Gasco M, Royse DJ. Improvement of yield
of Pleurotus eryngii var. eryngii by
substrate supplementation and use of a
casing overlay. Bioresource Technology.
2009;100:5270–5276.
16. Eslaminezhad Z, Emaratpardaz J,
Panahandeh J. The effect of nutritional
supplement addition and use of casing
Siddhant and Ukaogo; AJAAR, 4(1): 1-5, 2017; Article no.AJAAR.38476
5
overlay to substrate on yield of oyster
mushroom (Pleurotus florida). International
Journal of Agronomy and Agricultural
Research. 2015;7(4):61-67.
17. Olfati JA, Rasouli F. Casing with leached
vermicompost improve oyster mushroom
biological efficiency. Iran Agricultural
Research. 2016;35(1):33-40.
© 2017 Siddhant and Ukaogo; This is an Open Access article distributed under the terms of the Creative Commons Attribution
License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any
medium, provided the original work is properly cited.
Peer-review history:
The peer review history for this paper can be accessed here:
http://sciencedomain.org/review-history/22292

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Spawned Casing vs Simple Casing

  • 1. _____________________________________________________________________________________________________ *Corresponding author: Email: siddhant.ani@gmail.com; Asian Journal of Advances in Agricultural Research 4(1): 1-5, 2017; Article no.AJAAR.38476 ISSN: 2456-8864 Spawned Casing vs Simple Casing Siddhant1* and O. P. Ukaogo2 1 Department of Botany, Durgesh Nandini Degree College, Faizabad (U.P.), India. 2 Envirnmental and Analytical Units, Department of Industrial Chemistry, Abia State University, Nigeria. Authors’ contributions This work was carried out in collaboration between both authors. Author Siddhant designed the study, performed the statistical analysis, wrote the protocol and wrote the first draft of the manuscript. Authors Siddhant and OPU managed the analyses of the study. Author OPU managed the literature searches. Both authors read and approved the final manuscript. Article Information DOI: 10.9734/AJAAR/2017/38476 Editor(s): (1) Daniele De Wrachien, Professor, Department of Agricultural and Environmental Sciences,The State University of Milan, Italy. Reviewers: (1) Hasan HĂĽseyin DoÄźan, Biology, Selcuk University,Turkey. (2) Jayath P. Kirthisinghe, University of Peradeniya, Sri Lanka. Complete Peer review History: http://www.sciencedomain.org/review-history/22292 Received 28th November 2017 Accepted 7 th December 2017 Published 14 th December 2017 ABSTRACT Effect of spawned and simple casing on the biological efficiency of pink oyster mushroom Pleurotus eous was observed. The results exhibit that spawned casing not only takes lesser time for case run but also produces early primordial development. A positive response on mushroom biomass is also noticed in this technique. Keywords: Simple casing; spawned casing; Pleurotus eous; yield; biological efficiency. 1. INTRODUCTION The word 'casing' means covering of top of mushroom beds with a layer of soil [1]. Though the exact origin of this step in mushroom culture is not known, yet its use seems to have been more than two hundred year old. French were first to find it essential to cover compost with a casing layer, so as to stimulate vegetative mycelium phase to encourage fruit [2]. It regulates temperature and prevents quick drying of spawned compost. It also gives mechanical support to the mushroom sporophore. The spawned casing technique was developed in Original Research Article
  • 2. Siddhant and Ukaogo; AJAAR, 4(1): 1-5, 2017; Article no.AJAAR.38476 2 Ireland during 1960’s and reported for the first time by [3] in which small quantity of fully run spawn/compost are added to casing medium before spreading it over the mushroom beds. This result in early pin head formation and increase the yield [4]. This practice is widely used for the cultivation of button mushroom where pin is developed due to nutritional stress provided by casing soil. However, it is not necessary for oyster mushroom cultivation where primordia develop and economic optimum yield can be obtained without using casing application. Present investigation is an attempt to determine the effect of spawned and simple casing on the biological efficiency of pink oyster mushroom Pleurotus eous. 2. MATERIALS AND METHODS 2.1 Mushroom Culture The pure culture of Pleurotus eous was obtained from the Mushroom Section of Plant Pathology Department, Chandra Shekhar Azad University of Agriculture and Technology, Kanpur (U.P.) India. It was maintained on Potato Dextrose Agar medium (peeled, sliced and boiled potato, 200 g; dextrose, 20 g; agar, 20 g l -1 ) by using serial subculture method [5]. 2.2 Spawn Strategy 2.2.1 Spawn substrate Wheat grain (Triticum aestivum) was used as a spawn substrate which was purchased from the seed market of Faizabad. The spawn was prepared by the conventional method [5]. 2.2.2 Spawn dose Inoculation of substrate was made with spawn of P. eous @ 15% w/w on dry weight basis under aseptic conditions. 2.3 Substrate Preparation The wheat straw substrate was collected during threshing of harvested wheat crop by avoiding pieces of leaf and leaf sheath [6]. It was soaked in fresh water. When excess water was drained off, it was then pasteurized in the solution of Formaldehyde (500 ppm) and Bavistin (75 ppm) for 18 hours as suggested by [7]. 2.4 Method of Cultivation Plastic bag technology was employed in this experiment. The beds were prepared from pasteurized substrate by multilayered (3) spawning following the procedure adopted by [8]. In this method, the wheat straw was placed at the bottom of polythene bag. Later, a layer of mushroom spawn was sprinkled. In the same way, four layers of straw and three layer of spawn were kept in the polythene bag. The mouth of bags was then tightened with fibre thread. The treatments were replicated thrice. These bags were incubated in cultivation room at 22-30°C temperature for spawn run. Completely colonized substrate was cased with casing material. Watering was done at regular interval to maintain moisture. 2.5 Casing Practise 2.5.1 Casing soil preparation Farm yard manure and loam soil (1:1) were used as casing materials, which were collected from the village Madarahiya. These were properly mixed to a uniform texture. The pH of mixture was adjusted at 7.0-7.5 by addition of CaCO3. It was then treated with 2% formaldehyde solution and covered with the polythene sheet for next 72 hours. After this period, the mixture was uncovered to remove the extra trace of formaldehyde. It was then spread, collected and store for use. 2.5.2 Casing application Casing was applied on fully spawned run substrate. It was achieved by following ways. (1) Simple casing: In this method, the mouth of bag was opened after completion of spawn run which was then covered with 1- 1.25” thick layer of sterilized casing material. (2) Spawned casing: This was done by the method suggested by [3]. In this method, spawn was mixed to the casing soil @ 0.1% (w/w) at the time of casing. 2.6 Concerning Data 2.6.1 Data regarding mushroom development and yield parameters It included time lapsed in spawn and case run, fruit body initiation and maturation, number of flushes, total yield, biological efficiency and
  • 3. Siddhant and Ukaogo; AJAAR, 4(1): 1-5, 2017; Article no.AJAAR.38476 3 percent increase over control. The biological efficiency of mushroom was worked out as percentage yield of fresh mushroom in relation to dry weight of the substrate as suggested by [9]. 2.6.2 Statistical analysis Completely Randomized Design (CRD) was followed for the experiment. The data were statistically analysed by using the analysis of veriance (ANOVA) at p= 5%. The critical difference (CD) was worked out at five per cent probability level. 3. RESULTS 3.1 Mushroom Development All the sets took equal time (16 Days) for substrate colonization from the date of spawning. Once beds were fully covered with mushroom mycelium, casing was applied. Spawned casing seems to be significant in terms of early case run. It took least time (20 Days) as compare to simple casing (22 Days). Visual observations regarding mycelia characters also indicated that there was a compact mycelia growth with dense strand in case of spawned casing. Results also indicated that spawned casing produced early sporophore production in comparison to simple casing (Table 1). 3.2 Mushroom Yield The crop of mushroom was harvested in three flushes where yield and biological efficiency ranged 344-354 gm, 68.8-70.8% in both the casing techniques. Among them, spawned casing gave higher yield and biological efficiency (354 gm; 70.8%) over simple casing (344 gm; 68.8%), although, statistically both the casing techniques were at par to each other, but if choice is to be made between these, the spawned casing was preferred over simple casing due to early case run and primordial development along with positive response on mushroom biomass. The percent increase in yield was also noticed in spawned cased beds (Table 1). Table 1. Effect of simple and spawned casing on various parameters of mushroom production Casing Spawn run (days) Case run (days) Fruit body initiation (days) First harvest (days) Total yield from three flushes (gm/500 gm dry substrate) Biological efficiency (%) % increase over control Spawned casing 16 20 22 25 354 70.8 +2.90 Simple casing 16 22 25 28 344 68.8 0.0 SE - 0.52 - - 4.86 0.97 - CD (P=0.05) - 1.46 - - 13.51 2.70 - Average of three replications A) Spawned casing B) Simple casing Plate 1. Effect of casing techniques on cropping of Pleurotus eous
  • 4. Siddhant and Ukaogo; AJAAR, 4(1): 1-5, 2017; Article no.AJAAR.38476 4 4. DISCUSSION In our investigation, spawned casing produced early sporophore production in comparison to simple casing. It was due to evenly distributed inoculums in casing which equalized the mycelial growth thorough out the casing [10] and ensured all the mycelium on the bed surface at the same stage of development and had equal access to nutrients in the substrate [11] resulted early case run and pin head formation in spawned casing [4]. [12] suggested that specific bacterial populations in the casing layer play an important role in the formation of primordia and the development of basidiome in P. ostreatus. It is well established that casing in mushroom cultivation has been principally associated with aiding the change from the vegetative phase (mycelium) to a reproductive one e.g. fruiting [13]. In present investigation, spawned casing produced higher mushroom biomass. Similar observation has been made by [14,15,16] and [17] who reported higher yield of oyster mushroom from cased substrate. 5. CONCLUSION Pleurotus eous is one of the edible mushrooms that can be cultivated throughout the seasons in different climatic zones of India except arid and semi-arid regions. Simple cultivation technology, low capital input, attractive fruit-bodies and long shelf life are some of the qualities which makes it a better choice for mushroom growers and also consumers. The spawned casing results early commencement of this mushroom which simplifies the management of pre-fruiting period. This technique has also a potential of increasing the biological efficiency of mushroom and to get early crop over simple casing. COMPETING INTERESTS Authors have declared that no competing interests exist. REFERENCES 1. Kaul TN. Casing. Indian Mushroom Science. 1978;1:147-164. 2. Peerally A. Sporophore initiation in Agricus bisphorus and Agricus bitorquis in relation to bacteria and activated charcoal. Mushroom Science. 1979;10:611–639. 3. MacCanna C, Flanagan JB. Casing type and techniques. Mushroom Science. 1972; 8:727-731. 4. Shandilya TR, Seth PK, Munjal RL, Guleria DS. Treating casing soil with steam + benlate for better yield of mushrooms. Indian Journal of Mycology and Plant Pathology. 1976;6:5-7. 5. Naraian R, Sahu RK, Kumar S, Garg SK, Singh CS, Kanaujia RS. Influence of different nitrogen rich supplements during cultivation of Pleurotus florida on corn cob substrate. Environmentalist. 2009;29:1-7. 6. Siddhant, Yadav S, Ahmad A, Singh CS. Effect of wheat straw component on yield of Pleurotus eous. International Journal of Current Microbiology and Applied Sciences. 2013;2(8):221-225. 7. Vijay B, Sohi HS. Cultivation of Oyster mushroom Pleurotus sajor-caju (Fr.) Singer on chemically sterilized wheat straw. Mushroom Journal for the Tropics. 1987;7:67-75. 8. Bano Z. Cultivation of Pleurotus flabellatus. Second International Symposium on Plant Pathology Held at IARI, New Delhi. 1971; 135. 9. Chang ST, Miles PG. Edible mushrooms and their cultivation. Boca Raton: CRC Press. 1989;256-274. 10. MacCanna C. Spawned casing. Mushroom Journal. 1983;129:329-333. 11. Gupta Y, Vijay B, Sohi HS. Spawned casing: Effect on yield of Agaricus bisporus (Lang) Sing. Indian Journal of Mycology and Plant Pathology. 1989;19(2):225-227. 12. Cho YS, Weon HY, Joh JO, Lim JH, Kim KY, Son ES, et al. Effect of casing layer on growth promotion of the edible mushroom Pleurotus ostreatus. Mycobiology. 2008; 36(1):40-44. 13. Hayes WA, Nair HG. The cultivation of Agaricus bisporus and other edible mushroom. In: Smith JE, Berry OR, editors. The Filamentous Fungi. London: Edward Arnold; 1975. 14. Okhuoya JA, Okogbo FO. Cultivation of Pleurotus tuber-regium (Fr.) Sing on various farm wastes. Proc. Okla. Acad. Sci. 1991;71:1-3. 15. Rodriguez Estrada AE, Del Mar Jimenez Gasco M, Royse DJ. Improvement of yield of Pleurotus eryngii var. eryngii by substrate supplementation and use of a casing overlay. Bioresource Technology. 2009;100:5270–5276. 16. Eslaminezhad Z, Emaratpardaz J, Panahandeh J. The effect of nutritional supplement addition and use of casing
  • 5. Siddhant and Ukaogo; AJAAR, 4(1): 1-5, 2017; Article no.AJAAR.38476 5 overlay to substrate on yield of oyster mushroom (Pleurotus florida). International Journal of Agronomy and Agricultural Research. 2015;7(4):61-67. 17. Olfati JA, Rasouli F. Casing with leached vermicompost improve oyster mushroom biological efficiency. Iran Agricultural Research. 2016;35(1):33-40. © 2017 Siddhant and Ukaogo; This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Peer-review history: The peer review history for this paper can be accessed here: http://sciencedomain.org/review-history/22292