Upload
shyleshnair
View
42
Download
2
Embed Size (px)
Citation preview
Production of vermifertilizer from guar gum industrial wastesby using composting earthworm Perionyx sansibaricus (Perrier)
Surendra Suthar
Published online: 6 July 2007
� Springer Science+Business Media, LLC 2007
Abstract Efforts have been made to convert the guar gum
industrial waste into a value-added product, by employing a
new earthworm species for vermicomposting e.g. Perionyx
sansibaricus (Perrier) (Megascolecidae), under laboratory
conditions. Industrial lignocellulosic waste was amended
with other organic supplements (saw dust and cow dung);
and three types of vermibeds were prepared: guar gum
industrial waste + cow dung + saw dust in 40: 30: 30 ratio
(T1), guar gum industrial waste + cow dung + saw dust in
60: 20: 20 ratio (T2,), and guar gum industrial waste + cow
dung + saw dust in 75: 15: 10 ratio (T3). As compared to
initial concentrations, vermicomposts exhibited a decrease
in organic C content (5.0–11.3%) and C:N ratio (11.1–
24.4%) and an increase in total N (18.4–22.8%), available P
(39.7–92.4%), and exchangeable K (9.4–19.7%) contents,
after 150 days of vermicomposting. A vermicomposting
coefficient (VC) was used to compare of vermicomposting
with the experimental control (composting). P. sansibaricus
exhibited maximum value of mean individual live weight
(742.8 ± 21.1 mg), biomass gain (442.94 ± 21.8 mg),
growth rate (2.95 ± 0.15 mg day–1), cocoon numbers
(96.0 ± 5.1) and reproduction rate (cocoons worm–1 day–1)
(0.034 ± 0.001) in T2 treatment. In T3 maximum mortality
(30.0 ± 4.01 %) in earthworm population was observed.
Overall, T2 vermibed appeared as an ideal substrate to
manage guar gum industrial waste effectively. Vermicom-
posting can be proposed as a low-input basis technology to
convert industrial waste into value-added biofertilizer.
Keywords Earthworm � Vermicomposting � Perionyx
sansibaricus � Industrial waste � Cocoon � Cow dung �Saw dust
1 Introduction
Agriculture, food-processing, pulp and paper, or any cel-
lulose-based industry produces massive quantities of solid
and liquid waste materials. Disposal and environmental
friendly management of these industrial wastes has become
a serious global problem. The traditional disposal methods
such as open dumping and or/land filling practices of these
materials is not only increasingly expensive, but imprac-
tical as open space becomes limited. Therefore, in recent
years the focus has been to develop low input eco-friendly
technologies to manage industrial waste resources. Some
agro-industrial wastes contain a large amount of plant
nutrients. These materials can be utilized efficiently as soil
conditioner for sustainable soil fertility management by
converting the waste to a resource.
Some species of epigeic earthworms can live in decay-
ing organic waste materials and convert it to odor free, fine
particulate materials high in available nutrient (Marsh
et al., 2005; Suthar 2006; 2007a). Earthworm accelerates
the transformation of organic waste material into more
stabilized forms by aeration and bioturvation, by their
excreta and qualitative or quantitative influence upon the
telluric microflora (Vinceslas-Akpa and Loquest 1997).
The utility of epigeic earthworms for successful degrada-
tion of organic wastes is well documented for different
industries such as: paper and pulp (Elvira et al. 1997;
1998); dairy (Gratelly et al. 1996); sugar processing (Kale
1998; Reddy and Shantaram 2005); winery and distillery
(Nogales et al. 2005); wood and wood chips (Maboeta and
S. Suthar (&)
Environmental Biology Lab, Post Graduate Department
of Zoology, S.G.N. Khalsa (PG) College, Sri Ganganagar,
Rajasthan 335 001, India
e-mail: [email protected]
123
Environmentalist (2007) 27:329–335
DOI 10.1007/s10669-007-9032-9
van Rensburg 2003); textile mills (Kaushik and Garg 2004;
Garg and Kaushik 2005); oil (Benitez et al. 2002) and
power (fly ash) (Gupta et al. 2005). However, compared to
thermal composting, vermicomposting with earthworms
often produces a product with a lower mass, lower pro-
cessing time, humus content, phytotoxicity is less likely,
more N is released, fertilizer value is usually greater, and
an additional product (earthworms), which can have other
uses is produced (Lorimor et al. 2001). Therefore, vermi-
composting seems to be more appropriate and an efficient
technology to convert industrial waste to a valuable com-
munity resources at low input basis.
However, the composting efficiency and biology of only
a few epigeic earthworm species has been studied e.g.
Eisenia foetida (Maboeta and van Rensburg 2003; Kaushik
and Garg 2004; Gupta et al. 2005), E. andrei (Elvira et al.
1997, 1998; Nogales et al. 2005; Benitez et al. 2002) and
Eudrilus eugeniae (Kale 1998). Unfortunately, the poten-
tial of some commonly distributed tropical earthworms
for industrial waste degradation has not been explored.
Perionyx sansibaricus (Perrier) is an epigeic earthworm,
considered endemic to Indian soils, and commonly dis-
tributed in many natural soil ecosystems. Recently Suthar
(2007a) reported on the vermicomposting potential of this
species to address issue of waste generated from different
industries i.e. crop residues, animal dung from dairy,
household waste, municipal waste.
The guar gum is an agricultural based industrial product. It
is mainly acquired from a cereal plant i.e. Cyamposis tetrag-
onoloba Linn. There are more than 2000 guar gum industrial
units only in Rajasthan State, India producing guar gum
for use in pharmaceutical and chemical industries. These
guar gum industries are producing a great quantity of lingo-
cellulogic waste material, that could be transformed from an
expensive disposal problem to suitable vermistabilised humus
for food production and soil restoration.
The objectives of this study were, to test the potential
of a new earthworm species for vermicomposting i.e.
P. sansibaricus (Perrier) to manage industrial waste
resources and to establish an appropriate technology (ver-
mitechnolgy) to manage the lignocelluloses waste gener-
ated from a guar gum industry. Ultimately, we wanted to
produce vermicompost of high nutritive value, with a
sustainable population of earthworm.
2 Materials and methods
2.1 Earthworm culture
The Perionyx sansibaricus (Perrier) (Oligochaeta, Megas-
colecidae) used in this study were collected from a
sewage sludge situated in Nehru garden, Jodhpur city,
India. Collected worms were brought to the laboratory in
plastic circular containers, and were cultured on partially
composted organic material (cow dung mixed with leaf
litter of Mangifera indica). When the population reached a
sufficient size (after one months), the earthworms were
used for experimentation.
2.2 Industrial waste and other supplement material
The industrial waste was collected from Rajasthan Guar gum
Ltd., RICCO Industrial Area, Jodhpur, India. It was collected
in large plastic containers and brought to the laboratory. The
main characteristics of guar gum industrial waste were: 7.10
pH, 454.46 g kg–1 organic C, 28.17 g kg–1 total N,
15.6 g kg–1 available P, 3.92 g kg–1 exchangeable K, and
16.2 C:N ratio. The excess moisture was removed by shade
drying for about 3 days. After shade drying, material was
dried at 60�C in hot air oven, chopped and sieved (<2 mm).
The Cow dung was obtained from Boranada Dairy Farm,
Ghanchi Colony, Jodhpur, India. The saw dust used was
collected from Jodhpur Timbers, RICCO industrial area,
Jodhpur, India. These materials were chopped and sieved and
shade dried prior to use in vermicomposting trials.
2.3 Vermicomposting experimental
Plastic circular containers (28 cm diameter and 30 cm in
depth) with pierced lids for aeration were used for labo-
ratory screening of guar gum industrial wastes. The guar
gum industrial waste was mixed with the supplements (saw
dust and cow dung) in different ratios to provide three
treatments (Table 1). The organic substrate served as
bedding as well as food for the earthworms. Experimental
beddings were kept in triplicate for each treatment, and
same another triplicate for each treatment without earth-
worms served as the experimental control. All beddings
were kept for 2 weeks prior to experimentation for thermal
stabilization, initiation of microbial degradation and soft-
ening of waste. Twenty 4-wk old clitellate, P. sansibaricus
(live weight of individual �300 mg) were collected from
the stock culture and released into different containers
containing 750 g (on dry weight basis) of substrate mate-
rial. The moisture level of containers was maintained about
65–70%, throughout the study period by periodic sprin-
kling of adequate quantity of tap water. To prevent mois-
ture loss, the experimental pots were covered with paddy
straw. Containers were placed in a humid and dark room at
a temperature 26.3 ± 0.39�C (average of the temperature
recorded during experimental duration ± SEm). Vermibeds
were analyzed for chemical changes (organic C, total N,
available P, exchangeable K and C:N ratio) after each
30 day interval up to 150 days. Different growth parame-
ters like earthworm biomass; total cocoon production and
330 Environmentalist (2007) 27:329–335
123
total mortality in different experimental containers were
measured at the same interval.
The vermicomposting coefficients for different chemical
parameters were calculated by following formula (Suthar 2006):
2.4 Chemical analysis
The chemical parameters of the bedding material (Table 2)
and vermicompost produced during experiment were ana-
lyzed by using standard methods. Organic carbon was
determined by the partially-oxidation method (Walkley and
Black 1934). Total Kjeldhal nitrogen was measure by
following method as described by Anderson and Ingram
(1993). Potassium was determined after extracting the
sample using ammonium acetate and analyzing of with a
Perkin-Elmer model 3110 double beam atomic absorption
spectrophotometer (AAS).
2.5 Statistical analysis
One-way ANOVA procedures were applied to the data to
determine significant differences. Duncan’s multiple-ran-
ged test was also performed to identify the homogeneous
type of the treatments for the various assessment variables.
These variables included chemical properties and earth-
worm growth parameters (earthworm weight gain, indi-
vidual growth rate, total cocoons numbers, cocoon
production rate, and total population mortality.
3 Results and discussions
3.1 Chemical changes during vermicomposting
As summarized in Table 3, the vermicomposting process
caused significant changes (P < 0.01) in the chemistry of
the three treatments, after 150 days of experimentation. As
compared to the initial values (Table 2), pH of the substrate
declined in the order 10.53% (T3) > 6.39% (T2) > 2.83%
(T1). As compared to control bedding vermicomposted
material showed about 664.9, 231.1 and 1383.1 % more
reduction in pH values of the T1, T2 and T3 treatment,
respectively. It is concluded that the shifting in pH could be
attributed to microbial decomposition during the process of
vermicomposting. Elvira et al. (1998) suggested that pro-
duction of CO2 and organic acids by microbial decompo-
sition during vermicomposting lowers the pH of substrate.
Similarly, Ndegwa et al. (2000) pointed out that shifting of
pH could be related to the mineralization of the nitrogen and
phosphorous into nitrites/nitrates and orthophosphates and
Table 1 Composition of experimental bedding
Treatment Treatment description Guar gum industrial
waste (g)
Cow dung
(g)
Saw dust
(g)
T1 GIWa (40%)d + CDb (30%) + SDc (30%) 300.0 225.0 225.0
T2 GIWa (60%)c + CDb (20%) + SD (20%) 450.0 150.0 150.0
T3 GIWa (75%)c + CDb (15%) + SD (10%) 562.5 112.5 75.0
a Guar gum industrial waste (GIW)b Cow dung (CD)c Saw dust (SD)d The figures in parentheses indicates the percent content in the initial substrate material
Table 2 Chemical composition (g kg–1) of different treatments (n = 3, mean ± SEm) used for experiment
Treatment pH Organic C Total N Available P Exchangeable K C:N ratio C:P ratio
T1* 8.12 ± 0.8 481.9 ± 1.1 15.4 ± 0.1 2.5 ± 0.0 11.5 ± 0.2 31.3 ± 0.1 192.0 ± 1.4
T1* 8.29 ± 0.2 463.3 ± 0.5 19.8 ± 0.1 2.6 ± 0.2 15.6 ± 0.4 23.4 ± 0.4 175.5 ± 1.2
T3* 8.45 ± 0.3 436.4 ± 0.8 20.1 ± 0.1 2.8 ± 0.2 18.6 ± 0.3 18.9 ± 0.1 154.6 ± 0.6
* Refer to Table 1, for explanation of treatments
VC ¼ Total increase=decrease in during vermicomposting ðtreatmentÞTotal increase=decrease in during composting ðcontrolÞ
Environmentalist (2007) 27:329–335 331
123
bioconversion of the organic material into intermediate
species of the organic acids. In T3 mortality of worms
occurred and highly contributed to the pH shift possibly due
to higher content of ammonium N. Earthworm tissues may
be efficient source of nitrogen when cells lyses.
Vermicomposting decreased organic C content in the
three treatments. Comparatively organic C loss (as com-
pared to the initial levels (Table 2)) was 11.3% in
T2 treatment, 10.42% in T1, and 4.98% in T3 treatments.
Vermicomposting efficiency of P. sansibaricus was also
evaluated by using a vermicomposting coefficient (VC).
VCcarbon was highest in T3 (Table 4). Vermicomposting
refers to the breakdown of organic matter by earthworm
and subsequent microbial degradation. Earthworm modify
substrate conditions, which consequently affects carbon
losses from substrates through microbial respiration in the
form of CO2 and even through mineralization of organic C.
Body fluids and excreta, secreted by earthworms, (e.g.
mucous, high concentration of organic matter, ammonium
and urea) promote microbial communities in vermicom-
posting sub-system. Earthworm activity significantly
decrease organic C levels in waste and accelerates waste
stabilization process (Suthar 2006, 2007a; Garg and
Kaushik 2004).
At the end of the experiment, the total N content in
vermicompost was higher than that in the initial material.
Comparatively the maximum increase in total N content
occurred in T3 (22.81%), followed by T1 (18.42%), and T2
treatment (22.81%) (Table 3). Vermicomposting coeffi-
cient for total N (VCnitrogen) was highest in T1 treatment
(Table 4). Earthworms enrich the vermibed with nitrogen
through excretory products, mucous, enzymes, and growth
stimulating hormones and even by decaying earthworm
tissue after their death. Studies revealed that decomposition
of organic material by earthworms accelerates the N min-
eralization process and subsequently changes the N profile
of the substrate (Elvira et al. 1997; Benitez et al. 2002;
Suthar 2007a). However, the greater concentration of total
N in T3 treatment was not related to decomposition or
nitrification activity. It was related more likely to the
higher earthworm mortality that enriched the bedding with
N content due to decaying earthworm tissue. In general,
earthworm contains about 60–70% (of dry mass) protein in
their body tissue, and this pool of N returned to the soil
upon mineralization. Satchell (1967) reported that over
70% of the N in the tissues of dead earthworm was min-
eralized in less than 20 days. However, decomposition
activities and nitrogen enrichment by earthworms also
depend upon the quality of the substrate material.
After vermicomposting, all vermibeds showed higher
concentrations of available P in end product. Available P
was highest in T2 treatment (92.42% increase) followed by
T1 (54.98%) and T3 (39.72%) (Table 3). According to LeeTa
ble
3C
hem
ical
com
po
siti
on
of
con
tro
l(c
om
po
st)
and
exp
erim
ent
(ver
mic
om
po
st)
atth
een
d(n
=3
,m
ean
±S
Em
)
Tre
atm
ent
pH
Org
anic
CT
ota
lN
Av
aila
ble
P
1C
on
tro
l2E
xp
erim
ent
Co
ntr
ol
Ex
per
imen
tC
on
tro
lE
xp
erim
ent
Co
ntr
ol
Ex
per
imen
t
T1*
8.0
9±
0.8
07
.89
±0
.50
b4
11
.6±
0.6
94
31
.7±
0.4
5b
15
.8±
0.0
31
8.3
±0
.03
a3
.2±
0.0
23
.9±
0.0
2a
T2*
8.1
3±
0.4
27
.76
±0
.82
b4
03
.1±
0.4
74
10
.7±
5.0
3a
20
.3±
0.0
82
3.1
±0
.83
b3
.5±
0.0
35
.1±
0.0
5b
T3*
8.3
9±
0.1
17
.56
±0
.94
a3
89
.7±
2.0
44
14
.6±
2.2
0a
23
.6±
0.0
42
4.7
±0
.03
b3
.5±
0.0
33
.9±
0.0
2b
Tre
atm
ent
Ex
chan
gea
ble
KC
:Nra
tio
C:P
rati
o
1C
on
tro
l2E
xp
erim
ent
Co
ntr
ol
Ex
per
imen
tC
on
tro
lE
xp
erim
ent
T1*
12
.9±
0.0
31
3.2
±0
.03
b2
6.0
±0
.09
23
.6±
0.0
2b
12
7.1
±0
.64
11
1.0
±0
.38
b
T1*
17
.2±
0.0
31
8.6
±0
.26
a1
9.4
±0
.06
17
.9±
0.8
1a
11
3.9
±1
.03
80
.9±
1.5
6a
T3*
19
.9±
0.0
32
0.4
±0
.06
a1
6.5
±0
.05
16
.3±
0.0
4a
10
9.1
±0
.64
10
3.8
±0
.07
a
*R
efer
toT
able
1,
for
exp
lan
atio
no
ftr
eatm
ents
Mea
nv
alu
esfo
llo
wed
by
dif
fere
nt
lett
ers
are
stat
isti
call
yd
iffe
ren
t(A
NO
VA
,D
un
can
mu
ltip
le-r
ang
edte
st;
P<
0.0
51
Co
ntr
ol–
com
po
stp
roce
edw
ith
ou
tw
orm
s2
Ex
per
imen
t–v
erm
ico
mp
ost
pro
ceed
wit
hw
orm
s
332 Environmentalist (2007) 27:329–335
123
(1992) the passes of organic residue through the gut of
earthworm, results in phosphorous converted to forms,
which are more available to plants. The release of phos-
phorous in forms available to plants is mediated by phos-
phatages, which are produced in earthworm’s gut. Further
release of P may occur by P-solubilizing bacteria in casts.
Recently Suthar (2007a) reported about 36–115% incre-
ment in available P content, after inoculation of wastes
(some agriculture and municipal waste resources) with
earthworms. Earthworm gut flora provides enzymes
required for P metabolism. These enzymes release phos-
phorous form ingested waste material. However, the ver-
micomposting coefficient for phosphorous (VCphosphorous)
was highest in T2, which clearly indicates the suitability of
this industrial waste treatment for better recovery of plant
metabolites.
Potassium increase for different vermibeds was regis-
tered in the order: T2 (19.67%) > T1 (15.53%) > T3 treat-
ment (9.39%), after 150 days of vermicomposting
(Table 3). The vermicomposting coefficient for potassium
(VCpotassium) was highest in T2 (Table 4). It is clear that
plant nutrients in organic material are released by the
combined action of earthworm and microorganisms during
mineralization process, in vermicomposting system. Del-
gado et al. (1995) reported higher potassium content in
vermicompost produced from sewage sludge. The present
result is similar to those by Suthar (2007a), who reported
excellent increase in exchangeable content in vermicom-
post. The C:N ratio is considered as an important indicator
of compost maturity. In this study maximum decrease in
the value of C:N ratio was noted in T1 (24.35% decrease)
followed by T2 (23.59%), and T3 (11.08%). The C:N ratio
in end product reflects the decreasing of C and simulta-
neously enhancement of higher proportion of total N and
ionic protein content in the vermicompost. It is concluded
that in vermicomposting sub system, the loss of carbon as
carbon dioxide due to respiratory activities of earthworms
and associated microflora, and simultaneously increment in
N-content of substrate through earthworm’s activities (i.e.
production of mucus, enzymes and nitrogenous excre-
ments) lowers the C:N ratio of the substrate (Kale 1998;
Garg and Kaushik 2005; Suthar 2007b.
3.2 Earthworm growth, cocoon production
and mortality during experimentation
Vermicomposting is also considered in terms of production
patterns of earthworm biomass and numbers of cocoon.
Vermicomposting converts a portion of the organics matter
(OM) into worm biomass and respiration products, and
excrete some of the ingested on as partially stabilized
product i.e., vermicompost. For this study, mean individual
live weight (F = 85.92, P < 0.01), mean growth rate of an
individual (mg/day) (F = 93.75, P < 0.01), individual
biomass gain (F = 99.97, P < 0.01), total cocoon numbers
(42.24, P < 0.01), and reproduction rate (cocoon worm–1
day–1) (F = 17.39, P < 0.01) varied substantially among
different treatments. As summarized in Table 5, the live
weight (742.80 ± 21.1 mg) of earthworms as well as
growth rate (mg wt. worm day–1) 2.95 ± 0.15 were highest
in T2 treatment. P. sansibaricus exhibited highest weight
gain in T2 followed by T1 and T3 (Table 5). The weight
gain for individuals in T2 treatment was �45 and 84%
higher than for those in T1 and T3, respectively. Studies
revealed that the factors relating to the growth of earth-
worms may also be considered in terms of physiochemical
and nutrient characteristics of waste feed stocks (Kale
1998; Edwards et al. 1998; Suthar 2007b). Organic waste
palatability for earthworms is directly related to the
chemical nature of the waste material that consequently
Table 5 Individual biomass, mean growth rate and mortality in different treatments (n = 3, mean ± SEm)
Treatment Mean individual biomass (mg) Net weight gain
earthworm–1 (mg)
Mean growth
of individual
(mg day–1)
Total population
mortality (%)Start End
T1* 304.2 ± 2.7 610.8 ± 10.3b 306.6 ± 7.6b 2.0 ± 0.1b 16.7 ± 2.4b
T2* 299.9 ± 1.0 742.8 ± 21.1c 442.9 ± 21.8c 3.0 ± 0.2c 5.0 ± 4.1a
T3* 302.8 ± 3.0 546.0 ± 12.3a 241.2 ± 10.1a 1.7 ± 0.1a 30.0 ± 4.0c
* Refer to Table 1, for explanation of treatments
Mean values followed by different letters are statistically different (ANOVA, Duncan multiple-ranged test; P < 0.05)
Table 4 Vermicomposting
coefficient (VC) for different
chemical parameters
* Refer to Table 1, for
explanation of treatments
Treatment VC Carbon VC Nitrogen VC Phosphorous VC Potassium VC C-to-N VC C-to-P
T1* 1.05 1.15 1.20 1.03 1.10 1.14
T2* 1.02 1.14 1.44 1.08 1.08 1.41
T3* 1.06 1.05 1.13 1.03 1.01 1.05
Environmentalist (2007) 27:329–335 333
123
affects the earthworm growth and reproduction parameters.
Garg and Kaushik (2005) concluded that growth perfor-
mance of Eisenia foetida was related directly to the quality
of the feed stock. Numbers of cocoons produced during
vermicomposting varied significantly among the different
beddings. In T2 treatment the cocoon numbers for
P. sansibaricus (96.0 ± 5.10) (Table 6) were �80 and
146% higher than for worms in T1 and T3, respectively.
Despite noticeable differences between T1 and T3 but they
were not statistically different (F = 0.068). The cocoon
production rate (cocoon worm–1 day–1) was highest
(0.034 ± 0.15) in T2. The difference in cocoon production
rate between T1 and T3 was not statistically significant
(F = 0.348). Edwards et al. (1998) and Suthar (2006)
concluded that the important difference between the rates
of cocoon production in the two organic wastes must be
related to the quality of the waste. The variability in
earthworm biomass gain and reproduction rate different
treatments was probably related to the palatability, micro-
biology as well as the chemistry of the feeding stuff. The
difference in cocoon production patterns among different
treatment suggest a physiological trade-off (Streans 1992)
related to N-limitations. Recently Suthar (2007a) demon-
strated that earthworm growth and reproduction rate is
related to initial N-content of the substrate. Present results
are confirmatory.
3.3 Treatment for optimum results of industrial waste
treatment
During the process of vermicomposting, the suitability of
the tested substrate mainly depends on fold increase in
essential plant nutrients, lowering of toxicants, earthworm
biomass as well as reproduction performance, and even less
mortality in tested earthworm species. Of the five chemical
parameters measured, three were highest in T2 vermibeds
as reflected by the vermicomposting coefficient (Table 4).
Moreover, the earthworms’ individual live weight and
biomass gain, cocoon numbers, and individual reproduc-
tion rates were also highest for the T2 bedding. This clearly
indicates that the biochemical environment in this bedding
was more acceptable than that for the other two treatments.
T2 treatment was found to be an ideal for humification and
mineralization of plant metabolites. We suggest that
nitrogen; organic matter content and microbial populations
in this vermibed enhance conditions for earthworms. Result
also suggests that proportions of amendment materials
(cow dung and saw dust) were more acceptable to earth-
worms in terms of palatability. Guar gum industrial wastes
contain a relatively high concentration of ammonia that
adversely affects earthworms. Ammonium levels could be
tempered by supplementing the waste with materials of
high C:N ratio such as saw dust.
4 Conclusions
Recycling of guar gum industrial waste through vermi-
composting not only accelerated the mineralization of
complex nutrients into more available forms for plants. The
waste when amended with sawdust or cow dung for a
mixture there was a good growth media for earthworms.
These organic supplements create a favorable chemical
environment which consequently affects the waste reduc-
tion by increasing efficiency of earthworm. Vermicompo-
sting transfers energy rich and complex organic substances
into a product which has a relatively high content of
humus-like compounds for sustainable plant production
and land restoration practices.
Acknowledgements The author is grateful to three anonymous
reviewers for valuable comments and careful revision of the manu-
script.
References
Anderson, J. M., & Ingram, J. S. I. (1993). Soil organic matter and
organic carbon. In J. M., Anderson, J. S. I., Ingram (Eds.),
Tropical soil biology and fertility (pp. 62–66). Wallingford, UK:
CAB Internationals
Benitez, E., Saizn, H., Melayar, R., & Nogales, R. (2002). Vermi-
composting of a lignocellulosic waste from olive oil industry: A
pilot scale study. Waste Management and Research, 20, 134–142
Delgado, M., Bigeriego, M., Walter, I., & Calbo, R. (1995). Use of
California red worm in sewage sludge transformation. Turrialba,45, 33–41
Edwards, C. A., Dominguez, J., & Neuhauser, E. F. (1998). Growth
and reproduction of Perionyx excavatus (Perr.) (Megascolecidae)
Table 6 Reproduction pattern of P. sansibaricus (mean ± SD, n = 3) in different treatments
Bedding Total number of
cocoons produced
Cocoon production
(cocoon worm–1)
Net reproduction rate
(cocoon worm–1 day–1)
T1* 53.3 ± 8.4a 3.2 ± 0.5a 0.02 ± 0.004a
T2* 96.0 ± 5.1b 5.1 ± 0.1b 0.03 ± 0.001b
T3* 39.0 ± 5.4a 2.8 ± 0.5a 0.02 ± 0.003a
* Refer to Table 1, for explanation of treatments
Mean Value followed by different letters is statistically different (ANOVA; Duncan multiple-ranged test, P < 0.05)
334 Environmentalist (2007) 27:329–335
123
as factors in organic waste management. Biology and Fertility ofSoils, 27, 155–161
Elvira, C., Sampedro, L., Benitez, E., & Nogales, R. (1998).
Vermicomposting of sludges from paper mill and dairy indus-
tries with Eisenia andrei: A pilot scale study’. BioresourceTechnology 63, 205–211
Elvira, C., Sampedro, L., Domingnez, J., & Mato, S. (1997). Vermi-
composting of water stable sludge from paper pulp industry with
nitrogen rich material. Soil Biology and Biochemistry 29, 759–762
Garg, V. K., & Kaushik, P. (2005). Vermistabilization of textile mill
sludge spiked with poultry droppings by an epigeic earthworm
Eisenia fetida, Bioresource Technology, 96, 1063–1071
Gratelly, P., Benitez, E., Elvira, C., Polo, A., & Nogales R. (1996).
Stabilization of sludge from a diary processing plant using
vermicomposting. In C. Rodriguez-Barrueco (Ed.), Fertilizersand environment (pp. 341–343). The Netherlands: Kluwer
Gupta, S. K., Tewari, A., Srivastava, R., Murthy, R. C., &
Chandra, S. (2005). Potential of Eisenia foetida for sustainable
and efficient vermicomposting of fly ash. Water, Air, and SoilPollution, 163, 293–302
Kale, R. D. (1998) Earthworms: Nature’s gift for utilization of
organic wastes In C. A., Edwards (Ed.), Earthworm ecology(pp. 355–373). Ankeny, Lowa St. Lucie Press, New York
Kaushik, P., & Garg, V. K. (2004). Dynamics of biological and
chemical parameters during vermicomposting of solid textile
mill sludge mixed with cow dung and agricultural residues.
Bioresource Technology, 94, 203–209
Lee, K. E. (1992). Some trends opportunities in earthworm research
or: Darwin’s children. The future of our discipline. Soil Biologyand Biochemistry, 24, 1765–1771
Lorimor, J., Fulhage, C., Zhang, R., Funk, T., Sheffield, R., Sheppard,
C., & Newton, G.L. (2001). Manure management strategies/
technologies, White paper on animal agriculture and the
environment for national center for manure and animal waste
management. MWPS, Ames, IA, 52 p (2001)
Maboeta, M. S., & van Rensburg, L. (2003). Vermicomposting of
industrially produced woodchips and sewage sludge utilizing
Eisenia fetida. Ecotoxicology and Environment Safety, 56,
256–270
Marsh, L., Subler, S., Mishra, S., & Marini, M. (2005). Suitability of
aquaculture effluent solid mixed with cardboard as a feedstock
for vermicomposting. Bioresource Technology, 96, 413–418
Ndegwa, P. M., Thompson, S. A., & Das, K. C. (2000) Effects of
stocking density and feeding rate on vermicomposting of
biosolids, Bioresource Technology, 71, 5–12
Nogales, R., Cifuentes, C., & Benitez, E. (2005). Vermicomposting of
winery waste: a laboratory study. Journal of EnvironmentalScience and Health B, 40, 659–673
Reddy, K. S., & Shantaram, M. V. (2005). Potential of earthworm in
composting of sugarcane byproducts. Asian Journal Microbiol-ogy and Biotechnology Environmental Science, 7, 483–487
Satchell, J. E. (1967). Lumbricidae. In A. Burger, F. Raw (Ed.), Soilbiology (pp. 259–322). London: Academic Press
Strearns, S. C. (1992). The evolution of life histories. New York,
United States: Oxford University press, pp. 72–90
Suthar, S. (2006). Potential utilization of guargum industrial waste
in vermicompost production. Bioresource Technology 97,
2474–2477
Suthar, S. (2007a). Vermicomposting potential of Perionyx sansi-baricus (Perrier) in different waste Materials. BioresourceTechnology, 98, 1231–1237
Suthar, S. (2007b). Nutrient changes and biodynamics of epigeic
earthworm Perionyx excavatus (Perrier) during recycling
of some agricultural wastes. Bioresource Technology, 98,
1608–1614
Vinceslas-Akpa, M., & Loquest, M. (1997). Organic matter transfor-
mation in lignocellulosic waste products composted or vermi-
composed (Eisenia fetida andrei): Chemical analysis and C13
CPMAS, NMR spectroscopy. Soil Biology and Biochemistry, 29,
751–758
Walkley, A., & Black, I. A. (1934). An examination of the degtjareff
method for determining soil organic matter and prepared
modification of the chronic acid titration method. Soil Science34, 29–38
Environmentalist (2007) 27:329–335 335
123